Variant report

Variant	nsv530928
Chromosome Location	chr9:472086-602792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1375)
CpG islands
(count:490)
Chromatin interactive
region (count:40)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1375 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:489187-489524	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:504390-504746	K562	blood:	n/a	n/a
3	ARID3A	chr9:495829-496174	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
5	ATF1	chr9:491995-492195	K562	blood:	n/a	n/a
6	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
7	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:503882-504954	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:503516-503574	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:505331-505595	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr9:489067-489648	A549	lung:	n/a	n/a
13	BCL3	chr9:503842-504488	A549	lung:	n/a	chr9:504175-504184 chr9:504327-504340 chr9:504456-504469
14	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
15	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
16	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
17	BHLHE40	chr9:504376-504833	GM12878	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
18	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
19	BHLHE40	chr9:494860-495111	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:503924-504891	K562	blood:	n/a	chr9:504430-504446 chr9:504607-504623 chr9:504604-504620 chr9:504606-504622
21	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
22	BRCA1	chr9:504440-504580	HepG2	liver:	n/a	n/a
23	CCNT2	chr9:503997-505117	K562	blood:	n/a	chr9:504819-504828
24	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
25	CEBPB	chr9:489177-489772	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:599948-600356	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
27	CEBPB	chr9:489122-489760	A549	lung:	n/a	n/a
28	CEBPB	chr9:489180-489720	MCF-7	breast:	n/a	n/a
29	CEBPB	chr9:599836-600408	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
30	CEBPB	chr9:599936-600319	K562	blood:	n/a	chr9:600087-600098 chr9:600123-600134
31	CEBPB	chr9:504299-504587	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr9:599942-600395	HepG2	liver:	n/a	chr9:600087-600098 chr9:600123-600134
33	CEBPB	chr9:486108-486526	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
35	CEBPB	chr9:589903-590000	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
37	CEBPB	chr9:495311-495494	IMR90	lung:	n/a	n/a
38	CEBPB	chr9:599943-600381	IMR90	lung:	n/a	chr9:600087-600098 chr9:600123-600134
39	CEBPB	chr9:495243-495543	A549	lung:	n/a	n/a
40	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
41	CEBPB	chr9:561371-561765	A549	lung:	n/a	n/a
42	CEBPB	chr9:486090-486669	A549	lung:	n/a	n/a
43	CEBPB	chr9:489357-489758	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:599945-600321	H1-hESC	embryonic stem cell:	n/a	chr9:600087-600098 chr9:600123-600134
45	CEBPB	chr9:573656-573820	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr9:599907-600250	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
47	CEBPB	chr9:599844-600456	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
48	CEBPB	chr9:561219-561918	A549	lung:	n/a	n/a
49	CEBPB	chr9:573616-573837	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:505235-505285	HRCEpiC	kidney:	n/a
2	chr9:505235-505285	HAEpiC	amniotic membrane:	n/a
3	chr9:505235-505285	HRCEpiC	kidney:	n/a
4	chr9:505235-505285	HAEpiC	amniotic membrane:	n/a
5	chr9:505571-505621	GM12892	blood:	n/a
6	chr9:505721-505771	HNPCEpiC	eye:	n/a
7	chr9:505721-505771	SK-N-SH	brain:	n/a
8	chr9:505721-505771	BJ	skin:	n/a
9	chr9:503937-503987	GM12892	blood:	n/a
10	chr9:505571-505621	H1-hESC	embryonic stem cell:	embryo
11	chr9:505235-505285	HepG2	liver:	n/a
12	chr9:505721-505771	K562	blood:	n/a
13	chr9:507411-507461	RPTEC	kidney:	n/a
14	chr9:574312-574362	K562	blood:	n/a
15	chr9:574312-574362	MCF-7	breast:	n/a
16	chr9:574312-574362	ovcar-3	ovarian:	n/a
17	chr9:472966-473016	GM12892	blood:	n/a
18	chr9:504774-504824	U87	brain:	n/a
19	chr9:503937-503987	HRE	kidney:	n/a
20	chr9:503937-503987	HEK293	kidney:	embryo
21	chr9:503937-503987	A549	lung:	n/a
22	chr9:505571-505621	IMR90	lung:	fetal
23	chr9:507411-507461	AG09309	skin:	n/a
24	chr9:574312-574362	NHBE	bronchial:	n/a
25	chr9:504774-504824	ECC-1	luminal epithelium:	n/a
26	chr9:503937-503987	GM12891	blood:	n/a
27	chr9:507411-507461	NHDF-neo	bronchial:	n/a
28	chr9:505721-505771	U87	brain:	n/a
29	chr9:505235-505285	SKMC	muscle:	n/a
30	chr9:505571-505621	NT2-D1	testis:	n/a
31	chr9:505571-505621	GM06990	blood:	n/a
32	chr9:574312-574362	SK-N-SH	brain:	n/a
33	chr9:505235-505285	SK-N-SH_RA	brain:	n/a
34	chr9:505721-505771	HL-60	blood:	n/a
35	chr9:505235-505285	NT2-D1	testis:	n/a
36	chr9:505571-505621	HPAEpiC	pulmonary alveolar:	n/a
37	chr9:504774-504824	HCT-116	colon:	n/a
38	chr9:504774-504824	AG04450	lung:	fetal
39	chr9:507411-507461	HRE	kidney:	n/a
40	chr9:574312-574362	HNPCEpiC	eye:	n/a
41	chr9:472966-473016	T-47D	breast:	n/a
42	chr9:505721-505771	PrEC	prostate:	n/a
43	chr9:504774-504824	MCF-7	breast:	n/a
44	chr9:504774-504824	HUVEC	blood vessel:	n/a
45	chr9:505721-505771	HCF	heart:	n/a
46	chr9:472966-473016	SAEC	small airway:	n/a
47	chr9:505721-505771	RPTEC	kidney:	n/a
48	chr9:504774-504824	GM12878	blood:	n/a
49	chr9:472966-473016	HAEpiC	amniotic membrane:	n/a
50	chr9:472966-473016	GM06990	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
2	chr9:487771..490019-chr9:514331..516293,2	MCF-7	breast:
3	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
