| Tag | Content |
|---|
EnhancerAtlas ID | HS177-18212 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:110216010-110216540 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr5:110216216-110216227 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr5:110216216-110216227 | CATGAGTCACC | - | 6.02 | | MEOX2 | MA0706.1 | chr5:110216337-110216347 | AGTAATTAAC | + | 6.02 | | NFYA | MA0060.3 | chr5:110216324-110216335 | TCTGATTGGCT | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr5:110216156-110216171 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH05I110880 | chr5 | 110216201 | 110216370 |
|
Enhancer Sequence | TGCCTCCTGG GTTCAAGCAA TTCTCCTGCC TTAGCCTCTT GAATAGCTGG GATTACAGGC 60
ACCCACCAAC ATGCCCGGCT TTTTTTTTTT TTTTTTTTTG TATTTTTAGT AGAGATAGGG 120
TTTTGCCATT TTGGCCAGGC TAGTCTTGAA CTCCTGACCT CAAGTGATTT GCCCGCCTCA 180
GTCTTCCAAA GTGCTGGGAT TACAGGCATG AGTCACCATG GGCCAGATTT GTGTTTTGAT 240
CCAAGTTTCC TTGAACAAAT TTCTGATCCA AACTGGGTTT GGAAGTCATG ACAGAAACTG 300
GACTGGGTCC AGGATCTGAT TGGCTCCAGT AATTAACTGG CTTGGATCCA GTTAGAGGCC 360
TCTTACATCT GAGTGAGTCA GAAAGAAACT GGTTGTAAAT GGCAATGGAA ATTCGCAGAG 420
ATTTTTGTGT TCTAACCTCT TGTTTTCATT TTTACTGTGT GCTCAGGCAG GAAAAATATC 480
ACTGTGTGAG GTGATCAAGG TAACCTGAGA GTAAAGCCAA TATTTGAGGT 530
|
