Variant report

Variant	esv3341942
Chromosome Location	chr4:110354303-110356451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:110354211-110354931	HepG2	liver:	n/a	n/a
2	ATF2	chr4:110354473-110355010	GM12878	blood:	n/a	n/a
3	ATF3	chr4:110354491-110354811	A549	lung:	n/a	n/a
4	ATF3	chr4:110354590-110355029	K562	blood:	n/a	n/a
5	BACH1	chr4:110355512-110355621	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:110354710-110354946	K562	blood:	n/a	n/a
7	BACH1	chr4:110354432-110355016	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr4:110354396-110355310	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
9	BCLAF1	chr4:110354481-110355062	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
10	BHLHE40	chr4:110355545-110356014	GM12878	blood:	n/a	chr4:110355801-110355817
11	BHLHE40	chr4:110354288-110355032	K562	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
12	BHLHE40	chr4:110355604-110356009	K562	blood:	n/a	chr4:110355801-110355817
13	BHLHE40	chr4:110354469-110355120	HepG2	liver:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
14	BHLHE40	chr4:110355440-110355810	HepG2	liver:	n/a	n/a
15	BHLHE40	chr4:110354543-110355029	GM12878	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
16	BHLHE40	chr4:110354627-110354827	A549	lung:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
17	BRCA1	chr4:110354689-110354889	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:110354583-110354804	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr4:110354768-110354947	GM12878	blood:	n/a	n/a
20	CBX3	chr4:110354275-110355033	K562	blood:	n/a	n/a
21	CCNT2	chr4:110354501-110355331	K562	blood:	n/a	n/a
22	CEBPB	chr4:110353476-110354386	Hela-S3	cervix:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
23	CEBPB	chr4:110354600-110354908	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:110354588-110355000	Hela-S3	cervix:	n/a	n/a
25	CEBPD	chr4:110354505-110355207	HepG2	liver:	n/a	n/a
26	CHD1	chr4:110354216-110354720	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr4:110354529-110354915	GM12878	blood:	n/a	n/a
28	CHD1	chr4:110355474-110355809	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr4:110354486-110354971	K562	blood:	n/a	n/a
30	CHD2	chr4:110355466-110355836	GM12878	blood:	n/a	n/a
31	CHD2	chr4:110354553-110355068	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr4:110354495-110354992	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr4:110354399-110355043	GM12878	blood:	n/a	n/a
34	CHD2	chr4:110354323-110355067	HepG2	liver:	n/a	n/a
35	CREB1	chr4:110354409-110355456	HepG2	liver:	n/a	n/a
36	CREB1	chr4:110354544-110355262	K562	blood:	n/a	n/a
37	CREB1	chr4:110354551-110355299	A549	lung:	n/a	n/a
38	CREB1	chr4:110354428-110355277	GM12878	blood:	n/a	n/a
39	CREB1	chr4:110354403-110355296	K562	blood:	n/a	n/a
40	CREB1	chr4:110354509-110355241	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr4:110354429-110355267	HepG2	liver:	n/a	n/a
42	CREB1	chr4:110354488-110355154	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr4:110354442-110355227	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:110354560-110354982	MCF-7	breast:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
45	CTCF	chr4:110354620-110354770	GM12864	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
46	CTCF	chr4:110354413-110355054	GM12878	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
47	CTCF	chr4:110354620-110354770	HL-60	blood:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
48	CTCF	chr4:110354680-110354830	RPTEC	kidney:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731
49	CTCF	chr4:110354880-110355030	HAc	cerebellar:	n/a	n/a
50	CTCF	chr4:110354570-110354896	ProgFib	skin:	n/a	chr4:110354711-110354724 chr4:110354716-110354732 chr4:110354715-110354733 chr4:110354718-110354731

