| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00610 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:23710060-23710830 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr1:23710211-23710221 | GCACGTGACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27061 | chr1:23710018-23711255 | Esophagus | | SE_50618 | chr1:23709942-23711264 | Sigmoid_Colon | | SE_53272 | chr1:23709967-23711232 | Small_Intestine | | SE_65133 | chr1:23709934-23711086 | NHEK |
|
| | 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 |
| GH01I023383 | chr1 | 23710092 | 23712491 |
|
Enhancer Sequence | GGCAGAATGG GACCTGAAAC CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT 60
TAGAACTTTT GGAGCACCTG CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC 120
AAGTCAGAGA GCAGTTGGAA ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA 180
GACTTGGCAG GAAGGAGCAC TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA 240
AAACTTCTGC CTTTGCAGGA GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA 300
GAGCTTCCTT AGGAGGGAAG GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG 360
GGCTCAGCCT TCCTGTTTCC CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG 420
TGGAAGCACT TTCCAAAGAG GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG 480
ATCTCAGGAA GCCGATTCCA TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA 540
TGTGGGCTGC TGCCCCCACC CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG 600
TTCTCTCCCC ACCTCCCCAA CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT 660
GTGCAGGCTG GCAAGTGCTG CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC 720
CTTATGCGGG CGAGGTATGT GGATAACAGG GAAGGGGGAA ATACATAAAC 770
|
