Variant report

Variant	esv3415289
Chromosome Location	chr4:57063312-57236755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:902)
CpG islands
(count:1468)
Chromatin interactive
region (count:42)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:57114045-57114227	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:57081401-57082148	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:57107554-57107968	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:57107052-57107212	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:57111691-57112264	HepG2	liver:	n/a	chr4:57111730-57111746
6	BACH1	chr4:57167646-57167929	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:57125431-57125435	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:57167644-57167862	K562	blood:	n/a	n/a
9	BHLHE40	chr4:57119849-57120144	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:57168481-57168576	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:57197036-57197049	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:57167717-57168033	K562	blood:	n/a	n/a
13	BHLHE40	chr4:57120001-57120070	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:57167699-57168008	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:57196862-57197221	K562	blood:	n/a	chr4:57197047-57197060
16	BHLHE40	chr4:57107741-57108159	HepG2	liver:	n/a	n/a
17	BHLHE40	chr4:57196932-57197164	A549	lung:	n/a	chr4:57197047-57197060
18	BRCA1	chr4:57167709-57167955	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:57186729-57186795	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr4:57229510-57229859	K562	blood:	n/a	n/a
21	CBX3	chr4:57081976-57082493	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:57117002-57117173	A549	lung:	n/a	n/a
23	CEBPB	chr4:57214735-57215072	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:57186511-57186787	A549	lung:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
25	CEBPB	chr4:57078179-57078320	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:57079886-57079990	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:57173432-57174003	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr4:57173394-57173928	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr4:57081527-57081945	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:57186498-57186708	K562	blood:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
31	CEBPB	chr4:57186422-57186787	IMR90	lung:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
32	CEBPB	chr4:57186495-57186755	HepG2	liver:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
33	CEBPB	chr4:57186451-57186846	Hela-S3	cervix:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
34	CEBPB	chr4:57226292-57226551	IMR90	lung:	n/a	n/a
35	CEBPB	chr4:57173608-57173818	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:57209408-57209535	K562	blood:	n/a	n/a
37	CEBPB	chr4:57193642-57193767	K562	blood:	n/a	n/a
38	CEBPB	chr4:57173524-57174030	HCT-116	colon:	n/a	n/a
39	CEBPB	chr4:57111902-57112145	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:57113815-57114131	HepG2	liver:	n/a	chr4:57113962-57113973
41	CEBPB	chr4:57081439-57081670	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:57111020-57111065	K562	blood:	n/a	n/a
43	CEBPB	chr4:57096927-57097147	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:57186407-57186852	A549	lung:	n/a	chr4:57186611-57186624 chr4:57186595-57186606
45	CREB1	chr4:57167741-57167934	A549	lung:	n/a	n/a
46	CTCF	chr4:57122100-57122250	GM12873	blood:	n/a	n/a
47	CTCF	chr4:57167760-57167910	GM12865	blood:	n/a	chr4:57167823-57167844 chr4:57167828-57167846 chr4:57167833-57167841
48	CTCF	chr4:57214800-57214950	GM12868	blood:	n/a	n/a
49	CTCF	chr4:57167420-57167570	GM12872	blood:	n/a	chr4:57167520-57167530
50	CTCF	chr4:57152906-57152979	K562	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57178051-57178101	AG09319	gingival:	n/a
2	chr4:57181518-57181568	GM19239	blood:	n/a
3	chr4:57181855-57181905	U87	brain:	n/a
4	chr4:57092248-57092298	NH-A	brain:	n/a
5	chr4:57178051-57178101	AG09319	gingival:	n/a
6	chr4:57181518-57181568	GM19239	blood:	n/a
7	chr4:57181855-57181905	U87	brain:	n/a
8	chr4:57092248-57092298	NH-A	brain:	n/a
9	chr4:57182417-57182467	ovcar-3	ovarian:	n/a
10	chr4:57180335-57180385	MCF10A-Er-Src	breast:	n/a
11	chr4:57182417-57182467	HAEpiC	amniotic membrane:	n/a
12	chr4:57181855-57181905	RPTEC	kidney:	n/a
13	chr4:57092248-57092298	HMEC	breast:	n/a
14	chr4:57203352-57203402	A549	lung:	n/a
15	chr4:57181042-57181092	AG04449	skin:	fetal
16	chr4:57181042-57181092	HMEC	breast:	n/a
17	chr4:57082806-57082856	HUVEC	blood vessel:	n/a
