Variant report

Variant	esv3390669
Chromosome Location	chr16:70363244-70400179
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	chr16:70380541-70381311	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:70380544-70380928	K562	blood:	n/a	n/a
3	ATF1	chr16:70380532-70381183	K562	blood:	n/a	n/a
4	ATF2	chr16:70380414-70381037	GM12878	blood:	n/a	chr16:70380761-70380772
5	ATF2	chr16:70380395-70381061	H1-hESC	embryonic stem cell:	n/a	chr16:70380761-70380772
6	ATF2	chr16:70380407-70381374	GM12878	blood:	n/a	chr16:70380761-70380772
7	ATF2	chr16:70380507-70381065	H1-hESC	embryonic stem cell:	n/a	chr16:70380761-70380772
8	ATF3	chr16:70380546-70380950	H1-hESC	embryonic stem cell:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
9	ATF3	chr16:70380558-70381059	HepG2	liver:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
10	ATF3	chr16:70380510-70380964	GM12878	blood:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
11	ATF3	chr16:70380526-70381036	A549	lung:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
12	ATF3	chr16:70380604-70380786	GM12878	blood:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
13	ATF3	chr16:70380576-70380928	K562	blood:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
14	ATF3	chr16:70380428-70381024	A549	lung:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
15	ATF3	chr16:70380609-70380847	H1-hESC	embryonic stem cell:	n/a	chr16:70380763-70380770 chr16:70380762-70380782 chr16:70380763-70380773 chr16:70380761-70380774 chr16:70380760-70380773 chr16:70380761-70380772 chr16:70380759-70380772 chr16:70380763-70380771 chr16:70380761-70380772
16	BACH1	chr16:70379624-70379630	K562	blood:	n/a	n/a
17	BACH1	chr16:70380587-70380977	K562	blood:	n/a	n/a
18	BACH1	chr16:70366614-70366935	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr16:70380541-70381106	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr16:70366599-70366943	K562	blood:	n/a	n/a
21	BATF	chr16:70380626-70380931	GM12878	blood:	n/a	n/a
22	BATF	chr16:70398264-70398549	GM12878	blood:	n/a	chr16:70398416-70398424
23	BCL3	chr16:70380490-70381129	A549	lung:	n/a	chr16:70380785-70380794
24	BCL3	chr16:70380410-70381447	A549	lung:	n/a	chr16:70380785-70380794
25	BCLAF1	chr16:70380481-70381226	K562	blood:	n/a	chr16:70380785-70380794
26	BCLAF1	chr16:70380542-70381072	GM12878	blood:	n/a	chr16:70380785-70380794
27	BCLAF1	chr16:70380389-70380989	GM12878	blood:	n/a	chr16:70380785-70380794
28	BHLHE40	chr16:70366773-70366821	K562	blood:	n/a	n/a
29	BHLHE40	chr16:70380582-70381261	HepG2	liver:	n/a	n/a
30	BHLHE40	chr16:70380563-70380977	K562	blood:	n/a	n/a
31	BHLHE40	chr16:70379002-70379300	HepG2	liver:	n/a	n/a
32	BHLHE40	chr16:70380539-70381024	GM12878	blood:	n/a	n/a
33	BRCA1	chr16:70380505-70381103	HepG2	liver:	n/a	n/a
34	BRCA1	chr16:70380503-70380944	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr16:70380464-70381463	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr16:70380515-70380995	GM12878	blood:	n/a	n/a
37	CBX3	chr16:70380279-70381215	K562	blood:	n/a	n/a
38	CBX3	chr16:70380486-70380941	K562	blood:	n/a	n/a
39	CCNT2	chr16:70380581-70381022	K562	blood:	n/a	n/a
40	CEBPB	chr16:70380619-70381006	A549	lung:	n/a	n/a
41	CEBPB	chr16:70377878-70377990	HepG2	liver:	n/a	chr16:70377945-70377956
42	CEBPB	chr16:70380636-70381023	IMR90	lung:	n/a	n/a
43	CEBPB	chr16:70380560-70381030	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr16:70380610-70380925	K562	blood:	n/a	n/a
45	CEBPB	chr16:70380467-70381067	K562	blood:	n/a	n/a
46	CEBPB	chr16:70396273-70396415	A549	lung:	n/a	chr16:70396332-70396344
47	CEBPB	chr16:70377861-70377993	K562	blood:	n/a	chr16:70377945-70377956
48	CEBPB	chr16:70377835-70377982	A549	lung:	n/a	chr16:70377945-70377956
49	CEBPB	chr16:70380351-70380935	GM12878	blood:	n/a	n/a
50	CEBPB	chr16:70375681-70375856	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70365800-70365850	PrEC	prostate:	n/a
2	chr16:70381052-70381102	BE2_C	brain:	n/a
3	chr16:70378263-70378313	T-47D	breast:	n/a
4	chr16:70380729-70380779	Hela-S3	cervix:	n/a
5	chr16:70380729-70380779	LNCaP	prostate:	n/a
6	chr16:70384335-70384385	HNPCEpiC	eye:	n/a
7	chr16:70378263-70378313	SAEC	small airway:	n/a
8	chr16:70380888-70380938	AoSMC	blood vessel:	n/a
9	chr16:70381052-70381102	GM06990	blood:	n/a
10	chr16:70380615-70380665	NHDF-neo	bronchial:	n/a
11	chr16:70380649-70380699	AG10803	skin:	n/a
12	chr16:70380558-70380608	AoSMC	blood vessel:	n/a
13	chr16:70380649-70380699	PFSK-1	brain:	n/a
14	chr16:70380615-70380665	GM12892	blood:	n/a
15	chr16:70380649-70380699	HL-60	blood:	n/a
16	chr16:70384335-70384385	SAEC	small airway:	n/a
17	chr16:70380729-70380779	K562	blood:	n/a
18	chr16:70380649-70380699	SK-N-SH	brain:	n/a
19	chr16:70380649-70380699	NHDF-neo	bronchial:	n/a
20	chr16:70380474-70380524	LNCaP	prostate:	n/a
21	chr16:70365800-70365850	AG09309	skin:	n/a
