Tag | Content |
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EnhancerAtlas ID | HS038-01667 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:205662240-205663510 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr1:205662564-205662574 | TTCAAGTGGT | - | 6.02 | ZNF263 | MA0528.1 | chr1:205662538-205662559 | GAAGGACAAGGGGAAAGAAGG | + | 6.08 | ZNF263 | MA0528.1 | chr1:205662534-205662555 | GGAGGAAGGACAAGGGGAAAG | + | 6.14 | ZNF263 | MA0528.1 | chr1:205662531-205662552 | GGTGGAGGAAGGACAAGGGGA | + | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 205662575 | 205662757 | chr1 | 205662373 | 205663200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205693 | chr1 | 205662729 | 205662928 |
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Enhancer Sequence | GACAGGTATC ATTATATGAG GGAAATGTAA ACTTAGAGAA GTAGTGGCTC GCCCACGAAG 60 CCACTCAGTG TTGGAACACG TCCTCAACTT CTAGTTATCC ATCCAGATCT ACTCCTAAGG 120 AAGATGACCC AAGGGGGAAG AGGCTGCTGG ATGCTTGGAA CTGGGGATGC TGAGAAAGGA 180 CAATGTTCTA CCTTTGTTAC CTGAGAAGTC TGGTAAAACA GGACTTTTCT TCCCTGCAGG 240 GAGCAGGGCA GTGGTGGGGG CTCGGCCCAG CCCTCCAGAC TTCCCAGAGA TGGTGGAGGA 300 AGGACAAGGG GAAAGAAGGA AGCATTCAAG TGGTGGGCTG GCTGCACGGC CACACTCCTG 360 CACTGCACTG CACTGTGCCC TAGCCCCCGC ACTTAGGAGG GCAGCCGGTG TTTCCTCCTA 420 CTTTCAACTT CCTGTTCATC CCCAGTACCC TGGCCTTTGC AAGGACAGAG CCTTTGCGTT 480 TGCATTTAAA TTCCTGTCCC TTCTCTGCAC AGCCCTGTGA ATTTGCACAC ATACCCCCAC 540 CCCCAAGGCC ACACAGCAGC CTTCTTCAAT GTCGTTGGCT CCATCAGCCC TGGTGTCTCT 600 GCCACACGAA GGGGGAGCCT CCCACGGTGA TTATAAGCTC CCTAGAGAGA GAGACCTGTC 660 ATTAGGAGCA GACTTTCCAC CTCCCTGAAG CGGCTGGCTC TCCTGCTTTT CCTAAGAATA 720 ATCTACCAGG GCTCTCGCAG ACTGCCCGCC TACATGGGGC CTGCAGTGCG GATGTGCAAC 780 AGCCTCTGGG AGGAGAGAGG GTTCCCAGGG CTCCCACTTG GGGTGGGTCG CCTCTGTCTT 840 GGAGAGCTGA TGTCTGGAAG TCCAGCTACT TTAACCATGC CACCCTCCCT ACCTTCTGGA 900 GAAAACTAAG CCCAGGAAAA AGGGAGGTCA GAGGAGCTGC CACAGGGCAA GTGGCTCCTG 960 GGGGGGCTTC CCTCTGTGGG GGCTTCCCTC TGGGGGCTCC TTCCCTAAAA CGCTTAGGAG 1020 GTGTACAGCT CCCTCAAGCT CTCTCTGGGC TCCAGGAGGC TGGCAGTGCC TCTGCAGCCA 1080 GAGGTAAAAC AGAACCTTCT GAAGCATGCA GCAGAGAGCC CTGAAAGAGA AACAGTCCCC 1140 TGAGGTTGGC CTGTCCTCTC CTTGCCACCA TGCAGTCTCT TAGACAAGCT CCTTATTAGA 1200 ATCCGTAAAG AGTCAGATGG GAAATATTGC AGGGGCTATA TGGTCTCCAT CGCAACTACT 1260 CACCTCTGTG 1270
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