Tag | Content |
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EnhancerAtlas ID | HS062-07410 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr17:74294710-74296020 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:74295400-74295419 | TGGCGCCACCAAGTGGCCA | - | 6.82 | RARA | MA0729.1 | chr17:74295601-74295619 | GAGGTCAGAAGTTCGAGC | + | 6.44 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTAAGACA GAGTCTCGCT CTGTCGCCCA GGCTGGAGTT CAGTGGCGCG ATCTCGGCTC 60 ACTGCAACCT CTGCCTCCCG GGTTCAAGCG ATTCTCCTGC CTCGGCCTCC CGAGTAGCTG 120 GGATTACAGG CGCATGCCAC CACGCCCGGC TAATTTTTAT ATTTTTAGTA GAGATGGGGC 180 TTCACCATAT TGGTCAGGCT GGTCTCAAAT TCCCGACCTC AAGTGATCCG TCTGCCTCGG 240 CTTCCCAAAG TGCTGGAATT ATAGGTGTGA GCCACAGCGC CCGGCCCTGA GTGTAGTTTT 300 TATTTGCTTT TGTAGCTTTT CAAACTTTCT TTACAGTCTG TCCTGAAATG CAGGGATCTT 360 TCCTTATTAG TGGGCCATGG TGACAGACCC TGGAAATAAA ACTTCTGTAG GGGGCCCTCT 420 GCTGATGGCA ACTTTTGCAC ACAGGCATGC ATCTGTCTGT CTTGAGACAG TGTACAGATG 480 ACCAAATTGT TTTCCGATCG CCAACCTACC TTCACCTGAA TAAAATCAAG CTGAATATGT 540 TCAAATGGCC CTCAAAGATG AGGCTTAACT TCCCTTTTGG TCTTGACATC CCTCCCGCTG 600 GCTTTGGGCT AGTGGGTTAT CAAAACAAGC AAGCCAACTT TGAGGGCCAT TTGAAAATGT 660 AGACGGAAGC AGGGTGAAGA GTAAAGCTTT TGGCGCCACC AAGTGGCCAT CTTGGGGAGC 720 GCCAAATATC TGGGTACAAA AGACAACCTG GGATCTCCAG GACCATTTTC TGATTTCAGG 780 GCTCATTCTC AGAGGAAAGC GGCATCAGAA AGATGTTGCA AGAGGGGCCG GGCGCGGTGG 840 CTCCAGCCTG TAATCCTAGC ACTTTGGGAA GCCGAGGCGG GCGGATCACC TGAGGTCAGA 900 AGTTCGAGCC CAGCCTGGAC AACATGGTGA AACCCTGTCC CTAGTAAAAA TACAAAAATT 960 AGCTGGGCGT GATGGTGGGC GCCTGTAATC TCAGCTACTC GGGAGACTGA GGCAGGAGAA 1020 TCATTTGAAC CCAGGAGGTG AACGTTGCAG TGAGCCAAGA TTGCGCCACT GCACTCCAGC 1080 ATGGGCGACA AAGCAAGACT GTCTCAAAAA ACAAAACTAA ACGATATTGC AAGAGGACCC 1140 TGAACACAAA AGGAATGGAC TAGAAAAAAG TGGCCTCCAC TTTCACTTTT TTAAAGCCAA 1200 ACCTTTTTTT TTTTTGAGAC GGAGTTTCGC TCTTGTTGCC CAGGCTGGAG TGCAGTGATG 1260 CGATCTCGGC TCACTGCAAC CTCCGCCTTC CGGTGGTTTC AAGCGAGTCT 1310
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