Variant report

Variant	nsv533450
Chromosome Location	chr16:70929925-71196477
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2825)
CpG islands
(count:1284)
Chromatin interactive
region (count:332)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2825 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70971786-70971832	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:71021049-71021536	K562	blood:	n/a	n/a
3	ARID3A	chr16:71135528-71135631	K562	blood:	n/a	n/a
4	ARID3A	chr16:71155214-71155415	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:70961655-70961897	K562	blood:	n/a	n/a
6	ARID3A	chr16:70956273-70956284	HepG2	liver:	n/a	n/a
7	ATF1	chr16:70977109-70977159	K562	blood:	n/a	n/a
8	ATF1	chr16:70987738-70988064	K562	blood:	n/a	n/a
9	ATF1	chr16:71117539-71117895	K562	blood:	n/a	n/a
10	ATF1	chr16:70990674-70991056	K562	blood:	n/a	n/a
11	ATF1	chr16:71115100-71115287	K562	blood:	n/a	n/a
12	ATF1	chr16:71184717-71184907	K562	blood:	n/a	n/a
13	ATF1	chr16:71187867-71187907	K562	blood:	n/a	n/a
14	ATF1	chr16:70980043-70980287	K562	blood:	n/a	n/a
15	ATF1	chr16:71112061-71112067	K562	blood:	n/a	n/a
16	ATF1	chr16:71088250-71088569	K562	blood:	n/a	n/a
17	ATF1	chr16:71128261-71128310	K562	blood:	n/a	n/a
18	ATF1	chr16:71142323-71142501	K562	blood:	n/a	n/a
19	ATF1	chr16:71021180-71021685	K562	blood:	n/a	n/a
20	ATF1	chr16:71120453-71120767	K562	blood:	n/a	n/a
21	ATF1	chr16:71076132-71076230	K562	blood:	n/a	n/a
22	ATF1	chr16:70992165-70992287	K562	blood:	n/a	n/a
23	ATF2	chr16:71186718-71187702	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr16:70987603-70988175	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr16:71043362-71044048	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr16:71042989-71044337	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr16:71061483-71062714	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr16:71186893-71187728	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr16:71061713-71062433	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr16:71187076-71187578	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr16:71187125-71187485	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr16:71021188-71021575	K562	blood:	n/a	n/a
33	BACH1	chr16:71021074-71021564	K562	blood:	n/a	n/a
34	BACH1	chr16:71184315-71184498	K562	blood:	n/a	n/a
35	BACH1	chr16:71112932-71113088	K562	blood:	n/a	n/a
36	BACH1	chr16:71173649-71173792	K562	blood:	n/a	n/a
37	BACH1	chr16:71165544-71165704	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr16:70937028-70937453	K562	blood:	n/a	n/a
39	BACH1	chr16:71061535-71062530	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr16:71020996-71021702	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr16:70969729-70969731	K562	blood:	n/a	n/a
42	BATF	chr16:70963263-70963562	GM12878	blood:	n/a	n/a
43	BCL11A	chr16:71061909-71062286	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL11A	chr16:71043533-71043780	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL11A	chr16:71061959-71062411	H1-hESC	embryonic stem cell:	n/a	n/a
46	BCL3	chr16:70973768-70974260	GM12878	blood:	n/a	chr16:70974079-70974088
47	BCL3	chr16:70976321-70976732	GM12878	blood:	n/a	n/a
48	BCL3	chr16:70973830-70974232	GM12878	blood:	n/a	chr16:70974079-70974088
49	BCL3	chr16:70983386-70983627	GM12878	blood:	n/a	n/a
50	BCL3	chr16:70976273-70976645	GM12878	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:71088536-71088586	AG04449	skin:	fetal
2	chr16:71168874-71168924	HCF	heart:	n/a
3	chr16:71115142-71115192	ovcar-3	ovarian:	n/a
4	chr16:71088536-71088586	AG04449	skin:	fetal
5	chr16:71168874-71168924	HCF	heart:	n/a
6	chr16:71115142-71115192	ovcar-3	ovarian:	n/a
7	chr16:70955879-70955929	Caco-2	colon:	n/a
8	chr16:71043770-71043820	HCT-116	colon:	n/a
9	chr16:70955223-70955273	AG09309	skin:	n/a
10	chr16:71043770-71043820	A549	lung:	n/a
11	chr16:71071560-71071610	PFSK-1	brain:	n/a
12	chr16:71011407-71011457	HIPEpiC	eye:	n/a
13	chr16:71008732-71008782	GM12878	blood:	n/a
14	chr16:71008050-71008100	RPTEC	kidney:	n/a
15	chr16:71162835-71162885	HIPEpiC	eye:	n/a
16	chr16:71071560-71071610	GM06990	blood:	n/a
17	chr16:71115142-71115192	AG10803	skin:	n/a
18	chr16:71168874-71168924	GM12891	blood:	n/a
19	chr16:70955223-70955273	PFSK-1	brain:	n/a
20	chr16:71187554-71187604	NT2-D1	testis:	n/a
21	chr16:70955879-70955929	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:70955223-70955273	HRCEpiC	kidney:	n/a
23	chr16:71008063-71008113	SK-N-SH	brain:	n/a
24	chr16:71034828-71034878	PFSK-1	brain:	n/a
25	chr16:71008732-71008782	A549	lung:	n/a
26	chr16:71098674-71098724	SK-N-SH	brain:	n/a
27	chr16:71034828-71034878	RPTEC	kidney:	n/a
28	chr16:70955865-70955915	GM19239	blood:	n/a
29	chr16:71043770-71043820	HEEpiC	esophagus:	n/a
