Variant report

Variant	rs34901222
Chromosome Location	chr3:145786573-145786574
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs13065572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13066226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13075648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13079521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13088659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13095139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16857900	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs34041519	0.87[AMR][1000 genomes]
rs34092280	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34201307	1.00[AFR][1000 genomes]
rs34248972	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34298175	1.00[AMR][1000 genomes]
rs34392701	1.00[AFR][1000 genomes]
rs34589717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34695557	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35017529	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35020806	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35080774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35479343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35520151	1.00[AFR][1000 genomes]
rs35687630	1.00[AFR][1000 genomes]
rs35880277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35969739	1.00[AMR][1000 genomes]
rs62272613	1.00[AFR][1000 genomes]
rs71300372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71300373	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71300374	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71300375	0.84[EUR][1000 genomes]
rs71300377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs71300378	1.00[AMR][1000 genomes]
rs71300379	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71300380	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71300381	1.00[AFR][1000 genomes]
rs71300383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71621137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]

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	nsv877584	chr3:144903957-145833232	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv525829	chr3:145614317-145863779	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv4046	chr3:145693249-145880189	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145768800-145788400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:145774600-145787200	Weak transcription	Esophagus	oesophagus
3	chr3:145774600-145795400	Weak transcription	Aorta	Aorta
4	chr3:145775400-145786600	Weak transcription	HepG2	liver
5	chr3:145776600-145787200	Weak transcription	HMEC	breast
6	chr3:145777000-145819400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:145778200-145817200	Weak transcription	Fetal Stomach	stomach
8	chr3:145778600-145789000	Weak transcription	Left Ventricle	heart
9	chr3:145778800-145788400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr3:145779000-145789600	Weak transcription	Fetal Heart	heart
11	chr3:145779400-145788800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr3:145779600-145820600	Weak transcription	Fetal Kidney	kidney
13	chr3:145780000-145815600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr3:145780600-145820400	Weak transcription	Placenta	Placenta
15	chr3:145780800-145786600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr3:145780800-145793800	Weak transcription	Ovary	ovary
17	chr3:145780800-145793800	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr3:145780800-145819800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr3:145781000-145788400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:145781000-145788800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr3:145781800-145831800	Weak transcription	Psoas Muscle	Psoas
22	chr3:145782800-145843200	Weak transcription	Pancreas	Pancrea
23	chr3:145784000-145789400	Weak transcription	Colon Smooth Muscle	Colon
24	chr3:145784000-145811800	Weak transcription	Rectal Smooth Muscle	rectum
25	chr3:145784400-145788400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:145784600-145790400	Weak transcription	NHLF	lung
27	chr3:145784600-145848800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr3:145784800-145789600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr3:145784800-145794000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr3:145785000-145788000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr3:145785000-145789600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr3:145785200-145788400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:145785200-145806400	Weak transcription	Colonic Mucosa	Colon
34	chr3:145785200-145819400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr3:145785400-145787000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:145785400-145788600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:145785400-145789400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:145785400-145790400	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr3:145785400-145791800	Strong transcription	HSMM	muscle
40	chr3:145785400-145796800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr3:145785600-145790800	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr3:145785600-145790800	Weak transcription	NHDF-Ad	bronchial
43	chr3:145785600-145798600	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr3:145785800-145786800	Strong transcription	HSMMtube	muscle
45	chr3:145785800-145789400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr3:145785800-145790000	Strong transcription	Osteobl	bone
47	chr3:145786000-145786800	Strong transcription	Stomach Smooth Muscle	stomach
48	chr3:145786000-145787000	Strong transcription	NH-A	brain
49	chr3:145786000-145788600	Weak transcription	Fetal Muscle Leg	muscle
50	chr3:145786000-145789000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links