Variant report

Variant	nsv427983
Chromosome Location	chr16:47316866-47606287
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2464)
CpG islands
(count:1343)
Chromatin interactive
region (count:155)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2464 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47509336-47510111	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47499795-47500033	K562	blood:	n/a	n/a
3	ARID3A	chr16:47500293-47502483	K562	blood:	n/a	n/a
4	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
5	ARID3A	chr16:47484519-47484647	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
7	ARID3A	chr16:47572269-47572803	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
9	ARID3A	chr16:47421094-47421294	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47507738-47508382	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:47482890-47483076	K562	blood:	n/a	n/a
12	ARID3A	chr16:47498536-47498645	K562	blood:	n/a	n/a
13	ARID3A	chr16:47426038-47426363	K562	blood:	n/a	n/a
14	ARID3A	chr16:47357253-47357463	HepG2	liver:	n/a	n/a
15	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
16	ARID3A	chr16:47428252-47428453	HepG2	liver:	n/a	n/a
17	ARID3A	chr16:47431618-47431623	HepG2	liver:	n/a	n/a
18	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
19	ARID3A	chr16:47519386-47519410	HepG2	liver:	n/a	n/a
20	ARID3A	chr16:47507313-47507485	HepG2	liver:	n/a	n/a
21	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
22	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
23	ARID3A	chr16:47495283-47496261	K562	blood:	n/a	n/a
24	ARID3A	chr16:47494825-47496228	HepG2	liver:	n/a	n/a
25	ATF1	chr16:47495611-47496214	K562	blood:	n/a	n/a
26	ATF1	chr16:47426003-47426482	K562	blood:	n/a	n/a
27	ATF1	chr16:47554214-47554593	K562	blood:	n/a	n/a
28	ATF1	chr16:47422668-47422993	K562	blood:	n/a	n/a
29	ATF1	chr16:47501985-47502361	K562	blood:	n/a	n/a
30	ATF1	chr16:47599472-47599607	K562	blood:	n/a	n/a
31	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
32	ATF1	chr16:47427309-47427338	K562	blood:	n/a	n/a
33	ATF2	chr16:47344576-47345243	GM12878	blood:	n/a	n/a
34	ATF2	chr16:47351722-47352080	GM12878	blood:	n/a	n/a
35	ATF2	chr16:47557169-47557724	GM12878	blood:	n/a	n/a
36	ATF2	chr16:47526273-47527368	GM12878	blood:	n/a	n/a
37	ATF3	chr16:47494735-47495286	K562	blood:	n/a	n/a
38	ATF3	chr16:47494883-47495224	GM12878	blood:	n/a	n/a
39	ATF3	chr16:47494783-47495259	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF3	chr16:47494770-47495381	GM12878	blood:	n/a	n/a
41	ATF3	chr16:47494797-47495311	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr16:47494617-47495423	HepG2	liver:	n/a	n/a
43	ATF3	chr16:47494755-47495369	HepG2	liver:	n/a	n/a
44	ATF3	chr16:47501997-47502334	K562	blood:	n/a	n/a
45	ATF3	chr16:47494801-47495349	K562	blood:	n/a	n/a
46	BACH1	chr16:47495724-47496205	K562	blood:	n/a	n/a
47	BACH1	chr16:47495881-47496208	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr16:47538552-47539389	K562	blood:	n/a	n/a
49	BACH1	chr16:47502025-47502424	K562	blood:	n/a	n/a
50	BACH1	chr16:47502056-47502356	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47495113-47495163	PFSK-1	brain:	n/a
2	chr16:47495113-47495163	PFSK-1	brain:	n/a
3	chr16:47338451-47338501	U87	brain:	n/a
4	chr16:47495110-47495160	ProgFib	skin:	n/a
5	chr16:47494711-47494761	NHDF-neo	bronchial:	n/a
6	chr16:47494258-47494308	PrEC	prostate:	n/a
7	chr16:47495541-47495591	Jurkat	blood:	n/a
8	chr16:47527034-47527084	RPTEC	kidney:	n/a
9	chr16:47494735-47494785	HPAEpiC	pulmonary alveolar:	n/a
10	chr16:47494258-47494308	ECC-1	luminal epithelium:	n/a
11	chr16:47495445-47495495	HEK293	kidney:	embryo
12	chr16:47495541-47495591	SK-N-SH	brain:	n/a
13	chr16:47495768-47495818	HCM	heart:	n/a
14	chr16:47494711-47494761	MCF10A-Er-Src	breast:	n/a
15	chr16:47588660-47588710	PrEC	prostate:	n/a
16	chr16:47494711-47494761	HPAEpiC	pulmonary alveolar:	n/a
17	chr16:47539137-47539187	AG09309	skin:	n/a
18	chr16:47539203-47539253	CMK	blood:	n/a
19	chr16:47539166-47539216	AG04449	skin:	fetal
20	chr16:47495746-47495796	GM12892	blood:	n/a
21	chr16:47494258-47494308	AG04450	lung:	fetal
22	chr16:47588660-47588710	AG04449	skin:	fetal
23	chr16:47338451-47338501	SK-N-MC	brain:	n/a
24	chr16:47494258-47494308	HepG2	liver:	n/a
25	chr16:47344826-47344876	BJ	skin:	n/a
26	chr16:47495541-47495591	HCPEpiC	choroid plexus:	n/a
27	chr16:47527034-47527084	Jurkat	blood:	n/a
28	chr16:47527034-47527084	Hela-S3	cervix:	n/a
29	chr16:47539203-47539253	RPTEC	kidney:	n/a
30	chr16:47495768-47495818	HUVEC	blood vessel:	n/a
31	chr16:47492286-47492336	NHBE	bronchial:	n/a
32	chr16:47338451-47338501	AoSMC	blood vessel:	n/a
