Variant report

Variant	rs11598212
Chromosome Location	chr10:49977746-49977747
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:49973164..49974775-chr10:49975647..49977758,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10508908	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10776643	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11101469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11101470	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11101471	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11595065	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12768835	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs17836440	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs1904603	0.86[JPT][hapmap]
rs2620888	0.86[EUR][1000 genomes]
rs2620889	0.86[EUR][1000 genomes]
rs2663031	0.85[JPT][hapmap]
rs2663043	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2683610	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2940707	0.82[JPT][hapmap]
rs2947344	0.86[JPT][hapmap]
rs2947345	0.86[JPT][hapmap]
rs730591	0.96[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7904251	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[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:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49962400-49980600	Strong transcription	Primary B cells from cord blood	blood
2	chr10:49967600-49977800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:49967600-50000000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
4	chr10:49967800-49978200	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:49967800-49979000	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr10:49967800-50006800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr10:49968600-49978600	Weak transcription	Adipose Nuclei	Adipose
8	chr10:49969400-49989800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr10:49971400-49982600	Weak transcription	Spleen	Spleen
10	chr10:49975200-49982400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:49976400-49981200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr10:49976800-49980000	Strong transcription	GM12878-XiMat	blood
13	chr10:49977000-49979000	Weak transcription	Fetal Stomach	stomach
14	chr10:49977000-49990400	Weak transcription	Fetal Brain Male	brain
15	chr10:49977200-49978000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr10:49977200-49978200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr10:49977200-49978200	Strong transcription	Primary hematopoietic stem cells	blood
18	chr10:49977200-49978400	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr10:49977400-49979400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr10:49977400-49981200	Weak transcription	Fetal Thymus	thymus

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