Variant report

Variant	nsv1030163
Chromosome Location	chr8:48468835-48544495
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48531522-48531916	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48521014-48521055	K562	blood:	n/a	n/a
3	ARID3A	chr8:48469558-48470236	K562	blood:	n/a	n/a
4	ATF1	chr8:48469791-48470208	K562	blood:	n/a	n/a
5	ATF2	chr8:48513192-48513727	GM12878	blood:	n/a	n/a
6	ATF2	chr8:48510596-48510973	GM12878	blood:	n/a	n/a
7	ATF2	chr8:48510510-48511070	GM12878	blood:	n/a	n/a
8	ATF3	chr8:48510675-48511007	K562	blood:	n/a	n/a
9	BACH1	chr8:48520911-48521193	K562	blood:	n/a	n/a
10	BATF	chr8:48513237-48513650	GM12878	blood:	n/a	chr8:48513437-48513448
11	BATF	chr8:48513236-48513693	GM12878	blood:	n/a	chr8:48513437-48513448
12	BATF	chr8:48510570-48510905	GM12878	blood:	n/a	n/a
13	BATF	chr8:48510586-48511006	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:48510615-48510929	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:48486889-48487113	GM12878	blood:	n/a	n/a
16	BCL11A	chr8:48513234-48513581	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:48510631-48510906	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:48510587-48511026	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:48486816-48487206	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:48515128-48515535	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:48513269-48513679	GM12878	blood:	n/a	n/a
22	BHLHE40	chr8:48469788-48470117	K562	blood:	n/a	n/a
23	CBX3	chr8:48525057-48525544	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:48469664-48470193	K562	blood:	n/a	n/a
25	CCNT2	chr8:48469803-48470196	K562	blood:	n/a	chr8:48469952-48469972
26	CEBPB	chr8:48513700-48513901	K562	blood:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
27	CEBPB	chr8:48501316-48501609	IMR90	lung:	n/a	chr8:48501484-48501495
28	CEBPB	chr8:48513569-48514018	MCF-7	breast:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
29	CEBPB	chr8:48513623-48513989	HepG2	liver:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
30	CEBPB	chr8:48501324-48501652	K562	blood:	n/a	chr8:48501484-48501495
31	CEBPB	chr8:48513576-48514028	A549	lung:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
32	CEBPB	chr8:48540218-48540700	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:48469768-48470172	K562	blood:	n/a	n/a
34	CEBPB	chr8:48501337-48501644	HepG2	liver:	n/a	chr8:48501484-48501495
35	CEBPB	chr8:48524821-48525171	IMR90	lung:	n/a	chr8:48524997-48525008
36	CEBPB	chr8:48524887-48525168	Hela-S3	cervix:	n/a	chr8:48524997-48525008
37	CEBPB	chr8:48513625-48513994	A549	lung:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
38	CEBPB	chr8:48501327-48501645	A549	lung:	n/a	chr8:48501484-48501495
39	CEBPB	chr8:48522638-48523064	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:48513589-48514005	ECC-1	luminal epithelium:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
41	CEBPB	chr8:48513575-48514006	MCF-7	breast:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
42	CEBPB	chr8:48513606-48513962	H1-hESC	embryonic stem cell:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
43	CEBPB	chr8:48543166-48543451	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:48501463-48501545	H1-hESC	embryonic stem cell:	n/a	chr8:48501484-48501495
45	CEBPB	chr8:48524880-48525080	H1-hESC	embryonic stem cell:	n/a	chr8:48524997-48525008
46	CEBPB	chr8:48524922-48525149	HepG2	liver:	n/a	chr8:48524997-48525008
47	CEBPB	chr8:48513349-48513997	IMR90	lung:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
48	CEBPB	chr8:48513622-48513997	K562	blood:	n/a	chr8:48513805-48513816 chr8:48513805-48513818 chr8:48513805-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513807-48513818 chr8:48513807-48513816 chr8:48513807-48513816 chr8:48513805-48513818
49	CEBPB	chr8:48469807-48470195	K562	blood:	n/a	n/a
50	CEBPD	chr8:48469676-48470295	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48523498-48523548	ovcar-3	ovarian:	n/a
2	chr8:48517420-48517470	H1-hESC	embryonic stem cell:	embryo
3	chr8:48523498-48523548	GM12892	blood:	n/a
4	chr8:48486091-48486141	PFSK-1	brain:	n/a
5	chr8:48486091-48486141	HUVEC	blood vessel:	n/a
6	chr8:48523498-48523548	LNCaP	prostate:	n/a
7	chr8:48523498-48523548	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:48523498-48523548	Hepatocyte	liver:	n/a
