| Tag | Content |
|---|
EnhancerAtlas ID | HS116-19832 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:191583310-191584190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr2:191583762-191583777 | ATTTCCCAGGAAAGG | - | 6.15 |
|
| | 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 |
| GH02I190717 | chr2 | 191582084 | 191584601 |
|
Enhancer Sequence | AAAATAAACT TTCTAAATTA ACCGAGCCCT GTCTCAGACC TTCAGCGTTC ACAGACTATA 60
CCGAATCGGG CTGTTAATCT TTGAAAGTGA CTGGAACCCT AGAGATCTAA CCAAGATATT 120
GTCAGGGAAC TCAGCAGAGA GATCGTGAAC ATGGCAGAAC TGAAGGCAAG TGACTGTAGA 180
AAAATAAATT ATTTCACGCC TGTACTTCCT ACGAACAAGG ATTGTTTAGT AAACTAGATG 240
TGGTAGCCAC GATTTTCATG ATCAACAGAG TGGCAACAGG CAAGACTGAA TGATGGGGCT 300
TTGGGGAATT GCACTGGCGA TGAATCACCC TGAGATTATG CAGGTGGGGT TTCCCCTGAA 360
GGGACTGGAA CTGCTCACTG CCAGCTGTCC TCAGAAGAGG TCAGTCATGG GGCGGGAAAT 420
CAGAATGCTG GGACTAGAGT CAGTCTGACT GGATTTCCCA GGAAAGGTGA CTGTTGAGTC 480
CCCAGGGCAC TTCCTCCTGG AGGGGGAAGG ACCTGTGCCT GGCACTGACT TATTCTCTGT 540
TTTCTGTTTC CTTTCCATTG TCCCTGAACC TTTATTGTGA TCTGATCAGT GTCTCAAATA 600
TTTTGACTTC TGATGTCCTG AGAGGAATTA AGGGGAAAGG TCCACAACCA ACCCCTGAGG 660
CAAAGCAGAG GAGGGTTATG ACTTCTGTCC TCAGGCCACA GCAGTGGTGG CAGCCACAGG 720
CACCAGCTGA GAACAGCTTT GCCCCAGAGG GACCAGTTTC TGAATACACA TGACAGAGCA 780
CCTTGAGAGA GTCTCAAGAT TCTTTAGCAG AACAGGGGAC ACTGGGAGTA GGGGCAGAGG 840
GCACTCATTT TTGTCAATAA AACTAGTGTG AGTCAAACTA 880
|
