Variant report

Variant	nsv1060621
Chromosome Location	chr16:80532848-80980616
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4705)
CpG islands
(count:2138)
Chromatin interactive
region (count:391)
LncRNA
region (count:75)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4705 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:80948054-80948715	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:80862419-80862797	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:80902859-80902964	K562	blood:	n/a	n/a
4	ARID3A	chr16:80574685-80574999	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:80917098-80917501	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:80944278-80944659	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:80619268-80619298	K562	blood:	n/a	n/a
8	ARID3A	chr16:80858664-80859023	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:80560288-80560610	K562	blood:	n/a	n/a
10	ATF1	chr16:80972031-80972090	K562	blood:	n/a	n/a
11	ATF1	chr16:80944704-80944828	K562	blood:	n/a	n/a
12	ATF1	chr16:80810260-80810424	K562	blood:	n/a	n/a
13	ATF1	chr16:80828045-80828147	K562	blood:	n/a	n/a
14	ATF1	chr16:80662065-80662113	K562	blood:	n/a	n/a
15	ATF1	chr16:80861785-80861816	K562	blood:	n/a	n/a
16	ATF2	chr16:80710211-80710838	GM12878	blood:	n/a	n/a
17	ATF2	chr16:80660888-80661407	GM12878	blood:	n/a	n/a
18	ATF2	chr16:80619521-80620087	GM12878	blood:	n/a	n/a
19	ATF2	chr16:80617355-80617881	GM12878	blood:	n/a	n/a
20	ATF2	chr16:80661013-80661386	GM12878	blood:	n/a	n/a
21	ATF2	chr16:80574210-80574981	GM12878	blood:	n/a	n/a
22	ATF2	chr16:80603410-80603973	GM12878	blood:	n/a	n/a
23	ATF2	chr16:80754470-80755094	GM12878	blood:	n/a	n/a
24	ATF2	chr16:80613833-80614842	GM12878	blood:	n/a	n/a
25	ATF2	chr16:80696936-80697430	GM12878	blood:	n/a	n/a
26	ATF2	chr16:80754391-80755239	GM12878	blood:	n/a	n/a
27	ATF2	chr16:80709941-80710969	GM12878	blood:	n/a	n/a
28	ATF2	chr16:80613819-80615001	GM12878	blood:	n/a	n/a
29	ATF3	chr16:80645856-80646059	K562	blood:	n/a	n/a
30	ATF3	chr16:80574509-80575067	A549	lung:	n/a	n/a
31	ATF3	chr16:80648931-80649088	K562	blood:	n/a	n/a
32	ATF3	chr16:80645849-80646122	K562	blood:	n/a	n/a
33	ATF3	chr16:80648800-80649063	K562	blood:	n/a	n/a
34	BACH1	chr16:80574490-80574811	K562	blood:	n/a	n/a
35	BACH1	chr16:80837137-80837466	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr16:80927684-80927727	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr16:80570224-80570506	K562	blood:	n/a	n/a
38	BACH1	chr16:80561196-80561651	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr16:80561231-80561543	K562	blood:	n/a	n/a
40	BACH1	chr16:80574421-80575076	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr16:80907272-80907341	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr16:80690745-80691103	GM12878	blood:	n/a	n/a
43	BATF	chr16:80617452-80617785	GM12878	blood:	n/a	chr16:80617555-80617565 chr16:80617554-80617565
44	BATF	chr16:80710228-80710684	GM12878	blood:	n/a	n/a
45	BATF	chr16:80561267-80561526	GM12878	blood:	n/a	chr16:80561414-80561425 chr16:80561415-80561425
46	BATF	chr16:80661035-80661347	GM12878	blood:	n/a	chr16:80661236-80661246
47	BATF	chr16:80923667-80923938	GM12878	blood:	n/a	n/a
48	BATF	chr16:80617386-80617795	GM12878	blood:	n/a	chr16:80617555-80617565 chr16:80617554-80617565
49	BATF	chr16:80697093-80697335	GM12878	blood:	n/a	n/a
50	BATF	chr16:80690803-80691123	GM12878	blood:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:80934340-80934390	BJ	skin:	n/a
2	chr16:80654763-80654813	ProgFib	skin:	n/a
3	chr16:80584461-80584511	HCPEpiC	choroid plexus:	n/a
4	chr16:80934340-80934390	BJ	skin:	n/a
5	chr16:80654763-80654813	ProgFib	skin:	n/a
6	chr16:80584461-80584511	HCPEpiC	choroid plexus:	n/a
7	chr16:80969861-80969911	SKMC	muscle:	n/a
8	chr16:80966860-80966910	AG04450	lung:	fetal
9	chr16:80574553-80574603	HepG2	liver:	n/a
10	chr16:80966033-80966083	HCT-116	colon:	n/a
11	chr16:80969861-80969911	NH-A	brain:	n/a
12	chr16:80584461-80584511	PFSK-1	brain:	n/a
13	chr16:80969861-80969911	HUVEC	blood vessel:	n/a
14	chr16:80966279-80966329	HEEpiC	esophagus:	n/a
15	chr16:80966763-80966813	AG09309	skin:	n/a
16	chr16:80966703-80966753	BE2_C	brain:	n/a
17	chr16:80571499-80571549	SK-N-SH	brain:	n/a
18	chr16:80972238-80972288	GM19239	blood:	n/a
19	chr16:80966118-80966168	AoSMC	blood vessel:	n/a
20	chr16:80574926-80574976	HNPCEpiC	eye:	n/a
