Tag | Content |
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EnhancerAtlas ID | HS053-02557 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:152139170-152141660 |
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) |
RUNX1 | MA0002.2 | chr1:152140098-152140109 | CTCTGTGGTTT | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 152140920 | 152141203 | chr1 | 152141371 | 152141421 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I152166 | chr1 | 152139369 | 152141102 |
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Enhancer Sequence | TCTTGCCTCT GAATTAGATG ACGAATTCTC TGAGGGAAGA GTCCTTGATT TCTCCTTCTG 60 ATTCTCCCAT GAGCCCTGCC ATAGTGCTGG GACCCCAGTA GGTGACTGAA CTGGATGATG 120 TTTCACCTCC ACAAGTCCAT GCCCCCTGAG CAGTATTCTT TTGGGATTTA GAACTTATTT 180 GCAACTTGTT GGCTCTTGGA AATAAAAAAG AATAATGTGT GAAAATTCTA GAGCCTTACA 240 GAGTATGGGG CAGGAAGATG GTGTTGGTAG ATGAACCAGT GGTGGGCTGT GATAATTTCA 300 GGAGGTTTGG GAGATGGCTG CTGGTATCTT GAAGAGTTTA CATGCAGAAA TAACAGAGGA 360 ACTGCTTTAG TTTCTCCAGA AATATCTGGA TGCTAAAGTT TCCAGGCCAA ACTGAGAGGT 420 GGGACTTGAG GCACAGCCCA AGAGCCCCAG CTGTCACCAG CAGGGAAGCT GAATGTGGTC 480 ATGTGTACCG GGAGCAGCAG GCAAGTTGAA AGCAGTGATT GGTCAGAAGC AGATTCATCA 540 GGGCTTCTAA AGATCATCTT GCCCTGCTTC TGACCCAGGT AGGTCAGTGC CCAGTCCATT 600 CTTTGTAGGT GTCAATTCAA AGACTCCCCA GAGGAGCAGA TGGCCCACTG TCCCCAAGAA 660 GCTCATGCCT GTGTCTTATT CCCTTAGCTG TCAGGCATAG TAGGATGCCA GATCCAGGCA 720 TCTGGCAGGG ATGAGAAAGC AGGCAGAGAG AGCAGGGAGA GAAAATCAGG TAATGCCAGG 780 GAGCTTTCAT GAGGGATTGA GTAAGGAAAG TAATCCTTCT GAGGTCTTTG CCAGTAAAGC 840 ACAGCGAGAG TAGTAGAGGC TACTAGGGGA TGGTGTAAGG GCTTTGGTGG AGATTATCTG 900 GGACTGGGGA GGGGTGCTGT CCCCAGTCCT CTGTGGTTTA TTGCCTGGTC CCATAAGTGG 960 GGGCAGTTGA TGCTTGCATA ATACACCTAC TTGTCATGTC CACCTAGCAA AATCTTGGTG 1020 TAGTCAAGAA ACAAGAAGAT ATGATCGAGG GGTTGGAAAT CAAGTAAGAG TTTTCTCCAC 1080 TGGTTGCCTA GTTCATTGAT TCACTTATTC ATTTATCTTC CTGACGAATG CTTAGTGAGG 1140 AAGATAGAAC TGTTAACAGT CAAAAGGATT CTGGGAAGAG CTTATGGCAG AGCTGCAGCC 1200 ACGTTGGAGT AAGAACAAAA TTTCATCATC ATCAATTCTT CTCACACAGT GGGACTAGCC 1260 CAGACAAGTG CTCTCTCTTC TGCTGCTCTT GCCCCTGATG CTTACACCAC AGTGGCTTCA 1320 CACCCTTCTG CATGCCTGAG CCATGACTTG GCTAAATTAC CACACCACTT TGCCATGGGA 1380 ATTCTGCCTA ATCATCCTCC TTTAATCTTC AATCTCTTTA TTGTGGTCAC AAATGCTCCA 1440 CATGGCCCCA GTCACCCTGC AGAAAAGAAA TCATCAGCTT TCTGCAGCAT CAGACTTAGC 1500 AGCATCTTCC TGTCCCAAGA GAAGAGGGGA TGGGAGGATG GCATGGTTCA GGGCTTAGGG 1560 GAGGATAGGG GAGAAAAAGT GGAAGCAAAG GGAGAGGCCC AGGAAGGATT TTGTTGCGAC 1620 ATGTTACCTG GGCTGCACCT GCTGTATGCA AGAGAAGAGG CTGGGAGTCC CCTCTGCAGG 1680 GTGTTCATGC CCCATCTCTG TGCCACGAGG AGTTGGGCTG CTGAAGGTGA GTACAGGGAG 1740 GTTCCCTGTC ATCTCAAACC TCTCAGGCTC CACAGTACTG TTTCAAGTAT CCAGAGCTTT 1800 CCTGCCTTTG AAAAGCAAAA AGTTGTCTCA GGAGAGACAG TGTGATTTTT GCAAGGTCAT 1860 GCAGGGTCAC ACAAGTTAAT AGCAAAACTA TAGTCAGAAT TCAGACTTTC TAACACAAGC 1920 ATATGACATG TATACTTGTC CCAGGACTCT ATGTTCTATG TTTTCCTCTT GTCACATTTA 1980 TGGATCCAGT CCAAGGCAGA GAGAACATGA CTCTGAGGTC AGGCAGATCT GCAAGGGAAT 2040 AGCAGTTCTT CTCAGGATTG TTGAAGAAAT TAAATGAGCT CGAATATGTG AGTGCCTAGC 2100 CTAGTACCTG GCATGGGGGG TTATGCATTC AGTGTGTTGC TCTCCTTCCC TTCCAAGGTA 2160 GCCTGGCTGT TATCTCCTTT CTGGAAACTC ATTGAGCATC AGAGATCTTG ACCTCCTTGG 2220 GCACACTCCT GAGTTTATTT AGGCCTACAT TTATAGGATG TGTCAGGAGC TCAAGTACTT 2280 TATGAACAGA GATTAATTGC TCTTATGATT TAATGCATTG GCCACCCACA CTGGTGAGAT 2340 GCTCCCTGAA CTATGCTATT TGAGAAACAA TGAAGGAACT TTGTGAGGCT AATAAGATTT 2400 GTGCTGTTAA TTTAAGTCTT GAGGATGTGG ACTACAGAGA GTATAACATT TTATAGAATT 2460 TGTTTAAAGC TACACTCTCA TCTTTGCCAT 2490
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