| Tag | Content |
|---|
EnhancerAtlas ID | HS116-24342 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:119289980-119291250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr3:119289994-119290004 | ACCACTTGAG | + | 6.02 | | NR3C1 | MA0113.3 | chr3:119290338-119290355 | AGGAACAAAATGTCCCC | - | 6.13 | | NR3C1 | MA0113.3 | chr3:119290338-119290355 | AGGAACAAAATGTCCCC | + | 6.41 | | NR3C2 | MA0727.1 | chr3:119290338-119290355 | AGGAACAAAATGTCCCC | - | 6.21 | | NR3C2 | MA0727.1 | chr3:119290338-119290355 | AGGAACAAAATGTCCCC | + | 6.8 | | Nr2f6(var.2) | MA0728.1 | chr3:119291151-119291166 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 119289984 | 119290439 | | chr3 | 119290588 | 119290758 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I119570 | chr3 | 119288848 | 119290846 |
|
Enhancer Sequence | CGAGAAGGAA TTTGACCACT TGAGGGCCTG ATTTATACAA GTACCACATG ATGAAGAACA 60
GGATTTTATG GAGTGAAGAT CCTTAACAGC ACTCTCAGAT TGAATCTCTC CTGAGCCTTG 120
AACTGATTTC TCCAGTGGCC ACTGGGGTTG CGTGACTCCT CCAATGGCCC CAGACACAAC 180
TAAGAAATGT GCCTAAACTG GCTGCCATTT GAAACCTTTT GGTGTCCTTT GTTTAGATGC 240
CCCACCCTAA ACTTCAGGAG TTCTCTCCAG AGAGTAATTT TAGGAATGAA TGCCAGAGAC 300
CAAGGGATGA GGGACTGTTG CCTCATCAGA GGGGGAAGGA GCTTGCTGGA AAAACAAGAG 360
GAACAAAATG TCCCCTGACT AGATTTTTCT TTACCTTTTG TCTCAAGGAC TCTTCTAGAA 420
ATAGAAATAA GAGTAGATTC ATGTACATTT GCCCAGGTTG ACCCCAGTGG AGGAATTGTG 480
GGGCAGAAAG AATGATAACA TGAAAGAAAG ATAATTTCAG TAAGGCCCCC CAAACTTTTG 540
GTTTAGGGAG CAGTCACTTT TTGTTTCCTA GAAGCTGTAT TTTCACCTAC TGAGATTCTA 600
GCAGGCAGTG AAGTCCCCTT AGGATGGGAC CGTGTGCAAG AGCATTGCTG TTTCATTGTA 660
AACCCTGGAA GCGGAACTTA GGACTCAGCT GGCCAGCTGA GCTTCTCTTC CTGTGGGAAA 720
TCCCAGCGAA ACCAGGAGAA AGGGAGCAAC AGAGGTCATC TGCCAGGAAA TGTACCAAAG 780
AAGATTTGAA AATTACTGGT GGATCTCCAG AGCAAAGGCT GGAAAGCCCT GACCTACAGG 840
AGCGGGCTAC TGCATTGTTG GGAGGAGCAG GATTCACATC CACATGGACT TCCCTCGGGT 900
CTCTTTCTGC TCTGCAGAGA GGGGTGGAAG CTGCTCCTAG GGTTTTTTTT TTGTTTTTTG 960
TTTTTTGTTT TAAGATGGAG TCTCGGTCTG TCGTCCAGGC TACAGTGTAG TGGCACGATC 1020
TTGGCTCACT GCAACCTCTG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC AGCCTCCCGA 1080
GTAGCTGGGA TTACAGGCAT GCACCACCAT GCCCGGCTAA TTTTGTATTC TTAGTAGAGA 1140
GGAGGTTTCA CCATGTTGGC CAGGCTGGTC TTGAACTCCT GACCTCATGA TCCGCCTGCC 1200
TCGGCCTTCC AAAGTGCTGG GATTACAGGT GTGAGCCACC GCACCTGGCC ACTCCTAGGT 1260
TTTAAAACAC 1270
|
