Variant report

Variant	nsv457821
Chromosome Location	chr17:45419139-45547078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:366)
Chromatin interactive
region (count:29)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:45439691-45439792	K562	blood:	n/a	n/a
2	ARID3A	chr17:45505316-45506040	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:45430312-45430555	K562	blood:	n/a	n/a
4	ATF1	chr17:45430319-45430519	K562	blood:	n/a	n/a
5	BCL11A	chr17:45504891-45505246	GM12878	blood:	n/a	n/a
6	CBX3	chr17:45439646-45439988	K562	blood:	n/a	n/a
7	CBX3	chr17:45439597-45439937	K562	blood:	n/a	n/a
8	CBX3	chr17:45450400-45450697	K562	blood:	n/a	n/a
9	CBX3	chr17:45450397-45450796	HCT-116	colon:	n/a	n/a
10	CBX3	chr17:45450369-45450751	K562	blood:	n/a	n/a
11	CCNT2	chr17:45430296-45430403	K562	blood:	n/a	n/a
12	CCNT2	chr17:45428613-45428764	K562	blood:	n/a	n/a
13	CEBPB	chr17:45453915-45454146	K562	blood:	n/a	chr17:45454038-45454049
14	CEBPB	chr17:45493466-45493668	HepG2	liver:	n/a	chr17:45493564-45493575
15	CEBPB	chr17:45493445-45493683	A549	lung:	n/a	chr17:45493564-45493575
16	CEBPB	chr17:45482269-45482596	HepG2	liver:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
17	CEBPB	chr17:45482316-45482557	A549	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
18	CEBPB	chr17:45482340-45482579	IMR90	lung:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
19	CEBPB	chr17:45493468-45493688	K562	blood:	n/a	chr17:45493564-45493575
20	CEBPB	chr17:45505310-45505563	HepG2	liver:	n/a	n/a
21	CEBPB	chr17:45491776-45491931	K562	blood:	n/a	n/a
22	CEBPB	chr17:45482271-45482609	K562	blood:	n/a	chr17:45482429-45482440 chr17:45482429-45482442 chr17:45482429-45482442 chr17:45482431-45482440 chr17:45482431-45482442
23	CEBPB	chr17:45453922-45454159	HepG2	liver:	n/a	chr17:45454038-45454049
24	CTCF	chr17:45439660-45439810	HVMF	connective:	n/a	n/a
25	CTCF	chr17:45433980-45434130	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr17:45439640-45439790	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr17:45439572-45439917	K562	blood:	n/a	n/a
28	CTCF	chr17:45501240-45501390	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr17:45439637-45439861	MCF-7	breast:	n/a	n/a
30	CTCF	chr17:45545592-45545679	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr17:45439562-45439885	K562	blood:	n/a	n/a
32	CTCF	chr17:45439620-45439902	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr17:45439640-45439790	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr17:45513628-45513693	Lung_OC	lung:	n/a	n/a
35	CTCF	chr17:45439624-45439845	LNCaP	prostate:	n/a	n/a
36	CTCF	chr17:45439278-45440129	A549	lung:	n/a	n/a
37	CTCF	chr17:45439630-45439861	Fibrobl	skin:	n/a	n/a
38	CTCF	chr17:45439628-45439838	GM19240	blood:	n/a	n/a
39	CTCF	chr17:45439629-45439878	MCF-7	breast:	n/a	n/a
40	CTCF	chr17:45439640-45439790	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr17:45439640-45439790	HAc	cerebellar:	n/a	n/a
42	CTCF	chr17:45439660-45439810	GM12875	blood:	n/a	n/a
43	CTCF	chr17:45439640-45439790	NHLF	lung:	n/a	n/a
44	CTCF	chr17:45439624-45439831	GM13977	blood:	n/a	n/a
45	CTCF	chr17:45439680-45439830	HAc	cerebellar:	n/a	n/a
46	CTCF	chr17:45439645-45439779	Lung_OC	lung:	n/a	n/a
47	CTCF	chr17:45545460-45545610	BJ	skin:	n/a	n/a
48	CTCF	chr17:45439587-45439956	SK-N-SH	brain:	n/a	n/a
49	CTCF	chr17:45439560-45439710	GM12870	blood:	n/a	n/a
50	CTCF	chr17:45439620-45439770	AG09319	gingival:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45502151-45502201	Hela-S3	cervix:	n/a
2	chr17:45505249-45505299	H1-hESC	embryonic stem cell:	embryo
3	chr17:45501030-45501080	GM12878	blood:	n/a
4	chr17:45501242-45501292	Hepatocyte	liver:	n/a
5	chr17:45505249-45505299	SK-N-SH_RA	brain:	n/a
6	chr17:45501697-45501747	U87	brain:	n/a
7	chr17:45501697-45501747	SK-N-MC	brain:	n/a
8	chr17:45501030-45501080	Hela-S3	cervix:	n/a
9	chr17:45505249-45505299	T-47D	breast:	n/a
10	chr17:45501242-45501292	PFSK-1	brain:	n/a
11	chr17:45501697-45501747	HEK293	kidney:	embryo
12	chr17:45505249-45505299	HCT-116	colon:	n/a
13	chr17:45505249-45505299	ovcar-3	ovarian:	n/a
14	chr17:45501697-45501747	HCPEpiC	choroid plexus:	n/a
15	chr17:45501628-45501678	T-47D	breast:	n/a
