Variant report

Variant	nsv970467
Chromosome Location	chr7:39605971-39615006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:458)
CpG islands
(count:488)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39605696-39606077	HepG2	liver:	n/a	n/a
2	ATF2	chr7:39605695-39606255	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:39605695-39606256	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr7:39605532-39606336	A549	lung:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
5	BCLAF1	chr7:39605565-39606356	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
6	BCLAF1	chr7:39605624-39606257	GM12878	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
7	BCLAF1	chr7:39605736-39606198	K562	blood:	n/a	chr7:39605874-39605887 chr7:39605878-39605891
8	BHLHE40	chr7:39605211-39606254	K562	blood:	n/a	n/a
9	BHLHE40	chr7:39605270-39606262	GM12878	blood:	n/a	n/a
10	BRCA1	chr7:39605671-39606201	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr7:39605572-39606302	K562	blood:	n/a	n/a
12	CCNT2	chr7:39605686-39606555	K562	blood:	n/a	n/a
13	CEBPB	chr7:39605220-39606506	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr7:39613568-39613984	K562	blood:	n/a	n/a
15	CEBPD	chr7:39605695-39606303	HepG2	liver:	n/a	n/a
16	CEBPD	chr7:39605701-39606201	K562	blood:	n/a	n/a
17	CHD1	chr7:39606491-39606570	GM12878	blood:	n/a	n/a
18	CHD1	chr7:39605536-39606553	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr7:39605466-39606231	GM12878	blood:	n/a	n/a
20	CHD2	chr7:39605718-39606262	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr7:39605720-39606252	HepG2	liver:	n/a	n/a
22	CHD2	chr7:39605546-39606199	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr7:39605635-39606154	K562	blood:	n/a	n/a
24	CHD2	chr7:39605448-39606546	GM12878	blood:	n/a	n/a
25	CREB1	chr7:39605705-39606292	A549	lung:	n/a	n/a
26	CREB1	chr7:39605529-39606464	HepG2	liver:	n/a	n/a
27	CREB1	chr7:39605608-39606392	GM12878	blood:	n/a	n/a
28	CTCF	chr7:39605860-39606010	AG04449	skin:	n/a	n/a
29	CTCF	chr7:39605832-39605995	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr7:39607060-39607210	GM06990	blood:	n/a	n/a
31	CTCF	chr7:39606080-39606230	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr7:39605673-39606018	GM12878	blood:	n/a	n/a
33	CTCF	chr7:39605221-39606086	K562	blood:	n/a	n/a
34	CTCF	chr7:39605906-39605999	Lung_OC	lung:	n/a	n/a
35	CUX1	chr7:39605174-39606010	K562	blood:	n/a	n/a
36	E2F4	chr7:39605422-39606219	MCF10A-Er-Src	breast:	n/a	chr7:39605876-39605886
37	E2F6	chr7:39605551-39606361	K562	blood:	n/a	chr7:39605876-39605886
38	E2F6	chr7:39606028-39606280	K562	blood:	n/a	n/a
39	E2F6	chr7:39605475-39606422	A549	lung:	n/a	chr7:39605876-39605886
40	E2F6	chr7:39605742-39606127	K562	blood:	n/a	chr7:39605876-39605886
41	E2F6	chr7:39605677-39606025	K562	blood:	n/a	chr7:39605876-39605886
42	EBF1	chr7:39606019-39606463	GM12878	blood:	n/a	chr7:39606255-39606266 chr7:39606254-39606267 chr7:39606256-39606265 chr7:39606256-39606266
43	EBF1	chr7:39605645-39606417	GM12878	blood:	n/a	chr7:39606255-39606266 chr7:39606254-39606267 chr7:39606256-39606265 chr7:39606256-39606266
44	EBF1	chr7:39605759-39606516	GM12878	blood:	n/a	chr7:39606255-39606266 chr7:39606254-39606267 chr7:39606256-39606265 chr7:39606256-39606266
45	EGR1	chr7:39605729-39606066	K562	blood:	n/a	chr7:39605899-39605912 chr7:39605896-39605910
46	EGR1	chr7:39605787-39606054	GM12878	blood:	n/a	chr7:39605899-39605912 chr7:39605896-39605910
47	EGR1	chr7:39605780-39606019	GM12878	blood:	n/a	chr7:39605899-39605912 chr7:39605896-39605910
48	EGR1	chr7:39605648-39606137	K562	blood:	n/a	chr7:39605899-39605912 chr7:39605896-39605910
49	EGR1	chr7:39605485-39606345	HCT-116	colon:	n/a	chr7:39605899-39605912 chr7:39605896-39605910
50	ELF1	chr7:39605749-39606145	HepG2	liver:	n/a	chr7:39605979-39605992 chr7:39605901-39605910

