Variant report

Variant	rs2857982
Chromosome Location	chr4:3358665-3358666
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:3356602..3361196-chr4:3388835..3391854,4	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10155132	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10937924	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13104157	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13150241	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2236052	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2239725	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2748447	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2749778	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2749780	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2749781	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2749782	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2749783	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3129308	0.82[EUR][1000 genomes]
rs3129327	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3129328	0.81[EUR][1000 genomes]
rs3129334	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3135145	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3135146	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60181496	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60208975	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6819202	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7435601	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs881816	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs881817	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs910568	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes];0.81[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	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	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
4	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
5	nsv878462	chr4:3311548-3505448	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	nsv1007847	chr4:3317904-3527357	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	nsv537001	chr4:3317904-3527357	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3334000-3370600	Weak transcription	Right Atrium	heart
2	chr4:3344400-3362400	Weak transcription	HSMMtube	muscle
3	chr4:3344400-3367600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:3346600-3363800	Weak transcription	Fetal Brain Female	brain
5	chr4:3346600-3364600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr4:3347400-3360800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:3347400-3364800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:3348200-3367400	Weak transcription	Fetal Heart	heart
9	chr4:3348400-3360600	Weak transcription	HSMM	muscle
10	chr4:3348400-3367600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:3350400-3364000	Weak transcription	Spleen	Spleen
12	chr4:3350800-3364200	Weak transcription	Pancreas	Pancrea
13	chr4:3350800-3367600	Weak transcription	Ovary	ovary
14	chr4:3351000-3358800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:3352400-3363200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr4:3354200-3363800	Weak transcription	Brain Germinal Matrix	brain
17	chr4:3354600-3364600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:3354800-3368200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr4:3355000-3367800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr4:3355200-3368400	Weak transcription	Fetal Intestine Small	intestine
21	chr4:3356000-3361600	Weak transcription	Lung	lung
22	chr4:3356000-3365000	Weak transcription	Fetal Stomach	stomach
23	chr4:3356200-3359000	Weak transcription	Primary T cells from cord blood	blood
24	chr4:3356400-3360000	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr4:3356600-3364200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:3356600-3368000	Weak transcription	Fetal Intestine Large	intestine
27	chr4:3357400-3359400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr4:3357400-3360000	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr4:3357600-3359800	Weak transcription	Liver	Liver
30	chr4:3357600-3359800	Weak transcription	HUVEC	blood vessel
31	chr4:3357600-3360000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr4:3357600-3361200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr4:3358000-3358800	Strong transcription	Fetal Lung	lung
34	chr4:3358200-3367800	Weak transcription	HepG2	liver
35	chr4:3358400-3358800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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