Variant report

Variant	nsv522860
Chromosome Location	chr8:11253879-11330364
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2953)
CpG islands
(count:1588)
Chromatin interactive
region (count:76)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2953 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11316723-11316731	K562	blood:	n/a	n/a
2	ATF2	chr8:11324016-11324675	GM12878	blood:	n/a	chr8:11324301-11324315
3	ATF2	chr8:11324764-11325260	GM12878	blood:	n/a	n/a
4	ATF2	chr8:11274346-11276085	GM12878	blood:	n/a	chr8:11274443-11274454
5	ATF2	chr8:11279080-11280560	GM12878	blood:	n/a	n/a
6	ATF2	chr8:11275318-11275829	GM12878	blood:	n/a	n/a
7	ATF2	chr8:11323929-11324646	GM12878	blood:	n/a	chr8:11324301-11324315
8	ATF2	chr8:11324173-11324549	H1-hESC	embryonic stem cell:	n/a	chr8:11324301-11324315
9	ATF2	chr8:11279079-11280817	GM12878	blood:	n/a	n/a
10	ATF2	chr8:11315230-11315949	GM12878	blood:	n/a	n/a
11	ATF2	chr8:11315280-11316048	GM12878	blood:	n/a	n/a
12	ATF2	chr8:11282883-11283890	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr8:11324094-11324537	A549	lung:	n/a	chr8:11324303-11324316 chr8:11324303-11324314
14	ATF3	chr8:11315223-11315952	A549	lung:	n/a	n/a
15	ATF3	chr8:11324145-11324449	K562	blood:	n/a	chr8:11324303-11324316 chr8:11324303-11324314
16	ATF3	chr8:11315223-11315713	A549	lung:	n/a	n/a
17	BACH1	chr8:11325083-11325410	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr8:11281249-11281559	K562	blood:	n/a	n/a
19	BACH1	chr8:11267189-11267272	K562	blood:	n/a	n/a
20	BACH1	chr8:11324297-11324869	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:11281229-11281554	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr8:11309352-11309615	GM12878	blood:	n/a	n/a
23	BATF	chr8:11280097-11280511	GM12878	blood:	n/a	n/a
24	BATF	chr8:11306463-11306721	GM12878	blood:	n/a	n/a
25	BATF	chr8:11275313-11275910	GM12878	blood:	n/a	n/a
26	BATF	chr8:11279101-11279992	GM12878	blood:	n/a	n/a
27	BATF	chr8:11315333-11315981	GM12878	blood:	n/a	chr8:11315647-11315658
28	BATF	chr8:11315460-11315847	GM12878	blood:	n/a	chr8:11315647-11315658
29	BATF	chr8:11279150-11279899	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:11279119-11279958	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:11280161-11280728	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:11275326-11275768	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:11324115-11324617	GM12878	blood:	n/a	chr8:11324201-11324214
34	BCL11A	chr8:11279109-11279944	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:11315340-11315826	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:11274809-11275187	GM12878	blood:	n/a	n/a
37	BCL11A	chr8:11280048-11280701	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:11324299-11324584	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:11275293-11275786	GM12878	blood:	n/a	n/a
40	BCL3	chr8:11314572-11315907	A549	lung:	n/a	chr8:11314807-11314816 chr8:11314808-11314817
41	BCL3	chr8:11323781-11324619	GM12878	blood:	n/a	chr8:11324201-11324214 chr8:11324071-11324084 chr8:11324068-11324081 chr8:11324074-11324087 chr8:11324104-11324113 chr8:11324077-11324086
42	BCL3	chr8:11324188-11324646	A549	lung:	n/a	chr8:11324201-11324214
43	BCL3	chr8:11313823-11314324	A549	lung:	n/a	n/a
44	BCL3	chr8:11315168-11315821	A549	lung:	n/a	n/a
45	BCL3	chr8:11280032-11280582	GM12878	blood:	n/a	n/a
46	BCL3	chr8:11315296-11316136	GM12878	blood:	n/a	n/a
47	BCL3	chr8:11254759-11255021	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:11271137-11271639	GM12878	blood:	n/a	n/a
49	BCLAF1	chr8:11279067-11279641	GM12878	blood:	n/a	n/a
50	BCLAF1	chr8:11275336-11275807	GM12878	blood:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11302243-11302293	GM12892	blood:	n/a
2	chr8:11283299-11283349	GM12891	blood:	n/a
3	chr8:11302243-11302293	GM12892	blood:	n/a
