Variant report

Variant	nsv905722
Chromosome Location	chr16:30168507-30199571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1073)
CpG islands
(count:1039)
Chromatin interactive
region (count:39)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:30182291-30182531	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:30194725-30194739	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:30182745-30182862	HepG2	liver:	n/a	n/a
4	ATF1	chr16:30198455-30198718	K562	blood:	n/a	n/a
5	ATF2	chr16:30198423-30199069	GM12878	blood:	n/a	n/a
6	ATF2	chr16:30198083-30199160	GM12878	blood:	n/a	n/a
7	ATF2	chr16:30196503-30197466	GM12878	blood:	n/a	n/a
8	ATF2	chr16:30177440-30178013	GM12878	blood:	n/a	n/a
9	ATF2	chr16:30195156-30197910	GM12878	blood:	n/a	n/a
10	ATF2	chr16:30193876-30194374	GM12878	blood:	n/a	n/a
11	ATF2	chr16:30177517-30177990	GM12878	blood:	n/a	n/a
12	ATF2	chr16:30195759-30196132	GM12878	blood:	n/a	n/a
13	ATF2	chr16:30194769-30195107	GM12878	blood:	n/a	n/a
14	BACH1	chr16:30198613-30198914	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr16:30198003-30198007	K562	blood:	n/a	n/a
16	BACH1	chr16:30198528-30198904	K562	blood:	n/a	n/a
17	BATF	chr16:30177505-30177828	GM12878	blood:	n/a	n/a
18	BCL11A	chr16:30177543-30177899	GM12878	blood:	n/a	n/a
19	BCL11A	chr16:30197818-30198265	GM12878	blood:	n/a	n/a
20	BCL11A	chr16:30177528-30177966	GM12878	blood:	n/a	n/a
21	BCL3	chr16:30195266-30195671	GM12878	blood:	n/a	chr16:30195642-30195655
22	BCL3	chr16:30198207-30199080	A549	lung:	n/a	n/a
23	BCLAF1	chr16:30177489-30178005	GM12878	blood:	n/a	n/a
24	BCLAF1	chr16:30195097-30199113	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180
25	BCLAF1	chr16:30177501-30177945	GM12878	blood:	n/a	n/a
26	BCLAF1	chr16:30194548-30199158	GM12878	blood:	n/a	chr16:30195642-30195655 chr16:30197167-30197180 chr16:30194870-30194879 chr16:30194825-30194838
27	BCLAF1	chr16:30194550-30195085	GM12878	blood:	n/a	chr16:30194870-30194879 chr16:30194825-30194838
28	BHLHE40	chr16:30182399-30182672	HepG2	liver:	n/a	n/a
29	BHLHE40	chr16:30193847-30194404	GM12878	blood:	n/a	n/a
30	BHLHE40	chr16:30194613-30195046	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:30198454-30198956	K562	blood:	n/a	n/a
32	BHLHE40	chr16:30177509-30177916	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:30182321-30182749	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:30189943-30190272	HepG2	liver:	n/a	n/a
35	BHLHE40	chr16:30198633-30198880	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:30194857-30194946	K562	blood:	n/a	n/a
37	BHLHE40	chr16:30197995-30198979	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:30196426-30197505	GM12878	blood:	n/a	chr16:30197435-30197451
39	BHLHE40	chr16:30182386-30182725	HepG2	liver:	n/a	n/a
40	BHLHE40	chr16:30195302-30196027	GM12878	blood:	n/a	n/a
41	BHLHE40	chr16:30177645-30177846	K562	blood:	n/a	n/a
42	BRCA1	chr16:30198502-30198547	HepG2	liver:	n/a	n/a
43	BRCA1	chr16:30195351-30195364	GM12878	blood:	n/a	n/a
44	CBX3	chr16:30198527-30198990	K562	blood:	n/a	n/a
45	CBX3	chr16:30198506-30198929	K562	blood:	n/a	n/a
46	CCNT2	chr16:30198456-30198847	K562	blood:	n/a	n/a
47	CCNT2	chr16:30194744-30195127	K562	blood:	n/a	chr16:30194810-30194819
48	CEBPB	chr16:30177836-30178086	HepG2	liver:	n/a	chr16:30177998-30178009
49	CEBPB	chr16:30177937-30178024	H1-hESC	embryonic stem cell:	n/a	chr16:30177998-30178009
50	CEBPB	chr16:30188497-30188593	IMR90	lung:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30196023-30196073	BE2_C	brain:	n/a
2	chr16:30198517-30198567	A549	lung:	n/a
3	chr16:30196023-30196073	BE2_C	brain:	n/a
4	chr16:30198517-30198567	A549	lung:	n/a
5	chr16:30194717-30194767	GM12891	blood:	n/a
6	chr16:30195067-30195117	GM12892	blood:	n/a
7	chr16:30194888-30194938	ECC-1	luminal epithelium:	n/a
8	chr16:30194815-30194865	NHBE	bronchial:	n/a
9	chr16:30195318-30195368	HepG2	liver:	n/a
10	chr16:30197211-30197261	GM12891	blood:	n/a
11	chr16:30194888-30194938	T-47D	breast:	n/a
12	chr16:30194416-30194466	NHBE	bronchial:	n/a
13	chr16:30194776-30194826	GM12892	blood:	n/a
14	chr16:30194484-30194534	AG04450	lung:	fetal
15	chr16:30198370-30198420	SAEC	small airway:	n/a
16	chr16:30194776-30194826	HAEpiC	amniotic membrane:	n/a
17	chr16:30194888-30194938	HCT-116	colon:	n/a
18	chr16:30195318-30195368	SAEC	small airway:	n/a
19	chr16:30195318-30195368	PANC-1	pancreas:	n/a
20	chr16:30194484-30194534	SK-N-SH_RA	brain:	n/a
21	chr16:30198517-30198567	K562	blood:	n/a
22	chr16:30198517-30198567	HNPCEpiC	eye:	n/a
23	chr16:30198509-30198559	CMK	blood:	n/a
