Tag | Content |
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EnhancerAtlas ID | HS095-07973 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:122948180-122950010 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122949825-122949846 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 | Nr2f6(var.2) | MA0728.1 | chr12:122949276-122949291 | AAGGTCAGGAGTTCA | + | 6.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27577 | chr12:122948145-122949851 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 122948493 | 122949277 | chr12 | 122948284 | 122949772 | chr12 | 122949342 | 122949777 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122463 | chr12 | 122948038 | 122949938 |
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Enhancer Sequence | AAAAAAAAGA GTTGGAAGGA ACCTTAGTGA TCACTGAGTT CAAACTCTTA CCCTGAGCAC 60 CAATCTACTT AGACCTCAGC CAATCTCTAA AAGGTAATAT ACAAGTAGGC TATTTTAACC 120 TTTGAATCTA GTCACTTGCT CAACAAAATT TTTTTTTCTT AGGAGACAGG GTCTGTCTCT 180 GACCCAGGCT GAAGTTCAAT GTCACGATCA CAGTCCACTG CAGCCTCGAC CGTCCTCCTA 240 TCTCAGCCTT CCGAGCAGTT GGGACCACGG GTGTGTACCA CCACACCAAG CTAATTTTGT 300 TTATTTTTTG TAGAGACAGG TCTCGAACCT TGCTATGTTG CCAAGACTGG TCTCAAACTA 360 CTGGCCTCAA CCTATCCTCT TGTCTTGGCC TCCCAAAGCA TTGGGATTAC AGGCGTGAGC 420 CACCACATCC AGCCCTGCTG CAAGGTTCTT AACTGGGGGT CCACGGACCT TCTGGATAGA 480 ATTCAGGGAA ATTTGACATT TCCTTCAATT ATGACTGTAG GCAAACATTC TGTTTCTACC 540 ACATGCCTGC TATGCCTGTC CTAATCCTTG ACTCTCTAAA GTCATGAACC CTATTAGATT 600 TCAACTACCC TCATATAGTA GGTGTTCAGT ATTCCTCCAA ATGTTCTAAA TAAAAACTTA 660 GTAGAATGGG CCAGTACAAT GAACAGAGTT GTAATTGGTT TGAAGAATCC AAGATCAGGA 720 CTGTGGTAGG AACAGAAGGA AACTTGTTCC AAGTCTGTGA GAAATTTGCC CCAGGTCCAA 780 TCCCACAACC TGTTCCAATC CAGTTTCATT TGTCATTCTC ACTTATGACT AATGAATTTG 840 CTTCCATGAC GGAAAACATT AAGAAATCAC TCTGGCATGA GGTCACCCTA CAAAGGAGCA 900 ATCTCAGCTG CCCGGAATGT CAGCGTTCAG TAAGGGCCAC ACCCCTTGCC TTTTCAGTAA 960 TTCCTCCTAT TACAAAATTC CAAATGCAGC CATATTGTTG ATAGGAAATT TTGTTTAAAA 1020 AATACATTTC TTAGGCCGGG CGCGGTAGCT CGTGCCTGTA ATCCCAGCAC TTTGGGAGGC 1080 TGAGGTGGCG GATCACAAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 1140 CATCTCTACT AAAAATACAA AAAAATTATC CAGGCATGGT GGCATGCACT TGCAGTCCCA 1200 GCTACTAGGG AGGCTGTGGC AGGAGAATCG CTTGAACCTG GGAGGCAGAG GTTGCAGTGA 1260 GCTGAGATTG CGCCACTGAG ATTGCGCCAC TGCACTCCAG CCTGGGTGAC GGAGCGAGAC 1320 TCCATCTCAT AAATAAATAA ATAAATAATT TTTTTGCGGA ACGTGGTGGT TCGTGGTTAT 1380 AATTCTGACA CTGTGGGAGG CTAAGGCGGG TGGATCTCCT GAGCCCAGGA GTTAAAGACC 1440 AGCCTGGGTA ATGTAGGGAG ACCCCATCAC AATGAAAATT ATTAACATAA GCTAGGTGTG 1500 GTGACACATG CCTGTTGTCC CTGCTATTTA AGAGGTTGAG GTAGGAGGAT TGTTTGAGCC 1560 CAGGAGGTCG AGTACCCTAG CCTGGACAAC AGAGTGAAAC CCTATCTCGA GAAAACACAC 1620 ACACACACAC ACAAATCCCA CATTTCTTTT CTTTCTTTTT TTTTTTTTTT TTTTTTTTGA 1680 GATGGAGTCT CGCTCTGTTG CCCAGACTGG AGTGCAGTGG CGTGATCTTG GCTCACTGCA 1740 ACCTGCGCCT CTCAGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGATTA 1800 CTCCTTCTCA AATTAAAAAA AAAAAAATTT 1830
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