30	chr16:71115142-71115192	H1-hESC	embryonic stem cell:	embryo
31	chr16:71009778-71009828	HRE	kidney:	n/a
32	chr16:71168874-71168924	SK-N-SH_RA	brain:	n/a
33	chr16:71061931-71061981	T-47D	breast:	n/a
34	chr16:71115142-71115192	NHBE	bronchial:	n/a
35	chr16:71008063-71008113	IMR90	lung:	fetal
36	chr16:71008454-71008504	HL-60	blood:	n/a
37	chr16:71009778-71009828	ProgFib	skin:	n/a
38	chr16:71008454-71008504	HMEC	breast:	n/a
39	chr16:71008063-71008113	HRE	kidney:	n/a
40	chr16:71098674-71098724	HMEC	breast:	n/a
41	chr16:70955879-70955929	HCM	heart:	n/a
42	chr16:70967321-70967371	ECC-1	luminal epithelium:	n/a
43	chr16:70967321-70967371	HEK293	kidney:	embryo
44	chr16:71008063-71008113	NH-A	brain:	n/a
45	chr16:70955223-70955273	HCM	heart:	n/a
46	chr16:71008050-71008100	NB4	blood:	n/a
47	chr16:71071560-71071610	Hepatocyte	liver:	n/a
48	chr16:71061931-71061981	MCF10A-Er-Src	breast:	n/a
49	chr16:71162835-71162885	Hela-S3	cervix:	n/a
50	chr16:71009778-71009828	K562	blood:	n/a

(count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr16:71013218..71015708-chr16:71098677..71101219,2	MCF-7	breast:
2	chr16:70941298..70941798-chr6:91092581..91093084,2	Hela-S3	cervix:
3	chr1:146713329..146715162-chr16:71157129..71158866,2	K562	blood:
4	chr16:71127059..71128576-chr16:71174423..71176284,2	MCF-7	breast:
5	chr16:71065152..71067149-chr16:71070441..71072492,2	K562	blood:
6	chr1:146555074..146557107-chr16:71070862..71072402,2	K562	blood:
7	chr16:71040507..71041294-chr16:71052633..71053472,2	MCF-7	breast:
8	chr16:71061201..71063992-chr16:71068444..71070337,2	K562	blood:
9	chr16:71145606..71148394-chr16:71150978..71154581,3	K562	blood:
10	chr16:71034614..71035398-chr16:71445849..71446753,2	MCF-7	breast:
11	chr16:71001861..71002521-chr4:43883310..43883810,2	MCF-7	breast:
12	chr16:71095052..71096842-chr16:71128333..71130815,2	MCF-7	breast:
13	chr16:71033120..71035273-chr16:71039747..71041751,2	MCF-7	breast:
14	chr16:71021462..71023279-chr16:71026554..71028512,2	MCF-7	breast:
15	chr1:144532657..144535351-chr16:70953867..70956114,2	K562	blood:
16	chr16:71188987..71192929-chr16:71194834..71197955,4	MCF-7	breast:
17	chr16:71051562..71054023-chr16:71056905..71058672,3	K562	blood:
18	chr16:71084915..71086652-chr16:71089188..71090873,2	MCF-7	breast:
19	chr16:71072688..71075243-chr16:71094843..71097442,2	K562	blood:
20	chr16:71192483..71194543-chr16:71195143..71197017,2	MCF-7	breast:
21	chr16:71176614..71178323-chr16:71181138..71183405,2	K562	blood:
22	chr16:71006242..71008260-chr16:71011364..71013883,2	K562	blood:
23	chr16:71051562..71054023-chr16:71056905..71058672,3	K562	blood:
24	chr16:71016144..71018459-chr16:71020187..71022011,2	MCF-7	breast:
25	chr1:149222095..149224018-chr16:71054423..71057770,3	MCF-7	breast:
26	chr16:71151955..71154632-chr16:71157353..71159392,2	MCF-7	breast:
27	chr16:71033616..71034231-chr16:71400920..71401907,2	MCF-7	breast:
28	chr1:146551738..146553728-chr16:71003126..71004713,2	K562	blood:
29	chr1:147726894..147727805-chr16:71044140..71044879,2	MCF-7	breast:
30	chr16:71043873..71044605-chr5:87436587..87437176,2	MCF-7	breast:
31	chr16:71112561..71115215-chr16:71117868..71120109,2	K562	blood:
32	chr16:71133984..71136804-chr16:71138409..71140730,2	K562	blood:
33	chr16:71153052..71156401-chr16:71159001..71163450,6	K562	blood:
34	chr16:71131509..71134073-chr16:71136851..71139801,2	K562	blood:
35	chr16:71076131..71077699-chr16:71081158..71083457,2	MCF-7	breast:
36	chr16:71030533..71033114-chr16:71033879..71035665,2	K562	blood:
37	chr16:71169222..71171433-chr16:71173024..71177252,4	K562	blood:
38	chr16:71169999..71172997-chr16:71175859..71177965,3	MCF-7	breast:
39	chr16:71033432..71034748-chr16:71345163..71346194,8	MCF-7	breast:
40	chr16:71107666..71109248-chr16:71109772..71111296,2	K562	blood:
41	chr16:70973640..70974283-chr16:71001999..71002517,2	MCF-7	breast:
42	chr16:71158993..71163306-chr16:71165421..71171777,6	MCF-7	breast:
43	chr1:144534131..144535903-chr16:71032462..71035841,3	K562	blood:
44	chr16:71015461..71020683-chr16:71023504..71027533,5	K562	blood:
45	chr16:71158993..71163306-chr16:71165421..71171777,6	MCF-7	breast:
46	chr16:70974977..70976783-chr16:70983975..70986129,4	K562	blood:
47	chr12:49657789..49659866-chr16:71035354..71037246,2	MCF-7	breast:
48	chr16:71137230..71139618-chr16:71153836..71156298,2	MCF-7	breast:
49	chr16:71091520..71094181-chr16:71101967..71103897,2	K562	blood:
50	chr16:71051562..71054023-chr16:71057022..71058672,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALB2-4	chr16:71124086-71124278	ENSG00000259833.1
2	lnc-CALB2-4	chr16:71127494-71127570	ENSG00000259833.1
3	lnc-CALB2-4	chr16:71124359-71125289	ucscGeneNc_uc002fci_1
4	lnc-CALB2-3	chr16:71147708-71147903	ENSG00000259798.1
5	lnc-CALB2-3	chr16:71147255-71147541	ENSG00000259798.1