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110354923-110354973	IMR90	lung:	fetal
2	chr4:110354923-110354973	IMR90	lung:	fetal
3	chr4:110354443-110354493	GM12878	blood:	n/a
4	chr4:110355525-110355575	LNCaP	prostate:	n/a
5	chr4:110354354-110354404	HCPEpiC	choroid plexus:	n/a
6	chr4:110354354-110354404	AG10803	skin:	n/a
7	chr4:110354923-110354973	SK-N-SH	brain:	n/a
8	chr4:110354923-110354973	Hela-S3	cervix:	n/a
9	chr4:110355680-110355730	GM06990	blood:	n/a
10	chr4:110354820-110354870	HIPEpiC	eye:	n/a
11	chr4:110355525-110355575	Jurkat	blood:	n/a
12	chr4:110354354-110354404	HAEpiC	amniotic membrane:	n/a
13	chr4:110355680-110355730	Caco-2	colon:	n/a
14	chr4:110355525-110355575	GM12891	blood:	n/a
15	chr4:110355680-110355730	HEK293	kidney:	embryo
16	chr4:110354820-110354870	MCF10A-Er-Src	breast:	n/a
17	chr4:110355447-110355497	HEEpiC	esophagus:	n/a
18	chr4:110355525-110355575	HCF	heart:	n/a
19	chr4:110355680-110355730	GM12891	blood:	n/a
20	chr4:110355525-110355575	AoSMC	blood vessel:	n/a
21	chr4:110354923-110354973	H1-hESC	embryonic stem cell:	embryo
22	chr4:110354923-110354973	AG09309	skin:	n/a
23	chr4:110354896-110354946	HUVEC	blood vessel:	n/a
24	chr4:110354896-110354946	NHBE	bronchial:	n/a
25	chr4:110354923-110354973	HMEC	breast:	n/a
26	chr4:110355525-110355575	GM12878	blood:	n/a
27	chr4:110354354-110354404	AG04449	skin:	fetal
28	chr4:110355447-110355497	U87	brain:	n/a
29	chr4:110354896-110354946	Caco-2	colon:	n/a
30	chr4:110355525-110355575	SKMC	muscle:	n/a
31	chr4:110354896-110354946	AG04449	skin:	fetal
32	chr4:110355447-110355497	GM12892	blood:	n/a
33	chr4:110355447-110355497	HIPEpiC	eye:	n/a
34	chr4:110355680-110355730	HIPEpiC	eye:	n/a
35	chr4:110355472-110355522	AoSMC	blood vessel:	n/a
36	chr4:110354354-110354404	SAEC	small airway:	n/a
37	chr4:110354443-110354493	NHBE	bronchial:	n/a
38	chr4:110354820-110354870	Caco-2	colon:	n/a
39	chr4:110355472-110355522	LNCaP	prostate:	n/a
40	chr4:110354923-110354973	AG04449	skin:	fetal
41	chr4:110354896-110354946	NHDF-neo	bronchial:	n/a
42	chr4:110355525-110355575	GM19239	blood:	n/a
43	chr4:110354354-110354404	HIPEpiC	eye:	n/a
44	chr4:110354443-110354493	HUVEC	blood vessel:	n/a
45	chr4:110354923-110354973	LNCaP	prostate:	n/a
46	chr4:110354923-110354973	GM06990	blood:	n/a
47	chr4:110355680-110355730	HEEpiC	esophagus:	n/a
48	chr4:110354923-110354973	MCF-7	breast:	n/a
49	chr4:110355472-110355522	AG04450	lung:	fetal
50	chr4:110354820-110354870	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:110353323..110356452-chr4:110478874..110481567,4	MCF-7	breast:
2	chr14:105261712..105263242-chr4:110355266..110356786,2	MCF-7	breast:
3	chr4:109540362..109542277-chr4:110353620..110356489,2	K562	blood:
4	chr4:110352891..110355275-chr4:110649929..110651520,2	MCF-7	breast:
5	chr4:110354680..110356371-chr4:110650734..110652526,2	MCF-7	breast:
6	chr4:110351897..110354482-chr4:110431012..110433361,3	MCF-7	breast:
7	chr4:110353269..110354820-chr4:110577196..110580148,2	MCF-7	breast:
8	chr4:109542488..109544674-chr4:110355892..110357950,2	K562	blood:
9	chr4:110353826..110356085-chr4:110735938..110738635,3	MCF-7	breast:
10	chr4:110354421..110354923-chr7:44084218..44084744,2	Hela-S3	cervix:
11	chr4:110351870..110353542-chr4:110355047..110357946,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL25A1-1	chr4:110354890-110354939	ENSG00000247950
2	lnc-COL25A1-1	chr4:110354890-110354973	ENSG00000247950
3	lnc-COL25A1-1	chr4:110354890-110354920	ENSG00000247950

Variant related genes	Relation type
SEC24B-AS1	TF binding region
SEC24B	TF binding region
SEC24B-AS1	CpG island
SEC24B	CpG island
ENSG00000123739	chromatin interactions
ENSG00000272795	chromatin interactions
ENSG00000136279	chromatin interactions
ENSG00000109534	chromatin interactions
ENSG00000109475	chromatin interactions
ENSG00000234492	chromatin interactions
ENSG00000005059	chromatin interactions
ENSG00000142208	chromatin interactions
CCNG1	miRNA target sites
ATP6V1C1	miRNA target sites
G3BP1	miRNA target sites

