Variant report

Variant	rs4653645
Chromosome Location	chr1:224058745-224058746
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	chr1:224048345..224051041-chr1:224057644..224060087,2	K562	blood:
2	chr1:224032494..224036254-chr1:224057433..224064259,8	K562	blood:

Variant related genes	Relation type
ENSG00000143514	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10799327	0.95[EUR][1000 genomes]
rs10915882	0.95[EUR][1000 genomes]
rs10915892	0.95[EUR][1000 genomes]
rs10915917	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10915946	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10915948	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10915950	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10915956	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1124943	0.91[EUR][1000 genomes]
rs11801971	0.96[EUR][1000 genomes]
rs11802505	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11806886	0.88[EUR][1000 genomes]
rs12021759	0.98[EUR][1000 genomes]
rs12021785	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12024535	0.99[EUR][1000 genomes]
rs12026098	0.99[EUR][1000 genomes]
rs12026835	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12027539	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12030094	0.93[EUR][1000 genomes]
rs12032261	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12038299	0.82[EUR][1000 genomes]
rs12040633	0.84[EUR][1000 genomes]
rs12042503	0.84[EUR][1000 genomes]
rs12045776	0.95[EUR][1000 genomes]
rs12730520	0.95[EUR][1000 genomes]
rs12731254	0.93[EUR][1000 genomes]
rs12745879	0.83[EUR][1000 genomes]
rs12747926	0.87[EUR][1000 genomes]
rs17559050	0.95[EUR][1000 genomes]
rs2014441	0.95[EUR][1000 genomes]
rs2126389	0.98[EUR][1000 genomes]
rs2169459	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34124959	0.99[EUR][1000 genomes]
rs35634773	0.95[EUR][1000 genomes]
rs3856161	0.95[EUR][1000 genomes]
rs4653644	0.97[EUR][1000 genomes]
rs56280097	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59866505	0.84[EUR][1000 genomes]
rs61823593	0.95[EUR][1000 genomes]
rs61823594	0.95[EUR][1000 genomes]
rs61823595	0.95[EUR][1000 genomes]
rs61824002	0.82[EUR][1000 genomes]
rs6658752	0.97[EUR][1000 genomes]
rs6677956	0.93[EUR][1000 genomes]
rs6678103	0.84[EUR][1000 genomes]
rs6688246	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6693324	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6702843	0.98[EUR][1000 genomes]
rs723999	0.98[EUR][1000 genomes]
rs745697	0.95[EUR][1000 genomes]
rs7516059	0.98[EUR][1000 genomes]
rs7519753	0.97[EUR][1000 genomes]
rs7533614	0.95[EUR][1000 genomes]
rs7554109	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9728094	0.81[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	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1008800	chr1:223904653-224061032	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	esv2757772	chr1:223935220-224363163	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2759000	chr1:223935220-224363163	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	esv1793921	chr1:224048131-224105965	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv945313	chr1:224048561-224060636	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv1817834	chr1:224052449-224095114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1803377	chr1:224052449-224108920	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4653645	RP11-504P24.3	cis	Nerve Tibial	GTEx

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224057800-224059400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:224057800-224059400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:224057800-224060600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:224057800-224062000	Enhancers	K562	blood
5	chr1:224058000-224059400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:224058000-224059400	Enhancers	Placenta	Placenta
7	chr1:224058200-224058800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:224058200-224059200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr1:224058200-224059200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:224058200-224059200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:224058400-224058800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:224058400-224058800	Enhancers	Dnd41	blood
13	chr1:224058400-224059000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr1:224058400-224059000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr1:224058400-224059000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr1:224058400-224059200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr1:224058400-224059200	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr1:224058400-224059200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:224058400-224059400	Bivalent/Poised TSS	HepG2	liver
20	chr1:224058600-224058800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:224058600-224058800	Enhancers	Placenta Amnion	Placenta Amnion
22	chr1:224058600-224059000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:224058600-224059000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
24	chr1:224058600-224059000	Enhancers	Primary B cells from cord blood	blood
25	chr1:224058600-224059000	Active TSS	Pancreas	Pancrea
26	chr1:224058600-224059200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr1:224058600-224059400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links