Variant report

Variant	nsv1056946
Chromosome Location	chr16:76599511-77084651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2359)
CpG islands
(count:367)
Chromatin interactive
region (count:63)
LncRNA
region (count:14)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2359 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76934165-76934485	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76980885-76981085	K562	blood:	n/a	n/a
5	ARID3A	chr16:76673948-76674099	K562	blood:	n/a	n/a
6	ARID3A	chr16:76913373-76913653	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:76608141-76609300	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:76668888-76668938	K562	blood:	n/a	n/a
9	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
10	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
11	ATF1	chr16:76668805-76669470	K562	blood:	n/a	n/a
12	ATF1	chr16:76614425-76614592	K562	blood:	n/a	n/a
13	ATF2	chr16:76839037-76839302	GM12878	blood:	n/a	n/a
14	ATF2	chr16:77010103-77010377	GM12878	blood:	n/a	n/a
15	ATF3	chr16:76980721-76981225	A549	lung:	n/a	n/a
16	ATF3	chr16:77003970-77004466	A549	lung:	n/a	n/a
17	ATF3	chr16:76980737-76981284	A549	lung:	n/a	n/a
18	ATF3	chr16:76668818-76669064	K562	blood:	n/a	n/a
19	ATF3	chr16:76980774-76981124	K562	blood:	n/a	n/a
20	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr16:76980722-76981230	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr16:76980807-76981126	K562	blood:	n/a	n/a
24	BACH1	chr16:77057336-77057341	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr16:76617883-76618255	GM12878	blood:	n/a	chr16:76618063-76618074
26	BATF	chr16:76610960-76611272	GM12878	blood:	n/a	n/a
27	BATF	chr16:76838975-76839411	GM12878	blood:	n/a	n/a
28	BATF	chr16:76980823-76981049	GM12878	blood:	n/a	chr16:76980965-76980976
29	BATF	chr16:76610931-76611290	GM12878	blood:	n/a	n/a
30	BATF	chr16:76838952-76839361	GM12878	blood:	n/a	n/a
31	BATF	chr16:76856386-76856604	GM12878	blood:	n/a	n/a
32	BATF	chr16:76980831-76981097	GM12878	blood:	n/a	chr16:76980965-76980976
33	BATF	chr16:76617930-76618131	GM12878	blood:	n/a	chr16:76618063-76618074
34	BATF	chr16:76850433-76850727	GM12878	blood:	n/a	chr16:76850562-76850573
35	BATF	chr16:76966490-76966773	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
36	BATF	chr16:76966506-76966724	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
37	BATF	chr16:76850471-76850665	GM12878	blood:	n/a	chr16:76850562-76850573
38	BATF	chr16:76856327-76856649	GM12878	blood:	n/a	n/a
39	BCL11A	chr16:77010106-77010349	GM12878	blood:	n/a	n/a
40	BCL11A	chr16:76839121-76839299	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
41	BCL11A	chr16:76839015-76839347	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
42	BCL3	chr16:76980667-76981333	A549	lung:	n/a	n/a
43	BHLHE40	chr16:76937293-76937310	HepG2	liver:	n/a	n/a
44	BHLHE40	chr16:76668642-76669184	K562	blood:	n/a	n/a
45	BHLHE40	chr16:76608424-76608923	HepG2	liver:	n/a	n/a
46	BHLHE40	chr16:76981970-76981973	HepG2	liver:	n/a	n/a
47	BHLHE40	chr16:76968723-76968754	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:76980800-76981182	K562	blood:	n/a	n/a
49	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
50	BHLHE40	chr16:76610846-76611310	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76666860-76666910	PANC-1	pancreas:	n/a
2	chr16:76666860-76666910	PANC-1	pancreas:	n/a
3	chr16:76708064-76708114	AoSMC	blood vessel:	n/a
4	chr16:76668836-76668886	ECC-1	luminal epithelium:	n/a
5	chr16:76670197-76670247	NHDF-neo	bronchial:	n/a
6	chr16:76666860-76666910	HRPEpiC	eye:	n/a
7	chr16:76670197-76670247	GM12892	blood:	n/a
8	chr16:76670197-76670247	SK-N-SH	brain:	n/a
9	chr16:76708064-76708114	HCM	heart:	n/a
10	chr16:76708064-76708114	SAEC	small airway:	n/a
11	chr16:76669151-76669201	RPTEC	kidney:	n/a
12	chr16:76668836-76668886	NH-A	brain:	n/a
13	chr16:76665665-76665715	LNCaP	prostate:	n/a
14	chr16:76666860-76666910	H1-hESC	embryonic stem cell:	embryo
15	chr16:76669151-76669201	ovcar-3	ovarian:	n/a
16	chr16:76708064-76708114	Caco-2	colon:	n/a
17	chr16:76666860-76666910	SK-N-SH	brain:	n/a
18	chr16:76670197-76670247	A549	lung:	n/a
19	chr16:76665665-76665715	HAEpiC	amniotic membrane:	n/a
20	chr16:76665665-76665715	AG10803	skin:	n/a
21	chr16:76708064-76708114	GM12878	blood:	n/a
22	chr16:76669151-76669201	AG09319	gingival:	n/a
23	chr16:76666860-76666910	AG10803	skin:	n/a
24	chr16:76668836-76668886	GM12878	blood:	n/a
25	chr16:76708064-76708114	HUVEC	blood vessel:	n/a
26	chr16:76668836-76668886	U87	brain:	n/a
27	chr16:76669151-76669201	NH-A	brain:	n/a
28	chr16:76666860-76666910	BE2_C	brain:	n/a
29	chr16:76669151-76669201	HNPCEpiC	eye:	n/a
30	chr16:76708064-76708114	MCF-7	breast:	n/a
