| Tag | Content |
|---|
EnhancerAtlas ID | HS116-32072 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr7:129630150-129631080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr7:129630533-129630545 | TCTAAAAATAGA | + | 7.22 | | MEF2C | MA0497.1 | chr7:129630531-129630546 | TGTCTAAAAATAGAA | + | 7.17 | | RARA | MA0729.1 | chr7:129630382-129630400 | CATTGACCTTCTGCCCCT | - | 6.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH07I129991 | chr7 | 129630321 | 129630470 | | GH07I129990 | chr7 | 129630601 | 129630750 |
|
Enhancer Sequence | CCTGGGTGAC AGAGCGAGAC TCTGTCTCAA AAAAAAAACA AAAACAAAAA CAAAAATCCT 60
AGGGCTATGA GACTATGAGA GGCCTTGAAC TGGGCCCTGG AGGGGCAGAA GGCTTGGGAG 120
GACTGTGATC ACATCTCTGC TTAGGCACAG TGGGCTGGGT TTGGACCAGA TCATCCATGA 180
AAAGCCACCA TTCATCTCTG GCCAAGACCT GCCCTTGTGA GAGGCAGCTG AACATTGACC 240
TTCTGCCCCT TACTGTAACC TTTTGGTTTT CTGCTCTTTG GTCAGTTCTG GGGAAGAGAC 300
AAACATATCC CTGAGGTGCT GAAAATTCTG CTGGTGCCTT GGGAGCATGT TCAGGACTGG 360
AGATCATCCA ACCTACCACA GTGTCTAAAA ATAGAATCAA GCCAGTGAGA AGCCAGCTAG 420
TTGGGGATCC TGAGGTCTCC CCAGTGATGG AGAGGCCTCT GAGGAGTTGG TGCTCCAGGG 480
AATGACAGCC TTCTCTCAAG CACTGCTCCT CGCAGCTCCT GCAGCTTCCG GTAGCCAGCA 540
CCTGACCCCA AAACAAAGCC ACTCTTCTCC AGAGCAGCCA GACAAGCAGG CAGGCTGGCG 600
GGCTGGGAGA TTCAGCCCCA CTGCCACATT GGGCCAGCTA GGCTGCGGTG TGCCTTGCAA 660
GCTTGCCCTG GCCACCAGGA GGGCTCTATT TTAAATCACG AGAATATGGT CCCCATGAAA 720
CGGCTGAAGT GAGAACTTAA GACAGAGGGC CCTGTGTTTC CTGTGCCCCT CTTGCTCAGC 780
TGACTTCGCA CACCCCGCTG CTGCCCACCT GCCAGAAAGG GAACTGCCTC TGAGTCTTGT 840
ACTGTGGGGA ACCAAAGCCC AAGGGGAGAC ATGATCACAG TGAAAGTCCC CAAGAGGAAG 900
GCAAGGAGCT GGTGTCTAAG CAGACGCGAG 930
|
