Tag | Content |
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EnhancerAtlas ID | HS177-07796 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr15:70446360-70447750 |
Target genes | |
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) |
FOXF2 | MA0030.1 | chr15:70447258-70447272 | TGAACATAAACAAT | + | 6.03 | NFAT5 | MA0606.1 | chr15:70446617-70446627 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr15:70446617-70446627 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr15:70446617-70446627 | AATGGAAAAT | - | 6.02 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I070153 | chr15 | 70446290 | 70447946 |
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Enhancer Sequence | ACTCTCCCCA TCCTCTCCGT CCTGTGTGCG ATTCACCTGC CTATGACTGG GGCAAGGCCT 60 AGATTTGTGG GAAAGGATCC CGGCGCTGGG ATCATGATGA ACGGCAACCT CCCTGCAGCA 120 GCCCCCTCCC CCAACAACAC ACGCACATCA GAGCTCGGGG GGGAGGCAGA GGGCCCTCCT 180 TGCTCAAAAT AGCTCTGTGT TATTAGCTGC ATTTAATTGA AGGTGTTTCG AGGGCAGCCT 240 CCACCGGGCC CAAACCAAAT GGAAAATGAC ACACTGTCAA ATTAATGTCC CCAGACCATG 300 ATAAATGTCC GGGCTTGGTG AGTAATGCTT CCATTTCTTG TTTTAAAGGA GAAGGATGCA 360 GCCAGGCTCC GCGCGTCTGT CCCTGTTGTG CGGGGAAAGG TCAGGGGCAT CCTCGGGATA 420 AATAGCATTC CTCGCTGGCC CGCCCACCCA GGCTGGGCTT CTCCGGCTTC TGCTGAGCTC 480 TGCTTTCTCT CTCTTCCTGT CTCTTGAGGC TGGCAAGATT GCTGAACAGC TTGTGAGCCT 540 CCCGGCCAAT GTCCAGGGAG GAAGGAGCTG GAGATAAGAC TAATCCTCAC CATCCACCCG 600 TACTTTATAC CTTCCAGAGT GCAGTCACCT CGGTTATAGC GTGTGTTAGT TGGCATTCGA 660 GGCCTGCTCC TGACCTCCAG CTGCACGCCT CACTGCCATG CCCTTGGTTC AGCCATACTG 720 ATTCCTCAAA CCCGCCCTGC ACACCCCAGC CTCTTGGACT ATGTGGAACA CAACTGCTAA 780 AGCGCCTGCT CTGTGCCGGG CTCTGGGCTC TGGGCTCAGC CCCTGCCCTG GAGGACAGAC 840 AGCCCCTGAG AGCCGGAGCT GCCCTGGCAT TCCCAGCCTG GCTGCGGTAA TCTCTTATTG 900 AACATAAACA ATTTCCCAGA ATATAAACAT CAGACAAGGC CACAAGCAAG ACGAAAACAA 960 GACCACTCCG TAATTGTGTC TGAACACAGA CAAAAACAAG AACACTGTCC AAACCACAAA 1020 GATCACCAAA CACCCCCCTG TCCTGGCGAA CATCAGGGAC TACTGCTTCT TTACCAATTA 1080 CAGCTTCAGC TGTGCTCTCT GCTTCCCTCC TTCTAGATAA GATCCCCAGA CACAGAATTA 1140 CTCCCCACCA CTTTCTTCCT GATAGCACTC CCTCCAGAAC CAAGCTCTGC TCCCTGGAGC 1200 ACCTCACACT AGCCCAGATC CTGTAACTCA TTTCCAGCAC TCTCTCACTG AGCTGCCTCG 1260 CCATTCCCTG TGGCGCGTGT TCTCCCTGTT GCAATGGGTA ATACACCCGC CTTTGTTCAA 1320 ATATAGATGT GTTTCTGGCA GCTTGGGCTG GAAGGCACTG GCACCACCAA TATGGCCACA 1380 GAGCTGGGCA 1390
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