Variant report

Variant	nsv1057300
Chromosome Location	chr16:31862900-31959992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1984)
CpG islands
(count:979)
Chromatin interactive
region (count:89)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1984 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:31884911-31885138	K562	blood:	n/a	n/a
2	ARID3A	chr16:31880586-31880614	K562	blood:	n/a	n/a
3	ARID3A	chr16:31886881-31887081	K562	blood:	n/a	n/a
4	ARID3A	chr16:31879953-31880241	K562	blood:	n/a	n/a
5	ARID3A	chr16:31884916-31885514	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:31879879-31880246	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:31885742-31886117	K562	blood:	n/a	n/a
8	ARID3A	chr16:31891824-31892260	K562	blood:	n/a	n/a
9	ATF1	chr16:31888829-31889078	K562	blood:	n/a	n/a
10	ATF1	chr16:31891787-31892308	K562	blood:	n/a	n/a
11	ATF1	chr16:31921392-31921528	K562	blood:	n/a	n/a
12	ATF2	chr16:31888206-31889246	GM12878	blood:	n/a	n/a
13	ATF2	chr16:31885649-31886302	GM12878	blood:	n/a	n/a
14	ATF2	chr16:31888350-31889261	GM12878	blood:	n/a	n/a
15	ATF2	chr16:31885760-31886384	GM12878	blood:	n/a	n/a
16	ATF2	chr16:31880725-31881266	GM12878	blood:	n/a	n/a
17	ATF3	chr16:31891747-31892237	K562	blood:	n/a	n/a
18	BATF	chr16:31880850-31881259	GM12878	blood:	n/a	chr16:31880947-31880956
19	BATF	chr16:31885852-31886180	GM12878	blood:	n/a	n/a
20	BATF	chr16:31882172-31882412	GM12878	blood:	n/a	n/a
21	BATF	chr16:31891801-31892172	GM12878	blood:	n/a	chr16:31892009-31892020
22	BATF	chr16:31888608-31889175	GM12878	blood:	n/a	n/a
23	BATF	chr16:31880832-31881160	GM12878	blood:	n/a	chr16:31880947-31880956
24	BATF	chr16:31885684-31886193	GM12878	blood:	n/a	n/a
25	BATF	chr16:31891771-31892321	GM12878	blood:	n/a	chr16:31892009-31892020
26	BATF	chr16:31888714-31889189	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:31884828-31885187	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:31885621-31886215	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:31888635-31889205	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:31885672-31886229	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:31888801-31889128	GM12878	blood:	n/a	n/a
32	BCL3	chr16:31888623-31889192	GM12878	blood:	n/a	n/a
33	BCL3	chr16:31885753-31886218	GM12878	blood:	n/a	n/a
34	BCL3	chr16:31930017-31930282	GM12878	blood:	n/a	n/a
35	BCLAF1	chr16:31931788-31931977	GM12878	blood:	n/a	n/a
36	BCLAF1	chr16:31870747-31871023	GM12878	blood:	n/a	n/a
37	BCLAF1	chr16:31888523-31889248	GM12878	blood:	n/a	n/a
38	BCLAF1	chr16:31885015-31886418	GM12878	blood:	n/a	chr16:31885440-31885449 chr16:31885463-31885476
39	BCLAF1	chr16:31884894-31885431	GM12878	blood:	n/a	n/a
40	BCLAF1	chr16:31885670-31886252	GM12878	blood:	n/a	n/a
41	BCLAF1	chr16:31930908-31931183	GM12878	blood:	n/a	n/a
42	BCLAF1	chr16:31888636-31889431	GM12878	blood:	n/a	n/a
43	BHLHE40	chr16:31880064-31880226	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:31880852-31881118	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:31886911-31887058	K562	blood:	n/a	n/a
46	BHLHE40	chr16:31880767-31881250	GM12878	blood:	n/a	n/a
47	BHLHE40	chr16:31885052-31885333	K562	blood:	n/a	n/a
48	BHLHE40	chr16:31888194-31889248	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:31880824-31881177	K562	blood:	n/a	n/a
50	BHLHE40	chr16:31885929-31886113	K562	blood:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:31885481-31885531	SAEC	small airway:	n/a
2	chr16:31884740-31884790	ECC-1	luminal epithelium:	n/a
3	chr16:31885406-31885456	HRE	kidney:	n/a
4	chr16:31885481-31885531	SAEC	small airway:	n/a
5	chr16:31884740-31884790	ECC-1	luminal epithelium:	n/a
6	chr16:31885406-31885456	HRE	kidney:	n/a
7	chr16:31886923-31886973	A549	lung:	n/a
8	chr16:31885058-31885108	HCPEpiC	choroid plexus:	n/a
9	chr16:31884740-31884790	NHBE	bronchial:	n/a
10	chr16:31886923-31886973	MCF10A-Er-Src	breast:	n/a
11	chr16:31885014-31885064	ovcar-3	ovarian:	n/a
12	chr16:31886070-31886120	A549	lung:	n/a
13	chr16:31885014-31885064	AG10803	skin:	n/a
14	chr16:31886923-31886973	HCT-116	colon:	n/a
15	chr16:31885058-31885108	Jurkat	blood:	n/a
16	chr16:31885014-31885064	HL-60	blood:	n/a
17	chr16:31891978-31892028	HCF	heart:	n/a
18	chr16:31884589-31884639	CMK	blood:	n/a
19	chr16:31885481-31885531	PFSK-1	brain:	n/a
20	chr16:31884699-31884749	CMK	blood:	n/a
21	chr16:31885058-31885108	GM12878	blood:	n/a
22	chr16:31886070-31886120	GM06990	blood:	n/a
23	chr16:31885058-31885108	HEK293	kidney:	embryo
24	chr16:31885058-31885108	NT2-D1	testis:	n/a
25	chr16:31884740-31884790	Jurkat	blood:	n/a
26	chr16:31885091-31885141	PANC-1	pancreas:	n/a
27	chr16:31888794-31888844	T-47D	breast:	n/a
28	chr16:31888794-31888844	K562	blood:	n/a
29	chr16:31885014-31885064	HCF	heart:	n/a
30	chr16:31885481-31885531	GM12891	blood:	n/a
