Variant report

Variant	nsv569428
Chromosome Location	chr15:53069874-53140045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1170)
CpG islands
(count:4338)
Chromatin interactive
region (count:28)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:53082218-53082726	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53077296-53077584	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:53072684-53073202	HepG2	liver:	n/a	n/a
4	ATF2	chr15:53096969-53097302	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:53076172-53076686	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:53072294-53073257	GM12878	blood:	n/a	n/a
7	ATF2	chr15:53072301-53073212	GM12878	blood:	n/a	n/a
8	BACH1	chr15:53083442-53084110	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:53082775-53083015	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:53080571-53080771	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:53078728-53078986	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:53076053-53076451	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:53098308-53098367	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:53080077-53080277	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:53075540-53075823	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:53086711-53087039	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:53082150-53082339	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:53097811-53098098	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:53096002-53096582	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr15:53072306-53073200	GM12878	blood:	n/a	n/a
21	BATF	chr15:53072392-53072765	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:53072219-53072910	GM12878	blood:	n/a	chr15:53072401-53072409
23	BCL11A	chr15:53072380-53072869	GM12878	blood:	n/a	chr15:53072401-53072409
24	BCLAF1	chr15:53072432-53073030	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:53082092-53082932	HepG2	liver:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082462-53082478 chr15:53082455-53082471 chr15:53082734-53082743
26	BHLHE40	chr15:53082647-53082860	GM12878	blood:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082734-53082743
27	BHLHE40	chr15:53082633-53082846	K562	blood:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082734-53082743
28	BRCA1	chr15:53071977-53072011	GM12878	blood:	n/a	n/a
29	BRCA1	chr15:53106288-53106461	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr15:53076203-53076415	K562	blood:	n/a	n/a
31	CCNT2	chr15:53082422-53082718	K562	blood:	n/a	chr15:53082631-53082640
32	CEBPB	chr15:53072274-53072957	GM12878	blood:	n/a	chr15:53072565-53072576
33	CEBPB	chr15:53116686-53117039	MCF-7	breast:	n/a	chr15:53116969-53116980
34	CEBPB	chr15:53116803-53117002	HepG2	liver:	n/a	chr15:53116969-53116980
35	CEBPB	chr15:53072314-53073009	H1-hESC	embryonic stem cell:	n/a	chr15:53072565-53072576
36	CEBPB	chr15:53116834-53117087	HepG2	liver:	n/a	chr15:53116969-53116980
37	CEBPB	chr15:53094449-53094491	K562	blood:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
38	CEBPB	chr15:53116289-53117061	MCF-7	breast:	n/a	chr15:53116969-53116980
39	CEBPB	chr15:53116784-53117148	HepG2	liver:	n/a	chr15:53116969-53116980
40	CEBPB	chr15:53094308-53094599	HepG2	liver:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
41	CEBPB	chr15:53116901-53117119	A549	lung:	n/a	chr15:53116969-53116980
42	CEBPB	chr15:53116777-53117151	HepG2	liver:	n/a	chr15:53116969-53116980
43	CEBPB	chr15:53075756-53076401	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr15:53072470-53073069	A549	lung:	n/a	chr15:53072565-53072576
45	CEBPB	chr15:53094304-53094546	A549	lung:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
46	CEBPD	chr15:53078674-53079064	HepG2	liver:	n/a	n/a
47	CEBPD	chr15:53082328-53082849	HepG2	liver:	n/a	n/a
48	CEBPD	chr15:53116757-53117027	HepG2	liver:	n/a	n/a
49	CEBPD	chr15:53116877-53117012	HepG2	liver:	n/a	n/a
50	CEBPD	chr15:53081999-53082244	HepG2	liver:	n/a	n/a

(count:4338 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53096248-53096298	AG04450	lung:	fetal
2	chr15:53098257-53098307	SK-N-SH	brain:	n/a
3	chr15:53077010-53077060	HIPEpiC	eye:	n/a
4	chr15:53100108-53100158	HNPCEpiC	eye:	n/a
5	chr15:53095984-53096034	AoSMC	blood vessel:	n/a
6	chr15:53097649-53097699	HNPCEpiC	eye:	n/a
7	chr15:53097649-53097699	PFSK-1	brain:	n/a
8	chr15:53096248-53096298	AG04450	lung:	fetal
9	chr15:53098257-53098307	SK-N-SH	brain:	n/a
10	chr15:53077010-53077060	HIPEpiC	eye:	n/a
11	chr15:53100108-53100158	HNPCEpiC	eye:	n/a
12	chr15:53095984-53096034	AoSMC	blood vessel:	n/a
