Tag | Content |
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EnhancerAtlas ID | HS098-04732 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:205677680-205678840 |
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 | chr1:205678399-205678410 | TATAAACAATA | - | 6.32 | RORA(var.2) | MA0072.1 | chr1:205678517-205678531 | GTTAATTAGGTCAG | + | 6.05 | SCRT1 | MA0743.1 | chr1:205677681-205677696 | GAACACCTGTTGCAC | - | 7.26 | SCRT2 | MA0744.1 | chr1:205677683-205677696 | ACACCTGTTGCAC | - | 6.92 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 205678020 | 205678075 | chr1 | 205678054 | 205678200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205708 | chr1 | 205677998 | 205678648 |
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Enhancer Sequence | GGAACACCTG TTGCACTTTT TATACTATTC ACATACATTA CCTGGAATAC TCCAGTTTTC 60 AACATTGTCT GCTTCAGTCC CTTAAACCAT AGAAGTATCC AGACATGCCA ATATCATGAG 120 AACCAAACTA TACCTTAAAC TGTTTTTCCT GTTGAGGAAT ATGAAAGAAC TCTTCATTGT 180 AGCACAGATC CCAATTTTTG GTGGAATATA GTCACCACAA TTTTCATTGT CAATAAATAT 240 TGCTGGCTAA TTCAGAGGTG ACCTGTGGAA GCAACACGTG CTCTAAGAAC TCCTGTTTCC 300 ACTGTCTGGT ATTATTAGTG TGTCCTTACT TAGACTTAGC TCTCCCAGAG AGAGAGCCAT 360 CTGCTTCTCT CATTGCACAG TGACTGTGCA ATGGTGTTGA CTTCTAGAGA AGAGTAGCCC 420 AAGAGCTAAA TATTAGAGGT CTTATTGCTT CCCTTAAGTG CATGGCAAGA GAAAGGAAAG 480 CAAGGTGAGA AAAGGACTGA CTTGCTTTGC CAATGGCCCA GGACTGGTGA TTTTATAAGG 540 TTTAGCACAA AAACCACTCT TTTGAACTAG ATACTGTGTA TATCCTGTGT ACTTCAAGTC 600 ACACCAGCAT TCCCTACAAC AGAGCTTAGG AATGCTATTT ATCTTGTACT CAGGCCAACT 660 GTGTGGCTCT CTACCGAACA GCTGGTTCCC CATCCACCTC TAGGACTATC TAGTTGATGT 720 ATAAACAATA TTTTTGCCTC AAAAACGCTA ACCCCATGGA AACTAACTGT TCATCCACAC 780 ACACACACAC ACACACACAC ACGCACACAT ACACACACGA AGGAAAAGAA AGATGGGGTT 840 AATTAGGTCA GAAGCAGGAG GAAAAGACAA AACAGGGGGA GCTTGGGGTT TGTAACTGAG 900 ATGTGGCATG CATTAGATTT GAAGTCAGGT TACTGAAGCC CCAGATTATG TTCCAAGGTC 960 TAAACAGAAC GTCCATTGAG TCTTTGATTC CTAAAGACAT TTAGTGCCTT ATAAAAGAGC 1020 TTAGCTATAT CATTATTCCT GATTACCTTA GAAGTAAAAC GATATTTTTA AAGTGTTTAG 1080 TATTTGTATT CCTCTAGGCT GAATTAGTGA ACCACAAGAG ACCCAATTTA TAGCCACAAA 1140 ATGAGGATCC AGTGTGGGTC 1160
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