Variant report

Variant	rs9634728
Chromosome Location	chr13:76048125-76048126
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1050235	0.87[CEU][hapmap]
rs10507830	1.00[CHB][hapmap]
rs11148993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12146901	0.81[EUR][1000 genomes]
rs12146907	0.81[EUR][1000 genomes]
rs12146936	0.80[EUR][1000 genomes]
rs12855863	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs12865529	0.82[CEU][hapmap]
rs12869081	0.87[CEU][hapmap]
rs1325463	0.82[ASN][1000 genomes]
rs1359502	0.82[ASN][1000 genomes]
rs17064454	1.00[CHB][hapmap]
rs17064554	0.82[ASN][1000 genomes]
rs17064647	0.82[CEU][hapmap]
rs2031505	1.00[CHB][hapmap]
rs2031506	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs2146981	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3825440	0.82[ASN][1000 genomes]
rs4885295	1.00[CHB][hapmap]
rs4885298	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4885299	0.82[CEU][hapmap];0.85[EUR][1000 genomes]
rs7999938	0.82[ASN][1000 genomes]
rs9318351	0.83[EUR][1000 genomes]
rs9318352	0.82[ASN][1000 genomes]
rs9543938	0.93[CEU][hapmap];0.85[EUR][1000 genomes]
rs9543941	0.99[EUR][1000 genomes]
rs9543942	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9543943	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs9543948	0.83[EUR][1000 genomes]
rs9543949	0.83[EUR][1000 genomes]
rs9543952	0.82[CEU][hapmap]
rs9593081	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9593086	0.83[EUR][1000 genomes]
rs9600482	0.83[EUR][1000 genomes]
rs9634729	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs975435	0.82[ASN][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	esv2761803	chr13:75943309-76161774	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv455987	chr13:75972846-76090084	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv562346	chr13:75972846-76090084	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76020400-76054400	Weak transcription	A549	lung
2	chr13:76028400-76054800	Weak transcription	Esophagus	oesophagus
3	chr13:76031800-76053400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr13:76039400-76052000	Weak transcription	Right Ventricle	heart
5	chr13:76039600-76053600	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr13:76039800-76054200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr13:76040200-76054800	Weak transcription	Pancreas	Pancrea
8	chr13:76042400-76052000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr13:76043000-76051800	Weak transcription	Liver	Liver
10	chr13:76043000-76053000	Weak transcription	NHDF-Ad	bronchial
11	chr13:76043600-76053600	Weak transcription	Hela-S3	cervix
12	chr13:76043800-76053600	Weak transcription	NHEK	skin
13	chr13:76044600-76049000	Weak transcription	HepG2	liver
14	chr13:76045200-76049200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr13:76045800-76049200	Weak transcription	GM12878-XiMat	blood
16	chr13:76045800-76052000	Weak transcription	Right Atrium	heart
17	chr13:76045800-76054600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr13:76046000-76052000	Weak transcription	Left Ventricle	heart
19	chr13:76046000-76053600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr13:76046600-76048200	Enhancers	Adipose Nuclei	Adipose
21	chr13:76046600-76048400	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr13:76046800-76048400	Enhancers	Fetal Heart	heart
23	chr13:76047000-76048200	Enhancers	Fetal Lung	lung
24	chr13:76047400-76051000	Weak transcription	Ovary	ovary
25	chr13:76047400-76052000	Weak transcription	Psoas Muscle	Psoas
26	chr13:76047400-76052200	Weak transcription	Fetal Muscle Leg	muscle
27	chr13:76047800-76048400	Enhancers	Colon Smooth Muscle	Colon
28	chr13:76048000-76049200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr13:76048000-76049200	Weak transcription	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links