Variant report

Variant	rs11757612
Chromosome Location	chr6:33574488-33574489
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33567572..33569907-chr6:33573549..33575919,2	MCF-7	breast:
2	chr6:33562478..33565325-chr6:33572841..33575005,2	MCF-7	breast:
3	chr6:33574216..33577618-chr6:33579266..33582393,4	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10456420	0.86[AFR][1000 genomes]
rs10947415	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10947418	1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10947426	0.86[AFR][1000 genomes]
rs11755257	1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11756772	0.83[AFR][1000 genomes]
rs11757379	1.00[AFR][1000 genomes]
rs11758330	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12153870	0.86[AFR][1000 genomes]
rs12195409	0.86[AFR][1000 genomes]
rs12195707	0.86[AFR][1000 genomes]
rs12200154	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12204620	0.86[AFR][1000 genomes]
rs12204992	0.86[AFR][1000 genomes]
rs12205667	0.86[AFR][1000 genomes]
rs12206173	0.86[EUR][1000 genomes]
rs12211490	0.86[AFR][1000 genomes]
rs12211554	0.86[AFR][1000 genomes]
rs12211565	0.86[AFR][1000 genomes]
rs12214476	0.86[AFR][1000 genomes]
rs12214669	0.86[AFR][1000 genomes]
rs12660955	0.86[AFR][1000 genomes]
rs13195024	0.81[AMR][1000 genomes]
rs13195171	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs13200063	0.86[AFR][1000 genomes]
rs13206228	0.86[AFR][1000 genomes]
rs13219209	0.90[AMR][1000 genomes]
rs13220421	0.86[AFR][1000 genomes]
rs2227925	1.00[AFR][1000 genomes]
rs2296749	0.86[AFR][1000 genomes]
rs34339105	0.86[AFR][1000 genomes]
rs34376580	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34460651	0.86[AFR][1000 genomes]
rs34472165	0.86[AFR][1000 genomes]
rs34517899	0.86[AFR][1000 genomes]
rs34869648	0.86[AFR][1000 genomes]
rs35088242	0.86[AFR][1000 genomes]
rs35274562	0.86[AFR][1000 genomes]
rs35445446	0.86[AFR][1000 genomes]
rs35721478	0.86[AFR][1000 genomes]
rs35797388	0.86[AFR][1000 genomes]
rs36097803	0.86[AFR][1000 genomes]
rs36122085	0.86[AFR][1000 genomes]
rs4559081	0.86[AFR][1000 genomes]
rs66670017	0.86[AFR][1000 genomes]
rs68168863	0.86[AFR][1000 genomes]
rs71565393	1.00[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs755239	0.86[AFR][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	nsv462896	chr6:33534880-33588147	Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv602833	chr6:33534880-33588147	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885770	chr6:33543409-33614127	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	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
5	nsv5250	chr6:33565017-33598370	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	24 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	chr6:33567600-33575800	Weak transcription	Right Atrium	heart
2	chr6:33567600-33575800	Weak transcription	Right Ventricle	heart
3	chr6:33567800-33575000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:33567800-33575400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:33571600-33579000	Enhancers	Placenta	Placenta
6	chr6:33571800-33574800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:33572200-33574600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:33572200-33576800	Weak transcription	Lung	lung
9	chr6:33572400-33574600	Weak transcription	Hela-S3	cervix
10	chr6:33572600-33575000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:33573200-33574600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:33573200-33574800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:33573200-33576600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:33573400-33574600	Weak transcription	Duodenum Mucosa	Duodenum
15	chr6:33573400-33574800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:33573400-33575000	Weak transcription	A549	lung
17	chr6:33573400-33575400	Weak transcription	NHDF-Ad	bronchial
18	chr6:33573400-33575800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr6:33573400-33575800	Weak transcription	HSMM	muscle
20	chr6:33573400-33576200	Weak transcription	HSMMtube	muscle
21	chr6:33573400-33577200	Weak transcription	Fetal Intestine Large	intestine
22	chr6:33573400-33577600	Weak transcription	Colonic Mucosa	Colon
23	chr6:33574200-33576000	Enhancers	HepG2	liver
24	chr6:33574200-33577000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:33574400-33574600	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr6:33574400-33574800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:33574400-33575200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr6:33574400-33575600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:33574400-33575600	Enhancers	NHEK	skin
30	chr6:33574400-33575800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr6:33574400-33576000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr6:33574400-33578600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:33574400-33579000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr6:33574400-33579400	Enhancers	Spleen	Spleen
35	chr6:33574400-33579600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr6:33574400-33579600	Enhancers	Stomach Mucosa	stomach
37	chr6:33574400-33583200	Enhancers	HMEC	breast

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