Variant report

Variant	rs472487
Chromosome Location	chr11:9816447-9816448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10118	0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs10770062	0.89[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1392026	0.88[ASN][1000 genomes]
rs183110	0.84[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1875030	0.86[ASN][1000 genomes]
rs2173030	0.91[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2645017	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2645029	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs360120	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs360124	0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs360127	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs360129	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs360130	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs360131	0.87[ASN][1000 genomes]
rs360132	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs360140	0.85[JPT][hapmap]
rs360141	0.87[ASN][1000 genomes]
rs360142	0.90[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs360143	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs360146	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs360150	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs360151	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs380806	0.91[CEU][hapmap];0.89[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs391304	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs394315	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs405449	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs432849	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs438151	0.91[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs446760	1.00[CEU][hapmap];0.80[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs634680	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6483726	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1053369	chr11:9647837-9876054	Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS 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	39 gene(s)	inside rSNPs	diseases
3	nsv553468	chr11:9667828-9827871	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS 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	35 gene(s)	inside rSNPs	diseases
4	nsv896987	chr11:9759918-9885849	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	esv3384280	chr11:9766350-9911228	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9797400-9821800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr11:9799600-9823400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:9800200-9823800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:9801600-9823800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:9803000-9823400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:9803000-9823400	Weak transcription	Psoas Muscle	Psoas
7	chr11:9803200-9828600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:9803200-9828600	Weak transcription	Gastric	stomach
9	chr11:9803200-9828800	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr11:9806800-9821400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:9806800-9828600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr11:9807200-9823200	Weak transcription	Fetal Heart	heart
13	chr11:9808400-9828800	Weak transcription	Fetal Kidney	kidney
14	chr11:9809600-9823000	Weak transcription	HMEC	breast
15	chr11:9809600-9828600	Weak transcription	Esophagus	oesophagus
16	chr11:9809600-9832600	Weak transcription	Colonic Mucosa	Colon
17	chr11:9809800-9819800	Weak transcription	Pancreas	Pancrea
18	chr11:9809800-9823200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:9809800-9828000	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr11:9809800-9828600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr11:9810000-9818400	Weak transcription	Aorta	Aorta
22	chr11:9810000-9822400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:9810000-9823200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr11:9810000-9823200	Weak transcription	NH-A	brain
25	chr11:9810000-9829200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr11:9810200-9819800	Weak transcription	Hela-S3	cervix
27	chr11:9810200-9821000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr11:9810200-9822600	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr11:9810200-9828400	Weak transcription	Primary T cells from cord blood	blood
30	chr11:9810200-9829200	Weak transcription	Fetal Brain Male	brain
31	chr11:9810800-9818200	Weak transcription	Spleen	Spleen
32	chr11:9810800-9820800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr11:9810800-9823200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr11:9810800-9828600	Weak transcription	Duodenum Mucosa	Duodenum
35	chr11:9810800-9829000	Weak transcription	Right Ventricle	heart
36	chr11:9811000-9828600	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:9811200-9824000	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr11:9811600-9816800	Weak transcription	Fetal Brain Female	brain
39	chr11:9811600-9822800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr11:9811600-9823000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr11:9811600-9823400	Weak transcription	Brain Hippocampus Middle	brain
42	chr11:9811600-9824000	Weak transcription	Brain Substantia Nigra	brain
43	chr11:9811600-9828000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:9811600-9828600	Weak transcription	Dnd41	blood
45	chr11:9811600-9828600	Weak transcription	HUVEC	blood vessel
46	chr11:9811600-9828800	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr11:9811600-9828800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr11:9811800-9818200	Weak transcription	Adipose Nuclei	Adipose
49	chr11:9811800-9818200	Weak transcription	Left Ventricle	heart
50	chr11:9811800-9818400	Weak transcription	Primary B cells from cord blood	blood

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