Variant report

Variant	nsv882461
Chromosome Location	chr5:99745767-99927338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1469)
CpG islands
(count:1041)
Chromatin interactive
region (count:25)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1469 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:99913247-99913398	HepG2	liver:	n/a	n/a
2	ATF1	chr5:99870740-99871206	K562	blood:	n/a	n/a
3	ATF2	chr5:99805499-99805973	GM12878	blood:	n/a	n/a
4	ATF2	chr5:99870721-99871127	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
5	ATF2	chr5:99870739-99871221	GM12878	blood:	n/a	chr5:99870979-99870990
6	ATF2	chr5:99870731-99871119	H1-hESC	embryonic stem cell:	n/a	chr5:99870979-99870990
7	ATF2	chr5:99870603-99871255	GM12878	blood:	n/a	chr5:99870979-99870990
8	ATF3	chr5:99870861-99871135	K562	blood:	n/a	chr5:99870978-99870988 chr5:99870981-99870989 chr5:99870978-99870988 chr5:99870981-99870988 chr5:99870979-99870990 chr5:99870981-99870992 chr5:99870977-99870992 chr5:99870979-99870990 chr5:99870978-99870991 chr5:99870981-99870991 chr5:99870977-99870990 chr5:99870978-99870989
9	BATF	chr5:99805639-99805821	GM12878	blood:	n/a	n/a
10	BATF	chr5:99805585-99805811	GM12878	blood:	n/a	n/a
11	BATF	chr5:99886169-99886390	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:99919773-99920253	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:99805489-99805819	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:99805514-99805830	GM12878	blood:	n/a	n/a
15	BCL11A	chr5:99886437-99886629	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:99919820-99920240	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:99886248-99886772	GM12878	blood:	n/a	n/a
18	BCLAF1	chr5:99870672-99871419	GM12878	blood:	n/a	chr5:99871059-99871068
19	BCLAF1	chr5:99765967-99766325	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:99871514-99871882	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:99766143-99766219	K562	blood:	n/a	n/a
22	BHLHE40	chr5:99919902-99920215	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:99870720-99871139	K562	blood:	n/a	n/a
24	BHLHE40	chr5:99805437-99805794	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:99870679-99871193	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr5:99870828-99871275	HepG2	liver:	n/a	n/a
27	BRCA1	chr5:99869580-99869678	GM12878	blood:	n/a	n/a
28	BRCA1	chr5:99870674-99871232	GM12878	blood:	n/a	n/a
29	BRCA1	chr5:99836226-99836426	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr5:99871514-99871714	K562	blood:	n/a	n/a
31	CEBPB	chr5:99870850-99871310	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:99890906-99891108	IMR90	lung:	n/a	n/a
33	CEBPB	chr5:99784002-99784355	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:99886551-99886855	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:99852928-99853520	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:99870900-99871110	K562	blood:	n/a	n/a
37	CEBPB	chr5:99841938-99842358	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:99853145-99853522	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr5:99891070-99891104	A549	lung:	n/a	n/a
40	CEBPB	chr5:99829791-99830035	HepG2	liver:	n/a	chr5:99829921-99829932
41	CEBPB	chr5:99870650-99871585	Hela-S3	cervix:	n/a	chr5:99870837-99870848
42	CEBPB	chr5:99784028-99784357	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:99784056-99784276	MCF-7	breast:	n/a	n/a
44	CEBPB	chr5:99898160-99898375	A549	lung:	n/a	n/a
45	CEBPB	chr5:99784033-99784358	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:99853275-99853404	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPD	chr5:99759761-99760095	K562	blood:	n/a	n/a
48	CHD1	chr5:99870636-99871628	GM12878	blood:	n/a	n/a
49	CHD2	chr5:99870788-99871395	HepG2	liver:	n/a	n/a
50	CHD2	chr5:99871489-99871707	Hela-S3	cervix:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:99870957-99871007	GM12892	blood:	n/a
2	chr5:99870957-99871007	HIPEpiC	eye:	n/a
3	chr5:99871073-99871123	HCT-116	colon:	n/a
4	chr5:99922152-99922202	ECC-1	luminal epithelium:	n/a
5	chr5:99870957-99871007	GM12892	blood:	n/a
6	chr5:99870957-99871007	HIPEpiC	eye:	n/a
7	chr5:99871073-99871123	HCT-116	colon:	n/a
8	chr5:99922152-99922202	ECC-1	luminal epithelium:	n/a
9	chr5:99886768-99886818	ovcar-3	ovarian:	n/a
10	chr5:99870957-99871007	LNCaP	prostate:	n/a
