Variant report

Variant	nsv906958
Chromosome Location	chr16:77535643-77684529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1010)
CpG islands
(count:62)
Chromatin interactive
region (count:105)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:77618132-77618516	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:77590057-77590105	HepG2	liver:	n/a	n/a
3	BACH1	chr16:77619774-77620152	H1-hESC	embryonic stem cell:	n/a	chr16:77619957-77619971
4	BATF	chr16:77548515-77548734	GM12878	blood:	n/a	n/a
5	BATF	chr16:77619799-77620106	GM12878	blood:	n/a	chr16:77619932-77619942 chr16:77619960-77619971 chr16:77619961-77619971 chr16:77619931-77619942
6	BATF	chr16:77548505-77548705	GM12878	blood:	n/a	n/a
7	BCL3	chr16:77613148-77613482	GM12878	blood:	n/a	n/a
8	BCL3	chr16:77565743-77566001	GM12878	blood:	n/a	n/a
9	BHLHE40	chr16:77624625-77624932	HepG2	liver:	n/a	n/a
10	BHLHE40	chr16:77590052-77590574	HepG2	liver:	n/a	n/a
11	BHLHE40	chr16:77590106-77590357	K562	blood:	n/a	n/a
12	BHLHE40	chr16:77590168-77590439	HepG2	liver:	n/a	n/a
13	CEBPB	chr16:77542747-77542998	HepG2	liver:	n/a	chr16:77542880-77542893 chr16:77542866-77542877
14	CEBPB	chr16:77624733-77625007	HepG2	liver:	n/a	chr16:77624969-77624982 chr16:77624971-77624982 chr16:77624971-77624982 chr16:77624969-77624982
15	CEBPB	chr16:77549051-77549315	MCF-7	breast:	n/a	chr16:77549193-77549206
16	CEBPB	chr16:77558423-77558588	HepG2	liver:	n/a	n/a
17	CEBPB	chr16:77618080-77618468	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr16:77617936-77618536	MCF-7	breast:	n/a	n/a
19	CEBPB	chr16:77618068-77618437	IMR90	lung:	n/a	n/a
20	CEBPB	chr16:77637609-77638332	MCF-7	breast:	n/a	n/a
21	CEBPB	chr16:77583993-77584208	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr16:77618018-77618491	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr16:77613171-77613516	HepG2	liver:	n/a	n/a
24	CEBPB	chr16:77618087-77618501	A549	lung:	n/a	n/a
25	CEBPB	chr16:77652445-77652591	HepG2	liver:	n/a	chr16:77652544-77652555 chr16:77652545-77652556 chr16:77652544-77652557
26	CEBPB	chr16:77538187-77538370	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr16:77617985-77618528	MCF-7	breast:	n/a	n/a
28	CEBPB	chr16:77618049-77618479	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr16:77618096-77618481	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr16:77618081-77618407	K562	blood:	n/a	n/a
31	CEBPB	chr16:77624671-77624921	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr16:77618083-77618424	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:77644103-77644378	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:77618065-77618466	A549	lung:	n/a	n/a
35	CEBPB	chr16:77629511-77629666	A549	lung:	n/a	n/a
36	CEBPB	chr16:77604931-77604998	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:77644123-77644405	A549	lung:	n/a	n/a
38	CEBPB	chr16:77637633-77638369	MCF-7	breast:	n/a	n/a
39	CEBPB	chr16:77590213-77590586	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:77618188-77618339	HepG2	liver:	n/a	n/a
41	CEBPB	chr16:77559605-77559709	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:77613074-77613723	A549	lung:	n/a	n/a
43	CEBPB	chr16:77618090-77618425	K562	blood:	n/a	n/a
44	CEBPB	chr16:77590258-77590384	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:77629555-77629771	HepG2	liver:	n/a	chr16:77629667-77629676 chr16:77629665-77629676
46	CEBPB	chr16:77629518-77629792	IMR90	lung:	n/a	chr16:77629667-77629676 chr16:77629665-77629676
47	CEBPB	chr16:77619313-77619368	IMR90	lung:	n/a	n/a
48	CEBPB	chr16:77618085-77618563	A549	lung:	n/a	n/a
49	CEBPB	chr16:77570031-77570185	HepG2	liver:	n/a	chr16:77570134-77570145
50	CEBPB	chr16:77613157-77613574	A549	lung:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:77574072-77574122	AG10803	skin:	n/a
2	chr16:77574072-77574122	AG10803	skin:	n/a
3	chr16:77574072-77574122	HIPEpiC	eye:	n/a
4	chr16:77574072-77574122	MCF10A-Er-Src	breast:	n/a
5	chr16:77574072-77574122	HPAEpiC	pulmonary alveolar:	n/a
6	chr16:77574072-77574122	NT2-D1	testis:	n/a
7	chr16:77574072-77574122	HCT-116	colon:	n/a
8	chr16:77574072-77574122	HCPEpiC	choroid plexus:	n/a
9	chr16:77574072-77574122	SK-N-MC	brain:	n/a
10	chr16:77574072-77574122	BE2_C	brain:	n/a
11	chr16:77574072-77574122	AG04449	skin:	fetal
12	chr16:77574072-77574122	HAEpiC	amniotic membrane:	n/a
13	chr16:77574072-77574122	NB4	blood:	n/a
14	chr16:77574072-77574122	HL-60	blood:	n/a
15	chr16:77574072-77574122	AG09309	skin:	n/a
16	chr16:77574072-77574122	ProgFib	skin:	n/a
17	chr16:77574072-77574122	NHDF-neo	bronchial:	n/a
