| Tag | Content |
|---|
EnhancerAtlas ID | HS145-13184 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr2:122456880-122457950 | 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 | CCTGTAGTCC CAGCTACTTC AGAGGCTGAG GTGGGAGGAC GGTTTGAATC CTGGAGGTGG 60
AGGCTGCAGT GAGCAGAGAT GGTTCCACTG TACTCCAGCC TTGGCAACAG AGTGAGACCC 120
TGTCTCAAAA AAATATGCAT TTTAGGTATA TTTACCCCAC ACACACACAT ACAAATAGGC 180
CAGTGCAAGA TGAGCCAGAA GAGAGCTGCT TCGTTCAGTC TGAGTGACTA AGAGTGATGA 240
TGCCATCCAC CCAGACAGGA AGCAGACCGG GTGAGCGGGT TTGTGGGGAG AGATGAGGTC 300
AGCTCTCAGA GGTGACAACG CTCCTAATGA TCAAACCCTC AGTAGAGGCC CACTGTGCCC 360
GCATGGGAGG TGCTTTGCCC CCACCTCCCT CAGCCTTGCA AGGTGAAGGC TCTTGCTTTC 420
ATTTCACAGG GAAGCTAACG GTGTTTAGCC AGTATGACCC AGATTTGTCC AGCCCACTGT 480
GCCTGTCTGG GTTCGGGTGC TGAGGGCCAT TCCTTGTGAT GCGGCCAGCA AGCAAGGGGC 540
GACCTGGAGC TGAGAGAGGA GGTGAGAGTC AGAGGAGCTG CAACATTTCC TGCACTGAGA 600
TCCTGGTAAA GCCACAGGCA TGGCTTGGCC CCCGCAGGAA GGAAGCAAGA GGGAGAGAAG 660
GGGGAAGCCC TACATGTAAG ACACTCTCTC TACTGAGTCC TGCCGATCAC AGCAGCTCCT 720
CCTGGAGAAA TGTCCACCCC AGTGTCGCCA AGTTAAGACC TCGGCCTTGC TCAGCACCTG 780
CCCAGCAGCT GATGCTAGGA CCTCTGCCAA GCATGAGGAG AGGAGCCAGC TCAGAGTGAC 840
TCATTGTACA TCAGCCTGGC TCCATGGATC CGGATCAACG CCCTGGACCT CACCTGGCAG 900
TGAGGAACCA GTGGGAAGAG AGGTGCGTGC TGGACTCCAC TGGACAGCAC GTAGTCTCTC 960
GGTGGAAGCA AAGACACCAG CCTTGCACCG AGCCAGCCCA GCCAGGGAAG AGTGGAGAGG 1020
AGGCAAGGCT GGGGGCTGGT GGGTGACTGT GTAATTCCCA AGCCAGGTGA 1070
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