| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00499 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:22644830-22645760 |
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 | TATCTCTTTC TTGAGACTTT TGCTGTTGGC GTGGGGGCCG CATGCTGGTA CAGTGGGCAC 60
AGAGGTGTCT TATGGGATGG GTGGGGGCAG GGGCCTCCAG CAGCTCTGAG GGTGGCCTGG 120
AGGGGCCTCT TCCTGCCCAC CCTGCACACG CATCCGAGTC CAAGCAGGGG CCCCAGGGGC 180
GGTGGGAACA GGGAGACCCT CTCAGCTCTC CCCTGTGCAT CTCGTGGGCT TGGAGTAGTC 240
CCATAAATCG TCTGCCCGGA GTCAGGGGCA TAGAACTCCC TGATTTATGC CCCGCCAGGT 300
CCGCCCCCTC TGCCTCCCTC TCGGGCTTTG TGGGGCCAAG GCCTGGCAGG CTGCTGGCTC 360
CAGACGGCCC CTGCGGTTGC CGTGGCGACA GGTTCAGGCT GGGCCATTAT CCCGGCTCCC 420
TCACCGCTTC CCGCCCTCAG GCAACCCTCC CTCCCTCGCT CGCATCAGGG CTGGCATTTG 480
AACAGCACCG CGGGCTTCTT CTCCATAAGC CTGGCCCCTC CTGCAGGATG CCCCCCAAGT 540
CCAGTGGGAC CCATGCATCC CTGTCACAGT GAAGTGCAGA CTTGGAACTC ACTAAGGCAA 600
GGAAGGGGTG CTGAGCAAGT GCCTGGCCAG CATGCGGATC CCGCTTCTCC ACTTCAAGGC 660
TGGCCGTCGC AGTACCAGCC TCATGGGCTC ACTGTAAAGA ACTCGTGAGG GTCTACAGGG 720
AAAGGGCTGG TCCCTGAGAC CCCTGCAAGT CTCCATTGCC TCATCTGTAA AGTGAGTGTA 780
ATGACATTCA CATTCATTGC TCTCTCCCAG GACCTGCAGC AGTGTCGGGC ACACGGTAGG 840
TGCTCAATGG ATGTGAGTGG ATAAATGAAT CCCATAGATC ATTGTAAAAG TTCTTAAATG 900
AGAACATAAG CATGGCGAGT TGAAGGTGGC 930
|
