Variant report

Variant	esv3338953
Chromosome Location	chr7:6144176-6145774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:819)
CpG islands
(count:795)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6144216-6144499	K562	blood:	n/a	n/a
2	ARID3A	chr7:6144020-6144574	HepG2	liver:	n/a	n/a
3	ATF1	chr7:6144054-6144615	K562	blood:	n/a	n/a
4	ATF2	chr7:6143973-6144554	GM12878	blood:	n/a	n/a
5	ATF2	chr7:6143969-6144475	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:6143963-6144389	GM12878	blood:	n/a	n/a
7	ATF3	chr7:6143916-6144364	A549	lung:	n/a	chr7:6144238-6144247
8	ATF3	chr7:6144175-6144636	H1-hESC	embryonic stem cell:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
9	ATF3	chr7:6144173-6144629	HepG2	liver:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
10	ATF3	chr7:6144003-6144589	A549	lung:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
11	ATF3	chr7:6144063-6144497	H1-hESC	embryonic stem cell:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
12	ATF3	chr7:6143966-6144624	GM12878	blood:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
13	ATF3	chr7:6144239-6144555	GM12878	blood:	n/a	chr7:6144358-6144369
14	ATF3	chr7:6144119-6144750	K562	blood:	n/a	chr7:6144238-6144247 chr7:6144358-6144369
15	BACH1	chr7:6144078-6144449	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr7:6143876-6144448	A549	lung:	n/a	chr7:6144233-6144246
17	BCLAF1	chr7:6143958-6144586	GM12878	blood:	n/a	chr7:6144233-6144246
18	BCLAF1	chr7:6143976-6144609	GM12878	blood:	n/a	chr7:6144233-6144246
19	BHLHE40	chr7:6145410-6146494	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:6144032-6144593	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:6145264-6146399	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:6144020-6144538	K562	blood:	n/a	n/a
23	BHLHE40	chr7:6144159-6144652	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:6144086-6144519	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:6144167-6144503	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr7:6144073-6144492	HepG2	liver:	n/a	n/a
27	CBX3	chr7:6143832-6144479	K562	blood:	n/a	n/a
28	CCNT2	chr7:6144077-6145397	K562	blood:	n/a	chr7:6145165-6145174
29	CEBPB	chr7:6144055-6144537	Hela-S3	cervix:	n/a	chr7:6144318-6144326
30	CEBPB	chr7:6144216-6144477	H1-hESC	embryonic stem cell:	n/a	chr7:6144318-6144326
31	CEBPB	chr7:6144198-6144352	HepG2	liver:	n/a	chr7:6144318-6144326
32	CEBPD	chr7:6143958-6144528	HepG2	liver:	n/a	n/a
33	CEBPD	chr7:6144048-6144445	HepG2	liver:	n/a	n/a
34	CHD1	chr7:6144040-6144331	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr7:6144040-6144289	GM12878	blood:	n/a	n/a
36	CHD1	chr7:6145359-6145671	GM12878	blood:	n/a	n/a
37	CHD2	chr7:6144081-6144509	K562	blood:	n/a	n/a
38	CHD2	chr7:6144033-6144561	HepG2	liver:	n/a	n/a
39	CHD2	chr7:6144031-6144721	GM12878	blood:	n/a	n/a
40	CHD2	chr7:6145331-6145604	GM12878	blood:	n/a	n/a
41	CHD2	chr7:6144949-6145140	Hela-S3	cervix:	n/a	chr7:6145123-6145133
42	CHD2	chr7:6144023-6144696	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr7:6144018-6144501	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr7:6145170-6145343	HepG2	liver:	n/a	n/a
45	CREB1	chr7:6144054-6144712	A549	lung:	n/a	n/a
46	CREB1	chr7:6143921-6144872	HepG2	liver:	n/a	n/a
47	CREB1	chr7:6143929-6144742	K562	blood:	n/a	n/a
48	CREB1	chr7:6143910-6144753	GM12878	blood:	n/a	n/a
49	CREB1	chr7:6143944-6144667	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr7:6143971-6144642	ECC-1	luminal epithelium:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6145057-6145107	MCF10A-Er-Src	breast:	n/a
2	chr7:6145105-6145155	ovcar-3	ovarian:	n/a
3	chr7:6145057-6145107	MCF10A-Er-Src	breast:	n/a
4	chr7:6145105-6145155	ovcar-3	ovarian:	n/a
5	chr7:6144367-6144417	HRCEpiC	kidney:	n/a
6	chr7:6145114-6145164	Caco-2	colon:	n/a
7	chr7:6144367-6144417	SK-N-SH_RA	brain:	n/a
8	chr7:6144127-6144177	T-47D	breast:	n/a
9	chr7:6145057-6145107	HUVEC	blood vessel:	n/a
10	chr7:6144308-6144358	ovcar-3	ovarian:	n/a
11	chr7:6145114-6145164	Hela-S3	cervix:	n/a
12	chr7:6144298-6144348	Caco-2	colon:	n/a
13	chr7:6144399-6144449	HNPCEpiC	eye:	n/a
14	chr7:6145595-6145645	HRCEpiC	kidney:	n/a
15	chr7:6145168-6145218	AoSMC	blood vessel:	n/a
16	chr7:6145057-6145107	AG04449	skin:	fetal
17	chr7:6144367-6144417	IMR90	lung:	fetal
18	chr7:6145114-6145164	BE2_C	brain:	n/a
