Variant report

Variant	rs72772386
Chromosome Location	chr10:5846692-5846693
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:5841980..5844348-chr10:5846040..5847807,2	MCF-7	breast:
2	chr10:5831602..5838072-chr10:5842540..5850784,8	MCF-7	breast:
3	chr10:5846433..5848237-chr10:5929478..5933162,3	MCF-7	breast:
4	chr10:5841240..5842768-chr10:5845770..5847273,2	K562	blood:

Variant related genes	Relation type
ENSG00000134461	Chromatin interaction
ENSG00000134452	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs72772362	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72774107	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72774112	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72774114	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	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
3	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
4	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
5	nsv831775	chr10:5804335-6000849	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv515935	chr10:5820394-5869839	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv549896	chr10:5820394-5880066	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5768000-5849400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:5797400-5847400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:5818000-5854200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:5827800-5848800	Weak transcription	Stomach Mucosa	stomach
5	chr10:5827800-5851200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:5828800-5847000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:5832000-5848000	Weak transcription	Fetal Heart	heart
8	chr10:5834600-5853600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr10:5837800-5847000	Weak transcription	Psoas Muscle	Psoas
10	chr10:5837800-5854200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr10:5838000-5851400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr10:5838600-5851200	Weak transcription	Brain Angular Gyrus	brain
13	chr10:5838600-5851400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr10:5838800-5847400	Weak transcription	Hela-S3	cervix
15	chr10:5838800-5848800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr10:5838800-5849400	Weak transcription	Brain Substantia Nigra	brain
17	chr10:5838800-5851600	Weak transcription	Fetal Brain Male	brain
18	chr10:5840600-5851800	Weak transcription	Colonic Mucosa	Colon
19	chr10:5840800-5851600	Weak transcription	Fetal Kidney	kidney
20	chr10:5841400-5851400	Weak transcription	Aorta	Aorta
21	chr10:5841400-5851800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr10:5841400-5853400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:5841600-5848800	Weak transcription	Right Ventricle	heart
24	chr10:5841600-5848800	Weak transcription	Spleen	Spleen
25	chr10:5841600-5849600	Weak transcription	Lung	lung
26	chr10:5841600-5851400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr10:5841600-5853400	Weak transcription	Esophagus	oesophagus
28	chr10:5841800-5847600	Weak transcription	Left Ventricle	heart
29	chr10:5841800-5851200	Weak transcription	Brain Germinal Matrix	brain
30	chr10:5842000-5851200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr10:5842400-5847000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:5842400-5847400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr10:5842400-5847400	Weak transcription	Colon Smooth Muscle	Colon
34	chr10:5842400-5851400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr10:5842600-5847000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr10:5842600-5847200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr10:5842600-5847200	Weak transcription	Placenta	Placenta
38	chr10:5842600-5847600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:5842600-5847600	Weak transcription	NH-A	brain
40	chr10:5842600-5848000	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr10:5842600-5848200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr10:5842600-5848600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:5842600-5848800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr10:5842600-5849400	Weak transcription	Fetal Brain Female	brain
45	chr10:5842600-5850000	Weak transcription	Brain Hippocampus Middle	brain
46	chr10:5842600-5851400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr10:5842600-5851600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr10:5842600-5853200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr10:5842600-5853200	Weak transcription	HSMMtube	muscle
50	chr10:5842800-5847000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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