Variant report

Variant	esv3375545
Chromosome Location	chr13:54517432-54908108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:1220)
Chromatin interactive
region (count:14)
LncRNA
region (count:50)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:54603310-54603730	GM12878	blood:	n/a	n/a
2	BACH1	chr13:54608215-54608549	K562	blood:	n/a	chr13:54608373-54608387
3	BACH1	chr13:54608194-54608544	H1-hESC	embryonic stem cell:	n/a	chr13:54608373-54608387
4	BATF	chr13:54603353-54603674	GM12878	blood:	n/a	chr13:54603503-54603514 chr13:54603500-54603510
5	BHLHE40	chr13:54841375-54841570	K562	blood:	n/a	n/a
6	CCNT2	chr13:54841369-54841576	K562	blood:	n/a	n/a
7	CEBPB	chr13:54784789-54785162	MCF-7	breast:	n/a	n/a
8	CEBPB	chr13:54546458-54546730	A549	lung:	n/a	chr13:54546576-54546587
9	CEBPB	chr13:54687589-54687822	H1-hESC	embryonic stem cell:	n/a	chr13:54687764-54687776 chr13:54687700-54687711 chr13:54687629-54687646
10	CEBPB	chr13:54603845-54604179	HepG2	liver:	n/a	chr13:54604009-54604020
11	CEBPB	chr13:54813050-54813332	HepG2	liver:	n/a	chr13:54813217-54813228
12	CEBPB	chr13:54815858-54816140	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr13:54855795-54855944	HepG2	liver:	n/a	chr13:54855917-54855928
14	CEBPB	chr13:54603879-54604175	H1-hESC	embryonic stem cell:	n/a	chr13:54604009-54604020
15	CEBPB	chr13:54660289-54660602	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:54578495-54578853	HepG2	liver:	n/a	chr13:54578691-54578702 chr13:54578653-54578666 chr13:54578654-54578665 chr13:54578691-54578704
17	CEBPB	chr13:54884041-54884241	K562	blood:	n/a	chr13:54884186-54884197
18	CEBPB	chr13:54813135-54813273	H1-hESC	embryonic stem cell:	n/a	chr13:54813217-54813228
19	CEBPB	chr13:54642798-54643108	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:54603899-54604203	ECC-1	luminal epithelium:	n/a	chr13:54604009-54604020
21	CEBPB	chr13:54849401-54849525	HepG2	liver:	n/a	chr13:54849410-54849421 chr13:54849408-54849419
22	CEBPB	chr13:54725214-54725221	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr13:54578538-54578810	A549	lung:	n/a	chr13:54578691-54578702 chr13:54578653-54578666 chr13:54578654-54578665 chr13:54578691-54578704
24	CEBPB	chr13:54546404-54546747	ECC-1	luminal epithelium:	n/a	chr13:54546576-54546587
25	CEBPB	chr13:54784939-54785095	HepG2	liver:	n/a	n/a
26	CEBPB	chr13:54784873-54785176	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr13:54656746-54656974	HepG2	liver:	n/a	chr13:54656868-54656879
28	CEBPB	chr13:54884025-54884331	IMR90	lung:	n/a	chr13:54884186-54884197
29	CEBPB	chr13:54547171-54547443	HepG2	liver:	n/a	chr13:54547312-54547323
30	CEBPB	chr13:54750821-54751091	ECC-1	luminal epithelium:	n/a	chr13:54750934-54750945
31	CEBPB	chr13:54784761-54785163	MCF-7	breast:	n/a	n/a
32	CEBPB	chr13:54546426-54546737	HepG2	liver:	n/a	chr13:54546576-54546587
33	CEBPB	chr13:54784834-54785264	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr13:54833321-54833412	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr13:54719060-54719258	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr13:54644090-54644338	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr13:54523024-54523224	HepG2	liver:	n/a	chr13:54523109-54523120
38	CEBPB	chr13:54660363-54660452	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:54546497-54546664	H1-hESC	embryonic stem cell:	n/a	chr13:54546576-54546587
40	CEBPB	chr13:54573797-54574012	H1-hESC	embryonic stem cell:	n/a	chr13:54573850-54573863 chr13:54573852-54573863 chr13:54573850-54573863 chr13:54573847-54573864
41	CEBPB	chr13:54546447-54546726	ECC-1	luminal epithelium:	n/a	chr13:54546576-54546587
42	CEBPB	chr13:54687616-54687812	HepG2	liver:	n/a	chr13:54687764-54687776 chr13:54687700-54687711 chr13:54687629-54687646
43	CEBPB	chr13:54884015-54884265	HepG2	liver:	n/a	chr13:54884186-54884197
44	CEBPB	chr13:54750785-54751096	HepG2	liver:	n/a	chr13:54750934-54750945
45	CEBPB	chr13:54753352-54753369	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:54625790-54626036	HepG2	liver:	n/a	chr13:54625909-54625920 chr13:54625909-54625922
47	CEBPB	chr13:54815763-54816209	ECC-1	luminal epithelium:	n/a	chr13:54815801-54815812
48	CEBPB	chr13:54884004-54884338	H1-hESC	embryonic stem cell:	n/a	chr13:54884186-54884197
49	CEBPB	chr13:54744391-54744583	H1-hESC	embryonic stem cell:	n/a	chr13:54744558-54744571
50	CEBPB	chr13:54906665-54906963	HepG2	liver:	n/a	chr13:54906812-54906823 chr13:54906792-54906803

