Variant report

Variant	rs12672132
Chromosome Location	chr7:102086891-102086892
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:102054913..102058097-chr7:102085637..102088433,3	MCF-7	breast:
2	chr7:102079057..102082389-chr7:102085865..102088701,3	K562	blood:
3	chr7:102085518..102087165-chr7:102088201..102092179,3	K562	blood:
4	chr7:102077007..102082389-chr7:102085865..102088715,6	K562	blood:
5	chr7:102085208..102087796-chr7:102094817..102096828,2	K562	blood:
6	chr7:102035707..102037927-chr7:102085118..102087010,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000128563	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10233236	0.83[EUR][1000 genomes]
rs10237343	0.83[EUR][1000 genomes]
rs10243209	0.81[EUR][1000 genomes]
rs10246324	0.83[EUR][1000 genomes]
rs10268289	0.81[EUR][1000 genomes]
rs10268970	0.81[EUR][1000 genomes]
rs10276094	0.83[EUR][1000 genomes]
rs10277996	0.83[EUR][1000 genomes]
rs10278274	0.83[EUR][1000 genomes]
rs1131384	0.81[EUR][1000 genomes]
rs11538919	0.92[EUR][1000 genomes]
rs11982980	0.81[EUR][1000 genomes]
rs11983129	0.83[EUR][1000 genomes]
rs12381	0.81[EUR][1000 genomes]
rs17135197	0.83[EUR][1000 genomes]
rs1983476	0.81[EUR][1000 genomes]
rs1997164	0.81[EUR][1000 genomes]
rs2103229	0.83[EUR][1000 genomes]
rs2411005	0.81[EUR][1000 genomes]
rs28427402	0.83[EUR][1000 genomes]
rs28879187	0.83[EUR][1000 genomes]
rs35310665	0.85[EUR][1000 genomes]
rs4481505	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4729789	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6465859	0.81[EUR][1000 genomes]
rs6465864	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs6951185	0.81[EUR][1000 genomes]
rs6953087	0.83[EUR][1000 genomes]
rs6958795	0.81[EUR][1000 genomes]
rs6968325	0.81[EUR][1000 genomes]
rs7384178	0.81[EUR][1000 genomes]
rs7385200	0.81[EUR][1000 genomes]
rs7787493	0.81[EUR][1000 genomes]
rs9632724	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1814780	chr7:101912320-102375950	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv1819566	chr7:101912320-102375950	Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv1822347	chr7:101912320-102375950	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
4	esv1825708	chr7:101912320-102375950	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	esv1842898	chr7:101912320-102375950	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
6	esv1847418	chr7:101912320-102375950	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription 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 miRNA target site	61 gene(s)	inside rSNPs	diseases
7	nsv427798	chr7:101912320-102375950	Flanking Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv428182	chr7:101912320-102375950	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
9	nsv1016563	chr7:101912320-102695860	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
10	nsv1028438	chr7:101912320-102704135	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
11	nsv1029079	chr7:101939998-102112371	Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
12	esv1818954	chr7:101957513-102328097	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	esv1828190	chr7:101966669-102439077	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
14	esv1829377	chr7:101970299-102330884	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv831083	chr7:101981005-102295869	Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	esv1806297	chr7:101981544-102330884	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
17	esv1810415	chr7:101993063-102375950	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
18	esv1811751	chr7:101993063-102375950	Enhancers Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
19	esv1829118	chr7:101993063-102375950	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
20	esv1833155	chr7:101993063-102375950	Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
21	esv1832541	chr7:102072448-102328097	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
22	nsv1025363	chr7:102072448-102471485	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
23	esv1803868	chr7:102080919-102109591	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
24	nsv888831	chr7:102082286-102274889	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
25	esv1817154	chr7:102083909-102329872	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
26	esv1847127	chr7:102085576-102329872	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
27	esv1822399	chr7:102085576-102335217	Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12672132	ORAI2	cis	Whole Blood	GTEx

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102075000-102099800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:102075000-102104000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:102075200-102087000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:102075200-102092000	Weak transcription	Esophagus	oesophagus
5	chr7:102075200-102095200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:102075200-102097600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:102075200-102104200	Weak transcription	Fetal Kidney	kidney
8	chr7:102075400-102087000	Weak transcription	Placenta	Placenta
9	chr7:102075400-102087000	Weak transcription	Pancreas	Pancrea
10	chr7:102075400-102087000	Weak transcription	Dnd41	blood
11	chr7:102075400-102097000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr7:102075600-102103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:102075800-102103600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr7:102076000-102097600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr7:102076000-102104200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr7:102076600-102090000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:102076600-102091200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:102076600-102091400	Strong transcription	Fetal Stomach	stomach
19	chr7:102081000-102087000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr7:102081000-102087200	Weak transcription	Colon Smooth Muscle	Colon
21	chr7:102081000-102088800	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr7:102081000-102091800	Weak transcription	HSMMtube	muscle
23	chr7:102081200-102087600	Weak transcription	Right Ventricle	heart
24	chr7:102081200-102091600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:102081200-102091800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:102081200-102091800	Weak transcription	HMEC	breast
27	chr7:102081200-102091800	Weak transcription	NHDF-Ad	bronchial
28	chr7:102081200-102092000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:102081200-102092000	Weak transcription	HSMM	muscle
30	chr7:102081200-102095600	Weak transcription	Brain Substantia Nigra	brain
31	chr7:102081200-102096200	Weak transcription	Left Ventricle	heart
32	chr7:102081200-102098000	Weak transcription	Small Intestine	intestine
33	chr7:102081200-102104200	Weak transcription	Right Atrium	heart
34	chr7:102081400-102087000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:102081400-102087000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr7:102081400-102087000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr7:102081400-102087800	Weak transcription	NH-A	brain
38	chr7:102081400-102098200	Weak transcription	Hela-S3	cervix
39	chr7:102081600-102087600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:102082400-102088400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr7:102082400-102091800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr7:102082400-102091800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr7:102082600-102087000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr7:102082600-102087000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr7:102082600-102096600	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr7:102082800-102087400	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr7:102084400-102104000	Weak transcription	Fetal Brain Male	brain
48	chr7:102084800-102087000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
49	chr7:102085000-102087600	Genic enhancers	Primary B cells from peripheral blood	blood
50	chr7:102085000-102087800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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