Tag | Content |
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EnhancerAtlas ID | HS147-35934 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr6:47451510-47452970 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr6:47452241-47452252 | AATAAACAATG | - | 6.02 | ONECUT1 | MA0679.1 | chr6:47452317-47452331 | GTTATCGATTTTTT | - | 7.73 | ONECUT2 | MA0756.1 | chr6:47452317-47452331 | GTTATCGATTTTTT | - | 7.82 | ONECUT3 | MA0757.1 | chr6:47452317-47452331 | GTTATCGATTTTTT | - | 7.38 |
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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 |
GH06I047483 | chr6 | 47450878 | 47453110 |
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Enhancer Sequence | AGGGATTTGA TGTGCCTGTT TTTTTTTTTT TTTTTTGCTC CTGTCTCTTT TTCACCTAGG 60 TTCCTTTTCC TTTCATACCC AATGTGAAGC AGATTACAAA ACCTCAGCAT ATCCTTCTGT 120 TTCAGAAACA AGTACACAAT CCTTCAGGGT GTTAAGCAGT TATAACTGCA AATATAATAA 180 ATGACCAAGT AAGGCAGAAG AAACTTGAAA GTATTAGTAA TTATCAGTCT CTTGGTTTCA 240 CTGAAGTGGT GGTTGGCTAG TTATTAGAAA GACCTTTTTT GTTGTTGCTT TTTAAATTTT 300 TTTTTGGTAA TGTGTACCTG TCTTTGGCAA TACTCCCTCA TACTCCTCCC AGCTTTTGTT 360 TATTTTGGCT TACGTTAGGT AGATCTTTAG ACAGTAGCTC ACAGTAGAGA CATTTATTAT 420 GTCTCTTAAA CAGATAAAAT TTTATTGGGA CTTCACTAAC CTGAGACCAT GCTGTACTCA 480 TTTTTGAATC ATAACCTTGG TTTTAACCAC AAATGAAGTA GGCATTTTCC TTCTGGGCTC 540 CTAAATGTTT TCTTTGGACT AAACTTGATA TTACCTCTTT TTTTTTTTTT TGTTATGTTT 600 TGGTTTTTGT TTCTGAAGGT CTCAGCTTCC TAGATGTTCT ACACTCTTCC TGACCATTTT 660 CACTGAACCC TATTTGATTT ACTGAAAGCA TATTTACTAA TTGTTTGCAC TTAAAGGTGC 720 TTTTATCCTA GAATAAACAA TGCTTTTAAA ACAATTCACT ATTCTAAATT GATACTGGCT 780 TAAGATGTTG TTCCAGTGTC AGGTATTGTT ATCGATTTTT TCTTTCCTAG AACCTGTCCT 840 TTCCAGTGGC TCCAGTAGAC TTGTATTTTA TAATCTTTCA AATATTATGT AGCTTGTTAA 900 ACTTCCCATC ATGATCTTGT TCAGTTTCTC AACTCATTTG CAAAAGAGAT GACTAGCATG 960 GGAGCCTGGA TTCCAGTATC TGTTTTAGTG CCTTATTAGT GCCTCTTAGC TTAGGTTCTT 1020 TTTGATGATT CAGCGTCCAG ATAATTCCAA GGGAGTGACT GTAATCATTA GGGGTTTCTA 1080 GTAGAATGCA ATCATGAGCC CCTTAGGAAT GTTTTGGTCA ATAATAAACC ACACATAGGG 1140 TGGTGGTCCC CTAAGATTAT AATGAAGCTA GAAAATTCCT CTTCCCTAGT GAGTTGTAGC 1200 CATCCCACAC TATAGTAGTG CAACGCGTTA CTCACTGTGT TTGTGATGAT GCTGGTGTCA 1260 ACAAACCCGC ACTACCAGTT GTATAAAAGT ATAGCATGTA CATACATTTA TATGTAGTAC 1320 ATATATTGAT AATAAATGGC TGTGTTACTG GCTTATGTAT TTACTATGTT TTTTAATTGT 1380 TATTTTACAG AGTACATCTT CTACTTATTA AAAGAAGTTA ACTGTAAAAC ATCCTCAGGC 1440 AGGTCCTTCA GGGGGTATTC 1460
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