6	lnc-CALB2-4	chr16:71114769-71114884	ENSG00000259833.1
7	lnc-IL34-4	chr16:71017348-71020288	ucscGeneNc_uc002fch_1
8	lnc-CALB2-4	chr16:71020753-71021463	ucscGeneNc_uc002fci_1
9	lnc-CALB2-4	chr16:71121629-71121793	ENSG00000259833.1
10	lnc-CALB2-4	chr16:71114772-71114884	ENSG00000259833.1
11	lnc-CALB2-4	chr16:71121629-71121793	ENSG00000259833.1
12	lnc-CALB2-4	chr16:71124086-71124393	ENSG00000259833.1

No data

Variant related genes	Relation type
ENSG00000259798	TF binding region
HYDIN	TF binding region
ENSG00000259833	TF binding region
ENSG00000259798	CpG island
HYDIN	CpG island
ENSG00000259833	CpG island
ENSG00000259833	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000260593	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000157423	chromatin interactions
ENSG00000143363	chromatin interactions
ENSG00000259798	chromatin interactions
ENSG00000172137	chromatin interactions
ENSG00000271721	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000230832	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000180917	chromatin interactions
ENSG00000140832	chromatin interactions
ENSG00000272426	chromatin interactions

Extended variants
information (count: 9750 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:9750 , 50 per page) page: 1 2 3 4 5 6 7 ... 195

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565129136	chr16:70929997-70929998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1774439	chr16:70930002-70930003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9939429	chr16:70930044-70930045	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs2795773	chr16:70930060-70930061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs75375189	chr16:70930066-70930067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149491206	chr16:70930068-70930069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143963122	chr16:70930069-70930070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371866933	chr16:70930096-70930097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112948637	chr16:70930116-70930117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530205096	chr16:70930171-70930172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542037071	chr16:70930217-70930218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560775235	chr16:70930234-70930235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527957891	chr16:70930252-70930253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60603701	chr16:70930316-70930317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188432555	chr16:70930318-70930319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181375783	chr16:70930319-70930320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3003564	chr16:70930341-70930342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3003565	chr16:70930348-70930349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs56212732	chr16:70930370-70930371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3003566	chr16:70930387-70930388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549873532	chr16:70930394-70930395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148236134	chr16:70930415-70930416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2938742	chr16:70930416-70930417	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs61188880	chr16:70930421-70930422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116178425	chr16:70930429-70930430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553987206	chr16:70930443-70930444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3003567	chr16:70930451-70930452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13334276	chr16:70930460-70930461	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs539339704	chr16:70930490-70930491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369320884	chr16:70930527-70930528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1774440	chr16:70930547-70930548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537455459	chr16:70930560-70930561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71894448	chr16:70930567-70930568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558039276	chr16:70930568-70930569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72211609	chr16:70930575-70930576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113438527	chr16:70930577-70930578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1798459	chr16:70930637-70930638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11639921	chr16:70930737-70930738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577119544	chr16:70930746-70930747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544223107	