| Tag | Content |
|---|
EnhancerAtlas ID | HS047-19697 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr2:122456890-122457940 | 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 | CAGCTACTTC AGAGGCTGAG GTGGGAGGAC GGTTTGAATC CTGGAGGTGG AGGCTGCAGT 60
GAGCAGAGAT GGTTCCACTG TACTCCAGCC TTGGCAACAG AGTGAGACCC TGTCTCAAAA 120
AAATATGCAT TTTAGGTATA TTTACCCCAC ACACACACAT ACAAATAGGC CAGTGCAAGA 180
TGAGCCAGAA GAGAGCTGCT TCGTTCAGTC TGAGTGACTA AGAGTGATGA TGCCATCCAC 240
CCAGACAGGA AGCAGACCGG GTGAGCGGGT TTGTGGGGAG AGATGAGGTC AGCTCTCAGA 300
GGTGACAACG CTCCTAATGA TCAAACCCTC AGTAGAGGCC CACTGTGCCC GCATGGGAGG 360
TGCTTTGCCC CCACCTCCCT CAGCCTTGCA AGGTGAAGGC TCTTGCTTTC ATTTCACAGG 420
GAAGCTAACG GTGTTTAGCC AGTATGACCC AGATTTGTCC AGCCCACTGT GCCTGTCTGG 480
GTTCGGGTGC TGAGGGCCAT TCCTTGTGAT GCGGCCAGCA AGCAAGGGGC GACCTGGAGC 540
TGAGAGAGGA GGTGAGAGTC AGAGGAGCTG CAACATTTCC TGCACTGAGA TCCTGGTAAA 600
GCCACAGGCA TGGCTTGGCC CCCGCAGGAA GGAAGCAAGA GGGAGAGAAG GGGGAAGCCC 660
TACATGTAAG ACACTCTCTC TACTGAGTCC TGCCGATCAC AGCAGCTCCT CCTGGAGAAA 720
TGTCCACCCC AGTGTCGCCA AGTTAAGACC TCGGCCTTGC TCAGCACCTG CCCAGCAGCT 780
GATGCTAGGA CCTCTGCCAA GCATGAGGAG AGGAGCCAGC TCAGAGTGAC TCATTGTACA 840
TCAGCCTGGC TCCATGGATC CGGATCAACG CCCTGGACCT CACCTGGCAG TGAGGAACCA 900
GTGGGAAGAG AGGTGCGTGC TGGACTCCAC TGGACAGCAC GTAGTCTCTC GGTGGAAGCA 960
AAGACACCAG CCTTGCACCG AGCCAGCCCA GCCAGGGAAG AGTGGAGAGG AGGCAAGGCT 1020
GGGGGCTGGT GGGTGACTGT GTAATTCCCA 1050
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