Variant report

Variant	nsv885797
Chromosome Location	chr6:34791027-34980601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2915)
CpG islands
(count:2320)
Chromatin interactive
region (count:206)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2915 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34867597-34867797	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:34802936-34803203	K562	blood:	n/a	n/a
3	ARID3A	chr6:34979641-34979707	K562	blood:	n/a	n/a
4	ARID3A	chr6:34807829-34807953	K562	blood:	n/a	n/a
5	ARID3A	chr6:34856773-34857038	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:34832879-34833479	K562	blood:	n/a	n/a
7	ARID3A	chr6:34954566-34954923	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:34855719-34856923	K562	blood:	n/a	n/a
9	ARID3A	chr6:34913180-34913516	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:34921206-34922396	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:34954572-34954906	K562	blood:	n/a	n/a
12	ATF1	chr6:34979412-34979789	K562	blood:	n/a	n/a
13	ATF1	chr6:34855487-34856397	K562	blood:	n/a	chr6:34855838-34855852
14	ATF1	chr6:34874691-34874810	K562	blood:	n/a	n/a
15	ATF1	chr6:34803008-34803279	K562	blood:	n/a	n/a
16	ATF1	chr6:34832863-34833326	K562	blood:	n/a	n/a
17	ATF1	chr6:34921512-34921692	K562	blood:	n/a	n/a
18	ATF1	chr6:34950737-34951033	K562	blood:	n/a	n/a
19	ATF1	chr6:34827687-34828162	K562	blood:	n/a	n/a
20	ATF1	chr6:34856679-34857207	K562	blood:	n/a	n/a
21	ATF2	chr6:34880420-34880916	GM12878	blood:	n/a	n/a
22	ATF2	chr6:34855474-34856393	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
23	ATF2	chr6:34855555-34856110	GM12878	blood:	n/a	chr6:34855838-34855852
24	ATF2	chr6:34856633-34857098	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:34855549-34856136	H1-hESC	embryonic stem cell:	n/a	chr6:34855838-34855852
26	ATF2	chr6:34979119-34979993	GM12878	blood:	n/a	n/a
27	ATF2	chr6:34855528-34856206	GM12878	blood:	n/a	chr6:34855838-34855852
28	ATF2	chr6:34979083-34979953	GM12878	blood:	n/a	n/a
29	ATF2	chr6:34856545-34857022	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr6:34937401-34937669	K562	blood:	n/a	n/a
31	ATF3	chr6:34855569-34856012	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
32	ATF3	chr6:34855584-34856143	HepG2	liver:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
33	ATF3	chr6:34855564-34856045	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
34	ATF3	chr6:34855626-34856017	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
35	ATF3	chr6:34855575-34856023	H1-hESC	embryonic stem cell:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
36	ATF3	chr6:34855611-34856089	A549	lung:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
37	ATF3	chr6:34855565-34856126	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
38	ATF3	chr6:34869076-34869473	K562	blood:	n/a	n/a
39	ATF3	chr6:34855595-34856148	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
40	ATF3	chr6:34856802-34857214	K562	blood:	n/a	n/a
41	ATF3	chr6:34855553-34856043	K562	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
42	ATF3	chr6:34869194-34869500	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF3	chr6:34855748-34855947	GM12878	blood:	n/a	chr6:34855830-34855850 chr6:34855839-34855852 chr6:34855838-34855853
44	BACH1	chr6:34842743-34842837	K562	blood:	n/a	n/a
45	BACH1	chr6:34856735-34857116	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr6:34807714-34807998	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr6:34807689-34808041	K562	blood:	n/a	n/a
48	BACH1	chr6:34937468-34937748	K562	blood:	n/a	chr6:34937563-34937577
49	BATF	chr6:34923346-34923637	GM12878	blood:	n/a	n/a
50	BATF	chr6:34979078-34979815	GM12878	blood:	n/a	chr6:34979570-34979579

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34856897-34856947	HRPEpiC	eye:	n/a
2	chr6:34880181-34880231	HRCEpiC	kidney:	n/a
3	chr6:34856897-34856947	HRPEpiC	eye:	n/a
4	chr6:34880181-34880231	HRCEpiC	kidney:	n/a
5	chr6:34919755-34919805	HCM	heart:	n/a
6	chr6:34843579-34843629	MCF10A-Er-Src	breast:	n/a
7	chr6:34856135-34856185	HEK293	kidney:	embryo
8	chr6:34856897-34856947	H1-hESC	embryonic stem cell:	embryo
9	chr6:34856135-34856185	HRCEpiC	kidney:	n/a
10	chr6:34954867-34954917	ovcar-3	ovarian:	n/a
11	chr6:34880181-34880231	HepG2	liver:	n/a
12	chr6:34855797-34855847	HEK293	kidney:	embryo
13	chr6:34855789-34855839	ECC-1	luminal epithelium:	n/a
14	chr6:34941065-34941115	RPTEC	kidney:	n/a
15	chr6:34855887-34855937	NHBE	bronchial:	n/a
16	chr6:34855797-34855847	HCF	heart:	n/a
17	chr6:34954030-34954080	HEEpiC	esophagus:	n/a
