Variant report

Variant	nsv869584
Chromosome Location	chr4:3759068-3791709
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1068)
CpG islands
(count:1953)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1068 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3783057-3783426	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3786329-3786786	HepG2	liver:	n/a	n/a
3	ATF2	chr4:3768564-3769140	H1-hESC	embryonic stem cell:	n/a	chr4:3768787-3768801
4	ATF2	chr4:3789773-3790104	GM12878	blood:	n/a	n/a
5	ATF2	chr4:3789801-3789982	GM12878	blood:	n/a	n/a
6	BACH1	chr4:3785434-3785441	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3785649-3785677	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3769358-3769598	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3768715-3769081	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr4:3783096-3783585	K562	blood:	n/a	n/a
11	BHLHE40	chr4:3776114-3776532	HepG2	liver:	n/a	n/a
12	BHLHE40	chr4:3786213-3786960	HepG2	liver:	n/a	chr4:3786250-3786266
13	BHLHE40	chr4:3789727-3790087	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3783236-3783622	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:3775276-3775555	HepG2	liver:	n/a	chr4:3775401-3775410 chr4:3775399-3775412 chr4:3775400-3775409 chr4:3775401-3775410 chr4:3775402-3775411 chr4:3775395-3775416
16	BHLHE40	chr4:3786234-3786555	HepG2	liver:	n/a	chr4:3786250-3786266
17	BHLHE40	chr4:3775222-3775557	K562	blood:	n/a	chr4:3775401-3775410 chr4:3775399-3775412 chr4:3775400-3775409 chr4:3775401-3775410 chr4:3775402-3775411 chr4:3775395-3775416
18	BHLHE40	chr4:3786773-3786782	K562	blood:	n/a	n/a
19	BHLHE40	chr4:3776122-3776615	K562	blood:	n/a	n/a
20	BRCA1	chr4:3789723-3790088	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:3783738-3783775	HepG2	liver:	n/a	n/a
22	BRCA1	chr4:3782784-3782905	HepG2	liver:	n/a	n/a
23	CBX3	chr4:3783038-3783736	K562	blood:	n/a	n/a
24	CBX3	chr4:3783345-3783657	K562	blood:	n/a	n/a
25	CCNT2	chr4:3784091-3784220	K562	blood:	n/a	n/a
26	CCNT2	chr4:3767173-3768168	K562	blood:	n/a	chr4:3768060-3768069
27	CEBPB	chr4:3786323-3786664	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:3776401-3776638	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:3784753-3784882	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:3789858-3790003	GM12878	blood:	n/a	n/a
31	CEBPB	chr4:3776514-3776574	K562	blood:	n/a	n/a
32	CEBPB	chr4:3786242-3786707	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:3783052-3783191	HepG2	liver:	n/a	n/a
34	CEBPD	chr4:3767448-3767956	HepG2	liver:	n/a	n/a
35	CEBPD	chr4:3786240-3786661	HepG2	liver:	n/a	n/a
36	CEBPD	chr4:3768042-3768292	HepG2	liver:	n/a	n/a
37	CHD1	chr4:3788364-3788411	GM12878	blood:	n/a	n/a
38	CHD2	chr4:3768617-3769097	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:3786309-3786424	HepG2	liver:	n/a	n/a
40	CHD2	chr4:3782244-3782324	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr4:3785749-3785903	HepG2	liver:	n/a	n/a
42	CHD2	chr4:3783653-3783772	HepG2	liver:	n/a	n/a
43	CHD2	chr4:3767139-3767236	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr4:3789727-3790089	GM12878	blood:	n/a	n/a
45	CHD2	chr4:3769391-3769621	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr4:3782192-3782909	HepG2	liver:	n/a	n/a
47	CREB1	chr4:3768574-3769520	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:3787960-3788110	HRPEpiC	eye:	n/a	chr4:3788092-3788100
49	CTCF	chr4:3785560-3785710	HPF	lung:	n/a	n/a
50	CTCF	chr4:3769380-3769530	HBMEC	blood vessel:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3772769-3772819	AG09309	skin:	n/a
2	chr4:3772769-3772819	AG09309	skin:	n/a
3	chr4:3767169-3767219	GM12878	blood:	n/a
4	chr4:3770608-3770658	SK-N-SH_RA	brain:	n/a
5	chr4:3767073-3767123	SK-N-SH	brain:	n/a
6	chr4:3773815-3773865	HAEpiC	amniotic membrane:	n/a
7	chr4:3776301-3776351	BJ	skin:	n/a
8	chr4:3785927-3785977	HRPEpiC	eye:	n/a
9	chr4:3769558-3769608	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:3775898-3775948	AG04449	skin:	fetal
11	chr4:3785772-3785822	PANC-1	pancreas:	n/a
12	chr4:3775898-3775948	SK-N-MC	brain:	n/a
13	chr4:3773996-3774046	A549	lung:	n/a
14	chr4:3768081-3768131	HRCEpiC	kidney:	n/a
15	chr4:3773933-3773983	A549	lung:	n/a
16	chr4:3768638-3768688	RPTEC	kidney:	n/a
17	chr4:3769468-3769518	K562	blood:	n/a
