Variant report

Variant	rs7061
Chromosome Location	chr3:50114515-50114516
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 112 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs10049087	0.81[JPT][hapmap]
rs1061474	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1062633	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs11130228	0.81[JPT][hapmap]
rs11130233	0.89[JPT][hapmap]
rs1138536	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11709573	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs12107768	0.95[ASN][1000 genomes]
rs12496973	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs12634780	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs13060128	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs13071931	0.91[LWK][hapmap];1.00[YRI][hapmap]
rs13077403	0.80[ASN][1000 genomes]
rs13079006	0.80[ASN][1000 genomes]
rs13082703	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13095697	0.87[AFR][1000 genomes]
rs17304079	0.91[LWK][hapmap];1.00[YRI][hapmap]
rs17657664	0.94[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.94[YRI][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17657688	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2013208	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2014004	0.88[YRI][hapmap]
rs2230590	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240326	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240327	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2240328	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2240329	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2247510	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2252833	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2280406	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2352969	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2352984	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs2353579	0.82[JPT][hapmap]
rs2526397	0.81[ASW][hapmap];0.81[YRI][hapmap]
rs2526747	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2526748	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2526749	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2526750	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2526751	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2526754	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2624815	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2624817	0.98[ASN][1000 genomes]
rs2624819	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2624821	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2624822	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2624826	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2624829	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2624832	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2624834	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2624843	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2624847	0.82[JPT][hapmap]
rs2624848	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2624853	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs2681776	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2681779	1.00[CHB][hapmap];0.94[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs2856234	0.90[CHD][hapmap]
rs2856236	0.81[LWK][hapmap];0.89[MKK][hapmap]
rs2856237	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2856238	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2883057	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs34312088	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3774733	0.82[JPT][hapmap]
rs3774734	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3774759	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs4688688	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4688689	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688690	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688753	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4688754	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4688755	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs4688758	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs55924524	0.86[AFR][1000 genomes]
rs62263602	0.83[AFR][1000 genomes]
rs6446192	0.81[ASN][1000 genomes]
rs6446193	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6446194	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6446195	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6446197	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6762477	1.00[ASW][hapmap];0.92[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6765484	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6771546	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6772095	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6774354	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs6785500	0.81[YRI][hapmap]
rs6792892	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs6793528	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6799579	0.95[ASN][1000 genomes]
rs6808044	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7430334	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7613875	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7615206	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs7615318	0.97[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs7621026	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7621352	0.82[JPT][hapmap]
rs7627864	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7628058	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs7634441	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7635601	0.91[LWK][hapmap];1.00[YRI][hapmap]
rs7648174	0.83[ASN][1000 genomes]
rs7648652	0.88[AFR][1000 genomes]
rs868891	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs9311446	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs9682295	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9814664	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs9844201	0.86[ASN][1000 genomes]
rs9861216	0.90[CHD][hapmap];0.82[JPT][hapmap]
rs9866695	0.90[CHD][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876767	chr3:49918751-50153356	Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv460527	chr3:50028385-50153356	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv590249	chr3:50028385-50153356	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers 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	24 gene(s)	inside rSNPs	diseases
5	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers 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 lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv432418	chr3:50114496-50224196	Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs7061	RNF123	cis	parietal	SCAN
rs7061	RBM6	Cis_1M	lymphoblastoid	RTeQTL
rs7061	RBM6	cis	Artery Tibial	GTEx
rs7061	RBM6	cis	multi-tissue	Pritchard
rs7061	RBM6	cis	parietal	SCAN
rs7061	RNF123	cis	cerebellum	SCAN
rs7061	RBM6	cis	Skin Sun Exposed Lower leg	GTEx
rs7061	RBM6	cis	Nerve Tibial	GTEx
rs7061	RBM6	cis	lung	GTEx
rs7061	RBM6	cis	Thyroid	GTEx
rs7061	RBM6	cis	Esophagus Muscularis	GTEx
rs7061	RBM6	cis	Adipose Subcutaneous	GTEx
rs7061	QRICH1	cis	cerebellum	SCAN
rs7061	HYAL3	cis	multi-tissue	Pritchard
rs7061	RBM6	cis	Esophagus Mucosa	GTEx
rs7061	ARIH2	cis	cerebellum	SCAN
rs7061	RBM6	cis	Whole Blood	GTEx
rs7061	RBM6	cis	Artery Aorta	GTEx
rs7061	RBM6	cis	Heart Left Ventricle	GTEx
rs7061	RBM6	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50082000-50115600	Strong transcription	Fetal Intestine Large	intestine
2	chr3:50082200-50116000	Strong transcription	Fetal Muscle Leg	muscle
3	chr3:50082400-50115800	Strong transcription	Fetal Muscle Trunk	muscle
4	chr3:50082400-50116200	Strong transcription	Fetal Thymus	thymus
5	chr3:50082600-50116200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:50084000-50114800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:50084000-50114800	Strong transcription	Primary T cells fromperipheralblood	blood
8	chr3:50084200-50115000	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr3:50084200-50116600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:50084400-50115800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:50084600-50114600	Strong transcription	Adipose Nuclei	Adipose
12	chr3:50085000-50114800	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr3:50085000-50115800	Strong transcription	Liver	Liver
14	chr3:50085200-50115800	Strong transcription	Duodenum Smooth Muscle	Duodenum
15	chr3:50087200-50115800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr3:50087800-50115800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:50088200-50115200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:50088400-50115800	Strong transcription	Thymus	Thymus
19	chr3:50088600-50115400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr3:50089000-50115400	Strong transcription	Skeletal Muscle Female	skeletal muscle
21	chr3:50089200-50116000	Strong transcription	Brain Germinal Matrix	brain
22	chr3:50089200-50116200	Strong transcription	Duodenum Mucosa	Duodenum
23	chr3:50089200-50116400	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr3:50089400-50116000	Strong transcription	Stomach Smooth Muscle	stomach
25	chr3:50089800-50115800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr3:50090400-50115800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr3:50091000-50114800	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr3:50091200-50115400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr3:50093800-50116000	Strong transcription	Fetal Brain Female	brain
30	chr3:50094200-50115600	Strong transcription	Fetal Stomach	stomach
31	chr3:50095000-50114800	Strong transcription	Brain Hippocampus Middle	brain
32	chr3:50095000-50115000	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr3:50095000-50116000	Strong transcription	Brain Angular Gyrus	brain
34	chr3:50095200-50114600	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr3:50096000-50115800	Strong transcription	Lung	lung
36	chr3:50097200-50116200	Strong transcription	Brain Cingulate Gyrus	brain
37	chr3:50097600-50115800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:50104000-50115800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr3:50104200-50123400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:50105800-50115400	Strong transcription	Right Ventricle	heart
41	chr3:50105800-50116200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:50105800-50116200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:50105800-50116400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:50106000-50116000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr3:50106000-50116200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:50106200-50115400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr3:50106200-50116000	Strong transcription	Osteobl	bone
48	chr3:50106200-50125800	Weak transcription	Stomach Mucosa	stomach
49	chr3:50106400-50115800	Strong transcription	HSMM	muscle
50	chr3:50106400-50116000	Strong transcription	Fetal Intestine Small	intestine

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