Variant report

Variant	rs954313
Chromosome Location	chr19:44981318-44981319
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:77)
CpG islands
(count:0)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:77 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr19:44980550-44981751	A549	lung:	n/a	n/a
2	TEAD4	chr19:44980700-44981679	K562	blood:	n/a	n/a
3	ELF1	chr19:44980554-44981689	A549	lung:	n/a	n/a
4	SP1	chr19:44980615-44981763	A549	lung:	n/a	n/a
5	USF1	chr19:44981284-44981703	A549	lung:	n/a	n/a
6	ZNF274	chr19:44980580-44981772	Hela-S3	cervix:	n/a	n/a
7	USF1	chr19:44980677-44981660	A549	lung:	n/a	n/a
8	TRIM28	chr19:44981299-44981740	K562	blood:	n/a	n/a
9	RCOR1	chr19:44980215-44981892	IMR90	lung:	n/a	n/a
10	TCF12	chr19:44980414-44981825	A549	lung:	n/a	n/a
11	POLR2A	chr19:44980613-44981614	GM12892	blood:	n/a	n/a
12	ZBTB33	chr19:44980582-44981677	A549	lung:	n/a	n/a
13	KAP1	chr19:44980120-44982096	HEK293	kidney:	n/a	n/a
14	USF2	chr19:44981287-44981511	Hela-S3	cervix:	n/a	n/a
15	SETDB1	chr19:44978505-44985135	K562	blood:	n/a	n/a
16	ZC3H11A	chr19:44980770-44981469	K562	blood:	n/a	n/a
17	ZBTB33	chr19:44980620-44981596	A549	lung:	n/a	n/a
18	POLR2A	chr19:44980574-44981871	HL-60	blood:	n/a	n/a
19	USF1	chr19:44980646-44981721	ECC-1	luminal epithelium:	n/a	n/a
20	KAP1	chr19:44979715-44982298	K562	blood:	n/a	n/a
21	ZNF274	chr19:44980077-44982157	HepG2	liver:	n/a	n/a
22	TCF12	chr19:44980599-44981866	ECC-1	luminal epithelium:	n/a	n/a
23	POLR2A	chr19:44978768-44981780	K562	blood:	n/a	n/a
24	ZNF143	chr19:44980575-44981732	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr19:44980756-44981745	HCT-116	colon:	n/a	n/a
26	POLR2A	chr19:44980630-44981332	H1-hESC	embryonic stem cell:	n/a	n/a
27	GATA3	chr19:44980650-44981810	A549	lung:	n/a	n/a
28	SETDB1	chr19:44978818-44983161	U2OS	brain:	n/a	n/a
29	ETS1	chr19:44980687-44981697	K562	blood:	n/a	n/a
30	POLR2A	chr19:44981306-44981628	K562	blood:	n/a	n/a
31	GTF2F1	chr19:44980686-44981730	H1-hESC	embryonic stem cell:	n/a	n/a
32	TCF12	chr19:44979878-44982187	A549	lung:	n/a	n/a
33	ATF3	chr19:44980461-44981688	A549	lung:	n/a	n/a
34	TRIM28	chr19:44980501-44981878	K562	blood:	n/a	n/a
35	POLR2A	chr19:44980582-44981594	SK-N-MC	brain:	n/a	n/a
36	TCF12	chr19:44980557-44981822	SK-N-SH	brain:	n/a	n/a
37	SETDB1	chr19:44980597-44981861	K562	blood:	n/a	n/a
38	ZNF143	chr19:44980559-44981727	K562	blood:	n/a	n/a
39	KAP1	chr19:44980176-44982083	U2OS	brain:	n/a	n/a
40	ZNF274	chr19:44980289-44981979	GM12878	blood:	n/a	n/a
41	MAX	chr19:44980564-44981796	A549	lung:	n/a	n/a
42	USF1	chr19:44980481-44981828	A549	lung:	n/a	n/a
43	ZNF274	chr19:44979731-44982378	H1-hESC	embryonic stem cell:	n/a	n/a
44	TEAD4	chr19:44980717-44981410	K562	blood:	n/a	n/a
45	TCF12	chr19:44980462-44981887	ECC-1	luminal epithelium:	n/a	n/a
46	POLR2A	chr19:44981245-44981684	K562	blood:	n/a	n/a
47	EP300	chr19:44980561-44981742	A549	lung:	n/a	n/a
48	TCF12	chr19:44980471-44981579	MCF-7	breast:	n/a	n/a
49	USF1	chr19:44980604-44981783	ECC-1	luminal epithelium:	n/a	n/a
50	GATA3	chr19:44980538-44981763	SK-N-SH	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:44969208..44972041-chr19:44979244..44981448,2	K562	blood:
2	chr19:44765918..44767537-chr19:44979922..44981810,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000267242	TF binding region
ENSG00000176761	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11881628	0.85[ASN][1000 genomes]
rs12611267	0.89[ASN][1000 genomes]
rs12975841	1.00[AFR][1000 genomes]
rs1434577	1.00[AFR][1000 genomes]
rs17727484	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2020083	1.00[ASN][1000 genomes]
rs2293164	1.00[ASN][1000 genomes]
rs2571056	0.84[ASN][1000 genomes]
rs2571108	0.86[ASN][1000 genomes]
rs2571109	0.86[ASN][1000 genomes]
rs2686759	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2686779	0.82[ASN][1000 genomes]
rs3745146	0.98[ASN][1000 genomes]
rs3745147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4141695	1.00[ASN][1000 genomes]
rs45562836	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs566838	0.82[ASN][1000 genomes]
rs60625660	0.91[ASN][1000 genomes]
rs612890	0.82[ASN][1000 genomes]
