Variant report

Variant	rs28846396
Chromosome Location	chr4:121760861-121760862
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10003374	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10026006	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11933936	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11941156	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1511310	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1588522	1.00[EUR][1000 genomes]
rs17051242	0.91[EUR][1000 genomes]
rs17051245	1.00[EUR][1000 genomes]
rs17051255	0.83[AMR][1000 genomes]
rs28362092	1.00[EUR][1000 genomes]
rs28545211	0.89[AMR][1000 genomes]
rs56998648	0.81[AMR][1000 genomes]
rs58187778	0.89[AMR][1000 genomes]
rs58779616	0.91[EUR][1000 genomes]
rs59281550	0.91[EUR][1000 genomes]
rs60371752	1.00[EUR][1000 genomes]
rs6818794	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6826221	0.96[EUR][1000 genomes]
rs6826227	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73845482	0.87[EUR][1000 genomes]
rs73845483	0.83[EUR][1000 genomes]
rs73845486	0.91[EUR][1000 genomes]
rs9992625	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9996180	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9998810	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879852	chr4:121108734-121768496	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv998094	chr4:121504565-122374203	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv461634	chr4:121623057-121765527	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv595334	chr4:121623057-121765527	Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1013704	chr4:121657648-121791601	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121729600-121770400	Weak transcription	Stomach Smooth Muscle	stomach
2	chr4:121743800-121765400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:121750400-121768400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr4:121751600-121762000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr4:121753400-121762600	Weak transcription	Osteobl	bone
6	chr4:121755800-121774600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr4:121756000-121762200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:121756000-121762200	Weak transcription	Fetal Lung	lung
9	chr4:121756600-121763600	Weak transcription	Esophagus	oesophagus
10	chr4:121756800-121779800	Weak transcription	Aorta	Aorta
11	chr4:121758200-121765000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:121758200-121770400	Weak transcription	HSMM	muscle
13	chr4:121758200-121774600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr4:121758400-121761800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:121758800-121763000	Weak transcription	Colon Smooth Muscle	Colon
16	chr4:121759400-121762800	Weak transcription	NHLF	lung
17	chr4:121759600-121761600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr4:121759600-121762200	Strong transcription	Fetal Stomach	stomach
19	chr4:121759600-121775400	Weak transcription	Gastric	stomach
20	chr4:121759800-121761000	Strong transcription	Fetal Muscle Trunk	muscle
21	chr4:121759800-121761400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:121759800-121762000	Strong transcription	Fetal Intestine Small	intestine
23	chr4:121760000-121761200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr4:121760000-121761200	Genic enhancers	Right Ventricle	heart
25	chr4:121760000-121761200	ZNF genes & repeats	Spleen	Spleen
26	chr4:121760000-121761400	Strong transcription	Fetal Intestine Large	intestine
27	chr4:121760000-121761800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr4:121760000-121762000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:121760000-121762400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr4:121760000-121765400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr4:121760200-121761200	Strong transcription	Fetal Muscle Leg	muscle
32	chr4:121760400-121761400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:121760400-121762000	Enhancers	Fetal Heart	heart
34	chr4:121760400-121775800	Weak transcription	Lung	lung
35	chr4:121760600-121761800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:121760600-121765000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:121760600-121765600	Weak transcription	Ovary	ovary
38	chr4:121760800-121761000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:121760800-121761200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:121760800-121761200	Enhancers	Pancreas	Pancrea
41	chr4:121760800-121761400	Enhancers	Left Ventricle	heart
42	chr4:121760800-121761800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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