Variant report

Variant	rs10843994
Chromosome Location	chr12:31823218-31823219
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:31819291..31822149-chr12:31822447..31825439,3	K562	blood:
2	chr12:31820306..31823293-chr12:31823300..31825334,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1072778	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10743763	0.90[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10771864	0.90[ASN][1000 genomes]
rs10843998	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs11051539	0.91[ASN][1000 genomes]
rs11051550	0.95[EUR][1000 genomes]
rs1115971	0.94[ASN][1000 genomes]
rs12316119	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2200232	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2374171	0.91[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2388926	0.84[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs4272863	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.95[GIH][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap]
rs4931537	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7133297	0.97[EUR][1000 genomes]
rs7295568	0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];0.88[ASN][1000 genomes]
rs73090337	0.91[AFR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7309916	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7953032	0.94[ASN][1000 genomes]
rs7957042	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7966525	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7968792	0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs7970095	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7980264	0.91[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.92[JPT][hapmap];1.00[LWK][hapmap];0.89[MKK][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs900609	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs900610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[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	esv2760267	chr12:31626732-31909908	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
2	nsv1043010	chr12:31798446-32143151	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv541446	chr12:31798446-32143151	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv3432694	chr12:31801467-32109828	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv898966	chr12:31810126-31944985	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31812800-31823800	Weak transcription	Small Intestine	intestine
2	chr12:31813000-31826000	Weak transcription	Gastric	stomach
3	chr12:31813200-31837000	Weak transcription	Fetal Brain Male	brain
4	chr12:31813400-31825200	Weak transcription	Aorta	Aorta
5	chr12:31813400-31825400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr12:31813400-31825600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:31813400-31826600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr12:31813400-31835200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:31813400-31835600	Weak transcription	Brain Angular Gyrus	brain
10	chr12:31813400-31836200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr12:31815200-31840600	Weak transcription	Pancreas	Pancrea
12	chr12:31815800-31826200	Weak transcription	Brain Substantia Nigra	brain
13	chr12:31817400-31850400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr12:31821600-31823800	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
15	chr12:31822400-31823400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr12:31822400-31823800	Strong transcription	Primary T cells from cord blood	blood
17	chr12:31822400-31823800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr12:31822400-31824600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr12:31822400-31825000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr12:31822400-31827200	Weak transcription	Fetal Stomach	stomach
21	chr12:31822400-31828600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:31822400-31835600	Weak transcription	Fetal Lung	lung
23	chr12:31822400-31836600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:31822400-31840600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr12:31822600-31823400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr12:31822600-31823800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr12:31822600-31824000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:31822600-31824000	Weak transcription	Adipose Nuclei	Adipose
29	chr12:31822600-31824200	Weak transcription	Liver	Liver
30	chr12:31822600-31825600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:31822600-31826000	Weak transcription	Left Ventricle	heart
32	chr12:31822600-31826200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr12:31822600-31826200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:31822600-31827800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:31822600-31828000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:31822600-31829600	Weak transcription	Brain Hippocampus Middle	brain
37	chr12:31822600-31830400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:31822600-31830800	Weak transcription	HSMMtube	muscle
39	chr12:31822600-31835200	Weak transcription	Ovary	ovary
40	chr12:31822600-31835600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:31822600-31835600	Weak transcription	Fetal Brain Female	brain
42	chr12:31822600-31835600	Weak transcription	Fetal Muscle Leg	muscle
43	chr12:31822600-31836000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr12:31822600-31836400	Weak transcription	Brain Anterior Caudate	brain
45	chr12:31822600-31862000	Weak transcription	Rectal Smooth Muscle	rectum
46	chr12:31822600-31874200	Weak transcription	Right Ventricle	heart
47	chr12:31822800-31826400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr12:31822800-31826600	Weak transcription	HSMM	muscle
49	chr12:31822800-31826800	Weak transcription	Placenta	Placenta
50	chr12:31822800-31827200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links