Variant report

Variant	esv10189
Chromosome Location	chr16:74337046-74464266
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	chr16:74343761-74344069	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:74402200-74402343	K562	blood:	n/a	n/a
3	ARID3A	chr16:74343777-74343987	K562	blood:	n/a	n/a
4	ARID3A	chr16:74340614-74340822	K562	blood:	n/a	n/a
5	ATF1	chr16:74402006-74402375	K562	blood:	n/a	chr16:74402193-74402207
6	ATF2	chr16:74464112-74464462	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr16:74402079-74402253	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232
8	ATF3	chr16:74401853-74402428	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
9	ATF3	chr16:74401940-74402325	GM12878	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
10	ATF3	chr16:74401950-74402248	HepG2	liver:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
11	ATF3	chr16:74401896-74402310	K562	blood:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
12	ATF3	chr16:74402012-74402314	H1-hESC	embryonic stem cell:	n/a	chr16:74402196-74402216 chr16:74402212-74402232 chr16:74402077-74402086
13	BACH1	chr16:74402015-74402440	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr16:74398509-74398539	K562	blood:	n/a	n/a
15	BACH1	chr16:74356288-74356302	K562	blood:	n/a	n/a
16	BATF	chr16:74463982-74464267	GM12878	blood:	n/a	n/a
17	BATF	chr16:74340348-74340594	GM12878	blood:	n/a	n/a
18	BATF	chr16:74363304-74363522	GM12878	blood:	n/a	n/a
19	BCL3	chr16:74339512-74340098	A549	lung:	n/a	n/a
20	BCL3	chr16:74338505-74339423	A549	lung:	n/a	n/a
21	BCL3	chr16:74340156-74341682	A549	lung:	n/a	n/a
22	BCL3	chr16:74339747-74340167	K562	blood:	n/a	n/a
23	BHLHE40	chr16:74464001-74464283	A549	lung:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
24	BHLHE40	chr16:74463926-74464447	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
25	BHLHE40	chr16:74401879-74402451	HepG2	liver:	n/a	n/a
26	BHLHE40	chr16:74363293-74363678	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
27	BHLHE40	chr16:74401653-74402419	HepG2	liver:	n/a	n/a
28	BHLHE40	chr16:74363300-74363595	A549	lung:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
29	BHLHE40	chr16:74401987-74402336	A549	lung:	n/a	n/a
30	BHLHE40	chr16:74343759-74344160	K562	blood:	n/a	n/a
31	BHLHE40	chr16:74363329-74363542	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
32	BHLHE40	chr16:74363303-74363604	GM12878	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
33	BHLHE40	chr16:74463888-74464257	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
34	BHLHE40	chr16:74464015-74464235	HepG2	liver:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
35	BHLHE40	chr16:74401724-74402378	GM12878	blood:	n/a	n/a
36	BHLHE40	chr16:74445450-74445698	HepG2	liver:	n/a	n/a
37	BHLHE40	chr16:74363081-74363537	HepG2	liver:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
38	BHLHE40	chr16:74463908-74464447	K562	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
39	BHLHE40	chr16:74343713-74344036	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:74363294-74363668	K562	blood:	n/a	chr16:74363462-74363471 chr16:74363461-74363470 chr16:74363459-74363472 chr16:74363461-74363470
41	BHLHE40	chr16:74338044-74338054	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:74401339-74402424	K562	blood:	n/a	n/a
43	BHLHE40	chr16:74401340-74401505	GM12878	blood:	n/a	n/a
44	BHLHE40	chr16:74463983-74464410	GM12878	blood:	n/a	chr16:74464136-74464149 chr16:74464138-74464147 chr16:74464139-74464148 chr16:74464138-74464147
45	BRCA1	chr16:74402135-74402375	H1-hESC	embryonic stem cell:	n/a	chr16:74402243-74402252
46	BRCA1	chr16:74398022-74398270	HepG2	liver:	n/a	n/a
47	BRCA1	chr16:74464034-74464229	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr16:74402134-74402393	GM12878	blood:	n/a	chr16:74402243-74402252
49	BRCA1	chr16:74402144-74402372	HepG2	liver:	n/a	chr16:74402243-74402252
50	BRCA1	chr16:74402132-74402385	Hela-S3	cervix:	n/a	chr16:74402243-74402252

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74401547-74401597	A549	lung:	n/a
2	chr16:74456200-74456250	Jurkat	blood:	n/a
3	chr16:74401794-74401844	NHDF-neo	bronchial:	n/a
4	chr16:74401547-74401597	A549	lung:	n/a
5	chr16:74456200-74456250	Jurkat	blood:	n/a
6	chr16:74401794-74401844	NHDF-neo	bronchial:	n/a
7	chr16:74455140-74455190	BJ	skin:	n/a
8	chr16:74455448-74455498	GM19239	blood:	n/a
9	chr16:74441639-74441689	GM19239	blood:	n/a
10	chr16:74441639-74441689	MCF-7	breast:	n/a
11	chr16:74401794-74401844	RPTEC	kidney:	n/a
12	chr16:74441639-74441689	Jurkat	blood:	n/a
13	chr16:74401794-74401844	MCF10A-Er-Src	breast:	n/a
14	chr16:74402336-74402386	MCF-7	breast:	n/a
15	chr16:74402329-74402379	MCF-7	breast:	n/a
