Variant report

Variant	nsv879682
Chromosome Location	chr4:102859835-103088491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1350)
CpG islands
(count:184)
Chromatin interactive
region (count:43)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:102874997-102875510	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:102875018-102875480	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:102928871-102929419	GM12878	blood:	n/a	n/a
4	ATF3	chr4:102891559-102892187	A549	lung:	n/a	n/a
5	BATF	chr4:102929090-102929345	GM12878	blood:	n/a	chr4:102929197-102929205
6	BATF	chr4:102929053-102929342	GM12878	blood:	n/a	chr4:102929197-102929205
7	BCL3	chr4:102891602-102892411	A549	lung:	n/a	chr4:102891937-102891944
8	BCL3	chr4:102891662-102892194	A549	lung:	n/a	chr4:102891937-102891944
9	BCL3	chr4:102889110-102889709	A549	lung:	n/a	n/a
10	BCL3	chr4:102898097-102898669	A549	lung:	n/a	n/a
11	BCL3	chr4:102898061-102898877	A549	lung:	n/a	n/a
12	BRCA1	chr4:102864499-102864545	GM12878	blood:	n/a	n/a
13	BRCA1	chr4:103024539-103024540	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr4:102875169-102875556	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr4:102897789-102898772	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr4:102889042-102889556	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr4:103041942-103042346	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:102898123-102898750	HCT-116	colon:	n/a	n/a
19	CBX3	chr4:102902726-102903369	HCT-116	colon:	n/a	n/a
20	CBX3	chr4:103061062-103061620	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:103060273-103060730	HCT-116	colon:	n/a	n/a
22	CCNT2	chr4:103063078-103063392	K562	blood:	n/a	chr4:103063145-103063165
23	CEBPB	chr4:102939394-102939672	A549	lung:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
24	CEBPB	chr4:102898157-102898779	HCT-116	colon:	n/a	n/a
25	CEBPB	chr4:102859908-102860460	ECC-1	luminal epithelium:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
26	CEBPB	chr4:102898141-102898612	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:103042484-103042541	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:102889118-102889418	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:103079069-103079533	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr4:102939368-102939687	HepG2	liver:	n/a	chr4:102939534-102939547 chr4:102939535-102939546 chr4:102939534-102939547 chr4:102939534-102939545
31	CEBPB	chr4:102859965-102860440	Hela-S3	cervix:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
32	CEBPB	chr4:103007322-103007591	IMR90	lung:	n/a	chr4:103007450-103007461
33	CEBPB	chr4:102964391-102964639	IMR90	lung:	n/a	chr4:102964520-102964531
34	CEBPB	chr4:102958722-102958968	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:102962532-102962662	H1-hESC	embryonic stem cell:	n/a	chr4:102962623-102962634 chr4:102962622-102962639 chr4:102962623-102962636
36	CEBPB	chr4:102859976-102860454	ECC-1	luminal epithelium:	n/a	chr4:102860203-102860214 chr4:102860253-102860266
37	CEBPB	chr4:102891767-102892148	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:103075895-103076127	HepG2	liver:	n/a	chr4:103075994-103076005
39	CEBPB	chr4:102874953-102875505	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:103061133-103061474	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:102969012-102969231	HepG2	liver:	n/a	chr4:102969164-102969175 chr4:102969113-102969126 chr4:102969113-102969126 chr4:102969113-102969124 chr4:102969113-102969124 chr4:102969114-102969125
42	CEBPB	chr4:103079044-103079609	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr4:103060381-103060826	HCT-116	colon:	n/a	chr4:103060671-103060688 chr4:103060674-103060687
44	CEBPB	chr4:103060390-103060870	Hela-S3	cervix:	n/a	chr4:103060671-103060688 chr4:103060674-103060687
45	CEBPB	chr4:102875003-102875504	A549	lung:	n/a	n/a
46	CEBPB	chr4:102921643-102921978	HepG2	liver:	n/a	chr4:102921801-102921812
47	CEBPB	chr4:103060390-103060862	ECC-1	luminal epithelium:	n/a	chr4:103060671-103060688 chr4:103060674-103060687
48	CEBPB	chr4:102862850-102863632	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr4:102898283-102898601	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr4:103075889-103076144	K562	blood:	n/a	chr4:103075994-103076005

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102995477-102995527	Hepatocyte	liver:	n/a
2	chr4:102995477-102995527	Hepatocyte	liver:	n/a
3	chr4:102875309-102875359	SK-N-MC	brain:	n/a
4	chr4:102995477-102995527	BE2_C	brain:	n/a
5	chr4:102995477-102995527	NHBE	bronchial:	n/a
6	chr4:102878132-102878182	HCM	heart:	n/a
7	chr4:102878132-102878182	MCF-7	breast:	n/a
8	chr4:102995477-102995527	GM06990	blood:	n/a
