Variant report

Variant	nsv978435
Chromosome Location	chr17:45758314-45761310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr17:45761258-45762330	K562	blood:	n/a	chr17:45762320-45762329 chr17:45761498-45761507
2	BCL3	chr17:45761066-45765975	A549	lung:	n/a	chr17:45762320-45762329 chr17:45761498-45761507
3	BCLAF1	chr17:45761159-45761555	K562	blood:	n/a	chr17:45761498-45761507
4	GATA3	chr17:45759593-45759697	SH-SY5Y	brain:	n/a	n/a
5	MAFF	chr17:45759553-45759870	K562	blood:	n/a	chr17:45759695-45759713
6	MAFF	chr17:45759514-45759879	HepG2	liver:	n/a	chr17:45759695-45759713
7	MAFK	chr17:45759515-45759885	HepG2	liver:	n/a	chr17:45759701-45759712 chr17:45759696-45759711 chr17:45759701-45759712 chr17:45759699-45759713 chr17:45759696-45759712 chr17:45759700-45759711
8	MAFK	chr17:45759570-45759852	K562	blood:	n/a	chr17:45759701-45759712 chr17:45759696-45759711 chr17:45759701-45759712 chr17:45759699-45759713 chr17:45759696-45759712 chr17:45759700-45759711
9	MAFK	chr17:45759528-45759859	IMR90	lung:	n/a	chr17:45759701-45759712 chr17:45759696-45759711 chr17:45759701-45759712 chr17:45759699-45759713 chr17:45759696-45759712 chr17:45759700-45759711
10	MAFK	chr17:45759571-45759802	Hela-S3	cervix:	n/a	chr17:45759701-45759712 chr17:45759696-45759711 chr17:45759701-45759712 chr17:45759699-45759713 chr17:45759696-45759712 chr17:45759700-45759711
11	MAFK	chr17:45759522-45759875	HepG2	liver:	n/a	chr17:45759701-45759712 chr17:45759696-45759711 chr17:45759701-45759712 chr17:45759699-45759713 chr17:45759696-45759712 chr17:45759700-45759711
12	MTA3	chr17:45761054-45763668	GM12878	blood:	n/a	n/a
13	NFATC1	chr17:45761304-45763295	GM12878	blood:	n/a	n/a
14	NFATC1	chr17:45761035-45763870	GM12878	blood:	n/a	n/a
15	NR2F2	chr17:45761158-45761504	K562	blood:	n/a	n/a
16	PML	chr17:45761034-45762236	K562	blood:	n/a	n/a
17	PML	chr17:45761117-45763912	GM12878	blood:	n/a	n/a
18	POLR2A	chr17:45760971-45765833	K562	blood:	n/a	n/a
19	POLR2A	chr17:45760763-45762718	GM12878	blood:	n/a	n/a
20	POLR2A	chr17:45759085-45759201	GM12878	blood:	n/a	n/a
21	POLR2A	chr17:45759091-45759524	HL-60	blood:	n/a	n/a
22	POLR2A	chr17:45757198-45758558	GM12892	blood:	n/a	n/a
23	POLR2A	chr17:45760881-45765759	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr17:45758069-45758502	GM12878	blood:	n/a	n/a
25	POLR2A	chr17:45759361-45760472	GM12878	blood:	n/a	n/a
26	POLR2A	chr17:45760700-45764174	GM12891	blood:	n/a	n/a
27	POLR2A	chr17:45760028-45760414	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr17:45761166-45766789	SK-N-MC	brain:	n/a	n/a
29	POLR2A	chr17:45757884-45760003	HepG2	liver:	n/a	n/a
30	POLR2A	chr17:45759822-45760348	K562	blood:	n/a	n/a
31	POLR2A	chr17:45760984-45765870	U87	brain:	n/a	n/a
32	POLR2A	chr17:45761242-45762582	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr17:45761123-45765686	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr17:45761148-45763557	K562	blood:	n/a	n/a
35	POLR2A	chr17:45759005-45760432	SK-N-MC	brain:	n/a	n/a
36	POLR2A	chr17:45761106-45762863	GM12891	blood:	n/a	n/a
37	POLR2A	chr17:45759983-45760400	GM12891	blood:	n/a	n/a
38	POLR2A	chr17:45759548-45759748	HepG2	liver:	n/a	n/a
39	POLR2A	chr17:45760022-45760354	K562	blood:	n/a	n/a
40	POLR2A	chr17:45757138-45758580	GM12892	blood:	n/a	n/a
41	POLR2A	chr17:45759842-45760479	GM12891	blood:	n/a	n/a
42	POLR2A	chr17:45760728-45765897	A549	lung:	n/a	n/a
43	POLR2A	chr17:45759385-45760521	GM12892	blood:	n/a	n/a
44	POLR2A	chr17:45760032-45760399	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr17:45757237-45758645	PANC-1	pancreas:	n/a	n/a
46	POLR2A	chr17:45761280-45762448	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr17:45760900-45762822	K562	blood:	n/a	n/a
48	POLR2A	chr17:45759479-45760487	GM12892	blood:	n/a	n/a
49	POLR2A	chr17:45761138-45762573	HepG2	liver:	n/a	n/a
50	POLR2A	chr17:45761030-45763732	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45759987-45760037	MCF-7	breast:	n/a
2	chr17:45759987-45760037	NHBE	bronchial:	n/a