11	chr5:99871651-99871701	NB4	blood:	n/a
12	chr5:99870887-99870937	Jurkat	blood:	n/a
13	chr5:99871065-99871115	HEEpiC	esophagus:	n/a
14	chr5:99870926-99870976	A549	lung:	n/a
15	chr5:99871065-99871115	HCF	heart:	n/a
16	chr5:99871651-99871701	HUVEC	blood vessel:	n/a
17	chr5:99871683-99871733	HMEC	breast:	n/a
18	chr5:99871065-99871115	H1-hESC	embryonic stem cell:	embryo
19	chr5:99875156-99875206	AG09309	skin:	n/a
20	chr5:99870957-99871007	NH-A	brain:	n/a
21	chr5:99870926-99870976	H1-hESC	embryonic stem cell:	embryo
22	chr5:99871233-99871283	PFSK-1	brain:	n/a
23	chr5:99871651-99871701	AG10803	skin:	n/a
24	chr5:99875156-99875206	HCPEpiC	choroid plexus:	n/a
25	chr5:99870926-99870976	HL-60	blood:	n/a
26	chr5:99871683-99871733	AG09309	skin:	n/a
27	chr5:99871555-99871605	NH-A	brain:	n/a
28	chr5:99869796-99869846	HCT-116	colon:	n/a
29	chr5:99869796-99869846	GM12891	blood:	n/a
30	chr5:99870887-99870937	NH-A	brain:	n/a
31	chr5:99922152-99922202	SK-N-SH_RA	brain:	n/a
32	chr5:99869796-99869846	MCF10A-Er-Src	breast:	n/a
33	chr5:99871651-99871701	Hepatocyte	liver:	n/a
34	chr5:99869840-99869890	GM12878	blood:	n/a
35	chr5:99870961-99871011	MCF-7	breast:	n/a
36	chr5:99871026-99871076	HRCEpiC	kidney:	n/a
37	chr5:99871065-99871115	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:99870887-99870937	AG09319	gingival:	n/a
39	chr5:99871683-99871733	GM19239	blood:	n/a
40	chr5:99871026-99871076	HIPEpiC	eye:	n/a
41	chr5:99871073-99871123	PANC-1	pancreas:	n/a
42	chr5:99870961-99871011	U87	brain:	n/a
43	chr5:99871065-99871115	T-47D	breast:	n/a
44	chr5:99870955-99871005	HL-60	blood:	n/a
45	chr5:99869796-99869846	NH-A	brain:	n/a
46	chr5:99871073-99871123	ovcar-3	ovarian:	n/a
47	chr5:99871683-99871733	HCM	heart:	n/a
48	chr5:99871651-99871701	ovcar-3	ovarian:	n/a
49	chr5:99870926-99870976	T-47D	breast:	n/a
50	chr5:99870961-99871011	HPAEpiC	pulmonary alveolar:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:99843783..99845513-chr5:99845985..99848114,2	MCF-7	breast:
2	chr2:61371675..61372208-chr5:99870468..99871213,2	NB4	blood:
3	chr5:99870165..99872574-chr5:99872902..99874413,2	MCF-7	breast:
4	chr5:99814517..99815454-chr5:100725734..100726727,3	MCF-7	breast:
5	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:
6	chr5:99901928..99904752-chr5:99911773..99913756,2	MCF-7	breast:
7	chr5:99871520..99873605-chr5:99874648..99876676,2	MCF-7	breast:
8	chr5:99840638..99843580-chr5:99851710..99854340,2	MCF-7	breast:
9	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
10	chr4:32147186..32148048-chr5:99775915..99776706,2	MCF-7	breast:
11	chr5:99880455..99883115-chr5:99884041..99887018,2	MCF-7	breast:
12	chr5:99843783..99845513-chr5:99845985..99848114,2	MCF-7	breast:
13	chr5:99872854..99874470-chr5:99877624..99879735,2	K562	blood:
14	chr5:99814495..99815041-chr5:100726099..100726630,2	MCF-7	breast:
15	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
16	chr5:99813306..99815252-chr5:99818447..99820144,2	K562	blood:
17	chr5:99872854..99874470-chr5:99877624..99879735,2	K562	blood:
18	chr5:99840638..99843580-chr5:99851710..99854340,2	MCF-7	breast:
19	chr5:99871520..99873605-chr5:99874648..99876676,2	MCF-7	breast:
20	chr16:71322807..71323430-chr5:99870828..99871340,2	Hela-S3	cervix:
21	chr5:99861679..99863597-chr5:99869149..99871005,2	MCF-7	breast:
22	chr5:99901928..99904752-chr5:99911773..99913756,2	MCF-7	breast:
23	chr5:99852863..99854851-chr5:99869315..99872165,2	MCF-7	breast:
24	chr5:99763910..99766552-chr5:99768110..99770337,2	MCF-7	breast:
25	chr5:99862444..99865055-chr5:99868858..99871762,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST8SIA4-3	chr5:99869784-99869856	NONHSAT103002
2	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
3	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
4	lnc-FAM174A-1	chr5:99755149-99755217	XLOC_004490
5	lnc-FAM174A-1	chr5:99755954-99756452	XLOC_004490
6	lnc-ST8SIA4-3	chr5:99870865-99870890	ENSG00000247877
7	lnc-ST8SIA4-3	chr5:99785458-99786801	ENSG00000247877
8	lnc-FAM174A-1	chr5:99755149-99755217	NONHSAT103000
9	lnc-ST8SIA4-3	chr5:99785458-99786801	NONHSAT103002
10	lnc-ST8SIA4-3	chr5:99854234-99854315	NONHSAT103002
11	lnc-ST8SIA4-3	chr5:99862010-99862053	NONHSAT103002
12	lnc-ST8SIA4-3	chr5:99792761-99792828	ENSG00000247877
13	lnc-ST8SIA4-3	chr5:99862010-99862053	ENSG00000247877
14	lnc-ST8SIA4-3	chr5:99854234-99854315	ENSG00000247877
