Tag | Content |
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EnhancerAtlas ID | HS053-12878 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr14:93251690-93253080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr14:93252156-93252170 | AGAAAGTGACTCAG | + | 6.07 | JUN(var.2) | MA0489.1 | chr14:93252697-93252711 | AGGAAATGACTCAG | + | 6.73 | NFE2L1 | MA0089.2 | chr14:93252700-93252715 | AAATGACTCAGCACA | + | 6.91 | Nfe2l2 | MA0150.2 | chr14:93252698-93252713 | GGAAATGACTCAGCA | + | 6.41 | ZNF410 | MA0752.1 | chr14:93251706-93251723 | TAGTATTATGGGAGGGG | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 93251690 | 93252906 | chr14 | 93252078 | 93252440 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I092784 | chr14 | 93251285 | 93253158 |
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Enhancer Sequence | TGAAAGGCCG TAAGATTAGT ATTATGGGAG GGGCCTACAC CTGCTAAGAT ATAAGTGTAG 60 TTAAACTATA ACTAGCCATT GTTCTGGAGG TCACAATATT TGTAACCTCC CCGTTTGCTC 120 CTGTAGACAC CACCACTATT GTTAAAATCT GAGATTGGTG TTGATGGCAT TTTTCAGACC 180 CCGTATTCTG ATGGACCAGC TGGTGTTGTT GTAGTCTCAC CAACGCACCA CAGTGTAGTG 240 ATCTCTCTTG TGAGGTATCA CTCGGAGTTC TTTATCTCAT GTCCAAGATG ATTAAGGAGC 300 ACAGACACAA GGGTGAGGTG GGAGCGAAAG TTTAATAAGC GAAAGACGAA AACTCTCCTC 360 CAGCAGAGAG GGAAGCCTGA ATGGGTTGCC CACTAGGAGG CTGGGGTTCA GGGATTTTAT 420 AAACTGGGAA GGGGAAGGAA TGTGCTTAGT CTGTGGGCTG TCTTGGAGAA AGTGACTCAG 480 CTTGGCCCAA GGACCTTAGC CTGGGACCAA TCAGGGGCTG AAGTGATGAT TCATAGAGGC 540 TAGTCTCACA ATCCAAAAAG GAAAGGAAAA GTGCCCACCA GAACCCACCA GAGCCCACTG 600 TGTTCATGTC CTAAAAAGGA GAAGAAACTT TTTCCCAGGA GCCCACTGAT TATGAAAAGA 660 AAAAGTCATT TCTATGTCAG GCCTTGTTCC CTTATCTGAG TGAGCTGGAG GTTTGTGCAA 720 GTTTTTATCT GAACGGGCTG GAGGTTCTCC TATCTGTGAA GCCTCGGGCA TGTCTCCAGG 780 CACAGCCCTC TGTGCTAGTT CCCTTGTTGT TGCTTGCAGC TTGATTTTTT TCCCAGGCTG 840 CTTTTTCTGT TATGTGGGGA TGAGACAGGT CATCCCCTGT GGGTTGGGGG CTCTCTGGGG 900 ACCCTTCCCT TGCTGTCTAC ATAAGGCAAG CTGGCTAACT CCTCTCAGTG CCACCTGGAC 960 CTGTAACCCA TACCAAGAAA CTGGCTCATC TGGTCTTGCG ATCCACCAGG AAATGACTCA 1020 GCACAAGAAG ATAGCTTTGA CCCTCTATGA TTTCATCCCC AACCCAACCA GTCAACATCC 1080 TTCATTCCCT AGACCCCAGG CCACCAAGCT ATCTTTAAGA AACCCTCACC TCCAAATTTT 1140 CAGGGAGACT GATTTCAAGT AATAAGCTCC CATCTTCCAC TTGGCTAGCC TTGTGTTAAT 1200 TAAACTCTTT CTCTACTGCA ATACTGCTGT CTCAGTAAAT CTGTGCAGTG GGCAAGAAGA 1260 ACCTGTCAGG CAATTACAAA ATCACACTAT ATACACCATT ATTTTCCTTT TGTGTTTTTT 1320 TCTAATTTAA CATATATTCT TAAGATCTTA GAGCTTTTTT CGTATCCTTG CATAAGACAT 1380 CCTTTTTCTT 1390
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