13	chr15:53097649-53097699	HNPCEpiC	eye:	n/a
14	chr15:53097649-53097699	PFSK-1	brain:	n/a
15	chr15:53078121-53078171	SKMC	muscle:	n/a
16	chr15:53087232-53087282	HCM	heart:	n/a
17	chr15:53083587-53083637	CMK	blood:	n/a
18	chr15:53086857-53086907	SK-N-SH_RA	brain:	n/a
19	chr15:53075825-53075875	MCF10A-Er-Src	breast:	n/a
20	chr15:53077010-53077060	NH-A	brain:	n/a
21	chr15:53096248-53096298	Caco-2	colon:	n/a
22	chr15:53076806-53076856	HEEpiC	esophagus:	n/a
23	chr15:53098475-53098525	PANC-1	pancreas:	n/a
24	chr15:53100108-53100158	CMK	blood:	n/a
25	chr15:53083587-53083637	A549	lung:	n/a
26	chr15:53096481-53096531	HRCEpiC	kidney:	n/a
27	chr15:53096035-53096085	HCT-116	colon:	n/a
28	chr15:53078121-53078171	ProgFib	skin:	n/a
29	chr15:53087232-53087282	Hela-S3	cervix:	n/a
30	chr15:53080933-53080983	U87	brain:	n/a
31	chr15:53076188-53076238	SKMC	muscle:	n/a
32	chr15:53077913-53077963	HepG2	liver:	n/a
33	chr15:53083532-53083582	U87	brain:	n/a
34	chr15:53077609-53077659	LNCaP	prostate:	n/a
35	chr15:53087487-53087537	SK-N-MC	brain:	n/a
36	chr15:53080933-53080983	HCPEpiC	choroid plexus:	n/a
37	chr15:53086726-53086776	HEEpiC	esophagus:	n/a
38	chr15:53087887-53087937	NHBE	bronchial:	n/a
39	chr15:53082249-53082299	SK-N-SH	brain:	n/a
40	chr15:53077913-53077963	RPTEC	kidney:	n/a
41	chr15:53087887-53087937	NHDF-neo	bronchial:	n/a
42	chr15:53090807-53090857	PANC-1	pancreas:	n/a
43	chr15:53086968-53087018	CMK	blood:	n/a
44	chr15:53079445-53079495	SK-N-SH_RA	brain:	n/a
45	chr15:53079445-53079495	AG09319	gingival:	n/a
46	chr15:53083135-53083185	HUVEC	blood vessel:	n/a
47	chr15:53080459-53080509	HCT-116	colon:	n/a
48	chr15:53098475-53098525	SKMC	muscle:	n/a
49	chr15:53098257-53098307	Jurkat	blood:	n/a
50	chr15:53082902-53082952	AG09319	gingival:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53076988..53078899-chr16:3071890..3073813,2	MCF-7	breast:
2	chr15:53081655..53083909-chr15:53083926..53085751,2	K562	blood:
3	chr15:53088202..53091601-chr15:53093551..53096557,3	MCF-7	breast:
4	chr15:53072756..53074429-chr15:53080987..53082654,2	MCF-7	breast:
5	chr15:53079161..53080673-chr15:53143168..53145503,2	MCF-7	breast:
6	chr15:53098934..53100673-chr15:53103575..53106101,2	MCF-7	breast:
7	chr15:53072756..53074429-chr15:53080987..53082654,2	MCF-7	breast:
8	chr15:53093578..53096252-chr15:53138309..53141218,2	MCF-7	breast:
9	chr15:53072465..53075963-chr15:53080706..53083147,3	MCF-7	breast:
10	chr15:51844973..51847549-chr15:53093703..53095676,2	MCF-7	breast:
11	chr15:53093578..53096252-chr15:53138309..53141218,2	MCF-7	breast:
12	chr15:53075751..53076563-chr15:53489418..53490178,2	K562	blood:
13	chr15:53104829..53105653-chr15:53489336..53490188,3	MCF-7	breast:
14	chr15:53127363..53130328-chr15:53159239..53161065,2	MCF-7	breast:
15	chr15:53060401..53062540-chr15:53070993..53073276,2	MCF-7	breast:
16	chr15:53098934..53100673-chr15:53103575..53106101,2	MCF-7	breast:
17	chr15:53081717..53084310-chr15:53084763..53086372,2	MCF-7	breast:
18	chr13:45913793..45915528-chr15:53082604..53084932,2	MCF-7	breast:
19	chr15:53091716..53093481-chr15:53093879..53095531,2	MCF-7	breast:
20	chr15:52611004..52613000-chr15:53076080..53077962,2	K562	blood:
21	chr15:53091716..53093481-chr15:53093879..53095531,2	MCF-7	breast:
22	chr15:53072465..53075963-chr15:53080706..53083147,3	MCF-7	breast:
23	chr15:53079651..53082730-chr15:53114348..53117214,3	MCF-7	breast:
24	chr15:53088202..53091601-chr15:53093551..53096557,3	MCF-7	breast:
25	chr15:53139577..53141179-chr15:53147410..53150139,2	MCF-7	breast:
26	chr15:53072513..53073379-chr15:53804086..53804809,3	MCF-7	breast:
27	chr15:53072253..53073288-chr15:54008890..54009735,3	MCF-7	breast:
28	chr15:53078999..53085478-chr15:53088216..53096885,9	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ONECUT1-1	chr15:53092221-53093114	XLOC_011481
2	lnc-ONECUT1-1	chr15:53096691-53097142	XLOC_011481
3	lnc-MAPK6-18	chr15:53136240-53136402	l_1157_chr15:53136239-53171611_testes
4	lnc-FAM214A-1	chr15:53079204-53079324	NONHSAT043947
5	lnc-ONECUT1-1	chr15:53096691-53097139	ENSG00000259203.1
6	lnc-ONECUT1-1	chr15:53098245-53098609	NONHSAT043955
7	lnc-FAM214A-1	chr15:53079958-53080605	NONHSAT043947
8	lnc-ONECUT1-1	chr15:53096691-53096992	NONHSAT043955
9	lnc-ONECUT1-1	chr15:53096691-53096992	XLOC_011481
10	lnc-ONECUT1-1	chr15:53095448-53096044	NONHSAT043955
11	lnc-FAM214A-1	chr15:53077922-53078166	NONHSAT043947
12	lnc-ONECUT1-1	chr15:53093811-53093844	ENSG00000259203.1
13	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
14	lnc-ONECUT1-1	chr15:53092407-53093114	XLOC_011481
15	lnc-ONECUT1-1	chr15:53096691-53096992	XLOC_011481
