| Tag | Content |
|---|
EnhancerAtlas ID | HS144-00062 |
Organism | Homo sapiens |
Tissue/cell | NH-A |
Coordinate | chr1:11882860-11883760 |
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 | chr1:11883076-11883097 | GGAGGAAAAAAGGGGGAAAGG | + | 6.05 | | ZNF263 | MA0528.1 | chr1:11882909-11882930 | CTCCTTTTCCCCACCTCCTTC | - | 6.12 | | ZNF263 | MA0528.1 | chr1:11883073-11883094 | GGGGGAGGAAAAAAGGGGGAA | + | 6.96 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGTGGTTT GGATTCACCT GCTCGCTTAG GAGGTTTTAG AGTCCCGCAC TCCTTTTCCC 60
CACCTCCTTC CAGAATGTCA GGAAACTGAG AATGCAGATT CCTGCAGAAA GTGGCCTCTT 120
GTTCACTAAA GGTAAAGGTT TCACCTCTGG TGAGATTAAA GAAGAAAGGC CTCCCAGGTG 180
ATGCTCATTC ACAGGGAACT TGTACAGATT CTGGGGGGAG GAAAAAAGGG GGAAAGGGCT 240
GAAAACAAAA CTGTTGGGTG CCATGCGCAC TACCTGGGTG ACAGGATCAT TCATGTCCCA 300
AACCTCAGCA TCATGCAATA TACCCTCGTA ACATACCTGT ACATGCAATC CCTGAACCTA 360
AAATAAAAGT GGAAATTATT TTTCTTTAAA AAGTGCAAGT CTGGCCACTT TGGGAGGCCA 420
AGGCGGGCAG ATCACCTAAG ATCGGGAGTT TGAGACCATT CTGACCAGTG TAGAGAAACC 480
CTGTCTCTAG TAAAAATACA AAATTAGCCG GTAAAAATAC AAAATTAGCC GGGCGTGGTG 540
GCGCATGCCT GTAATCCCAG CTACTCGGGC GACTGAGGCA GGGGAATTGC TGGAACCCAG 600
AAGGCGGAGG TTGCAATGAG TGGAGATTGT GCCATTGCAC TCCAGCCTGG GCAACAAGAG 660
TGAAACTCTA CCTCAAAAAA AAAAAAGAAA AAAAAGTGCA AGTCCTCCCA TTGCCCCTCA 720
GACCTCCTGA GTCAGATCCT CTGGAGTGGG GCCCAGCAGC TGTGGTTCTG CAAGCCCTCC 780
AGGTGACGCT CACGCTGCTA ATGAAGGTGG CCAGCTCTCC CTCTTCCGCC GCCCAGATTG 840
TTGAGGGTAA GCCAGAGAAC CAATGGATTT CGAGTTATGG GTGTGCCTGC TCTCCTCCAT 900
|