3	chr17:45759987-45760037	HPAEpiC	pulmonary alveolar:	n/a
4	chr17:45759987-45760037	PANC-1	pancreas:	n/a
5	chr17:45759987-45760037	ProgFib	skin:	n/a
6	chr17:45759987-45760037	HRPEpiC	eye:	n/a
7	chr17:45759987-45760037	Jurkat	blood:	n/a
8	chr17:45759987-45760037	HEK293	kidney:	embryo
9	chr17:45759987-45760037	GM12891	blood:	n/a
10	chr17:45759987-45760037	HRE	kidney:	n/a
11	chr17:45759987-45760037	HAEpiC	amniotic membrane:	n/a
12	chr17:45759987-45760037	NT2-D1	testis:	n/a
13	chr17:45759987-45760037	SK-N-SH	brain:	n/a
14	chr17:45759987-45760037	Hepatocyte	liver:	n/a
15	chr17:45759987-45760037	AG09319	gingival:	n/a
16	chr17:45759987-45760037	HCPEpiC	choroid plexus:	n/a
17	chr17:45759987-45760037	HRCEpiC	kidney:	n/a
18	chr17:45759987-45760037	AG04450	lung:	fetal
19	chr17:45759987-45760037	ovcar-3	ovarian:	n/a
20	chr17:45759987-45760037	HIPEpiC	eye:	n/a
21	chr17:45759987-45760037	HCT-116	colon:	n/a
22	chr17:45759987-45760037	AG10803	skin:	n/a
23	chr17:45759987-45760037	SK-N-MC	brain:	n/a
24	chr17:45759987-45760037	HNPCEpiC	eye:	n/a
25	chr17:45759987-45760037	AoSMC	blood vessel:	n/a
26	chr17:45759987-45760037	LNCaP	prostate:	n/a
27	chr17:45759987-45760037	SAEC	small airway:	n/a
28	chr17:45759987-45760037	HMEC	breast:	n/a
29	chr17:45759987-45760037	A549	lung:	n/a
30	chr17:45759987-45760037	Hela-S3	cervix:	n/a
31	chr17:45759987-45760037	NH-A	brain:	n/a
32	chr17:45759987-45760037	U87	brain:	n/a
33	chr17:45759987-45760037	HCF	heart:	n/a
34	chr17:45759987-45760037	T-47D	breast:	n/a
35	chr17:45759987-45760037	PrEC	prostate:	n/a
36	chr17:45759987-45760037	HL-60	blood:	n/a
37	chr17:45759987-45760037	GM12892	blood:	n/a
38	chr17:45759987-45760037	AG04449	skin:	fetal
39	chr17:45759987-45760037	HEEpiC	esophagus:	n/a
40	chr17:45759987-45760037	AG09309	skin:	n/a
41	chr17:45759987-45760037	CMK	blood:	n/a
42	chr17:45759987-45760037	HepG2	liver:	n/a
43	chr17:45759987-45760037	GM06990	blood:	n/a
44	chr17:45759987-45760037	SK-N-SH_RA	brain:	n/a
45	chr17:45759987-45760037	HCM	heart:	n/a
46	chr17:45759987-45760037	MCF10A-Er-Src	breast:	n/a
47	chr17:45759987-45760037	BE2_C	brain:	n/a
48	chr17:45759987-45760037	HUVEC	blood vessel:	n/a
49	chr17:45759987-45760037	H1-hESC	embryonic stem cell:	embryo
50	chr17:45759987-45760037	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45759280..45761453-chr17:45769227..45771829,2	MCF-7	breast:
2	chr17:45759177..45766275-chr17:45767435..45773662,12	K562	blood:
3	chr17:45760258..45764544-chr17:45769222..45773538,5	MCF-7	breast:
4	chr17:45757714..45759244-chr17:45760827..45763039,2	MCF-7	breast:
5	chr17:45757423..45758947-chr17:48941374..48943875,2	MCF-7	breast:
6	chr17:45752623..45755412-chr17:45757645..45762048,4	K562	blood:
7	chr17:45749677..45752105-chr17:45758082..45761229,3	MCF-7	breast:
8	chr17:45758194..45759902-chr17:45762797..45765497,2	K562	blood:
9	chr17:45752642..45755741-chr17:45755945..45758372,4	MCF-7	breast:
10	chr17:45725427..45729938-chr17:45759883..45763405,4	K562	blood:
11	chr17:45751990..45755538-chr17:45760652..45765275,4	MCF-7	breast:
12	chr17:45756856..45759143-chr17:45760653..45762664,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSBPL7-1	chr17:45759783-45760049	ENSG00000264558.1

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KPNB1	hsa-miR-181b-5p	chr17:45760646-45760653
2	KPNB1	hsa-miR-128-3p	chr17:45760146-45760168
3	KPNB1	hsa-miR-181b-5p	chr17:45759849-45759868
4	KPNB1	hsa-miR-128-3p	chr17:45760627-45760648
5	KPNB1	hsa-miR-181b-5p	chr17:45759861-45759867
6	KPNB1	hsa-miR-181b-5p	chr17:45760631-45760653

Variant related genes	Relation type
ENSG00000264558	TF binding region
ENSG00000264558	CpG island
ENSG00000198933	chromatin interactions
ENSG00000263766	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000141232	chromatin interactions
ITM2B	miRNA target sites

Extended variants
