Variant report

Variant	nsv906947
Chromosome Location	chr16:76682263-77160626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1999)
CpG islands
(count:183)
Chromatin interactive
region (count:61)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1999 , 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	chr16:76684292-76684820	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:76934165-76934485	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:76913373-76913653	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:76687350-76687721	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:76980885-76981085	K562	blood:	n/a	n/a
6	ATF1	chr16:76687134-76687664	K562	blood:	n/a	n/a
7	ATF1	chr16:76789952-76789998	K562	blood:	n/a	n/a
8	ATF2	chr16:77010103-77010377	GM12878	blood:	n/a	n/a
9	ATF2	chr16:76839037-76839302	GM12878	blood:	n/a	n/a
10	ATF3	chr16:76980774-76981124	K562	blood:	n/a	n/a
11	ATF3	chr16:76980737-76981284	A549	lung:	n/a	n/a
12	ATF3	chr16:76687346-76687640	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr16:77003970-77004466	A549	lung:	n/a	n/a
14	ATF3	chr16:76980721-76981225	A549	lung:	n/a	n/a
15	BACH1	chr16:76980722-76981230	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr16:76703299-76703491	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr16:76980807-76981126	K562	blood:	n/a	n/a
18	BACH1	chr16:77057336-77057341	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr16:76850471-76850665	GM12878	blood:	n/a	chr16:76850562-76850573
20	BATF	chr16:76966490-76966773	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
21	BATF	chr16:76850433-76850727	GM12878	blood:	n/a	chr16:76850562-76850573
22	BATF	chr16:76856327-76856649	GM12878	blood:	n/a	n/a
23	BATF	chr16:76856386-76856604	GM12878	blood:	n/a	n/a
24	BATF	chr16:76980823-76981049	GM12878	blood:	n/a	chr16:76980965-76980976
25	BATF	chr16:76838975-76839411	GM12878	blood:	n/a	n/a
26	BATF	chr16:76966506-76966724	GM12878	blood:	n/a	chr16:76966611-76966622 chr16:76966612-76966622
27	BATF	chr16:76838952-76839361	GM12878	blood:	n/a	n/a
28	BATF	chr16:76980831-76981097	GM12878	blood:	n/a	chr16:76980965-76980976
29	BCL11A	chr16:77010106-77010349	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:76839015-76839347	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
31	BCL11A	chr16:76839121-76839299	GM12878	blood:	n/a	chr16:76839215-76839224 chr16:76839226-76839235
32	BCL3	chr16:76980667-76981333	A549	lung:	n/a	n/a
33	BHLHE40	chr16:76981970-76981973	HepG2	liver:	n/a	n/a
34	BHLHE40	chr16:76980800-76981182	K562	blood:	n/a	n/a
35	BHLHE40	chr16:76968723-76968754	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:76937293-76937310	HepG2	liver:	n/a	n/a
37	BHLHE40	chr16:76704362-76704737	K562	blood:	n/a	chr16:76704597-76704606
38	BRCA1	chr16:77146758-77147111	Hela-S3	cervix:	n/a	n/a
39	CCNT2	chr16:76980827-76981168	K562	blood:	n/a	n/a
40	CEBPB	chr16:76777685-76778008	A549	lung:	n/a	chr16:76777865-76777876
41	CEBPB	chr16:76944923-76945036	K562	blood:	n/a	n/a
