Variant report

Variant	rs17010062
Chromosome Location	chr1:221631207-221631208
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11118737	0.84[JPT][hapmap]
rs11118740	1.00[YRI][hapmap]
rs12565312	0.81[ASN][1000 genomes]
rs1585327	0.84[JPT][hapmap]
rs17010134	0.97[ASN][1000 genomes]
rs17010167	0.97[ASN][1000 genomes]
rs17010220	0.85[ASN][1000 genomes]
rs56015767	0.94[ASN][1000 genomes]
rs56205442	0.85[ASN][1000 genomes]
rs57205860	0.91[ASN][1000 genomes]
rs74144285	0.91[ASN][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	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221615600-221635000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:221623800-221631600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:221628200-221631800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:221629800-221633200	Enhancers	Fetal Lung	lung
5	chr1:221630400-221631600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:221630400-221631600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:221630400-221631600	Enhancers	NHDF-Ad	bronchial
8	chr1:221630600-221632200	Enhancers	Fetal Muscle Leg	muscle
9	chr1:221630800-221631600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:221631000-221631800	Enhancers	Psoas Muscle	Psoas
11	chr1:221631000-221631800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr1:221631000-221632200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:221631000-221632200	Enhancers	Osteobl	bone
14	chr1:221631000-221632400	Enhancers	Fetal Stomach	stomach
15	chr1:221631000-221632400	Enhancers	HSMMtube	muscle
16	chr1:221631000-221632400	Enhancers	NHLF	lung
17	chr1:221631000-221632600	Enhancers	Rectal Smooth Muscle	rectum
18	chr1:221631000-221632600	Enhancers	Hela-S3	cervix
19	chr1:221631000-221632600	Enhancers	HSMM	muscle
20	chr1:221631000-221632800	Enhancers	Colon Smooth Muscle	Colon
21	chr1:221631200-221631600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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