| Tag | Content |
|---|
EnhancerAtlas ID | HS195-03112 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr18:24336890-24337970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | - | 6.2 | | HNF1A | MA0046.2 | chr18:24337538-24337553 | AGTTAATCATTAGCA | + | 6.4 | | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | + | 6.17 | | HNF1B | MA0153.2 | chr18:24337539-24337552 | GTTAATCATTAGC | - | 6.32 | | ZNF263 | MA0528.1 | chr18:24337896-24337917 | TCCCCATTTTCCTTCTCCTTT | - | 6.01 |
|
| | 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 |
| GH18I026757 | chr18 | 24337288 | 24338050 |
|
Enhancer Sequence | TCTTCCAAGG TGAACATGAG CTGTTAGGCA GTGCTCATGA AGCAATTGTT TGGCTTATAT 60
ACCAAAATTT TCTCACATTC TTGCAGGACT GATTTTCTTC ATGCCAAGCA CAAAAAATGC 120
TGTTCAATAC ACTTTCTCCT TTTCTCCTTG TGTAGTAAAG GAAGGATTCT TGGATATTTA 180
TCCAAAGTTT TGTCACACTG AAAAGAGAAG ACTGCATTGA GGTGATGCTC CAAAAGGAGC 240
AGCTTTGATG CAAAAGAAGC AAAACCCTTT TGTTTCTTGG GCTTATACGA AGGTACTTCC 300
TTTAGATCAG AGTCGGGATG CATACACACT ACAAAAACTG GAATGAAAAA GGCAAACCAT 360
TTTTACTCAA CAGAATTCTC TGTACAGGTC AAGGAAATGC CAAACTTAAC AGATGTCTTA 420
GACTGTGCCC TGCAGGTCAA TAAATTAGAG TTTTGTTGAA CCAGGAAGAG GAAGGAATTC 480
CAGGACTTCA GGTCCCCAAA TGGAAATGCC CCTTAGGACA AGTCTAAACT AGGCAAATAG 540
CACTGGAGCT CCTCCAAGTC AGTTGGCTCA GTCTCGTGTA ACTCATTTCT GGCCCCCCTG 600
AAGCTGTTTG TTCAACTGTG CCTTCTACAA CGCTACAGTG TCAAAGAGAG TTAATCATTA 660
GCAAGTGTGA ATAATGTCAG TGTAACGCAG CATGATTGCA GTTCAGTCTG TTTTGACAAA 720
ATTCTAAGCA TTTGTCAGAG TTTACCAAAA AACAAAAAAC AACATGACCA CAGAATGTTA 780
AAATAGCATG AAGTTTGGGG AGCAGTTAAT TCACTTTCTA GCATTTTACA TCACCATTCT 840
CATCGTTTTC CCAGAGGAGA GTGTTGGGTG AGGCCCTCCA GGTGATGCAG TATTACTGAC 900
TGGCCTGGTA TGGTCTGATT CAGTTCAAGT CAGCTTAATG CAGCTCACCT CCAGAGATCC 960
AGGCTTTGGA GAATGATCTA AAGGTTTAGG TGTAGGGTCC TTAACCTCCC CATTTTCCTT 1020
CTCCTTTGTC AGAGCCACCT ACTGCCATAG AATTAATATG GACCCATCTG TGATGCAGAG 1080
|
