Variant report

Variant	rs11674250
Chromosome Location	chr2:98167017-98167018
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10177127	0.86[AMR][1000 genomes]
rs10181934	0.80[AMR][1000 genomes]
rs10182018	0.81[AMR][1000 genomes]
rs10191071	0.81[AMR][1000 genomes]
rs10192821	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10195004	0.83[AFR][1000 genomes]
rs10199389	0.82[AMR][1000 genomes]
rs10209395	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11123815	0.81[AMR][1000 genomes]
rs11676277	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11683920	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11684898	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11688491	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11688544	0.81[AMR][1000 genomes]
rs11690658	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12712050	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12990187	0.86[AMR][1000 genomes]
rs12993579	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12994535	0.84[AMR][1000 genomes]
rs13000078	0.82[AMR][1000 genomes]
rs13001728	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13009263	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13017744	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13027550	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13033336	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13034553	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13034764	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs13395166	0.86[AMR][1000 genomes]
rs13417653	0.83[AMR][1000 genomes]
rs13427163	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1814505	0.80[AMR][1000 genomes]
rs1868445	0.84[AMR][1000 genomes]
rs1972985	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28415903	0.84[AMR][1000 genomes]
rs3925996	0.82[EUR][1000 genomes]
rs4069526	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4086889	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4434044	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs56226039	0.86[AMR][1000 genomes]
rs62154337	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6542895	0.83[AFR][1000 genomes]
rs6718109	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6725692	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6742337	0.80[AFR][1000 genomes]
rs6744616	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6745810	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6750197	0.81[EUR][1000 genomes]
rs6756674	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs7577439	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7579570	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7592057	0.80[ASN][1000 genomes]
rs9653462	0.84[AMR][1000 genomes]
rs9677078	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9677087	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9677528	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9678893	0.85[ASN][1000 genomes]
rs9679287	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9679293	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:46 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757819	chr2:97571109-98336507	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
2	esv2759077	chr2:97571109-98336507	Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	64 gene(s)	inside rSNPs	diseases
3	nsv431402	chr2:97669032-98281634	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
4	nsv535831	chr2:97671335-98270990	Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
5	esv2752937	chr2:97708611-98269110	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
6	esv2756939	chr2:97708611-98274527	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
7	esv2763630	chr2:97731133-98279050	Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv431413	chr2:97753585-98274527	Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers 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	33 gene(s)	inside rSNPs	diseases
9	nsv1004229	chr2:97758953-98225437	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS 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	29 gene(s)	inside rSNPs	diseases
10	nsv522486	chr2:97768178-98265491	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
11	nsv869602	chr2:97820572-98263438	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
12	nsv874695	chr2:97845100-98253816	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	esv1838312	chr2:97852832-98240470	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
14	esv1845945	chr2:97859833-98202258	Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
15	nsv1005903	chr2:97872625-98264679	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
16	nsv999118	chr2:97886322-98264679	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	nsv1011958	chr2:97886322-98269110	Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
18	nsv1001249	chr2:97972600-98274527	Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	nsv1005846	chr2:97972600-98281634	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
20	nsv1010905	chr2:98013814-98269110	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
21	nsv1003384	chr2:98013814-98270884	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers 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	20 gene(s)	inside rSNPs	diseases
22	nsv1010167	chr2:98013814-98273619	Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
23	nsv999627	chr2:98013814-98274527	Enhancers Weak transcription Strong transcription 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	20 gene(s)	inside rSNPs	diseases
24	nsv1009263	chr2:98013814-98281634	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats 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	33 gene(s)	inside rSNPs	diseases
25	esv32869	chr2:98141231-98192553	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
26	nsv1004566	chr2:98146258-98216777	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
