Tag | Content |
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EnhancerAtlas ID | HS098-47436 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:3151160-3152720 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr6:3152090-3152101 | GACAGCTGCAG | + | 6.62 | Sox3 | MA0514.1 | chr6:3151469-3151479 | AAAACAAAGG | - | 6.02 | Tcf12 | MA0521.1 | chr6:3152090-3152101 | GACAGCTGCAG | + | 6.14 |
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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 |
GH06I003151 | chr6 | 3151630 | 3152819 |
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Enhancer Sequence | CCCATATTTT AATGAAGGGA ACCTCATTTT TATTTCCCCA AGATCTAGAG ATTAGGAAGA 60 GTGCAGACAG TGCTGAACGG CTAAAAAGAA ACGATTCACA GCGAGGTTCT CCTTCCTTCC 120 TTATGGGAAA CCAACAAATC ATAGCCAGAT AGGCTGGACT GTCTACAGAG AAAGACTTCA 180 CATGTGGCAG GCTGGGGATT CCCTGCCTCC CAGTCCAGCT TAGTGCAGAT TAGGGGATGC 240 AATTTAGCCT ATACGTGACC TTCTATGACC TCGCAGCATC CTTGGCAATT CGTTCTTTCC 300 TGTTTCCTGA AAACAAAGGC CTTGAGTGTC CCTGCAAGCC CTGTTCCTTG TGTAGGCAAC 360 TGGGATCCTA TCTCTGGGGT GGGTGCAACT CATCCTTCTT TTCTGAATAG TGTTAAAGTT 420 GAATTTAGAA TGTCGTGATT GTTAGTAATA GCATTACTAA TGTTCCAAGG CCCTCGGAAA 480 GGTCCCAACA ATATGTCTTC CTTTCAAGTT GATTCTCTTG GTACCCCATT CCCACCCCCA 540 ATGTGGTGGC TGAGTTGGAA GAGGCCCAGC ATCTTCCAAG CACAGCTCCC TGCCCCACAG 600 TTCCTCCCTC GCACCTACTG AGGTTCTGAG CTGTCAGCCC CCCAGTATTG AAACTCAAAA 660 AATTAGGGAA CATGATAACG CATTCTGCCC TAATATTGTC CTTTTAATGT CTAATTATCA 720 TTGTAGACAA AGTGGCTTGA ACTTAGGCTT TCATCCTAGA AGCTTTACCA CTTTTACTGT 780 TTCTATACTT TTGTAGCTAA TAAGTCAAAT GTAGAACAAA GAGAAGGCTG CATTTGTTCA 840 GGAAACTGTA AATCTGTCCC ATTTGATCAC AATCCTGTTG AAAGGAAGAA GCCTTACGAG 900 GACAGTGTGT TTGCTACAAT GCTGAGCCGT GACAGCTGCA GCAGCGGCTC CTGGAGCACA 960 GGGCTGCTGG CATGGGCTCA CCACCCTCAC AGCCATTTGT CTGGCGGCTT GTATTCAGAT 1020 GTATTTGTTC AGTAATCCAA AAATGGAAGG GTGATTTGGA ACCTTGAGCA GCAGGCTGGG 1080 GATGGCTGTG AATTCTGCTT TGCACTTGCC CACTACATCA ACACGCCAAG AAACTCACCT 1140 GCCCCATCCC AGTGCATTCT GAACATTTCT TATTTTTATC TTCTTACCAA CCTTCTCTCT 1200 TAAAATCAGC TTCATTAAAA TGGATTTTTC TAGAGTAACC ACCAGATCAC CTCCCCCACT 1260 CTCAGTCCGT TTTCCAGTCA AACCATTTGT TACTTGATTC AGTTCCAAAT ATAATGTGTG 1320 TCTGCTACTG TTAAGTCATT GCCTTATAGT CAACCTCAAG GGTAGTCATA AACTCCAAGA 1380 GTTTCACGTG TCTGACTATA TTCTTAGGAG ATTGATGGGT TACATTTTTC TCCTCGATAG 1440 TGGTCATGGG GGAAATGTGT TAATTTTTCA CTTTAGATGT TTGTGAAATG TTGGGGAGAG 1500 TGAGGGGTTT GTTCTTAAGT GGTGGGCCAT TGACCCAAAG TATTTTTAAT TCCTTTTTTA 1560
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