Variant report

Variant	rs73599586
Chromosome Location	chr19:36420781-36420782
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:36208876..36211502-chr19:36420769..36422543,2	K562	blood:
2	chr19:36247011..36249990-chr19:36420044..36422413,2	K562	blood:
3	chr19:36379793..36382037-chr19:36419529..36422363,2	MCF-7	breast:
4	chr19:36389300..36392686-chr19:36419635..36422381,3	MCF-7	breast:
5	chr19:36420760..36422359-chr19:36480786..36482872,2	K562	blood:
6	chr19:36415212..36417969-chr19:36419526..36423356,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167595	Chromatin interaction
ENSG00000272333	Chromatin interaction
ENSG00000004776	Chromatin interaction
ENSG00000167604	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10221486	0.86[EUR][1000 genomes]
rs1057265	0.90[EUR][1000 genomes]
rs11878444	0.90[EUR][1000 genomes]
rs11878880	0.82[EUR][1000 genomes]
rs11879537	0.86[EUR][1000 genomes]
rs11881157	0.86[EUR][1000 genomes]
rs11882386	0.90[EUR][1000 genomes]
rs13382036	0.86[EUR][1000 genomes]
rs2242590	0.90[EUR][1000 genomes]
rs34933126	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56744930	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56922307	0.90[EUR][1000 genomes]
rs57068163	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57094555	0.90[EUR][1000 genomes]
rs57412339	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57516855	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57962062	0.86[EUR][1000 genomes]
rs58161969	0.90[EUR][1000 genomes]
rs58456578	0.86[EUR][1000 genomes]
rs58504183	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58551711	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58622306	1.00[ASN][1000 genomes]
rs58976020	0.86[EUR][1000 genomes]
rs59150589	0.86[EUR][1000 genomes]
rs59399698	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59416903	0.86[EUR][1000 genomes]
rs59478831	0.89[EUR][1000 genomes]
rs59534183	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60073802	0.90[EUR][1000 genomes]
rs60935148	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61660311	0.90[EUR][1000 genomes]
rs61672461	1.00[EUR][1000 genomes]
rs7246259	0.86[EUR][1000 genomes]
rs7246541	0.86[EUR][1000 genomes]
rs7247000	0.86[EUR][1000 genomes]
rs7252526	0.86[EUR][1000 genomes]
rs7253086	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7254335	0.86[EUR][1000 genomes]
rs7256280	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7256433	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7257789	0.86[EUR][1000 genomes]
rs7257911	0.86[EUR][1000 genomes]
rs7258914	0.86[EUR][1000 genomes]
rs7260613	0.89[EUR][1000 genomes]
rs73590883	0.89[EUR][1000 genomes]
rs73590895	0.85[EUR][1000 genomes]
rs73599539	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73599540	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73599546	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73599554	0.86[EUR][1000 genomes]
rs73599561	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73599565	0.90[EUR][1000 genomes]
rs73599577	0.90[EUR][1000 genomes]
rs73599600	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73599602	0.90[EUR][1000 genomes]
rs73928364	0.86[EUR][1000 genomes]
rs8110868	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs909135	0.95[EUR][1000 genomes]
rs909136	0.95[EUR][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	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv911638	chr19:36265508-36537959	Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv3526489	chr19:36306483-36741945	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	esv3526490	chr19:36306483-36741945	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
5	esv1831737	chr19:36324324-36690874	Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
6	nsv833812	chr19:36331913-36507594	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
7	nsv833813	chr19:36341181-36499431	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:36414200-36421400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr19:36417200-36422000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr19:36417800-36421800	Enhancers	Primary B cells from cord blood	blood
4	chr19:36418400-36422000	Enhancers	Primary B cells from peripheral blood	blood
5	chr19:36418400-36422000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr19:36419000-36420800	Enhancers	GM12878-XiMat	blood
7	chr19:36419000-36422000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr19:36419200-36422000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr19:36419400-36420800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr19:36419400-36420800	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr19:36419400-36420800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:36419400-36422000	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr19:36419400-36422000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr19:36419600-36420800	Enhancers	Primary T cells from cord blood	blood
15	chr19:36419600-36420800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
16	chr19:36419600-36421400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
17	chr19:36419600-36422000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:36419600-36422000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:36420000-36422000	Weak transcription	Fetal Kidney	kidney
20	chr19:36420200-36421800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr19:36420400-36422000	Enhancers	Primary hematopoietic stem cells	blood
22	chr19:36420400-36423000	Enhancers	Fetal Thymus	thymus
23	chr19:36420600-36421000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr19:36420600-36421000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
25	chr19:36420600-36421000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:36420600-36421000	Enhancers	Duodenum Mucosa	Duodenum
27	chr19:36420600-36421200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr19:36420600-36421200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr19:36420600-36422000	Enhancers	Dnd41	blood
30	chr19:36420600-36422400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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