4	chr8:11283299-11283349	GM12891	blood:	n/a
5	chr8:11324244-11324294	SAEC	small airway:	n/a
6	chr8:11324687-11324737	NT2-D1	testis:	n/a
7	chr8:11324448-11324498	HCM	heart:	n/a
8	chr8:11324327-11324377	SKMC	muscle:	n/a
9	chr8:11311868-11311918	U87	brain:	n/a
10	chr8:11327014-11327064	GM12892	blood:	n/a
11	chr8:11320112-11320162	Caco-2	colon:	n/a
12	chr8:11304273-11304323	SK-N-SH_RA	brain:	n/a
13	chr8:11324327-11324377	HMEC	breast:	n/a
14	chr8:11327014-11327064	PANC-1	pancreas:	n/a
15	chr8:11324666-11324716	PFSK-1	brain:	n/a
16	chr8:11311868-11311918	ovcar-3	ovarian:	n/a
17	chr8:11327014-11327064	HEK293	kidney:	embryo
18	chr8:11324327-11324377	PrEC	prostate:	n/a
19	chr8:11304273-11304323	K562	blood:	n/a
20	chr8:11302030-11302080	GM12892	blood:	n/a
21	chr8:11302983-11303033	U87	brain:	n/a
22	chr8:11327014-11327064	GM12878	blood:	n/a
23	chr8:11327014-11327064	AoSMC	blood vessel:	n/a
24	chr8:11303039-11303089	H1-hESC	embryonic stem cell:	embryo
25	chr8:11324446-11324496	HepG2	liver:	n/a
26	chr8:11323474-11323524	PANC-1	pancreas:	n/a
27	chr8:11327014-11327064	HAEpiC	amniotic membrane:	n/a
28	chr8:11324327-11324377	GM12892	blood:	n/a
29	chr8:11302030-11302080	HEK293	kidney:	embryo
30	chr8:11323474-11323524	AG10803	skin:	n/a
31	chr8:11284912-11284962	HCF	heart:	n/a
32	chr8:11327014-11327064	SKMC	muscle:	n/a
33	chr8:11296980-11297030	SK-N-SH	brain:	n/a
34	chr8:11324817-11324867	HUVEC	blood vessel:	n/a
35	chr8:11303828-11303878	LNCaP	prostate:	n/a
36	chr8:11324687-11324737	HRCEpiC	kidney:	n/a
37	chr8:11304273-11304323	SK-N-MC	brain:	n/a
38	chr8:11324666-11324716	BE2_C	brain:	n/a
39	chr8:11302243-11302293	Caco-2	colon:	n/a
40	chr8:11287657-11287707	SK-N-SH_RA	brain:	n/a
41	chr8:11283299-11283349	HEK293	kidney:	embryo
42	chr8:11302243-11302293	SAEC	small airway:	n/a
43	chr8:11324048-11324098	AG04450	lung:	fetal
44	chr8:11324687-11324737	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:11296980-11297030	AG04450	lung:	fetal
46	chr8:11324666-11324716	K562	blood:	n/a
47	chr8:11324244-11324294	NH-A	brain:	n/a
48	chr8:11324806-11324856	Hela-S3	cervix:	n/a
49	chr8:11303039-11303089	GM12891	blood:	n/a
50	chr8:11324666-11324716	HEK293	kidney:	embryo

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11301164..11304076-chr8:11323710..11325324,2	K562	blood:
2	chr8:11328896..11331385-chr8:11333353..11335506,3	K562	blood:
3	chr8:11312294..11314584-chr8:11324898..11327052,2	K562	blood:
4	chr8:11269234..11272216-chr8:11272728..11274513,2	K562	blood:
5	chr8:11301164..11304076-chr8:11323710..11325324,2	K562	blood:
6	chr8:11277465..11279000-chr8:11280296..11282136,2	K562	blood:
7	chr8:11268709..11269611-chr8:11315574..11316471,2	K562	blood:
8	chr8:11312570..11318244-chr8:11320573..11323970,6	K562	blood:
9	chr8:11271149..11271854-chr8:11412541..11413131,2	MCF-7	breast:
10	chr8:11203206..11204716-chr8:11251549..11254468,2	K562	blood:
11	chr8:11269234..11272216-chr8:11272728..11274513,2	K562	blood:
12	chr8:11270864..11271417-chr8:11324839..11325370,2	K562	blood:
13	chr8:11303566..11306251-chr8:11321499..11323964,2	MCF-7	breast:
14	chr8:11173378..11174004-chr8:11266732..11267373,2	MCF-7	breast:
15	chr8:11204194..11206548-chr8:11284736..11287319,2	K562	blood:
16	chr8:11270954..11271858-chr8:11324416..11325957,6	MCF-7	breast:
17	chr8:11311333..11313794-chr8:11324898..11327371,2	K562	blood:
18	chr8:11268286..11268904-chr8:11447156..11448012,2	K562	blood:
19	chr8:11268366..11270477-chr8:11325534..11327747,2	MCF-7	breast:
20	chr8:11303566..11306251-chr8:11321499..11323964,2	MCF-7	breast:
21	chr8:11270794..11271511-chr8:11421638..11422402,4	MCF-7	breast:
22	chr8:11322451..11325795-chr8:11329496..11335044,6	MCF-7	breast:
23	chr8:11269226..11269868-chr8:11286430..11287417,2	K562	blood:
24	chr8:11159367..11162691-chr8:11316510..11321033,4	K562	blood:
25	chr8:11313214..11317170-chr8:11317580..11320923,5	K562	blood:
26	chr8:11306300..11308613-chr8:11308996..11313515,5	K562	blood:
27	chr8:11268366..11270477-chr8:11325534..11327747,2	MCF-7	breast:
28	chr8:11270968..11271833-chr8:11411148..11411819,2	MCF-7	breast:
29	chr8:11242265..11244818-chr8:11252582..11254482,2	MCF-7	breast:
30	chr8:11268882..11269661-chr8:11411000..11411902,2	MCF-7	breast:
31	chr8:11291994..11295873-chr8:11300373..11305945,6	K562	blood:
32	chr8:11286965..11287640-chr8:11410754..11411417,2	MCF-7	breast:
33	chr8:11278797..11280380-chr8:11316966..11319071,2	K562	blood:
34	chr8:11273893..11276099-chr8:11313214..11316137,2	MCF-7	breast:
35	chr8:11322451..11325795-chr8:11329496..11335044,6	MCF-7	breast:
36	chr8:11306364..11309144-chr8:11311400..11314118,3	MCF-7	breast:
37	chr8:11294217..11296027-chr8:11297947..11300867,2	MCF-7	breast:
38	chr8:11269226..11269868-chr8:11286430..11287417,2	K562	blood:
39	chr8:11313788..11316536-chr8:11322548..11325766,4	MCF-7	breast:
40	chr8:11277465..11279000-chr8:11280296..11282136,2	K562	blood:
41	chr8:11194174..11194960-chr8:11325192..11325823,2	K562	blood:
42	chr8:11271761..11274397-chr8:11330948..11333721,2	MCF-7	breast:
43	chr8:11319006..11321957-chr8:11323524..11325949,2	MCF-7	breast:
44	chr8:11141824..11143509-chr8:11265608..11267420,2	MCF-7	breast:
45	chr8:11306364..11309144-chr8:11311400..11314118,3	MCF-7	breast:
46	chr8:11297376..11298167-chr8:11588230..11588817,3	MCF-7	breast:
47	chr8:11299743..11301452-chr8:11307305..11309157,2	MCF-7	breast:
48	chr8:11266403..11269696-chr8:11413780..11416893,3	MCF-7	breast:
49	chr8:11266732..11267234-chr8:11421696..11422273,2	K562	blood:
50	chr8:11302281..11304397-chr8:11308190..11310452,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf12-1	chr8:11291429-11291644	NONHSAT125054
2	lnc-C8orf12-1	chr8:11263321-11263371	ucscGeneNc_uc003wtu_2
3	lnc-C8orf12-1	chr8:11258575-11258674	NONHSAT125056
4	lnc-C8orf12-1	chr8:11262050-11262211	NONHSAT125056
5	lnc-RP11-148O21.3.1-3	chr8:11324135-11324244	NONHSAT125061
6	lnc-RP11-148O21.3.1-3	chr8:11302929-11303079	NONHSAT125061
7	lnc-RP11-148O21.3.1-3	chr8:11303912-11304130	NONHSAT125061
8	lnc-C8orf12-1	chr8:11292339-11292611	NR_026814
9	lnc-C8orf12-1	chr8:11295945-11296166	NONHSAT125056
10	lnc-C8orf12-1	chr8:11328839-11329054	ucscGeneNc_uc003wtu_2
11	lnc-C8orf12-1	chr8:11292339-11292510	NONHSAT125054
12	lnc-C8orf12-1	chr8:11295985-11296084	ucscGeneNc_uc003wtu_2
13	lnc-BLK-2	chr8:11279007-11280419	NONHSAT125057
14	lnc-C8orf12-1	chr8:11295549-11295719	NONHSAT125056
15	lnc-C8orf12-1	chr8:11329749-11330021	ucscGeneNc_uc003wtu_2
16	lnc-BLK-2	chr8:11280428-11280443	NONHSAT125057
17	lnc-C8orf12-1	chr8:11295549-11295719	NR_026814
18	lnc-C8orf12-1	chr8:11291429-11291644	NONHSAT125056
19	lnc-C8orf12-1	chr8:11278732-11278920	ucscGeneNc_uc003wtu_2
20	lnc-C8orf12-1	chr8:11291429-11291644	NR_026814
21	lnc-C8orf12-1	chr8:11295945-11296166	NR_026814
22	lnc-C8orf12-1	chr8:11258575-11258674	NR_026814
23	lnc-C8orf12-1	chr8:11292339-11292611	NONHSAT125056
24	lnc-RP11-148O21.3.1-3	chr8:11302086-11302317	NONHSAT125061
25	lnc-C8orf12-1	chr8:11258575-11258674	NONHSAT125054

No data

Variant related genes	Relation type
C8orf12	TF binding region
RNU6-1084P	TF binding region
FAM167A	TF binding region
C8orf12	CpG island
RNU6-1084P	CpG island
FAM167A	CpG island
ENSG00000255518	chromatin interactions
ENSG00000254774	chromatin interactions
ENSG00000154316	chromatin interactions
ENSG00000154319	chromatin interactions
ENSG00000255020	chromatin interactions
ENSG00000104643	chromatin interactions

Extended variants
