Variant report

Variant	rs62110447
Chromosome Location	chr19:52801386-52801387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HEY1	chr19:52800351-52801420	K562	blood:	n/a	n/a
2	POLR2A	chr19:52800329-52801682	GM12878	blood:	n/a	n/a
3	MAZ	chr19:52799619-52801613	IMR90	lung:	n/a	n/a
4	MAX	chr19:52800363-52801565	K562	blood:	n/a	n/a
5	POLR2A	chr19:52799967-52801511	GM12878	blood:	n/a	n/a
6	POLR2A	chr19:52800362-52801595	GM12878	blood:	n/a	n/a
7	REST	chr19:52799805-52801604	H1-neurons	neurons:	n/a	chr19:52800663-52800676 chr19:52800568-52800581 chr19:52800838-52800845 chr19:52801431-52801444 chr19:52800751-52800764 chr19:52801427-52801437
8	MXI1	chr19:52799569-52801627	SK-N-SH	brain:	n/a	n/a
9	POLR2A	chr19:52801207-52801635	K562	blood:	n/a	n/a
10	SIN3A	chr19:52801331-52801413	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr19:52800309-52801570	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr19:52800028-52801511	IMR90	lung:	n/a	n/a
13	MXI1	chr19:52799779-52801694	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:52776723..52778376-chr19:52800239..52801922,2	K562	blood:
2	chr19:52799793..52802447-chr19:52803288..52807131,4	MCF-7	breast:
3	chr19:52772363..52775107-chr19:52799601..52802037,4	MCF-7	breast:
4	chr19:52799531..52802059-chr19:52803187..52805101,2	K562	blood:
5	chr19:52800699..52803892-chr19:52837325..52840976,3	MCF-7	breast:

Variant related genes	Relation type
ZNF480	TF binding region
ENSG00000269102	TF binding region
ENSG00000196214	Chromatin interaction
ENSG00000198464	Chromatin interaction
ENSG00000167554	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1048399	1.00[ASN][1000 genomes]
rs55783720	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56186790	1.00[ASN][1000 genomes]
rs62109258	1.00[ASN][1000 genomes]
rs62110407	1.00[ASN][1000 genomes]
rs62110409	1.00[ASN][1000 genomes]
rs62110410	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62110415	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065410	chr19:52103914-52889530	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	596 gene(s)	inside rSNPs	diseases
2	esv3366000	chr19:52491073-52842946	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv1066015	chr19:52502213-52890308	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	nsv544059	chr19:52502213-52890308	Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv833873	chr19:52788939-52937281	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv912299	chr19:52795985-52832830	ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:52799600-52801400	Active TSS	H9 Cell Line	embryonic stem cell
2	chr19:52799600-52801400	Active TSS	Fetal Intestine Small	intestine
3	chr19:52799600-52801400	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr19:52799600-52801400	Active TSS	GM12878-XiMat	blood
5	chr19:52799600-52801600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr19:52799600-52801600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr19:52799600-52801600	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr19:52799600-52801600	Active TSS	Fetal Kidney	kidney
9	chr19:52799600-52801800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:52799600-52801800	Active TSS	Colonic Mucosa	Colon
11	chr19:52799800-52801400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr19:52799800-52801400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr19:52799800-52801400	Active TSS	Aorta	Aorta
14	chr19:52799800-52801400	Active TSS	Ovary	ovary
15	chr19:52799800-52801600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr19:52799800-52801600	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr19:52799800-52801600	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr19:52799800-52801600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:52799800-52801600	Active TSS	Fetal Intestine Large	intestine
20	chr19:52799800-52801600	Active TSS	HSMM	muscle
21	chr19:52799800-52801600	Active TSS	NHDF-Ad	bronchial
22	chr19:52799800-52801800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr19:52800000-52801400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr19:52800000-52801400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr19:52800000-52801400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:52800000-52801400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr19:52800000-52801400	Active TSS	NHEK	skin
28	chr19:52800000-52801600	Active TSS	Fetal Brain Female	brain
29	chr19:52800000-52802000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr19:52800200-52801400	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr19:52800200-52801600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:52800400-52801400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr19:52800600-52801400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
34	chr19:52800600-52801400	Flanking Active TSS	Primary B cells from peripheral blood	blood
35	chr19:52800600-52801400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
36	chr19:52800600-52801600	Flanking Active TSS	Primary B cells from cord blood	blood
37	chr19:52800600-52801600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr19:52800600-52801600	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr19:52800600-52802600	Transcr. at gene 5' and 3'	Dnd41	blood
40	chr19:52800800-52801400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
41	chr19:52800800-52801400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr19:52800800-52801400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr19:52800800-52801400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
44	chr19:52800800-52801400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr19:52800800-52801400	Flanking Active TSS	Thymus	Thymus
46	chr19:52800800-52801400	Flanking Active TSS	Hela-S3	cervix
47	chr19:52800800-52801400	Flanking Active TSS	HSMMtube	muscle
48	chr19:52800800-52801600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
49	chr19:52800800-52801600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
50	chr19:52800800-52801600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood

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