| Tag | Content |
|---|
EnhancerAtlas ID | HS067-00009 |
Organism | Homo sapiens |
Tissue/cell | GM18522 |
Coordinate | chr1:1615140-1616150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | | ERG | MA0474.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | | FEV | MA0156.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr1:1615755-1615765 | ACCGGAAGTG | + | 6.02 | | GLI2 | MA0734.2 | chr1:1615868-1615883 | GGACCACCCACAACC | + | 6.19 | | Zfx | MA0146.2 | chr1:1615990-1616004 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_32013 | chr1:1614622-1615903 | Gastric | | SE_52422 | chr1:1614441-1616065 | Small_Intestine | | SE_65325 | chr1:1613532-1616277 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1615717 | 1615777 | | chr1 | 1615180 | 1615915 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001683 | chr1 | 1614749 | 1615855 |
|
Enhancer Sequence | CCCCCCTACC CCCGCTCTCC AGGGCCCCAC CCCCTGCCTC ATCAGCATAA GCTCAGGTGT 60
GATCAGCATA AGCTCCGGGG TGATCTGAAC CACTCCTGTC ACTCAGGAAA TTCCAAGGCT 120
TCGAGGAGCT TCTGTGCCAG GAACCAGGAA CAAAGACCAA ACACATTTCA TATCAGAGCA 180
CAAGTGCAAA ACATCATGGT TGGAAACAGG GTCTCAGAGT CCTCCAGGTG CAGGTGCCTG 240
TTCAGACCAG AGACCACAAA GTTGTAAGTC AAACCTTCAT GTTTGGCCAG CGGCGGTGGC 300
CCACACCTAG AACCCCAGTA CTTTGGAAGG CCGAGGAGGG AGGATCGCTT GCTGTCCACT 360
CACGTCTGGG GCACAGCCCA GGAGACCCGT GGGCCGCAGG GTAGACACTC AGCAGTCGTG 420
AGACGCTTGC CCCAGTGCAC TGTCTTTTCA AGGCCACTGA CATCTCCACA GACAGCCCCC 480
AGCCCGTCCT TTGGCTCTTA ATGTGCCTCA TCCACCTCCG CGTGCTGACA CCCACATCAG 540
TGACATTTGG GCTAAGCCGC CTAATGCAGA GTGGCTATAA GCGCGCTGAG CCGCTCGTGA 600
AATTCAGACA ACCCCACCGG AAGTGAGAGA GAGGACGGCT GTGAGCTCAG GGCAGCGTTT 660
CTGCTGAAGG CGTTTGCTTT CCCACCATCA TAAAGTCAGA AAATCACAAC TCAGACCATG 720
GTAAGTGGGG ACCACCCACA ACCCAAGTGG GCCTTGGAAA TTAAGAATAG GAGGCCGGGC 780
GCGGGGGCTC ACGCCTGTCA TCCCAGGAGG CTGGGCACAG TGGCTCACGC CTGTCATCCC 840
AGCACTGTGG GAGGCCGAGG CGGGTGGATC ACAAGGTCAG GAGATTGAGA CCATCCTGGC 900
CTACATGGTG AAACCCCGTC TCCACTAAAA ATACAAAAAT TAGCTGGGCG TGGTGGTGGG 960
TGCCTGCAGT CCCAGCTACT TGGCAGGCTG AGGCAGAAGA ATGGCGTGAA 1010
|
