| Tag | Content |
|---|
EnhancerAtlas ID | HS073-08560 | Organism | Homo sapiens | Tissue/cell | GM19238 | Coordinate | chr2:122456920-122457900 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:122457521-122457542 | GAAGCAAGAGGGAGAGAAGGG | + | 6.5 |
| | | 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 |
| GH02I121698 | chr2 | 122456236 | 122459153 |
| Enhancer Sequence | GGTTTGAATC CTGGAGGTGG AGGCTGCAGT GAGCAGAGAT GGTTCCACTG TACTCCAGCC 60
TTGGCAACAG AGTGAGACCC TGTCTCAAAA AAATATGCAT TTTAGGTATA TTTACCCCAC 120
ACACACACAT ACAAATAGGC CAGTGCAAGA TGAGCCAGAA GAGAGCTGCT TCGTTCAGTC 180
TGAGTGACTA AGAGTGATGA TGCCATCCAC CCAGACAGGA AGCAGACCGG GTGAGCGGGT 240
TTGTGGGGAG AGATGAGGTC AGCTCTCAGA GGTGACAACG CTCCTAATGA TCAAACCCTC 300
AGTAGAGGCC CACTGTGCCC GCATGGGAGG TGCTTTGCCC CCACCTCCCT CAGCCTTGCA 360
AGGTGAAGGC TCTTGCTTTC ATTTCACAGG GAAGCTAACG GTGTTTAGCC AGTATGACCC 420
AGATTTGTCC AGCCCACTGT GCCTGTCTGG GTTCGGGTGC TGAGGGCCAT TCCTTGTGAT 480
GCGGCCAGCA AGCAAGGGGC GACCTGGAGC TGAGAGAGGA GGTGAGAGTC AGAGGAGCTG 540
CAACATTTCC TGCACTGAGA TCCTGGTAAA GCCACAGGCA TGGCTTGGCC CCCGCAGGAA 600
GGAAGCAAGA GGGAGAGAAG GGGGAAGCCC TACATGTAAG ACACTCTCTC TACTGAGTCC 660
TGCCGATCAC AGCAGCTCCT CCTGGAGAAA TGTCCACCCC AGTGTCGCCA AGTTAAGACC 720
TCGGCCTTGC TCAGCACCTG CCCAGCAGCT GATGCTAGGA CCTCTGCCAA GCATGAGGAG 780
AGGAGCCAGC TCAGAGTGAC TCATTGTACA TCAGCCTGGC TCCATGGATC CGGATCAACG 840
CCCTGGACCT CACCTGGCAG TGAGGAACCA GTGGGAAGAG AGGTGCGTGC TGGACTCCAC 900
TGGACAGCAC GTAGTCTCTC GGTGGAAGCA AAGACACCAG CCTTGCACCG AGCCAGCCCA 960
GCCAGGGAAG AGTGGAGAGG 980
|
| |
|
|
|
