Variant report

Variant	rs10831050
Chromosome Location	chr11:93230475-93230476
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:93215734..93218245-chr11:93228402..93230678,2	MCF-7	breast:
2	chr11:93225464..93227548-chr11:93228029..93230930,2	MCF-7	breast:
3	chr11:93226135..93229081-chr11:93229518..93231367,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10831051	0.88[CHB][hapmap]
rs10831053	0.85[MKK][hapmap]
rs11020380	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11020381	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11020385	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11020386	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs11020387	0.88[CHB][hapmap]
rs11020388	0.88[CHB][hapmap]
rs11020391	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11020397	0.82[ASN][1000 genomes]
rs11020398	0.82[ASN][1000 genomes]
rs11020399	0.82[ASN][1000 genomes]
rs11020400	0.82[ASN][1000 genomes]
rs11020401	0.88[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11020402	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11820614	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16834	0.83[CEU][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2045313	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2045459	0.85[EUR][1000 genomes]
rs2045461	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2045462	0.87[CEU][hapmap];0.87[LWK][hapmap];0.92[MKK][hapmap];0.90[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2198797	0.85[MKK][hapmap]
rs2605591	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2605592	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2605594	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2605595	0.83[CEU][hapmap];0.85[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2605598	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2605599	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2605601	0.83[CEU][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2605602	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2605605	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2608273	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2608277	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2608278	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2658794	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2658795	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2658796	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2658800	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2658802	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2939621	0.82[EUR][1000 genomes]
rs3750951	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6483246	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7114771	0.92[CEU][hapmap];0.82[LWK][hapmap];0.96[MKK][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7124358	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7928401	0.88[CHB][hapmap]

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	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1039623	chr11:93141461-93328739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription 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 target site	13 gene(s)	inside rSNPs	diseases
3	esv2760208	chr11:93172673-93266594	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10831050	C11orf75	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93207000-93239000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr11:93209000-93231400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:93209000-93235200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:93210600-93231600	Weak transcription	A549	lung
5	chr11:93211000-93253400	Weak transcription	Primary T cells from cord blood	blood
6	chr11:93211600-93243800	Weak transcription	Fetal Thymus	thymus
7	chr11:93212200-93234800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:93214800-93234400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr11:93218600-93254400	Weak transcription	Hela-S3	cervix
10	chr11:93218800-93231800	Weak transcription	Ovary	ovary
11	chr11:93218800-93238200	Weak transcription	Esophagus	oesophagus
12	chr11:93218800-93245800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr11:93220600-93230600	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr11:93220600-93230800	Weak transcription	Colon Smooth Muscle	Colon
15	chr11:93220600-93232000	Weak transcription	Left Ventricle	heart
16	chr11:93220800-93235400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr11:93222000-93231600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:93222200-93232000	Weak transcription	Spleen	Spleen
19	chr11:93222400-93238000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr11:93222800-93231800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr11:93222800-93236000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr11:93223000-93242800	Weak transcription	Adipose Nuclei	Adipose
23	chr11:93224800-93230600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr11:93224800-93230600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:93225400-93242800	Weak transcription	GM12878-XiMat	blood
26	chr11:93225600-93230600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:93225600-93230800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:93225600-93231800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:93225600-93248800	Weak transcription	Fetal Muscle Leg	muscle
30	chr11:93225800-93232800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:93226000-93230600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr11:93226000-93235000	Weak transcription	Small Intestine	intestine
33	chr11:93226400-93257400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr11:93226600-93238000	Weak transcription	Fetal Lung	lung
35	chr11:93226800-93233600	Weak transcription	Stomach Mucosa	stomach
36	chr11:93227000-93231600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:93227000-93234600	Weak transcription	Gastric	stomach
38	chr11:93227000-93243800	Weak transcription	Lung	lung
39	chr11:93227200-93231600	Weak transcription	Aorta	Aorta
40	chr11:93227200-93257600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr11:93227400-93239800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr11:93227600-93232800	Strong transcription	Fetal Stomach	stomach
43	chr11:93227800-93231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr11:93227800-93235000	Weak transcription	Pancreas	Pancrea
45	chr11:93228200-93230600	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr11:93228200-93230600	Weak transcription	Fetal Intestine Small	intestine
47	chr11:93228200-93231000	Weak transcription	Fetal Kidney	kidney
48	chr11:93228200-93234000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:93228200-93243400	Weak transcription	Right Ventricle	heart
50	chr11:93228200-93248200	Weak transcription	Brain Hippocampus Middle	brain

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