| Tag | Content |
|---|
EnhancerAtlas ID | HS145-11326 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:77385090-77386070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr18:77385810-77385822 | GGGCACGTGGCC | - | 7.22 | | SPI1 | MA0080.4 | chr18:77385412-77385426 | AAAAACCGGAAGTT | + | 6.81 |
|
| | 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 |
| GH18I079624 | chr18 | 77384325 | 77386000 |
|
Enhancer Sequence | ACTGGTTCCT TTTTAAAGCC TACCTCTCTG CAGTAAGAGA CTATTTAATA ATGACAACAA 60
CAATATGCTT GTGAGAGCAA ACGAGGGTTG CAGCTCCAAT TCAAGAGGCC AACCATGGCT 120
AATCTTGAAG ATTTTCACTC ATTAGCTTTT TAAGGAGCTG TTAACTGCAA ACGTGGGACT 180
CAGAGCTTCG GGGACTTTCC GTGTTGAGTG TTCCGCCAGC AGTGCTTGCA TGTCTCAGCA 240
GCACAGAGCT ATTTCTGGGG AAAGCAGAAA TAATAAACTC ACTGAAAATA CCCATGATTG 300
ATCCAAGCTT CCTCTTTCAA AGAAAAACCG GAAGTTCCTC CTTCCGTATT CTTGTGGAAA 360
GCTTTGCAGG TGCAGGGCCA TGCGGCCGGG GAGACTGGGG AGCAGCCCTC CTGCCGCTGA 420
CGGGTCAGGC CGGCTCCGTG AGTGATTAAT TCCCAGGTCA CATTTCTGTC CACAGCTGGG 480
AGACGATGAT TAAAACTTGA GTGTGTTTAT TCCTTTGCAT TGGAACTTGA AAACATCAAT 540
TTTTATTTCT TGGATAAGTA ATCAGAAAAG TAAAACAAGA TGAAAGAAAG GAGAGTTTGT 600
GCTACGGACA CAGTCAAAGA CGTAGAAAGG CACAGTCCTG GAAGGAGTGT GGGAGCAGCT 660
TGAGAGCAGA TGGACGGAAA GAGCCACAGT GGAGGCAGCC CAGAGACACC TGGAGATTAG 720
GGGCACGTGG CCCAGGCCAC ATTTCAAACC ACAGGCAAGA GAATGGCTGA TTTGATCCCT 780
GGAATAGAGA CCATTTTGGA AAGTTAATTT GGAAGCCTGT AAGATGCAAA TTCCAAGCAG 840
ATTAAAGTTT GTAGTGATGG GGTTTTCTGT AGACAGACTT TTTCTAGATG TCCAAAGAGC 900
TGATCGGGCA CGGGGCTCCT GATCCGCCTG CCGGGCTCCA CGGGAAGAGC CTCAAGGTTC 960
CATTCGGTGC TGAGGCCGAG 980
|
