Variant report

Variant	rs1726755
Chromosome Location	chr11:73736801-73736802
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:73724598..73727385-chr11:73734984..73736826,2	MCF-7	breast:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1095419	0.85[AFR][1000 genomes]
rs1095420	0.85[AFR][1000 genomes]
rs1095421	0.88[AFR][1000 genomes]
rs1095423	1.00[ASW][hapmap];1.00[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1095426	1.00[AMR][1000 genomes]
rs1095428	0.88[AFR][1000 genomes]
rs11235979	0.83[YRI][hapmap]
rs12285706	1.00[YRI][hapmap]
rs12286971	0.97[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs12291461	0.83[YRI][hapmap]
rs1617256	0.83[YRI][hapmap]
rs1618253	0.83[YRI][hapmap]
rs1632245	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1685341	0.83[YRI][hapmap]
rs1685342	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1685343	0.83[YRI][hapmap]
rs17132602	0.83[YRI][hapmap]
rs1726742	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1726756	1.00[ASW][hapmap];0.94[MKK][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790383	1.00[YRI][hapmap];0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790402	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790408	1.00[ASW][hapmap];0.95[LWK][hapmap];0.85[MKK][hapmap];1.00[YRI][hapmap]
rs1790409	1.00[YRI][hapmap]
rs1944971	0.80[LWK][hapmap];1.00[YRI][hapmap]
rs28604496	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2950412	1.00[YRI][hapmap]
rs826032	0.85[AFR][1000 genomes]
rs826034	0.85[AFR][1000 genomes]
rs826036	0.85[AFR][1000 genomes]
rs826037	0.86[AFR][1000 genomes]
rs826038	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826040	0.85[AFR][1000 genomes]
rs826041	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs826043	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs826045	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs826046	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826047	1.00[ASW][hapmap];0.91[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs826049	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826052	0.85[AFR][1000 genomes]
rs826053	0.85[AFR][1000 genomes]
rs826070	0.95[YRI][hapmap];0.82[AFR][1000 genomes]
rs826074	0.95[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826076	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826077	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826084	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs826086	1.00[ASW][hapmap];0.91[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs826088	1.00[ASW][hapmap];0.91[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs826090	0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs861144	0.85[AFR][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	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
2	nsv976527	chr11:73728292-73738902	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv3428878	chr11:73736186-73737649	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73710600-73741800	Weak transcription	Fetal Kidney	kidney
2	chr11:73710600-73748800	Weak transcription	Fetal Brain Male	brain
3	chr11:73712200-73743600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:73712200-73743800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr11:73712800-73743400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:73720000-73743400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr11:73721800-73743000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:73722000-73744000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr11:73722200-73767200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr11:73724800-73746800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:73725400-73740200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr11:73728000-73741200	Weak transcription	Aorta	Aorta
13	chr11:73728000-73755000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:73728400-73738400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr11:73728600-73738600	Weak transcription	Dnd41	blood
16	chr11:73729000-73742000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr11:73729200-73740000	Weak transcription	Fetal Lung	lung
18	chr11:73730400-73737800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr11:73730400-73738400	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr11:73730600-73741400	Weak transcription	Hela-S3	cervix
21	chr11:73730600-73743400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:73730800-73742800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:73730800-73745400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:73730800-73800800	Weak transcription	Fetal Heart	heart
25	chr11:73731000-73742600	Weak transcription	Esophagus	oesophagus
26	chr11:73731200-73743800	Weak transcription	Rectal Smooth Muscle	rectum
27	chr11:73731200-73744800	Weak transcription	HepG2	liver
28	chr11:73731400-73739000	Weak transcription	Pancreas	Pancrea
29	chr11:73731400-73741400	Weak transcription	Brain Angular Gyrus	brain
30	chr11:73731400-73741400	Weak transcription	Gastric	stomach
31	chr11:73731400-73743800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:73731400-73744000	Weak transcription	Colon Smooth Muscle	Colon
33	chr11:73731400-73750800	Strong transcription	Fetal Muscle Leg	muscle
34	chr11:73731800-73738600	Weak transcription	Right Atrium	heart
35	chr11:73731800-73740000	Weak transcription	Right Ventricle	heart
36	chr11:73732000-73752400	Weak transcription	Small Intestine	intestine
37	chr11:73732200-73739000	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr11:73732200-73741600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr11:73732200-73744000	Weak transcription	Colonic Mucosa	Colon
40	chr11:73732600-73741400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr11:73733000-73737800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr11:73733600-73740000	Weak transcription	Brain Anterior Caudate	brain
43	chr11:73734000-73741400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr11:73734000-73743000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:73734400-73743600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr11:73734600-73737000	Weak transcription	Fetal Intestine Small	intestine
47	chr11:73734600-73737000	Weak transcription	Fetal Muscle Trunk	muscle
48	chr11:73734600-73754400	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr11:73735000-73738400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:73735000-73738600	Enhancers	HUVEC	blood vessel

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