Variant report

Variant	nsv1059039
Chromosome Location	chr16:32872263-33528744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5166)
CpG islands
(count:2748)
Chromatin interactive
region (count:12)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5166 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:33502987-33503033	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:33293788-33294209	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
4	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
5	ATF1	chr16:33446622-33446661	K562	blood:	n/a	n/a
6	ATF3	chr16:33240952-33241267	HepG2	liver:	n/a	n/a
7	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
8	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
9	ATF3	chr16:32993758-32993903	K562	blood:	n/a	n/a
10	ATF3	chr16:33293710-33294426	HepG2	liver:	n/a	n/a
11	BACH1	chr16:33293845-33294023	K562	blood:	n/a	n/a
12	BATF	chr16:33042934-33043504	GM12878	blood:	n/a	n/a
13	BATF	chr16:33521180-33521433	GM12878	blood:	n/a	n/a
14	BATF	chr16:33043855-33044053	GM12878	blood:	n/a	n/a
15	BATF	chr16:33041862-33042137	GM12878	blood:	n/a	n/a
16	BATF	chr16:33365611-33366045	GM12878	blood:	n/a	n/a
17	BATF	chr16:33328184-33328483	GM12878	blood:	n/a	chr16:33328300-33328311
18	BATF	chr16:33331077-33331251	GM12878	blood:	n/a	n/a
19	BATF	chr16:32993933-32994319	GM12878	blood:	n/a	n/a
20	BATF	chr16:33521242-33521484	GM12878	blood:	n/a	n/a
21	BATF	chr16:33048704-33048907	GM12878	blood:	n/a	n/a
22	BATF	chr16:33092972-33093212	GM12878	blood:	n/a	n/a
23	BATF	chr16:33042313-33042791	GM12878	blood:	n/a	n/a
24	BATF	chr16:32951300-32951515	GM12878	blood:	n/a	chr16:32951446-32951457
25	BATF	chr16:33524710-33524926	GM12878	blood:	n/a	chr16:33524743-33524752
26	BATF	chr16:33051640-33051829	GM12878	blood:	n/a	n/a
27	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
28	BATF	chr16:33052311-33052561	GM12878	blood:	n/a	n/a
29	BATF	chr16:33087692-33087910	GM12878	blood:	n/a	n/a
30	BATF	chr16:33369625-33369914	GM12878	blood:	n/a	n/a
31	BATF	chr16:33077153-33077342	GM12878	blood:	n/a	n/a
32	BATF	chr16:33517629-33517889	GM12878	blood:	n/a	n/a
33	BATF	chr16:33448799-33449188	GM12878	blood:	n/a	chr16:33449053-33449063
34	BATF	chr16:33002452-33002671	GM12878	blood:	n/a	n/a
35	BATF	chr16:33082292-33082557	GM12878	blood:	n/a	n/a
36	BATF	chr16:33431461-33431755	GM12878	blood:	n/a	chr16:33431606-33431617
37	BATF	chr16:33046042-33046353	GM12878	blood:	n/a	n/a
38	BATF	chr16:33524553-33524907	GM12878	blood:	n/a	chr16:33524743-33524752
39	BATF	chr16:33044181-33044885	GM12878	blood:	n/a	chr16:33044727-33044738
40	BATF	chr16:33044491-33044914	GM12878	blood:	n/a	chr16:33044727-33044738
41	BATF	chr16:33002463-33002715	GM12878	blood:	n/a	n/a
42	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
43	BATF	chr16:33458798-33459290	GM12878	blood:	n/a	n/a
44	BATF	chr16:33087718-33087908	GM12878	blood:	n/a	n/a
45	BATF	chr16:33020846-33021096	GM12878	blood:	n/a	n/a
46	BATF	chr16:33448828-33449178	GM12878	blood:	n/a	chr16:33449053-33449063
47	BATF	chr16:33445748-33446186	GM12878	blood:	n/a	chr16:33445964-33445975 chr16:33445982-33445990
48	BATF	chr16:33091390-33091661	GM12878	blood:	n/a	n/a
49	BATF	chr16:33365688-33366003	GM12878	blood:	n/a	n/a
50	BATF	chr16:33364185-33364651	GM12878	blood:	n/a	chr16:33364440-33364451

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:33040275-33040325	LNCaP	prostate:	n/a
2	chr16:33040206-33040256	PANC-1	pancreas:	n/a
3	chr16:33302523-33302573	HPAEpiC	pulmonary alveolar:	n/a
4	chr16:33040275-33040325	LNCaP	prostate:	n/a
5	chr16:33040206-33040256	PANC-1	pancreas:	n/a
6	chr16:33302523-33302573	HPAEpiC	pulmonary alveolar:	n/a
7	chr16:33319610-33319660	Hela-S3	cervix:	n/a
8	chr16:32937057-32937107	T-47D	breast:	n/a
9	chr16:33481620-33481670	HRE	kidney:	n/a
10	chr16:33319610-33319660	LNCaP	prostate:	n/a
11	chr16:33357151-33357201	HMEC	breast:	n/a
12	chr16:33319610-33319660	AG10803	skin:	n/a
13	chr16:33481620-33481670	U87	brain:	n/a
14	chr16:33509523-33509573	HCPEpiC	choroid plexus:	n/a
15	chr16:33038657-33038707	GM12878	blood:	n/a
16	chr16:33483299-33483349	A549	lung:	n/a
17	chr16:32898433-32898483	AG04449	skin:	fetal
18	chr16:33510089-33510139	T-47D	breast:	n/a
19	chr16:33039897-33039947	AG09309	skin:	n/a
20	chr16:33070632-33070682	RPTEC	kidney:	n/a
21	chr16:32936895-32936945	HRPEpiC	eye:	n/a
22	chr16:33483462-33483512	ProgFib	skin:	n/a
23	chr16:33071657-33071707	A549	lung:	n/a
24	chr16:33509523-33509573	HRPEpiC	eye:	n/a
25	chr16:33317852-33317902	HPAEpiC	pulmonary alveolar:	n/a
26	chr16:33374131-33374181	HCPEpiC	choroid plexus:	n/a
27	chr16:33509523-33509573	A549	lung:	n/a
28	chr16:33483244-33483294	BJ	skin:	n/a
29	chr16:33356843-33356893	Hepatocyte	liver:	n/a
30	chr16:33483591-33483641	HEK293	kidney:	embryo
31	chr16:33319362-33319412	AoSMC	blood vessel:	n/a
32	chr16:32898433-32898483	GM12878	blood:	n/a
