Variant report

Variant	rs41271255
Chromosome Location	chr6:33650411-33650412
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33648020..33651730-chr6:33656230..33658624,3	MCF-7	breast:
2	chr6:33645251..33648923-chr6:33649815..33652997,4	MCF-7	breast:
3	chr6:33644740..33654543-chr6:33656969..33664772,16	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269490	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10214667	1.00[EUR][1000 genomes]
rs11967163	1.00[EUR][1000 genomes]
rs11970477	1.00[EUR][1000 genomes]
rs28488940	1.00[EUR][1000 genomes]
rs28589816	1.00[EUR][1000 genomes]
rs55897728	1.00[EUR][1000 genomes]
rs56085633	1.00[EUR][1000 genomes]
rs56122765	1.00[EUR][1000 genomes]
rs56124649	1.00[EUR][1000 genomes]
rs56148814	1.00[EUR][1000 genomes]
rs56226140	1.00[EUR][1000 genomes]
rs56875788	1.00[EUR][1000 genomes]
rs57104544	1.00[EUR][1000 genomes]
rs57290518	1.00[EUR][1000 genomes]
rs58043092	1.00[EUR][1000 genomes]
rs58058146	1.00[EUR][1000 genomes]
rs58312523	1.00[EUR][1000 genomes]
rs58566767	1.00[EUR][1000 genomes]
rs59401679	1.00[EUR][1000 genomes]
rs60263379	1.00[EUR][1000 genomes]
rs60289279	1.00[EUR][1000 genomes]
rs60854312	1.00[EUR][1000 genomes]
rs61138871	1.00[EUR][1000 genomes]
rs61348385	1.00[EUR][1000 genomes]
rs61589902	1.00[EUR][1000 genomes]
rs73402380	1.00[EUR][1000 genomes]
rs73402381	1.00[EUR][1000 genomes]
rs73402386	1.00[EUR][1000 genomes]
rs73414139	1.00[EUR][1000 genomes]
rs73414141	1.00[EUR][1000 genomes]
rs73741932	1.00[EUR][1000 genomes]
rs73743206	1.00[EUR][1000 genomes]
rs73743207	1.00[EUR][1000 genomes]
rs7742848	1.00[EUR][1000 genomes]
rs7754339	1.00[EUR][1000 genomes]
rs9461865	1.00[EUR][1000 genomes]
rs9461866	1.00[EUR][1000 genomes]
rs9461871	1.00[EUR][1000 genomes]
rs9461872	1.00[EUR][1000 genomes]
rs9469441	1.00[EUR][1000 genomes]
rs9469442	1.00[EUR][1000 genomes]
rs9469444	1.00[EUR][1000 genomes]
rs9469445	1.00[EUR][1000 genomes]
rs9469446	1.00[EUR][1000 genomes]
rs9469468	1.00[EUR][1000 genomes]
rs9469473	1.00[EUR][1000 genomes]
rs9469474	1.00[EUR][1000 genomes]
rs9469476	1.00[EUR][1000 genomes]
rs9469477	1.00[EUR][1000 genomes]
rs9469478	1.00[EUR][1000 genomes]
rs9469479	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830638	chr6:33551202-33711346	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
2	nsv830639	chr6:33592022-33711346	Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	30 gene(s)	inside rSNPs	diseases
3	nsv602838	chr6:33624733-33650743	Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	nsv885771	chr6:33626717-33660143	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv885772	chr6:33638180-33767727	Bivalent Enhancer Genic enhancers Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33613000-33659400	Strong transcription	Fetal Intestine Small	intestine
2	chr6:33613200-33660400	Strong transcription	Thymus	Thymus
3	chr6:33615000-33660800	Strong transcription	Fetal Intestine Large	intestine
4	chr6:33619600-33660800	Strong transcription	Rectal Mucosa Donor 29	rectum
5	chr6:33621000-33659400	Strong transcription	Duodenum Mucosa	Duodenum
6	chr6:33621400-33662200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr6:33621400-33672600	Strong transcription	Dnd41	blood
8	chr6:33622000-33660000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:33624600-33664800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr6:33629000-33662800	Weak transcription	Colon Smooth Muscle	Colon
11	chr6:33630200-33651000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr6:33630400-33650800	Weak transcription	Ovary	ovary
13	chr6:33630400-33660800	Strong transcription	Rectal Mucosa Donor 31	rectum
14	chr6:33631600-33667000	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr6:33631800-33661200	Weak transcription	Liver	Liver
16	chr6:33636600-33660600	Strong transcription	Colonic Mucosa	Colon
17	chr6:33636800-33660200	Strong transcription	Lung	lung
18	chr6:33636800-33661400	Strong transcription	Sigmoid Colon	Sigmoid Colon
19	chr6:33637400-33661600	Strong transcription	Esophagus	oesophagus
20	chr6:33638000-33652200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr6:33638200-33659200	Weak transcription	Right Atrium	heart
22	chr6:33638800-33650800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
23	chr6:33639600-33659200	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:33640000-33669200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:33641000-33650600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr6:33641000-33667800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
27	chr6:33641200-33658600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:33641200-33659600	Strong transcription	H1 Cell Line	embryonic stem cell
29	chr6:33641200-33661600	Strong transcription	NHEK	skin
30	chr6:33641400-33659200	Strong transcription	HMEC	breast
31	chr6:33641400-33660200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:33641400-33668000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr6:33641800-33661800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr6:33642400-33654000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:33642400-33659600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:33642400-33660600	Weak transcription	Brain Germinal Matrix	brain
37	chr6:33643600-33654200	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:33643800-33654000	Weak transcription	Fetal Brain Male	brain
39	chr6:33643800-33659800	Strong transcription	Adipose Nuclei	Adipose
40	chr6:33644000-33659400	Weak transcription	HSMMtube	muscle
41	chr6:33644000-33660600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:33644000-33662000	Weak transcription	Fetal Kidney	kidney
43	chr6:33644600-33659600	Strong transcription	Gastric	stomach
44	chr6:33645400-33657000	Weak transcription	Left Ventricle	heart
45	chr6:33645400-33659400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:33645600-33650800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr6:33645600-33650800	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr6:33645600-33651000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:33645600-33651000	Weak transcription	NH-A	brain
50	chr6:33645600-33659400	Strong transcription	NHLF	lung

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