Variant report

Variant	esv3354637
Chromosome Location	chr6:33377724-33379522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:728)
CpG islands
(count:1589)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:728 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:33377459-33378281	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:33377354-33378298	K562	blood:	n/a	n/a
3	ATF1	chr6:33377456-33378622	K562	blood:	n/a	n/a
4	ATF2	chr6:33377783-33378358	GM12878	blood:	n/a	chr6:33378125-33378136
5	ATF2	chr6:33377787-33378421	H1-hESC	embryonic stem cell:	n/a	chr6:33378125-33378136
6	ATF2	chr6:33377956-33378389	GM12878	blood:	n/a	chr6:33378125-33378136
7	ATF2	chr6:33377756-33378341	H1-hESC	embryonic stem cell:	n/a	chr6:33378125-33378136
8	ATF3	chr6:33377976-33378351	K562	blood:	n/a	chr6:33378125-33378138 chr6:33378127-33378137 chr6:33378126-33378146 chr6:33378123-33378138 chr6:33378125-33378136
9	ATF3	chr6:33377591-33377875	A549	lung:	n/a	n/a
10	BACH1	chr6:33377722-33378484	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr6:33377877-33378447	GM12878	blood:	n/a	n/a
12	BCL3	chr6:33377432-33378520	A549	lung:	n/a	chr6:33377704-33377712
13	BCL3	chr6:33377546-33378667	A549	lung:	n/a	chr6:33377704-33377712
14	BCL3	chr6:33377904-33378649	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:33377697-33378299	GM12878	blood:	n/a	chr6:33377704-33377712
16	BHLHE40	chr6:33379179-33379309	K562	blood:	n/a	n/a
17	BHLHE40	chr6:33377882-33378715	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:33377721-33379028	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:33377710-33378706	K562	blood:	n/a	n/a
20	BRCA1	chr6:33377677-33378306	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr6:33377880-33378164	HepG2	liver:	n/a	n/a
22	BRCA1	chr6:33377785-33377960	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr6:33377952-33378149	GM12878	blood:	n/a	n/a
24	CBX3	chr6:33377963-33378304	K562	blood:	n/a	n/a
25	CBX3	chr6:33377136-33378708	K562	blood:	n/a	n/a
26	CCNT2	chr6:33377730-33379160	K562	blood:	n/a	chr6:33377839-33377848 chr6:33378424-33378433 chr6:33378456-33378465 chr6:33377939-33377948
27	CEBPB	chr6:33377968-33378269	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:33377980-33378304	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:33377843-33378308	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr6:33377959-33378259	K562	blood:	n/a	n/a
31	CEBPB	chr6:33377989-33378341	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr6:33377734-33378261	K562	blood:	n/a	n/a
33	CEBPD	chr6:33377986-33378315	HepG2	liver:	n/a	n/a
34	CEBPD	chr6:33377676-33379035	HepG2	liver:	n/a	n/a
35	CEBPD	chr6:33377628-33378754	K562	blood:	n/a	n/a
36	CHD1	chr6:33378504-33378686	GM12878	blood:	n/a	n/a
37	CHD1	chr6:33377460-33378125	GM12878	blood:	n/a	n/a
38	CHD1	chr6:33378936-33378938	GM12878	blood:	n/a	n/a
39	CHD2	chr6:33377816-33379088	GM12878	blood:	n/a	chr6:33378144-33378154
40	CHD2	chr6:33378962-33379018	HepG2	liver:	n/a	n/a
41	CHD2	chr6:33377769-33379082	Hela-S3	cervix:	n/a	chr6:33378144-33378154
42	CHD2	chr6:33377700-33378591	HepG2	liver:	n/a	chr6:33378144-33378154
43	CHD2	chr6:33377751-33379244	K562	blood:	n/a	chr6:33378144-33378154
44	CHD2	chr6:33377866-33378624	H1-hESC	embryonic stem cell:	n/a	chr6:33378144-33378154
45	CREB1	chr6:33377949-33378386	A549	lung:	n/a	chr6:33378124-33378137
46	CREB1	chr6:33377217-33379234	HepG2	liver:	n/a	chr6:33378124-33378137
47	CREB1	chr6:33377662-33378701	GM12878	blood:	n/a	chr6:33378124-33378137
48	CREB1	chr6:33377589-33378593	K562	blood:	n/a	chr6:33378124-33378137
49	CREB1	chr6:33377866-33378426	ECC-1	luminal epithelium:	n/a	chr6:33378124-33378137
50	CREB1	chr6:33377666-33378584	H1-hESC	embryonic stem cell:	n/a	chr6:33378124-33378137

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33378305-33378355	HAEpiC	amniotic membrane:	n/a
2	chr6:33379155-33379205	SKMC	muscle:	n/a
3	chr6:33378305-33378355	ovcar-3	ovarian:	n/a
4	chr6:33378305-33378355	HAEpiC	amniotic membrane:	n/a
5	chr6:33379155-33379205	SKMC	muscle:	n/a
6	chr6:33378305-33378355	ovcar-3	ovarian:	n/a
7	chr6:33378951-33379001	PFSK-1	brain:	n/a
8	chr6:33379287-33379337	Caco-2	colon:	n/a
