Tag | Content |
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EnhancerAtlas ID | HS044-01132 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:209606190-209607500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GRHL1 | MA0647.1 | chr1:209606750-209606762 | AAAACCGGTTTT | + | 7.22 | GRHL1 | MA0647.1 | chr1:209606750-209606762 | AAAACCGGTTTT | - | 7.22 | TFCP2 | MA0145.3 | chr1:209606751-209606761 | AAACCGGTTT | + | 6.02 | TFCP2 | MA0145.3 | chr1:209606751-209606761 | AAACCGGTTT | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26692 | chr1:209600232-209607903 | Esophagus | SE_33755 | chr1:209600227-209609871 | HCC1954 | SE_35814 | chr1:209600232-209609482 | HMEC | SE_64219 | chr1:209600308-209609442 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I209427 | chr1 | 209600485 | 209609310 |
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Enhancer Sequence | GCAGATTGCA GATATTTCCG ATGCTATACA AGATATATCT CATAGTATGG GTGTAGATTC 60 TGCAAAGGTT AATGCAGTTA AACATATTTG ACACATAAAA ATGTCAGATC CAACATTAAT 120 CATTCACCAA TTGTAATTGC CTTTCTATGG GTCTCTTCTC CCCAAGACAT AGCTTAAAAC 180 ACCAGGCTCG GTAGAAATCT GGGAGGAAAA AAGCAAATAA TACCTCTCAG CTGTCAGGGT 240 CTATGATACG CTTTGATAGA TTTAGCACTG ATTTCATTCT CTTTACAATT CAGTGTGATT 300 GGGTGTGCGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTTACT CCATGTTTCT 360 CCTTTTTAAG GAAGGAGAAG GTGTGGAACA AGAGAAAGTT CCTAAGTCTG AAGGAAGTCC 420 AACCCAGTTA TGAAGGGAAT GCCATCCACA AGCCTTTTTT ATAATTGGCC CCTGCCTCAG 480 GTAAAGGGGT CTCCTTTAAG GAGCCAGTCT GGCTAAATTG GCAGATTCTG AACAAAGCCT 540 GGCCCTGACA AGTCTTCAGA AAAACCGGTT TTCACCTCCA GAATGTGCCC CAGGCAGCAA 600 AATACAATAG CTCTCCTTGG CTGAGTGGTG TTTTTCTTAG GAGCTCACTC TAAAGGAGAT 660 TCCAGCTTTG CAGATGGATA CCGATCACTT GAATGGCCAA GCCCTGCCCC CCAGCCAGTG 720 ACCTCTGAGG GGGATAGGTC TCTTCACCTT CCCCCAACCC TTCCCTGGTT TTTGACCCCT 780 GAGGGTCCCA GATTGCCAGC AGGAACTAAA AGGAATAAAC CTTTCTCCAA AATATTTTTC 840 TGTGTCAAGT TAATACAGAT TTAAAACCTA GTTTCTGTCA CCCCCACCCC TTCATTCCAA 900 GACCCACAGG CAACAAAAGG ATGAAGAAGC CAAGCCACAG GCATTTTTTA AAAACATGTT 960 TACTCATAAA AATTGCGTAG CAAATCCAAC TGTGGGGTGC TGTTTGTCCA GCAAACTCCT 1020 AGTTAACCAG CAAACACCTC CCATTCAAGG TCTGAAACAA GCCCTGAGAT CAGAACAAAA 1080 AGCACACGAC AGACACGATG TGGCACTTTT ATTTGCAGCT TGGTTTGAGC CCTATGACCT 1140 GGAATCTTTT TATAGGAGAT AAGTGCTTGT GTATTTATGT GCCACCTGGC CCAGGTGGAG 1200 GCAGGAACCA AAATGGCCAA CAATGGTGAC CAGAGGGTAG ACTGTCAAAC ACTAGCCAGG 1260 GCACAATGCT GTGACTACAA AAGGTTCTAC CTGATGTGCT GTTGGGTTCC 1310
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