Variant report

Variant	rs1074886
Chromosome Location	chr2:231237573-231237574
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	chr2:231235932..231237817-chr2:231243056..231245722,2	K562	blood:

Extended variants
information (count: 114 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs11675127	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11675135	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11676089	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11676310	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11677269	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11677462	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11677512	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11677646	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11679026	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11681234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11681358	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11687964	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11688362	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11692506	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap]
rs11692527	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11692602	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11693767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11694346	0.91[ASN][1000 genomes]
rs11694422	0.81[ASN][1000 genomes]
rs11694428	0.81[ASN][1000 genomes]
rs11695277	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs12694865	0.85[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1427284	0.87[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs17273079	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17332171	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17332742	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17333189	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2303608	0.85[ASN][1000 genomes]
rs35919859	0.81[ASN][1000 genomes]
rs3752431	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs3754940	0.87[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3754941	0.87[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs3754942	0.87[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3754943	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3769849	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3815885	0.85[ASN][1000 genomes]
rs3893836	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs55637456	0.91[ASN][1000 genomes]
rs55770359	0.85[ASN][1000 genomes]
rs55893188	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55964110	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56007282	0.85[ASN][1000 genomes]
rs56044062	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56052963	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56105857	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56108366	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56251216	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56270546	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56303947	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56401027	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6436933	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6706167	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6713447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6713465	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6722656	0.82[ASN][1000 genomes]
rs6725726	0.82[ASN][1000 genomes]
rs6732684	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6732940	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6748339	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6748445	0.96[CEU][hapmap];0.88[GIH][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6750712	0.85[ASN][1000 genomes]
rs6753500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6759292	0.85[ASN][1000 genomes]
rs6761255	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs68096532	0.91[ASN][1000 genomes]
rs72495174	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495175	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495176	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495180	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495181	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495182	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72495183	0.91[ASN][1000 genomes]
rs72495185	0.85[ASN][1000 genomes]
rs725202	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72994332	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72996270	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72996292	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72998203	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72998264	0.91[ASN][1000 genomes]
rs72998283	0.91[ASN][1000 genomes]
rs73000239	0.85[ASN][1000 genomes]
rs73000253	0.85[ASN][1000 genomes]
rs73000268	0.85[ASN][1000 genomes]
rs7559665	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7563909	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7565654	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7568128	0.91[ASN][1000 genomes]
rs7585646	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7585731	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7589948	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7597033	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7606804	0.91[ASN][1000 genomes]
rs999888	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498047	chr2:230951712-231250489	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	esv3417154	chr2:231159789-231258938	Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3348338	chr2:231160124-231259498	Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv875945	chr2:231172642-231267925	Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv869708	chr2:231173700-231267616	Genic enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1004183	chr2:231174420-231258603	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	esv3486129	chr2:231175581-231265831	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3486131	chr2:231175581-231265831	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1013738	chr2:231176856-231258603	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv584667	chr2:231177822-231258450	Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv460119	chr2:231178876-231258450	Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv584668	chr2:231178876-231258450	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	esv2751844	chr2:231179495-231280495	Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv1001929	chr2:231179884-231258603	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv1006206	chr2:231179884-231268938	Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv584669	chr2:231183321-231258150	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	nsv584670	chr2:231183786-231241276	ZNF genes & repeats Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
19	nsv875946	chr2:231184106-231277567	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	esv3374323	chr2:231186424-231244177	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
21	nsv875947	chr2:231190446-231281286	Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs1074886	B3GNT7	cis	parietal	SCAN
rs1074886	SP140L	cis	lymphoblastoid	seeQTL
rs1074886	SCARNA6	cis	parietal	SCAN
rs1074886	LOC93349	cis	multi-tissue	Pritchard
rs1074886	LOC93349	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231212800-231253600	Weak transcription	Gastric	stomach
2	chr2:231212800-231253600	Weak transcription	HMEC	breast
3	chr2:231212800-231259200	Weak transcription	Small Intestine	intestine
4	chr2:231212800-231262400	Weak transcription	K562	blood
5	chr2:231213000-231237600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:231220000-231275800	Weak transcription	Stomach Mucosa	stomach
7	chr2:231222200-231253400	Weak transcription	Colonic Mucosa	Colon
8	chr2:231222200-231273200	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr2:231223200-231237600	Weak transcription	Right Ventricle	heart
10	chr2:231223200-231253600	Weak transcription	NHLF	lung
11	chr2:231223400-231257800	Weak transcription	NH-A	brain
12	chr2:231223600-231263600	Weak transcription	Fetal Kidney	kidney
13	chr2:231224200-231254000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:231225200-231268000	Weak transcription	Colon Smooth Muscle	Colon
15	chr2:231225600-231244600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:231226600-231245600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:231226600-231253800	Weak transcription	Fetal Stomach	stomach
18	chr2:231226800-231237800	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:231226800-231249800	Weak transcription	Lung	lung
20	chr2:231226800-231253600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:231226800-231253600	Weak transcription	Pancreas	Pancrea
22	chr2:231227000-231251400	Weak transcription	HSMMtube	muscle
23	chr2:231227200-231242400	Weak transcription	HSMM	muscle
24	chr2:231228800-231260000	Strong transcription	Primary B cells from peripheral blood	blood
25	chr2:231228800-231275600	Weak transcription	Psoas Muscle	Psoas
26	chr2:231231400-231243600	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr2:231231600-231246600	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr2:231232200-231238400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr2:231232200-231260400	Weak transcription	Fetal Lung	lung
30	chr2:231232400-231239600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr2:231232400-231243400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:231232800-231241000	Strong transcription	Liver	Liver
33	chr2:231233000-231238600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
34	chr2:231233200-231238800	Strong transcription	Primary B cells from cord blood	blood
35	chr2:231233400-231238400	Strong transcription	Dnd41	blood
36	chr2:231233600-231239600	Strong transcription	Primary T cells from cord blood	blood
37	chr2:231233800-231238400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr2:231233800-231238600	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr2:231233800-231239600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr2:231234000-231242200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:231234200-231238600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:231234200-231249600	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr2:231234200-231253600	Weak transcription	Esophagus	oesophagus
44	chr2:231234200-231274400	Weak transcription	Brain Hippocampus Middle	brain
45	chr2:231234400-231238600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr2:231234400-231239200	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr2:231234400-231239400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr2:231234400-231259400	Weak transcription	Fetal Intestine Small	intestine
49	chr2:231234800-231238400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr2:231234800-231238600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood

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