Variant report

Variant	rs7606279
Chromosome Location	chr2:99902066-99902067
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:99900352..99903264-chr2:99910186..99913049,2	K562	blood:

Extended variants
information (count: 142 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:116)

rs_ID	r²[population]
rs10173883	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10175852	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10176205	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10179343	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10179435	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10179697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10180138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10180688	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10182492	0.90[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs10186223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10191001	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10207435	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10210257	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10210346	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10469848	0.83[EUR][1000 genomes]
rs10496337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10865030	0.80[CEU][hapmap]
rs11123769	0.84[EUR][1000 genomes]
rs11123776	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123778	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11123783	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11123784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs12162367	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12617324	0.93[EUR][1000 genomes]
rs12623835	1.00[CEU][hapmap];0.95[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12989521	0.83[EUR][1000 genomes]
rs12992356	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12993310	0.87[EUR][1000 genomes]
rs13001438	0.90[EUR][1000 genomes]
rs13003899	0.81[AFR][1000 genomes]
rs13017843	0.90[EUR][1000 genomes]
rs13028722	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13032885	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13384665	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs13394927	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs13401163	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13402784	0.89[CEU][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs13405400	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13409359	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13415713	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13416265	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13419448	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13420087	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13420293	0.90[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs13426758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13427424	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13429185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13429806	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs13430662	0.94[ASN][1000 genomes]
rs13430962	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13432046	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1487271	0.87[EUR][1000 genomes]
rs1565054	0.89[EUR][1000 genomes]
rs17022653	0.90[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs17022663	0.90[CEU][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1843807	0.87[EUR][1000 genomes]
rs1882598	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1922625	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1922626	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs1922627	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1948101	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2309577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2309615	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2309616	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28369949	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28382945	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28382947	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28745279	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3087399	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3792151	0.89[CEU][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap]
rs3828162	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4522654	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4850896	0.82[CEU][hapmap]
rs4850902	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4851189	0.80[CEU][hapmap];0.80[EUR][1000 genomes]
rs4851191	0.90[CEU][hapmap];0.87[EUR][1000 genomes]
rs4851194	0.87[EUR][1000 genomes]
rs4851197	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4851199	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4851201	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4851202	0.82[EUR][1000 genomes]
rs6542871	0.80[EUR][1000 genomes]
rs6542876	0.84[EUR][1000 genomes]
rs6542877	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6706425	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6712137	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6721031	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6726711	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6728723	0.80[CEU][hapmap]
rs6744199	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6745645	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6749029	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72815074	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7567230	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7567462	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7569805	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7579143	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7579171	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7579999	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs7581337	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7582085	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7582133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7584022	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7584705	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7585532	0.81[EUR][1000 genomes]
rs7586635	0.82[CEU][hapmap]
rs7595318	0.91[AFR][1000 genomes]
rs7599384	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7599843	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7602401	0.87[EUR][1000 genomes]
rs7603388	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9308819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9308821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9308822	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9308823	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9973846	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431424	chr2:99652682-100494682	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer 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
2	nsv515702	chr2:99827733-99922967	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
3	nsv458685	chr2:99827733-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
4	nsv582519	chr2:99827733-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv874698	chr2:99827733-99924918	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
6	nsv1001784	chr2:99838079-99910328	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv535840	chr2:99838079-99910328	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv458696	chr2:99838203-99922967	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
9	nsv582520	chr2:99838203-99922967	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
10	nsv997436	chr2:99840131-99916886	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
11	nsv1009872	chr2:99840131-99924543	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
12	nsv1001194	chr2:99840131-99928323	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
13	esv2762746	chr2:99840143-99916898	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
14	nsv1005118	chr2:99841951-99924543	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
15	nsv1001736	chr2:99846306-99916886	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
16	nsv1009459	chr2:99846306-99918895	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
17	nsv1002169	chr2:99846306-99924543	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
18	esv2751904	chr2:99847882-99913998	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
19	nsv1001235	chr2:99847890-99913998	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
20	nsv582521	chr2:99847890-99922967	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
21	nsv1007566	chr2:99847890-99924543	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
22	nsv999059	chr2:99847890-99926934	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
23	nsv1007249	chr2:99855978-99916886	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
24	nsv1004291	chr2:99855978-99919999	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
25	nsv1003262	chr2:99858556-99924543	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
26	nsv874699	chr2:99898998-100010044	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS 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	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7606279	LYG1	cis	Whole Blood	GTEx

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99879000-99933600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr2:99880400-99907400	Weak transcription	Right Ventricle	heart
3	chr2:99889000-99906000	Weak transcription	Aorta	Aorta
4	chr2:99892400-99918600	Weak transcription	Brain Anterior Caudate	brain
5	chr2:99892400-99935000	Weak transcription	Brain Angular Gyrus	brain
6	chr2:99894000-99902400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr2:99894200-99934800	Weak transcription	Gastric	stomach
8	chr2:99895400-99935000	Weak transcription	Pancreas	Pancrea
9	chr2:99895800-99914400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr2:99895800-99921000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:99895800-99933600	Weak transcription	HSMM	muscle
12	chr2:99895800-99933600	Weak transcription	HSMMtube	muscle
13	chr2:99896800-99933400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:99897000-99907200	Weak transcription	A549	lung
15	chr2:99897000-99918400	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr2:99897000-99933600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:99897200-99914600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:99897200-99918400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:99897200-99933800	Weak transcription	Fetal Intestine Small	intestine
20	chr2:99897400-99933800	Weak transcription	HepG2	liver
21	chr2:99897600-99902600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:99897600-99918800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:99897800-99907400	Weak transcription	Adipose Nuclei	Adipose
24	chr2:99898200-99918800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr2:99898200-99934000	Weak transcription	Small Intestine	intestine
26	chr2:99898400-99938600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr2:99898600-99933800	Weak transcription	Colon Smooth Muscle	Colon
28	chr2:99899200-99918400	Weak transcription	Spleen	Spleen
29	chr2:99899400-99902200	Strong transcription	Left Ventricle	heart
30	chr2:99899400-99902200	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:99899400-99902200	Weak transcription	GM12878-XiMat	blood
32	chr2:99899400-99902400	Strong transcription	Primary T cells from cord blood	blood
33	chr2:99899400-99918600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr2:99899400-99933800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr2:99899600-99918600	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr2:99899600-99933000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr2:99899800-99935000	Weak transcription	Esophagus	oesophagus
38	chr2:99900000-99902200	Strong transcription	Stomach Smooth Muscle	stomach
39	chr2:99900000-99902200	Strong transcription	Dnd41	blood
40	chr2:99900000-99902400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:99900000-99902800	Strong transcription	Fetal Muscle Leg	muscle
42	chr2:99900000-99933600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr2:99900400-99902200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr2:99900400-99933800	Weak transcription	Colonic Mucosa	Colon
45	chr2:99900600-99902600	Weak transcription	Primary B cells from peripheral blood	blood
46	chr2:99900800-99902400	Strong transcription	Fetal Muscle Trunk	muscle
47	chr2:99901000-99918600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr2:99901200-99933400	Weak transcription	Primary B cells from cord blood	blood
49	chr2:99901200-99936600	Weak transcription	Fetal Brain Male	brain
50	chr2:99901400-99906400	Weak transcription	Liver	Liver

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