19	chr7:6145057-6145107	AG09309	skin:	n/a
20	chr7:6145168-6145218	NT2-D1	testis:	n/a
21	chr7:6145057-6145107	BE2_C	brain:	n/a
22	chr7:6144367-6144417	U87	brain:	n/a
23	chr7:6145105-6145155	H1-hESC	embryonic stem cell:	embryo
24	chr7:6144308-6144358	NT2-D1	testis:	n/a
25	chr7:6144308-6144358	ProgFib	skin:	n/a
26	chr7:6144367-6144417	BE2_C	brain:	n/a
27	chr7:6144372-6144422	HIPEpiC	eye:	n/a
28	chr7:6145114-6145164	Jurkat	blood:	n/a
29	chr7:6144399-6144449	HL-60	blood:	n/a
30	chr7:6144308-6144358	HAEpiC	amniotic membrane:	n/a
31	chr7:6144367-6144417	RPTEC	kidney:	n/a
32	chr7:6144399-6144449	GM19239	blood:	n/a
33	chr7:6145168-6145218	GM19239	blood:	n/a
34	chr7:6145168-6145218	IMR90	lung:	fetal
35	chr7:6144399-6144449	HEK293	kidney:	embryo
36	chr7:6145595-6145645	AG09309	skin:	n/a
37	chr7:6144369-6144419	PANC-1	pancreas:	n/a
38	chr7:6144308-6144358	Hela-S3	cervix:	n/a
39	chr7:6144399-6144449	GM12891	blood:	n/a
40	chr7:6144399-6144449	ProgFib	skin:	n/a
41	chr7:6145105-6145155	NHBE	bronchial:	n/a
42	chr7:6145309-6145359	HCM	heart:	n/a
43	chr7:6144372-6144422	BE2_C	brain:	n/a
44	chr7:6145595-6145645	HEEpiC	esophagus:	n/a
45	chr7:6144308-6144358	HCPEpiC	choroid plexus:	n/a
46	chr7:6145309-6145359	HIPEpiC	eye:	n/a
47	chr7:6145309-6145359	ProgFib	skin:	n/a
48	chr7:6144127-6144177	HMEC	breast:	n/a
49	chr7:6144372-6144422	K562	blood:	n/a
50	chr7:6145309-6145359	SK-N-SH	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6065831..6068709-chr7:6141820..6144838,4	MCF-7	breast:
2	chr7:6145063..6147709-chr7:6164403..6167299,2	MCF-7	breast:
3	chr7:6064661..6068184-chr7:6142795..6145849,5	MCF-7	breast:
4	chr5:176830787..176831503-chr7:6143819..6144569,2	Hela-S3	cervix:
5	chr7:6055317..6057272-chr7:6144133..6145966,2	K562	blood:
6	chr7:6100114..6101811-chr7:6141887..6144361,2	K562	blood:
7	chr7:6145257..6148014-chr7:6162760..6164511,2	K562	blood:
8	chr1:38061256..38061780-chr7:6143823..6144821,2	NB4	blood:
9	chr7:6048826..6049627-chr7:6143766..6144544,2	HCT-116	colon:
10	chr7:6055602..6058271-chr7:6142750..6144893,2	MCF-7	breast:
11	chr13:103248649..103249379-chr7:6143733..6144282,2	NB4	blood:
12	chr10:17243122..17243935-chr7:6143879..6144532,2	HCT-116	colon:
13	chr7:6119521..6122293-chr7:6142698..6146719,8	K562	blood:
14	chr7:6141805..6147526-chr7:6152442..6159269,12	MCF-7	breast:
15	chr7:6119410..6124898-chr7:6141396..6145150,7	MCF-7	breast:
16	chr7:6054308..6057610-chr7:6144384..6145966,3	K562	blood:
17	chr7:6054346..6056159-chr7:6142852..6144380,2	K562	blood:
18	chr11:537982..538482-chr7:6143933..6144434,2	HCT-116	colon:
19	chr7:6143403..6145262-chr7:6310829..6313708,2	MCF-7	breast:
20	chr19:17516059..17516719-chr7:6143769..6144365,2	NB4	blood:
21	chr2:135675640..135676288-chr7:6143525..6144422,2	Hela-S3	cervix:
22	chr7:6094946..6099638-chr7:6140891..6146239,12	K562	blood:
23	chr1:117601936..117602864-chr7:6143842..6144663,2	Hela-S3	cervix:
24	chr7:6096763..6100631-chr7:6141376..6146373,15	MCF-7	breast:
25	chr7:6143900..6146202-chr7:6155214..6157141,2	MCF-7	breast:
26	chr7:6096872..6099965-chr7:6142845..6147736,5	MCF-7	breast:
27	chr7:6143877..6144677-chr9:134000320..134001058,2	Hela-S3	cervix:
28	chr7:6118710..6122632-chr7:6142742..6146844,10	K562	blood:
29	chr7:6144993..6146575-chr7:6155330..6157057,2	K562	blood:
30	chr7:6094497..6101614-chr7:6140891..6145784,14	K562	blood:
31	chr17:34136464..34136998-chr7:6144143..6144663,2	Hela-S3	cervix:
32	chr7:6047026..6051403-chr7:6141746..6146462,7	K562	blood:
33	chr7:6142905..6144683-chr7:6522279..6524664,2	MCF-7	breast:
34	chr7:6047404..6049912-chr7:6142714..6146343,4	MCF-7	breast:
35	chr17:56708604..56709142-chr7:6143631..6144302,2	Hela-S3	cervix:
36	chr3:73160101..73161088-chr7:6143657..6144592,2	Hela-S3	cervix:
37	chr7:6046967..6050535-chr7:6141219..6149580,10	K562	blood:
38	chr7:6143696..6144293-chr7:73153152..73153874,2	Hela-S3	cervix:
39	chr7:6118878..6122850-chr7:6140823..6146720,14	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2AK1-1	chr7:6144054-6144254	NONHSAT118982

No data

Variant related genes	Relation type
USP42	TF binding region
USP42	CpG island
ENSG00000207217	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000130303	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000224043	chromatin interactions
