| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21113 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:110216060-110216580 |
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 | | Stat6 | MA0520.1 | chr5:110216556-110216571 | ATTTCTGAAGAAATG | - | 6.67 |
|
| | 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 | GATTACAGGC ACCCACCAAC ATGCCCGGCT TTTTTTTTTT TTTTTTTTTG TATTTTTAGT 60
AGAGATAGGG TTTTGCCATT TTGGCCAGGC TAGTCTTGAA CTCCTGACCT CAAGTGATTT 120
GCCCGCCTCA GTCTTCCAAA GTGCTGGGAT TACAGGCATG AGTCACCATG GGCCAGATTT 180
GTGTTTTGAT CCAAGTTTCC TTGAACAAAT TTCTGATCCA AACTGGGTTT GGAAGTCATG 240
ACAGAAACTG GACTGGGTCC AGGATCTGAT TGGCTCCAGT AATTAACTGG CTTGGATCCA 300
GTTAGAGGCC TCTTACATCT GAGTGAGTCA GAAAGAAACT GGTTGTAAAT GGCAATGGAA 360
ATTCGCAGAG ATTTTTGTGT TCTAACCTCT TGTTTTCATT TTTACTGTGT GCTCAGGCAG 420
GAAAAATATC ACTGTGTGAG GTGATCAAGG TAACCTGAGA GTAAAGCCAA TATTTGAGGT 480
AAAAATGGGA TCCTTAATTT CTGAAGAAAT GAGTTCCTTC 520
|
