Variant report

Variant	esv2759310
Chromosome Location	chr4:187261330-187422342
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:895)
CpG islands
(count:1525)
Chromatin interactive
region (count:33)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187393967-187394511	K562	blood:	n/a	n/a
2	ARID3A	chr4:187394041-187394370	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187421894-187422344	K562	blood:	n/a	n/a
4	ATF1	chr4:187420491-187420916	K562	blood:	n/a	n/a
5	ATF1	chr4:187272198-187272476	K562	blood:	n/a	n/a
6	ATF3	chr4:187394371-187394479	GM12878	blood:	n/a	n/a
7	ATF3	chr4:187421950-187422165	K562	blood:	n/a	n/a
8	BACH1	chr4:187356907-187357919	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:187392859-187392959	K562	blood:	n/a	n/a
10	BCL11A	chr4:187354074-187354310	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:187266370-187266656	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr4:187327155-187327407	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:187362735-187362783	K562	blood:	n/a	n/a
14	BHLHE40	chr4:187421756-187422525	K562	blood:	n/a	n/a
15	BRCA1	chr4:187346073-187346283	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
17	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
18	CBX3	chr4:187373146-187373490	K562	blood:	n/a	n/a
19	CBX3	chr4:187285262-187285641	K562	blood:	n/a	n/a
20	CBX3	chr4:187373072-187373601	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:187284185-187284627	K562	blood:	n/a	n/a
22	CBX3	chr4:187373086-187373652	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:187354461-187354780	K562	blood:	n/a	n/a
24	CBX3	chr4:187373144-187373570	K562	blood:	n/a	n/a
25	CBX3	chr4:187285282-187285592	K562	blood:	n/a	n/a
26	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
27	CCNT2	chr4:187362847-187363236	K562	blood:	n/a	n/a
28	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
29	CEBPB	chr4:187361028-187361112	A549	lung:	n/a	n/a
30	CEBPB	chr4:187316995-187317220	K562	blood:	n/a	n/a
31	CEBPB	chr4:187378227-187378457	IMR90	lung:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
32	CEBPB	chr4:187394195-187394430	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr4:187375448-187375609	A549	lung:	n/a	chr4:187375528-187375539
34	CEBPB	chr4:187371106-187371462	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
35	CEBPB	chr4:187371132-187371388	MCF-7	breast:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
36	CEBPB	chr4:187371124-187371436	Hela-S3	cervix:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
37	CEBPB	chr4:187371144-187371490	HepG2	liver:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
38	CEBPB	chr4:187421769-187422320	K562	blood:	n/a	n/a
39	CEBPB	chr4:187371108-187371409	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
40	CEBPB	chr4:187361057-187361080	HepG2	liver:	n/a	n/a
41	CEBPB	chr4:187371126-187371469	H1-hESC	embryonic stem cell:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
42	CEBPB	chr4:187379564-187379739	A549	lung:	n/a	n/a
43	CEBPB	chr4:187325690-187326036	A549	lung:	n/a	n/a
44	CEBPB	chr4:187378219-187378507	K562	blood:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
45	CEBPB	chr4:187375483-187375595	HepG2	liver:	n/a	chr4:187375528-187375539
46	CEBPB	chr4:187360936-187361199	K562	blood:	n/a	n/a
47	CEBPB	chr4:187420609-187420949	K562	blood:	n/a	n/a
48	CEBPB	chr4:187371127-187371481	IMR90	lung:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
49	CEBPB	chr4:187371179-187371335	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
50	CEBPB	chr4:187371090-187371490	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187404958-187405008	IMR90	lung:	fetal
2	chr4:187404923-187404973	GM12878	blood:	n/a
3	chr4:187404988-187405038	HNPCEpiC	eye:	n/a
4	chr4:187418419-187418469	PrEC	prostate:	n/a
5	chr4:187291940-187291990	NH-A	brain:	n/a
6	chr4:187394380-187394430	AG04449	skin:	fetal
7	chr4:187404958-187405008	HEK293	kidney:	embryo
8	chr4:187422114-187422164	AG04449	skin:	fetal
9	chr4:187418419-187418469	CMK	blood:	n/a
10	chr4:187293592-187293642	AG04450	lung:	fetal
11	chr4:187349131-187349181	GM06990	blood:	n/a
12	chr4:187293521-187293571	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:187349131-187349181	HRCEpiC	kidney:	n/a
14	chr4:187293418-187293468	SK-N-SH	brain:	n/a
15	chr4:187360860-187360910	HRE	kidney:	n/a
16	chr4:187349665-187349715	ECC-1	luminal epithelium:	n/a
17	chr4:187291940-187291990	Caco-2	colon:	n/a
18	chr4:187349131-187349181	HRE	kidney:	n/a
19	chr4:187289264-187289314	BJ	skin:	n/a
20	chr4:187349714-187349764	HNPCEpiC	eye:	n/a
21	chr4:187422091-187422141	Hepatocyte	liver:	n/a
22	chr4:187422005-187422055	GM12891	blood:	n/a
