Variant report

Variant	rs59582367
Chromosome Location	chr6:149726545-149726546
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs17085985	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17086054	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34024129	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35391071	1.00[EUR][1000 genomes]
rs35507156	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55763048	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56126528	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56390023	1.00[EUR][1000 genomes]
rs56836556	1.00[EUR][1000 genomes]
rs57234155	1.00[EUR][1000 genomes]
rs57240808	1.00[EUR][1000 genomes]
rs58467138	1.00[EUR][1000 genomes]
rs59090184	0.87[AMR][1000 genomes]
rs59181586	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60598581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60923183	1.00[EUR][1000 genomes]
rs6926168	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6926360	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6934491	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73604793	1.00[EUR][1000 genomes]
rs73779304	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779305	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779307	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779311	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779312	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779313	1.00[EUR][1000 genomes]
rs73779314	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779330	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73779333	1.00[EUR][1000 genomes]
rs73779345	1.00[EUR][1000 genomes]
rs73779346	1.00[EUR][1000 genomes]
rs73779354	1.00[EUR][1000 genomes]
rs73779366	1.00[EUR][1000 genomes]
rs73779373	1.00[EUR][1000 genomes]
rs73779376	1.00[EUR][1000 genomes]
rs7740647	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7760102	1.00[EUR][1000 genomes]
rs7761612	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs935386	1.00[AMR][1000 genomes];1.00[EUR][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	nsv1024106	chr6:149622349-149745053	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv522875	chr6:149643709-149762537	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv530444	chr6:149654540-149848997	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv969455	chr6:149720845-149727255	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149700400-149728400	Weak transcription	Hela-S3	cervix
2	chr6:149700400-149732400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:149700600-149730800	Weak transcription	Fetal Brain Male	brain
4	chr6:149700800-149732800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:149701400-149730800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:149701400-149734200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:149701600-149733600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:149703400-149730600	Weak transcription	Brain Germinal Matrix	brain
9	chr6:149703600-149730400	Weak transcription	NHLF	lung
10	chr6:149705200-149734600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:149709400-149733000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr6:149709600-149729800	Weak transcription	Fetal Heart	heart
13	chr6:149709600-149750200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:149711400-149726600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr6:149712000-149727200	Strong transcription	Primary hematopoietic stem cells	blood
16	chr6:149713800-149735400	Weak transcription	Small Intestine	intestine
17	chr6:149714000-149728000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:149714800-149730800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr6:149715000-149728200	Strong transcription	Fetal Thymus	thymus
20	chr6:149715400-149732600	Strong transcription	Dnd41	blood
21	chr6:149715600-149733600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:149716000-149728000	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr6:149716000-149728200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:149716400-149728600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr6:149717200-149726800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:149717400-149726600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:149717400-149728200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:149717400-149728400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr6:149717400-149733200	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr6:149717600-149727000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:149717600-149727600	Strong transcription	Primary B cells from cord blood	blood
32	chr6:149717800-149732200	Strong transcription	GM12878-XiMat	blood
33	chr6:149718600-149727200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr6:149718600-149727800	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr6:149718800-149727200	Strong transcription	HUES48 Cell Line	embryonic stem cell
36	chr6:149718800-149727600	Weak transcription	Stomach Mucosa	stomach
37	chr6:149718800-149727800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr6:149718800-149728400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:149718800-149732800	Strong transcription	HSMM	muscle
40	chr6:149719000-149727400	Strong transcription	NH-A	brain
41	chr6:149720200-149727800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr6:149720400-149726600	Strong transcription	Liver	Liver
43	chr6:149721600-149726600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr6:149721800-149730400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:149721800-149730400	Weak transcription	Gastric	stomach
46	chr6:149721800-149730600	Weak transcription	Esophagus	oesophagus
47	chr6:149721800-149730800	Weak transcription	Aorta	Aorta
48	chr6:149721800-149730800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr6:149721800-149730800	Weak transcription	Colonic Mucosa	Colon
50	chr6:149721800-149730800	Weak transcription	Spleen	Spleen

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