ENSG00000172660	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000134697	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000269640	chromatin interactions
ENSG00000082258	chromatin interactions
ENSG00000252929	chromatin interactions
ENSG00000134900	chromatin interactions
ENSG00000107614	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000131187	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000106077	chromatin interactions
ENSG00000236137	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000126883	chromatin interactions
ENSG00000264605	chromatin interactions
ENSG00000141971	chromatin interactions
ENSG00000106346	chromatin interactions

Extended variants
information (count: 56 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:56 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370638229	chr7:6144214-6144215	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	27 gene(s)	Overlapped CNVs	n/a
2	rs547297913	chr7:6144272-6144273	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	27 gene(s)	Overlapped CNVs	n/a
3	rs571998029	chr7:6144293-6144294	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	26 gene(s)	Overlapped CNVs	n/a
4	rs532861308	chr7:6144298-6144299	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
5	rs550665728	chr7:6144299-6144300	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
6	rs61753115	chr7:6144308-6144309	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536304456	chr7:6144315-6144316	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
8	rs554690868	chr7:6144336-6144337	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
9	rs61753116	chr7:6144348-6144349	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
10	rs61753117	chr7:6144359-6144360	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	25 gene(s)	Overlapped CNVs	n/a
11	rs552830187	chr7:6144372-6144373	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
12	rs577488451	chr7:6144387-6144388	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
13	rs113876284	chr7:6144475-6144476	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
14	rs545305604	chr7:6144512-6144513	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
15	rs186647247	chr7:6144520-6144521	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
16	rs573243927	chr7:6144545-6144546	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
17	rs191083247	chr7:6144602-6144603	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs575240808	chr7:6144604-6144605	Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs542347605	chr7:6144700-6144701	Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs10277939	chr7:6145161-6145162	Weak transcription Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs528673568	chr7:6145172-6145173	Weak transcription Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs540800034	chr7:6145174-6145175	Weak transcription Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs76647311	chr7:6145218-6145219	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs112495046	chr7:6145223-6145224	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs570893173	chr7:6145234-6145235	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs551260088	chr7:6145243-6145244	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs182974213	chr7:6145249-6145250	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs530150564	chr7:6145252-6145253	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs552191417	chr7:6145278-6145279	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs566654903	chr7:6145296-6145297	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs534050738	chr7:6145311-6145312	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs376282709	chr7:6145337-6145338	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs552718436	chr7:6145347-6145348	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs571420952	chr7:6145348-6145349	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs116295029	chr7:6145362-6145363	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs186630865	chr7:6145389-6145390	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs575113660	chr7:6145397-6145398	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs536280601	chr7:6145418-6145419	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs554626339	chr7:6145440-6145441	