21	chr16:80578423-80578473	AG04450	lung:	fetal
22	chr16:80969861-80969911	LNCaP	prostate:	n/a
23	chr16:80575018-80575068	PANC-1	pancreas:	n/a
24	chr16:80839183-80839233	LNCaP	prostate:	n/a
25	chr16:80584461-80584511	NHBE	bronchial:	n/a
26	chr16:80574580-80574630	HRCEpiC	kidney:	n/a
27	chr16:80972238-80972288	AG04449	skin:	fetal
28	chr16:80575018-80575068	K562	blood:	n/a
29	chr16:80969861-80969911	HRE	kidney:	n/a
30	chr16:80574649-80574699	AG04449	skin:	fetal
31	chr16:80574580-80574630	MCF-7	breast:	n/a
32	chr16:80574580-80574630	NHBE	bronchial:	n/a
33	chr16:80575723-80575773	AG04449	skin:	fetal
34	chr16:80966118-80966168	A549	lung:	n/a
35	chr16:80952459-80952509	GM06990	blood:	n/a
36	chr16:80969861-80969911	GM12878	blood:	n/a
37	chr16:80578423-80578473	AoSMC	blood vessel:	n/a
38	chr16:80962864-80962914	GM19239	blood:	n/a
39	chr16:80966491-80966541	H1-hESC	embryonic stem cell:	embryo
40	chr16:80972238-80972288	PFSK-1	brain:	n/a
41	chr16:80575723-80575773	GM12892	blood:	n/a
42	chr16:80966192-80966242	HEK293	kidney:	embryo
43	chr16:80966703-80966753	GM12878	blood:	n/a
44	chr16:80574553-80574603	NT2-D1	testis:	n/a
45	chr16:80966118-80966168	GM12892	blood:	n/a
46	chr16:80575723-80575773	NT2-D1	testis:	n/a
47	chr16:80574553-80574603	HRCEpiC	kidney:	n/a
48	chr16:80838738-80838788	NT2-D1	testis:	n/a
49	chr16:80838738-80838788	Hepatocyte	liver:	n/a
50	chr16:80969861-80969911	AG09319	gingival:	n/a

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr16:80957146..80959233-chr16:80965352..80966876,2	MCF-7	breast:
2	chr16:80886274..80886849-chr16:80933809..80934549,2	MCF-7	breast:
3	chr16:80582632..80584948-chr16:80633817..80635436,2	MCF-7	breast:
4	chr16:80831187..80832847-chr16:80836382..80838874,2	MCF-7	breast:
5	chr16:80589493..80592966-chr16:80593921..80596964,3	MCF-7	breast:
6	chr11:65272537..65273491-chr16:80966234..80966909,2	Hela-S3	cervix:
7	chr16:80560979..80561850-chr16:80982503..80983251,4	MCF-7	breast:
8	chr16:80826716..80830460-chr16:80836759..80839570,3	MCF-7	breast:
9	chr16:80723055..80725180-chr16:80728525..80730099,2	MCF-7	breast:
10	chr16:80789011..80790811-chr16:80792089..80794243,2	MCF-7	breast:
11	chr16:80838427..80840322-chr16:80885425..80887354,2	MCF-7	breast:
12	chr16:80654095..80656173-chr16:80667578..80669313,2	MCF-7	breast:
13	chr16:80826270..80828360-chr16:80833260..80835837,2	MCF-7	breast:
14	chr16:80561006..80561873-chr16:80858356..80858913,3	K562	blood:
15	chr16:80533745..80536579-chr16:80846654..80849245,2	MCF-7	breast:
16	chr16:80573192..80575392-chr16:80605742..80608359,2	MCF-7	breast:
17	chr16:80648695..80650960-chr16:80752549..80754538,2	MCF-7	breast:
18	chr16:80772543..80774780-chr16:80838144..80840162,2	MCF-7	breast:
19	chr16:80829092..80831427-chr16:80833348..80835042,2	MCF-7	breast:
20	chr16:80943433..80946323-chr16:80947532..80951132,3	K562	blood:
21	chr16:80812055..80815396-chr16:80837025..80838979,4	MCF-7	breast:
22	chr16:80841190..80844369-chr16:80857041..80859496,3	MCF-7	breast:
23	chr16:80826433..80828352-chr16:80832808..80835900,4	MCF-7	breast:
24	chr16:80601424..80603816-chr16:80622383..80625289,2	MCF-7	breast:
25	chr16:80657950..80660118-chr16:80836861..80838846,2	MCF-7	breast:
26	chr16:80742029..80744707-chr16:80834367..80837032,2	MCF-7	breast:
27	chr16:80690433..80692139-chr16:80693277..80695460,2	K562	blood:
28	chr16:80836267..80838116-chr16:81067816..81069508,2	MCF-7	breast:
29	chr16:80884292..80886767-chr16:80887725..80889575,2	K562	blood:
30	chr16:80858781..80859754-chr16:80885898..80886889,3	MCF-7	breast:
31	chr16:80573192..80575392-chr16:80605742..80608359,2	MCF-7	breast:
32	chr16:80653589..80657400-chr16:80657593..80661612,3	K562	blood:
33	chr16:80963937..80967554-chr16:80967751..80972204,4	K562	blood:
34	chr16:80745711..80747675-chr16:80834808..80837555,2	MCF-7	breast:
35	chr16:80572758..80574587-chr16:80801032..80802655,2	MCF-7	breast:
36	chr16:80653589..80657400-chr16:80657593..80661612,3	K562	blood:
37	chr16:80756751..80759614-chr16:80770866..80773817,2	MCF-7	breast:
38	chr16:80732152..80734988-chr16:80742943..80745813,2	MCF-7	breast:
39	chr16:80807863..80810063-chr16:80836867..80839644,2	MCF-7	breast:
40	chr16:80903251..80907289-chr16:80908287..80911628,3	K562	blood:
41	chr16:80650331..80653317-chr16:80787913..80789751,2	MCF-7	breast:
42	chr16:80852508..80854176-chr16:80857247..80859304,2	K562	blood:
43	chr16:80697075..80698922-chr16:80836578..80838205,2	MCF-7	breast:
44	chr16:80560059..80562846-chr16:80837762..80839641,2	MCF-7	breast:
45	chr16:80785744..80787464-chr16:80788203..80790386,2	MCF-7	breast:
46	chr16:80593040..80595743-chr16:80600736..80603732,2	K562	blood:
47	chr16:80791934..80794867-chr16:80796683..80798258,2	K562	blood:
48	chr16:80577485..80580342-chr16:80689346..80691790,2	MCF-7	breast:
49	chr16:80826270..80828360-chr16:80833260..80835837,2	MCF-7	breast:
50	chr16:80622034..80624182-chr16:80626322..80628140,2	MCF-7	breast:

(count:75 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDYL2-6	chr16:80562541-80562683	XLOC_012019
2	lnc-DYNLRB2-1	chr16:80775995-80776202	ENSG00000260594.1
3	lnc-CDYL2-2	chr16:80602704-80602795	ENSG00000260737.1
4	lnc-CDYL2-6	chr16:80560736-80560915	ENSG00000259867.1
5	lnc-CDYL2-6	chr16:80573869-80574385	XLOC_012019
6	lnc-CDYL2-2	chr16:80601476-80601656	NONHSAT143899
7	lnc-CDYL2-2	chr16:80603122-80603167	ENSG00000260737.1
8	lnc-CDYL2-2	chr16:80606531-80606705	ENSG00000260737.1
9	lnc-CDYL2-2	chr16:80602704-80602793	NONHSAT143899
10	lnc-CDYL2-2	chr16:80601845-80602010	NONHSAT143893
11	lnc-CDYL2-2	chr16:80604029-80604412	NONHSAT143901
12	lnc-CDYL2-2	chr16:80601452-80601656	NR_104665
13	lnc-CDYL2-4	chr16:80926402-80926457	ENSG00000260896.1
14	lnc-CDYL2-4	chr16:80862435-80864654	XLOC_012021
15	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
16	lnc-CDYL2-2	chr16:80595134-80595182	NONHSAT143893
17	lnc-CDYL2-4	chr16:80864428-80864654	ENSG00000260896.1
18	lnc-CDYL2-6	chr16:80574747-80574844	ENSG00000259867.1
19	lnc-CDYL2-4	chr16:80871829-80871942	ENSG00000260896.1
20	lnc-CDYL2-4	chr16:80864391-80864654	ENSG00000260896.1
21	lnc-CDYL2-2	chr16:80600691-80600990	ENSG00000250904
22	lnc-CDYL2-2	chr16:80601845-80602010	NONHSAT143899
23	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
24	lnc-CDYL2-6	chr16:80596926-80597032	ENSG00000259867.1
25	lnc-CDYL2-6	chr16:80574747-80574850	ENSG00000259867.1
26	lnc-CDYL2-6	chr16:80541466-80541666	ENSG00000259867.1
27	lnc-CDYL2-4	chr16:80871829-80871942	ENSG00000260896.1
28	lnc-CDYL2-2	chr16:80601452-80601656	ENSG00000260737.1
29	lnc-CDYL2-2	chr16:80603122-80603566	NONHSAT143899
30	lnc-CDYL2-2	chr16:80602704-80602793	NR_104665
31	lnc-CDYL2-6	chr16:80562539-80562683	ENSG00000259867.1
32	lnc-CDYL2-2	chr16:80603088-80603495	NONHSAT143901
33	lnc-CDYL2-2	chr16:80601845-80602010	ENSG00000260737.1
34	lnc-CDYL2-6	chr16:80574747-80574767	ENSG00000259867.1
35	lnc-CDYL2-2	chr16:80602713-80602875	XLOC_012020
36	lnc-DYNLRB2-1	chr16:80770257-80770412	ENSG00000260594.1
37	lnc-CDYL2-2	chr16:80601000-80601413	ENSG00000260737.1
38	lnc-CDYL2-6	chr16:80562539-80562683	ENSG00000259867.1
39	lnc-CDYL2-4	chr16:80864323-80864654	ENSG00000260896.1
40	lnc-CDYL2-2	chr16:80603122-80603581	XLOC_012020
41	lnc-CDYL2-2	chr16:80594621-80594776	NONHSAT143893
42	lnc-CDYL2-2	chr16:80603122-80603566	NONHSAT143893
43	lnc-CDYL2-4	chr16:80874016-80874119	ENSG00000260896.1
44	lnc-CDYL2-2	chr16:80603122-80603507	NR_104665
45	lnc-CDYL2-4	chr16:80926402-80926492	ENSG00000260896.1
46	lnc-CDYL2-2	chr16:80601845-80602010	ENSG00000260737.1
47	lnc-CDYL2-6	chr16:80562539-80562683	ENSG00000259867.1
48	lnc-CDYL2-2	chr16:80601845-80602010	ENSG00000250904
49	lnc-CDYL2-6	chr16:80574747-80574764	ENSG00000259867.1
50	lnc-CDYL2-2	chr16:80600941-80600990	XLOC_012020

No data

Variant related genes	Relation type
ENSG00000260594	TF binding region
CDYL2	TF binding region
ENSG00000260737	TF binding region
ENSG00000265341	TF binding region
ENSG00000259867	TF binding region
DYNLRB2	TF binding region
ENSG00000260064	TF binding region
ENSG00000260183	TF binding region
ENSG00000260896	TF binding region
ENSG00000260594	CpG island
CDYL2	CpG island
ENSG00000260737	CpG island
ENSG00000265341	CpG island
ENSG00000259867	CpG island
DYNLRB2	CpG island
ENSG00000260064	CpG island
ENSG00000260183	CpG island
ENSG00000260896	CpG island
ENSG00000133316	chromatin interactions
ENSG00000196374	chromatin interactions
ENSG00000166446	chromatin interactions
ENSG00000028116	chromatin interactions
ENSG00000135930	chromatin interactions
ENSG00000265341	chromatin interactions
ENSG00000259867	chromatin interactions
ENSG00000182611	chromatin interactions
ENSG00000221944	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000260183	chromatin interactions
ENSG00000260064	chromatin interactions
