Variant report

Variant	rs846777
Chromosome Location	chr6:101323741-101323742
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:101316563..101319212-chr6:101321882..101324252,3	K562	blood:
2	chr6:101321078..101323999-chr6:101327365..101330497,3	K562	blood:
3	chr6:101321574..101324468-chr6:101327088..101328680,2	MCF-7	breast:
4	chr6:101315511..101317723-chr6:101321403..101323944,2	K562	blood:
5	chr6:101319726..101322538-chr6:101323434..101327261,5	K562	blood:

Variant related genes	Relation type
ENSG00000260000	Chromatin interaction
ENSG00000112249	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1069049	0.81[EUR][1000 genomes]
rs1099911	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11155720	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4454144	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4840159	0.94[ASN][1000 genomes]
rs592436	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs618919	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6570972	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6931410	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs705589	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs705591	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs705592	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs705593	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs705596	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs705599	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs705600	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs705603	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705604	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705605	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705606	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs705607	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705608	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs705610	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7771570	0.92[ASN][1000 genomes]
rs846771	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs846772	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs846773	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs846775	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs846781	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs846782	0.90[EUR][1000 genomes]
rs846785	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs846794	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs846797	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs846798	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs865318	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9322294	0.82[ASN][1000 genomes]
rs9377239	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9498420	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer 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	8 gene(s)	inside rSNPs	diseases
7	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' 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
8	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101269200-101326600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:101285600-101326600	Weak transcription	NHLF	lung
3	chr6:101291200-101326400	Weak transcription	Brain Anterior Caudate	brain
4	chr6:101294600-101325400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:101294600-101328600	Weak transcription	Spleen	Spleen
6	chr6:101294800-101325600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:101295000-101325800	Weak transcription	Brain Angular Gyrus	brain
8	chr6:101295000-101325800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr6:101296800-101323800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:101297000-101327200	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:101297000-101328200	Weak transcription	Ovary	ovary
12	chr6:101300200-101326600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:101300200-101328400	Weak transcription	Esophagus	oesophagus
14	chr6:101300200-101328400	Weak transcription	Lung	lung
15	chr6:101302600-101327800	Weak transcription	Stomach Mucosa	stomach
16	chr6:101303800-101325600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr6:101304200-101326600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr6:101304400-101327800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr6:101304800-101325400	Weak transcription	Brain Substantia Nigra	brain
20	chr6:101305000-101327800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr6:101309800-101326600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:101311600-101326400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:101311600-101327800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr6:101311800-101326400	Weak transcription	Duodenum Mucosa	Duodenum
25	chr6:101311800-101326600	Weak transcription	Pancreas	Pancrea
26	chr6:101311800-101326600	Weak transcription	Thymus	Thymus
27	chr6:101311800-101328200	Weak transcription	Aorta	Aorta
28	chr6:101311800-101328400	Weak transcription	Fetal Muscle Trunk	muscle
29	chr6:101311800-101328400	Weak transcription	Left Ventricle	heart
30	chr6:101313000-101327200	Weak transcription	Fetal Intestine Large	intestine
31	chr6:101314800-101326400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:101314800-101326800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr6:101315000-101325600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:101315200-101327800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr6:101315600-101327200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr6:101315800-101325600	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr6:101315800-101325800	Weak transcription	NHEK	skin
38	chr6:101315800-101326400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:101315800-101327200	Weak transcription	Adipose Nuclei	Adipose
40	chr6:101315800-101327200	Weak transcription	Placenta	Placenta
41	chr6:101315800-101327800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr6:101316000-101324200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:101316000-101325000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:101316000-101325600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:101316000-101325600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr6:101316000-101325600	Weak transcription	Hela-S3	cervix
47	chr6:101316000-101325600	Weak transcription	NH-A	brain
48	chr6:101316000-101325800	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr6:101316000-101325800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr6:101316000-101325800	Weak transcription	Muscle Satellite Cultured Cells	--

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