9	chr6:33378508-33378558	SKMC	muscle:	n/a
10	chr6:33378936-33378986	NB4	blood:	n/a
11	chr6:33378345-33378395	IMR90	lung:	fetal
12	chr6:33378912-33378962	ProgFib	skin:	n/a
13	chr6:33378340-33378390	RPTEC	kidney:	n/a
14	chr6:33378912-33378962	HEEpiC	esophagus:	n/a
15	chr6:33377848-33377898	H1-hESC	embryonic stem cell:	embryo
16	chr6:33377958-33378008	AoSMC	blood vessel:	n/a
17	chr6:33377958-33378008	Jurkat	blood:	n/a
18	chr6:33379265-33379315	SK-N-MC	brain:	n/a
19	chr6:33378130-33378180	A549	lung:	n/a
20	chr6:33378502-33378552	NB4	blood:	n/a
21	chr6:33379155-33379205	HEEpiC	esophagus:	n/a
22	chr6:33377795-33377845	CMK	blood:	n/a
23	chr6:33378305-33378355	SAEC	small airway:	n/a
24	chr6:33379330-33379380	AoSMC	blood vessel:	n/a
25	chr6:33378340-33378390	GM12878	blood:	n/a
26	chr6:33378502-33378552	MCF10A-Er-Src	breast:	n/a
27	chr6:33378936-33378986	GM12892	blood:	n/a
28	chr6:33378130-33378180	NHBE	bronchial:	n/a
29	chr6:33379287-33379337	AG04450	lung:	fetal
30	chr6:33377739-33377789	HCF	heart:	n/a
31	chr6:33377848-33377898	BE2_C	brain:	n/a
32	chr6:33378345-33378395	HRCEpiC	kidney:	n/a
33	chr6:33378516-33378566	PFSK-1	brain:	n/a
34	chr6:33379287-33379337	K562	blood:	n/a
35	chr6:33378130-33378180	T-47D	breast:	n/a
36	chr6:33377739-33377789	NB4	blood:	n/a
37	chr6:33378340-33378390	GM12892	blood:	n/a
38	chr6:33379155-33379205	HRPEpiC	eye:	n/a
39	chr6:33378951-33379001	AG09309	skin:	n/a
40	chr6:33378345-33378395	SAEC	small airway:	n/a
41	chr6:33378951-33379001	Caco-2	colon:	n/a
42	chr6:33379267-33379317	AG10803	skin:	n/a
43	chr6:33377795-33377845	GM12892	blood:	n/a
44	chr6:33378340-33378390	HRCEpiC	kidney:	n/a
45	chr6:33378951-33379001	AG09319	gingival:	n/a
46	chr6:33377795-33377845	BJ	skin:	n/a
47	chr6:33378936-33378986	HCPEpiC	choroid plexus:	n/a
48	chr6:33377933-33377983	BE2_C	brain:	n/a
49	chr6:33378010-33378060	HEK293	kidney:	embryo
50	chr6:33377990-33378040	HCPEpiC	choroid plexus:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33280795..33292485-chr6:33374786..33387605,31	K562	blood:
2	chr6:33377496..33379251-chr6:33661661..33664420,2	MCF-7	breast:
3	chr6:33279489..33293095-chr6:33375317..33398824,56	K562	blood:
4	chr16:25268976..25269623-chr6:33377932..33378898,2	Hela-S3	cervix:
5	chr6:33261265..33262842-chr6:33377823..33379768,2	K562	blood:
6	chr6:33215707..33217514-chr6:33377026..33379165,2	K562	blood:
7	chr6:33166881..33169550-chr6:33376292..33379063,3	K562	blood:
8	chr17:75283611..75284123-chr6:33378111..33378909,2	Hela-S3	cervix:
9	chr6:33167104..33169096-chr6:33376083..33378504,2	K562	blood:
10	chr6:27114748..27115280-chr6:33378038..33378746,2	Hela-S3	cervix:
11	chr6:32938764..32940269-chr6:33377609..33379519,2	MCF-7	breast:
12	chr6:33358222..33360525-chr6:33377821..33380717,3	MCF-7	breast:
13	chr6:33261342..33263204-chr6:33376924..33379323,2	K562	blood:
14	chr1:28974856..28975665-chr6:33378255..33378960,2	Hela-S3	cervix:
15	chr10:134145639..134146221-chr6:33378370..33378986,2	Hela-S3	cervix:
16	chr12:52444856..52445551-chr6:33378224..33378869,2	Hela-S3	cervix:
17	chr6:33357351..33361150-chr6:33373102..33380127,12	MCF-7	breast:
18	chr6:33356271..33363521-chr6:33371085..33380351,32	K562	blood:
19	chr6:33359285..33360429-chr6:33377538..33378244,3	K562	blood:
20	chr6:33237079..33247876-chr6:33369927..33381738,26	K562	blood:
21	chr6:33237157..33241221-chr6:33375922..33380109,6	MCF-7	breast:
22	chr6:33280452..33282497-chr6:33377188..33378997,2	MCF-7	breast:
23	chr6:33263073..33268205-chr6:33376944..33380191,7	MCF-7	breast:
24	chr6:33256889..33260224-chr6:33374160..33378303,4	K562	blood:
25	chr6:33256522..33259302-chr6:33375799..33380992,5	MCF-7	breast:
26	chr6:33377727..33378412-chr7:64838619..64839491,2	Hela-S3	cervix:
27	chr6:33244680..33251060-chr6:33375427..33382644,12	MCF-7	breast:
28	chr6:33237328..33248026-chr6:33370896..33379989,29	K562	blood:
29	chr6:33242863..33248981-chr6:33374531..33379553,10	MCF-7	breast:
30	chr6:33255152..33256710-chr6:33377924..33379590,2	K562	blood:
31	chr6:30710804..30712449-chr6:33376908..33379450,2	MCF-7	breast:
32	chr6:33366608..33368247-chr6:33376462..33378479,2	MCF-7	breast:
33	chr6:33255490..33258967-chr6:33375507..33378634,5	MCF-7	breast:
34	chr6:33377039..33379614-chr6:33421781..33424452,2	K562	blood:

No data

Variant related genes	Relation type
PHF1	TF binding region
PHF1	CpG island
ENSG00000227057	chromatin interactions
ENSG00000236104	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000235863	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000232940	chromatin interactions
ENSG00000204231	chromatin interactions
ENSG00000202441	chromatin interactions
ENSG00000204220	chromatin interactions
ENSG00000231925	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000155592	chromatin interactions
ENSG00000269490	chromatin interactions
ENSG00000146757	chromatin interactions
ENSG00000237441	chromatin interactions
ENSG00000148814	chromatin interactions
ENSG00000237649	chromatin interactions
ENSG00000213588	chromatin interactions
ENSG00000112473	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000204209	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000184640	chromatin interactions

Extended variants
information (count: 37 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185611277	chr6:33377739-33377740	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
2	rs562814276	chr6:33377750-33377751	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
3	rs73741833	chr6:33377784-33377785	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs545454270	chr6:33377789-33377790	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
5	rs554324129	chr6:33377796-33377797	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
6	rs560487735	chr6:33377831-33377832	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
7	rs189344915	chr6:33377885-33377886	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
8	rs141323325	chr6:33377911-33377912	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
9	rs144977635	chr6:33377974-33377975	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
10	rs561929268	chr6:33377983-33377984	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
11	rs376690709	chr6:33377990-33377991	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
12	rs529041898	chr6:33378058-33378059	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
13	rs112889929	chr6:33378083-33378084	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
14	rs180850031	chr6:33378099-33378100	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
15	rs568885830	chr6:33378158-33378159	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
16	rs542734689	chr6:33378236-33378237	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
17	rs539502052	chr6:33378237-33378238	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
18	rs551010707	chr6:33378322-33378323	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
19	rs199931674	chr6:33378346-33378347	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
20	rs568201930	chr6:33378347-33378348	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
21	rs185295374	chr6:33378392-33378393	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
22	rs566086431	chr6:33378496-33378497	Active TSS Weak transcription	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
23	rs534233188	chr6:33378880-33378881	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
24	rs555608864	chr6:33378958-33378959	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
25	rs561383534	chr6:33379018-33379019	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
26	rs567871066	chr6:33379019-33379020	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
27	rs73416053	chr6:33379102-33379103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
28	rs565691549	chr6:33379239-33379240	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs188693894	chr6:33379270-33379271	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs576352183	chr6:33379333-33379334	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs538085022	chr6:33379380-33379381	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs141218981	chr6:33379482-33379483	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs372908240	chr6:33379483-33379484	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs556703274	chr6:33379487-33379488	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs181543604	chr6:33379488-33379489	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs545513651	chr6:33379502-33379503	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs554211449	chr6:33379509-33379510	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	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
