Tag | Content |
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EnhancerAtlas ID | HS179-04456 | Organism | Homo sapiens | Tissue/cell | SkMC | Coordinate | chr10:34864820-34866180 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr10:34866101-34866111 | TCTAATTAAA | + | 6.02 | IRF1 | MA0050.2 | chr10:34864828-34864849 | AAAAAGAAAAAGAAAGAAAGA | - | 6.87 | SOX10 | MA0442.2 | chr10:34866067-34866078 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr10:34866067-34866077 | AAAACAAAGG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 34865493 | 34865699 | chr10 | 34865809 | 34866128 |
| Enhancer Sequence | TCTCAAAAAA AAAGAAAAAG AAAGAAAGAA AATCAGGTAT TTGAGCTCTT CTCTGTAGGT 60 TCTAACTGAG ATGCACCAGG CATAGGCTTA GCCATCTTTC TTTTCTACTG ACTCATAAGA 120 ACGAGTCAGG GAAATGTGTG TTGCTTCTTC AAGCTCTGCA GGCAATGGTT ATGTGCAGTC 180 TTGAATGAAT AAGCAGCAGA ATCACTGATG TTTGCCAGAG AAGTACAGGG TAAGCCCTCC 240 CCCACAAAGT CTCAATCTAT TACTTTCAAT GGGAATCCAT GATAAAGTAT AACAAAAGAC 300 ACTATGCTTA AATATACACA TCCACTTAGA TGCTGTGGAG GACAAAATCC TAAACAACAT 360 AATACAGTTC GCTTGCCTCT GGCCTCTCTT CCTCACCCCA ATTCTCGCCA TCCCGACCTT 420 CCAGAGGGGC TGTCTGCTTG CTTGTGCATT CTCTCATCAG CAATGTTTGT TTCACCTTTT 480 AAAAGTTGTT AATAGCCAAA TCAAGGAATC TTTAAAAATA AATACAAGTC AAATTAAATC 540 ACCCATAGAA ACACACTGCA CTCTTTACAT GTTAAGGCAA GAAATTTTTG AAGAAGATGA 600 TCTGAAAAGA ACAGGGACAA AAGAAAAAAA AAAGACAAAA GCTTTTTTTG GACCATATAA 660 AATTATAGGT AAGCAGATAA CAGCTGGTTT CCATTTCACC CCTCTGCCCA CCCCTAATTT 720 AGTGTGTCAC CCCCTGACTG CACTAATCAG AACTCTATTG AAGGAGATGA CTGTGTGAAT 780 TTACTGGGAA CTAAAGAAAT CACTACAGAA ACAGTCTCCA ACCCAAAGAT AATCCTGTAA 840 GCTGACCAGT GTCAAGATCT GAATATAAAA CATACAAAAC CAAATTTAGA TACCTCTATG 900 ATATTTTTAG TTACAGTGGA ATGAACATGT CACTGTATAG CTTCTCTGCA TCTAATGCAT 960 AAAAATGAAA GGAAATCTGG TTTTCAACAT CACACTCCCA CTAAAACAAC TTGCAATCAA 1020 TTAACGTCAT CAGCAGTAAA ACTCAATTTT CTCCCCTGCG TGTGGGGGTG AACATACAGC 1080 ACAGATTGAT AATTCCCGTT GAGAGTGTGG CTAAGTGTTT CTAAGCAACC TTGCTCCATC 1140 ATCTTCTCTG ACAAAAACAA GGGAAAGGGT TTGAACTGCA GGCTGATGGA GCTCTGAATA 1200 CTAATGACTA GGCAAAGAGG AATGGTTCAT TACTGACTTC AGGCAGAAAA ACAAAGGAGC 1260 AGCTTCGAGC TGTAAATAAA TTCTAATTAA AACTTAGCCT GCATTTCATA TACCTGAACT 1320 CAAGCCTACA TATGAAGTTC CCTCAGTGAC TGTCCATTCA 1360
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