| Tag | Content |
|---|
EnhancerAtlas ID | HS060-23064 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr22:30616760-30618160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:30617365-30617383 | TGAAGGGAGGAAGGAAAC | + | 6.4 | | IRF9 | MA0653.1 | chr22:30617277-30617292 | ATCGAAACAGAAACA | + | 6.1 | | ZNF263 | MA0528.1 | chr22:30617393-30617414 | AGAGGAAGCGAGAGAGGAGGG | + | 6.17 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_57361 | chr22:30616828-30617253 | VACO_503 |
|
| | 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 |
| GH22I030220 | chr22 | 30616158 | 30618014 |
|
Enhancer Sequence | AGCTTGGGTG AAGGGAGAGG CAATCCAGGA AGGCTTCCTA GAGCAGGTGC CATTGGGCTG 60
AGTCCTGAAA AATGAGTCAG GCAAGAAAGC AAGAGGCAGA AGAAGATGTC ACAGGTGAAA 120
AGGGTGGAAG CCTACTCAGG GAATGTTCTG GGTGGAGGTT GGGGTGTGAC AGGGAGGAGA 180
ATCCTGCCTG GTGTCCTGGG AAGGACAGTC CCCCGACATC TACCTCTACC CCCTGTGTTT 240
CTTCAAGCAA GCCCTTGCCC CTCTCTGGGC CTGGGTTCTA ACAAAAGCCC TTCCATCTCT 300
GAGGCTGAGA GTCTCTGGGG CTCAGGTTGG AGTGATGAGG GCAAAGGGAG GGCAGACGGG 360
GAATCAGGAG GAGGGGATGT CGTCGGGTGT CAGGGCCTGG AGACAGAGGG ACCGAGGCTT 420
CTATGGCCTT CGTGGCCACA GAGCCGGACC TGCTGCCCAG GGGCCACGTC CCCGCTACCC 480
TCAGGCCTCC CCAGGAAACA GAAGTGCCTG GGGAGGAATC GAAACAGAAA CACAGGTGTC 540
TCTCCCTGGG CAGATTCCAA GAAAAAAAAA GAAAGTGGCC TCTAGAGAAG AGAACTTGTG 600
AGCTTTGAAG GGAGGAAGGA AACCCAAGCC GCGAGAGGAA GCGAGAGAGG AGGGTAGGTG 660
TGAGAGAGAA GCAGGTGCCC CAGGCGCAGG CCACACCGGC CACGGCCCAC GGCCATGCCA 720
CCAGTCAGGC TTGTGGAACC CAACCGCAGG CAGCTTTGAG GGGGCACAAG AAGTGTGTGG 780
AGGAGGAGCG GGCCCTGATG ACGGTCCCCA GTGGTGCCAC CAGCTTCCTG TCTCCTCGGC 840
CCTGATACTC TCTTGGTCTC CCCAAGTCAC CGTGGCCCTG GCACTAATGA GTCCTGAATT 900
TGGAGTCATG GGGTCTCCTT TTGGCTTTTT GGAGAGTTCA GCCTTTTGGC CCCACCATGT 960
GTGATTTGCA GTCTCTGAGC CTCAGTTTGC TTGTCTGTAA AATGGGGACC GCCAGTGCTG 1020
CTCTCCCTCT GCCGTCGGGG AGCACAGAGT GTGCACTGGA GGAAGACAAA GCAATGTGCA 1080
TGAAAACACC TGGCCATGCA GACCTAAGGG ATGGGAGGAT CGTGGGCATG ATGATATTAA 1140
CCTCTTGTAT GGTGATGGTA TCCATTTCTT GGATGGTGAG GATATCAACC TCTTCGTGCA 1200
GTGTTTTCAC CTTTCTGAAG CATCTTCTCA TTACTTACCT CCTCTGAGCC TCACAGTGCC 1260
GAGTGCAAAA GGCCAGGTGG GTGTCCTTAT ACCCATTTGA CAGGAGATAA AACTGAGGCT 1320
TGGAGAAGCA GCATCACGGA GCAGGCAGGA GAACCATGGG GATGTTGGGC TCCTGGGGCC 1380
TGGACATCAC CACCCACCTC 1400
|
