Variant report

Variant	rs17076613
Chromosome Location	chr6:147379956-147379957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17076400	1.00[AMR][1000 genomes]
rs17076616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17076618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17076629	1.00[AMR][1000 genomes]
rs17076639	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs6900567	1.00[AMR][1000 genomes]
rs6911338	1.00[AMR][1000 genomes]
rs73582223	1.00[AMR][1000 genomes]
rs73582235	1.00[AMR][1000 genomes]
rs73582237	1.00[AMR][1000 genomes]
rs73582240	1.00[AMR][1000 genomes]
rs73582241	1.00[AMR][1000 genomes]
rs73582243	1.00[AMR][1000 genomes]
rs7774882	1.00[AMR][1000 genomes]
rs927670	1.00[AMR][1000 genomes]
rs927671	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019245	chr6:147350834-147609776	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv538467	chr6:147350834-147609776	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886751	chr6:147354092-147490398	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147375400-147380000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:147375600-147380000	Weak transcription	HepG2	liver
3	chr6:147375600-147384400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:147377200-147381800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr6:147377400-147381600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:147377400-147385000	Weak transcription	Pancreas	Pancrea
7	chr6:147378600-147381200	Weak transcription	Fetal Brain Male	brain
8	chr6:147378800-147381000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr6:147379000-147381000	Enhancers	Pancreatic Islets	Pancreatic Islet

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links