| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01079 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:22644780-22645710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:22645255-22645266 | GCTTCCCGCCC | - | 6.02 | | ZNF410 | MA0752.1 | chr1:22644894-22644911 | GTGTCTTATGGGATGGG | - | 6.03 |
|
| | 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 |
| GH01I022318 | chr1 | 22645181 | 22645330 |
|
Enhancer Sequence | AGAACAGAAT AAGATAGAAA ATATCAGCAT GCATTTCAAG AATTTAGAGG TATCTCTTTC 60
TTGAGACTTT TGCTGTTGGC GTGGGGGCCG CATGCTGGTA CAGTGGGCAC AGAGGTGTCT 120
TATGGGATGG GTGGGGGCAG GGGCCTCCAG CAGCTCTGAG GGTGGCCTGG AGGGGCCTCT 180
TCCTGCCCAC CCTGCACACG CATCCGAGTC CAAGCAGGGG CCCCAGGGGC GGTGGGAACA 240
GGGAGACCCT CTCAGCTCTC CCCTGTGCAT CTCGTGGGCT TGGAGTAGTC CCATAAATCG 300
TCTGCCCGGA GTCAGGGGCA TAGAACTCCC TGATTTATGC CCCGCCAGGT CCGCCCCCTC 360
TGCCTCCCTC TCGGGCTTTG TGGGGCCAAG GCCTGGCAGG CTGCTGGCTC CAGACGGCCC 420
CTGCGGTTGC CGTGGCGACA GGTTCAGGCT GGGCCATTAT CCCGGCTCCC TCACCGCTTC 480
CCGCCCTCAG GCAACCCTCC CTCCCTCGCT CGCATCAGGG CTGGCATTTG AACAGCACCG 540
CGGGCTTCTT CTCCATAAGC CTGGCCCCTC CTGCAGGATG CCCCCCAAGT CCAGTGGGAC 600
CCATGCATCC CTGTCACAGT GAAGTGCAGA CTTGGAACTC ACTAAGGCAA GGAAGGGGTG 660
CTGAGCAAGT GCCTGGCCAG CATGCGGATC CCGCTTCTCC ACTTCAAGGC TGGCCGTCGC 720
AGTACCAGCC TCATGGGCTC ACTGTAAAGA ACTCGTGAGG GTCTACAGGG AAAGGGCTGG 780
TCCCTGAGAC CCCTGCAAGT CTCCATTGCC TCATCTGTAA AGTGAGTGTA ATGACATTCA 840
CATTCATTGC TCTCTCCCAG GACCTGCAGC AGTGTCGGGC ACACGGTAGG TGCTCAATGG 900
ATGTGAGTGG ATAAATGAAT CCCATAGATC 930
|
