Variant report

Variant	esv7375
Chromosome Location	chr6:150324114-150388625
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1368)
CpG islands
(count:3236)
Chromatin interactive
region (count:37)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:150338070-150338270	HepG2	liver:	n/a	n/a
2	ATF1	chr6:150326501-150326880	K562	blood:	n/a	n/a
3	ATF1	chr6:150336933-150337019	K562	blood:	n/a	n/a
4	ATF2	chr6:150325826-150326122	GM12878	blood:	n/a	n/a
5	ATF2	chr6:150328002-150328596	GM12878	blood:	n/a	n/a
6	ATF2	chr6:150328091-150328518	GM12878	blood:	n/a	n/a
7	ATF2	chr6:150325436-150325936	GM12878	blood:	n/a	n/a
8	ATF3	chr6:150326273-150326742	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
9	ATF3	chr6:150326401-150326606	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
10	ATF3	chr6:150326376-150326975	H1-hESC	embryonic stem cell:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
11	ATF3	chr6:150326327-150326877	K562	blood:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
12	ATF3	chr6:150326345-150326945	H1-hESC	embryonic stem cell:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
13	ATF3	chr6:150326347-150326676	HepG2	liver:	n/a	chr6:150326500-150326509 chr6:150326563-150326583 chr6:150326489-150326509 chr6:150326500-150326520
14	BACH1	chr6:150326284-150326697	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr6:150328116-150328490	GM12878	blood:	n/a	n/a
16	BATF	chr6:150346621-150346888	GM12878	blood:	n/a	chr6:150346723-150346734 chr6:150346728-150346738 chr6:150346724-150346734
17	BATF	chr6:150328171-150328476	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:150328125-150328471	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
19	BCL11A	chr6:150328061-150328481	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
20	BCL3	chr6:150328101-150328407	GM12878	blood:	n/a	chr6:150328226-150328235
21	BCLAF1	chr6:150325804-150326446	GM12878	blood:	n/a	chr6:150326058-150326067
22	BCLAF1	chr6:150328046-150328455	GM12878	blood:	n/a	chr6:150328226-150328235 chr6:150328420-150328429
23	BHLHE40	chr6:150334502-150334672	K562	blood:	n/a	n/a
24	BHLHE40	chr6:150328197-150328464	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:150381236-150381439	K562	blood:	n/a	n/a
26	BHLHE40	chr6:150326114-150327095	HepG2	liver:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
27	BHLHE40	chr6:150325516-150326816	GM12878	blood:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
28	BHLHE40	chr6:150326209-150326949	K562	blood:	n/a	chr6:150326500-150326509 chr6:150326499-150326508 chr6:150326500-150326509 chr6:150326501-150326510 chr6:150326498-150326511 chr6:150326494-150326515
29	BHLHE40	chr6:150336771-150337140	K562	blood:	n/a	n/a
30	BHLHE40	chr6:150381181-150381607	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:150329735-150330023	K562	blood:	n/a	n/a
32	BHLHE40	chr6:150381363-150381384	HepG2	liver:	n/a	n/a
33	BRCA1	chr6:150326801-150326903	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr6:150326274-150326876	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr6:150326263-150326443	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr6:150336795-150337204	K562	blood:	n/a	n/a
37	CBX3	chr6:150325861-150326760	K562	blood:	n/a	n/a
38	CBX3	chr6:150326784-150327232	K562	blood:	n/a	n/a
39	CBX3	chr6:150388339-150388656	K562	blood:	n/a	n/a
40	CCNT2	chr6:150336957-150337116	K562	blood:	n/a	n/a
41	CCNT2	chr6:150326066-150326830	K562	blood:	n/a	chr6:150326773-150326782
42	CEBPB	chr6:150336946-150337113	K562	blood:	n/a	n/a
43	CEBPB	chr6:150338040-150338363	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr6:150338074-150338240	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr6:150338050-150338338	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:150326311-150326551	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:150339733-150339933	Hela-S3	cervix:	n/a	chr6:150339786-150339797
48	CEBPB	chr6:150339700-150339896	HepG2	liver:	n/a	chr6:150339786-150339797
49	CEBPB	chr6:150353985-150354064	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:150329675-150329997	Hela-S3	cervix:	n/a	n/a

(count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150346921-150346971	NH-A	brain:	n/a
2	chr6:150346816-150346866	SK-N-SH	brain:	n/a
3	chr6:150331562-150331612	AG04450	lung:	fetal
4	chr6:150346921-150346971	NH-A	brain:	n/a
5	chr6:150346816-150346866	SK-N-SH	brain:	n/a
6	chr6:150331562-150331612	AG04450	lung:	fetal
7	chr6:150327687-150327737	A549	lung:	n/a
8	chr6:150336524-150336574	GM06990	blood:	n/a
9	chr6:150326316-150326366	PrEC	prostate:	n/a
10	chr6:150346497-150346547	NHBE	bronchial:	n/a
