Variant report

Variant	nsv961291
Chromosome Location	chr19:39324891-39329561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:560 , 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	chr19:39328365-39328607	HepG2	liver:	n/a	n/a
2	ATF2	chr19:39326167-39327035	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr19:39326050-39326583	GM12878	blood:	n/a	n/a
4	ATF2	chr19:39326047-39326522	GM12878	blood:	n/a	n/a
5	ATF2	chr19:39326609-39326890	GM12878	blood:	n/a	n/a
6	ATF3	chr19:39327445-39328793	A549	lung:	n/a	n/a
7	ATF3	chr19:39325878-39326580	A549	lung:	n/a	n/a
8	BCL11A	chr19:39326178-39326527	GM12878	blood:	n/a	n/a
9	BCL3	chr19:39326133-39326993	K562	blood:	n/a	n/a
10	BCL3	chr19:39325180-39326963	A549	lung:	n/a	n/a
11	BCL3	chr19:39325179-39327051	A549	lung:	n/a	n/a
12	BCL3	chr19:39329047-39329529	K562	blood:	n/a	n/a
13	BCL3	chr19:39329044-39330454	A549	lung:	n/a	n/a
14	BCL3	chr19:39327798-39329016	A549	lung:	n/a	chr19:39328370-39328379
15	BCL3	chr19:39327233-39330842	A549	lung:	n/a	chr19:39328370-39328379
16	BCLAF1	chr19:39326077-39327012	GM12878	blood:	n/a	n/a
17	BCLAF1	chr19:39325985-39326542	GM12878	blood:	n/a	n/a
18	BRCA1	chr19:39329443-39329556	HepG2	liver:	n/a	n/a
19	CCNT2	chr19:39326525-39326869	K562	blood:	n/a	n/a
20	CEBPB	chr19:39325407-39325543	Hela-S3	cervix:	n/a	chr19:39325512-39325523
21	CEBPB	chr19:39325394-39325600	H1-hESC	embryonic stem cell:	n/a	chr19:39325512-39325523
22	CEBPB	chr19:39325365-39325670	IMR90	lung:	n/a	chr19:39325512-39325523
23	CEBPB	chr19:39326068-39326366	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:39325381-39325660	K562	blood:	n/a	chr19:39325512-39325523
25	CEBPB	chr19:39328449-39328969	MCF-7	breast:	n/a	n/a
26	CEBPB	chr19:39325434-39325635	HepG2	liver:	n/a	chr19:39325512-39325523
27	CEBPB	chr19:39328207-39328981	MCF-7	breast:	n/a	n/a
28	CEBPB	chr19:39326178-39326218	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:39325350-39325679	A549	lung:	n/a	chr19:39325512-39325523
30	CHD2	chr19:39326757-39326856	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr19:39326341-39326342	HepG2	liver:	n/a	n/a
32	CREB1	chr19:39327891-39328353	A549	lung:	n/a	n/a
33	CTCF	chr19:39329560-39329710	A549	lung:	n/a	n/a
34	CTCF	chr19:39328920-39329070	SAEC	small airway:	n/a	n/a
35	CTCF	chr19:39328745-39328772	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr19:39329400-39329624	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:39329460-39329610	NHEK	skin:	n/a	n/a
38	CTCF	chr19:39329420-39329570	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr19:39328820-39328970	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr19:39329400-39329550	RPTEC	kidney:	n/a	n/a
41	CTCF	chr19:39329440-39329590	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:39329020-39329170	SAEC	small airway:	n/a	n/a
43	CTCF	chr19:39329306-39329670	NHEK	skin:	n/a	n/a
44	CTCF	chr19:39328996-39329159	K562	blood:	n/a	n/a
45	CTCF	chr19:39329455-39329584	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:39329440-39329594	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:39329441-39329584	MCF-7	breast:	n/a	n/a
48	CTCF	chr19:39329300-39329450	A549	lung:	n/a	n/a
49	CTCF	chr19:39329434-39329606	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr19:39328967-39329143	NHEK	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39325721-39325771	A549	lung:	n/a
2	chr19:39325721-39325771	AG04449	skin:	fetal
3	chr19:39327196-39327246	HIPEpiC	eye:	n/a
4	chr19:39327196-39327246	HNPCEpiC	eye:	n/a
5	chr19:39325721-39325771	HMEC	breast:	n/a
6	chr19:39325721-39325771	GM12891	blood:	n/a
7	chr19:39325721-39325771	Caco-2	colon:	n/a
8	chr19:39327196-39327246	GM12892	blood:	n/a
9	chr19:39325721-39325771	MCF10A-Er-Src	breast:	n/a
10	chr19:39325721-39325771	HAEpiC	amniotic membrane:	n/a
11	chr19:39327196-39327246	NH-A	brain:	n/a
12	chr19:39327196-39327246	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:39327196-39327246	GM19239	blood:	n/a
14	chr19:39325721-39325771	HNPCEpiC	eye:	n/a
15	chr19:39325721-39325771	HEK293	kidney:	embryo
16	chr19:39325721-39325771	SAEC	small airway:	n/a
17	chr19:39325721-39325771	ProgFib	skin:	n/a
18	chr19:39325721-39325771	HRCEpiC	kidney:	n/a
19	chr19:39325721-39325771	SK-N-SH	brain:	n/a
20	chr19:39327196-39327246	CMK	blood:	n/a
21	chr19:39325721-39325771	Jurkat	blood:	n/a
22	chr19:39325721-39325771	SK-N-SH_RA	brain:	n/a
23	chr19:39325721-39325771	HCF	heart:	n/a
24	chr19:39325721-39325771	HIPEpiC	eye:	n/a
25	chr19:39327196-39327246	Caco-2	colon:	n/a
26	chr19:39327196-39327246	Jurkat	blood:	n/a
27	chr19:39327196-39327246	AG04449	skin:	fetal
28	chr19:39325721-39325771	GM12892	blood:	n/a
29	chr19:39325721-39325771	GM06990	blood:	n/a
30	chr19:39325721-39325771	HRPEpiC	eye:	n/a
31	chr19:39325721-39325771	BJ	skin:	n/a
32	chr19:39327196-39327246	ProgFib	skin:	n/a
33	chr19:39327196-39327246	U87	brain:	n/a
34	chr19:39325721-39325771	AG09309	skin:	n/a
35	chr19:39327196-39327246	K562	blood:	n/a
36	chr19:39325721-39325771	AG09319	gingival:	n/a
37	chr19:39327196-39327246	GM12891	blood:	n/a
38	chr19:39327196-39327246	MCF10A-Er-Src	breast:	n/a
39	chr19:39327196-39327246	HCPEpiC	choroid plexus:	n/a
40	chr19:39327196-39327246	SKMC	muscle:	n/a
41	chr19:39325721-39325771	HCT-116	colon:	n/a
42	chr19:39325721-39325771	HCM	heart:	n/a
43	chr19:39327196-39327246	MCF-7	breast:	n/a
44	chr19:39327196-39327246	HepG2	liver:	n/a