information (count: 124 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:124 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147421799	chr17:45758378-45758379	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs112270020	chr17:45758416-45758417	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs578043253	chr17:45758419-45758420	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs9897288	chr17:45758421-45758422	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs10602429	chr17:45758422-45758423	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75668026	chr17:45758423-45758424	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs71141924	chr17:45758445-45758446	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs75807639	chr17:45758450-45758451	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs34775547	chr17:45758455-45758456	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553633109	chr17:45758530-45758531	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528169969	chr17:45758531-45758532	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186055082	chr17:45758550-45758551	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567947483	chr17:45758594-45758595	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs545535844	chr17:45758631-45758632	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564429552	chr17:45758632-45758633	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530864359	chr17:45758634-45758635	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs201741253	chr17:45758649-45758650	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs189251683	chr17:45758660-45758661	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570382122	chr17:45758673-45758674	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139789175	chr17:45758674-45758675	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181632993	chr17:45758676-45758677	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs552706247	chr17:45758698-45758699	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs367609567	chr17:45758711-45758712	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535560501	chr17:45758715-45758716	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs555757456	chr17:45758724-45758725	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs367783530	chr17:45758728-45758729	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575569955	chr17:45758729-45758730	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574994633	chr17:45758740-45758741	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs558496883	chr17:45758889-45758890	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs60014739	chr17:45758917-45758918	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs140775662	chr17:45758918-45758919	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs186370789	chr17:45759003-45759004	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201370926	chr17:45759013-45759014	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75325493	chr17:45759053-45759054	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs112475736	chr17:45759056-45759057	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199753019	chr17:45759058-45759059	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541538466	chr17:45759063-45759064	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12601310	chr17:45759064-45759065	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78194523	chr17:45759074-45759075	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs75248948	chr17:45759075-45759076	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs59222945	chr17:45759076-45759077	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371516513	chr17:45759078-45759079	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs9904230	chr17:45759079-45759080	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149680589	chr17:45759093-45759094	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576235175	chr17:45759113-45759114	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368009016	chr17:45759191-45759192	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs146698519	chr17:45759220-45759221	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534676886	chr17:45759275-45759276	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550121302	chr17:45759286-45759287	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs570419686	chr17:45759309-45759310	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45728800-45762800	Strong transcription	Fetal Stomach	stomach
