Variant report

Variant	rs11253444
Chromosome Location	chr10:836115-836116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:739318..742202-chr10:834057..836421,2	MCF-7	breast:
2	chr10:835663..837203-chr10:849697..852402,2	MCF-7	breast:
3	chr10:556492..557579-chr10:835209..836234,4	MCF-7	breast:
4	chr10:829650..833485-chr10:834016..837949,4	MCF-7	breast:
5	chr10:734067..736710-chr10:835595..837174,2	MCF-7	breast:
6	chr10:835224..837627-chr10:1092339..1094785,2	MCF-7	breast:
7	chr10:733781..736812-chr10:835046..837380,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151240	Chromatin interaction
ENSG00000067064	Chromatin interaction

Extended variants
information (count: 122 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs1013504	0.88[CEU][hapmap]
rs1013505	0.88[CEU][hapmap]
rs10508208	0.94[CEU][hapmap]
rs10904581	0.89[CEU][hapmap]
rs10904583	0.89[CEU][hapmap]
rs10904584	0.89[CEU][hapmap]
rs1106064	0.89[CEU][hapmap]
rs11253443	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253445	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253446	1.00[CEU][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11253458	0.94[CEU][hapmap]
rs11253459	1.00[CEU][hapmap]
rs11253460	0.94[CEU][hapmap]
rs11253467	0.94[CEU][hapmap]
rs11253468	0.94[CEU][hapmap]
rs11253475	0.94[CEU][hapmap]
rs11253485	0.94[CEU][hapmap]
rs11253488	1.00[CEU][hapmap]
rs11253492	0.94[CEU][hapmap]
rs11253493	0.94[CEU][hapmap]
rs11253494	0.94[CEU][hapmap]
rs11253495	0.94[CEU][hapmap]
rs11253504	0.87[CEU][hapmap]
rs11253509	0.89[CEU][hapmap]
rs11253517	0.89[CEU][hapmap]
rs11253520	0.89[CEU][hapmap]
rs11253521	0.89[CEU][hapmap]
rs11813210	0.94[CEU][hapmap]
rs11815185	0.94[CEU][hapmap]
rs11816064	0.94[CEU][hapmap]
rs11817793	0.94[CEU][hapmap]
rs12249828	0.94[CEU][hapmap]
rs12250936	0.94[CEU][hapmap]
rs12250937	0.94[CEU][hapmap]
rs12254002	0.94[CEU][hapmap]
rs12259338	0.89[CEU][hapmap]
rs12259801	0.89[CEU][hapmap]
rs12260800	0.94[CEU][hapmap]
rs12264390	0.89[CEU][hapmap]
rs12354639	0.89[CEU][hapmap]
rs12357633	0.88[CEU][hapmap]
rs12761180	0.89[EUR][1000 genomes]
rs12761424	0.89[CEU][hapmap]
rs12762228	0.87[EUR][1000 genomes]
rs12763396	0.94[CEU][hapmap]
rs12764024	0.82[CEU][hapmap]
rs12768348	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12769002	1.00[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs12769873	0.94[CEU][hapmap]
rs12770190	0.88[CEU][hapmap]
rs12771179	0.89[EUR][1000 genomes]
rs12774985	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs12776659	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12778271	0.83[EUR][1000 genomes]
rs12781100	0.93[EUR][1000 genomes]
rs13377166	1.00[CEU][hapmap]
rs1341741	0.94[CEU][hapmap]
rs1539174	0.89[CEU][hapmap]
rs1555899	0.94[CEU][hapmap]
rs17159950	0.92[CEU][hapmap]
rs17159970	0.94[CEU][hapmap]
rs2050944	0.89[CEU][hapmap]
rs34251037	0.91[EUR][1000 genomes]
rs34278722	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34318754	0.87[EUR][1000 genomes]
rs34405399	0.89[CEU][hapmap]
rs34487581	0.88[EUR][1000 genomes]
rs34527494	0.85[EUR][1000 genomes]
rs34885925	0.87[EUR][1000 genomes]
rs34982663	0.81[EUR][1000 genomes]
rs35370435	0.87[EUR][1000 genomes]
rs35443149	0.87[EUR][1000 genomes]
rs35666723	0.91[EUR][1000 genomes]
rs35667562	0.84[EUR][1000 genomes]
rs35957139	0.87[EUR][1000 genomes]
rs35967867	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4522091	0.94[CEU][hapmap]
rs55697724	0.87[EUR][1000 genomes]
rs55708963	0.84[EUR][1000 genomes]
rs56222464	0.91[EUR][1000 genomes]
rs61830900	0.89[EUR][1000 genomes]
rs61830926	0.86[EUR][1000 genomes]
rs61830931	0.84[EUR][1000 genomes]
rs61830933	0.81[EUR][1000 genomes]
rs61831436	0.93[EUR][1000 genomes]
rs7067865	0.94[CEU][hapmap]
rs7074642	0.94[CEU][hapmap]
rs7077278	0.94[CEU][hapmap]
rs7088956	0.87[EUR][1000 genomes]
rs72776479	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72778228	0.84[EUR][1000 genomes]
rs765867	0.94[CEU][hapmap]
rs7908138	0.89[CEU][hapmap]
rs7914758	1.00[CEU][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916591	chr10:224406-1088734	Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv540386	chr10:224406-1197416	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1050252	chr10:375035-839594	Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv540397	chr10:375035-839594	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1048859	chr10:442805-887622	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
6	nsv1039958	chr10:450753-889167	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
7	nsv540400	chr10:450753-889167	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer 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	19 gene(s)	inside rSNPs	diseases
8	nsv549753	chr10:458477-894838	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
9	nsv1044857	chr10:577396-856059	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
