Variant report

Variant	rs1695
Chromosome Location	chr11:67352689-67352690
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:67352580-67352730	A549	lung:	n/a	n/a
2	BHLHE40	chr11:67352357-67352710	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:67350846-67356110	GM12878	blood:	n/a	n/a
4	POLR2A	chr11:67352313-67352851	A549	lung:	n/a	n/a
5	MAZ	chr11:67352464-67352689	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:67350880-67353764	K562	blood:	n/a	n/a
7	CTCF	chr11:67352560-67352710	HPAF	blood vessel:	n/a	n/a
8	POLR2A	chr11:67352465-67352785	K562	blood:	n/a	n/a
9	POLR2A	chr11:67350853-67353368	GM12892	blood:	n/a	n/a
10	POLR2A	chr11:67352253-67352753	A549	lung:	n/a	n/a
11	POLR2A	chr11:67351526-67354804	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:67352540-67352690	HRE	kidney:	n/a	n/a
13	JUN	chr11:67350726-67353062	K562	blood:	n/a	chr11:67351214-67351226 chr11:67351216-67351224 chr11:67351215-67351225 chr11:67351237-67351246
14	POLR2A	chr11:67350864-67353228	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr11:67352363-67353348	HUVEC	blood vessel:	n/a	n/a
16	MAX	chr11:67352367-67352758	K562	blood:	n/a	n/a
17	POLR2A	chr11:67350934-67352733	IMR90	lung:	n/a	n/a
18	ZNF143	chr11:67352505-67352712	GM12878	blood:	n/a	n/a
19	MXI1	chr11:67350857-67352796	IMR90	lung:	n/a	n/a
20	USF1	chr11:67352406-67352708	K562	blood:	n/a	n/a
21	POLR2A	chr11:67350852-67354306	K562	blood:	n/a	n/a
22	POLR2A	chr11:67350830-67352763	MCF10A-Er-Src	breast:	n/a	n/a
23	CTCF	chr11:67352560-67352710	HEEpiC	esophagus:	n/a	n/a
24	POLR2A	chr11:67351717-67355895	K562	blood:	n/a	n/a
25	CTCF	chr11:67352540-67352690	HRPEpiC	eye:	n/a	n/a
26	POLR2A	chr11:67351525-67352829	H1-hESC	embryonic stem cell:	n/a	n/a
27	STAT3	chr11:67352667-67352719	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:67351090-67355966	GM12878	blood:	n/a	n/a
29	MTA3	chr11:67350790-67352916	GM12878	blood:	n/a	n/a
30	POLR2A	chr11:67350236-67352722	K562	blood:	n/a	n/a
31	MYC	chr11:67352583-67352760	K562	blood:	n/a	n/a
32	POLR2A	chr11:67350654-67355306	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr11:67350877-67352992	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr11:67352560-67352710	HEK293	kidney:	n/a	n/a
35	MAX	chr11:67352444-67352736	K562	blood:	n/a	n/a
36	CTCF	chr11:67352560-67352710	HepG2	liver:	n/a	n/a
37	MAZ	chr11:67350681-67352885	IMR90	lung:	n/a	n/a
38	CTCF	chr11:67352620-67352770	SAEC	small airway:	n/a	n/a
39	CTCF	chr11:67352520-67352789	T-47D	breast:	n/a	n/a
40	POLR2A	chr11:67349901-67357618	K562	blood:	n/a	n/a
41	POLR2A	chr11:67350930-67353427	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:67350861-67352933	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:67352580-67352730	SK-N-SH_RA	brain:	n/a	n/a
44	POLR2A	chr11:67350823-67352716	GM12878	blood:	n/a	n/a
45	CTCF	chr11:67352540-67352690	HBMEC	blood vessel:	n/a	n/a
46	POLR2A	chr11:67350880-67356064	GM12892	blood:	n/a	n/a
47	USF2	chr11:67352395-67352748	GM12878	blood:	n/a	n/a
48	POLR2A	chr11:67350874-67352858	GM12878	blood:	n/a	n/a
49	BHLHE40	chr11:67352425-67352701	K562	blood:	n/a	n/a
50	POLR2A	chr11:67352581-67352789	HCT-116	colon:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67349088..67352896-chr11:67377453..67387652,15	K562	blood:
2	chr11:67348020..67353194-chr11:67379787..67385803,14	K562	blood:
3	chr11:67269844..67272585-chr11:67351352..67354034,3	K562	blood:
4	chr11:67347575..67355744-chr11:67372717..67376912,13	K562	blood:
5	chr11:67347249..67355748-chr11:67372717..67377095,16	K562	blood:
6	chr11:67344360..67352769-chr11:67395394..67400721,12	K562	blood:
7	chr11:67269985..67274388-chr11:67349964..67354078,4	K562	blood:
8	chr11:67169390..67171344-chr11:67351281..67353180,2	K562	blood:
9	chr11:67348847..67353254-chr11:67396059..67399206,10	K562	blood:
10	chr11:67351259..67353873-chr11:67373020..67375265,2	MCF-7	breast:
11	chr11:67274528..67277767-chr11:67349958..67353064,4	K562	blood:

No data

Variant related genes	Relation type
GSTP1	TF binding region
ENSG00000255119	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000167797	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000231793	Chromatin interaction
ENSG00000167799	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10896186	0.81[CEU][hapmap]
rs11601325	0.86[JPT][hapmap]
rs11603735	0.89[EUR][1000 genomes]
rs11603991	0.92[CEU][hapmap];0.92[CHB][hapmap]
rs12421329	0.92[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.83[TSI][hapmap]
rs12790798	0.92[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.81[TSI][hapmap]
rs12793832	0.92[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.83[TSI][hapmap]
rs1531514	0.81[CEU][hapmap]
rs1871034	1.00[JPT][hapmap]
rs1871042	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.92[TSI][hapmap];0.91[EUR][1000 genomes]
rs1871043	0.92[CEU][hapmap];0.92[CHB][hapmap]
rs2370141	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs2514022	0.87[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap]
rs3765088	0.81[CEU][hapmap]
rs4024254	0.92[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.81[TSI][hapmap]
rs4084113	0.86[JPT][hapmap]
rs4148959	0.84[CEU][hapmap];0.92[CHB][hapmap];0.93[CHD][hapmap]
rs4320958	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs4465371	0.86[JPT][hapmap]
rs4891	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4930210	0.85[CEU][hapmap]
rs4930430	1.00[JPT][hapmap]
rs4930431	1.00[JPT][hapmap]
rs4930436	0.83[ASN][1000 genomes]
rs596603	0.81[CEU][hapmap]
rs6591245	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6591251	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs6591252	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs6591256	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs6591258	0.90[EUR][1000 genomes]
rs7103632	0.92[CEU][hapmap];0.92[CHB][hapmap]
rs7106423	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs7106675	1.00[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs7108149	0.84[EUR][1000 genomes]
rs7114510	0.86[JPT][hapmap]
rs749174	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.92[TSI][hapmap];0.92[EUR][1000 genomes]
rs762803	0.90[CHB][hapmap]
rs7941395	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs7941648	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs7948073	0.88[CEU][hapmap];0.92[CHB][hapmap]
rs7952081	1.00[CHB][hapmap];0.87[CHD][hapmap];0.88[JPT][hapmap];0.82[ASN][1000 genomes]
rs7952248	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs917570	0.86[JPT][hapmap]
rs947895	1.00[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.86[JPT][hapmap];0.92[TSI][hapmap];0.91[EUR][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	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
4	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
5	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
6	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
7	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
8	nsv1041988	chr11:67319916-67749246	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
9	nsv897814	chr11:67339949-67460529	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv1050463	chr11:67343421-67717338	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
11	nsv1038189	chr11:67345320-67749246	Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
12	nsv1047236	chr11:67345320-67764068	Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
13	nsv555268	chr11:67346743-67752972	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
14	nsv1036101	chr11:67346813-67828351	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
15	nsv541079	chr11:67346813-67828351	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	139 gene(s)	inside rSNPs	diseases
16	nsv897815	chr11:67347595-67408791	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv1053811	chr11:67349444-67749246	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
18	esv1817852	chr11:67349899-67626567	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
19	nsv468606	chr11:67352689-67816936	Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
20	nsv555269	chr11:67352689-67816936	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs1695	DOC2GP	cis	Skin Sun Exposed Lower leg	GTEx
rs1695	PTPRCAP	cis	Nerve Tibial	GTEx
rs1695	GSTP1	cis	parietal	SCAN
rs1695	RPS6KB2	cis	lymphoblastoid	seeQTL
rs1695	NDUFV1	cis	parietal	SCAN
rs1695	RP11-655M14.12	cis	Muscle Skeletal	GTEx
rs1695	GSTP1	cis	cerebellum	SCAN
rs1695	SLC29A2	cis	parietal	SCAN
rs1695	NUDT8	cis	Heart Left Ventricle	GTEx
rs1695	DOC2GP	cis	Artery Tibial	GTEx
rs1695	ATG2A	cis	parietal	SCAN
rs1695	NDUFV1	cis	cerebellum	SCAN
rs1695	RTN3	cis	parietal	SCAN

