Variant report

Variant	esv3355881
Chromosome Location	chr4:1209202-1211700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

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	CEBPB	chr4:1209147-1209683	GM12878	blood:	n/a	n/a
7	CEBPB	chr4:1209279-1209582	GM12878	blood:	n/a	n/a
8	CHD1	chr4:1209884-1210032	GM12878	blood:	n/a	n/a
9	CHD2	chr4:1209215-1209552	GM12878	blood:	n/a	n/a
10	CTCF	chr4:1210720-1210870	GM12874	blood:	n/a	n/a
11	CTCF	chr4:1210780-1210930	GM12868	blood:	n/a	n/a
12	CTCF	chr4:1210560-1210830	GM12869	blood:	n/a	n/a
13	CTCF	chr4:1210620-1210870	GM12801	blood:	n/a	n/a
14	CTCF	chr4:1210680-1210830	GM12873	blood:	n/a	n/a
15	CTCF	chr4:1210660-1210810	GM12865	blood:	n/a	n/a
16	CTCF	chr4:1210720-1210870	GM12867	blood:	n/a	n/a
17	CTCF	chr4:1210660-1210810	HPF	lung:	n/a	n/a
18	CTCF	chr4:1210740-1210890	GM12865	blood:	n/a	n/a
19	CTCF	chr4:1210740-1210890	GM12871	blood:	n/a	n/a
20	CTCF	chr4:1210760-1210910	GM12873	blood:	n/a	n/a
21	CTCF	chr4:1210800-1210950	GM12875	blood:	n/a	n/a
22	CTCF	chr4:1210196-1210250	GM19239	blood:	n/a	n/a
23	CTCF	chr4:1210720-1210870	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr4:1210660-1210810	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr4:1210790-1210833	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:1210187-1210189	GM19239	blood:	n/a	n/a
27	CTCF	chr4:1210780-1210930	GM12872	blood:	n/a	n/a
28	CTCF	chr4:1210740-1210890	GM12873	blood:	n/a	n/a
29	CTCF	chr4:1210700-1210850	GM12864	blood:	n/a	n/a
30	CTCF	chr4:1209249-1209364	GM12891	blood:	n/a	n/a
31	CTCF	chr4:1210720-1210870	GM06990	blood:	n/a	n/a
32	CTCF	chr4:1210680-1210830	GM12864	blood:	n/a	n/a
33	CTCF	chr4:1210620-1210770	GM12869	blood:	n/a	n/a
34	CTCF	chr4:1209386-1209466	GM12891	blood:	n/a	n/a
35	CTCF	chr4:1210740-1210890	GM12866	blood:	n/a	n/a
36	CTCF	chr4:1210780-1210930	GM12866	blood:	n/a	n/a
37	CTCF	chr4:1210635-1210656	GM10248	blood:	n/a	n/a
38	CTCF	chr4:1210760-1210910	GM12875	blood:	n/a	n/a
39	CTCF	chr4:1210723-1210895	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr4:1209205-1209374	GM12892	blood:	n/a	chr4:1209223-1209236
41	CTCF	chr4:1210780-1210930	GM12874	blood:	n/a	n/a
42	CTCF	chr4:1210680-1210830	AG04450	lung:	n/a	n/a
43	EBF1	chr4:1210586-1210942	GM12878	blood:	n/a	n/a
44	EBF1	chr4:1209224-1209653	GM12878	blood:	n/a	n/a
45	EBF1	chr4:1209359-1209563	GM12878	blood:	n/a	n/a
46	EGR1	chr4:1210672-1210864	GM12878	blood:	n/a	n/a
47	EGR1	chr4:1208932-1209567	GM12878	blood:	n/a	chr4:1209071-1209086 chr4:1209249-1209260 chr4:1209247-1209262 chr4:1209072-1209085 chr4:1209245-1209259