rs8104374	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv912112	chr19:44853707-45011727	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv912114	chr19:44858776-45002563	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1061350	chr19:44869075-45035469	Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv912115	chr19:44957508-44995990	ZNF genes & repeats Weak transcription Strong transcription Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv960853	chr19:44958445-44982821	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv978867	chr19:44963452-44982821	ZNF genes & repeats Strong transcription Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44966800-44992400	ZNF genes & repeats	Liver	Liver
2	chr19:44967200-44992800	ZNF genes & repeats	Adipose Nuclei	Adipose
3	chr19:44969800-44992200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:44971600-44992200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
5	chr19:44972600-44992200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
6	chr19:44975200-44992200	ZNF genes & repeats	Fetal Brain Female	brain
7	chr19:44975400-44992200	ZNF genes & repeats	Brain Hippocampus Middle	brain
8	chr19:44975600-44990000	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
9	chr19:44975600-44992200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
10	chr19:44975800-44992200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
11	chr19:44975800-44992200	ZNF genes & repeats	Brain Anterior Caudate	brain
12	chr19:44976000-44992400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
13	chr19:44976400-44992000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:44976400-44992000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
15	chr19:44976600-44992000	ZNF genes & repeats	Rectal Smooth Muscle	rectum
16	chr19:44976600-44992200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
17	chr19:44976600-44992200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
18	chr19:44976600-44992400	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
19	chr19:44977000-44989800	ZNF genes & repeats	Brain Angular Gyrus	brain
20	chr19:44977000-44990200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
21	chr19:44977000-44992000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
22	chr19:44977000-44992200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
23	chr19:44977000-44992200	ZNF genes & repeats	Brain Substantia Nigra	brain
24	chr19:44977000-44992400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
25	chr19:44977000-44992400	ZNF genes & repeats	Primary T killer memory cells from peripheral blood	blood
26	chr19:44977200-44987600	ZNF genes & repeats	Left Ventricle	heart
27	chr19:44977200-44991800	ZNF genes & repeats	Colon Smooth Muscle	Colon
28	chr19:44977200-44992000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
29	chr19:44977200-44992000	ZNF genes & repeats	Stomach Smooth Muscle	stomach
30	chr19:44977200-44992200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
31	chr19:44977200-44992800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr19:44977400-44987600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:44977400-44989600	ZNF genes & repeats	Right Ventricle	heart
34	chr19:44977400-44990000	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr19:44977400-44992000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
36	chr19:44977400-44992200	ZNF genes & repeats	Fetal Lung	lung
37	chr19:44977400-44992400	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
38	chr19:44977400-44992400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr19:44977600-44981600	ZNF genes & repeats	Right Atrium	heart
40	chr19:44977600-44989800	ZNF genes & repeats	Ovary	ovary
41	chr19:44977600-44992000	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr19:44977600-44992200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr19:44977800-44989200	ZNF genes & repeats	NH-A	brain
44	chr19:44977800-44989600	ZNF genes & repeats	Fetal Brain Male	brain
45	chr19:44977800-44992000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
46	chr19:44977800-44992000	ZNF genes & repeats	Brain Germinal Matrix	brain
47	chr19:44977800-44992200	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:44977800-44992200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr19:44977800-44992600	ZNF genes & repeats	Primary B cells from peripheral blood	blood
50	chr19:44977800-44992600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood

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