| Tag | Content |
|---|
EnhancerAtlas ID | HS116-21600 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr21:37801020-37802450 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr21:37802028-37802038 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr21:37802028-37802038 | GGCACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38121 | chr21:37800618-37805882 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGATGACATT TAAGCCAGTA GAGGCTTGAA ATACAAAGAG AAGTGGAGGC GGGCATTTCA 60
GGCACAGGAA ATAGCCAGAA GGCCTTGAAA TGGGAAGACC TGGCCTATTT GAGGAACAGA 120
CAGACAGACA CTCGTGTGGC TGGAGCTTTG TGCGGCAGCA GGCAGAGAGT GTGTGCTGAG 180
GACAGACGGG AGTCGAGTGT ATTCACAGCA CACAGGGGAC TCCTCATCTG CATTTTAGAA 240
AGAGCTCTCT GGATGCCATG TGGGCAATGA ACTGTGGACA GAATCCTAGC CAGGCAGTGA 300
CTGCAATAGT CCAGACAGCG GGGACGGACC TGGGCCAGAT GCTGGCTTGC AGGGTGGAGG 360
GATAGGCGCA TTTGAGGGGT GTTTTGGAGC TCAAGATGGC AGTCATGACT TTGCTGATGA 420
TGTGAAATTT TAGGACTGTG TTATTGGAGA GGCCTTAGAG ATTTGAATTT TACAGCCAGA 480
AGCAGCCAAC CCAGTGGGAT TGCCCATGTC TGCCCAGTTT CCCTGAACTC CCCTTCTGGG 540
TGAAGAAGGG ACGGCGGCCT GGGAAGGGTA GGTGCTTGTG TTGATCTGTC CAAGGAGCAG 600
ACACCAAATT CGCTTTCAAG GAAGTGGAGC CCAGGGCTGG GCTATTTTCC TCTTTTCCAC 660
AAGGGACACT TTTCACATAA CCCACCCTCC TTCCAACACA GGGATACCGT TCACTCCATC 720
GTGCTTCGTC TCACTCAGCC TCAGCTTGAA GCCCTCTGGC AACGGGGAGC TCATCACTTT 780
GTGAGCTCAG CCCTAGACAC TTTTCCCAGT CAGCCCTAGG CAGGCACCTC CTCCACATGT 840
GGAATCAAAA CCCAGCTCTT TGGTCAGGCG CGGTGGCGCA CGCCTGTAAT CCCAGCACTT 900
TGGGGGGCCA GGGCAGGCAG ACTGCTTGAG CCCAGGAGTT CAAGACCAGC CTGGACAACA 960
TGGTGAAACC CTGTCTCTAC AAATTACAAA AAATTAGCCA GATGTGGTGG CACGTGCCTG 1020
TAGTCCCAGC TTCTCAGGAG GCTAAGGTGG GAGGATCATC TGAGCCCAGC GAGGTTGAGG 1080
CTGCAGTGAG CCGAGATCGC ACCACTGTGC TGCAGCCTGG GCAACAGAGT GAGAACAAAA 1140
CCCCAGCTCT AGGTGTGCCC TCGGCCCCTC CAGGCAGCCT GTGTCCTCTC CCCAGGATTT 1200
AAGATCATGC CGCTCTTGTT TTGGGCTTTT TCAGGACAGT TAACTCTTAG GAAGAAGGGA 1260
CCTCCAAACC TCTAAGTCGC CAAACCACCG CACCGCCCTG GGTGGAAGAA ACCGCTTCGG 1320
CAGCAGAGGA AACAGCAGCT TCGCAGAGCA GCCTGGCCCG AGTGGCTACA CCGGGTCTGT 1380
CTGGTCTCAG CTCTGGCCTC TGAGTCATTA GCGTTGTTTT CTTCTGAGGC 1430
|
