Variant report

Variant	rs7306387
Chromosome Location	chr12:50989352-50989353
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:50948499..50950319-chr12:50987447..50990082,2	K562	blood:
2	chr12:50988872..50990700-chr12:51006546..51009118,2	MCF-7	breast:
3	chr12:50975463..50977998-chr12:50988989..50993005,3	K562	blood:
4	chr12:50974754..50976788-chr12:50985941..50989901,3	MCF-7	breast:
5	chr12:50984035..50986586-chr12:50986718..50989992,3	MCF-7	breast:
6	chr12:50987041..50990767-chr12:51006413..51009565,3	K562	blood:
7	chr12:50979886..50981797-chr12:50988399..50990199,2	MCF-7	breast:

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs10506293	0.90[EUR][1000 genomes]
rs10506296	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10735826	0.84[ASN][1000 genomes]
rs10783367	0.80[ASN][1000 genomes]
rs10783368	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10876041	0.82[ASN][1000 genomes]
rs10876044	0.82[ASN][1000 genomes]
rs10876048	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10876054	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10876057	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10876082	0.86[EUR][1000 genomes]
rs10876083	0.86[EUR][1000 genomes]
rs10876088	0.86[EUR][1000 genomes]
rs11169422	0.90[EUR][1000 genomes]
rs11169553	0.86[EUR][1000 genomes]
rs11614911	0.82[ASN][1000 genomes]
rs12099511	0.90[EUR][1000 genomes]
rs12099615	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12296379	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12307602	0.90[EUR][1000 genomes]
rs12320201	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13328926	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1402693	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1521515	0.86[EUR][1000 genomes]
rs1521517	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17119774	0.90[EUR][1000 genomes]
rs17124672	0.90[EUR][1000 genomes]
rs17124888	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17124907	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1815010	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1996750	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2246840	0.86[EUR][1000 genomes]
rs2252595	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2684886	0.86[EUR][1000 genomes]
rs2684890	0.86[EUR][1000 genomes]
rs2684891	0.86[EUR][1000 genomes]
rs2684902	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2684906	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2700486	0.86[EUR][1000 genomes]
rs28414775	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28479152	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2947617	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3803181	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3825401	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4129355	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4132432	0.90[AMR][1000 genomes]
rs4143663	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4257057	0.90[EUR][1000 genomes]
rs4306347	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4450234	0.90[EUR][1000 genomes]
rs4517607	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4562889	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4768885	0.82[ASN][1000 genomes]
rs4768886	0.82[ASN][1000 genomes]
rs4768887	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4768894	0.81[ASN][1000 genomes]
rs4768915	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4768920	0.86[EUR][1000 genomes]
rs56671180	0.90[EUR][1000 genomes]
rs56753963	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56818625	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57283487	0.90[EUR][1000 genomes]
rs57293958	0.90[EUR][1000 genomes]
rs57328764	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57512759	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57578212	0.90[EUR][1000 genomes]
rs57811009	0.90[EUR][1000 genomes]
rs57828015	0.90[EUR][1000 genomes]
rs58301497	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58500867	0.90[EUR][1000 genomes]
rs58869591	0.85[EUR][1000 genomes]
rs58888905	0.90[EUR][1000 genomes]
rs58915267	0.85[EUR][1000 genomes]
rs58916974	0.90[EUR][1000 genomes]
rs58943330	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59194948	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59284993	0.90[EUR][1000 genomes]
rs59683461	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59696942	0.90[EUR][1000 genomes]
rs59968707	0.90[EUR][1000 genomes]
rs60010359	0.90[EUR][1000 genomes]
rs60198651	0.90[EUR][1000 genomes]
rs60201334	0.90[EUR][1000 genomes]
rs60239257	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60242613	0.90[EUR][1000 genomes]
rs60396677	0.90[EUR][1000 genomes]
rs60420087	0.90[EUR][1000 genomes]
rs60494920	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60743903	0.90[EUR][1000 genomes]
rs60908906	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61578731	0.90[EUR][1000 genomes]
rs6580766	0.86[EUR][1000 genomes]
rs6580767	0.86[EUR][1000 genomes]
rs6580768	0.86[EUR][1000 genomes]
rs7131993	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7132443	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7135222	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7301125	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7302749	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7303202	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7304262	0.90[EUR][1000 genomes]
rs7310507	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7487645	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7953880	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7955176	0.90[EUR][1000 genomes]
rs7955310	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7969251	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7974480	0.90[EUR][1000 genomes]
rs7978443	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7979184	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7979474	0.86[EUR][1000 genomes]
rs865490	0.81[EUR][1000 genomes]
rs939631	0.86[EUR][1000 genomes]
rs951591	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9634264	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9738596	0.85[ASN][1000 genomes]
rs9804759	0.87[EUR][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	esv1820967	chr12:50856613-51002088	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv1816169	chr12:50973897-51002088	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv1817171	chr12:50973897-51002088	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1821299	chr12:50973897-51002088	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv1822840	chr12:50973897-51015509	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	3 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	chr12:50967400-50991200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr12:50967400-50991200	Weak transcription	Aorta	Aorta
3	chr12:50968800-50997400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr12:50969600-50997400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr12:50969800-50989600	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:50974000-51011800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr12:50975600-50991200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:50975800-50989400	Weak transcription	HepG2	liver
9	chr12:50975800-50990200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr12:50975800-50991400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr12:50976000-50993400	Weak transcription	Fetal Lung	lung
12	chr12:50976200-50991200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:50977800-50989400	Weak transcription	Brain Angular Gyrus	brain
14	chr12:50977800-50990400	Weak transcription	Left Ventricle	heart
15	chr12:50978000-50991200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr12:50979200-50991200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr12:50979200-51013800	Weak transcription	Fetal Stomach	stomach
18	chr12:50979400-50991200	Weak transcription	Right Ventricle	heart
19	chr12:50979400-50991600	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr12:50979400-50997200	Weak transcription	Pancreas	Pancrea
21	chr12:50979400-50997200	Weak transcription	Spleen	Spleen
22	chr12:50979600-50991400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr12:50979800-50991000	Weak transcription	A549	lung
24	chr12:50980000-50989600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:50980000-50991200	Weak transcription	Primary B cells from cord blood	blood
26	chr12:50981200-50989600	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr12:50981400-50991200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:50981400-50997400	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr12:50981800-50991200	Weak transcription	Liver	Liver
30	chr12:50983600-50990200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr12:50983600-50991000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr12:50983600-50991200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr12:50983600-50991200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr12:50983600-50991200	Weak transcription	NHLF	lung
35	chr12:50983600-50991600	Weak transcription	HSMMtube	muscle
36	chr12:50983800-50989800	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr12:50983800-50991000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:50983800-50991200	Weak transcription	Primary B cells from peripheral blood	blood
39	chr12:50983800-50991200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr12:50983800-50991200	Weak transcription	GM12878-XiMat	blood
41	chr12:50983800-50991400	Weak transcription	Adipose Nuclei	Adipose
42	chr12:50984000-50990200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr12:50984000-50991000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr12:50984000-50991000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr12:50984000-50991200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:50984000-50991200	Weak transcription	Primary T cells from cord blood	blood
47	chr12:50984000-50991200	Weak transcription	NH-A	brain
48	chr12:50984000-50991400	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr12:50984200-50990800	Weak transcription	NHEK	skin
50	chr12:50984200-50991000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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