Variant report

Variant	esv2830024
Chromosome Location	chr16:32511914-32975525
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2852)
CpG islands
(count:1647)
Chromatin interactive
region (count:4)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2852 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:32817100-32817669	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:32818363-32818754	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:32876710-32876890	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:32657798-32657972	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:32655940-32657281	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:32547652-32548159	K562	blood:	n/a	n/a
7	ARID3A	chr16:32590243-32590613	K562	blood:	n/a	n/a
8	ARID3A	chr16:32817496-32817662	K562	blood:	n/a	n/a
9	ATF1	chr16:32521319-32521519	K562	blood:	n/a	n/a
10	ATF1	chr16:32583782-32583972	K562	blood:	n/a	n/a
11	ATF1	chr16:32559923-32560294	K562	blood:	n/a	n/a
12	ATF1	chr16:32547497-32547620	K562	blood:	n/a	n/a
13	ATF1	chr16:32549843-32550009	K562	blood:	n/a	n/a
14	ATF1	chr16:32873309-32873509	K562	blood:	n/a	n/a
15	ATF1	chr16:32558594-32558903	K562	blood:	n/a	n/a
16	ATF1	chr16:32550785-32551178	K562	blood:	n/a	n/a
17	ATF1	chr16:32526924-32527721	K562	blood:	n/a	n/a
18	ATF1	chr16:32832855-32832989	K562	blood:	n/a	n/a
19	ATF1	chr16:32515726-32516011	K562	blood:	n/a	n/a
20	ATF1	chr16:32568174-32568349	K562	blood:	n/a	n/a
21	ATF3	chr16:32909214-32909368	K562	blood:	n/a	n/a
22	ATF3	chr16:32876765-32876921	K562	blood:	n/a	n/a
23	BACH1	chr16:32553830-32554374	K562	blood:	n/a	n/a
24	BACH1	chr16:32590237-32590618	K562	blood:	n/a	n/a
25	BACH1	chr16:32531668-32531907	K562	blood:	n/a	n/a
26	BACH1	chr16:32639174-32639436	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr16:32805422-32805612	GM12878	blood:	n/a	n/a
28	BATF	chr16:32944783-32945170	GM12878	blood:	n/a	n/a
29	BATF	chr16:32848099-32848439	GM12878	blood:	n/a	n/a
30	BATF	chr16:32805420-32805638	GM12878	blood:	n/a	n/a
31	BATF	chr16:32652784-32652999	GM12878	blood:	n/a	n/a
32	BATF	chr16:32652782-32652951	GM12878	blood:	n/a	n/a
33	BATF	chr16:32801669-32801940	GM12878	blood:	n/a	n/a
34	BATF	chr16:32846943-32847213	GM12878	blood:	n/a	n/a
35	BATF	chr16:32727057-32727270	GM12878	blood:	n/a	n/a
36	BATF	chr16:32815984-32816173	GM12878	blood:	n/a	n/a
37	BATF	chr16:32909165-32909547	GM12878	blood:	n/a	n/a
38	BATF	chr16:32799795-32800035	GM12878	blood:	n/a	n/a
39	BATF	chr16:32847350-32847649	GM12878	blood:	n/a	n/a
40	BATF	chr16:32800340-32800564	GM12878	blood:	n/a	n/a
41	BATF	chr16:32951300-32951515	GM12878	blood:	n/a	chr16:32951446-32951457
42	BCL11A	chr16:32808250-32808438	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:32828470-32828650	GM12878	blood:	n/a	n/a
44	BCL11A	chr16:32816660-32816835	GM12878	blood:	n/a	n/a
45	BCL11A	chr16:32944851-32945232	GM12878	blood:	n/a	n/a
46	BCL11A	chr16:32722318-32722491	GM12878	blood:	n/a	n/a
47	BCL11A	chr16:32727141-32727357	GM12878	blood:	n/a	n/a
48	BCL11A	chr16:32819672-32819869	GM12878	blood:	n/a	n/a
49	BCL11A	chr16:32811597-32811895	GM12878	blood:	n/a	n/a
50	BCL11A	chr16:32847030-32847596	GM12878	blood:	n/a	n/a

