| Tag | Content |
|---|
EnhancerAtlas ID | HS113-39465 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chrX:135435560-135437140 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6 | MA0677.1 | chrX:135435581-135435595 | TGGGTCAAAGGGCA | + | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI136352 | chrX | 135435097 | 135437466 |
| Enhancer Sequence | GTATGTGAAT GACATTTACT GTGGGTCAAA GGGCAATTTG AGGGCATTTT GGGTCTGTTC 60
CTATCTGGAG GGGATGTCCT ATGTTTATGT CTGAGATTTA GGGCTGCCAC ATTTTTAGTT 120
GCATCTTCCT TCCTGAGTAG GTTCTTTTTG GCATGAGGAA AAAAATTGTA TTACTATTGT 180
AGGGCACAAA GCCAATGGGA GAACAAAACA AAAGAAAATC AATAGGGGAA GTCATGCAGT 240
TAGACTGAGT TACCTCTAAT GCCCTTTTCA TCTCTAAGTT TCTATGAATC TGTGATTTAT 300
ACAAAAATCA TGCTTTGAAG TGCTATGTAT GGACAATGCA CGAGGATTTA TAAGGCCTTT 360
TATTTTGGAA TGATTCACTT TCAGAAAAGA GAAATTCCAA AGTGAACTTG AAATGTCTAA 420
AGCAAGAATG TTGACTAATC CAAGATTTGC TTGGGGCACA AATTTCGAAA GGTGATTGCA 480
GTGAAATGGG CAGGCACTGA GTAGTATCAT GGAAACTATG GCAAAGGCAA TTGCTCACCT 540
GAGAAGTATT TCCTGTATTC TTTCGCTGCA CATATACTAG TCCTCTGTAA AGGGACACCC 600
CGCAGAAGCT CTTTGAAAAA TAGGCATGGC TCTGTTAAGC CATGGCAAAC TGATTTTTAA 660
AACATAAAAT GCTACTGCCT GTCTTCTGTA CACTGGGACT TTGGTTTCTC TTACATATCC 720
AAGTATTAAT TATTAATCAA GTATTAATTC ATATACATAT TAATAGGTTC AAGAAAATTC 780
ATATAAATGA ATGGAGGTAA ATGTACGGTA GGTTATTGTC TTAGTCAGTT TTGAGTTACT 840
ATAACAAAAA TGCTATAGAC TAGGTGGCTT AAGCCACAGA AATTTATTGC TCACAGTTCC 900
GGAGGCTGGG AAGTCCAAGA TCAAGGTGTT GGCAGGTTCA GTGTCTGGTG ATGGCCCTCT 960
TCTTGCTGTG CCCTCAAGTG GCAGAAAGCA GAGAGACAGA AAGCTCTCCT GTCTCTTCTT 1020
ATAAGGGTAC TGTTTCAAAA AAATTCAAAC TGTTTTTTTT CCTCTGTTGT CATACCAACA 1080
CAACAATCAA TATAGAAGAC TTCTACGACC AAACGTGTGG GGATTTTCCC CCAACACACC 1140
AAGCAGCTGA CACCAGCTGG TTGTTCTCTA CTTCAATTCT ATTCTGGTGT TATCCTCTCA 1200
AAAATAGCTT CAGATCTCAC AGGTCCCCAA GACTGCCCCT CACCCCAGAC ACTAGTCAAA 1260
AGTCCAGGCC TCCAGAACTT CTGACTAACT GACTTCAACT TGGGGTTCCC GTGACCCACT 1320
CTTTGAGCTT GATTAATTTG CTAGAGCAGC TCAAAGAACT CAGGTAAATA CTTATGTGCA 1380
TTGGTTTATT ATAAAGGATA CTGCAGAAGA TACGAATGAA GAGATGTGTA AGGCGAGGTA 1440
AGGGACAAGG GGAATGGAGC TTCTATGATC TCCCTGGGTG CACCACCCTC CAGGAACCTC 1500
CATGTATTCA GCTCTTGGGA AGCTCTCCAA ACCCAGTCTT CTTGGGATTT TATGGAAACA 1560
TCATTATGTC AGCATTCCTT 1580
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