Variant report

Variant	nsv879676
Chromosome Location	chr4:102202285-102340930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2024)
CpG islands
(count:1588)
Chromatin interactive
region (count:66)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2024 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:102266883-102267082	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:102268870-102269129	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:102277128-102278568	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:102206748-102207057	HepG2	liver:	n/a	chr4:102206940-102206956
5	ARID3A	chr4:102270051-102270246	HepG2	liver:	n/a	n/a
6	ATF2	chr4:102339134-102339737	GM12878	blood:	n/a	n/a
7	ATF2	chr4:102276346-102276818	GM12878	blood:	n/a	n/a
8	ATF2	chr4:102340441-102340905	GM12878	blood:	n/a	n/a
9	ATF2	chr4:102276329-102276842	GM12878	blood:	n/a	n/a
10	ATF2	chr4:102249182-102249856	GM12878	blood:	n/a	n/a
11	ATF2	chr4:102249102-102249943	GM12878	blood:	n/a	n/a
12	ATF2	chr4:102339234-102339683	GM12878	blood:	n/a	n/a
13	BACH1	chr4:102278170-102278287	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:102268296-102268651	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:102269007-102269398	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:102234818-102234843	K562	blood:	n/a	n/a
17	BACH1	chr4:102266603-102267217	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr4:102339200-102339646	GM12878	blood:	n/a	n/a
19	BATF	chr4:102256033-102256341	GM12878	blood:	n/a	n/a
20	BATF	chr4:102249517-102249840	GM12878	blood:	n/a	n/a
21	BATF	chr4:102339267-102339612	GM12878	blood:	n/a	n/a
22	BATF	chr4:102249135-102249874	GM12878	blood:	n/a	n/a
23	BATF	chr4:102249224-102249502	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:102339255-102339648	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:102339259-102339562	GM12878	blood:	n/a	n/a
26	BCL3	chr4:102269133-102269684	A549	lung:	n/a	chr4:102269314-102269327 chr4:102269500-102269508 chr4:102269334-102269347 chr4:102269310-102269323
27	BCL3	chr4:102277222-102277839	A549	lung:	n/a	n/a
28	BCL3	chr4:102269158-102269648	A549	lung:	n/a	chr4:102269314-102269327 chr4:102269500-102269508 chr4:102269334-102269347 chr4:102269310-102269323
29	BCL3	chr4:102333047-102333465	A549	lung:	n/a	n/a
30	BCLAF1	chr4:102269101-102269432	GM12878	blood:	n/a	chr4:102269314-102269327 chr4:102269334-102269347 chr4:102269310-102269323
31	BCLAF1	chr4:102339132-102339714	GM12878	blood:	n/a	n/a
32	BCLAF1	chr4:102340390-102340904	GM12878	blood:	n/a	chr4:102340518-102340527
33	BHLHE40	chr4:102267821-102267970	K562	blood:	n/a	n/a
34	BHLHE40	chr4:102340516-102340716	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:102268204-102268609	K562	blood:	n/a	n/a
36	BHLHE40	chr4:102266870-102267476	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:102277311-102277417	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:102276360-102276798	GM12878	blood:	n/a	n/a
39	BHLHE40	chr4:102249227-102249995	GM12878	blood:	n/a	n/a
40	BHLHE40	chr4:102277318-102278000	HepG2	liver:	n/a	n/a
41	BHLHE40	chr4:102339219-102339605	GM12878	blood:	n/a	n/a
42	BHLHE40	chr4:102226332-102226631	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:102227391-102227696	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:102268064-102269557	GM12878	blood:	n/a	chr4:102269313-102269329 chr4:102269324-102269340 chr4:102269316-102269332
45	BHLHE40	chr4:102268827-102269533	K562	blood:	n/a	chr4:102269313-102269329 chr4:102269324-102269340 chr4:102269316-102269332
46	BRCA1	chr4:102267814-102267862	GM12878	blood:	n/a	n/a
47	BRCA1	chr4:102267314-102267339	GM12878	blood:	n/a	chr4:102267314-102267323
48	BRCA1	chr4:102314320-102314648	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr4:102277481-102277934	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr4:102267844-102267962	Hela-S3	cervix:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102340823-102340873	GM12891	blood:	n/a
2	chr4:102272871-102272921	AG04450	lung:	fetal
3	chr4:102340823-102340873	GM12891	blood:	n/a
4	chr4:102272871-102272921	AG04450	lung:	fetal
5	chr4:102268075-102268125	MCF-7	breast:	n/a
6	chr4:102267974-102268024	AG04450	lung:	fetal
7	chr4:102268957-102269007	AG09319	gingival:	n/a
8	chr4:102267974-102268024	SK-N-MC	brain:	n/a
9	chr4:102267189-102267239	Hepatocyte	liver:	n/a
10	chr4:102227740-102227790	Jurkat	blood:	n/a
11	chr4:102268125-102268175	NB4	blood:	n/a
12	chr4:102268854-102268904	HMEC	breast:	n/a
13	chr4:102267189-102267239	AG10803	skin:	n/a
14	chr4:102272871-102272921	AG10803	skin:	n/a
15	chr4:102268957-102269007	HNPCEpiC	eye:	n/a
16	chr4:102268854-102268904	HNPCEpiC	eye:	n/a
17	chr4:102207435-102207485	ProgFib	skin:	n/a
18	chr4:102272871-102272921	HEK293	kidney:	embryo
19	chr4:102267189-102267239	NHDF-neo	bronchial:	n/a
