| Tag | Content |
|---|
EnhancerAtlas ID | HS041-19036 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr8:27440530-27442020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr8:27441404-27441418 | TGTCCCTGGGGAGT | - | 6.05 | | Klf1 | MA0493.1 | chr8:27440894-27440905 | TGGGTGTGGCC | - | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28379 | chr8:27440292-27443297 | Fetal_Intestine | | SE_47912 | chr8:27440730-27441251 | Pancreas | | SE_47912 | chr8:27441395-27442601 | Pancreas | | SE_65621 | chr8:27440297-27442598 | Pancreatic_islets |
|
| | 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 |
| GH08I027583 | chr8 | 27440586 | 27443184 |
|
Enhancer Sequence | CCGCTTCAGC CTCCCGGAGT GCTGGGATTC CAGACGTGAG CTACTGAACC CAGCCAGCAG 60
CTAAAGGTTT AAATGTACCA CGTGTTCTTT GTATGCCAGG CCTGCACTGG GTGTGTCATT 120
CCTTTTAATT TTTGCAGCAT CCCTAGAAAG TGACACATTG CCCTTACTTT ACAGATGAGG 180
AAACTGAGGC TCAGAGAGGT ATCTCCAGAG GGTCTGTGAT GAGCAGCCAG GATGGGATCA 240
TAGGACTCAC TGGCTCCAGC TGAGCCCTAG GCTGGGCTGT AGTGTTTTCT CCCAAGCCAG 300
GCAGCCCGAC AGAGTCCACA CCAGCAGCAG AGCCTGGGGG ACCCACTGGA GTTCATGGCA 360
TTTCTGGGTG TGGCCAAGAT TGTTCCGCTT TAGGTCTGAA CCAGGAATCA AGGGACAAGT 420
CGGCCTCTTT CCTCCAGAGG ATCGGCCTCT CCCCAGGGGA GGGGGACTAC AGGTGGCACT 480
AGAGGGACCC CACTAAACAA ACCATGAGGA AGACTAACTG CCTGAAAGGT GCTGGGAAGT 540
GAAACACAAG AAGCCACGTA TTGGATCTGG GCAGGGAAGG GCCAAAGAGC AGTGAGGGAG 600
ACCAGCCCAA AGGCCTTGCT CTGTCTGGGT TACAGATTTG GGGTGAGAAT GGAAAGGGCC 660
CCGCAGGCTT TCTCTCTGTG GCCTCAGCTC CAACACAGCT GACAGCTTTA TGTGCCTGTG 720
TCTGTAGAGC CGGAGCTGAG CCAGGGAGCT TCCCAATAAA TTAAACTCTA AATCACACCT 780
GCCACCTTCC GGCGAACAGC CAGAAGCTCC AAGAGAGCTC CAGGGCCTCT GAGCTCAGCC 840
CACGTGGCTC TCCGGCTTAG CAGCTTCAGC AAACTGTCCC TGGGGAGTGA GCCAGGGCCA 900
GAGACACACT CAGCGCCTGT GGTTAGAATA ACCCTGTGCC CTGGGGCCTG TGGAAGCTCT 960
GCCATGGCCA GGCTGGTCCC CAAGACACCA CAGAGCATCT GCCTAGAAAG AGGCAAGTGC 1020
CCCTCCCCAG TGTGTACTCT GCATATACCC AGACCTGATG CCCAGAAACT CTGGCTCCTT 1080
GGGACAGTGG AAGATGCCCA GGCTGTGGAT TCAAGTGGAC TTAGCCTCTG ATCCTCGCCC 1140
CTCACTTACC TGCTGTGTGA CTCTAGGTAA ATCGCTCTGC CTCTCTGAGC TGTGGTTTGC 1200
CCATATATAA AGTAAAGCTG GTAGCAACAA TTGGGGTTGG GAGGATTCAG CGTCTAGTCC 1260
GCATGAAGGG TGCTCACCAG ATGTGCCCTC CCTTCTCACT ATGATAAACA AAGATTCTTC 1320
ATTCTCCATA CAAGACCCCC ACCTCTGGTG TCATCTGAAA CCCCACAGGA GGTGCCCTGG 1380
GCATCTGGTT TATGGCCCAC AGTGAGATGG CAAGGATGGG ACAGTGGGAC AGGCTTGTGG 1440
GGTGGGAGGG GGCGAACGAC CTCTCCAGTG AATCCAGAGG AGGGGCTGGG 1490
|