42	CEBPB	chr16:77117695-77117820	K562	blood:	n/a	chr16:77117765-77117776
43	CEBPB	chr16:76980741-76981163	A549	lung:	n/a	chr16:76980793-76980804
44	CEBPB	chr16:76734183-76734406	K562	blood:	n/a	n/a
45	CEBPB	chr16:76825079-76825413	HepG2	liver:	n/a	chr16:76825240-76825251
46	CEBPB	chr16:76946769-76947111	A549	lung:	n/a	chr16:76946917-76946930 chr16:76946917-76946930 chr16:76946918-76946929
47	CEBPB	chr16:77117642-77117884	HepG2	liver:	n/a	chr16:77117765-77117776
48	CEBPB	chr16:76921714-76921937	H1-hESC	embryonic stem cell:	n/a	chr16:76921782-76921793
49	CEBPB	chr16:77127191-77127532	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr16:77127169-77127545	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:76708064-76708114	NT2-D1	testis:	n/a
2	chr16:76708064-76708114	HNPCEpiC	eye:	n/a
3	chr16:76708064-76708114	AG09319	gingival:	n/a
4	chr16:77103259-77103309	MCF10A-Er-Src	breast:	n/a
5	chr16:77098093-77098143	HCPEpiC	choroid plexus:	n/a
6	chr16:76708064-76708114	AG10803	skin:	n/a
7	chr16:76708064-76708114	HUVEC	blood vessel:	n/a
8	chr16:77103259-77103309	NH-A	brain:	n/a
9	chr16:77103259-77103309	HUVEC	blood vessel:	n/a
10	chr16:77098093-77098143	NH-A	brain:	n/a
11	chr16:77098093-77098143	U87	brain:	n/a
12	chr16:77098093-77098143	Hela-S3	cervix:	n/a
13	chr16:77103259-77103309	U87	brain:	n/a
14	chr16:76708064-76708114	BJ	skin:	n/a
15	chr16:77098093-77098143	CMK	blood:	n/a
16	chr16:77103259-77103309	ProgFib	skin:	n/a
17	chr16:77103259-77103309	HepG2	liver:	n/a
18	chr16:77103259-77103309	SK-N-MC	brain:	n/a
19	chr16:76708064-76708114	HepG2	liver:	n/a
20	chr16:77103259-77103309	NT2-D1	testis:	n/a
21	chr16:77098093-77098143	SK-N-MC	brain:	n/a
22	chr16:77103259-77103309	Caco-2	colon:	n/a
23	chr16:76708064-76708114	SK-N-SH	brain:	n/a
24	chr16:76708064-76708114	Caco-2	colon:	n/a
25	chr16:77098093-77098143	PrEC	prostate:	n/a
26	chr16:77098093-77098143	AG04450	lung:	fetal
27	chr16:77098093-77098143	HIPEpiC	eye:	n/a
28	chr16:76708064-76708114	SKMC	muscle:	n/a
29	chr16:77103259-77103309	HEEpiC	esophagus:	n/a
30	chr16:77103259-77103309	LNCaP	prostate:	n/a
31	chr16:77098093-77098143	PFSK-1	brain:	n/a
32	chr16:76708064-76708114	RPTEC	kidney:	n/a
33	chr16:76708064-76708114	LNCaP	prostate:	n/a
34	chr16:76708064-76708114	Jurkat	blood:	n/a
35	chr16:77098093-77098143	HepG2	liver:	n/a
36	chr16:76708064-76708114	Hela-S3	cervix:	n/a
37	chr16:76708064-76708114	AG09309	skin:	n/a
38	chr16:76708064-76708114	HCF	heart:	n/a
39	chr16:76708064-76708114	NHBE	bronchial:	n/a
40	chr16:77098093-77098143	MCF-7	breast:	n/a
41	chr16:77098093-77098143	HRPEpiC	eye:	n/a
42	chr16:77098093-77098143	HMEC	breast:	n/a
43	chr16:76708064-76708114	MCF-7	breast:	n/a
44	chr16:77098093-77098143	Hepatocyte	liver:	n/a
45	chr16:77103259-77103309	CMK	blood:	n/a
46	chr16:77103259-77103309	IMR90	lung:	fetal
47	chr16:77103259-77103309	AoSMC	blood vessel:	n/a
48	chr16:77103259-77103309	HMEC	breast:	n/a
49	chr16:77103259-77103309	PANC-1	pancreas:	n/a
50	chr16:77103259-77103309	AG04449	skin:	fetal