16	chr16:74402737-74402787	HRCEpiC	kidney:	n/a
17	chr16:74340046-74340096	ovcar-3	ovarian:	n/a
18	chr16:74441639-74441689	GM12892	blood:	n/a
19	chr16:74402336-74402386	BJ	skin:	n/a
20	chr16:74401794-74401844	HCM	heart:	n/a
21	chr16:74340046-74340096	NH-A	brain:	n/a
22	chr16:74446218-74446268	MCF-7	breast:	n/a
23	chr16:74402737-74402787	HMEC	breast:	n/a
24	chr16:74398168-74398218	IMR90	lung:	fetal
25	chr16:74402336-74402386	HCPEpiC	choroid plexus:	n/a
26	chr16:74446218-74446268	CMK	blood:	n/a
27	chr16:74456200-74456250	NB4	blood:	n/a
28	chr16:74403516-74403566	HCM	heart:	n/a
29	chr16:74455360-74455410	GM19239	blood:	n/a
30	chr16:74401986-74402036	Hela-S3	cervix:	n/a
31	chr16:74455360-74455410	HMEC	breast:	n/a
32	chr16:74400946-74400996	HL-60	blood:	n/a
33	chr16:74406059-74406109	MCF-7	breast:	n/a
34	chr16:74455448-74455498	GM06990	blood:	n/a
35	chr16:74402336-74402386	NB4	blood:	n/a
36	chr16:74456200-74456250	HPAEpiC	pulmonary alveolar:	n/a
37	chr16:74455448-74455498	SK-N-SH	brain:	n/a
38	chr16:74398168-74398218	PFSK-1	brain:	n/a
39	chr16:74456200-74456250	GM12891	blood:	n/a
40	chr16:74455542-74455592	HL-60	blood:	n/a
41	chr16:74401794-74401844	AoSMC	blood vessel:	n/a
42	chr16:74402329-74402379	HPAEpiC	pulmonary alveolar:	n/a
43	chr16:74406059-74406109	PFSK-1	brain:	n/a
44	chr16:74402329-74402379	Caco-2	colon:	n/a
45	chr16:74455542-74455592	RPTEC	kidney:	n/a
46	chr16:74401794-74401844	CMK	blood:	n/a
47	chr16:74455360-74455410	PFSK-1	brain:	n/a
48	chr16:74455448-74455498	LNCaP	prostate:	n/a
49	chr16:74401547-74401597	ovcar-3	ovarian:	n/a
50	chr16:74402329-74402379	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:74345519..74347436-chr16:74350317..74352101,2	MCF-7	breast:
2	chr16:74333029..74335675-chr16:74353488..74356515,3	K562	blood:
3	chr16:74343323..74344029-chr16:74656867..74657812,2	MCF-7	breast:
4	chr13:96705422..96706004-chr16:74337665..74338558,2	NB4	blood:
5	chr16:74349759..74351336-chr16:74353263..74355191,2	MCF-7	breast:
6	chr16:74349759..74351336-chr16:74353263..74355191,2	MCF-7	breast:
7	chr16:74353334..74355532-chr16:74355748..74357983,4	K562	blood:
8	chr16:74463888..74464834-chr16:74487133..74487740,2	MCF-7	breast:
9	chr16:74329306..74331523-chr16:74400690..74402975,2	MCF-7	breast:
10	chr16:74338414..74342140-chr16:74346350..74349350,4	K562	blood:
11	chr16:74338496..74341325-chr16:74351538..74353061,2	MCF-7	breast:
12	chr16:74338496..74341325-chr16:74351538..74353061,2	MCF-7	breast:
13	chr16:74394116..74395645-chr3:9438342..9440027,2	MCF-7	breast:
14	chr16:74348919..74351200-chr16:74353361..74355371,2	K562	blood:
15	chr16:74338418..74341376-chr16:74345812..74348805,2	MCF-7	breast:
16	chr16:74338484..74340832-chr16:74341734..74345070,5	MCF-7	breast:
17	chr16:74343804..74344312-chr16:74363008..74363532,2	MCF-7	breast:
18	chr16:74276279..74277864-chr16:74338868..74341244,2	K562	blood:
19	chr16:74396107..74397775-chr16:74400703..74403254,2	K562	blood:
20	chr16:70185001..70186006-chr16:74463672..74464734,4	MCF-7	breast:
21	chr16:74348919..74351200-chr16:74353361..74355371,2	K562	blood:
22	chr16:74353334..74355532-chr16:74355748..74357983,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC18B-5	chr16:74346507-74346617	NONHSAT143673
2	lnc-PSMD7-1	chr16:74349044-74349532	ENSG00000260884.1
3	lnc-CLEC18B-5	chr16:74349041-74349919	NONHSAT143674
4	lnc-CLEC18B-5	chr16:74353763-74354252	NONHSAT143674
5	lnc-NPIPL2-2	chr16:74456028-74456340	ENSG00000261170.1
6	lnc-CLEC18B-5	chr16:74351443-74352311	NONHSAT143674
7	lnc-CLEC18B-1	chr16:74411388-74411587	XLOC_012009
8	lnc-CLEC18B-2	chr16:74343998-74344032	ENSG00000259972.1
9	lnc-CLEC18B-5	chr16:74346927-74347288	NONHSAT143673
10	lnc-NPIPL2-3	chr16:74389382-74389428	l_1361_chr16:74389381-74506276_brain
11	lnc-CLEC18B-2	chr16:74400933-74401582	NONHSAT143681
12	lnc-CLEC18B-2	chr16:74401963-74402046	NONHSAT143681
13	lnc-PSMD7-1	chr16:74347235-74347258	ENSG00000260884.1
14	lnc-CLEC18B-5	chr16:74347204-74347745	NONHSAT143674
15	lnc-PSMD7-2	chr16:74362373-74362939	NONHSAT143677
16	lnc-NPIPL2-1	chr16:74401360-74403724	ENSG00000261079.1
17	lnc-NPIPL2-2	chr16:74456018-74456340	ENSG00000261170.1
18	lnc-CLEC18B-5	chr16:74359871-74360683	NONHSAT143674
19	lnc-CLEC18B-5	chr16:74349938-74350415	NONHSAT143674
20	lnc-CLEC18B-1	chr16:74411642-74411717	XLOC_012009
21	lnc-CLEC18B-5	chr16:74356132-74356732	NONHSAT143674
22	lnc-CLEC18B-2	chr16:74368790-74369244	ENSG00000259972.1
23	lnc-CLEC18B-5	chr16:74347924-74348600	NONHSAT143674

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PSMD7	hsa-miR-15b-5p	chr16:74339691-74339698
2	PSMD7	hsa-miR-15b-5p	chr16:74339679-74339698

Variant related genes	Relation type
