Variant report

Variant	rs12505746
Chromosome Location	chr4:106114071-106114072
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:106064689..106068216-chr4:106113083..106116896,4	MCF-7	breast:
2	chr4:106065192..106067810-chr4:106113392..106115229,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000168769	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10003144	0.89[ASN][1000 genomes]
rs10006632	0.89[ASN][1000 genomes]
rs10006721	0.89[ASN][1000 genomes]
rs10008189	0.89[ASN][1000 genomes]
rs10017522	0.89[ASN][1000 genomes]
rs10018267	0.97[ASN][1000 genomes]
rs10022126	0.89[ASN][1000 genomes]
rs10022891	0.89[ASN][1000 genomes]
rs10023701	0.97[ASN][1000 genomes]
rs10026237	0.97[ASN][1000 genomes]
rs10027791	0.89[ASN][1000 genomes]
rs10033325	0.89[ASN][1000 genomes]
rs11932794	0.87[ASN][1000 genomes]
rs11938493	0.97[ASN][1000 genomes]
rs11941838	0.89[ASN][1000 genomes]
rs11943394	0.89[ASN][1000 genomes]
rs11944001	0.89[ASN][1000 genomes]
rs11944085	0.89[ASN][1000 genomes]
rs11947617	0.89[ASN][1000 genomes]
rs12499227	0.84[EUR][1000 genomes]
rs17430167	0.86[EUR][1000 genomes]
rs17508289	0.86[EUR][1000 genomes]
rs2017763	0.89[ASN][1000 genomes]
rs2214407	0.86[EUR][1000 genomes]
rs28394039	0.89[ASN][1000 genomes]
rs28707121	0.97[ASN][1000 genomes]
rs3733609	0.89[ASN][1000 genomes]
rs3796927	0.89[ASN][1000 genomes]
rs4235413	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55793049	0.89[ASN][1000 genomes]
rs58862751	0.90[ASN][1000 genomes]
rs59339947	0.83[ASN][1000 genomes]
rs59806714	0.89[ASN][1000 genomes]
rs60886348	0.89[ASN][1000 genomes]
rs6826102	0.89[ASN][1000 genomes]
rs6831247	0.89[ASN][1000 genomes]
rs6831445	0.89[ASN][1000 genomes]
rs6833560	0.97[ASN][1000 genomes]
rs6835030	0.89[ASN][1000 genomes]
rs6839609	0.89[ASN][1000 genomes]
rs6843141	0.89[ASN][1000 genomes]
rs6857812	0.89[ASN][1000 genomes]
rs72955167	0.89[ASN][1000 genomes]
rs72955198	0.89[ASN][1000 genomes]
rs73836047	0.97[ASN][1000 genomes]
rs73836048	0.97[ASN][1000 genomes]
rs73836052	0.93[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs73836055	0.93[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs73838074	0.89[ASN][1000 genomes]
rs7662448	0.89[ASN][1000 genomes]
rs7696287	0.89[ASN][1000 genomes]
rs7696337	0.89[ASN][1000 genomes]
rs7698398	0.97[ASN][1000 genomes]
rs7698522	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7700148	0.89[ASN][1000 genomes]
rs871215	0.89[ASN][1000 genomes]
rs9985622	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs9993497	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs9998069	0.89[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	nsv461609	chr4:105869548-106366209	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv470063	chr4:105869548-106366209	Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv595007	chr4:105869548-106366209	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv830025	chr4:105988876-106137946	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106069400-106114200	Weak transcription	Esophagus	oesophagus
2	chr4:106084800-106127400	Weak transcription	Brain Germinal Matrix	brain
3	chr4:106099000-106114200	Weak transcription	Gastric	stomach
4	chr4:106101000-106146600	Weak transcription	Spleen	Spleen
5	chr4:106102800-106127400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:106104800-106117400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:106105200-106117800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr4:106106000-106135000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:106106200-106114200	Weak transcription	Small Intestine	intestine
10	chr4:106106200-106118600	Weak transcription	Thymus	Thymus
11	chr4:106106200-106155000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr4:106106600-106125800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr4:106108000-106115400	Weak transcription	HMEC	breast
14	chr4:106108000-106123000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:106108400-106114200	Weak transcription	Pancreas	Pancrea
16	chr4:106110200-106114600	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr4:106110600-106118600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:106110800-106114400	Enhancers	Colon Smooth Muscle	Colon
19	chr4:106110800-106114600	Enhancers	Rectal Smooth Muscle	rectum
20	chr4:106111000-106118800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:106111200-106117200	Genic enhancers	Primary monocytes fromperipheralblood	blood
22	chr4:106111400-106114600	Enhancers	Adipose Nuclei	Adipose
23	chr4:106111800-106127400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:106112200-106114200	Weak transcription	Liver	Liver
25	chr4:106112200-106127200	Weak transcription	Primary T cells from cord blood	blood
26	chr4:106112400-106114200	Weak transcription	Aorta	Aorta
27	chr4:106112400-106114400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:106112400-106114600	Enhancers	Fetal Heart	heart
29	chr4:106112400-106115400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:106112400-106115600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:106112400-106116600	Enhancers	Osteobl	bone
32	chr4:106112400-106127000	Weak transcription	Fetal Muscle Leg	muscle
33	chr4:106112600-106114200	Enhancers	A549	lung
34	chr4:106112600-106114200	Enhancers	NHLF	lung
35	chr4:106112600-106114400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr4:106112600-106114400	Genic enhancers	Fetal Lung	lung
37	chr4:106112600-106114600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:106112600-106114800	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr4:106112600-106117000	Genic enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:106112800-106114400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:106112800-106114400	Enhancers	HSMMtube	muscle
42	chr4:106112800-106114600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr4:106112800-106114600	Enhancers	HSMM	muscle
44	chr4:106112800-106114800	Enhancers	Primary hematopoietic stem cells	blood
45	chr4:106112800-106115000	Enhancers	HUVEC	blood vessel
46	chr4:106112800-106116400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:106112800-106116400	Enhancers	NHDF-Ad	bronchial
48	chr4:106112800-106116400	Enhancers	NHEK	skin
49	chr4:106112800-106127400	Weak transcription	Placenta	Placenta
50	chr4:106113000-106114200	Weak transcription	Fetal Intestine Large	intestine

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