Tag | Content |
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EnhancerAtlas ID | HS051-23533 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:41735980-41737470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr6:41736830-41736851 | GGAGGAGGAGGAGAGAGGCAG | + | 6.36 | ZNF263 | MA0528.1 | chr6:41736824-41736845 | AGAGGAGGAGGAGGAGGAGAG | + | 9.28 | ZNF263 | MA0528.1 | chr6:41736827-41736848 | GGAGGAGGAGGAGGAGAGAGG | + | 9.5 |
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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 |
GH06I041766 | chr6 | 41734169 | 41737506 |
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Enhancer Sequence | GTCAGGACAG GTCTCTTAAG CCAGCCTCTG GCTACCCCAT CATAGTATCT GTCCATCGAT 60 AAGGCGGAGC CTGCACTGAC CCATGAGTCA CAAACACGGC CAGGACCCCT AAGCCTGGTC 120 CCGGCATAGC CATACCTGCC CCCACATATC CACCCTCCTG TTTGGAGACA CCCACCACCC 180 CAACTGTGGA GGTCATGAGT AGTAGCAGGG GTAGTGTATG TGGACATCCA AACAGAATTG 240 AGCTGCTTGG TAAGGCTGCA GAGAGAAGAC AGCATTTCCC TACTACAGTG TGGAAAACTG 300 CAATGAATCC AGCCTGCAGC AGGTGACCCC TCTGGTCCAG AGATCAAAAG GATATAAGGG 360 GGAGAAGGGT TTGGTGCCAG CTCTGGGGTT GTGGCAGCTG CCCTCTTGAG CTCTGCTGGG 420 CCCCACTCGA AGGGCCTTTT CACATCCTGT TGTGGCCAGT CGTCACTGCC CATTTCACTG 480 ACAGAAAGTG ACACCTGAGG TCGGGGGGTC TGAAAGCTTC CAGTCCAACC CCCACTCAGA 540 GGAGGTAGGA TCCAGGAAAT GAGGCCCAGG CAGCAGTGTC CTGGACAGTA GGAGGGGGAG 600 GGAACTGGGT GGGGTGTCTC GCCTGGGCTT GTTTCCTTGG TGACGAAGAG GACAGGTCTG 660 CTTGCTCCAC AGGACAGGGA GCTGGAGCAC AAACAGTGAC AAGGCTTTTC CCCAAGTTGG 720 ACAAACACAA CTCTCATTCT TCACCTGGGC CCTGAGTGGC TTATCACAAA AGCAGCATTT 780 CCTTTAGATG AACCGCACTG GGGTTTCAGA CAGAAATGGA GTCTTGGAGG AAAGGAAGCC 840 AGCAAGAGGA GGAGGAGGAG GAGAGAGGCA GCCTCATGAC AGAGAAAGGA GCTCCTGGAA 900 CAGATCAGCA CTAGGTTGTG TGTGCAGCAC AGCCCCGCTG GACCCTGTGC TTCCAGGCAG 960 GTGCTCCAAT GTGGCGGCTC TGTTAGCGCC CAGCCTTGTG GCAGGGTAGA GGCATCCTAA 1020 CAGTCCATTC CTGAAGGGAC GTTCTCTAGG AAAGACACTT AGCAAGCCAG ATTATCTAGT 1080 TACACATTAC ACTGTATTTT TTCATTTTGC TATAATCCTA GGATTTTAGT AAAGTCCTGT 1140 TTAAAGGTTT GGTCTTGACT CAGCCATGCT GGGGGCAGCT AAGGAGGATC CAGGATCCAT 1200 CTCTGGGCCA AGGTGGTAAA GGACAGCAGT GCCCTTTGGG GCCTGCCTAT TGGCAGGGGC 1260 GTCAGTGAGG GCTCCCCAAG AAGGCGAAGG TGTCTCTTCT GTAGCTGTGC CCGCTCCGCT 1320 GCACTCCTCA CCTGTTACCA GCCTCAGAGG GCTGGGCTCT ACCTCATTAG GGCAGTCCTC 1380 ACAGGCTCCC CTTTTGGCTT CTAGGACTCC AGCCATCCCA CCCCTTTCCT TCAACAGAGC 1440 ATCCATCCCT GGCAACTGTA GGTTCATGAC CAGGGCTTCT TGGAGGAGAA 1490
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