Tag | Content |
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EnhancerAtlas ID | HS158-14569 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr12:122948350-122949690 |
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) |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122463 | chr12 | 122948038 | 122949938 |
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Enhancer Sequence | GTCTGTCTCT GACCCAGGCT GAAGTTCAAT GTCACGATCA CAGTCCACTG CAGCCTCGAC 60 CGTCCTCCTA TCTCAGCCTT CCGAGCAGTT GGGACCACGG GTGTGTACCA CCACACCAAG 120 CTAATTTTGT TTATTTTTTG TAGAGACAGG TCTCGAACCT TGCTATGTTG CCAAGACTGG 180 TCTCAAACTA CTGGCCTCAA CCTATCCTCT TGTCTTGGCC TCCCAAAGCA TTGGGATTAC 240 AGGCGTGAGC CACCACATCC AGCCCTGCTG CAAGGTTCTT AACTGGGGGT CCACGGACCT 300 TCTGGATAGA ATTCAGGGAA ATTTGACATT TCCTTCAATT ATGACTGTAG GCAAACATTC 360 TGTTTCTACC ACATGCCTGC TATGCCTGTC CTAATCCTTG ACTCTCTAAA GTCATGAACC 420 CTATTAGATT TCAACTACCC TCATATAGTA GGTGTTCAGT ATTCCTCCAA ATGTTCTAAA 480 TAAAAACTTA GTAGAATGGG CCAGTACAAT GAACAGAGTT GTAATTGGTT TGAAGAATCC 540 AAGATCAGGA CTGTGGTAGG AACAGAAGGA AACTTGTTCC AAGTCTGTGA GAAATTTGCC 600 CCAGGTCCAA TCCCACAACC TGTTCCAATC CAGTTTCATT TGTCATTCTC ACTTATGACT 660 AATGAATTTG CTTCCATGAC GGAAAACATT AAGAAATCAC TCTGGCATGA GGTCACCCTA 720 CAAAGGAGCA ATCTCAGCTG CCCGGAATGT CAGCGTTCAG TAAGGGCCAC ACCCCTTGCC 780 TTTTCAGTAA TTCCTCCTAT TACAAAATTC CAAATGCAGC CATATTGTTG ATAGGAAATT 840 TTGTTTAAAA AATACATTTC TTAGGCCGGG CGCGGTAGCT CGTGCCTGTA ATCCCAGCAC 900 TTTGGGAGGC TGAGGTGGCG GATCACAAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT 960 GGTGAAACCC CATCTCTACT AAAAATACAA AAAAATTATC CAGGCATGGT GGCATGCACT 1020 TGCAGTCCCA GCTACTAGGG AGGCTGTGGC AGGAGAATCG CTTGAACCTG GGAGGCAGAG 1080 GTTGCAGTGA GCTGAGATTG CGCCACTGAG ATTGCGCCAC TGCACTCCAG CCTGGGTGAC 1140 GGAGCGAGAC TCCATCTCAT AAATAAATAA ATAAATAATT TTTTTGCGGA ACGTGGTGGT 1200 TCGTGGTTAT AATTCTGACA CTGTGGGAGG CTAAGGCGGG TGGATCTCCT GAGCCCAGGA 1260 GTTAAAGACC AGCCTGGGTA ATGTAGGGAG ACCCCATCAC AATGAAAATT ATTAACATAA 1320 GCTAGGTGTG GTGACACATG 1340
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