| Tag | Content |
|---|
EnhancerAtlas ID | HS098-55639 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:102092520-102093560 |
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 | TGGGCAATGG CTGTGAGGGA GAGCTCAGGA AATGGGAAGG CCACCAGTGT GGCCCAGGGC 60
AGAGAGGTCA GGGGACCAGG CAGGAGACAG GATGTGGGGG GAGGCCAGTG CAGAGCACCT 120
GGGCCACAGC CACGGGTCAA GTTCGTGTTT ATGCTGGGAG CCTGGGGAAG CCGGCGAGAG 180
ACTGGAGTAG GAGTGGCCTT CAGGTCTTGG GGCGCCCAGT ACAGTGCAAG TGATGGGCTG 240
GGGCCCCTCC GCCCTCCTTG TCAAGCAGTG TCCACGGATA AGGGCGTCCC GGGGCGGGGG 300
GGGGACGTGG GCGAGGAGAT GGTGGAGCTG GGGGAAGGGA CAGGGACAGA AGGCAGAAGA 360
GTCACCCTCA GCGTCACCTT CTCTCCCCTC CCTACTCCGG AGGCCAAGCG CCCCAGCGGG 420
AGGCTTCCCT GCCCGCCTCG GCCTCGCTTA CACCGCAGGT GCTGTGAGTC ACCCACCTGC 480
GTGGTGAGTC AGGGGAGGAG GCCGAGAAGG CAGGTGGGCG GCGCGGCAGG GCGCCGGGCT 540
TCGCGGGGAG GGGAGCGCTG TCTCCCCACG CGCCCCTCCC CCACGAGCGG CTTCCAGAAA 600
CCCGTTTGCC CATCCCCGGC AGGAGGCCTC CGCCCGGCTT CTCGCTCCCT CTTCCCTCTC 660
CCCGACCCCC TCCCGGGCTG TCAGCCGACT GCCACCGTCA CCATGGCTAC GCGGCTCCCG 720
CTCAGTTCCA CAGTCAGCAG GAGTCGAGCA GGGGAGGCGG CTGTCTCCTT GGTCTTCCTG 780
CTGCACCGGG TTCTTTGAAA ATCAGCTCCT GACTGCATGT TGCGGATTCC AGGCCCAGCC 840
CCCTTACCTG GAAGGCTCAC CTTGAAAGAC GGCAGGATGA GACCAGGAAA CGGGGCCACA 900
GGCATACCAA GGAAGCTTAT TTTGCCTGGC TTCCCTTTTT AAGCACGGAT GCATACCGGT 960
GTGTTGGACA TGACTGATGA ACCAAGATTT GAGGAAGGCC ACCCACTGAG TGACTGGAGG 1020
TAGACGTGGA AGGCTTTGGT 1040
|