31	chr16:31884761-31884811	H1-hESC	embryonic stem cell:	embryo
32	chr16:31885091-31885141	HEEpiC	esophagus:	n/a
33	chr16:31885481-31885531	HNPCEpiC	eye:	n/a
34	chr16:31885406-31885456	NT2-D1	testis:	n/a
35	chr16:31884589-31884639	HepG2	liver:	n/a
36	chr16:31885014-31885064	PFSK-1	brain:	n/a
37	chr16:31885194-31885244	SAEC	small airway:	n/a
38	chr16:31884740-31884790	HEEpiC	esophagus:	n/a
39	chr16:31884699-31884749	A549	lung:	n/a
40	chr16:31885194-31885244	HEEpiC	esophagus:	n/a
41	chr16:31885481-31885531	HRE	kidney:	n/a
42	chr16:31885091-31885141	HepG2	liver:	n/a
43	chr16:31885091-31885141	NHDF-neo	bronchial:	n/a
44	chr16:31885118-31885168	BE2_C	brain:	n/a
45	chr16:31885406-31885456	AG04449	skin:	fetal
46	chr16:31885058-31885108	NHDF-neo	bronchial:	n/a
47	chr16:31885014-31885064	ECC-1	luminal epithelium:	n/a
48	chr16:31885194-31885244	K562	blood:	n/a
49	chr16:31888794-31888844	NT2-D1	testis:	n/a
50	chr16:31884699-31884749	HMEC	breast:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:31481310..31483531-chr16:31880897..31883874,2	MCF-7	breast:
2	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:
3	chr16:31878665..31883270-chr16:31884134..31887533,7	K562	blood:
4	chr16:31730337..31731972-chr16:31892630..31894181,2	MCF-7	breast:
5	chr16:31722786..31725985-chr16:31883201..31886521,4	MCF-7	breast:
6	chr16:31717471..31719103-chr16:31884292..31886617,2	MCF-7	breast:
7	chr16:31873078..31876399-chr16:31883790..31886310,4	MCF-7	breast:
8	chr16:31888939..31890909-chr16:31894661..31896622,2	MCF-7	breast:
9	chr16:31884910..31885705-chr6:35656392..35657131,2	Hela-S3	cervix:
10	chr16:31724410..31726103-chr16:31891793..31894409,2	MCF-7	breast:
11	chr16:31886296..31887801-chr16:31893665..31896214,2	MCF-7	breast:
12	chr16:31711684..31713887-chr16:31887236..31889001,2	MCF-7	breast:
13	chr16:31893208..31894819-chr16:31924723..31927123,2	K562	blood:
14	chr16:31926933..31929361-chr16:31930312..31932712,3	K562	blood:
15	chr16:31870465..31871190-chr21:47082634..47083160,4	MCF-7	breast:
16	chr16:31469205..31472299-chr16:31879583..31882157,3	MCF-7	breast:
17	chr16:31884754..31886636-chr16:31917954..31920190,2	MCF-7	breast:
18	chr16:31884716..31885620-chr19:3572981..3573761,2	Hela-S3	cervix:
19	chr16:31897518..31899829-chr16:31901532..31903567,2	K562	blood:
20	chr16:31880244..31883180-chr16:31883770..31886607,4	K562	blood:
21	chr16:31722890..31726571-chr16:31866772..31870403,3	MCF-7	breast:
22	chr16:31873078..31876399-chr16:31883790..31886310,4	MCF-7	breast:
23	chr16:31893208..31894819-chr16:31924723..31927123,2	K562	blood:
24	chr16:31870846..31873491-chr16:31890033..31893376,3	K562	blood:
25	chr16:31930170..31932707-chr16:31934024..31936447,2	K562	blood:
26	chr16:31724092..31726599-chr16:31882160..31884520,2	K562	blood:
27	chr16:31711865..31714581-chr16:31881690..31883987,3	MCF-7	breast:
28	chr16:31929972..31932646-chr16:31933691..31936236,4	MCF-7	breast:
29	chr16:31931465..31935999-chr16:31936605..31940603,7	K562	blood:
30	chr16:31888939..31890909-chr16:31894661..31896622,2	MCF-7	breast:
31	chr16:31518488..31520792-chr16:31884835..31887460,2	MCF-7	breast:
32	chr16:31517832..31520648-chr16:31892374..31894301,2	K562	blood:
33	chr16:30967440..30970238-chr16:31885707..31887923,2	MCF-7	breast:
34	chr16:31869060..31871109-chr16:31885651..31887862,2	MCF-7	breast:
35	chr16:31900905..31903577-chr16:31904504..31907027,3	K562	blood:
36	chr16:31723093..31725658-chr16:31880416..31882671,2	MCF-7	breast:
37	chr16:31926933..31929361-chr16:31930312..31932712,3	K562	blood:
38	chr16:31870536..31871564-chr16:31879727..31880499,3	MCF-7	breast:
39	chr16:31461549..31464190-chr16:31877877..31881538,3	MCF-7	breast:
40	chr16:31870536..31871564-chr16:31879727..31880499,3	MCF-7	breast:
41	chr16:31884665..31885467-chr2:88315813..88316421,2	Hela-S3	cervix:
42	chr16:31870203..31874358-chr16:31883750..31887952,5	K562	blood:
43	chr16:31876300..31879894-chr16:31880296..31883851,5	K562	blood:
44	chr16:31468715..31471317-chr16:31890566..31892808,2	MCF-7	breast:
45	chr16:31880244..31883180-chr16:31883770..31886607,4	K562	blood:
46	chr16:31885246..31885797-chr4:6695588..6696329,2	Hela-S3	cervix:
47	chr16:31932903..31935520-chr16:31946813..31948460,2	K562	blood:
48	chr16:31878665..31883270-chr16:31884134..31887533,7	K562	blood:
49	chr16:31932491..31936311-chr16:31936605..31941493,6	K562	blood:
50	chr1:110090809..110091593-chr16:31885003..31885525,2	Hela-S3	cervix:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF720-2	chr16:31895819-31895945	NR_049749
2	lnc-ZNF267-2	chr16:31874954-31876197	NONHSAT141973
3	lnc-C16orf58-11	chr16:31882208-31882445	NONHSAT141974
4	lnc-ZNF720-2	chr16:31901528-31901571	NR_049749
5	lnc-ZNF720-2	chr16:31896482-31896577	NR_049749
6	lnc-ZNF720-2	chr16:31925797-31928629	NR_049749
