Variant report

Variant	rs2252205
Chromosome Location	chr10:93729989-93729990
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10748573	0.93[AFR][1000 genomes]
rs10748574	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1418789	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1776206	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2066175	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2066176	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2676810	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2676818	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2792026	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4933221	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4933223	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4933702	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6583796	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7078187	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7914187	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7919043	0.83[AMR][1000 genomes]
rs833371	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs833377	0.83[AFR][1000 genomes];1.00[AMR][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	nsv1051226	chr10:93711296-93915586	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv540745	chr10:93711296-93915586	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1042818	chr10:93715483-93855032	Strong transcription ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93685800-93735200	Weak transcription	Fetal Heart	heart
2	chr10:93690800-93742400	Weak transcription	Stomach Mucosa	stomach
3	chr10:93691800-93741400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:93696800-93735600	Weak transcription	Pancreas	Pancrea
5	chr10:93697000-93735600	Weak transcription	Esophagus	oesophagus
6	chr10:93697800-93748800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:93699600-93750600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr10:93704800-93807400	Weak transcription	Gastric	stomach
9	chr10:93708000-93732600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr10:93708600-93730600	Strong transcription	Liver	Liver
11	chr10:93708600-93733200	Strong transcription	Primary B cells from peripheral blood	blood
12	chr10:93709000-93771800	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr10:93709200-93731000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:93709400-93740000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr10:93710000-93750200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr10:93710400-93736600	Strong transcription	Fetal Thymus	thymus
17	chr10:93710600-93730400	Strong transcription	Fetal Intestine Large	intestine
18	chr10:93710800-93736200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr10:93711000-93730200	Strong transcription	Placenta	Placenta
20	chr10:93711000-93730600	Strong transcription	HepG2	liver
21	chr10:93711000-93731000	Strong transcription	Duodenum Mucosa	Duodenum
22	chr10:93711000-93731200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:93711000-93732400	Strong transcription	Adipose Nuclei	Adipose
24	chr10:93711000-93732600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr10:93711200-93731200	Strong transcription	Primary T helper cells PMA-I stimulated	--
26	chr10:93713600-93733200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr10:93713600-93744400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr10:93714000-93732400	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr10:93714000-93734400	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr10:93714400-93743800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr10:93714600-93768000	Weak transcription	Right Ventricle	heart
32	chr10:93715400-93741400	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr10:93716200-93731200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:93718400-93734200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:93718400-93774000	Weak transcription	Spleen	Spleen
36	chr10:93719000-93734200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr10:93719400-93761000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr10:93720000-93735400	Weak transcription	Brain Hippocampus Middle	brain
39	chr10:93720000-93741400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr10:93720000-93757400	Weak transcription	Small Intestine	intestine
41	chr10:93720200-93734200	Weak transcription	NHLF	lung
42	chr10:93720200-93741400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr10:93720400-93741800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr10:93720400-93757400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr10:93720600-93742600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr10:93720600-93742800	Weak transcription	Brain Cingulate Gyrus	brain
47	chr10:93721200-93734200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr10:93721200-93741200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr10:93721200-93742000	Weak transcription	Fetal Kidney	kidney
50	chr10:93721400-93742000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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