Variant report

Variant	rs12298110
Chromosome Location	chr12:50387601-50387602
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	chr1:17230410..17232111-chr12:50386405..50387926,2	K562	blood:

Variant related genes	Relation type
ENSG00000272426	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10161020	0.98[EUR][1000 genomes]
rs10161120	0.98[EUR][1000 genomes]
rs10875992	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10875993	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11169232	0.86[EUR][1000 genomes]
rs11169234	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11169247	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11169256	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11169259	0.98[EUR][1000 genomes]
rs11169260	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11835014	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11836389	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12311010	0.96[EUR][1000 genomes]
rs12317586	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17124264	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2291612	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2292720	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs378943	0.96[EUR][1000 genomes]
rs4297542	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55634523	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55652312	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55802497	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55936104	0.98[EUR][1000 genomes]
rs55990533	0.98[EUR][1000 genomes]
rs56099252	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56159935	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56232366	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs56259551	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57014171	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57045365	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60000653	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60042968	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60456498	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60905953	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs611434	0.94[EUR][1000 genomes]
rs615382	0.96[EUR][1000 genomes]
rs629754	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs661823	0.83[EUR][1000 genomes]
rs694851	0.92[EUR][1000 genomes]
rs7131715	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7303531	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7306035	0.96[EUR][1000 genomes]
rs7308994	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7309480	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7309940	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7309966	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73119648	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73119651	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73119660	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73119664	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73119671	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73119681	0.98[EUR][1000 genomes]
rs73119688	0.98[EUR][1000 genomes]
rs73119690	0.98[EUR][1000 genomes]
rs7961683	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7972522	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7979958	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9325146	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9669608	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045327	chr12:49975040-50551375	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
2	nsv541490	chr12:49975040-50551375	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	170 gene(s)	inside rSNPs	diseases
3	nsv522972	chr12:50196394-50410831	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv530671	chr12:50233858-50708991	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
5	nsv832407	chr12:50243268-50412236	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv558835	chr12:50275137-50433234	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription 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	36 gene(s)	inside rSNPs	diseases
7	nsv469374	chr12:50349765-50467769	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Active TSS 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	28 gene(s)	inside rSNPs	diseases
8	nsv469375	chr12:50349765-50467769	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers 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	28 gene(s)	inside rSNPs	diseases
9	nsv558837	chr12:50349765-50467769	Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50367400-50401200	Weak transcription	Gastric	stomach
2	chr12:50369600-50418200	Weak transcription	Colonic Mucosa	Colon
3	chr12:50372400-50404800	Weak transcription	Spleen	Spleen
4	chr12:50377600-50403200	Weak transcription	Ovary	ovary
5	chr12:50377600-50405600	Strong transcription	Fetal Thymus	thymus
6	chr12:50377800-50399800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr12:50377800-50400800	Strong transcription	Thymus	Thymus
8	chr12:50378000-50399000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:50378200-50399200	Weak transcription	Fetal Brain Male	brain
10	chr12:50378200-50400000	Weak transcription	HSMMtube	muscle
11	chr12:50378600-50391800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr12:50378600-50400600	Strong transcription	A549	lung
13	chr12:50378600-50412800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr12:50378800-50396000	Weak transcription	Right Ventricle	heart
15	chr12:50378800-50401400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:50379000-50388200	Strong transcription	NHEK	skin
17	chr12:50379000-50405800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr12:50379200-50401400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:50379400-50401400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr12:50379400-50405600	Strong transcription	Hela-S3	cervix
21	chr12:50379600-50396600	Strong transcription	Fetal Muscle Trunk	muscle
22	chr12:50379600-50398200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr12:50379600-50400200	Strong transcription	GM12878-XiMat	blood
24	chr12:50379600-50403800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr12:50379800-50400600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:50379800-50401200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr12:50379800-50401600	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr12:50379800-50405400	Strong transcription	Dnd41	blood
29	chr12:50380200-50400800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:50380200-50404800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr12:50380400-50410600	Weak transcription	Aorta	Aorta
32	chr12:50380800-50394000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr12:50381000-50389000	Strong transcription	HMEC	breast
34	chr12:50381200-50395400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr12:50381200-50396600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr12:50381200-50401400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
37	chr12:50381400-50396400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr12:50381400-50401600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr12:50381600-50402000	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr12:50381600-50404000	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr12:50381800-50393200	Strong transcription	HUVEC	blood vessel
42	chr12:50381800-50410400	Weak transcription	Small Intestine	intestine
43	chr12:50382000-50393600	Strong transcription	Fetal Lung	lung
44	chr12:50382000-50396200	Strong transcription	Fetal Muscle Leg	muscle
45	chr12:50382000-50400800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:50382000-50414800	Weak transcription	Psoas Muscle	Psoas
47	chr12:50382200-50387800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:50382200-50395600	Strong transcription	Duodenum Mucosa	Duodenum
49	chr12:50382400-50388800	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr12:50382400-50396800	Weak transcription	Colon Smooth Muscle	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links