| Tag | Content |
|---|
EnhancerAtlas ID | HS116-23652 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr3:49333890-49335300 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr3:49334417-49334428 | TGGGTGTGGCT | - | 6.14 | | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr3:49334834-49334844 | AACAGCTGTT | - | 6.02 |
|
| | 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 |
| GH03I049296 | chr3 | 49334281 | 49334430 |
|
Enhancer Sequence | GCTAACACGG TGAAGCCCTG GCTCTACTAA AAATACCAAA AATGAGCCAG GCGTGGTGGC 60
GGGTGCCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGA AAAATGGCAT GAACCCGGGA 120
GGCAGAGCTT GCAGTGAGCC GAGATTGCGC CACTGCACTC CTGCCTGGGA GACAGAGCGA 180
GACTCCGTCT AAAAAAATAA AATAAAATAA AATAAAAATA CCAGATGCTA CTATTGCTTT 240
CATAAAACAA TTGTCAATTC AAATTCATCT ATAAAAGAAT TTGTTTTTCC AATGGTTGGC 300
CCATAGGCCC TCTGAAAATT CCTTTGTTGG TGGTCTGCTA AGCTCCCCAC AGGGTAATCC 360
TCCAGTTCCT TTCAGCTCAG GTGTGTGAAA ACACTACTTT CTGGAATTTA CAGAGACCAT 420
GTTAAGGGCT TGGGGTTATA TGTGAAAGTG GACTTTCCCA TGTTCTAGCC CTTGGCACAG 480
TGTCAGCTCT TGGCTGTGTC TGTGCAAGTG AGAACAGAAA TAGATCTTGG GTGTGGCTAG 540
GAACTATTCC TTTTAGAGAG ATCTAGAAGT CATAGGCCCA AAAATGTAAA GGGAAGGAAC 600
TATCTCCTTT ACATACTGAA TTCCTCAGCC AAAAACAAAA ACCAAAACAA AATCCTAAAA 660
CCCTTTCTCA GCAGAGGCAA GTTCCTGAGT GAGAGGTAAA GAGGGAGGGA CAGTACGGCT 720
GTGCTCCATA CTTCCTGGGC AAGTGGCTGC CTGGGAGCAG CAGGCAAGTT CATGTATGGG 780
AGCAGCCGGC AAGTTATTAC ACCACTGTGC CTGGAAGAGG GACACACACA CAATTACACA 840
GAGCAGCCAT GAAGCAGCAT GTGGGAAGGC AGAGGAGGCC TTTGTATTGT CCTCACAGAG 900
ATGAAGAAAC TCAGTCTCAG AGCTTACAGA ATGTTTGAGC TGAAAACAGC TGTTTAAATC 960
AGCCCTGTCA TTTCTGCATT GGGGATGGTA GTATCATGGT ACTCGCTGAG AAGCTACAGC 1020
CTGTGGCAGA GAAAGGACAA GATCCTTCCG TACCACACCC CTACTACCAT CTTCCCATCA 1080
CACAGCTGGG ATTCCTCTTA AGAAAGGCAT CTCTGATGGT AGGACCATCT GTAGGAGCAG 1140
TGATTTGGCC TTCTTCATAG GCAAAACTGT TGAAAAAAGG CTGTGGCTGT GCTGAGGAGA 1200
GTTATCAGAA TGTTTAGCTC TGCAGGGCAG GAGGGGTTGA GCACTGATGG CTGCCCACGA 1260
TGCCCTCAAT ACCCATCTCT TGCACCCAGG GGTCAGGGCC AATCCACATG AGCAATGACT 1320
GCCCACATTT TTGTTCTGGA GATATGAATG CAGCAAAGTC TCTAGAATGT GTCCTCTGAC 1380
CTGACCTGCA GCAGAAACTG CTGAGTACTC 1410
|