(count:1647 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:32857923-32857973	HMEC	breast:	n/a
2	chr16:32662543-32662593	HRPEpiC	eye:	n/a
3	chr16:32857872-32857922	Hela-S3	cervix:	n/a
4	chr16:32936895-32936945	T-47D	breast:	n/a
5	chr16:32820218-32820268	Hepatocyte	liver:	n/a
6	chr16:32857347-32857397	GM19239	blood:	n/a
7	chr16:32937057-32937107	HUVEC	blood vessel:	n/a
8	chr16:32822392-32822442	HNPCEpiC	eye:	n/a
9	chr16:32858846-32858896	K562	blood:	n/a
10	chr16:32822612-32822662	BE2_C	brain:	n/a
11	chr16:32823584-32823634	AG04450	lung:	fetal
12	chr16:32599433-32599483	IMR90	lung:	fetal
13	chr16:32857007-32857057	PANC-1	pancreas:	n/a
14	chr16:32857872-32857922	A549	lung:	n/a
15	chr16:32940983-32941033	H1-hESC	embryonic stem cell:	embryo
16	chr16:32823584-32823634	HRPEpiC	eye:	n/a
17	chr16:32857923-32857973	ProgFib	skin:	n/a
18	chr16:32936664-32936714	H1-hESC	embryonic stem cell:	embryo
19	chr16:32822612-32822662	HIPEpiC	eye:	n/a
20	chr16:32857872-32857922	AG04449	skin:	fetal
21	chr16:32823584-32823634	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:32823584-32823634	SAEC	small airway:	n/a
23	chr16:32936664-32936714	HCPEpiC	choroid plexus:	n/a
24	chr16:32823289-32823339	HRPEpiC	eye:	n/a
25	chr16:32857347-32857397	HEK293	kidney:	embryo
26	chr16:32599417-32599467	SK-N-SH	brain:	n/a
27	chr16:32857347-32857397	HMEC	breast:	n/a
28	chr16:32857007-32857057	NT2-D1	testis:	n/a
29	chr16:32662543-32662593	K562	blood:	n/a
30	chr16:32820218-32820268	HRE	kidney:	n/a
31	chr16:32822612-32822662	PANC-1	pancreas:	n/a
32	chr16:32940983-32941033	SKMC	muscle:	n/a
33	chr16:32822612-32822662	IMR90	lung:	fetal
34	chr16:32853952-32854002	Jurkat	blood:	n/a
35	chr16:32823000-32823050	HCPEpiC	choroid plexus:	n/a
36	chr16:32898433-32898483	T-47D	breast:	n/a
37	chr16:32662543-32662593	Caco-2	colon:	n/a
38	chr16:32822480-32822530	HIPEpiC	eye:	n/a
39	chr16:32823289-32823339	MCF10A-Er-Src	breast:	n/a
40	chr16:32822612-32822662	Hela-S3	cervix:	n/a
41	chr16:32822480-32822530	SK-N-MC	brain:	n/a
42	chr16:32822392-32822442	K562	blood:	n/a
43	chr16:32659887-32659937	SK-N-SH	brain:	n/a
44	chr16:32822392-32822442	SK-N-SH_RA	brain:	n/a
45	chr16:32823000-32823050	IMR90	lung:	fetal
46	chr16:32940983-32941033	HIPEpiC	eye:	n/a
47	chr16:32599417-32599467	MCF-7	breast:	n/a
48	chr16:32936895-32936945	SK-N-MC	brain:	n/a
49	chr16:32858241-32858291	ProgFib	skin:	n/a
50	chr16:32937057-32937107	Hela-S3	cervix:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
2	chr16:32951293..32951850-chr16:33618657..33619267,2	MCF-7	breast:
3	chr16:32876380..32877212-chr16:32951315..32951834,2	MCF-7	breast:
4	chr16:32876653..32877208-chr16:33618895..33619446,2	MCF-7	breast:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1277H1.1.1-11	chr16:32926544-32926857	NONHSAT142052
2	lnc-AC133485.1.1-3	chr16:32676974-32677014	ENSG00000260311.1
3	lnc-AC133485.1.1-2	chr16:32616957-32617035	NONHSAT142021
4	lnc-AC133485.1.1-3	chr16:32677470-32677854	ENSG00000260311.1
5	lnc-RP11-1277H1.1.1-4	chr16:32897547-32898093	ENSG00000214614.2
6	lnc-RP11-1277H1.1.1-4	chr16:32897778-32897912	ENSG00000214614.2
7	lnc-AC133485.1.1-2	chr16:32626287-32626324	NONHSAT142022
8	lnc-AC133485.1.1-2	chr16:32619006-32619076	NONHSAT142022
9	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898880	ENSG00000214614.2
10	lnc-AC133485.1.1-3	chr16:32660514-32660649	ENSG00000261569.1
11	lnc-AC133485.1.1-2	chr16:32613844-32613953	NONHSAT142021
12	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142022
13	lnc-TP53TG3-17	chr16:32943089-32943890	NONHSAT142053
14	lnc-RP11-1277H1.1.1-4	chr16:32896515-32896578	ENSG00000214614.2
15	lnc-TP53TG3-11	chr16:32751296-32751487	NONHSAT142041
16	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
17	lnc-AC133485.1.1-3	chr16:32674902-32675277	ENSG00000261569.1
18	lnc-AC133485.1.1-2	chr16:32626903-32626960	NONHSAT142022
19	lnc-RP11-1277H1.1.1-4	chr16:32898658-32898850	ENSG00000214614.2
20	lnc-RP11-1277H1.1.1-4	chr16:32898371-32898495	ENSG00000214614.2
21	lnc-AC133485.1.1-3	chr16:32661076-32661211	ENSG00000261569.1
22	lnc-AC133485.1.1-2	chr16:32626742-32626953	XLOC_011694
23	lnc-AC133485.1.1-2	chr16:32626088-32626324	XLOC_011694
24	lnc-AC133485.1.1-2	chr16:32611620-32611754	NONHSAT142021
25	lnc-TP53TG3-1	chr16:32752331-32752415	ENSG00000260845.1
26	lnc-AC133485.1.1-3	chr16:32661463-32661540	ENSG00000261569.1
27	lnc-RP11-1277H1.1.1-4	chr16:32899139-32900195	ENSG00000214614.2
28	lnc-AC133485.1.1-2	chr16:32618849-32619005	NONHSAT142021
29	lnc-AC133485.1.1-4	chr16:32689961-32690152	ENSG00000260974.1
30	lnc-AC133485.1.1-2	chr16:32619515-32619547	NONHSAT142021
31	lnc-AC133485.1.1-2	chr16:32613896-32614018	NONHSAT142022
32	lnc-AC133485.1.1-2	chr16:32616227-32616285	NONHSAT142021
33	lnc-RP11-1277H1.1.1-4	chr16:32898658-32899949	ENSG00000214614.2
34	lnc-AC133485.1.1-3	chr16:32661637-32661722	ENSG00000261569.1
35	lnc-AC133485.1.1-4	chr16:32686358-32686427	ENSG00000260974.1
36	lnc-TP53TG3-1	chr16:32747230-32748010	ENSG00000260845.1
37	lnc-RP11-1277H1.1.1-4	chr16:32897796-32898008	ENSG00000214614.2
38	lnc-TP53TG3-11	chr16:32750948-32750981	NONHSAT142041
39	lnc-AC133485.1.1-2	chr16:32619515-32619545	NONHSAT142022
40	lnc-RP11-1277H1.1.1-11	chr16:32926395-32926440	NONHSAT142052
41	lnc-AC133485.1.1-2	chr16:32626742-32626807	NONHSAT142022

