Variant report

Variant	rs73038930
Chromosome Location	chr19:39209286-39209287
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:39197861..39200154-chr19:39208243..39210310,2	MCF-7	breast:
2	chr19:39207119..39209379-chr19:39340963..39342887,2	K562	blood:
3	chr19:39141347..39144030-chr19:39208371..39211834,3	MCF-7	breast:
4	chr19:39207779..39209795-chr19:39227154..39229627,2	MCF-7	breast:
5	chr19:39202818..39205555-chr19:39206868..39209450,2	K562	blood:
6	chr19:39207862..39211804-chr19:39330654..39334530,3	MCF-7	breast:
7	chr19:39196541..39198571-chr19:39208360..39211296,2	K562	blood:
8	chr19:39151274..39153019-chr19:39209216..39212183,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000182472	Chromatin interaction
ENSG00000130402	Chromatin interaction
ENSG00000104824	Chromatin interaction
ENSG00000267892	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11553600	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12052046	1.00[ASN][1000 genomes]
rs17589415	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17665451	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41482151	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45468197	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4616403	1.00[ASN][1000 genomes]
rs4802744	1.00[ASN][1000 genomes]
rs4802747	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4802775	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67438539	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67953948	1.00[ASN][1000 genomes]
rs7258742	1.00[ASN][1000 genomes]
rs73032668	1.00[ASN][1000 genomes]
rs73032691	1.00[ASN][1000 genomes]
rs73032697	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73034621	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038909	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038918	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038924	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038932	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73038936	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73038948	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7351086	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8103824	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8182484	0.86[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs888995	1.00[ASN][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	nsv833828	chr19:39084759-39257979	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv817834	chr19:39174332-39237950	Enhancers Flanking Active TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv911668	chr19:39174669-39291771	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	esv1826260	chr19:39178364-39248836	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
6	esv1837023	chr19:39190588-39425722	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
7	nsv911669	chr19:39196745-39231548	Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr19:39182200-39214200	Genic enhancers	Fetal Muscle Trunk	muscle
2	chr19:39182200-39225200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:39186400-39213400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr19:39189400-39223400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr19:39189800-39222800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr19:39190000-39218400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr19:39190200-39222600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr19:39190200-39222800	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr19:39190400-39212000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr19:39190400-39212200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr19:39190400-39217000	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr19:39190400-39218000	Strong transcription	Primary T cells from cord blood	blood
13	chr19:39190400-39222400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:39190400-39222600	Strong transcription	Dnd41	blood
15	chr19:39190600-39216400	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr19:39190600-39217000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr19:39190600-39219600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr19:39190600-39222800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr19:39190800-39220400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr19:39190800-39222600	Strong transcription	Primary B cells from peripheral blood	blood
21	chr19:39190800-39222600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr19:39190800-39222800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr19:39190800-39223000	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr19:39190800-39223000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:39191000-39222400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr19:39191000-39222600	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr19:39191400-39209400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr19:39191400-39218800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
29	chr19:39192400-39221200	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr19:39192800-39209600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr19:39193400-39210200	Strong transcription	Brain Germinal Matrix	brain
32	chr19:39199000-39215600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:39199000-39220400	Strong transcription	Rectal Mucosa Donor 31	rectum
34	chr19:39199400-39215400	Weak transcription	Fetal Kidney	kidney
35	chr19:39199800-39214600	Strong transcription	HUVEC	blood vessel
36	chr19:39200200-39209400	Strong transcription	Fetal Intestine Large	intestine
37	chr19:39200400-39217200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr19:39202400-39209400	Strong transcription	Colonic Mucosa	Colon
39	chr19:39202800-39221400	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr19:39203200-39209400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr19:39203400-39218600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr19:39204000-39209600	Strong transcription	Osteobl	bone
43	chr19:39204200-39223400	Strong transcription	H9 Cell Line	embryonic stem cell
44	chr19:39204600-39209600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr19:39204600-39209600	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr19:39204600-39211800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr19:39205000-39209400	Strong transcription	Fetal Stomach	stomach
48	chr19:39205000-39209400	Strong transcription	HepG2	liver
49	chr19:39205000-39210600	Strong transcription	Fetal Lung	lung
50	chr19:39205000-39221000	Strong transcription	Duodenum Mucosa	Duodenum

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