Tag | Content |
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EnhancerAtlas ID | HS165-01634 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr10:24911690-24913150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:24912621-24912642 | AAAGGAGGATGGGGGAGAGGA | + | 7.39 | ZNF263 | MA0528.1 | chr10:24912624-24912645 | GGAGGATGGGGGAGAGGAGGT | + | 7.51 |
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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 |
GH10I024622 | chr10 | 24911430 | 24912716 |
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Enhancer Sequence | GCTAGCAGAA AATAGGAAAA CATAGTAGAA GCTGCTTACT GATATAAAGA CAAAATCATG 60 TTGTCATATT GATGCTGGAA ACGGCAAGCT AAAAATACAT CTATACTTGT TTCTCTGGAA 120 GGTACCAAGA GAGGTAAAGG GCAGTGAAGC ATAAAGAATA ACTCCAGTAT TCTTCTGAAC 180 ATCTTTTTCT CAGGCTTTTA TCTGATTCTT GTTTGATGTG TCTACCATTC TTGAAAGCAA 240 AATACATCTG GTGACATGCA TTCCTAACAG ATATTTTCTT CAATATGCAC TGCTGTCTGA 300 TAACATGCTA CAAAGCTTCC CTCCACGAAA GCAACAGTGA TGTCTCTCAT TTCCCCCCAG 360 CTTCTTCCAT CTCTGCTTCC AGATGACGAA ACGAATGCTC TATTATGCAT TTAAAATAGT 420 ACAACCTCCT CCTTCCCCAG TAAATCAGAG CATAACCACA AGCTGTCAGC AGACTGCAGC 480 TGCCTTTACA CTAAGATTCA GGGGGGAAAA TGACTTCTTT TAAGTAAGTT TCACTCAAAA 540 ATTAAGATCT TTCAACACTG TGCCTTTTGT ACTATTGTAT TAGTTTGCAA AAATAACTAC 600 TGGATAGACA TAAAAATATT ACTTCCAGAG TAATTCTTGT TAACCTATAA TAAATATTAT 660 AGAACAGAGA CTAGAATGCA GTGACAAATT AAAGCTAGCC ATATAAAATA AAATATGTCT 720 ACATAGTATT TTTATGGCAT GAATACAGTT AATCCCAACA TGCATTTTGG GTGTGTGCAT 780 TGACACACCA AGTCTATCTT TTCCATGCTG ATTAGAATCA TACCAATACT TTTCTGCAAT 840 AGGAAAATTG TGTCTGGATG AGAGAATACT GTACTGTCTG GTACAGCATT TCCCACAACA 900 TCCTTGTGTA GTTTTATTAT ATACCACCTG AAAAGGAGGA TGGGGGAGAG GAGGTCCCTA 960 TGGTCAATGA TGTAGGGCCA CTTGGCAAGC TTTTTGATTT CTCAAAACCA CGACGACACT 1020 AATGTACATT GTGAAATTCG AAAGGAAAAT ATAAACTTAT TCACCATGGA GGCCATTTTT 1080 TTCCCAGAGG TTTTAACATA ATTAGAATAT CTACTTGGGT AATGCTATTC TAGAACTAAT 1140 ATTTTAAAGA TGACTCCTTT ATTCAAATTT GGGAAGAAAT ATTACTGTTT AGTAATAGAA 1200 GTATACGGCT GGAACTATTA AAACTTGAGA ATATTTTACA TACTTCAGAC ATCTCTAATA 1260 TTCCTGTATG GCAATTCTAA ATGCTAAATA GTCTACATTA CAGTCACAGG TCCCCACTTC 1320 TGAGTTAAGT TATCACAAGG GGCCCTGAAA TCCATACAAA TGCAGGCATT AACAGTGAAC 1380 ATCTCACACA TGCAGTACTA TTATCTAATG TAAGCAGATA TGGTTGAGAT AAAATATGAA 1440 TTCATTCAAG AACATTTTTC 1460
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