| Tag | Content |
|---|
EnhancerAtlas ID | HS050-32164 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr18:77384940-77385950 |
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 | TCCTGCTGTA TGGCTTGTAA AGATTGGCTA TTCGCAGGTT CCTGCGAGGA GGAATTTCAC 60
TGACACCACT GTTGCGGCAC TTATTTTTCT GTGCATAAAG ACTACTAATT TAGGACTTTA 120
TATCCACCAC AGAAAAGTCA ATTTTATGAG ACTGGTTCCT TTTTAAAGCC TACCTCTCTG 180
CAGTAAGAGA CTATTTAATA ATGACAACAA CAATATGCTT GTGAGAGCAA ACGAGGGTTG 240
CAGCTCCAAT TCAAGAGGCC AACCATGGCT AATCTTGAAG ATTTTCACTC ATTAGCTTTT 300
TAAGGAGCTG TTAACTGCAA ACGTGGGACT CAGAGCTTCG GGGACTTTCC GTGTTGAGTG 360
TTCCGCCAGC AGTGCTTGCA TGTCTCAGCA GCACAGAGCT ATTTCTGGGG AAAGCAGAAA 420
TAATAAACTC ACTGAAAATA CCCATGATTG ATCCAAGCTT CCTCTTTCAA AGAAAAACCG 480
GAAGTTCCTC CTTCCGTATT CTTGTGGAAA GCTTTGCAGG TGCAGGGCCA TGCGGCCGGG 540
GAGACTGGGG AGCAGCCCTC CTGCCGCTGA CGGGTCAGGC CGGCTCCGTG AGTGATTAAT 600
TCCCAGGTCA CATTTCTGTC CACAGCTGGG AGACGATGAT TAAAACTTGA GTGTGTTTAT 660
TCCTTTGCAT TGGAACTTGA AAACATCAAT TTTTATTTCT TGGATAAGTA ATCAGAAAAG 720
TAAAACAAGA TGAAAGAAAG GAGAGTTTGT GCTACGGACA CAGTCAAAGA CGTAGAAAGG 780
CACAGTCCTG GAAGGAGTGT GGGAGCAGCT TGAGAGCAGA TGGACGGAAA GAGCCACAGT 840
GGAGGCAGCC CAGAGACACC TGGAGATTAG GGGCACGTGG CCCAGGCCAC ATTTCAAACC 900
ACAGGCAAGA GAATGGCTGA TTTGATCCCT GGAATAGAGA CCATTTTGGA AAGTTAATTT 960
GGAAGCCTGT AAGATGCAAA TTCCAAGCAG ATTAAAGTTT GTAGTGATGG 1010
|
