| Tag | Content |
|---|
EnhancerAtlas ID | HS116-29275 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:32211610-32212780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | - | 6.41 | | Ar | MA0007.3 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | + | 6.6 | | NR3C1 | MA0113.3 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | - | 6.53 | | NR3C1 | MA0113.3 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | + | 6.59 | | NR3C2 | MA0727.1 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | - | 6.52 | | NR3C2 | MA0727.1 | chr6:32212316-32212333 | GAGGACACAGTGTTCCT | + | 6.79 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 32211686 | 32211736 | | chr6 | 32212081 | 32212257 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I032243 | chr6 | 32211768 | 32213200 |
|
Enhancer Sequence | TCCCCAACCT GGCACAGTCA TGGGTCAAGG GCTGCCTGTT CCTCACCTGC CTTCCTCACG 60
GGGCTTCTGA GCCTAGCCTT GCTTCGGGCA TTAGGAGAGT CTGCCTGGAA GGCTCTCTGG 120
CCCCCAATGC CCTGCCCTCC AAGGCTCCCA GTCTAGGTGG GAGAGACATA CAGAACAAAT 180
AGCATCGTGG GGGTGGTGGG AGGTGGTGTG AACATGTCTC CTGCAAGCTC TGGGAAGAAG 240
CTGTGGCCAC ACAATGGAAT GTCTCCAGCC CTGACCTCTC CTTGGAACTC AGACCTTTCT 300
GCCTCTCTCG CCAAACTATA CGGAGCACCT GGTAAGGATA GAGGACTGTC GGATGTGTTT 360
TCAGTGGAAT CACTGTTTTC TTCACATTCT TCACATCAGC CACCTCCTCC ACTCCCCACC 420
AGGATGTCAA CTGAAACATG TCTCAGTCCA AATTCTTTAT TCCCTGCTTC TGCAGCTATT 480
CCCTCCCTCC CCGCAATCCT GGCACAGCGT ATTGCTTAGG CTGGACTACG CTGTGAATGT 540
GTCTCCCAAA ATTCATGTGT TGGAAATTTA ATTCCCATGC AACTGTTGGA AGGTGGGGCC 600
TTTTGGGAGG GCCTTTTGGC AGGGCCTGCA TGAATGGATT AATGTCATTA TAAAAGGACT 660
TGATGGAAAG AGTTCATCCC TTTTGCCCTT CCACTCCCTG CCACGTGAGG ACACAGTGTT 720
CCTCCCCTCC AGAGGATGAA GCAACAGATG CCACATTGGA AGCAGAGAAC AGCCCTCACC 780
AGGCAGTAGT GCCTTGATCT CAGGTTTTCT GGCCTCTAGA ACTGTGAGAA AAGACATTTC 840
TTTTCTTTTT TCTTTTTTTT TTTTTTTTAA GACAGAGTCT TACTCTGTTG CCCAGGCTGG 900
AGTGTAGTGG CATGATCTTG GCTCACTGCA ACCTCCGCCT TCCGGGTTCA AGCGATTTCC 960
GGCTAATTTT TGTATTTTTA GTAGGGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTCA 1020
AACTCTTGAC CTCAAGTGAT CCGCCCGCTT CAGCCTCCCA AAGTGCTAGG ATTACAGGCA 1080
TGAGCCACTG CGCCCGCCTC GTTTTGCTAT TCTTCAACTT CGCATGTTTG GATTGCTACA 1140
GCTTGAGGTC TTTAGTGTCT GGTTTCCTTC 1170
|
