Variant report

Variant	nsv967996
Chromosome Location	chr4:74902400-74920659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:618)
CpG islands
(count:916)
Chromatin interactive
region (count:28)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:74920131-74920265	K562	blood:	n/a	n/a
2	ARID3A	chr4:74905097-74905553	K562	blood:	n/a	n/a
3	ARID3A	chr4:74904679-74904879	K562	blood:	n/a	n/a
4	ARID3A	chr4:74903695-74903769	K562	blood:	n/a	n/a
5	ATF1	chr4:74906895-74907485	K562	blood:	n/a	n/a
6	BACH1	chr4:74904237-74904832	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:74902964-74902965	K562	blood:	n/a	n/a
8	BHLHE40	chr4:74904181-74905422	K562	blood:	n/a	n/a
9	BHLHE40	chr4:74919899-74920053	K562	blood:	n/a	n/a
10	BHLHE40	chr4:74908958-74909031	K562	blood:	n/a	n/a
11	BHLHE40	chr4:74902865-74903376	K562	blood:	n/a	n/a
12	BRCA1	chr4:74904351-74905411	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr4:74904165-74904495	K562	blood:	n/a	n/a
14	CBX3	chr4:74912859-74913199	K562	blood:	n/a	n/a
15	CCNT2	chr4:74904145-74904900	K562	blood:	n/a	chr4:74904527-74904536
16	CCNT2	chr4:74905122-74905373	K562	blood:	n/a	n/a
17	CEBPB	chr4:74909801-74909981	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:74903443-74903524	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:74917034-74917198	A549	lung:	n/a	n/a
20	CEBPB	chr4:74918530-74918750	IMR90	lung:	n/a	chr4:74918666-74918679 chr4:74918667-74918678
21	CEBPB	chr4:74918529-74918742	HepG2	liver:	n/a	chr4:74918666-74918679 chr4:74918667-74918678
22	CEBPB	chr4:74917056-74917160	K562	blood:	n/a	n/a
23	CEBPB	chr4:74909679-74910082	IMR90	lung:	n/a	n/a
24	CEBPB	chr4:74918500-74918772	K562	blood:	n/a	chr4:74918666-74918679 chr4:74918667-74918678
25	CEBPD	chr4:74904146-74904971	K562	blood:	n/a	n/a
26	CHD2	chr4:74904254-74904827	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr4:74904689-74904775	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:74904323-74904325	K562	blood:	n/a	n/a
29	CREB1	chr4:74904134-74904759	A549	lung:	n/a	n/a
30	CREB1	chr4:74904355-74904774	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr4:74907020-74907655	K562	blood:	n/a	n/a
32	CTCF	chr4:74908583-74908592	GM19239	blood:	n/a	n/a
33	CTCF	chr4:74908504-74908655	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:74908511-74908643	K562	blood:	n/a	n/a
35	CTCF	chr4:74920456-74920517	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:74904320-74904470	HCT-116	colon:	n/a	n/a
37	CTCF	chr4:74904300-74904450	GM12868	blood:	n/a	n/a
38	CTCF	chr4:74903940-74904090	GM12875	blood:	n/a	n/a
39	CTCF	chr4:74904161-74904405	GM19240	blood:	n/a	n/a
40	CTCF	chr4:74908480-74908630	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:74903900-74904050	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr4:74902940-74903090	HRE	kidney:	n/a	n/a
43	CTCF	chr4:74903960-74904110	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:74904153-74904434	GM19238	blood:	n/a	n/a
45	CTCF	chr4:74904196-74904386	GM12892	blood:	n/a	n/a
46	CTCF	chr4:74903300-74903450	AG04449	skin:	n/a	n/a
47	CTCF	chr4:74920429-74920528	LNCaP	prostate:	n/a	n/a
48	CTCF	chr4:74903500-74903650	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr4:74902962-74903038	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr4:74908529-74908634	A549	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:74904765-74904815	U87	brain:	n/a
2	chr4:74904765-74904815	U87	brain:	n/a
3	chr4:74904714-74904764	A549	lung:	n/a
4	chr4:74904359-74904409	Caco-2	colon:	n/a
5	chr4:74904583-74904633	AG04449	skin:	fetal
6	chr4:74904675-74904725	PFSK-1	brain:	n/a
7	chr4:74904714-74904764	GM06990	blood:	n/a
8	chr4:74904106-74904156	H1-hESC	embryonic stem cell:	embryo
9	chr4:74907683-74907733	ProgFib	skin:	n/a
10	chr4:74904397-74904447	BE2_C	brain:	n/a
11	chr4:74904714-74904764	HEEpiC	esophagus:	n/a
12	chr4:74904583-74904633	IMR90	lung:	fetal
13	chr4:74904675-74904725	HepG2	liver:	n/a
14	chr4:74904765-74904815	PrEC	prostate:	n/a
15	chr4:74902951-74903001	ProgFib	skin:	n/a
16	chr4:74907683-74907733	CMK	blood:	n/a
