Variant report

Variant	rs2267162
Chromosome Location	chr22:31010997-31010998
allele	C/T
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	NR2F2	chr22:31010884-31011317	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:31001608..31004689-chr22:31008894..31012791,3	K562	blood:
2	chr22:31002585..31007249-chr22:31007343..31011235,4	K562	blood:
3	chr22:31009106..31011344-chr22:31017330..31018949,2	K562	blood:

Variant related genes	Relation type
TCN2	TF binding region
ENSG00000100029	Chromatin interaction
ENSG00000185339	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11913239	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs16988855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16988936	0.86[CHB][hapmap];0.88[JPT][hapmap];0.92[EUR][1000 genomes]
rs2009857	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2013928	0.92[EUR][1000 genomes]
rs2072195	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.84[YRI][hapmap];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2267165	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2267166	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2283873	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs5994329	0.83[JPT][hapmap]
rs5997719	0.92[EUR][1000 genomes]
rs5997722	0.83[JPT][hapmap]
rs72558391	0.86[ASN][1000 genomes]
rs7288385	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7288627	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7289549	0.93[YRI][hapmap];0.91[AFR][1000 genomes]
rs7290898	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73396379	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73396395	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73398305	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8135450	0.92[EUR][1000 genomes]
rs8141515	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9606762	0.82[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	nsv829171	chr22:30598030-31043578	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv915818	chr22:30708245-31346302	Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv834175	chr22:30976624-31089545	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31003200-31031200	Weak transcription	Aorta	Aorta
2	chr22:31003800-31030600	Weak transcription	Thymus	Thymus
3	chr22:31004200-31013400	Weak transcription	Pancreas	Pancrea
4	chr22:31004400-31020200	Weak transcription	Fetal Kidney	kidney
5	chr22:31005000-31022200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr22:31005600-31012200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr22:31006000-31019200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr22:31006000-31020800	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr22:31006000-31023200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr22:31006000-31023200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr22:31006000-31030400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr22:31006000-31030600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr22:31006000-31030600	Weak transcription	Colonic Mucosa	Colon
14	chr22:31006200-31017400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr22:31006200-31017400	Strong transcription	Fetal Stomach	stomach
16	chr22:31006200-31019400	Strong transcription	H9 Cell Line	embryonic stem cell
17	chr22:31006200-31023800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr22:31006200-31030600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr22:31006400-31013600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr22:31006400-31015000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr22:31006400-31017000	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr22:31006400-31023000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr22:31006400-31023200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:31006400-31023400	Strong transcription	Fetal Intestine Small	intestine
25	chr22:31006600-31017000	Strong transcription	Brain Germinal Matrix	brain
26	chr22:31006600-31020000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr22:31006600-31030400	Weak transcription	Duodenum Mucosa	Duodenum
28	chr22:31006800-31030200	Weak transcription	Placenta	Placenta
29	chr22:31007000-31012200	Strong transcription	Fetal Intestine Large	intestine
30	chr22:31007000-31017200	Strong transcription	Liver	Liver
31	chr22:31007000-31030600	Weak transcription	Fetal Brain Male	brain
32	chr22:31007200-31019200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr22:31007600-31011000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr22:31007600-31011200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr22:31007600-31030200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr22:31007800-31011800	Strong transcription	Lung	lung
37	chr22:31008000-31030400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr22:31008400-31023200	Strong transcription	Adipose Nuclei	Adipose
39	chr22:31008600-31011800	Strong transcription	Left Ventricle	heart
40	chr22:31008600-31012000	Strong transcription	Fetal Brain Female	brain
41	chr22:31008600-31012200	Strong transcription	Duodenum Smooth Muscle	Duodenum
42	chr22:31008600-31014000	Strong transcription	Brain Substantia Nigra	brain
43	chr22:31008800-31011400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr22:31008800-31011800	Strong transcription	Right Ventricle	heart
45	chr22:31008800-31012000	Strong transcription	Brain Cingulate Gyrus	brain
46	chr22:31008800-31012000	Strong transcription	Brain Hippocampus Middle	brain
47	chr22:31008800-31013800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr22:31008800-31019000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr22:31009000-31012200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr22:31009200-31011200	Weak transcription	Fetal Muscle Leg	muscle

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