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54740236-54740286	GM12892	blood:	n/a
2	chr13:54604033-54604083	SK-N-MC	brain:	n/a
3	chr13:54821786-54821836	MCF10A-Er-Src	breast:	n/a
4	chr13:54898133-54898183	LNCaP	prostate:	n/a
5	chr13:54887997-54888047	SK-N-MC	brain:	n/a
6	chr13:54708344-54708394	GM12891	blood:	n/a
7	chr13:54887288-54887338	H1-hESC	embryonic stem cell:	embryo
8	chr13:54875232-54875282	GM12891	blood:	n/a
9	chr13:54861089-54861139	IMR90	lung:	fetal
10	chr13:54887314-54887364	ProgFib	skin:	n/a
11	chr13:54758149-54758199	A549	lung:	n/a
12	chr13:54847234-54847284	K562	blood:	n/a
13	chr13:54604033-54604083	HEK293	kidney:	embryo
14	chr13:54817511-54817561	IMR90	lung:	fetal
15	chr13:54887288-54887338	RPTEC	kidney:	n/a
16	chr13:54887314-54887364	GM12878	blood:	n/a
17	chr13:54758149-54758199	ovcar-3	ovarian:	n/a
18	chr13:54604033-54604083	U87	brain:	n/a
19	chr13:54708344-54708394	AG04449	skin:	fetal
20	chr13:54875232-54875282	ProgFib	skin:	n/a
21	chr13:54817511-54817561	SKMC	muscle:	n/a
22	chr13:54888141-54888191	HRE	kidney:	n/a
23	chr13:54758149-54758199	PFSK-1	brain:	n/a
24	chr13:54887997-54888047	MCF10A-Er-Src	breast:	n/a
25	chr13:54887314-54887364	SKMC	muscle:	n/a
26	chr13:54774189-54774239	Hepatocyte	liver:	n/a
27	chr13:54817511-54817561	Hela-S3	cervix:	n/a
28	chr13:54888141-54888191	HAEpiC	amniotic membrane:	n/a
29	chr13:54847234-54847284	NHBE	bronchial:	n/a
30	chr13:54604033-54604083	HIPEpiC	eye:	n/a
31	chr13:54883769-54883819	LNCaP	prostate:	n/a
32	chr13:54821786-54821836	PrEC	prostate:	n/a
33	chr13:54875232-54875282	LNCaP	prostate:	n/a
34	chr13:54883769-54883819	HMEC	breast:	n/a
35	chr13:54774189-54774239	HUVEC	blood vessel:	n/a
36	chr13:54707971-54708021	HCT-116	colon:	n/a
37	chr13:54604033-54604083	HRE	kidney:	n/a
38	chr13:54887369-54887419	H1-hESC	embryonic stem cell:	embryo
39	chr13:54821786-54821836	HRE	kidney:	n/a
40	chr13:54707971-54708021	CMK	blood:	n/a
41	chr13:54758149-54758199	AoSMC	blood vessel:	n/a
42	chr13:54719190-54719240	BJ	skin:	n/a
43	chr13:54883769-54883819	BE2_C	brain:	n/a
44	chr13:54887369-54887419	GM12891	blood:	n/a
45	chr13:54740236-54740286	HMEC	breast:	n/a
46	chr13:54740236-54740286	K562	blood:	n/a
47	chr13:54887997-54888047	PANC-1	pancreas:	n/a
48	chr13:54887997-54888047	SK-N-SH	brain:	n/a
49	chr13:54719190-54719240	MCF-7	breast:	n/a
50	chr13:54861089-54861139	GM12891	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:54766693..54769398-chr13:54785918..54788383,2	MCF-7	breast:
2	chr13:54688466..54689986-chr6:86385107..86388002,2	K562	blood:
3	chr13:54780172..54782257-chr13:54783482..54785302,2	MCF-7	breast:
4	chr13:54759630..54760543-chr13:55804447..55805083,2	MCF-7	breast:
5	chr13:54831947..54834177-chr13:54836785..54838998,2	MCF-7	breast:
6	chr13:54758846..54760838-chr13:54765685..54768244,2	K562	blood:
7	chr13:54693602..54695448-chr13:54696284..54698888,2	MCF-7	breast:
8	chr13:54758846..54760838-chr13:54765685..54768244,2	K562	blood:
9	chr13:54766693..54769398-chr13:54785918..54788383,2	MCF-7	breast:
10	chr13:54831947..54834177-chr13:54836785..54838998,2	MCF-7	breast:
11	chr13:54693602..54695448-chr13:54696284..54698888,2	MCF-7	breast:
12	chr13:54636455..54636955-chr3:194041864..194042378,2	Hela-S3	cervix:
13	chr13:54780172..54782257-chr13:54783482..54785302,2	MCF-7	breast:
14	chr13:54628019..54628961-chr16:83370704..83371434,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH8-7	chr13:54678118-54678348	NONHSAT034022
2	lnc-PCDH8-7	chr13:54679850-54679912	NONHSAT034022
3	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
4	lnc-PCDH8-5	chr13:54698459-54698890	ENSG00000234787.3
5	lnc-OLFM4-4	chr13:54843168-54843542	NONHSAT034030
6	lnc-PCDH8-5	chr13:54689924-54690344	ENSG00000234787.3
7	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
8	lnc-PCDH8-5	chr13:54699284-54699407	ENSG00000234787.3
9	lnc-PCDH8-5	chr13:54698459-54698890	NR_108062
10	lnc-PCDH8-5	chr13:54699284-54699407	ENSG00000234787
11	lnc-PCDH8-5	chr13:54706748-54706954	ENSG00000234787.3
12	lnc-OLFM4-11	chr13:54690611-54690986	NONHSAT034026
13	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787
14	lnc-PCDH8-5	chr13:54701415-54701564	NR_108062
15	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787.3
16	lnc-PCDH8-5	chr13:54695071-54695179	ENSG00000234787
17	lnc-PCDH8-5	chr13:54700998-54701564	NR_108063
18	lnc-OLFM4-4	chr13:54813174-54813188	NONHSAT034030
19	lnc-PCDH8-5	chr13:54705009-54705206	NONHSAT034028
20	lnc-PCDH8-5	chr13:54706748-54706997	ENSG00000234787.3
21	lnc-PCDH8-5	chr13:54689984-54690344	ENSG00000234787.3
22	lnc-PCDH8-5	chr13:54695075-54695179	ENSG00000234787.3
23	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
24	lnc-PCDH8-5	chr13:54706748-54707001	NONHSAT034028
25	lnc-PCDH8-5	chr13:54705009-54705206	NR_108062
26	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787.3
27	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787.3
28	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787
29	lnc-PCDH8-5	chr13:54706748-54706986	ENSG00000234787.3
30	lnc-PCDH8-5	chr13:54701415-54701564	NONHSAT034028
31	lnc-PCDH8-5	chr13:54699130-54699407	ENSG00000234787.3
32	lnc-OLFM4-4	chr13:54817929-54818572	NONHSAT034030
33	lnc-PCDH8-5	chr13:54706748-54707006	NR_108062
34	lnc-PCDH8-5	chr13:54698462-54698890	NONHSAT034028
35	lnc-PCDH8-5	chr13:54701415-54701478	ENSG00000234787.3
36	lnc-PCDH8-5	chr13:54706748-54707006	NR_108063
37	lnc-OLFM4-4	chr13:54813124-54813153	NONHSAT034030
38	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787
39	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787
40	lnc-PCDH8-5	chr13:54689924-54690344	ENSG00000234787
41	lnc-OLFM4-4	chr13:54817928-54819360	NONHSAT034031
42	lnc-PCDH8-5	chr13:54701415-54701564	ENSG00000234787.3
43	lnc-PCDH8-5	chr13:54705009-54705206	NR_108063
44	lnc-PCDH8-5	chr13:54705009-54705206	ENSG00000234787
45	lnc-PCDH8-5	chr13:54706497-54706748	ENSG00000234787
46	lnc-OLFM4-4	chr13:54812998-54813118	NONHSAT034030
47	lnc-PCDH8-5	chr13:54706748-54707001	ENSG00000234787
48	lnc-PCDH8-5	chr13:54700997-54701564	ENSG00000234787
49	lnc-PCDH8-5	chr13:54698948-54699407	ENSG00000234787.3
50	lnc-PCDH8-5	chr13:54698459-54698890	ENSG00000234787