27	nsv1010893	chr2:98146258-98225437	Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
28	esv1825324	chr2:98154449-98168868	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
29	esv1836995	chr2:98155850-98240470	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
30	esv1838952	chr2:98155850-98240470	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
31	esv1842036	chr2:98155850-98257451	Weak transcription Active TSS Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
32	nsv499474	chr2:98156052-98167874	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
33	esv1842956	chr2:98156626-98168363	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
34	esv1817664	chr2:98156626-98169910	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
35	esv1847638	chr2:98156826-98168165	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
36	esv1798385	chr2:98162246-98167979	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
37	esv1833304	chr2:98162246-98167979	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
38	esv1851214	chr2:98162246-98167979	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
39	esv1796348	chr2:98162246-98168363	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
40	esv1819349	chr2:98162246-98169480	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
41	esv3460305	chr2:98162620-98168618	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
42	esv3460306	chr2:98162620-98168618	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
43	esv3415663	chr2:98164520-98167818	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
44	nsv979247	chr2:98164562-98167992	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
45	esv3347700	chr2:98164620-98167718	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
46	esv3354089	chr2:98164620-98167718	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs11674250	ANKRD36B	cis	Nerve Tibial	GTEx
rs11674250	ANKRD36B	cis	Thyroid	GTEx
rs11674250	ANKRD36B	cis	Adipose Subcutaneous	GTEx
rs11674250	ANKRD36B	cis	Esophagus Mucosa	GTEx
rs11674250	ANKRD36B	cis	Stomach	GTEx
rs11674250	AC017099.3	cis	Muscle Skeletal	GTEx
rs11674250	ANKRD36B	cis	Artery Aorta	GTEx
rs11674250	ANKRD36B	cis	Skin Sun Exposed Lower leg	GTEx
rs11674250	ANKRD36B	cis	Artery Tibial	GTEx
rs11674250	ANKRD36B	cis	lung	GTEx

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98140800-98187600	Weak transcription	Fetal Stomach	stomach
2	chr2:98142000-98168000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:98142800-98171400	Weak transcription	Fetal Intestine Small	intestine
4	chr2:98142800-98174800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:98142800-98177800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:98143600-98167600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:98143600-98205600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:98147800-98168000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr2:98149600-98167600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr2:98153400-98189800	Weak transcription	Colon Smooth Muscle	Colon
11	chr2:98153600-98178600	Weak transcription	Rectal Smooth Muscle	rectum
12	chr2:98153800-98167200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr2:98154200-98168000	Weak transcription	Fetal Intestine Large	intestine
14	chr2:98154200-98185200	Weak transcription	Fetal Kidney	kidney
15	chr2:98154200-98187000	Weak transcription	Left Ventricle	heart
16	chr2:98154800-98169600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:98154800-98174800	Weak transcription	Placenta	Placenta
18	chr2:98155200-98176600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:98156200-98205600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:98156400-98168000	Weak transcription	Ovary	ovary
21	chr2:98156800-98168000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr2:98156800-98168000	Weak transcription	HSMM	muscle
23	chr2:98156800-98204200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr2:98158200-98167400	Weak transcription	Osteobl	bone
25	chr2:98160200-98205800	Weak transcription	K562	blood
26	chr2:98160800-98175800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr2:98161000-98167600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr2:98161200-98171000	Weak transcription	HMEC	breast
29	chr2:98161400-98167400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr2:98161400-98167400	Weak transcription	Brain Hippocampus Middle	brain
31	chr2:98161400-98167600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr2:98161400-98168000	Weak transcription	NHDF-Ad	bronchial
33	chr2:98161400-98171000	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:98161400-98172600	Weak transcription	Aorta	Aorta
35	chr2:98161400-98174400	Weak transcription	Pancreas	Pancrea
36	chr2:98161400-98174800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:98161400-98176600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr2:98161400-98176600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:98161400-98176800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:98161400-98177400	Weak transcription	Brain Substantia Nigra	brain
41	chr2:98161400-98178400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr2:98161400-98185800	Weak transcription	NHEK	skin
43	chr2:98161600-98170000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr2:98161800-98170800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr2:98162200-98176400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr2:98162400-98172600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:98162600-98173400	Strong transcription	Primary T cells from cord blood	blood
48	chr2:98162600-98177000	Weak transcription	Lung	lung
49	chr2:98163000-98168000	Weak transcription	Adipose Nuclei	Adipose
50	chr2:98163400-98167600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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