Variant report

Variant	rs10843475
Chromosome Location	chr12:29829065-29829066
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:29827022..29829541-chr12:29831461..29833182,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10128913	0.82[CEU][hapmap];0.84[EUR][1000 genomes]
rs10743669	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10771560	0.84[EUR][1000 genomes]
rs10771561	0.82[CEU][hapmap];0.84[EUR][1000 genomes]
rs10771564	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs10771566	0.81[CEU][hapmap];0.84[EUR][1000 genomes]
rs10771567	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11050352	0.83[EUR][1000 genomes]
rs11050353	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12228730	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12229802	0.83[CEU][hapmap]
rs2003607	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2033027	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs2033028	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs2033029	0.83[EUR][1000 genomes]
rs2033031	0.83[EUR][1000 genomes]
rs2033032	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs2033033	0.84[EUR][1000 genomes]
rs2033035	0.82[CEU][hapmap];0.84[EUR][1000 genomes]
rs2033036	0.82[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2033037	0.82[CEU][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2033040	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2033041	0.82[CHB][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4617668	0.82[CEU][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7298533	0.85[EUR][1000 genomes]
rs759887	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs759888	0.82[CHB][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs759890	0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7964894	0.83[CEU][hapmap];0.83[EUR][1000 genomes]
rs7965351	0.88[CEU][hapmap];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053641	chr12:29268813-29854413	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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 target site	40 gene(s)	inside rSNPs	diseases
2	nsv529328	chr12:29692414-30246209	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:29794400-29831800	Weak transcription	Ovary	ovary
2	chr12:29794800-29829400	Weak transcription	Hela-S3	cervix
3	chr12:29806800-29829200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:29816600-29840400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr12:29820200-29851600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:29820400-29844200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:29821200-29829600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr12:29821400-29829800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr12:29822400-29840200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:29823000-29829400	Weak transcription	Right Atrium	heart
11	chr12:29825400-29829400	Weak transcription	Spleen	Spleen
12	chr12:29825400-29833200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr12:29825400-29847800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr12:29825800-29829400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr12:29825800-29832800	Weak transcription	Small Intestine	intestine
16	chr12:29826000-29829400	Weak transcription	Stomach Smooth Muscle	stomach
17	chr12:29826000-29829400	Weak transcription	HSMMtube	muscle
18	chr12:29826000-29829600	Weak transcription	Fetal Muscle Leg	muscle
19	chr12:29826000-29829800	Weak transcription	Fetal Heart	heart
20	chr12:29826200-29829400	Weak transcription	HMEC	breast
21	chr12:29826400-29829400	Weak transcription	Osteobl	bone
22	chr12:29827000-29830600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr12:29827600-29829200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr12:29827600-29829200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:29827600-29829400	Weak transcription	Psoas Muscle	Psoas
26	chr12:29827600-29830200	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr12:29827800-29829400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr12:29827800-29829400	Weak transcription	Left Ventricle	heart
29	chr12:29828400-29829400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:29828400-29829400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr12:29828600-29829400	Weak transcription	HSMM	muscle
32	chr12:29828600-29830000	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr12:29828600-29854000	Weak transcription	Aorta	Aorta
34	chr12:29828800-29829200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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