18	chr4:3766151-3766201	U87	brain:	n/a
19	chr4:3773815-3773865	H1-hESC	embryonic stem cell:	embryo
20	chr4:3766875-3766925	U87	brain:	n/a
21	chr4:3769558-3769608	HCT-116	colon:	n/a
22	chr4:3767402-3767452	HEEpiC	esophagus:	n/a
23	chr4:3769558-3769608	HAEpiC	amniotic membrane:	n/a
24	chr4:3773996-3774046	LNCaP	prostate:	n/a
25	chr4:3772769-3772819	HMEC	breast:	n/a
26	chr4:3773933-3773983	NB4	blood:	n/a
27	chr4:3768555-3768605	HepG2	liver:	n/a
28	chr4:3768097-3768147	HL-60	blood:	n/a
29	chr4:3766656-3766706	HRE	kidney:	n/a
30	chr4:3775898-3775948	SAEC	small airway:	n/a
31	chr4:3770608-3770658	SAEC	small airway:	n/a
32	chr4:3773815-3773865	CMK	blood:	n/a
33	chr4:3767169-3767219	Caco-2	colon:	n/a
34	chr4:3768458-3768508	AG04449	skin:	fetal
35	chr4:3766151-3766201	SAEC	small airway:	n/a
36	chr4:3766875-3766925	AG04450	lung:	fetal
37	chr4:3775898-3775948	NHDF-neo	bronchial:	n/a
38	chr4:3776301-3776351	HCPEpiC	choroid plexus:	n/a
39	chr4:3770608-3770658	HEEpiC	esophagus:	n/a
40	chr4:3775787-3775837	T-47D	breast:	n/a
41	chr4:3767402-3767452	CMK	blood:	n/a
42	chr4:3767402-3767452	Hepatocyte	liver:	n/a
43	chr4:3772769-3772819	PFSK-1	brain:	n/a
44	chr4:3785772-3785822	HCPEpiC	choroid plexus:	n/a
45	chr4:3768458-3768508	A549	lung:	n/a
46	chr4:3769810-3769860	H1-hESC	embryonic stem cell:	embryo
47	chr4:3770608-3770658	NHDF-neo	bronchial:	n/a
48	chr4:3768458-3768508	BE2_C	brain:	n/a
49	chr4:3769468-3769518	HRPEpiC	eye:	n/a
50	chr4:3766151-3766201	HEEpiC	esophagus:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3757289..3759766-chr4:3767491..3769392,2	MCF-7	breast:
2	chr4:3787711..3790485-chr4:3795544..3797629,2	K562	blood:
3	chr4:3741522..3743412-chr4:3768536..3771001,2	MCF-7	breast:
4	chr4:3784876..3787026-chr4:3792827..3794730,2	K562	blood:
5	chr4:3777218..3779189-chr4:3782437..3784740,2	K562	blood:
6	chr4:3773333..3775875-chr4:3781745..3785058,3	MCF-7	breast:
7	chr4:3773333..3775875-chr4:3781745..3785058,3	MCF-7	breast:
8	chr4:3484374..3487460-chr4:3786826..3789487,3	MCF-7	breast:
9	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
10	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
11	chr4:3772497..3774575-chr4:3777624..3779393,2	MCF-7	breast:
12	chr4:3533743..3535319-chr4:3783998..3786670,2	MCF-7	breast:
13	chr4:3767980..3770496-chr4:3782004..3784205,2	MCF-7	breast:
14	chr4:3774460..3776998-chr4:3955638..3958181,2	K562	blood:
15	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
16	chr4:3784430..3786032-chr4:3804329..3807090,2	K562	blood:
17	chr4:3747628..3750191-chr4:3756565..3759403,2	K562	blood:
18	chr4:3749442..3749991-chr4:3785209..3785794,2	MCF-7	breast:
19	chr4:3784486..3786605-chr4:3826007..3828204,2	MCF-7	breast:
20	chr4:3767732..3769957-chr4:3773146..3775340,2	MCF-7	breast:
21	chr4:3771642..3772558-chr4:3785244..3785866,2	MCF-7	breast:
22	chr4:3757965..3759799-chr4:3762426..3765280,2	MCF-7	breast:
23	chr4:3783567..3786061-chr4:3828338..3831241,3	MCF-7	breast:
24	chr4:3533020..3535005-chr4:3786672..3788250,2	MCF-7	breast:
25	chr4:3769693..3772648-chr4:3773478..3776740,3	MCF-7	breast:
26	chr4:3596211..3598668-chr4:3781245..3783965,2	K562	blood:
27	chr19:54974695..54977436-chr4:3766258..3768919,2	MCF-7	breast:
28	chr4:3784436..3787283-chr4:3790083..3791949,2	MCF-7	breast:
29	chr4:3767078..3767943-chr4:3882124..3882913,2	MCF-7	breast:
30	chr17:41400219..41402369-chr4:3774076..3775596,3	K562	blood:
31	chr4:3767101..3767926-chr4:3787451..3788371,3	MCF-7	breast:
32	chr4:3785291..3787678-chr4:3788137..3789890,2	MCF-7	breast:
33	chr4:3754355..3758397-chr4:3760571..3763729,4	K562	blood:
34	chr4:3786308..3789117-chr4:3789630..3791634,2	K562	blood:
35	chr4:3532933..3534970-chr4:3765784..3768236,2	MCF-7	breast:
36	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
37	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
38	chr4:3774394..3778170-chr4:3784395..3787889,4	MCF-7	breast:
39	chr4:3772497..3774575-chr4:3777624..3779393,2	MCF-7	breast:
40	chr4:3774394..3778170-chr4:3784395..3787889,4	MCF-7	breast:
41	chr4:3767665..3768566-chr4:3785108..3786011,4	MCF-7	breast:
42	chr4:3767671..3769192-chr4:3769796..3772388,2	MCF-7	breast:
43	chr4:3764851..3771480-chr4:3778154..3785249,14	MCF-7	breast:
44	chr4:3785291..3787678-chr4:3788137..3789890,2	MCF-7	breast:
45	chr4:3770762..3772814-chr4:3782317..3785191,2	K562	blood:
46	chr4:3748965..3749720-chr4:3785547..3786123,2	MCF-7	breast:
47	chr14:41952601..41955142-chr4:3784821..3786920,2	MCF-7	breast:
48	chr4:3769000..3769555-chr4:3785283..3786137,2	MCF-7	breast:
49	chr4:3774123..3777050-chr4:3780900..3782661,2	K562	blood:
50	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-3	chr4:3761872-3765117	XLOC_003862
2	lnc-LRPAP1-3	chr4:3760475-3761753	XLOC_003862

No data

Variant related genes	Relation type
ENSG00000250986	TF binding region
ADRA2C	TF binding region
ENSG00000250986	CpG island
ADRA2C	CpG island
ENSG00000251669	chromatin interactions
ENSG00000113430	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000250986	chromatin interactions
ENSG00000182909	chromatin interactions
ENSG00000250681	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000216560	chromatin interactions

Extended variants
information (count: 1555 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78353318	chr4:3759083-3759084	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558067775	chr4:3759086-3759087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571695104	chr4:3759118-3759119	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537563729	chr4:3759142-3759143	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557143009	chr4:3759146-3759147	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576208584	chr4:3759147-3759148	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541637208	chr4:3759163-3759164	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs140144072	chr4:3759181-3759182	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7435018	chr4:3759184-3759185	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs572364740	chr4:3759198-3759199	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs541075980	chr4:3759202-3759203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564076443	chr4:3759203-3759204	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72215514	chr4:3759205-3759206	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs183294899	chr4:3759220-3759221	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543518348	chr4:3759239-3759240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563205898	chr4:3759253-3759254	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs55792167	chr4:3759260-3759261	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540023078	chr4:3759285-3759286	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561584976	chr4:3759318-3759319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542274759	chr4:3759384-3759385	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549148911	chr4:3759390-3759391	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566071993	chr4:3759398-3759399	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs528756078	chr4:3759424-3759425	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs79208395	chr4:3759443-3759444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571632066	chr4:3759447-3759448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187872599	chr4:3759458-3759459	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573033047	chr4:3759479-3759480	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs189775777	chr4:3759494-3759495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs557456734	chr4:3759509-3759510	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs3934515	chr4:3759538-3759539	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372472632	chr4:3759543-3759544	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs182153558	chr4:3759584-3759585	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139087565	chr4:3759585-3759586	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs7677577	chr4:3759586-3759587	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562302309	chr4:3759590-3759591	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7674251	chr4:3759617-3759618	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs187869964	chr4:3759633-3759634	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs376753673	chr4:3759641-3759642	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs192451531	chr4:3759648-3759649	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532961489	