Variant report

Variant	rs28835689
Chromosome Location	chr7:64464998-64464999
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:64463794..64465655-chr7:64465725..64468714,2	MCF-7	breast:
2	chr7:64433625..64435948-chr7:64463259..64466229,2	K562	blood:
3	chr7:64464158..64466866-chr7:64514284..64516776,2	MCF-7	breast:
4	chr7:64365308..64368250-chr7:64464896..64466671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERV3-1-2	chr7:64464047-64465572	NONHSAT121063

Variant related genes	Relation type
ENSG00000152926	Chromatin interaction
ENSG00000213462	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 37 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10229485	0.84[AMR][1000 genomes]
rs10237971	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10243523	0.85[AMR][1000 genomes]
rs10252925	0.80[AMR][1000 genomes]
rs1060383	0.83[EUR][1000 genomes]
rs10949955	0.83[EUR][1000 genomes]
rs11760504	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11764811	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11769801	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11771269	0.85[EUR][1000 genomes]
rs11771529	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11978852	0.85[EUR][1000 genomes]
rs12056025	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12056103	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12333999	0.82[AFR][1000 genomes]
rs12530729	0.83[EUR][1000 genomes]
rs12538992	0.82[EUR][1000 genomes]
rs12670240	0.84[EUR][1000 genomes]
rs13222578	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13226855	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13229762	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13233376	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13238842	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13243536	0.82[EUR][1000 genomes]
rs13244300	0.85[EUR][1000 genomes]
rs13245077	0.85[EUR][1000 genomes]
rs1540833	0.83[EUR][1000 genomes]
rs1709515	0.80[AMR][1000 genomes]
rs1852026	0.85[EUR][1000 genomes]
rs2091224	0.85[EUR][1000 genomes]
rs2103146	0.84[EUR][1000 genomes]
rs2103148	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2419256	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28510371	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28872832	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3088174	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34171289	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34362307	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34636014	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34639489	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34897549	0.80[AMR][1000 genomes]
rs35079894	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35189858	0.84[EUR][1000 genomes]
rs35281840	0.83[EUR][1000 genomes]
rs35408058	0.81[AFR][1000 genomes]
rs35586133	0.81[EUR][1000 genomes]
rs35679667	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35953728	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3807068	0.83[EUR][1000 genomes]
rs3807069	0.82[EUR][1000 genomes]
rs3823471	0.83[EUR][1000 genomes]
rs3982216	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4266535	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4379351	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4481471	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4499978	0.80[EUR][1000 genomes]
rs4718177	0.83[EUR][1000 genomes]
rs4718178	0.84[EUR][1000 genomes]
rs4718180	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4718187	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4718188	0.83[AMR][1000 genomes]
rs55762719	0.83[AMR][1000 genomes]
rs55959098	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56294715	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56303509	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56340521	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57449421	0.83[AMR][1000 genomes]
rs58134413	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62455989	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62455992	0.85[ASN][1000 genomes]
rs62456481	0.81[AFR][1000 genomes]
rs62457195	0.83[AMR][1000 genomes]
rs6460216	0.84[EUR][1000 genomes]
rs66688157	0.82[AMR][1000 genomes]
rs67499519	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs67896886	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6947903	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6950807	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6955268	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6961678	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6962429	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6965099	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6965753	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6968439	0.84[EUR][1000 genomes]
rs6971128	0.81[AMR][1000 genomes]
rs6974079	0.81[AMR][1000 genomes]
rs6978332	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7780100	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7789394	0.85[EUR][1000 genomes]
rs7803542	0.85[EUR][1000 genomes]
rs7806567	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7807855	0.85[EUR][1000 genomes]
rs9638216	0.83[EUR][1000 genomes]
rs9638417	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9647852	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9770557	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9770631	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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 miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
8	esv3506582	chr7:64323055-64563984	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	esv3506583	chr7:64323055-64563984	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
10	nsv1019180	chr7:64329889-64512842	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv888283	chr7:64343985-64511564	Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	esv2752165	chr7:64345822-65208605	Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
13	nsv888284	chr7:64406439-64562139	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
14	nsv970505	chr7:64441807-64494987	ZNF genes & repeats Weak transcription Active TSS Genic enhancers Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1033517	chr7:64443052-64942418	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
16	nsv538893	chr7:64443052-64942418	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
17	nsv1034625	chr7:64456197-64850413	Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
18	nsv1019089	chr7:64456197-64874187	Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
19	nsv1023699	chr7:64456197-64942418	Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
20	nsv517778	chr7:64462326-65326821	ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:37)