7	lnc-ZNF720-2	chr16:31885079-31885290	NR_049749
8	lnc-ZNF720-2	chr16:31923175-31928172	ENSG00000262657.1

No data

Variant related genes	Relation type
RBM22P13	TF binding region
ENSG00000261289	TF binding region
ZNF267	TF binding region
ENSG00000259950	TF binding region
ENSG00000259874	TF binding region
RBM22P13	CpG island
ENSG00000261289	CpG island
ZNF267	CpG island
ENSG00000259950	CpG island
ENSG00000259874	CpG island
ENSG00000222724	chromatin interactions
ENSG00000099381	chromatin interactions
ENSG00000131797	chromatin interactions
ENSG00000259874	chromatin interactions
ENSG00000163993	chromatin interactions
ENSG00000259950	chromatin interactions
ENSG00000260625	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000260568	chromatin interactions
ENSG00000161091	chromatin interactions
ENSG00000140688	chromatin interactions
ENSG00000140682	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000065135	chromatin interactions
ENSG00000261284	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000064961	chromatin interactions
ENSG00000197302	chromatin interactions
ENSG00000261731	chromatin interactions
ENSG00000185947	chromatin interactions
ENSG00000175130	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000089280	chromatin interactions

Extended variants
information (count: 2641 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:2641 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564610516	chr16:31862909-31862910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575875038	chr16:31862915-31862916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532056744	chr16:31862934-31862935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376363360	chr16:31862967-31862968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10871460	chr16:31862982-31862983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371776901	chr16:31862989-31862990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567243447	chr16:31863014-31863015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558453437	chr16:31863071-31863072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576711912	chr16:31863123-31863124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540893366	chr16:31863130-31863131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534464796	chr16:31863131-31863132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546676104	chr16:31863229-31863230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571323663	chr16:31863239-31863240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539250190	chr16:31863246-31863247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557560964	chr16:31863289-31863290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569599814	chr16:31863341-31863342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569343811	chr16:31863360-31863361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536932052	chr16:31863396-31863397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75730775	chr16:31863407-31863408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188093460	chr16:31863422-31863423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574333432	chr16:31863519-31863520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181455960	chr16:31863533-31863534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573189174	chr16:31863549-31863550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373264541	chr16:31863550-31863551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138102381	chr16:31863570-31863571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76315127	chr16:31863586-31863587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80094509	chr16:31863694-31863695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576894936	chr16:31863716-31863717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544829188	chr16:31863721-31863722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563123646	chr16:31863774-31863775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74568892	chr16:31863840-31863841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs61376545	chr16:31863872-31863873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567448223	chr16:31863919-31863920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184639870	chr16:31863942-31863943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560978591	chr16:31863956-31863957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528096709	chr16:31863966-31863967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546244190	chr16:31864011-31864012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571387167	chr16:31864045-31864046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532223929	chr16:31864138-31864139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551230556	