| Tag | Content |
|---|
EnhancerAtlas ID | HS176-21520 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr2:122456810-122457950 | 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 | CCTGGGTAAC ATGGTGAAAC CTTGTCTCTA CAAAAAAAAT ACAAAAATTA GCTGGGCGTG 60
GTGGTATGCA CCTGTAGTCC CAGCTACTTC AGAGGCTGAG GTGGGAGGAC GGTTTGAATC 120
CTGGAGGTGG AGGCTGCAGT GAGCAGAGAT GGTTCCACTG TACTCCAGCC TTGGCAACAG 180
AGTGAGACCC TGTCTCAAAA AAATATGCAT TTTAGGTATA TTTACCCCAC ACACACACAT 240
ACAAATAGGC CAGTGCAAGA TGAGCCAGAA GAGAGCTGCT TCGTTCAGTC TGAGTGACTA 300
AGAGTGATGA TGCCATCCAC CCAGACAGGA AGCAGACCGG GTGAGCGGGT TTGTGGGGAG 360
AGATGAGGTC AGCTCTCAGA GGTGACAACG CTCCTAATGA TCAAACCCTC AGTAGAGGCC 420
CACTGTGCCC GCATGGGAGG TGCTTTGCCC CCACCTCCCT CAGCCTTGCA AGGTGAAGGC 480
TCTTGCTTTC ATTTCACAGG GAAGCTAACG GTGTTTAGCC AGTATGACCC AGATTTGTCC 540
AGCCCACTGT GCCTGTCTGG GTTCGGGTGC TGAGGGCCAT TCCTTGTGAT GCGGCCAGCA 600
AGCAAGGGGC GACCTGGAGC TGAGAGAGGA GGTGAGAGTC AGAGGAGCTG CAACATTTCC 660
TGCACTGAGA TCCTGGTAAA GCCACAGGCA TGGCTTGGCC CCCGCAGGAA GGAAGCAAGA 720
GGGAGAGAAG GGGGAAGCCC TACATGTAAG ACACTCTCTC TACTGAGTCC TGCCGATCAC 780
AGCAGCTCCT CCTGGAGAAA TGTCCACCCC AGTGTCGCCA AGTTAAGACC TCGGCCTTGC 840
TCAGCACCTG CCCAGCAGCT GATGCTAGGA CCTCTGCCAA GCATGAGGAG AGGAGCCAGC 900
TCAGAGTGAC TCATTGTACA TCAGCCTGGC TCCATGGATC CGGATCAACG CCCTGGACCT 960
CACCTGGCAG TGAGGAACCA GTGGGAAGAG AGGTGCGTGC TGGACTCCAC TGGACAGCAC 1020
GTAGTCTCTC GGTGGAAGCA AAGACACCAG CCTTGCACCG AGCCAGCCCA GCCAGGGAAG 1080
AGTGGAGAGG AGGCAAGGCT GGGGGCTGGT GGGTGACTGT GTAATTCCCA AGCCAGGTGA 1140
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