| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00447 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:36947280-36948410 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:36947683-36947704 | GAGGGAGGAGGGGGCTGGGAA | + | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATAGCAGGTC AGCAGCTCAC AGAATCCAGC ACAGTTCAGT TTTCCCCTCA CCCCTGCCTC 60
CCTCACAGCC TGTGTGGTCA CACCTCCCAG GACTGCCACC TTGCTTTTGT CTGTGCCACA 120
CTGCGCAGTT CCAAAGCCCC CTTTCTGGAT CCTCTCCTCC TAACTCCTGG GCCCCCTGGC 180
CCTCCTGTCA CTGCGGCCAT CTCTGCTGGG CTCTGCAGGT GCTCACTCCT GTGGCCCAGC 240
ACAGCTCGAT GTCTCCTGGG CTGGCTGCCT TCACATTCCC TCTTTCTGTT TCTCCCTCAT 300
CACGCTCAGC CCTCTCCCCT CACACTCTCT TCCCCACTTC ACACCCCTCG CTCCCTTGCT 360
GTTTCTACTC TCACCTCGAG ATTCTTTCTG TGGGAAGGGT GGGGAGGGAG GAGGGGGCTG 420
GGAATAAACA GAGGGGAGAG GCATTTCCAG ATATGCTGCA GATAAAGAAA AAGAGAGAGC 480
AACAGGAAGA GTGACAGAGT GAGGCGGTGA CTGAAATCCA CACAGACTGA AACGACAGAG 540
AGACTCGCCA AGAGGACGAT TGAGGCCAGA GAGATATCGA GAGACAGAGA AAAAGGGCCC 600
AATGTACGCC GACCCAGAGA GTGGGCGGGG GGGGGGCACT CGGAGGCCTG GAGCCCGGGA 660
AGCGTCTGTT ACCGAGAGTT TAAGATTCAA GAGATAGCAG GAAATATGCG AGACAGAGAA 720
ACTCAGAGAG ATAGCAAGCC AGAGAGAAGC TGAGGAGGAA AGATGGAAAC AGAGAGTGAA 780
ATAGAGACCC AGACGGGGAG GGGTTGCGCG GCTGGAACTC ACAGACACAC ACGTCCTGAG 840
AGACAGAGGC ATGGGGAGGG GAGAATGATT ATGCCTGTCC CCAGCCCAGC TCAGTGTCCC 900
CAAGGAGATA CTTGGCTGTG AGTGACTTCC CTGGTGCAAT ACCCCCAAAA GTAGGGGCAT 960
CCTGTGAAAA GAGACTCAGT GTCCAGGGCT GGGGTTCCAA AGGACGAATC CCGGGCCCCA 1020
GGCCTAGGAC CCCGGACATG AACACTTGGC AGAGCTGTGG GGAGTGGCCC CAGGATTCCA 1080
GCTCTCCATC AAGCCCAAGG CTCAGCCCCT CTCTAGGGAT CCCCTACTCA 1130
|