33	chr16:47495768-47495818	AG04450	lung:	fetal
34	chr16:47539166-47539216	GM12878	blood:	n/a
35	chr16:47494711-47494761	NH-A	brain:	n/a
36	chr16:47495768-47495818	NH-A	brain:	n/a
37	chr16:47344826-47344876	PrEC	prostate:	n/a
38	chr16:47539166-47539216	HCT-116	colon:	n/a
39	chr16:47494711-47494761	T-47D	breast:	n/a
40	chr16:47420506-47420556	LNCaP	prostate:	n/a
41	chr16:47344826-47344876	AG09319	gingival:	n/a
42	chr16:47497822-47497872	Jurkat	blood:	n/a
43	chr16:47495541-47495591	GM12878	blood:	n/a
44	chr16:47495768-47495818	HPAEpiC	pulmonary alveolar:	n/a
45	chr16:47494258-47494308	HRPEpiC	eye:	n/a
46	chr16:47495113-47495163	HCM	heart:	n/a
47	chr16:47539137-47539187	ECC-1	luminal epithelium:	n/a
48	chr16:47494824-47494874	AG09309	skin:	n/a
49	chr16:47362879-47362929	SKMC	muscle:	n/a
50	chr16:47539137-47539187	Hela-S3	cervix:	n/a

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:47419086..47421518-chr16:47425690..47428678,2	K562	blood:
2	chr16:47493966..47496755-chr16:47501403..47504796,3	MCF-7	breast:
3	chr16:47538608..47539232-chr19:24184323..24185236,2	MCF-7	breast:
4	chr16:47500342..47506721-chr16:47514207..47520673,8	K562	blood:
5	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
6	chr16:47418744..47420370-chr16:47492976..47495384,2	K562	blood:
7	chr16:47481523..47483741-chr16:47529384..47531603,2	K562	blood:
8	chr16:47517170..47520211-chr16:47526974..47528925,3	K562	blood:
9	chr16:47464879..47466397-chr16:47504717..47506667,2	K562	blood:
10	chr16:47538686..47539206-chr5:50081215..50081735,2	MCF-7	breast:
11	chr16:47426138..47427741-chr16:47428449..47430981,2	K562	blood:
12	chr16:47500342..47506721-chr16:47514207..47520673,8	K562	blood:
13	chr16:47439487..47441195-chr16:47493204..47494931,2	K562	blood:
14	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
15	chr16:47449583..47451141-chr16:47452818..47455615,2	K562	blood:
16	chr16:47516457..47520432-chr16:47524851..47526977,4	K562	blood:
17	chr16:47449583..47451141-chr16:47452818..47455615,2	K562	blood:
18	chr16:47502099..47504584-chr16:47526951..47528627,3	K562	blood:
19	chr16:47483080..47485293-chr16:47494461..47496130,2	K562	blood:
20	chr16:47441890..47444403-chr16:47493696..47496197,3	K562	blood:
21	chr16:47533842..47536233-chr16:47541991..47544849,2	K562	blood:
22	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
23	chr16:47439487..47441195-chr16:47493204..47494931,2	K562	blood:
24	chr16:47506877..47508386-chr16:47511006..47513909,2	K562	blood:
25	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
26	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
27	chr16:47535504..47537200-chr16:47537688..47539463,2	K562	blood:
28	chr16:47560964..47562749-chr16:47565268..47567477,2	K562	blood:
29	chr16:47503547..47505420-chr16:47506732..47508518,2	K562	blood:
30	chr16:47416227..47418087-chr16:47500282..47502102,2	K562	blood:
31	chr16:47177492..47179325-chr16:47500185..47502883,2	K562	blood:
32	chr1:192021477..192022058-chr16:47435294..47435896,2	MCF-7	breast:
33	chr16:47343363..47345915-chr16:47349595..47352299,2	K562	blood:
34	chr16:47486141..47491798-chr16:47493044..47496709,8	MCF-7	breast:
35	chr16:47386165..47387733-chr16:47392448..47394557,2	K562	blood:
36	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
37	chr16:47386165..47387733-chr16:47392448..47394557,2	K562	blood:
38	chr16:47416227..47418087-chr16:47500282..47502102,2	K562	blood:
39	chr16:47176885..47177462-chr16:47479483..47480444,2	K562	blood:
40	chr16:47421435..47423287-chr16:47429426..47431466,2	MCF-7	breast:
41	chr16:47503547..47505420-chr16:47506732..47508518,2	K562	blood:
42	chr16:47495155..47497057-chr16:47571448..47573039,2	K562	blood:
43	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
44	chr16:47594118..47597140-chr16:47598345..47602068,5	K562	blood:
45	chr16:47505221..47508195-chr16:47519032..47520673,2	K562	blood:
46	chr16:47165353..47167030-chr16:47501273..47503652,2	K562	blood:
47	chr16:47479859..47483126-chr16:47518741..47522601,4	K562	blood:
48	chr16:47521997..47524877-chr16:47525537..47527944,2	K562	blood:
49	chr16:47514435..47516490-chr16:47516541..47519935,3	K562	blood:
50	chr12:25403374..25403874-chr16:47495157..47495674,2	Hela-S3	cervix:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITFG1-1	chr16:47595218-47596391	NONHSAT142300
2	lnc-PHKB-1	chr16:47333358-47333859	ENSG00000261369.1
3	lnc-GPT2-4	chr16:47563101-47563152	ENSG00000262038.1
4	lnc-GPT2-12	chr16:47497009-47497433	NONHSAT142295
5	lnc-GPT2-4	chr16:47563386-47563827	NONHSAT142298
6	lnc-GPT2-12	chr16:47495240-47495337	NONHSAT142295
7	lnc-GPT2-4	chr16:47563387-47563827	ENSG00000262038.1
