Variant report

Variant	nsv542394
Chromosome Location	chr15:57232111-57344561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:954)
CpG islands
(count:733)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57263403-57263635	K562	blood:	n/a	n/a
2	ARID3A	chr15:57271204-57271795	HepG2	liver:	n/a	chr15:57271527-57271543
3	ARID3A	chr15:57281883-57282101	K562	blood:	n/a	n/a
4	ARID3A	chr15:57308127-57308446	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57252427-57252618	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57264390-57264853	K562	blood:	n/a	n/a
7	ARID3A	chr15:57257894-57258148	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:57275254-57275472	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:57262164-57262398	HepG2	liver:	n/a	n/a
10	ARID3A	chr15:57281407-57282155	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:57325925-57326378	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:57249593-57250337	HepG2	liver:	n/a	n/a
13	ARID3A	chr15:57309332-57309533	K562	blood:	n/a	n/a
14	ARID3A	chr15:57280562-57280984	HepG2	liver:	n/a	n/a
15	ATF1	chr15:57323514-57323525	K562	blood:	n/a	n/a
16	ATF1	chr15:57295750-57295894	K562	blood:	n/a	n/a
17	ATF1	chr15:57311748-57311868	K562	blood:	n/a	n/a
18	ATF1	chr15:57264660-57264913	K562	blood:	n/a	n/a
19	ATF2	chr15:57252057-57252784	GM12878	blood:	n/a	n/a
20	ATF2	chr15:57252188-57252761	GM12878	blood:	n/a	n/a
21	ATF2	chr15:57256206-57256858	GM12878	blood:	n/a	n/a
22	ATF2	chr15:57243166-57243752	GM12878	blood:	n/a	n/a
23	ATF2	chr15:57243165-57243623	GM12878	blood:	n/a	n/a
24	ATF3	chr15:57323970-57324162	K562	blood:	n/a	n/a
25	BACH1	chr15:57265992-57266005	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr15:57243148-57243483	GM12878	blood:	n/a	n/a
27	BATF	chr15:57252379-57252719	GM12878	blood:	n/a	chr15:57252539-57252550
28	BATF	chr15:57252297-57252772	GM12878	blood:	n/a	chr15:57252539-57252550
29	BATF	chr15:57337923-57338340	GM12878	blood:	n/a	n/a
30	BATF	chr15:57337860-57338323	GM12878	blood:	n/a	n/a
31	BCL11A	chr15:57252328-57252744	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:57243148-57243555	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:57337958-57338293	GM12878	blood:	n/a	n/a
34	BCL11A	chr15:57243289-57243499	GM12878	blood:	n/a	n/a
35	BCL3	chr15:57256319-57256601	GM12878	blood:	n/a	n/a
36	BCL3	chr15:57252199-57252677	GM12878	blood:	n/a	n/a
37	BCL3	chr15:57271054-57271868	A549	lung:	n/a	n/a
38	BCLAF1	chr15:57252291-57252683	GM12878	blood:	n/a	n/a
39	BCLAF1	chr15:57243099-57243697	GM12878	blood:	n/a	n/a
40	BHLHE40	chr15:57243277-57243596	GM12878	blood:	n/a	n/a
41	BHLHE40	chr15:57311754-57312028	K562	blood:	n/a	n/a
42	BHLHE40	chr15:57281904-57282089	K562	blood:	n/a	n/a
43	BHLHE40	chr15:57233777-57234029	K562	blood:	n/a	n/a
44	BHLHE40	chr15:57250100-57250554	HepG2	liver:	n/a	n/a
45	BHLHE40	chr15:57263440-57263705	K562	blood:	n/a	n/a
46	BRCA1	chr15:57317615-57318275	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr15:57263356-57263717	K562	blood:	n/a	n/a
48	CBX3	chr15:57308112-57308484	HCT-116	colon:	n/a	n/a
49	CBX3	chr15:57319806-57320145	K562	blood:	n/a	n/a
50	CBX3	chr15:57238369-57238650	K562	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57324333-57324383	Jurkat	blood:	n/a
2	chr15:57324333-57324383	Jurkat	blood:	n/a
3	chr15:57272441-57272491	NT2-D1	testis:	n/a
4	chr15:57324333-57324383	GM19239	blood:	n/a
5	chr15:57309541-57309591	PANC-1	pancreas:	n/a
6	chr15:57341718-57341768	SAEC	small airway:	n/a
7	chr15:57341718-57341768	HepG2	liver:	n/a
8	chr15:57332446-57332496	HL-60	blood:	n/a
9	chr15:57272441-57272491	CMK	blood:	n/a
10	chr15:57256372-57256422	AoSMC	blood vessel:	n/a
11	chr15:57272441-57272491	HRCEpiC	kidney:	n/a
12	chr15:57332446-57332496	AG09309	skin:	n/a
13	chr15:57250375-57250425	GM12878	blood:	n/a
14	chr15:57332446-57332496	NHBE	bronchial:	n/a
15	chr15:57324333-57324383	LNCaP	prostate:	n/a
16	chr15:57277634-57277684	NT2-D1	testis:	n/a
17	chr15:57250375-57250425	HUVEC	blood vessel:	n/a
18	chr15:57309541-57309591	SK-N-SH_RA	brain:	n/a
19	chr15:57341718-57341768	HNPCEpiC	eye:	n/a
20	chr15:57317980-57318030	HCF	heart:	n/a
21	chr15:57256372-57256422	HRCEpiC	kidney:	n/a
22	chr15:57324333-57324383	T-47D	breast:	n/a
23	chr15:57309541-57309591	AG04450	lung:	fetal
24	chr15:57250375-57250425	Caco-2	colon:	n/a
25	chr15:57324333-57324383	NT2-D1	testis:	n/a
