Tag | Content |
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EnhancerAtlas ID | HS017-31568 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr8:27259770-27263880 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr8:27262529-27262547 | CCTCCCTTCCTCTCTTTC | - | 6.11 | NFAT5 | MA0606.1 | chr8:27260400-27260410 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr8:27260400-27260410 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr8:27260400-27260410 | ATTTTCCATT | + | 6.02 | SREBF1 | MA0595.1 | chr8:27261948-27261958 | ATCACCCCAC | + | 6.02 | ZNF263 | MA0528.1 | chr8:27261296-27261317 | TCCTCCTCTTCTTCTTTCTTT | - | 6.03 | ZNF263 | MA0528.1 | chr8:27262535-27262556 | TTCCTCTCTTTCTCTTCCTCT | - | 6.05 | ZNF263 | MA0528.1 | chr8:27261440-27261461 | TCCTTCTCTGCCTCCTCTTCC | - | 6.09 | ZNF263 | MA0528.1 | chr8:27261434-27261455 | TCCTTCTCCTTCTCTGCCTCC | - | 6.2 | ZNF263 | MA0528.1 | chr8:27261398-27261419 | TTCCTTTTCTTCTCTTCCTCC | - | 6.32 | ZNF263 | MA0528.1 | chr8:27261428-27261449 | TCTTTCTCCTTCTCCTTCTCT | - | 6.49 | ZNF263 | MA0528.1 | chr8:27261290-27261311 | TCCTCCTCCTCCTCTTCTTCT | - | 6.54 | ZNF263 | MA0528.1 | chr8:27261293-27261314 | TCCTCCTCCTCTTCTTCTTTC | - | 6.73 | ZNF263 | MA0528.1 | chr8:27261452-27261473 | TCCTCTTCCTCCTACTTCTCC | - | 6.97 | ZNF263 | MA0528.1 | chr8:27262516-27262537 | CCCTCTCCCCCTCCCTCCCTT | - | 6.97 | ZNF263 | MA0528.1 | chr8:27261413-27261434 | TCCTCCTCCTCCTCTTCTTTC | - | 6.9 | ZNF263 | MA0528.1 | chr8:27261443-27261464 | TTCTCTGCCTCCTCTTCCTCC | - | 7.07 | ZNF263 | MA0528.1 | chr8:27261437-27261458 | TTCTCCTTCTCTGCCTCCTCT | - | 7.2 | ZNF263 | MA0528.1 | chr8:27261410-27261431 | TCTTCCTCCTCCTCCTCTTCT | - | 7.31 | ZNF263 | MA0528.1 | chr8:27262521-27262542 | TCCCCCTCCCTCCCTTCCTCT | - | 7.39 | ZNF263 | MA0528.1 | chr8:27261422-27261443 | TCCTCTTCTTTCTCCTTCTCC | - | 7.41 | ZNF263 | MA0528.1 | chr8:27261461-27261482 | TCCTACTTCTCCTCCTCCTCT | - | 7.49 | ZNF263 | MA0528.1 | chr8:27261425-27261446 | TCTTCTTTCTCCTTCTCCTTC | - | 7.52 | ZNF263 | MA0528.1 | chr8:27262512-27262533 | CTCTCCCTCTCCCCCTCCCTC | - | 7.61 | ZNF263 | MA0528.1 | chr8:27261287-27261308 | TCCTCCTCCTCCTCCTCTTCT | - | 7.64 | ZNF263 | MA0528.1 | chr8:27261416-27261437 | TCCTCCTCCTCTTCTTTCTCC | - | 