Variant report

Variant	esv2752152
Chromosome Location	chr7:16863727-16946225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:656)
CpG islands
(count:1040)
Chromatin interactive
region (count:62)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16886912-16887247	HepG2	liver:	n/a	n/a
2	ATF1	chr7:16920513-16920521	K562	blood:	n/a	n/a
3	ATF1	chr7:16938123-16938126	K562	blood:	n/a	n/a
4	ATF3	chr7:16886801-16887449	A549	lung:	n/a	n/a
5	ATF3	chr7:16886770-16887562	A549	lung:	n/a	n/a
6	ATF3	chr7:16944740-16945401	A549	lung:	n/a	n/a
7	BCL3	chr7:16944794-16945427	A549	lung:	n/a	n/a
8	BCL3	chr7:16886665-16887601	A549	lung:	n/a	n/a
9	BCL3	chr7:16944766-16945589	A549	lung:	n/a	n/a
10	BCL3	chr7:16886626-16887591	A549	lung:	n/a	n/a
11	BRCA1	chr7:16886387-16887480	Hela-S3	cervix:	n/a	chr7:16886665-16886672
12	CEBPB	chr7:16895239-16895386	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:16939841-16940183	HepG2	liver:	n/a	chr7:16940012-16940023
14	CEBPB	chr7:16939879-16940162	K562	blood:	n/a	chr7:16940012-16940023
15	CEBPB	chr7:16886971-16887172	K562	blood:	n/a	chr7:16887030-16887041
16	CEBPB	chr7:16934284-16934399	A549	lung:	n/a	n/a
17	CEBPB	chr7:16939849-16940196	A549	lung:	n/a	chr7:16940012-16940023
18	CEBPB	chr7:16886263-16887556	MCF-7	breast:	n/a	chr7:16887030-16887041
19	CEBPB	chr7:16903709-16903939	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:16886566-16887551	A549	lung:	n/a	chr7:16887030-16887041
21	CEBPB	chr7:16886822-16887457	A549	lung:	n/a	chr7:16887030-16887041
22	CEBPB	chr7:16939862-16940157	H1-hESC	embryonic stem cell:	n/a	chr7:16940012-16940023
23	CEBPB	chr7:16939825-16940248	MCF-7	breast:	n/a	chr7:16940012-16940023
24	CEBPB	chr7:16886843-16887410	A549	lung:	n/a	chr7:16887030-16887041
25	CEBPB	chr7:16939841-16940168	IMR90	lung:	n/a	chr7:16940012-16940023
26	CEBPB	chr7:16934273-16934451	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:16886171-16887513	MCF-7	breast:	n/a	chr7:16887030-16887041
28	CEBPB	chr7:16944788-16945468	A549	lung:	n/a	n/a
29	CEBPB	chr7:16886925-16887186	IMR90	lung:	n/a	chr7:16887030-16887041
30	CEBPB	chr7:16939900-16940158	Hela-S3	cervix:	n/a	chr7:16940012-16940023
31	CEBPB	chr7:16895188-16895415	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:16886195-16887591	Hela-S3	cervix:	n/a	chr7:16887030-16887041
33	CEBPB	chr7:16886891-16887218	HepG2	liver:	n/a	chr7:16887030-16887041
34	CHD2	chr7:16886926-16887519	Hela-S3	cervix:	n/a	n/a
35	CREB1	chr7:16886905-16887254	A549	lung:	n/a	n/a
36	CREB1	chr7:16886947-16887300	A549	lung:	n/a	n/a
37	CTCF	chr7:16890880-16891030	HRE	kidney:	n/a	chr7:16890893-16890906 chr7:16891017-16891030
38	CTCF	chr7:16931080-16931230	GM12865	blood:	n/a	chr7:16931142-16931163
39	CTCF	chr7:16930946-16931354	GM12878	blood:	n/a	chr7:16931142-16931163
40	CTCF	chr7:16931040-16931190	GM12878	blood:	n/a	chr7:16931142-16931163
41	CTCF	chr7:16881640-16881790	AG04449	skin:	n/a	n/a
42	CTCF	chr7:16930942-16931341	IMR90	lung:	n/a	chr7:16931142-16931163
43	CTCF	chr7:16931023-16931269	NHEK	skin:	n/a	chr7:16931142-16931163
44	CTCF	chr7:16931080-16931230	NHDF-neo	bronchial:	n/a	chr7:16931142-16931163
45	CTCF	chr7:16931780-16931930	NHEK	skin:	n/a	n/a
46	CTCF	chr7:16930851-16931444	SK-N-SH	brain:	n/a	chr7:16931142-16931163
47	CTCF	chr7:16930897-16931342	A549	lung:	n/a	chr7:16931142-16931163
48	CTCF	chr7:16931025-16931262	LNCaP	prostate:	n/a	chr7:16931142-16931163
49	CTCF	chr7:16931000-16931290	BE2_C	brain:	n/a	chr7:16931142-16931163
50	CTCF	chr7:16931080-16931230	GM12864	blood:	n/a	chr7:16931142-16931163

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16945442-16945492	GM12891	blood:	n/a
2	chr7:16945442-16945492	AG04450	lung:	fetal
3	chr7:16890431-16890481	A549	lung:	n/a
4	chr7:16945442-16945492	GM12891	blood:	n/a
5	chr7:16945442-16945492	AG04450	lung:	fetal
6	chr7:16890431-16890481	A549	lung:	n/a
7	chr7:16890879-16890929	HEEpiC	esophagus:	n/a
8	chr7:16892988-16893038	Hepatocyte	liver:	n/a
9	chr7:16879330-16879380	HIPEpiC	eye:	n/a
10	chr7:16892988-16893038	AoSMC	blood vessel:	n/a
11	chr7:16890879-16890929	HCT-116	colon:	n/a
12	chr7:16921699-16921749	NHBE	bronchial:	n/a
13	chr7:16893769-16893819	PrEC	prostate:	n/a
14	chr7:16890769-16890819	H1-hESC	embryonic stem cell:	embryo
15	chr7:16922421-16922471	ProgFib	skin:	n/a
16	chr7:16892988-16893038	HepG2	liver:	n/a
17	chr7:16890973-16891023	Hela-S3	cervix:	n/a
18	chr7:16922421-16922471	HRE	kidney:	n/a
