Variant report

Variant	nsv1043387
Chromosome Location	chr15:50822035-50940979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:427)
Chromatin interactive
region (count:97)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:698 , 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	chr15:50888476-50888556	K562	blood:	n/a	n/a
2	ARID3A	chr15:50914579-50914778	K562	blood:	n/a	n/a
3	ARID3A	chr15:50834985-50835658	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:50885990-50886949	K562	blood:	n/a	n/a
5	ATF1	chr15:50886574-50886849	K562	blood:	n/a	n/a
6	ATF1	chr15:50916939-50917053	K562	blood:	n/a	n/a
7	ATF1	chr15:50837432-50837566	K562	blood:	n/a	n/a
8	ATF2	chr15:50844379-50844831	GM12878	blood:	n/a	n/a
9	BACH1	chr15:50869845-50869896	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:50869823-50869907	K562	blood:	n/a	n/a
11	CCNT2	chr15:50933565-50933899	K562	blood:	n/a	n/a
12	CCNT2	chr15:50886474-50886898	K562	blood:	n/a	n/a
13	CEBPB	chr15:50905849-50906159	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:50905848-50906147	A549	lung:	n/a	n/a
15	CEBPB	chr15:50830541-50830820	HepG2	liver:	n/a	chr15:50830673-50830684
16	CEBPB	chr15:50830539-50830840	K562	blood:	n/a	chr15:50830673-50830684
17	CEBPB	chr15:50916859-50917181	K562	blood:	n/a	n/a
18	CEBPB	chr15:50879839-50880023	HepG2	liver:	n/a	chr15:50879905-50879916
19	CEBPB	chr15:50881597-50881743	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:50916897-50917199	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr15:50894818-50895097	HepG2	liver:	n/a	n/a
22	CEBPB	chr15:50889075-50889077	K562	blood:	n/a	n/a
23	CEBPB	chr15:50834942-50835448	HepG2	liver:	n/a	n/a
24	CEBPB	chr15:50929889-50930144	A549	lung:	n/a	chr15:50930024-50930035
25	CEBPB	chr15:50879756-50879976	A549	lung:	n/a	chr15:50879905-50879916
26	CEBPB	chr15:50905719-50906245	MCF-7	breast:	n/a	n/a
27	CEBPB	chr15:50905830-50906159	K562	blood:	n/a	n/a
28	CEBPB	chr15:50916905-50917183	A549	lung:	n/a	n/a
29	CEBPB	chr15:50905827-50906151	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:50880374-50880513	K562	blood:	n/a	chr15:50880463-50880474
31	CEBPB	chr15:50931692-50932047	A549	lung:	n/a	n/a
32	CEBPB	chr15:50916902-50917200	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:50830531-50830802	IMR90	lung:	n/a	chr15:50830673-50830684
34	CEBPB	chr15:50861954-50862152	A549	lung:	n/a	n/a
35	CEBPB	chr15:50889065-50889265	IMR90	lung:	n/a	n/a
36	CEBPB	chr15:50905894-50906111	A549	lung:	n/a	n/a
37	CEBPB	chr15:50894829-50895045	A549	lung:	n/a	n/a
38	CEBPB	chr15:50858006-50858029	K562	blood:	n/a	n/a
39	CEBPB	chr15:50931794-50931833	K562	blood:	n/a	n/a
40	CEBPB	chr15:50830561-50830780	A549	lung:	n/a	chr15:50830673-50830684
41	CEBPB	chr15:50881475-50881754	K562	blood:	n/a	chr15:50881581-50881594 chr15:50881581-50881594
42	CEBPB	chr15:50905825-50906178	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:50881732-50881885	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr15:50880400-50880451	A549	lung:	n/a	n/a
45	CEBPB	chr15:50886533-50886784	K562	blood:	n/a	n/a
46	CEBPB	chr15:50929899-50930169	HepG2	liver:	n/a	chr15:50930024-50930035
47	CEBPB	chr15:50905809-50906222	A549	lung:	n/a	n/a
48	CEBPB	chr15:50836795-50836995	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:50874149-50874329	HepG2	liver:	n/a	chr15:50874215-50874226
50	CEBPB	chr15:50827802-50827830	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50839463-50839513	ovcar-3	ovarian:	n/a
2	chr15:50839502-50839552	SKMC	muscle:	n/a
3	chr15:50839463-50839513	AG04450	lung:	fetal
4	chr15:50838905-50838955	HRE	kidney:	n/a
5	chr15:50838905-50838955	HL-60	blood:	n/a
6	chr15:50839502-50839552	PANC-1	pancreas:	n/a
7	chr15:50838805-50838855	ECC-1	luminal epithelium:	n/a
8	chr15:50920452-50920502	GM06990	blood:	n/a
9	chr15:50839463-50839513	IMR90	lung:	fetal
10	chr15:50853806-50853856	AG10803	skin:	n/a
11	chr15:50839502-50839552	HUVEC	blood vessel:	n/a
12	chr15:50839326-50839376	HUVEC	blood vessel:	n/a
13	chr15:50839502-50839552	HRE	kidney:	n/a
14	chr15:50838905-50838955	AG09319	gingival:	n/a
15	chr15:50853806-50853856	HCT-116	colon:	n/a
16	chr15:50839502-50839552	NHDF-neo	bronchial:	n/a
17	chr15:50839463-50839513	A549	lung:	n/a
18	chr15:50838905-50838955	BJ	skin:	n/a
19	chr15:50839463-50839513	LNCaP	prostate:	n/a
20	chr15:50838905-50838955	RPTEC	kidney:	n/a
21	chr15:50838805-50838855	HCT-116	colon:	n/a
22	chr15:50839326-50839376	HPAEpiC	pulmonary alveolar:	n/a
23	chr15:50839463-50839513	HEK293	kidney:	embryo
24	chr15:50839463-50839513	HNPCEpiC	eye:	n/a
25	chr15:50839463-50839513	GM06990	blood:	n/a
26	chr15:50839502-50839552	IMR90	lung:	fetal
27	chr15:50839463-50839513	RPTEC	kidney:	n/a