2	chr17:45728800-45765600	Strong transcription	Fetal Muscle Trunk	muscle
3	chr17:45729200-45760400	Strong transcription	Fetal Muscle Leg	muscle
4	chr17:45729200-45760600	Strong transcription	Fetal Brain Female	brain
5	chr17:45729200-45763800	Strong transcription	Placenta	Placenta
6	chr17:45729600-45762600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr17:45729800-45761600	Strong transcription	HSMM	muscle
8	chr17:45730400-45764800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr17:45730400-45765000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr17:45730800-45760600	Strong transcription	Lung	lung
11	chr17:45731200-45762200	Strong transcription	Fetal Lung	lung
12	chr17:45731200-45763800	Strong transcription	K562	blood
13	chr17:45731400-45762000	Strong transcription	NH-A	brain
14	chr17:45732400-45762600	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr17:45732600-45760200	Strong transcription	Brain Germinal Matrix	brain
16	chr17:45732600-45760400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr17:45732600-45762000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr17:45732600-45762200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr17:45732800-45760200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr17:45732800-45760600	Strong transcription	Fetal Intestine Large	intestine
21	chr17:45732800-45762200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr17:45732800-45762200	Strong transcription	Adipose Nuclei	Adipose
23	chr17:45732800-45762600	Strong transcription	Brain Anterior Caudate	brain
24	chr17:45733000-45759200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr17:45733000-45759400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr17:45733000-45761600	Strong transcription	HepG2	liver
27	chr17:45733000-45763600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr17:45733200-45760200	Strong transcription	Brain Cingulate Gyrus	brain
29	chr17:45733200-45760400	Strong transcription	Hela-S3	cervix
30	chr17:45733200-45762400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr17:45733200-45763400	Strong transcription	NHEK	skin
32	chr17:45733200-45765000	Strong transcription	HMEC	breast
33	chr17:45736200-45763600	Strong transcription	Dnd41	blood
34	chr17:45737000-45762400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr17:45737800-45762600	Strong transcription	Thymus	Thymus
36	chr17:45737800-45764200	Strong transcription	Duodenum Mucosa	Duodenum
37	chr17:45738000-45760200	Strong transcription	Rectal Smooth Muscle	rectum
38	chr17:45738000-45762600	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr17:45738000-45763800	Strong transcription	Liver	Liver
40	chr17:45738400-45762800	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr17:45738400-45763600	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr17:45738400-45765600	Strong transcription	Primary T cells from cord blood	blood
43	chr17:45738600-45762600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr17:45738800-45762600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:45739000-45760400	Strong transcription	Ovary	ovary
46	chr17:45739000-45760400	Strong transcription	Spleen	Spleen
47	chr17:45740000-45763400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr17:45741600-45762200	Strong transcription	Stomach Smooth Muscle	stomach
49	chr17:45741600-45763600	Strong transcription	Primary T cells fromperipheralblood	blood
50	chr17:45741800-45760200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood

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