Variant report

Variant	rs17055563
Chromosome Location	chr6:128609514-128609515
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17055598	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17055628	0.85[YRI][hapmap]
rs17055630	0.83[YRI][hapmap]
rs17055694	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17055702	1.00[AMR][1000 genomes]
rs17055737	1.00[AMR][1000 genomes]
rs17055770	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs2039754	1.00[AMR][1000 genomes]
rs9491936	1.00[AMR][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	nsv1033443	chr6:128306654-128899203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv538440	chr6:128306654-128899203	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886649	chr6:128399657-128808054	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
4	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128585200-128617600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:128593000-128631600	Weak transcription	Left Ventricle	heart
3	chr6:128596800-128623600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:128597800-128625000	Weak transcription	HSMM	muscle
5	chr6:128598200-128613800	Weak transcription	HUVEC	blood vessel
6	chr6:128598600-128621200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:128598800-128612400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:128602400-128632400	Weak transcription	Pancreas	Pancrea
9	chr6:128603000-128617200	Weak transcription	Fetal Intestine Small	intestine
10	chr6:128603000-128642800	Weak transcription	Fetal Intestine Large	intestine
11	chr6:128604400-128630600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:128604400-128633200	Weak transcription	Fetal Thymus	thymus
13	chr6:128604600-128612600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr6:128605600-128616600	Weak transcription	Ovary	ovary
15	chr6:128605800-128612200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr6:128605800-128627400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:128605800-128631200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:128606200-128630600	Weak transcription	Fetal Heart	heart
19	chr6:128606400-128616600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:128607400-128611400	Weak transcription	Stomach Smooth Muscle	stomach
21	chr6:128609000-128609600	Enhancers	Fetal Lung	lung
22	chr6:128609000-128646000	Weak transcription	NH-A	brain

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