Variant report

Variant	esv2761916
Chromosome Location	chr16:77277005-77555833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1812)
CpG islands
(count:1832)
Chromatin interactive
region (count:49)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1812 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:77440675-77440938	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:77392464-77393533	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:77338735-77339097	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:77440704-77440882	K562	blood:	n/a	n/a
5	ATF1	chr16:77310381-77310453	K562	blood:	n/a	n/a
6	ATF1	chr16:77306707-77306708	K562	blood:	n/a	n/a
7	ATF2	chr16:77361518-77362088	GM12878	blood:	n/a	n/a
8	ATF2	chr16:77442492-77442850	GM12878	blood:	n/a	n/a
9	ATF3	chr16:77332259-77333052	A549	lung:	n/a	n/a
10	ATF3	chr16:77392876-77393442	A549	lung:	n/a	n/a
11	ATF3	chr16:77392831-77393401	A549	lung:	n/a	n/a
12	ATF3	chr16:77387390-77387946	A549	lung:	n/a	n/a
13	ATF3	chr16:77323119-77323849	A549	lung:	n/a	n/a
14	ATF3	chr16:77387406-77387935	A549	lung:	n/a	n/a
15	ATF3	chr16:77323094-77323609	A549	lung:	n/a	n/a
16	ATF3	chr16:77332521-77333151	A549	lung:	n/a	n/a
17	BACH1	chr16:77296164-77296240	K562	blood:	n/a	n/a
18	BACH1	chr16:77496736-77496798	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr16:77370568-77370892	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr16:77468868-77469068	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:77364729-77364750	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr16:77469290-77469530	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr16:77468365-77468638	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr16:77361605-77362055	GM12878	blood:	n/a	n/a
25	BATF	chr16:77548515-77548734	GM12878	blood:	n/a	n/a
26	BATF	chr16:77361667-77361962	GM12878	blood:	n/a	n/a
27	BATF	chr16:77548505-77548705	GM12878	blood:	n/a	n/a
28	BATF	chr16:77442505-77442763	GM12878	blood:	n/a	chr16:77442619-77442630
29	BCL11A	chr16:77370621-77370777	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr16:77361671-77362022	GM12878	blood:	n/a	n/a
31	BCL11A	chr16:77442480-77442825	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:77442458-77442818	GM12878	blood:	n/a	n/a
33	BCL3	chr16:77392767-77393412	A549	lung:	n/a	n/a
34	BCL3	chr16:77448744-77449184	A549	lung:	n/a	n/a
35	BCL3	chr16:77329827-77330201	A549	lung:	n/a	n/a
36	BCL3	chr16:77387257-77388009	A549	lung:	n/a	n/a
37	BCL3	chr16:77361644-77361903	GM12878	blood:	n/a	n/a
38	BCL3	chr16:77331990-77333064	A549	lung:	n/a	chr16:77332174-77332181
39	BCL3	chr16:77332232-77333037	A549	lung:	n/a	n/a
40	BCL3	chr16:77334052-77334620	A549	lung:	n/a	n/a
41	BCL3	chr16:77392824-77393588	A549	lung:	n/a	n/a
42	BCL3	chr16:77387277-77387969	A549	lung:	n/a	n/a
43	BHLHE40	chr16:77392876-77393379	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:77442539-77442831	GM12878	blood:	n/a	n/a
45	BHLHE40	chr16:77355073-77355181	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:77364267-77364567	GM12878	blood:	n/a	n/a
47	BHLHE40	chr16:77322150-77322378	A549	lung:	n/a	n/a
48	BRCA1	chr16:77410410-77410539	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr16:77362884-77362892	GM12878	blood:	n/a	n/a
50	BRCA1	chr16:77332371-77333025	Hela-S3	cervix:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77469998-77470048	HNPCEpiC	eye:	n/a
2	chr16:77468277-77468327	HIPEpiC	eye:	n/a
3	chr16:77469998-77470048	HNPCEpiC	eye:	n/a
4	chr16:77468277-77468327	HIPEpiC	eye:	n/a
5	chr16:77468893-77468943	ECC-1	luminal epithelium:	n/a
6	chr16:77468486-77468536	RPTEC	kidney:	n/a
7	chr16:77353824-77353874	HepG2	liver:	n/a
8	chr16:77469998-77470048	HRPEpiC	eye:	n/a
9	chr16:77477150-77477200	A549	lung:	n/a
10	chr16:77472697-77472747	PFSK-1	brain:	n/a
11	chr16:77322779-77322829	HRCEpiC	kidney:	n/a
12	chr16:77469583-77469633	HEEpiC	esophagus:	n/a
13	chr16:77468277-77468327	Caco-2	colon:	n/a
14	chr16:77469540-77469590	AG04449	skin:	fetal
15	chr16:77469538-77469588	BJ	skin:	n/a
16	chr16:77370171-77370221	GM19239	blood:	n/a
17	chr16:77397865-77397915	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:77469667-77469717	SAEC	small airway:	n/a
19	chr16:77397865-77397915	NT2-D1	testis:	n/a
20	chr16:77465215-77465265	Hepatocyte	liver:	n/a
21	chr16:77307863-77307913	HRCEpiC	kidney:	n/a
22	chr16:77398740-77398790	ECC-1	luminal epithelium:	n/a
23	chr16:77468373-77468423	IMR90	lung:	fetal
24	chr16:77469540-77469590	HRCEpiC	kidney:	n/a
25	chr16:77370171-77370221	HIPEpiC	eye:	n/a