16	lnc-ONECUT1-1	chr15:53095405-53096044	XLOC_011481
17	lnc-ONECUT1-1	chr15:53097866-53097962	XLOC_011481
18	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
19	lnc-ONECUT1-1	chr15:53097866-53097962	XLOC_011481
20	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
21	lnc-ONECUT1-1	chr15:53096406-53096494	ENSG00000259203.1
22	lnc-MAPK6-11	chr15:53086548-53087549	XLOC_011257
23	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
24	lnc-ONECUT1-1	chr15:53096406-53096494	NONHSAT043955
25	lnc-MAPK6-11	chr15:53084847-53084886	XLOC_011257
26	lnc-ONECUT1-1	chr15:53096691-53097142	XLOC_011481
27	lnc-ONECUT1-1	chr15:53095593-53096044	XLOC_011481

No data

Variant related genes	Relation type
ONECUT1	TF binding region
ENSG00000259203	TF binding region
ONECUT1	CpG island
ENSG00000259203	CpG island
ENSG00000273149	chromatin interactions
ENSG00000133112	chromatin interactions
ENSG00000169856	chromatin interactions
ENSG00000170919	chromatin interactions
LPHN2	miRNA target sites
HLA-A	miRNA target sites
FBXO28	miRNA target sites
CCND1	miRNA target sites

Extended variants
information (count: 2427 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2427 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17543338	chr15:53069874-53069875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369734028	chr15:53069895-53069896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539823142	chr15:53069916-53069917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200121358	chr15:53069930-53069931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200691262	chr15:53069932-53069933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111323288	chr15:53069933-53069934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs78935952	chr15:53069934-53069935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57187579	chr15:53069935-53069936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78549952	chr15:53069936-53069937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533813246	chr15:53069941-53069942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555212772	chr15:53069945-53069946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558499657	chr15:53069957-53069958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28461901	chr15:53069973-53069974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182351656	chr15:53070016-53070017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371364750	chr15:53070017-53070018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537603429	chr15:53070029-53070030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186580185	chr15:53070074-53070075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577658806	chr15:53070122-53070123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7180600	chr15:53070141-53070142	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368448813	chr15:53070146-53070147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553784988	chr15:53070181-53070182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370340409	chr15:53070214-53070215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573609358	chr15:53070256-53070257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540951268	chr15:53070258-53070259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191826195	chr15:53070303-53070304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142952212	chr15:53070340-53070341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544433200	chr15:53070385-53070386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114955693	chr15:53070400-53070401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553039895	chr15:53070433-53070434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151119690	chr15:53070472-53070473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184838395	chr15:53070478-53070479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75223709	chr15:53070493-53070494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527642966	chr15:53070499-53070500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548874327	chr15:53070541-53070542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs62023486	chr15:53070589-53070590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs538087725	chr15:53070634-53070635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556074151	chr15:53070699-53070700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140887961	chr15:53070746-53070747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74369848	chr15:53070862-53070863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538335476	