Variant report

Variant	rs10875070
Chromosome Location	chr1:97814644-97814645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10875071	0.92[ASN][1000 genomes]
rs11165865	0.83[EUR][1000 genomes]
rs12022799	0.83[EUR][1000 genomes]
rs12024103	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12030174	0.83[EUR][1000 genomes]
rs12038518	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12039093	0.83[EUR][1000 genomes]
rs12040045	0.83[EUR][1000 genomes]
rs12046771	0.92[ASN][1000 genomes]
rs12047456	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12048663	0.81[EUR][1000 genomes]
rs12070583	0.83[EUR][1000 genomes]
rs12750945	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1879375	0.83[ASN][1000 genomes]
rs4434871	0.83[EUR][1000 genomes]
rs6690620	0.83[EUR][1000 genomes]
rs74104367	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs74104372	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74104373	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74105110	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74105111	0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs74105145	0.83[EUR][1000 genomes]
rs74105146	0.83[EUR][1000 genomes]
rs74105150	0.83[EUR][1000 genomes]
rs74105153	0.83[EUR][1000 genomes]
rs7512213	0.83[EUR][1000 genomes]
rs9783115	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[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	nsv491816	chr1:97266403-98223619	Enhancers Strong transcription ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer 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	nsv530048	chr1:97457175-98031501	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1007950	chr1:97466488-98021146	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv533039	chr1:97665736-98343102	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97781600-97822200	Weak transcription	Primary T cells from cord blood	blood
2	chr1:97789800-97823600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr1:97791800-97823600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:97792800-97820800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr1:97794600-97848200	Weak transcription	Left Ventricle	heart
6	chr1:97795600-97823600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr1:97795600-97830000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:97801200-97822400	Weak transcription	Primary B cells from cord blood	blood
9	chr1:97802200-97823200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:97802200-97848600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr1:97803200-97843200	Weak transcription	Spleen	Spleen
12	chr1:97804200-97823400	Weak transcription	Esophagus	oesophagus
13	chr1:97805200-97823200	Weak transcription	Fetal Lung	lung
14	chr1:97805800-97816400	Weak transcription	Dnd41	blood
15	chr1:97805800-97846800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:97807200-97815800	Weak transcription	HSMM	muscle
17	chr1:97807600-97815600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr1:97813800-97814800	Enhancers	Fetal Heart	heart
19	chr1:97814200-97814800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:97814400-97815000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:97814400-97815600	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr1:97814400-97816200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:97814400-97816800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr1:97814400-97818400	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr1:97814400-97818400	Weak transcription	Brain Anterior Caudate	brain
26	chr1:97814400-97818400	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:97814400-97818600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr1:97814400-97818800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr1:97814400-97823600	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr1:97814400-97824600	Weak transcription	Right Ventricle	heart
31	chr1:97814600-97815600	Weak transcription	Adipose Nuclei	Adipose
32	chr1:97814600-97816000	Weak transcription	NH-A	brain
33	chr1:97814600-97818200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:97814600-97818400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr1:97814600-97818400	Weak transcription	Brain Substantia Nigra	brain

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