15	lnc-FAM174A-1	chr5:99759095-99759158	NONHSAT103000
16	lnc-ST8SIA4-3	chr5:99786639-99786801	ENSG00000247877
17	lnc-FAM174A-1	chr5:99755954-99756151	NONHSAT103000
18	lnc-ST8SIA4-3	chr5:99869784-99869856	ENSG00000247877
19	lnc-ST8SIA4-3	chr5:99870865-99870966	ENSG00000247877

No data

Variant related genes	Relation type
FAM174A	TF binding region
ENSG00000247877	TF binding region
FAM174A	CpG island
ENSG00000247877	CpG island
ENSG00000174132	chromatin interactions
ENSG00000180917	chromatin interactions
ENSG00000247877	chromatin interactions
ENSG00000212978	chromatin interactions
NOTCH2	miRNA target sites
TTLL12	miRNA target sites
RLF	miRNA target sites
LPGAT1	miRNA target sites
EIF2B1	miRNA target sites
ZBTB38	miRNA target sites
TJAP1	miRNA target sites
FRZB	miRNA target sites
FAM190B	miRNA target sites
CLDN12	miRNA target sites
HSPC159	miRNA target sites

Extended variants
information (count: 4315 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4315 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11738482	chr5:99745767-99745768	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs77798373	chr5:99745798-99745799	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs538957973	chr5:99745838-99745839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116112419	chr5:99745864-99745865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192569809	chr5:99745923-99745924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113995853	chr5:99745933-99745934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550421031	chr5:99745995-99745996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183253276	chr5:99746001-99746002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201029629	chr5:99746010-99746011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199559970	chr5:99746011-99746012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72060945	chr5:99746012-99746013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78660727	chr5:99746013-99746014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535611638	chr5:99746059-99746060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553935127	chr5:99746100-99746101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572349067	chr5:99746146-99746147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539496198	chr5:99746165-99746166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557598802	chr5:99746168-99746169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575967071	chr5:99746184-99746185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146768297	chr5:99746189-99746190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561979340	chr5:99746190-99746191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569881347	chr5:99746196-99746197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140227110	chr5:99746214-99746215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541385589	chr5:99746261-99746262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116420639	chr5:99746262-99746263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs145276454	chr5:99746290-99746291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552606484	chr5:99746336-99746337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564445378	chr5:99746432-99746433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188170614	chr5:99746462-99746463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6866895	chr5:99746472-99746473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549915565	chr5:99746473-99746474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531045262	chr5:99746484-99746485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568154805	chr5:99746489-99746490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374395645	chr5:99746506-99746507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564673718	chr5:99746508-99746509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535741163	chr5:99746528-99746529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535110815	chr5:99746532-99746533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202169341	chr5:99746639-99746640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192652651	chr5:99746668-99746669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565915798	