Tag | Content |
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EnhancerAtlas ID | HS050-17795 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:131117920-131119300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr12:131118596-131118607 | AATGAGTCACA | - | 6.62 | TFAP2A | MA0003.3 | chr12:131118991-131119002 | AGCCTCAGGCA | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65354 | chr12:131116633-131120869 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I130632 | chr12 | 131116586 | 131119946 |
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Enhancer Sequence | AACTGTTCCC ACCAGAACGG TGAATTCCTG AGGGAGGAAA GTTGGAGGGA CAAATAACCG 60 GACACCCAGC CCTTGCCTTT CCTCCTGAAC CACATCCTAT CCCGAGTGTC CCGCCCACAG 120 CCCACCGAAA CTGATCCTCG AGACCAAGGG TCTTTTCTAG CCTGATACAA GGCCTGAGGA 180 CAGATTTGGA ACAGCATACC CACAGGGTAG TAACAGTGAT TTGAGCCACA ATTAAGACCC 240 AAAGGTTTAG AAACCAGGGG TTATCACAAC CCCTTGAGGC TGGAAATGCC TCTTCCCACC 300 TCTCAGCCCA GAAAACAACC CTTGCTCTAC AGCCCACAGC CTAGAAAGAG ATTGATTTCC 360 CGTCTGTGTC TAAGCTGTAT CTCATTAACC CACGGGGCTC TTTCCCCAGC CCCAGAAGCA 420 GGTACTTACA AGGCACCGGA GATTAGTGGT CTAGTGGACC AGACAGACTG GTCCAGGCCT 480 CCCCGCCGGC CCCCCTTCCG GTCCCCGTGG ACGCCAGCCT CTCTGAGCCT CGGATGTTTG 540 TGCTCGGCAC CAGGCTGGAA GGCTATTTAC TTATTCATGG GCTGCCCAAG CCGGCCAGGA 600 ACTGCTTTGT GTCAGCTGAA TAGGATGGTA ATTCAATCTG CGAATGGGAG CCGTTGGCAC 660 ACAGCACGCC TGTCATAATG AGTCACAGGG GGGACAAGCA CCCAGCGTTC AGAGCCACTG 720 GGAACCTGTC CTTCGACAAC GAGCTGTGTC ACAAGACACC ACCTTCCTTT CCTCAGTCGC 780 TCTCTTCCCC CCGAATCTCC CCACCCCTGA TCAACTCTCC TGGAGATGCA TGACACAGAA 840 TTACATATCC TTGGGAGCGG AGACGGGGAG GCGGGTAATG CCACCTGTTC TCTTGAGCTG 900 TATACATGGA AATAGAGGAG ACAGAAGTGT TGGGAAGGAA TCTGAAGCAA GAAACGCGGA 960 GTGAGGAAGC GGGAGGAAAA GCTCACCTGC ACCAGGAGTC CTCAGGTTTA ATGTTTTCTA 1020 TGCCCTATCT CACACACTCC TCATCAAAGC CCTTGGAGCA AATGAACAAT TAGCCTCAGG 1080 CAGGTTAACA ATCACACCCG AAGTCTCTGA CTGGGGGTCT TTGAGCCCTG GTCCATCTCA 1140 CGTCACAAGC CACATGCTGC CTTTGGTCCA GCACGTCACA TCATCCAATG CAAAGAAACC 1200 TGCCTCTCTT TAAAGATGAC TTTTTTTTTT TTTCCAGACA AGGTCTCATT CTGCCACCTA 1260 GGCTGAAGTG CAGTGGCGTG ATCTCAGCTC ACTGCAGCCT CGACCTCCCA GCTTCAAGCT 1320 ATCCTTCCAC CTCAGCCTCC CAAGTAGCTG AGGCTACCAG TGCTTACCAC CATGCCTGGC 1380
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