Variant report

Variant	nsv966246
Chromosome Location	chr4:1205017-1210824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:1041)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:1208963-1209677	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:1209157-1209563	GM12878	blood:	n/a	n/a
3	BCLAF1	chr4:1208969-1209695	GM12878	blood:	n/a	chr4:1209624-1209633
4	BHLHE40	chr4:1210702-1211061	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:1209295-1209629	GM12878	blood:	n/a	n/a
6	CCNT2	chr4:1208033-1208121	K562	blood:	n/a	n/a
7	CEBPB	chr4:1209147-1209683	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:1209279-1209582	GM12878	blood:	n/a	n/a
9	CHD1	chr4:1209884-1210032	GM12878	blood:	n/a	n/a
10	CHD2	chr4:1209215-1209552	GM12878	blood:	n/a	n/a
11	CTCF	chr4:1210187-1210189	GM19239	blood:	n/a	n/a
12	CTCF	chr4:1210620-1210770	GM12869	blood:	n/a	n/a
13	CTCF	chr4:1210635-1210656	GM10248	blood:	n/a	n/a
14	CTCF	chr4:1210780-1210930	GM12874	blood:	n/a	n/a
15	CTCF	chr4:1210680-1210830	GM12873	blood:	n/a	n/a
16	CTCF	chr4:1210700-1210850	GM12864	blood:	n/a	n/a
17	CTCF	chr4:1206210-1206245	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr4:1208940-1209090	HCPEpiC	choroid plexus:	n/a	n/a
19	CTCF	chr4:1210660-1210810	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr4:1208880-1209030	HMF	breast:	n/a	n/a
21	CTCF	chr4:1210720-1210870	GM12867	blood:	n/a	n/a
22	CTCF	chr4:1205836-1205919	LNCaP	prostate:	n/a	n/a
23	CTCF	chr4:1210740-1210890	GM12871	blood:	n/a	n/a
24	CTCF	chr4:1208980-1209130	GM12867	blood:	n/a	n/a
25	CTCF	chr4:1210720-1210870	GM12874	blood:	n/a	n/a
26	CTCF	chr4:1210780-1210930	GM12866	blood:	n/a	n/a
27	CTCF	chr4:1210720-1210870	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr4:1210660-1210810	GM12865	blood:	n/a	n/a
29	CTCF	chr4:1210660-1210810	HPF	lung:	n/a	n/a
30	CTCF	chr4:1210620-1210870	GM12801	blood:	n/a	n/a
31	CTCF	chr4:1210680-1210830	AG04450	lung:	n/a	n/a
32	CTCF	chr4:1209000-1209150	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr4:1210720-1210870	GM06990	blood:	n/a	n/a
34	CTCF	chr4:1210680-1210830	GM12864	blood:	n/a	n/a
35	CTCF	chr4:1208720-1208870	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr4:1210800-1210950	GM12875	blood:	n/a	n/a
37	CTCF	chr4:1210723-1210895	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr4:1209020-1209170	GM12865	blood:	n/a	n/a
39	CTCF	chr4:1208980-1209130	HPF	lung:	n/a	n/a
40	CTCF	chr4:1210760-1210910	GM12875	blood:	n/a	n/a
41	CTCF	chr4:1209205-1209374	GM12892	blood:	n/a	chr4:1209223-1209236
42	CTCF	chr4:1210780-1210930	GM12872	blood:	n/a	n/a
43	CTCF	chr4:1210196-1210250	GM19239	blood:	n/a	n/a
44	CTCF	chr4:1210740-1210890	GM12866	blood:	n/a	n/a
45	CTCF	chr4:1205855-1205942	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:1209386-1209466	GM12891	blood:	n/a	n/a
47	CTCF	chr4:1208640-1208790	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr4:1210790-1210833	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:1210740-1210890	GM12873	blood:	n/a	n/a
50	CTCF	chr4:1209249-1209364	GM12891	blood:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1209971-1210021	HL-60	blood:	n/a
2	chr4:1208310-1208360	Hela-S3	cervix:	n/a
