Variant report

Variant	rs56215298
Chromosome Location	chr15:73498371-73498372
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:73493630..73495142-chr15:73497332..73499715,2	K562	blood:
2	chr15:73463612..73466544-chr15:73496830..73498478,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs1023924	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1038137	0.84[ASN][1000 genomes]
rs10467948	0.80[ASN][1000 genomes]
rs11072403	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11072406	0.96[ASN][1000 genomes]
rs1116880	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634084	0.83[EUR][1000 genomes]
rs11634147	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12050658	0.87[EUR][1000 genomes]
rs12050685	0.87[EUR][1000 genomes]
rs12050774	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12902768	0.95[ASN][1000 genomes]
rs1479338	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1479339	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1479340	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1564345	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17762516	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17762600	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17829830	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17829836	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17829957	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1812835	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1871385	0.89[ASN][1000 genomes]
rs2127277	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2169951	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2415147	0.88[ASN][1000 genomes]
rs2415148	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2899784	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34013312	0.83[ASN][1000 genomes]
rs35450875	0.88[ASN][1000 genomes]
rs3736510	0.88[ASN][1000 genomes]
rs3784801	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3985587	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3985588	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4545783	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4777598	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55646651	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55836604	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55853625	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55868723	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55925663	0.82[ASN][1000 genomes]
rs55939596	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56269104	0.81[ASN][1000 genomes]
rs56348595	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56377702	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58060856	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59066156	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62015460	0.94[EUR][1000 genomes]
rs62015484	0.86[EUR][1000 genomes]
rs62015499	0.85[EUR][1000 genomes]
rs62015500	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62015502	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62015504	0.83[EUR][1000 genomes]
rs62016806	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62016809	0.80[ASN][1000 genomes]
rs62016811	0.81[EUR][1000 genomes]
rs62016814	0.80[ASN][1000 genomes]
rs62016849	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62016851	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62016853	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62016854	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62016856	0.92[EUR][1000 genomes]
rs62016857	0.87[EUR][1000 genomes]
rs62016858	0.92[EUR][1000 genomes]
rs62017774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62017776	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7169083	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7172021	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7172396	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs74022925	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74025262	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs747872	0.89[ASN][1000 genomes]
rs747873	0.89[ASN][1000 genomes]
rs7497992	0.87[EUR][1000 genomes]
rs8024575	0.96[ASN][1000 genomes]
rs8035925	0.83[ASN][1000 genomes]
rs8042700	0.96[ASN][1000 genomes]
rs9806496	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9972347	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525462	chr15:73349633-73563495	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv904340	chr15:73375847-73524629	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv904342	chr15:73390790-73524629	Enhancers ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv904343	chr15:73396760-73775043	Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73455200-73500400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:73472200-73504600	Weak transcription	Left Ventricle	heart
3	chr15:73474200-73523800	Weak transcription	Esophagus	oesophagus
4	chr15:73474600-73500600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:73475200-73517600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:73476200-73506200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:73477600-73503800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr15:73477800-73499200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr15:73482000-73504600	Weak transcription	Aorta	Aorta
10	chr15:73483600-73505800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr15:73487200-73519800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr15:73489000-73502200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:73492200-73518000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr15:73492400-73516200	Weak transcription	Fetal Brain Male	brain
15	chr15:73493400-73504400	Weak transcription	Fetal Intestine Small	intestine
16	chr15:73493400-73528600	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr15:73495000-73499000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr15:73495600-73502600	Weak transcription	Small Intestine	intestine
19	chr15:73495600-73504600	Weak transcription	Psoas Muscle	Psoas
20	chr15:73495800-73507400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr15:73496200-73506200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:73496400-73500000	Strong transcription	Fetal Intestine Large	intestine
23	chr15:73496800-73507400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr15:73497000-73499600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr15:73497000-73517600	Weak transcription	Brain Hippocampus Middle	brain
26	chr15:73497400-73504400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:73497400-73505800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:73497800-73541800	Weak transcription	Fetal Kidney	kidney
29	chr15:73498000-73501000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr15:73498000-73502200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr15:73498000-73502400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr15:73498000-73505200	Weak transcription	Ovary	ovary
33	chr15:73498000-73515200	Weak transcription	Fetal Lung	lung
34	chr15:73498200-73505600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links