28	chr15:50838805-50838855	SAEC	small airway:	n/a
29	chr15:50838905-50838955	HMEC	breast:	n/a
30	chr15:50920452-50920502	Hela-S3	cervix:	n/a
31	chr15:50839326-50839376	Hela-S3	cervix:	n/a
32	chr15:50838905-50838955	NB4	blood:	n/a
33	chr15:50839463-50839513	HIPEpiC	eye:	n/a
34	chr15:50839502-50839552	HEK293	kidney:	embryo
35	chr15:50839326-50839376	MCF-7	breast:	n/a
36	chr15:50853806-50853856	Hela-S3	cervix:	n/a
37	chr15:50920452-50920502	GM19239	blood:	n/a
38	chr15:50839502-50839552	HRPEpiC	eye:	n/a
39	chr15:50838905-50838955	Jurkat	blood:	n/a
40	chr15:50839326-50839376	CMK	blood:	n/a
41	chr15:50920452-50920502	HRE	kidney:	n/a
42	chr15:50839502-50839552	SAEC	small airway:	n/a
43	chr15:50839502-50839552	HCM	heart:	n/a
44	chr15:50838905-50838955	AG04450	lung:	fetal
45	chr15:50838905-50838955	HAEpiC	amniotic membrane:	n/a
46	chr15:50839502-50839552	AoSMC	blood vessel:	n/a
47	chr15:50838905-50838955	HUVEC	blood vessel:	n/a
48	chr15:50838805-50838855	HRPEpiC	eye:	n/a
49	chr15:50920452-50920502	BE2_C	brain:	n/a
50	chr15:50839326-50839376	HEK293	kidney:	embryo

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:50859308..50861522-chr15:50879370..50881097,2	K562	blood:
2	chr15:50872498..50875116-chr15:50878753..50881368,3	K562	blood:
3	chr15:50832514..50835250-chr15:50836851..50839622,2	MCF-7	breast:
4	chr15:50824175..50826190-chr15:50832683..50834926,2	K562	blood:
5	chr15:50894679..50897378-chr15:50902879..50904659,2	MCF-7	breast:
6	chr15:50869972..50871677-chr15:51057056..51058734,2	MCF-7	breast:
7	chr15:50647415..50649249-chr15:50862816..50866408,3	MCF-7	breast:
8	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
9	chr15:50714902..50717197-chr15:50911765..50913524,2	MCF-7	breast:
10	chr15:50925249..50927102-chr15:51201168..51202804,2	MCF-7	breast:
11	chr15:50646177..50648161-chr15:50884558..50887057,2	K562	blood:
12	chr15:50878762..50881023-chr15:50884773..50886938,2	K562	blood:
13	chr15:50646294..50648601-chr15:50837515..50839531,2	MCF-7	breast:
14	chr15:50647510..50649094-chr15:50844767..50846494,2	MCF-7	breast:
15	chr15:50897808..50900573-chr15:50902086..50904020,3	K562	blood:
16	chr15:50890587..50894134-chr15:50900500..50903052,3	MCF-7	breast:
17	chr15:50881070..50883291-chr15:50976406..50979005,2	MCF-7	breast:
18	chr15:50842951..50845112-chr15:50852235..50854464,2	MCF-7	breast:
19	chr15:50939543..50942459-chr15:50946221..50948158,2	K562	blood:
20	chr15:50646500..50650701-chr15:50853140..50859875,5	MCF-7	breast:
21	chr15:50840672..50844284-chr15:50844552..50846855,4	K562	blood:
22	chr15:50885676..50889608-chr15:50891608..50893462,3	K562	blood:
23	chr15:50551676..50553333-chr15:50885793..50888407,2	K562	blood:
24	chr15:50714805..50717547-chr15:50833179..50836070,2	MCF-7	breast:
25	chr15:50932446..50935258-chr15:50953275..50954778,2	K562	blood:
26	chr15:50840672..50844284-chr15:50844552..50846855,4	K562	blood:
27	chr15:50900703..50903174-chr15:51177027..51179659,2	K562	blood:
28	chr15:50869586..50872138-chr15:50874488..50876598,3	K562	blood:
29	chr15:50826682..50828335-chr15:50833156..50835191,2	K562	blood:
30	chr15:50929757..50931631-chr15:50935588..50938584,2	MCF-7	breast:
31	chr15:50864188..50868322-chr15:50872346..50875460,4	MCF-7	breast:
32	chr15:50914714..50916559-chr15:50917058..50919826,2	K562	blood:
33	chr15:50872361..50874197-chr15:50874784..50877011,2	K562	blood:
34	chr15:50646177..50649955-chr15:50884558..50888661,4	K562	blood:
35	chr15:50866589..50868103-chr15:50868342..50870495,2	K562	blood:
36	chr15:50929757..50931631-chr15:50935588..50938584,2	MCF-7	breast:
37	chr15:50918354..50921026-chr15:51021586..51024072,2	MCF-7	breast:
38	chr15:50882354..50884324-chr15:50884736..50886650,2	MCF-7	breast:
39	chr15:50646822..50648460-chr15:50870305..50871829,2	MCF-7	breast:
40	chr15:50889435..50893254-chr15:50893944..50897716,3	K562	blood:
41	chr15:50645350..50647759-chr15:50913615..50916284,2	K562	blood:
42	chr15:50822298..50825180-chr15:50846070..50848811,2	MCF-7	breast:
43	chr15:50843592..50846048-chr8:116105548..116107246,2	MCF-7	breast:
44	chr15:50861509..50865180-chr15:50865318..50870216,6	K562	blood:
45	chr15:50872361..50874007-chr15:50875166..50877011,2	K562	blood:
46	chr15:50842296..50845000-chr15:50847608..50850215,3	MCF-7	breast:
47	chr15:50871076..50873819-chr15:50876627..50878202,2	MCF-7	breast:
48	chr15:50856695..50857215-chr19:16191667..16192187,2	MCF-7	breast:
49	chr15:50714621..50716242-chr15:50826547..50828170,2	MCF-7	breast:
50	chr15:50914710..50917387-chr15:50934928..50936647,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP50-5	chr15:50883698-50883786	l_1156_chr15:50879698-50884434_liver
2	lnc-USP50-5	chr15:50882478-50883336	l_1156_chr15:50879698-50884434_liver
