Variant report

Variant	rs73131157
Chromosome Location	chr1:224020875-224020876
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	chr1:223998652..224000420-chr1:224020765..224022326,2	MCF-7	breast:
2	chr1:224017359..224022811-chr1:224031085..224036329,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000143514	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12038706	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16842157	1.00[AMR][1000 genomes]
rs16842168	1.00[AMR][1000 genomes]
rs16842198	1.00[AMR][1000 genomes]
rs28370148	1.00[AMR][1000 genomes]
rs28370168	1.00[AMR][1000 genomes]
rs28370180	1.00[AMR][1000 genomes]
rs28370183	1.00[AMR][1000 genomes]
rs56831338	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57108544	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57153784	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58391315	1.00[AMR][1000 genomes]
rs59173114	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60245976	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60799191	0.98[AFR][1000 genomes]
rs60956486	1.00[AMR][1000 genomes]
rs73114404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73114482	1.00[AMR][1000 genomes]
rs73114500	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73114501	0.80[AFR][1000 genomes]
rs73115632	1.00[AMR][1000 genomes]
rs73116403	0.82[AFR][1000 genomes]
rs73116433	1.00[AMR][1000 genomes]
rs73116444	1.00[AMR][1000 genomes]
rs73116448	1.00[AMR][1000 genomes]
rs73127419	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73127431	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73127434	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73127439	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73128039	1.00[AMR][1000 genomes]
rs73128040	1.00[AMR][1000 genomes]
rs73128044	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73131132	1.00[AMR][1000 genomes]
rs73131150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73131162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73131164	0.98[AFR][1000 genomes];1.00[AMR][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	esv3361888	chr1:223725597-224114846	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv1007380	chr1:223834380-224042190	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv535310	chr1:223834380-224042190	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	esv34082	chr1:223851018-224144509	Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
5	nsv1008800	chr1:223904653-224061032	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	esv2757772	chr1:223935220-224363163	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	esv2759000	chr1:223935220-224363163	Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223960200-224025400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:224002000-224023800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:224007000-224024000	Weak transcription	Fetal Intestine Small	intestine
4	chr1:224009400-224023800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr1:224010200-224026400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr1:224013800-224021600	Weak transcription	Ovary	ovary
7	chr1:224014200-224021400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr1:224014200-224023400	Weak transcription	Thymus	Thymus
9	chr1:224014200-224023400	Weak transcription	Dnd41	blood
10	chr1:224014200-224024400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:224015200-224023800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr1:224015400-224023600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr1:224015400-224025000	Weak transcription	Fetal Stomach	stomach
14	chr1:224015800-224024200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr1:224017000-224021200	Weak transcription	Primary B cells from cord blood	blood
16	chr1:224017600-224022600	Weak transcription	Fetal Kidney	kidney
17	chr1:224017600-224026800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:224019000-224026400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr1:224019400-224021000	Enhancers	Fetal Lung	lung
20	chr1:224019400-224021000	Enhancers	Hela-S3	cervix
21	chr1:224019400-224021000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr1:224019400-224021200	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr1:224019400-224021800	Enhancers	Primary hematopoietic stem cells	blood
24	chr1:224019400-224021800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr1:224019400-224022400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr1:224019400-224022600	Enhancers	Brain Anterior Caudate	brain
27	chr1:224019400-224022600	Enhancers	K562	blood
28	chr1:224019400-224023400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr1:224019400-224024800	Enhancers	Brain Hippocampus Middle	brain
30	chr1:224019400-224025400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr1:224019400-224025600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:224019400-224026400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr1:224019400-224026400	Enhancers	Primary T cells from cord blood	blood
34	chr1:224019400-224027000	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr1:224019600-224021000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr1:224019600-224024600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr1:224019600-224024600	Enhancers	Brain Cingulate Gyrus	brain
38	chr1:224019600-224027400	Enhancers	Fetal Heart	heart
39	chr1:224019800-224021200	Enhancers	Colon Smooth Muscle	Colon
40	chr1:224019800-224022400	Enhancers	NHDF-Ad	bronchial
41	chr1:224019800-224025400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr1:224019800-224026600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr1:224020000-224021000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr1:224020000-224024800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr1:224020200-224021000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr1:224020200-224021000	Enhancers	Pancreas	Pancrea
47	chr1:224020200-224021000	Enhancers	Psoas Muscle	Psoas
48	chr1:224020200-224022200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:224020200-224022400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:224020200-224026400	Enhancers	HUVEC	blood vessel

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