19	chr7:16921699-16921749	NHDF-neo	bronchial:	n/a
20	chr7:16921699-16921749	HCPEpiC	choroid plexus:	n/a
21	chr7:16892988-16893038	MCF-7	breast:	n/a
22	chr7:16891079-16891129	SAEC	small airway:	n/a
23	chr7:16891079-16891129	GM19239	blood:	n/a
24	chr7:16890769-16890819	SK-N-SH_RA	brain:	n/a
25	chr7:16890973-16891023	AG04449	skin:	fetal
26	chr7:16913845-16913895	RPTEC	kidney:	n/a
27	chr7:16879330-16879380	SK-N-SH	brain:	n/a
28	chr7:16890775-16890825	SK-N-MC	brain:	n/a
29	chr7:16891079-16891129	T-47D	breast:	n/a
30	chr7:16921699-16921749	GM06990	blood:	n/a
31	chr7:16890775-16890825	PFSK-1	brain:	n/a
32	chr7:16922326-16922376	HEK293	kidney:	embryo
33	chr7:16879330-16879380	HNPCEpiC	eye:	n/a
34	chr7:16890879-16890929	HCM	heart:	n/a
35	chr7:16887412-16887462	H1-hESC	embryonic stem cell:	embryo
36	chr7:16945442-16945492	BJ	skin:	n/a
37	chr7:16892988-16893038	AG09319	gingival:	n/a
38	chr7:16891079-16891129	HRPEpiC	eye:	n/a
39	chr7:16893769-16893819	PFSK-1	brain:	n/a
40	chr7:16887412-16887462	HEEpiC	esophagus:	n/a
41	chr7:16945442-16945492	HCPEpiC	choroid plexus:	n/a
42	chr7:16945442-16945492	AG10803	skin:	n/a
43	chr7:16890879-16890929	NHDF-neo	bronchial:	n/a
44	chr7:16890879-16890929	AG09309	skin:	n/a
45	chr7:16891079-16891129	RPTEC	kidney:	n/a
46	chr7:16890769-16890819	BJ	skin:	n/a
47	chr7:16922421-16922471	AG10803	skin:	n/a
48	chr7:16920271-16920321	HAEpiC	amniotic membrane:	n/a
49	chr7:16879330-16879380	HRCEpiC	kidney:	n/a
50	chr7:16922492-16922542	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:16852860..16855364-chr7:16884704..16887275,2	MCF-7	breast:
2	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
3	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
4	chr7:16944903..16947549-chr7:16951008..16952763,2	MCF-7	breast:
5	chr7:16847748..16852819-chr7:16884544..16888713,8	MCF-7	breast:
6	chr7:16944622..16945221-chr7:16961355..16961992,2	MCF-7	breast:
7	chr7:16882638..16888125-chr7:16917806..16922749,7	MCF-7	breast:
8	chr7:16862568..16864717-chr7:16882217..16883862,2	MCF-7	breast:
9	chr7:16892686..16894527-chr7:16894873..16896897,2	MCF-7	breast:
10	chr7:16882221..16884477-chr7:16885403..16887201,3	MCF-7	breast:
11	chr7:16929547..16932168-chr7:17718216..17720768,2	MCF-7	breast:
12	chr7:16843687..16847356-chr7:16880969..16885089,4	MCF-7	breast:
13	chr7:16862568..16864717-chr7:16882217..16883862,2	MCF-7	breast:
14	chr7:16843625..16845723-chr7:16926394..16928363,2	MCF-7	breast:
15	chr7:16842671..16846672-chr7:16872970..16875840,3	MCF-7	breast:
16	chr7:16883300..16885078-chr7:16885250..16887314,2	K562	blood:
17	chr7:16825159..16826158-chr7:16919904..16920435,2	MCF-7	breast:
18	chr7:16930864..16931608-chr7:16957731..16958689,3	MCF-7	breast:
19	chr7:16840256..16845659-chr7:16882127..16888432,10	MCF-7	breast:
20	chr7:16882221..16884477-chr7:16885403..16887201,3	MCF-7	breast:
21	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
22	chr7:16842139..16846678-chr7:16885089..16889372,16	MCF-7	breast:
23	chr7:16922993..16923881-chr9:94630482..94631276,2	MCF-7	breast:
24	chr7:16842935..16845400-chr7:16919121..16922153,4	MCF-7	breast:
25	chr7:16880852..16883494-chr7:16885535..16888915,3	MCF-7	breast:
26	chr7:16930587..16933448-chr7:16954480..16956101,2	MCF-7	breast:
27	chr7:16859226..16861036-chr7:16864531..16866470,3	MCF-7	breast:
28	chr7:16878823..16881693-chr7:16881989..16884135,2	K562	blood:
29	chr7:16895265..16896877-chr7:16900259..16902475,2	MCF-7	breast:
30	chr7:16878823..16881693-chr7:16881989..16884135,2	K562	blood:
31	chr7:16895265..16896877-chr7:16900259..16902475,2	MCF-7	breast:
32	chr7:16834464..16837381-chr7:16917250..16920233,2	MCF-7	breast:
33	chr7:16856551..16859411-chr7:16862546..16864505,2	MCF-7	breast:
34	chr7:16795433..16797720-chr7:16943125..16945595,2	MCF-7	breast:
35	chr7:16839543..16841251-chr7:16918984..16920555,2	MCF-7	breast:
36	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
37	chr7:16920618..16921311-chr8:99380929..99381723,2	MCF-7	breast:
38	chr7:16918898..16922214-chr7:16923893..16926911,3	MCF-7	breast:
39	chr7:16793190..16795518-chr7:16923523..16926249,2	MCF-7	breast:
40	chr7:16885425..16887633-chr7:16956037..16959031,2	MCF-7	breast:
41	chr7:16876778..16878697-chr7:16884099..16885965,2	MCF-7	breast:
42	chr7:16843068..16844721-chr7:16868529..16870557,2	MCF-7	breast:
43	chr7:16931815..16932543-chr7:16957591..16958753,3	MCF-7	breast:
44	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