3	lnc-USP8-1	chr15:50852196-50852697	ENSG00000259684.1
4	lnc-USP8-1	chr15:50849798-50849895	ENSG00000259684.1
5	lnc-USP8-3	chr15:50872074-50872178	l_1155_chr15:50872073-50874894_testes
6	lnc-USP8-3	chr15:50873840-50874894	l_1155_chr15:50872073-50874894_testes
7	lnc-USP8-1	chr15:50850820-50850825	ENSG00000259684.1
8	lnc-USP50-5	chr15:50883983-50884434	l_1156_chr15:50879698-50884434_liver
9	lnc-USP50-5	chr15:50879699-50880406	l_1156_chr15:50879698-50884434_liver

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TRPM7	hsa-miR-10a-5p	chr15:50896593-50896615
2	TRPM7	hsa-miR-9-5p	chr15:50853543-50853537
3	TRPM7	hsa-miR-9-5p	chr15:50853004-50853026
4	TRPM7	hsa-miR-10a-5p	chr15:50853328-50853352
5	TRPM7	hsa-miR-21-5p	chr15:50852616-50852636
6	TRPM7	hsa-miR-10a-5p	chr15:50896505-50896530
7	TRPM7	hsa-miR-9-5p	chr15:50853009-50853003
8	TRPM7	hsa-miR-9-5p	chr15:50853537-50853560
9	TRPM7	hsa-miR-21-5p	chr15:50852622-50852616

Variant related genes	Relation type
USP50	TF binding region
TRPM7	TF binding region
ENSG00000259684	TF binding region
USP50	CpG island
TRPM7	CpG island
ENSG00000259684	CpG island
ENSG00000104064	chromatin interactions
ENSG00000179218	chromatin interactions
ENSG00000138600	chromatin interactions
ENSG00000081014	chromatin interactions
ENSG00000259684	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000092439	chromatin interactions
ENSG00000170236	chromatin interactions

Extended variants
information (count: 4879 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4879 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571432071	chr15:50822071-50822072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557823387	chr15:50822088-50822089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373904683	chr15:50822106-50822107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538961652	chr15:50822124-50822125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367711727	chr15:50822168-50822169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62019151	chr15:50822178-50822179	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs572280781	chr15:50822198-50822199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141101722	chr15:50822215-50822216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79153765	chr15:50822218-50822219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201441632	chr15:50822219-50822220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534240590	chr15:50822243-50822244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs3109896	chr15:50822277-50822278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs145489809	chr15:50822333-50822334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544265087	chr15:50822340-50822341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562928508	chr15:50822477-50822478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556579812	chr15:50822481-50822482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578186313	chr15:50822551-50822552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183355960	chr15:50822552-50822553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148850701	chr15:50822555-50822556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527882126	chr15:50822638-50822639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548640538	chr15:50822645-50822646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113578139	chr15:50822658-50822659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558042599	chr15:50822688-50822689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560833546	chr15:50822713-50822714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374385986	chr15:50822722-50822723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3105599	chr15:50822735-50822736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146419369	chr15:50822768-50822769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562986315	chr15:50822779-50822780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543432392	chr15:50822794-50822795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140833906	chr15:50822796-50822797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547719347	chr15:50822799-50822800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148172654	chr15:50822800-50822801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78911096	chr15:50822805-50822806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536468363	chr15:50822855-50822856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554784047	chr15:50822915-50822916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3098201	chr15:50822931-50822932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs538384793	