Tag | Content |
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EnhancerAtlas ID | HS187-21733 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:130348950-130351370 |
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) |
ZNF263 | MA0528.1 | chr6:130350957-130350978 | TCCCCTGCCCTGCCCTCCTCT | - | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 130349511 | 130349612 | chr6 | 130349129 | 130349778 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I130027 | chr6 | 130349141 | 130349290 |
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Enhancer Sequence | ATATTTAGCA TATGCATAGA AATATCTGTG TCAGGTTCTT GTTCTTTTTA TGGCCCTTGA 60 ATCCCTCTAA TGGGTGTAAA ATTTCTATTA TTACCCTTCT AGTATAGTAT GTTGATGATA 120 TGCTAGCACT TTAAAAAATA TGTCTGACTC AAATTGAGGT ATAGTCTGCA CGTTGAACAT 180 GAATTTAAAA TAAAAGCATT TAATGAGAGT CTATTAAATA TGCCATAGGC CCATTAATGT 240 CAGTTTGTGA TTTCACTTTC TGTGTACCTT TTTTTTTTTT TTTCTTGAAA GGCATTTTTC 300 ATTTTCTGTT CCTTCTTTAG AGGAAGTAAG TAGGTTAGGC CACAGAATCT CAAATAATTC 360 ATCCTTCTTA CAGTAACACA GAAGGGCAGG AAGTTGAGAT TTTGTAAAGG TTACCTTTGG 420 TGACTACCCT TTCTTTGCAC ATGATCTCCA TGGCAGACAA GGTAGCAAAT CAGAGAGACC 480 ATTGCAACAT TATAAATAGG ATCATTCACA TTAAAATATG ACTAGCTGAT AAAGGGACAG 540 TGTTTTTGAG AAAATATCAA TAAGATGGAA CCGCTGTAAT GACTGATTTC ATGTTTAAAG 600 GCAGCATGGA TTAGTTCACA CTCAGGTGTC TCCTCTGCAG GGATGGATGA GAACAGAAGA 660 CCCAACTTCT CAAGGATTTG TTCTTGATGC TGCTAAGATT TCAGTTCTCA CATTGAAATA 720 ATGATCTAGA GTTTTTCCTG CCTAAAATCT ATGAACTTAG GTCCTTAGGA CAGATTTCAC 780 ATCTCTCCAC AACAGACCTT AATTCCAATA TATGTGTGAT TCAGAGTACT TATCAGGCAG 840 GATGAGTAGC ATATCAAAGG TGGTCTCTGT CATGCTTGAT TTGAAAGGAA TATTTTTCTT 900 CATAGCAATG TGTGTTTGTT GAGAGATGCT TCAAGTGTGA GTTTAGATTT TCTCTTATCC 960 TTATTGAATA AGTCTGTTTA AGAGGTTTGA ATTTAACTTC TTTTGATGTG TTCTCCACTG 1020 ACACTTATAT AAGGAGAGTT TCTTGGAGTG GTGATGTTAT GCTTCTGCCA AAGAGGTAAA 1080 CAAATACTTA GCAGCCTAGT TGTTAGAATT TTCACTGGAG AATATGAGCT AGATGGACAG 1140 ATGAAGGTCT TTCCCTGATT TTTCCTCTCC CCAAGCCCCT TCCATTCCCC TCCAGTAGTG 1200 TATTGTATTT TCCTCTTCTC TTTTATTGAT TCATTTGGTA AGTTTTATCA ATACCTACTA 1260 TAGATATTCA TAAGAGATAA CAAAATGGGT AAATCAAGGT CTCTGTGCTT CAAAACCTCC 1320 TATAAGTAGA TGATCAAGAT ACAGTGTCAT AAGCATTATA ATCAGTGTAT AGATTCTGTC 1380 CTCCCAGCCC CACTTATGTC CTGGTCCTGG CATCTTACTT GCACGTACAT ACTCCAGTGC 1440 TCCTATAGAG AAACACTCCC ACTGTAGCCC CTTTGGGGAT GATGACGCAG AGCTTTCATC 1500 TCTCTTTTTC ATACTGGCCT CTTGCTTTAA TCTCTCACAG CACTTTCTGT TTGCCTGTGT 1560 ACCAGCTCTC TTGAAAGCAG GTCCTGGAAC CACATTTGGT ACATGAGGAC GTTTTTATGC 1620 CTCCTCAGCA AAAACGTCAC AGTAAGGTTG CGAATGGCCT AGTCCTGAGT AGTTTCTCAG 1680 AAATTACGTC CTTTTTATTT TGTTGGCAGT TAAATTTTTT TTCTTTATAA GAACTTGGCA 1740 AAACTAACAG CTATTGACCT TACATCGGTC TCCCAAATTC ACTTTGAAGT CTACTTGTCC 1800 ATGAAATCTG AGTCATACCA TTGTTCTTGA CTGCCCTGCT GCCCACCTTT CCTGTCCTCA 1860 TCTCTGGACT CCTGAGAAAT TAAATAGGCC TTTTTTGATG TAAAGGTATT GGCCTTCGCA 1920 CAGTTTTCAT TCCTCTGCCC TGTGAGACTT CAGAGATCTG ATAAACTGGT TCTTGGAGGG 1980 CATGTGGACC CTGGAGAGCC CCTCCCCTCC CCTGCCCTGC CCTCCTCTTT TTGAGACAGA 2040 GTCTCAGTCT GTCACCCAGG CTGGAGTGCA GTGGGTGGTA CAATCTTGGT TCACTGCAAC 2100 TTCTGCCTCC TGGGTTCAAG CGATTCTCGT GCTTCAGCAT CTGGAGTAGC TGGGACTAGA 2160 GGCATGCACC ACCACGCCCA ACTAATTTTT GTATTTTCAG TCACCACCAC ACCCAGCTAA 2220 TTTTTGTATT TTCAGTAGAG ATAGGGTTTC ACCATGTTGA CCAGGCTGGT CTTGAACTCC 2280 TGACCATTTT TGATTCACCT GCCTCGGTCT CCCAAAGTGC TAGGATTACA GAAGTGAGCC 2340 ACCTCTCCCG GCCGCTTGTC TTTTCTTTAG AATAACTGTA ACTTTTACAT ACCAAGCATT 2400 CACTGTGTGC AAAGCACTCT 2420
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