chr4:3759709-3759710	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543026826	chr4:3759719-3759720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12507607	chr4:3759773-3759774	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs373130466	chr4:3759780-3759781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7663765	chr4:3759820-3759821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77616588	chr4:3759831-3759832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7656272	chr4:3759889-3759890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542858462	chr4:3759892-3759893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559523012	chr4:3759915-3759916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7679361	chr4:3759935-3759936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528628562	chr4:3759936-3759937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3750000-3763200	Weak transcription	Pancreas	Pancrea
2	chr4:3756200-3764000	Weak transcription	Fetal Kidney	kidney
3	chr4:3757600-3762000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:3758000-3760200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr4:3758600-3761000	Weak transcription	Aorta	Aorta
6	chr4:3759600-3761400	Weak transcription	Spleen	Spleen
7	chr4:3760200-3761400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:3760800-3761200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:3761000-3762000	Strong transcription	Aorta	Aorta
10	chr4:3761400-3762200	ZNF genes & repeats	Spleen	Spleen
11	chr4:3761400-3762600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr4:3761800-3766600	Weak transcription	HSMM	muscle
13	chr4:3762000-3762200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr4:3762000-3763000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:3762000-3765800	Weak transcription	Aorta	Aorta
16	chr4:3762200-3762400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:3762200-3762600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:3762200-3765400	Weak transcription	Spleen	Spleen
19	chr4:3762400-3763200	Enhancers	Fetal Brain Male	brain
20	chr4:3762400-3766800	Weak transcription	Right Atrium	heart
21	chr4:3762600-3763000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3762600-3763800	Bivalent Enhancer	Fetal Stomach	stomach
23	chr4:3762600-3765400	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr4:3763000-3763200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr4:3763000-3763200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:3763000-3763200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr4:3763000-3765400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr4:3763000-3766800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr4:3763200-3764000	Enhancers	Pancreas	Pancrea
30	chr4:3763200-3765200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:3763800-3764000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr4:3764000-3764200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr4:3764000-3764400	ZNF genes & repeats	Fetal Kidney	kidney
34	chr4:3764000-3766000	Weak transcription	Pancreas	Pancrea
35	chr4:3764400-3764600	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
36	chr4:3764400-3767400	Weak transcription	Fetal Kidney	kidney
37	chr4:3764600-3766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr4:3764800-3765800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:3765000-3765400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:3765200-3765400	Bivalent Enhancer	Fetal Stomach	stomach
41	chr4:3765200-3766000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:3765400-3765600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr4:3765400-3765800	Bivalent Enhancer	Fetal Muscle Leg	muscle
44	chr4:3765400-3766000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr4:3765400-3766000	Enhancers	Spleen	Spleen
46	chr4:3765400-3766800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
47	chr4:3765800-3766000	Enhancers	Aorta	Aorta
48	chr4:3765800-3766000	Enhancers	Brain Anterior Caudate	brain
49	chr4:3765800-3766200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
50	chr4:3765800-3766200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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