chr16:31864146-31864147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375802495	chr16:31864154-31864155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35357661	chr16:31864173-31864174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536590963	chr16:31864205-31864206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555248696	chr16:31864312-31864313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143676156	chr16:31864323-31864324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117940787	chr16:31864339-31864340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576955845	chr16:31864383-31864384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545389816	chr16:31864389-31864390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563392254	chr16:31864474-31864475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78032453	chr16:31864513-31864514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	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
Breast cancer	22522925	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:2588 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31862000-31866400	Weak transcription	Gastric	stomach
2	chr16:31864200-31865000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr16:31866000-31866800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:31866200-31866400	Enhancers	Spleen	Spleen
5	chr16:31866400-31866600	Genic enhancers	Gastric	stomach
6	chr16:31866400-31867000	Weak transcription	Spleen	Spleen
7	chr16:31866400-31870800	Weak transcription	Esophagus	oesophagus
8	chr16:31866600-31867000	Weak transcription	Gastric	stomach
9	chr16:31870800-31871000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr16:31870800-31871200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr16:31870800-31871200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr16:31870800-31871400	Enhancers	Primary T cells fromperipheralblood	blood
13	chr16:31870800-31871400	Enhancers	Esophagus	oesophagus
14	chr16:31870800-31873000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr16:31871000-31871200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr16:31871000-31871200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr16:31871000-31871200	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr16:31871000-31871200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr16:31871000-31871200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr16:31871000-31871200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr16:31871000-31871200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr16:31871000-31871200	Enhancers	K562	blood
23	chr16:31871000-31871400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr16:31871000-31871400	Enhancers	Lung	lung
25	chr16:31871200-31872200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr16:31871200-31872400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr16:31871200-31872400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr16:31871200-31872400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr16:31871200-31872600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr16:31871200-31872600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr16:31871400-31872400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr16:31871400-31872400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr16:31871400-31872600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr16:31871400-31872600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr16:31871400-31872800	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr16:31872200-31874000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr16:31872400-31873000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chr16:31872400-31873600	Enhancers	Primary T cells from cord blood	blood
39	chr16:31872400-31873800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr16:31872400-31874000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr16:31872400-31874000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr16:31872400-31874000	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr16:31872400-31874200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr16:31872600-31873400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr16:31872600-31873800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr16:31872600-31873800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr16:31872600-31874000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr16:31872600-31874000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr16:31872800-31873200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr16:31872800-31874000	Enhancers	Primary T cells fromperipheralblood	blood

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