Variant report

Variant	rs56405130
Chromosome Location	chr2:127859010-127859011
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:127825324..127826896-chr2:127856890..127859750,2	MCF-7	breast:
2	chr2:127857696..127862567-chr2:127862895..127866178,8	MCF-7	breast:
3	chr2:127852372..127854342-chr2:127858358..127859956,2	MCF-7	breast:
4	chr2:127823166..127825424-chr2:127856557..127859034,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136717	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11554586	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11678744	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11682186	1.00[ASN][1000 genomes]
rs11685593	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11689089	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11694264	1.00[ASN][1000 genomes]
rs1583647	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35114168	0.92[ASN][1000 genomes]
rs4663104	0.83[EUR][1000 genomes]
rs55646068	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55654668	1.00[ASN][1000 genomes]
rs55669136	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55828408	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56026783	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56117224	1.00[ASN][1000 genomes]
rs56193035	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57109420	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57724183	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58402148	0.80[EUR][1000 genomes]
rs59176034	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs59253801	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60447541	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60572885	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs60692476	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61308109	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6714558	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72838215	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72838226	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72838284	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72838285	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72838287	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72838288	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72846701	0.80[EUR][1000 genomes]
rs749007	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999422	chr2:127464647-127956543	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1004930	chr2:127477369-127938234	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv1003730	chr2:127794288-127860830	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1003461	chr2:127794288-127862257	Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv516759	chr2:127796666-127859441	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv1000994	chr2:127797089-127860830	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
7	esv1825024	chr2:127798138-127864285	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription 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	5 gene(s)	inside rSNPs	diseases
8	nsv459241	chr2:127800981-127868435	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv583033	chr2:127800981-127868435	Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv875011	chr2:127800981-127868435	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv875012	chr2:127800981-127895573	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1002673	chr2:127801964-127860830	Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv1010577	chr2:127801964-127862257	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1011224	chr2:127802375-127860830	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv1003887	chr2:127802375-127862257	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv1009309	chr2:127802730-127862257	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	nsv1014290	chr2:127805366-127860830	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
18	nsv1010084	chr2:127805366-127862257	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	nsv1002124	chr2:127810478-127860830	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
20	nsv1014118	chr2:127814781-127860830	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
21	nsv999224	chr2:127821207-127860830	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	nsv1001064	chr2:127828941-127862257	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv1006112	chr2:127830117-128032546	Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
24	esv2757832	chr2:127830943-128006514	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
25	esv2759090	chr2:127830943-128006514	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
26	nsv1005149	chr2:127841930-127880106	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
27	nsv1011378	chr2:127841930-128020546	Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
28	nsv999809	chr2:127841930-128032546	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
29	nsv1010669	chr2:127848860-128032546	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
30	nsv10142	chr2:127855764-127859277	Transcr. at gene 5' and 3' Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127845200-127859400	Enhancers	Brain Anterior Caudate	brain
2	chr2:127852400-127859800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:127853000-127861600	Weak transcription	NHDF-Ad	bronchial
4	chr2:127853200-127862000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr2:127853200-127862200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:127853200-127862400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:127853200-127862600	Weak transcription	NHLF	lung
8	chr2:127853200-127863000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr2:127853400-127859600	Weak transcription	Ovary	ovary
10	chr2:127853400-127862400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr2:127853600-127862200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr2:127854200-127862400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr2:127854400-127859600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:127854800-127860200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr2:127854800-127862400	Weak transcription	Right Atrium	heart
16	chr2:127855200-127859200	Enhancers	Colonic Mucosa	Colon
17	chr2:127855200-127860800	Weak transcription	Right Ventricle	heart
18	chr2:127855400-127859800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:127856600-127860000	Strong transcription	Fetal Stomach	stomach
20	chr2:127856600-127860800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr2:127856600-127861800	Weak transcription	Brain Germinal Matrix	brain
22	chr2:127856600-127862200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:127856800-127859600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:127856800-127860600	Weak transcription	Esophagus	oesophagus
25	chr2:127856800-127860800	Weak transcription	Colon Smooth Muscle	Colon
26	chr2:127856800-127862200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:127857000-127859400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr2:127857000-127859600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:127857400-127860000	Enhancers	Psoas Muscle	Psoas
30	chr2:127857400-127860800	Enhancers	Adipose Nuclei	Adipose
31	chr2:127857400-127862600	Genic enhancers	Fetal Intestine Small	intestine
32	chr2:127857600-127860400	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
33	chr2:127857600-127860800	Bivalent Enhancer	Placenta	Placenta
34	chr2:127857600-127862600	Enhancers	Fetal Intestine Large	intestine
35	chr2:127857600-127863000	Enhancers	Gastric	stomach
36	chr2:127857800-127859400	Genic enhancers	Brain Substantia Nigra	brain
37	chr2:127857800-127859600	Enhancers	Brain Cingulate Gyrus	brain
38	chr2:127857800-127859600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr2:127857800-127859600	Enhancers	Stomach Mucosa	stomach
40	chr2:127857800-127860200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr2:127857800-127861400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:127857800-127862800	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:127857800-127863000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr2:127858000-127859200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr2:127858000-127859200	Enhancers	Lung	lung
46	chr2:127858000-127859400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr2:127858000-127859400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr2:127858000-127860200	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr2:127858000-127860600	Enhancers	Liver	Liver
50	chr2:127858000-127863600	Enhancers	Spleen	Spleen

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