11	chr6:150379479-150379529	A549	lung:	n/a
12	chr6:150326762-150326812	HCF	heart:	n/a
13	chr6:150331562-150331612	BJ	skin:	n/a
14	chr6:150381200-150381250	ProgFib	skin:	n/a
15	chr6:150347012-150347062	SAEC	small airway:	n/a
16	chr6:150346863-150346913	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:150346721-150346771	HIPEpiC	eye:	n/a
18	chr6:150358985-150359035	HRE	kidney:	n/a
19	chr6:150346721-150346771	HL-60	blood:	n/a
20	chr6:150359130-150359180	CMK	blood:	n/a
21	chr6:150326776-150326826	HCF	heart:	n/a
22	chr6:150331562-150331612	U87	brain:	n/a
23	chr6:150326596-150326646	AG04449	skin:	fetal
24	chr6:150346886-150346936	AG09309	skin:	n/a
25	chr6:150326453-150326503	NH-A	brain:	n/a
26	chr6:150376218-150376268	U87	brain:	n/a
27	chr6:150326334-150326384	ovcar-3	ovarian:	n/a
28	chr6:150325970-150326020	NB4	blood:	n/a
29	chr6:150346863-150346913	PFSK-1	brain:	n/a
30	chr6:150326394-150326444	NHDF-neo	bronchial:	n/a
31	chr6:150388100-150388150	PANC-1	pancreas:	n/a
32	chr6:150378881-150378931	AG10803	skin:	n/a
33	chr6:150346886-150346936	AG04450	lung:	fetal
34	chr6:150326021-150326071	PrEC	prostate:	n/a
35	chr6:150347053-150347103	K562	blood:	n/a
36	chr6:150346787-150346837	LNCaP	prostate:	n/a
37	chr6:150336524-150336574	HEK293	kidney:	embryo
38	chr6:150376218-150376268	CMK	blood:	n/a
39	chr6:150346816-150346866	GM12891	blood:	n/a
40	chr6:150362502-150362552	Hela-S3	cervix:	n/a
41	chr6:150378881-150378931	Caco-2	colon:	n/a
42	chr6:150325970-150326020	GM12891	blood:	n/a
43	chr6:150326334-150326384	AG04449	skin:	fetal
44	chr6:150326394-150326444	HAEpiC	amniotic membrane:	n/a
45	chr6:150329845-150329895	ECC-1	luminal epithelium:	n/a
46	chr6:150336015-150336065	GM06990	blood:	n/a
47	chr6:150326323-150326373	T-47D	breast:	n/a
48	chr6:150362502-150362552	MCF-7	breast:	n/a
49	chr6:150358985-150359035	AoSMC	blood vessel:	n/a
50	chr6:150357289-150357339	NHDF-neo	bronchial:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150328123..150330822-chr6:150332783..150334807,2	MCF-7	breast:
2	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
3	chr6:150283429..150285848-chr6:150336024..150337757,2	MCF-7	breast:
4	chr6:150379821..150382555-chr6:150387863..150390602,3	MCF-7	breast:
5	chr6:150380000..150382934-chr6:150383185..150385012,2	MCF-7	breast:
6	chr6:150384794..150386662-chr6:150388680..150390331,2	MCF-7	breast:
7	chr6:150380000..150382934-chr6:150383185..150385012,2	MCF-7	breast:
8	chr6:150370900..150373661-chr6:150377798..150379934,2	K562	blood:
9	chr6:150370900..150376205-chr6:150377396..150379934,4	K562	blood:
10	chr6:150350371..150352271-chr6:150387708..150390265,2	MCF-7	breast:
11	chr6:150258514..150260378-chr6:150337573..150339969,2	MCF-7	breast:
12	chr6:150384115..150385944-chr6:150388643..150390347,3	MCF-7	breast:
13	chr6:150378922..150380433-chr6:150385877..150388167,2	K562	blood:
14	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
15	chr6:150246157..150249113-chr6:150336737..150339289,2	K562	blood:
16	chr6:150255064..150255979-chr6:150337750..150338789,5	K562	blood:
17	chr6:150328123..150330822-chr6:150332783..150334807,2	MCF-7	breast:
18	chr6:150323301..150326870-chr6:150337464..150339739,3	MCF-7	breast:
19	chr6:150378184..150381057-chr6:150388223..150390154,2	MCF-7	breast:
20	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
21	chr6:150274811..150275321-chr6:150336040..150336549,2	MCF-7	breast:
22	chr6:150354931..150357925-chr6:150386556..150388661,2	K562	blood:
23	chr6:150351052..150353254-chr6:150355645..150357982,2	K562	blood:
24	chr6:150355810..150358323-chr6:150360175..150362251,2	K562	blood:
25	chr6:150378184..150381057-chr6:150388223..150390154,2	MCF-7	breast:
26	chr6:150250322..150251340-chr6:150337738..150338572,3	K562	blood:
27	chr6:150155381..150157771-chr6:150346025..150347800,2	MCF-7	breast:
28	chr6:150324211..150327033-chr6:150387350..150388851,2	K562	blood:
29	chr6:150154861..150155845-chr6:150337730..150338274,2	K562	blood:
30	chr6:150370900..150376205-chr6:150377396..150379934,4	K562	blood:
31	chr6:150345687..150347890-chr6:150385680..150387900,2	MCF-7	breast:
32	chr6:150386654..150388325-chr6:150388815..150391248,2	MCF-7	breast:
33	chr6:150283785..150286352-chr6:150326807..150328312,2	MCF-7	breast:
34	chr6:150261749..150263311-chr6:150348518..150350047,2	MCF-7	breast:
35	chr6:150354901..150357527-chr6:150362159..150364156,2	MCF-7	breast:
36	chr6:150378922..150380433-chr6:150385877..150388167,2	K562	blood:
37	chr6:150370900..150373661-chr6:150377798..150379934,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ULBP1-2	chr6:150354375-150354702	NONHSAT115530