45	chr7:16840041..16842170-chr7:16902969..16904527,2	MCF-7	breast:
46	chr7:16843304..16845867-chr7:16878790..16881977,4	MCF-7	breast:
47	chr7:16791779..16793290-chr7:16881466..16883566,2	MCF-7	breast:
48	chr7:16891035..16893983-chr7:16905819..16908710,2	MCF-7	breast:
49	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
50	chr7:16853700..16855388-chr7:16865354..16867185,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGR2-1	chr7:16918134-16918269	NONHSAT119307
2	lnc-TSPAN13-1	chr7:16928245-16928509	NONHSAT119308
3	lnc-AGR2-1	chr7:16913040-16913467	NONHSAT119307
4	lnc-AGR2-1	chr7:16921568-16921597	NONHSAT119307

No data

Variant related genes	Relation type
AGR2	TF binding region
ENSG00000270593	TF binding region
AGR3	TF binding region
ENSG00000227965	TF binding region
RAD17P1	TF binding region
AGR2	CpG island
ENSG00000270593	CpG island
AGR3	CpG island
ENSG00000227965	CpG island
RAD17P1	CpG island
ENSG00000228675	chromatin interactions
ENSG00000106537	chromatin interactions
ENSG00000173467	chromatin interactions
ENSG00000106541	chromatin interactions
ENSG00000232400	chromatin interactions

Extended variants
information (count: 3958 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:3958 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11768848	chr7:16863727-16863728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73078127	chr7:16863753-16863754	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs560184921	chr7:16863758-16863759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181714349	chr7:16863771-16863772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138138964	chr7:16863775-16863776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142635754	chr7:16863808-16863809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1404974	chr7:16863812-16863813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144989586	chr7:16863828-16863829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545147825	chr7:16863873-16863874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565035875	chr7:16863881-16863882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559142737	chr7:16863904-16863905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577720464	chr7:16863914-16863915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11768938	chr7:16863920-16863921	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs560157048	chr7:16863992-16863993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572324488	chr7:16864009-16864010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185793494	chr7:16864038-16864039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550637518	chr7:16864046-16864047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564046408	chr7:16864050-16864051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73078130	chr7:16864069-16864070	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs567253349	chr7:16864072-16864073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376895278	chr7:16864077-16864078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531245134	chr7:16864119-16864120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1404973	chr7:16864159-16864160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564993949	chr7:16864162-16864163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532556410	chr7:16864208-16864209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189467710	chr7:16864209-16864210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138681289	chr7:16864216-16864217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536930292	chr7:16864225-16864226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548941576	chr7:16864346-16864347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570063840	chr7:16864458-16864459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537447685	chr7:16864500-16864501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149387814	chr7:16864515-16864516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373142629	chr7:16864516-16864517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570942402	chr7:16864552-16864553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374397621	chr7:16864557-16864558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112074659	chr7:16864634-16864635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181775077	