45	chr19:39325721-39325771	NH-A	brain:	n/a
46	chr19:39325721-39325771	AoSMC	blood vessel:	n/a
47	chr19:39325721-39325771	GM12878	blood:	n/a
48	chr19:39325721-39325771	ovcar-3	ovarian:	n/a
49	chr19:39325721-39325771	HRE	kidney:	n/a
50	chr19:39327196-39327246	SAEC	small airway:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39303539..39306224-chr19:39328570..39331543,2	MCF-7	breast:
2	chr19:39221972..39229243-chr19:39319630..39326763,11	K562	blood:
3	chr19:39325391..39328182-chr19:39375242..39377449,2	K562	blood:
4	chr19:39138022..39142840-chr19:39322070..39325450,5	MCF-7	breast:
5	chr19:39325997..39327543-chr19:39409428..39411815,2	K562	blood:
6	chr19:39328103..39328842-chr19:39339617..39340595,2	MCF-7	breast:
7	chr19:39324931..39327493-chr19:39358939..39361060,2	MCF-7	breast:
8	chr19:39218553..39228703-chr19:39324875..39331730,17	MCF-7	breast:
9	chr19:39183521..39187102-chr19:39327849..39329398,3	MCF-7	breast:
10	chr19:39326367..39329872-chr19:39419342..39422625,3	MCF-7	breast:
11	chr19:38805271..38808237-chr19:39322535..39325453,2	K562	blood:
12	chr19:39326299..39328674-chr19:39389140..39390810,2	K562	blood:
13	chr19:39326299..39328911-chr19:39388226..39390640,3	K562	blood:
14	chr19:39216544..39219007-chr19:39328306..39331285,2	MCF-7	breast:
15	chr19:39204938..39205721-chr19:39328551..39329336,2	MCF-7	breast:
16	chr19:39315714..39318484-chr19:39324884..39327703,2	K562	blood:
17	chr19:39223964..39228282-chr19:39327392..39332302,8	MCF-7	breast:
18	chr19:39137584..39140325-chr19:39327324..39331607,4	MCF-7	breast:
19	chr19:39138050..39138858-chr19:39328433..39329173,2	MCF-7	breast:
20	chr19:39328430..39329992-chr19:39354096..39356995,2	MCF-7	breast:
21	chr19:39137231..39139589-chr19:39329369..39331157,2	MCF-7	breast:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HNRNPL	hsa-miR-106b-5p	chr19:39327134-39327154
2	HNRNPL	hsa-miR-23b-3p	chr19:39327112-39327132
3	HNRNPL	hsa-miR-16-5p	chr19:39327078-39327099
4	HNRNPL	hsa-miR-615-3p	chr19:39329515-39329529

Variant related genes	Relation type
HNRNPL	TF binding region
ECH1	TF binding region
HNRNPL	CpG island
ECH1	CpG island
ENSG00000182472	chromatin interactions
ENSG00000104825	chromatin interactions
ENSG00000130402	chromatin interactions
ENSG00000171747	chromatin interactions
ENSG00000104824	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000267892	chromatin interactions
ENSG00000187994	chromatin interactions
ENSG00000167645	chromatin interactions
ENSG00000267375	chromatin interactions
ENSG00000104835	chromatin interactions
ENSG00000068903	chromatin interactions
ENSG00000269050	chromatin interactions

Extended variants
information (count: 265 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570787077	chr19:39324903-39324904	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs118075766	chr19:39324905-39324906	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs10418221	chr19:39324957-39324958	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs543851533	chr19:39324977-39324978	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs535672134	chr19:39325029-39325030	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs373073925	chr19:39325044-39325045	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs147718884	chr19:39325052-39325053	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs112602239	chr19:39325098-39325099	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs376819288	chr19:39325129-39325130	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs569271077	chr19:39325144-39325145	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs539795747	chr19:39325145-39325146	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs557897604	chr19:39325177-39325178	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs186836590	chr19:39325186-39325187	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs10418861	chr19:39325264-39325265	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs555583760	chr19:39325275-39325276	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs570682422	chr19:39325278-39325279	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs374496758	chr19:39325326-39325327	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs368757719	chr19:39325327-39325328	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs192955867	chr19:39325416-39325417	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs143397884	chr19:39325442-39325443	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs563367641	chr19:39325456-39325457	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs373895832	chr19:39325457-39325458	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs545767551	chr19:39325462-39325463	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs538018453	chr19:39325488-39325489	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs563776469	chr19:39325533-39325534	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs528754229	chr19:39325567-39325568	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs11668766	chr19:39325610-39325611	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs184163646	chr19:39325649-39325650	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs568558360	chr19:39325705-39325706	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs148364535	chr19:39325707-39325708	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs141426350	chr19:39325708-39325709	