2	lnc-ULBP1-2	chr6:150353905-150354172	NONHSAT115530
3	lnc-RAET1L-1	chr6:150361683-150362309	XLOC_005876
4	lnc-RAET1L-1	chr6:150362917-150363169	XLOC_005876
5	lnc-RAET1L-2	chr6:150326209-150326280	NONHSAT115529

No data

Variant related genes	Relation type
PHBP1	TF binding region
RAET1L	TF binding region
RAET1M	TF binding region
RAET1K	TF binding region
ENSG00000235972	TF binding region
PHBP1	CpG island
RAET1L	CpG island
RAET1M	CpG island
RAET1K	CpG island
ENSG00000235972	CpG island
ENSG00000131019	chromatin interactions
ENSG00000216621	chromatin interactions
ENSG00000131015	chromatin interactions
ENSG00000155918	chromatin interactions
ENSG00000111981	chromatin interactions
ENSG00000213091	chromatin interactions
ENSG00000218358	chromatin interactions
ENSG00000120256	chromatin interactions
ENSG00000235972	chromatin interactions
INTS6	miRNA target sites
WDR11	miRNA target sites

Extended variants
information (count: 2800 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2800 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375931212	chr6:150324122-150324123	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs147226432	chr6:150324165-150324166	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs199674600	chr6:150324168-150324169	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs10644722	chr6:150324169-150324170	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs113270331	chr6:150324170-150324171	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs369089348	chr6:150324173-150324174	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs372022190	chr6:150324174-150324175	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs375754614	chr6:150324205-150324206	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs185096198	chr6:150324206-150324207	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs188391501	chr6:150324213-150324214	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs370106420	chr6:150324218-150324219	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs564134182	chr6:150324264-150324265	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs562131550	chr6:150324268-150324269	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs181265143	chr6:150324295-150324296	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs367788877	chr6:150324297-150324298	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs12196573	chr6:150324329-150324330	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs9479371	chr6:150324335-150324336	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs141660283	chr6:150324342-150324343	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs186875012	chr6:150324357-150324358	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs377066618	chr6:150324361-150324362	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs375028935	chr6:150324388-150324389	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs530786164	chr6:150324407-150324408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191726815	chr6:150324412-150324413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3963990	chr6:150324424-150324425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs550671711	chr6:150324440-150324441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397832813	chr6:150324447-150324448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570840381	chr6:150324479-150324480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1762124	chr6:150324486-150324487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539480857	chr6:150324504-150324505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563423579	chr6:150324533-150324534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566868399	chr6:150324549-150324550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532391661	chr6:150324583-150324584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535640595	chr6:150324588-150324589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56023615	chr6:150324628-150324629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575224059	chr6:150324635-150324636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12523689	chr6:150324636-150324637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557604673	chr6:150324645-150324646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577691145	chr6:150324701-150324702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552401070	chr6:150324717-150324718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34792200	chr6:150324735-150324736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1762126	chr6:150324817-150324818	