Variant report

Variant	rs10155548
Chromosome Location	chr5:126880558-126880559
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:126880553-126880560	ProgFib	skin:	n/a	n/a
2	POLR2A	chr5:126880072-126880606	H1-hESC	embryonic stem cell:	n/a	n/a

Variant related genes	Relation type
PRRC1	TF binding region

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10043977	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10063277	1.00[AMR][1000 genomes]
rs10063666	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10155578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10452551	1.00[AMR][1000 genomes]
rs10478768	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13361500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13436184	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13436211	1.00[AFR][1000 genomes]
rs13436719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28439085	1.00[AMR][1000 genomes]
rs28514390	1.00[AMR][1000 genomes]
rs28535011	1.00[AMR][1000 genomes]
rs58086571	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61631930	1.00[AMR][1000 genomes]
rs73331301	1.00[AMR][1000 genomes]
rs73333106	1.00[AMR][1000 genomes]
rs73333162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73335012	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73335024	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73335031	1.00[AMR][1000 genomes]
rs73335039	1.00[AMR][1000 genomes]
rs73335045	1.00[AMR][1000 genomes]
rs73783903	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73786118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327441	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327444	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9327445	1.00[AMR][1000 genomes]
rs9327446	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1019821	chr5:126658200-126934917	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537894	chr5:126658200-126934917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv830478	chr5:126721368-126937408	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv830479	chr5:126849254-127053121	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:126855400-126883200	Weak transcription	Stomach Mucosa	stomach
2	chr5:126860600-126889400	Weak transcription	Esophagus	oesophagus
3	chr5:126870600-126898000	Weak transcription	Colon Smooth Muscle	Colon
4	chr5:126871000-126892800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr5:126871200-126883600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr5:126871200-126889400	Weak transcription	Aorta	Aorta
7	chr5:126871200-126889400	Weak transcription	Gastric	stomach
8	chr5:126871200-126889400	Weak transcription	Pancreas	Pancrea
9	chr5:126871200-126889400	Weak transcription	Spleen	Spleen
10	chr5:126871200-126896800	Weak transcription	Colonic Mucosa	Colon
11	chr5:126871400-126887600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr5:126871400-126891600	Weak transcription	Right Ventricle	heart
13	chr5:126871600-126887400	Weak transcription	Brain Angular Gyrus	brain
14	chr5:126871600-126888000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr5:126871600-126889000	Weak transcription	Small Intestine	intestine
16	chr5:126871800-126901400	Weak transcription	Brain Substantia Nigra	brain
17	chr5:126875200-126886400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr5:126875200-126887400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr5:126875400-126883400	Weak transcription	HMEC	breast
20	chr5:126875600-126887400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:126875600-126889000	Weak transcription	NHEK	skin
22	chr5:126875800-126883000	Weak transcription	HepG2	liver
23	chr5:126875800-126887400	Weak transcription	Brain Hippocampus Middle	brain
24	chr5:126875800-126887400	Weak transcription	Fetal Kidney	kidney
25	chr5:126875800-126887400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr5:126875800-126889600	Weak transcription	Psoas Muscle	Psoas
27	chr5:126876000-126881600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr5:126876000-126885600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr5:126876000-126886200	Weak transcription	Brain Anterior Caudate	brain
30	chr5:126876000-126891400	Weak transcription	Fetal Heart	heart
31	chr5:126876000-126898000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:126876200-126881600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:126876200-126884800	Weak transcription	NHLF	lung
34	chr5:126876200-126887400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:126876400-126881400	Weak transcription	Primary B cells from peripheral blood	blood
36	chr5:126876400-126881400	Weak transcription	HSMM	muscle
37	chr5:126876400-126881600	Weak transcription	NH-A	brain
38	chr5:126876400-126881600	Weak transcription	Osteobl	bone
39	chr5:126876400-126881800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr5:126876400-126882000	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr5:126876400-126883400	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr5:126876400-126883400	Weak transcription	A549	lung
43	chr5:126876400-126883400	Weak transcription	Hela-S3	cervix
44	chr5:126876400-126883400	Weak transcription	HSMMtube	muscle
45	chr5:126876400-126883400	Weak transcription	HUVEC	blood vessel
46	chr5:126876400-126883600	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr5:126876400-126883800	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr5:126876400-126884000	Weak transcription	Primary B cells from cord blood	blood
49	chr5:126876400-126885200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr5:126876400-126885200	Weak transcription	Fetal Lung	lung

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