26	chr15:57332446-57332496	CMK	blood:	n/a
27	chr15:57277634-57277684	IMR90	lung:	fetal
28	chr15:57332446-57332496	HCT-116	colon:	n/a
29	chr15:57256372-57256422	HCPEpiC	choroid plexus:	n/a
30	chr15:57250375-57250425	NH-A	brain:	n/a
31	chr15:57309541-57309591	LNCaP	prostate:	n/a
32	chr15:57295758-57295808	MCF10A-Er-Src	breast:	n/a
33	chr15:57317980-57318030	NHBE	bronchial:	n/a
34	chr15:57341718-57341768	CMK	blood:	n/a
35	chr15:57324333-57324383	HRPEpiC	eye:	n/a
36	chr15:57251471-57251521	GM12891	blood:	n/a
37	chr15:57341718-57341768	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:57251471-57251521	ECC-1	luminal epithelium:	n/a
39	chr15:57256372-57256422	NB4	blood:	n/a
40	chr15:57341718-57341768	HRPEpiC	eye:	n/a
41	chr15:57341718-57341768	AG09319	gingival:	n/a
42	chr15:57251471-57251521	HCT-116	colon:	n/a
43	chr15:57256372-57256422	HCT-116	colon:	n/a
44	chr15:57251471-57251521	SK-N-MC	brain:	n/a
45	chr15:57317980-57318030	HUVEC	blood vessel:	n/a
46	chr15:57277634-57277684	T-47D	breast:	n/a
47	chr15:57324333-57324383	NH-A	brain:	n/a
48	chr15:57250375-57250425	RPTEC	kidney:	n/a
49	chr15:57332446-57332496	SKMC	muscle:	n/a
50	chr15:57250375-57250425	AG04449	skin:	fetal

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:57310993..57315176-chr15:57315668..57319705,4	K562	blood:
2	chr15:57333982..57335700-chr15:57337723..57339646,2	K562	blood:
3	chr15:57208974..57212376-chr15:57299847..57301988,3	MCF-7	breast:
4	chr15:57315197..57318733-chr15:57320688..57324516,3	K562	blood:
5	chr15:57265601..57267263-chr15:57271593..57273612,2	K562	blood:
6	chr15:57253721..57256073-chr15:57262899..57264820,2	K562	blood:
7	chr15:57277263..57280006-chr15:57281828..57283970,2	K562	blood:
8	chr15:57210057..57212896-chr15:57260738..57263139,2	MCF-7	breast:
9	chr15:57263359..57266200-chr15:57266241..57268315,2	K562	blood:
10	chr15:57300673..57301307-chr5:172483325..172483972,2	MCF-7	breast:
11	chr15:57326879..57327856-chr15:57438827..57439782,2	K562	blood:
12	chr15:57277206..57280483-chr15:57280538..57284418,3	K562	blood:
13	chr15:57265601..57267263-chr15:57271593..57273612,2	K562	blood:
14	chr15:57333982..57335700-chr15:57337723..57339646,2	K562	blood:
15	chr15:57269633..57272065-chr15:57273062..57274627,2	K562	blood:
16	chr15:57262336..57264742-chr15:57265375..57267744,2	K562	blood:
17	chr15:57263359..57266200-chr15:57266241..57268315,2	K562	blood:
18	chr15:57242148..57243813-chr15:57244143..57246252,2	MCF-7	breast:
19	chr15:57325288..57327004-chr15:57330879..57332478,2	K562	blood:
20	chr15:57273239..57275335-chr15:57275612..57277322,2	K562	blood:
21	chr15:57285454..57287142-chr15:57328507..57331190,2	K562	blood:
22	chr15:57212275..57213860-chr15:57281190..57283282,2	K562	blood:
23	chr15:57325288..57327004-chr15:57330879..57332478,2	K562	blood:
24	chr15:57179564..57182313-chr15:57232225..57234178,2	K562	blood:
25	chr15:57281787..57284402-chr15:57285432..57287690,2	K562	blood:
26	chr15:57316485..57318733-chr15:57320688..57323136,2	K562	blood:
27	chr15:57210017..57214406-chr15:57230340..57233852,4	K562	blood:
28	chr15:57331807..57334195-chr15:57336717..57338701,2	K562	blood:
29	chr15:57273239..57275335-chr15:57275612..57277322,2	K562	blood:
30	chr15:57254284..57256820-chr15:57279086..57281932,2	K562	blood:
31	chr15:57331807..57334195-chr15:57336717..57338701,2	K562	blood:
32	chr15:57277206..57280483-chr15:57280538..57284418,3	K562	blood:
33	chr15:57209364..57212331-chr15:57308276..57309947,2	MCF-7	breast:
34	chr15:57253721..57256073-chr15:57262899..57264820,2	K562	blood:
35	chr15:57210198..57214861-chr15:57238728..57241582,5	K562	blood:
36	chr15:57243814..57246675-chr15:57249324..57251467,2	K562	blood:
37	chr15:57210716..57212486-chr15:57263351..57264921,2	K562	blood:
38	chr15:57254985..57258076-chr15:57265765..57268821,3	K562	blood:
39	chr15:57209175..57210784-chr15:57308733..57311658,2	K562	blood:
40	chr15:57269633..57272065-chr15:57273062..57274627,2	K562	blood:
41	chr15:57242148..57243813-chr15:57244143..57246252,2	MCF-7	breast:
42	chr15:57275197..57277151-chr15:57278136..57281602,3	K562	blood:
43	chr15:57277263..57280006-chr15:57281828..57283970,2	K562	blood:
44	chr15:57208582..57210610-chr15:57249153..57251996,2	K562	blood:
45	chr15:57254985..57258076-chr15:57265765..57268821,3	K562	blood:
46	chr15:57179828..57184056-chr15:57314164..57317264,3	K562	blood:
47	chr15:57281787..57284402-chr15:57285432..57287690,2	K562	blood:
48	chr15:57285454..57287142-chr15:57328507..57331190,2	K562	blood:
49	chr15:57210623..57212439-chr15:57268070..57269704,2	MCF-7	breast:
50	chr15:57310993..57315176-chr15:57315668..57319705,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000222586	TF binding region
ENSG00000222586	CpG island
ENSG00000137871	chromatin interactions
ENSG00000164463	chromatin interactions
ENSG00000140262	chromatin interactions

Extended variants
information (count: 4564 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4564 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2899600	chr15:57232130-57232131	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181105079	chr15:57232147-57232148	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs573159285	chr15:57232161-57232162	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201646655	chr15:57232166-57232167	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542467986	chr15:57232178-57232179	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs71113035	chr15:57232189-57232190	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs184609266	chr15:57232251-57232252	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573483536	chr15:57232357-57232358	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs575328824	chr15:57232386-57232387	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs531128235	chr15:57232468-57232469	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550787786	chr15:57232527-57232528	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs563821401	chr15:57232578-57232579	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72749416	chr15:57232636-57232637	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140177247	chr15:57232641-57232642	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs546294338	chr15:57232658-57232659	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs574379483	chr15:57232663-57232664	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566424519	chr15:57232669-57232670	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs539672168	chr15:57232676-57232677	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs74889504	chr15:57232679-57232680	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2543674	chr15:57232697-57232698	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569085400	chr15:57232701-57232702	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs538022789	chr15:57232706-57232707	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558004423	chr15:57232709-57232710	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573337051	chr15:57232721-57232722	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146596227	chr15:57232728-57232729	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs571489598	chr15:57232733-57232734	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539893544	chr15:57232736-57232737	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553199382	chr15:57232762-57232763	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372805592	chr15:57232763-57232764	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs540736706	chr15:57232772-57232773	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141360881	chr15:57232799-57232800	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562013310	chr15:57232815-57232816	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182575511	chr15:57232826-57232827	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs2435895	chr15:57232859-57232860	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546048622	chr15:57232887-57232888	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575881527	chr15:57232913-57232914	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544518321	chr15:57232918-57232919	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564295411	chr15:57232921-57232922	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs2439921	chr15:57232934-57232935	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539934103	chr15:57232935-57232936	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs79838790	chr15:57232936-57232937	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs72073466	chr15:57232943-57232944	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs74668253	chr15:57232963-57232964	Weak transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191910344	