Variant report

Variant	esv3324958
Chromosome Location	chr6:109803709-109805707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:109803773-109804079	HepG2	liver:	n/a	n/a
2	ATF3	chr6:109804214-109804545	GM12878	blood:	n/a	n/a
3	ATF3	chr6:109804272-109804511	HepG2	liver:	n/a	n/a
4	ATF3	chr6:109804313-109804523	K562	blood:	n/a	n/a
5	ATF3	chr6:109804341-109804533	GM12878	blood:	n/a	n/a
6	BACH1	chr6:109804377-109804382	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr6:109803784-109804534	K562	blood:	n/a	n/a
8	BHLHE40	chr6:109803848-109804593	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:109803838-109804534	HepG2	liver:	n/a	n/a
10	BRCA1	chr6:109804357-109804472	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr6:109803978-109805009	K562	blood:	n/a	chr6:109804230-109804239
12	CEBPB	chr6:109803655-109804135	K562	blood:	n/a	chr6:109803942-109803953
13	CEBPB	chr6:109803632-109804219	H1-hESC	embryonic stem cell:	n/a	chr6:109803942-109803953
14	CEBPB	chr6:109803728-109804148	HepG2	liver:	n/a	chr6:109803942-109803953
15	CEBPB	chr6:109803672-109804137	A549	lung:	n/a	chr6:109803942-109803953
16	CEBPB	chr6:109803681-109804099	ECC-1	luminal epithelium:	n/a	chr6:109803942-109803953
17	CEBPB	chr6:109803647-109804548	HepG2	liver:	n/a	chr6:109803942-109803953
18	CEBPB	chr6:109803635-109804179	HepG2	liver:	n/a	chr6:109803942-109803953
19	CEBPB	chr6:109803625-109804159	K562	blood:	n/a	chr6:109803942-109803953
20	CEBPB	chr6:109803635-109804193	IMR90	lung:	n/a	chr6:109803942-109803953
21	CEBPB	chr6:109803676-109803852	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:109803664-109804196	MCF-7	breast:	n/a	chr6:109803942-109803953
23	CEBPB	chr6:109803666-109804180	MCF-7	breast:	n/a	chr6:109803942-109803953
24	CEBPB	chr6:109803603-109804124	ECC-1	luminal epithelium:	n/a	chr6:109803942-109803953
25	CEBPB	chr6:109803658-109804023	K562	blood:	n/a	chr6:109803942-109803953
26	CEBPB	chr6:109803637-109804501	Hela-S3	cervix:	n/a	chr6:109803942-109803953
27	CEBPD	chr6:109804162-109804527	HepG2	liver:	n/a	n/a
28	CHD1	chr6:109803863-109804345	GM12878	blood:	n/a	n/a
29	CHD1	chr6:109803793-109804085	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:109804045-109805000	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:109804346-109804526	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:109804239-109804423	K562	blood:	n/a	n/a
33	CHD2	chr6:109804381-109804432	HepG2	liver:	n/a	n/a
34	CHD2	chr6:109803758-109804561	GM12878	blood:	n/a	n/a
35	CHD2	chr6:109804986-109805001	GM12878	blood:	n/a	n/a
36	CREB1	chr6:109804214-109804619	A549	lung:	n/a	n/a
37	CREB1	chr6:109804091-109804719	HepG2	liver:	n/a	n/a
38	CTBP2	chr6:109803683-109804343	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr6:109804360-109804510	GM12867	blood:	n/a	chr6:109804493-109804502
40	CTCF	chr6:109804426-109804451	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:109804389-109804504	Spleen_OC	spleen:	n/a	chr6:109804493-109804502
42	CTCF	chr6:109804363-109804541	GM12878	blood:	n/a	chr6:109804493-109804502
43	CTCF	chr6:109804360-109804510	AG04449	skin:	n/a	chr6:109804493-109804502
44	CTCF	chr6:109804120-109804270	GM12875	blood:	n/a	chr6:109804141-109804150
45	CTCF	chr6:109804419-109804425	Lung_OC	lung:	n/a	n/a
46	CTCFL	chr6:109804367-109804507	K562	blood:	n/a	n/a
47	E2F1	chr6:109804076-109804632	Hela-S3	cervix:	n/a	chr6:109804344-109804353 chr6:109804450-109804465 chr6:109804352-109804361 chr6:109804400-109804410 chr6:109804195-109804205 chr6:109804119-109804128
48	E2F4	chr6:109804350-109804482	GM12878	blood:	n/a	chr6:109804450-109804465 chr6:109804352-109804361 chr6:109804400-109804410
49	E2F4	chr6:109803828-109804600	MCF10A-Er-Src	breast:	n/a	chr6:109804344-109804353 chr6:109804450-109804465 chr6:109804352-109804361 chr6:109804400-109804410 chr6:109804195-109804205 chr6:109804119-109804128
50	E2F6	chr6:109804243-109804672	H1-hESC	embryonic stem cell:	n/a	chr6:109804344-109804353 chr6:109804450-109804465 chr6:109804352-109804361 chr6:109804400-109804410

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109804376-109804426	GM12892	blood:	n/a
