Variant report

Variant	rs10483153
Chromosome Location	chr22:29402751-29402752
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:29392383..29394290-chr22:29401537..29403639,2	MCF-7	breast:
2	chr22:29401603..29404388-chr22:29410754..29413254,2	K562	blood:
3	chr22:29395298..29397330-chr22:29401566..29403212,2	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11912498	0.89[EUR][1000 genomes]
rs12628368	1.00[JPT][hapmap]
rs16986814	1.00[JPT][hapmap]
rs16986873	0.88[ASN][1000 genomes]
rs16986951	0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs16986993	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16987090	0.89[EUR][1000 genomes]
rs1986295	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41341948	1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4820793	0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4822999	0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4823001	0.86[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4823004	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5752851	0.90[EUR][1000 genomes]
rs7286026	0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs8137589	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9625657	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064079	chr22:29065528-29456059	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv531586	chr22:29252132-29902266	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29398800-29405000	Weak transcription	HSMMtube	muscle
2	chr22:29399400-29403200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr22:29399600-29403400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr22:29400600-29412000	Weak transcription	A549	lung
5	chr22:29400600-29425400	Weak transcription	NHEK	skin
6	chr22:29400800-29405000	Weak transcription	Aorta	Aorta
7	chr22:29401000-29403600	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr22:29401200-29403000	Enhancers	Duodenum Mucosa	Duodenum
9	chr22:29401200-29403200	Enhancers	Fetal Intestine Small	intestine
10	chr22:29401200-29403400	Enhancers	Fetal Intestine Large	intestine
11	chr22:29401200-29413400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr22:29401400-29403400	Enhancers	H1 Cell Line	embryonic stem cell
13	chr22:29401400-29403400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr22:29401400-29405000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr22:29401400-29405000	Weak transcription	Ovary	ovary
16	chr22:29401400-29407200	Weak transcription	Right Atrium	heart
17	chr22:29401400-29414800	Weak transcription	Esophagus	oesophagus
18	chr22:29401400-29419200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr22:29401400-29425000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr22:29401600-29402800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr22:29401600-29402800	Weak transcription	Fetal Kidney	kidney
22	chr22:29401600-29402800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr22:29401600-29403000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:29401600-29403200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr22:29401600-29403200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr22:29401600-29403400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr22:29401600-29403800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr22:29401600-29404200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr22:29401600-29404200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr22:29401600-29404200	Weak transcription	Psoas Muscle	Psoas
31	chr22:29401600-29404800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr22:29401600-29405000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr22:29401600-29407000	Weak transcription	Brain Germinal Matrix	brain
34	chr22:29401600-29407000	Weak transcription	Brain Hippocampus Middle	brain
35	chr22:29401600-29407200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr22:29401600-29407600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr22:29401800-29402800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr22:29401800-29402800	Enhancers	HepG2	liver
39	chr22:29401800-29403400	Weak transcription	Left Ventricle	heart
40	chr22:29401800-29404200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr22:29401800-29404200	Weak transcription	Stomach Mucosa	stomach
42	chr22:29401800-29404400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr22:29401800-29404400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr22:29401800-29406400	Weak transcription	Brain Substantia Nigra	brain
45	chr22:29401800-29406400	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr22:29401800-29407000	Weak transcription	Fetal Lung	lung
47	chr22:29401800-29407200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr22:29401800-29407200	Weak transcription	Liver	Liver
49	chr22:29401800-29407200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr22:29401800-29407200	Weak transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links