7.72 | ZNF263 | MA0528.1 | chr8:27261455-27261476 | TCTTCCTCCTACTTCTCCTCC | - | 8.03 | ZNF263 | MA0528.1 | chr8:27261284-27261305 | TGCTCCTCCTCCTCCTCCTCT | - | 8.08 | ZNF263 | MA0528.1 | chr8:27261458-27261479 | TCCTCCTACTTCTCCTCCTCC | - | 8.21 | ZNF263 | MA0528.1 | chr8:27261401-27261422 | CTTTTCTTCTCTTCCTCCTCC | - | 8.23 | ZNF263 | MA0528.1 | chr8:27261419-27261440 | TCCTCCTCTTCTTTCTCCTTC | - | 8.28 | ZNF263 | MA0528.1 | chr8:27261407-27261428 | TTCTCTTCCTCCTCCTCCTCT | - | 8.69 | ZNF263 | MA0528.1 | chr8:27261404-27261425 | TTCTTCTCTTCCTCCTCCTCC | - | 9.01 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_09156 | chr8:27241158-27268637 | CD14 | SE_10267 | chr8:27261756-27267418 | CD19_Primary | SE_10868 | chr8:27181046-27285079 | CD20 | SE_17600 | chr8:27259508-27267110 | CD4p_CD25-_CD45RAp_Naive | SE_18325 | chr8:27259402-27272992 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20066 | chr8:27261082-27267374 | CD56 | SE_22414 | chr8:27260059-27267410 | CD8_primiary | SE_31168 | chr8:27261696-27263957 | Fetal_Thymus | SE_32488 | chr8:27262009-27263300 | GM12878 | SE_43522 | chr8:27260188-27266669 | MM1S | SE_50221 | chr8:27261374-27263786 | Sigmoid_Colon | SE_52630 | chr8:27261366-27263232 | Small_Intestine | SE_53591 | chr8:27261400-27263882 | Spleen | SE_55148 | chr8:27261661-27264166 | Thymus | SE_60867 | chr8:27217627-27263346 | DHL6 | SE_62276 | chr8:27181124-27271753 | Tonsil | SE_67171 | chr8:27260188-27266669 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr8 | 27262000 | 27263476 | chr8 | 27261517 | 27261874 | chr8 | 27261537 | 27262078 | chr8 | 27261971 | 27263654 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I027403 | chr8 | 27261056 | 27264581 |
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Enhancer Sequence | GAAGAATGGC AGCCCTGGTC TGGGTGGTCA GGGTCCCATT GCCTAAGATG AGAAACACTG 60 GAGGAGAAAT CCACTGCAGA GTGGGGAGTT CACATGCCCA GTTTTGGACC TGTGGAGTAC 120 AATTGAGACA CATTAACATC TTCACATGGA AATGCTGAGT AGATCCTTGG ATACATAATT 180 CTGGAGGAGG GAGCCAGGTT GGTCGTAGAC ACTTGAGTGA GGTCAGTCCA ACCATCTGGT 240 GGTTGAAGCA TGGCTGTGAA TGAGATCATT TGGGAAAGGG TTCTGAATTA CTCCATCATC 300 CACTCCACAA ATGTTTGTTG GATCCTTCCA TGTGCCTGGC ATCATGGTAG CATGGCCTAG 360 GGTATTAGCA TATCCCAAAA CACAGGTGTA