Variant report

Variant	rs11758353
Chromosome Location	chr6:35436429-35436430
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:3261385..3261959-chr6:35436177..35436756,2	HCT-116	colon:
2	chr17:66508673..66509254-chr6:35436145..35436972,2	Hela-S3	cervix:
3	chr6:26056308..26057054-chr6:35436068..35436860,2	Hela-S3	cervix:
4	chr12:54366608..54368151-chr6:35435475..35437868,2	MCF-7	breast:
5	chr10:114711341..114712330-chr6:35436015..35436846,2	Hela-S3	cervix:
6	chr6:35226066..35229330-chr6:35434346..35438215,4	K562	blood:
7	chr6:35259383..35261485-chr6:35435927..35437799,2	MCF-7	breast:
8	chr13:50017638..50018206-chr6:35436122..35436718,2	NB4	blood:
9	chr6:35435945..35437939-chr6:35694170..35698146,4	MCF-7	breast:
10	chr6:34855314..34856910-chr6:35435686..35437650,2	MCF-7	breast:
11	chr6:35308405..35313609-chr6:35434054..35440248,12	K562	blood:
12	chr6:35410187..35412214-chr6:35434908..35436495,2	K562	blood:
13	chr6:35260730..35269335-chr6:35433870..35444063,22	MCF-7	breast:
14	chr6:35434857..35438603-chr6:35692996..35696802,4	K562	blood:
15	chr6:35436322..35437059-chr9:75766687..75767366,2	Hela-S3	cervix:
16	chr6:26045293..26047313-chr6:35435617..35437589,2	MCF-7	breast:
17	chr19:39342287..39343048-chr6:35436123..35436710,2	HCT-116	colon:
18	chr16:31519299..31520039-chr6:35435669..35436598,2	HCT-116	colon:
19	chr6:35270811..35278072-chr6:35434777..35439344,8	MCF-7	breast:
20	chr1:22109654..22110213-chr6:35435641..35436558,2	Hela-S3	cervix:
21	chr6:35308378..35313609-chr6:35433550..35439145,12	K562	blood:
22	chr6:35309215..35314259-chr6:35432456..35439068,10	MCF-7	breast:
23	chr6:35227094..35229802-chr6:35433183..35436613,4	K562	blood:
24	chr6:35265067..35266084-chr6:35435395..35436525,11	K562	blood:
25	chr6:35415017..35416617-chr6:35436362..35437925,2	MCF-7	breast:
26	chr16:53536981..53537865-chr6:35435748..35436675,2	NB4	blood:
27	chr6:35436149..35436774-chr8:48173185..48173690,2	HCT-116	colon:
28	chr6:35435012..35436668-chr6:35752247..35755003,2	MCF-7	breast:
29	chr6:35265112..35265974-chr6:35435522..35436961,5	MCF-7	breast:
30	chr15:55700055..55700776-chr6:35435724..35436851,3	Hela-S3	cervix:
31	chr6:35264065..35266185-chr6:35435418..35437067,2	MCF-7	breast:
32	chr1:207924892..207925541-chr6:35435801..35436654,2	Hela-S3	cervix:
33	chr6:35309667..35310668-chr6:35435356..35436547,17	K562	blood:
34	chr11:2397606..2400001-chr6:35434655..35437647,2	K562	blood:
35	chr6:35435995..35436585-chr7:26239889..26240720,2	HCT-116	colon:
36	chr6:35434775..35437842-chr6:35701549..35705876,5	MCF-7	breast:
37	chr6:35418617..35424875-chr6:35434196..35438070,12	MCF-7	breast:
38	chr19:39926523..39927127-chr6:35436191..35436721,2	HCT-116	colon:
39	chr6:35226330..35228825-chr6:35434969..35437843,3	MCF-7	breast:
40	chr6:35360426..35363519-chr6:35436261..35438354,3	K562	blood:
41	chr17:41150274..41150856-chr6:35435959..35436552,2	HCT-116	colon:
42	chr6:35257372..35267692-chr6:35433856..35438688,25	K562	blood:
43	chr6:35435616..35437664-chrX:153627963..153630833,2	K562	blood:
44	chr6:35415818..35424678-chr6:35432486..35440672,36	K562	blood:
45	chr6:35433822..35437754-chr6:35703135..35706478,6	K562	blood:
46	chr6:35257372..35267871-chr6:35433266..35439192,25	K562	blood:
47	chr6:35436419..35438425-chr6:35888772..35891148,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000064995	Chromatin interaction
ENSG00000117335	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000110651	Chromatin interaction
ENSG00000112039	Chromatin interaction
ENSG00000118680	Chromatin interaction
ENSG00000157343	Chromatin interaction
ENSG00000260916	Chromatin interaction
ENSG00000090686	Chromatin interaction
ENSG00000065029	Chromatin interaction
ENSG00000096060	Chromatin interaction
ENSG00000140688	Chromatin interaction
ENSG00000023892	Chromatin interaction
ENSG00000096063	Chromatin interaction
ENSG00000147403	Chromatin interaction
ENSG00000264235	Chromatin interaction
ENSG00000166971	Chromatin interaction
ENSG00000164808	Chromatin interaction
ENSG00000238184	Chromatin interaction
ENSG00000207165	Chromatin interaction
ENSG00000261652	Chromatin interaction
ENSG00000196235	Chromatin interaction
ENSG00000135046	Chromatin interaction
ENSG00000105193	Chromatin interaction
ENSG00000232909	Chromatin interaction
ENSG00000233547	Chromatin interaction
ENSG00000123388	Chromatin interaction
ENSG00000204140	Chromatin interaction
ENSG00000227154	Chromatin interaction
ENSG00000112033	Chromatin interaction
ENSG00000104824	Chromatin interaction
ENSG00000260625	Chromatin interaction
ENSG00000131469	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000122566	Chromatin interaction
ENSG00000108946	Chromatin interaction
ENSG00000102547	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1076655	0.94[ASN][1000 genomes]
rs11756089	0.94[ASN][1000 genomes]
