Variant report

Variant	rs10772245
Chromosome Location	chr12:10381873-10381874
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:10373969..10375781-chr12:10380719..10382478,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10743876	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10772244	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10772246	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10845077	0.84[AFR][1000 genomes]
rs11834167	0.82[ASN][1000 genomes]
rs12310669	0.87[ASN][1000 genomes]
rs2417582	0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs2417584	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2537800	0.86[ASN][1000 genomes]
rs2537801	0.86[ASN][1000 genomes]
rs2900385	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4764332	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4764333	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4764337	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4764342	0.88[AMR][1000 genomes]
rs55823125	0.81[ASN][1000 genomes]
rs58510785	0.82[ASN][1000 genomes]
rs59389382	0.95[ASN][1000 genomes]
rs59511495	0.97[ASN][1000 genomes]
rs59761822	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60221429	0.81[ASN][1000 genomes]
rs6488277	0.86[ASN][1000 genomes]
rs6488279	0.86[ASN][1000 genomes]
rs66996903	0.81[ASN][1000 genomes]
rs7137304	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7302157	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7302532	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs73053363	0.81[ASN][1000 genomes]
rs73053368	0.81[ASN][1000 genomes]
rs73060081	0.97[ASN][1000 genomes]
rs73062005	0.97[ASN][1000 genomes]
rs73068064	0.86[ASN][1000 genomes]
rs73068080	0.86[ASN][1000 genomes]
rs7315203	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7959312	0.86[ASN][1000 genomes]
rs7959512	0.86[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	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1054811	chr12:10350587-10440005	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10366800-10386600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:10373400-10382200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:10376400-10386600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr12:10376400-10386600	Weak transcription	Brain Substantia Nigra	brain
5	chr12:10376400-10388600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:10376400-10395000	Weak transcription	Pancreas	Pancrea
7	chr12:10376400-10397600	Weak transcription	Aorta	Aorta
8	chr12:10376600-10382400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:10376600-10385600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr12:10376800-10385800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:10377000-10382800	Weak transcription	Right Ventricle	heart
12	chr12:10377000-10385000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr12:10377000-10386600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr12:10377200-10383000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:10377200-10384200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr12:10377200-10385200	Weak transcription	Lung	lung
17	chr12:10377200-10386000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr12:10377200-10386000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr12:10377200-10386000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr12:10377200-10386800	Weak transcription	HSMMtube	muscle
21	chr12:10377200-10389000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:10377200-10394200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:10377200-10394600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr12:10377200-10399000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr12:10377600-10386800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:10377600-10386800	Weak transcription	Liver	Liver
27	chr12:10377600-10386800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr12:10377800-10404400	Weak transcription	Left Ventricle	heart
29	chr12:10378800-10386200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:10380000-10386600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:10380200-10395800	Weak transcription	Thymus	Thymus
32	chr12:10380600-10382000	Strong transcription	Placenta	Placenta

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