4	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
5	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
6	chr9:468995..471572-chr9:503851..506185,2	MCF-7	breast:
7	chr9:495605..498122-chr9:502386..505122,3	MCF-7	breast:
8	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
9	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
10	chr9:490701..492635-chr9:494682..497058,2	K562	blood:
11	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
12	chr9:468933..471416-chr9:484729..487754,3	MCF-7	breast:
13	chr9:494848..496689-chr9:501659..504144,2	MCF-7	breast:
14	chr9:490052..492255-chr9:502875..504712,2	MCF-7	breast:
15	chr9:468830..470676-chr9:503247..506779,4	MCF-7	breast:
16	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
17	chr9:470985..473419-chr9:489407..491415,2	MCF-7	breast:
18	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
19	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
20	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
21	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
22	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
23	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
24	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
25	chr9:490052..492255-chr9:502875..504712,2	MCF-7	breast:
26	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
27	chr9:469030..473266-chr9:476113..479118,4	MCF-7	breast:
28	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
29	chr9:469030..473266-chr9:476113..479118,4	MCF-7	breast:
30	chr9:512039..514160-chr9:515791..519174,3	K562	blood:
31	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
32	chr9:504296..504898-chr9:21802481..21802992,2	HCT-116	colon:
33	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
34	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
35	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
36	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
37	chr9:469974..471479-chr9:511045..512830,2	K562	blood:
38	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
39	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
40	chr9:500269..502662-chr9:502681..505040,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-1	chr9:495238-495610	ENSG00000228115.1
2	lnc-C9orf66-8	chr9:507258-507553	NONHSAT129930
3	lnc-DOCK8-5	chr9:484282-484491	NONHSAT129926
4	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
5	lnc-DOCK8-5	chr9:476628-476769	NONHSAT129927
6	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931
7	lnc-DOCK8-5	chr9:473194-473273	NONHSAT129927
8	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931
9	lnc-C9orf66-2	chr9:488957-489066	ENSG00000227155.3
10	lnc-C9orf66-2	chr9:492084-492112	ENSG00000227155.3
11	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1
12	lnc-C9orf66-7	chr9:503057-504746	NONHSAT129929
13	lnc-DOCK8-5	chr9:473194-473273	NONHSAT129926
14	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
15	lnc-DOCK8-1	chr9:487774-487803	ENSG00000228115.1
16	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
RN7SL412P	TF binding region
ENSG00000228115	TF binding region
ENSG00000227155	TF binding region
KANK1	TF binding region
ENSG00000235330	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
RN7SL412P	CpG island
ENSG00000228115	CpG island
ENSG00000227155	CpG island
KANK1	CpG island
ENSG00000235330	CpG island
ENSG00000107104	chromatin interactions
ENSG00000227155	chromatin interactions
ENSG00000235330	chromatin interactions
ENSG00000264545	chromatin interactions
ENSG00000228115	chromatin interactions
ENSG00000099810	chromatin interactions

Extended variants
information (count: 7230 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:7230 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558426788	chr9:472153-472154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs555659419	chr9:472157-472158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569214540	chr9:472162-472163	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116726076	chr9:472188-472189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145258913	chr9:472217-472218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs114671226	chr9:472274-472275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371711018	chr9:472281-472282	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186703720	chr9:472286-472287	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs540686767	chr9:472308-472309	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553867880	chr9:472329-472330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576988889	chr9:472409-472410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573846820	chr9:472416-472417	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145416036	chr9:472442-472443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs57500851	chr9:472443-472444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147606742	chr9:472474-472475	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs566926249	chr9:472480-472481	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562841544	chr9:472506-472507	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs142292822	chr9:472534-472535	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs10974690	chr9:472591-472592	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs369092744	chr9:472598-472599	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs556157784	chr9:472622-472623	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564075641	chr9:472645-472646	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs138384292	chr9:472674-472675	