Variant report

Variant	rs61075731
Chromosome Location	chr10:49984658-49984659
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10776644	1.00[ASN][1000 genomes]
rs10776646	0.83[ASN][1000 genomes]
rs10857640	1.00[ASN][1000 genomes]
rs10857642	0.83[ASN][1000 genomes]
rs10857643	0.83[ASN][1000 genomes]
rs10857646	0.83[ASN][1000 genomes]
rs10857647	0.83[ASN][1000 genomes]
rs11101486	0.83[ASN][1000 genomes]
rs11101491	0.83[ASN][1000 genomes]
rs11101492	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11101493	0.83[ASN][1000 genomes]
rs11101494	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11101495	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11101500	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11101501	0.83[ASN][1000 genomes]
rs11101504	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11101506	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11101508	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11101509	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12217548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12217755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12220888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12250158	1.00[ASN][1000 genomes]
rs1871602	0.83[ASN][1000 genomes]
rs41282005	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs41282013	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4838650	1.00[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895374	chr10:49969556-49990081	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49967600-50000000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:49967800-50006800	Strong transcription	Primary B cells from peripheral blood	blood
3	chr10:49969400-49989800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr10:49977000-49990400	Weak transcription	Fetal Brain Male	brain
5	chr10:49979400-49989200	Strong transcription	Primary hematopoietic stem cells	blood
6	chr10:49979600-49990600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:49979800-49991000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr10:49979800-49992400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr10:49980000-49990400	Weak transcription	Right Atrium	heart
10	chr10:49981200-49991000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr10:49981400-50007200	Strong transcription	Primary B cells from cord blood	blood
12	chr10:49981800-49989000	Strong transcription	GM12878-XiMat	blood
13	chr10:49982000-49992200	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr10:49982400-49991400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr10:49982400-50000800	Weak transcription	Fetal Thymus	thymus
16	chr10:49982600-49988800	Strong transcription	Spleen	Spleen
17	chr10:49982600-50006800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr10:49983000-49986000	Weak transcription	Lung	lung
19	chr10:49983600-49985800	Enhancers	Fetal Lung	lung
20	chr10:49984000-49985400	Enhancers	Right Ventricle	heart
21	chr10:49984200-49985200	Enhancers	Fetal Muscle Trunk	muscle
22	chr10:49984400-49985000	Bivalent Enhancer	Fetal Stomach	stomach
23	chr10:49984600-49985400	Enhancers	Fetal Muscle Leg	muscle

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