| Tag | Content |
|---|
EnhancerAtlas ID | HS109-08105 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr16:1294700-1296010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr16:1295643-1295654 | CCTTCCCGCCC | - | 6.62 | | GLI2 | MA0734.2 | chr16:1294851-1294866 | CCTGGTGGGTGGTCA | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr16 | 1295489 | 1295973 | | chr16 | 1295495 | 1295885 | | chr16 | 1294888 | 1295037 | | chr16 | 1295534 | 1295914 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I001244 | chr16 | 1294874 | 1295973 |
|
Enhancer Sequence | GAGGGTGTCC GGCCGTGGGT GCACTGCTGG CCCCGCATGC TGGTGTTGTC CTTATTGGTC 60
ACCAGGAAAA ACACTGAACC TCCAGTTCTG AGCCTTGGCT ACCCCACGTG CTGGCGTGCA 120
GACAGCCACG TCTGTGCCCG GGAGGCCACA TCCTGGTGGG TGGTCAGGCA ACTCCCCCCC 180
ACCAGTGCCT CAGTTTCCCC ACATCAAAGA GGGATCCCTG ACCTAGAGGG TCTCAGCCGG 240
ACCCTCCAGC CTGGCCTGTG ATTTGGATCT GGGGAGGGCG GCAGGAAAGT CCTGGGCGCT 300
GCCCAGGGCC CCTAATCAGC TGAGTCATCA GGCTGGGGCA GCCAGGACGG TTAGGAAGGG 360
CCAACCCAGG CTGGGCCGTG AAGCGGTGCC CATCTGATCT GCCGCGCGAC CACAGGACCT 420
GCTGCCGGAT GTGGGGACAG GGACTTCTCA AAGGGTGGTT GTCACGAGGG CCTGAGCTGT 480
CTCCAAAGGG CTGCTGGGCC TGGAAGTATT TCTGTGTCTT TTTATTTAAA ATACACTTAT 540
TATTTTAGGA CAGGTTTAGA TTTATGGAAA AGTTTCGAAG ATAGTATAAC AGAGCTACCC 600
GCATGCCCCG GGCCCGCTTC CCATTCTTCC TCAGGAAAGG CTCATTGGCC ATAACGGACG 660
AACCAGCAGG ATTCGTTACA TTAACTGAAG CCCGGAGCTT ACTTGGGTTT CCTTACTCTC 720
CTTAACCTCC CGTTCCTGTC CCAGGACCTC ACCCCGGATC CTCCTGTCTC CTCCGGCTCC 780
TCTTGGCTGT GACCGTTTCT CTGGCTTCCC TTGCTTTTGA CCATGTTGAG GAGGGTTGGT 840
CAGCGATTTT GTAGAGTGCC AATCAATGGG GATTTGTCTG ACGTTGTTCT CATGCTTGGC 900
CTGAGGCCGT GGGTTTTAAA AGGAAGGGCA CGGAGGTAAA GTGCCTTCCC GCCCGTGTGG 960
TGGGGTCGCG TGGGGTTGCA TGGCGTCGCG AGCCGTCAAC CTGATTTACC CCCAGCTCAG 1020
GCGTAGCTGG TTCCTCACCG TGCAGCCCCT CCCTGCCAGC CTCAGTACCA CAGTGCCCGT 1080
GGAGGTGGGG TCGCCAGCCA TCAACCTGAT TTACCCCTGC CTCAGGCGTA GCTGGTTCCT 1140
CACCGTGCAG CCCCTCCCTG CTGGCCTCAG TGCTTCAGTG TTTGGAAGGA AGTTCCCCTG 1200
AACAGCCAGG TGGGGGTTGG GGGTTCCACT GTGCCCTGCC TCCATGAGAG GGGAGGGCTG 1260
TGACATTATT TTGAATTCTG CGTGGAGATT TGTCTCTTCT CCCCACTTAT 1310
|