chr15:50822989-50822990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs28558235	chr15:50823054-50823055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs577623897	chr15:50823065-50823066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545248651	chr15:50823128-50823129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201196444	chr15:50823142-50823143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3109897	chr15:50823205-50823206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs72739001	chr15:50823225-50823226	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs3109898	chr15:50823288-50823289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187698588	chr15:50823294-50823295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191070917	chr15:50823304-50823305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182165614	chr15:50823308-50823309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532169460	chr15:50823309-50823310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547683159	chr15:50823310-50823311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79938649	chr15:50823317-50823318	Weak transcription	n/a	n/a	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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2498 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50816600-50827800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr15:50817000-50830600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr15:50821200-50824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:50823600-50823800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr15:50823800-50824000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr15:50823800-50824000	Enhancers	Osteobl	bone
7	chr15:50823800-50824400	Enhancers	HUVEC	blood vessel
8	chr15:50823800-50824600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr15:50824000-50824200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:50824000-50824600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr15:50824000-50824600	Active TSS	Osteobl	bone
12	chr15:50824000-50824800	Enhancers	HepG2	liver
13	chr15:50824200-50824600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:50824400-50824600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
15	chr15:50824400-50824800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:50824400-50824800	Enhancers	K562	blood
17	chr15:50824600-50824800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:50824600-50824800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr15:50824600-50825000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr15:50824600-50833800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr15:50824800-50836800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr15:50825000-50826200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:50830600-50830800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:50830600-50830800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr15:50833200-50833400	Enhancers	K562	blood
26	chr15:50833200-50833400	Flanking Active TSS	NHDF-Ad	bronchial
27	chr15:50833200-50833800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:50833200-50834200	Enhancers	Fetal Kidney	kidney
29	chr15:50833400-50833600	Enhancers	Fetal Stomach	stomach
30	chr15:50833400-50835000	Weak transcription	K562	blood
31	chr15:50833400-50836200	Enhancers	NHDF-Ad	bronchial
32	chr15:50833600-50834200	Weak transcription	Fetal Stomach	stomach
33	chr15:50833600-50835200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr15:50833800-50834000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:50833800-50835200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:50833800-50835400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr15:50833800-50836200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr15:50834000-50834400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr15:50834000-50834600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr15:50834000-50835600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr15:50834200-50834600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr15:50834200-50834600	Enhancers	HSMMtube	muscle
43	chr15:50834200-50835200	Weak transcription	Fetal Kidney	kidney
44	chr15:50834200-50835200	Enhancers	Fetal Stomach	stomach
45	chr15:50834200-50835800	Enhancers	Osteobl	bone
46	chr15:50834400-50834800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:50834400-50835200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr15:50834400-50835600	Enhancers	GM12878-XiMat	blood
49	chr15:50834400-50836000	Enhancers	HepG2	liver
50	chr15:50834400-50837000	Enhancers	Placenta	Placenta

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