23	chr4:187394380-187394430	NT2-D1	testis:	n/a
24	chr4:187293114-187293164	GM19239	blood:	n/a
25	chr4:187266705-187266755	A549	lung:	n/a
26	chr4:187293418-187293468	HEK293	kidney:	embryo
27	chr4:187349665-187349715	HEEpiC	esophagus:	n/a
28	chr4:187407036-187407086	ovcar-3	ovarian:	n/a
29	chr4:187349665-187349715	ProgFib	skin:	n/a
30	chr4:187291940-187291990	HMEC	breast:	n/a
31	chr4:187293592-187293642	GM12892	blood:	n/a
32	chr4:187296698-187296748	NHBE	bronchial:	n/a
33	chr4:187422119-187422169	HRE	kidney:	n/a
34	chr4:187291940-187291990	AG10803	skin:	n/a
35	chr4:187404923-187404973	A549	lung:	n/a
36	chr4:187422091-187422141	K562	blood:	n/a
37	chr4:187422119-187422169	ovcar-3	ovarian:	n/a
38	chr4:187422119-187422169	U87	brain:	n/a
39	chr4:187291940-187291990	RPTEC	kidney:	n/a
40	chr4:187357928-187357978	AG09319	gingival:	n/a
41	chr4:187293418-187293468	NB4	blood:	n/a
42	chr4:187296698-187296748	GM19239	blood:	n/a
43	chr4:187266705-187266755	HEEpiC	esophagus:	n/a
44	chr4:187394380-187394430	HL-60	blood:	n/a
45	chr4:187422005-187422055	GM19239	blood:	n/a
46	chr4:187422005-187422055	HRCEpiC	kidney:	n/a
47	chr4:187293418-187293468	LNCaP	prostate:	n/a
48	chr4:187293592-187293642	SKMC	muscle:	n/a
49	chr4:187349131-187349181	K562	blood:	n/a
50	chr4:187422114-187422164	NH-A	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
2	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
3	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
4	chr4:187250299..187252105-chr4:187259927..187262894,2	K562	blood:
5	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
6	chr4:187332246..187335061-chr4:187336434..187338116,2	K562	blood:
7	chr4:187336442..187338955-chr4:187341117..187342706,2	K562	blood:
8	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
9	chr4:187339945..187342685-chr4:187344135..187346623,2	K562	blood:
10	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
11	chr4:187332850..187335061-chr4:187335595..187338116,3	K562	blood:
12	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
13	chr4:187339945..187342685-chr4:187344135..187346623,2	K562	blood:
14	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
15	chr4:187414357..187416175-chr4:187420876..187423477,2	MCF-7	breast:
16	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
17	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
18	chr4:187327492..187329160-chr4:187332412..187335274,2	K562	blood:
19	chr4:187336442..187338955-chr4:187341117..187342706,2	K562	blood:
20	chr10:56621759..56622362-chr4:187295967..187296841,2	MCF-7	breast:
21	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
22	chr4:187327492..187329160-chr4:187332412..187335274,2	K562	blood:
23	chr4:187393785..187394637-chr4:187475328..187475950,2	MCF-7	breast:
24	chr4:187394722..187395443-chr4:187508309..187509281,2	MCF-7	breast:
25	chr4:187400808..187402522-chr4:187420720..187422452,2	MCF-7	breast:
26	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
27	chr4:187393992..187394694-chr4:187476207..187476860,2	MCF-7	breast:
28	chr4:187402656..187405583-chr4:187422037..187423656,2	K562	blood:
29	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
30	chr4:187332246..187335061-chr4:187336434..187338116,2	K562	blood:
31	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
32	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
33	chr11:67069270..67069773-chr4:187272896..187273396,2	NB4	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187345244-187345390	NONHSAT099658
2	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
3	lnc-MTNR1A-1	chr4:187349859-187350004	ENSG00000251165.1
4	lnc-MTNR1A-1	chr4:187347391-187348252	ENSG00000251165.1
5	lnc-MTNR1A-1	chr4:187352772-187352922	NONHSAT099658
6	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
7	lnc-MTNR1A-1	chr4:187421999-187422212	NONHSAT099658
8	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1
9	lnc-MTNR1A-1	chr4:187344883-187344986	NONHSAT099658
10	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
11	lnc-FAT1-5	chr4:187409184-187409778	predAs_chen_AV690772_1
12	lnc-MTNR1A-1	chr4:187353299-187353392	ENSG00000251165.1
13	lnc-MTNR1A-1	chr4:187337280-187337490	NONHSAT099658
14	lnc-MTNR1A-1	chr4:187348128-187348252	ENSG00000251165.1
15	lnc-MTNR1A-1	chr4:187345244-187345390	ENSG00000251165.1
16	lnc-MTNR1A-1	chr4:187353299-187353392	NONHSAT099658
17	lnc-MTNR1A-1	chr4:187347391-187348252	NONHSAT099658
18	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
19	lnc-MTNR1A-1	chr4:187347391-187347447	ENSG00000251165.1
20	lnc-MTNR1A-1	chr4:187344882-187344986	ENSG00000251165.1
21	lnc-MTNR1A-1	chr4:187352772-187352922	ENSG00000251165.1

