Tag | Content |
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EnhancerAtlas ID | HS043-44507 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr9:135965400-135966980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr9:135966723-135966739 | GGGGGCAAAGTCCTGC | + | 6.09 | Myog | MA0500.1 | chr9:135965646-135965657 | CTGCAGCTGTC | - | 6.62 | RARA(var.2) | MA0730.1 | chr9:135966530-135966547 | TGACCTCACCATGGCCT | - | 6.04 | Tcf12 | MA0521.1 | chr9:135965646-135965657 | CTGCAGCTGTC | - | 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 |
GH09I133090 | chr9 | 135966034 | 135967223 |
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Enhancer Sequence | TTCATTCTTT TGTTACTTTG TGAGTTTTGT TCACTTCTTT GTTCAATACA CCAAGAACCT 60 GGACAACTCA GTCAGGACCT TCCATCCTAT AACACCTCAA CCTCGGACTT CTCAGCCTTC 120 ATAACTGTGA GAAATTCCTT TTCTTTATAA ATTACCCGGT TTTAGGTATT CTGTTATAAG 180 CAACAGAAAA TCTACTTTAA AAGCCTCCAT GGCACAGGTG AGCCCTGCAG TGTGTCTGGG 240 TGATGCCTGC AGCTGTCGAG AGGGAGGAGA CAGCTCAGAG TCACCTGCAA TCTGGCTCTT 300 GCCATTACAG ACTCCAGATG ATGAAGTTGA AAATACTGAC AGGCTGGAGG CCATCTGGGG 360 TCCTGCTGGC TCCCAGTTCC AGGAAGCCTG GAAGAGCACT GGGGTGAGCT CGGGCCAGCG 420 CATGTTTACT GTCACAGGGG ACATGTTTCA GCACTTTCAT TGTAAGGCTG TGGCCTTCTG 480 TGCTTGTGGA TCCTCAGTCT CAGTGGCCTT CCTCTTCCCC CCACCCCAAC TCCTGTGTTG 540 CGTGTTTAAC ACACCTACGC CCAACCGGGA CATAACTAAA TCCTAGACTG TGGACAAAGA 600 ATACAGTCAC CTCAGGGGGC TGCGAGCTCT AAAGGCTCAG GGCCCAGCTA CCCCTTTAGG 660 ATGGGTCAGT AACAACACGA CTGACTCTGT AAATTGGTGA TCACCTGAGA CTGGACCTCA 720 GCACCACACG GACCTGTGCT TCACCTTGGC CATCGGGGGA GAGTATGGAG GTCTTTTGCT 780 GGCAGGAATC AGCACCCTTA TCCTGGCAAT CAGCACTCAC TGGCCATTCA TGAGGCTCCA 840 GCAGGACGAG TGGCCACAGT GTGCAGGGCA CAGGGGATGG GGCTTTCCAA GGTGTTTCTG 900 GATGACATCA ATCACACAAG GAGTTGTAGG AATGCTGGCA TCCTGGTTCA CGGGTAGACG 960 CCAGAGGATG CCAAGGGTGC TGGGTAGAAA GCAGAGGATG CCAAGGGTGC TGGGTGGTGG 1020 GCCCCTTGGG GGTGCCCAAT GGCTCTGGCA GAGTTGTTGG GGCAGAGTCG GGACCACCCC 1080 CACCTCTTCC GGGTCCAAGC CCAGGCACTG CACTGAGCAC TTGATGAGCC TGACCTCACC 1140 ATGGCCTTGT GACGTGGGCA CTGTGGGCAG GAATGCTTAT GGAATGAGGC CCACTGTAAC 1200 CCTAACACAG CATCACAAGT CTTTCCCCAG AGAGAAAACG CACAGGCAAT GGAAATCTAT 1260 GGTTAGGAAC AAAGATTCCC GTCTAAGAAA AAGGGTGGAC CACGGGCCTC TAGAAGGGAC 1320 TGAGGGGGCA AAGTCCTGCC CGTGCACTGG CTAACACTCT TCCTTTAGCT TTTCCCCCCC 1380 ACTTTCCATA TTGTACATTT TATCTGTTTA TAATTTTTCT TAGTGCTGAC TAAATTCCAG 1440 AGTTAGACCT TGAAATCCAC AAGTTCCTAA TTGGTGGTCA ACAGAAACCT CAGCAAGACA 1500 AGCAGAAAAT GCTCCTCTTC CCCTAAAGCT GTAGAAAGGC AGCCACCAAC CTGGGCTAGG 1560 AAATGGTCCT TACAGATACT 1580
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