Variant report

Variant	rs61731327
Chromosome Location	chr10:5781800-5781801
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5775178..5776755-chr10:5781337..5783023,2	K562	blood:
2	chr10:5780274..5783194-chr10:5784148..5786108,3	K562	blood:
3	chr10:5781284..5783375-chr10:5788559..5791168,2	MCF-7	breast:
4	chr10:5781025..5783578-chr10:5784148..5786676,3	K562	blood:

Variant related genes	Relation type
ENSG00000226647	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10905101	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11253740	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11254891	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12247193	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12263390	1.00[EUR][1000 genomes]
rs12263869	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12269174	1.00[EUR][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:144 , 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	chr10:5762200-5783000	Weak transcription	Stomach Mucosa	stomach
4	chr10:5762200-5795400	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:5762400-5794600	Strong transcription	Primary T helper cells PMA-I stimulated	--
6	chr10:5762600-5843400	Strong transcription	Dnd41	blood
7	chr10:5762800-5793000	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr10:5762800-5843000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr10:5763000-5795000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr10:5763400-5788600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr10:5767200-5792800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr10:5768000-5788400	Weak transcription	Fetal Brain Male	brain
13	chr10:5768000-5849400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:5768600-5786400	Strong transcription	GM12878-XiMat	blood
15	chr10:5769400-5784200	Weak transcription	Psoas Muscle	Psoas
16	chr10:5771800-5790000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr10:5773000-5788400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr10:5773400-5781800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr10:5773600-5784200	Weak transcription	Small Intestine	intestine
20	chr10:5773600-5786000	Weak transcription	Right Ventricle	heart
21	chr10:5773800-5781800	Weak transcription	Brain Angular Gyrus	brain
22	chr10:5773800-5785800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:5773800-5788200	Weak transcription	Fetal Kidney	kidney
24	chr10:5774000-5781800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr10:5774000-5781800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr10:5774000-5781800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr10:5774000-5781800	Weak transcription	Colon Smooth Muscle	Colon
28	chr10:5774000-5788200	Weak transcription	Gastric	stomach
29	chr10:5774200-5781800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr10:5774200-5783800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr10:5774200-5786800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr10:5774400-5781800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr10:5774400-5781800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr10:5774400-5781800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr10:5774400-5781800	Weak transcription	Brain Anterior Caudate	brain
36	chr10:5774400-5781800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr10:5774400-5781800	Weak transcription	Brain Germinal Matrix	brain
38	chr10:5774400-5781800	Weak transcription	Brain Hippocampus Middle	brain
39	chr10:5774400-5781800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr10:5774400-5781800	Weak transcription	Spleen	Spleen
41	chr10:5774400-5782000	Weak transcription	Hela-S3	cervix
42	chr10:5774400-5785200	Weak transcription	NHLF	lung
43	chr10:5774400-5788200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr10:5774400-5788200	Weak transcription	Pancreas	Pancrea
45	chr10:5774400-5788400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr10:5774800-5788200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr10:5775000-5781800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr10:5775000-5785600	Weak transcription	Fetal Heart	heart
49	chr10:5775200-5794400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:5775400-5786200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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