48	EGR1	chr4:1208975-1209294	GM12878	blood:	n/a	chr4:1209071-1209086 chr4:1209249-1209260 chr4:1209247-1209262 chr4:1209072-1209085 chr4:1209245-1209259
49	EGR1	chr4:1210646-1210856	GM12878	blood:	n/a	n/a
50	EGR1	chr4:1209311-1209535	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1209971-1210021	BJ	skin:	n/a
2	chr4:1209971-1210021	ProgFib	skin:	n/a
3	chr4:1209844-1209894	HCM	heart:	n/a
4	chr4:1209971-1210021	CMK	blood:	n/a
5	chr4:1211419-1211469	HRPEpiC	eye:	n/a
6	chr4:1210066-1210116	RPTEC	kidney:	n/a
7	chr4:1211419-1211469	Hepatocyte	liver:	n/a
8	chr4:1209971-1210021	MCF-7	breast:	n/a
9	chr4:1209844-1209894	AoSMC	blood vessel:	n/a
10	chr4:1209971-1210021	AG04450	lung:	fetal
11	chr4:1209971-1210021	HAEpiC	amniotic membrane:	n/a
12	chr4:1210478-1210528	NHDF-neo	bronchial:	n/a
13	chr4:1209971-1210021	SKMC	muscle:	n/a
14	chr4:1209971-1210021	AoSMC	blood vessel:	n/a
15	chr4:1210066-1210116	ProgFib	skin:	n/a
16	chr4:1209844-1209894	HNPCEpiC	eye:	n/a
17	chr4:1209844-1209894	SK-N-SH	brain:	n/a
18	chr4:1210066-1210116	GM19239	blood:	n/a
19	chr4:1209844-1209894	HEEpiC	esophagus:	n/a
20	chr4:1210066-1210116	HCF	heart:	n/a
21	chr4:1209971-1210021	K562	blood:	n/a
22	chr4:1210066-1210116	HEEpiC	esophagus:	n/a
23	chr4:1209844-1209894	PFSK-1	brain:	n/a
24	chr4:1210478-1210528	A549	lung:	n/a
25	chr4:1209844-1209894	HepG2	liver:	n/a
26	chr4:1210478-1210528	RPTEC	kidney:	n/a
27	chr4:1209844-1209894	SKMC	muscle:	n/a
28	chr4:1210478-1210528	GM06990	blood:	n/a
29	chr4:1209844-1209894	HL-60	blood:	n/a
30	chr4:1210066-1210116	HepG2	liver:	n/a
31	chr4:1209844-1209894	HAEpiC	amniotic membrane:	n/a
32	chr4:1209971-1210021	SK-N-SH_RA	brain:	n/a
33	chr4:1210478-1210528	HL-60	blood:	n/a
34	chr4:1211419-1211469	PANC-1	pancreas:	n/a
35	chr4:1210478-1210528	HRPEpiC	eye:	n/a
36	chr4:1210066-1210116	Hepatocyte	liver:	n/a
37	chr4:1210478-1210528	NHBE	bronchial:	n/a
38	chr4:1210066-1210116	AG04450	lung:	fetal
39	chr4:1209971-1210021	HCM	heart:	n/a
40	chr4:1210478-1210528	GM12891	blood:	n/a
41	chr4:1210478-1210528	Hepatocyte	liver:	n/a
42	chr4:1211419-1211469	HCF	heart:	n/a
43	chr4:1210478-1210528	HNPCEpiC	eye:	n/a
44	chr4:1210066-1210116	HRPEpiC	eye:	n/a
45	chr4:1209844-1209894	AG09319	gingival:	n/a
46	chr4:1209844-1209894	PrEC	prostate:	n/a
47	chr4:1210478-1210528	SKMC	muscle:	n/a
48	chr4:1209971-1210021	GM12892	blood:	n/a
49	chr4:1211419-1211469	SK-N-SH	brain:	n/a
50	chr4:1209844-1209894	IMR90	lung:	fetal