20	chr4:102269779-102269829	HRE	kidney:	n/a
21	chr4:102340691-102340741	SK-N-SH_RA	brain:	n/a
22	chr4:102268799-102268849	SK-N-SH_RA	brain:	n/a
23	chr4:102267366-102267416	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:102266325-102266375	GM12891	blood:	n/a
25	chr4:102269425-102269475	HCF	heart:	n/a
26	chr4:102268245-102268295	MCF10A-Er-Src	breast:	n/a
27	chr4:102340691-102340741	RPTEC	kidney:	n/a
28	chr4:102277629-102277679	NT2-D1	testis:	n/a
29	chr4:102268957-102269007	H1-hESC	embryonic stem cell:	embryo
30	chr4:102227740-102227790	CMK	blood:	n/a
31	chr4:102267974-102268024	PrEC	prostate:	n/a
32	chr4:102268957-102269007	HIPEpiC	eye:	n/a
33	chr4:102268821-102268871	NHBE	bronchial:	n/a
34	chr4:102268245-102268295	HNPCEpiC	eye:	n/a
35	chr4:102227740-102227790	MCF-7	breast:	n/a
36	chr4:102269779-102269829	Hepatocyte	liver:	n/a
37	chr4:102269779-102269829	GM19239	blood:	n/a
38	chr4:102269779-102269829	MCF-7	breast:	n/a
39	chr4:102267189-102267239	ECC-1	luminal epithelium:	n/a
40	chr4:102268854-102268904	GM12878	blood:	n/a
41	chr4:102258631-102258681	HIPEpiC	eye:	n/a
42	chr4:102340823-102340873	MCF10A-Er-Src	breast:	n/a
43	chr4:102267189-102267239	U87	brain:	n/a
44	chr4:102264326-102264376	PrEC	prostate:	n/a
45	chr4:102268821-102268871	MCF-7	breast:	n/a
46	chr4:102268854-102268904	PANC-1	pancreas:	n/a
47	chr4:102227740-102227790	GM12891	blood:	n/a
48	chr4:102268622-102268672	AG04450	lung:	fetal
49	chr4:102268854-102268904	NT2-D1	testis:	n/a
50	chr4:102269779-102269829	H1-hESC	embryonic stem cell:	embryo

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:102191153..102193723-chr4:102199346..102202643,3	MCF-7	breast:
2	chr4:102205631..102207880-chr4:102239422..102240935,2	MCF-7	breast:
3	chr4:102229146..102231940-chr4:102232073..102233783,2	K562	blood:
4	chr4:102238335..102240230-chr4:102246275..102248377,2	MCF-7	breast:
5	chr4:102234738..102237332-chr4:102239450..102241192,2	MCF-7	breast:
6	chr4:102238335..102240230-chr4:102246275..102248377,2	MCF-7	breast:
7	chr4:102269774..102272032-chr4:102277264..102279804,2	K562	blood:
8	chr4:102277055..102279316-chr4:102287621..102289577,3	MCF-7	breast:
9	chr4:102242973..102245664-chr4:102246576..102249048,2	MCF-7	breast:
10	chr4:102114465..102117225-chr4:102221024..102223068,2	MCF-7	breast:
11	chr4:102229146..102231940-chr4:102232073..102233783,2	K562	blood:
12	chr4:102249081..102251620-chr4:102269591..102272220,2	MCF-7	breast:
13	chr4:102090213..102092693-chr4:102253077..102255174,2	MCF-7	breast:
14	chr4:102252145..102254033-chr4:102258356..102260817,2	MCF-7	breast:
15	chr4:102211391..102213772-chr4:102219486..102221204,2	MCF-7	breast:
16	chr11:113966492..113967012-chr4:102236344..102236864,2	Hela-S3	cervix:
17	chr4:102252145..102254033-chr4:102258356..102260817,2	MCF-7	breast:
18	chr4:102160648..102162431-chr4:102260568..102262904,2	MCF-7	breast:
19	chr4:102202182..102203692-chr4:102205246..102206935,2	MCF-7	breast:
20	chr4:102277040..102279542-chr4:102281591..102284231,2	MCF-7	breast:
21	chr4:102269774..102272032-chr4:102277264..102279804,2	K562	blood:
22	chr4:102265718..102267485-chr4:103187307..103189886,2	MCF-7	breast:
23	chr4:102263328..102265199-chr4:102265515..102267436,2	K562	blood:
24	chr4:102242973..102245664-chr4:102246576..102249048,2	MCF-7	breast:
25	chr4:102226380..102228700-chr4:102233879..102237672,3	MCF-7	breast:
26	chr4:101039108..101041675-chr4:102229054..102231223,2	K562	blood:
27	chr4:102228684..102230512-chr4:102715753..102717632,2	K562	blood:
28	chr4:102198153..102200394-chr4:102259165..102261544,2	MCF-7	breast:
29	chr4:102226021..102228958-chr4:102267685..102270990,3	MCF-7	breast:
30	chr4:102277055..102279316-chr4:102287621..102289577,3	MCF-7	breast:
31	chr4:102226380..102228700-chr4:102233879..102237672,3	MCF-7	breast:
32	chr4:102263328..102265199-chr4:102265515..102267436,2	K562	blood:
33	chr4:102248729..102250846-chr4:102268529..102271038,2	K562	blood:
34	chr4:102276355..102278194-chr4:102281593..102284291,2	MCF-7	breast:
35	chr4:102244312..102246286-chr4:102248183..102250301,2	K562	blood:
36	chr4:102129139..102132021-chr4:102226843..102229507,2	MCF-7	breast:
37	chr4:102205631..102207880-chr4:102239422..102240935,2	MCF-7	breast:
38	chr4:102278096..102281241-chr4:102294142..102296404,3	MCF-7	breast:
39	chr4:102208778..102209725-chr4:102317892..102318526,2	MCF-7	breast:
40	chr4:102244312..102246286-chr4:102248183..102250301,2	K562	blood:
41	chr4:102202182..102203692-chr4:102205246..102206935,2	MCF-7	breast:
42	chr4:102219978..102222828-chr4:102224431..102227610,3	MCF-7	breast:
43	chr4:102276355..102278194-chr4:102281593..102284291,2	MCF-7	breast:
44	chr4:102048414..102050219-chr4:102262763..102264265,2	MCF-7	breast:
45	chr4:102206850..102209343-chr4:102209669..102211406,2	MCF-7	breast:
46	chr4:102277040..102279542-chr4:102281591..102284231,2	MCF-7	breast:
47	chr4:102221934..102223732-chr4:102258287..102261196,2	MCF-7	breast:
48	chr4:102229250..102230989-chr4:102267695..102270675,2	MCF-7	breast:
49	chr4:102278096..102281241-chr4:102294142..102296404,3	MCF-7	breast:
50	chr4:102234738..102237332-chr4:102239450..102241192,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EMCN-2	chr4:102218141-102219108	NONHSAT097569
2	lnc-AP001816.1.1-1	chr4:102269481-102270040	NR_033874
3	lnc-EMCN-3	chr4:102265025-102267178	NONHSAT097571
4	lnc-BANK1-1	chr4:102333336-102333506	NONHSAT097572
5	lnc-BANK1-1	chr4:102332443-102332593	NONHSAT097572
6	lnc-AP001816.1.1-1	chr4:102268934-102269166	NR_033874

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1255a	chr4:102251522-102251544	MIMAT0005906

No data

Variant related genes	Relation type
MIR1255A	TF binding region
ENSG00000254531	TF binding region
PPP3CA	TF binding region
BANK1	TF binding region
MIR1255A	CpG island
ENSG00000254531	CpG island
PPP3CA	CpG island
BANK1	CpG island
ENSG00000254531	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000138814	chromatin interactions
ENSG00000221265	chromatin interactions

Extended variants
information (count: 5044 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:5044 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2850976	chr4:102202285-102202286	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184362155	chr4:102202353-102202354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562568390	chr4:102202357-102202358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542900739	chr4:102202399-102202400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536764172	chr4:102202447-102202448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554636558	chr4:102202471-102202472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572926578	chr4:102202499-102202500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534208634	chr4:102202547-102202548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11736443	chr4:102202564-102202565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367707902	chr4:102202593-102202594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376519546	chr4:102202606-102202607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577021311	chr4:102202607-102202608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533234909	chr4:102202621-102202622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544435024	chr4:102202623-102202624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563108086	chr4:102202699-102202700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11454628	chr4:102202737-102202738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34791348	chr4:102202759-102202760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189292063	chr4:102202809-102202810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541931328	chr4:102202865-102202866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560168985	chr4:102202868-102202869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181328133	chr4:102202899-102202900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115835705	chr4:102202954-102202955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564325335	chr4:102203000-102203001	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs9998913	chr4:102203022-102203023	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549673824	chr4:102203024-102203025	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568266570	chr4:102203031-102203032	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs536324889	chr4:102203046-102203047	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548694465	chr4:102203052-102203053	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs566521631	chr4:102203140-102203141	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs533981106	chr4:102203149-102203150	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs558534038	chr4:102203156-102203157	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs80208621	chr4:102203188-102203189	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs549353536	chr4:102203243-102203244	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs199991310	chr4:102203332-102203333	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs28491829	chr4:102203385-102203386	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73835913	chr4:102203409-102203410	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369951453	chr4:102203442-102203443	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75562815	chr4:102203461-102203462	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184045067	chr4:102203499-102203500	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189172733	chr4:102203598-102203599	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181540132	