Variant report

Variant	rs12822436
Chromosome Location	chr12:21658316-21658317
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:21657807..21659744-chr12:21755887..21758843,2	MCF-7	breast:
2	chr12:21655984..21659478-chr12:21666041..21668591,3	K562	blood:

Variant related genes	Relation type
ENSG00000111713	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10492117	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10770819	0.84[CEU][hapmap];0.84[CHB][hapmap];0.84[EUR][1000 genomes]
rs10841835	0.89[CEU][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10841836	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10841837	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10841839	0.85[CHB][hapmap]
rs10841840	0.85[CHB][hapmap]
rs11046089	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11046093	0.85[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.87[YRI][hapmap];0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs11046095	0.80[AFR][1000 genomes]
rs11046098	0.85[CHB][hapmap]
rs12582513	1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs12582514	0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs2110159	0.89[CEU][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2284394	0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs2284395	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2300211	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs2300212	0.83[ASN][1000 genomes]
rs2417991	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34965831	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35538394	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3782661	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4762834	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4762835	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61926331	0.83[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	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:4)

SNP	Gene	Cis/trans	Tissue	Source
rs12822436	RECQL	Cis_1M	lymphoblastoid	RTeQTL
rs12822436	LOC642732	Cis_1M	lymphoblastoid	RTeQTL
rs12822436	PYROXD1	Cis_1M	lymphoblastoid	RTeQTL
rs12822436	LOC642732///PYROXD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21655400-21674800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:21655600-21659400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:21655600-21660800	Weak transcription	Left Ventricle	heart
4	chr12:21655600-21661800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr12:21655600-21666000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr12:21656000-21658800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr12:21656000-21658800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:21656000-21659400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr12:21656000-21660000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr12:21656000-21660400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:21656000-21660800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr12:21656000-21660800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr12:21656000-21661000	Weak transcription	Fetal Intestine Large	intestine
14	chr12:21656000-21671800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:21656000-21672800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr12:21656000-21674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr12:21656000-21674600	Weak transcription	Fetal Kidney	kidney
18	chr12:21656200-21658600	Enhancers	Primary T cells from cord blood	blood
19	chr12:21656200-21658800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr12:21656200-21660000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr12:21656200-21660000	Weak transcription	Placenta	Placenta
22	chr12:21656200-21660200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr12:21656200-21660600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:21656200-21660800	Weak transcription	Primary B cells from cord blood	blood
25	chr12:21656200-21660800	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr12:21656200-21660800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr12:21656200-21660800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr12:21656200-21662000	Weak transcription	Fetal Intestine Small	intestine
29	chr12:21656200-21662000	Weak transcription	Fetal Stomach	stomach
30	chr12:21656200-21662200	Weak transcription	HSMM	muscle
31	chr12:21656200-21664000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:21656200-21665000	Weak transcription	HSMMtube	muscle
33	chr12:21656200-21665200	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr12:21656200-21665600	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr12:21656200-21666200	Weak transcription	Colonic Mucosa	Colon
36	chr12:21656200-21669800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr12:21656200-21671800	Weak transcription	Thymus	Thymus
38	chr12:21656200-21680000	Weak transcription	Right Ventricle	heart
39	chr12:21656400-21659200	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr12:21656400-21660600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr12:21656400-21660600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr12:21656400-21660800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr12:21656400-21661000	Weak transcription	Primary B cells from peripheral blood	blood
44	chr12:21656400-21662600	Weak transcription	Brain Germinal Matrix	brain
45	chr12:21656400-21668000	Weak transcription	Fetal Lung	lung
46	chr12:21656400-21680200	Weak transcription	Aorta	Aorta
47	chr12:21656600-21660600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr12:21656600-21663800	Weak transcription	NHLF	lung
49	chr12:21656600-21665200	Weak transcription	NHEK	skin
50	chr12:21656600-21665400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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