Variant report

Variant	rs2797484
Chromosome Location	chr10:5778945-5778946
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5772075..5775852-chr10:5776811..5780345,4	K562	blood:
2	chr10:5727335..5729854-chr10:5777449..5779108,2	K562	blood:
3	chr10:5725557..5727727-chr10:5778800..5780889,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108021	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1057943	0.81[EUR][1000 genomes]
rs10737018	0.86[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10905029	0.96[ASN][1000 genomes]
rs10905066	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11592993	0.81[EUR][1000 genomes]
rs11593876	0.81[EUR][1000 genomes]
rs11594505	0.81[EUR][1000 genomes]
rs11594846	0.83[EUR][1000 genomes]
rs11595421	0.83[EUR][1000 genomes]
rs11599810	0.80[EUR][1000 genomes]
rs2254067	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2380209	0.83[ASN][1000 genomes]
rs2386620	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2386664	0.93[EUR][1000 genomes]
rs2669135	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2669137	0.84[ASN][1000 genomes]
rs2797486	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2797487	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2797491	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2797493	0.97[ASN][1000 genomes]
rs2797494	0.93[ASN][1000 genomes]
rs2797501	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3736460	0.81[EUR][1000 genomes]
rs4423100	0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs45549643	0.83[EUR][1000 genomes]
rs56352451	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61832759	0.81[EUR][1000 genomes]
rs61832860	0.83[EUR][1000 genomes]
rs61832863	0.83[EUR][1000 genomes]
rs61832864	0.93[EUR][1000 genomes]
rs61832865	0.83[EUR][1000 genomes]
rs61832866	0.80[EUR][1000 genomes]
rs61832870	0.83[EUR][1000 genomes]
rs61832872	0.80[EUR][1000 genomes]
rs61832874	0.80[EUR][1000 genomes]
rs61836362	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7093027	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72772369	0.81[EUR][1000 genomes]
rs72774084	0.84[EUR][1000 genomes]
rs7475869	0.81[EUR][1000 genomes]
rs7902987	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7907687	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2758209	chr10:5637111-5804780	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	esv34147	chr10:5726821-6105717	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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	42 gene(s)	inside rSNPs	diseases
5	esv34061	chr10:5726821-6225187	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv1050663	chr10:5737979-5785918	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5753800-5783400	Weak transcription	Brain Substantia Nigra	brain
2	chr10:5753800-5787000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:5754400-5781600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr10:5762200-5783000	Weak transcription	Stomach Mucosa	stomach
5	chr10:5762200-5795400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr10:5762400-5794600	Strong transcription	Primary T helper cells PMA-I stimulated	--
7	chr10:5762600-5843400	Strong transcription	Dnd41	blood
8	chr10:5762800-5779800	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr10:5762800-5793000	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr10:5762800-5843000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:5763000-5795000	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr10:5763200-5779000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr10:5763400-5788600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr10:5767200-5792800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr10:5768000-5788400	Weak transcription	Fetal Brain Male	brain
16	chr10:5768000-5849400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr10:5768600-5786400	Strong transcription	GM12878-XiMat	blood
18	chr10:5769400-5784200	Weak transcription	Psoas Muscle	Psoas
19	chr10:5769600-5781600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr10:5771800-5779600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr10:5771800-5790000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr10:5772200-5779600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr10:5773000-5788400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:5773400-5781400	Weak transcription	HSMMtube	muscle
25	chr10:5773400-5781800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:5773600-5784200	Weak transcription	Small Intestine	intestine
27	chr10:5773600-5786000	Weak transcription	Right Ventricle	heart
28	chr10:5773800-5781600	Weak transcription	Aorta	Aorta
29	chr10:5773800-5781600	Weak transcription	Colonic Mucosa	Colon
30	chr10:5773800-5781600	Weak transcription	Ovary	ovary
31	chr10:5773800-5781600	Weak transcription	HUVEC	blood vessel
32	chr10:5773800-5781800	Weak transcription	Brain Angular Gyrus	brain
33	chr10:5773800-5785800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:5773800-5788200	Weak transcription	Fetal Kidney	kidney
35	chr10:5774000-5781800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr10:5774000-5781800	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr10:5774000-5781800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:5774000-5781800	Weak transcription	Colon Smooth Muscle	Colon
39	chr10:5774000-5788200	Weak transcription	Gastric	stomach
40	chr10:5774200-5781600	Weak transcription	NHDF-Ad	bronchial
41	chr10:5774200-5781800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr10:5774200-5783800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr10:5774200-5786800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr10:5774400-5781000	Weak transcription	NHEK	skin
45	chr10:5774400-5781400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:5774400-5781600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr10:5774400-5781600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr10:5774400-5781600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr10:5774400-5781600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:5774400-5781600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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