Variant report

Variant	nsv831084
Chromosome Location	chr7:102778908-102964970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2367)
CpG islands
(count:2933)
Chromatin interactive
region (count:94)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2367 , 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	chr7:102792428-102792755	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102937667-102937974	K562	blood:	n/a	n/a
3	ARID3A	chr7:102789008-102789693	K562	blood:	n/a	n/a
4	ARID3A	chr7:102894620-102894913	K562	blood:	n/a	n/a
5	ARID3A	chr7:102937529-102937991	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:102790767-102790966	HepG2	liver:	n/a	n/a
7	ATF1	chr7:102839766-102839968	K562	blood:	n/a	n/a
8	ATF1	chr7:102940212-102940384	K562	blood:	n/a	n/a
9	ATF1	chr7:102792752-102793085	K562	blood:	n/a	n/a
10	ATF1	chr7:102894715-102894811	K562	blood:	n/a	n/a
11	ATF2	chr7:102937635-102938156	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:102937710-102938168	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:102937607-102938130	GM12878	blood:	n/a	n/a
14	ATF2	chr7:102789822-102790521	GM12878	blood:	n/a	n/a
15	ATF2	chr7:102789695-102790643	GM12878	blood:	n/a	n/a
16	ATF3	chr7:102937691-102938207	K562	blood:	n/a	n/a
17	ATF3	chr7:102940027-102940367	K562	blood:	n/a	n/a
18	BACH1	chr7:102789324-102790184	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:102937582-102937999	K562	blood:	n/a	n/a
20	BACH1	chr7:102785515-102785682	K562	blood:	n/a	n/a
21	BACH1	chr7:102789017-102789662	K562	blood:	n/a	n/a
22	BACH1	chr7:102937572-102937898	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:102872627-102872850	GM12878	blood:	n/a	n/a
24	BATF	chr7:102863528-102863901	GM12878	blood:	n/a	n/a
25	BATF	chr7:102863497-102863908	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:102863536-102863866	GM12878	blood:	n/a	chr7:102863703-102863712
27	BCL3	chr7:102789718-102790534	A549	lung:	n/a	n/a
28	BCL3	chr7:102950443-102950988	K562	blood:	n/a	n/a
29	BCL3	chr7:102951624-102952580	K562	blood:	n/a	n/a
30	BCL3	chr7:102906588-102906815	GM12878	blood:	n/a	n/a
31	BCL3	chr7:102937480-102938123	A549	lung:	n/a	n/a
32	BCLAF1	chr7:102937583-102938278	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:102920684-102921045	GM12878	blood:	n/a	chr7:102920916-102920929
34	BCLAF1	chr7:102789333-102790625	GM12878	blood:	n/a	n/a
35	BCLAF1	chr7:102937555-102938301	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:102789393-102790394	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:102863630-102863788	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:102920337-102921182	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:102789344-102790726	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:102937620-102938177	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:102894632-102894890	K562	blood:	n/a	n/a
42	BHLHE40	chr7:102789312-102790958	K562	blood:	n/a	n/a
43	BHLHE40	chr7:102937698-102938370	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:102787017-102787266	K562	blood:	n/a	n/a
45	BHLHE40	chr7:102937658-102938338	K562	blood:	n/a	n/a
46	BRCA1	chr7:102839762-102839912	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr7:102789382-102789738	GM12878	blood:	n/a	chr7:102789633-102789640
48	BRCA1	chr7:102789950-102790189	GM12878	blood:	n/a	n/a
49	BRCA1	chr7:102789348-102789815	HepG2	liver:	n/a	chr7:102789633-102789640
50	BRCA1	chr7:102937664-102938583	Hela-S3	cervix:	n/a	n/a

(count:2933 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102937993-102938043	A549	lung:	n/a
2	chr7:102921643-102921693	AG04449	skin:	fetal
3	chr7:102787173-102787223	HRE	kidney:	n/a
4	chr7:102937788-102937838	PANC-1	pancreas:	n/a
5	chr7:102792783-102792833	HNPCEpiC	eye:	n/a
6	chr7:102937993-102938043	A549	lung:	n/a
7	chr7:102921643-102921693	AG04449	skin:	fetal
8	chr7:102787173-102787223	HRE	kidney:	n/a
9	chr7:102937788-102937838	PANC-1	pancreas:	n/a
10	chr7:102792783-102792833	HNPCEpiC	eye:	n/a
11	chr7:102941673-102941723	SKMC	muscle:	n/a
12	chr7:102920962-102921012	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:102937814-102937864	SK-N-MC	brain:	n/a
14	chr7:102921001-102921051	GM12892	blood:	n/a
15	chr7:102918709-102918759	SK-N-MC	brain:	n/a
16	chr7:102789948-102789998	Hela-S3	cervix:	n/a
17	chr7:102782124-102782174	GM12892	blood:	n/a
18	chr7:102782124-102782174	A549	lung:	n/a
19	chr7:102954408-102954458	NHDF-neo	bronchial:	n/a
20	chr7:102937749-102937799	Hepatocyte	liver:	n/a
21	chr7:102783873-102783923	Hela-S3	cervix:	n/a
22	chr7:102920777-102920827	ovcar-3	ovarian:	n/a
23	chr7:102920771-102920821	AG04449	skin:	fetal
24	chr7:102920980-102921030	SKMC	muscle:	n/a
25	chr7:102937535-102937585	K562	blood:	n/a
26	chr7:102921052-102921102	SK-N-SH_RA	brain:	n/a
27	chr7:102784027-102784077	CMK	blood:	n/a