abnormal development	18461090	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
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33361200-33377800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:33376600-33380000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:33377000-33377800	Flanking Active TSS	HepG2	liver
4	chr6:33377000-33378000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:33377000-33378000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:33377000-33378000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr6:33377000-33379600	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr6:33377200-33377800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr6:33377200-33377800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:33377200-33377800	Enhancers	Spleen	Spleen
11	chr6:33377200-33377800	Flanking Active TSS	Hela-S3	cervix
12	chr6:33377200-33377800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr6:33377200-33378000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr6:33377200-33378000	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr6:33377200-33378000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr6:33377200-33378000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
17	chr6:33377200-33378000	Enhancers	Fetal Heart	heart
18	chr6:33377200-33378000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
19	chr6:33377200-33378000	Flanking Active TSS	GM12878-XiMat	blood
20	chr6:33377200-33379200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:33377200-33379200	Active TSS	Colonic Mucosa	Colon
22	chr6:33377200-33379400	Active TSS	Rectal Smooth Muscle	rectum
23	chr6:33377200-33379600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr6:33377200-33379600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:33377200-33379800	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr6:33377200-33379800	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr6:33377200-33380000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:33377400-33377800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:33377400-33377800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:33377400-33377800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:33377400-33377800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
32	chr6:33377400-33377800	Flanking Active TSS	Primary T cells from cord blood	blood
33	chr6:33377400-33377800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr6:33377400-33377800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
35	chr6:33377400-33377800	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr6:33377400-33378000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr6:33377400-33378000	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr6:33377400-33378000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr6:33377400-33378000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr6:33377400-33378000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr6:33377400-33378000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr6:33377400-33378000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr6:33377400-33378000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr6:33377400-33378000	Flanking Active TSS	Liver	Liver
45	chr6:33377400-33378000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
46	chr6:33377400-33378000	Flanking Active TSS	Fetal Intestine Small	intestine
47	chr6:33377400-33378000	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr6:33377400-33378000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr6:33377400-33378000	Transcr. at gene 5' and 3'	Dnd41	blood
50	chr6:33377400-33378000	Flanking Active TSS	HMEC	breast

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