| Tag | Content |
|---|
EnhancerAtlas ID | HS062-14038 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr6:39133920-39134860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:39134359-39134378 | TGACCACAAGGGGGCAGTG | + | 7.67 | | KLF5 | MA0599.1 | chr6:39134576-39134586 | GGGGCGGGGC | - | 6.02 |
|
| | 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 |
| GH06I039166 | chr6 | 39134301 | 39134470 |
|
Enhancer Sequence | CCTGGCAGAA GCCTTCCAGC CTCACCCCTC TCTGCCCAGG GCTTTTTGCA AAAGGTGTCT 60
CACAAGCCCT CGCAACAGCT CCTGAGGCCT GTGGGATGGG AACTGTGAGT CTCATTTTAT 120
AAACAAGAAC ATGGAGGCTC AGAGAGGTTA TCAGACTTAT CCAAGTCACA CAGCATGTTG 180
AGGACAGCAG TATTCACGCC CTGGTCTCTA TACTCCCAGG CCGGAGCTGG ACACACCGCA 240
CCACGTGGCT TTGGTTTCTG ATGGTTCTTG CTTTGGGAGC CTTGGCCTGA AGGAGAAAGG 300
GAAGCCAGAG GCAGATTCCC TGAGTTATCT GGTTCTGATC CCAGCCAGAG AGCATCTGGC 360
TTTGGGGGAG GTCTTCGTCC TCCAGGCACT TAGAGCATCC CCACTGCAGG GACAGGACGC 420
TTCGGCTTTG CTGGCGGCAT GACCACAAGG GGGCAGTGGC GCTGCATGTG ACGATCTACG 480
GGCGGGAGGG ACTCGAGGTC TCCAGAGACG GGCAGGTGGC TCTGCTTCCC TGCGACACCC 540
TCAGAGCCCC CAGCTGCCAG CATCCTGCCC AGACACCTCT CCTCCAATGA GCGCTCATCA 600
GCCTTCAGAA TACATAACTT TGACTCTCAA TGGTCTCTTC TGGGTTTCCC TTAGCTGGGG 660
CGGGGCTTGC TGCTGGAGAA GCCTCCATCT CCCACCACAA ACTCCCACAT TCAGCCCCGA 720
CTCGAAATTA CTGGAGTCCC CTTCACTCCA TGCTTCCTCC TCCTTCTCTC CCCTTCCTCG 780
GGAGCTTAGA ATTTGAAGAG GACAGCTCCT CCAGGTGTTC TCAAAGTGGG TTCCACAGAG 840
CCTGTGAGAT CCCTAAGGGA ACCCCCTAGG AACGTGTGGG GAGCAAGGTG GGCTGGACAG 900
GGACTTGGAA CTGTTGGAAG AAGAGTCCAA AAGTCCATGC 940
|
