| Tag | Content |
|---|
EnhancerAtlas ID | HS116-06892 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:85435960-85437040 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr11:85436787-85436804 | TAACCTTTGGATGAACT | - | 6.24 |
|
| | 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 |
| GH11I085725 | chr11 | 85436056 | 85438034 |
|
Enhancer Sequence | TTCCACTTCC TGAGGGAGGC CTTTGCCATA TTGAGCAACA ATGGAAGCAA ATGAGCTAAG 60
CGTCTGGTCT GATGGAGACA TTTGGGCAGC TAAATAAGAT CCAACTTCAT GAGTTTTATC 120
AGGAACTACA TTGGAGGAAT AAAAATCCTT CCTGTCTGGA ACTATGGTGT CCATCGTAGC 180
CCATGGTGAT ATCACTCCTG GAGGATTTAG GGGGCTACAT ACTGGCTGTA CTGCTTCAGG 240
AAATTCTGGG TTCACTTCTC CAGGACCTAC TTCCCTTCCA GCTGGATAAC TTAACCATAC 300
TTCTCCACAC AGCTTCTGTA ATGCAGCACT TACATCATTC AATACAGGTC TGGGTGGAAG 360
AATGACTTTC TCTACAGTCT CCGAAATTTC CGTTTGAGAA GGGTGTACCC TAGCCTGGGG 420
AACAAGATGA GCATCCTGGG GAAAAAGCAT ATCTTGGGGA GGGCTGGCCA CATCCCCAAA 480
AGAACCCTTT CTGGAAAGCT GGGAAGTTGG ATCCAATGGA TGAGAATCTT CTGCAGCCAT 540
CTGAATCAAA TTCTGTGTGC TTAGCTGGCA CTCACCACTT TCAGCTTTCT TGAGGAGAGC 600
TGTATTTCCA AAAGTTTCAT CTCTCACTGG AAAAGGAGCT AGTATTTCTC TCTTATCAGC 660
TGAAGTATTG TGACTCTGTT CTATCCCTTT TCCAAAAAAT CTCCCCTCTT CCAGCTTAGA 720
GTTGGTTCCA GTGATAACAG GCGCCAACTT GGCTTGCAAG GGAGAGGGTG AAGTTCCAGT 780
TGCTTCCTTC AGGAGTTTGT CTAGACTAGC AGTCAAAGAG TTCCGTTTAA CCTTTGGATG 840
AACTACTGTT TTGTCAACAT GCTCATTAAT GATCTTCTCA GGTCCTTTGA CTTCTTCCTC 900
AGTATCAGCA AAATCTGTTT TTTGAGGCCA TGTCCTATTT TCAGAAACAC TTGGTTCAAG 960
CACTTGTTTT CCATGAACTT TTCCACCAGA GGGTTGAATT GCTGGTGTTG AGGTTTCTGA 1020
AAGCAGTTTC TGCAAGCTGT CATTAAAAGT GTCTTTGCAG TCTTTAGACA AAACATTGGT 1080
|