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67350400-67352800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr11:67350800-67352800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:67350800-67352800	Active TSS	Aorta	Aorta
4	chr11:67351600-67353200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:67351600-67353600	Transcr. at gene 5' and 3'	Dnd41	blood
6	chr11:67351800-67353200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr11:67351800-67353200	Flanking Active TSS	Fetal Brain Female	brain
8	chr11:67351800-67353400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
9	chr11:67351800-67353400	Weak transcription	Small Intestine	intestine
10	chr11:67351800-67353800	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
11	chr11:67351800-67354000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:67351800-67354400	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:67351800-67358600	Weak transcription	Primary T cells from cord blood	blood
14	chr11:67352000-67352800	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:67352000-67352800	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr11:67352000-67352800	Flanking Active TSS	Rectal Smooth Muscle	rectum
17	chr11:67352000-67353000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
18	chr11:67352000-67353000	Transcr. at gene 5' and 3'	Stomach Mucosa	stomach
19	chr11:67352000-67353000	Flanking Active TSS	HUVEC	blood vessel
20	chr11:67352000-67353000	Flanking Active TSS	Osteobl	bone
21	chr11:67352000-67353400	Transcr. at gene 5' and 3'	Esophagus	oesophagus
22	chr11:67352000-67353800	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
23	chr11:67352000-67354000	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:67352000-67354000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
25	chr11:67352000-67354000	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr11:67352000-67354000	Transcr. at gene 5' and 3'	A549	lung
27	chr11:67352000-67354200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:67352200-67352800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr11:67352200-67352800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr11:67352200-67352800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr11:67352200-67352800	Genic enhancers	Sigmoid Colon	Sigmoid Colon
32	chr11:67352200-67353000	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:67352200-67353000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:67352200-67353000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:67352200-67353000	Flanking Active TSS	NH-A	brain
36	chr11:67352200-67353200	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
37	chr11:67352200-67353200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:67352200-67353200	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
39	chr11:67352200-67353200	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
40	chr11:67352200-67353200	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
41	chr11:67352200-67353200	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr11:67352200-67353200	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
43	chr11:67352200-67353200	Enhancers	Fetal Brain Male	brain
44	chr11:67352200-67353400	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
45	chr11:67352200-67353400	Weak transcription	Ovary	ovary
46	chr11:67352200-67353400	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
47	chr11:67352200-67353600	Genic enhancers	Primary B cells from peripheral blood	blood
48	chr11:67352200-67353600	Weak transcription	Thymus	Thymus
49	chr11:67352200-67353800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr11:67352200-67353800	Genic enhancers	Placenta Amnion	Placenta Amnion

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