Variant report

Variant	rs26748
Chromosome Location	chr5:16676549-16676550
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10060275	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10060411	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11738070	0.93[ASN][1000 genomes]
rs1560087	0.93[ASN][1000 genomes]
rs1560088	0.92[ASN][1000 genomes]
rs2288432	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288433	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288434	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288435	0.96[ASN][1000 genomes]
rs2288436	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2288437	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2303703	0.95[ASN][1000 genomes]
rs2401987	0.95[ASN][1000 genomes]
rs26745	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs26746	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs26749	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs26750	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs26757	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs26758	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs27350	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs27501	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs27553	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs27880	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28056	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28057	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs399833	0.96[ASN][1000 genomes]
rs4702166	0.81[ASN][1000 genomes]
rs6881621	0.93[ASN][1000 genomes]
rs6889243	0.95[ASN][1000 genomes]
rs7735007	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869660	chr5:16651289-16766428	Genic enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv522062	chr5:16670618-16679966	Genic enhancers Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv516145	chr5:16673685-16679966	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16661600-16689400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:16661800-16700000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:16663000-16712400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:16663400-16676600	Strong transcription	A549	lung
5	chr5:16663600-16695400	Strong transcription	Fetal Intestine Small	intestine
6	chr5:16663800-16676600	Strong transcription	Duodenum Mucosa	Duodenum
7	chr5:16663800-16690800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr5:16663800-16694400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:16663800-16698000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:16663800-16702400	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr5:16663800-16713400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr5:16664000-16676800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:16664000-16701000	Strong transcription	Fetal Intestine Large	intestine
14	chr5:16664000-16702000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr5:16664000-16702200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr5:16664000-16702400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr5:16664200-16702200	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:16664600-16690600	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr5:16664800-16677600	Strong transcription	H9 Cell Line	embryonic stem cell
20	chr5:16665600-16676800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr5:16665600-16699200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr5:16666200-16676800	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr5:16666200-16680600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:16667400-16683600	Weak transcription	Liver	Liver
25	chr5:16667600-16676600	Strong transcription	HSMMtube	muscle
26	chr5:16667800-16677400	Strong transcription	Rectal Mucosa Donor 31	rectum
27	chr5:16667800-16680000	Weak transcription	Rectal Smooth Muscle	rectum
28	chr5:16667800-16701000	Weak transcription	Right Ventricle	heart
29	chr5:16670200-16676800	Strong transcription	Fetal Muscle Leg	muscle
30	chr5:16670200-16678000	Weak transcription	Fetal Heart	heart
31	chr5:16670400-16677200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:16670600-16676800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:16670600-16676800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:16670600-16676800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr5:16670600-16676800	Strong transcription	HepG2	liver
36	chr5:16670600-16677400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr5:16670800-16677000	Strong transcription	Lung	lung
38	chr5:16670800-16677200	Strong transcription	NH-A	brain
39	chr5:16670800-16677200	Strong transcription	Osteobl	bone
40	chr5:16670800-16686000	Strong transcription	Fetal Stomach	stomach
41	chr5:16671000-16676600	Strong transcription	NHLF	lung
42	chr5:16671000-16691000	Strong transcription	Fetal Muscle Trunk	muscle
43	chr5:16671200-16676600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr5:16671200-16676600	Strong transcription	Hela-S3	cervix
45	chr5:16671200-16690200	Strong transcription	HUVEC	blood vessel
46	chr5:16671800-16685400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:16672800-16676800	Strong transcription	Ovary	ovary
48	chr5:16673000-16679400	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr5:16673800-16680400	Weak transcription	Fetal Brain Male	brain
50	chr5:16673800-16713400	Weak transcription	Psoas Muscle	Psoas

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links