28	chr7:102789617-102789667	MCF10A-Er-Src	breast:	n/a
29	chr7:102937788-102937838	NB4	blood:	n/a
30	chr7:102937765-102937815	BJ	skin:	n/a
31	chr7:102921643-102921693	GM19239	blood:	n/a
32	chr7:102936381-102936431	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:102782124-102782174	GM19239	blood:	n/a
34	chr7:102789396-102789446	GM12878	blood:	n/a
35	chr7:102937659-102937709	HMEC	breast:	n/a
36	chr7:102921513-102921563	HCT-116	colon:	n/a
37	chr7:102790119-102790169	NHBE	bronchial:	n/a
38	chr7:102920962-102921012	GM19239	blood:	n/a
39	chr7:102921643-102921693	H1-hESC	embryonic stem cell:	embryo
40	chr7:102921001-102921051	H1-hESC	embryonic stem cell:	embryo
41	chr7:102920323-102920373	PFSK-1	brain:	n/a
42	chr7:102921442-102921492	Jurkat	blood:	n/a
43	chr7:102793411-102793461	GM19239	blood:	n/a
44	chr7:102783873-102783923	AG04450	lung:	fetal
45	chr7:102789948-102789998	SAEC	small airway:	n/a
46	chr7:102787173-102787223	HRCEpiC	kidney:	n/a
47	chr7:102920980-102921030	GM06990	blood:	n/a
48	chr7:102792783-102792833	HMEC	breast:	n/a
49	chr7:102789948-102789998	HCM	heart:	n/a
50	chr7:102792783-102792833	NB4	blood:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:102963743..102965327-chr7:102981901..102984611,2	K562	blood:
2	chr7:102955140..102957635-chr7:102980256..102982685,2	MCF-7	breast:
3	chr7:102779926..102783136-chr7:102788446..102789979,3	MCF-7	breast:
4	chr7:102953286..102955465-chr7:102961116..102963832,3	MCF-7	breast:
5	chr7:102928821..102931248-chr7:102936716..102938968,2	MCF-7	breast:
6	chr7:102939410..102942182-chr7:102954318..102956590,2	K562	blood:
7	chr7:102737570..102739269-chr7:102784132..102785986,2	K562	blood:
8	chr7:102774358..102779744-chr7:102786583..102790988,10	MCF-7	breast:
9	chr7:102754783..102757571-chr7:102779422..102781825,2	MCF-7	breast:
10	chr7:102936986..102939329-chr7:102943274..102946072,3	MCF-7	breast:
11	chr7:102940663..102947555-chr7:102980823..102987452,8	K562	blood:
12	chr21:34144018..34144738-chr7:102788853..102789789,2	Hela-S3	cervix:
13	chr7:102940048..102941783-chr7:102957595..102959414,2	K562	blood:
14	chr7:102788301..102790522-chr7:102804564..102807525,2	K562	blood:
15	chr7:102799119..102800765-chr7:102801413..102803528,2	MCF-7	breast:
16	chr7:102952502..102955468-chr7:102982681..102986530,4	K562	blood:
17	chr7:102954023..102956070-chr7:102962172..102966045,3	K562	blood:
18	chr7:102799119..102800765-chr7:102801413..102803528,2	MCF-7	breast:
19	chr7:102789004..102789710-chr7:102937583..102938403,2	MCF-7	breast:
20	chr7:102946587..102948728-chr7:103004817..103007123,2	MCF-7	breast:
21	chr7:102789004..102789710-chr7:102937583..102938403,2	MCF-7	breast:
22	chr7:102775653..102777256-chr7:102783186..102785613,2	K562	blood:
23	chr7:102714786..102716772-chr7:102789401..102791256,2	MCF-7	breast:
24	chr3:73160043..73160592-chr7:102789631..102790426,2	HCT-116	colon:
25	chr7:102949416..102952354-chr7:102981636..102984074,3	K562	blood:
26	chr7:102759033..102762956-chr7:102787889..102791523,5	K562	blood:
27	chr7:102945838..102949503-chr7:103019550..103022202,3	K562	blood:
28	chr7:102931004..102933961-chr7:102984506..102986894,2	K562	blood:
29	chr7:102784051..102785716-chr7:102793385..102795157,2	K562	blood:
30	chr7:102941619..102944987-chr7:102988206..102992263,4	K562	blood:
31	chr7:102939410..102942182-chr7:102954318..102956590,2	K562	blood:
32	chr7:102788341..102791545-chr7:102935934..102939308,4	K562	blood:
33	chr19:58200030..58201680-chr7:102943117..102944705,2	MCF-7	breast:
34	chr7:102953286..102955465-chr7:102961116..102963832,3	MCF-7	breast:
35	chr7:102938125..102939951-chr7:102963643..102966218,2	K562	blood:
36	chr7:102937219..102940435-chr7:102985734..102988691,4	MCF-7	breast:
37	chr7:102787809..102789430-chr7:102937893..102939792,2	MCF-7	breast:
38	chr7:102759379..102762894-chr7:102787802..102793821,6	K562	blood:
39	chr7:102937260..102939405-chr7:102983367..102989226,6	MCF-7	breast:
40	chr7:102941816..102944695-chr7:102945655..102947787,3	K562	blood:
41	chr7:102788463..102790768-chr7:102937238..102939346,3	K562	blood:
42	chr7:102936363..102940498-chr7:102983696..102986201,5	K562	blood:
43	chr7:102714022..102717631-chr7:102788669..102792237,6	MCF-7	breast:
44	chr7:102784051..102785716-chr7:102793385..102795157,2	K562	blood:
45	chr7:102956158..102958455-chr7:102994162..102996871,2	MCF-7	breast:
46	chr7:102780818..102786371-chr7:102786977..102791342,10	K562	blood:
47	chr7:102777685..102779366-chr7:102784071..102785694,2	K562	blood:
48	chr7:102936782..102939322-chr7:102944870..102947708,2	K562	blood:
49	chr7:102779926..102783136-chr7:102788446..102789979,3	MCF-7	breast:
50	chr7:102789022..102791029-chr7:102804564..102807367,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAPEPLD-5	chr7:102918669-102918793	NONHSAT122547
