| Tag | Content |
|---|
EnhancerAtlas ID | HS176-18716 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:13080800-13081510 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:13081462-13081480 | CTTTCTTTCTTTCCTTTC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr19:13081466-13081484 | CTTTCTTTCCTTTCTTTC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr19:13081470-13081488 | CTTTCCTTTCTTTCTTTC | - | 6.34 | | IRF1 | MA0050.2 | chr19:13081396-13081417 | TCTTTCTTTCTTTTTCTCTTT | + | 6.96 | | SOX10 | MA0442.2 | chr19:13081432-13081443 | TTCTTTGTTTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGTGGGTGG GTGTGGGGAG GAGAGGGCTG GGTCTCACCA TTGGCAGAAG GCACAGGCTG 60
TGGCCCAAGA AAGATTTGGG TTCAAGTCCT GTATCCTCCA CCTGAATGTC TCGGTGCCTC 120
AGTTTCCTCC CTTGTAAAAT GCGACCCAAG CCTCCTCTAT CCTGGTCTCC TTGATTCCAC 180
TATCATGCCC CTCTCCACCC CCCAGTCTAT TTTTCCACTC AGCAGCCAGA GGGTGCCTGT 240
GAACACCAGA GTCAGATCTG GTTCCCCCTC CCCCTAGAAC CTTGCATGGC TCCCACTTTA 300
CTCAGAACAA AAGCCCAAGT CCTCTTCACA GCCCACAAAT TTCTGTACTC TCTGATCCTG 360
TTACCTCCCT GATTTCACCT CCTCCCACTC TCCCCCTCAG TTACTTTGCT TCTACACATC 420
AGCCTCCTTT TCCTCAGACA CCAACTTTCT TTCTGTTTTT TTAGACACGG GAGTCTCGCT 480
ATGTTGCCCA AGCTAGTCTT GAGCTTCTGG CCTCAAGCAA TCCTCCCACC TCAGCCTCCT 540
GAGTTCTAGG TGTGAGCCCG TCTCTTGCTT GATATACCAA CTTTCTTTCT TTTCTTTCTT 600
TCTTTCTTTT TCTCTTTCTT TCTTTCTTTT CTTTCTTTGT TTTTCTTTTT TTCTCTTTCT 660
TTCTTTCTTT CTTTCCTTTC TTTCTTTCTT TTCTCTCTCT CTCTTTCTTT 710
|