17	chr4:74904765-74904815	RPTEC	kidney:	n/a
18	chr4:74904397-74904447	HMEC	breast:	n/a
19	chr4:74904607-74904657	HCPEpiC	choroid plexus:	n/a
20	chr4:74904765-74904815	Hepatocyte	liver:	n/a
21	chr4:74904359-74904409	A549	lung:	n/a
22	chr4:74904583-74904633	HEK293	kidney:	embryo
23	chr4:74902951-74903001	ECC-1	luminal epithelium:	n/a
24	chr4:74904106-74904156	AG09309	skin:	n/a
25	chr4:74907683-74907733	NHBE	bronchial:	n/a
26	chr4:74904359-74904409	NB4	blood:	n/a
27	chr4:74904583-74904633	MCF10A-Er-Src	breast:	n/a
28	chr4:74907683-74907733	GM19239	blood:	n/a
29	chr4:74907683-74907733	PrEC	prostate:	n/a
30	chr4:74904397-74904447	U87	brain:	n/a
31	chr4:74904498-74904548	NH-A	brain:	n/a
32	chr4:74904583-74904633	HRCEpiC	kidney:	n/a
33	chr4:74903507-74903557	HCT-116	colon:	n/a
34	chr4:74904397-74904447	K562	blood:	n/a
35	chr4:74904607-74904657	HEK293	kidney:	embryo
36	chr4:74902951-74903001	PANC-1	pancreas:	n/a
37	chr4:74904521-74904571	GM06990	blood:	n/a
38	chr4:74903507-74903557	CMK	blood:	n/a
39	chr4:74904790-74904840	RPTEC	kidney:	n/a
40	chr4:74920559-74920609	ProgFib	skin:	n/a
41	chr4:74920559-74920609	GM06990	blood:	n/a
42	chr4:74920559-74920609	AG10803	skin:	n/a
43	chr4:74904359-74904409	SK-N-SH	brain:	n/a
44	chr4:74904397-74904447	CMK	blood:	n/a
45	chr4:74904583-74904633	HCT-116	colon:	n/a
46	chr4:74920559-74920609	HL-60	blood:	n/a
47	chr4:74904583-74904633	RPTEC	kidney:	n/a
48	chr4:74904607-74904657	HAEpiC	amniotic membrane:	n/a
49	chr4:74903507-74903557	IMR90	lung:	fetal
50	chr4:74904498-74904548	AG09319	gingival:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:74902918..74906977-chr4:74963214..74968788,8	K562	blood:
2	chr4:74913574..74916451-chr4:74961099..74963523,2	K562	blood:
3	chr4:74902434..74906647-chr4:74918639..74924896,12	K562	blood:
4	chr4:74855916..74858178-chr4:74901845..74903855,2	K562	blood:
5	chr4:74874915..74877444-chr4:74902823..74905015,2	K562	blood:
6	chr4:74920487..74923421-chr4:75023614..75026198,3	K562	blood:
7	chr4:74902434..74906647-chr4:74918639..74924896,12	K562	blood:
8	chr4:74904625..74906220-chr4:74906808..74908780,2	MCF-7	breast:
9	chr4:74905779..74908851-chr4:74974510..74977216,3	K562	blood:
10	chr4:74902406..74903926-chr4:74946680..74949073,2	K562	blood:
11	chr4:74913657..74916615-chr4:74960329..74961922,2	K562	blood:
12	chr4:74904625..74906220-chr4:74906808..74908780,2	MCF-7	breast:
13	chr4:74902071..74908104-chr4:74918639..74927051,16	K562	blood:
14	chr4:74906392..74908851-chr4:74974510..74976154,2	K562	blood:
15	chr4:74903038..74905484-chr4:74963526..74965321,3	K562	blood:
16	chr4:74903817..74904810-chr4:74964503..74965118,2	HCT-116	colon:
17	chr4:74902531..74904905-chr4:74978906..74980803,2	K562	blood:
18	chr4:74908077..74910007-chr4:74941278..74943027,2	K562	blood:
19	chr4:74764548..74766659-chr4:74904527..74906987,2	K562	blood:
20	chr4:74902984..74906659-chr4:74908263..74910717,4	K562	blood:
21	chr4:74907375..74910324-chr4:74936842..74940272,3	K562	blood:
22	chr4:74918446..74926481-chr4:74958079..74968779,32	K562	blood:
23	chr4:74902071..74908104-chr4:74918639..74927051,16	K562	blood:
24	chr4:74906693..74909434-chr4:74919569..74922539,3	K562	blood:
25	chr4:74917982..74919932-chr4:75041196..75043826,2	K562	blood:
26	chr4:74901269..74902961-chr4:74935972..74938903,2	K562	blood:
27	chr4:74904496..74906866-chr4:74952202..74954701,2	K562	blood:
28	chr4:74917692..74925936-chr4:74958187..74967502,26	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXCL3-1	chr4:74904229-74904524	NONHSAT096879
2	lnc-CXCL3-2	chr4:74919992-74920127	NONHSAT096881
3	lnc-CXCL3-1	chr4:74902786-74904130	NONHSAT096879
4	lnc-CXCL3-2	chr4:74920420-74920537	NONHSAT096881
5	lnc-CXCL3-2	chr4:74919758-74919849	NONHSAT096881
6	lnc-CXCL3-2	chr4:74919755-74921116	NONHSAT096880

No data

Variant related genes	Relation type
PPBPP2	TF binding region
CXCL3	TF binding region
PPBPP2	CpG island
CXCL3	CpG island
ENSG00000081041	chromatin interactions
ENSG00000163738	chromatin interactions
ENSG00000244194	chromatin interactions
