Variant report

Variant	rs2122290
Chromosome Location	chr2:74358901-74358902
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBP	chr2:74358841-74359340	K562	blood:	n/a	n/a
2	EP300	chr2:74358889-74359405	K562	blood:	n/a	n/a
3	CTCF	chr2:74358797-74359205	K562	blood:	n/a	n/a
4	CBX3	chr2:74358757-74359435	K562	blood:	n/a	n/a
5	TAL1	chr2:74358866-74359435	K562	blood:	n/a	chr2:74359226-74359237 chr2:74359225-74359240
6	RCOR1	chr2:74358877-74359386	K562	blood:	n/a	n/a
7	GTF2F1	chr2:74358788-74358956	K562	blood:	n/a	n/a
8	NR2F2	chr2:74358870-74359665	K562	blood:	n/a	n/a
9	CTCF	chr2:74358900-74359050	K562	blood:	n/a	n/a
10	CTCF	chr2:74358860-74359363	K562	blood:	n/a	n/a
11	CTCF	chr2:74358800-74358950	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr2:74358900-74359050	MCF-7	breast:	n/a	n/a
13	GATA1	chr2:74358771-74359773	PBDE	blood:	n/a	chr2:74359205-74359214 chr2:74359210-74359220

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:74345800..74349275-chr2:74357385..74359321,6	MCF-7	breast:
2	chr2:74357697..74362841-chr2:74424131..74428670,5	K562	blood:
3	chr2:74356615..74359477-chr2:74372011..74374139,2	MCF-7	breast:
4	chr2:74285218..74287266-chr2:74357972..74359990,2	K562	blood:
5	chr2:74224937..74227638-chr2:74357477..74359947,2	MCF-7	breast:
6	chr2:74235618..74237940-chr2:74357623..74360543,2	MCF-7	breast:
7	chr2:74210918..74212665-chr2:74357393..74359886,2	MCF-7	breast:
8	chr2:74347023..74350379-chr2:74357531..74361133,4	K562	blood:
9	chr2:74357599..74359894-chr2:74425001..74426947,2	K562	blood:
10	chr2:74356810..74359552-chr2:74365465..74371208,7	MCF-7	breast:
11	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
12	chr2:74356746..74359023-chr2:74373471..74375958,3	MCF-7	breast:
13	chr2:74357326..74359137-chr2:74360563..74363969,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000217702	TF binding region
ENSG00000235499	Chromatin interaction
ENSG00000225439	Chromatin interaction
ENSG00000257800	Chromatin interaction
ENSG00000163170	Chromatin interaction
ENSG00000065911	Chromatin interaction
ENSG00000217702	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1026150	0.91[JPT][hapmap]
rs1095969	0.90[JPT][hapmap]
rs11675066	0.93[ASN][1000 genomes]
rs12465641	0.82[CHB][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs12478482	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12619982	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13025827	0.86[JPT][hapmap]
rs1667615	0.86[JPT][hapmap]
rs1667616	0.86[JPT][hapmap]
rs1667622	0.86[JPT][hapmap]
rs2177707	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2280642	0.94[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2280643	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2280644	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4429500	0.89[CEU][hapmap];0.86[CHB][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.85[EUR][1000 genomes]
rs4452177	0.91[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4563249	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4852329	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4853010	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4853011	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4853012	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58759652	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59570457	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60330274	0.85[EUR][1000 genomes]
rs60705299	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60964317	0.84[EUR][1000 genomes]
rs61521879	0.83[EUR][1000 genomes]
rs6546891	0.82[MEX][hapmap]
rs6707619	0.86[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6715351	0.85[EUR][1000 genomes]
rs6731793	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6758220	0.86[JPT][hapmap]
rs702463	0.86[JPT][hapmap]
rs702464	0.86[JPT][hapmap]
rs72911122	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72915068	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7570950	0.81[GIH][hapmap];0.90[MEX][hapmap]
rs828841	0.86[JPT][hapmap]
rs828847	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874286	chr2:74323500-74436721	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv3427010	chr2:74351730-74813541	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
3	nsv525117	chr2:74358901-74374641	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs2122290	FNBP1P1	cis	Skin Sun Exposed Lower leg	GTEx
rs2122290	FNBP1P1	cis	Artery Aorta	GTEx
rs2122290	MGC10955	cis	Nerve Tibial	GTEx
rs2122290	MGC10955	cis	Esophagus Muscularis	GTEx
rs2122290	PCGF1	cis	parietal	SCAN
rs2122290	MGC10955	cis	lung	GTEx
rs2122290	MGC10955	cis	Artery Tibial	GTEx
rs2122290	FNBP1P1	cis	Esophagus Muscularis	GTEx
rs2122290	MGC10955	cis	Skin Sun Exposed Lower leg	GTEx
rs2122290	NAT8	cis	parietal	SCAN
rs2122290	FBXO41	cis	cerebellum	SCAN
rs2122290	FNBP1P1	cis	Artery Tibial	GTEx
rs2122290	MGC10955	cis	Artery Aorta	GTEx
rs2122290	MGC10955	cis	Thyroid	GTEx
rs2122290	MGC10955	cis	Adipose Subcutaneous	GTEx
rs2122290	MGC10955	cis	Esophagus Mucosa	GTEx

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74348200-74360400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr2:74348200-74367600	Weak transcription	Brain Anterior Caudate	brain
3	chr2:74348600-74361800	Weak transcription	Hela-S3	cervix
4	chr2:74348800-74360400	Weak transcription	Primary T cells from cord blood	blood
5	chr2:74350800-74360400	Weak transcription	Brain Substantia Nigra	brain
6	chr2:74353400-74360400	Weak transcription	Dnd41	blood
7	chr2:74353600-74360400	Weak transcription	A549	lung
8	chr2:74354200-74359400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr2:74354400-74373800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:74354800-74360400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:74355200-74373800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr2:74356400-74361400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:74357000-74360400	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:74357200-74361200	Weak transcription	NHLF	lung
15	chr2:74357600-74359400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:74357600-74361200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr2:74357600-74361200	Weak transcription	Fetal Thymus	thymus
18	chr2:74357600-74361800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:74357600-74361800	Weak transcription	Right Ventricle	heart
20	chr2:74357600-74373800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr2:74357800-74360400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:74357800-74360400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr2:74357800-74361200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:74357800-74361400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:74357800-74361800	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr2:74357800-74367600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:74357800-74373600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:74358000-74360400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:74358000-74361200	Weak transcription	HMEC	breast
30	chr2:74358000-74361600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:74358200-74360400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr2:74358200-74360600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr2:74358200-74361600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr2:74358200-74364800	Weak transcription	Esophagus	oesophagus
35	chr2:74358200-74373800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr2:74358400-74359400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:74358400-74360400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr2:74358400-74360400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:74358400-74360600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr2:74358400-74361200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr2:74358600-74359600	Flanking Active TSS	K562	blood
42	chr2:74358600-74360400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr2:74358600-74360400	Weak transcription	Fetal Brain Female	brain
44	chr2:74358600-74360600	Weak transcription	Left Ventricle	heart
45	chr2:74358600-74360600	Weak transcription	HepG2	liver
46	chr2:74358600-74360600	Weak transcription	NHEK	skin
47	chr2:74358600-74367800	Weak transcription	Osteobl	bone
48	chr2:74358600-74368800	Weak transcription	NHDF-Ad	bronchial
49	chr2:74358800-74360400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr2:74358800-74360400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links