Variant report

Variant	rs2691561
Chromosome Location	chr7:17948590-17948591
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:17946487..17949983-chr7:17978237..17982024,4	MCF-7	breast:
2	chr7:17945292..17946912-chr7:17947838..17950371,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000071189	Chromatin interaction

Extended variants
information (count: 106 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10216315	0.88[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.98[TSI][hapmap];0.82[YRI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10227224	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10227501	0.95[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.91[ASN][1000 genomes]
rs10227582	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10231926	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10233816	0.89[ASW][hapmap];0.92[CEU][hapmap];0.87[JPT][hapmap];0.91[LWK][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes]
rs10265373	0.94[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10447542	0.92[CEU][hapmap]
rs11768866	0.82[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs11973277	0.92[CEU][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11983260	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12699918	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs12699919	0.92[CEU][hapmap];0.87[JPT][hapmap]
rs1357796	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs1404414	0.82[GIH][hapmap]
rs1404422	0.82[GIH][hapmap]
rs1404424	0.89[ASN][1000 genomes]
rs1464804	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs1524775	0.86[CHB][hapmap];0.95[CHD][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs1524776	0.82[CHB][hapmap];0.84[CHD][hapmap];0.82[GIH][hapmap];0.86[JPT][hapmap]
rs1568815	1.00[CEU][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1568817	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1568818	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2103144	0.90[ASN][1000 genomes]
rs2177652	0.82[CHB][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs2691555	0.81[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2691557	0.89[ASN][1000 genomes]
rs2691558	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691559	0.85[CHB][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2691560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691562	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691563	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691564	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691565	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2691566	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691567	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691568	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691569	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691570	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691571	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2691572	0.88[CEU][hapmap];0.87[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2691574	0.92[CEU][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap]
rs2691575	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2691576	0.94[ASW][hapmap];0.92[CEU][hapmap];0.87[JPT][hapmap];0.93[LWK][hapmap];0.95[MEX][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2691577	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2691578	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2691579	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2691580	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2691583	0.82[GIH][hapmap]
rs2691600	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs2691601	0.82[GIH][hapmap]
rs2691609	0.82[CHB][hapmap];0.81[CHD][hapmap];0.86[JPT][hapmap]
rs2691611	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2691612	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2691615	0.86[JPT][hapmap]
rs2714853	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2714854	0.94[ASW][hapmap];0.92[CEU][hapmap];0.87[JPT][hapmap];0.93[LWK][hapmap];0.95[MEX][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2714855	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2714856	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2714857	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2714858	0.83[ASW][hapmap];0.92[CEU][hapmap];0.87[JPT][hapmap];0.93[LWK][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs2714859	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2714860	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714861	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714862	0.81[LWK][hapmap]
rs2714863	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2714864	0.82[ASW][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.80[MKK][hapmap];0.85[YRI][hapmap];1.00[ASN][1000 genomes]
rs2714865	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714866	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714867	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2714868	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714869	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2714870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2714871	1.00[CHB][hapmap];0.83[CHD][hapmap];0.81[LWK][hapmap];0.86[ASN][1000 genomes]
rs2714872	1.00[CHB][hapmap];0.83[CHD][hapmap];0.89[ASN][1000 genomes]
rs2714878	0.96[CEU][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2723494	0.82[GIH][hapmap]
rs2723501	0.82[GIH][hapmap]
rs2723502	0.82[GIH][hapmap]
rs2723515	0.82[GIH][hapmap]
rs2723540	0.82[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs2723553	0.82[GIH][hapmap]
rs35819944	0.86[ASN][1000 genomes]
rs4532510	0.87[ASN][1000 genomes]
rs4543433	0.82[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs4719525	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4721670	0.80[AFR][1000 genomes]
rs4721671	0.91[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6952907	0.92[CEU][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs6955984	0.84[ASN][1000 genomes]
rs6962380	0.92[CEU][hapmap];0.87[JPT][hapmap]
rs6973480	0.84[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs7802343	0.92[CEU][hapmap];0.86[JPT][hapmap];0.86[LWK][hapmap];0.89[YRI][hapmap]
rs949451	0.81[GIH][hapmap]
rs9942602	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021524	chr7:17251148-17963307	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats 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 miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
5	nsv830913	chr7:17848480-18034218	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
8	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active 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	16 gene(s)	inside rSNPs	diseases
9	nsv887808	chr7:17920613-18150005	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1018517	chr7:17926468-18127372	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2691561	SNX13	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17900400-17956600	Weak transcription	A549	lung
2	chr7:17903600-17953000	Weak transcription	Thymus	Thymus
3	chr7:17903800-17949000	Weak transcription	NHEK	skin
4	chr7:17907200-17954800	Weak transcription	Spleen	Spleen
5	chr7:17911400-17977400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:17913000-17955800	Weak transcription	K562	blood
7	chr7:17927200-17955000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:17929200-17951400	Weak transcription	Fetal Intestine Large	intestine
9	chr7:17929200-17952200	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:17929800-17949200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:17929800-17951600	Weak transcription	Fetal Thymus	thymus
12	chr7:17929800-17954000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:17930000-17949200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:17930000-17950200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr7:17930000-17950200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr7:17930000-17952400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr7:17930200-17950200	Weak transcription	NHDF-Ad	bronchial
18	chr7:17930200-17951800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:17930200-17954200	Weak transcription	Placenta	Placenta
20	chr7:17934800-17949400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr7:17938200-17951800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:17938800-17952800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:17940200-17950800	Weak transcription	Fetal Stomach	stomach
24	chr7:17941000-17951600	Weak transcription	Right Ventricle	heart
25	chr7:17941000-17952400	Weak transcription	Ovary	ovary
26	chr7:17941200-17952400	Weak transcription	Gastric	stomach
27	chr7:17941400-17949200	Weak transcription	Fetal Intestine Small	intestine
28	chr7:17941400-17951000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr7:17941400-17958400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr7:17942600-17949600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:17942800-17951800	Weak transcription	Left Ventricle	heart
32	chr7:17942800-17954800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:17942800-17954800	Weak transcription	Pancreas	Pancrea
34	chr7:17943200-17952400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr7:17943400-17951400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr7:17943800-17952400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:17943800-17956000	Weak transcription	Primary T cells from cord blood	blood
38	chr7:17944000-17953800	Weak transcription	Liver	Liver
39	chr7:17944000-17955400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr7:17944600-17952000	Weak transcription	Fetal Heart	heart
41	chr7:17944800-17955200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr7:17947000-17955200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:17947200-17949600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:17947200-17954800	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:17947200-17955400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr7:17947400-17951800	Weak transcription	Psoas Muscle	Psoas
47	chr7:17947400-17954800	Weak transcription	Small Intestine	intestine
48	chr7:17947400-17956600	Weak transcription	Fetal Lung	lung
49	chr7:17947400-17957400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:17947600-17953600	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links