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:76887924..76888465-chr16:77203271..77204023,2	MCF-7	breast:
2	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
3	chr16:76312246..76313469-chr16:76687103..76688657,6	MCF-7	breast:
4	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
5	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
6	chr16:77092274..77095002-chr16:77096388..77098456,2	MCF-7	breast:
7	chr16:75835108..75835786-chr16:76687075..76687822,2	MCF-7	breast:
8	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
9	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
10	chr16:76319924..76320753-chr16:76686923..76687617,2	MCF-7	breast:
11	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
12	chr16:76687235..76688893-chr16:76692839..76694713,2	K562	blood:
13	chr16:76878928..76880909-chr16:76882753..76884640,2	K562	blood:
14	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
15	chr16:76972133..76974493-chr16:76974679..76976840,2	MCF-7	breast:
16	chr16:76844876..76847420-chr19:45599129..45600971,2	MCF-7	breast:
17	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
18	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
19	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
20	chr16:76773881..76775450-chr16:76881262..76882791,2	MCF-7	breast:
21	chr16:76747877..76750802-chr16:76754682..76756382,2	K562	blood:
22	chr16:77078662..77079429-chr16:77203303..77204211,3	MCF-7	breast:
23	chr16:75834944..75835823-chr16:76687371..76688062,3	MCF-7	breast:
24	chr16:76887896..76888842-chr16:77076469..77077719,11	MCF-7	breast:
25	chr16:76756661..76759781-chr16:76761311..76764642,3	K562	blood:
26	chr16:76699506..76700441-chr16:77205329..77206242,3	MCF-7	breast:
27	chr16:77117943..77120097-chr16:77124904..77127006,2	MCF-7	breast:
28	chr16:76784883..76787638-chr16:76787899..76789936,2	MCF-7	breast:
29	chr16:76699516..76700310-chr16:77203606..77204151,2	MCF-7	breast:
30	chr16:76887896..76888842-chr16:77076469..77077719,11	MCF-7	breast:
31	chr16:76741969..76744727-chr16:76747101..76748627,2	K562	blood:
32	chr16:76846196..76848121-chr16:76848521..76851117,2	MCF-7	breast:
33	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
34	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
35	chr16:76886880..76887748-chr16:77077328..77078325,2	MCF-7	breast:
36	chr16:76701550..76704283-chr16:76707898..76709517,2	K562	blood:
37	chr16:76669652..76671358-chr16:76701917..76703611,2	K562	blood:
38	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
39	chr16:76881611..76883954-chr16:76887729..76889678,2	MCF-7	breast:
40	chr16:77044641..77046687-chr16:77049304..77051697,2	K562	blood:
41	chr16:77092274..77095002-chr16:77096388..77098456,2	MCF-7	breast:
42	chr16:77059610..77062396-chr16:77260233..77262257,2	K562	blood:
43	chr16:77129914..77131450-chr16:77133881..77136315,2	K562	blood:
44	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:
45	chr16:76741499..76743675-chr16:76746368..76748815,2	K562	blood:
46	chr16:76687186..76688106-chr16:76857078..76857671,2	MCF-7	breast:
47	chr16:76817240..76820216-chr16:76820936..76823507,2	K562	blood:
48	chr16:76699528..76700343-chr16:77076632..77077627,2	MCF-7	breast:
49	chr16:76703589..76705752-chr16:76708591..76711050,2	MCF-7	breast:
50	chr16:76856883..76857419-chr16:77076804..77077643,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-58C22.1.1-4	chr16:76961793-76962066	ENSG00000259995.1
2	lnc-ADAMTS18-2	chr16:77028205-77028433	XLOC_012014
3	lnc-RP11-58C22.1.1-3	chr16:76803213-76803278	XLOC_011793
4	lnc-RP11-58C22.1.1-1	chr16:76689454-76689561	ENSG00000250514
5	lnc-RP11-58C22.1.1-3	chr16:76806570-76806959	XLOC_011793
6	lnc-RP11-58C22.1.1-4	chr16:76770239-76770376	ENSG00000259995.1
7	lnc-RP11-58C22.1.1-1	chr16:76690565-76692375	ENSG00000250514
8	lnc-ADAMTS18-8	chr16:76912171-76912833	NONHSAT143788
9	lnc-RP11-58C22.1.1-2	chr16:76733678-76734033	XLOC_011792
10	lnc-MON1B-2	chr16:77118307-77118365	NONHSAT143790
11	lnc-RP11-58C22.1.1-4	chr16:76946252-76946305	ENSG00000259995.1
12	lnc-ADAMTS18-2	chr16:77042061-77042204	XLOC_012014
13	lnc-RP11-58C22.1.1-2	chr16:76737141-76737172	XLOC_011792