ENSG00000251017	chromatin interactions
ENSG00000163734	chromatin interactions
ENSG00000248848	chromatin interactions
ENSG00000269559	chromatin interactions

Extended variants
information (count: 761 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200113321	chr4:74902412-74902413	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200931739	chr4:74902416-74902417	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545469277	chr4:74902424-74902425	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201745827	chr4:74902440-74902441	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199936057	chr4:74902446-74902447	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201223860	chr4:74902457-74902458	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs202150150	chr4:74902463-74902464	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200245948	chr4:74902465-74902466	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs201068516	chr4:74902482-74902483	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201824210	chr4:74902497-74902498	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200396970	chr4:74902509-74902510	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113503574	chr4:74902519-74902520	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs551729161	chr4:74902527-74902528	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199517714	chr4:74902528-74902529	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs200320368	chr4:74902538-74902539	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201623624	chr4:74902540-74902541	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538109513	chr4:74902561-74902562	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs199778175	chr4:74902567-74902568	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200716830	chr4:74902574-74902575	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs201735236	chr4:74902592-74902593	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs199743689	chr4:74902597-74902598	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543086648	chr4:74902611-74902612	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs13150258	chr4:74902664-74902665	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192662858	chr4:74902665-74902666	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112785228	chr4:74902674-74902675	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201862278	chr4:74902706-74902707	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199876137	chr4:74902716-74902717	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201055105	chr4:74902717-74902718	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs202015979	chr4:74902750-74902751	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200151056	chr4:74902752-74902753	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201127219	chr4:74902775-74902776	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201791349	chr4:74902776-74902777	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs200253429	chr4:74902826-74902827	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs200886112	chr4:74902832-74902833	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs201879346	chr4:74902833-74902834	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs528751164	chr4:74902844-74902845	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs200262907	chr4:74902847-74902848	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs201421057	chr4:74902857-74902858	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs151083701	chr4:74902868-74902869	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs565439920	chr4:74902869-74902870	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs199753671	chr4:74902894-74902895	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs200565678	chr4:74902904-74902905	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs201483390	chr4:74902914-74902915	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs199509809	chr4:74902925-74902926	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs200611108	