Tag | Content |
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EnhancerAtlas ID | HS051-17065 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr20:11666600-11668270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr20:11667100-11667121 | GGAGGAAGTGAAAGAGGAGGA | + | 6.82 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTACTGGA AGAAACACAA AAACAGTTTT TCGATGAATG CCTATCTTCA TCCTTGGGAG 60 GCTCAGCTGT GGGCCTGGCT TCCTATGTCA CAGCCTTCCC TGCATGTTTA CGGACCATGG 120 CAGGTTCTTC TGCTGGCCCC CTCTGGTACT CAGAGGGGTT CAGGCAGGAA ACAGATGCTT 180 TTGAATACTT ACTGCCCCAC TTTTCGTGCT CTTTGAAGGA CGCAAGAAAA AGGAGTCAAT 240 CTTTACATGC TTCCCAATTA CAAAAAGTAG CTAGGATGGC AACAATCTGT CTTGACTTCC 300 CCTGTGTTTA CATCCTCCAA CCCAGACCTG AGAAATGACT GTGAAATTCT GACCAAGACT 360 CACTGTTTTG GCAGCTTCCT TTTCCTTTAT TTGCTCCCCA TCCAAAATTC TCCTCCCTCT 420 TAGGGATGTC TAATTTATAC AATTTGTCTA GCAGGTATGG TACTGGTTTA GGCTACATTT 480 GGGAATTCCA GCTGGGGCTG GGAGGAAGTG AAAGAGGAGG ACGGTTCCCA GAAGGCGCAT 540 AACAGGCATT TTCAGTGGGG GCTTTCCTTC TGCCACTCCG ATAAGCCCCT CGAGTTCCTG 600 CCTCCTCCCT AGGAAAGGGT AAGCAAGACA GAAGAAAAGG TCAACAACCA CAACCTAGAC 660 AGTGAAAATG TCTCTGCCAA TTTCGCTGGG GCCCTCCAGG GCTAGTAACC CTCCAACCCA 720 CTTAATGAAT TTAGAGACAC ATTAGATTCA TTTACATAAC AATATTTTAA AGACCACACG 780 ATTGCTTTGG AAAATTGTCT TATTTTTTTT TCCTTCCTCA AACTGAACTG CAGAGTTACA 840 AATACCCTCC CAGAGAGCCT CAGAGGAGGC AAACTTGGCA GAGGAGAGAA CGGAGAAAAA 900 TCCATCCCTT GCAAATGCCA AGCGGAAGAA CAATCCCGTT AGGCGGCCAG TTGATGCTTA 960 ACTGCGGGAC TGGGGGCTCG GGCAGGGATC TTAAACATCA TTTCGCGTAG GGAAACAGGC 1020 ACTCTCCTCT CCCGGAAGAC AAGGCTGCGC GTAGGTTTAT CTCGGCCTCC TGGAGGACCT 1080 GTAGTTTTTG GGAGAGCAGC TGCGAGGGGA CAGAATGCTT CGCTGTGGTG GTTCCGCCGC 1140 GGGCTCCGCT GCCAGGAGGC CGGCGTGCGC GCAGCTCTGC GGCGGGGCAG GCTGCCAGGG 1200 CCCGGGGAGC AGCGGCAGTC TTCCTTGGAG GAGCACCTGT TCTTCCTCTC CCTGCGCCGG 1260 AAACGTGCCA CCTTCCCCCA CCCCATGCTG CTTTCCCCTG CGTGGCTCCA TTTTGTCTTT 1320 CCTGATGGCA GATACCCCCG CGGCCTTCCT CTCGAACACT TGCGGGGCGC TGGGGGAGGG 1380 GACGGCCACG TCAGGCGCAT CCCTTTTCCC AACACCCCAA GGTAGCAGCA GCAGCAGGTG 1440 CTGTGACATT ATGACAAACA CTCAGGTCCC CCGTGACTGG ATGCGTCACA CACTATGTCT 1500 AACAGTCGCT GACATCTCAT CAATCACGGC CTTGATTATG CTGCTGGGGT CCCTGGGCTC 1560 AACTTTGGGC TCTGAACAGA ATTTACTGCA AACTGAACAT CCTTATTTCC AACGTAGGCA 1620 AGCCCGTCTT GTTTATAATG GCATAATCCA GCTGGAAGAT CACACTGGCA 1670
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