Variant report

Variant	rs4849007
Chromosome Location	chr2:112856165-112856166
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:112854247..112856297-chr2:112866128..112867747,2	K562	blood:
2	chr2:112848431..112851658-chr2:112853970..112857290,3	MCF-7	breast:
3	chr2:112854980..112857744-chr2:112857881..112859739,2	K562	blood:

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10165845	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10175143	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10178449	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10182333	0.87[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.83[MKK][hapmap];0.93[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1045300	0.92[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.85[GIH][hapmap];0.90[JPT][hapmap];0.91[MEX][hapmap];0.89[TSI][hapmap];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10779884	0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10864898	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.90[JPT][hapmap];0.83[MEX][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11675437	0.81[EUR][1000 genomes]
rs12618637	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4241121	0.87[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4257409	0.87[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.93[YRI][hapmap];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4613287	0.85[CHD][hapmap];1.00[JPT][hapmap]
rs4848993	0.82[ASW][hapmap];0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.83[MKK][hapmap];0.86[TSI][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4849044	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6707397	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6730057	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6731563	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6737707	0.86[CHD][hapmap]
rs7577442	0.97[ASN][1000 genomes]
rs7580507	1.00[ASN][1000 genomes]
rs7581849	0.90[JPT][hapmap]
rs7591702	0.82[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.89[MKK][hapmap];0.93[TSI][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7595574	0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9308669	1.00[ASW][hapmap];0.89[CEU][hapmap];0.86[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9653401	0.93[ASW][hapmap];0.92[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.96[LWK][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9653422	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874863	chr2:112591224-113157344	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv874864	chr2:112617280-113104142	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv874865	chr2:112623098-113049274	Enhancers Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	nsv1013218	chr2:112645633-112908416	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	esv3333591	chr2:112669320-112892618	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv1002027	chr2:112679182-112861534	Weak transcription Genic enhancers Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv1014787	chr2:112679182-112908416	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv535893	chr2:112679182-112908416	Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4849007	POLR1B	cis	parietal	SCAN

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112814200-112859800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr2:112816600-112866200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr2:112816800-112871400	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr2:112822800-112876800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr2:112832000-112866000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr2:112834600-112871200	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr2:112835800-112883200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:112836000-112874400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:112838200-112866200	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr2:112838200-112866400	Strong transcription	Rectal Mucosa Donor 31	rectum
11	chr2:112838600-112858200	Strong transcription	Fetal Intestine Large	intestine
12	chr2:112843000-112869400	Weak transcription	Fetal Heart	heart
13	chr2:112845000-112856200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr2:112845400-112856200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr2:112845400-112875200	Weak transcription	Right Ventricle	heart
16	chr2:112845600-112856400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:112845600-112865400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:112845800-112856200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr2:112846000-112856200	Weak transcription	Fetal Brain Female	brain
20	chr2:112846000-112856400	Weak transcription	Brain Germinal Matrix	brain
21	chr2:112846200-112865800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr2:112847800-112856200	Weak transcription	Colon Smooth Muscle	Colon
23	chr2:112847800-112856400	Weak transcription	Brain Angular Gyrus	brain
24	chr2:112847800-112867200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr2:112848000-112856200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr2:112848200-112856200	Weak transcription	Brain Anterior Caudate	brain
27	chr2:112848200-112856400	Weak transcription	Aorta	Aorta
28	chr2:112848400-112856400	Weak transcription	A549	lung
29	chr2:112850200-112856200	Weak transcription	HMEC	breast
30	chr2:112850400-112856200	Weak transcription	Lung	lung
31	chr2:112850400-112856400	Weak transcription	Spleen	Spleen
32	chr2:112851000-112866400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:112851000-112867600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr2:112851200-112881600	Weak transcription	Stomach Mucosa	stomach
35	chr2:112851600-112856400	Weak transcription	NHLF	lung
36	chr2:112852000-112871200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr2:112852800-112858000	Strong transcription	Fetal Muscle Leg	muscle
38	chr2:112852800-112858000	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr2:112852800-112866000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr2:112853200-112858000	Strong transcription	HepG2	liver
41	chr2:112853200-112864600	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr2:112853200-112865600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr2:112853200-112866000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr2:112853200-112866200	Strong transcription	Liver	Liver
45	chr2:112853200-112866600	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr2:112853200-112871200	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr2:112853200-112871200	Strong transcription	Duodenum Mucosa	Duodenum
48	chr2:112853400-112857000	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr2:112853400-112857200	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr2:112853400-112857400	Strong transcription	Fetal Stomach	stomach

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