Variant report

Variant	rs11964758
Chromosome Location	chr6:15418953-15418954
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:15418815..15421161-chr6:15421182..15423587,2	MCF-7	breast:
2	chr6:15417534..15419132-chr6:15421621..15423962,2	K562	blood:
3	chr6:15417100..15419181-chr6:15441212..15443490,2	K562	blood:
4	chr6:15324221..15325970-chr6:15417466..15419567,2	K562	blood:

Variant related genes	Relation type
ENSG00000201519	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10484354	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11961516	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11961748	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11961827	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11963285	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11965505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11969359	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16876316	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16876327	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16876361	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35438327	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35801290	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60535196	1.00[AFR][1000 genomes]
rs6905116	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365205	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365227	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365229	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73365234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73367315	1.00[AMR][1000 genomes]
rs7743283	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7757154	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7769123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027010	chr6:15201803-15425629	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong 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	27 gene(s)	inside rSNPs	diseases
2	nsv538140	chr6:15217899-15547127	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1030558	chr6:15234675-15449137	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv538141	chr6:15234675-15509163	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv949448	chr6:15279490-15449441	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1025512	chr6:15291551-15452395	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv538143	chr6:15291551-15452395	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1019927	chr6:15351240-15419257	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv538145	chr6:15351240-15419257	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15401200-15426200	Weak transcription	Pancreas	Pancrea
2	chr6:15403000-15422000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr6:15404600-15420800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:15404600-15421200	Weak transcription	Spleen	Spleen
5	chr6:15404800-15427600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:15404800-15429000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr6:15405600-15422000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:15405800-15421200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:15409200-15426200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr6:15410600-15422000	Weak transcription	Gastric	stomach
11	chr6:15412200-15421600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr6:15413000-15420800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr6:15413600-15421200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr6:15414200-15421000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:15414200-15421000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr6:15414200-15421200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr6:15414200-15422000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr6:15414200-15422000	Weak transcription	Right Ventricle	heart
19	chr6:15414200-15427200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr6:15414200-15427400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr6:15414200-15429200	Weak transcription	HSMM	muscle
22	chr6:15414400-15420000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr6:15414600-15419600	Weak transcription	Fetal Kidney	kidney
24	chr6:15414600-15420800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:15414600-15427800	Weak transcription	Fetal Brain Male	brain
26	chr6:15414800-15419000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr6:15414800-15419600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:15415000-15419000	Weak transcription	Fetal Lung	lung
29	chr6:15415000-15419600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:15415000-15419600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:15415000-15421200	Weak transcription	Psoas Muscle	Psoas
32	chr6:15415000-15422200	Weak transcription	Brain Hippocampus Middle	brain
33	chr6:15415400-15420400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
34	chr6:15415600-15423400	Weak transcription	Right Atrium	heart
35	chr6:15415800-15421000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:15416200-15420400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:15416400-15420000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chr6:15416400-15420400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:15416800-15419000	ZNF genes & repeats	Fetal Thymus	thymus
40	chr6:15417000-15419000	Strong transcription	Primary B cells from cord blood	blood
41	chr6:15417000-15419000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:15417000-15419000	Enhancers	HMEC	breast
43	chr6:15417000-15419000	Enhancers	NHEK	skin
44	chr6:15417000-15420400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:15417000-15420400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
46	chr6:15417000-15420400	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:15417000-15420400	ZNF genes & repeats	Dnd41	blood
48	chr6:15417000-15420400	ZNF genes & repeats	K562	blood
49	chr6:15417000-15420600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
50	chr6:15417000-15420800	ZNF genes & repeats	GM12878-XiMat	blood

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