| Tag | Content |
|---|
EnhancerAtlas ID | HS105-78780 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:102092560-102093580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | - | 6.68 | | RFX1 | MA0509.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | + | 6.69 | | RFX2 | MA0600.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | + | 6.39 | | RFX2 | MA0600.2 | chr8:102093215-102093231 | CGTCACCATGGCTACG | - | 6.63 | | Zfx | MA0146.2 | chr8:102092951-102092965 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_25430 | chr8:102089963-102095749 | DND41 | | SE_27458 | chr8:102090078-102093744 | Esophagus | | SE_36229 | chr8:102091981-102094113 | HMEC | | SE_64657 | chr8:102092135-102093972 | 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 |
| GH08I101077 | chr8 | 102089241 | 102094190 |
|
Enhancer Sequence | CCACCAGTGT GGCCCAGGGC AGAGAGGTCA GGGGACCAGG CAGGAGACAG GATGTGGGGG 60
GAGGCCAGTG CAGAGCACCT GGGCCACAGC CACGGGTCAA GTTCGTGTTT ATGCTGGGAG 120
CCTGGGGAAG CCGGCGAGAG ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT 180
ACAGTGCAAG TGATGGGCTG GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG TCCACGGATA 240
AGGGCGTCCC GGGGCGGGGG GGGGACGTGG GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA 300
CAGGGACAGA AGGCAGAAGA GTCACCCTCA GCGTCACCTT CTCTCCCCTC CCTACTCCGG 360
AGGCCAAGCG CCCCAGCGGG AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA CACCGCAGGT 420
GCTGTGAGTC ACCCACCTGC GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG 480
GCGCGGCAGG GCGCCGGGCT TCGCGGGGAG GGGAGCGCTG TCTCCCCACG CGCCCCTCCC 540
CCACGAGCGG CTTCCAGAAA CCCGTTTGCC CATCCCCGGC AGGAGGCCTC CGCCCGGCTT 600
CTCGCTCCCT CTTCCCTCTC CCCGACCCCC TCCCGGGCTG TCAGCCGACT GCCACCGTCA 660
CCATGGCTAC GCGGCTCCCG CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG 720
CTGTCTCCTT GGTCTTCCTG CTGCACCGGG TTCTTTGAAA ATCAGCTCCT GACTGCATGT 780
TGCGGATTCC AGGCCCAGCC CCCTTACCTG GAAGGCTCAC CTTGAAAGAC GGCAGGATGA 840
GACCAGGAAA CGGGGCCACA GGCATACCAA GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT 900
AAGCACGGAT GCATACCGGT GTGTTGGACA TGACTGATGA ACCAAGATTT GAGGAAGGCC 960
ACCCACTGAG TGACTGGAGG TAGACGTGGA AGGCTTTGGT TGCCATAGGC AACTTGGGGC 1020
|
