Variant report

Variant	rs9491951
Chromosome Location	chr6:128775139-128775140
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr6:128775082-128775218	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:128773075..128776512-chr6:128778434..128782134,3	MCF-7	breast:
2	chr6:128769204..128770819-chr6:128773712..128776222,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182404	TF binding region
ENSG00000182404	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12332836	1.00[EUR][1000 genomes]
rs12717181	0.82[EUR][1000 genomes]
rs13196790	1.00[CEU][hapmap]
rs13216847	1.00[CEU][hapmap]
rs1341597	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1341598	1.00[TSI][hapmap]
rs1341599	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1891150	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs28531950	1.00[EUR][1000 genomes]
rs61143917	0.82[EUR][1000 genomes]
rs71568904	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7775722	1.00[EUR][1000 genomes]
rs9482890	1.00[TSI][hapmap]
rs9491950	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9491964	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs9491970	1.00[CEU][hapmap]
rs9491971	1.00[CEU][hapmap]
rs9491972	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 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
6	nsv830800	chr6:128710631-128878435	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128740800-128777000	Weak transcription	Fetal Intestine Small	intestine
2	chr6:128753200-128777000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:128756400-128776600	Weak transcription	Fetal Intestine Large	intestine
4	chr6:128759800-128786800	Weak transcription	Left Ventricle	heart
5	chr6:128761400-128775600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:128761400-128778000	Weak transcription	Small Intestine	intestine
7	chr6:128763600-128775200	Weak transcription	Psoas Muscle	Psoas
8	chr6:128765600-128775200	Weak transcription	Pancreas	Pancrea
9	chr6:128765800-128777000	Weak transcription	HepG2	liver
10	chr6:128767800-128785200	Weak transcription	NHEK	skin
11	chr6:128768200-128785000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:128770000-128776400	Weak transcription	Brain Hippocampus Middle	brain
13	chr6:128770000-128776600	Weak transcription	Fetal Heart	heart
14	chr6:128770400-128777000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:128773400-128795200	Weak transcription	HSMMtube	muscle
16	chr6:128774200-128775400	Enhancers	Brain Substantia Nigra	brain
17	chr6:128774600-128775400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr6:128774600-128786800	Weak transcription	Right Ventricle	heart
19	chr6:128774800-128775200	Enhancers	Ovary	ovary
20	chr6:128774800-128777000	Weak transcription	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links