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546628808	chr9:472680-472681	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs11788982	chr9:472702-472703	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112894317	chr9:472748-472749	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549244322	chr9:472749-472750	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192613512	chr9:472762-472763	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs538172123	chr9:472769-472770	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112826128	chr9:472775-472776	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542638410	chr9:472807-472808	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184228270	chr9:472816-472817	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs137955931	chr9:472817-472818	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs80079439	chr9:472834-472835	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553843024	chr9:472840-472841	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs573846691	chr9:472842-472843	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs77840001	chr9:472852-472853	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558161987	chr9:472868-472869	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs193078009	chr9:472874-472875	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs184706559	chr9:472875-472876	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543431389	chr9:472920-472921	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112400586	chr9:472921-472922	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs563710924	chr9:472966-472967	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs577526794	chr9:472995-472996	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142433967	chr9:473010-473011	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs146129512	chr9:473011-473012	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs35707414	chr9:473013-473014	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529024524	chr9:473014-473015	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs73639544	chr9:473048-473049	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138926059	chr9:473081-473082	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:2641 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:470800-472600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:470800-477400	Weak transcription	Aorta	Aorta
3	chr9:470800-477800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:471000-472400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:471000-472400	Enhancers	Esophagus	oesophagus
6	chr9:471000-472600	Enhancers	HepG2	liver
7	chr9:471000-472800	Enhancers	Placenta	Placenta
8	chr9:471000-473000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr9:471000-473200	Enhancers	Fetal Thymus	thymus
10	chr9:471000-477600	Weak transcription	Fetal Stomach	stomach
11	chr9:471200-472600	Enhancers	Spleen	Spleen
12	chr9:471200-474400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr9:471200-476600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr9:471400-472200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:471400-472400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr9:471400-472400	Weak transcription	Lung	lung
17	chr9:471400-472600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr9:471400-472600	Enhancers	Duodenum Mucosa	Duodenum
19	chr9:471400-473200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr9:471400-473200	Enhancers	Pancreas	Pancrea
21	chr9:471400-474200	Weak transcription	Primary T cells from cord blood	blood
22	chr9:471400-474400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr9:471400-474800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:471400-475200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr9:471400-475200	Weak transcription	Fetal Muscle Leg	muscle
26	chr9:471400-476200	Weak transcription	Gastric	stomach
27	chr9:471400-476400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr9:471400-476600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:471400-477800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:471400-480000	Weak transcription	Brain Substantia Nigra	brain
31	chr9:471600-472800	Weak transcription	Fetal Kidney	kidney
32	chr9:471600-475000	Weak transcription	Fetal Intestine Large	intestine
33	chr9:471600-475600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr9:471600-486000	Weak transcription	A549	lung
35	chr9:471800-472400	Weak transcription	Fetal Lung	lung
36	chr9:471800-474600	Weak transcription	Fetal Intestine Small	intestine
37	chr9:471800-475400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr9:472000-474000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:472000-476600	Weak transcription	Stomach Mucosa	stomach
40	chr9:472200-472800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr9:472400-472600	Enhancers	Fetal Lung	lung
42	chr9:472400-472600	Enhancers	Lung	lung
43	chr9:472400-472800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr9:472400-473000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr9:472400-473200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr9:472400-479800	Weak transcription	Esophagus	oesophagus
47	chr9:472600-477600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr9:472600-478000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:472800-473000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr9:472800-473200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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