ENSG00000047346	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000168589	chromatin interactions
ENSG00000260737	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000166451	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000103363	chromatin interactions
ENSG00000260896	chromatin interactions
RBM10	miRNA target sites
AK3	miRNA target sites
TNPO1	miRNA target sites
CSDA	miRNA target sites
RAB3IL1	miRNA target sites

Extended variants
information (count: 22025 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:22025 , 50 per page) page: 1 2 3 4 5 6 7 ... 441

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140987846	chr16:80532848-80532849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559497730	chr16:80532933-80532934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150357678	chr16:80532995-80532996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375040863	chr16:80533000-80533001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549953916	chr16:80533025-80533026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192179369	chr16:80533051-80533052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532426963	chr16:80533057-80533058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185706220	chr16:80533066-80533067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116321495	chr16:80533071-80533072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573063295	chr16:80533091-80533092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138009907	chr16:80533119-80533120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72822225	chr16:80533131-80533132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs377329073	chr16:80533138-80533139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140971955	chr16:80533144-80533145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144907244	chr16:80533152-80533153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59617944	chr16:80533177-80533178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs189361732	chr16:80533181-80533182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533563927	chr16:80533203-80533204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138729932	chr16:80533232-80533233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538697443	chr16:80533260-80533261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553743812	chr16:80533315-80533316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571917709	chr16:80533339-80533340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117098909	chr16:80533352-80533353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542593266	chr16:80533385-80533386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149248290	chr16:80533390-80533391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553335784	chr16:80533394-80533395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576325347	chr16:80533410-80533411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111532245	chr16:80533449-80533450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565099042	chr16:80533467-80533468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573441762	chr16:80533486-80533487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542309995	chr16:80533495-80533496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148020711	chr16:80533505-80533506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547548096	chr16:80533512-80533513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192224266	chr16:80533566-80533567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184669239	chr16:80533597-80533598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548551407	chr16:80533635-80533636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs16953527	chr16:80533636-80533637	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs141673304	chr16:80533642-80533643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147156972	chr16:80533696-80533697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140941046	chr16:80533705-80533706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12444376	chr16:80533726-80533727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79491740	chr16:80533740-80533741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553612691	chr16:80533751-80533752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs8045647	