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1209494..1211546-chr4:1218177..1220594,3	MCF-7	breast:
2	chr4:1208349..1210341-chr4:1211100..1213340,2	MCF-7	breast:
3	chr4:1203383..1207466-chr4:1208474..1210757,3	K562	blood:
4	chr4:1207031..1209440-chr4:1241875..1243998,2	K562	blood:
5	chr2:86422281..86424225-chr4:1209194..1210696,2	K562	blood:
6	chr4:1207031..1209938-chr4:1240960..1243998,4	K562	blood:
7	chr2:86422601..86423306-chr4:1209197..1209717,2	MCF-7	breast:
8	chr4:1199021..1202194-chr4:1205945..1209496,3	K562	blood:
9	chr4:1211126..1212834-chr4:1216389..1218243,2	K562	blood:
10	chr4:1210297..1212921-chr4:1219688..1223007,3	K562	blood:
11	chr4:1210359..1211936-chr4:1235947..1237642,2	K562	blood:
12	chr4:1160724..1161481-chr4:1208619..1209214,2	K562	blood:

No data

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

Extended variants
information (count: 143 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:143 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560876424	chr4:1209213-1209214	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs529578439	chr4:1209228-1209229	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs528337327	chr4:1209230-1209231	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs143293917	chr4:1209272-1209273	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs571044094	chr4:1209289-1209290	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs189416949	chr4:1209310-1209311	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs113781022	chr4:1209368-1209369	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs550133500	chr4:1209373-1209374	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs3755951	chr4:1209383-1209384	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs537304306	chr4:1209440-1209441	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs556027914	chr4:1209446-1209447	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs567755130	chr4:1209447-1209448	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs535259278	chr4:1209481-1209482	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs111337493	chr4:1209489-1209490	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs578162440	chr4:1209498-1209499	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs545538023	chr4:1209502-1209503	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs563220557	chr4:1209521-1209522	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs557353420	chr4:1209528-1209529	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs547234468	chr4:1209552-1209553	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs182017336	chr4:1209592-1209593	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs542556923	chr4:1209639-1209640	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs561278483	chr4:1209650-1209651	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs141426450	chr4:1209663-1209664	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs73793116	chr4:1209688-1209689	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs73793118	chr4:1209725-1209726	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs375999937	chr4:1209742-1209743	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs143129857	chr4:1209788-1209789	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs147464431	chr4:1209797-1209798	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs369657048	chr4:1209821-1209822	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs139911392	chr4:1209827-1209828	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs374344295	chr4:1209830-1209831	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs529740572	chr4:1209883-1209884	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs377714722	chr4:1209899-1209900	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs371355192	chr4:1209900-1209901	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs567980949	chr4:1209918-1209919	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs372599555	chr4:1209938-1209939	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs142670248	chr4:1209952-1209953	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs370377200	chr4:1209953-1209954	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs370649780	chr4:1209958-1209959	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs186090455	chr4:1209971-1209972	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs376681305	chr4:1209989-1209990	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs374755819	chr4:1209996-1209997	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs571881989	chr4:1209999-1210000	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375283311	chr4:1210002-1210003	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs201816175	chr4:1210009-1210010	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs372153693	chr4:1210040-1210041	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs557479089	chr4:1210047-1210048	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs371816731	chr4:1210058-1210059	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs551371217	chr4:1210111-1210112	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112053976	chr4:1210123-1210124	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region 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:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1195200-1214600	Weak transcription	A549	lung
2	chr4:1196400-1209800	Weak transcription	Primary B cells from cord blood	blood
3	chr4:1198000-1211200	Genic enhancers	Fetal Stomach	stomach
4	chr4:1201600-1211600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:1201800-1210000	Strong transcription	Thymus	Thymus
6	chr4:1202400-1210000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr4:1202600-1210200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr4:1202800-1210200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr4:1202800-1218000	Weak transcription	Fetal Brain Male	brain
10	chr4:1203000-1209600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr4:1203000-1210200	Strong transcription	Primary neutrophils fromperipheralblood	blood
12	chr4:1203200-1217800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr4:1203400-1210200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr4:1203400-1213000	Weak transcription	Fetal Kidney	kidney
15	chr4:1203800-1223000	Strong transcription	Osteobl	bone
16	chr4:1204000-1209400	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr4:1204000-1211600	Genic enhancers	Esophagus	oesophagus
18	chr4:1204000-1218000	Weak transcription	K562	blood
19	chr4:1204200-1212600	Genic enhancers	Fetal Muscle Leg	muscle
20	chr4:1204400-1210000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:1204400-1210400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr4:1204400-1210800	Strong transcription	Fetal Intestine Large	intestine
23	chr4:1204400-1211600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:1204400-1211600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:1204400-1211600	Genic enhancers	Fetal Muscle Trunk	muscle
26	chr4:1204400-1212000	Strong transcription	NHEK	skin
27	chr4:1204400-1227200	Strong transcription	Fetal Intestine Small	intestine
28	chr4:1204400-1235800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr4:1204600-1210000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr4:1204600-1210200	Weak transcription	Fetal Heart	heart
31	chr4:1204600-1220400	Strong transcription	Liver	Liver
32	chr4:1204600-1236200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:1204800-1211000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:1204800-1212000	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr4:1204800-1213800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:1204800-1226400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:1204800-1237000	Weak transcription	Psoas Muscle	Psoas
38	chr4:1205000-1210000	Strong transcription	Sigmoid Colon	Sigmoid Colon
39	chr4:1205000-1210200	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr4:1205000-1210600	Weak transcription	Small Intestine	intestine
41	chr4:1205000-1211000	Weak transcription	Right Atrium	heart
42	chr4:1205000-1213400	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr4:1205000-1226200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr4:1205200-1210000	Strong transcription	Right Ventricle	heart
45	chr4:1205200-1210400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr4:1205200-1211800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr4:1205200-1218000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr4:1205400-1226800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:1205600-1210000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr4:1205800-1210400	Strong transcription	H9 Cell Line	embryonic stem cell

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