Variant report

Variant	rs11935128
Chromosome Location	chr4:3015617-3015618
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	chr4:3014192..3017069-chr4:3021177..3023631,3	MCF-7	breast:

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11947255	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34854780	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35248769	1.00[AMR][1000 genomes]
rs35492582	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35970030	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41264719	1.00[AMR][1000 genomes]
rs56733257	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57294059	1.00[AMR][1000 genomes]
rs57447128	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57779369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57812385	1.00[AMR][1000 genomes]
rs58036497	1.00[AMR][1000 genomes]
rs58202885	1.00[AMR][1000 genomes]
rs58376060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58643792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58782413	1.00[AMR][1000 genomes]
rs58966302	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58998372	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6812433	0.81[AFR][1000 genomes]
rs6813002	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6813023	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6826590	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6832730	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6845680	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73073038	1.00[AMR][1000 genomes]
rs73073070	1.00[AMR][1000 genomes]
rs73074803	1.00[AMR][1000 genomes]
rs73084106	0.90[AFR][1000 genomes]
rs73084115	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73086132	1.00[AMR][1000 genomes]
rs73088165	1.00[AMR][1000 genomes]
rs7696059	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 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	nsv461163	chr4:2906285-3234980	Enhancers Strong transcription Flanking Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
4	nsv593437	chr4:2906285-3234980	Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv1008436	chr4:2947160-3031195	Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv536998	chr4:2947160-3031195	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv593438	chr4:2948456-3030097	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv1008527	chr4:2957814-3019042	Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv878453	chr4:2963222-3021383	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1008781	chr4:2964080-3019042	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv870141	chr4:2982146-3021346	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv1013440	chr4:2993130-3053503	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	esv2439437	chr4:3015613-3015620	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv2055103	chr4:3015613-3015621	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2979600-3025000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:2983600-3032000	Weak transcription	Fetal Brain Female	brain
3	chr4:2991400-3024600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr4:3003800-3024600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:3005000-3018600	Weak transcription	Left Ventricle	heart
6	chr4:3005800-3038600	Weak transcription	Right Ventricle	heart
7	chr4:3007000-3020600	Weak transcription	Brain Germinal Matrix	brain
8	chr4:3007600-3024600	Weak transcription	Brain Angular Gyrus	brain
9	chr4:3011800-3039600	Weak transcription	Right Atrium	heart
10	chr4:3012800-3024800	Weak transcription	Aorta	Aorta
11	chr4:3013200-3022600	Weak transcription	Ovary	ovary
12	chr4:3013400-3022200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:3013600-3018600	Weak transcription	HSMMtube	muscle
14	chr4:3013800-3018600	Weak transcription	HSMM	muscle
15	chr4:3013800-3022600	Weak transcription	Adipose Nuclei	Adipose
16	chr4:3014600-3026200	Weak transcription	Fetal Brain Male	brain
17	chr4:3014800-3015800	Enhancers	Stomach Mucosa	stomach
18	chr4:3014800-3025000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr4:3015000-3016000	Enhancers	Liver	Liver
20	chr4:3015200-3015800	Enhancers	Fetal Intestine Small	intestine
21	chr4:3015200-3016000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:3015200-3016200	Enhancers	Pancreas	Pancrea
23	chr4:3015200-3016200	Flanking Active TSS	GM12878-XiMat	blood
24	chr4:3015400-3015800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:3015400-3015800	Bivalent Enhancer	HepG2	liver
26	chr4:3015400-3016000	Enhancers	Fetal Heart	heart
27	chr4:3015400-3016000	Enhancers	K562	blood
28	chr4:3015600-3015800	Flanking Active TSS	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links