Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44355270..44357315-chr10:44376908..44378969,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11238720	1.00[ASN][1000 genomes]
rs11238721	1.00[ASN][1000 genomes]
rs12264669	1.00[ASN][1000 genomes]
rs12266918	1.00[ASN][1000 genomes]
rs1254856	1.00[ASN][1000 genomes]
rs1270513	1.00[ASN][1000 genomes]
rs1578855	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17154499	1.00[ASN][1000 genomes]
rs17154520	1.00[ASN][1000 genomes]
rs17154571	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1947673	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2025622	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2025623	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2209487	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2613103	1.00[ASN][1000 genomes]
rs2798994	1.00[ASN][1000 genomes]
rs2798995	1.00[ASN][1000 genomes]
rs28475171	1.00[ASN][1000 genomes]
rs2863233	1.00[ASN][1000 genomes]
rs28654354	1.00[ASN][1000 genomes]
rs61861590	1.00[ASN][1000 genomes]
rs7071492	1.00[ASN][1000 genomes]
rs7075076	1.00[ASN][1000 genomes]
rs7075813	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7078623	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7079939	1.00[ASN][1000 genomes]
rs7086449	1.00[ASN][1000 genomes]
rs7087019	1.00[ASN][1000 genomes]
rs7096797	1.00[ASN][1000 genomes]
rs73267817	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7918642	1.00[ASN][1000 genomes]
rs984001	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051921	chr10:44378011-44458880	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44360000-44392200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:44374400-44383400	Weak transcription	NHLF	lung
3	chr10:44375800-44387400	Weak transcription	Left Ventricle	heart
4	chr10:44377200-44378600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr10:44377400-44379000	Enhancers	Osteobl	bone
6	chr10:44377600-44378800	Weak transcription	Right Ventricle	heart
7	chr10:44377600-44387600	Weak transcription	Right Atrium	heart
8	chr10:44377800-44383800	Weak transcription	HSMMtube	muscle
9	chr10:44378000-44380000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr10:44378000-44382600	Weak transcription	NHDF-Ad	bronchial
11	chr10:44378000-44383800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:44378200-44383200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr10:44378200-44387000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:44378400-44378600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:44378400-44378800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr10:44378400-44378800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:44378400-44378800	Enhancers	HUVEC	blood vessel
18	chr10:44378400-44379000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr10:44378400-44379000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:44378400-44379200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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