Variant report

Variant	rs6909581
Chromosome Location	chr6:33629600-33629601
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33625658..33632208-chr6:33632440..33635133,7	MCF-7	breast:
2	chr6:33480361..33482958-chr6:33629089..33631311,2	K562	blood:
3	chr6:33627824..33631151-chr6:33635216..33637671,3	MCF-7	breast:
4	chr6:33628674..33633402-chr6:33634889..33637916,6	MCF-7	breast:
5	chr6:33625809..33628481-chr6:33628600..33630329,2	K562	blood:
6	chr6:33626651..33628941-chr6:33628944..33631916,2	MCF-7	breast:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1536041	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3736893	0.88[ASN][1000 genomes]
rs41271249	0.82[ASN][1000 genomes]
rs4713651	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73408252	0.85[ASN][1000 genomes]
rs7752472	0.83[ASN][1000 genomes]
rs9357163	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9366827	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9380372	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs942638	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs942639	0.85[EUR][1000 genomes];0.91[ASN][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	nsv470811	chr6:33622933-33647651	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	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
5	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

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33602400-33636400	Weak transcription	HSMMtube	muscle
2	chr6:33602600-33631600	Weak transcription	Osteobl	bone
3	chr6:33603400-33640400	Weak transcription	HUVEC	blood vessel
4	chr6:33603400-33641200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:33605200-33636400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:33606600-33633000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:33606800-33646600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:33608200-33640800	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:33611400-33643400	Weak transcription	Left Ventricle	heart
10	chr6:33613000-33659400	Strong transcription	Fetal Intestine Small	intestine
11	chr6:33613200-33660400	Strong transcription	Thymus	Thymus
12	chr6:33613400-33635400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:33613600-33635000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr6:33614400-33636200	Strong transcription	Primary B cells from peripheral blood	blood
15	chr6:33615000-33660800	Strong transcription	Fetal Intestine Large	intestine
16	chr6:33616600-33631400	Weak transcription	GM12878-XiMat	blood
17	chr6:33619000-33632800	Strong transcription	NHEK	skin
18	chr6:33619400-33629600	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr6:33619600-33660800	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr6:33620000-33632400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:33621000-33659400	Strong transcription	Duodenum Mucosa	Duodenum
22	chr6:33621200-33636200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr6:33621200-33636400	Strong transcription	Primary T cells from cord blood	blood
24	chr6:33621200-33636400	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:33621400-33635800	Strong transcription	Colonic Mucosa	Colon
26	chr6:33621400-33636400	Strong transcription	Lung	lung
27	chr6:33621400-33643400	Strong transcription	Spleen	Spleen
28	chr6:33621400-33662200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:33621400-33672600	Strong transcription	Dnd41	blood
30	chr6:33622000-33660000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:33622200-33630000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:33622400-33644400	Strong transcription	Gastric	stomach
33	chr6:33623000-33629600	Strong transcription	Muscle Satellite Cultured Cells	--
34	chr6:33623000-33635200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:33623200-33634800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr6:33623200-33635600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr6:33623200-33636200	Strong transcription	HMEC	breast
38	chr6:33623200-33649000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr6:33623400-33641000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr6:33623400-33644000	Strong transcription	Fetal Stomach	stomach
41	chr6:33623600-33629800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:33624200-33636200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:33624200-33639200	Strong transcription	NHLF	lung
44	chr6:33624600-33635800	Weak transcription	HepG2	liver
45	chr6:33624600-33664800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr6:33624800-33630200	Weak transcription	Small Intestine	intestine
47	chr6:33624800-33639400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:33625200-33634800	Weak transcription	Placenta	Placenta
49	chr6:33625200-33645200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr6:33625600-33636200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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