Variant report

Variant	rs9373834
Chromosome Location	chr6:106577694-106577695
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:106562594..106564776-chr6:106574919..106578759,3	K562	blood:
2	chr6:106576961..106578620-chr6:106582173..106584108,2	MCF-7	breast:
3	chr6:106570219..106573350-chr6:106576379..106579233,4	K562	blood:
4	chr6:106572499..106574358-chr6:106575871..106578205,2	MCF-7	breast:
5	chr6:106549886..106552780-chr6:106576798..106578575,2	MCF-7	breast:
6	chr6:106574758..106578826-chr6:106580489..106584982,7	K562	blood:

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs4946726	0.84[ASN][1000 genomes]
rs504045	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs693612	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72943407	0.94[ASN][1000 genomes]
rs72943419	0.95[EUR][1000 genomes]
rs9480643	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1025231	chr6:106451012-106634389	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv830755	chr6:106461705-106624202	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1025900	chr6:106529777-106898421	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv1018270	chr6:106531658-106908606	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv538399	chr6:106531658-106908606	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	esv1832544	chr6:106539914-106642993	Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	nsv1035110	chr6:106557281-106802212	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv538400	chr6:106557281-106802212	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv1022855	chr6:106570926-106802072	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
11	nsv538401	chr6:106570926-106802072	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106553600-106584000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:106568800-106578000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:106575000-106582400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr6:106576800-106578000	Flanking Active TSS	Hela-S3	cervix
5	chr6:106576800-106578000	Enhancers	K562	blood
6	chr6:106576800-106578400	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr6:106576800-106578400	Enhancers	GM12878-XiMat	blood
8	chr6:106576800-106578400	Enhancers	HMEC	breast
9	chr6:106577000-106577800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:106577000-106577800	Enhancers	Stomach Mucosa	stomach
11	chr6:106577000-106578000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr6:106577000-106578000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr6:106577000-106578000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr6:106577000-106578000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:106577000-106578000	Enhancers	Sigmoid Colon	Sigmoid Colon
16	chr6:106577000-106578000	Flanking Active TSS	A549	lung
17	chr6:106577000-106578000	Enhancers	HSMMtube	muscle
18	chr6:106577000-106578000	Flanking Active TSS	NHEK	skin
19	chr6:106577000-106578000	Flanking Active TSS	NHLF	lung
20	chr6:106577000-106578400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr6:106577000-106579000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:106577200-106577800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:106577200-106577800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr6:106577200-106578000	Enhancers	Dnd41	blood
25	chr6:106577200-106578000	Flanking Active TSS	NH-A	brain
26	chr6:106577200-106578400	Flanking Active TSS	Osteobl	bone
27	chr6:106577400-106577800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr6:106577400-106577800	Enhancers	Duodenum Mucosa	Duodenum
29	chr6:106577400-106578000	Enhancers	Fetal Intestine Small	intestine
30	chr6:106577400-106578600	Enhancers	HSMM	muscle
31	chr6:106577600-106577800	Enhancers	NHDF-Ad	bronchial
32	chr6:106577600-106578000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:106577600-106578400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr6:106577600-106578600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:106577600-106579600	Weak transcription	Placenta	Placenta
36	chr6:106577600-106580200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr6:106577600-106582000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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