24	chr16:30198517-30198567	AG09319	gingival:	n/a
25	chr16:30194416-30194466	AoSMC	blood vessel:	n/a
26	chr16:30194815-30194865	RPTEC	kidney:	n/a
27	chr16:30192587-30192637	U87	brain:	n/a
28	chr16:30192587-30192637	LNCaP	prostate:	n/a
29	chr16:30198509-30198559	Jurkat	blood:	n/a
30	chr16:30192587-30192637	HUVEC	blood vessel:	n/a
31	chr16:30194416-30194466	PFSK-1	brain:	n/a
32	chr16:30194815-30194865	NHDF-neo	bronchial:	n/a
33	chr16:30195067-30195117	ovcar-3	ovarian:	n/a
34	chr16:30195318-30195368	LNCaP	prostate:	n/a
35	chr16:30195067-30195117	SK-N-SH_RA	brain:	n/a
36	chr16:30194888-30194938	MCF10A-Er-Src	breast:	n/a
37	chr16:30196023-30196073	ECC-1	luminal epithelium:	n/a
38	chr16:30194903-30194953	HepG2	liver:	n/a
39	chr16:30196023-30196073	SK-N-SH	brain:	n/a
40	chr16:30198505-30198555	HUVEC	blood vessel:	n/a
41	chr16:30198370-30198420	K562	blood:	n/a
42	chr16:30197211-30197261	Hepatocyte	liver:	n/a
43	chr16:30196023-30196073	Caco-2	colon:	n/a
44	chr16:30198370-30198420	HEEpiC	esophagus:	n/a
45	chr16:30198505-30198555	BJ	skin:	n/a
46	chr16:30194886-30194936	GM12892	blood:	n/a
47	chr16:30198505-30198555	NT2-D1	testis:	n/a
48	chr16:30194776-30194826	CMK	blood:	n/a
49	chr16:30198517-30198567	HepG2	liver:	n/a
50	chr16:30198370-30198420	T-47D	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30080041..30082622-chr16:30171672..30174574,2	MCF-7	breast:
2	chr16:30185936..30188220-chr16:30197826..30199753,2	MCF-7	breast:
3	chr16:30121828..30124583-chr16:30196625..30198544,2	MCF-7	breast:
4	chr1:12399202..12400121-chr16:30198326..30198844,2	K562	blood:
5	chr16:30087286..30089339-chr16:30194884..30196555,2	MCF-7	breast:
6	chr16:29815002..29817643-chr16:30193444..30196373,3	MCF-7	breast:
7	chr16:30127849..30129805-chr16:30193188..30195789,2	MCF-7	breast:
8	chr16:30134390..30135940-chr16:30193438..30196422,2	MCF-7	breast:
9	chr16:30099194..30104975-chr16:30193189..30199409,9	MCF-7	breast:
10	chr16:30173126..30174657-chr16:30193076..30195048,2	MCF-7	breast:
11	chr16:30193615..30195273-chr16:30388746..30390987,2	K562	blood:
12	chr16:30102992..30108322-chr16:30194679..30199860,7	K562	blood:
13	chr11:60691741..60692731-chr16:30194046..30194929,2	HCT-116	colon:
14	chr16:30196751..30201052-chr16:30379113..30382636,3	MCF-7	breast:
15	chr16:30122202..30125558-chr16:30192872..30196155,3	MCF-7	breast:
16	chr16:30105196..30108316-chr16:30196676..30200078,3	MCF-7	breast:
17	chr16:30164181..30165686-chr16:30171890..30174652,2	K562	blood:
18	chr16:30123508..30126853-chr16:30193449..30196569,3	MCF-7	breast:
19	chr16:30073832..30076686-chr16:30197424..30199809,3	MCF-7	breast:
20	chr16:30077452..30079715-chr16:30197226..30200095,2	MCF-7	breast:
21	chr16:30122556..30125865-chr16:30196040..30198997,3	K562	blood:
22	chr16:30132897..30136323-chr16:30193309..30196336,5	MCF-7	breast:
23	chr16:30194484..30196796-chr16:30455955..30457567,2	K562	blood:
24	chr16:30079070..30081233-chr16:30194915..30196655,2	MCF-7	breast:
25	chr16:30194030..30196796-chr16:30455949..30457567,2	K562	blood:
26	chr16:30197384..30200120-chr16:30417665..30420072,2	K562	blood:
27	chr16:30132759..30134974-chr16:30196981..30199413,2	MCF-7	breast:
28	chr16:30076811..30079031-chr16:30197360..30200413,3	K562	blood:
29	chr16:30075111..30080393-chr16:30194482..30199026,7	MCF-7	breast:
30	chr16:30122445..30125435-chr16:30197147..30198801,2	K562	blood:
31	chr16:30124210..30124751-chr16:30198102..30199056,2	MCF-7	breast:
32	chr16:30102283..30103884-chr16:30194608..30196819,2	MCF-7	breast:
33	chr16:30086324..30089424-chr16:30196059..30198552,4	MCF-7	breast:
34	chr16:30102992..30106412-chr16:30196223..30199425,3	K562	blood:
35	chr16:30075696..30078954-chr16:30197360..30200413,3	K562	blood:
36	chr16:30194759..30196474-chr16:30708321..30710929,2	K562	blood:
37	chr16:30198315..30198870-chr16:30420884..30421401,2	MCF-7	breast:
38	chr16:30197720..30200168-chr16:30772376..30774510,2	MCF-7	breast:
39	chr16:30197379..30199709-chr16:30708853..30710594,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BOLA2B-1	chr16:30196153-30196278	ENSG00000261416.1
2	lnc-BOLA2B-1	chr16:30195825-30195860	ENSG00000261416.1
3	lnc-BOLA2B-1	chr16:30195383-30195740	ENSG00000261416.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CORO1A	hsa-miR-24-3p	chr16:30198442-30198465

Variant related genes	Relation type
CORO1A	TF binding region
ENSG00000261416	TF binding region
CORO1A	CpG island
ENSG00000261416	CpG island
ENSG00000102879	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000102882	chromatin interactions