9	chr4:102995477-102995527	SAEC	small airway:	n/a
10	chr4:102995477-102995527	SK-N-SH_RA	brain:	n/a
11	chr4:102878132-102878182	GM06990	blood:	n/a
12	chr4:102995477-102995527	U87	brain:	n/a
13	chr4:102878132-102878182	HRE	kidney:	n/a
14	chr4:102995477-102995527	AG04450	lung:	fetal
15	chr4:102878132-102878182	RPTEC	kidney:	n/a
16	chr4:102878132-102878182	LNCaP	prostate:	n/a
17	chr4:102995477-102995527	PFSK-1	brain:	n/a
18	chr4:102878132-102878182	Caco-2	colon:	n/a
19	chr4:102875309-102875359	A549	lung:	n/a
20	chr4:102875309-102875359	SKMC	muscle:	n/a
21	chr4:102995477-102995527	NT2-D1	testis:	n/a
22	chr4:102995477-102995527	RPTEC	kidney:	n/a
23	chr4:102875309-102875359	HCF	heart:	n/a
24	chr4:102875309-102875359	HRE	kidney:	n/a
25	chr4:102875309-102875359	AG04449	skin:	fetal
26	chr4:102875309-102875359	HRPEpiC	eye:	n/a
27	chr4:102995477-102995527	Caco-2	colon:	n/a
28	chr4:102878132-102878182	BJ	skin:	n/a
29	chr4:102995477-102995527	AG04449	skin:	fetal
30	chr4:102875309-102875359	CMK	blood:	n/a
31	chr4:102995477-102995527	HL-60	blood:	n/a
32	chr4:102995477-102995527	HNPCEpiC	eye:	n/a
33	chr4:102878132-102878182	Jurkat	blood:	n/a
34	chr4:102995477-102995527	ECC-1	luminal epithelium:	n/a
35	chr4:102995477-102995527	HMEC	breast:	n/a
36	chr4:102878132-102878182	HMEC	breast:	n/a
37	chr4:102878132-102878182	BE2_C	brain:	n/a
38	chr4:102878132-102878182	K562	blood:	n/a
39	chr4:102995477-102995527	SK-N-SH	brain:	n/a
40	chr4:102995477-102995527	T-47D	breast:	n/a
41	chr4:102995477-102995527	NB4	blood:	n/a
42	chr4:102995477-102995527	NHDF-neo	bronchial:	n/a
43	chr4:102875309-102875359	AG04450	lung:	fetal
44	chr4:102878132-102878182	HEK293	kidney:	embryo
45	chr4:102878132-102878182	ECC-1	luminal epithelium:	n/a
46	chr4:102875309-102875359	Hela-S3	cervix:	n/a
47	chr4:102995477-102995527	GM19239	blood:	n/a
48	chr4:102878132-102878182	NB4	blood:	n/a
49	chr4:102878132-102878182	GM12878	blood:	n/a
50	chr4:102875309-102875359	HEK293	kidney:	embryo

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:102853526..102855448-chr4:102860047..102862482,2	K562	blood:
2	chr4:103046022..103047684-chr4:103082977..103085283,2	K562	blood:
3	chr4:102872789..102875813-chr4:102887302..102889181,3	MCF-7	breast:
4	chr4:102842276..102843131-chr4:102874015..102874871,3	MCF-7	breast:
5	chr4:102905542..102907916-chr4:102924446..102926465,2	K562	blood:
6	chr4:102926272..102927803-chr4:102933320..102936106,2	K562	blood:
7	chr4:102889946..102892052-chr4:102899600..102901567,2	MCF-7	breast:
8	chr4:103026061..103028758-chr4:103046881..103048973,2	K562	blood:
9	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
10	chr4:103081624..103084608-chr4:103098581..103101497,2	MCF-7	breast:
11	chr4:102929581..102932403-chr4:102937190..102939421,2	K562	blood:
12	chr17:56735383..56737967-chr4:102987580..102990239,2	MCF-7	breast:
13	chr4:102984591..102987150-chr4:102995563..102997735,2	MCF-7	breast:
14	chr4:102926272..102927803-chr4:102933320..102936106,2	K562	blood:
15	chr4:103026061..103028758-chr4:103046881..103048973,2	K562	blood:
16	chr4:102929581..102932403-chr4:102937190..102939421,2	K562	blood:
17	chr4:102913976..102916173-chr4:102919455..102922403,2	MCF-7	breast:
18	chr4:103006830..103008574-chr4:103015934..103018544,2	K562	blood:
19	chr4:102860897..102862820-chr4:102873982..102876353,2	MCF-7	breast:
20	chr4:102889946..102892052-chr4:102899600..102901567,2	MCF-7	breast:
21	chr4:102951568..102953598-chr4:102955632..102958106,2	K562	blood:
22	chr4:103064909..103066909-chr4:103071089..103073966,2	MCF-7	breast:
23	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
24	chr4:103056824..103059784-chr4:103061536..103063846,2	K562	blood:
25	chr4:102935717..102937290-chr4:102939556..102941946,2	K562	blood:
26	chr4:103056824..103059784-chr4:103061536..103063846,2	K562	blood:
27	chr4:102860897..102862820-chr4:102873982..102876353,2	MCF-7	breast:
28	chr4:103006830..103008574-chr4:103015934..103018544,2	K562	blood:
29	chr4:102874020..102874843-chr4:102891401..102892080,2	MCF-7	breast:
30	chr4:102983408..102985207-chr4:102988825..102991000,2	MCF-7	breast:
31	chr4:102880000..102881759-chr4:102886736..102889314,2	MCF-7	breast:
32	chr1:173794005..173794756-chr4:102954358..102954878,2	Hela-S3	cervix:
33	chr4:102905542..102907916-chr4:102924446..102926465,2	K562	blood:
34	chr4:103087475..103090012-chr4:103094577..103097148,2	MCF-7	breast:
35	chr4:102935717..102937290-chr4:102939556..102941946,2	K562	blood:
36	chr4:103046022..103047684-chr4:103082977..103085283,2	K562	blood:
37	chr4:103087412..103089274-chr4:103106235..103108167,2	MCF-7	breast:
38	chr4:102913976..102916173-chr4:102919455..102922403,2	MCF-7	breast:
39	chr4:102880000..102881759-chr4:102886736..102889314,2	MCF-7	breast:
40	chr4:103064909..103066909-chr4:103071089..103073966,2	MCF-7	breast:
41	chr4:102874020..102874843-chr4:102891401..102892080,2	MCF-7	breast:
42	chr3:64045097..64045973-chr4:102874042..102874640,2	MCF-7	breast:
43	chr4:102872789..102875813-chr4:102887302..102889181,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC39A8-2	chr4:102957839-102958060	ENSG00000251309.1
2	lnc-NFKB1-5	chr4:102992432-102992461	NONHSAT097576
3	lnc-NFKB1-6	chr4:102893580-102893955	NONHSAT097574
4	lnc-NFKB1-5	chr4:102994841-102994905	NONHSAT097576
5	lnc-NFKB1-5	chr4:102993502-102993557	NONHSAT097576
6	lnc-NFKB1-5	chr4:102995162-102995377	NONHSAT097576
7	lnc-NFKB1-5	chr4:102982573-102984295	NONHSAT097576
8	lnc-SLC39A8-2	chr4:102953366-102953539	ENSG00000251309.1
9	lnc-SLC39A8-2	chr4:102898051-102898257	ENSG00000251309.1

No data

Variant related genes	Relation type
BANK1	TF binding region
ENSG00000251309	TF binding region
MTND5P5	TF binding region
BANK1	CpG island
ENSG00000251309	CpG island
MTND5P5	CpG island
ENSG00000202077	chromatin interactions
ENSG00000251309	chromatin interactions

Extended variants
information (count: 5998 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:5998 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6858108	chr4:102859835-102859836	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572496873	chr4:102859901-102859902	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs539258385	chr4:102859907-102859908	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72686769	chr4:102859949-102859950	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184424184	chr4:102859959-102859960	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561425134	chr4:102860007-102860008	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73836675	chr4:102860010-102860011	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs572910140	chr4:102860028-102860029	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142064534	chr4:102860037-102860038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147758554	chr4:102860166-102860167	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189349430	chr4:102860167-102860168	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550780321	chr4:102860183-102860184	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs562565648	chr4:102860206-102860207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374432118	chr4:102860214-102860215	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548199534	chr4:102860223-102860224	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566430353	chr4:102860269-102860270	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533816055	chr4:102860393-102860394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552290676	chr4:102860419-102860420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181808930	chr4:102860442-102860443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538832735	chr4:102860443-102860444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186406355	chr4:102860445-102860446	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144535720	chr4:102860628-102860629	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188800220	chr4:102860629-102860630	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181605441	chr4:102860715-102860716	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536908814	chr4:102860720-102860721	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544362243	chr4:102860757-102860758	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554891230	chr4:102860791-102860792	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572893817	chr4:102860792-102860793	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540265793	chr4:102860803-102860804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147151901	chr4:102861003-102861004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527515859	chr4:102861004-102861005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186194451	chr4:102861012-102861013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576901120	chr4:102861076-102861077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368993079	chr4:102861084-102861085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544397889	chr4:102861167-102861168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141119898	chr4:102861275-102861276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529854248	chr4:102861362-102861363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546767599	chr4:102861407-102861408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5860704	chr4:102861408-102861409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs397719936	