Variant report

Variant	rs72805481
Chromosome Location	chr2:55863868-55863869
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:55857547..55860047-chr2:55862706..55864207,2	MCF-7	breast:
2	chr2:55862409..55864848-chr2:55873720..55876031,2	K562	blood:
3	chr2:54201384..54203059-chr2:55863159..55864990,2	K562	blood:

Variant related genes	Relation type
ENSG00000138035	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10496045	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28451828	0.87[EUR][1000 genomes]
rs72805471	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805472	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805484	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805490	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805494	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805500	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72805501	0.87[EUR][1000 genomes]
rs72807608	0.87[EUR][1000 genomes]
rs72807616	0.87[EUR][1000 genomes]
rs72807624	0.87[EUR][1000 genomes]
rs72812157	0.81[EUR][1000 genomes]
rs72812162	0.81[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	nsv520581	chr2:55622825-55903016	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv531374	chr2:55653723-56299784	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv834080	chr2:55741036-55927928	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	esv2757798	chr2:55747239-55981074	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	esv2759050	chr2:55747239-55981074	Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv1008452	chr2:55809191-55987274	Strong transcription Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 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	chr2:55846400-55870000	Weak transcription	Aorta	Aorta
2	chr2:55846600-55870000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:55846600-55870000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:55846800-55919800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:55847400-55911000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr2:55847600-55864200	Weak transcription	Brain Germinal Matrix	brain
7	chr2:55847600-55870000	Weak transcription	Colonic Mucosa	Colon
8	chr2:55847600-55870000	Weak transcription	Psoas Muscle	Psoas
9	chr2:55847600-55886600	Weak transcription	Stomach Mucosa	stomach
10	chr2:55848000-55872600	Weak transcription	Small Intestine	intestine
11	chr2:55849200-55865200	Weak transcription	Gastric	stomach
12	chr2:55849200-55865600	Weak transcription	Fetal Brain Female	brain
13	chr2:55849200-55867400	Weak transcription	Lung	lung
14	chr2:55849200-55868200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:55849200-55868200	Weak transcription	Right Ventricle	heart
16	chr2:55849200-55869400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:55849200-55873200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr2:55849400-55867400	Weak transcription	Thymus	Thymus
19	chr2:55849800-55869400	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr2:55849800-55882800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:55851400-55870000	Weak transcription	Spleen	Spleen
22	chr2:55852000-55865800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr2:55852000-55872400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr2:55853200-55864000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr2:55853600-55882400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr2:55857000-55873800	Strong transcription	Fetal Thymus	thymus
27	chr2:55857600-55869800	Weak transcription	Brain Angular Gyrus	brain
28	chr2:55858200-55920400	Weak transcription	Fetal Heart	heart
29	chr2:55858600-55871600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:55858800-55873400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr2:55858800-55875600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr2:55858800-55877200	Strong transcription	Dnd41	blood
33	chr2:55859000-55876800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:55859000-55877000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:55859000-55877200	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr2:55859200-55874000	Weak transcription	Pancreas	Pancrea
37	chr2:55859400-55875600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:55859400-55877600	Strong transcription	HUES48 Cell Line	embryonic stem cell
39	chr2:55859800-55871200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr2:55859800-55871400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:55859800-55873200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr2:55859800-55873600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
43	chr2:55860200-55864000	Weak transcription	HMEC	breast
44	chr2:55860400-55905400	Weak transcription	Fetal Brain Male	brain
45	chr2:55860600-55869800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr2:55860800-55871200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr2:55861800-55865400	Strong transcription	Rectal Mucosa Donor 29	rectum
48	chr2:55861800-55868000	Strong transcription	Liver	Liver
49	chr2:55861800-55875000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr2:55861800-55875800	Strong transcription	Primary monocytes fromperipheralblood	blood

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