Variant report

Variant	rs73523072
Chromosome Location	chr19:18538834-18538835
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:18538551-18551124	K562	blood:	n/a	n/a
2	POLR2A	chr19:18534926-18553479	K562	blood:	n/a	n/a

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18538215..18540689-chr19:18541318..18544057,3	MCF-7	breast:
2	chr19:18527431..18533703-chr19:18536573..18544512,11	MCF-7	breast:
3	chr19:18384108..18395354-chr19:18534355..18544725,18	K562	blood:
4	chr19:18401175..18404023-chr19:18537863..18539807,2	K562	blood:
5	chr19:18537918..18539910-chr19:18546510..18549015,3	MCF-7	breast:
6	chr19:18483975..18485616-chr19:18538435..18540189,2	K562	blood:
7	chr19:18388633..18392429-chr19:18537213..18541674,5	K562	blood:
8	chr19:18385704..18387487-chr19:18538825..18541635,2	K562	blood:

No data

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000130513	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000130511	Chromatin interaction
ENSG00000105655	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10403002	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11574806	1.00[EUR][1000 genomes]
rs16982418	0.87[EUR][1000 genomes]
rs16982427	0.87[EUR][1000 genomes]
rs16982429	0.87[EUR][1000 genomes]
rs16982485	0.87[EUR][1000 genomes]
rs2314669	1.00[EUR][1000 genomes]
rs34078075	0.87[EUR][1000 genomes]
rs34868531	0.87[EUR][1000 genomes]
rs35328461	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs58410315	0.87[EUR][1000 genomes]
rs58604797	0.87[EUR][1000 genomes]
rs58723610	0.87[EUR][1000 genomes]
rs58842178	0.87[EUR][1000 genomes]
rs59511380	0.87[EUR][1000 genomes]
rs59549953	0.87[EUR][1000 genomes]
rs60687616	0.87[EUR][1000 genomes]
rs61743938	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61743954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73523074	1.00[EUR][1000 genomes]
rs8101976	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
2	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
3	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
4	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
6	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription 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	61 gene(s)	inside rSNPs	diseases
7	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
8	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
9	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
11	nsv911278	chr19:18526536-18550276	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	39 gene(s)	inside rSNPs	diseases
12	nsv911279	chr19:18533642-18550276	Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
13	nsv911280	chr19:18533642-18552139	Genic enhancers Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv532615	chr19:18534867-18796031	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18531200-18540000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr19:18531400-18539400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr19:18531400-18539600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:18531400-18539800	Weak transcription	Brain Substantia Nigra	brain
5	chr19:18531400-18543000	Enhancers	Fetal Brain Male	brain
6	chr19:18531800-18539600	Genic enhancers	Fetal Stomach	stomach
7	chr19:18532400-18539400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr19:18532400-18539600	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr19:18532800-18547600	Weak transcription	HepG2	liver
10	chr19:18533800-18539200	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr19:18533800-18541000	Enhancers	Placenta	Placenta
12	chr19:18534000-18539400	Weak transcription	Primary B cells from cord blood	blood
13	chr19:18534000-18539600	Enhancers	Primary T cells fromperipheralblood	blood
14	chr19:18534000-18539600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr19:18534000-18539600	Weak transcription	HUVEC	blood vessel
16	chr19:18534200-18540200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr19:18534400-18539200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:18534400-18539400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:18534600-18539800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr19:18534800-18539000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr19:18534800-18539200	Weak transcription	Dnd41	blood
22	chr19:18535000-18539400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:18535200-18539000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr19:18535200-18539200	Weak transcription	Stomach Mucosa	stomach
25	chr19:18535200-18539600	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr19:18535400-18539200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr19:18535400-18539600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr19:18535600-18539000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:18535800-18539400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr19:18535800-18539600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr19:18535800-18539600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr19:18535800-18539800	Weak transcription	Small Intestine	intestine
33	chr19:18536200-18539600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr19:18536200-18539600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr19:18536200-18539600	Enhancers	A549	lung
36	chr19:18536200-18541200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr19:18536400-18539200	Genic enhancers	Fetal Brain Female	brain
38	chr19:18536600-18539600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr19:18536600-18539600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr19:18536600-18542200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr19:18536800-18539000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr19:18537000-18539000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr19:18537000-18539200	Weak transcription	Fetal Lung	lung
44	chr19:18537000-18539400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr19:18537000-18539600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr19:18537000-18540000	Weak transcription	Pancreas	Pancrea
47	chr19:18537200-18539200	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr19:18537400-18539000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr19:18537400-18539000	Weak transcription	Brain Germinal Matrix	brain
50	chr19:18537400-18539200	Strong transcription	Gastric	stomach

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