information (count: 4134 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:4134 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10105588	chr8:11253879-11253880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372157455	chr8:11253881-11253882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528383582	chr8:11253895-11253896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs75702868	chr8:11253929-11253930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375560262	chr8:11253933-11253934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562125294	chr8:11253944-11253945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529265221	chr8:11253956-11253957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192238419	chr8:11253957-11253958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183570096	chr8:11253981-11253982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188572379	chr8:11254071-11254072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192043787	chr8:11254125-11254126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567042199	chr8:11254129-11254130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534498609	chr8:11254133-11254134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138429591	chr8:11254236-11254237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555743599	chr8:11254303-11254304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184228893	chr8:11254315-11254316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374618292	chr8:11254339-11254340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34128921	chr8:11254365-11254366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187008901	chr8:11254366-11254367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570461204	chr8:11254397-11254398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs397891411	chr8:11254400-11254401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34198094	chr8:11254401-11254402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149279908	chr8:11254443-11254444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368256519	chr8:11254497-11254498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144541696	chr8:11254502-11254503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572662858	chr8:11254515-11254516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540563550	chr8:11254559-11254560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546209508	chr8:11254560-11254561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561834253	chr8:11254594-11254595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148046941	chr8:11254600-11254601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544264942	chr8:11254615-11254616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141737647	chr8:11254624-11254625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533487262	chr8:11254668-11254669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563505926	chr8:11254673-11254674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191608927	chr8:11254736-11254737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566159191	chr8:11254738-11254739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184439928	chr8:11254740-11254741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535345771	chr8:11254742-11254743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73536174	chr8:11254753-11254754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549697336	chr8:11254781-11254782	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs117908970	chr8:11254787-11254788	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535464262	chr8:11254793-11254794	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556696273	chr8:11254794-11254795	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs568482529	chr8:11254812-11254813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs568708837	chr8:11254818-11254819	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs539158566	chr8:11254846-11254847	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs113961022	chr8:11254853-11254854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs143558879	chr8:11254854-11254855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs190523622	chr8:11254861-11254862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs73536179	chr8:11254868-11254869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1923 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11251800-11254600	Weak transcription	Pancreas	Pancrea