No data

Variant related genes	Relation type
ENSG00000260864	TF binding region
IGHV2OR16-5	TF binding region
ENSG00000261263	TF binding region
TP53TG3	TF binding region
ENSG00000259966	TF binding region
ENSG00000261108	TF binding region
ENSG00000260610	TF binding region
ENSG00000260158	TF binding region
IGHV3OR16-15	TF binding region
ENSG00000261719	TF binding region
ENSG00000261391	TF binding region
ENSG00000260974	TF binding region
ENSG00000261111	TF binding region
ENSG00000214614	TF binding region
ENSG00000260047	TF binding region
SLC6A10P	TF binding region
HERC2P5	TF binding region
IGHV3OR16-6	TF binding region
ENSG00000261569	TF binding region
ENSG00000262187	TF binding region
ENSG00000260845	TF binding region
ENSG00000259934	TF binding region
ENSG00000260311	TF binding region
ENSG00000260864	CpG island
IGHV2OR16-5	CpG island
ENSG00000261263	CpG island
TP53TG3	CpG island
ENSG00000259966	CpG island
ENSG00000261108	CpG island
ENSG00000260610	CpG island
ENSG00000260158	CpG island
IGHV3OR16-15	CpG island
ENSG00000261719	CpG island
ENSG00000261391	CpG island
ENSG00000260974	CpG island
ENSG00000261111	CpG island
ENSG00000214614	CpG island
ENSG00000260047	CpG island
SLC6A10P	CpG island
HERC2P5	CpG island
IGHV3OR16-6	CpG island
ENSG00000261569	CpG island
ENSG00000262187	CpG island
ENSG00000260845	CpG island
ENSG00000259934	CpG island
ENSG00000260311	CpG island

Extended variants
information (count: 13072 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:13072 , 50 per page) page: 1 2 3 4 5 6 7 ... 262

