Variant report

Variant	rs11211307
Chromosome Location	chr1:47044509-47044510
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	chr1:47036966..47039803-chr1:47043494..47046451,2	K562	blood:

Variant related genes	Relation type
ENSG00000079277	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11211305	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11211308	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11211310	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211311	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211313	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211314	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211315	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211316	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211318	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11211322	1.00[YRI][hapmap]
rs12074458	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12080601	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12083666	1.00[YRI][hapmap]
rs12088719	1.00[CEU][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12090191	1.00[YRI][hapmap]
rs12092171	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12093618	1.00[YRI][hapmap]
rs12095096	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12096548	1.00[CEU][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs3766235	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs41305866	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56089465	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61783115	1.00[EUR][1000 genomes]
rs61783117	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61783120	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61783122	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61783123	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61783125	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001455	chr1:46828004-47326539	Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv534950	chr1:46828004-47326539	Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1015045	chr1:46910546-47067492	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv534952	chr1:46910546-47067492	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1009193	chr1:46939999-47085667	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1009899	chr1:47007765-47062737	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv534954	chr1:47007765-47062737	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv1008246	chr1:47007844-47069845	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
9	nsv1011892	chr1:47010519-47067492	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
10	nsv870392	chr1:47040676-47095097	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47020800-47047400	Weak transcription	Brain Germinal Matrix	brain
2	chr1:47021000-47057000	Weak transcription	Fetal Brain Male	brain
3	chr1:47021200-47045000	Weak transcription	K562	blood
4	chr1:47021800-47054600	Weak transcription	A549	lung
5	chr1:47022400-47053600	Strong transcription	Thymus	Thymus
6	chr1:47022600-47051400	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:47022600-47051600	Strong transcription	Liver	Liver
8	chr1:47023000-47047400	Strong transcription	Primary T cells from cord blood	blood
9	chr1:47023200-47046600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr1:47023200-47047200	Strong transcription	Fetal Thymus	thymus
11	chr1:47023200-47051200	Strong transcription	Fetal Muscle Leg	muscle
12	chr1:47023200-47060000	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:47023400-47044600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr1:47023800-47045200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr1:47023800-47053200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr1:47024000-47054800	Weak transcription	HUVEC	blood vessel
17	chr1:47025600-47062400	Weak transcription	Fetal Heart	heart
18	chr1:47027200-47047600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr1:47028800-47044800	Weak transcription	Stomach Mucosa	stomach
20	chr1:47030800-47046000	Weak transcription	Psoas Muscle	Psoas
21	chr1:47031200-47045600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr1:47032600-47046200	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr1:47034200-47044800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:47035200-47044800	Strong transcription	Placenta	Placenta
25	chr1:47035200-47047600	Weak transcription	NHDF-Ad	bronchial
26	chr1:47035200-47048000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr1:47035200-47053000	Strong transcription	Spleen	Spleen
28	chr1:47035600-47053400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr1:47036000-47047400	Weak transcription	Fetal Lung	lung
30	chr1:47036000-47056400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr1:47036000-47060000	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr1:47036200-47045000	Weak transcription	Fetal Kidney	kidney
33	chr1:47036400-47053200	Strong transcription	Fetal Stomach	stomach
34	chr1:47036600-47045600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:47037000-47046400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:47037800-47047400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr1:47037800-47057000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr1:47038400-47053200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:47038600-47050800	Strong transcription	Primary B cells from peripheral blood	blood
40	chr1:47039000-47052600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:47039000-47054800	Weak transcription	Hela-S3	cervix
42	chr1:47039200-47046400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:47039200-47048200	Weak transcription	Brain Substantia Nigra	brain
44	chr1:47039200-47053000	Weak transcription	Right Atrium	heart
45	chr1:47039200-47060400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:47039400-47044800	Strong transcription	Adipose Nuclei	Adipose
47	chr1:47039400-47050200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:47039600-47052400	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr1:47039600-47060000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:47040000-47044600	Strong transcription	Primary hematopoietic stem cells	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links