18	chr6:34843579-34843629	Hela-S3	cervix:	n/a
19	chr6:34857018-34857068	SK-N-SH_RA	brain:	n/a
20	chr6:34853620-34853670	Jurkat	blood:	n/a
21	chr6:34857162-34857212	A549	lung:	n/a
22	chr6:34856217-34856267	HAEpiC	amniotic membrane:	n/a
23	chr6:34855834-34855884	AG04449	skin:	fetal
24	chr6:34855887-34855937	HL-60	blood:	n/a
25	chr6:34856158-34856208	AG04449	skin:	fetal
26	chr6:34843579-34843629	RPTEC	kidney:	n/a
27	chr6:34954867-34954917	U87	brain:	n/a
28	chr6:34856704-34856754	AG09319	gingival:	n/a
29	chr6:34880181-34880231	SK-N-SH	brain:	n/a
30	chr6:34941065-34941115	K562	blood:	n/a
31	chr6:34856927-34856977	HPAEpiC	pulmonary alveolar:	n/a
32	chr6:34895360-34895410	PrEC	prostate:	n/a
33	chr6:34856217-34856267	AoSMC	blood vessel:	n/a
34	chr6:34843579-34843629	SK-N-SH_RA	brain:	n/a
35	chr6:34852903-34852953	CMK	blood:	n/a
36	chr6:34855885-34855935	Hepatocyte	liver:	n/a
37	chr6:34857281-34857331	HCM	heart:	n/a
38	chr6:34856704-34856754	LNCaP	prostate:	n/a
39	chr6:34852903-34852953	MCF10A-Er-Src	breast:	n/a
40	chr6:34857162-34857212	HEEpiC	esophagus:	n/a
41	chr6:34856217-34856267	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:34856135-34856185	HepG2	liver:	n/a
43	chr6:34855789-34855839	AG10803	skin:	n/a
44	chr6:34856217-34856267	MCF10A-Er-Src	breast:	n/a
45	chr6:34858220-34858270	ovcar-3	ovarian:	n/a
46	chr6:34856135-34856185	HCM	heart:	n/a
47	chr6:34857162-34857212	Jurkat	blood:	n/a
48	chr6:34879081-34879131	GM06990	blood:	n/a
49	chr6:34855635-34855685	Jurkat	blood:	n/a
50	chr6:34855797-34855847	U87	brain:	n/a

(count:206 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:34854042..34857854-chr6:34876810..34882352,6	K562	blood:
2	chr6:34880699..34884444-chr6:34885944..34888970,5	K562	blood:
3	chr6:34893290..34895416-chr6:34950224..34952119,2	K562	blood:
4	chr6:34779065..34780836-chr6:34797089..34799244,2	K562	blood:
5	chr6:34953914..34956313-chr6:34963882..34965683,2	MCF-7	breast:
6	chr6:34947461..34949129-chr6:34952748..34955327,2	MCF-7	breast:
7	chr6:34828677..34833050-chr6:34855355..34860063,5	K562	blood:
8	chr6:34832033..34834649-chr6:34867129..34869415,2	K562	blood:
9	chr6:34836775..34838347-chr6:34941205..34942985,2	MCF-7	breast:
10	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
11	chr6:34884853..34887138-chr6:34887416..34892086,4	K562	blood:
12	chr6:34856018..34858760-chr6:34873113..34875329,3	K562	blood:
13	chr6:34834250..34837156-chr6:34851105..34853013,3	MCF-7	breast:
14	chr6:34892877..34895013-chr6:34901039..34903046,2	K562	blood:
15	chr15:91446501..91447001-chr6:34954264..34955087,2	HCT-116	colon:
16	chr6:34833067..34835129-chr6:34854541..34856066,2	K562	blood:
17	chr6:34940687..34943018-chr6:34944838..34946831,2	K562	blood:
18	chr6:34835870..34838689-chr6:34843706..34845674,2	K562	blood:
19	chr6:34758169..34761129-chr6:34802765..34804303,2	K562	blood:
20	chr6:34759748..34761318-chr6:34832739..34834824,2	K562	blood:
21	chr17:56708594..56709416-chr6:34855776..34856394,2	Hela-S3	cervix:
22	chr6:34874014..34875640-chr6:34878716..34880730,2	K562	blood:
23	chr6:34828049..34830008-chr6:34830119..34831858,2	K562	blood:
24	chr6:34873430..34875640-chr6:34878874..34880730,2	K562	blood:
25	chr6:34838773..34840454-chr6:34842472..34845232,2	MCF-7	breast:
26	chr6:34803335..34805787-chr6:34806399..34809385,2	K562	blood:
27	chr6:34891666..34893180-chr6:34904331..34907073,2	K562	blood:
28	chr6:34887280..34889976-chr6:34890282..34893090,2	K562	blood:
29	chr6:34723520..34726444-chr6:34854512..34857469,3	MCF-7	breast:
30	chr6:34836775..34838347-chr6:34941205..34942985,2	MCF-7	breast:
31	chr4:2419677..2420373-chr6:34855480..34855994,2	Hela-S3	cervix:
32	chr6:34759044..34761512-chr6:34840299..34841904,2	K562	blood:
33	chr6:34875439..34878531-chr6:34883509..34886060,3	MCF-7	breast:
34	chr6:34856224..34858095-chr6:35226235..35229197,2	MCF-7	breast:
35	chr6:34832033..34834649-chr6:34867129..34869415,2	K562	blood:
36	chr6:34937846..34940693-chr6:34953607..34956913,3	K562	blood:
37	chr6:34786614..34789043-chr6:34809197..34812183,2	K562	blood:
38	chr6:34869119..34871903-chr6:34874576..34877464,3	K562	blood:
39	chr17:73285374..73286157-chr6:34855342..34855976,2	Hela-S3	cervix:
40	chr6:34392549..34394826-chr6:34874788..34877623,2	MCF-7	breast:
41	chr6:34865959..34867467-chr6:34869062..34871406,2	K562	blood:
42	chr6:34938891..34940598-chr6:35202108..35204116,2	K562	blood:
43	chr6:27798350..27799895-chr6:34855095..34857385,2	K562	blood:
44	chr6:34825507..34827584-chr6:34840818..34842443,2	MCF-7	breast:
45	chr6:34951005..34953968-chr6:34956984..34958726,3	MCF-7	breast:
46	chr6:34854944..34856631-chr6:34874568..34876971,2	MCF-7	breast:
47	chr6:34878922..34882866-chr6:34883896..34887915,4	MCF-7	breast:
48	chr6:34835870..34838689-chr6:34843706..34845674,2	K562	blood:
49	chr6:34954072..34954818-chr6:35208589..35209528,2	MCF-7	breast:
50	chr6:34857055..34859091-chr6:34938202..34940889,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UHRF1BP1	hsa-let-7e-5p	chr6:34843708-34843714
2	UHRF1BP1	hsa-let-7e-5p	chr6:34825126-34825148

Variant related genes	Relation type
ANKS1A	TF binding region
TAF11	TF binding region
ANKS1A	CpG island
TAF11	CpG island
ENSG00000064999	chromatin interactions
ENSG00000159733	chromatin interactions
ENSG00000264241	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000174197	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000125454	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000197914	chromatin interactions
ENSG00000065029	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000137309	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000272374	chromatin interactions

Extended variants
information (count: 6706 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:6706 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7774697	chr6:34791027-34791028	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368358653	chr6:34791040-34791041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192913090	chr6:34791059-34791060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs370789136	chr6:34791086-34791087	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs200279224	chr6:34791089-34791090	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563270535	chr6:34791108-34791109	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530864945	chr6:34791110-34791111	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184575469	chr6:34791162-34791163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570686187	chr6:34791171-34791172	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs565865034	chr6:34791239-34791240	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534786149	chr6:34791248-34791249	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560432104	chr6:34791250-34791251	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs62402661	chr6:34791259-34791260	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141532162	chr6:34791271-34791272	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371886251	chr6:34791333-34791334	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112732340	chr6:34791334-34791335	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62402662	chr6:34791336-34791337	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs367924051	chr6:34791353-34791354	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543310556	chr6:34791358-34791359	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs58796631	chr6:34791401-34791402	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111951738	chr6:34791414-34791415	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537376848	chr6:34791443-34791444	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558799238	chr6:34791450-34791451	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs9469897	chr6:34791465-34791466	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs541572506	chr6:34791502-34791503	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187122902	chr6:34791532-34791533	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369692271	chr6:34791567-34791568	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192336324	chr6:34791611-34791612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs541550677	chr6:34791670-34791671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs563304715	chr6:34791715-34791716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184444784	chr6:34791732-34791733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552518930	chr6:34791741-34791742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189596867	chr6:34791833-34791834	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11755575	chr6:34791859-34791860	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150864643	chr6:34791945-34791946	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181989314	chr6:34791997-34791998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567246278	chr6:34792037-34792038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530246957	chr6:34792047-34792048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548255495	chr6:34792048-34792049	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184494639	