16	chr17:45501697-45501747	IMR90	lung:	fetal
17	chr17:45501030-45501080	RPTEC	kidney:	n/a
18	chr17:45501697-45501747	AG09309	skin:	n/a
19	chr17:45501628-45501678	MCF-7	breast:	n/a
20	chr17:45502151-45502201	HRCEpiC	kidney:	n/a
21	chr17:45501030-45501080	Jurkat	blood:	n/a
22	chr17:45501030-45501080	MCF10A-Er-Src	breast:	n/a
23	chr17:45505249-45505299	HNPCEpiC	eye:	n/a
24	chr17:45505249-45505299	HCPEpiC	choroid plexus:	n/a
25	chr17:45501628-45501678	GM12878	blood:	n/a
26	chr17:45501030-45501080	HNPCEpiC	eye:	n/a
27	chr17:45501242-45501292	HCM	heart:	n/a
28	chr17:45502151-45502201	T-47D	breast:	n/a
29	chr17:45502151-45502201	BE2_C	brain:	n/a
30	chr17:45501242-45501292	HMEC	breast:	n/a
31	chr17:45501697-45501747	ECC-1	luminal epithelium:	n/a
32	chr17:45501242-45501292	A549	lung:	n/a
33	chr17:45505249-45505299	U87	brain:	n/a
34	chr17:45501030-45501080	NH-A	brain:	n/a
35	chr17:45501697-45501747	GM12892	blood:	n/a
36	chr17:45501628-45501678	HRE	kidney:	n/a
37	chr17:45501242-45501292	PrEC	prostate:	n/a
38	chr17:45501628-45501678	Hepatocyte	liver:	n/a
39	chr17:45505249-45505299	ProgFib	skin:	n/a
40	chr17:45501628-45501678	AG09309	skin:	n/a
41	chr17:45501628-45501678	HRPEpiC	eye:	n/a
42	chr17:45501030-45501080	AG09319	gingival:	n/a
43	chr17:45505249-45505299	LNCaP	prostate:	n/a
44	chr17:45505249-45505299	ECC-1	luminal epithelium:	n/a
45	chr17:45501030-45501080	H1-hESC	embryonic stem cell:	embryo
46	chr17:45501697-45501747	NHBE	bronchial:	n/a
47	chr17:45501242-45501292	NH-A	brain:	n/a
48	chr17:45501030-45501080	K562	blood:	n/a
49	chr17:45501697-45501747	NT2-D1	testis:	n/a
50	chr17:45501030-45501080	HRE	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
2	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
3	chr17:45499733..45501782-chr17:45502052..45504438,2	K562	blood:
4	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:
5	chr17:45422002..45424871-chr17:45443232..45445313,2	MCF-7	breast:
6	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
7	chr17:45417186..45419360-chr17:45433473..45435862,2	K562	blood:
8	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
9	chr17:45450399..45452853-chr17:45453985..45455878,3	K562	blood:
10	chr17:45433817..45436270-chr17:45439623..45442042,2	K562	blood:
11	chr17:45450230..45451965-chr17:45515633..45517209,2	K562	blood:
12	chr17:45463722..45466707-chr17:45470914..45473396,3	K562	blood:
13	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
14	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
15	chr17:45433817..45436270-chr17:45439623..45442042,2	K562	blood:
16	chr17:45399518..45402231-chr17:45418878..45421613,2	K562	blood:
17	chr17:45417186..45419360-chr17:45433473..45435862,2	K562	blood:
18	chr17:45469114..45472029-chr17:45476038..45478353,2	K562	blood:
19	chr17:45474211..45476724-chr17:45477326..45478919,2	MCF-7	breast:
20	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
21	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
22	chr17:45489885..45492541-chr17:45494163..45496455,2	MCF-7	breast:
23	chr17:45445857..45448249-chr17:45449955..45451934,2	MCF-7	breast:
24	chr17:45468184..45470293-chr17:45471127..45473354,2	MCF-7	breast:
25	chr17:45485568..45487998-chr17:45490186..45492096,2	K562	blood:
26	chr17:45422002..45424871-chr17:45443232..45445313,2	MCF-7	breast:
27	chr17:45443966..45446911-chr17:45490626..45492639,2	K562	blood:
28	chr17:45414278..45416918-chr17:45428922..45430523,2	K562	blood:
29	chr17:45443966..45446911-chr17:45490507..45492639,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C17orf57-1	chr17:45522601-45522883	NONHSAT054305
2	lnc-AC040934.1-1	chr17:45500728-45500892	ENSG00000253347.1
3	lnc-ITGB3-1	chr17:45446982-45447290	NONHSAT054302
4	lnc-MYL4-4	chr17:45419287-45419393	NONHSAT054299
5	lnc-ITGB3-1	chr17:45447803-45447874	NONHSAT054302
6	lnc-AC040934.1-1	chr17:45486688-45487035	ENSG00000253347.1
7	lnc-ITGB3-1	chr17:45451838-45452004	NONHSAT054302

No data

Variant related genes	Relation type
EFCAB13	TF binding region
ENSG00000253347	TF binding region
EFCAB13	CpG island
ENSG00000253347	CpG island
ENSG00000263293	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000253347	chromatin interactions