2	lnc-NAPEPLD-5	chr7:102920280-102920411	NONHSAT122547
3	lnc-NAPEPLD-2	chr7:102792541-102792772	NONHSAT122538
4	lnc-NAPEPLD-2	chr7:102792454-102792486	NONHSAT122538
5	lnc-FBXL13-1	chr7:102781717-102782850	NR_026660
6	lnc-NAPEPLD-4	chr7:102802394-102803107	NONHSAT122539
7	lnc-ARMC10-2	chr7:102789571-102791089	NONHSAT122537

No data

Variant related genes	Relation type
S100A11P1	TF binding region
DNAJC2	TF binding region
PMPCB	TF binding region
NAPEPLD	TF binding region
RPL19P12	TF binding region
DPY19L2P2	TF binding region
ENSG00000236848	TF binding region
S100A11P1	CpG island
DNAJC2	CpG island
PMPCB	CpG island
NAPEPLD	CpG island
RPL19P12	CpG island
DPY19L2P2	CpG island
ENSG00000236848	CpG island
ENSG00000222011	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000236848	chromatin interactions
ENSG00000161048	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000235354	chromatin interactions
ENSG00000105819	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000170615	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000159086	chromatin interactions
ENSG00000161057	chromatin interactions
ENSG00000234715	chromatin interactions
ENSG00000224415	chromatin interactions
ENSG00000205930	chromatin interactions
ENSG00000105821	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000239569	chromatin interactions
CREB5	miRNA target sites

Extended variants
information (count: 4319 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4319 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555919683	chr7:102778917-102778918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs114342490	chr7:102778920-102778921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs397702999	chr7:102778932-102778933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370701668	chr7:102778933-102778934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182357202	chr7:102778973-102778974	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577451329	chr7:102779027-102779028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186137959	chr7:102779032-102779033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77901601	chr7:102779054-102779055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs560210666	chr7:102779079-102779080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150908507	chr7:102779081-102779082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369289219	chr7:102779106-102779107	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544783964	chr7:102779153-102779154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569665915	chr7:102779163-102779164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189854597	chr7:102779164-102779165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182117058	chr7:102779183-102779184	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10224485	chr7:102779197-102779198	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs71519141	chr7:102779212-102779213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149640119	chr7:102779221-102779222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563055279	chr7:102779239-102779240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147310752	chr7:102779249-102779250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373435791	chr7:102779335-102779336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56075230	chr7:102779363-102779364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185754961	chr7:102779388-102779389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190124347	chr7:102779464-102779465	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183121907	chr7:102779481-102779482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549108179	chr7:102779497-102779498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1477159	chr7:102779639-102779640	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs537934374	chr7:102779687-102779688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556254744	chr7:102779692-102779693	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140909167	chr7:102779717-102779718	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs538458453	chr7:102779788-102779789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371277247	chr7:102779903-102779904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532267580	chr7:102779905-102779906	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536670707	chr7:102779941-102779942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115980270	chr7:102779970-102779971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542954683	chr7:102779986-102779987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563269023	chr7:102780080-102780081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554242991	