33	chr16:33302523-33302573	ECC-1	luminal epithelium:	n/a
34	chr16:33298952-33299002	HRCEpiC	kidney:	n/a
35	chr16:33483299-33483349	HL-60	blood:	n/a
36	chr16:33040275-33040325	Caco-2	colon:	n/a
37	chr16:33040275-33040325	GM12892	blood:	n/a
38	chr16:33358227-33358277	GM12891	blood:	n/a
39	chr16:33006163-33006213	HEEpiC	esophagus:	n/a
40	chr16:33483297-33483347	T-47D	breast:	n/a
41	chr16:33510089-33510139	HL-60	blood:	n/a
42	chr16:33483462-33483512	HIPEpiC	eye:	n/a
43	chr16:33040275-33040325	AG10803	skin:	n/a
44	chr16:33297688-33297738	A549	lung:	n/a
45	chr16:32936664-32936714	A549	lung:	n/a
46	chr16:33483244-33483294	SAEC	small airway:	n/a
47	chr16:33374161-33374211	SAEC	small airway:	n/a
48	chr16:33070632-33070682	AG04449	skin:	fetal
49	chr16:33044270-33044320	U87	brain:	n/a
50	chr16:33319610-33319660	HCPEpiC	choroid plexus:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
2	chr16:32993835..32994354-chr16:33619041..33619624,2	MCF-7	breast:
3	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
4	chr12:123886567..123888097-chr16:33420189..33423186,2	K562	blood:
5	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
6	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:
7	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
8	chr16:33501621..33504383-chr16:33506713..33508666,2	K562	blood:
9	chr16:33362493..33363428-chr3:73095698..73096500,2	MCF-7	breast:
10	chr16:33357445..33357965-chrX:123093937..123094556,2	MCF-7	breast:
11	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:
12	chr16:33374454..33377112-chr16:33390580..33392185,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC136428.1.1-5	chr16:33272554-33272594	ENSG00000261009.1
2	lnc-AC136428.1.1-6	chr16:33231324-33231409	ENSG00000261507.1
3	lnc-RP11-1277H1.1.1-1	chr16:33140637-33140721	ENSG00000261682.1
4	lnc-RP11-1277H1.1.1-4	chr16:32897547-32898093	ENSG00000214614.2
5	lnc-CTD-2144E22.5.1-37	chr16:33263182-33263470	NONHSAT142077
6	lnc-AC136428.1.1-6	chr16:33231506-33231583	ENSG00000261507.1
7	lnc-TP53TG3-5	chr16:33102620-33102910	ENSG00000260141.1
8	lnc-CTD-2144E22.5.1-37	chr16:33263683-33264006	NONHSAT142077
9	lnc-RP11-1277H1.1.1-9	chr16:32989782-32989827	NONHSAT142058
10	lnc-RP11-1277H1.1.1-7	chr16:33141556-33141763	NONHSAT142067
11	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898880	ENSG00000214614.2
12	lnc-RP11-1277H1.1.1-3	chr16:33007600-33008091	ENSG00000260921.1
13	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
14	lnc-CTD-2144E22.5.1-37	chr16:33262848-33262894	NONHSAT142077
15	lnc-RP11-1277H1.1.1-9	chr16:32989910-32990212	NONHSAT142058
16	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
17	lnc-RP11-1277H1.1.1-3	chr16:33007112-33007188	ENSG00000260921.1
18	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
19	lnc-AC136428.1.1-7	chr16:33202882-33203073	ENSG00000260419.1
20	lnc-AC136428.1.1-6	chr16:33215175-33215559	ENSG00000260827.1
21	lnc-AC136428.1.1-4	chr16:33336283-33336630	ENSG00000260626.1
22	lnc-RP11-1277H1.1.1-4	chr16:32897796-32898008	ENSG00000214614.2
23	lnc-TP53TG3-17	chr16:32943089-32943890	NONHSAT142053
24	lnc-RP11-1277H1.1.1-2	chr16:33340193-33341795	XLOC_011696
25	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
26	lnc-RP11-1277H1.1.1-3	chr16:33006858-33006938	ENSG00000260921.1
27	lnc-AC136428.1.1-4	chr16:33337232-33337443	ENSG00000260626.1
28	lnc-AC136428.1.1-6	chr16:33216015-33216055	ENSG00000260827.1
29	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
30	lnc-TP53TG3-5	chr16:33054930-33055459	ENSG00000260141.1
31	lnc-AC136428.1.1-5	chr16:33271714-33272098	ENSG00000261009.1
32	lnc-RP11-1277H1.1.1-11	chr16:32926395-32926440	NONHSAT142052
33	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
34	lnc-AC136428.1.1-7	chr16:33206606-33206675	ENSG00000260419.1
35	lnc-RP11-1277H1.1.1-1	chr16:33145040-33145820	ENSG00000261682.1
36	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
37	lnc-RP11-1277H1.1.1-2	chr16:33342943-33343609	XLOC_011696
38	lnc-AC136428.1.1-6	chr16:33217752-33218127	ENSG00000261507.1

No data

Variant related genes	Relation type
IGHV3OR16-8	TF binding region
ENSG00000263337	TF binding region
ENSG00000260419	TF binding region
ENSG00000262090	TF binding region
ENSG00000214614	TF binding region
IGHV3OR16-10	TF binding region
ENSG00000260047	TF binding region
ENSG00000260414	TF binding region
ENSG00000259882	TF binding region
ENSG00000263277	TF binding region
ENSG00000261682	TF binding region
ENSG00000260827	TF binding region
ENSG00000261466	TF binding region
ENSG00000261405	TF binding region
SLC6A10P	TF binding region
ENSG00000261259	TF binding region
ENSG00000261507	TF binding region
ENSG00000260626	TF binding region
IGHV1OR16-2	TF binding region
TP53TG3B	TF binding region
ENSG00000263204	TF binding region
ENSG00000260610	TF binding region
ENSG00000261536	TF binding region