chr16:70930799-70930800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200004284	chr16:70930911-70930912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146370634	chr16:70930984-70930985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556207736	chr16:70930989-70930990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139809862	chr16:70931060-70931061	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1774441	chr16:70931067-70931068	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541949085	chr16:70931083-70931084	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs560517056	chr16:70931087-70931088	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12102325	chr16:70931126-70931127	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541018289	chr16:70931134-70931135	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546140528	chr16:70931167-70931168	Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	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 myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70908800-70933400	Weak transcription	Fetal Brain Male	brain
2	chr16:70921400-70939400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr16:70921600-70939400	Weak transcription	Fetal Kidney	kidney
4	chr16:70921800-70933000	Weak transcription	Brain Substantia Nigra	brain
5	chr16:70922600-70933600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr16:70922600-70949400	Weak transcription	Pancreas	Pancrea
7	chr16:70922800-70933200	Weak transcription	Fetal Intestine Small	intestine
8	chr16:70923200-70931400	Weak transcription	Brain Angular Gyrus	brain
9	chr16:70923400-70933400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr16:70926200-70932200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr16:70926800-70931200	Weak transcription	Brain Hippocampus Middle	brain
12	chr16:70928400-70931000	Weak transcription	Fetal Stomach	stomach
13	chr16:70928400-70931200	Weak transcription	Brain Anterior Caudate	brain
14	chr16:70928400-70932400	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr16:70928600-70930200	Enhancers	K562	blood
16	chr16:70929200-70932000	Weak transcription	Fetal Brain Female	brain
17	chr16:70929600-70931400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr16:70929800-70932000	Weak transcription	Brain Germinal Matrix	brain
19	chr16:70929800-70933200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr16:70930200-70934800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr16:70930200-70937800	Weak transcription	Spleen	Spleen
22	chr16:70931000-70931200	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr16:70931000-70931600	Genic enhancers	Fetal Stomach	stomach
24	chr16:70931200-70931800	ZNF genes & repeats	Stomach Smooth Muscle	stomach
25	chr16:70931200-70935200	Strong transcription	Brain Anterior Caudate	brain
26	chr16:70931200-70935200	Strong transcription	Brain Hippocampus Middle	brain
27	chr16:70931400-70931600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr16:70931400-70935000	Strong transcription	Brain Angular Gyrus	brain
29	chr16:70931600-70934200	Strong transcription	Fetal Stomach	stomach
30	chr16:70931800-70933000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr16:70932000-70933000	Weak transcription	Fetal Intestine Large	intestine
32	chr16:70932000-70935200	Strong transcription	Fetal Brain Female	brain
33	chr16:70932000-70935400	Strong transcription	Brain Germinal Matrix	brain
34	chr16:70932200-70932400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr16:70932200-70935200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr16:70932400-70935000	Strong transcription	Brain Inferior Temporal Lobe	brain
37	chr16:70933000-70933600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr16:70933000-70934000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
39	chr16:70933000-70934600	Strong transcription	Stomach Smooth Muscle	stomach
40	chr16:70933000-70935000	Strong transcription	Fetal Intestine Large	intestine
41	chr16:70933000-70935200	Strong transcription	Brain Substantia Nigra	brain
42	chr16:70933200-70934200	Strong transcription	Fetal Intestine Small	intestine
43	chr16:70933200-70935000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:70933200-70935000	Weak transcription	Fetal Muscle Leg	muscle
45	chr16:70933400-70935000	ZNF genes & repeats	Aorta	Aorta
46	chr16:70933400-70935000	Strong transcription	Fetal Brain Male	brain
47	chr16:70933400-70935200	Strong transcription	Brain Cingulate Gyrus	brain
48	chr16:70933600-70934800	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr16:70933600-70934800	Strong transcription	Pancreatic Islets	Pancreatic Islet
50	chr16:70933800-70934000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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