26	chr16:77322779-77322829	BJ	skin:	n/a
27	chr16:77353824-77353874	MCF-7	breast:	n/a
28	chr16:77353810-77353860	U87	brain:	n/a
29	chr16:77353824-77353874	PANC-1	pancreas:	n/a
30	chr16:77469998-77470048	Jurkat	blood:	n/a
31	chr16:77353810-77353860	SK-N-SH	brain:	n/a
32	chr16:77468893-77468943	AG09309	skin:	n/a
33	chr16:77468486-77468536	ECC-1	luminal epithelium:	n/a
34	chr16:77467409-77467459	IMR90	lung:	fetal
35	chr16:77469667-77469717	HRPEpiC	eye:	n/a
36	chr16:77370171-77370221	A549	lung:	n/a
37	chr16:77421693-77421743	AG10803	skin:	n/a
38	chr16:77469540-77469590	HEK293	kidney:	embryo
39	chr16:77469167-77469217	NHBE	bronchial:	n/a
40	chr16:77469167-77469217	SAEC	small airway:	n/a
41	chr16:77469167-77469217	GM12891	blood:	n/a
42	chr16:77477150-77477200	HIPEpiC	eye:	n/a
43	chr16:77353824-77353874	NHBE	bronchial:	n/a
44	chr16:77468277-77468327	HAEpiC	amniotic membrane:	n/a
45	chr16:77307863-77307913	BJ	skin:	n/a
46	chr16:77307863-77307913	SK-N-SH	brain:	n/a
47	chr16:77467409-77467459	SK-N-MC	brain:	n/a
48	chr16:77469998-77470048	U87	brain:	n/a
49	chr16:77307863-77307913	T-47D	breast:	n/a
50	chr16:77467409-77467459	GM12891	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:77427682..77431642-chr16:77432418..77435564,3	K562	blood:
2	chr16:77545100..77546949-chr16:77551989..77554470,2	MCF-7	breast:
3	chr16:77435097..77437524-chr16:77437651..77440031,2	K562	blood:
4	chr16:77333024..77336055-chr16:77337376..77340346,3	MCF-7	breast:
5	chr16:77471559..77472162-chr16:77617897..77618748,2	MCF-7	breast:
6	chr16:77396978..77399255-chr16:77401512..77403029,2	K562	blood:
7	chr16:77470494..77473466-chr16:77473923..77475786,2	K562	blood:
8	chr16:77273435..77275318-chr16:77277806..77279543,2	K562	blood:
9	chr12:75336977..75337697-chr16:77358943..77359755,2	MCF-7	breast:
10	chr16:77269656..77270610-chr16:77471829..77472511,2	MCF-7	breast:
11	chr16:77502736..77504722-chr16:77511149..77514131,2	K562	blood:
12	chr16:77473576..77476044-chr16:77476229..77478435,2	MCF-7	breast:
13	chr16:77376619..77379177-chr16:77392341..77394728,2	MCF-7	breast:
14	chr16:77318927..77321221-chr16:77323637..77325291,2	MCF-7	breast:
15	chr16:77468850..77470466-chr16:77476156..77478006,2	MCF-7	breast:
16	chr16:77320544..77323017-chr16:77325949..77328291,2	K562	blood:
17	chr16:77435097..77437524-chr16:77437651..77440031,2	K562	blood:
18	chr16:77376619..77379177-chr16:77392341..77394728,2	MCF-7	breast:
19	chr16:77396978..77399255-chr16:77401512..77403029,2	K562	blood:
20	chr16:77502736..77504722-chr16:77511149..77514131,2	K562	blood:
21	chr16:77364104..77366895-chr16:77412752..77415656,2	K562	blood:
22	chr16:77269758..77270518-chr16:77334286..77335046,2	MCF-7	breast:
23	chr16:77269912..77270651-chr16:77440233..77440965,2	MCF-7	breast:
24	chr16:77470494..77473466-chr16:77473923..77475786,2	K562	blood:
25	chr16:77364163..77366855-chr16:77389238..77390900,2	MCF-7	breast:
26	chr16:77269710..77270493-chr16:77407930..77408448,2	MCF-7	breast:
27	chr16:77333024..77336055-chr16:77337376..77340346,3	MCF-7	breast:
28	chr16:77284002..77285688-chr16:77295972..77298884,2	K562	blood:
29	chr16:77531888..77534312-chr16:77536499..77538354,2	K562	blood:
30	chr16:77427682..77431642-chr16:77432418..77435564,3	K562	blood:
31	chr16:77542643..77546674-chr16:77547761..77549967,3	K562	blood:
32	chr16:77273139..77275298-chr16:77332609..77335095,2	MCF-7	breast:
33	chr16:77545100..77546949-chr16:77551989..77554470,2	MCF-7	breast:
34	chr16:77364104..77366895-chr16:77412752..77415656,2	K562	blood:
35	chr16:77364163..77366855-chr16:77389238..77390900,2	MCF-7	breast:
36	chr16:77542643..77546674-chr16:77547761..77549967,3	K562	blood:
37	chr16:77318927..77321221-chr16:77323637..77325291,2	MCF-7	breast:
38	chr16:77499344..77501262-chr16:77505118..77507842,2	MCF-7	breast:
39	chr16:77499344..77501262-chr16:77505118..77507842,2	MCF-7	breast:
40	chr16:77320544..77323017-chr16:77325949..77328291,2	K562	blood:
41	chr16:77269653..77270243-chr16:77410066..77410842,2	MCF-7	breast:
42	chr16:77531888..77534312-chr16:77536499..77538354,2	K562	blood:
43	chr16:77428869..77431642-chr16:77432418..77434289,2	K562	blood:
44	chr16:77471508..77472616-chr16:77617706..77618810,7	MCF-7	breast:
45	chr16:77428869..77431642-chr16:77432418..77434289,2	K562	blood:
46	chr16:77471519..77472123-chr16:77694084..77694927,2	MCF-7	breast:
47	chr16:77284002..77285688-chr16:77295972..77298884,2	K562	blood:
48	chr16:77278039..77279706-chr16:77282947..77285823,2	K562	blood:
49	chr16:77473576..77476044-chr16:77476229..77478435,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SYCE1L-2	chr16:77477742-77477968	NONHSAT143803