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

No data

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

Extended variants
information (count: 12787 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:12787 , 50 per page) page: 1 2 3 4 5 6 7 ... 256

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34113077	chr16:76684422-76684423	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs547468150	chr16:76684451-76684452	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184382491	chr16:76684497-76684498	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs371740229	chr16:76684536-76684537	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs532293591	chr16:76684562-76684563	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147992050	chr16:76684584-76684585	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs568743695	chr16:76684587-76684588	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs571570637	chr16:76684636-76684637	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548310876	chr16:76684641-76684642	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568052694	chr16:76684652-76684653	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534053241	chr16:76684678-76684679	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187685758	chr16:76684681-76684682	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553492121	chr16:76684708-76684709	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553365852	chr16:76684710-76684711	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191261873	chr16:76684719-76684720	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549247091	chr16:76684726-76684727	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566045968	chr16:76684747-76684748	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540158392	chr16:76684757-76684758	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556873220	chr16:76684768-76684769	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535992303	chr16:76684819-76684820	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576743468	chr16:76684826-76684827	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141627689	chr16:76684834-76684835	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369292607	chr16:76684846-76684847	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562254578	chr16:76684873-76684874	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373181948	chr16:76684888-76684889	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572448598	chr16:76684893-76684894	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555570247	chr16:76684913-76684914	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150596234	chr16:76684960-76684961	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564347530	chr16:76684980-76684981	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557690860	chr16:76684987-76684988	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184123505	chr16:76685062-76685063	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188473967	chr16:76685087-76685088	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562433855	chr16:76685091-76685092	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181615541	chr16:76685109-76685110	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548086405	chr16:76685147-76685148	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568206013	chr16:76685150-76685151	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185156317	chr16:76685154-76685155	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547440851	chr16:76685182-76685183	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138635211	chr16:76685208-76685209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539422978	chr16:76685251-76685252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575290852	chr16:76685265-76685266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140256395	chr16:76685276-76685277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76586486	chr16:76685288-76685289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7205389	chr16:76685292-76685293	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141761399	chr16:76685328-76685329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77219805	chr16:76685397-76685398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543471122	chr16:76686601-76686602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146088107	chr16:76686634-76686635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573950035	chr16:76686683-76686684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190014914	chr16:76686690-76686691	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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	20164919	CNVD
Neuroblastoma	18923524	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20581869	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:76684400-76685200	Flanking Active TSS	A549	lung
2	chr16:76684600-76685200	Enhancers	HepG2	liver
3	chr16:76685200-76685400	Enhancers	A549	lung
4	chr16:76686600-76687000	Enhancers	Fetal Brain Male	brain
5	chr16:76687200-76687800	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr16:76687200-76688000	Enhancers	Brain Substantia Nigra	brain
7	chr16:76687200-76688200	Enhancers	Fetal Lung	lung
8	chr16:76687600-76688200	Enhancers	Brain Hippocampus Middle	brain
9	chr16:76687600-76689600	Enhancers	Brain Germinal Matrix	brain
10	chr16:76688200-76690600	Weak transcription	Fetal Lung	lung
11	chr16:76689600-76690400	Weak transcription	Brain Germinal Matrix	brain
12	chr16:76690000-76692000	Enhancers	Primary hematopoietic stem cells	blood
13	chr16:76690400-76692000	Enhancers	Brain Germinal Matrix	brain
14	chr16:76690600-76691800	Enhancers	Fetal Lung	lung
15	chr16:76690600-76692000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr16:76690600-76692000	Enhancers	Fetal Muscle Leg	muscle
17	chr16:76691400-76692000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr16:76692000-76694600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr16:76693400-76694000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr16:76694000-76699400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr16:76694600-76696400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr16:76695000-76696200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr16:76696600-76714800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr16:76699400-76699600	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr16:76699600-76704000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr16:76699800-76700400	Enhancers	Primary hematopoietic stem cells	blood
27	chr16:76700400-76703200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr16:76703200-76703400	Active TSS	Primary hematopoietic stem cells	blood
29	chr16:76703400-76703600	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr16:76703600-76704600	Enhancers	Primary hematopoietic stem cells	blood
31	chr16:76703800-76704800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr16:76704000-76705200	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr16:76704800-76709400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr16:76707400-76708200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr16:76707600-76708000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr16:76708000-76709800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr16:76708000-76710800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr16:76708200-76710200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr16:76708600-76711400	Enhancers	Placenta Amnion	Placenta Amnion
40	chr16:76708800-76709000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr16:76708800-76709600	Enhancers	Fetal Lung	lung
42	chr16:76708800-76710800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr16:76709000-76710200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr16:76709200-76711200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:76709200-76711400	Enhancers	HMEC	breast
46	chr16:76709400-76711000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr16:76709400-76711400	Enhancers	Placenta	Placenta
48	chr16:76709800-76710600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr16:76710000-76710800	Enhancers	H9 Cell Line	embryonic stem cell
50	chr16:76710200-76710800	Enhancers	HUES48 Cell Line	embryonic stem cell

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