31	chr16:76669151-76669201	GM12892	blood:	n/a
32	chr16:76666860-76666910	Jurkat	blood:	n/a
33	chr16:76665665-76665715	ovcar-3	ovarian:	n/a
34	chr16:76669151-76669201	NT2-D1	testis:	n/a
35	chr16:76669151-76669201	HRE	kidney:	n/a
36	chr16:76665665-76665715	Hepatocyte	liver:	n/a
37	chr16:76670197-76670247	HIPEpiC	eye:	n/a
38	chr16:76668836-76668886	RPTEC	kidney:	n/a
39	chr16:76665665-76665715	HUVEC	blood vessel:	n/a
40	chr16:76666860-76666910	ProgFib	skin:	n/a
41	chr16:76669151-76669201	HUVEC	blood vessel:	n/a
42	chr16:76668836-76668886	HAEpiC	amniotic membrane:	n/a
43	chr16:76668836-76668886	AoSMC	blood vessel:	n/a
44	chr16:76670197-76670247	AG09309	skin:	n/a
45	chr16:76708064-76708114	NHDF-neo	bronchial:	n/a
46	chr16:76708064-76708114	HRCEpiC	kidney:	n/a
47	chr16:76666860-76666910	NHBE	bronchial:	n/a
48	chr16:76666860-76666910	GM12892	blood:	n/a
49	chr16:76668836-76668886	PANC-1	pancreas:	n/a
50	chr16:76668836-76668886	SAEC	small airway:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
2	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
3	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
4	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
5	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
6	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
7	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
8	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
9	chr16:77076688..77077729-chr16:77203577..77204202,3	MCF-7	breast:
10	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
11	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
12	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
13	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
14	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
15	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
16	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
17	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
18	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
19	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
20	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
21	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
22	chr16:76887878..76888800-chr16:77205307..77205910,4	MCF-7	breast:
23	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
24	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
25	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
26	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
27	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
28	chr16:76665227..76667688-chr16:76668445..76671290,2	K562	blood:
29	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
30	chr16:76844876..76847420-chr19:45599129..45600971,2	MCF-7	breast:
31	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
32	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
33	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
34	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
35	chr16:76607256..76609840-chr16:76614807..76617382,2	K562	blood:
36	chr16:76887394..76888672-chr16:77203188..77204165,5	MCF-7	breast:
37	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
38	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
39	chr16:76679307..76681357-chr16:76683795..76685911,2	MCF-7	breast:
40	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
41	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
42	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
43	chr16:76636023..76638622-chr16:76652291..76654068,2	K562	blood:
44	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
45	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
46	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
47	chr16:76886880..76887748-chr16:77077328..77078325,2	MCF-7	breast:
48	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
49	chr16:77078662..77079429-chr16:77203303..77204211,3	MCF-7	breast:
50	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792
2	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
3	lnc-ADAMTS18-2	chr16:77028205-77028433	XLOC_012014
4	lnc-RP11-58C22.1.1-3	chr16:76803213-76803278	XLOC_011793
5	lnc-ADAMTS18-8	chr16:76912171-76912833	NONHSAT143788
6	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
7	lnc-RP11-58C22.1.1-4	chr16:76961793-76962066	ENSG00000259995.1
8	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
9	lnc-RP11-58C22.1.1-3	chr16:76806570-76806959	XLOC_011793
10	lnc-RP11-58C22.1.1-4	chr16:76946252-76946305	ENSG00000259995.1
11	lnc-ADAMTS18-2	chr16:77042061-77042204	XLOC_012014
12	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
13	lnc-RP11-58C22.1.1-1	chr16:76669394-76669520	ENSG00000250514
14	lnc-RP11-58C22.1.1-1	chr16:76668895-76669046	ENSG00000250514

