Tag | Content |
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EnhancerAtlas ID | HS116-17773 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr2:23892260-23893450 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr2:23892657-23892671 | CAGGCCTGGCCCCG | - | 6.24 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 23892318 | 23892426 | chr2 | 23892400 | 23893211 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I023669 | chr2 | 23891880 | 23893663 |
| Enhancer Sequence | GGGAATAGCC TAGGTGCCAC CCTCCTCTTC CAGGCTCCCA CGCAGCCTCC GTTTCCCTTC 60 CACACAGTCC TGCCCCACAG AGTAGATAAC TGTACATGCA GAGAAGACTC CCTAGGGCAG 120 AAAGCCAGAT TGTTGCATCA CTTCTGCCCC CTGCACAGGG CCCGGCACAC AGTGGGGGCT 180 CCCTGAGTGC TGGGTACCCC GTGAGCAGCA CCCGTGGCCC GTGCTGGACA CAGCCTGTTG 240 GGGAGACTGG TCCTTCTCAG CGTTTGTGTT CACGTAGGGG ATGGTCCCCC CTCTGTGTGG 300 CTGCCCTGCC ACCCCCAGTC AGCCTCTGAG CACAGTGGCC GGTGCCCAGC TCATTTAGAG 360 CTGAGGCCCC CAGAACCCAG GGCTGCAGCC GAGTACACAG GCCTGGCCCC GCCAGCGCAG 420 GACAGCAACT CTTGGGTAAC TGTGTCCATT GGATTTGTAA AAACAGGGCC GTGGTATTAT 480 CACAGAATCT GGTAGGTTCT GCTTCCAAGA AAAACAGACT GTCAAGTTAA ATACATGTGG 540 GTAGGGACCC AAGCAGAGAG GGGTGTCAGT AAAGCCAGAA GCTCAGCTGA AATGGTAGGG 600 ACCCATGAAA AGTCCCATGC AGGGAGAATT GAGCCAGAAG GCCCCAGAGC ATGGGCCGTG 660 TGCCCAGTTA GGCCTCTCCT TCCTGCATCT GGGTTCTCAG GCGTGTAGAT CGTCACGTGG 720 AGCCCAGTGA GTGCCAGAGG CTGCACAGGG CTCTGGGAAT ATCGGGGGAG GGAAAGGCGG 780 CGGCTCCACC TACCTGAGCT CGCGGGCTAA CTGGAAGACA GGATTCAGCA GGCAAAGATC 840 ACACACCCAG GAGGAGGGAT TGGCCTGGGA CGCAGGGAGA CCAGGCACAA CCTGGGGGTT 900 GGGAGGACGG GGGTGTCAGT ACAGCCCACC TGTTGGTCCT TTCTGGGACC TCATGAGACC 960 AGGCCGGGTG CCTCCTCACA AGCTGGGGCA CGACTGGACT CGCCGACCGG TGTGATGGGC 1020 AGGGGGGTGT GCTGGGCACC GTGCCTGCTA CACAGGGGCA CCGAAGCAGT GTTCCACCCT 1080 TGGCAGGATG AGGGGCTGAC TCCCAACTGT TGCATGGTCC CCCCAACCCC CAGGCCTGAC 1140 ATAGGCCTCC TAAGGCAGAC CTGACTCCCT GACTCTGTGC CAGGGCCTGC 1190
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