22	chr16:70380593-70380643	NHDF-neo	bronchial:	n/a
23	chr16:70380593-70380643	SKMC	muscle:	n/a
24	chr16:70380649-70380699	AG04449	skin:	fetal
25	chr16:70380729-70380779	AG10803	skin:	n/a
26	chr16:70380649-70380699	T-47D	breast:	n/a
27	chr16:70380474-70380524	BJ	skin:	n/a
28	chr16:70384335-70384385	ovcar-3	ovarian:	n/a
29	chr16:70365800-70365850	HRCEpiC	kidney:	n/a
30	chr16:70367582-70367632	HRE	kidney:	n/a
31	chr16:70380615-70380665	SKMC	muscle:	n/a
32	chr16:70380615-70380665	AG04450	lung:	fetal
33	chr16:70380649-70380699	HRCEpiC	kidney:	n/a
34	chr16:70365800-70365850	HEEpiC	esophagus:	n/a
35	chr16:70380888-70380938	A549	lung:	n/a
36	chr16:70367582-70367632	Caco-2	colon:	n/a
37	chr16:70380649-70380699	GM12878	blood:	n/a
38	chr16:70384335-70384385	GM12878	blood:	n/a
39	chr16:70380615-70380665	HCT-116	colon:	n/a
40	chr16:70380474-70380524	HL-60	blood:	n/a
41	chr16:70380649-70380699	GM12892	blood:	n/a
42	chr16:70380474-70380524	ovcar-3	ovarian:	n/a
43	chr16:70380615-70380665	PANC-1	pancreas:	n/a
44	chr16:70384335-70384385	H1-hESC	embryonic stem cell:	embryo
45	chr16:70381052-70381102	SK-N-SH_RA	brain:	n/a
46	chr16:70380729-70380779	Jurkat	blood:	n/a
47	chr16:70380888-70380938	NH-A	brain:	n/a
48	chr16:70380729-70380779	AG04450	lung:	fetal
49	chr16:70381052-70381102	MCF-7	breast:	n/a
50	chr16:70380593-70380643	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:70383544..70387219-chr16:70393401..70395517,4	K562	blood:
2	chr16:70365097..70367956-chr16:70382920..70385112,3	K562	blood:
3	chr16:70321381..70324414-chr16:70379252..70382918,7	MCF-7	breast:
4	chr16:70321837..70323481-chr16:70366163..70367690,2	K562	blood:
5	chr16:70374148..70377902-chr16:70377991..70380820,4	K562	blood:
6	chr16:70378223..70384231-chr16:70413255..70416872,7	MCF-7	breast:
7	chr16:70390592..70393385-chr16:70487447..70489700,3	MCF-7	breast:
8	chr16:70388743..70391309-chr16:70392278..70395068,2	K562	blood:
9	chr16:70318554..70325188-chr16:70378714..70382302,15	K562	blood:
10	chr16:70381919..70383634-chr16:70512388..70514213,2	K562	blood:
11	chr16:70362677..70365574-chr16:70378421..70380660,2	K562	blood:
12	chr16:70356920..70359897-chr16:70366133..70369094,2	K562	blood:
13	chr16:70365097..70367956-chr16:70382920..70385112,3	K562	blood:
14	chr16:70379526..70383319-chr16:70470652..70474068,4	K562	blood:
15	chr14:58711561..58712466-chr16:70380477..70381118,2	Hela-S3	cervix:
16	chr16:70366563..70368241-chr16:70379128..70380680,2	MCF-7	breast:
17	chr16:70359039..70361319-chr16:70373919..70375711,2	MCF-7	breast:
18	chr16:70321709..70323528-chr16:70379604..70382270,2	MCF-7	breast:
19	chr16:70375788..70377818-chr16:70381402..70383532,2	K562	blood:
20	chr16:70320088..70322419-chr16:70366268..70367885,2	K562	blood:
21	chr16:70358390..70361005-chr16:70361905..70363847,2	MCF-7	breast:
22	chr16:70383544..70387219-chr16:70393401..70395517,4	K562	blood:
23	chr16:70380684..70382606-chr16:70382776..70384424,3	MCF-7	breast:
24	chr16:70373940..70375897-chr16:70406795..70408435,2	MCF-7	breast:
25	chr16:70368628..70371487-chr16:70373484..70375931,2	MCF-7	breast:
26	chr11:61583398..61584153-chr16:70380735..70381273,2	Hela-S3	cervix:
27	chr16:70366698..70368203-chr16:70543911..70546004,2	K562	blood:
28	chr16:70333101..70334676-chr16:70365140..70367684,2	MCF-7	breast:
29	chr16:70365124..70367009-chr16:70367397..70369284,2	K562	blood:
30	chr12:46765086..46765689-chr16:70380707..70381691,2	Hela-S3	cervix:
31	chr16:70379206..70382816-chr16:70556059..70558953,4	K562	blood:
32	chr16:70380316..70381242-chr7:44886810..44887807,2	Hela-S3	cervix:
33	chr16:70367181..70369957-chr16:70373031..70374921,2	K562	blood:
34	chr16:70379903..70382135-chr16:70398083..70399782,2	MCF-7	breast:
35	chr16:70380168..70380677-chr5:180632256..180632782,2	Hela-S3	cervix:
36	chr16:70382995..70385484-chr16:70556876..70560677,3	MCF-7	breast:
37	chr16:70338862..70341028-chr16:70375885..70378298,2	MCF-7	breast:
38	chr16:70382796..70385300-chr16:70408811..70411389,2	K562	blood:
39	chr16:70386987..70389423-chr16:70409457..70411415,2	MCF-7	breast:
40	chr16:70383005..70385826-chr16:70388585..70390141,2	MCF-7	breast:
41	chr16:70380612..70382422-chr16:70687697..70689426,2	MCF-7	breast:
42	chr16:70374149..70377957-chr16:70378674..70382168,7	MCF-7	breast:
43	chr16:70379064..70380688-chr16:70557670..70559331,2	MCF-7	breast:
44	chr16:70380243..70381157-chr7:72936224..72937111,2	Hela-S3	cervix:
45	chr16:11836059..11836968-chr16:70380587..70381246,2	Hela-S3	cervix:
46	chr16:70380684..70382354-chr16:70595667..70598602,2	MCF-7	breast:
47	chr16:70380932..70385143-chr16:70404657..70409914,6	MCF-7	breast:
48	chr16:70379157..70381349-chr16:70561785..70563465,2	MCF-7	breast:
49	chr16:70338003..70340478-chr16:70365568..70367994,2	K562	blood:
50	chr16:70322056..70324677-chr16:70375656..70378564,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AARS-1	chr16:70367686-70367863	ENSG00000261777.1
2	lnc-AARS-1	chr16:70367723-70367863	ENSG00000261777.1
3	lnc-AARS-1	chr16:70367723-70367863	ENSG00000245206
4	lnc-AARS-1	chr16:70375843-70376002	ENSG00000261777.1
5	lnc-AARS-1	chr16:70380102-70380650	ENSG00000261777.1
6	lnc-AARS-1	chr16:70375843-70376002	ENSG00000261777.1
7	lnc-AARS-1	chr16:70375843-70376002	ENSG00000245206
8	lnc-AARS-1	chr16:70380102-70380650	ENSG00000261777.1
9	lnc-AARS-1	chr16:70380102-70380650	ENSG00000245206

Variant related genes	Relation type
DDX19A	TF binding region
ENSG00000261777	TF binding region
DDX19A	CpG island
ENSG00000261777	CpG island
ENSG00000157353	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000157350	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000260111	chromatin interactions
ENSG00000009954	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000221514	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000105968	chromatin interactions
ENSG00000261777	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000223496	chromatin interactions
ENSG00000260537	chromatin interactions
ENSG00000168872	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000157349	chromatin interactions
ENSG00000146054	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000157368	chromatin interactions
ENSG00000100567	chromatin interactions
ERLIN1	miRNA target sites
SURF4	miRNA target sites
HNRNPUL1	miRNA target sites

Extended variants
information (count: 1503 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1503 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138232298	chr16:70363285-70363286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs143802195	chr16:70363325-70363326	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201224231	chr16:70363334-70363335	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369244897	chr16:70363372-70363373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200700862	chr16:70363383-70363384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149381034	chr16:70363405-70363406	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377609980	chr16:70363420-70363421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547898778	chr16:70363441-70363442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116873214	chr16:70363446-70363447	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370143314	chr16:70363473-70363474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566691698	chr16:70363510-70363511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11864890	chr16:70363519-70363520	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558736584	chr16:70363520-70363521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374526997	chr16:70363551-70363552	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544288688	chr16:70363554-70363555	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs556019082	chr16:70363572-70363573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567676895	chr16:70363592-70363593	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574352544	chr16:70363594-70363595	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77870639	chr16:70363621-70363622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189455055	chr16:70363623-70363624	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527940065	chr16:70363647-70363648	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371206714	chr16:70363656-70363657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74024200	chr16:70363670-70363671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181426540	chr16:70363672-70363673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs531805699	chr16:70363677-70363678	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs116155420	chr16:70363680-70363681	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs562071479	chr16:70363681-70363682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200110458	chr16:70363693-70363694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs529276130	chr16:70363702-70363703	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376956522	chr16:70363706-70363707	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371590664	chr16:70363717-70363718	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147242047	chr16:70363770-70363771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367757760	chr16:70363828-70363829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566066316	chr16:70363927-70363928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530175934	chr16:70363937-70363938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs150748407	chr16:70363993-70363994	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534051026	