Variant report

Variant	rs10135836
Chromosome Location	chr14:71518596-71518597
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10132278	0.91[AFR][1000 genomes]
rs10132657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10133398	0.91[AFR][1000 genomes]
rs10135131	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10136593	0.91[AFR][1000 genomes]
rs10137584	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10138314	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10139870	0.91[AFR][1000 genomes]
rs10142606	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10144526	0.91[AFR][1000 genomes]
rs10144763	1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs10145450	0.87[AFR][1000 genomes]
rs10146200	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10147846	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10148594	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10150003	0.91[AFR][1000 genomes]
rs10150435	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10150628	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10151876	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10438024	0.92[AFR][1000 genomes]
rs12385922	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28401611	0.91[AFR][1000 genomes]
rs28444741	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28448751	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28453676	0.91[AFR][1000 genomes]
rs28552942	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28556569	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28617460	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28623756	1.00[AMR][1000 genomes]
rs28659887	0.91[AFR][1000 genomes]
rs28771184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28793135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28800773	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28807752	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28824190	0.91[AFR][1000 genomes]
rs28842770	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28867199	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28896292	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1035416	chr14:71212882-71623271	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv542126	chr14:71212882-71623271	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1037839	chr14:71263886-71625114	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv542127	chr14:71263886-71625114	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv1039769	chr14:71310954-71525720	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv542128	chr14:71310954-71525720	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
10	nsv565043	chr14:71395604-71625112	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
12	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71495800-71546200	Weak transcription	Stomach Mucosa	stomach
2	chr14:71497000-71554200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:71499600-71540800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:71503000-71526400	Weak transcription	Gastric	stomach
5	chr14:71503400-71524400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr14:71503400-71526600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:71503400-71527200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr14:71503600-71519400	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:71506600-71520800	Strong transcription	Liver	Liver
10	chr14:71506800-71520400	Weak transcription	HSMMtube	muscle
11	chr14:71507000-71531600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr14:71508000-71524200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:71508000-71530800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr14:71508400-71524200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr14:71510000-71526800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:71510000-71531600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr14:71510000-71531800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr14:71510000-71532600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr14:71510200-71526400	Weak transcription	Right Ventricle	heart
20	chr14:71510200-71532000	Strong transcription	Primary B cells from peripheral blood	blood
21	chr14:71510200-71538200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr14:71510400-71530000	Strong transcription	Dnd41	blood
23	chr14:71510800-71531200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:71511000-71530600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr14:71511200-71526600	Weak transcription	Fetal Brain Male	brain
26	chr14:71511200-71526600	Weak transcription	Fetal Heart	heart
27	chr14:71511400-71519000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr14:71511400-71519400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr14:71511400-71524200	Weak transcription	Brain Substantia Nigra	brain
30	chr14:71511400-71527000	Weak transcription	Brain Angular Gyrus	brain
31	chr14:71511600-71518600	Weak transcription	Fetal Stomach	stomach
32	chr14:71511600-71518800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:71511600-71518800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr14:71511600-71519600	Weak transcription	Hela-S3	cervix
35	chr14:71511600-71521400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr14:71511600-71524200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr14:71511600-71524200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:71511600-71524200	Weak transcription	Brain Cingulate Gyrus	brain
39	chr14:71511600-71524400	Weak transcription	Brain Germinal Matrix	brain
40	chr14:71511600-71524800	Weak transcription	Aorta	Aorta
41	chr14:71511600-71526400	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:71511600-71526400	Weak transcription	Esophagus	oesophagus
43	chr14:71511600-71526400	Weak transcription	Small Intestine	intestine
44	chr14:71511600-71526400	Weak transcription	Spleen	Spleen
45	chr14:71511600-71527600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:71511600-71527800	Weak transcription	Colonic Mucosa	Colon
47	chr14:71511600-71540800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr14:71511600-71541000	Weak transcription	Pancreas	Pancrea
49	chr14:71511800-71527800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr14:71512200-71519000	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links