18	chr4:57186067-57186117	LNCaP	prostate:	n/a
19	chr4:57181518-57181568	NB4	blood:	n/a
20	chr4:57182146-57182196	NB4	blood:	n/a
21	chr4:57178318-57178368	HCF	heart:	n/a
22	chr4:57215479-57215529	NHDF-neo	bronchial:	n/a
23	chr4:57092248-57092298	HIPEpiC	eye:	n/a
24	chr4:57195432-57195482	T-47D	breast:	n/a
25	chr4:57082806-57082856	Caco-2	colon:	n/a
26	chr4:57182417-57182467	GM12891	blood:	n/a
27	chr4:57181369-57181419	Hepatocyte	liver:	n/a
28	chr4:57179371-57179421	GM12878	blood:	n/a
29	chr4:57203352-57203402	ECC-1	luminal epithelium:	n/a
30	chr4:57178051-57178101	BJ	skin:	n/a
31	chr4:57180053-57180103	GM12892	blood:	n/a
32	chr4:57180053-57180103	BE2_C	brain:	n/a
33	chr4:57179371-57179421	PFSK-1	brain:	n/a
34	chr4:57203352-57203402	MCF-7	breast:	n/a
35	chr4:57181252-57181302	GM12891	blood:	n/a
36	chr4:57215479-57215529	SK-N-SH_RA	brain:	n/a
37	chr4:57180029-57180079	HRCEpiC	kidney:	n/a
38	chr4:57182146-57182196	GM12892	blood:	n/a
39	chr4:57183618-57183668	ECC-1	luminal epithelium:	n/a
40	chr4:57186067-57186117	HCM	heart:	n/a
41	chr4:57180387-57180437	SAEC	small airway:	n/a
42	chr4:57182417-57182467	SK-N-SH_RA	brain:	n/a
43	chr4:57203385-57203435	ECC-1	luminal epithelium:	n/a
44	chr4:57082806-57082856	HEK293	kidney:	embryo
45	chr4:57178051-57178101	H1-hESC	embryonic stem cell:	embryo
46	chr4:57181042-57181092	ECC-1	luminal epithelium:	n/a
47	chr4:57181042-57181092	AG09309	skin:	n/a
48	chr4:57112570-57112620	Hela-S3	cervix:	n/a
49	chr4:57180335-57180385	H1-hESC	embryonic stem cell:	embryo
50	chr4:57215479-57215529	IMR90	lung:	fetal

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:57175601..57178505-chr4:57178570..57181893,3	K562	blood:
2	chr4:57142987..57144545-chr4:57152460..57154348,2	MCF-7	breast:
3	chr4:57162080..57164576-chr4:57166169..57168503,2	MCF-7	breast:
4	chr4:56814043..56816033-chr4:57177641..57180439,2	K562	blood:
5	chr4:57210332..57213092-chr4:57213871..57215383,2	K562	blood:
6	chr4:57114307..57117265-chr4:57118392..57119918,2	K562	blood:
7	chr4:57130565..57132897-chr4:57276076..57278023,2	K562	blood:
8	chr4:57097502..57100938-chr4:57102922..57104816,3	K562	blood:
9	chr4:57208608..57209402-chrX:86554266..86554924,2	MCF-7	breast:
10	chr4:57210332..57213092-chr4:57213871..57215383,2	K562	blood:
11	chr4:57121307..57123223-chr4:57154482..57156026,2	MCF-7	breast:
12	chr4:56995235..56996245-chr4:57167093..57168027,4	MCF-7	breast:
13	chr4:57127130..57129997-chr4:57137802..57139341,2	K562	blood:
14	chr4:57209917..57212599-chr4:57213686..57216147,2	MCF-7	breast:
15	chr4:56994960..56996210-chr4:57167032..57168215,14	MCF-7	breast:
16	chr4:57097502..57100938-chr4:57102922..57104816,3	K562	blood:
17	chr4:57215250..57218405-chr4:57219428..57221610,3	K562	blood:
18	chr4:56814547..56815433-chr4:57167339..57168281,5	MCF-7	breast:
19	chr4:57142987..57144545-chr4:57152460..57154348,2	MCF-7	breast:
20	chr4:57132745..57135392-chr4:57140286..57142322,2	MCF-7	breast:
21	chr4:57210170..57212119-chr4:57222013..57224651,2	K562	blood:
22	chr4:57093123..57095590-chr4:57097803..57099999,2	K562	blood:
23	chr4:57218340..57220899-chr4:57253048..57255780,3	K562	blood:
24	chr4:57116209..57117787-chr4:57119886..57122042,2	K562	blood:
25	chr4:57182829..57184444-chr4:57184985..57187563,2	K562	blood:
26	chr4:57116209..57117787-chr4:57119886..57122042,2	K562	blood:
27	chr4:57114307..57117265-chr4:57118392..57119918,2	K562	blood:
28	chr4:57097271..57099309-chr4:57112147..57113822,2	MCF-7	breast:
29	chr4:57110581..57112837-chr4:57332810..57334755,2	K562	blood:
30	chr4:57215250..57218405-chr4:57219428..57221610,3	K562	blood:
31	chr4:57171966..57174118-chr4:57176983..57178637,2	K562	blood:
32	chr4:56812961..56814619-chr4:57166848..57168708,2	K562	blood:
33	chr4:57182829..57184444-chr4:57184985..57187563,2	K562	blood:
34	chr4:57093123..57095590-chr4:57097803..57099999,2	K562	blood:
35	chr4:57162080..57164576-chr4:57166169..57168503,2	MCF-7	breast:
36	chr4:57175601..57178505-chr4:57178570..57181893,3	K562	blood:
37	chr4:57209917..57212599-chr4:57213686..57216147,2	MCF-7	breast:
38	chr4:57188347..57191240-chr4:57253035..57255608,2	K562	blood:
39	chr4:57132745..57135392-chr4:57140286..57142322,2	MCF-7	breast:
40	chr4:57054944..57056829-chr4:57061059..57063842,2	MCF-7	breast:
41	chr4:57223936..57226086-chr4:57238093..57240180,2	K562	blood:
42	chr4:57171966..57174118-chr4:57176983..57178637,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1211-1	chr4:57222301-57223098	NONHSAT096499
2	lnc-AASDH-2	chr4:57186885-57187500	NONHSAT096496
3	lnc-AASDH-1	chr4:57112518-57112587	NONHSAT096490