chr16:70364002-70364003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201092171	chr16:70364004-70364005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370359923	chr16:70364008-70364009	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374022327	chr16:70364010-70364011	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200333329	chr16:70364016-70364017	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs74024201	chr16:70364019-70364020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs115132510	chr16:70364039-70364040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568706808	chr16:70364061-70364062	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556220428	chr16:70364071-70364072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574488319	chr16:70364076-70364077	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183629578	chr16:70364105-70364106	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188288583	chr16:70364106-70364107	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113742194	chr16:70364141-70364142	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs181908152	chr16:70364147-70364148	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1522 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70333800-70367800	Weak transcription	Small Intestine	intestine
2	chr16:70334000-70368400	Weak transcription	Fetal Heart	heart
3	chr16:70334200-70379800	Weak transcription	Stomach Mucosa	stomach
4	chr16:70335800-70366400	Weak transcription	Psoas Muscle	Psoas
5	chr16:70335800-70374200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr16:70339000-70366400	Weak transcription	K562	blood
7	chr16:70339200-70367600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr16:70339400-70365000	Weak transcription	A549	lung
9	chr16:70339400-70367400	Weak transcription	HMEC	breast
10	chr16:70345600-70366600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr16:70346200-70367600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr16:70346200-70376000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:70346400-70369600	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr16:70347400-70371000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr16:70348200-70367800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:70348200-70371000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr16:70348400-70371000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr16:70348800-70365200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr16:70348800-70370600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr16:70348800-70371000	Strong transcription	Liver	Liver
21	chr16:70349400-70369400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr16:70349400-70370600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr16:70349400-70371200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:70349400-70372000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr16:70349600-70379800	Weak transcription	Fetal Brain Male	brain
26	chr16:70349800-70367600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:70349800-70370400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr16:70349800-70372600	Strong transcription	Fetal Muscle Trunk	muscle
29	chr16:70349800-70373200	Strong transcription	Fetal Stomach	stomach
30	chr16:70349800-70374600	Strong transcription	Fetal Muscle Leg	muscle
31	chr16:70350200-70365800	Weak transcription	NHEK	skin
32	chr16:70350600-70369800	Strong transcription	Fetal Brain Female	brain
33	chr16:70351800-70363400	Weak transcription	Esophagus	oesophagus
34	chr16:70351800-70365000	Weak transcription	Fetal Kidney	kidney
35	chr16:70351800-70365800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr16:70351800-70367800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr16:70351800-70367800	Weak transcription	NH-A	brain
38	chr16:70352000-70366000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr16:70352800-70373000	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr16:70354400-70363400	Weak transcription	Aorta	Aorta
41	chr16:70356600-70370600	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr16:70356800-70364200	Strong transcription	Duodenum Smooth Muscle	Duodenum
43	chr16:70356800-70370200	Strong transcription	Placenta	Placenta
44	chr16:70357200-70380200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr16:70357800-70370200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr16:70358000-70363400	Weak transcription	NHLF	lung
47	chr16:70358000-70367400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr16:70358600-70363400	Weak transcription	Pancreas	Pancrea
49	chr16:70359000-70364800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr16:70359000-70364800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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