ENSG00000239763	TF binding region
NPIPB15	TF binding region
ENSG00000259972	TF binding region
ENSG00000261079	TF binding region
CLEC18B	TF binding region
PSMD7	TF binding region
ENSG00000260884	TF binding region
ENSG00000261170	TF binding region
ENSG00000214331	TF binding region
ENSG00000239763	CpG island
NPIPB15	CpG island
ENSG00000259972	CpG island
ENSG00000261079	CpG island
CLEC18B	CpG island
PSMD7	CpG island
ENSG00000260884	CpG island
ENSG00000261170	CpG island
ENSG00000214331	CpG island
ENSG00000261079	chromatin interactions
ENSG00000214331	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000260884	chromatin interactions
ENSG00000102595	chromatin interactions
ENSG00000168137	chromatin interactions
ENSG00000259972	chromatin interactions
ENSG00000239763	chromatin interactions
ENSG00000103035	chromatin interactions
ENSG00000206573	chromatin interactions

Extended variants
information (count: 5453 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:5453 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569456683	chr16:74337064-74337065	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs564245087	chr16:74337069-74337070	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1201628	chr16:74337086-74337087	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs548730420	chr16:74337098-74337099	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs17336867	chr16:74337104-74337105	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs534891413	chr16:74337135-74337136	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs557785022	chr16:74337199-74337200	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs138062731	chr16:74337203-74337204	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs537079084	chr16:74337222-74337223	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143531747	chr16:74337240-74337241	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574226192	chr16:74337249-74337250	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187064515	chr16:74337284-74337285	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116200441	chr16:74337291-74337292	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370051193	chr16:74337331-74337332	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374623169	chr16:74337384-74337385	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573490823	chr16:74337399-74337400	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545667280	chr16:74337448-74337449	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs565466683	chr16:74337485-74337486	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532936410	chr16:74337514-74337515	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs80331868	chr16:74337521-74337522	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs562951815	chr16:74337547-74337548	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191543841	chr16:74337549-74337550	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548693810	chr16:74337595-74337596	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs559088843	chr16:74337623-74337624	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs570609139	chr16:74337627-74337628	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs183729013	chr16:74337631-74337632	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188062729	chr16:74337635-74337636	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs3785310	chr16:74337665-74337666	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs113940583	chr16:74337670-74337671	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs537444986	chr16:74337680-74337681	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs147156243	chr16:74337695-74337696	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567685585	chr16:74337702-74337703	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140525417	chr16:74337707-74337708	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs553536869	chr16:74337745-74337746	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554867342	chr16:74337803-74337804	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs193252249	chr16:74337810-74337811	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs367589329	chr16:74337854-74337855	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542130825	chr16:74337856-74337857	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528351277	chr16:74337878-74337879	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs538907279	chr16:74337916-74337917	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113758793	chr16:74337921-74337922	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs149290611	chr16:74337930-74337931	