| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11936 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:89734790-89735600 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:89735275-89735288 | TTCTAGAACATTC | + | 7.52 |
|
| | 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 |
| GH16I089668 | chr16 | 89735009 | 89735208 |
|
Enhancer Sequence | GTTCGTGAGC TACCAAGTGT CCCCACAAAG CTGTAAAACA ACATGACCAC TGTAGTTACG 60
TTTCTGTAAA AAGGTGACTG AGTCTTCTAA CCCTGACCAC ACATATGTGT GCAGAGAGAG 120
CCAGCTCCAT CCTGCTCTCC CAGAAGCCTG AACAGCTGTG CCCTAGCTCG TAGCAGTGGC 180
ACTCCAGGAA GGGGGCGGGC GGCTGTGCCC GAGCTCGTAG CAGTGGCACT CCAGGAAGGG 240
GGCGGGCGGC TGTGTCTGAG CTCGTAGCAG TGGCACTCCA CGAAGGGGGT GGGCGGCTGT 300
GCCCGAGCTT GTAGCAGTGG CACTCCAGGA AGGGGCGGCC GGCCAGCCAG GAGAGCAGCC 360
GGTGAAGGAG CACTTTTGCT TTGTACGTGG CAACGCTCGG CAGGCTCAGC AGTTTCACAG 420
GTCTCAGGCG TTCCTTGTAA CCTTAACAGG TTTAAGAAAA TGTGAGCAAC ATCAGACATG 480
TCCATTTCTA GAACATTCTA ATGGATGAAG TTCTGTACAG AGGGCTTTAG CAGAATTAGA 540
GACCTTTGGA GTGGAAATGA TGTCTCTGAA CCTTGAGCTC TGAGGCGGTT CCTGCCTGGA 600
CGTGTGCCCT CCCTCCTTCC TTTGCTGGTC GCCCTGACAC CATCCTGCCA CGGATAGTGG 660
AAGTGTTTCT CCTGTTTTCT TCCCTGAAAA AGGGTGTCCA GCATCAGCAA CCTTCATGGC 720
TGAGTTGCAC ATCCCTTAAG CCCTGTAATG TTCATGGACA GTTTTGATCA CTTTTGGACT 780
CACCCATTTT TTCTGCTAAC CATACATCTT 810
|
