| Tag | Content |
|---|
EnhancerAtlas ID | HS116-01172 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:46504750-46505740 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:46504933-46504947 | 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 |
| GH01I046039 | chr1 | 46504935 | 46505626 |
|
Enhancer Sequence | ACGGCCTCAG CTCACTGCAA CCCCTGCATC CCAGGTTCAA GCAATTCTCA TGCCTCAGCC 60
TCCCGAGTAG CTGGGATTAC AGGTGCATGC TACCACGCCC AGCTAATTTT TGTACTTTTA 120
GTAGAGACGG GGTTTCACCA CGTTGGCCAG GCTGTTCTCG AACTCCTGAC CTCAGGTGAT 180
CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCA TGAGCCACCA CGCCCAGCCC 240
CAAGTAAACA AGTTTGAAGT GTCGGTGAGA TACCCAGGAG CCCAGTGGAA ACATCCAGCC 300
AGCGGGTAGA GTTCAGAAGA AAGAACTGGG AAGGAGCTAG GAATTTGAGC ATCCTAAACA 360
CAGAAGTGCG AACAACTCTG GGATTAGGAG AAATCCATAG TTCCTGGCAG TGGTCTTGGG 420
ATGCTGTGTA GCTAAAGTGT AGTGGGGAGA AAAGACATAG GCAAGGTCAC TTAGAACAAC 480
AGGCTGTTCC CTGCCCAATC TGACTTATTT ATAATTGAGT ACACATGGGT GGGGCCTGAG 540
ACATGGATGA GCGCTGCAAT ATCCTATGCA ACAAGAGGTT ATCGCATGTT GGCTCATTAC 600
GTTCCCAGAA TACAGGAAGC TCAACAGTGT GCCTTGGCAG GAGATGACAA GGGCCTGGGG 660
CAATAAGAGG ATAGATTATA AAGCTGGGCC CATTTCCCCC TCCCCCAGAG TAGAATGTGG 720
AAACACTTCA TTCTGGGCAG AAATATGAGA ACCAATAAAC AGCTTATTAG GAGTGGGCAG 780
TGAGGTGTGG AGGAAATGGC ATTCAGTTTT AATTTTCTCA GAGTCAGTAT CTAAGACTTC 840
TGTGTCTGTG TTCGGTGGAC AGGACTCTGG CATCATGCCT AGTTGGAGTC AATGTCCTCC 900
CCTAGGAAGA AAAGAGCCTC TGGCTGCCCC AGTACTAGTC TTTTGGTGCT TACTGGAGAG 960
AAGGTTTGGA AGTTTCAAGG GCTGTTCAAC 990
|
