Tag | Content |
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EnhancerAtlas ID | HS195-02673 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr17:17348960-17350400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK4 | MA0076.2 | chr17:17349661-17349672 | GCACTTCCGGC | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr17:17349357-17349375 | CCTTCCTTCCCTTTTGCC | - | 6.03 | EWSR1-FLI1 | MA0149.1 | chr17:17349353-17349371 | CTTTCCTTCCTTCCCTTT | - | 6.23 | EWSR1-FLI1 | MA0149.1 | chr17:17349349-17349367 | TTTCCTTTCCTTCCTTCC | - | 6.2 | ZBTB7A | MA0750.2 | chr17:17349660-17349673 | GGCACTTCCGGCT | - | 6.48 |
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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 |
GH17I017444 | chr17 | 17347707 | 17350904 |
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Enhancer Sequence | AAGCCCCGCA CACAGGCTCC AGCCCATCCT CAGGTCTCTG CCTCCTGCTC CGGCTCTGGC 60 TTCCTCCGCA TGTTGGATTC GTATGGGTTG GTCCCCAGCT GCCCTGTGAG GCAAGGCAGG 120 CCTTGATGTT CACTTGCCAT ATCAGGTCCC GCCTGCCTCT GCAGAAAAAT TTTAGGCTCC 180 TCAAGGTCTG GGTCCACTTC TACTCCTCCT ATCAGAGTGT AAATAAAAAC AGTCTCCTCA 240 TCCTGCCCCT GCTCATATAA CCTCTGTGAC AGGATGCTCA CTACTTGGAG AAGTAACTCT 300 TTTTGCGGAG CTGGTCTCCG CCCCTTCTGT GACTGCCACC CACTGGGCCA GTTCTGCCTA 360 ATAGCAAAGA ACACTGCTCA CCAATCTTCT TTCCTTTCCT TCCTTCCCTT TTGCCCATAA 420 GTCACCGATG GATGGACTGG ACCCATGGGC AACGTCTGTG GATGACGCTG TGTTTGTCCT 480 TCCACAGGGC GTGGGGCTCC TCCACCCTGC ATCAGGCACA AGCCTGCTTT TGGGGAAAGT 540 CCCACCATCT CATTTTCCCT TGCCTAAAAT AGCTACTTCC TTTATGGGGA ATGCAGTGTG 600 GTGGGGAGCA ATGAAAGGGA TGAGGTAAGT CATCCACAGA TGCCTGGTTT GGAATCATTC 660 CTGAAAAGGT CAGCGTTTTC ATCAGCCAAA CAGGAGGCAG GGCACTTCCG GCTGGTCATT 720 AACCAAGGCA AACAGCGTGG CGGGGAAAGT CAAAGCCATA GCCAACCACA AACAAACAAG 780 TCATGTATCC TCTGTGGAGG TGACTTTCTT CTGAAGGAAT GTGTGGTTGT TTGCAGATAA 840 TATCAAATCC ATTTCACGTC AGATCAGGAT GACAGACAGC CAGAGGCTAT TGGGGTCTCA 900 CATTAAATGG CTCTTTTATG GTAATAAATT GTTTCCTTTT CACGGTTGCA TGAGCAATCT 960 CAAGTTTTAT TTTGAGGTGT CAACTGCCCT CAGGGACACC TGCCACAGGT GGGATCTTGG 1020 GTCCTGGCCA CCATATGTGA GAGAGCAGAC CCTGGCTGAG TCACTCAGCT GTGGTCGCAT 1080 CACCTCTGTC CCTGCCCCAC TGCTCAGCCC CATGCAGGCT GGCAGGGGAG GCCTCCTCTC 1140 CCCCATGGGG TCTCCCTTTC TTCCTCTCAC ACTGATCATT GGAAAGAGTG GCTTGCATTT 1200 GCCACAGTGC TGAGGGCTGT CAGTCTTCAC AGCTGAGGAA ATGACATGAT TTGTTGGGAG 1260 CCACTTGAAA TAACCAGTTC CCCAGCTGGT CTCGCTGTCC CTGTGCTGGC AGCCCTGCTG 1320 ACGTGGGGCC TGGCTAGACA GAGGTGGGCC TTCTGTGCCC TCACCTGGGC CATCCCCACC 1380 ATGCGGTGAG GTTGGGTTGC ATCCAGCCAG GAGGCAGCTG GCAGGGCCCT GTGGCTTGTC 1440
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