Variant report

Variant	rs60921905
Chromosome Location	chr4:3266128-3266129
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:3265031..3267765-chr4:3268616..3271432,2	K562	blood:
2	chr4:3195952..3197606-chr4:3265003..3267231,2	K562	blood:

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

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

rs_ID	r²[population]
rs41264719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41264741	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57294059	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57346236	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57812385	1.00[AMR][1000 genomes]
rs58782413	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73073038	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73073070	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73074803	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73074829	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73074831	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73074857	1.00[AMR][1000 genomes]
rs73074859	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73074885	1.00[AFR][1000 genomes]
rs73074892	1.00[AMR][1000 genomes]
rs73077119	1.00[AMR][1000 genomes]
rs73077132	0.86[AFR][1000 genomes]
rs73086119	0.86[AFR][1000 genomes]
rs73086132	1.00[AMR][1000 genomes]
rs73088165	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv998290	chr4:3176454-3355758	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv524211	chr4:3215835-3270488	Strong transcription Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv470003	chr4:3215835-3275484	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv878454	chr4:3215835-3305739	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv878455	chr4:3215835-3344891	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv878456	chr4:3215835-3467519	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
9	nsv428106	chr4:3226182-3752322	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv878457	chr4:3231661-3278517	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
11	nsv878458	chr4:3235518-3303976	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
12	nsv878459	chr4:3235518-3310831	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
13	nsv878460	chr4:3260154-3303976	Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
2	chr4:3247600-3268400	Weak transcription	Primary T cells from cord blood	blood
3	chr4:3252400-3271400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:3255800-3271000	Weak transcription	Brain Hippocampus Middle	brain
5	chr4:3257000-3271800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr4:3258400-3271000	Weak transcription	Brain Anterior Caudate	brain
7	chr4:3258400-3271000	Weak transcription	Right Ventricle	heart
8	chr4:3258400-3271000	Weak transcription	Stomach Smooth Muscle	stomach
9	chr4:3258600-3269600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr4:3259200-3269600	Weak transcription	Fetal Intestine Small	intestine
11	chr4:3259200-3270000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr4:3259400-3269400	Weak transcription	Fetal Brain Female	brain
13	chr4:3259600-3269600	Weak transcription	Gastric	stomach
14	chr4:3259600-3269800	Weak transcription	Brain Germinal Matrix	brain
15	chr4:3260000-3270200	Weak transcription	Pancreas	Pancrea
16	chr4:3260000-3270200	Weak transcription	Spleen	Spleen
17	chr4:3260200-3269400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:3260200-3278200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr4:3264200-3273000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:3265000-3269400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:3265200-3269200	Weak transcription	Fetal Stomach	stomach
22	chr4:3265600-3270000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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