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs185390361	chr16:74337946-74337947	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs562919198	chr16:74337947-74337948	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371799922	chr16:74337948-74337949	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544226845	chr16:74337965-74337966	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs144639916	chr16:74337977-74337978	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542301627	chr16:74338006-74338007	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564115176	chr16:74338050-74338051	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559052119	chr16:74338052-74338053	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	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
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:2518 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74331800-74366400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:74332000-74342000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:74332200-74340600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr16:74332400-74340400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
5	chr16:74332400-74340600	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr16:74332400-74340800	Strong transcription	H9 Cell Line	embryonic stem cell
7	chr16:74332400-74340800	Strong transcription	Osteobl	bone
8	chr16:74332400-74341200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr16:74332400-74341400	Strong transcription	NH-A	brain
10	chr16:74332400-74341600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr16:74332400-74341800	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr16:74332400-74342000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr16:74332400-74342400	Strong transcription	Fetal Thymus	thymus
14	chr16:74332400-74342600	Strong transcription	HUES64 Cell Line	embryonic stem cell
15	chr16:74332600-74340600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
16	chr16:74332600-74341000	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr16:74332600-74341400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr16:74332600-74341600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr16:74332600-74341600	Strong transcription	Brain Inferior Temporal Lobe	brain
20	chr16:74332600-74341600	Strong transcription	K562	blood
21	chr16:74332600-74342000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr16:74332600-74342000	Strong transcription	Primary B cells from peripheral blood	blood
23	chr16:74332600-74342000	Strong transcription	Primary hematopoietic stem cells	blood
24	chr16:74332600-74342000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr16:74332600-74342400	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr16:74332600-74342600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr16:74332600-74342600	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr16:74332600-74342800	Strong transcription	Brain Substantia Nigra	brain
29	chr16:74332800-74338000	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr16:74332800-74340000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr16:74332800-74340000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr16:74332800-74340400	Strong transcription	Muscle Satellite Cultured Cells	--
33	chr16:74332800-74340600	Strong transcription	Brain Cingulate Gyrus	brain
34	chr16:74332800-74341600	Strong transcription	NHEK	skin
35	chr16:74332800-74342400	Strong transcription	Fetal Intestine Large	intestine
36	chr16:74332800-74342400	Strong transcription	Fetal Stomach	stomach
37	chr16:74332800-74342400	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr16:74332800-74342400	Strong transcription	Thymus	Thymus
39	chr16:74332800-74342600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr16:74332800-74342600	Strong transcription	Fetal Brain Female	brain
41	chr16:74332800-74342600	Strong transcription	Fetal Muscle Leg	muscle
42	chr16:74332800-74401200	Weak transcription	Stomach Mucosa	stomach
43	chr16:74333000-74341000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr16:74333000-74341600	Strong transcription	NHLF	lung
45	chr16:74333000-74342400	Strong transcription	Liver	Liver
46	chr16:74333200-74340800	Strong transcription	Primary T killer memory cells from peripheral blood	blood
47	chr16:74333200-74341400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr16:74333200-74341600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr16:74333200-74341600	Strong transcription	NHDF-Ad	bronchial
50	chr16:74333200-74341800	Strong transcription	Spleen	Spleen

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