Variant report

Variant	rs10841833
Chromosome Location	chr12:21637225-21637226
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:21635310..21637987-chr12:21651998..21654175,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1029931	0.94[CEU][hapmap];0.85[CHB][hapmap];0.89[CHD][hapmap];0.92[TSI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10492117	0.86[CHD][hapmap]
rs10770819	0.86[CHD][hapmap]
rs10841835	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs10841837	0.86[CHD][hapmap];0.90[JPT][hapmap]
rs10841839	1.00[ASW][hapmap];0.87[CEU][hapmap];0.82[GIH][hapmap]
rs10841840	1.00[ASW][hapmap];0.87[CEU][hapmap];0.84[GIH][hapmap]
rs11046089	0.83[CHD][hapmap]
rs11046093	0.86[CHD][hapmap];0.90[JPT][hapmap]
rs11046098	1.00[ASW][hapmap];0.87[CEU][hapmap];0.83[CHD][hapmap]
rs11046100	0.87[CEU][hapmap]
rs12231436	0.83[CHB][hapmap];0.89[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.86[ASN][1000 genomes]
rs12423412	1.00[ASW][hapmap];0.94[CEU][hapmap];0.83[CHB][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12424924	0.81[CEU][hapmap]
rs12582514	0.80[CHD][hapmap]
rs12829302	0.83[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs12833589	0.94[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17682462	0.80[CEU][hapmap]
rs2110159	0.83[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap]
rs2159944	0.93[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];0.83[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2284393	0.82[CEU][hapmap];0.94[CHB][hapmap];0.97[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.80[TSI][hapmap];0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2284394	0.84[CHD][hapmap];0.94[JPT][hapmap]
rs2300211	0.82[CHB][hapmap];0.84[CHD][hapmap];0.94[JPT][hapmap]
rs4762834	0.83[CHD][hapmap]

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	nsv898896	chr12:21561645-21695584	Strong transcription Bivalent Enhancer Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1043936	chr12:21562673-21979030	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv557741	chr12:21578559-22169854	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv1054220	chr12:21612158-21692103	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1036084	chr12:21631009-21792756	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10841833	PYROXD1	cis	Esophagus Muscularis	GTEx
rs10841833	PYROXD1	cis	parietal	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21595800-21650000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:21607000-21645800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:21611000-21652800	Weak transcription	Small Intestine	intestine
4	chr12:21611000-21653600	Weak transcription	Esophagus	oesophagus
5	chr12:21611200-21640800	Weak transcription	Fetal Heart	heart
6	chr12:21614800-21652800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:21617000-21653000	Weak transcription	Colonic Mucosa	Colon
8	chr12:21619800-21638400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:21619800-21652200	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr12:21619800-21652400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:21619800-21652400	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr12:21620200-21652600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:21620400-21637800	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:21620600-21652200	Strong transcription	Primary B cells from peripheral blood	blood
15	chr12:21623200-21649400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:21623800-21638000	Strong transcription	Placenta	Placenta
17	chr12:21623800-21639000	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr12:21623800-21639600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr12:21624000-21637600	Strong transcription	Adipose Nuclei	Adipose
20	chr12:21624000-21638200	Strong transcription	Primary B cells from cord blood	blood
21	chr12:21624200-21639800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:21624400-21638000	Strong transcription	Primary T cells from cord blood	blood
23	chr12:21624400-21638000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr12:21625000-21637400	Strong transcription	A549	lung
25	chr12:21626600-21641000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr12:21628200-21649200	Weak transcription	HepG2	liver
27	chr12:21629000-21637400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr12:21630400-21652000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:21630400-21652400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:21631600-21637400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:21632000-21649000	Weak transcription	Psoas Muscle	Psoas
32	chr12:21632600-21646800	Weak transcription	Fetal Intestine Small	intestine
33	chr12:21632800-21639400	Strong transcription	NH-A	brain
34	chr12:21633600-21642000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr12:21633800-21641000	Weak transcription	Brain Angular Gyrus	brain
36	chr12:21633800-21641800	Weak transcription	NHEK	skin
37	chr12:21633800-21642000	Weak transcription	Brain Substantia Nigra	brain
38	chr12:21633800-21645400	Weak transcription	Gastric	stomach
39	chr12:21633800-21645600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:21633800-21645600	Weak transcription	Fetal Stomach	stomach
41	chr12:21633800-21645600	Weak transcription	Right Ventricle	heart
42	chr12:21633800-21647000	Weak transcription	Pancreas	Pancrea
43	chr12:21633800-21647000	Weak transcription	Spleen	Spleen
44	chr12:21633800-21647400	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr12:21633800-21648600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr12:21634000-21642000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:21634200-21649000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:21635200-21646200	Weak transcription	Fetal Kidney	kidney
49	chr12:21635600-21641800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr12:21635600-21642400	Weak transcription	Lung	lung

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