chr4:102203614-102203615	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561225341	chr4:102203662-102203663	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs28551487	chr4:102203688-102203689	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572173901	chr4:102203718-102203719	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17031119	chr4:102203784-102203785	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549787943	chr4:102203798-102203799	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79500763	chr4:102203808-102203809	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541932709	chr4:102203813-102203814	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs73835914	chr4:102203824-102203825	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs531476762	chr4:102203848-102203849	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	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
Hirschsprung''s Disease	21712996	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
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2518 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102180600-102203000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr4:102184000-102203200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr4:102188800-102203200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr4:102192800-102208600	Weak transcription	Fetal Kidney	kidney
5	chr4:102193000-102203400	Weak transcription	Brain Angular Gyrus	brain
6	chr4:102194000-102205200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr4:102194200-102203000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr4:102195400-102203400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr4:102196600-102203000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:102197400-102203600	Weak transcription	Left Ventricle	heart
11	chr4:102197400-102203600	Weak transcription	Pancreas	Pancrea
12	chr4:102198400-102206800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:102198600-102203400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:102198800-102203200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr4:102198800-102207800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:102199600-102203600	Weak transcription	Small Intestine	intestine
17	chr4:102199600-102205200	Enhancers	Primary B cells from peripheral blood	blood
18	chr4:102199600-102210400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr4:102199800-102202400	Weak transcription	Primary T cells from cord blood	blood
20	chr4:102199800-102203000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr4:102199800-102206800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:102200000-102211800	Weak transcription	HMEC	breast
23	chr4:102200200-102206200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:102200400-102202600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:102200600-102203000	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr4:102200600-102211800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:102200800-102202400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:102200800-102204400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr4:102200800-102206200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:102200800-102206200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:102200800-102209000	Weak transcription	Aorta	Aorta
32	chr4:102201000-102203200	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr4:102201000-102203400	Weak transcription	Psoas Muscle	Psoas
34	chr4:102201000-102203400	Weak transcription	Right Atrium	heart
35	chr4:102201000-102203600	Weak transcription	Fetal Thymus	thymus
36	chr4:102201000-102203600	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr4:102201000-102206200	Weak transcription	Ovary	ovary
38	chr4:102201000-102206800	Weak transcription	Gastric	stomach
39	chr4:102201000-102207000	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr4:102201000-102213000	Weak transcription	Fetal Heart	heart
41	chr4:102201200-102203000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr4:102201200-102203200	Weak transcription	Primary B cells from cord blood	blood
43	chr4:102201200-102203400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:102201200-102205200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr4:102201200-102205200	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr4:102201200-102205600	Weak transcription	HUVEC	blood vessel
47	chr4:102201200-102207800	Weak transcription	Adipose Nuclei	Adipose
48	chr4:102201200-102218200	Weak transcription	NHEK	skin
49	chr4:102201400-102203600	Weak transcription	GM12878-XiMat	blood
50	chr4:102201400-102204800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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