Tag | Content |
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EnhancerAtlas ID | HS066-00010 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr1:1615190-1616150 |
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 |
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| 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001683 | chr1 | 1614749 | 1615855 |
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Enhancer Sequence | GCTCAGGTGT GATCAGCATA AGCTCCGGGG TGATCTGAAC CACTCCTGTC ACTCAGGAAA 60 TTCCAAGGCT TCGAGGAGCT TCTGTGCCAG GAACCAGGAA CAAAGACCAA ACACATTTCA 120 TATCAGAGCA CAAGTGCAAA ACATCATGGT TGGAAACAGG GTCTCAGAGT CCTCCAGGTG 180 CAGGTGCCTG TTCAGACCAG AGACCACAAA GTTGTAAGTC AAACCTTCAT GTTTGGCCAG 240 CGGCGGTGGC CCACACCTAG AACCCCAGTA CTTTGGAAGG CCGAGGAGGG AGGATCGCTT 300 GCTGTCCACT CACGTCTGGG GCACAGCCCA GGAGACCCGT GGGCCGCAGG GTAGACACTC 360 AGCAGTCGTG AGACGCTTGC CCCAGTGCAC TGTCTTTTCA AGGCCACTGA CATCTCCACA 420 GACAGCCCCC AGCCCGTCCT TTGGCTCTTA ATGTGCCTCA TCCACCTCCG CGTGCTGACA 480 CCCACATCAG TGACATTTGG GCTAAGCCGC CTAATGCAGA GTGGCTATAA GCGCGCTGAG 540 CCGCTCGTGA AATTCAGACA ACCCCACCGG AAGTGAGAGA GAGGACGGCT GTGAGCTCAG 600 GGCAGCGTTT CTGCTGAAGG CGTTTGCTTT CCCACCATCA TAAAGTCAGA AAATCACAAC 660 TCAGACCATG GTAAGTGGGG ACCACCCACA ACCCAAGTGG GCCTTGGAAA TTAAGAATAG 720 GAGGCCGGGC GCGGGGGCTC ACGCCTGTCA TCCCAGGAGG CTGGGCACAG TGGCTCACGC 780 CTGTCATCCC AGCACTGTGG GAGGCCGAGG CGGGTGGATC ACAAGGTCAG GAGATTGAGA 840 CCATCCTGGC CTACATGGTG AAACCCCGTC TCCACTAAAA ATACAAAAAT TAGCTGGGCG 900 TGGTGGTGGG TGCCTGCAGT CCCAGCTACT TGGCAGGCTG AGGCAGAAGA ATGGCGTGAA 960
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