Variant report

Variant	rs13217619
Chromosome Location	chr6:28306671-28306672
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28305023..28307714-chr6:28355958..28358291,2	K562	blood:
2	chr6:28191649..28195458-chr6:28301378..28307708,9	K562	blood:
3	chr6:28099723..28110178-chr6:28301599..28306918,14	K562	blood:
4	chr6:28302870..28305047-chr6:28305335..28307557,3	MCF-7	breast:
5	chr6:28245880..28256877-chr6:28299741..28307557,21	K562	blood:
6	chr6:28103055..28111556-chr6:28296771..28308203,17	K562	blood:
7	chr6:28306214..28308475-chr6:28356791..28358478,2	K562	blood:
8	chr6:28233221..28238495-chr6:28301018..28307259,12	K562	blood:
9	chr6:28184981..28190782-chr6:28297491..28307222,23	K562	blood:
10	chr6:28233528..28236356-chr6:28305759..28308573,2	K562	blood:
11	chr6:28182366..28191375-chr6:28300021..28306741,17	K562	blood:
12	chr6:28220144..28224072-chr6:28306303..28309254,3	K562	blood:
13	chr6:28304462..28306809-chr6:28341388..28343447,2	K562	blood:
14	chr6:27857690..27865363-chr6:28300493..28306970,14	K562	blood:

No data

Variant related genes	Relation type
ENSG00000198315	Chromatin interaction
ENSG00000269293	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000261839	Chromatin interaction
ENSG00000137338	Chromatin interaction
ENSG00000137185	Chromatin interaction
ENSG00000197062	Chromatin interaction
ENSG00000176933	Chromatin interaction
ENSG00000238610	Chromatin interaction
ENSG00000235109	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs13190888	0.88[EUR][1000 genomes]
rs13191038	0.82[EUR][1000 genomes]
rs13191786	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13195291	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs13197633	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs13198809	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13201308	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs13201681	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13203816	1.00[AFR][1000 genomes]
rs13204012	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13205211	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13205911	1.00[CEU][hapmap];1.00[AFR][1000 genomes]
rs13207345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13208096	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13211507	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs13213152	0.83[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13213986	0.83[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13214023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2232423	0.83[CEU][hapmap];0.86[EUR][1000 genomes]
rs2232426	0.83[CEU][hapmap];0.86[EUR][1000 genomes]
rs2232429	0.83[CEU][hapmap];0.86[EUR][1000 genomes]
rs33932084	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34218844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34243448	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34371502	1.00[AFR][1000 genomes]
rs34396849	0.93[EUR][1000 genomes]
rs34505829	1.00[AFR][1000 genomes]
rs34546986	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34588114	1.00[AFR][1000 genomes]
rs34661125	0.93[EUR][1000 genomes]
rs34676049	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34691223	0.93[EUR][1000 genomes]
rs34832585	1.00[AFR][1000 genomes]
rs34871267	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34878803	0.93[EUR][1000 genomes]
rs34950484	0.93[EUR][1000 genomes]
rs35001169	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35016036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35017208	0.89[EUR][1000 genomes]
rs35030260	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35072899	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35098436	1.00[AFR][1000 genomes]
rs35345226	1.00[AFR][1000 genomes]
rs35353359	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35656932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35744819	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs35781323	1.00[AFR][1000 genomes]
rs35883476	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs36092177	0.86[EUR][1000 genomes]
rs55690788	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56075693	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56189111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs66886492	1.00[AFR][1000 genomes]
rs67340775	0.95[EUR][1000 genomes]
rs67381177	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67981811	0.86[EUR][1000 genomes]
rs67998226	0.93[EUR][1000 genomes]
rs68188794	1.00[AFR][1000 genomes]
rs72846780	1.00[AFR][1000 genomes]
rs72846794	1.00[AFR][1000 genomes]
rs72854513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7752448	0.90[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	nsv830620	chr6:28173997-28348033	Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs13217619	ZFP57	Cis_chr	lymphoblastoid	RTeQTL
rs13217619	BTN3A2	Cis_chr	lymphoblastoid	RTeQTL
rs13217619	AL022393.7	cis	Muscle Skeletal	GTEx
rs13217619	BTN3A2///BTN3A3	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28304400-28317400	Weak transcription	Pancreas	Pancrea
2	chr6:28304800-28317200	Weak transcription	Aorta	Aorta
3	chr6:28305000-28310000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:28305000-28317200	Weak transcription	Brain Anterior Caudate	brain
5	chr6:28305000-28317200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr6:28305200-28308000	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr6:28305200-28308000	Weak transcription	Fetal Stomach	stomach
8	chr6:28305200-28311800	Weak transcription	Brain Angular Gyrus	brain
9	chr6:28305200-28313800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr6:28305200-28317000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr6:28305200-28317000	Weak transcription	NHEK	skin
12	chr6:28305200-28317200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:28305200-28317200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr6:28305200-28317200	Weak transcription	HSMMtube	muscle
15	chr6:28305400-28306800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:28305800-28317200	Weak transcription	Stomach Smooth Muscle	stomach

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