Variant report

Variant	rs4838421
Chromosome Location	chr10:49769527-49769528
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10491040	0.87[ASN][1000 genomes]
rs10776614	0.91[ASN][1000 genomes]
rs10776615	0.91[ASN][1000 genomes]
rs10776616	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10857596	0.91[ASN][1000 genomes]
rs10857598	0.87[ASN][1000 genomes]
rs11101377	0.93[ASN][1000 genomes]
rs11101381	0.91[ASN][1000 genomes]
rs11101384	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12358311	0.91[ASN][1000 genomes]
rs12358315	0.91[ASN][1000 genomes]
rs12412164	0.93[ASN][1000 genomes]
rs1345104	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1345109	0.91[ASN][1000 genomes]
rs1345110	0.91[ASN][1000 genomes]
rs1345111	0.91[ASN][1000 genomes]
rs1348633	0.82[ASN][1000 genomes]
rs1445148	0.91[ASN][1000 genomes]
rs1473323	0.83[ASN][1000 genomes]
rs1814469	0.82[ASN][1000 genomes]
rs1838568	0.91[ASN][1000 genomes]
rs1838569	0.91[ASN][1000 genomes]
rs1838570	0.91[ASN][1000 genomes]
rs1838573	0.80[ASN][1000 genomes]
rs1838574	0.82[ASN][1000 genomes]
rs1838579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1900021	0.80[ASN][1000 genomes]
rs1965170	0.91[ASN][1000 genomes]
rs2077152	0.91[ASN][1000 genomes]
rs2120910	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4084916	0.87[ASN][1000 genomes]
rs4101278	0.80[ASN][1000 genomes]
rs4838418	0.82[ASN][1000 genomes]
rs4838422	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4838617	0.93[ASN][1000 genomes]
rs4838623	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56058334	0.91[ASN][1000 genomes]
rs56080723	0.80[ASN][1000 genomes]
rs56248718	0.80[ASN][1000 genomes]
rs6537568	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7071095	0.91[ASN][1000 genomes]
rs7071480	0.91[ASN][1000 genomes]
rs7072237	0.82[ASN][1000 genomes]
rs7074631	0.91[ASN][1000 genomes]
rs7085183	0.91[ASN][1000 genomes]
rs7085335	0.89[ASN][1000 genomes]
rs7088010	0.91[ASN][1000 genomes]
rs7094216	0.91[ASN][1000 genomes]
rs7096053	0.90[ASN][1000 genomes]
rs7098068	0.91[ASN][1000 genomes]
rs7350424	0.91[ASN][1000 genomes]
rs7350439	0.91[ASN][1000 genomes]
rs747533	0.90[ASN][1000 genomes]
rs7894707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7894971	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7896644	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7904456	0.91[ASN][1000 genomes]
rs7905247	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916108	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs935271	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49742600-49774800	Weak transcription	Aorta	Aorta
2	chr10:49751200-49771600	Weak transcription	Pancreas	Pancrea
3	chr10:49757400-49782200	Weak transcription	HSMMtube	muscle
4	chr10:49759200-49770400	Weak transcription	NH-A	brain
5	chr10:49761600-49780600	Weak transcription	HUVEC	blood vessel
6	chr10:49762600-49772600	Weak transcription	Brain Angular Gyrus	brain
7	chr10:49763200-49780800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:49763800-49772600	Weak transcription	Brain Substantia Nigra	brain
9	chr10:49764400-49777800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:49765000-49773400	Weak transcription	NHLF	lung
11	chr10:49765000-49776400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:49765400-49774000	Weak transcription	NHDF-Ad	bronchial
13	chr10:49766000-49776800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:49766200-49772600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr10:49767400-49769800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:49767400-49770600	Strong transcription	HSMM	muscle
17	chr10:49767400-49772000	Weak transcription	Osteobl	bone
18	chr10:49767600-49770400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:49767600-49770600	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr10:49768400-49770000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr10:49769200-49771200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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