Tag | Content |
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EnhancerAtlas ID | HS134-00135 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:8241700-8243120 |
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) |
FOXP2 | MA0593.1 | chr1:8242600-8242611 | TTTGTTTACTT | - | 6.62 | IRF2 | MA0051.1 | chr1:8242750-8242768 | AGAAAGCGAAAGCATTCA | + | 6.14 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_33918 | chr1:8241396-8243905 | HCC1954 | SE_34231 | chr1:8240249-8246041 | HCT-116 | SE_34786 | chr1:8240946-8245641 | HeLa | SE_47106 | chr1:8240454-8246507 | Panc1 | SE_57530 | chr1:8241904-8242444 | VACO_503 | SE_65889 | chr1:8242598-8243711 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I008180 | chr1 | 8240803 | 8245776 |
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Enhancer Sequence | TATTTTTGGT GTCTTTTCCC CACCTTTTGC TTTCAACTTT TCCATGTCCT TTTGCTTTAG 60 ATGGCTCCCT AACAGGGTTT ATCCAAGGAT GATAATGTCT GCTTTTTAAC TCAATGAGTT 120 TGACCCATTT ATATTTTGGG GGACGATGAA TACTGTGATA CGTAAGTTTC CAACATCTCA 180 CTGTAGGGGA TACTGGAAAG TATGAGCGTC AAGATCATGT ATCTTTTCCA GGAATCAAAG 240 CACGTAGTGT GGCAATTCAG ATATGTTGGT TGCCTTGACT CTTCTTCAAC AGAATTAACA 300 GTTTTGGATC TTGAGAAAAT GTTATTTTCT GGCTAAGTAT AGGGGTAAAA TGAAATCTTT 360 GGGAAATTAG TGAATTCTCA TGATTTCTCA AAGCTTTTCT TGGGTAACTC CAAGAGGCAG 420 CCTGGTGGAG TGAAAGCATG GACTCCAGTG CCCCATTCTC TAGCTGCGTG ATTTGGAGTA 480 AATTCCTTAT CTCAGTGACT CTGTGTCTCC ATCTTGAAAT TGAGAATAAT CACACCGGCC 540 TGAGATTTTT TTACCATGTG AATGGAAGCA CGTGGCACAT AGCAGGGACT GAATGAATGT 600 GCCCATGTCC GCTCTCCCTC CTCTTTCTAG GGCTGCGGCC TTGGTGATGT CAAGAACATT 660 TTGTAAATAT TACAAGTAAG ATAAGGCATT GTGACTATTA CTCGTTAAAA TCACTTTGTT 720 TCCTGACTTA GGTGATTCAC TGCAACCCAG AGAAAGTTTT GTGTTGTGTT CTGGCTGGCG 780 AAACTTCTGC AAACAACGAA TGCTTCTTTT CATCAGCCTA TTCTGCGTTG GTTGGTAGGA 840 TGTCAGTCTA TAACCACATC AATTTCAGGT AATAACAAGT GTGTGAGCTT TCTGAAGCTT 900 TTTGTTTACT TATTTGTTTT AGGGTTGTTC AAGTGTGACT CATGTAGTAG CACTGCATTC 960 TTGAGAATTC ACAGAGATCG AAACACAGAT ATGAAACAGG GCCAGAAAGA ATAAGGCGTT 1020 CCCAATATAT GAGAGTAAAA AAAAAGCACA AGAAAGCGAA AGCATTCAAT GTCTGCATCC 1080 TGTATAGATG AGAAACTTAG CAGTATCCTC TTTTCTTTTT GGACCAATCA TATGCTGATA 1140 AAACAGGGTC TCGCTGCTTT CCCCCCATTT TTAACATCTT CAAACATTCT GAGAGCCTAC 1200 GGGAATAGAG GCAAACAGGT TTGATGTGAC TGGTCATTTG GCCAAAGGTA TTTTACTCTG 1260 CGCTCAGCAT TTTGTTTCGT TCATGCTCTC TAGCAGTTTG GAATCTAAAA AGGAAAGATT 1320 AGATAGAGGA AGTGTGAAAA TGCATACGCA ATGTGGGAAA CCAGGCCATG AACTTGAGTT 1380 TTTAAATGCA TGGTATAAGG CCGGGCTCAG TGGCTCACGC 1420
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