9	chr8:48517420-48517470	PrEC	prostate:	n/a
10	chr8:48523498-48523548	GM12878	blood:	n/a
11	chr8:48523498-48523548	HIPEpiC	eye:	n/a
12	chr8:48517420-48517470	AG09309	skin:	n/a
13	chr8:48474400-48474450	T-47D	breast:	n/a
14	chr8:48474400-48474450	HEK293	kidney:	embryo
15	chr8:48474400-48474450	Caco-2	colon:	n/a
16	chr8:48517420-48517470	AG10803	skin:	n/a
17	chr8:48523498-48523548	NHBE	bronchial:	n/a
18	chr8:48486091-48486141	NH-A	brain:	n/a
19	chr8:48474400-48474450	NHBE	bronchial:	n/a
20	chr8:48517420-48517470	CMK	blood:	n/a
21	chr8:48474400-48474450	BJ	skin:	n/a
22	chr8:48523498-48523548	NB4	blood:	n/a
23	chr8:48517420-48517470	HCPEpiC	choroid plexus:	n/a
24	chr8:48523498-48523548	HAEpiC	amniotic membrane:	n/a
25	chr8:48486091-48486141	NHDF-neo	bronchial:	n/a
26	chr8:48486091-48486141	HRCEpiC	kidney:	n/a
27	chr8:48517420-48517470	GM12892	blood:	n/a
28	chr8:48486091-48486141	SK-N-MC	brain:	n/a
29	chr8:48474400-48474450	SK-N-SH_RA	brain:	n/a
30	chr8:48517420-48517470	Hepatocyte	liver:	n/a
31	chr8:48517420-48517470	SK-N-MC	brain:	n/a
32	chr8:48474400-48474450	HMEC	breast:	n/a
33	chr8:48517420-48517470	PANC-1	pancreas:	n/a
34	chr8:48474400-48474450	HCF	heart:	n/a
35	chr8:48486091-48486141	T-47D	breast:	n/a
36	chr8:48474400-48474450	PFSK-1	brain:	n/a
37	chr8:48517420-48517470	K562	blood:	n/a
38	chr8:48517420-48517470	GM12891	blood:	n/a
39	chr8:48474400-48474450	BE2_C	brain:	n/a
40	chr8:48523498-48523548	MCF10A-Er-Src	breast:	n/a
41	chr8:48523498-48523548	GM19239	blood:	n/a
42	chr8:48523498-48523548	AoSMC	blood vessel:	n/a
43	chr8:48486091-48486141	NHBE	bronchial:	n/a
44	chr8:48486091-48486141	PANC-1	pancreas:	n/a
45	chr8:48523498-48523548	NHDF-neo	bronchial:	n/a
46	chr8:48486091-48486141	HL-60	blood:	n/a
47	chr8:48486091-48486141	IMR90	lung:	fetal
48	chr8:48523498-48523548	A549	lung:	n/a
49	chr8:48517420-48517470	SAEC	small airway:	n/a
50	chr8:48474400-48474450	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:48521758..48524505-chr8:48647961..48649849,2	MCF-7	breast:
2	chr8:48529361..48531739-chr8:48533390..48535611,4	K562	blood:
3	chr8:48516911..48521430-chr8:48646759..48650653,4	K562	blood:
4	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
5	chr8:48467740..48469374-chr8:48475967..48477813,2	K562	blood:
6	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
7	chr8:48489348..48491815-chr8:48492654..48494861,2	K562	blood:
8	chr8:48467740..48469374-chr8:48475967..48477813,2	K562	blood:
9	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
10	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
11	chr8:48529413..48532601-chr8:48533499..48535653,4	K562	blood:
12	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
13	chr8:48467560..48471011-chr8:48644906..48648230,3	MCF-7	breast:
14	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
15	chr8:48493400..48495648-chr8:48645566..48647459,2	MCF-7	breast:
16	chr6:54711853..54714484-chr8:48522444..48524308,2	MCF-7	breast:
17	chr8:48524955..48527562-chr8:48528831..48532011,3	K562	blood:
18	chr8:48343800..48344570-chr8:48513956..48514755,2	MCF-7	breast:
19	chr8:48492450..48494081-chr8:48504159..48506029,2	K562	blood:
20	chr8:48468813..48471018-chr8:48483021..48485795,2	K562	blood:
21	chr8:48492643..48494808-chr8:48494843..48497616,2	K562	blood:
22	chr8:48490247..48491813-chr8:48492932..48495527,2	MCF-7	breast:
23	chr8:48489348..48491815-chr8:48492654..48494861,2	K562	blood:
24	chr8:48518671..48521335-chr8:48522262..48524014,3	MCF-7	breast:
25	chr8:48529219..48530791-chr8:48540316..48542801,2	MCF-7	breast:
26	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:
27	chr8:48468813..48471018-chr8:48483021..48485795,2	K562	blood:
28	chr8:48507124..48508721-chr8:48509922..48512866,2	MCF-7	breast:
29	chr8:48513464..48515742-chr8:48650061..48652115,2	MCF-7	breast:
30	chr8:48489915..48491427-chr8:48495181..48498031,2	MCF-7	breast:
31	chr8:48516477..48519191-chr8:48648055..48649779,2	MCF-7	breast:
32	chr8:48529361..48531739-chr8:48533390..48535611,4	K562	blood:
33	chr1:234744778..234747020-chr8:48484752..48487431,2	MCF-7	breast:
34	chr8:48524955..48527562-chr8:48528831..48532011,3	K562	blood:
35	chr8:48493147..48494925-chr8:48494980..48497854,3	MCF-7	breast:
36	chr8:48529219..48530791-chr8:48540316..48542801,2	MCF-7	breast:
37	chr8:48518004..48520090-chr8:48648537..48650198,2	K562	blood:
38	chr8:48544030..48546745-chr8:48645753..48648082,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEBPD-2	chr8:48504709-48505171	NONHSAT126451

Variant related genes	Relation type
ENSG00000254065	TF binding region
ENSG00000254065	CpG island
ENSG00000164808	chromatin interactions
ENSG00000254065	chromatin interactions
ENSG00000168264	chromatin interactions
ENSG00000221869	chromatin interactions

Extended variants
information (count: 2441 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10090740	chr8:48468835-48468836	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191603272	chr8:48468867-48468868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181216645	chr8:48468875-48468876	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557076756	chr8:48468889-48468890	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371756771	chr8:48468946-48468947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575197386	chr8:48468996-48468997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs542615258	chr8:48469044-48469045	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532792229	chr8:48469102-48469103	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561598735	chr8:48469145-48469146	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185345896	chr8:48469231-48469232	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs540957632	chr8:48469296-48469297	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565314550	chr8:48469401-48469402	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs189657245	chr8:48469405-48469406	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371594518	chr8:48469413-48469414	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140972202	chr8:48469441-48469442	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563380688	chr8:48469451-48469452	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183466465	chr8:48469456-48469457	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549079425	chr8:48469457-48469458	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs16927869	chr8:48469542-48469543	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs567515940	chr8:48469622-48469623	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116998514	chr8:48469810-48469811	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188914447	chr8:48469822-48469823	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs73567507	chr8:48469832-48469833	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs535105937	chr8:48469847-48469848	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191894615	chr8:48469855-48469856	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551933520	chr8:48469891-48469892	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs556991093	chr8:48469902-48469903	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148752521	chr8:48469981-48469982	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536211941	chr8:48470015-48470016	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142392284	chr8:48470043-48470044	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146861269	chr8:48470047-48470048	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs183848553	chr8:48470050-48470051	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs565610628	chr8:48470082-48470083	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs367562716	chr8:48470146-48470147	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577472890	chr8:48470180-48470181	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544822063	chr8:48470186-48470187	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532680932	chr8:48470200-48470201	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188346395	chr8:48470231-48470232	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549094433	chr8:48470298-48470299	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs554589766	chr8:48470302-48470303	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139753531	chr8:48470313-48470314	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs144517978	chr8:48470331-48470332	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs546540499	chr8:48470349-48470350	