Variant report

Variant	rs12249190
Chromosome Location	chr10:23109973-23109974
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:23108692..23110534-chr10:23308268..23309848,2	K562	blood:
2	chr10:23108350..23110476-chr10:23111720..23113681,2	K562	blood:
3	chr10:23108350..23110546-chr10:23110740..23113681,3	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10466082	0.95[EUR][1000 genomes]
rs10828339	0.83[AFR][1000 genomes]
rs11596079	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1970447	0.83[AFR][1000 genomes]
rs4747446	0.81[AFR][1000 genomes]
rs61013475	0.94[EUR][1000 genomes]
rs7073439	0.97[EUR][1000 genomes]
rs7093263	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72812424	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72812426	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902635	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7922263	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894960	chr10:23049139-23113841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv894961	chr10:23049139-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv466833	chr10:23050683-23110797	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv894962	chr10:23050683-23113841	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv894963	chr10:23050683-23121820	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv894964	chr10:23050683-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv894965	chr10:23071128-23113841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv2764013	chr10:23087298-23239345	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv894966	chr10:23090535-23202522	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23100200-23114400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:23104800-23112800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:23106000-23113200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:23106200-23111800	Weak transcription	A549	lung
5	chr10:23106400-23110200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:23106400-23113200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:23106600-23110000	Weak transcription	HUVEC	blood vessel
8	chr10:23106600-23110200	Weak transcription	NH-A	brain
9	chr10:23106600-23110200	Weak transcription	NHDF-Ad	bronchial
10	chr10:23106600-23110400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr10:23106600-23110400	Weak transcription	HSMMtube	muscle
12	chr10:23106600-23110400	Weak transcription	Osteobl	bone
13	chr10:23106600-23111600	Weak transcription	NHEK	skin
14	chr10:23106600-23111800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr10:23106600-23111800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:23106600-23111800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:23106600-23111800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr10:23106600-23111800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:23106600-23111800	Weak transcription	Hela-S3	cervix
20	chr10:23106600-23111800	Weak transcription	HMEC	breast
21	chr10:23106600-23111800	Weak transcription	HSMM	muscle
22	chr10:23106600-23112000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr10:23106800-23110200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr10:23109200-23110800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr10:23109800-23110400	Weak transcription	NHLF	lung
26	chr10:23109800-23115200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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