No data

Variant related genes	Relation type
F11-AS1	TF binding region
RNU6-1055P	TF binding region
F11-AS1	CpG island
RNU6-1055P	CpG island
ENSG00000272297	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000168412	chromatin interactions
ENSG00000213332	chromatin interactions

Extended variants
information (count: 5294 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5294 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75892058	chr4:187261333-187261334	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568770280	chr4:187261335-187261336	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375782054	chr4:187261406-187261407	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs143361832	chr4:187261420-187261421	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs576373281	chr4:187261429-187261430	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542070645	chr4:187261491-187261492	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555581639	chr4:187261497-187261498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577979424	chr4:187261529-187261530	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572082666	chr4:187261592-187261593	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs545467290	chr4:187261646-187261647	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114807765	chr4:187261661-187261662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139237772	chr4:187261684-187261685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143342434	chr4:187261717-187261718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs542974528	chr4:187261728-187261729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs62350302	chr4:187261744-187261745	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563654436	chr4:187261831-187261832	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147109644	chr4:187261843-187261844	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529515608	chr4:187261844-187261845	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77804005	chr4:187261894-187261895	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559504397	chr4:187261898-187261899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs116462026	chr4:187261947-187261948	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73873793	chr4:187261951-187261952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571601136	chr4:187261970-187261971	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113911709	chr4:187261981-187261982	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200744134	chr4:187261989-187261990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138518824	chr4:187261994-187261995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs550968551	chr4:187262127-187262128	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543245267	chr4:187262159-187262160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569996902	chr4:187262161-187262162	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77174595	chr4:187262235-187262236	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369484086	chr4:187262276-187262277	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs116289508	chr4:187262291-187262292	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376364925	chr4:187262295-187262296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572203093	chr4:187262389-187262390	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185137659	chr4:187262394-187262395	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534471823	chr4:187262436-187262437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557843874	chr4:187262474-187262475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190876948	chr4:187262479-187262480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs10032695	chr4:187262489-187262490	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562921336	chr4:187262506-187262507	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141850721	chr4:187262507-187262508	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs58321536	chr4:187262602-187262603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs59116022	chr4:187262643-187262644	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs376517580	chr4:187262648-187262649	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528685187	chr4:187262675-187262676	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115273876	chr4:187262728-187262729	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs117923488	chr4:187262747-187262748	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
48	rs532805789	chr4:187262799-187262800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs150602785	chr4:187262821-187262822	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34606402	chr4:187262833-187262834	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

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
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
Acute lymphoblastic leukemia	20067559	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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187263200-187264000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:187264000-187264200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:187264000-187264400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:187265200-187265600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr4:187265800-187267000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr4:187266000-187266600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
7	chr4:187266200-187266400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr4:187266200-187266800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
9	chr4:187266200-187267000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
10	chr4:187266200-187267000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
11	chr4:187266600-187266800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
12	chr4:187266600-187266800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
13	chr4:187266600-187266800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
14	chr4:187266600-187266800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:187266600-187266800	Enhancers	Fetal Stomach	stomach
16	chr4:187266600-187267000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr4:187266600-187267000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr4:187266600-187267000	Enhancers	Duodenum Mucosa	Duodenum
19	chr4:187266600-187267000	Enhancers	Fetal Intestine Large	intestine
20	chr4:187266600-187267000	Enhancers	Fetal Intestine Small	intestine
21	chr4:187266800-187267000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr4:187266800-187267000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:187267800-187268000	Enhancers	Pancreas	Pancrea
24	chr4:187268000-187269000	Weak transcription	Pancreas	Pancrea
25	chr4:187268800-187269400	Enhancers	Fetal Kidney	kidney
26	chr4:187269000-187269400	Active TSS	Pancreas	Pancrea
27	chr4:187269200-187269400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr4:187269200-187269400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
29	chr4:187269200-187269800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr4:187269400-187270200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr4:187269400-187272400	Enhancers	Pancreas	Pancrea
32	chr4:187269600-187269800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
33	chr4:187269600-187269800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
34	chr4:187272400-187278800	Weak transcription	Pancreas	Pancrea
35	chr4:187273800-187274000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr4:187273800-187274000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:187278800-187279000	Enhancers	Pancreas	Pancrea
38	chr4:187285000-187285600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr4:187285000-187286200	ZNF genes & repeats	Adipose Nuclei	Adipose
40	chr4:187285000-187287800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:187285200-187286200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
42	chr4:187285200-187286200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
43	chr4:187285800-187286200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:187286200-187289200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:187289000-187289600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:187289000-187289600	Enhancers	HMEC	breast
47	chr4:187289200-187289800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr4:187289200-187289800	Enhancers	NHEK	skin
49	chr4:187289200-187290200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:187289200-187290200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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