3	chr4:1206045-1206095	A549	lung:	n/a
4	chr4:1205914-1205964	AoSMC	blood vessel:	n/a
5	chr4:1209971-1210021	HL-60	blood:	n/a
6	chr4:1208310-1208360	Hela-S3	cervix:	n/a
7	chr4:1206045-1206095	A549	lung:	n/a
8	chr4:1205914-1205964	AoSMC	blood vessel:	n/a
9	chr4:1205447-1205497	AG09309	skin:	n/a
10	chr4:1205914-1205964	NHBE	bronchial:	n/a
11	chr4:1205359-1205409	PANC-1	pancreas:	n/a
12	chr4:1205447-1205497	BE2_C	brain:	n/a
13	chr4:1208301-1208351	PFSK-1	brain:	n/a
14	chr4:1206045-1206095	HepG2	liver:	n/a
15	chr4:1208301-1208351	HNPCEpiC	eye:	n/a
16	chr4:1210066-1210116	GM06990	blood:	n/a
17	chr4:1205447-1205497	Jurkat	blood:	n/a
18	chr4:1205447-1205497	T-47D	breast:	n/a
19	chr4:1208147-1208197	ovcar-3	ovarian:	n/a
20	chr4:1205914-1205964	MCF-7	breast:	n/a
21	chr4:1206045-1206095	BE2_C	brain:	n/a
22	chr4:1208737-1208787	SKMC	muscle:	n/a
23	chr4:1208960-1209010	Hepatocyte	liver:	n/a
24	chr4:1208675-1208725	HAEpiC	amniotic membrane:	n/a
25	chr4:1208675-1208725	CMK	blood:	n/a
26	chr4:1206004-1206054	H1-hESC	embryonic stem cell:	embryo
27	chr4:1208147-1208197	RPTEC	kidney:	n/a
28	chr4:1208147-1208197	SAEC	small airway:	n/a
29	chr4:1206045-1206095	HEK293	kidney:	embryo
30	chr4:1208737-1208787	NH-A	brain:	n/a
31	chr4:1209971-1210021	A549	lung:	n/a
32	chr4:1205359-1205409	HepG2	liver:	n/a
33	chr4:1205447-1205497	H1-hESC	embryonic stem cell:	embryo
34	chr4:1206004-1206054	HepG2	liver:	n/a
35	chr4:1208960-1209010	ovcar-3	ovarian:	n/a
36	chr4:1208301-1208351	HepG2	liver:	n/a
37	chr4:1208675-1208725	HEEpiC	esophagus:	n/a
38	chr4:1208675-1208725	HepG2	liver:	n/a
39	chr4:1208699-1208749	AG09319	gingival:	n/a
40	chr4:1208147-1208197	AG09319	gingival:	n/a
41	chr4:1210478-1210528	HRPEpiC	eye:	n/a
42	chr4:1208301-1208351	AG04450	lung:	fetal
43	chr4:1208737-1208787	LNCaP	prostate:	n/a
44	chr4:1206150-1206200	HRE	kidney:	n/a
45	chr4:1205359-1205409	Jurkat	blood:	n/a
46	chr4:1208301-1208351	HRE	kidney:	n/a
47	chr4:1208310-1208360	PANC-1	pancreas:	n/a
48	chr4:1206045-1206095	MCF-7	breast:	n/a
49	chr4:1208699-1208749	HRCEpiC	kidney:	n/a
50	chr4:1208147-1208197	SKMC	muscle:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1199380..1201260-chr4:1203296..1206173,2	MCF-7	breast:
2	chr4:1203383..1207466-chr4:1208474..1210757,3	K562	blood:
3	chr4:1207031..1209440-chr4:1241875..1243998,2	K562	blood:
4	chr4:1203383..1207466-chr4:1208474..1210757,3	K562	blood:
5	chr4:1204791..1207603-chr4:1281765..1283856,2	MCF-7	breast:
6	chr4:1205834..1208746-chr4:1226457..1228401,2	K562	blood:
7	chr4:1204218..1206634-chr4:1220495..1222901,2	MCF-7	breast:
8	chr4:1204863..1206646-chr4:1239464..1241348,2	K562	blood:
9	chr2:86422281..86424225-chr4:1209194..1210696,2	K562	blood:
10	chr4:1160724..1161481-chr4:1208619..1209214,2	K562	blood:
11	chr2:86422601..86423306-chr4:1209197..1209717,2	MCF-7	breast:
12	chr4:1209494..1211546-chr4:1218177..1220594,3	MCF-7	breast:
13	chr4:1198351..1202176-chr4:1203916..1208029,5	K562	blood:
14	chr4:1210297..1212921-chr4:1219688..1223007,3	K562	blood:
15	chr4:1199021..1202194-chr4:1205945..1209496,3	K562	blood:
16	chr4:1210359..1211936-chr4:1235947..1237642,2	K562	blood:
17	chr4:1207031..1209938-chr4:1240960..1243998,4	K562	blood:

