| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20119 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:191583230-191584130 |
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 | CAAGCTGTGC CCCGACCACA TTGGGCACAT GTCTTCAGGA CTTCCTGAGG CTGTGTCATG 60
GGTGCATCCT CAACCTTGGC AAAATAAACT TTCTAAATTA ACCGAGCCCT GTCTCAGACC 120
TTCAGCGTTC ACAGACTATA CCGAATCGGG CTGTTAATCT TTGAAAGTGA CTGGAACCCT 180
AGAGATCTAA CCAAGATATT GTCAGGGAAC TCAGCAGAGA GATCGTGAAC ATGGCAGAAC 240
TGAAGGCAAG TGACTGTAGA AAAATAAATT ATTTCACGCC TGTACTTCCT ACGAACAAGG 300
ATTGTTTAGT AAACTAGATG TGGTAGCCAC GATTTTCATG ATCAACAGAG TGGCAACAGG 360
CAAGACTGAA TGATGGGGCT TTGGGGAATT GCACTGGCGA TGAATCACCC TGAGATTATG 420
CAGGTGGGGT TTCCCCTGAA GGGACTGGAA CTGCTCACTG CCAGCTGTCC TCAGAAGAGG 480
TCAGTCATGG GGCGGGAAAT CAGAATGCTG GGACTAGAGT CAGTCTGACT GGATTTCCCA 540
GGAAAGGTGA CTGTTGAGTC CCCAGGGCAC TTCCTCCTGG AGGGGGAAGG ACCTGTGCCT 600
GGCACTGACT TATTCTCTGT TTTCTGTTTC CTTTCCATTG TCCCTGAACC TTTATTGTGA 660
TCTGATCAGT GTCTCAAATA TTTTGACTTC TGATGTCCTG AGAGGAATTA AGGGGAAAGG 720
TCCACAACCA ACCCCTGAGG CAAAGCAGAG GAGGGTTATG ACTTCTGTCC TCAGGCCACA 780
GCAGTGGTGG CAGCCACAGG CACCAGCTGA GAACAGCTTT GCCCCAGAGG GACCAGTTTC 840
TGAATACACA TGACAGAGCA CCTTGAGAGA GTCTCAAGAT TCTTTAGCAG AACAGGGGAC 900
|