SNP	Gene	Cis/trans	Tissue	Source
rs28835689	CCT6P3	cis	Esophagus Mucosa	GTEx
rs28835689	RP11-797H7.5	cis	Adipose Subcutaneous	GTEx
rs28835689	RP11-460N20.5	cis	Thyroid	GTEx
rs28835689	RP11-460N20.5	cis	lung	GTEx
rs28835689	RP11-797H7.3	cis	Thyroid	GTEx
rs28835689	RP11-460N20.4	cis	Nerve Tibial	GTEx
rs28835689	RP11-460N20.5	cis	Artery Aorta	GTEx
rs28835689	RP11-797H7.3	cis	Nerve Tibial	GTEx
rs28835689	RP11-460N20.4	cis	Adipose Subcutaneous	GTEx
rs28835689	INTS4L1	cis	Skin Sun Exposed Lower leg	GTEx
rs28835689	RP11-460N20.4	cis	Esophagus Mucosa	GTEx
rs28835689	CCT6P3	cis	Skin Sun Exposed Lower leg	GTEx
rs28835689	RP11-460N20.5	cis	Nerve Tibial	GTEx
rs28835689	RP11-667F9.1	cis	Adipose Subcutaneous	GTEx
rs28835689	ZNF273	cis	lung	GTEx
rs28835689	ERV3	cis	multi-tissue	Pritchard
rs28835689	ERV3-1	cis	Artery Aorta	GTEx
rs28835689	RP11-460N20.5	cis	Artery Tibial	GTEx
rs28835689	CCT6P3	cis	Adipose Subcutaneous	GTEx
rs28835689	RP11-797H7.3	cis	Artery Tibial	GTEx
rs28835689	CCT6P3	cis	Nerve Tibial	GTEx
rs28835689	RP11-667F9.1	cis	Nerve Tibial	GTEx
rs28835689	RP11-797H7.5	cis	Thyroid	GTEx
rs28835689	RP11-797H7.3	cis	lung	GTEx
rs28835689	RP11-460N20.4	cis	lung	GTEx
rs28835689	ZNF273	cis	Thyroid	GTEx
rs28835689	RP11-797H7.5	cis	lung	GTEx
rs28835689	INTS4L1	cis	Esophagus Muscularis	GTEx
rs28835689	RP11-460N20.5	cis	Esophagus Mucosa	GTEx
rs28835689	INTS4L1	cis	Adipose Subcutaneous	GTEx
rs28835689	RP11-797H7.3	cis	Adipose Subcutaneous	GTEx
rs28835689	CCT6P3	cis	lung	GTEx
rs28835689	INTS4L1	cis	Nerve Tibial	GTEx
rs28835689	RP11-460N20.5	cis	Adipose Subcutaneous	GTEx
rs28835689	RP11-460N20.5	cis	Whole Blood	GTEx
rs28835689	AC104057.1	cis	Adipose Subcutaneous	GTEx
rs28835689	RP11-460N20.4	cis	Esophagus Muscularis	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64433400-64465600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:64438600-64465200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:64441800-64465000	Weak transcription	Brain Angular Gyrus	brain
4	chr7:64449000-64465200	ZNF genes & repeats	Fetal Brain Female	brain
5	chr7:64450200-64465400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:64451200-64465400	Weak transcription	Brain Substantia Nigra	brain
7	chr7:64453800-64465200	Weak transcription	Brain Anterior Caudate	brain
8	chr7:64453800-64465400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr7:64453800-64465400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:64458600-64465200	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
11	chr7:64458600-64466200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr7:64459400-64465400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr7:64459600-64465000	Weak transcription	Psoas Muscle	Psoas
14	chr7:64459600-64465000	Weak transcription	Small Intestine	intestine
15	chr7:64459600-64466000	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr7:64459600-64466000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:64459600-64466000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr7:64459600-64466000	Weak transcription	HSMMtube	muscle
19	chr7:64459800-64465000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr7:64459800-64465000	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:64459800-64465400	Weak transcription	NHEK	skin
22	chr7:64459800-64465800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr7:64459800-64466000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr7:64459800-64466400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:64460000-64465000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr7:64460000-64465000	Weak transcription	Rectal Smooth Muscle	rectum
27	chr7:64460000-64465200	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:64460000-64465400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:64460200-64465000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr7:64460600-64465400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:64460800-64465600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr7:64460800-64465600	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr7:64461200-64465600	ZNF genes & repeats	Primary B cells from cord blood	blood
34	chr7:64461600-64465000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:64461600-64466000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr7:64461800-64465000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr7:64461800-64465400	Weak transcription	Hela-S3	cervix
38	chr7:64462000-64465000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:64462000-64465000	Weak transcription	Lung	lung
40	chr7:64462000-64465000	Weak transcription	Osteobl	bone
41	chr7:64462000-64465400	Weak transcription	Stomach Mucosa	stomach
42	chr7:64462000-64466000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:64462000-64466200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:64462200-64465000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr7:64462200-64465000	Strong transcription	Fetal Lung	lung
46	chr7:64462200-64465000	Weak transcription	Left Ventricle	heart
47	chr7:64462200-64465000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr7:64462200-64465000	Weak transcription	Right Ventricle	heart
49	chr7:64462200-64465000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr7:64462200-64465400	Weak transcription	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links