ENSG00000006118	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000102886	chromatin interactions
ENSG00000196118	chromatin interactions
ENSG00000090238	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000103549	chromatin interactions
ENSG00000149923	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000103495	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000179965	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000169221	chromatin interactions
ENSG00000250616	chromatin interactions

Extended variants
information (count: 1025 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:1025 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542691383	chr16:30168565-30168566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560794181	chr16:30168573-30168574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571102677	chr16:30168607-30168608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528204846	chr16:30168626-30168627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs28877870	chr16:30168682-30168683	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564875391	chr16:30168709-30168710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553050334	chr16:30168731-30168732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532442683	chr16:30168745-30168746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142085112	chr16:30168750-30168751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550933337	chr16:30168777-30168778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186075742	chr16:30168883-30168884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117866142	chr16:30168946-30168947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548389843	chr16:30168965-30168966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574792033	chr16:30168979-30168980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146472842	chr16:30168980-30168981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566821003	chr16:30169001-30169002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368549250	chr16:30169073-30169074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142466675	chr16:30169116-30169117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372221542	chr16:30169123-30169124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548981523	chr16:30169126-30169127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs570559639	chr16:30169136-30169137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538140411	chr16:30169141-30169142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556473071	chr16:30169167-30169168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535527884	chr16:30169210-30169211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12931219	chr16:30169217-30169218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143277140	chr16:30169229-30169230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190193227	chr16:30169256-30169257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148317124	chr16:30169267-30169268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540373985	chr16:30169278-30169279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575823468	chr16:30169338-30169339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12927190	chr16:30169393-30169394	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs12926100	chr16:30169472-30169473	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs372820893	chr16:30169480-30169481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555141934	chr16:30169506-30169507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562615523	chr16:30169624-30169625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576651080	chr16:30169628-30169629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530019575	chr16:30169638-30169639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71389447	chr16:30169701-30169702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7195182	chr16:30169761-30169762	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs182557480	chr16:30169874-30169875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35679339	chr16:30169878-30169879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376051557	chr16:30169904-30169905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34582355	chr16:30169924-30169925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs147380847	chr16:30169925-30169926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62055378	chr16:30169927-30169928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62055379	chr16:30169930-30169931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35411666	chr16:30169950-30169951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs527782628	chr16:30170022-30170023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139396157	chr16:30170024-30170025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72791244	chr16:30170027-30170028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

