Tag | Content |
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EnhancerAtlas ID | HS141-10684 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr2:122456850-122458350 | 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: 2 | Chromosome | Start | End |
chr2 | 122456992 | 122457582 | chr2 | 122458148 | 122458329 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I121698 | chr2 | 122456236 | 122459153 |
| Enhancer Sequence | ACAAAAATTA GCTGGGCGTG GTGGTATGCA CCTGTAGTCC CAGCTACTTC AGAGGCTGAG 60 GTGGGAGGAC GGTTTGAATC CTGGAGGTGG AGGCTGCAGT GAGCAGAGAT GGTTCCACTG 120 TACTCCAGCC TTGGCAACAG AGTGAGACCC TGTCTCAAAA AAATATGCAT TTTAGGTATA 180 TTTACCCCAC ACACACACAT ACAAATAGGC CAGTGCAAGA TGAGCCAGAA GAGAGCTGCT 240 TCGTTCAGTC TGAGTGACTA AGAGTGATGA TGCCATCCAC CCAGACAGGA AGCAGACCGG 300 GTGAGCGGGT TTGTGGGGAG AGATGAGGTC AGCTCTCAGA GGTGACAACG CTCCTAATGA 360 TCAAACCCTC AGTAGAGGCC CACTGTGCCC GCATGGGAGG TGCTTTGCCC CCACCTCCCT 420 CAGCCTTGCA AGGTGAAGGC TCTTGCTTTC ATTTCACAGG GAAGCTAACG GTGTTTAGCC 480 AGTATGACCC AGATTTGTCC AGCCCACTGT GCCTGTCTGG GTTCGGGTGC TGAGGGCCAT 540 TCCTTGTGAT GCGGCCAGCA AGCAAGGGGC GACCTGGAGC TGAGAGAGGA GGTGAGAGTC 600 AGAGGAGCTG CAACATTTCC TGCACTGAGA TCCTGGTAAA GCCACAGGCA TGGCTTGGCC 660 CCCGCAGGAA GGAAGCAAGA GGGAGAGAAG GGGGAAGCCC TACATGTAAG ACACTCTCTC 720 TACTGAGTCC TGCCGATCAC AGCAGCTCCT CCTGGAGAAA TGTCCACCCC AGTGTCGCCA 780 AGTTAAGACC TCGGCCTTGC TCAGCACCTG CCCAGCAGCT GATGCTAGGA CCTCTGCCAA 840 GCATGAGGAG AGGAGCCAGC TCAGAGTGAC TCATTGTACA TCAGCCTGGC TCCATGGATC 900 CGGATCAACG CCCTGGACCT CACCTGGCAG TGAGGAACCA GTGGGAAGAG AGGTGCGTGC 960 TGGACTCCAC TGGACAGCAC GTAGTCTCTC GGTGGAAGCA AAGACACCAG CCTTGCACCG 1020 AGCCAGCCCA GCCAGGGAAG AGTGGAGAGG AGGCAAGGCT GGGGGCTGGT GGGTGACTGT 1080 GTAATTCCCA AGCCAGGTGA AAATCTGTAC AGGTTTTGAG GAGGAGGTCA CTTCTCAGCT 1140 CCAAATAATA GAAGCATCCA GAAGGAAATA ACCAGAGGCT TCTGCCAATT GATCTGGAGA 1200 CTGGGAAAAG GTCCCACAGT TATTAATAAC CTCTGTGTTC TGGGAACTGA TTTCATGCAC 1260 CAGACAAAGG GATTAAAAAG TTGCTGGTGA AGGCAAAGTG GTTTCAGCCA AAGCTCTCCT 1320 TTCTGTCTCC CAATAAATGA GCATTTTTCT CCACAGAAAC CCTTAGAGCT GATTGGCCCT 1380 TTGACAAATC TGGTGAGCTG GGAGCTGTGT GGCTGATTGG CATATTTTGA TAACCACTCT 1440 GTCGTCGTGA AGCACTTTCT TCCGGCAACC CCCATTTCAC TCGCTCTGAG TATGGGGGTG 1500
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