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1297	chr13:54886116-54886132	MIMAT0005886

No data

Variant related genes	Relation type
ENSG00000271652	TF binding region
LINC00458	TF binding region
ENSG00000271652	CpG island
LINC00458	CpG island
ENSG00000203875	chromatin interactions
POU5F1	lncRNA
TRIB2	Mature miRNA region

Extended variants
information (count: 10368 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:10368 , 50 per page) page: 1 2 3 4 5 6 7 ... 208

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187338070	chr13:54520611-54520612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577881665	chr13:54520657-54520658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150128913	chr13:54520670-54520671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76236442	chr13:54520687-54520688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9316680	chr13:54520694-54520695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149375202	chr13:54520695-54520696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562499725	chr13:54520718-54520719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531248613	chr13:54520792-54520793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2446169	chr13:54520877-54520878	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs145663849	chr13:54520885-54520886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77197391	chr13:54520975-54520976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190955522	chr13:54520990-54520991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577303975	chr13:54527408-54527409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184955838	chr13:54527463-54527464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552257138	chr13:54527464-54527465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145583649	chr13:54527473-54527474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528925258	chr13:54527497-54527498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376902240	chr13:54527511-54527512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188167896	chr13:54527517-54527518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192968835	chr13:54527575-54527576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534835821	chr13:54527580-54527581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140349441	chr13:54527600-54527601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551986674	chr13:54527606-54527607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554629406	chr13:54527630-54527631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553533940	chr13:54527776-54527777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571895810	chr13:54527786-54527787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144082716	chr13:54527983-54527984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547949719	chr13:54528064-54528065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185341217	chr13:54528093-54528094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146577960	chr13:54528169-54528170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141276851	chr13:54528194-54528195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575413567	chr13:54528196-54528197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112242251	chr13:54528198-54528199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557508818	chr13:54528217-54528218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537245138	chr13:54528218-54528219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577461824	chr13:54528273-54528274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116159884	chr13:54528364-54528365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564369506	chr13:54528423-54528424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1125084	chr13:54528432-54528433	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs181886644	chr13:54528447-54528448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541923254	chr13:54528468-54528469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542233181	chr13:54528474-54528475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184671502	chr13:54528513-54528514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577424408	chr13:54528525-54528526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375623171	chr13:54528558-54528559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78516814	chr13:54528625-54528626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs76939285	chr13:54528642-54528643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528981225	chr13:54528648-54528649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527846561	chr13:54528649-54528650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571720502	chr13:54528719-54528720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Urothelial carcinoma	21177765	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54520600-54521000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:54527400-54527800	Enhancers	Fetal Brain Female	brain
3	chr13:54527400-54527800	Enhancers	Fetal Stomach	stomach
4	chr13:54527400-54528600	Enhancers	Rectal Smooth Muscle	rectum
5	chr13:54527600-54528200	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr13:54527600-54528800	Enhancers	Fetal Heart	heart
7	chr13:54528600-54530600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr13:54530600-54530800	Enhancers	Rectal Smooth Muscle	rectum
9	chr13:54540200-54541000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:54540400-54541000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr13:54541000-54543000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:54543000-54543600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr13:54545600-54545800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:54545800-54546000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr13:54546000-54547200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:54546200-54549200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:54551600-54552600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr13:54551800-54552600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:54568400-54568800	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr13:54572000-54578200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr13:54578200-54578800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:54578400-54578800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr13:54578400-54579200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:54578800-54580200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:54580200-54580600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:54580600-54603200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:54588800-54589000	Enhancers	Fetal Brain Male	brain
28	chr13:54589000-54590400	Weak transcription	Fetal Brain Male	brain
29	chr13:54590400-54592200	Enhancers	Fetal Brain Male	brain
30	chr13:54590600-54591200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:54591200-54591800	Enhancers	Fetal Brain Female	brain
32	chr13:54591800-54592400	Weak transcription	Fetal Brain Female	brain
33	chr13:54592400-54592600	Enhancers	Fetal Brain Female	brain
34	chr13:54600000-54604000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:54602800-54604200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr13:54603000-54603800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr13:54603200-54603600	Enhancers	Rectal Smooth Muscle	rectum
38	chr13:54603200-54603800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:54603200-54603800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:54603200-54603800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr13:54603200-54604000	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr13:54603200-54604000	Enhancers	NH-A	brain
43	chr13:54603200-54604200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr13:54603200-54604200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:54603200-54604400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr13:54603200-54604600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr13:54603400-54603800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr13:54603400-54603800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr13:54603600-54604000	Enhancers	Brain Germinal Matrix	brain
50	chr13:54603600-54604400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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