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs572940041	chr7:6145442-6145443	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs570384412	chr7:6145451-6145452	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs540339896	chr7:6145488-6145489	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs550330105	chr7:6145500-6145501	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs565433063	chr7:6145532-6145533	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs577414093	chr7:6145553-6145554	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs73333498	chr7:6145565-6145566	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs573504575	chr7:6145569-6145570	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs370270252	chr7:6145570-6145571	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs568249327	chr7:6145643-6145644	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs183264055	chr7:6145680-6145681	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6142800-6144400	Active TSS	iPS-18 Cell Line	embryonic stem cell
2	chr7:6143200-6144400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:6143200-6144400	Active TSS	A549	lung
4	chr7:6143200-6145200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:6143200-6145600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:6143200-6146200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:6143200-6146200	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr7:6143200-6146200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:6143200-6146400	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr7:6143400-6144200	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr7:6143400-6144200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
12	chr7:6143400-6144200	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr7:6143400-6144200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr7:6143400-6144200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr7:6143400-6144400	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr7:6143400-6144400	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr7:6143400-6144400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:6143400-6144400	Active TSS	Brain Hippocampus Middle	brain
19	chr7:6143400-6144400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr7:6143400-6144400	Active TSS	Brain Substantia Nigra	brain
21	chr7:6143400-6144400	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr7:6143400-6144400	Active TSS	Fetal Kidney	kidney
23	chr7:6143400-6144400	Active TSS	NHDF-Ad	bronchial
24	chr7:6143400-6145400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:6143400-6145400	Active TSS	Brain Angular Gyrus	brain
26	chr7:6143400-6145800	Active TSS	H9 Cell Line	embryonic stem cell
27	chr7:6143400-6146000	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr7:6143400-6146000	Active TSS	Muscle Satellite Cultured Cells	--
29	chr7:6143400-6146000	Active TSS	Brain Anterior Caudate	brain
30	chr7:6143400-6146000	Active TSS	Rectal Smooth Muscle	rectum
31	chr7:6143400-6146200	Active TSS	H1 Cell Line	embryonic stem cell
32	chr7:6143400-6146400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:6143400-6146400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr7:6143400-6146400	Active TSS	HSMM	muscle
35	chr7:6143400-6146800	Active TSS	HSMMtube	muscle
36	chr7:6143600-6144200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr7:6143600-6144200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:6143600-6144400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr7:6143600-6144400	Active TSS	Brain Cingulate Gyrus	brain
40	chr7:6143600-6144400	Active TSS	Placenta Amnion	Placenta Amnion
41	chr7:6143600-6144400	Active TSS	GM12878-XiMat	blood
42	chr7:6143600-6144400	Active TSS	K562	blood
43	chr7:6143600-6144400	Active TSS	NHEK	skin
44	chr7:6143600-6145200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr7:6143600-6145600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr7:6143600-6145600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:6143600-6145600	Active TSS	Gastric	stomach
48	chr7:6143600-6145800	Active TSS	Sigmoid Colon	Sigmoid Colon
49	chr7:6143600-6146000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr7:6143600-6146000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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