Extended variants
information (count: 54 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:54 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs151143846	chr4:110354418-110354419	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs540622048	chr4:110354433-110354434	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs77326245	chr4:110354456-110354457	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs189459377	chr4:110354492-110354493	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs560185560	chr4:110354493-110354494	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs532173387	chr4:110354538-110354539	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs79665044	chr4:110354557-110354558	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs562456698	chr4:110354593-110354594	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs531326472	chr4:110354632-110354633	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs76023249	chr4:110354682-110354683	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs567551528	chr4:110354721-110354722	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs536423717	chr4:110354739-110354740	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs180697394	chr4:110354790-110354791	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs567063509	chr4:110354793-110354794	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs185054241	chr4:110354819-110354820	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs371131199	chr4:110354821-110354822	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs534049793	chr4:110354873-110354874	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs71603023	chr4:110354889-110354890	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs575677521	chr4:110354899-110354900	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
20	rs538377411	chr4:110354966-110354967	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
21	rs72896632	chr4:110354973-110354974	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs570129880	chr4:110355097-110355098	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs574733736	chr4:110355129-110355130	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs540044361	chr4:110355136-110355137	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs553890452	chr4:110355176-110355177	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs577065985	chr4:110355305-110355306	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs13103419	chr4:110355351-110355352	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs546049130	chr4:110355410-110355411	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs115096670	chr4:110355463-110355464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs531190289	chr4:110355486-110355487	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs541550304	chr4:110355493-110355494	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs190301923	chr4:110355546-110355547	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs527347571	chr4:110355553-110355554	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs546883957	chr4:110355582-110355583	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs181123724	chr4:110355750-110355751	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs565364003	chr4:110355754-110355755	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs532711829	chr4:110355771-110355772	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs552820812	chr4:110355779-110355780	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs569303036	chr4:110355781-110355782	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs538240356	chr4:110355852-110355853	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs368340573	chr4:110355882-110355883	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs140064705	chr4:110355948-110355949	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs371163442	chr4:110355971-110355972	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs568577311	chr4:110356060-110356061	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs150327298	chr4:110356068-110356069	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs368844743	chr4:110356088-110356089	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs553705634	chr4:110356107-110356108	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs34984365	chr4:110356118-110356119	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs186005931	chr4:110356179-110356180	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs545810979	chr4:110356192-110356193	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110346000-110354400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:110351000-110354400	Weak transcription	Pancreas	Pancrea
3	chr4:110353400-110354400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr4:110353400-110354600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:110353400-110356600	Active TSS	K562	blood
6	chr4:110353600-110354400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr4:110353600-110354400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr4:110353600-110354400	Flanking Active TSS	Brain Hippocampus Middle	brain
9	chr4:110353600-110354600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr4:110353600-110354600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:110353600-110354600	Flanking Active TSS	HUVEC	blood vessel
12	chr4:110353600-110354600	Flanking Active TSS	Osteobl	bone
13	chr4:110353600-110354800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr4:110353600-110357000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:110353800-110354400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:110353800-110354400	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr4:110353800-110354400	Flanking Active TSS	Primary hematopoietic stem cells	blood
18	chr4:110353800-110354400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr4:110353800-110354400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
20	chr4:110353800-110354400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
21	chr4:110353800-110354400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:110353800-110354400	Flanking Active TSS	Liver	Liver
23	chr4:110353800-110354400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
24	chr4:110353800-110354400	Flanking Active TSS	Colon Smooth Muscle	Colon
25	chr4:110353800-110354400	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr4:110353800-110354400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr4:110353800-110354400	Flanking Active TSS	Stomach Mucosa	stomach
28	chr4:110353800-110354400	Flanking Active TSS	Dnd41	blood
29	chr4:110353800-110354600	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr4:110353800-110354600	Flanking Active TSS	GM12878-XiMat	blood
31	chr4:110353800-110356000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:110353800-110356000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:110353800-110356000	Active TSS	Fetal Intestine Large	intestine
34	chr4:110353800-110356400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr4:110353800-110356400	Active TSS	HSMM	muscle
36	chr4:110353800-110356600	Active TSS	H1 Cell Line	embryonic stem cell
37	chr4:110353800-110356800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr4:110353800-110357000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:110354000-110354400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
40	chr4:110354000-110354400	Flanking Active TSS	Brain Cingulate Gyrus	brain
41	chr4:110354000-110354400	Flanking Active TSS	Fetal Brain Male	brain
42	chr4:110354000-110354400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr4:110354000-110354400	Flanking Active TSS	Rectal Smooth Muscle	rectum
44	chr4:110354000-110354400	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr4:110354000-110354400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr4:110354000-110354600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr4:110354000-110354600	Flanking Active TSS	Primary B cells from cord blood	blood
48	chr4:110354000-110354600	Flanking Active TSS	Primary B cells from peripheral blood	blood
49	chr4:110354000-110354600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr4:110354000-110354600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland

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