| Tag | Content |
|---|
EnhancerAtlas ID | HS046-00485 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:23710000-23710830 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
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 | GAAAGGCATT ATTATTACTC TTTTGCTCAA TGAGGTGAGT AACATGCTCA GCATGAGTAG 60
GGCAGAATGG GACCTGAAAC CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT 120
TAGAACTTTT GGAGCACCTG CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC 180
AAGTCAGAGA GCAGTTGGAA ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA 240
GACTTGGCAG GAAGGAGCAC TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA 300
AAACTTCTGC CTTTGCAGGA GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA 360
GAGCTTCCTT AGGAGGGAAG GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG 420
GGCTCAGCCT TCCTGTTTCC CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG 480
TGGAAGCACT TTCCAAAGAG GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG 540
ATCTCAGGAA GCCGATTCCA TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA 600
TGTGGGCTGC TGCCCCCACC CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG 660
TTCTCTCCCC ACCTCCCCAA CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT 720
GTGCAGGCTG GCAAGTGCTG CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC 780
CTTATGCGGG CGAGGTATGT GGATAACAGG GAAGGGGGAA ATACATAAAC 830
|
