Tag | Content |
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EnhancerAtlas ID | HS098-47847 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:17031920-17034320 |
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) |
MEF2A | MA0052.3 | chr6:17032416-17032428 | CCTAAAAATAGA | + | 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 |
chr6 | 17032639 | 17033791 | chr6 | 17033300 | 17033417 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I017031 | chr6 | 17031936 | 17034166 |
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Enhancer Sequence | TGAAAAGGAT ACTGAGGCCA CTCGTTTGCT TCTACTTGAG GACAAGCAGG TGCCTCTCTT 60 CCCGCTTCTT TCTCCTTACT GCTGCTGCCA CCCACACAGC CCCCAGGCTT GTCCTAGAGG 120 GCTCTGGAGG TACACGCGAG GCCGGCGAGT TGTCATGGCA GGGAAGTTGT GGGGAGGGTG 180 GAAATGGCGA TTTCCATTCC TTTTTTCCTA TTTCATGTCC TGCCTGGAAC ATGAAACAAA 240 ACAAAACAAA ACAAGACCAA ATGCCCTTGG TCAAAACACC TCTGCATCCA AATAGCCTCT 300 GAGGCAAGGC AGCTTCTGAG GCAAGGCGGG GCATCGCCGC ACAGAGGCTT GGAGCCTTTG 360 AGGAACAAAG AGGGCTTCAG AGCGCGCTGG CACTCCTTGG CTCACCCATT GATTTTCATT 420 TGCACAGACG CAGGCCCTCT TTTTGTAATC AGAGGGGGGA AAGCAGATCT GTGGAAGGCA 480 AATCTACCAT CAGCTGCCTA AAAATAGACC CGCCGCCTCA CCACCGTGCA AAACAGGCGC 540 CGGCCCGCTG CTGTGCGCTG GTTGCAGCAT GAATTCGCTG GGCAGGGATT TGCAGTATAG 600 ACGTAGAGTT GTTCTGGCCT CTGATGCTGC GCCCGGGCCT TAAATGGAAT CGCGGTCTGT 660 GATAACTTTT GACAAGAGCT GGCAAGCTGA GCCTTTCTTT GAAATGCACT GGGGGGCTCT 720 CGCACAAGAG CCAGGGCTTT CCAACAGGTG TGAGCTAGGG GGTAGGCCCT ACAGATTATT 780 AGGAGGGAAA GTTGTCTATG GTAAATTACC AACTGGGGGA GGTCAGAGTC AAAATCTCCA 840 TAGCAGAATT ATTACTAATT GTGAAGCGCC AAGATCGTAA GAGAAGAAAC CATTCTGACG 900 TGTCATTTTT CCCAGGCCAC GACATCTCTG TTAAACAAAA GAGACTCATA TTTGAAGTGA 960 TGAAAAAGCC ATGAAACATA ATTTGAAAAT TATGTCATGC CCAGCTTTGC CTTCCCTCAA 1020 GGCAAATAAA AGCCTCGGAA TAAAAACGTT TCTATTTATT TTCAAATATT TGCATGGGTT 1080 GCCCCTTTAA TCATCCATTC CCTCTAATAT TAGTCACAAG CAGTTTAAAT GGAAGCTGTT 1140 AGCATGAATG AACACTCCTT AATGGCTGGA TCACTGGAGG AAGTGAGCTG TAAAGCCCAA 1200 ACAGTCAGAT GAAGAAAAGC AATTAATAAA ATTTGCCTTT ATCTCAAAGA AACTAGGATG 1260 TTTTAACTGC AGTTATGTTT TGAAGGAAAC AAATATGATG GTTGATTATC ACGGAAAATA 1320 GACTGAAGCC TGCCCACTTG TAAATTCACA AACTCACTTC AAGTGGAAAA CCCAAGTCTG 1380 CATCCTCGAG GAATTGTACA AATGTGCATC ACGAGACAAG ATCTGGCCCA ATGCCTAGAA 1440 GCTGGTGAGG TCACCAAACT CATTACTCAG AAAATCAGCT GTGAGCCAAG CCCTCATTCC 1500 GTTGCATTTC ACATAGAATG GAGATTCCTC CGTCTTTCCC ATGCTCCCAC CTCCCATCAT 1560 TAGAAGAAAA ATGGGATTCC CAGGTATTTA ACTTTAGGAA TCTTACAGAG ATCCAACATG 1620 GACGCTTTCA CGCCACATCC TGATTTTAGC TGTGGCTCTT CTTGCTCTGT CTGGAGGCAT 1680 CTCAGCAGTT AATGGGAGTG ATTCACATGA TCCTACTCCA ATTCCTGCTA TTTTAGGATA 1740 CTTAGCTTTT CTTAGCCATG GATTTCTTCT GTCTAAATCT GCCCGACTGA ATTGGAAGCT 1800 GCCCAGAATC TTCTTCTTTG GAAATTACAT TTGTGCATCT AGGGTATATT TGTCGTTCCG 1860 CCCACGCTCC AGCCACTTTT TGAGAAGTGC AGAGCGAGTC ATGTGACAGC CATCAGTGTA 1920 TTTGCACCCT TTTTTGTTTA AAAACATAAT CTGCATTACA AATTGCACCA ATTCCTGTAT 1980 GTAGTAAGTC ATCATTCAAT AAAAAGCACA AATGTATGCC TGTCACATTC AACATAATAA 2040 ACTGCAAGTA AATACATCTT TTCTTAGTCC AAATCAGTCA GTAAATGATG TCTTTATTTT 2100 CTCTGTTATG CACCAAGTTT GCAATCAGCT TTATTCTTGA TTCTCTCAGG CCAAGCCTAC 2160 ACAGCGTTAA CTGCAGTGGA AGATTGTGCT TTTATCAGAA GCAGCTGAAC ACCTGAGGAC 2220 AGGAACATGG CTGAAGCAAT TCATTTCTCC AATTCACTTT GTTCTACTTT ATCATCATCA 2280 TTCCGGTATT ATCATCATGT TCATCAGATT CTCCATCTAA AAAAGATTTA TCACAGTGTC 2340 TGCATCTGCA GGCGATACTA CAATATAGAT AAAACCATTG CTCCCTGCCT GCTCCGGATG 2400
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