Extended variants
information (count: 4271 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:4271 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11652957	chr17:45419139-45419140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567613557	chr17:45419286-45419287	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs374908244	chr17:45419298-45419299	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs138179179	chr17:45419305-45419306	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs367806543	chr17:45419313-45419314	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs373155023	chr17:45419364-45419365	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs201668575	chr17:45419369-45419370	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs139217839	chr17:45419375-45419376	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs375109457	chr17:45419436-45419437	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560451526	chr17:45419448-45419449	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs77018363	chr17:45419467-45419468	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543162581	chr17:45419475-45419476	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs562952476	chr17:45419487-45419488	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530596431	chr17:45419542-45419543	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs550717389	chr17:45419683-45419684	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs80335564	chr17:45419846-45419847	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs532666126	chr17:45419872-45419873	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145368946	chr17:45419877-45419878	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114842527	chr17:45419924-45419925	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs148740354	chr17:45420037-45420038	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs186665485	chr17:45420051-45420052	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs549127231	chr17:45420081-45420082	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568976885	chr17:45420083-45420084	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537924117	chr17:45420097-45420098	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs144263503	chr17:45420182-45420183	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs557863521	chr17:45420268-45420269	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577603762	chr17:45420286-45420287	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs533979307	chr17:45420290-45420291	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs553885527	chr17:45420298-45420299	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574237100	chr17:45420360-45420361	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542969770	chr17:45420413-45420414	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs563070428	chr17:45420430-45420431	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs565745613	chr17:45420441-45420442	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs544309176	chr17:45420499-45420500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs193226432	chr17:45420520-45420521	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533062645	chr17:45420524-45420525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546578683	chr17:45420533-45420534	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs546730629	chr17:45420537-45420538	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs559907467	chr17:45420538-45420539	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs529158412	chr17:45420618-45420619	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs185620218	chr17:45420652-45420653	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577474077	chr17:45420668-45420669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190185450	chr17:45420716-45420717	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568277396	chr17:45420774-45420775	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs143663128	chr17:45420783-45420784	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs146815547	chr17:45420820-45420821	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs557269500	chr17:45420834-45420835	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534039022	chr17:45420898-45420899	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs79872574	chr17:45420906-45420907	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573976404	chr17:45420945-45420946	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

