Variant report

Variant	rs34304845
Chromosome Location	chr11:73106186-73106187
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73102189..73103729-chr11:73105258..73107363,2	K562	blood:
2	chr11:73065745..73068475-chr11:73103301..73106275,2	MCF-7	breast:
3	chr11:73104835..73106451-chr11:73106455..73108482,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000266866	Chromatin interaction
ENSG00000110237	Chromatin interaction
ENSG00000256928	Chromatin interaction
ENSG00000054967	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1002127	0.80[AFR][1000 genomes]
rs11823289	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12146658	0.93[AMR][1000 genomes]
rs17851510	0.82[AFR][1000 genomes]
rs55727935	0.81[AMR][1000 genomes]
rs55940558	0.81[AMR][1000 genomes]
rs56045329	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56057109	0.81[AMR][1000 genomes]
rs56135026	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56187614	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56193465	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56205113	0.81[AMR][1000 genomes]
rs56260110	0.81[AMR][1000 genomes]
rs56262837	0.81[AMR][1000 genomes]
rs56332879	0.81[AMR][1000 genomes]
rs56407713	0.81[AMR][1000 genomes]
rs56701090	0.81[AMR][1000 genomes]
rs56834522	0.91[EUR][1000 genomes]
rs57288336	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs57727431	0.83[EUR][1000 genomes]
rs58062099	0.94[AFR][1000 genomes]
rs58619954	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs58658035	1.00[EUR][1000 genomes]
rs58850636	0.81[AMR][1000 genomes]
rs59199852	0.81[AMR][1000 genomes]
rs59212255	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs59250186	0.81[AMR][1000 genomes]
rs59912809	0.81[AMR][1000 genomes]
rs60578483	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61236919	0.81[AMR][1000 genomes]
rs61361454	0.81[AMR][1000 genomes]
rs61527032	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6592525	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7105000	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7105567	0.81[AMR][1000 genomes]
rs7105802	0.81[AMR][1000 genomes]
rs7105824	0.81[AMR][1000 genomes]
rs7109601	0.81[EUR][1000 genomes]
rs7119049	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7120131	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7120967	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7128786	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7128980	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7131044	0.81[AMR][1000 genomes]
rs7924394	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7928848	0.85[AMR][1000 genomes]
rs7931840	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7932197	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7933274	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7945735	0.81[AMR][1000 genomes]
rs7945984	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7949882	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821041	chr11:72937162-73113080	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases
2	nsv897911	chr11:73044351-73108276	Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	esv3395161	chr11:73084616-73461577	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73095200-73116200	Weak transcription	Liver	Liver
2	chr11:73096200-73130200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:73097200-73117600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:73097400-73106400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:73097400-73113000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:73097600-73106800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:73097600-73110200	Weak transcription	NHDF-Ad	bronchial
8	chr11:73098600-73126000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr11:73098600-73132400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr11:73098800-73113000	Weak transcription	Fetal Brain Female	brain
11	chr11:73099200-73106600	Strong transcription	Fetal Intestine Small	intestine
12	chr11:73099200-73112400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:73099200-73139800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr11:73099200-73141000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr11:73099400-73109600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:73099400-73112400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr11:73099400-73113200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:73099600-73119200	Weak transcription	Fetal Lung	lung
19	chr11:73100000-73116600	Weak transcription	Pancreas	Pancrea
20	chr11:73100000-73118400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr11:73100200-73106400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr11:73100200-73117400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:73100400-73109600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:73100400-73109800	Weak transcription	Right Atrium	heart
25	chr11:73100600-73118600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr11:73100800-73109800	Weak transcription	HSMM	muscle
27	chr11:73100800-73115800	Weak transcription	HMEC	breast
28	chr11:73101000-73116200	Weak transcription	Brain Angular Gyrus	brain
29	chr11:73101000-73116400	Weak transcription	Brain Substantia Nigra	brain
30	chr11:73101200-73124800	Weak transcription	Psoas Muscle	Psoas
31	chr11:73101400-73110400	Strong transcription	GM12878-XiMat	blood
32	chr11:73101400-73112600	Weak transcription	HSMMtube	muscle
33	chr11:73101600-73107200	Strong transcription	Brain Cingulate Gyrus	brain
34	chr11:73101800-73110000	Strong transcription	Thymus	Thymus
35	chr11:73101800-73110200	Strong transcription	Dnd41	blood
36	chr11:73102200-73107000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
37	chr11:73103000-73106600	Strong transcription	NHLF	lung
38	chr11:73103000-73106800	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr11:73103200-73108800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr11:73103600-73109400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr11:73103600-73118400	Weak transcription	Esophagus	oesophagus
42	chr11:73103800-73109400	Strong transcription	Fetal Thymus	thymus
43	chr11:73103800-73116600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr11:73104000-73106400	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr11:73104000-73109400	Weak transcription	Right Ventricle	heart
46	chr11:73104000-73116200	Weak transcription	Brain Anterior Caudate	brain
47	chr11:73104400-73108200	Strong transcription	Hela-S3	cervix
48	chr11:73104400-73109800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:73104400-73111000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr11:73104600-73106400	Weak transcription	Primary hematopoietic stem cells	blood

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