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
low-grade B-cell lymphoma tumor	18367492	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
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Epilepsy	20502679	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
autism	21731881	CNVD
Developmental delay	22909776	CNVD
speech impairment	22909776	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:897 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30168200-30168800	Enhancers	HepG2	liver
2	chr16:30168800-30171000	Weak transcription	HepG2	liver
3	chr16:30170000-30170400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr16:30170000-30170400	Enhancers	Placenta	Placenta
5	chr16:30171000-30171400	Enhancers	HepG2	liver
6	chr16:30171400-30182200	Weak transcription	HepG2	liver
7	chr16:30171600-30172000	Enhancers	Fetal Brain Male	brain
8	chr16:30172000-30174800	Weak transcription	Fetal Brain Male	brain
9	chr16:30172400-30172600	Enhancers	Primary T cells fromperipheralblood	blood
10	chr16:30172600-30173600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr16:30173200-30173400	Active TSS	Gastric	stomach
12	chr16:30173600-30179000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr16:30174200-30179000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:30174600-30175000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr16:30174600-30175200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr16:30174800-30175000	Enhancers	Primary T cells from cord blood	blood
17	chr16:30174800-30175000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr16:30174800-30175000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr16:30174800-30175000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
20	chr16:30174800-30175200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr16:30174800-30175200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr16:30174800-30175200	Enhancers	Fetal Brain Male	brain
23	chr16:30174800-30177600	Enhancers	GM12878-XiMat	blood
24	chr16:30175000-30175200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr16:30175000-30175200	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr16:30175000-30175200	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr16:30175000-30177600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr16:30175200-30176600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr16:30175200-30176600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr16:30175200-30177000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr16:30175400-30176600	Weak transcription	Primary T cells from cord blood	blood
32	chr16:30175400-30176600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr16:30175600-30176800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr16:30175800-30177400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr16:30175800-30179800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr16:30176200-30179000	Enhancers	Primary B cells from peripheral blood	blood
37	chr16:30176400-30177400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr16:30176400-30179000	Enhancers	Primary B cells from cord blood	blood
39	chr16:30176600-30178600	Enhancers	Primary T cells from cord blood	blood
40	chr16:30176600-30178600	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr16:30176600-30178600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr16:30176600-30178600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr16:30176600-30178800	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr16:30176600-30179000	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr16:30176600-30179000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr16:30176800-30177200	Enhancers	Spleen	Spleen
47	chr16:30176800-30178800	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr16:30177000-30177400	Enhancers	Primary hematopoietic stem cells	blood
49	chr16:30177000-30178200	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr16:30177000-30178400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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