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4719	chr16:76902885-76902906	MIMAT0019832

No data

Variant related genes	Relation type
MIR4719	TF binding region
ENSG00000250514	TF binding region
ENSG00000260797	TF binding region
ENSG00000259995	TF binding region
MIR4719	CpG island
ENSG00000250514	CpG island
ENSG00000260797	CpG island
ENSG00000259995	CpG island
ENSG00000250514	chromatin interactions
QARS	miRNA target sites
DDX3Y	miRNA target sites
CDV3	miRNA target sites
CDKN1A	miRNA target sites
PYGO2	miRNA target sites
SPRYD3	miRNA target sites

Extended variants
information (count: 11321 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:11321 , 50 per page) page: 1 2 3 4 5 6 7 ... 227

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370943194	chr16:76599512-76599513	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs554616828	chr16:76599538-76599539	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs533243671	chr16:76599554-76599555	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550069419	chr16:76599557-76599558	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs569879004	chr16:76599584-76599585	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535602578	chr16:76599681-76599682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114734916	chr16:76599703-76599704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183426240	chr16:76599734-76599735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565763683	chr16:76599736-76599737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534361161	chr16:76599746-76599747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557719616	chr16:76599790-76599791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144020517	chr16:76599796-76599797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148424920	chr16:76607223-76607224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556943000	chr16:76607237-76607238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565145018	chr16:76607247-76607248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190400098	chr16:76607300-76607301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542089715	chr16:76607312-76607313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs60072161	chr16:76607317-76607318	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs572517701	chr16:76607319-76607320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541138706	chr16:76607334-76607335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564233808	chr16:76607363-76607364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533203414	chr16:76607398-76607399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549745201	chr16:76607413-76607414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562674923	chr16:76607435-76607436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531651288	chr16:76607530-76607531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548158040	chr16:76607573-76607574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117288713	chr16:76607588-76607589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147133171	chr16:76607619-76607620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7186700	chr16:76607635-76607636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs570559008	chr16:76607723-76607724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539465181	chr16:76607727-76607728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556177783	chr16:76607732-76607733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367755814	chr16:76607761-76607762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562081017	chr16:76607790-76607791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180709737	chr16:76607844-76607845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536167066	chr16:76607874-76607875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555745575	chr16:76607877-76607878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572641884	chr16:76607886-76607887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4243125	chr16:76607888-76607889	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs377467317	chr16:76607902-76607903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564270882	chr16:76607933-76607934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547053971	chr16:76607956-76607957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577700717	chr16:76607982-76607983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543477244	chr16:76608020-76608021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs111527568	chr16:76608036-76608037	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs111440034	chr16:76608042-76608043	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs373250601	chr16:76608050-76608051	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs144475458	chr16:76608083-76608084	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs561824161	chr16:76608091-76608092	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs368438306	chr16:76608095-76608096	Enhancers Flanking Active TSS	n/a	n/a	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Cancer	20581869	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	17363583	CNVD