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548883849	chr8:48470369-48470370	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571214503	chr8:48470400-48470401	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371360013	chr8:48470475-48470476	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192936268	chr8:48470493-48470494	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs72646358	chr8:48470529-48470530	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs536327344	chr8:48470578-48470579	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555091163	chr8:48470607-48470608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	17142309	CNVD
22q11 deletion syndrome	20357662	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48466800-48479200	Weak transcription	Stomach Mucosa	stomach
2	chr8:48466800-48522600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:48467200-48474200	Weak transcription	Pancreas	Pancrea
4	chr8:48467200-48478800	Weak transcription	Psoas Muscle	Psoas
5	chr8:48467400-48471400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:48467400-48473000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:48467400-48473600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:48467400-48474400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:48467400-48475200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:48467400-48475600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:48467400-48475800	Weak transcription	Fetal Intestine Small	intestine
12	chr8:48467400-48475800	Weak transcription	Fetal Stomach	stomach
13	chr8:48467400-48476000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:48467400-48476000	Weak transcription	Lung	lung
15	chr8:48467400-48478200	Weak transcription	Spleen	Spleen
16	chr8:48467400-48479400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:48467400-48480000	Weak transcription	Primary B cells from cord blood	blood
18	chr8:48467400-48480800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr8:48467400-48481400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:48467400-48482400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr8:48467400-48484600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:48467400-48485400	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr8:48467400-48485800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr8:48467400-48486000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr8:48467400-48486000	Weak transcription	Esophagus	oesophagus
26	chr8:48467400-48486000	Weak transcription	Gastric	stomach
27	chr8:48467400-48486000	Weak transcription	Ovary	ovary
28	chr8:48467400-48492400	Weak transcription	Left Ventricle	heart
29	chr8:48467600-48471800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:48467600-48477600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr8:48467600-48479000	Weak transcription	Primary B cells from peripheral blood	blood
32	chr8:48467600-48479000	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr8:48467600-48480800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr8:48467800-48480800	Weak transcription	Dnd41	blood
35	chr8:48468200-48469200	Strong transcription	Primary T cells from cord blood	blood
36	chr8:48468400-48469200	Enhancers	K562	blood
37	chr8:48468600-48471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr8:48468800-48472800	Weak transcription	Fetal Muscle Leg	muscle
39	chr8:48469000-48481600	Weak transcription	GM12878-XiMat	blood
40	chr8:48469200-48470600	Flanking Active TSS	K562	blood
41	chr8:48469200-48471600	Weak transcription	Primary T cells from cord blood	blood
42	chr8:48469200-48472800	Weak transcription	Small Intestine	intestine
43	chr8:48470600-48472600	Enhancers	K562	blood
44	chr8:48470600-48474200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr8:48470800-48474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:48470800-48474800	Weak transcription	Placenta	Placenta
47	chr8:48470800-48478800	Weak transcription	Adipose Nuclei	Adipose
48	chr8:48471200-48474600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr8:48471400-48472200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr8:48471400-48472200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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