Variant report

Variant	rs4885345
Chromosome Location	chr13:76318453-76318454
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:76317185..76320050-chr13:76322503..76324953,2	K562	blood:

Extended variants
information (count: 46 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1092601	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1108412	0.88[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1323712	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1408060	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1535730	0.86[ASN][1000 genomes]
rs1830760	0.85[EUR][1000 genomes]
rs1924214	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2025354	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2328953	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2328954	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2328956	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2761398	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34545980	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs479824	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs480929	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs502171	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs504273	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs508596	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs528783	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs560069	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs562940	0.83[EUR][1000 genomes]
rs585233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs603274	0.81[EUR][1000 genomes]
rs607095	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626182	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs634729	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs636505	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs636580	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7320216	0.84[CEU][hapmap]
rs7331527	0.81[CEU][hapmap]
rs7336908	0.86[ASN][1000 genomes]
rs776527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7986141	0.86[ASN][1000 genomes]
rs7991448	0.85[CEU][hapmap]
rs8002635	0.86[ASN][1000 genomes]
rs9530463	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9544028	0.86[ASN][1000 genomes]
rs9544029	0.87[ASN][1000 genomes]
rs9544034	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9544035	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9565195	0.83[EUR][1000 genomes]
rs9573627	0.86[ASN][1000 genomes]
rs9573647	0.80[AMR][1000 genomes];0.88[EUR][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	nsv949152	chr13:76211453-76366622	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1091	chr13:76282392-76327906	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv832646	chr13:76300428-76483102	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4885345	TBC1D4	cis	cerebellum	SCAN
rs4885345	KCTD12	cis	cerebellum	SCAN
rs4885345	COMMD6	cis	cerebellum	SCAN

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76294800-76321800	Weak transcription	NH-A	brain
2	chr13:76298600-76318800	Weak transcription	Gastric	stomach
3	chr13:76306200-76330600	Weak transcription	Thymus	Thymus
4	chr13:76308200-76324800	Weak transcription	Left Ventricle	heart
5	chr13:76308200-76345200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:76313600-76324800	Weak transcription	Psoas Muscle	Psoas
7	chr13:76313800-76323600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr13:76314000-76319000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr13:76314000-76323600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:76314000-76323800	Weak transcription	Fetal Heart	heart
11	chr13:76314200-76323200	Weak transcription	NHLF	lung
12	chr13:76314600-76318800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr13:76314600-76321800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:76314600-76321800	Weak transcription	HSMMtube	muscle
15	chr13:76315000-76319200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr13:76316600-76322600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr13:76317200-76319400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr13:76317800-76318600	Enhancers	Osteobl	bone
19	chr13:76317800-76318800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr13:76317800-76319400	Enhancers	Muscle Satellite Cultured Cells	--
21	chr13:76318000-76319000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr13:76318200-76318600	Enhancers	NHDF-Ad	bronchial
23	chr13:76318200-76319000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr13:76318200-76320400	Strong transcription	HSMM	muscle
25	chr13:76318400-76319000	Enhancers	NHEK	skin

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