4	lnc-PAICS-5	chr4:57136428-57136558	l_2649_chr4:57120311-57136558_testes
5	lnc-PAICS-4	chr4:57177374-57177787	NONHSAT096493
6	lnc-AASDH-1	chr4:57095800-57097193	NONHSAT096490
7	lnc-PAICS-4	chr4:57176832-57176900	NONHSAT096493
8	lnc-PAICS-4	chr4:57177038-57177235	NONHSAT096493
9	lnc-PAICS-5	chr4:57120312-57120443	l_2649_chr4:57120311-57136558_testes
10	lnc-PAICS-4	chr4:57175095-57175275	NONHSAT096493

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	KIAA1211	hsa-miR-27b-3p	chr4:57177038-57177052
2	KIAA1211	hsa-miR-27b-3p	chr4:57194884-57194904
3	KIAA1211	hsa-miR-27b-3p	chr4:57176894-57176900

Variant related genes	Relation type
KIAA1211	TF binding region
RPL7AP31	TF binding region
RNU6-197P	TF binding region
MRPL22P1	TF binding region
RNA5SP162	TF binding region
KIAA1211	CpG island
RPL7AP31	CpG island
RNU6-197P	CpG island
MRPL22P1	CpG island
RNA5SP162	CpG island
ENSG00000109265	chromatin interactions
ENSG00000157426	chromatin interactions
ENSG00000250324	chromatin interactions
ENSG00000174780	chromatin interactions
ENSG00000269921	chromatin interactions
ENSG00000268171	chromatin interactions
ENSG00000174799	chromatin interactions
ENSG00000252489	chromatin interactions
ENSG00000242083	chromatin interactions

Extended variants
information (count: 6941 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:6941 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190372514	chr4:57063313-57063314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562357497	chr4:57063344-57063345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574136157	chr4:57063350-57063351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559453316	chr4:57063376-57063377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528528532	chr4:57063388-57063389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145987784	chr4:57063397-57063398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139921547	chr4:57063418-57063419	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs181238564	chr4:57063434-57063435	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs75729497	chr4:57063482-57063483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542710968	chr4:57063534-57063535	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs12501286	chr4:57063639-57063640	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs533399787	chr4:57063661-57063662	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs73158787	chr4:57063673-57063674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs373838161	chr4:57063675-57063676	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs528428839	chr4:57063699-57063700	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs187969346	chr4:57063773-57063774	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs17086420	chr4:57063790-57063791	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs180878599	chr4:57063807-57063808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs17745069	chr4:57063809-57063810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs542152435	chr4:57063850-57063851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568875287	chr4:57063865-57063866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537436673	chr4:57063876-57063877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554873604	chr4:57063879-57063880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565547371	chr4:57063883-57063884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111973841	chr4:57063903-57063904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111829615	chr4:57063913-57063914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553524035	chr4:57063941-57063942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573007031	chr4:57063943-57063944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186123847	chr4:57063948-57063949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565228599	chr4:57063997-57063998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575640642	chr4:57064012-57064013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544258918	chr4:57064033-57064034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561661453	chr4:57064034-57064035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530384537	chr4:57064042-57064043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532712022	chr4:57064044-57064045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192044116	chr4:57064059-57064060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560627628	chr4:57064064-57064065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551293032	chr4:57064085-57064086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573905494	