| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00311 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:27969920-27971160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:27970081-27970099 | GGAATGAAGGAAGGACAA | + | 6.2 | | SREBF1 | MA0595.1 | chr1:27970870-27970880 | ATCACCCCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_20210 | chr1:27970184-27971289 | CD56 | | SE_25377 | chr1:27969875-27971753 | DND41 | | SE_39434 | chr1:27970139-27971232 | Jurkat | | SE_62470 | chr1:27916580-27996594 | Tonsil | | SE_66376 | chr1:27970139-27971232 | Jurkat |
|
| | 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 |
| GH01I027643 | chr1 | 27970001 | 27970965 |
|
Enhancer Sequence | GACCCAACTA TCATTGTGCA TATTAGTTGA TGTGTTTTTC TCTCTCCTTC CTTGACTTTG 60
GGCTCCACTA GGTTTCGTCG CTTTAACTTA GCATAGTTCA ACCAGCATCT TGCAGCGTCT 120
GGCACCCACT AGGTGCTTAA TAAAGACCGA CTGAGAAAAC AGGAATGAAG GAAGGACAAA 180
ACTTTGCCTA GTGGAGAGGG ATGACGTCTC AGAGGATTCT GAAGGACAAA CAGGTTGCCC 240
ACAGGTGAAA TCTCTGATTC AGCCTCCCAC TCAGTGGCTC TAGTGCCAGA CATGACACTC 300
ATTTTTGGGG AACCCAAACA GCAGAACTCT GACCAGCGGG TGGAGACTCG AGCAGGGAGG 360
ATTTCAGCTC AGGAGCAGGA AGAACTACAG CCGTGGGAAT AGCTCAGCAG CAGAATAGCT 420
GGTCTCGGGA GGTACCAAGG TGAGCATGCA GAGGGGACTC ACACGGACTG ACCTCATGCA 480
CAGGCAGGGA ATGCACCTGC ATGGTGACCC CGACCACAAG TCCCACCACC AAGCCTTTGC 540
CCAAAGGTCC TCCCACCTGG CAGCCTCTCT GTCCCCTTTT TTGCCCAGGC TTAGCCTCCG 600
AGAGAGCGGT ATTTTCTCCC TTCTCTAAGC CCTGAGCACT TCTTCTCTGC ACCACCAGGG 660
GTCCTGTGGC ACGATGTGCC TTTTTCGGGC AGGCATCTCT GCCTGGATAA GAAGCAAGGC 720
CTCTGACAGG TTGTGCGAAC TTGACCAAGT GTCTGCCTCT CTCTGGGCCC CTGTTTCCTT 780
TTTTGTACAA GGATAAGGTG GGACAAGATG CCCCAAGAAG CCTGTTTAAC CTTCAAATGT 840
CTTTCTTGGA GTCTGGTCCT CTAGTCCTCT ATGGCATTGG GGACTCCTAG GGGACAGGGA 900
CGATACTGGC TGAGGCCCCT GCCAGGACCC CCCAGGAACA GACCCAGCTT ATCACCCCAC 960
AGTGTGGACA TGCTGTGGTG ATACTCTCAC CTCCATTCTT GCTAAAGGCA GCGTGGCTCA 1020
AATTTAGGAC CCACAAGTTA CTGGCTGTGT GATCTTAGGC AAATGTCTTA ACAACTCTGG 1080
GCTTTAGTTT CCACACCGAT AAAACTAGAA CAGTAATATC TGATTATCAG GATGAGGAGT 1140
AAAGGAAATG ATGGCTTCGA AAGTATCTTG TACATAGCGG GTATACAAAA AGCTGTCAGG 1200
AGCCAGGGAG GGAGGTCTGA TGAGGAGTTT TGGAATCTCT 1240
|