chr7:102780085-102780086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs552064078	chr7:102780119-102780120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs116348562	chr7:102780153-102780154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543505245	chr7:102780161-102780162	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564992140	chr7:102780164-102780165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs533526571	chr7:102780201-102780202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs114309988	chr7:102780202-102780203	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560787540	chr7:102780217-102780218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145162291	chr7:102780237-102780238	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549685417	chr7:102780242-102780243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs567289643	chr7:102780247-102780248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531617991	chr7:102780266-102780267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs80275650	chr7:102780294-102780295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:2417 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102747400-102781800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:102747600-102789200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:102760600-102782000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:102760600-102782200	Weak transcription	HSMM	muscle
5	chr7:102764000-102781800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:102764200-102787000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr7:102767200-102786000	Weak transcription	GM12878-XiMat	blood
8	chr7:102768800-102781800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:102768800-102782000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr7:102768800-102782000	Weak transcription	Pancreas	Pancrea
11	chr7:102768800-102786000	Weak transcription	Brain Germinal Matrix	brain
12	chr7:102768800-102786200	Weak transcription	Fetal Heart	heart
13	chr7:102768800-102786600	Weak transcription	Lung	lung
14	chr7:102768800-102788600	Weak transcription	Right Ventricle	heart
15	chr7:102769000-102781400	Weak transcription	Dnd41	blood
16	chr7:102769000-102782000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:102769000-102786000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:102769000-102786000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:102769000-102786000	Weak transcription	Fetal Brain Male	brain
20	chr7:102769000-102786600	Weak transcription	Stomach Smooth Muscle	stomach
21	chr7:102769000-102786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr7:102769000-102787000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr7:102769200-102781200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr7:102769200-102781800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:102769200-102781800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr7:102769200-102781800	Weak transcription	Fetal Thymus	thymus
27	chr7:102769200-102786000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr7:102769200-102786600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr7:102769200-102786800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr7:102769200-102787000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:102769200-102787000	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr7:102769200-102787000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:102769200-102787200	Weak transcription	Adipose Nuclei	Adipose
34	chr7:102769200-102787800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr7:102769200-102788200	Weak transcription	Primary B cells from cord blood	blood
36	chr7:102769200-102788400	Weak transcription	Thymus	Thymus
37	chr7:102770400-102781200	Weak transcription	Fetal Intestine Large	intestine
38	chr7:102770800-102781800	Weak transcription	Primary T cells from cord blood	blood
39	chr7:102771000-102786600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:102771000-102788800	Weak transcription	Small Intestine	intestine
41	chr7:102771200-102783000	Weak transcription	A549	lung
42	chr7:102771600-102784000	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr7:102772400-102781200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr7:102772600-102781800	Weak transcription	Fetal Intestine Small	intestine
45	chr7:102772600-102781800	Weak transcription	Fetal Stomach	stomach
46	chr7:102774000-102782000	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:102774000-102782600	Weak transcription	Spleen	Spleen
48	chr7:102774000-102783800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr7:102774000-102788600	Weak transcription	HSMMtube	muscle
50	chr7:102774200-102781200	Weak transcription	K562	blood

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