Tag | Content |
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EnhancerAtlas ID | HS175-13391 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr19:44256080-44258800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr19:44257542-44257554 | TTCTGTTTACTG | - | 6.02 | JUN(var.2) | MA0489.1 | chr19:44257365-44257379 | GGAAAATGACTCAT | + | 6.76 | KLF16 | MA0741.1 | chr19:44258732-44258743 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:44258733-44258743 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr19:44258731-44258746 | CGGGGGCGGGGCCTG | - | 6.11 | SP4 | MA0685.1 | chr19:44258729-44258746 | GGCGGGGGCGGGGCCTG | - | 6.26 | Zfx | MA0146.2 | chr19:44258732-44258746 | GGGGGCGGGGCCTG | + | 6.19 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_02767 | chr19:44256100-44260167 | Astrocytes | SE_09619 | chr19:44255368-44262466 | CD14 | SE_10575 | chr19:44256833-44260060 | CD19_Primary | SE_11483 | chr19:44255253-44262275 | CD20 | SE_13735 | chr19:44255931-44257680 | CD34_Primary_RO01536 | SE_13735 | chr19:44257681-44261073 | CD34_Primary_RO01536 | SE_14657 | chr19:44256014-44261046 | CD4_Memory_Primary_7pool | SE_18182 | chr19:44255605-44260321 | CD4p_CD25-_CD45ROp_Memory | SE_18680 | chr19:44255276-44260362 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19217 | chr19:44256242-44260273 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20985 | chr19:44256876-44261109 | CD8_Memory_7pool | SE_23510 | chr19:44257834-44261164 | Colon_Crypt_1 | SE_23897 | chr19:44258182-44260089 | Colon_Crypt_2 | SE_27247 | chr19:44256975-44262719 | Esophagus | SE_31804 | chr19:44257590-44260338 | Gastric | SE_32542 | chr19:44255365-44264271 | GM12878 | SE_33868 | chr19:44256868-44261203 | HCC1954 | SE_34298 | chr19:44255426-44256716 | HCT-116 | SE_34298 | chr19:44256799-44272203 | HCT-116 | SE_34813 | chr19:44256968-44262677 | HeLa | SE_36558 | chr19:44255760-44264581 | HMEC | SE_37675 | chr19:44254852-44262981 | HSMMtube | SE_39921 | chr19:44256960-44261248 | K562 | SE_50403 | chr19:44256946-44260066 | Sigmoid_Colon | SE_53073 | chr19:44256976-44257621 | Small_Intestine | SE_53073 | chr19:44257665-44260035 | Small_Intestine | SE_53761 | chr19:44256508-44260208 | Spleen | SE_56117 | chr19:44257406-44262941 | u87 | SE_59025 | chr19:44248893-44290143 | Ly3 | SE_60730 | chr19:44257018-44289948 | DHL6 | SE_62525 | chr19:44242576-44303622 | Tonsil | SE_64692 | chr19:44256932-44264220 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | ACTCACAGGG GCAAGTTCAC ATAAAAATAG GATATTCTCC TTACCAAAAT GCAGCAAGGC 60 ATTTGCTTAC AAACCAGCAA TGTGATCCTC AGTCCAACAG CTACTCTTGA TTAGTCATTA 120 CTAGTGTATG TCATGGTGGG GCTCCAGCCA CTTACTAGTG TATGTCATGG TGAGGTTCCA 180 ACACTCAAGG GCCTATTTTC ACCTGGTATC CCACTACATT TCAGTGTCTG TCTGTCTTCC 240 GTTCCTGACG GTCTGCCTTC CCTCACAGTG AATTTCATTT CAAGGTGTCT CCAGTGTTTA 300 TTCTATTTGA GATGTTATAT AATGTCTGGC TACCTATGCA ACCCACTCTC