Variant report

Variant	rs73784730
Chromosome Location	chr6:161477688-161477689
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:161474546..161476528-chr6:161476872..161479203,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs55683369	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55813371	1.00[AMR][1000 genomes]
rs55925816	1.00[EUR][1000 genomes]
rs56024080	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56288506	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56335955	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56655389	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56691844	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57028833	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57850413	1.00[EUR][1000 genomes]
rs58008940	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59028741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59165451	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59302035	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59413458	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60747861	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6939921	1.00[EUR][1000 genomes]
rs73782389	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73782393	1.00[EUR][1000 genomes]
rs73782398	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73782399	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784708	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784709	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784712	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784723	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784725	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784733	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784739	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784742	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784743	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784750	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784754	1.00[EUR][1000 genomes]
rs73784788	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73784791	1.00[EUR][1000 genomes]
rs73784796	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73786003	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	nsv1030045	chr6:161359075-161562255	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv886817	chr6:161371621-161846654	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv3381361	chr6:161373617-161864101	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1023982	chr6:161382188-161549831	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161435000-161490400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:161443800-161478600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:161449000-161494400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr6:161452800-161489400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:161453600-161506600	Weak transcription	Small Intestine	intestine
6	chr6:161455200-161495800	Weak transcription	Fetal Brain Male	brain
7	chr6:161456400-161501600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr6:161456800-161485800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:161459400-161488800	Weak transcription	Brain Angular Gyrus	brain
10	chr6:161459400-161508800	Weak transcription	Hela-S3	cervix
11	chr6:161459800-161496600	Weak transcription	Fetal Kidney	kidney
12	chr6:161459800-161502800	Weak transcription	HUVEC	blood vessel
13	chr6:161460000-161499200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:161460400-161487200	Weak transcription	Colon Smooth Muscle	Colon
15	chr6:161460400-161488800	Weak transcription	Fetal Heart	heart
16	chr6:161460600-161495600	Weak transcription	HSMMtube	muscle
17	chr6:161462000-161478400	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr6:161462800-161478400	Weak transcription	Esophagus	oesophagus
19	chr6:161462800-161485800	Weak transcription	Aorta	Aorta
20	chr6:161462800-161497200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr6:161462800-161497800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:161462800-161508200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:161463000-161489000	Weak transcription	Fetal Brain Female	brain
24	chr6:161463000-161491600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
25	chr6:161463200-161488000	Weak transcription	Ovary	ovary
26	chr6:161463400-161491600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr6:161463600-161495600	Weak transcription	Pancreas	Pancrea
28	chr6:161463800-161499200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:161465400-161478200	Weak transcription	NHEK	skin
30	chr6:161470400-161478400	Weak transcription	HMEC	breast
31	chr6:161470400-161495000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr6:161470600-161488800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr6:161470600-161492000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:161470600-161493800	Weak transcription	Fetal Thymus	thymus
35	chr6:161470600-161508000	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr6:161470800-161478600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr6:161470800-161484400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:161470800-161485800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr6:161470800-161485800	Weak transcription	Gastric	stomach
40	chr6:161470800-161485800	Weak transcription	Thymus	Thymus
41	chr6:161470800-161491600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr6:161470800-161491600	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:161471000-161478200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:161471000-161481400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:161471000-161481600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:161471000-161485800	Weak transcription	Dnd41	blood
47	chr6:161471000-161487200	Weak transcription	NHDF-Ad	bronchial
48	chr6:161471000-161490400	Weak transcription	Lung	lung
49	chr6:161471000-161491600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:161471000-161503800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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