IGHV3OR16-15	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261200	TF binding region
ENSG00000260141	TF binding region
ENSG00000261009	TF binding region
ENSG00000260921	TF binding region
ENSG00000260900	TF binding region
ENSG00000259800	TF binding region
TP53TG3C	TF binding region
IGHV1OR16-4	TF binding region
BMS1P8	TF binding region
HERC2P8	TF binding region
IGHV3OR16-8	CpG island
ENSG00000263337	CpG island
ENSG00000260419	CpG island
ENSG00000262090	CpG island
ENSG00000214614	CpG island
IGHV3OR16-10	CpG island
ENSG00000260047	CpG island
ENSG00000260414	CpG island
ENSG00000259882	CpG island
ENSG00000263277	CpG island
ENSG00000261682	CpG island
ENSG00000260827	CpG island
ENSG00000261466	CpG island
ENSG00000261405	CpG island
SLC6A10P	CpG island
ENSG00000261259	CpG island
ENSG00000261507	CpG island
ENSG00000260626	CpG island
IGHV1OR16-2	CpG island
TP53TG3B	CpG island
ENSG00000263204	CpG island
ENSG00000260610	CpG island
ENSG00000261536	CpG island
IGHV3OR16-15	CpG island
IGHV3OR16-6	CpG island
ENSG00000261200	CpG island
ENSG00000260141	CpG island
ENSG00000261009	CpG island
ENSG00000260921	CpG island
ENSG00000260900	CpG island
ENSG00000259800	CpG island
TP53TG3C	CpG island
IGHV1OR16-4	CpG island
BMS1P8	CpG island
HERC2P8	CpG island
ENSG00000101972	chromatin interactions
UHMK1	miRNA target sites

Extended variants
information (count: 8914 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:8914 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558586481	chr16:32876601-32876602	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs1651608	chr16:32876656-32876657	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576927644	chr16:32876704-32876705	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs191615604	chr16:32876794-32876795	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs3097301	chr16:32876795-32876796	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs3094331	chr16:32876811-32876812	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs3097302	chr16:32876828-32876829	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs575009382	chr16:32876834-32876835	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs542135163	chr16:32876850-32876851	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183473680	chr16:32876852-32876853	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs527244532	chr16:32876870-32876871	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs188851544	chr16:32876873-32876874	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs564119647	chr16:32876898-32876899	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs116810617	chr16:32876899-32876900	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201969105	chr16:32876966-32876967	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568140224	chr16:32877011-32877012	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs529107996	chr16:32877027-32877028	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs547340685	chr16:32877028-32877029	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs78041799	chr16:32877041-32877042	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs565647352	chr16:32877078-32877079	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533886515	chr16:32877096-32877097	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs558525447	chr16:32877122-32877123	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570551302	chr16:32877139-32877140	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2905124	chr16:32877165-32877166	Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs144312071	chr16:32877208-32877209	Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs148453648	chr16:32877251-32877252	Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs1820207	chr16:32877271-32877272	Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs556644122	chr16:32877292-32877293	Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs113579091	chr16:32877360-32877361	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs201718499	chr16:32877363-32877364	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs11860281	chr16:32877387-32877388	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs1989495	chr16:32877390-32877391	Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs150985109	chr16:32877426-32877427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs542422673	chr16:32877435-32877436	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs1820772	chr16:32877436-32877437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs683980	chr16:32877457-32877458	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554463055	chr16:32877478-32877479	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs572776713	chr16:32877484-32877485	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs1794032	chr16:32877488-32877489	