Variant report

Variant	rs17079521
Chromosome Location	chr6:150576650-150576651
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:150572423..150575831-chr6:150576136..150578517,3	MCF-7	breast:
2	chr6:150576059..150579717-chr6:150580532..150582490,4	K562	blood:
3	chr6:150571832..150575013-chr6:150575106..150579101,3	K562	blood:
4	chr6:150572452..150574254-chr6:150575448..150578031,3	K562	blood:
5	chr6:150571087..150575708-chr6:150576058..150580847,8	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11155716	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12662622	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs2880661	0.98[ASN][1000 genomes]
rs3734729	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3734730	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4870392	0.96[ASN][1000 genomes]
rs4870404	0.96[ASN][1000 genomes]
rs6557376	0.80[CHB][hapmap]
rs6936990	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs7741317	0.87[CEU][hapmap]
rs7749005	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs9322253	0.80[CHB][hapmap]
rs9322254	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9322255	0.88[ASN][1000 genomes]
rs9371362	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9371830	0.80[CHB][hapmap]
rs9371831	0.85[CEU][hapmap];0.80[CHB][hapmap]
rs9371833	0.80[CHB][hapmap]
rs9371834	0.80[CHB][hapmap]
rs9371844	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs9371852	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9383732	0.80[CHB][hapmap]
rs9383739	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9383740	0.96[ASN][1000 genomes]
rs9383747	0.98[ASN][1000 genomes]
rs9384259	0.80[CHB][hapmap]
rs9384261	0.80[CHB][hapmap]
rs9384262	0.80[CHB][hapmap]
rs9384264	0.87[CEU][hapmap];0.80[CHB][hapmap];0.81[JPT][hapmap]
rs9384270	0.93[ASN][1000 genomes]
rs9384299	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9397206	0.85[CEU][hapmap]
rs9397229	0.89[ASN][1000 genomes]
rs9397234	0.98[ASN][1000 genomes]
rs9397764	0.96[ASN][1000 genomes]
rs9397777	0.90[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs9397780	0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830843	chr6:150517411-150691173	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150569600-150576800	Weak transcription	Esophagus	oesophagus
2	chr6:150569800-150577000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:150570400-150577600	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr6:150571000-150576800	Enhancers	HMEC	breast
5	chr6:150571000-150579200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr6:150571400-150579400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:150571600-150576800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:150571600-150577200	Enhancers	Fetal Heart	heart
9	chr6:150572400-150576800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:150572600-150577000	Weak transcription	Lung	lung
11	chr6:150573600-150577000	Weak transcription	Gastric	stomach
12	chr6:150574200-150577000	Weak transcription	Hela-S3	cervix
13	chr6:150574200-150578800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr6:150574400-150576800	Enhancers	HSMMtube	muscle
15	chr6:150574400-150577400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr6:150574800-150576800	Weak transcription	Left Ventricle	heart
17	chr6:150574800-150577200	Weak transcription	NH-A	brain
18	chr6:150574800-150590800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:150575000-150576800	Weak transcription	Fetal Muscle Leg	muscle
20	chr6:150575000-150576800	Weak transcription	Right Atrium	heart
21	chr6:150575600-150576800	Weak transcription	Psoas Muscle	Psoas
22	chr6:150575600-150579000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:150575800-150576800	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr6:150576200-150576800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:150576200-150577800	Flanking Active TSS	NHEK	skin
26	chr6:150576400-150576800	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr6:150576400-150577000	Bivalent Enhancer	HSMM	muscle
28	chr6:150576400-150577400	Enhancers	Right Ventricle	heart
29	chr6:150576400-150579600	Weak transcription	K562	blood
30	chr6:150576400-150580400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:150576600-150577000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:150576600-150577600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr6:150576600-150577600	Enhancers	Placenta	Placenta
34	chr6:150576600-150578600	Weak transcription	Osteobl	bone

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