| Tag | Content |
|---|
EnhancerAtlas ID | HS098-28650 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:636580-637430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr2:637095-637106 | GGGCGGGAAGA | + | 6.14 |
|
| | 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 |
| GH02I000636 | chr2 | 636179 | 637357 |
|
Enhancer Sequence | GCCTGATGAC TCCATTTTGT CGCTGCGGAG GAGCCGCACC GAGTCCACAG CGCCAGTGCG 60
GGGGAGCCGC GCCGGGGAAG AGGGAGGAGG CGCGTCCACA GCAGCCTCGT GTCTCCACAT 120
GGGACGTTTC CTCGGCGGGG ACCCGGCGCG CCCAGGGGCT CAGGCTCGCT CAGGCCTACG 180
GAGGCGGGTG TATCCGCGTC CGGCCCGACT TGTGAGGAAA CAGCACACGT GAAGCGAGCG 240
GAGTCGGCGC AGCCTGGAAC AGGGTGAATC CGCAGAGTCC TCGGCCGCGC ATGGCGGCTC 300
TGTCAGCTCC AGGGACACAG GGACCGTCCC CGGGCCCATC AGCGCAATCG GGAGGGCGTC 360
CGTGTGCCCA CAGGCCCAGC TACACCTCCA CAAAGCTGGG AAAGACGAAC ACGGGCCACC 420
CTCAGCCACC TGCCCGGACC GCTGCGAGGC CCACGGGAGG GAAGACGCGC CCTGGCACGC 480
GGTGTGGTAA CCGCCCTTGG ACGCGGCGGC GCTTTGGGCG GGAAGAACCG CGAATTCCAG 540
AACATTTGGG ATCATTTGTT AAAAGAAAAA TCCTCGGGCG CCACCTAGCG CTGACATGCT 600
GCCTAACTCT TCTCAGCCCT CATTTTAGAG AACGGAAAAT GAAGCCCAAG TTATTGACTA 660
TAAAATGGGA AAAAACTAAA ACATTGCAAT ATGCAGATTG CATCACACAT ATTATCTTAG 720
CAGGTTTTCT TGCACTTGCC TTGCAGATAA ATAGGACATA TCTAGGTGGT GCTGTGTCCA 780
ATAAAATAAC ACATCTGAAC TCAGGTAAGG AAGGGTTCTC TCAACAGGGA GAGGTTCCAG 840
CCAGGAGACC 850
|