18	chr16:77574072-77574122	HEEpiC	esophagus:	n/a
19	chr16:77574072-77574122	NHBE	bronchial:	n/a
20	chr16:77574072-77574122	ECC-1	luminal epithelium:	n/a
21	chr16:77574072-77574122	GM12878	blood:	n/a
22	chr16:77574072-77574122	H1-hESC	embryonic stem cell:	embryo
23	chr16:77574072-77574122	HUVEC	blood vessel:	n/a
24	chr16:77574072-77574122	GM12892	blood:	n/a
25	chr16:77574072-77574122	PFSK-1	brain:	n/a
26	chr16:77574072-77574122	T-47D	breast:	n/a
27	chr16:77574072-77574122	HRCEpiC	kidney:	n/a
28	chr16:77574072-77574122	HCF	heart:	n/a
29	chr16:77574072-77574122	HEK293	kidney:	embryo
30	chr16:77574072-77574122	Caco-2	colon:	n/a
31	chr16:77574072-77574122	U87	brain:	n/a
32	chr16:77574072-77574122	BJ	skin:	n/a
33	chr16:77574072-77574122	SKMC	muscle:	n/a
34	chr16:77574072-77574122	PANC-1	pancreas:	n/a
35	chr16:77574072-77574122	AG04450	lung:	fetal
36	chr16:77574072-77574122	HepG2	liver:	n/a
37	chr16:77574072-77574122	ovcar-3	ovarian:	n/a
38	chr16:77574072-77574122	GM19239	blood:	n/a
39	chr16:77574072-77574122	GM06990	blood:	n/a
40	chr16:77574072-77574122	RPTEC	kidney:	n/a
41	chr16:77574072-77574122	HMEC	breast:	n/a
42	chr16:77574072-77574122	HCM	heart:	n/a
43	chr16:77574072-77574122	SK-N-SH_RA	brain:	n/a
44	chr16:77574072-77574122	Hela-S3	cervix:	n/a
45	chr16:77574072-77574122	K562	blood:	n/a
46	chr16:77574072-77574122	PrEC	prostate:	n/a
47	chr16:77574072-77574122	MCF-7	breast:	n/a
48	chr16:77574072-77574122	NH-A	brain:	n/a
49	chr16:77574072-77574122	IMR90	lung:	fetal
50	chr16:77574072-77574122	SAEC	small airway:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:77270739..77273458-chr16:77636094..77637749,2	MCF-7	breast:
2	chr16:77632750..77638052-chr16:77677805..77683228,7	MCF-7	breast:
3	chr16:77244991..77247286-chr16:77635984..77637881,2	MCF-7	breast:
4	chr16:77617063..77620231-chr16:77635961..77639482,4	MCF-7	breast:
5	chr16:77635739..77638106-chr16:78082889..78086047,4	MCF-7	breast:
6	chr16:77471559..77472162-chr16:77617897..77618748,2	MCF-7	breast:
7	chr16:77678330..77681247-chr16:77683040..77686814,3	K562	blood:
8	chr16:77666135..77671025-chr16:77671164..77674266,4	K562	blood:
9	chr16:77618149..77620811-chr16:77638039..77640626,2	MCF-7	breast:
10	chr16:77633668..77634317-chr16:77827464..77828066,2	K562	blood:
11	chr16:77627298..77629189-chr16:77688223..77690020,2	MCF-7	breast:
12	chr16:77269442..77270538-chr16:77616365..77617604,8	MCF-7	breast:
13	chr16:77633402..77634464-chr16:77694120..77694942,5	MCF-7	breast:
14	chr16:77531888..77534312-chr16:77536499..77538354,2	K562	blood:
15	chr16:77619452..77621182-chr16:77622487..77625423,2	MCF-7	breast:
16	chr16:77634214..77636366-chr16:77646332..77647931,2	MCF-7	breast:
17	chr16:77621448..77623074-chr16:77623868..77626822,2	MCF-7	breast:
18	chr16:77635631..77639665-chr16:78082151..78086401,6	MCF-7	breast:
19	chr16:77652245..77655116-chr16:77670753..77672397,2	MCF-7	breast:
20	chr16:77634214..77636366-chr16:77646332..77647931,2	MCF-7	breast:
21	chr16:77636182..77638707-chr16:77703957..77706105,3	MCF-7	breast:
22	chr16:77635946..77638059-chr16:77690308..77692551,2	MCF-7	breast:
23	chr16:77672608..77676304-chr16:77676785..77680142,3	MCF-7	breast:
24	chr16:77637560..77638380-chr16:77708753..77709733,3	MCF-7	breast:
25	chr16:77627723..77631345-chr16:77632470..77634432,3	MCF-7	breast:
26	chr16:77545100..77546949-chr16:77551989..77554470,2	MCF-7	breast:
27	chr16:77542643..77546674-chr16:77547761..77549967,3	K562	blood:
28	chr16:77631425..77634877-chr16:77636805..77640283,4	MCF-7	breast:
29	chr16:77622459..77625433-chr16:77633946..77636644,2	MCF-7	breast:
30	chr16:77614257..77616100-chr16:77616427..77619291,2	MCF-7	breast:
31	chr16:77675283..77677201-chr16:77679287..77681153,2	MCF-7	breast:
32	chr16:77619040..77621294-chr16:77626377..77629005,2	MCF-7	breast:
33	chr16:77657528..77659608-chr16:77662783..77664358,2	MCF-7	breast:
34	chr16:77626884..77631201-chr16:77634780..77638487,6	MCF-7	breast:
35	chr16:77619040..77621294-chr16:77626377..77629005,2	MCF-7	breast:
36	chr16:77587001..77589429-chr16:77614448..77616263,2	K562	blood:
37	chr16:77634889..77635492-chr16:78005438..78006098,2	MCF-7	breast:
38	chr16:77542643..77546674-chr16:77547761..77549967,3	K562	blood:
39	chr16:77678330..77681247-chr16:77683040..77686814,3	K562	blood:
40	chr16:77633435..77634605-chr16:77694012..77694839,5	MCF-7	breast:
41	chr16:77638698..77640543-chr16:78082140..78085063,3	MCF-7	breast:
42	chr16:77614257..77616100-chr16:77616427..77619291,2	MCF-7	breast:
43	chr16:77619466..77621855-chr16:77621914..77626371,4	MCF-7	breast:
44	chr16:77672608..77676304-chr16:77676785..77680142,3	MCF-7	breast:
45	chr16:77667748..77670064-chr16:77674734..77677404,2	MCF-7	breast:
46	chr16:77619730..77621519-chr16:77627821..77630581,2	MCF-7	breast:
47	chr16:77269705..77270364-chr16:77617639..77618395,2	MCF-7	breast:
48	chr16:77638173..77640324-chr16:78132312..78134748,3	MCF-7	breast:
49	chr16:77644345..77646917-chr16:77647534..77649296,2	MCF-7	breast:
50	chr16:77598841..77600943-chr16:77604716..77607641,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT7-2	chr16:77632982-77633140	ENSG00000261154.1
2	lnc-NUDT7-2	chr16:77644434-77644578	ENSG00000261154.1
3	lnc-NUDT7-2	chr16:77624703-77624817	ENSG00000261154.1

No data

Variant related genes	Relation type
ENSG00000261154	TF binding region
ENSG00000261154	CpG island
ENSG00000260731	chromatin interactions
ENSG00000205078	chromatin interactions
ENSG00000260922	chromatin interactions
ENSG00000261154	chromatin interactions
ENSG00000186153	chromatin interactions

Extended variants
information (count: 4960 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4960 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10514418	chr16:77535643-77535644	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568050753	chr16:77535650-77535651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530068538	chr16:77535658-77535659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540639581	chr16:77535660-77535661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116630120	chr16:77535678-77535679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532738115	chr16:77535719-77535720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552713887	chr16:77535721-77535722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12149270	chr16:77535745-77535746	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567374340	chr16:77535753-77535754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531800357	chr16:77535764-77535765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12149272	chr16:77535775-77535776	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs567821466	chr16:77535781-77535782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79713003	chr16:77535782-77535783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553529099	chr16:77535786-77535787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570723909	chr16:77535857-77535858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539380358	chr16:77535860-77535861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556308645	chr16:77535869-77535870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182670300	chr16:77535877-77535878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs8056964	chr16:77535882-77535883	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555058955	chr16:77535934-77535935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs66758255	chr16:77535940-77535941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540627091	chr16:77535956-77535957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560311442	chr16:77535957-77535958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143660215	chr16:77535983-77535984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370094938	chr16:77535984-77535985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563220819	chr16:77536044-77536045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9921323	chr16:77536078-77536079	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs549077272	chr16:77536092-77536093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs16945784	chr16:77536105-77536106	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs527433512	chr16:77536118-77536119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547349380	chr16:77536130-77536131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570387062	chr16:77536237-77536238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9921487	chr16:77536259-77536260	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs9928437	chr16:77536293-77536294	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs574815154	chr16:77536327-77536328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569975059	chr16:77536338-77536339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574943657	chr16:77536358-77536359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188062392	chr16:77536372-77536373	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555646847	chr16:77536399-77536400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116740118	