| Tag | Content |
|---|
EnhancerAtlas ID | HS104-25704 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr17:44862760-44863950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIA | MA0670.1 | chr17:44863725-44863735 | ACTTGGCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr17:44863639-44863660 | GGAGAAGCGGGGGATGGAGGG | + | 6.22 | | ZNF263 | MA0528.1 | chr17:44863480-44863501 | GGAGGAGGGTGCGAGAGAGGG | + | 6.63 | | ZNF263 | MA0528.1 | chr17:44863558-44863579 | GGAGGAGGAAAGAGAGTGGAA | + | 6.89 |
|
| | 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 |
| GH17I046785 | chr17 | 44863221 | 44863390 |
|
Enhancer Sequence | TATCCCAGGC AGTGATCCAC GCCATAGGAG AAAAACCCAT GCACACGGAG AAAAGATAAC 60
CAAGGAAAAA GCTATTCCTT CCCCTCCGAC AGGAGCCCCC GAGGACAGGC CCCAGGAGCC 120
CCGGAAACTC ACTAGCCCTG CTGGCCAAAT GACCACTTCT ACATGCTGTG GACGACTTTA 180
GCAACTCCCT TCTGCCCGCA GCTTCTGAAG GTTCCCTTTC AGGGCCACGA GGGGCCTTCC 240
GAGGAGGTGG CACAGCTCAG CTGCCAGGGA CCACCTGAGA GCCCGGGAGG ACCATGGTTC 300
TGGGCAGCCG TGGGGAGAAG GAAAGGGTGC GGGCAGGAGC TCAAAGCCAA GGGTTTGGCC 360
ACAGACTATA CCTCAGTCAG AGGGAAGAGG CTGCGGGCCC TGTGCTCCAT CCCAGGGAGC 420
CCTGTGGGAT GTTTCTTTGG GGAGAAAAGG GAAGGGAGGG AAGGGGTGTG GAGGGCGGGG 480
CAGTGCCTGG GCTGGAATGT TGCAGCTTCT GTTCTCCAAA GCAGCTCCTG GAGCGCCTGC 540
CTGCGGCTCT GGCTGATCTG ATAAGATGTG ACAAGACCGC CTGAAAAATG TTGAAACCTG 600
TAAAATGTTT AAACCTGTTT TTTGTTGTGT TGTGAGCATG AAGTGCTTTT TCTTTCTTTC 660
TTACCCACCC CCCCACCCCT TCATTTCACA GGAAAGTGAA GTTGATAAGC CTGGAAAAAG 720
GGAGGAGGGT GCGAGAGAGG GATTGTTGCC TTCAGCCAAA TTGTGGTCCG GGGCATGGAG 780
CAGTCTGGTG GGACCTGGGG AGGAGGAAAG AGAGTGGAAA CAGGAGGGAA GAGGGGACAA 840
GAGGTGAGAG GAGTCAAGGG TGGAAGAAGG AGGAGGACAG GAGAAGCGGG GGATGGAGGG 900
GTCCTGCACC CCTGGCCTGC TCAGCAGCCC CAGCCCATCC TCCCCAGGAC CAAACACAGT 960
CCCCCACTTG GCACCCCAGA GGAACCCCAG GGCTGTGGGT CTCTTCCTTC AGGCAGGGGA 1020
TTCACAGGGA AGGGCCTAGG CCCAGAGGGG TGTCCAGAGA CGGGTAAAAG GCAGGGACCT 1080
CACTCTTCAG ACCCCAGAGC GTCTCCCTGA GAGGCACCAA GCCCACAGGT GGGCAAGTGC 1140
TGCCTGGTGA CCACAGAGGG GAGCAGCTCC CAAGGACACA TGCTGAGAGC 1190
|