chr7:16864639-16864640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553906812	chr7:16864660-16864661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572178961	chr7:16864684-16864685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573256427	chr7:16864707-16864708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554488556	chr7:16864715-16864716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186172338	chr7:16864728-16864729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566536495	chr7:16864747-16864748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144731332	chr7:16864748-16864749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540372690	chr7:16864756-16864757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374918860	chr7:16864823-16864824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564794733	chr7:16864824-16864825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148567319	chr7:16864872-16864873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540803162	chr7:16864877-16864878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559889712	chr7:16864915-16864916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16862600-16865200	Weak transcription	A549	lung
2	chr7:16865200-16865400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:16865200-16865400	Enhancers	A549	lung
4	chr7:16865200-16866200	Enhancers	Placenta Amnion	Placenta Amnion
5	chr7:16865200-16866800	Enhancers	Placenta	Placenta
6	chr7:16865400-16866400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr7:16865400-16867600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr7:16866200-16872000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr7:16872000-16873800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:16873800-16875800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:16875800-16878400	Enhancers	Placenta Amnion	Placenta Amnion
12	chr7:16878000-16878600	Enhancers	A549	lung
13	chr7:16878000-16879800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:16878200-16878400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:16878200-16878400	Enhancers	HSMM	muscle
16	chr7:16878200-16878400	Enhancers	Osteobl	bone
17	chr7:16878200-16878800	Enhancers	Primary B cells from peripheral blood	blood
18	chr7:16878400-16879200	Weak transcription	HSMM	muscle
19	chr7:16878400-16879400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:16878400-16879600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:16878600-16878800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:16878600-16879000	Enhancers	Primary B cells from cord blood	blood
23	chr7:16878600-16879000	Weak transcription	A549	lung
24	chr7:16878600-16879600	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr7:16878600-16879600	Weak transcription	Osteobl	bone
26	chr7:16878800-16880000	Enhancers	NHDF-Ad	bronchial
27	chr7:16878800-16881200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr7:16879000-16880000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:16879000-16881400	Enhancers	A549	lung
30	chr7:16879200-16879400	Enhancers	HSMM	muscle
31	chr7:16879400-16882600	Enhancers	Placenta Amnion	Placenta Amnion
32	chr7:16879600-16879800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:16879600-16880000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:16879600-16880000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:16879600-16880000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:16879600-16880000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:16879600-16880000	Enhancers	Placenta	Placenta
38	chr7:16879600-16880000	Enhancers	NH-A	brain
39	chr7:16879600-16880200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:16879600-16880200	Enhancers	Osteobl	bone
41	chr7:16879800-16881200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr7:16880000-16881200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:16880000-16881200	Weak transcription	NHDF-Ad	bronchial
44	chr7:16880000-16881400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr7:16880000-16881400	Weak transcription	NH-A	brain
46	chr7:16880000-16886200	Weak transcription	Placenta	Placenta
47	chr7:16880200-16881200	Weak transcription	Osteobl	bone
48	chr7:16880400-16880800	Enhancers	Fetal Heart	heart
49	chr7:16880400-16881800	Enhancers	HSMMtube	muscle
50	chr7:16880400-16889600	Weak transcription	Gastric	stomach

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