chr16:80533761-80533762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535915784	chr16:80533806-80533807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34439994	chr16:80533814-80533815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147538605	chr16:80533828-80533829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576341363	chr16:80533840-80533841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543676806	chr16:80533851-80533852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188987043	chr16:80533853-80533854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Adrenocortical carcinoma	18281524	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
early-passage human iPS cells	21368824	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3648 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80531000-80534200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:80534600-80535000	Enhancers	Fetal Lung	lung
3	chr16:80534800-80535200	Enhancers	Fetal Brain Male	brain
4	chr16:80535000-80538000	Weak transcription	Fetal Lung	lung
5	chr16:80536600-80536800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr16:80537400-80537800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr16:80538000-80538200	Enhancers	Fetal Lung	lung
8	chr16:80538400-80538800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr16:80540600-80541800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr16:80540800-80542000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr16:80541400-80541600	Enhancers	Fetal Lung	lung
12	chr16:80543400-80544200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr16:80543600-80544200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr16:80543600-80544200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr16:80543600-80544200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:80543600-80544200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr16:80543800-80544000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr16:80543800-80544000	Enhancers	Fetal Kidney	kidney
19	chr16:80543800-80544200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr16:80544000-80544200	Enhancers	Fetal Muscle Leg	muscle
21	chr16:80544000-80547800	Weak transcription	Fetal Kidney	kidney
22	chr16:80544200-80552400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr16:80547200-80548000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr16:80547200-80552600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr16:80547400-80548000	Enhancers	Placenta	Placenta
26	chr16:80547800-80548200	Enhancers	Fetal Kidney	kidney
27	chr16:80547800-80548600	Enhancers	Ovary	ovary
28	chr16:80547800-80548800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr16:80548000-80552400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr16:80551800-80553400	Enhancers	Primary B cells from peripheral blood	blood
31	chr16:80551800-80553400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr16:80551800-80553800	Enhancers	Primary T cells from cord blood	blood
33	chr16:80551800-80553800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr16:80551800-80554000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr16:80552000-80553800	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr16:80552200-80552600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr16:80552200-80552600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr16:80552200-80552600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr16:80552200-80552600	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr16:80552200-80553000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr16:80552200-80553200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr16:80552200-80553600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr16:80552200-80553800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:80552200-80553800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr16:80552400-80552600	Enhancers	Aorta	Aorta
46	chr16:80552400-80552800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr16:80552400-80553200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr16:80552400-80553400	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr16:80552400-80553400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr16:80552400-80553400	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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