Variant report

Variant	rs11235956
Chromosome Location	chr11:73642361-73642362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73497522..73500464-chr11:73642315..73643944,2	K562	blood:
2	chr11:73336454..73337272-chr11:73642184..73642999,2	MCF-7	breast:
3	chr11:73336420..73337418-chr11:73642068..73642960,3	MCF-7	breast:
4	chr11:73371809..73372966-chr11:73642075..73643041,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175581	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10160362	0.85[ASN][1000 genomes]
rs10437752	0.83[ASN][1000 genomes]
rs1122373	0.91[ASN][1000 genomes]
rs11235921	0.86[ASN][1000 genomes]
rs11235924	0.89[ASN][1000 genomes]
rs11235940	0.93[ASN][1000 genomes]
rs11235941	0.91[ASN][1000 genomes]
rs11235944	0.91[ASN][1000 genomes]
rs11235948	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12269892	0.87[ASN][1000 genomes]
rs12280222	0.89[ASN][1000 genomes]
rs12284230	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12284235	0.85[ASN][1000 genomes]
rs12284670	0.89[ASN][1000 genomes]
rs12287418	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12291665	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12294934	0.91[ASN][1000 genomes]
rs12295206	0.91[ASN][1000 genomes]
rs12420040	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12421959	0.87[ASN][1000 genomes]
rs1670539	0.85[ASN][1000 genomes]
rs17132368	0.81[ASN][1000 genomes]
rs17132495	0.87[ASN][1000 genomes]
rs1976139	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2010583	0.91[ASN][1000 genomes]
rs2067913	0.83[ASN][1000 genomes]
rs3741138	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3741139	0.96[ASN][1000 genomes]
rs3926010	0.85[ASN][1000 genomes]
rs56006060	0.89[ASN][1000 genomes]
rs56380005	0.89[ASN][1000 genomes]
rs58695771	0.89[ASN][1000 genomes]
rs637028	0.80[ASN][1000 genomes]
rs694103	0.81[ASN][1000 genomes]
rs7116620	0.89[ASN][1000 genomes]
rs7119602	0.91[ASN][1000 genomes]
rs73549968	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs935985	0.85[ASN][1000 genomes]
rs935988	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530624	chr11:73114283-73646329	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
3	nsv1038105	chr11:73552023-73673836	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73602400-73644800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:73617600-73646000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:73618000-73646400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr11:73625200-73647200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr11:73625600-73646400	Strong transcription	Liver	Liver
6	chr11:73626600-73647800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:73628000-73646200	Strong transcription	Fetal Intestine Small	intestine
8	chr11:73628800-73646400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr11:73631000-73647200	Weak transcription	Psoas Muscle	Psoas
10	chr11:73633200-73652400	Weak transcription	Small Intestine	intestine
11	chr11:73634400-73643800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr11:73634600-73645600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr11:73635000-73643600	Strong transcription	Fetal Stomach	stomach
14	chr11:73635000-73644000	Strong transcription	Fetal Intestine Large	intestine
15	chr11:73635000-73646400	Strong transcription	Fetal Muscle Leg	muscle
16	chr11:73635400-73642800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:73637400-73642800	Strong transcription	Lung	lung
18	chr11:73637400-73644000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:73637400-73644200	Strong transcription	Fetal Muscle Trunk	muscle
20	chr11:73637800-73642600	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:73637800-73642600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:73637800-73644200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:73637800-73644400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:73637800-73645600	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr11:73638000-73645600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:73638800-73647200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr11:73639000-73645200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:73639000-73653000	Weak transcription	K562	blood
29	chr11:73639200-73645600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr11:73639200-73645600	Weak transcription	NHLF	lung
31	chr11:73639200-73650000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:73639400-73643200	Weak transcription	Fetal Brain Male	brain
33	chr11:73639400-73643600	Weak transcription	Colon Smooth Muscle	Colon
34	chr11:73639400-73643600	Weak transcription	Fetal Lung	lung
35	chr11:73639400-73643800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr11:73639400-73643800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:73639400-73643800	Weak transcription	Colonic Mucosa	Colon
38	chr11:73639400-73645200	Weak transcription	Aorta	Aorta
39	chr11:73639400-73647200	Weak transcription	NHEK	skin
40	chr11:73639400-73648000	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr11:73639400-73648000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:73639400-73648200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:73639400-73653200	Weak transcription	Gastric	stomach
44	chr11:73639400-73668000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:73639600-73643400	Weak transcription	Fetal Heart	heart
46	chr11:73639600-73643400	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr11:73639600-73643600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:73639600-73643600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr11:73639600-73644800	Weak transcription	HSMM	muscle
50	chr11:73639600-73645000	Weak transcription	Brain Cingulate Gyrus	brain

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