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CTBP1	hsa-miR-137	chr4:1205251-1205273
2	CTBP1	hsa-miR-137	chr4:1205316-1205310
3	CTBP1	hsa-miR-137	chr4:1205310-1205331

Variant related genes	Relation type
CTBP1	TF binding region
SPON2	TF binding region
CTBP1	CpG island
SPON2	CpG island
ENSG00000159674	chromatin interactions
ENSG00000090316	chromatin interactions
ENSG00000196810	chromatin interactions
ENSG00000273080	chromatin interactions
ENSG00000159692	chromatin interactions
ENSG00000132305	chromatin interactions

Extended variants
information (count: 323 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557477459	chr4:1205030-1205031	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs73793115	chr4:1205042-1205043	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs559569998	chr4:1205064-1205065	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs554632884	chr4:1205131-1205132	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573199490	chr4:1205134-1205135	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs149339505	chr4:1205149-1205150	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs369812683	chr4:1205154-1205155	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs565230395	chr4:1205338-1205339	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs532166377	chr4:1205339-1205340	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs544035199	chr4:1205369-1205370	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs574402308	chr4:1205377-1205378	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs533092925	chr4:1205385-1205386	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs529712088	chr4:1205390-1205391	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs147222661	chr4:1205418-1205419	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs372329092	chr4:1205455-1205456	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs566302187	chr4:1205458-1205459	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs564855534	chr4:1205472-1205473	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs372380097	chr4:1205473-1205474	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs527281344	chr4:1205474-1205475	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs563184205	chr4:1205475-1205476	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs77379446	chr4:1205521-1205522	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs572008054	chr4:1205569-1205570	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs76532252	chr4:1205579-1205580	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs11540633	chr4:1205583-1205584	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs140581613	chr4:1205592-1205593	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs569490067	chr4:1205645-1205646	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs186984898	chr4:1205650-1205651	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs555048849	chr4:1205659-1205660	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs1045480	chr4:1205667-1205668	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
30	rs374555956	chr4:1205669-1205670	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs190712719	chr4:1205679-1205680	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs376995762	chr4:1205687-1205688	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs4974572	chr4:1205737-1205738	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs576753551	chr4:1205764-1205765	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs544119555	chr4:1205783-1205784	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs181483701	chr4:1205827-1205828	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs562305900	chr4:1205877-1205878	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs1045470	chr4:1205892-1205893	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs529846447	chr4:1205913-1205914	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs541511602	chr4:1205933-1205934	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs1045469	chr4:1205949-1205950	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs115317882	chr4:1205975-1205976	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs551713236	chr4:1205977-1205978	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs1045466	chr4:1205991-1205992	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs368867475	chr4:1205992-1205993	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs371763271	chr4:1206001-1206002	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs375089554	chr4:1206005-1206006	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs552180452	chr4:1206023-1206024	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs145193058	chr4:1206045-1206046	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs532821312	chr4:1206058-1206059	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Wolf-Hirschhorn syndrome	21549014	CNVD
Breast cancer	21806811	CNVD
Wolf-Hirschhorn syndrome	22283845	CNVD
Wolf-Hirschhorn syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Wolf-Hirschhorn syndrome	22470819	CNVD
Wolf-Hirschhorn syndrome	18541967	CNVD
sporadic birth defects	19047251	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17142309	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	20932292	CNVD
Pancreatic cancer	17952125	CNVD
Type 2 diabetes	21754918	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1194200-1207800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:1195200-1214600	Weak transcription	A549	lung
3	chr4:1196400-1209800	Weak transcription	Primary B cells from cord blood	blood
4	chr4:1198000-1211200	Genic enhancers	Fetal Stomach	stomach
5	chr4:1198200-1205200	Enhancers	Stomach Mucosa	stomach
6	chr4:1198400-1207000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr4:1199000-1205800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr4:1199200-1207600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr4:1200000-1205200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:1200400-1206200	Enhancers	Ovary	ovary
11	chr4:1200400-1206400	Genic enhancers	Brain Germinal Matrix	brain
12	chr4:1200600-1205800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr4:1201000-1205200	Strong transcription	Fetal Brain Female	brain
14	chr4:1201200-1205200	Genic enhancers	Spleen	Spleen
15	chr4:1201400-1206000	Enhancers	NHDF-Ad	bronchial
16	chr4:1201600-1205200	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr4:1201600-1211600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:1201800-1209000	Strong transcription	Fetal Thymus	thymus
19	chr4:1201800-1210000	Strong transcription	Thymus	Thymus
20	chr4:1202000-1205200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:1202200-1206000	Weak transcription	HepG2	liver
22	chr4:1202200-1209000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:1202400-1206000	Genic enhancers	Lung	lung
24	chr4:1202400-1207000	Genic enhancers	Gastric	stomach
25	chr4:1202400-1208000	Genic enhancers	Pancreas	Pancrea
26	chr4:1202400-1210000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr4:1202600-1206400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:1202600-1210200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:1202800-1205200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr4:1202800-1210200	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr4:1202800-1218000	Weak transcription	Fetal Brain Male	brain
32	chr4:1203000-1205200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:1203000-1205200	Genic enhancers	Right Ventricle	heart
34	chr4:1203000-1207200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
35	chr4:1203000-1209600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr4:1203000-1210200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr4:1203200-1206000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:1203200-1206600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr4:1203200-1217800	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr4:1203400-1205200	Genic enhancers	Duodenum Mucosa	Duodenum
41	chr4:1203400-1205400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:1203400-1206200	Weak transcription	HUVEC	blood vessel
43	chr4:1203400-1207400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr4:1203400-1209200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:1203400-1210200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:1203400-1213000	Weak transcription	Fetal Kidney	kidney
47	chr4:1203600-1205200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr4:1203600-1206000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:1203600-1206200	Weak transcription	Primary hematopoietic stem cells	blood
50	chr4:1203600-1206200	Weak transcription	Aorta	Aorta

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