Tag | Content |
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EnhancerAtlas ID | HS116-11241 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:94507870-94509600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr14:94508829-94508849 | GGTTTGGGGGTGGGAGGGGG | - | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 94509158 | 94509472 | chr14 | 94508089 | 94508868 |
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| Number: 3 | ID | Chromosome | Start | End |
GH14I094041 | chr14 | 94508262 | 94508390 | GH14I094042 | chr14 | 94508441 | 94508590 | GH14I094043 | chr14 | 94509441 | 94510231 |
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Enhancer Sequence | TGGGCTCAGG CGGTCCTCCC TCCTCAGCCT GCATCTTCTT AACACAAAAA CCGAGACCAT 60 GTCACTCCCA AGCTTGAAAT ATGCCCCTGA CCTCTAGGAG CAGTGGAAAC CCCTGACACC 120 AACGCCCTCC ACACCAGGCC CCTGCCTCTC CTGCCCCGTT GCCTACCCAC CCTGAGTTCT 180 AGGCACAGGG ACTCACTTAT CCTACACACA CCAGAGCTTG CAGGCATGAC ATGCCGCCTG 240 ACGCTGCCTG GGCCTAGGTA GCCCTGCTTC TGACCCGGCT GTGGGTTCCT TGGGCCCCAG 300 GCAGGCTGCT TCACTCACTC CTCTGTAGCT CCTTTCCCCA GTTGAACAGT GGCCATAGCC 360 CTGTCACGGA CATTAAGTGA TTGACTCGTG AGCACTTGGA ACACTGACCT GGGGTGTTCC 420 GTGCTAGCTC TTAGCGTCAG CGTCATGCAT CCTCCACAAG CCACTGTCTC CCTGTGTGCA 480 GTGAGCCCAG AGCCACCCAG GCAGACACTT GTTCTCTGCT CAGTGCTGCT GCAGGGCTGG 540 AGCAAGCGTG TTGCAGCAGT ATGCTTGTTC CAGCCCTGTA TCTTGCATAC TTGCTCTAGA 600 AGTATGCGAA GTACTTGTGT GTGCCAGAGG CTTGGAGAAC ACGCGCCGCC TCTGAGGGCA 660 GCCACTGTTA CTACCACATC TGATGAGCAA ACAGAGCCTC ATAGAGGTCA AATGACTTGC 720 CAGAGGTCCC ACACAGGCTT GTGTGCAGCC CCAGCGGTCT GAACTTGCAC CCCCTCCAAG 780 CCCCAGTGCT ATCCTTCTCC CTATCCCTGG CTTGCCTCTC GGGGGTGCAT GTCCTGGCCT 840 GGGGGCTTGC CCCCTTCTGA CAGAGCCTAC GACTGCATGC TGCTTATCTC CGTGCCCCAG 900 TGCCTGGCAC AGAGGGGCCC ACAAGTCACT GGCGAGGAAT GAATGTGGAA TGAGGCAGAG 960 GTTTGGGGGT GGGAGGGGGG GCAGGAGAGC TGGGAGCAGA GCAGTGCACT TCATGGCCAT 1020 GCAGGGACAG AGTGGCTAGA AGAGGGTGCC GGCCCTTGGA GCAGCCCTGG AGGACTGCAG 1080 CTGCTTCCTG GAGCTGCTTC TAGTACTCTG GCCATGGGCC ACCTAGCCGC AGCTGAAGAC 1140 TGAACAGGGG GTGCTGATGA GGGTGGCTCC TGAGTGAGAG GCGTTAGCCA GCACTGACCA 1200 TCAGATCCTT GCCCTGGCCA GGAGGGGAAA CCTAGGCAGC AGGTACCACT GCAGTGGAGG 1260 CCTCGTCCTC CCAGGCAGCT CTCCGTTCGC CCTCAGCACC CCTGCAGTCA AGGCGTCATC 1320 ACCATCCACA CTTGCGCCAA AGTGGAGCTT ATGGCCAAAA GCCACAGGGG GACTTGACAG 1380 GGCTGGAGGG GACTGCGGCT AGAAGCCAGC ACAGGCTCCA TCCCTCCAAT CCAGGCACCT 1440 CACCCTGCAA TCAGGACAAA CTAGTCCTGG CCCAGGCAGG ACTGTTAGAT ATGCCAGGAC 1500 CAGGCAGGGG CAAGCGGCAT CTAGGCAAAT ACTCCTCCTT CTGAGTTAGG AGACCAGCTT 1560 CCCGTCCACA CCCACCACCT TCTCCCTCCT CACTGCCCCC TGTCCTCCTA CAAGGCACCA 1620 GGCTTTTCTG GAGCACAGCA CCTTCTGAGG TGGCCCAGGC CTCTGTATTC CCTTGTGAAC 1680 CTTCTGCCTC CTGGGTGCTG TCAGAGCCTC ATCTCCGTTC CCAGGCAAAG 1730
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