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11961011	chr6:150324826-150324827	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs9384029	chr6:150324829-150324830	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184014941	chr6:150324850-150324851	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187397781	chr6:150324853-150324854	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191036983	chr6:150324854-150324855	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551038126	chr6:150324858-150324859	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143217730	chr6:150324904-150324905	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9384030	chr6:150324908-150324909	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs9478350	chr6:150324914-150324915	Weak transcription Bivalent/Poised TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1262 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150315000-150324800	Weak transcription	Dnd41	blood
2	chr6:150318200-150325400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:150319800-150325600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:150320800-150324200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:150321400-150325200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:150321600-150325400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:150322400-150325000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:150322800-150325200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr6:150322800-150325200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr6:150323000-150325200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:150323000-150325200	Weak transcription	Thymus	Thymus
12	chr6:150323200-150324800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr6:150323200-150324800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr6:150323200-150325200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr6:150323200-150325400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr6:150323400-150324400	ZNF genes & repeats	GM12878-XiMat	blood
17	chr6:150323400-150325200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:150323400-150325400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr6:150323600-150325000	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr6:150324200-150324600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:150324600-150325600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:150324800-150325000	Enhancers	Dnd41	blood
23	chr6:150324800-150325400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr6:150324800-150325600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr6:150324800-150325600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr6:150325000-150325200	Weak transcription	GM12878-XiMat	blood
27	chr6:150325000-150325400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:150325000-150325600	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:150325000-150325600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr6:150325000-150325600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr6:150325000-150326000	Flanking Active TSS	Dnd41	blood
32	chr6:150325200-150325400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:150325200-150325400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr6:150325200-150325400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:150325200-150325400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
36	chr6:150325200-150325400	Bivalent Enhancer	Fetal Thymus	thymus
37	chr6:150325200-150325400	Enhancers	GM12878-XiMat	blood
38	chr6:150325200-150325600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:150325200-150325600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
40	chr6:150325200-150325600	Enhancers	Primary B cells from cord blood	blood
41	chr6:150325200-150325600	Enhancers	Primary T cells from cord blood	blood
42	chr6:150325200-150325600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr6:150325200-150325600	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr6:150325200-150325600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr6:150325200-150325600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr6:150325200-150325600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:150325200-150325800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr6:150325200-150326000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr6:150325200-150327000	Active TSS	Hela-S3	cervix
50	chr6:150325400-150325600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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