Variant report

Variant	rs9429089
Chromosome Location	chr1:46501599-46501600
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:46495760..46499404-chr1:46501029..46505549,6	K562	blood:
2	chr1:46501344..46502975-chr1:46637425..46639494,2	MCF-7	breast:
3	chr1:46500117..46505906-chr1:46642218..46647717,9	K562	blood:
4	chr1:46501490..46502010-chr1:46688870..46689796,2	K562	blood:
5	chr1:46500927..46503041-chr1:46594569..46596961,2	MCF-7	breast:
6	chr1:46501151..46503873-chr1:46689820..46692443,2	MCF-7	breast:
7	chr1:46501329..46503162-chr1:46604855..46606915,2	K562	blood:
8	chr1:46501155..46503229-chr1:46711979..46714694,2	K562	blood:
9	chr1:46501521..46503992-chr1:46598593..46600286,2	K562	blood:
10	chr1:46501257..46504423-chr1:46594631..46599309,4	MCF-7	breast:
11	chr1:46500166..46508245-chr1:46642169..46649663,17	K562	blood:
12	chr1:46499846..46501821-chr1:46501905..46505233,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000227857	Chromatin interaction
ENSG00000085999	Chromatin interaction
ENSG00000117461	Chromatin interaction
ENSG00000117472	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10749862	1.00[AFR][1000 genomes]
rs11211231	1.00[AFR][1000 genomes]
rs4279789	1.00[AFR][1000 genomes]
rs4409589	1.00[AFR][1000 genomes]
rs4420030	1.00[AFR][1000 genomes]
rs4660899	1.00[AFR][1000 genomes]
rs4660908	1.00[AFR][1000 genomes]
rs6688097	1.00[AFR][1000 genomes]
rs7549798	1.00[AFR][1000 genomes]
rs9429087	0.83[AFR][1000 genomes]
rs9919273	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
2	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
3	nsv871928	chr1:46024701-46609736	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	123 gene(s)	inside rSNPs	diseases
4	nsv1003517	chr1:46244432-46609881	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv1009527	chr1:46286329-46520127	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1009474	chr1:46320433-46557734	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1005189	chr1:46335186-46949309	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
8	nsv534946	chr1:46335186-46949309	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
9	esv2761743	chr1:46339858-47026743	Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv829737	chr1:46352900-46506424	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv1000557	chr1:46383876-46591182	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
12	esv2754420	chr1:46461580-46635180	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	esv1795204	chr1:46466373-46504466	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
14	esv1829371	chr1:46466373-46504466	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
15	nsv1007750	chr1:46471293-46552564	Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
16	nsv1006747	chr1:46476089-46655484	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
17	nsv534947	chr1:46476089-46655484	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
18	nsv515934	chr1:46493460-46502836	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46473600-46502600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr1:46474400-46502600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr1:46475600-46525000	Weak transcription	Fetal Kidney	kidney
4	chr1:46476200-46502600	Weak transcription	Stomach Mucosa	stomach
5	chr1:46476600-46515800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr1:46484800-46502000	Strong transcription	Fetal Intestine Small	intestine
7	chr1:46485000-46502000	Strong transcription	Fetal Stomach	stomach
8	chr1:46485800-46503000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:46486800-46502400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:46487000-46502000	Strong transcription	Fetal Muscle Trunk	muscle
11	chr1:46487200-46501600	Strong transcription	Fetal Brain Female	brain
12	chr1:46487600-46501600	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:46488800-46501800	Strong transcription	Fetal Muscle Leg	muscle
14	chr1:46488800-46505200	Weak transcription	HMEC	breast
15	chr1:46490200-46524600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:46490600-46505000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr1:46490600-46525200	Weak transcription	NH-A	brain
18	chr1:46492000-46507600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:46492600-46502000	Strong transcription	Fetal Intestine Large	intestine
20	chr1:46492800-46502000	Strong transcription	Brain Germinal Matrix	brain
21	chr1:46493000-46501600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:46493000-46502400	Strong transcription	Cortex derived primary cultured neurospheres	brain
23	chr1:46493000-46509200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:46493200-46501800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:46493200-46502200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:46493400-46502000	Strong transcription	Placenta	Placenta
27	chr1:46493600-46501800	Strong transcription	Stomach Smooth Muscle	stomach
28	chr1:46493600-46502800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr1:46494000-46501800	Strong transcription	Spleen	Spleen
30	chr1:46494000-46502000	Strong transcription	Thymus	Thymus
31	chr1:46494200-46505200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:46494400-46502200	Strong transcription	Esophagus	oesophagus
33	chr1:46495800-46505000	Weak transcription	HUVEC	blood vessel
34	chr1:46496000-46508600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:46496200-46505400	Weak transcription	Small Intestine	intestine
36	chr1:46497200-46501600	Strong transcription	Left Ventricle	heart
37	chr1:46497200-46502400	Weak transcription	Right Atrium	heart
38	chr1:46497400-46506600	Weak transcription	Fetal Thymus	thymus
39	chr1:46497600-46502200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr1:46497600-46506800	Weak transcription	Primary B cells from cord blood	blood
41	chr1:46497800-46502600	Weak transcription	Brain Angular Gyrus	brain
42	chr1:46498000-46528200	Weak transcription	Osteobl	bone
43	chr1:46498200-46501600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr1:46498200-46502600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr1:46498200-46528400	Weak transcription	Colon Smooth Muscle	Colon
46	chr1:46498400-46501600	Strong transcription	Right Ventricle	heart
47	chr1:46498400-46502200	Weak transcription	HSMMtube	muscle
48	chr1:46498400-46502400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr1:46498400-46502600	Weak transcription	Brain Cingulate Gyrus	brain
50	chr1:46498400-46502600	Weak transcription	Brain Hippocampus Middle	brain

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