Variant report

Variant	rs73334063
Chromosome Location	chr5:179265884-179265885
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr5:179265686-179265973	GM12878	blood:	n/a	n/a
2	POLR2A	chr5:179262507-179269414	PANC-1	pancreas:	n/a	n/a
3	POLR2A	chr5:179262587-179266982	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr5:179264312-179266003	A549	lung:	n/a	n/a
5	POLR2A	chr5:179262501-179268119	K562	blood:	n/a	n/a
6	POLR2A	chr5:179265544-179266012	GM12891	blood:	n/a	n/a
7	POLR2A	chr5:179262579-179266031	U87	brain:	n/a	n/a
8	ELF1	chr5:179265548-179266013	A549	lung:	n/a	n/a
9	POLR2A	chr5:179262980-179266031	U87	brain:	n/a	n/a
10	POLR2A	chr5:179265524-179265996	A549	lung:	n/a	n/a
11	POLR2A	chr5:179262538-179266058	GM12878	blood:	n/a	n/a
12	JUND	chr5:179264368-179267131	A549	lung:	n/a	n/a
13	POLR2A	chr5:179263086-179269260	IMR90	lung:	n/a	n/a
14	POLR2A	chr5:179263016-179266976	HepG2	liver:	n/a	n/a
15	POLR2A	chr5:179263338-179269338	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr5:179262885-179267061	PFSK-1	brain:	n/a	n/a
17	POLR2A	chr5:179262413-179266067	GM12892	blood:	n/a	n/a
18	TCF12	chr5:179265633-179267064	A549	lung:	n/a	chr5:179266813-179266823
19	POLR2A	chr5:179263085-179266079	MCF-7	breast:	n/a	n/a
20	POLR2A	chr5:179262516-179269530	A549	lung:	n/a	n/a
21	POLR2A	chr5:179263068-179266984	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr5:179265569-179265986	HepG2	liver:	n/a	n/a
23	POLR2A	chr5:179264249-179266062	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr5:179265725-179266013	GM12878	blood:	n/a	n/a
25	POLR2A	chr5:179265578-179265973	A549	lung:	n/a	n/a
26	POLR2A	chr5:179263161-179266048	K562	blood:	n/a	n/a
27	POLR2A	chr5:179262506-179266092	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr5:179262325-179266060	GM12892	blood:	n/a	n/a
29	POLR2A	chr5:179263029-179266942	K562	blood:	n/a	n/a
30	SIX5	chr5:179265650-179267039	A549	lung:	n/a	chr5:179266423-179266432
31	POLR2A	chr5:179262433-179266905	GM12891	blood:	n/a	n/a
32	POLR2A	chr5:179264226-179267122	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr5:179262474-179266063	GM12892	blood:	n/a	n/a
34	POLR2A	chr5:179262939-179269368	U87	brain:	n/a	n/a
35	BCL3	chr5:179262891-179267091	A549	lung:	n/a	n/a
36	POLR2A	chr5:179265500-179266063	GM12892	blood:	n/a	n/a
37	JUND	chr5:179265679-179266058	A549	lung:	n/a	n/a
38	POLR2A	chr5:179262545-179268187	HepG2	liver:	n/a	n/a
39	POLR2A	chr5:179265569-179265998	GM12878	blood:	n/a	n/a
40	POLR2A	chr5:179265785-179266018	HUVEC	blood vessel:	n/a	n/a
41	POLR2A	chr5:179265753-179265942	K562	blood:	n/a	n/a
42	POLR2A	chr5:179265533-179266004	GM12878	blood:	n/a	n/a
43	POLR2A	chr5:179262462-179266098	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr5:179264384-179266072	HUVEC	blood vessel:	n/a	n/a
45	PBX3	chr5:179265604-179266041	A549	lung:	n/a	n/a
46	POLR2A	chr5:179265537-179266044	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr5:179265585-179265971	A549	lung:	n/a	n/a
48	POLR2A	chr5:179262411-179266062	GM12878	blood:	n/a	n/a
49	POLR2A	chr5:179263187-179265973	GM19193	blood:	n/a	n/a
50	POLR2A	chr5:179262985-179266031	HCT-116	colon:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:179262940..179266304-chr5:179284329..179288957,4	K562	blood:
2	chr5:179265203..179267411-chr5:179270940..179272885,3	MCF-7	breast:

No data

Variant related genes	Relation type
C5orf45	TF binding region
ENSG00000161010	Chromatin interaction
ENSG00000222448	Chromatin interaction
ENSG00000245317	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs55782074	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55986721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56225166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57713691	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58652165	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58713160	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60403632	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60462250	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61613267	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61748794	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73334031	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73334055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73335948	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73351618	1.00[AMR][1000 genomes]
rs73810204	1.00[AMR][1000 genomes]
rs73810488	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949554	chr5:178832325-179309513	Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
2	nsv883270	chr5:178951106-179350387	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	312 gene(s)	inside rSNPs	diseases
3	nsv531997	chr5:179107599-179588082	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	339 gene(s)	inside rSNPs	diseases
4	nsv469579	chr5:179184831-179360191	Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
5	nsv883274	chr5:179186397-179310330	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
6	nsv883275	chr5:179193598-179267783	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
7	nsv883276	chr5:179193598-179310330	Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
8	nsv883277	chr5:179193598-179350387	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
9	nsv1030437	chr5:179235423-179649944	Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	189 gene(s)	inside rSNPs	diseases
10	nsv537982	chr5:179235423-179649944	Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	189 gene(s)	inside rSNPs	diseases
11	nsv948909	chr5:179249099-179772640	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers 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	175 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	chr5:179250200-179272000	Strong transcription	Fetal Muscle Leg	muscle
2	chr5:179250200-179272800	Weak transcription	Fetal Brain Male	brain
3	chr5:179251800-179267800	Strong transcription	Fetal Muscle Trunk	muscle
4	chr5:179255000-179268800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:179255200-179269000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:179255400-179266000	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr5:179258200-179274800	Weak transcription	Fetal Heart	heart
8	chr5:179261000-179266400	Weak transcription	Primary hematopoietic stem cells	blood
9	chr5:179262400-179266600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:179262400-179267000	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr5:179262400-179267400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr5:179262400-179268600	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr5:179262400-179269000	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr5:179262400-179269200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr5:179262400-179269400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:179262400-179269400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:179262400-179269400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:179262400-179269400	Strong transcription	Brain Angular Gyrus	brain
19	chr5:179262400-179271000	Strong transcription	Fetal Stomach	stomach
20	chr5:179262400-179271400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:179262400-179271600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr5:179262400-179272000	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:179262600-179266400	Strong transcription	Brain Cingulate Gyrus	brain
24	chr5:179262600-179269000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr5:179262600-179269000	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr5:179262600-179269200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr5:179262600-179279400	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr5:179262800-179266800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr5:179262800-179269200	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr5:179263000-179266000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr5:179263000-179266200	Genic enhancers	Pancreas	Pancrea
32	chr5:179263000-179266200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
33	chr5:179263000-179266200	Strong transcription	HSMM	muscle
34	chr5:179263000-179266400	Strong transcription	HMEC	breast
35	chr5:179263000-179267000	Genic enhancers	A549	lung
36	chr5:179263000-179268200	Strong transcription	Primary B cells from cord blood	blood
37	chr5:179263000-179269000	Strong transcription	Placenta Amnion	Placenta Amnion
38	chr5:179263000-179269200	Strong transcription	Primary T cells from cord blood	blood
39	chr5:179263000-179269800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr5:179263000-179271000	Strong transcription	Brain Germinal Matrix	brain
41	chr5:179263000-179271400	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr5:179263000-179271800	Strong transcription	Fetal Lung	lung
43	chr5:179263000-179279600	Strong transcription	Brain Anterior Caudate	brain
44	chr5:179263000-179279800	Strong transcription	Brain Hippocampus Middle	brain
45	chr5:179263000-179280400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr5:179263200-179266200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
47	chr5:179263200-179267200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr5:179263200-179268200	Strong transcription	Thymus	Thymus
49	chr5:179263200-179269000	Strong transcription	Brain Substantia Nigra	brain
50	chr5:179263200-179269600	Strong transcription	Fetal Brain Female	brain

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