Variant report

Variant	rs7234474
Chromosome Location	chr18:28854117-28854118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSG1-7	chr18:28853309-28855721	NONHSAT058813

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1365290	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961568	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961573	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16961579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961588	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961589	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961590	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16961592	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961601	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961609	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16961613	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16961641	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16961648	1.00[CEU][hapmap];0.82[AMR][1000 genomes]
rs16961657	1.00[CEU][hapmap]
rs16961679	1.00[CEU][hapmap]
rs17728162	0.81[ASN][1000 genomes]
rs17728400	0.88[EUR][1000 genomes]
rs17801172	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17801274	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2912319	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56697971	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59592286	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59593146	0.88[EUR][1000 genomes]
rs59844732	0.82[AMR][1000 genomes]
rs60220975	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62087706	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62087750	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62087751	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62087754	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62087755	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62087756	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62088669	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62088670	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62088672	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs62088673	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62088674	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62088676	0.82[EUR][1000 genomes]
rs62088713	0.88[EUR][1000 genomes]
rs6506905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6506907	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7237750	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8096678	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9966811	1.00[CEU][hapmap]

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	esv3360998	chr18:28693111-28881812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28848200-28854800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr18:28849400-28854200	Weak transcription	HMEC	breast
3	chr18:28849400-28854800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr18:28849400-28854800	Weak transcription	Hela-S3	cervix
5	chr18:28849400-28854800	Weak transcription	NH-A	brain
6	chr18:28849400-28855000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr18:28849600-28854200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr18:28849600-28854200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr18:28849600-28854200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr18:28849800-28854200	Weak transcription	NHEK	skin
11	chr18:28849800-28855000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr18:28850000-28855000	Weak transcription	Fetal Heart	heart
13	chr18:28850000-28855000	Weak transcription	Small Intestine	intestine
14	chr18:28850200-28854800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr18:28850200-28855000	Weak transcription	Stomach Mucosa	stomach
16	chr18:28853200-28855200	Enhancers	Fetal Intestine Large	intestine
17	chr18:28853800-28855200	Enhancers	A549	lung
18	chr18:28853800-28855400	Enhancers	Liver	Liver
19	chr18:28853800-28855800	Enhancers	Fetal Intestine Small	intestine
20	chr18:28853800-28859400	Enhancers	HepG2	liver

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