Variant report

Variant	rs9403470
Chromosome Location	chr6:143579237-143579238
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143578191..143580326-chr6:143614788..143617612,2	K562	blood:
2	chr6:143578203..143580061-chr6:143580169..143582946,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10484581	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10484582	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10484583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12055523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12055848	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12176429	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1424924	1.00[AFR][1000 genomes]
rs1593289	1.00[AFR][1000 genomes]
rs17072338	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17072347	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17072349	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs17072381	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17072390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17072404	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17072408	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17072410	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs17072450	1.00[AFR][1000 genomes]
rs17072501	1.00[AFR][1000 genomes]
rs17072541	1.00[AFR][1000 genomes]
rs17072544	1.00[AFR][1000 genomes]
rs2328475	1.00[AFR][1000 genomes]
rs4458714	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4482993	1.00[AFR][1000 genomes]
rs4895603	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs4895604	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4895608	1.00[AFR][1000 genomes]
rs4895610	1.00[AFR][1000 genomes]
rs4896625	0.88[AMR][1000 genomes]
rs4896630	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4896631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4896654	1.00[AFR][1000 genomes]
rs6932032	0.93[ASN][1000 genomes]
rs7452873	1.00[AFR][1000 genomes]
rs7765576	0.92[ASN][1000 genomes]
rs7769247	0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9321895	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9321896	1.00[AFR][1000 genomes]
rs9373380	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9373382	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9373383	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9376732	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9376733	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs9376734	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9376735	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9386028	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9386029	1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9390071	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9399431	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9399432	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9403465	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs9403467	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs9403469	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9403471	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9403472	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9403473	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9403474	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9403476	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9496541	0.93[ASN][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	nsv981344	chr6:143566840-143579617	Strong transcription Active TSS ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143545400-143588800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:143554200-143581400	Weak transcription	Psoas Muscle	Psoas
3	chr6:143563400-143579800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr6:143564200-143583000	Weak transcription	Pancreas	Pancrea
5	chr6:143565200-143579400	Weak transcription	Ovary	ovary
6	chr6:143569000-143592000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:143569200-143586600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr6:143569600-143588600	Weak transcription	Aorta	Aorta
9	chr6:143570000-143581600	Weak transcription	NHEK	skin
10	chr6:143570800-143609200	Weak transcription	Fetal Intestine Large	intestine
11	chr6:143571000-143579800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:143571400-143581800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:143574400-143583000	Weak transcription	Liver	Liver
14	chr6:143576000-143579400	Weak transcription	Fetal Intestine Small	intestine
15	chr6:143576200-143585800	Weak transcription	Fetal Lung	lung
16	chr6:143578400-143579400	Weak transcription	K562	blood
17	chr6:143579000-143579600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:143579000-143581800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:143579000-143585600	Weak transcription	Fetal Stomach	stomach

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