| Tag | Content |
|---|
EnhancerAtlas ID | HS145-18643 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr3:184209980-184210670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr3:184210031-184210042 | AGCCACACCCA | + | 6.14 | | ZNF263 | MA0528.1 | chr3:184210401-184210422 | AGGGGAGGACGGAGAGAGAGA | + | 6.32 | | ZNF263 | MA0528.1 | chr3:184210382-184210403 | AGAGGAGGAGAGAAGAGAGAG | + | 6.65 | | ZNF263 | MA0528.1 | chr3:184210385-184210406 | GGAGGAGAGAAGAGAGAGGGG | + | 6.82 | | ZNF263 | MA0528.1 | chr3:184210373-184210394 | GGGGGAGAGAGAGGAGGAGAG | + | 7.51 |
|
| | 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 |
| GH03I184492 | chr3 | 184209905 | 184210788 |
|
Enhancer Sequence | GGTTCAGTCC GGGGCGCCTG GACAGGTTGG CATTGGAAAG CGTGAGGAAG CAGCCACACC 60
CAGAGCGCAC TGCGGCTATC AGAGATGGGG TCTCCGGATC TGCGACTTCC ACGAGGCGCT 120
CGCGAGGGGG AAGTTAGGAA CTGGTTTCGC AAGGAAGGAT GCGGTTGGCA CACAGTGCGA 180
GGAGAAAGGG GTTCTTCGGG CTGAGCGCGG GCTCGCTCAG CTCAGCGTCA TCAAAGAATT 240
GCAAAGTAGA GAAGAAAGCG GCTGATTACC AAGGACGCCT TGGGCAGTGA GGAAGGGGGA 300
GGGTGAAGGG GAGCCAATAT ATGTGGGCTC CCAGGGTAGC CAGAAGGCGG CCCTCAGCAG 360
TATCTAGGGA GCGGGAGAGA GGGACAGGGG GTCGGGGGAG AGAGAGGAGG AGAGAAGAGA 420
GAGGGGAGGA CGGAGAGAGA GAAACCTGTG AGGATTCAGA CCGATGCCTG GGTGAGACTT 480
TGAGGGCTGG GGACCGTGAA TATGGCTCGC TAGCCTTCCT GTGGTCCCTT TTGCACTCAC 540
AGGCTAGTGA GCAGAGAGGG AACTGGATTT TCTTTTCTTT TCTTTTCTTT TTTTTTTTTT 600
TTTTTGATAC GGAGTCTAAC TGTGTAGCCC AGGCTGGAGT GCAGTGGCGC GATCTCGGCT 660
CACTGCAAGC TCCGCCTCCC GGGTTCACGC 690
|
