Tag | Content |
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EnhancerAtlas ID | HS037-20317 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr2:119953650-119954680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:119954279-119954300 | GGAGGAGAGGGAAGATAGGAG | + | 6.22 | ZNF263 | MA0528.1 | chr2:119954630-119954651 | GGTGGAGGGGGTGAGGGGAGG | + | 6.75 |
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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 |
GH02I119196 | chr2 | 119953621 | 119954623 |
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Enhancer Sequence | TTGGCACAGA ACTTTTCAGC TTGCTATGGG GAGTGCCAGC CACCGGCAAC AGGTGTGACT 60 GCAGGGGAAA GCCCCGTGCA GGTGAGAGAA AGGGGCCAGA ATGAGAAGGG CTTTGTAAGG 120 CTGGGACCAC TATGTTGGGT CTGCTATGGA GGGGGGAGCT CAGGAGTAGG CAGGGCAGAT 180 TTGAACATGG GAAGGGGAAA GCTGCTGCTG GAAGCAGTGG CCCATGCCCA GGTGCATGGA 240 GAAGAGAGCC TGGAAGCCTC TCTTGGTCCC TCTAGGCTGG CAGAGGCAGG GCCCCACATT 300 GGCAGTGGTG TGAACAATTT CCCCTCATCA TGGGGCTGCT CATGGCTGTG AAACATGGGA 360 TGGCACTAGA TTTGGTCATT AAGTAAATAG GATAAAGAAA TAATTGGAAA ATGGATCCCT 420 GCCTGGAAGG AGTGGAATTG TTCCTGGGGC TATTGTTGTC CGGCATCCTG CTTTCTGAGT 480 AATCTCCCGA GCCAGGCAAG GAAGGATGTC AGGCTTAGGG CTGATGAGAA ACTTACACTT 540 GAAAAGAGCT CAAAATTACC CATGACAATG GAAAAGCCTT TGTATCCTGA ACAGAGAGAG 600 GAAAAAGACT CTGAATCTTC TCTGGGGCGG GAGGAGAGGG AAGATAGGAG GGCAGTCTCG 660 AGTCACAGAA TGTCAAACCC AGGACCCCTG TGTCTTTCCA AGTTGGGGGC ACTGGCCAGG 720 GAAGGATCCT GGTTCTTCCG GTGTCTGGGA TGATGAGGCT GGTCCTCAGG CAGTGGGAGG 780 CTGGAGGAGG GGGAATGTGT GAAGACCACA TGCTTTCGCC TGCAAGAGCA TCCATCCATG 840 TCTTGGTCAC TGCAATTTAC ATCCTCCCAT TCAACCCTCA GCACACCCAC CAAACCAAGC 900 TCCTCCTTGC ACCTTGATGG GCAGAAAGTT GGAGTGATGA TTATCTAAGA CAGAGCCCTG 960 AGGTGAAGAA CTGGTTTTCT GGTGGAGGGG GTGAGGGGAG GATGGAGGGA GCTATCCCTT 1020 CCCTGTCCCC 1030
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