Variant report

Variant	rs60480849
Chromosome Location	chr1:97593599-97593600
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12069444	1.00[AMR][1000 genomes]
rs290823	1.00[AMR][1000 genomes]
rs55737241	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55890675	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55896709	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56116315	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56283857	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57607396	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58372929	1.00[AMR][1000 genomes]
rs59996661	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60455988	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61208874	1.00[AMR][1000 genomes]
rs72726671	1.00[EUR][1000 genomes]
rs74104255	1.00[AMR][1000 genomes]
rs74104256	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74104257	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74104259	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74104311	1.00[AMR][1000 genomes]
rs74104313	1.00[AMR][1000 genomes]
rs74104319	1.00[AMR][1000 genomes]
rs74104321	1.00[AMR][1000 genomes]
rs74106608	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106609	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106636	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106638	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106640	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106641	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106643	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106677	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106679	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106684	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74106701	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv530048	chr1:97457175-98031501	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1007950	chr1:97466488-98021146	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv830692	chr1:97501492-97625153	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97538000-97603600	Weak transcription	Psoas Muscle	Psoas
2	chr1:97560800-97603600	Weak transcription	Pancreas	Pancrea
3	chr1:97563600-97594000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:97563600-97619200	Weak transcription	Dnd41	blood
5	chr1:97564200-97632800	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr1:97565400-97603600	Weak transcription	Left Ventricle	heart
7	chr1:97566000-97599400	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr1:97570600-97603800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:97571200-97604000	Weak transcription	Primary B cells from cord blood	blood
10	chr1:97579000-97596800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:97580800-97595400	Weak transcription	Liver	Liver
12	chr1:97580800-97604400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr1:97583000-97596800	Weak transcription	Adipose Nuclei	Adipose
14	chr1:97585600-97621800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr1:97586000-97596600	Weak transcription	Brain Angular Gyrus	brain
16	chr1:97587600-97603400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:97587800-97597200	Weak transcription	Primary T cells from cord blood	blood
18	chr1:97587800-97603800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr1:97590000-97603600	Weak transcription	HSMM	muscle
20	chr1:97590000-97603600	Weak transcription	HSMMtube	muscle
21	chr1:97590200-97603800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr1:97590400-97603600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:97592000-97598000	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:97592200-97608800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:97592600-97597600	Strong transcription	Monocytes-CD14+_RO01746	blood

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