rs2072887	0.84[ASN][1000 genomes]
rs2076171	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3800379	0.84[ASN][1000 genomes]
rs41270066	0.97[ASN][1000 genomes]
rs41270070	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs45454199	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45464000	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs45472598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45624039	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713863	0.84[ASN][1000 genomes]
rs4713866	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4713870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713872	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6935950	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830641	chr6:35282534-35440603	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
2	nsv528351	chr6:35377922-35465786	Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
3	nsv885799	chr6:35378778-35442397	Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	54 gene(s)	inside rSNPs	diseases
4	nsv462908	chr6:35378778-35457396	Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
5	nsv602910	chr6:35378778-35457396	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
6	nsv519370	chr6:35378778-35537406	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	72 gene(s)	inside rSNPs	diseases
7	nsv984463	chr6:35432948-35477634	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35435200-35440200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr6:35435400-35436600	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr6:35435400-35436600	Active TSS	Fetal Brain Male	brain
4	chr6:35435400-35437000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr6:35435400-35437000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr6:35435400-35437000	Active TSS	Thymus	Thymus
7	chr6:35435400-35437200	Active TSS	Duodenum Smooth Muscle	Duodenum
8	chr6:35435600-35436800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:35435600-35436800	Active TSS	Colonic Mucosa	Colon
10	chr6:35435600-35436800	Active TSS	Esophagus	oesophagus
11	chr6:35435600-35437200	Active TSS	H9 Cell Line	embryonic stem cell
12	chr6:35435600-35437200	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr6:35435600-35437200	Active TSS	Primary T cells from cord blood	blood
14	chr6:35435600-35437200	Active TSS	Brain Hippocampus Middle	brain
15	chr6:35435600-35437200	Active TSS	Brain Substantia Nigra	brain
16	chr6:35435600-35437400	Active TSS	Colon Smooth Muscle	Colon
17	chr6:35435600-35437400	Active TSS	Left Ventricle	heart
18	chr6:35435600-35437400	Active TSS	Psoas Muscle	Psoas
19	chr6:35435600-35437400	Active TSS	Rectal Smooth Muscle	rectum
20	chr6:35435600-35437400	Active TSS	Right Ventricle	heart
21	chr6:35435600-35437600	Active TSS	Aorta	Aorta
22	chr6:35435600-35437600	Active TSS	Gastric	stomach
23	chr6:35435600-35437600	Active TSS	Sigmoid Colon	Sigmoid Colon
24	chr6:35435600-35437600	Active TSS	HSMMtube	muscle
25	chr6:35435600-35437600	Active TSS	NHDF-Ad	bronchial
26	chr6:35435600-35437800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr6:35435600-35437800	Active TSS	Ovary	ovary
28	chr6:35435600-35437800	Active TSS	Small Intestine	intestine
29	chr6:35435600-35438800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr6:35435800-35436600	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr6:35435800-35436600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:35435800-35436600	Active TSS	Primary T helper cells fromperipheralblood	blood
33	chr6:35435800-35436600	Active TSS	Fetal Intestine Small	intestine
34	chr6:35435800-35436600	Active TSS	Fetal Stomach	stomach
35	chr6:35435800-35436600	Transcr. at gene 5' and 3'	Right Atrium	heart
36	chr6:35435800-35436600	Active TSS	Spleen	Spleen
37	chr6:35435800-35436800	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr6:35435800-35436800	Active TSS	Primary B cells from peripheral blood	blood
39	chr6:35435800-35436800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:35435800-35436800	Active TSS	Fetal Brain Female	brain
41	chr6:35435800-35436800	Active TSS	Fetal Intestine Large	intestine
42	chr6:35435800-35436800	Active TSS	Monocytes-CD14+_RO01746	blood
43	chr6:35435800-35437000	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr6:35435800-35437000	Active TSS	Liver	Liver
45	chr6:35435800-35437000	Active TSS	Brain Anterior Caudate	brain
46	chr6:35435800-35437000	Active TSS	Hela-S3	cervix
47	chr6:35435800-35437200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:35435800-35437200	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr6:35435800-35437200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:35435800-35437200	Active TSS	Primary T killer memory cells from peripheral blood	blood

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