| Tag | Content |
|---|
EnhancerAtlas ID | HS165-15325 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr8:101920130-101921490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr8:101920239-101920256 | CAGGTCATCCTGACATC | - | 6.61 | | NFYB | MA0502.1 | chr8:101920315-101920330 | CTGATTGGTCCATGG | - | 6.98 | | SP2 | MA0516.2 | chr8:101920878-101920895 | AAGCGGGCGGGGCTTCG | - | 6.55 | | SPIC | MA0687.1 | chr8:101921475-101921489 | AAAATGAGGAAGCA | + | 6.04 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_10716 | chr8:101917592-101921965 | CD19_Primary | | SE_11102 | chr8:101916604-101922454 | CD20 |
|
| | 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 |
| GH08I100905 | chr8 | 101917929 | 101922028 |
|
Enhancer Sequence | CTCTCAGGAG ACCTGAAGTG GGTAGTTCCT TTCTGCAGGC ACGTGGTCCT GAGGAGTGTC 60
CAGCTCTCAG GGGAGAGGAG ACCCGGAGTG AGAAGCTCTT ATCCGCAGGC AGGTCATCCT 120
GACATCTCTC TGCGAGTCTA GCTGAGTCTG GGACTTCTAC GGGTTTTGAA GGGAGGAAGT 180
GTGTGCTGAT TGGTCCATGG GTGGCCATCG GCGGGGCTGG AAAAAACACC AAAAGTTCTC 240
ACTCCCGCGG TGGACTCCAC TGGGAACCGA CAGGCCCCAG GCCTCAGGTC GTCCCTGTCT 300
TCAAAGTGGG GCTTCACCGG GACCGCCCCT TTCCACCCGG GAACCTATCT GCCTCCTGCT 360
GCCATTGACA GGTTTGTCCA CCGCAATGCC CTGGCTATCC GTGCCATGGG GGACCTGCAG 420
GCCCCTTTCA GCCTTCCTCC CCGTGCTCGT TGGCACCCAA AGTCTGGAGG GGGCAGAGGC 480
GGCAGGGGGC TGGCATGGCA GGGCTGCCCC GAGTGTACGC ACACCCGGCC GGGTTGCAAA 540
GCGCCCGGAC TTGACCAAAA CTTTGCTCAG TCCCGGAGCA GACACTGGGA GTCTGGAGAA 600
GCCACGCATC TGGAGCAGGC ACTTCTGAGC CTGCAGAGGA AAGGGGACTT CCCGGGGCCC 660
CCGAGAGCAC AGGGATGCCC GGTTTGGGAG CCTTGGCTAG GCAGCTGCAG CTGCGCAGGA 720
GGGTGGGGCT TCCGCCCCGC CGACTCAGAA GCGGGCGGGG CTTCGGCCTC TTCCCGGCTC 780
CCGCCAGCTC CGTGGAGCCT GGAGCCCCAG CCGCGCCTCC CTGGCTGCAG CTGCTGTATT 840
CACAGCAGCC GCTTCAGGCG GGCCGCCACG GCGATCAGTT TTTCATGGCC TCCAGGTTCT 900
GATGAAGCGT GGGATTTTCT GCCCTGTACC CCTCAGAACA AGAAACCACC TTACTGCAGT 960
CTGTAAGTGG CTCCTCAGTA ACAGGGCACC CACAACTTTC ATGGCATCCG CCCGTTACTT 1020
TTGTGTCTTC CCTTCTGTGT GTGGGACCAG GAACCTGTGG AGCTGGCTCT CAGCTTACTG 1080
CTCTTTCTGC TATGTAAGCG ATCAACTGTC TGACTCTAAA AGTGACTCGT ATTTTTCCTT 1140
TTGAATCAGA CAGACCCTGA TCTGGGTTTT GCTTTGTGTT TTATGTGTGA GCTTTATACT 1200
CTGAAGTCGC TTTATATTTT ATTTTTTCAT TTATTAACAA ATATTTCTAT CATATTTCCT 1260
ATGGACCAAG CACTTTACAA AGTATTAATA CATTTAATAC TTGGTATAAC CCTATAAAGT 1320
CAGTGCTATT ATCACCCTCA CTTTAAAAAT GAGGAAGCAA 1360
|
