Tag | Content |
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EnhancerAtlas ID | HS074-01286 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:212124520-212125650 |
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 | CAAAGGCTGG GAATTGGGAA CTGAATGTTT GTGTTCCCCC AAATTCGTAT GTGGAAGCTG 60 CAACCCCCAA GGTAATGGCA TTTGGAGGTG GGCCCCCATG ATGGGATGAG TGTTTTTTTT 120 GTTTGTTTGT TTGGTTGGTT TTTTTTTGAG ACAGAGTCCT CGCTCTGTTG CCCGGGCTGG 180 AGTGCAGTGG CGCTATCTCA GCTCACTGCA ACCTCCGCCA CCCGGTTCAA GCGATTCTCC 240 TGCCTCAGCC GCCTGAGTAG CTGGGATTAC AGGCATGCGC CACCATGCCC AGCTAATTTT 300 TGCATTTTCA GTAGACACAG GGTTTCACCA TGTTAGTCAG GCTGGTCTCA AACTCCTGGC 360 CTCGTGATCT GCCCACCTCA CCCTCCCAAA GTGCTGAGAT TACAGGCGTG AGCCACCGCA 420 CCCGGCCAGG ATGAGTGTTC TTAAAGAAGA GGAAGAGTGA CCAGAGCTCT CGATCTCTCC 480 CTACCATGTG AAGATGTAAT AAGAAGGTGG CTGTCACCAG GGCCAGGAAG AAAGTCCTCA 540 CCAGGAACCG AATCTGCTGG CAGCTTGATA CTGGACTTTC CTGCCTCCAA AACTGTGAGA 600 AATAAATGTC TGTTGTTTAA GGTACCAAGC CTACGGCATT TTGTTATAAA ACCTGAGCAG 660 AGATACTGGG GAATGGTCAG ACAGGGAGGA GAAAATTTGG GTGAGAGTAT GTTAGCCTGT 720 CCTGTGACTG GGAAATCAGG GGAGAAGATA AAAAAAAGGG TGAGTGCTCT GAGAACTTCT 780 TAGGAAGTGC CAAAGGCAGC AGAGATTCAG CAGGGTAAAG GCTGAAGAGT GTACTGAAAG 840 GCATTAATGT CATCACCTGG TAGGAAATGA CTCATTGCCA GTCAGCCAAC AAGCCCTGTT 900 CTTTCTGTTT CAATTGTCCA GTGGTTCTCC CAACCATGGC AGCATGACAG AATCACCTGA 960 GTGTGTGTAA AACTACTAAT GCCTGGGCCA CAATTCCAGA AACTCAGAGT TAGCTGGTCA 1020 GGGGTGAGGC CTGTATATTA ATGTATTCTT TAAAAAGCCC TCAAAGTGAT TCTAATGTGT 1080 AGCCTGCGTT GAGAATTATT GCAACTTCAG TTAAATTGTT AAAAAAAGAA 1130
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