chr4:74902931-74902932	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs201781698	chr4:74902936-74902937	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs374315451	chr4:74902941-74902942	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs199810402	chr4:74902943-74902944	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs185155671	chr4:74902944-74902945	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs201732413	chr4:74902951-74902952	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Abnormal phenotypes	18644119	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20932292	CNVD

Chromatin state (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74890200-74903200	Weak transcription	Stomach Mucosa	stomach
2	chr4:74896600-74902600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr4:74896800-74902800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr4:74897800-74902800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr4:74897800-74902800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr4:74898000-74903000	Weak transcription	Gastric	stomach
7	chr4:74898200-74902800	Weak transcription	NHLF	lung
8	chr4:74898800-74903000	Weak transcription	Colonic Mucosa	Colon
9	chr4:74899000-74902600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:74899000-74903000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr4:74899000-74903000	Weak transcription	HUVEC	blood vessel
12	chr4:74899600-74902800	Weak transcription	Hela-S3	cervix
13	chr4:74900000-74902800	Weak transcription	NHDF-Ad	bronchial
14	chr4:74900000-74903200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:74900000-74903200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr4:74900000-74903600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:74900200-74902400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:74900200-74902400	Weak transcription	HMEC	breast
19	chr4:74900200-74902600	Weak transcription	HSMM	muscle
20	chr4:74900200-74902600	Weak transcription	NHEK	skin
21	chr4:74900200-74902800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:74900200-74902800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:74900200-74903800	Weak transcription	Esophagus	oesophagus
24	chr4:74900600-74903000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr4:74901400-74902800	Weak transcription	Osteobl	bone
26	chr4:74901800-74902400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:74901800-74903000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:74902000-74903200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:74902200-74902400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:74902200-74902800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:74902200-74902800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:74902200-74902800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:74902200-74902800	Active TSS	Muscle Satellite Cultured Cells	--
34	chr4:74902200-74902800	Active TSS	K562	blood
35	chr4:74902200-74905200	Active TSS	A549	lung
36	chr4:74902400-74902600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr4:74902400-74902600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:74902400-74902600	Active TSS	HMEC	breast
39	chr4:74902400-74902800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:74902400-74902800	Active TSS	Thymus	Thymus
41	chr4:74902600-74902800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:74902600-74902800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:74902600-74902800	Active TSS	NHEK	skin
44	chr4:74902600-74903000	Enhancers	Dnd41	blood
45	chr4:74902600-74903400	Flanking Active TSS	HMEC	breast
46	chr4:74902600-74904200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:74902600-74905000	Active TSS	HSMM	muscle
48	chr4:74902600-74905200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr4:74902600-74905800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:74902800-74903000	Enhancers	H9 Cell Line	embryonic stem cell

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