2	chr6:109804970-109805020	AG09319	gingival:	n/a
3	chr6:109804103-109804153	Jurkat	blood:	n/a
4	chr6:109804376-109804426	HRE	kidney:	n/a
5	chr6:109804376-109804426	AG10803	skin:	n/a
6	chr6:109805074-109805124	CMK	blood:	n/a
7	chr6:109804852-109804902	ovcar-3	ovarian:	n/a
8	chr6:109805074-109805124	GM12891	blood:	n/a
9	chr6:109804852-109804902	SK-N-MC	brain:	n/a
10	chr6:109804376-109804426	CMK	blood:	n/a
11	chr6:109804103-109804153	HL-60	blood:	n/a
12	chr6:109804376-109804426	ECC-1	luminal epithelium:	n/a
13	chr6:109804970-109805020	SK-N-SH_RA	brain:	n/a
14	chr6:109805074-109805124	HL-60	blood:	n/a
15	chr6:109805074-109805124	HRCEpiC	kidney:	n/a
16	chr6:109804852-109804902	HEEpiC	esophagus:	n/a
17	chr6:109805074-109805124	AG04449	skin:	fetal
18	chr6:109805074-109805124	BE2_C	brain:	n/a
19	chr6:109805074-109805124	NH-A	brain:	n/a
20	chr6:109805074-109805124	HCM	heart:	n/a
21	chr6:109804376-109804426	GM19239	blood:	n/a
22	chr6:109805074-109805124	Hela-S3	cervix:	n/a
23	chr6:109805074-109805124	A549	lung:	n/a
24	chr6:109804852-109804902	NH-A	brain:	n/a
25	chr6:109804376-109804426	AG09309	skin:	n/a
26	chr6:109805074-109805124	SAEC	small airway:	n/a
27	chr6:109804376-109804426	HL-60	blood:	n/a
28	chr6:109804376-109804426	SK-N-SH_RA	brain:	n/a
29	chr6:109804103-109804153	PrEC	prostate:	n/a
30	chr6:109804852-109804902	RPTEC	kidney:	n/a
31	chr6:109805074-109805124	T-47D	breast:	n/a
32	chr6:109804970-109805020	HNPCEpiC	eye:	n/a
33	chr6:109804376-109804426	HMEC	breast:	n/a
34	chr6:109804103-109804153	BE2_C	brain:	n/a
35	chr6:109804970-109805020	SKMC	muscle:	n/a
36	chr6:109804103-109804153	HRCEpiC	kidney:	n/a
37	chr6:109805074-109805124	K562	blood:	n/a
38	chr6:109804852-109804902	A549	lung:	n/a
39	chr6:109805074-109805124	PANC-1	pancreas:	n/a
40	chr6:109804103-109804153	ovcar-3	ovarian:	n/a
41	chr6:109804103-109804153	NT2-D1	testis:	n/a
42	chr6:109804970-109805020	NB4	blood:	n/a
43	chr6:109804376-109804426	AoSMC	blood vessel:	n/a
44	chr6:109805074-109805124	GM12878	blood:	n/a
45	chr6:109804852-109804902	HUVEC	blood vessel:	n/a
46	chr6:109804852-109804902	AG09309	skin:	n/a
47	chr6:109804970-109805020	GM12878	blood:	n/a
48	chr6:109804103-109804153	AoSMC	blood vessel:	n/a
49	chr6:109804970-109805020	H1-hESC	embryonic stem cell:	embryo
50	chr6:109804970-109805020	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:109702597..109705942-chr6:109803330..109806291,3	K562	blood:
2	chr6:109703226..109705290-chr6:109802868..109805423,2	K562	blood:
3	chr6:109802318..109804692-chr6:109827428..109829307,3	MCF-7	breast:
4	chr6:109804505..109806373-chr6:109808766..109811459,2	K562	blood:
5	chr6:109787055..109789260-chr6:109802525..109804653,2	K562	blood:
6	chr6:109760146..109763576-chr6:109804047..109805770,3	MCF-7	breast:
7	chr6:31782365..31783340-chr6:109804610..109805551,2	Hela-S3	cervix:
8	chr6:109759652..109764361-chr6:109800705..109806354,8	K562	blood:
9	chr6:109774016..109776250-chr6:109801827..109803875,2	K562	blood:
10	chr6:109759628..109764398-chr6:109803414..109806709,4	K562	blood:
11	chr6:109775795..109777582-chr6:109802976..109804493,2	MCF-7	breast:
12	chr6:109774750..109777186-chr6:109800628..109803875,3	K562	blood:
13	chr6:109700978..109703685-chr6:109804896..109807033,2	MCF-7	breast:
14	chr6:109804488..109806145-chr6:109811754..109813384,2	K562	blood:
15	chr6:109760182..109762059-chr6:109802883..109805670,2	MCF-7	breast:

Variant related genes	Relation type
ZBTB24	TF binding region
ENSG00000223537	TF binding region
ZBTB24	CpG island
ENSG00000223537	CpG island
ENSG00000260273	chromatin interactions
ENSG00000135587	chromatin interactions
ENSG00000135535	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000135596	chromatin interactions
ENSG00000185250	chromatin interactions
ENSG00000223537	chromatin interactions
ENSG00000155085	chromatin interactions
ENSG00000204390	chromatin interactions

Extended variants
