Variant report

Variant	rs10029437
Chromosome Location	chr4:143167307-143167308
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1907109	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1907113	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1907117	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1907119	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1948323	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2130685	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2172023	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2627812	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2627816	0.82[EUR][1000 genomes]
rs2627817	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2627834	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2627835	0.93[ASN][1000 genomes]
rs2627836	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636632	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636641	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636642	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636643	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636647	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636655	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636656	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636657	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636660	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2636679	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2636685	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3102436	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3102437	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3102438	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3102439	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3102443	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3102446	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3113511	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3113513	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3113515	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498005	chr4:142515689-143502988	Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1027781	chr4:142943485-143306567	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830098	chr4:143050143-143234384	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv595604	chr4:143077401-143228914	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv830099	chr4:143138257-143285055	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143058000-143181000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:143129200-143169600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr4:143135400-143184200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:143151000-143185000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr4:143151200-143174000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr4:143153800-143181000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr4:143157600-143173800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr4:143158200-143173600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr4:143158400-143174000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:143158600-143173800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr4:143159200-143181000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr4:143159200-143181000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr4:143160200-143171000	Weak transcription	NHEK	skin
14	chr4:143160400-143180000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr4:143160600-143185000	Weak transcription	HMEC	breast
16	chr4:143160600-143186400	Weak transcription	HSMM	muscle
17	chr4:143164000-143172800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr4:143164400-143168000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr4:143164400-143169000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr4:143164400-143169000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:143164400-143181000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:143164600-143176200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:143164600-143186000	Weak transcription	HSMMtube	muscle
24	chr4:143164800-143170000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:143164800-143170000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr4:143164800-143170000	Weak transcription	NHDF-Ad	bronchial
27	chr4:143164800-143170200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:143164800-143170800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:143164800-143172800	Weak transcription	Primary T cells from cord blood	blood
30	chr4:143166600-143173000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr4:143167200-143168200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links