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39609343-39609393	HL-60	blood:	n/a
2	chr7:39606002-39606052	HIPEpiC	eye:	n/a
3	chr7:39609343-39609393	PFSK-1	brain:	n/a
4	chr7:39606013-39606063	CMK	blood:	n/a
5	chr7:39606002-39606052	HNPCEpiC	eye:	n/a
6	chr7:39606002-39606052	RPTEC	kidney:	n/a
7	chr7:39606071-39606121	AG09319	gingival:	n/a
8	chr7:39606013-39606063	K562	blood:	n/a
9	chr7:39605996-39606046	MCF-7	breast:	n/a
10	chr7:39606013-39606063	NHBE	bronchial:	n/a
11	chr7:39606280-39606330	A549	lung:	n/a
12	chr7:39609343-39609393	Hela-S3	cervix:	n/a
13	chr7:39606002-39606052	MCF10A-Er-Src	breast:	n/a
14	chr7:39606280-39606330	HRPEpiC	eye:	n/a
15	chr7:39609343-39609393	MCF-7	breast:	n/a
16	chr7:39606280-39606330	HCM	heart:	n/a
17	chr7:39606280-39606330	GM12878	blood:	n/a
18	chr7:39606965-39607015	GM12878	blood:	n/a
19	chr7:39606965-39607015	U87	brain:	n/a
20	chr7:39606965-39607015	NT2-D1	testis:	n/a
21	chr7:39606965-39607015	HEEpiC	esophagus:	n/a
22	chr7:39609343-39609393	NB4	blood:	n/a
23	chr7:39606013-39606063	Hela-S3	cervix:	n/a
24	chr7:39606002-39606052	NHDF-neo	bronchial:	n/a
25	chr7:39606002-39606052	GM19239	blood:	n/a
26	chr7:39605996-39606046	BJ	skin:	n/a
27	chr7:39606013-39606063	H1-hESC	embryonic stem cell:	embryo
28	chr7:39606071-39606121	ovcar-3	ovarian:	n/a
29	chr7:39606002-39606052	A549	lung:	n/a
30	chr7:39605996-39606046	AoSMC	blood vessel:	n/a
31	chr7:39606002-39606052	HAEpiC	amniotic membrane:	n/a
32	chr7:39609343-39609393	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:39606965-39607015	HAEpiC	amniotic membrane:	n/a
34	chr7:39606071-39606121	SK-N-SH	brain:	n/a
35	chr7:39612363-39612413	K562	blood:	n/a
36	chr7:39606002-39606052	Caco-2	colon:	n/a
37	chr7:39606071-39606121	NH-A	brain:	n/a
38	chr7:39606965-39607015	SKMC	muscle:	n/a
39	chr7:39606280-39606330	HAEpiC	amniotic membrane:	n/a
40	chr7:39609343-39609393	HIPEpiC	eye:	n/a
41	chr7:39612363-39612413	CMK	blood:	n/a
42	chr7:39612363-39612413	HIPEpiC	eye:	n/a
43	chr7:39605996-39606046	H1-hESC	embryonic stem cell:	embryo
44	chr7:39609343-39609393	HEK293	kidney:	embryo
45	chr7:39606002-39606052	GM12878	blood:	n/a
46	chr7:39605996-39606046	HRE	kidney:	n/a
47	chr7:39606071-39606121	BJ	skin:	n/a
48	chr7:39605996-39606046	NH-A	brain:	n/a
49	chr7:39606280-39606330	PFSK-1	brain:	n/a
50	chr7:39609343-39609393	SAEC	small airway:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39613001..39614812-chr7:39768164..39770870,2	K562	blood:
2	chr7:39605618..39607861-chr7:39772706..39774759,2	K562	blood:
3	chr7:39610504..39612853-chr7:39613535..39615540,2	K562	blood:
4	chr7:39604710..39608797-chr7:39663149..39665225,4	K562	blood:
5	chr7:39606078..39608053-chr7:39609216..39613025,4	MCF-7	breast:
6	chr7:39612446..39614989-chr7:39616627..39618783,2	MCF-7	breast:
7	chr7:39603623..39606050-chr7:39662280..39665105,2	MCF-7	breast:
8	chr7:39608617..39610852-chr7:39611782..39613419,2	K562	blood:
9	chr7:39606078..39608053-chr7:39609216..39613025,4	MCF-7	breast:
10	chr7:39604590..39607851-chr7:39609967..39614867,7	K562	blood:
11	chr7:39609139..39613691-chr7:39613860..39617111,6	K562	blood:
12	chr7:39605969..39608430-chr7:39663149..39665540,3	K562	blood:
13	chr7:39610504..39612853-chr7:39613535..39615540,2	K562	blood:
14	chr12:120729013..120729820-chr7:39605948..39606462,2	Hela-S3	cervix:
15	chr7:39605012..39607338-chr7:39986740..39989686,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-14	chr7:39608975-39609797	NONHSAT120207