chr6:34792107-34792108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537014149	chr6:34792108-34792109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9469898	chr6:34792178-34792179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558832963	chr6:34792191-34792192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532884152	chr6:34792196-34792197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571077691	chr6:34792225-34792226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554782989	chr6:34792259-34792260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12177835	chr6:34792262-34792263	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs566294949	chr6:34792283-34792284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574916790	chr6:34792285-34792286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543604808	chr6:34792305-34792306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:5203 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34764000-34803800	Weak transcription	HSMM	muscle
2	chr6:34773200-34791400	Weak transcription	Gastric	stomach
3	chr6:34775400-34802400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:34779200-34797000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:34779200-34807400	Weak transcription	A549	lung
6	chr6:34779400-34796400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:34779400-34841000	Weak transcription	NH-A	brain
8	chr6:34779600-34791400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:34779600-34796200	Weak transcription	NHEK	skin
10	chr6:34780800-34794000	Weak transcription	Aorta	Aorta
11	chr6:34781000-34797000	Weak transcription	Colon Smooth Muscle	Colon
12	chr6:34781600-34791400	Weak transcription	Brain Substantia Nigra	brain
13	chr6:34781600-34824000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr6:34783200-34807400	Weak transcription	Psoas Muscle	Psoas
15	chr6:34785600-34802400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:34786600-34838800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr6:34787400-34791200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr6:34787600-34791400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:34787600-34802400	Weak transcription	Right Ventricle	heart
20	chr6:34787600-34807400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:34787800-34793200	Weak transcription	NHDF-Ad	bronchial
22	chr6:34787800-34803600	Weak transcription	Esophagus	oesophagus
23	chr6:34788000-34802600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr6:34788200-34791400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr6:34788200-34792400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr6:34788200-34802000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr6:34788200-34831800	Weak transcription	HUVEC	blood vessel
28	chr6:34788400-34796400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr6:34788400-34802000	Weak transcription	Small Intestine	intestine
30	chr6:34788400-34826600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr6:34788400-34826800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:34788400-34830800	Weak transcription	Fetal Heart	heart
33	chr6:34789000-34791800	Strong transcription	Primary B cells from cord blood	blood
34	chr6:34789000-34791800	Strong transcription	Primary T cells from cord blood	blood
35	chr6:34789000-34802400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr6:34789000-34811000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:34789000-34811800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr6:34789200-34791800	Strong transcription	Primary hematopoietic stem cells	blood
39	chr6:34789200-34798000	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr6:34789200-34798600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:34789200-34798800	Strong transcription	Placenta	Placenta
42	chr6:34789400-34791800	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:34789400-34791800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr6:34789400-34791800	Strong transcription	Brain Inferior Temporal Lobe	brain
45	chr6:34789400-34791800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr6:34789400-34792000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:34789400-34792000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:34789400-34792000	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr6:34789400-34792000	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr6:34789400-34792000	Strong transcription	Skeletal Muscle Female	skeletal muscle

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