CACCATTTCA 360 GTATCTGTTT ACAGGTCCTT AGAGAGTTTT CCCAGCTGTT CACACATCAG TCTAGGGTGG 420 TATTTGACTA CTTAACTGTT TGTAGAACTC AGTGGGGCTA TCTGCTCAAG CTCAGAAGTC 480 AGGTTGACAA AGTGTGGCCT AGGGGCCAAA TCTGGTCTGC TTTCTGTTTT TGTAAATAGA 540 AAGTTTTATC GGAACATGGC CACATCCATC AATTTAGAAA CTGTCTGTGG CTGCCTTCTT 600 GATGCAATGG CAGAGCTGAG ACAGACAATA CAGTCTGCAG GGCCTAAAAT AATTATTCTC 660 TGGCCTTAAC AGAAAGTTTT ACTGAATGGC CGAGTATGGT GGCTCACACC TGTAATCCCG 720 ACACTTTGGG AGGCCGAGAC AGGAGGACTG CTTCAGCCCA GGAGTTCGAG ACCAGCTTGG 780 GCAACATAGC AAGATCCTGT CTCTATATAA CATTTAAAAA AGAAAAAAGT AGCTGGGCGT 840 GGTGACATGC ACCTGTAGTC CCAGCTACTT GGGAGGCTGA GGTGGTGGGA TCACTTGAGC 900 CTGGGAGGTC AAGGCTGCCA TGATCATGCT GCACCACTGC ACTCTAGCCT GGGTAACAAA 960 GCAAGACCCT GTCTAAAAAA AAAAAAAAGC AGAACCCTGT CTCAAAAAAA CAGTTTGCTG 1020 ACCCTTGCTT AGCTTGGAAG TATCTGTTAA ATCCCTCCAT GAATCCTCCC CTGCCCCACC 1080 TCATAATGAC ATAAACAGGT CCCTCCGAGA CTCTCCAGAA TGGAAGGGTC TGTTTACAAG 1140 ATGCAGTCAT AATTTTGCTA GCCAGACAAG TGGCTTGTCT AGCTCCTCTC CTACTGTGCT 1200 ACATGACCTC TCCCAGAGCC ACAAGCCAGG CTGAAGACTG CTTTCCTAGA CAGAGGAGGA 1260 CAAGGGCCTG TTTACAGCTG CTTAGGGAAA ATGACTCATT CCATACCGAA ATGACTGCTT 1320 AGTCTGGGAT GGAGATTCTC CCCAGAATCT GAGACTCCTC CCTCACTTGC AATTAAGTGT 1380 CTTTACACAT TATTCTGAAA TCTACCCAGT GCTTAAGTAC TTGTCTTCAT GCCTCAATTG 1440 GGATACTGCC CAGCCCTGAG GTTTCTGTTT ACTGGCCTAT GAGGATGCCC TTTCCTGTGC 1500 AAAGTAAGCG CCCCTGTGTG AATGCTTTTC TTTTTTTTTT TTTTTTTTTT TTGAGACGGT 1560 CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT GGCACGATCT CAGCTGGCTG CGGCCTCTGC 1620 CTCCCGGGTT CAGGCAATTC TCCTGCCTCA GCCTCCCAAG TAGGTGGGAT TACAGGTGCA 1680 TACCACCAGG CCGGGCTAAG TTTTGCATTT TCAGTAGAGA CGGGGTTTCG CCATGTTGGC 1740 CAGGCTGGTA TCGAACTCCT GGCCTCAAGT GATTCGCCAG CCTCGGTCTC CCAAAGTGAT 1800 CGGATTCCCC GGGTAAGCCA CCGCACCTGG CCTCCCTGTG CCCTTTATTC TGGGAGCTTC 1860 CACAGTATCT GAATGTGGGG AGTTCCTTGG AACTTAAAAG CCCACCTAAA CCAGGTGTGG 1920 AGGATACAGT GAGCCGAGAT CGTGCCACTG CACTCCAGCC TGGGCGACAG AGCGAGACTC 1980 TTGTCTCAAA GAAAAAAAAA AAAAACCCCA CCCACATGCA AGCTGGGGAC TTCCAATGCT 2040 GTTTCCGGGC TCCTTTGGGG ATTACCCCCA AACTTAGGAA AGCTGGTCTA TTTAAGTGTC 2100 TGCTGATGGA CTTCTAGGGT GACTTCCCGA AAATTAACAA ATCGAATTTA CATATTTTTG 2160 GGGAGTGTCT CCTCAGTATT TAGGCATCGC TTCACACACT CCCTTCGGGG ATCTCCCAGA 2220 ACCTCACTAT TTGCAAATAT TTGGGGAGAC TCTCCCGATT CCTGAGTATG TAAGCCCACT 2280 TCGTGGGGCA CTCCCCAGCC CAGAACTGTA GTCGATTTGC ACATTTTCCT AAGGACTCCC 2340 TAGGATTTAA ACTTCTCTCT ACGGGGTTCT AGAAGGGAGC CTCCCCCGGA TTTAGGCATT 2400 GCTTTACAAA GCTTCCCTCG GGGAACCCAA CTCAAGTTTC TCGTTACACG TTATTGGGGC 2460 GGCCTCCCCA GTACTTGACG GGCAGTTTGC AGGCTGTACT TGGATCTCGC AGAGCATAAG 2520 TTTCTCATTT ACACGTTATT TCCGTCCCCC GCCCCCATTC CTGCCAACCC AGTATCGAAT 2580 TGACGGTCGC CGGCCCCCTA CTCAGTGCCG CACCCCCGCC GGACGTCCCA GCGACCTTTC 2640 AATGGCCAAG GCGGGGGCGG GGCCTGCCGG AGCGCCCCGC CCGCCGCCGG TGCGCTAGCC 2700 TCGCGCGGGC TCGCGGCCCC 2720
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