information (count: 58 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:58 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571946295	chr6:109803719-109803720	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs540978220	chr6:109803773-109803774	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs564236768	chr6:109803823-109803824	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs533026786	chr6:109803864-109803865	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs549591580	chr6:109803893-109803894	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs73520940	chr6:109803994-109803995	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189260136	chr6:109804044-109804045	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs151029482	chr6:109804050-109804051	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs531730743	chr6:109804058-109804059	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs374826159	chr6:109804060-109804061	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs548388537	chr6:109804080-109804081	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs568494579	chr6:109804103-109804104	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs533949636	chr6:109804105-109804106	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs547734977	chr6:109804112-109804113	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs535465846	chr6:109804129-109804130	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs13437135	chr6:109804172-109804173	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs540116468	chr6:109804184-109804185	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs556830776	chr6:109804227-109804228	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs576702716	chr6:109804247-109804248	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs535586118	chr6:109804248-109804249	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs13437139	chr6:109804311-109804312	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs572068699	chr6:109804320-109804321	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs540689524	chr6:109804341-109804342	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs557711471	chr6:109804355-109804356	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs577548432	chr6:109804366-109804367	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs543301440	chr6:109804402-109804403	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs563188860	chr6:109804414-109804415	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs529056535	chr6:109804518-109804519	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs71539090	chr6:109804681-109804682	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	mRNA abundance
30	rs71015583	chr6:109804770-109804771	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs542681510	chr6:109804860-109804861	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs374912401	chr6:109804880-109804881	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs115102479	chr6:109804897-109804898	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs367992367	chr6:109804914-109804915	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs181531196	chr6:109804925-109804926	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs185056048	chr6:109804926-109804927	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs144499019	chr6:109804927-109804928	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs533711960	chr6:109804948-109804949	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs190702449	chr6:109804954-109804955	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs570318902	chr6:109804996-109804997	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs74383532	chr6:109805036-109805037	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs555897151	chr6:109805079-109805080	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs374907248	chr6:109805086-109805087	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs565664046	chr6:109805125-109805126	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs67142735	chr6:109805141-109805142	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs398002583	chr6:109805142-109805143	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs181992466	chr6:109805180-109805181	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs77111861	chr6:109805235-109805236	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs577213501	chr6:109805249-109805250	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs542966491	chr6:109805264-109805265	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109799600-109803800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:109801400-109804400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
