Variant report

Variant	rs495381
Chromosome Location	chr15:55973398-55973399
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11853621	1.00[EUR][1000 genomes]
rs1344957	1.00[EUR][1000 genomes]
rs16976359	1.00[AMR][1000 genomes]
rs16976473	1.00[AMR][1000 genomes]
rs2196774	1.00[EUR][1000 genomes]
rs2414420	1.00[AMR][1000 genomes]
rs28680405	1.00[EUR][1000 genomes]
rs28702037	1.00[EUR][1000 genomes]
rs2917842	1.00[EUR][1000 genomes]
rs4774219	1.00[EUR][1000 genomes]
rs55974808	1.00[EUR][1000 genomes]
rs562086	1.00[EUR][1000 genomes]
rs58886852	1.00[EUR][1000 genomes]
rs59196369	1.00[AMR][1000 genomes]
rs59998724	1.00[EUR][1000 genomes]
rs60604532	1.00[EUR][1000 genomes]
rs61254561	1.00[EUR][1000 genomes]
rs61729647	1.00[EUR][1000 genomes]
rs61753409	1.00[EUR][1000 genomes]
rs7167185	1.00[EUR][1000 genomes]
rs7167804	1.00[EUR][1000 genomes]
rs7171082	1.00[EUR][1000 genomes]
rs7180984	1.00[EUR][1000 genomes]
rs73413205	1.00[EUR][1000 genomes]
rs74017524	1.00[EUR][1000 genomes]
rs74017548	1.00[AMR][1000 genomes]
rs8025181	1.00[EUR][1000 genomes]
rs8026616	1.00[EUR][1000 genomes]
rs8037279	1.00[EUR][1000 genomes]
rs8042087	1.00[EUR][1000 genomes]
rs9744860	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv948522	chr15:55639867-56032099	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv1049774	chr15:55759573-56044600	Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
7	nsv457158	chr15:55930542-55982257	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv569541	chr15:55930542-55982257	Strong transcription ZNF genes & repeats Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55911800-55977000	Weak transcription	Fetal Intestine Small	intestine
2	chr15:55920800-55987600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:55932600-55987000	Weak transcription	Ovary	ovary
4	chr15:55932800-55973400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:55942800-55974400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:55954000-55975400	Weak transcription	HSMM	muscle
7	chr15:55954000-55977400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr15:55954400-55987000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr15:55954600-55975000	Weak transcription	A549	lung
10	chr15:55955400-55980000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr15:55958200-55977600	Weak transcription	Fetal Muscle Trunk	muscle
12	chr15:55958800-55977400	Weak transcription	Left Ventricle	heart
13	chr15:55959000-55973800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr15:55960400-55977600	Weak transcription	Placenta	Placenta
15	chr15:55960800-55995800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:55962600-55974800	Weak transcription	Fetal Muscle Leg	muscle
17	chr15:55963400-55980200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:55964000-55977200	Weak transcription	HUVEC	blood vessel
19	chr15:55964200-55975600	Weak transcription	Fetal Stomach	stomach
20	chr15:55964800-55977200	Weak transcription	HepG2	liver
21	chr15:55966000-55974400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr15:55969000-55975600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr15:55969000-55976000	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr15:55969000-55976800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:55969000-55987000	Weak transcription	Fetal Lung	lung
26	chr15:55969200-55975600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr15:55969200-55980200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr15:55969200-55986000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr15:55969400-55980200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:55970400-55977800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:55970600-55974200	Weak transcription	Hela-S3	cervix
32	chr15:55970600-55976800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr15:55970800-55977400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:55971200-55976200	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr15:55972000-55986400	Weak transcription	Fetal Intestine Large	intestine
36	chr15:55972400-55973800	Weak transcription	Fetal Kidney	kidney
37	chr15:55972400-55974200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr15:55973000-55973600	Enhancers	Dnd41	blood
39	chr15:55973200-55974200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links