Variant report

Variant	rs7156770
Chromosome Location	chr14:35544300-35544301
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	chr14:35542856..35545379-chr14:35545884..35547837,2	K562	blood:

Extended variants
information (count: 108 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10146133	0.91[ASN][1000 genomes]
rs11156874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11848309	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11850487	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12100841	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12100944	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17103013	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs17103033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17103044	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17103047	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17386684	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs17456067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1807162	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs2008130	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143949	0.83[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2415258	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2899832	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34509212	0.91[ASN][1000 genomes]
rs4494460	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs55791227	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55833640	0.82[ASN][1000 genomes]
rs55890055	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56142562	0.80[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs56363117	0.96[ASN][1000 genomes]
rs57166048	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs57338667	0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs57411359	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61060564	1.00[ASN][1000 genomes]
rs61492899	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62625039	0.91[ASN][1000 genomes]
rs6571694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6571695	0.91[ASN][1000 genomes]
rs7140462	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7154292	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7154637	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7155697	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7156704	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7160889	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7218	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs72664814	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664816	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72664819	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72664820	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs72664829	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72664840	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72664843	0.91[ASN][1000 genomes]
rs72664849	0.84[ASN][1000 genomes]
rs72664854	0.91[ASN][1000 genomes]
rs72664855	0.91[ASN][1000 genomes]
rs72680622	0.87[ASN][1000 genomes]
rs72680641	0.87[ASN][1000 genomes]
rs72680648	0.96[ASN][1000 genomes]
rs72680652	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680655	1.00[ASN][1000 genomes]
rs72680657	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680662	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72680663	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7493705	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8004236	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8005079	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8007337	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8007346	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8007575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8008066	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8009666	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8011195	0.91[ASN][1000 genomes]
rs8011242	0.90[CEU][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8011549	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8012905	0.96[ASN][1000 genomes]
rs8014760	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8016140	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs8016541	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8017547	1.00[ASN][1000 genomes]
rs8018116	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8019182	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8019482	0.91[ASN][1000 genomes]
rs8019523	0.91[ASN][1000 genomes]
rs8019700	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs8019709	0.91[ASN][1000 genomes]
rs8019741	0.89[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9646144	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9888560	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9888561	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9888597	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901602	chr14:35367889-35571651	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	nsv1043470	chr14:35398522-35754029	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
4	nsv542031	chr14:35398522-35754029	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats 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 miRNA target site	65 gene(s)	inside rSNPs	diseases
5	nsv901608	chr14:35449467-35571651	Weak transcription ZNF genes & repeats Enhancers Strong transcription 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 miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv901609	chr14:35449467-35587767	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
7	nsv456204	chr14:35466584-35556498	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats 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	26 gene(s)	inside rSNPs	diseases
8	nsv564263	chr14:35466584-35556498	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats 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	26 gene(s)	inside rSNPs	diseases
9	nsv901612	chr14:35470049-35571651	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv901613	chr14:35470049-35587767	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Enhancers Flanking Active TSS 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	30 gene(s)	inside rSNPs	diseases
11	nsv564264	chr14:35482797-35732369	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
12	nsv901614	chr14:35485748-35571651	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv901615	chr14:35485748-35630175	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
14	nsv870305	chr14:35488290-35852349	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats 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 miRNA target site	50 gene(s)	inside rSNPs	diseases
15	nsv1052800	chr14:35509858-35607117	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats 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	37 gene(s)	inside rSNPs	diseases
16	nsv1044515	chr14:35510785-35756317	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
17	nsv564265	chr14:35512335-35624831	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers 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 miRNA target site	38 gene(s)	inside rSNPs	diseases
18	nsv1046992	chr14:35527239-35724227	Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
19	nsv1051274	chr14:35529529-35724227	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
20	nsv1048823	chr14:35537281-35724892	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking 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 miRNA target site	27 gene(s)	inside rSNPs	diseases
21	nsv542032	chr14:35537281-35724892	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
22	nsv1040540	chr14:35537481-35724753	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
23	nsv542033	chr14:35537481-35724753	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7156770	PPP2R3C	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35516400-35552600	Weak transcription	Spleen	Spleen
2	chr14:35516800-35551200	Weak transcription	Right Ventricle	heart
3	chr14:35516800-35552200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr14:35517200-35547200	Weak transcription	Brain Anterior Caudate	brain
5	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
6	chr14:35517600-35545800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr14:35517600-35554400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr14:35518000-35547400	Weak transcription	GM12878-XiMat	blood
9	chr14:35520200-35550800	Weak transcription	NHLF	lung
10	chr14:35521000-35559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:35526600-35547200	Weak transcription	Brain Angular Gyrus	brain
12	chr14:35526600-35552400	Weak transcription	Brain Substantia Nigra	brain
13	chr14:35528200-35547400	Weak transcription	Fetal Thymus	thymus
14	chr14:35528200-35552200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr14:35528200-35559400	Weak transcription	Colonic Mucosa	Colon
16	chr14:35528600-35552400	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr14:35528600-35552800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr14:35528800-35563200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:35529000-35552000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:35529400-35555800	Weak transcription	Aorta	Aorta
21	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
22	chr14:35530400-35550600	Weak transcription	Rectal Smooth Muscle	rectum
23	chr14:35530600-35547200	Weak transcription	HMEC	breast
24	chr14:35530600-35548000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr14:35530600-35550200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:35530600-35552400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr14:35530600-35563600	Weak transcription	Small Intestine	intestine
28	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
29	chr14:35530800-35552000	Weak transcription	Hela-S3	cervix
30	chr14:35531400-35547400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr14:35531400-35550800	Weak transcription	HUVEC	blood vessel
32	chr14:35531400-35552600	Weak transcription	Pancreas	Pancrea
33	chr14:35531400-35563400	Weak transcription	Gastric	stomach
34	chr14:35531800-35546000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr14:35532800-35544800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:35537600-35544400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr14:35537600-35545800	Weak transcription	NHDF-Ad	bronchial
38	chr14:35538200-35545800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr14:35538200-35546200	Weak transcription	Colon Smooth Muscle	Colon
40	chr14:35538200-35547000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr14:35538200-35547000	Weak transcription	HSMMtube	muscle
42	chr14:35538200-35547400	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr14:35538400-35544400	Strong transcription	Duodenum Mucosa	Duodenum
45	chr14:35538400-35546000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr14:35538400-35546200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr14:35538400-35546400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:35538400-35546800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr14:35538400-35547000	Weak transcription	Fetal Kidney	kidney
50	chr14:35538400-35547000	Weak transcription	NHEK	skin

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