Variant report

Variant	rs2453045
Chromosome Location	chr1:120504985-120504986
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:120499139..120500697-chr1:120503771..120505843,2	K562	blood:
2	chr1:120501693..120505181-chr1:120522270..120525046,3	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs17024243	1.00[EUR][1000 genomes]
rs17024274	1.00[EUR][1000 genomes]
rs2453043	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453054	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453057	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453060	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2493393	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2493395	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2493397	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2493399	1.00[EUR][1000 genomes]
rs2493409	1.00[ASW][hapmap];1.00[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2641341	1.00[EUR][1000 genomes]
rs2691751	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2793828	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2793924	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34996202	1.00[EUR][1000 genomes]
rs4274109	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59055697	1.00[EUR][1000 genomes]
rs60594933	1.00[EUR][1000 genomes]
rs6673881	1.00[EUR][1000 genomes]
rs6689706	1.00[EUR][1000 genomes]
rs6690032	1.00[EUR][1000 genomes]
rs6697236	1.00[EUR][1000 genomes]
rs74115097	1.00[EUR][1000 genomes]
rs74115360	1.00[EUR][1000 genomes]
rs74115365	1.00[EUR][1000 genomes]
rs7536072	1.00[EUR][1000 genomes]
rs7537153	1.00[EUR][1000 genomes]
rs7537385	1.00[EUR][1000 genomes]
rs7540526	1.00[EUR][1000 genomes]
rs835566	1.00[EUR][1000 genomes]
rs835567	1.00[EUR][1000 genomes]
rs835577	1.00[EUR][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	nsv428201	chr1:120267313-120697156	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS 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	20 gene(s)	inside rSNPs	diseases
2	esv2757750	chr1:120267313-121226013	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	esv2758965	chr1:120267313-121226013	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	esv1816057	chr1:120469050-120697156	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	esv1818054	chr1:120469050-120697156	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic 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	10 gene(s)	inside rSNPs	diseases
6	esv1844863	chr1:120469050-120697156	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active 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 target site	10 gene(s)	inside rSNPs	diseases
7	esv1850218	chr1:120469050-120697156	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
8	nsv427730	chr1:120469050-120697156	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:120468400-120506200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:120468400-120507400	Weak transcription	Right Ventricle	heart
3	chr1:120468600-120532800	Weak transcription	Stomach Mucosa	stomach
4	chr1:120476400-120507400	Weak transcription	Brain Angular Gyrus	brain
5	chr1:120478800-120508800	Weak transcription	A549	lung
6	chr1:120478800-120511000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr1:120479000-120511000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr1:120480400-120507800	Weak transcription	Fetal Brain Female	brain
9	chr1:120480600-120507400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:120484400-120506000	Weak transcription	Gastric	stomach
11	chr1:120484600-120505800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr1:120488800-120510400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr1:120490000-120512400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr1:120490000-120514400	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr1:120490000-120517600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:120490200-120512600	Strong transcription	Primary T cells from cord blood	blood
17	chr1:120490200-120512600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr1:120490200-120521000	Strong transcription	Primary B cells from cord blood	blood
19	chr1:120490400-120512600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr1:120490800-120515000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr1:120491200-120510800	Weak transcription	Brain Germinal Matrix	brain
22	chr1:120491200-120538800	Weak transcription	Fetal Brain Male	brain
23	chr1:120493400-120505800	Weak transcription	Colonic Mucosa	Colon
24	chr1:120493400-120507800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr1:120493600-120512200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:120494200-120506200	Weak transcription	Fetal Intestine Small	intestine
27	chr1:120495800-120506000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:120496200-120506000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr1:120497400-120506200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr1:120497800-120505600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:120497800-120506000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:120497800-120506400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:120497800-120508800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr1:120498000-120505200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:120498000-120505200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:120498000-120505400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:120498000-120505600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr1:120498000-120506000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr1:120498000-120506000	Weak transcription	Lung	lung
40	chr1:120498000-120506000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:120498000-120506200	Weak transcription	Spleen	Spleen
42	chr1:120498000-120507600	Weak transcription	Pancreas	Pancrea
43	chr1:120498000-120507800	Weak transcription	Ovary	ovary
44	chr1:120498000-120507800	Weak transcription	Small Intestine	intestine
45	chr1:120498000-120508000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr1:120498000-120508600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:120498000-120508600	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr1:120498200-120505400	Weak transcription	Fetal Intestine Large	intestine
49	chr1:120498200-120506000	Weak transcription	Hela-S3	cervix
50	chr1:120498200-120506200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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