chr16:77536408-77536409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540763075	chr16:77536422-77536423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149380214	chr16:77536427-77536428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552841473	chr16:77536445-77536446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563646809	chr16:77536484-77536485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577133099	chr16:77536497-77536498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546185666	chr16:77536500-77536501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1389521	chr16:77536529-77536530	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs576371980	chr16:77536588-77536589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542016887	chr16:77536641-77536642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546219328	chr16:77536672-77536673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:77532800-77536200	Enhancers	Adipose Nuclei	Adipose
2	chr16:77532800-77536200	Enhancers	Ovary	ovary
3	chr16:77533000-77536200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr16:77533200-77536000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr16:77533400-77535800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr16:77533400-77536000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr16:77533600-77537200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr16:77533600-77537400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr16:77533600-77537600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr16:77533800-77536000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr16:77533800-77536200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr16:77534000-77536000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr16:77534200-77536200	Enhancers	Fetal Kidney	kidney
14	chr16:77534600-77535800	Weak transcription	Fetal Lung	lung
15	chr16:77535200-77536000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr16:77535200-77536200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr16:77535200-77536800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr16:77535600-77535800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr16:77535600-77537000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr16:77536000-77536200	Enhancers	Fetal Lung	lung
21	chr16:77536000-77537000	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr16:77536000-77537000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr16:77536000-77537000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr16:77536200-77536600	Weak transcription	Fetal Kidney	kidney
25	chr16:77536600-77537400	Enhancers	Fetal Kidney	kidney
26	chr16:77537000-77537200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr16:77537000-77537200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr16:77537000-77537200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr16:77537000-77537400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr16:77537200-77537400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:77537400-77543800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr16:77537400-77543800	Weak transcription	Fetal Kidney	kidney
33	chr16:77543400-77544200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr16:77543400-77544600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr16:77543600-77544000	Active TSS	Brain Anterior Caudate	brain
36	chr16:77543600-77544000	Enhancers	Brain Substantia Nigra	brain
37	chr16:77543600-77544200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr16:77543600-77544200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr16:77543600-77544400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr16:77543600-77544600	Enhancers	Brain Germinal Matrix	brain
41	chr16:77543600-77545400	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr16:77543800-77544000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr16:77543800-77544000	Enhancers	Fetal Kidney	kidney
44	chr16:77543800-77544200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr16:77543800-77544400	Enhancers	Brain Cingulate Gyrus	brain
46	chr16:77543800-77544600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr16:77544000-77544200	Weak transcription	Brain Anterior Caudate	brain
48	chr16:77544000-77545200	Weak transcription	Brain Substantia Nigra	brain
49	chr16:77544200-77544800	Enhancers	Brain Hippocampus Middle	brain
50	chr16:77544200-77545000	Enhancers	Brain Anterior Caudate	brain

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