Tag | Content |
---|
EnhancerAtlas ID | HS148-01685 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:223917700-223920530 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr1:223919971-223919989 | GTAAAGTGAAAGCAAATT | + | 6.52 | ZNF263 | MA0528.1 | chr1:223919696-223919717 | GGAGAAAGAGAAGGAGGGGGC | + | 6 |
|
| Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223917623-223923297 | Adipose_Nuclei | SE_01908 | chr1:223918292-223919960 | Aorta | SE_02306 | chr1:223918166-223920027 | Astrocytes | SE_04026 | chr1:223918327-223919959 | Brain_Anterior_Caudate | SE_05036 | chr1:223918296-223919826 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223918153-223920025 | Brain_Hippocampus_Middle | SE_05972 | chr1:223920132-223922577 | Brain_Hippocampus_Middle | SE_07159 | chr1:223918575-223919801 | Brain_Hippocampus_Middle_150 | SE_07159 | chr1:223920244-223923166 | Brain_Hippocampus_Middle_150 | SE_09681 | chr1:223912826-223918041 | CD14 | SE_09681 | chr1:223918139-223920041 | CD14 | SE_23408 | chr1:223918840-223919937 | Colon_Crypt_1 | SE_24051 | chr1:223918949-223919614 | Colon_Crypt_2 | SE_25230 | chr1:223918779-223919775 | Colon_Crypt_3 | SE_26209 | chr1:223918227-223919614 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223918492-223919864 | Esophagus | SE_31491 | chr1:223918204-223920043 | Gastric | SE_31491 | chr1:223920239-223923646 | Gastric | SE_37129 | chr1:223917375-223920072 | HSMMtube | SE_38254 | chr1:223917692-223922239 | HUVEC | SE_38957 | chr1:223918328-223919928 | IMR90 | SE_41495 | chr1:223918394-223920179 | Left_Ventricle | SE_42269 | chr1:223918111-223920107 | Lung | SE_42269 | chr1:223920225-223923100 | Lung | SE_44530 | chr1:223917549-223919989 | NHDF-Ad | SE_44904 | chr1:223918045-223919953 | NHLF | SE_45872 | chr1:223917531-223920254 | Osteoblasts | SE_49408 | chr1:223918777-223919926 | Right_Atrium | SE_50365 | chr1:223918695-223919952 | Sigmoid_Colon | SE_51879 | chr1:223918137-223919804 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223918717-223919906 | Small_Intestine | SE_55958 | chr1:223918085-223920003 | u87 | SE_63671 | chr1:223918137-223919937 | HSMM | SE_65644 | chr1:223918515-223920092 | Pancreatic_islets | SE_67677 | chr1:223918085-223920003 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I223730 | chr1 | 223917704 | 223922480 |
|
Enhancer Sequence | TCCCAAAAAA CCAAAAAAAA AAAAAAAAAA AAAAAAACGA AAACCTGAAA TCAGTTGAAA 60 AGTGTGCCTG GGTTGAGATA AGAAGTTGTT AGAGACCAAG GTTTTTATTA TGTAGATGAA 120 GTCTCACAGA GGGCCACTCT CAAAGGCAAT AGATGGCAAA TGTTTTCTAT TCAGACCTTT 180 AAAAGGTGCT ACTAGATGCT CAGCTAATCT CTTCAGGATC AGAAAAAGAC CTGAAGGGAA 240 GGTGATTCTC TACATCAAGC TTGTCCAACC CTCGTGCTGC CCAGGATGGC TTTGAATGTG 300 GCCCAACACA AATTTGTGAA CTTTCTCAAA ATATTATGAG ATTTTTTTTT TTTTTAGCTC 360 ATCATCTATC ATTAGTGTCA GTGTATTTTA TGTGTGGCCC AAGACAATTC TTCTTCTTCC 420 