| Tag | Content |
|---|
EnhancerAtlas ID | HS095-21870 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:186314200-186315100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr3:186314855-186314868 | AGGATGATGTCAT | + | 7.34 | | JUND(var.2) | MA0492.1 | chr3:186314854-186314869 | GAGGATGATGTCATA | + | 7.14 | | Zfx | MA0146.2 | chr3:186314336-186314350 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH03I186596 | chr3 | 186314590 | 186314989 |
|
Enhancer Sequence | TGCCTCAGCC TCCCGTGTAG CTGGGACTAC AGGTGCCCGC CACCACGCCT GGCTAATTTT 60
TTTTTGTATT TTTTAGTAGC GACGGGGTTT CACTGTGTTA GCTAGGATGG TCTCGATCTC 120
CTGACCTCCT GATCCGCCCG CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 180
CCGCACCCTG CCACAAAGAA CATTTTTTAA AATGTTCCTC TATTTGCATG AAAGGGCACT 240
GCCTGCTGTG GAAAGGATGG ATCCGGTGCA CATTCTATCA ACTATGGAGA GTCATGCAGG 300
GAAACAGATT GGTTGCTGTC CAGCTTCCAG GTCATTCTAG TGTCATATTA ACTCCCCTTT 360
CCGAGTGCTG CCCGGGGCCT ATTCATGCCT ACCCCTCCCC ATATGACTCA GGGAGGGGCT 420
CTCTGTACTC TTGGCAGCCA GAGAAAAGCC CATGATCTCT GGTGTAGAGA TGAAGTGGGC 480
ACAATTACAT CAAAAGGAGA GAGGGAGAGC TCACTCGTGA AAGCTTTCAT TTGGTATAAA 540
GAAACAATCA GGGGGAGAAA CGAGATGGGG GTGAAGCTGG AGATATTTCG GATGATAATC 600
TACCTCACTT TCCCTGTGGC TATGTTCTGG GTTTCCAATC AGGCCGAGTG GTTTGAGGAT 660
GATGTCATAC AGCGCAAGAG GGAGCTGTGG CCACCTGAGA AGCTTCAAGA GTTAGAGGAA 720
TTCAAAGAGA GGTTACGGAA GCGGAAGCGG CGGGAGGAGA AGCTCCTTCG CGACGCCCAG 780
CAGAACTCCT GAGGCCTCCA AGTGGGAGTC CTAGCCCCTC CCCTGATGAA ATATACATAT 840
ACTCAGTTCC TTGTTATTCA AAAAAAAAAA AAAAAAAGAG AAAACATCAG GAGCAATTGT 900
|