CTCCCTGCTT TCGTAGGGCT TCCTGGCCAA 420 GAGTGAGACT GACATGGACT CACACTAATG AATGAACCTT CTCAATCTGA AGCATATGCT 480 CCTACAGGAA AACATAGGTC TTGTGAGAAC AGGTCACCAT CATCATCTCC ATGGCTACAA 540 CCTTCATTTA AGCTACTGTC ATCACTCATT TGATTCACTG TAATAGCCAC ATAACATCTT 600 CCCACATCCG TTCTTGCCTT TCTCCAAAGT ATTTTCCATT GTGTATCCCA AGTTATCTCT 660 AAAAAGCACA ACCTTATGTC ACTCCTAGGT TGTGAGAGCA AGACTGGGTT TACATGCAGA 720 GGAGCAGCTT TGCTGTGTAG TGCCTGTGTG GGGATGCAGT GTCCAGTTGG GAGTCTAAGC 780 CCAACTTCCT TGTCTGGGAC CCTCTTGGAG CAGCCCTTCT TCTCTCTGCT TCCTGACTTC 840 TTTTTGCAGT CTCCTTTCCT AGCTTGGCTT TATCCTTTGA TGGAGTTTTC TACTTCCATC 900 TTTGTATCTT CCTTTCCTCA TTTTCCCAGT ACTCAGAATG CTGCCAGCCC TTTCAAATTT 960 GCCAAGCACA TGTCCTTCCC CAAGAACACT TCTGAGATCC TGACACCCCC ACATAGGAGT 1020 GTCTGATCAA ATGGAAGCAG TCGCGAATCG CCCTGAACAG TCCACATGGC AACACATTTC 1080 CAAAACATAG TTACTCCATG CATATTTGCT GATTTCATGT TTTGGTCTTT ATTCTCTGCT 1140 TTTTTTTCTG CAGACGTAGT AGCTTCATTG TGATTTCTCC ATGTTGTAAA AAGCTTTGTG 1200 AATAAGCGCT GGCCCCTGTG CCTAGGACCT AAAAGAAATT AGGCAGGTGT TGCAGAGAAC 1260 AATGAGAAAT TGATTTTGCT CTTCTGGATT TTCTATTTCC TTTTTGTTTG ATATTCATAG 1320 GAAATTGTGT TTGTTTAGGA GCTCTGAATT TCTGGGGCAA GCAGAGGCTC ATATCATTAT 1380 ATTTTTCTCT ACAGTGCTAA TTTGCTTGTC TGGGAAAAGG GGTAAGATGA CACTCTGAAA 1440 ACAACTGGCA GAGTGGCACC CAGACGTGCC CACACAGGGC GGCTCTCTTT GGCTCTTGCT 1500 GCTGCTGCTG CTGCTGCTCC TCCTCCTCCT CCTCTTCTTC TTTCTTTGTT CTTCTTTCTT 1560 CTGTCTTCTT TCTTTTTTCT TCTTTCTTCT CTCTTCTTTC TTTTTTCTTC TTCTTTCTCC 1620 CTTCTTTCTT CCTTTTCTTC TCTTCCTCCT CCTCCTCTTC TTTCTCCTTC TCCTTCTCTG 1680 CCTCCTCTTC CTCCTACTTC TCCTCCTCCT CTCTCTGTCT ATCTCTCCTT CCTTTCCCTC 1740 TCCTTTCTCT TCTTCTCAAG CCATATGTCC TGATTTGTCT CATCCCCAGT TTCTATACAT 1800 TGCCCAGGGA TGACTATCCA CAGTGCCCCT GTCCTGCCAG TCTCAAATGT ATCATGATAT 1860 GGGTGACAAT GACACAATAA TGACATGGTC ACCTTCGTCT AAGGCCCTGC TCTCTCCTCT 1920 CCCTGCCTGG CACACTGACC GGCTGACTCA TGGTGTTTTC TCCCTCCAGC TTCCTCCAGT 1980 TGACCCACTC TTTTCATGTG CTCATCTCTG CCTATCACAA GACCATCTTT TCTCACCCAG 2040 GAAGACATTG AGCAGAAGCA GAGATATTCA TCTGGGGTAT GGTGTTGTTC AGAGGTGCCG 2100 ATGGAGTCCT CTCTCTCAGC CAGTTTCTAC CAAGCTGGAA ACCTAGGTTC AAGATTCATC 2160 CTTGTTTTGT CCTGAAGCAT CACCCCACTC AGAATTCACA TTCACATCCT CAGGAGGGGC 2220 AGAGGCTGCA GCCATCCTGT GCCCTCCCCA CCCAGTCTGG ATGCATCCCT CCCACCCGCA 2280 GCAGGGACTC