| Tag | Content |
|---|
EnhancerAtlas ID | HS088-35678 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr22:46763750-46764760 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:46763795-46763813 | GCTCCCTTCCTCCCTCCC | - | 6.09 | | EWSR1-FLI1 | MA0149.1 | chr22:46763799-46763817 | CCTTCCTCCCTCCCTCTC | - | 6.27 | | EWSR1-FLI1 | MA0149.1 | chr22:46763894-46763912 | CCTTGCTCCCTTCCTCCC | - | 7.28 | | ZNF263 | MA0528.1 | chr22:46763794-46763815 | TGCTCCCTTCCTCCCTCCCTC | - | 6.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65618 | chr22:46762292-46764682 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46764354 | 46764585 | | chr22 | 46764116 | 46764166 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046367 | chr22 | 46763601 | 46763790 |
|
Enhancer Sequence | AGCTGCGGGA GGGCAGGATC AGGCCTGTGC CCATCGCCAC CACCTGCTCC CTTCCTCCCT 60
CCCTCTCTGC ACGTCCACCT GTCCACCTGC CTGCCCGTCC GCCCATCTAT CTGTCCGTCC 120
ACCTGTCCAC CCAGCCATCA TCCACCTTGC TCCCTTCCTC CCCTCGTAGC CAGGTACGGA 180
CTCATCCGGG AACCAGACAG AGCTCGTGTT AGTGGGGGTG GTGGTGGAAT ACATTAGGAA 240
GCAAATGAGA AAACAGGAGC TGTGAGGACT ACACCAGGCC AAGGGGCCTG AGCCATGCCC 300
ATGGCTGCAC TAGCTCCCGT GAGATACCCT GTGGAGAGGC AAGAGGAAGA GCCCAGGACC 360
TGCCCTTGAG CTGTGACCCT GCAATCAGCT TCCTGAGCTC TGCCTCAGTC TCCCCATGTG 420
TACAAGGGGA AGACAAAGGC GCATCCCCTC CCAGGGTTCA GAGGGGATGG AGTGAATCCG 480
GGTGACAGAG CCCGCAAGGT CCACAGGTCG TGGATGGCAC TGAAGACGAG GAACTGACAA 540
GGCCCCAGAC CCCCCGTGCA CCCCCATATC CGGCCTTCCA GGCCACTCAC TGCCTCTCCC 600
TCTCTGCCCT ACCCCCCTTC AGACTCGGCT CTCTCCTCCC GGGCCGGGAG CCTCACACTC 660
CTCCTGACAC CCAGCCCCTG CGCAAGCATT ATCCCTTCGC CCATCCCTGG CTCAGTCCCA 720
TCTCAGCTAC CAGGTCACCA GGGGCTGGCC TTGTTGTCTG ACAGATGCCC CCGTCAACCC 780
CTCCTGACCC TGTCGTGGCT CCTGGACGCT GTGCTGAGTC CTCCCGCGGT GCCACCTGCT 840
CCTTTGGGGC CTCGAAGGTC CCCTCTCCTC CCTAGAACAC TGGAGGTTCC CTCTGTGCTG 900
GGCCCCTGTT CCACTGCACC CTCTGACAGT GGGGTGGGGG GGTCTCCTCC CCTCCAGTGG 960
CCTCAGCAAC ACCCTCACCA CCCACCAGAA AGTTTCATCT CCCCCACCCC 1010
|