chr4:57064090-57064091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568834860	chr4:57064099-57064100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs4334804	chr4:57064129-57064130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547840862	chr4:57064133-57064134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200285477	chr4:57064147-57064148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536892337	chr4:57064148-57064149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568033413	chr4:57064158-57064159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182506441	chr4:57064192-57064193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559586682	chr4:57064220-57064221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548295630	chr4:57064292-57064293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566578903	chr4:57064356-57064357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533003139	chr4:57064364-57064365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:57023000-57076000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:57050000-57076000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:57050000-57084600	Weak transcription	Fetal Brain Male	brain
4	chr4:57050200-57063600	Weak transcription	HepG2	liver
5	chr4:57050600-57075800	Weak transcription	Ovary	ovary
6	chr4:57053600-57074200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:57054200-57072400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr4:57054200-57077200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr4:57057000-57076000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:57057000-57076400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr4:57057600-57065400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr4:57057600-57077400	Weak transcription	Fetal Brain Female	brain
13	chr4:57057800-57070200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:57057800-57071000	Weak transcription	Brain Germinal Matrix	brain
15	chr4:57058000-57066000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:57058000-57068000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:57058000-57069200	Weak transcription	Fetal Stomach	stomach
18	chr4:57058000-57069400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr4:57059200-57072600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:57059400-57072400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:57062200-57063400	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr4:57062200-57064600	Enhancers	Fetal Intestine Small	intestine
23	chr4:57062200-57064800	Enhancers	Fetal Intestine Large	intestine
24	chr4:57062600-57063600	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr4:57062600-57064600	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:57062600-57066800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr4:57062800-57063600	Weak transcription	Small Intestine	intestine
28	chr4:57063000-57063600	Weak transcription	Rectal Smooth Muscle	rectum
29	chr4:57063000-57107800	Weak transcription	Fetal Kidney	kidney
30	chr4:57063400-57063800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:57063400-57063800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr4:57063600-57063800	Enhancers	Rectal Smooth Muscle	rectum
33	chr4:57063600-57063800	Enhancers	Small Intestine	intestine
34	chr4:57063600-57064400	Enhancers	HepG2	liver
35	chr4:57063600-57064600	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr4:57063800-57064600	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:57063800-57065000	Weak transcription	Small Intestine	intestine
38	chr4:57064600-57064800	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr4:57064600-57068400	Weak transcription	Fetal Intestine Small	intestine
40	chr4:57064800-57074200	Weak transcription	Fetal Intestine Large	intestine
41	chr4:57065000-57065200	Enhancers	Small Intestine	intestine
42	chr4:57065200-57065400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:57065200-57065400	Enhancers	GM12878-XiMat	blood
44	chr4:57065400-57066000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:57065400-57067600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr4:57066000-57066800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:57066000-57066800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:57066400-57067000	Enhancers	HUVEC	blood vessel
49	chr4:57066400-57067600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:57066800-57068000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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