Tag | Content |
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EnhancerAtlas ID | HS037-09303 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr12:103437200-103438400 |
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) |
Crx | MA0467.1 | chr12:103437485-103437496 | CTAATCCTCTC | - | 6.02 | RARA | MA0729.1 | chr12:103438084-103438102 | TAGGTCACAAGTTCAATC | + | 6.16 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I103043 | chr12 | 103437461 | 103437590 |
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Enhancer Sequence | GTTAAAAACA TGCAAATTGC TTTAGAGTAA TAGGTTAAGA TTCCCTCCCT CTTTTTTTTT 60 TTTTTTTTTT TTGCCAATCC CCGTATTTGG ATTATTTCAC CTATCCTATG TATTTTTTTC 120 CCTAAATAAT AGCAAAAACT CAAAAACTTT TTCAAGGGAC AAAGAAGAAA AAGATGAGTA 180 TCTGGAGGAG ATACTTCTCC CCCTTCACCT TACAGTCAGG CTTTTGCTGA TACTCAGTTT 240 TTTTCAGCCC TGTCAGCCCC TTTTCGGAGG AGTTGATGTG TAGCCCTAAT CCTCTCTGCT 300 GGCTGCCTCC CTATTCAGGA GGGTATGCAA ATACTTCCAA ACCAGAGCAT TTTAGACCTA 360 TTCAAGGCCC AAGACAACAC ACTTTTCATT AGCATTTGAA GTGTGAGGGC TGAAAAAGGG 420 GAATGGACAA CTTTTTTTCT TTTTTCTTTT TTTCCCTTTT GGCTCGAAGC TTTGGGGAGA 480 CTTGAAAATG TACGTTTTTC ATCCCTTTGC ACACATCAGC ATTGGCGCTA AACTTCAGAG 540 GGACGCATTG ACTGCCCTCA GGGGAAAGCA TTCAGGGGGA TTTTTACACA TACACGGAGG 600 GCCATCGCCT GAAATAAATC ACAGAAAGGA GGTGGCAGAG ATGAAGCGAG AGGGGTTCAA 660 CGCGGGCTAA GCTATGCGTC CAGAGGCATG AATTTAAATC GCGATTTATT TTCCTCTCGC 720 TCTGCACTTG CATGAACCTC AGTTTCTTAA TCTTCAGCAA TGGGGAGGGG GGCTTTGGGG 780 AGAAGCGGCA CAAGATTTAA AATGCAAGGC AAGTCTCCCA TCAGACAACC CTCTGGAGGT 840 GCTCTGTCTG TAGCCGTGAT GTTAGAGCCT GGCGCTCTGA AGCCTAGGTC ACAAGTTCAA 900 TCCCCTTCTG GGTCAGTTAG CTTTTCTCTG TTCCACAGCC ACAGACTAAA GGCCTGAGCC 960 CCTTATTCAG GCCAAATGTC TAACAAAATG TGTGTCCTTA GTCACTGCAC AAAACAGCCC 1020 AGCCAGAGCC TAGCAAATCC ATCCTTTACT GTTGGGGAGC CGTCAGGAAG CTAGCTGTCC 1080 TTGGAGGCCT ACAATCTCTG CACGGACAAG GTGAGAAGGT GAGAAGGTCA GAGGGAGGTA 1140 GTGTGTGGGT GCTGAAGATG GCCAGAACTT GGAGGAGATC GAGCCCAACA ACTTACTCTG 1200
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