Chromatin state (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76599400-76599600	Enhancers	Brain Cingulate Gyrus	brain
2	chr16:76599400-76599600	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr16:76599400-76599800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr16:76607200-76607600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr16:76607400-76608000	Enhancers	HepG2	liver
6	chr16:76608000-76608600	Enhancers	Fetal Intestine Small	intestine
7	chr16:76608000-76608800	Flanking Active TSS	HepG2	liver
8	chr16:76608400-76609400	Enhancers	Fetal Intestine Large	intestine
9	chr16:76608600-76609000	Enhancers	Liver	Liver
10	chr16:76608800-76610000	Enhancers	HepG2	liver
11	chr16:76610000-76610400	Weak transcription	HepG2	liver
12	chr16:76610200-76612200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr16:76610400-76611200	Enhancers	Fetal Lung	lung
14	chr16:76610400-76611200	Enhancers	HepG2	liver
15	chr16:76610400-76611400	Enhancers	Primary hematopoietic stem cells	blood
16	chr16:76610400-76611800	Enhancers	GM12878-XiMat	blood
17	chr16:76611200-76611800	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr16:76614400-76614600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr16:76615400-76616200	Enhancers	Brain Germinal Matrix	brain
20	chr16:76616200-76616800	Weak transcription	Brain Germinal Matrix	brain
21	chr16:76616800-76617800	Enhancers	Brain Germinal Matrix	brain
22	chr16:76616800-76618000	Enhancers	Fetal Brain Male	brain
23	chr16:76616800-76618200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr16:76616800-76618400	Enhancers	Fetal Brain Female	brain
25	chr16:76617000-76617200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr16:76617000-76617200	Enhancers	Brain Angular Gyrus	brain
27	chr16:76617000-76617400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr16:76617000-76618000	Enhancers	Fetal Lung	lung
29	chr16:76617200-76617400	Flanking Active TSS	Brain Angular Gyrus	brain
30	chr16:76617200-76617600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr16:76617200-76617600	Enhancers	Adipose Nuclei	Adipose
32	chr16:76617200-76617600	Enhancers	Fetal Muscle Leg	muscle
33	chr16:76617200-76617600	Enhancers	Fetal Stomach	stomach
34	chr16:76617200-76617800	Active TSS	Brain Anterior Caudate	brain
35	chr16:76617200-76617800	Active TSS	Brain Cingulate Gyrus	brain
36	chr16:76617200-76617800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr16:76617200-76617800	Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr16:76617200-76618000	Active TSS	Brain Hippocampus Middle	brain
39	chr16:76617200-76618200	Active TSS	Brain Inferior Temporal Lobe	brain
40	chr16:76617200-76618200	Active TSS	Brain Substantia Nigra	brain
41	chr16:76617400-76617800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr16:76617400-76617800	Active TSS	Brain Angular Gyrus	brain
43	chr16:76617600-76618000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr16:76617800-76618200	Active TSS	Brain Germinal Matrix	brain
45	chr16:76617800-76618400	Enhancers	Brain Cingulate Gyrus	brain
46	chr16:76618000-76618200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr16:76618000-76618400	Enhancers	Brain Angular Gyrus	brain
48	chr16:76618000-76621000	Weak transcription	Fetal Lung	lung
49	chr16:76618200-76619600	Enhancers	Brain Germinal Matrix	brain
50	chr16:76618800-76619800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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