| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09701 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr2:217106700-217108060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:217107813-217107834 | CCTTCCTCTGAGCCCTCCTCC | - | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 217107000 | 217107400 | | chr2 | 217107400 | 217107760 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I216242 | chr2 | 217106974 | 217107312 |
| Enhancer Sequence | CCAAGATTGC GCCACTGCAC TCCAGCCTGG GCGACAGAGC GAGACTCCGT CTCAAAAAAA 60
AAAAAAAAAA AGGTGGAAGG GGATATCATT TGACTAGAAA GGATGGAGCT TTTGATTTGG 120
GGGTAAGCAT CTGAGGACTG GAGGCTTGGT GTGAGCAGAC GAATAAGCTG ATTGTCCTTG 180
CTGGTGACCC AACAAGGATG CTGCAGTATC AGAGAGCACC TGGATGGTAA GCATCCCTGA 240
AACTGCTGTT TAGACTTAGT CTTTATGCAA GATGGTAACA GAAAGGCCAG AGAAAGGAAG 300
TAGTTTGGAC GAGGAATCAT CCTTTCAGTC ATGGCTGTTA CTGGTGGCTC TGCCATCTTG 360
CTCAATCGAC AGTGTTTTTC AGTGAAACTG TATTTACTGC TTTTTCTCAG AGCTCCCTCC 420
GCACCGTGTT TTCCCAGAGC CAGGGCGCTG AGCTGTGGGA ACTAGGTTTG GCCAGCTCCC 480
TGAAAACTTC CACCTGCTGA GAGCTCCAGT TGTCTCCCTG CCATCGTGAT GAACGTGCTG 540
CAGAGCGCAA AACTGGGGCA AGTGAAAAAA TGAATTGAAA TAAGGAAATG AAGCAACCTG 600
TAAAAAACCA GCAAACAAGA CTAAATCAGC AATGAAAATC AATGAGGCAA ACACCATCTG 660
GCCCTGAAAA TGAATGGAGC ACAAAAGGAG GCCTTGCCTC CTGGGGATTC CTGCTCCAAC 720
CAGGCAGAGT TACATTCATG CCTGCCTGAG ATAAGCCTGG GTTGGCAGCA AGTGCTGATG 780
TGTTTTTGCA GAGCAAGATG TTTGGGACAG GTGCTTTTTT CCCTTGACAA TATATCGGGG 840
TATATTTTTT ACCTAATGAA ACTCTAACAG GAATGAGTTA TGAGTTTCAT CAACACACAG 900
AGCAGAATTC AGAGATTTGA ATACAATGGA ACTGTCCCTG AGAGAGGTAC AGCTGGTTTG 960
CATCTGACCG CTTGCATTTA CTCATTCATT CCTTCACTTA TCCATCCTTC CATTCATCCA 1020
TCCCTCTCTT CCTCTCCGTT TCCACCACCA CTGATCTAGT CCACTCCACA GCACATCACT 1080
CCAAATGCTT GCTGGGGCCT CCTCTCCGGG CTGCCTTCCT CTGAGCCCTC CTCCACATGC 1140
CTCCAGAGCC TATTTTCCAA GCCCAAACCT GCTACACTTT CCTGATGTTA GCCTTTTAAT 1200
GTCCCTCCAC TGCTCACACG CAATGCCCAC CATAGCCAAG CTTCTGCCAA CCGGCCACAA 1260
CCTGCTGCAT TGTCCCCCCC TATCACTCCA TTCATGCAGA ATTACTTCCA GGTCCATTAA 1320
GGAGCTACAT GGACTCATGC TTTGGTGTGT TTTCTAATGC 1360
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