Variant report

Variant	rs4421433
Chromosome Location	chr9:27152339-27152340
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10511803	1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10967734	0.84[EUR][1000 genomes]
rs12337860	0.83[EUR][1000 genomes]
rs12340500	0.83[EUR][1000 genomes]
rs12343345	0.83[EUR][1000 genomes]
rs12350086	0.83[EUR][1000 genomes]
rs12352474	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17694796	0.83[EUR][1000 genomes]
rs17695026	1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17756599	0.83[EUR][1000 genomes]
rs17756667	0.83[EUR][1000 genomes]
rs17756685	0.83[EUR][1000 genomes]
rs2027124	1.00[JPT][hapmap]
rs4601425	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs62542752	0.81[EUR][1000 genomes]
rs62542753	0.81[EUR][1000 genomes]
rs62542755	0.83[EUR][1000 genomes]
rs62542757	0.83[EUR][1000 genomes]
rs62542758	0.83[EUR][1000 genomes]
rs62544592	0.83[EUR][1000 genomes]
rs62544599	0.83[EUR][1000 genomes]
rs62544600	0.83[EUR][1000 genomes]
rs62544602	0.84[EUR][1000 genomes]
rs62544604	0.84[EUR][1000 genomes]
rs62544652	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7854048	0.84[EUR][1000 genomes]
rs7856747	1.00[CHB][hapmap];0.84[ASN][1000 genomes]

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	nsv892862	chr9:26956663-27190655	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016733	chr9:27073650-27264576	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1022313	chr9:27083369-27250505	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1017802	chr9:27088160-27262682	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1019104	chr9:27088160-27358206	Enhancers Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv892863	chr9:27138898-27170934	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27147800-27155000	Weak transcription	Aorta	Aorta
2	chr9:27149400-27152400	Enhancers	Fetal Stomach	stomach
3	chr9:27149600-27152400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr9:27149600-27152400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr9:27149600-27152400	Enhancers	Rectal Smooth Muscle	rectum
6	chr9:27149600-27152600	Enhancers	Colon Smooth Muscle	Colon
7	chr9:27149600-27154600	Enhancers	HUVEC	blood vessel
8	chr9:27149600-27155400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:27150000-27152400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:27150200-27152400	Enhancers	Fetal Lung	lung
11	chr9:27150200-27152600	Enhancers	Fetal Heart	heart
12	chr9:27150200-27152800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:27150400-27152400	Enhancers	NHLF	lung
14	chr9:27150400-27152600	Enhancers	Muscle Satellite Cultured Cells	--
15	chr9:27150600-27152600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr9:27150600-27152600	Enhancers	HSMM	muscle
17	chr9:27150800-27152400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr9:27150800-27152400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr9:27150800-27152600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr9:27150800-27152600	Enhancers	HMEC	breast
21	chr9:27150800-27152600	Enhancers	Osteobl	bone
22	chr9:27150800-27153000	Enhancers	NHEK	skin
23	chr9:27150800-27153200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:27150800-27158000	Weak transcription	Spleen	Spleen
25	chr9:27151000-27152600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr9:27151000-27153200	Enhancers	HSMMtube	muscle
27	chr9:27151000-27154600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr9:27151000-27154800	Weak transcription	Placenta	Placenta
29	chr9:27151000-27155800	Enhancers	Placenta Amnion	Placenta Amnion
30	chr9:27151000-27158000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr9:27151000-27172800	Weak transcription	Left Ventricle	heart
32	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:27151200-27164800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr9:27151400-27152400	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr9:27151400-27152400	Enhancers	Hela-S3	cervix
36	chr9:27151400-27152600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:27151400-27152600	Enhancers	NH-A	brain
38	chr9:27151400-27154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:27151600-27152400	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr9:27151800-27152400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr9:27151800-27154200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:27151800-27154600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr9:27151800-27158000	Weak transcription	Lung	lung
44	chr9:27151800-27165000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr9:27152000-27152600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:27152000-27152800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr9:27152000-27155000	Weak transcription	Ovary	ovary
48	chr9:27152000-27174600	Weak transcription	Fetal Muscle Leg	muscle
49	chr9:27152200-27152400	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr9:27152200-27165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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