2	lnc-SYCE1L-2	chr16:77480430-77480469	NONHSAT143803
3	lnc-SYCE1L-2	chr16:77469122-77469237	NONHSAT143803
4	lnc-SYCE1L-2	chr16:77477742-77478233	ENSG00000260701.1
5	lnc-ADAMTS18-1	chr16:77283791-77283854	ENSG00000261063.1
6	lnc-SYCE1L-2	chr16:77467279-77467365	ENSG00000260701.1

No data

Variant related genes	Relation type
ENSG00000260701	TF binding region
ENSG00000216131	TF binding region
ADAMTS18	TF binding region
ENSG00000261063	TF binding region
ENSG00000260701	CpG island
ENSG00000216131	CpG island
ADAMTS18	CpG island
ENSG00000261063	CpG island
ENSG00000261063	chromatin interactions
ENSG00000140873	chromatin interactions
ENSG00000216131	chromatin interactions

Extended variants
information (count: 13387 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:13387 , 50 per page) page: 1 2 3 4 5 6 7 ... 268

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9674287	chr16:77277005-77277006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs199690097	chr16:77277029-77277030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527428911	chr16:77277040-77277041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369022099	chr16:77277051-77277052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9938871	chr16:77277057-77277058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558869154	chr16:77277058-77277059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567280210	chr16:77277062-77277063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72800050	chr16:77277067-77277068	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144363258	chr16:77277091-77277092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546640947	chr16:77277094-77277095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181205320	chr16:77277104-77277105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566466241	chr16:77277116-77277117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185347117	chr16:77277123-77277124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200724479	chr16:77277157-77277158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201693720	chr16:77277159-77277160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199949063	chr16:77277160-77277161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs397854862	chr16:77277164-77277165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375507197	chr16:77278084-77278085	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565515023	chr16:77278085-77278086	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553776101	chr16:77278102-77278103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs527342666	chr16:77278111-77278112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573936776	chr16:77278218-77278219	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9931400	chr16:77278241-77278242	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs539377769	chr16:77278286-77278287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186888165	chr16:77278304-77278305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2343041	chr16:77278316-77278317	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549830719	chr16:77278341-77278342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375333970	chr16:77278353-77278354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192132120	chr16:77278361-77278362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs572057563	chr16:77278381-77278382	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540960246	chr16:77278413-77278414	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs564367340	chr16:77278467-77278468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577173953	chr16:77278520-77278521	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs546153319	chr16:77278528-77278529	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs74025736	chr16:77278531-77278532	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531822490	chr16:77278538-77278539	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs184022983	chr16:77278584-77278585	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565869441	chr16:77278616-77278617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562262345	chr16:77278639-77278640	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147347695	chr16:77278672-77278673	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs28709511	chr16:77278695-77278696	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533999944	