| Tag | Content |
|---|
EnhancerAtlas ID | HS095-02700 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr1:204653280-204654440 | 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 | ACAGTGACCA AACTGGCAGG GAGTCACCTC TACTGCCCTG ACCTAGGGAG GCTGTTCTCC 60
TCACCACCCT AGGTCCTGGA GTTCTCAAGC AGAGGGCCTG TCAGTCCATC TCTGGCAACT 120
GAGCGCTGTG CCCAGCCCAC CCCCTCCAAC CCTGCCAGTC GCCCAGTTAG AAGCTGCGTT 180
GGCTCCAACA GATGGGAGCT GCGGCAGCCT GAGGAACAGA GCACAAAGCC CAGCTGACAT 240
TTTCCTTCCT GTTCGTTTGG GTGGGGGAGG AAGGGTAGGG AGCACAGTGC TACCCCCGGG 300
GCCCCTCCCC AGGTTCCGGG TCTCCTGCAC CTCTTTAGCT TCTCCGCTCG GCCCCAGATG 360
GAGCTCAGTT CCCTCACCCC GCGGCTCCTC GCCGGCTGGG CAGCCAGAGC CTGCGCCACC 420
CTTTGCCAGC AGGACAGACG GCCCACCTGT GGCTGGCCAG CCCATCCTGT CTCCTGGGTC 480
CTGCGGTGGG CTCAGAGCCA CCCTTCCGTT TCCGCTTCCC CCTGACCGAG TCCCCAGGCT 540
GAGCCCCAGG CCGGCCCATC CCCCACCCCA AAGGTCCCAT CCCAGGCTGC GGTCGGACCC 600
CAGCCAGCCG GCCCGGGAGG AGCCTAGCTC CTGGTTCCAG ATACTTCAGA CAGACCCAAG 660
GCCACCTTGT CCCTCCGCAC AGACTCGCGA GCTCCAAGGA GGAGAAAGTC CCCAGGCTCT 720
GGAGCGCTTC CAGCCTGCCA GTCCGCCCGT GTCACGCCCT CCCTAACCTC ACTGCCACCT 780
CTCGGCTCCT CCACATCTCC AGGGCCCCAC TCTACCCAGC AACAGTTTGG GGGAGGTTCT 840
GGCCTCTCCA GGCGAAGGCC CAGGCGCCCT CTCCCTGGCC GCTTCTGGGC ATTCTCCAGC 900
CCTCCGTCCC TCTGCCCCTC GGCCGCCTCC CTCTCCCAAG TCTCCGGCTC CCCCGCAGGC 960
GTCTCGGCGG AAGGCAGCGG CCGGCCCTCC TCTGGCCCCC ACCCGGGTCA GGCGGAGCTG 1020
CGGTGCCGGG GCAGGAGCCA GGAGCCCTGA GGCGGCTGCT CCGGCCGCTC CCGCCGCGTA 1080
CGCCTCGGCC ACGCCAGCGA CCTCGGTGTC CACGATTCCC CGGCGGCGGC GGCGCTGCCC 1140
AGGTCAGCCC CGAAGCTGCA 1160
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