Tag | Content |
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EnhancerAtlas ID | HS159-00504 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:212124170-212125910 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:212124640-212124652 | GTTTGTTTGTTT | + | 6.32 | JUN(var.2) | MA0489.1 | chr1:212125381-212125395 | AGGAAATGACTCAT | + | 8.12 | Stat6 | MA0520.1 | chr1:212125294-212125309 | ACTTCTTAGGAAGTG | - | 6.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27820 | chr1:212124787-212126227 | Fetal_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211951 | chr1 | 212124829 | 212126122 |
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Enhancer Sequence | TTCAATTCCA TCAAAATGAA GTTTGTTTAG CATCTATTTC ATTTTTTAGG ATGGAGCTTA 60 GAAGAATATG AAAATAACCA CTGTCTCACA CAGATGTGTG TATTTCTTTC AAAGACTGTC 120 TTTACACTCT CCCTTAGCAA ACAATGTCAC TGTCAAACAG CTGTCAATTC AATTCAGTAA 180 ATACTATTGA CAATTTTACA TGGAAAGCAA TATGTCAAAG GAATTGCCCA TCTTTAGATC 240 TAACCTAACT CTTTAATGAC ATCCTATTTA TTCTAAAACA CTTGATAAAG CATGAAAGTA 300 CAGAATGAGA AGAGCAGAAG CAGAAGAGAA ACTCTCCAAG GGGTAAAGTT CAAAGGCTGG 360 GAATTGGGAA CTGAATGTTT GTGTTCCCCC AAATTCGTAT GTGGAAGCTG CAACCCCCAA 420 GGTAATGGCA TTTGGAGGTG GGCCCCCATG ATGGGATGAG TGTTTTTTTT GTTTGTTTGT 480 TTGGTTGGTT TTTTTTTGAG ACAGAGTCCT CGCTCTGTTG CCCGGGCTGG AGTGCAGTGG 540 CGCTATCTCA GCTCACTGCA ACCTCCGCCA CCCGGTTCAA GCGATTCTCC TGCCTCAGCC 600 GCCTGAGTAG CTGGGATTAC AGGCATGCGC CACCATGCCC AGCTAATTTT TGCATTTTCA 660 GTAGACACAG GGTTTCACCA TGTTAGTCAG GCTGGTCTCA AACTCCTGGC CTCGTGATCT 720 GCCCACCTCA CCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGCA CCCGGCCAGG 780 ATGAGTGTTC TTAAAGAAGA GGAAGAGTGA CCAGAGCTCT CGATCTCTCC CTACCATGTG 840 AAGATGTAAT AAGAAGGTGG CTGTCACCAG GGCCAGGAAG AAAGTCCTCA CCAGGAACCG 900 AATCTGCTGG CAGCTTGATA CTGGACTTTC CTGCCTCCAA AACTGTGAGA AATAAATGTC 960 TGTTGTTTAA GGTACCAAGC CTACGGCATT TTGTTATAAA ACCTGAGCAG AGATACTGGG 1020 GAATGGTCAG ACAGGGAGGA GAAAATTTGG GTGAGAGTAT GTTAGCCTGT CCTGTGACTG 1080 GGAAATCAGG GGAGAAGATA AAAAAAAGGG TGAGTGCTCT GAGAACTTCT TAGGAAGTGC 1140 CAAAGGCAGC AGAGATTCAG CAGGGTAAAG GCTGAAGAGT GTACTGAAAG GCATTAATGT 1200 CATCACCTGG TAGGAAATGA CTCATTGCCA GTCAGCCAAC AAGCCCTGTT CTTTCTGTTT 1260 CAATTGTCCA GTGGTTCTCC CAACCATGGC AGCATGACAG AATCACCTGA GTGTGTGTAA 1320 AACTACTAAT GCCTGGGCCA CAATTCCAGA AACTCAGAGT TAGCTGGTCA GGGGTGAGGC 1380 CTGTATATTA ATGTATTCTT TAAAAAGCCC TCAAAGTGAT TCTAATGTGT AGCCTGCGTT 1440 GAGAATTATT GCAACTTCAG TTAAATTGTT AAAAAAAGAA AAAATTTTAT TTGCATTCTG 1500 GTAGAGCAGA TTTTTATATA TTAATATAAC TACGTAGCAG CTAGAGATGT GCTAAGTACT 1560 TTCATGGATT ATCTCATTTA CTCCCCACTA CAATGCTGTG AGGTAGGTAT TAACCCTGTT 1620 TTATGGATAA GGAAACAGGC ACAGAAAGGT TAATTTGTTG AACTCACACA GTAAGTGCCA 1680 TAAATGTATG AAAAACCCAC ATCCATACAA TAAAAGCTCA ATAAAACAAA TGCCACTTGC 1740
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