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	17142309	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
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45402000-45428600	Weak transcription	Spleen	Spleen
2	chr17:45402000-45442600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr17:45402200-45420400	Weak transcription	Pancreas	Pancrea
4	chr17:45402200-45446400	Weak transcription	Colon Smooth Muscle	Colon
5	chr17:45402200-45500800	Weak transcription	Aorta	Aorta
6	chr17:45402400-45419400	Weak transcription	Liver	Liver
7	chr17:45402400-45419600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr17:45402400-45421200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr17:45402400-45421400	Weak transcription	Fetal Kidney	kidney
10	chr17:45402400-45421600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr17:45402400-45423400	Weak transcription	NHDF-Ad	bronchial
12	chr17:45402400-45424200	Weak transcription	Fetal Brain Male	brain
13	chr17:45402400-45427200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr17:45402400-45428400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr17:45402400-45433600	Weak transcription	Fetal Heart	heart
16	chr17:45402400-45433600	Weak transcription	Fetal Intestine Small	intestine
17	chr17:45402400-45433600	Weak transcription	Fetal Stomach	stomach
18	chr17:45402400-45435800	Weak transcription	Rectal Smooth Muscle	rectum
19	chr17:45402400-45436000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr17:45402600-45422200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr17:45402600-45423000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr17:45402600-45423400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr17:45402600-45424600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr17:45402600-45428800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr17:45402800-45422400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr17:45402800-45440800	Weak transcription	Primary T cells from cord blood	blood
27	chr17:45403000-45429400	Weak transcription	Placenta	Placenta
28	chr17:45407600-45435800	Weak transcription	Fetal Intestine Large	intestine
29	chr17:45408200-45421000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr17:45409200-45425200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr17:45409400-45419600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr17:45411200-45424000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr17:45411400-45419800	Weak transcription	Fetal Lung	lung
34	chr17:45411600-45468200	Weak transcription	Left Ventricle	heart
35	chr17:45412400-45463400	Weak transcription	Gastric	stomach
36	chr17:45413400-45419200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr17:45413400-45419400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr17:45413400-45421600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr17:45413400-45423800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:45413400-45463800	Weak transcription	Ovary	ovary
41	chr17:45415200-45419600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr17:45415200-45421600	Weak transcription	Adipose Nuclei	Adipose
43	chr17:45415400-45421600	Weak transcription	Primary B cells from cord blood	blood
44	chr17:45417000-45423000	Weak transcription	Lung	lung
45	chr17:45418000-45420600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr17:45418600-45425000	Strong transcription	Primary B cells from peripheral blood	blood
47	chr17:45419000-45420000	Strong transcription	Primary hematopoietic stem cells	blood
48	chr17:45419200-45423200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr17:45419400-45420200	Strong transcription	Liver	Liver
50	chr17:45419400-45420400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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