Tag | Content |
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EnhancerAtlas ID | HS177-06268 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr13:51265290-51266780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr13:51265516-51265526 | CTCAAGTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr13:51266294-51266309 | TGACCTCTTTACCTC | - | 6.63 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I050691 | chr13 | 51265305 | 51266754 |
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Enhancer Sequence | TCACCTGATT TTCCTCACAG AGACCAGTGC AATGCAGAAA AGATCACATA AATATTCTTA 60 TCATTCAATT ATTAGAAAAA CTGGAATTTC CTTGGATTAT TCTGTGGAAT TTACCATCTC 120 CCAACCGCTA TTGCAATTAT TTGGTCAGCT GGTGGCCTGT CTCAACAGAG AGGGCAGGAA 180 AACAAACAAA AAAAACAAAA CTCTTGAGTA AAATTATCTT ATCAGTCTCA AGTGGTTAAA 240 GCTGCCATGC AGGGCCCTCT GTGTAAAGAA ATAGTTCTCC CCCTTCAACA ACTCTGAAAA 300 GTAAAAGAAC AAAACTGTGC TCTCTCCAAA AAGCATTAGT GACAGTTAGA AGGCGGAAGG 360 GGAGAGATCT GCTGACTTGA CAAACCATGA TTACTTTTTA CAGCTCATGA AACTGTCTTT 420 TTAAGAGCTG TGCTCTATGA CCTTAAGTTT ATTGCACTTA CGATTCTAGA AATGTCATCT 480 TTTGGAAAGA TGAGAAGCCT CAATGAGAAA AGACAAGATT AATAGCATAG CTTTTGCCCA 540 GTGCTAAGCA TCTTAGCATT TGTTGCCAAA CAGGGAAGAA AATGGAGAGC AAGTGTGCTG 600 CGGGGCTGTG CCATCTGTCA GCACAGACAA CCCCTAACCC CACTTCGTTC CTTAATAGCA 660 AGGTCTGTTA GTCTGCTCTG CTTTATAAAC TGATATATCA TGGCCTAGAT TGAATCACGG 720 CTTCCCTCCC TCATAGATGG TGACCTGGAA TACATCACAT TACTTTCTGT GAGTCCCCAT 780 TCCTTCTAGT ATAAAAAGAG GGTAGTAACG GCCTTCTCTC TGAGAGTTGG GATAATTGGC 840 AGCTAAAAAG ATCTTGATAA AATATGAGTC ACGTAATGTC ACTCCTTTAC TCAGAACCCT 900 TGAATGGCTG CCTGTGTCAC TCTGAGTAAA AGCTAAAATC CAGACAGTGG TCCACCAGCA 960 AGACCCAGCA GGATATGGAG CCCCATCCTC TCTGACCTTT TCTCTGACCT CTTTACCTCC 1020 AGCCGTGTTG GCTGCCTTAT TACTCAGGCA GGTCCCTGCT CATGGTTCTG CCTCAGGGCC 1080 TTGACACATA CTATTCCTTC TGCCTCGAGC TCTTCTCCCC TAAGTGTTTG CATGGCTTAG 1140 ATCCTGAGCT CTGAGGACCT CTACCCATAT ATCACCTTCT CAGGGATCCT ATCAACACTA 1200 TTCACAATTG CAAACTCTTT CCCCAACCCC TTTCCTCCTT TTCTGCTTCA TTTTTCTCCA 1260 GAGCACTTGT CACCAGATAA CATGTTTATT TTACTCATTT ATTATGTTTA TTATCTGCCT 1320 TTCTCTTCTT GAATGAAAGC CAGTGAGGGT AGGGATTTCT TTCTGTTCAC TGCTATATCC 1380 CAAGCACCTG GAATACTGTC TGGCACATGG CATTCAGTAA GTATGTGTTA GATGAATGGA 1440 TATTAAATAA TAACAAAATT AAAGCACATA GCACTGTGCC TTTGGTTAAA 1490
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