Variant report

Variant	rs9668146
Chromosome Location	chr11:9956840-9956841
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1044583	0.84[AFR][1000 genomes]
rs10506693	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12809241	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12825946	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1493796	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1493801	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1493810	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17113674	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17113675	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17113679	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17113748	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs17113750	0.81[ASN][1000 genomes]
rs1824539	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2061579	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs2126136	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2365919	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2605375	0.83[ASN][1000 genomes]
rs2605381	0.90[ASN][1000 genomes]
rs34706013	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35454023	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35957931	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36030036	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs36153793	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4547177	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4882643	0.80[ASN][1000 genomes]
rs58783285	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs590352	0.90[ASN][1000 genomes]
rs60905363	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67506065	0.81[ASN][1000 genomes]
rs7132047	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs725181	0.80[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7295970	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs7300059	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7304361	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7962722	0.93[EUR][1000 genomes];0.96[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	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	nsv896988	chr11:9912052-10012511	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv896989	chr11:9951968-10059623	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
2	chr11:9929200-9966800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:9943400-9980600	Weak transcription	Primary T cells from cord blood	blood
4	chr11:9944800-9961000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:9944800-9969000	Weak transcription	Ovary	ovary
6	chr11:9945000-9967600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:9945400-9964800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:9945600-9958400	Weak transcription	NHDF-Ad	bronchial
9	chr11:9950200-9980400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr11:9952600-9966600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr11:9952600-9968600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr11:9952800-9958400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr11:9952800-9967600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:9952800-9980200	Weak transcription	Aorta	Aorta
15	chr11:9952800-9980400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:9952800-9980600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:9952800-9980600	Weak transcription	Spleen	Spleen
18	chr11:9952800-9995200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:9953000-9962600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:9953000-9963600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:9953000-9963600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:9953000-9963600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr11:9953000-9969200	Weak transcription	Fetal Intestine Small	intestine
24	chr11:9953000-9978200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:9953000-9979600	Weak transcription	Fetal Stomach	stomach
26	chr11:9953000-9980200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:9953000-9980200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr11:9953000-9980400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:9953000-9980400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:9953000-9980400	Weak transcription	Esophagus	oesophagus
31	chr11:9953200-9963600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:9954400-9960800	Weak transcription	HepG2	liver

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