Variant report

Variant	rs4923840
Chromosome Location	chr15:40088314-40088315
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:40080849..40083373-chr15:40085760..40088536,2	K562	blood:
2	chr15:40086220..40089106-chr15:40229459..40231210,2	K562	blood:

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

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

rs_ID	r²[population]
rs10520147	1.00[ASN][1000 genomes]
rs1073675	1.00[ASN][1000 genomes]
rs16969662	1.00[ASN][1000 genomes]
rs16969663	1.00[ASN][1000 genomes]
rs16969664	1.00[ASN][1000 genomes]
rs16969666	1.00[ASN][1000 genomes]
rs16969672	1.00[ASN][1000 genomes]
rs16969679	1.00[ASN][1000 genomes]
rs16969680	1.00[ASN][1000 genomes]
rs16969688	1.00[ASN][1000 genomes]
rs17717859	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28625134	1.00[ASN][1000 genomes]
rs28626090	1.00[ASN][1000 genomes]
rs55674415	1.00[ASN][1000 genomes]
rs55899942	1.00[ASN][1000 genomes]
rs56862147	1.00[ASN][1000 genomes]
rs58878379	1.00[ASN][1000 genomes]
rs59628570	1.00[ASN][1000 genomes]
rs60613947	1.00[ASN][1000 genomes]
rs7172155	1.00[ASN][1000 genomes]
rs7173948	1.00[ASN][1000 genomes]
rs7181354	1.00[ASN][1000 genomes]
rs7181875	1.00[ASN][1000 genomes]
rs7182423	1.00[ASN][1000 genomes]
rs72727047	1.00[ASN][1000 genomes]
rs72727060	1.00[ASN][1000 genomes]
rs74008680	1.00[ASN][1000 genomes]
rs8041266	1.00[ASN][1000 genomes]
rs937961	1.00[ASN][1000 genomes]
rs937962	1.00[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	nsv832978	chr15:39899759-40094881	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv530816	chr15:40003136-40586792	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv832979	chr15:40041928-40218407	Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:40076000-40103200	Weak transcription	Right Atrium	heart
2	chr15:40076600-40090200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr15:40076600-40092600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:40077200-40092600	Weak transcription	NHEK	skin
5	chr15:40077200-40093200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr15:40077600-40094600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:40080000-40095600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:40080400-40095000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr15:40081000-40092400	Weak transcription	HSMMtube	muscle
10	chr15:40081200-40089600	Weak transcription	HSMM	muscle
11	chr15:40081200-40090400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:40081200-40092200	Weak transcription	NH-A	brain
13	chr15:40081200-40093400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:40081400-40088600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr15:40081400-40092800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr15:40081400-40100200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:40082400-40090400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr15:40082600-40091800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:40082600-40092000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr15:40083600-40089600	Weak transcription	Aorta	Aorta
21	chr15:40084800-40090600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:40085400-40089600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:40085400-40089800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:40085400-40090400	Weak transcription	Adipose Nuclei	Adipose
25	chr15:40085400-40091600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr15:40085400-40092200	Weak transcription	NHDF-Ad	bronchial
27	chr15:40086000-40088800	Weak transcription	Osteobl	bone
28	chr15:40086000-40090200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:40086000-40090400	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr15:40086000-40095600	Weak transcription	HUVEC	blood vessel
31	chr15:40086400-40090400	Weak transcription	NHLF	lung
32	chr15:40086400-40093600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr15:40086600-40089600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:40086600-40089600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:40087800-40088600	Enhancers	H1 Cell Line	embryonic stem cell
36	chr15:40087800-40090200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr15:40088000-40095000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links