| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06876 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:26821530-26822440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:26821897-26821916 | CAGCCACCAGGGGGCACCA | + | 8.56 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I028495 | chr17 | 26821601 | 26821658 | | GH17I028494 | chr17 | 26821821 | 26821990 |
|
Enhancer Sequence | GTGAGAGGCC CCCAGCCCCC TCCTCAGCCT GTGTGAGGGT GTCTCTGTGG CAGGGAGAGA 60
GGGGGCCCTG CTTCTGTCCC ACAGAGGGGA GACCTGGTCC CCACGTAGGA GCCTCTCGGG 120
TAGGCAGAGC CTTTGCAGCA GCTGGGAAGA CTTAGGTTAG AGCCCTCATG TGGGAGGAAG 180
AAACACAAGC CCTAGGGACC TCTTTGTTCA GTTCTCAAAG TCCAAGGGAA GGCAGGATTC 240
TCTGGTGGGC AGAGCCTGTT CTCAGAGACA AATGCCATCC CACCCCAGCC CTTTGCCCGC 300
TGCCAGAGCA CACAGTAGCA TCAGCACCAA AGTAATTGGG GGTTGTGTTG ACGCGGTCTG 360
CCCTCCGCAG CCACCAGGGG GCACCATGAT CACACCCACC CAGGCTCTGG GGACCAGAAC 420
ATCTTTCCCC AGAGCCTCCA TCCAAAAGAG GGAAATCCCT GACACGGCAT CCCTGGGCCT 480
CCGTGTTCTG GCTCAAACAG AAGGTGGCTG CCCAGGTCAG GGATCGGTGC AGGGGACTCC 540
TGGGTCTGTG GCATGTTCAT CCACTGACTG TGCCCAGTCC TGTGCTAGGC GCTGGCCCCA 600
CTGAGCGAGA TTAAGTCCCA CCTTACAGCC TGGCATTCCA GACGTGGGAA GGCAAGACCT 660
CGGAGCTCTT CTGACCCTGT GGACTGTCCC TGTCCTCCCA TTAGCCTCTT GCAGCCTCTG 720
TCAGGGTCCT CCCCCAACTT TCCCTCCCTG CCAGGAGCAA GGTTCCCTCT GCCCCAAGCC 780
ACTGGACTGG AAGGGGCAGG AAGAGGGCTA AGGTTGTCCA GGGACCTCCT GAGAGAGGTC 840
AGGAAGGCAG GAGTCAGTGC GGTCAAAGAT TTTTGCTCCC ACCAAGCCCC AAATTTCCCA 900
AGAAGGCCCT 910
|