chr15:53070871-53070872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144848324	chr15:53070908-53070909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572090332	chr15:53070931-53070932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542606455	chr15:53070941-53070942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35531895	chr15:53070994-53070995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1357	chr15:53071000-53071001	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79703436	chr15:53071082-53071083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79719072	chr15:53071093-53071094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545932069	chr15:53071128-53071129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533540735	chr15:53071129-53071130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545113567	chr15:53071156-53071157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:1908 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53045800-53070800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:53049600-53070600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:53059400-53072400	Weak transcription	HepG2	liver
4	chr15:53069200-53070600	Weak transcription	Liver	Liver
5	chr15:53069800-53073000	Weak transcription	Pancreas	Pancrea
6	chr15:53070400-53070800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr15:53070400-53071000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:53070600-53070800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr15:53070600-53071000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr15:53070600-53071200	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr15:53070600-53071400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr15:53070600-53073000	Enhancers	Liver	Liver
13	chr15:53070800-53071000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr15:53070800-53071000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:53070800-53071000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr15:53071000-53071200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr15:53071000-53072000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr15:53071000-53075400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:53071200-53072400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr15:53071400-53071800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr15:53071800-53072200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr15:53071800-53072600	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr15:53071800-53073000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:53072000-53072200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:53072000-53072200	Enhancers	GM12878-XiMat	blood
26	chr15:53072000-53072400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr15:53072000-53072400	Bivalent Enhancer	A549	lung
28	chr15:53072000-53072800	Enhancers	Primary B cells from peripheral blood	blood
29	chr15:53072000-53073400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:53072000-53073400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
31	chr15:53072200-53072600	Enhancers	Primary B cells from cord blood	blood
32	chr15:53072200-53072600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:53072200-53072600	Flanking Active TSS	GM12878-XiMat	blood
34	chr15:53072200-53072800	Enhancers	Primary hematopoietic stem cells	blood
35	chr15:53072200-53073400	Bivalent Enhancer	Colon Smooth Muscle	Colon
36	chr15:53072200-53073600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr15:53072400-53072600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
38	chr15:53072400-53072600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:53072400-53072600	Enhancers	Duodenum Mucosa	Duodenum
40	chr15:53072400-53072600	Bivalent Enhancer	Fetal Brain Female	brain
41	chr15:53072400-53072800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr15:53072400-53072800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
43	chr15:53072400-53072800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
44	chr15:53072400-53072800	Flanking Bivalent TSS/Enh	A549	lung
45	chr15:53072400-53073000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr15:53072400-53073000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
47	chr15:53072400-53073000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
48	chr15:53072400-53073000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
49	chr15:53072400-53073000	Bivalent Enhancer	Fetal Lung	lung
50	chr15:53072400-53073400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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