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs189389573	chr19:39325751-39325752	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs11672634	chr19:39325754-39325755	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs551790188	chr19:39325755-39325756	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs566919568	chr19:39325789-39325790	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs553887352	chr19:39325795-39325796	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs572370096	chr19:39325811-39325812	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs10425464	chr19:39325832-39325833	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs553265242	chr19:39325834-39325835	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs574805068	chr19:39325846-39325847	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs535616191	chr19:39325946-39325947	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs556910747	chr19:39325981-39325982	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs575288388	chr19:39326020-39326021	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs180987429	chr19:39326022-39326023	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs138353697	chr19:39326044-39326045	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs572462732	chr19:39326049-39326050	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs142834689	chr19:39326064-39326065	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs146012467	chr19:39326117-39326118	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs529590164	chr19:39326158-39326159	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs185680922	chr19:39326170-39326171	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39322400-39331800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr19:39322600-39325400	Weak transcription	Esophagus	oesophagus
3	chr19:39322600-39325600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr19:39322600-39326200	Weak transcription	Gastric	stomach
5	chr19:39322600-39326400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:39322600-39326600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr19:39322600-39327400	Weak transcription	Small Intestine	intestine
8	chr19:39322800-39326200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr19:39322800-39326400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr19:39323000-39325400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr19:39323000-39325400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr19:39323000-39325400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr19:39323000-39326000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr19:39323000-39326000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr19:39323000-39326000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr19:39323000-39326000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr19:39323000-39326000	Enhancers	Placenta	Placenta
18	chr19:39323000-39326200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr19:39323000-39326200	Weak transcription	Fetal Brain Male	brain
20	chr19:39323000-39326200	Weak transcription	Ovary	ovary
21	chr19:39323000-39327200	Weak transcription	Brain Angular Gyrus	brain
22	chr19:39323000-39334600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr19:39323200-39325200	Weak transcription	Primary T cells from cord blood	blood
24	chr19:39323200-39325400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr19:39323200-39325400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr19:39323200-39325400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr19:39323200-39325400	Weak transcription	Fetal Thymus	thymus
28	chr19:39323200-39325400	Weak transcription	Thymus	Thymus
29	chr19:39323200-39325600	Weak transcription	Osteobl	bone
30	chr19:39323200-39326000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr19:39323200-39326000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr19:39323200-39326000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr19:39323200-39326000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr19:39323200-39326000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr19:39323200-39326000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr19:39323200-39326000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr19:39323200-39326000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr19:39323200-39326000	Weak transcription	Brain Hippocampus Middle	brain
39	chr19:39323200-39326000	Weak transcription	Colon Smooth Muscle	Colon
40	chr19:39323200-39326000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr19:39323200-39326000	Weak transcription	HSMM	muscle
42	chr19:39323200-39326000	Weak transcription	NH-A	brain
43	chr19:39323200-39326200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr19:39323200-39326200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr19:39323200-39326200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr19:39323200-39326200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr19:39323200-39326200	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr19:39323200-39326200	Weak transcription	Brain Germinal Matrix	brain
49	chr19:39323200-39326200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr19:39323200-39326200	Weak transcription	Fetal Kidney	kidney

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