3	chr6:109801600-109804200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
4	chr6:109801800-109803800	Enhancers	Stomach Mucosa	stomach
5	chr6:109802600-109803800	Enhancers	Spleen	Spleen
6	chr6:109802800-109804000	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr6:109803000-109803800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:109803000-109804000	Flanking Active TSS	Adipose Nuclei	Adipose
9	chr6:109803000-109804200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr6:109803000-109805000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:109803200-109803800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
12	chr6:109803200-109803800	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
13	chr6:109803200-109803800	Flanking Active TSS	Brain Germinal Matrix	brain
14	chr6:109803200-109803800	Weak transcription	Gastric	stomach
15	chr6:109803200-109803800	Flanking Active TSS	Left Ventricle	heart
16	chr6:109803200-109803800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
17	chr6:109803200-109803800	Flanking Active TSS	HMEC	breast
18	chr6:109803200-109804000	Flanking Active TSS	Primary B cells from peripheral blood	blood
19	chr6:109803200-109804000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
20	chr6:109803200-109804000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
21	chr6:109803200-109804000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr6:109803200-109804200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr6:109803200-109804200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:109803200-109804200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr6:109803200-109804400	Flanking Active TSS	Primary B cells from cord blood	blood
26	chr6:109803200-109804400	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr6:109803200-109804800	Active TSS	HSMMtube	muscle
28	chr6:109803200-109805000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:109803200-109805000	Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr6:109803200-109805000	Active TSS	iPS-15b Cell Line	embryonic stem cell
31	chr6:109803200-109805000	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr6:109803200-109805000	Active TSS	Aorta	Aorta
33	chr6:109803200-109805000	Active TSS	Fetal Kidney	kidney
34	chr6:109803200-109805200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:109803200-109805400	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr6:109803400-109803800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:109803400-109803800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr6:109803400-109803800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:109803400-109803800	Flanking Active TSS	Brain Cingulate Gyrus	brain
40	chr6:109803400-109803800	Enhancers	Fetal Brain Male	brain
41	chr6:109803400-109803800	Flanking Active TSS	Lung	lung
42	chr6:109803400-109803800	Flanking Active TSS	Right Atrium	heart
43	chr6:109803400-109803800	Flanking Active TSS	Right Ventricle	heart
44	chr6:109803400-109803800	Flanking Active TSS	Dnd41	blood
45	chr6:109803400-109804000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
46	chr6:109803400-109804000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
47	chr6:109803400-109804000	Flanking Active TSS	Fetal Muscle Trunk	muscle
48	chr6:109803400-109804000	Flanking Active TSS	Fetal Muscle Leg	muscle
49	chr6:109803400-109804000	Flanking Active TSS	Fetal Thymus	thymus
50	chr6:109803400-109804000	Flanking Active TSS	Thymus	Thymus

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