Variant report

Variant	rs360087
Chromosome Location	chr1:226056913-226056914
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:226056196..226058584-chr1:226111610..226114032,2	MCF-7	breast:
2	chr1:226054269..226057848-chr1:226069122..226072255,3	K562	blood:
3	chr1:226038808..226040415-chr1:226055569..226057247,2	K562	blood:
4	chr1:226054613..226057085-chr1:226059205..226061185,3	K562	blood:
5	chr1:226055732..226058409-chr1:226119393..226121117,2	K562	blood:
6	chr1:226054600..226056714-chr1:226056820..226058465,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196187	Chromatin interaction
ENSG00000143811	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs12061043	0.90[ASN][1000 genomes]
rs12071072	0.90[ASN][1000 genomes]
rs12071104	0.90[ASN][1000 genomes]
rs12074209	0.90[ASN][1000 genomes]
rs12074247	0.90[ASN][1000 genomes]
rs12075664	1.00[ASN][1000 genomes]
rs184853	1.00[ASW][hapmap];1.00[YRI][hapmap]
rs2271544	0.97[ASN][1000 genomes]
rs2292556	1.00[ASN][1000 genomes]
rs2292559	0.99[ASN][1000 genomes]
rs2292560	1.00[ASN][1000 genomes]
rs2292561	1.00[ASN][1000 genomes]
rs2292568	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs28384447	0.91[ASN][1000 genomes]
rs360080	0.84[AFR][1000 genomes]
rs360084	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs360085	1.00[ASW][hapmap];1.00[LWK][hapmap];0.96[MKK][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs360086	0.92[AFR][1000 genomes]
rs360089	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs360090	0.84[AFR][1000 genomes]
rs3738050	0.99[ASN][1000 genomes]
rs3738051	1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[ASN][1000 genomes]
rs3753663	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs3753668	0.81[GIH][hapmap]
rs3766935	1.00[ASN][1000 genomes]
rs3766936	1.00[ASN][1000 genomes]
rs3766937	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.92[JPT][hapmap];1.00[ASN][1000 genomes]
rs3806258	0.91[ASN][1000 genomes]
rs41310561	0.91[ASN][1000 genomes]
rs4149227	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4149228	1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs4149230	0.99[ASN][1000 genomes]
rs45467394	0.99[ASN][1000 genomes]
rs56231004	0.87[ASN][1000 genomes]
rs56301120	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56325807	1.00[ASN][1000 genomes]
rs57095220	1.00[ASN][1000 genomes]
rs57932384	0.99[ASN][1000 genomes]
rs59728172	1.00[ASN][1000 genomes]
rs60943392	0.99[ASN][1000 genomes]
rs61033712	0.99[ASN][1000 genomes]
rs61227102	1.00[ASN][1000 genomes]
rs61295362	1.00[ASN][1000 genomes]
rs717759	0.82[AFR][1000 genomes]
rs74150536	1.00[ASN][1000 genomes]
rs805179	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1795046	chr1:225874059-226091150	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv1834932	chr1:225874059-226091150	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	esv1834948	chr1:225874059-226214882	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv524126	chr1:225973777-226210653	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv873231	chr1:226019653-226134471	Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	esv2762223	chr1:226025175-226201716	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv520628	chr1:226026406-226093362	Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226026800-226061600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:226033800-226067400	Strong transcription	H9 Cell Line	embryonic stem cell
3	chr1:226034000-226063000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:226034200-226062800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:226036600-226064600	Weak transcription	Fetal Heart	heart
6	chr1:226036800-226058600	Weak transcription	Brain Germinal Matrix	brain
7	chr1:226036800-226066600	Weak transcription	Fetal Brain Male	brain
8	chr1:226037600-226060600	Strong transcription	Placenta	Placenta
9	chr1:226037800-226065200	Weak transcription	Right Atrium	heart
10	chr1:226038400-226059600	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:226038800-226065800	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr1:226039000-226063200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:226039200-226064600	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr1:226039600-226059800	Strong transcription	Skeletal Muscle Male	skeletal muscle
15	chr1:226039600-226062200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:226039600-226063000	Strong transcription	Duodenum Smooth Muscle	Duodenum
17	chr1:226041400-226064600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:226044400-226062800	Strong transcription	Duodenum Mucosa	Duodenum
19	chr1:226044600-226065800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:226045000-226060800	Strong transcription	Liver	Liver
21	chr1:226046200-226057200	Strong transcription	K562	blood
22	chr1:226046200-226063000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:226046800-226057200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:226046800-226059400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr1:226047000-226057200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:226047600-226063200	Strong transcription	Left Ventricle	heart
27	chr1:226048000-226060000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:226048400-226062600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr1:226050200-226068600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:226051800-226066400	Genic enhancers	Primary T cells fromperipheralblood	blood
31	chr1:226052200-226059800	Strong transcription	NHLF	lung
32	chr1:226052600-226057000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr1:226052600-226057200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
34	chr1:226052600-226064200	Strong transcription	Right Ventricle	heart
35	chr1:226052800-226057000	Strong transcription	Colonic Mucosa	Colon
36	chr1:226052800-226057800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr1:226052800-226059400	Strong transcription	HepG2	liver
38	chr1:226052800-226059800	Strong transcription	Colon Smooth Muscle	Colon
39	chr1:226052800-226060000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr1:226053000-226057000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr1:226053000-226057200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr1:226053000-226057200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:226053000-226057200	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr1:226053000-226057200	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr1:226053000-226057400	Strong transcription	Aorta	Aorta
46	chr1:226053000-226059600	Strong transcription	Esophagus	oesophagus
47	chr1:226053200-226059600	Strong transcription	Rectal Smooth Muscle	rectum
48	chr1:226053200-226062000	Strong transcription	Fetal Intestine Large	intestine
49	chr1:226053200-226063600	Strong transcription	Ovary	ovary
50	chr1:226053400-226057000	Genic enhancers	Primary T cells from cord blood	blood

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