2	chr8:11254600-11254800	Enhancers	Pancreas	Pancrea
3	chr8:11264800-11265400	Enhancers	Stomach Mucosa	stomach
4	chr8:11265200-11265400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:11265400-11269200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:11267000-11267200	Enhancers	Brain Substantia Nigra	brain
7	chr8:11267000-11271400	Enhancers	Fetal Heart	heart
8	chr8:11267200-11267600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:11267200-11267600	Enhancers	A549	lung
10	chr8:11267400-11267600	Enhancers	Fetal Brain Male	brain
11	chr8:11267400-11268200	Enhancers	Fetal Brain Female	brain
12	chr8:11267600-11268000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:11267600-11268800	Weak transcription	A549	lung
14	chr8:11267800-11268000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr8:11267800-11268000	Enhancers	Brain Anterior Caudate	brain
16	chr8:11267800-11269200	Weak transcription	Fetal Brain Male	brain
17	chr8:11268000-11268200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:11268000-11268600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:11268000-11269200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:11268200-11269000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:11268200-11269200	Weak transcription	Fetal Brain Female	brain
22	chr8:11268600-11269000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:11268800-11269000	Enhancers	A549	lung
24	chr8:11268800-11269400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr8:11268800-11269600	Enhancers	HSMM	muscle
26	chr8:11269000-11269200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr8:11269000-11269200	Bivalent Enhancer	Brain Hippocampus Middle	brain
28	chr8:11269000-11269200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
29	chr8:11269000-11269200	Flanking Active TSS	A549	lung
30	chr8:11269000-11269200	Flanking Active TSS	HSMMtube	muscle
31	chr8:11269000-11269200	Enhancers	K562	blood
32	chr8:11269000-11269400	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr8:11269000-11269400	Bivalent Enhancer	Fetal Intestine Small	intestine
34	chr8:11269000-11269600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
35	chr8:11269000-11269600	Bivalent Enhancer	NH-A	brain
36	chr8:11269000-11269800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
37	chr8:11269000-11269800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:11269000-11269800	Enhancers	Brain Angular Gyrus	brain
39	chr8:11269000-11270000	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr8:11269000-11270200	Enhancers	Brain Substantia Nigra	brain
41	chr8:11269000-11271200	Enhancers	Brain Germinal Matrix	brain
42	chr8:11269000-11271400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:11269200-11269400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
44	chr8:11269200-11269400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr8:11269200-11269400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:11269200-11269400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:11269200-11269400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr8:11269200-11269400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr8:11269200-11269400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:11269200-11269400	Bivalent Enhancer	Adipose Nuclei	Adipose

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