| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02893 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:204652960-204654440 |
Target genes | |
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 | CTTCTGTTTC CATCGTTTCG CCACAACAGC ACCTGGCCAG GAAAGTGGGT CAGGCCACCC 60
ACATGTGGCT TTTTCTGGTA GCCACAGGGC CCAAAGGCAA GGGGGCTCCA GTGCCCAGTG 120
CAGAGCCCAC CTCTACCCTC CATGCCCAGT GCTCTTTTTT GAAGGGATCT TTAAGAAGCA 180
GTGGGCAATG GGAGGAGCTC CTGGCCTTCT TATTCAGGGA CAAAACGCTG GGCCAGAGCC 240
CATCCTAGAC TGGCGGGAAA GGGGGGCACG GAGCCTGCCA TCGGCCTGGG TGCATGGGGA 300
GACCTACATC TTCCCCTATG ACAGTGACCA AACTGGCAGG GAGTCACCTC TACTGCCCTG 360
ACCTAGGGAG GCTGTTCTCC TCACCACCCT AGGTCCTGGA GTTCTCAAGC AGAGGGCCTG 420
TCAGTCCATC TCTGGCAACT GAGCGCTGTG CCCAGCCCAC CCCCTCCAAC CCTGCCAGTC 480
GCCCAGTTAG AAGCTGCGTT GGCTCCAACA GATGGGAGCT GCGGCAGCCT GAGGAACAGA 540
GCACAAAGCC CAGCTGACAT TTTCCTTCCT GTTCGTTTGG GTGGGGGAGG AAGGGTAGGG 600
AGCACAGTGC TACCCCCGGG GCCCCTCCCC AGGTTCCGGG TCTCCTGCAC CTCTTTAGCT 660
TCTCCGCTCG GCCCCAGATG GAGCTCAGTT CCCTCACCCC GCGGCTCCTC GCCGGCTGGG 720
CAGCCAGAGC CTGCGCCACC CTTTGCCAGC AGGACAGACG GCCCACCTGT GGCTGGCCAG 780
CCCATCCTGT CTCCTGGGTC CTGCGGTGGG CTCAGAGCCA CCCTTCCGTT TCCGCTTCCC 840
CCTGACCGAG TCCCCAGGCT GAGCCCCAGG CCGGCCCATC CCCCACCCCA AAGGTCCCAT 900
CCCAGGCTGC GGTCGGACCC CAGCCAGCCG GCCCGGGAGG AGCCTAGCTC CTGGTTCCAG 960
ATACTTCAGA CAGACCCAAG GCCACCTTGT CCCTCCGCAC AGACTCGCGA GCTCCAAGGA 1020
GGAGAAAGTC CCCAGGCTCT GGAGCGCTTC CAGCCTGCCA GTCCGCCCGT GTCACGCCCT 1080
CCCTAACCTC ACTGCCACCT CTCGGCTCCT CCACATCTCC AGGGCCCCAC TCTACCCAGC 1140
AACAGTTTGG GGGAGGTTCT GGCCTCTCCA GGCGAAGGCC CAGGCGCCCT CTCCCTGGCC 1200
GCTTCTGGGC ATTCTCCAGC CCTCCGTCCC TCTGCCCCTC GGCCGCCTCC CTCTCCCAAG 1260
TCTCCGGCTC CCCCGCAGGC GTCTCGGCGG AAGGCAGCGG CCGGCCCTCC TCTGGCCCCC 1320
ACCCGGGTCA GGCGGAGCTG CGGTGCCGGG GCAGGAGCCA GGAGCCCTGA GGCGGCTGCT 1380
CCGGCCGCTC CCGCCGCGTA CGCCTCGGCC ACGCCAGCGA CCTCGGTGTC CACGATTCCC 1440
CGGCGGCGGC GGCGCTGCCC AGGTCAGCCC CGAAGCTGCA 1480
|