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs564057930	chr16:32877501-32877502	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374348342	chr16:32877536-32877537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544862473	chr16:32877537-32877538	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs1794031	chr16:32877540-32877541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs193216934	chr16:32877549-32877550	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs561838735	chr16:32877593-32877594	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529039686	chr16:32877605-32877606	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs587210	chr16:32877629-32877630	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs1651609	chr16:32877630-32877631	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs565584578	chr16:32877658-32877659	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs1651610	chr16:32877668-32877669	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Ductal carcinoma	22052326	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Autism	19287141	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Lung cancer	18438408	CNVD
Autism	21865298	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32876600-32876800	Enhancers	Skeletal Muscle Female	skeletal muscle
2	chr16:32876800-32877000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:32876800-32877000	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr16:32876800-32877200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr16:32876800-32881000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr16:32877000-32877400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
7	chr16:32877200-32877400	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr16:32877400-32877600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr16:32877400-32877800	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr16:32877600-32877800	Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr16:32877800-32878000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr16:32877800-32878200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr16:32878000-32878200	Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr16:32878200-32878600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
15	chr16:32878200-32880000	Active TSS	Skeletal Muscle Male	skeletal muscle
16	chr16:32878600-32879400	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr16:32879400-32879800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr16:32879800-32880200	Enhancers	Left Ventricle	heart
19	chr16:32879800-32881000	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr16:32880000-32880800	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr16:32880800-32883800	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr16:32881000-32881800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr16:32881000-32886000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr16:32883800-32884200	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr16:32884200-32885400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr16:32885400-32887600	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr16:32886000-32887400	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr16:32890600-32891000	Active TSS	HSMM	muscle
29	chr16:32957400-32957800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr16:33006000-33007200	Enhancers	Dnd41	blood
31	chr16:33039600-33040000	Bivalent Enhancer	Placenta	Placenta
32	chr16:33039600-33040800	Active TSS	K562	blood
33	chr16:33040000-33040400	Flanking Bivalent TSS/Enh	Placenta	Placenta
34	chr16:33040400-33040800	Bivalent Enhancer	Placenta	Placenta
35	chr16:33070400-33071000	Bivalent Enhancer	Placenta	Placenta
36	chr16:33070600-33071000	Active TSS	Psoas Muscle	Psoas
37	chr16:33070800-33071000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr16:33071400-33071600	Enhancers	Right Ventricle	heart
39	chr16:33140000-33140400	Active TSS	HSMM	muscle
40	chr16:33140200-33140400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr16:33140200-33140400	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr16:33236400-33241000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr16:33236600-33241600	Weak transcription	Fetal Lung	lung
44	chr16:33237400-33237600	Bivalent Enhancer	Placenta	Placenta
45	chr16:33237400-33237600	Enhancers	Right Ventricle	heart
46	chr16:33237400-33238000	Active TSS	Primary T helper naive cells from peripheral blood	blood
47	chr16:33237400-33238000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr16:33237400-33238200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr16:33237400-33238200	Active TSS	Primary T cells from cord blood	blood
50	chr16:33237400-33238200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum

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