Tag | Content |
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EnhancerAtlas ID | HS095-18218 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:11175790-11178320 |
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) |
NFIA | MA0670.1 | chr20:11176535-11176545 | ACTTGGCACC | - | 6.02 | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | + | 6.74 | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | - | 6.82 | ZNF263 | MA0528.1 | chr20:11176359-11176380 | TCCTCTCTCTTCCCCTCCTCT | - | 7.42 | ZNF740 | MA0753.2 | chr20:11176815-11176828 | CCGCCCCCCCCCC | + | 6.64 |
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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 |
GH20I011195 | chr20 | 11175658 | 11177760 |
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Enhancer Sequence | TAAGAGCTTT CAGACACATC TCTAGTCACA TCCTAAAAGC CTTCCTAGTT GTGTAGCTTA 60 GGTGCATCCG GTAGCACAGC CGTGTTCTGA TCTTCCTGGC AGATGTCATA ATTTACTGTC 120 ACCCCCATGC AGGAATGCAG GGCGAGGGGC CCCCATGCCG GCTCTGTGAT CCATTGCCTG 180 ACAAGTCCTG AGTGTCAACC TCAGGCAGGC CCAGCGGAGG TGGAACACCA TTTACCTGAT 240 AGTGCCTGTG ATAAAGTGGG CAATTAGACG CACTTGGAAA AGCCTGGCTG GAAACTGGCT 300 GGCATTTACA CAACATTACA GCCAAGTCAG GCTTCATAAA AGTTAATGGA GAAAAATGAA 360 GTCCTTCAAG ATCTACCTTG CTCTCTGAGG AAGTCAGGAA CACAGGACTC TGTAGCTTTA 420 TTTCTTTTTG TGTCTCTCCC ACCTTTTCAC TCTATTTCCC CCAGACAGGG TAATATATTC 480 TCATTGGAGA TGGGAGTAAA GGAAAGCGAA TTGAGAGTTG AGGTCTTAAG TGTTTGATCT 540 CAGAGGCATG TTATTTCTTT AGTCTTCAAT CCTCTCTCTT CCCCTCCTCT CTGTCTCTCT 600 CTCACACACA CACATGCACA CACACACACA CACTCTATAC TTCTATAGAG TATACACACT 660 CTATATTTCT CTGTCTTTCT GTCTCTGTCT CTCTCTCACA CACATGTGCG AGCACACACA 720 CACACAATCA CAGTGCTAGG ATTTAACTTG GCACCTTGGC TTACAATTTG CCTCTCACTG 780 GAGTTTCTGG AGTTTGGTGC CAGTTCAAGA GCATGATCTG TTTGACATGA ATTCTACAGC 840 CCTCTCTTCA TTTCCTCCTA ACTGGATAGC TTCAGTTTGC CGATGATTAA TGAGTCTGGA 900 AGGTGAGCGA CAGTTATCTT AAGGGCTCTC AAAAGTTTAT TTCAGAGACT AGCCAAACTC 960 TCCTGCTACA TTAACTGCAG CGAAGTTTCC TGTTTAACAG CCCATGGAAA ATAACTGCCT 1020 GACCCCCGCC CCCCCCCCAA ACCAAGCTGC CATGAGCGCA GCTCTGTTTA TTGGCCAACA 1080 GTGTGCATGT TCTCTCTATC GCTTCCTTTC AGGCAGACGA ACATTTTACC TATGAGAAGT 1140 AGGAAGTCCA TTGTGAGGCT GGTCCAATAC TGGACCTCAT TTGGATGTGG AGGATTTCTG 1200 AAATTGGAAA GTCAGGACTG ATCTGGAAAA TGTGCTTACA GATAGTGGAA CAGGAAAATG 1260 ATTCGCTCCC CAAGGCCAGT TCCTCCTCCT CTGCTGGGTG GAAAAGGTGG GAGGAAGGGA 1320 CAGGGTGTTC TGCCTGTGAT TGGAATTCCC CTGTAGAGTC ATAGAGGATG AGCAAGCCTT 1380 TGGTTTTCCT TTTTCATATT TTATTTTGCA CCTACAATAA TAAGCATGCA GAGAGGAGAC 1440 AGAGAGGCCT AAATGAGTTT TTTTCCTTTC TAAATAATGA CCAGCTCTGT ATCAATCTGA 1500 AGGCTACTGA GGGATGCTGG TGGCTGGATG GCGGGGCCTA TTTAGGGTTT TGGCCTGATT 1560 AAAAGTTAGT CCCAGGGACA TGCAGGCCTA CCAGGTGCAC ACTGGTGCCA GCCACTTCAG 1620 TGGGGTGGGG GAAATTACTG GGCCTGCTGT CTCAAGTTTG AGAGGACATC TGAGATTCGG 1680 GTCCGATAGG GTCACAATGT CTTCAACACG AATAAATAGG CAGTTGTAGG TTGGGGAAGG 1740 GAAAGCTAAA GTGGAAAATA AATAACTTAA GACACCAGAC AAGTTCTGGA GACTGAGGTA 1800 GAGAGATGAT GGAGTGCTCT TCACCCATGT ACACTTCAGC CTCTCATGTC ATCGTGGTGA 1860 TGCTGCCAAA ATAGACCCAA GTTACATTTT CCTTATGATC TCATTTTACT GGGCTTGAAG 1920 CCTACCTCAC TCAACATCTT TGGAGGGTAC ATTGAAACGA GCTGTTTGTA AGACAGTATT 1980 AAAGGAAGTG GCGTTATATG TGTGTGTATT TGTGTCATAT ACATATATGA AACAAAGATA 2040 TTTGAATATA TACATGTAGA TAGTTTCCCA AAAACCCATC TCCCTTGGGG AATAGTCTCA 2100 CCTTCAGGGA GAGGTGCTAG AGAGGGTCAG AGATTCTCCT GCTCTATGCC ATAAGACCAA 2160 AGATAGATTG TAATTATGAT CCCAATTCTT TGCCTCTCCT CTATCCGTGC TATTTGAAGC 2220 CCCTCCCATC AAGAGGTGAG GTCTGGGTCT ATTTCTCTAC TCTTTGATTA TTGATTGGCC 2280 TTGTGACACA GCTGGGCCTA TAGTGGAGGT TACACTGTGC CAGTTTTGTC TAAGCCCCGA 2340 GATGTCTTGT GTGTTTCCTC TTGCCCACTC AATCCCTGTA AGTTGCAGCC ATGACACTAT 2400 GCCCTGAATA GCCTTCTGTA GGATGAGACA TGAGGGACAG AGCCATGTCA TCCCAGTGGT 2460 TTTAGCGAAG GCTGTCCTAA ATCAGCCAAA GGCTAACTGA CCTCTGAAAT ATGAATGGGC 2520 CCAGCAGAGC 2530
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