CAGGTTGCAG GGGTGGCCTT GGGCATTGCT TGCCTGGTGC ATGAGGAAGG 2340 CTGTCCAGTT CCAAATGCAG CCTGGTCCAC ACACACCTGT CCTCACCACC ACCCGTGTGC 2400 ATTCAGTGAT CATACAATCC CTTCCAGAAA TCCCCAGAGG CAGACTGCAG ATGTCAGAAC 2460 CCATTGACTT TCCCCTTCGC TCCTTAAACC CATCACACAC TCATCCCAGT TAGCTTTGAG 2520 TTTAATCTAT TGTTACTCAA CCAGACACAA GGTGCACAGG GTGTTATGGA CTGGATATTT 2580 ATGTCCCCTC ACCCCCAATT CCATATGCTG ATGCCCTAAC ACCCAGTGTA ATGGTGTTTG 2640 AAGGTAGGGG TATTGAAAGG TAATTGGGCT TAGGTGAGGT CATGAGAGTG GGGGCCCTAT 2700 AATGGGATTA GTGTCCTTAT AAAAGAGGAA GAGGCTAGAT TCCTCTCCCT CTCCCCCTCC 2760 CTCCCTTCCT CTCTTTCTCT TCCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCTCTTAGC 2820 CATGTGAGGA CAGAAGGAGA AGGTGTACTT CTGTAAATGA GGAAGCTCAC ACCAGGAGCC 2880 AAATCTGCTG TACCTTGATC TTAGACTCCC AGCTCTAGAG CTGTTTAGAA ATAAATGCTT 2940 CTTGTTTAAG GCGCCCAGTC AGGGTGATTT GTTAGAGCAG CTCAAGATGA CCGGGACACA 3000 GGCCAGCAGT TCCCTGTGCC TGGAAGAGCA GTCTCAGGCA CACAGGCCAT TGGCTCAGGT 3060 TCTCTGTATC TGGAACAATC TCTGTCACCC TCCTTCAGAT GCTGCTAGAG TAGGGCCCAA 3120 GGTCACAGTG CAAGAGGTAG GGAGGAGGAG GTTACTTGTC CTGGTAAGTT GCCATTTTTG 3180 AAAGAAAAGT TACCCTAGAG AGAATAAAAT GGAAGCACAC AAGGCTGGTC TCCCATGCAT 3240 GAAAATAGTC CCTGAAAAAG AGGAAAGGGT TCATCCAGGA AACCACAACC CAGTGCCGCA 3300 GTATTTAAAA AGGTATATTC ACAAGGACCT TCTGCACCCC CTCCCTGTTT CCTGTGTGTG 3360 CTCTGCAGGC CAGCCCGCCC CCACACAGAC ACCTACAGAG GCCAGCACAA GGTAGACACG 3420 CAGGTTCCGG GCCTTTGTGG ATCTCCACGC CCACATTCAT TGCATCCACA AATTGGCAGT 3480 CAGGTGCCTG GGCTTTCATT TCTATTTTTA ATCTGGTAGT TGCATTGCTG AATGTCCTTG 3540 TTAGAGACTT TTATCACGTC AAAATGAATG CTTTCAGGGT GTTAAGTTAT GCTCACTTGT 3600 ATTATTTTGT TCTTCAATCA CTTATTTTAG AATGATCCCT TACATGTGTT GCAAACTCAG 3660 AAGGTATATA ACCAGTGTAT CAGTTTTCTA TGGCTGCCAC TGCAAATTAT CACAAACCTG 3720 GTGGCTTACA ATAGAAATGA TTCTCTCACA TTTCTGGAGG CCAGAAGTCC TAAATCAAGG 3780 TGTCAGCAGG GACTCAGTTC TCCTGAAGGC TCTAGGGGAG GATCTCTCCT TGCCTGTCCC 3840 AGCTTCTGGT AGCTCTAGGC ATTCGCAGCT TATGGATACT TCACTCCAAC TTCTGCTTCC 3900 ATCTTCACGT GGACTTCTCC TCTCTCTGTG TCTCTTTTCT GTATCTTTTA CAAGGATGCT 3960 TATCATTGGA TTTGGGGCCA CTCAGTCCAG AGTGATCTCA TCTTGAGATC CTTAACTTAA 4020 TTACATTTGC AAAGCCCCCC ATTTTTTTTT CCAAATGAGG TCACATTCAC AGATTCTGGG 4080 GTTAGGACAT GGACATATCT TTTGGGGGCC 4110
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