8	lnc-GPT2-4	chr16:47563101-47563152	NONHSAT142298
9	lnc-PHKB-1	chr16:47351460-47351725	ENSG00000261369.1
10	lnc-PHKB-1	chr16:47346550-47346651	ENSG00000261369.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47484216-47484236

Variant related genes	Relation type
EIF4BP5	TF binding region
RNA5SP424	TF binding region
ITFG1	TF binding region
ENSG00000262038	TF binding region
ENSG00000261369	TF binding region
ENSG00000259866	TF binding region
ENSG00000222767	TF binding region
PHKB	TF binding region
RNA5SP425	TF binding region
EIF4BP5	CpG island
RNA5SP424	CpG island
ITFG1	CpG island
ENSG00000262038	CpG island
ENSG00000261369	CpG island
ENSG00000259866	CpG island
ENSG00000222767	CpG island
PHKB	CpG island
RNA5SP425	CpG island
ENSG00000259918	chromatin interactions
ENSG00000212290	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000259866	chromatin interactions
ENSG00000261336	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000133703	chromatin interactions
ENSG00000222268	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000102893	chromatin interactions

Extended variants
information (count: 9505 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:9505 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539627951	chr16:47316894-47316895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558818064	chr16:47316906-47316907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551877378	chr16:47316922-47316923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184363428	chr16:47317003-47317004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566621312	chr16:47317029-47317030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142676233	chr16:47317117-47317118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189127499	chr16:47317149-47317150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181127041	chr16:47317168-47317169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186714589	chr16:47317185-47317186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556840013	chr16:47317187-47317188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs111441981	chr16:47317200-47317201	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138758301	chr16:47317262-47317263	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573229053	chr16:47317265-47317266	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540507824	chr16:47317338-47317339	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141781547	chr16:47317340-47317341	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532561334	chr16:47317343-47317344	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79548925	chr16:47317432-47317433	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562798065	chr16:47317461-47317462	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530120025	chr16:47317495-47317496	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548264388	chr16:47317497-47317498	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535709369	chr16:47317573-47317574	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566839059	chr16:47317589-47317590	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146236231	chr16:47317646-47317647	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552492325	chr16:47317666-47317667	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556961860	chr16:47317689-47317690	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570706451	chr16:47317731-47317732	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565641750	chr16:47317812-47317813	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539566601	chr16:47317814-47317815	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537993942	chr16:47317869-47317870	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370897522	chr16:47317991-47317992	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200019480	chr16:47318001-47318002	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200585253	chr16:47318004-47318005	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556232900	chr16:47318010-47318011	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568034153	chr16:47318023-47318024	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535511732	chr16:47318058-47318059	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139103351	chr16:47318070-47318071	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376419817	chr16:47318081-47318082	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571697880	chr16:47318145-47318146	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534264944	chr16:47318200-47318201	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370883027	