Variant report

Variant	rs2625196
Chromosome Location	chr5:16826986-16826987
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10045693	1.00[EUR][1000 genomes]
rs149110	1.00[MEX][hapmap]
rs16869070	1.00[TSI][hapmap]
rs253331	1.00[AMR][1000 genomes]
rs253332	1.00[AMR][1000 genomes]
rs253334	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs2560866	1.00[AMR][1000 genomes]
rs2625198	1.00[AMR][1000 genomes]
rs31504	1.00[AMR][1000 genomes]
rs55850620	1.00[EUR][1000 genomes]
rs58996233	1.00[EUR][1000 genomes]
rs59897191	1.00[EUR][1000 genomes]
rs73055131	1.00[EUR][1000 genomes]
rs747058	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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
7	esv2762500	chr5:16815489-16952565	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16795200-16829800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:16804400-16827200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:16812600-16829200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:16813800-16828200	Weak transcription	Fetal Intestine Small	intestine
5	chr5:16814200-16828000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:16818000-16832800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr5:16818000-16846600	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr5:16820000-16841600	Weak transcription	Fetal Kidney	kidney
9	chr5:16820200-16842600	Weak transcription	HMEC	breast
10	chr5:16820400-16827400	Weak transcription	Placenta	Placenta
11	chr5:16820400-16828000	Weak transcription	Gastric	stomach
12	chr5:16820400-16845400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr5:16820600-16838800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:16820600-16845000	Weak transcription	NH-A	brain
15	chr5:16820800-16827200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr5:16820800-16828000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr5:16820800-16829200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr5:16820800-16834000	Weak transcription	Osteobl	bone
19	chr5:16820800-16843000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:16820800-16855200	Weak transcription	HSMM	muscle
21	chr5:16822600-16828000	Weak transcription	A549	lung
22	chr5:16823600-16835800	Weak transcription	HSMMtube	muscle
23	chr5:16823600-16841600	Weak transcription	HUVEC	blood vessel
24	chr5:16825400-16842800	Weak transcription	NHLF	lung
25	chr5:16825600-16827000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:16825800-16828000	Weak transcription	Pancreas	Pancrea
27	chr5:16826000-16827000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:16826000-16828400	Weak transcription	Spleen	Spleen
29	chr5:16826000-16829600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:16826200-16828200	Weak transcription	Lung	lung
31	chr5:16826400-16827000	Active TSS	Brain Anterior Caudate	brain
32	chr5:16826600-16827000	Active TSS	Ovary	ovary
33	chr5:16826600-16827000	Strong transcription	NHEK	skin
34	chr5:16826600-16827200	Active TSS	Brain Angular Gyrus	brain
35	chr5:16826600-16827200	Enhancers	Fetal Stomach	stomach
36	chr5:16826600-16827200	Active TSS	Stomach Smooth Muscle	stomach
37	chr5:16826600-16827200	Flanking Active TSS	NHDF-Ad	bronchial
38	chr5:16826600-16827400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr5:16826600-16827600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr5:16826600-16828000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:16826800-16827000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr5:16826800-16827000	Enhancers	Brain Hippocampus Middle	brain
43	chr5:16826800-16827000	Active TSS	Fetal Brain Female	brain
44	chr5:16826800-16827200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:16826800-16827200	Active TSS	Brain Cingulate Gyrus	brain
46	chr5:16826800-16827200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
47	chr5:16826800-16827200	Flanking Active TSS	Fetal Brain Male	brain
48	chr5:16826800-16827600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:16826800-16829200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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