Variant report

Variant	rs17055714
Chromosome Location	chr6:128649123-128649124
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:128647886..128650591-chr6:128840783..128842601,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000152894	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17053277	0.83[YRI][hapmap];0.95[AFR][1000 genomes]
rs17055730	0.94[AFR][1000 genomes]
rs17055772	0.83[YRI][hapmap];0.94[AFR][1000 genomes]
rs57056055	0.90[AFR][1000 genomes]
rs60098660	1.00[AMR][1000 genomes]
rs61459271	1.00[AMR][1000 genomes]
rs6913849	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7755117	0.89[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	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:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128632000-128650600	Weak transcription	Psoas Muscle	Psoas
2	chr6:128632000-128650800	Weak transcription	Right Ventricle	heart
3	chr6:128632000-128658000	Weak transcription	Ovary	ovary
4	chr6:128632200-128665200	Weak transcription	Gastric	stomach
5	chr6:128635600-128672000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:128635800-128654200	Weak transcription	Liver	Liver
7	chr6:128639000-128660600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:128639000-128660800	Weak transcription	Small Intestine	intestine
9	chr6:128639800-128659000	Weak transcription	Fetal Stomach	stomach
10	chr6:128640000-128653200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:128640000-128660600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:128641400-128661400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:128641800-128657600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr6:128642000-128657000	Weak transcription	HepG2	liver
15	chr6:128643400-128659000	Weak transcription	NHEK	skin
16	chr6:128643400-128660600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:128643600-128653400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:128645000-128654800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:128646200-128657000	Weak transcription	Brain Anterior Caudate	brain
20	chr6:128648200-128650600	Weak transcription	Rectal Smooth Muscle	rectum
21	chr6:128648600-128649400	ZNF genes & repeats	Fetal Intestine Large	intestine
22	chr6:128648600-128649400	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr6:128648800-128649400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:128648800-128654400	Weak transcription	A549	lung
25	chr6:128649000-128649200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:128649000-128649200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr6:128649000-128649200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:128649000-128649200	ZNF genes & repeats	Left Ventricle	heart
29	chr6:128649000-128649200	Enhancers	Pancreas	Pancrea
30	chr6:128649000-128649200	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr6:128649000-128649400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:128649000-128649400	ZNF genes & repeats	Primary T cells from cord blood	blood
33	chr6:128649000-128649400	ZNF genes & repeats	Aorta	Aorta
34	chr6:128649000-128649400	ZNF genes & repeats	Fetal Lung	lung
35	chr6:128649000-128649400	ZNF genes & repeats	Fetal Thymus	thymus
36	chr6:128649000-128649400	ZNF genes & repeats	HSMM	muscle
37	chr6:128649000-128649400	ZNF genes & repeats	HSMMtube	muscle
38	chr6:128649000-128649600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr6:128649000-128649600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet

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