Variant report

Variant	rs17036320
Chromosome Location	chr2:47387187-47387188
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:47382524-47406811	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr2:47385615-47387337	K562	blood:	n/a	n/a
3	POLR2A	chr2:47382225-47405286	PFSK-1	brain:	n/a	n/a
4	POLR2A	chr2:47385491-47387192	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr2:47386477-47387205	GM12892	blood:	n/a	n/a
6	POLR2A	chr2:47386540-47387263	GM12878	blood:	n/a	n/a
7	POLR2A	chr2:47385318-47387857	HepG2	liver:	n/a	n/a
8	POLR2A	chr2:47382411-47391126	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr2:47386583-47387216	HepG2	liver:	n/a	n/a
10	POLR2A	chr2:47386421-47387193	K562	blood:	n/a	n/a
11	POLR2A	chr2:47382450-47387588	PANC-1	pancreas:	n/a	n/a
12	POLR2A	chr2:47386687-47387319	HepG2	liver:	n/a	n/a
13	TCF7L2	chr2:47386969-47387462	HepG2	liver:	n/a	n/a
14	POLR2A	chr2:47386361-47387336	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr2:47386587-47387554	GM12892	blood:	n/a	n/a
16	POLR2A	chr2:47386583-47387192	GM12891	blood:	n/a	n/a
17	MBD4	chr2:47386319-47387618	HepG2	liver:	n/a	n/a
18	POLR2A	chr2:47385530-47387721	HepG2	liver:	n/a	n/a
19	POLR2A	chr2:47382208-47387634	U87	brain:	n/a	n/a
20	POLR2A	chr2:47382271-47387210	U87	brain:	n/a	n/a
21	MYBL2	chr2:47387146-47387791	HepG2	liver:	n/a	n/a
22	POLR2A	chr2:47386653-47387196	GM12878	blood:	n/a	n/a
23	POLR2A	chr2:47386644-47387291	K562	blood:	n/a	n/a
24	POLR2A	chr2:47383059-47391091	K562	blood:	n/a	n/a
25	POLR2A	chr2:47386537-47387291	GM12892	blood:	n/a	n/a
26	POLR2A	chr2:47386629-47387248	K562	blood:	n/a	n/a
27	FOXA2	chr2:47387084-47387779	HepG2	liver:	n/a	n/a

No data

(count:1 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:47385656..47388232-chr2:47538182..47540860,2	MCF-7	breast:

No data

Variant related genes	Relation type
C2orf61	TF binding region

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11842	0.86[AMR][1000 genomes]
rs1693888	0.85[ASN][1000 genomes]
rs1693889	0.85[ASN][1000 genomes]
rs17036300	0.83[ASW][hapmap];1.00[CEU][hapmap];0.87[LWK][hapmap];0.94[MEX][hapmap];0.80[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs17036311	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036313	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036316	0.92[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17036325	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[YRI][hapmap];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1723485	0.85[ASN][1000 genomes]
rs2347617	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4953469	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4953470	0.83[ASW][hapmap];1.00[CEU][hapmap];0.87[LWK][hapmap];0.94[MEX][hapmap];0.80[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4953471	1.00[CEU][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes]
rs4953472	0.94[AMR][1000 genomes]
rs56875665	0.98[AMR][1000 genomes]
rs59415749	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6713257	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6749284	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs6760339	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs72810414	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72810415	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72810417	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs72810419	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72877054	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7583684	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs815812	0.85[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	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv457374	chr2:47313624-47448865	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases
4	nsv581754	chr2:47313624-47448865	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47366200-47397000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:47366800-47399400	Strong transcription	Fetal Thymus	thymus
3	chr2:47367000-47401200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr2:47367200-47402000	Weak transcription	Esophagus	oesophagus
5	chr2:47367600-47387400	Weak transcription	Pancreas	Pancrea
6	chr2:47369800-47391200	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr2:47370000-47389600	Strong transcription	Muscle Satellite Cultured Cells	--
8	chr2:47371200-47388200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:47371600-47389800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:47371800-47392200	Strong transcription	Osteobl	bone
11	chr2:47372600-47396800	Weak transcription	Small Intestine	intestine
12	chr2:47375600-47397400	Weak transcription	Fetal Brain Male	brain
13	chr2:47376000-47388000	Strong transcription	HSMM	muscle
14	chr2:47376400-47389800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr2:47378400-47392000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr2:47378600-47388000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:47378600-47389800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:47380200-47391400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr2:47380600-47388000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr2:47381400-47389600	Strong transcription	Fetal Brain Female	brain
21	chr2:47381600-47390400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr2:47382000-47391000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:47382200-47390000	Strong transcription	NHLF	lung
24	chr2:47382600-47391400	Strong transcription	NH-A	brain
25	chr2:47382600-47398200	Weak transcription	Aorta	Aorta
26	chr2:47382800-47390600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:47382800-47390600	Weak transcription	Spleen	Spleen
28	chr2:47383800-47388600	Weak transcription	Lung	lung
29	chr2:47383800-47390200	Strong transcription	Primary B cells from cord blood	blood
30	chr2:47384000-47388200	Strong transcription	Brain Cingulate Gyrus	brain
31	chr2:47384000-47389800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:47384400-47390000	Genic enhancers	A549	lung
33	chr2:47384400-47391800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:47384400-47397200	Weak transcription	Right Atrium	heart
35	chr2:47384600-47389800	Strong transcription	Duodenum Smooth Muscle	Duodenum
36	chr2:47384600-47390800	Strong transcription	HUVEC	blood vessel
37	chr2:47384600-47391000	Strong transcription	Fetal Muscle Trunk	muscle
38	chr2:47384600-47393200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:47384800-47390400	Strong transcription	GM12878-XiMat	blood
40	chr2:47384800-47397600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:47385000-47390400	Strong transcription	NHDF-Ad	bronchial
42	chr2:47385000-47390600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:47385000-47391000	Strong transcription	Fetal Lung	lung
44	chr2:47385000-47392400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:47385000-47398000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr2:47385200-47387200	Strong transcription	Fetal Intestine Small	intestine
47	chr2:47385200-47387200	Strong transcription	Fetal Stomach	stomach
48	chr2:47385200-47388200	Strong transcription	Brain Hippocampus Middle	brain
49	chr2:47385200-47388400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr2:47385200-47390200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--

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