Variant report

Variant	rs17868327
Chromosome Location	chr2:234600695-234600696
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:234600037-234600944	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:234356284..234357802-chr2:234598772..234601558,2	MCF-7	breast:
2	chr2:234599124..234606471-chr2:234613478..234621007,17	MCF-7	breast:
3	chr2:234473282..234477495-chr2:234598048..234603332,9	MCF-7	breast:
4	chr2:234388753..234400184-chr2:234596527..234603213,35	MCF-7	breast:
5	chr2:234600369..234602177-chr2:234775436..234777156,2	MCF-7	breast:
6	chr2:234393680..234401613-chr2:234597738..234605139,18	MCF-7	breast:
7	chr2:234472037..234477650-chr2:234599067..234602356,8	MCF-7	breast:
8	chr2:234597435..234606028-chr2:234613419..234620116,22	MCF-7	breast:
9	chr2:234387197..234390730-chr2:234600088..234603557,3	MCF-7	breast:
10	chr15:50714595..50716933-chr2:234599004..234601578,2	MCF-7	breast:

No data

Variant related genes	Relation type
UGT1A6	TF binding region
ENSG00000224287	Chromatin interaction
ENSG00000224814	Chromatin interaction
ENSG00000077044	Chromatin interaction
ENSG00000138592	Chromatin interaction
ENSG00000085982	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11892031	1.00[CHD][hapmap]
rs11893247	1.00[CHD][hapmap]
rs17862850	1.00[CEU][hapmap]
rs17862858	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs17863755	1.00[CEU][hapmap]
rs17863777	1.00[CEU][hapmap]
rs17863783	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17863786	1.00[CEU][hapmap]
rs17864687	1.00[CEU][hapmap]
rs17864690	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17868309	1.00[CEU][hapmap]
rs17868315	1.00[CEU][hapmap]
rs17868321	1.00[CEU][hapmap]
rs28900391	0.84[AMR][1000 genomes]
rs28948068	1.00[CEU][hapmap]
rs28948385	1.00[CEU][hapmap]
rs28969701	1.00[CEU][hapmap];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs45554333	1.00[ASN][1000 genomes]
rs6723506	1.00[MEX][hapmap];0.84[AMR][1000 genomes]
rs7569014	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	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv428072	chr2:234393609-234624769	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1010936	chr2:234549011-234640221	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv876016	chr2:234590527-234601669	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234597400-234600800	Enhancers	Rectal Mucosa Donor 29	rectum
2	chr2:234597400-234601000	Enhancers	Hela-S3	cervix
3	chr2:234597800-234608600	Weak transcription	Gastric	stomach
4	chr2:234599200-234601000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr2:234599400-234600800	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr2:234599400-234608000	Weak transcription	HUVEC	blood vessel
7	chr2:234599800-234601000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:234600000-234601000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr2:234600200-234600800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr2:234600200-234601400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:234600200-234601600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:234600200-234602600	Enhancers	A549	lung
13	chr2:234600400-234600800	Flanking Active TSS	HMEC	breast
14	chr2:234600400-234601000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:234600400-234601600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr2:234600400-234601800	Enhancers	Colonic Mucosa	Colon
17	chr2:234600400-234608200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:234600600-234600800	Flanking Active TSS	Stomach Mucosa	stomach
19	chr2:234600600-234601000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:234600600-234601200	Enhancers	Liver	Liver
21	chr2:234600600-234601200	Active TSS	Esophagus	oesophagus
22	chr2:234600600-234601400	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr2:234600600-234602000	Flanking Active TSS	NHEK	skin

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