AGTGTGGCCC AGGGAAGCCA AAAGATTGGA CACCCCTGCT ATAGAATGTA GATTTTCCCA 480 CAAGAGACAG CTTTCAGAGA CATTTCAAAA TCTGTCAGAA AAATATATTT TGGGCTAAAA 540 TACTTTGATT TCTTTCAGGG CCTGCTATCT GTCATGTGAT GCTCTACTAG AGTGTGGTTG 600 GAATTTGGTA TCTTATTGCT AGGAAGAGTC TGTTTTGTGA GTCTTAAGAT CTCTGTTTTC 660 AGTTAAGGCT GGTCAGCTGT GCCTGAATTC CTAAAGGAGG AGGATAAAAT GAGGCATGAC 720 GGACCTCCCT TCCCATCGTG GCCTGAACTT GTTTTTCAGG TTTACCTTGG AATCCCCTTG 780 ACTAAGGGGG CACCCATTCA GTTAGTTAAG GGGCTTAGAC TTTGATTTTT AGTTTACAGT 840 AGGCTGAGGT GTATTAAATG CATTTTCGAC TTGCAATATT TTCAACTTCT GATGGATTTG 900 TTCAGATGTA ACCCCGTTGT AAGTTAAGGA GCATGTATAC TTGTATCTAA TCCACTTTGG 960 GCATTGCTGC CAGAAAACCT GTCCTCAGGG AGCTATGGAA GTAGTGGAGG CAAATTATTA 1020 AATGGATGGA TTAATTCCAA GTTCAGATCA TGTTGGGAGT CAGCTGGGAG TCAGTGTGAG 1080 GATCTGGGAG GGGAACAGTA AGGGGTTAAG AGAGATACCC CAAAGGATGA TTAAGGAGGG 1140 AGAGTTGGAA GGAAGGTTTC CCACAAAGAG GAAGCAGGGA GTGATTCATT CTGAAAAAGG 1200 CAAATATTTT ATTATGCTTG GAGGGTCTGG TGCAGAAGGG GAAAGGAAGA GAAGGAAGTT 1260 TGGCTTAAAT TCCCTTAGGA GCCAGTTCAG ATTCCTAAGC TGGCCCGGAC ATCCAACCCA 1320 ATCCGCCTAG CCCCAGCCCT CTCCAGTTCC CAATGCCCAG CCCCACAATG CCCGTCCTGC 1380 TGCCTGCCTG TTCTGGACTC TGCACTTGAC CTTCCCTCTC CCTGAAAGTG CCCCTGCTCT 1440 TCCTCACCCA GCTCCCCGCT CTAAGCCTTC CTCGCCCACC CCAGCCCTCC TACAGTCCCA 1500 GTCTGCCCTG TTCAGACTCA AAGCCTCATG CTCACCACCA TCATCCACAA CCAGTTTCCA 1560 CGTCTGTCTC CTGCCGGCTG TGAGCTCACT GCCTCAGAAC CAGCGCCAGT CTCCTCTAGA 1620 CTGAGTACAG GCCTGGCACG GAGCCAGGAA TGCACCAACA AGGAGCCTGA GACTAGATTG 1680 GAGGGGAAAG AGACATGTCC TCCAGAGTTG ACTTACGCGA GGACAGAGGT GTGCAGAGGC 1740 ACGGCAAGCT GGGCCCCAGG CGAGAAGCAT GGAGTGAGGG ATGTGGAGGC AGCGGAAGGC 1800 ATCTGGGAGT CTGGGCTGCC CCGTAGCAGC TCTGTGTTCT GCCTGCTCTT CCTCCAAGAT 1860 GAGCTCCCTT GGCCAGTGTG TGAAACGTGT GTGTGAGTGT GTCACCGGTA AGCTGAGTTC 1920 TTTCCCTACT TGGTATCAGT TGCAAAGAAA GAACACTCAG TTGGAAAAAA AGGCAAGAGG 1980 GTTTTATTCC TGACCAGGAG AAAGAGAAGG AGGGGGCTCT TGCTCTAAAG ACACCTTCAC 2040 CCCGAGCCAT GGAAACTGGG GAGTTGTAAG GAGATAGGTG TGGGGCAGGG AGGTGTGTAA 2100 GCAGGTGTGG GGTCACGGTG TGGGGGTGGA GACCTCTAGA CGCTCAGGCC CAGGTCATAA 2160 ACATGCCTCT CCATACAATG CAAGATGTGT TACCAGAAAG GGGTCCTGAT CTAGAACTAA 2220 GAAAGGGTTC TTGGATCCCG CTCAAGAAAG AATTCAGGGT GAGTCCATAC AGTAAAGTGA 2280 AAGCAAATTT ATTATGAAAA TAAAGGAATA AAAGAAAATC TACTTCATAG AGCAGCCCTG 2340 AGGGCTGATG ATTGCCCATT TTTATGGTTA TTTCTTGATT ATATGCTAAA CTTCTTGATT 2400 ATATGCTAAA CAAGGGGTGG ATTATTCATG CCTCCTCTTT TTAGATCACG TAGGGTAACT 2460 TCCTGATGTT GCCATGGCAT CTGTAAACTG TCATGGCTCT GGTGGGAGTG TAGCAGTGAG 2520 GACGAGCAGA GGTCACTCTT GTCACCATCT TGGTTTTGGT AGGTTTTGGC CGGCTTCTTT 2580 ACTGCAACTG TTTTATCAGC AAGGTCTTTA TGACCTGTAT CTTGTGCCGA CTTCCTATCT 2640 CATCCTGTGA CTTAGAATGC CTTAACTGTC TGGGAATGCA GCCCAGTAGG TCTCAGCCTC 2700 ATTTTACTCA GCTCTTATTC AAGATGGAGT TGCTCTAGTT CACACGCCTC TGACACATGT 2760 TCAGAAATAA TGGTGATTTT CTTCTACAGG TGGGGACGTT AGCATTATAA TGACATGGTA 2820 AAGTTCTGAA 2830
|