Tag | Content |
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EnhancerAtlas ID | HS116-05028 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr10:99681130-99682560 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EGR4 | MA0733.1 | chr10:99681703-99681719 | AAATGCGTGGGTGTGC | - | 6.11 | RORA | MA0071.1 | chr10:99681208-99681218 | ATCAAGGTCA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr10 | 99681191 | 99681488 | chr10 | 99681546 | 99682195 | chr10 | 99682245 | 99682528 |
| Enhancer Sequence | AGGCGGAAGG TAAAAAGGCA TCTTCATTTT CAGGCAGGCA AGGTTCAATT CCTGGCTTTG 60 CCTGTTGCCT CATGTGTGAT CAAGGTCAAG TTGCCTAATT TCTCAAAACC TGAGTTTCCA 120 TATCTGTCAA ATCGGATAGT GACAGCATCT ACCTCATTGG TGTCTTATGA GGATTCAGTA 180 GGACGAGGCA GCTAAAGCAT GCAGCATAAG GCTCGGCATG TCCCTAGTGT AAGAGGTGTT 240 GGCTGTTACT GTTGTCCTTG CTCTCGTGTT TTCCTGCACC ATGCTGCATT CCTCTCTGTC 300 AACTTCCAGG CTGCCCTTGG CCTCTCTCCA TTCCTCCCCT GGCAGTCCTC AGGCCCCAGG 360 GATGGCCAAG GTGGTGGCTG GACTCAGAAA GCAACCCTCC TCTGCTGGCA GACTGACCAT 420 AGGGCTTCTT TCTAGTTCTC TGAGGCCTGG GAGACTGAAG TCAGGGGCTA AGCAGGGTGT 480 GAGCAAGCTT CTGGACGCCT GCCTCCTGTG CTGCAGTGCC AGGTCATCTT TTTTTTTTTT 540 TTTCATTTCA CATAGTGCCT TTGTCCTGTG GTTAAATGCG TGGGTGTGCA GATGACCTTG 600 TTAGGACAGA GTGCATCTCT TTGTGATTAA CCTGCATGCC TCTCCCCCCA GTTCTCTGAG 660 AAGTTGCCCA CGTTAGCTGA GTGTCAAAAG CCTTGGTCCT GAACGGGTGA GATGGGAAAC 720 CGGGAGGAGG CTGGGAAGAG GCCCCTAACC GTGACCAGGT CTGGCACCCC CCAGCTCCAC 780 CCCACACTCT GGGGCTGTTC ACAGAGCTGC CTTCCCATCT ACTCCCACCA GGCAGGAGTC 840 CAGGTGGCAC AGATTCAGGT CAGGCTAAAT GTGGCTTCAC AGCCCAGCTT GGCTTCTCTT 900 CCCAGCGCCA GCTTGTTAAG AAATAAATAT TTATACCTGG CACCTGCCTT CTCCCAAGGC 960 CTGGAGGCCC CTGCTGTAAA GATTCACACT GAATCCCCAA TCCCCTCGGT GCCATCTCAA 1020 TCCCAAAGTG AGCCAAACCT CTTGCCCCTG CCCCCAGAAT GGGGGCCATA GACACTCCTG 1080 TGGCAGCCGG GCAGCAGCTG GGCCCCTGAT TTAGTGATGA CTGTTTACAA AGCCAAGGAG 1140 GTGGGTGGCA GGGGAGCAGG TGACAGGAGG GATAAATCAC CTTTGCAGCA AGCTGCTGGC 1200 TCTGGCGAGG CCTGCTGGGA CCTAAGCCTG GGTGGGCGGC TGCCCCCTCA CCGGGCAGAT 1260 GGCTGCAGTG GCTCATGCCC CTTCCCACTC CGTCTTTCCT CCCCATCCAG TTTGGGTGGG 1320 GCACCTCTGT GTAGGGTGCA CTTGCAGAGC ATGAAAACGT TGGAGGAGCT ATTGATGAAC 1380 TAAAGTACTC GTATATTGAG GCAACCCTCC CTTCACCCAT CTAGGAACCC 1430
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