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28778587	chr16:32511914-32511915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs544228693	chr16:32511921-32511922	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs562437337	chr16:32511922-32511923	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs529700778	chr16:32512001-32512002	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs548929465	chr16:32512006-32512007	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs560766370	chr16:32512031-32512032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs62043435	chr16:32512040-32512041	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs552697691	chr16:32512060-32512061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs570860167	chr16:32512078-32512079	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs538309494	chr16:32512079-32512080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs549780236	chr16:32512086-32512087	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs568148712	chr16:32512099-32512100	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs535433672	chr16:32512103-32512104	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs554490428	chr16:32512106-32512107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs573081149	chr16:32512155-32512156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs28794273	chr16:32512192-32512193	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs558670087	chr16:32512193-32512194	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs576885721	chr16:32512225-32512226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs28877617	chr16:32512249-32512250	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs544359594	chr16:32512276-32512277	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs562550815	chr16:32512291-32512292	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs574534283	chr16:32512292-32512293	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs1911060	chr16:32512302-32512303	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs375902399	chr16:32512339-32512340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs188249231	chr16:32512348-32512349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs192960236	chr16:32512374-32512375	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs527940923	chr16:32512404-32512405	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs552519311	chr16:32512409-32512410	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs564669277	chr16:32512450-32512451	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs369012957	chr16:32512452-32512453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs143858949	chr16:32512470-32512471	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs549890470	chr16:32512475-32512476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs568211148	chr16:32512488-32512489	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs535496484	chr16:32512512-32512513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs547344150	chr16:32512548-32512549	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs182980349	chr16:32512553-32512554	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs1911059	chr16:32512556-32512557	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs534063154	chr16:32512566-32512567	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs558485902	chr16:32512593-32512594	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs548258077	chr16:32512598-32512599	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs538037135	chr16:32512610-32512611	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs111765668	chr16:32512620-32512621	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs556336932	chr16:32512621-32512622	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs1911058	chr16:32512634-32512635	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs1911057	chr16:32512669-32512670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs574546612	chr16:32512681-32512682	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs578019315	chr16:32512709-32512710	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs546028534	chr16:32512712-32512713	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs1847947	chr16:32512739-32512740	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs553700820	chr16:32512746-32512747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

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
Bladder cancer	21909424	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
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	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
Recurrent pregnancy loss	19789632	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Osteosarcoma	21215367	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	21509527	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:32511200-32562600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr16:32513800-32526800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr16:32513800-32564000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr16:32513800-32572000	ZNF genes & repeats	Liver	Liver
5	chr16:32514600-32561200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr16:32515200-32518000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr16:32515200-32562800	ZNF genes & repeats	Adipose Nuclei	Adipose
8	chr16:32515400-32516000	ZNF genes & repeats	Psoas Muscle	Psoas
9	chr16:32515400-32518400	ZNF genes & repeats	Brain Substantia Nigra	brain
10	chr16:32515600-32517800	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 2	blood
11	chr16:32515600-32521600	ZNF genes & repeats	Brain Anterior Caudate	brain
12	chr16:32515800-32518400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr16:32516200-32521600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr16:32516200-32524200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
15	chr16:32516800-32517400	Active TSS	Aorta	Aorta
16	chr16:32517000-32517600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
17	chr16:32517400-32519000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
18	chr16:32518000-32518600	ZNF genes & repeats	Fetal Brain Male	brain
19	chr16:32518200-32519000	Active TSS	Right Atrium	heart
20	chr16:32520200-32520400	ZNF genes & repeats	Brain Substantia Nigra	brain
21	chr16:32520400-32523400	ZNF genes & repeats	Psoas Muscle	Psoas
22	chr16:32520600-32523600	ZNF genes & repeats	Fetal Brain Male	brain
23	chr16:32521000-32524200	ZNF genes & repeats	Brain Substantia Nigra	brain
24	chr16:32521200-32521600	ZNF genes & repeats	Brain Hippocampus Middle	brain
25	chr16:32521800-32522000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr16:32521800-32522400	Active TSS	Right Atrium	heart
27	chr16:32523200-32523600	Bivalent/Poised TSS	Right Atrium	heart
28	chr16:32523600-32524200	Active TSS	Right Atrium	heart
29	chr16:32524200-32527800	Weak transcription	Right Atrium	heart
30	chr16:32525600-32527800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:32526000-32526400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
32	chr16:32526200-32526600	Active TSS	Aorta	Aorta
33	chr16:32526400-32526600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
34	chr16:32526600-32528000	Weak transcription	Aorta	Aorta
35	chr16:32526800-32530000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr16:32527800-32529000	Active TSS	Right Atrium	heart
37	chr16:32528000-32531600	Active TSS	Aorta	Aorta
38	chr16:32528200-32528400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
39	chr16:32529200-32530400	ZNF genes & repeats	Fetal Brain Male	brain
40	chr16:32529200-32530800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
41	chr16:32529200-32535200	ZNF genes & repeats	Psoas Muscle	Psoas
42	chr16:32529400-32530600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr16:32529400-32570400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
44	chr16:32529800-32536000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
45	chr16:32529800-32536800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
46	chr16:32530400-32531400	Weak transcription	Fetal Brain Male	brain
47	chr16:32531000-32531200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chr16:32531400-32534000	ZNF genes & repeats	Fetal Brain Male	brain
49	chr16:32531600-32535600	Weak transcription	Aorta	Aorta
50	chr16:32531600-32538800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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