Variant report

Variant	rs253365
Chromosome Location	chr5:16797415-16797416
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs153409	0.85[CEU][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap];0.81[AMR][1000 genomes]
rs185236	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs250349	0.83[EUR][1000 genomes]
rs250353	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs250356	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs253359	0.89[CEU][hapmap];0.82[CHB][hapmap];0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs253363	0.98[EUR][1000 genomes]
rs253366	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs253367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs253370	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28297	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[GIH][hapmap];0.98[TSI][hapmap];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs33401	0.96[CEU][hapmap];0.83[TSI][hapmap];0.84[EUR][1000 genomes]
rs33402	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs33405	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs385552	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs40020	0.96[CEU][hapmap];0.83[TSI][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs451009	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs496033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6888120	0.81[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025225	chr5:16714512-17234866	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	esv3529928	chr5:16748426-16856563	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS 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 miRNA target site	2 gene(s)	inside rSNPs	diseases
3	esv3529929	chr5:16748426-16856563	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv1030550	chr5:16748966-16872084	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1015247	chr5:16748966-17133274	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
6	nsv597309	chr5:16791857-16837862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16764600-16807400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr5:16778800-16800000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:16783400-16810000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:16784600-16809200	Weak transcription	Ovary	ovary
5	chr5:16785800-16804200	Weak transcription	HSMM	muscle
6	chr5:16788600-16799800	Weak transcription	Pancreas	Pancrea
7	chr5:16789400-16809200	Weak transcription	NHLF	lung
8	chr5:16791800-16800600	Weak transcription	Osteobl	bone
9	chr5:16791800-16807000	Weak transcription	Fetal Kidney	kidney
10	chr5:16791800-16807400	Weak transcription	Psoas Muscle	Psoas
11	chr5:16792600-16798800	Weak transcription	Esophagus	oesophagus
12	chr5:16793000-16807600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:16793200-16797600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:16793200-16805400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr5:16793400-16807600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:16795000-16799200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:16795000-16804000	Weak transcription	Lung	lung
18	chr5:16795000-16806800	Weak transcription	Fetal Stomach	stomach
19	chr5:16795000-16807000	Weak transcription	Fetal Lung	lung
20	chr5:16795000-16807400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:16795000-16807400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr5:16795200-16797800	Weak transcription	Fetal Intestine Large	intestine
23	chr5:16795200-16799400	Weak transcription	Fetal Muscle Leg	muscle
24	chr5:16795200-16799800	Weak transcription	Spleen	Spleen
25	chr5:16795200-16804000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:16795200-16804000	Weak transcription	Gastric	stomach
27	chr5:16795200-16806800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr5:16795200-16829800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:16795400-16797800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:16795400-16798000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:16795400-16798000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:16795400-16798200	Weak transcription	Fetal Intestine Small	intestine
33	chr5:16795600-16798000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr5:16796400-16799800	Weak transcription	Fetal Brain Male	brain
35	chr5:16796600-16798400	Enhancers	A549	lung
36	chr5:16796600-16798800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:16796600-16799200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr5:16796800-16798000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:16796800-16798400	Enhancers	NHEK	skin
40	chr5:16797000-16797800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:16797000-16800000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr5:16797000-16804200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr5:16797000-16809200	Weak transcription	NH-A	brain
44	chr5:16797200-16800600	Weak transcription	HUVEC	blood vessel
45	chr5:16797200-16806800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:16797400-16809800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr5:16797400-16817400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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