chr15:57233028-57233029	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568215834	chr15:57233070-57233071	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs181489553	chr15:57233087-57233088	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185779901	chr15:57233090-57233091	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115250229	chr15:57233095-57233096	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539031767	chr15:57233115-57233116	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75351839	chr15:57233116-57233117	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Pancreatic cancer	17952125	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3300 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57212400-57233400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:57212400-57256000	Weak transcription	Pancreas	Pancrea
3	chr15:57212600-57241000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr15:57213200-57256000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr15:57216400-57241800	Weak transcription	Fetal Brain Male	brain
6	chr15:57220400-57236400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:57222600-57233000	Weak transcription	Right Ventricle	heart
8	chr15:57222600-57250200	Weak transcription	NH-A	brain
9	chr15:57222800-57232600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr15:57222800-57240800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr15:57222800-57255000	Weak transcription	HMEC	breast
12	chr15:57223000-57236800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr15:57223200-57240400	Weak transcription	Aorta	Aorta
14	chr15:57224400-57234400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr15:57224400-57235200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr15:57224400-57238000	Weak transcription	Fetal Lung	lung
17	chr15:57224600-57233800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr15:57224600-57248600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr15:57225000-57239400	Weak transcription	Left Ventricle	heart
20	chr15:57225000-57244200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr15:57225000-57249000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr15:57225200-57238000	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr15:57226400-57234000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr15:57226400-57235200	Weak transcription	Colon Smooth Muscle	Colon
25	chr15:57226400-57242000	Weak transcription	HUVEC	blood vessel
26	chr15:57226600-57234600	Weak transcription	Fetal Heart	heart
27	chr15:57227000-57233000	Weak transcription	HSMMtube	muscle
28	chr15:57227000-57249800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr15:57227200-57234200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr15:57227200-57236800	Weak transcription	A549	lung
31	chr15:57227600-57234000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr15:57227600-57234000	Weak transcription	Brain Germinal Matrix	brain
33	chr15:57227600-57235400	Weak transcription	Dnd41	blood
34	chr15:57227600-57236000	Weak transcription	Psoas Muscle	Psoas
35	chr15:57227600-57260600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:57227800-57235200	Weak transcription	NHEK	skin
37	chr15:57228000-57233200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr15:57228000-57234600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:57228000-57235200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr15:57228000-57237600	Weak transcription	Primary B cells from peripheral blood	blood
41	chr15:57228000-57237600	Weak transcription	Fetal Intestine Large	intestine
42	chr15:57228000-57238000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr15:57228000-57242400	Weak transcription	Fetal Intestine Small	intestine
44	chr15:57228200-57235400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:57228200-57236800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr15:57228200-57238000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:57228200-57260600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr15:57228400-57236800	Weak transcription	Primary B cells from cord blood	blood
49	chr15:57228400-57237600	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:57228800-57234200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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