chr16:77278717-77278718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571079592	chr16:77278718-77278719	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539084035	chr16:77278728-77278729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139221454	chr16:77278749-77278750	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs553867493	chr16:77278762-77278763	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569440350	chr16:77278767-77278768	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567457670	chr16:77278801-77278802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535172406	chr16:77278819-77278820	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536227080	chr16:77278851-77278852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Lung cancer	24585490	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD
Ovarian cancer	21720365	CNVD
Bipolar disorder	19114987	CNVD
Barrett''s syndrome	19417022	CNVD
Gastric cancer	22315472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77273800-77277200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr16:77279400-77280800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr16:77279600-77280200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr16:77280000-77280600	Enhancers	Adipose Nuclei	Adipose
5	chr16:77280200-77280600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr16:77280600-77280800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr16:77280800-77284000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr16:77280800-77284000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr16:77281200-77282400	Enhancers	Osteobl	bone
10	chr16:77284000-77284400	Enhancers	Fetal Stomach	stomach
11	chr16:77284000-77284400	Enhancers	NHDF-Ad	bronchial
12	chr16:77284000-77284600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr16:77284000-77285000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr16:77284200-77284400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr16:77285400-77285600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr16:77285600-77302800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr16:77302800-77303200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr16:77303000-77303200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:77303000-77303600	Enhancers	Adipose Nuclei	Adipose
20	chr16:77303000-77304000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr16:77303000-77304000	Enhancers	Pancreas	Pancrea
22	chr16:77303200-77303400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr16:77303200-77303600	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr16:77303200-77315600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr16:77303400-77303800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr16:77303600-77303800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr16:77303600-77303800	Flanking Active TSS	Adipose Nuclei	Adipose
28	chr16:77303600-77305200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr16:77303800-77305600	Weak transcription	Adipose Nuclei	Adipose
30	chr16:77303800-77307800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:77304000-77305400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr16:77304000-77307800	Weak transcription	Pancreas	Pancrea
33	chr16:77305200-77306400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr16:77305400-77306200	Enhancers	Brain Angular Gyrus	brain
35	chr16:77305400-77306200	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr16:77305400-77306400	Enhancers	HepG2	liver
37	chr16:77305400-77307000	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr16:77305600-77306200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr16:77305600-77306200	Enhancers	Adipose Nuclei	Adipose
40	chr16:77305600-77306200	Enhancers	Brain Anterior Caudate	brain
41	chr16:77305600-77306200	Enhancers	Brain Cingulate Gyrus	brain
42	chr16:77305600-77306200	Enhancers	Brain Substantia Nigra	brain
43	chr16:77305600-77306400	Enhancers	Brain Germinal Matrix	brain
44	chr16:77305800-77306000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr16:77305800-77306200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr16:77305800-77306200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr16:77305800-77306400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr16:77305800-77309200	Enhancers	Dnd41	blood
49	chr16:77306200-77307800	Weak transcription	Adipose Nuclei	Adipose
50	chr16:77306200-77311000	Weak transcription	Brain Inferior Temporal Lobe	brain

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