chr4:102861417-102861418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542101195	chr4:102861424-102861425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560475235	chr4:102861425-102861426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191391060	chr4:102861437-102861438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183215603	chr4:102861465-102861466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185999418	chr4:102861512-102861513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146914909	chr4:102861528-102861529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549618787	chr4:102861612-102861613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533209950	chr4:102861619-102861620	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189994501	chr4:102861657-102861658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569542136	chr4:102861714-102861715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102836000-102868400	Strong transcription	Primary B cells from peripheral blood	blood
2	chr4:102855000-102865800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:102859600-102860800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:102859600-102872000	Strong transcription	Primary B cells from cord blood	blood
5	chr4:102859800-102860400	Enhancers	Hela-S3	cervix
6	chr4:102859800-102860800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr4:102860800-102873600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:102862400-102863600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr4:102863000-102863200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:102863200-102865600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:102864400-102867000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:102865200-102866800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr4:102865400-102865800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:102865400-102866200	Enhancers	H9 Cell Line	embryonic stem cell
15	chr4:102865400-102867000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:102865400-102867200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:102865400-102867600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr4:102865600-102866000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr4:102865600-102866400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr4:102865600-102866600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr4:102865600-102867000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr4:102865800-102866000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:102865800-102866200	Enhancers	NH-A	brain
24	chr4:102865800-102866400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:102865800-102871000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:102866000-102866200	Enhancers	HMEC	breast
27	chr4:102866000-102870200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr4:102866200-102875400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr4:102866400-102869800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr4:102866400-102870200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:102866400-102870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr4:102866600-102874200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:102866800-102874200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr4:102867000-102870200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr4:102867000-102871200	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr4:102867000-102871400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr4:102867200-102870200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr4:102867600-102871000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr4:102868400-102869400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr4:102869400-102889200	Strong transcription	Primary B cells from peripheral blood	blood
41	chr4:102869800-102872800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr4:102870200-102870400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:102870200-102870600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:102870200-102872400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:102870200-102872400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr4:102870200-102872800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:102870400-102875600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr4:102870600-102871800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr4:102870800-102872200	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr4:102871000-102872400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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