10	nsv540402	chr10:577396-856059	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
11	nsv528733	chr10:577444-838378	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1036675	chr10:600206-839594	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1054659	chr10:611444-1133578	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	43 gene(s)	inside rSNPs	diseases
14	nsv948602	chr10:708293-944641	Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv949063	chr10:708293-974870	Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
16	nsv466697	chr10:734229-1129527	ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
17	nsv549765	chr10:734229-1129527	Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv1036316	chr10:748848-849979	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
19	nsv894718	chr10:763714-861390	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
20	nsv1045119	chr10:766867-855251	Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
21	nsv1043812	chr10:776547-981126	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
22	nsv540406	chr10:776547-981126	Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
23	nsv530116	chr10:776548-1401075	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
24	nsv948978	chr10:813426-1019115	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv1048707	chr10:834439-915534	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
26	esv3356062	chr10:835552-839750	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
27	nsv466698	chr10:836115-888073	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
28	nsv549766	chr10:836115-888073	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:831400-850000	Weak transcription	Fetal Heart	heart
2	chr10:832800-836600	Bivalent Enhancer	Fetal Muscle Leg	muscle
3	chr10:834400-836200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:834800-836200	Flanking Active TSS	Duodenum Mucosa	Duodenum
5	chr10:834800-836200	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr10:835000-841800	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr10:835400-836200	Bivalent Enhancer	Placenta	Placenta
8	chr10:835400-838800	Weak transcription	NHDF-Ad	bronchial
9	chr10:835400-843000	Weak transcription	Aorta	Aorta
10	chr10:835600-836200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr10:835600-836200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:835600-836200	Enhancers	Liver	Liver
13	chr10:835600-836200	Enhancers	Esophagus	oesophagus
14	chr10:835600-836200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr10:835600-836200	Bivalent Enhancer	Fetal Stomach	stomach
16	chr10:835600-836200	Flanking Active TSS	Gastric	stomach
17	chr10:835600-836200	Enhancers	Spleen	Spleen
18	chr10:835600-836200	Enhancers	HSMM	muscle
19	chr10:835600-836400	Enhancers	Fetal Intestine Small	intestine
20	chr10:835600-836600	Enhancers	Stomach Mucosa	stomach
21	chr10:835600-837400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr10:835600-837600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr10:835600-837600	Weak transcription	Fetal Kidney	kidney
24	chr10:835600-838800	Weak transcription	NH-A	brain
25	chr10:835600-841400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:835600-841800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr10:835600-842800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr10:835600-853000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr10:835800-836200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr10:835800-836200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr10:835800-836200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:835800-836200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:835800-836200	Enhancers	Brain Cingulate Gyrus	brain
34	chr10:835800-836200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr10:835800-836200	Enhancers	Ovary	ovary
36	chr10:835800-836200	Enhancers	Pancreas	Pancrea
37	chr10:835800-836200	Enhancers	Stomach Smooth Muscle	stomach
38	chr10:835800-836600	Enhancers	Fetal Intestine Large	intestine
39	chr10:835800-837600	Weak transcription	Fetal Brain Male	brain
40	chr10:835800-838000	Weak transcription	HSMMtube	muscle
41	chr10:835800-838200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:835800-838800	Weak transcription	NHLF	lung
43	chr10:835800-839600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr10:835800-852800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr10:836000-836200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:836000-836200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr10:836000-836200	Enhancers	Muscle Satellite Cultured Cells	--
48	chr10:836000-836200	Enhancers	Adipose Nuclei	Adipose
49	chr10:836000-836200	Enhancers	Brain Anterior Caudate	brain
50	chr10:836000-836200	Enhancers	Brain Hippocampus Middle	brain

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