Variant report

Variant	rs12058182
Chromosome Location	chr1:172805122-172805123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10912480	1.00[AMR][1000 genomes]
rs12065145	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12074858	1.00[AMR][1000 genomes]
rs12076562	1.00[AMR][1000 genomes]
rs12079004	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12083050	1.00[AMR][1000 genomes]
rs6671377	1.00[AMR][1000 genomes]
rs7526843	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv947552	chr1:172794244-172807477	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172791200-172806200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:172796000-172806200	Weak transcription	HMEC	breast
3	chr1:172796000-172813800	Weak transcription	Small Intestine	intestine
4	chr1:172797800-172807000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:172797800-172807000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:172798200-172806600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:172801800-172806800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:172801800-172807000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr1:172801800-172808000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:172802000-172806800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr1:172803400-172806200	Weak transcription	NHEK	skin
12	chr1:172803400-172806400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:172803400-172806800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:172803600-172806800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:172803600-172806800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr1:172803600-172807400	Weak transcription	Dnd41	blood
17	chr1:172803800-172807200	Weak transcription	HSMM	muscle
18	chr1:172804800-172807000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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

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