Variant report

Variant	rs6735771
Chromosome Location	chr2:152273503-152273504
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:152272396-152274996	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:152265797..152267957-chr2:152272152..152274379,2	MCF-7	breast:
2	chr2:152143066..152145503-chr2:152272183..152273824,2	MCF-7	breast:

Variant related genes	Relation type
RIF1	TF binding region
ENSG00000080345	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10173699	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10175134	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10206635	0.85[EUR][1000 genomes]
rs1047957	0.86[AFR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10490521	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10497081	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10497082	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1061305	0.80[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs11675385	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12616688	0.83[EUR][1000 genomes]
rs12616740	0.85[EUR][1000 genomes]
rs12618981	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12994320	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13403719	0.91[ASN][1000 genomes]
rs13425170	0.81[ASN][1000 genomes]
rs13555	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17193268	0.86[EUR][1000 genomes]
rs17270233	0.81[ASN][1000 genomes]
rs17806204	0.86[EUR][1000 genomes]
rs2045025	0.87[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2288193	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2342911	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2432942	0.88[ASN][1000 genomes]
rs2432943	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2432945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432946	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2432953	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2432954	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2432956	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2432957	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2444256	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2444264	0.88[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2444267	0.84[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs4335940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4467261	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4500942	0.81[EUR][1000 genomes]
rs4592848	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4664438	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5024580	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6718372	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6718653	0.89[ASN][1000 genomes]
rs72860233	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7587301	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7608474	0.88[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	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1012891	chr2:152019809-152306897	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats 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 miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv1013484	chr2:152028515-152473913	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv535983	chr2:152028515-152473913	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv1012139	chr2:152114637-152389516	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv1011339	chr2:152114637-152392940	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv999748	chr2:152135514-152476396	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv834418	chr2:152205803-152385516	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6735771	RIF1	Cis_1M	lymphoblastoid	RTeQTL
rs6735771	RIF1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152267400-152276200	Weak transcription	Spleen	Spleen
2	chr2:152267600-152274800	Weak transcription	Thymus	Thymus
3	chr2:152267600-152276600	Weak transcription	Psoas Muscle	Psoas
4	chr2:152267600-152277400	Weak transcription	HSMMtube	muscle
5	chr2:152267600-152287000	Weak transcription	Colonic Mucosa	Colon
6	chr2:152267600-152379400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr2:152267800-152275600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr2:152267800-152276000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr2:152267800-152276200	Weak transcription	Aorta	Aorta
10	chr2:152267800-152276200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:152267800-152340400	Weak transcription	Stomach Mucosa	stomach
12	chr2:152268000-152274000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr2:152268000-152342800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:152268200-152276200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr2:152268200-152276200	Weak transcription	Fetal Brain Male	brain
16	chr2:152268200-152276800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr2:152268200-152278200	Strong transcription	HSMM	muscle
18	chr2:152268200-152278600	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr2:152268200-152279200	Weak transcription	Small Intestine	intestine
20	chr2:152268200-152279800	Strong transcription	Primary B cells from peripheral blood	blood
21	chr2:152268200-152282000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:152268200-152284200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:152268200-152303000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr2:152268200-152319400	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr2:152268200-152320800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr2:152268200-152327800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr2:152268200-152328400	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr2:152268200-152328600	Strong transcription	Fetal Thymus	thymus
29	chr2:152268400-152274200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr2:152268400-152274600	Strong transcription	Placenta	Placenta
31	chr2:152268400-152274600	Strong transcription	NHLF	lung
32	chr2:152268400-152280600	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr2:152268400-152282600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:152268400-152282600	Strong transcription	Osteobl	bone
35	chr2:152268400-152283200	Strong transcription	Duodenum Mucosa	Duodenum
36	chr2:152268400-152298200	Strong transcription	Fetal Intestine Large	intestine
37	chr2:152268400-152327800	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr2:152268600-152276200	Weak transcription	Fetal Heart	heart
39	chr2:152268600-152276800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr2:152268600-152278600	Strong transcription	Muscle Satellite Cultured Cells	--
41	chr2:152268600-152280400	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:152268600-152281800	Strong transcription	HUVEC	blood vessel
43	chr2:152268600-152283600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:152268600-152300200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr2:152268600-152319200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr2:152268600-152326800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
47	chr2:152268600-152327800	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr2:152268600-152334400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr2:152268600-152342600	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr2:152268800-152274800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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