| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11245 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:30634890-30636340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr16:30635107-30635128 | GGTCAGTTTCAGTTTCTCTGC | + | 6.54 | | IRF9 | MA0653.1 | chr16:30635111-30635126 | AGTTTCAGTTTCTCT | - | 6.28 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATAACAACCT CCTGCAGCAG CTTAGTGTTT GAGAACTAAC CTGAGCACCA GATTGTTTAA 60
GTAAAACTTT AAGCAACTGC ACATAATGTT GCTCCTCAGT TGACAAATTC TGCCCCACGT 120
TACCCTGATT CACAAACTTC CCACTCCCAG TATCTCTTTA GGGCACTGAC CTTATATCCT 180
CTGCCAGCAG ATTTGTCCTG GGGTTTCTCA CTCATCTGGT CAGTTTCAGT TTCTCTGCTC 240
CAGCAGATCT TCTTCCTTCA CGTCCCTGAT TAGGCACCAC TTGTGGCTGT TGGTTTGGGA 300
CTGAATGAAG GAGGACAAAC GCAGAAATGA AGACAAAGAC AAAAGGATCT GTTTTAAGGA 360
AGGGGTCAGG GGGCTCCTTG CTTCTAGGGA ATAAGGGCCC TGAGCTTCTA CAGCCCTTCG 420
TATTTATTAG GTAGAATCGA CAGGGAGGAC GAGGCAACGG TTGATCAGCT GCTTGATTTA 480
TCACAGGCTC ACATAATTGC TTTCTTTATA CAACAGGCTC CAGATGTTCC TATAGATAAC 540
CACAAAGAAC ACTTCACCTA CGGCATGACC ATCCTCAGCA TTCCTTCTGG CGGCAGATGC 600
AGTTGTCAGC TTGCCCACAT CCTGCATCCA TGAGAACAGT TTGCTGTTTG CTCATATAGC 660
CTCCAGTGGT ATACTGAGTT GGTCACAACC CTCATTCTTT CGGCCTCCAA CACACAAACA 720
TGGGGACGGT CACCAGAGTG GATTTCCTGG TATTGGACCA ACAGTGAGAT GGAGGCAAAG 780
AGCTGCCCAC GGTCAAGACA TGCCTACGGC TTCTCCCTCA TGTGTGTGCC TGTGGGTGGC 840
CAGAGCCCCA CTTGTTCGAA CACAGTGGCC ACTCTGGGGG CAGCAGCAGG GTGTCTCATC 900
TCTGTGGATG AATGAGCGGA TGCTGGAGCA GACCCTTGCT TTGAGGGGGT GGGCAGTTAC 960
AGGGAAGGGC TGCTCCAGCA AGTGGATTTG GAGGGGCTGC CCAGGAAGAG GAGGGAGCCA 1020
AAGCCACTGG AGCCTGAGTG CACTGTCACC TCATGGTTGA GGAGCCCCCA GGCCATGTCT 1080
GGCCACAGGC CCTGCAGATA GGGCCTTTGG CTTCTCCAGG GGTCCTGCTA CTTGTGACAT 1140
ACTGACCACT TCCTCACACA GGCCACATTC AGTTTCTTGA CCCCCATTTC TTTTTTTTAA 1200
GACAGAGTCT TGCTCTGTCG CCCAGGCTGG AGTGCAGTGG CGTGATCTCG GCTCACTGCA 1260
AGCTCCGCCT CCCAGGTTCA CGCCATTCTC CTGCCTCAGC CTCCCCAGTA GCTGGGACTA 1320
CAGGTGCCCG CCACAAGGCC GGCTAATTTT CTGTATTTTT AGTAGAGACG GGGTTTCACC 1380
GTGCTAGCCA GGATGGACTC GATCTCCTGA CCTCGTGATC TGCCCGTCTC GGCCTCCCAA 1440
AGTGCTGAGA 1450
|