chr16:47318207-47318208	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558777017	chr16:47318229-47318230	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149895110	chr16:47318335-47318336	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143877646	chr16:47318358-47318359	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190658012	chr16:47318362-47318363	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180997085	chr16:47318369-47318370	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148599451	chr16:47318495-47318496	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542295933	chr16:47318561-47318562	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560514294	chr16:47318599-47318600	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527684592	chr16:47318621-47318622	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs28495596	chr16:47318750-47318751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:6328 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47230000-47332600	Weak transcription	Thymus	Thymus
2	chr16:47264200-47321000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr16:47282200-47321000	Weak transcription	Brain Hippocampus Middle	brain
4	chr16:47289200-47320600	Weak transcription	Small Intestine	intestine
5	chr16:47292200-47317400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr16:47292200-47345600	Weak transcription	K562	blood
7	chr16:47292400-47317400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:47292400-47317400	Weak transcription	HSMM	muscle
9	chr16:47292600-47317200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr16:47292600-47317200	Weak transcription	Dnd41	blood
11	chr16:47292600-47317200	Weak transcription	HepG2	liver
12	chr16:47294600-47319600	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr16:47294600-47332600	Weak transcription	Pancreas	Pancrea
14	chr16:47294800-47332600	Weak transcription	Ovary	ovary
15	chr16:47295200-47317200	Weak transcription	Liver	Liver
16	chr16:47295200-47317400	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr16:47297400-47317200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr16:47297400-47317200	Weak transcription	Adipose Nuclei	Adipose
19	chr16:47297400-47317200	Weak transcription	Left Ventricle	heart
20	chr16:47297400-47319000	Weak transcription	Fetal Stomach	stomach
21	chr16:47297400-47319400	Weak transcription	Lung	lung
22	chr16:47297600-47317200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr16:47297600-47317400	Weak transcription	Fetal Intestine Large	intestine
24	chr16:47297600-47333200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:47304600-47317200	Weak transcription	Primary B cells from cord blood	blood
26	chr16:47304800-47317400	Weak transcription	Primary T cells from cord blood	blood
27	chr16:47305400-47332400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr16:47305400-47332400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr16:47306200-47317200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr16:47307200-47332400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr16:47307400-47325600	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr16:47308800-47319000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr16:47311400-47341800	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr16:47311400-47362200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr16:47313400-47319000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr16:47314000-47333800	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr16:47314200-47319600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr16:47314800-47324000	Weak transcription	Aorta	Aorta
39	chr16:47315800-47318800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr16:47316000-47317800	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr16:47316600-47318200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr16:47316600-47319200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr16:47316800-47317200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr16:47317200-47317400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:47317200-47317600	ZNF genes & repeats	Left Ventricle	heart
46	chr16:47317200-47318000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr16:47317200-47318200	ZNF genes & repeats	Primary B cells from cord blood	blood
48	chr16:47317200-47318200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
49	chr16:47317200-47318600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr16:47317200-47319000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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