Variant report

Variant	rs12911794
Chromosome Location	chr15:99654880-99654881
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	chr15:99653397..99656049-chr15:99657808..99660823,3	MCF-7	breast:
2	chr15:99652267..99657709-chr15:99661798..99664247,5	MCF-7	breast:

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12904860	0.81[AFR][1000 genomes]
rs1670237	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs1670246	0.81[ASN][1000 genomes]
rs1810091	0.91[CHB][hapmap];0.84[JPT][hapmap];0.87[ASN][1000 genomes]
rs1965866	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1965867	0.82[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2242076	0.91[CHB][hapmap];0.85[ASN][1000 genomes]
rs2663105	0.81[ASN][1000 genomes]
rs4965445	0.80[JPT][hapmap]
rs56009713	0.90[ASN][1000 genomes]
rs7162579	0.89[ASN][1000 genomes]
rs7164548	0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs8032817	0.91[CHB][hapmap];0.85[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs8037159	0.90[ASN][1000 genomes]
rs8041213	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs906760	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531079	chr15:98907913-99878547	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv1039575	chr15:98982045-99924685	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	nsv869529	chr15:99416774-99903351	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv533375	chr15:99443534-99696221	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1050982	chr15:99450004-99725825	Enhancers Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv530685	chr15:99452377-99713365	Bivalent/Poised TSS Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv1055008	chr15:99477144-100019861	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv1045124	chr15:99504843-99847210	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv1038870	chr15:99510479-99768374	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv904543	chr15:99513231-99991506	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
11	nsv533926	chr15:99519820-99997114	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
12	nsv915926	chr15:99519820-100138705	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
13	nsv904544	chr15:99524865-99655744	Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1051782	chr15:99621061-99792967	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv916822	chr15:99621061-99878564	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv949203	chr15:99621061-99932797	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
17	nsv817289	chr15:99621061-100138705	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
18	nsv431411	chr15:99621061-100143999	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
19	nsv570716	chr15:99629901-99916332	Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:99646400-99663200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr15:99646600-99662200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr15:99646800-99663600	Weak transcription	Ovary	ovary
4	chr15:99646800-99663600	Weak transcription	Spleen	Spleen
5	chr15:99647000-99662000	Weak transcription	HUVEC	blood vessel
6	chr15:99647000-99663200	Weak transcription	HSMM	muscle
7	chr15:99647600-99672400	Weak transcription	Esophagus	oesophagus
8	chr15:99648000-99658000	Weak transcription	Fetal Brain Female	brain
9	chr15:99648000-99663200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr15:99648200-99656200	Weak transcription	Hela-S3	cervix
11	chr15:99648200-99663000	Weak transcription	NHDF-Ad	bronchial
12	chr15:99648200-99663200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr15:99648600-99655400	Transcr. at gene 5' and 3'	Stomach Smooth Muscle	stomach
14	chr15:99649000-99663800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:99649200-99658400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:99650400-99663400	Weak transcription	HSMMtube	muscle
17	chr15:99650600-99663400	Weak transcription	Colonic Mucosa	Colon
18	chr15:99650800-99662000	Strong transcription	A549	lung
19	chr15:99651200-99659600	Weak transcription	Liver	Liver
20	chr15:99651200-99663200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr15:99651200-99663800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:99651400-99663200	Weak transcription	NH-A	brain
23	chr15:99651800-99655000	Weak transcription	Aorta	Aorta
24	chr15:99651800-99658600	Weak transcription	Fetal Heart	heart
25	chr15:99651800-99662800	Weak transcription	Primary T cells from cord blood	blood
26	chr15:99651800-99663200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:99651800-99663200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:99652000-99669800	Weak transcription	Thymus	Thymus
29	chr15:99652200-99663600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:99652400-99663200	Weak transcription	Fetal Intestine Large	intestine
31	chr15:99653400-99657400	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:99653400-99660600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:99653600-99656600	Strong transcription	Brain Cingulate Gyrus	brain
34	chr15:99653800-99655000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr15:99653800-99655000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr15:99653800-99655200	Genic enhancers	Rectal Smooth Muscle	rectum
37	chr15:99653800-99655400	Enhancers	Psoas Muscle	Psoas
38	chr15:99653800-99655400	Enhancers	Right Atrium	heart
39	chr15:99653800-99655600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:99653800-99656600	Strong transcription	Adipose Nuclei	Adipose
41	chr15:99653800-99657000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:99653800-99658000	Strong transcription	Brain Hippocampus Middle	brain
43	chr15:99653800-99658200	Strong transcription	Fetal Muscle Trunk	muscle
44	chr15:99653800-99659800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr15:99654000-99655000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:99654000-99655200	Strong transcription	Brain Angular Gyrus	brain
47	chr15:99654000-99655400	Strong transcription	Brain Substantia Nigra	brain
48	chr15:99654000-99655400	Strong transcription	NHLF	lung
49	chr15:99654000-99655600	Strong transcription	Fetal Intestine Small	intestine
50	chr15:99654000-99656600	Strong transcription	Fetal Stomach	stomach

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