chr5:99746678-99746679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539669696	chr5:99746695-99746696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs578180065	chr5:99746700-99746701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573811515	chr5:99746702-99746703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115873703	chr5:99746739-99746740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137895412	chr5:99746778-99746779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537193161	chr5:99746822-99746823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs149050362	chr5:99746827-99746828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112255396	chr5:99746831-99746832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541318007	chr5:99746858-99746859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183737826	chr5:99746859-99746860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577738226	chr5:99746863-99746864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:99744600-99746000	Enhancers	Fetal Lung	lung
2	chr5:99745400-99745800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:99745400-99745800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:99745400-99745800	Flanking Active TSS	Brain Germinal Matrix	brain
5	chr5:99745400-99745800	Flanking Active TSS	Fetal Brain Male	brain
6	chr5:99745600-99746000	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr5:99745800-99746000	Enhancers	Brain Germinal Matrix	brain
8	chr5:99745800-99747200	Enhancers	Fetal Brain Male	brain
9	chr5:99746000-99753200	Weak transcription	Fetal Lung	lung
10	chr5:99753200-99753400	Enhancers	Fetal Lung	lung
11	chr5:99753400-99760000	Weak transcription	Fetal Lung	lung
12	chr5:99753800-99765000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:99754000-99754200	Enhancers	Brain Germinal Matrix	brain
14	chr5:99754200-99756400	Weak transcription	Brain Germinal Matrix	brain
15	chr5:99754400-99755600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:99755600-99756400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:99758200-99758400	Enhancers	HSMM	muscle
18	chr5:99758200-99759200	Enhancers	HSMMtube	muscle
19	chr5:99758600-99759000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:99758800-99759200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr5:99759000-99759200	Enhancers	HSMM	muscle
22	chr5:99759000-99759600	Enhancers	Hela-S3	cervix
23	chr5:99759000-99759600	Enhancers	HUVEC	blood vessel
24	chr5:99759000-99760200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:99759600-99760000	Weak transcription	Hela-S3	cervix
26	chr5:99759600-99760000	Weak transcription	HUVEC	blood vessel
27	chr5:99760000-99760400	Enhancers	Hela-S3	cervix
28	chr5:99760000-99760400	Enhancers	HUVEC	blood vessel
29	chr5:99760000-99761000	ZNF genes & repeats	Fetal Lung	lung
30	chr5:99760000-99761600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr5:99760200-99760600	ZNF genes & repeats	Fetal Kidney	kidney
32	chr5:99760200-99761400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:99761600-99762200	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr5:99762200-99762400	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr5:99766200-99767000	Enhancers	Fetal Lung	lung
36	chr5:99766200-99767400	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr5:99767400-99769000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr5:99769000-99770800	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr5:99770400-99770800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr5:99770400-99770800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr5:99776400-99776800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:99782600-99786400	Enhancers	Fetal Lung	lung
43	chr5:99783800-99784400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:99783800-99784600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:99790200-99790800	Enhancers	HUVEC	blood vessel
46	chr5:99799600-99800000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr5:99800000-99800600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:99800000-99800600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr5:99800000-99800600	Enhancers	Osteobl	bone
50	chr5:99800600-99801000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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