| Tag | Content |
|---|
EnhancerAtlas ID | HS007-01261 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr1:204653220-204654440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:204653542-204653563 | GGGGGAGGAAGGGTAGGGAGC | + | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I204684 | chr1 | 204653343 | 204653636 |
| Enhancer Sequence | GGGGGGCACG GAGCCTGCCA TCGGCCTGGG TGCATGGGGA GACCTACATC TTCCCCTATG 60
ACAGTGACCA AACTGGCAGG GAGTCACCTC TACTGCCCTG ACCTAGGGAG GCTGTTCTCC 120
TCACCACCCT AGGTCCTGGA GTTCTCAAGC AGAGGGCCTG TCAGTCCATC TCTGGCAACT 180
GAGCGCTGTG CCCAGCCCAC CCCCTCCAAC CCTGCCAGTC GCCCAGTTAG AAGCTGCGTT 240
GGCTCCAACA GATGGGAGCT GCGGCAGCCT GAGGAACAGA GCACAAAGCC CAGCTGACAT 300
TTTCCTTCCT GTTCGTTTGG GTGGGGGAGG AAGGGTAGGG AGCACAGTGC TACCCCCGGG 360
GCCCCTCCCC AGGTTCCGGG TCTCCTGCAC CTCTTTAGCT TCTCCGCTCG GCCCCAGATG 420
GAGCTCAGTT CCCTCACCCC GCGGCTCCTC GCCGGCTGGG CAGCCAGAGC CTGCGCCACC 480
CTTTGCCAGC AGGACAGACG GCCCACCTGT GGCTGGCCAG CCCATCCTGT CTCCTGGGTC 540
CTGCGGTGGG CTCAGAGCCA CCCTTCCGTT TCCGCTTCCC CCTGACCGAG TCCCCAGGCT 600
GAGCCCCAGG CCGGCCCATC CCCCACCCCA AAGGTCCCAT CCCAGGCTGC GGTCGGACCC 660
CAGCCAGCCG GCCCGGGAGG AGCCTAGCTC CTGGTTCCAG ATACTTCAGA CAGACCCAAG 720
GCCACCTTGT CCCTCCGCAC AGACTCGCGA GCTCCAAGGA GGAGAAAGTC CCCAGGCTCT 780
GGAGCGCTTC CAGCCTGCCA GTCCGCCCGT GTCACGCCCT CCCTAACCTC ACTGCCACCT 840
CTCGGCTCCT CCACATCTCC AGGGCCCCAC TCTACCCAGC AACAGTTTGG GGGAGGTTCT 900
GGCCTCTCCA GGCGAAGGCC CAGGCGCCCT CTCCCTGGCC GCTTCTGGGC ATTCTCCAGC 960
CCTCCGTCCC TCTGCCCCTC GGCCGCCTCC CTCTCCCAAG TCTCCGGCTC CCCCGCAGGC 1020
GTCTCGGCGG AAGGCAGCGG CCGGCCCTCC TCTGGCCCCC ACCCGGGTCA GGCGGAGCTG 1080
CGGTGCCGGG GCAGGAGCCA GGAGCCCTGA GGCGGCTGCT CCGGCCGCTC CCGCCGCGTA 1140
CGCCTCGGCC ACGCCAGCGA CCTCGGTGTC CACGATTCCC CGGCGGCGGC GGCGCTGCCC 1200
AGGTCAGCCC CGAAGCTGCA 1220
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