No data

Variant related genes	Relation type
ENSG00000236015	TF binding region
YAE1D1	TF binding region
ENSG00000227172	TF binding region
ENSG00000236015	CpG island
YAE1D1	CpG island
ENSG00000227172	CpG island
ENSG00000259826	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000188185	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000241127	chromatin interactions
ENSG00000236015	chromatin interactions
ENSG00000227172	chromatin interactions

Extended variants
information (count: 353 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370478069	chr7:39605981-39605982	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs201699900	chr7:39605988-39605989	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs201220767	chr7:39605993-39605994	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs375353965	chr7:39605995-39605996	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs368248675	chr7:39605996-39605997	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs200260427	chr7:39605999-39606000	Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs372274583	chr7:39606002-39606003	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs202233622	chr7:39606003-39606004	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs375853820	chr7:39606005-39606006	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs573560764	chr7:39606009-39606010	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs143928572	chr7:39606036-39606037	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs146389256	chr7:39606041-39606042	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs116520088	chr7:39606054-39606055	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs7777434	chr7:39606074-39606075	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs17851965	chr7:39606080-39606081	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs1051162	chr7:39606107-39606108	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs142596038	chr7:39606133-39606134	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs369308164	chr7:39606163-39606164	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs200229728	chr7:39606187-39606188	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs532253635	chr7:39606215-39606216	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs552028918	chr7:39606216-39606217	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs207467801	chr7:39606220-39606221	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs373068336	chr7:39606223-39606224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs568852926	chr7:39606225-39606226	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs574749993	chr7:39606273-39606274	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs60155760	chr7:39606274-39606275	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs60581566	chr7:39606276-39606277	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs565823885	chr7:39606285-39606286	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs116390844	chr7:39606299-39606300	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs548271079	chr7:39606327-39606328	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs116041915	chr7:39606344-39606345	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs536888338	chr7:39606365-39606366	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs574591849	chr7:39606379-39606380	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs553581507	chr7:39606396-39606397	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs148342932	chr7:39606407-39606408	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs529776427	chr7:39606426-39606427	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs539356692	chr7:39606439-39606440	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs558944853	chr7:39606440-39606441	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs575595355	chr7:39606441-39606442	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs188170050	chr7:39606453-39606454	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs115688940	chr7:39606468-39606469	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs574578682	chr7:39606486-39606487	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs540067201	chr7:39606491-39606492	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs180889116	chr7:39606516-39606517	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs112002348	chr7:39606524-39606525	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs576596601	chr7:39606556-39606557	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs546087943	chr7:39606639-39606640	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs76986107	chr7:39606686-39606687	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs35097992	chr7:39606748-39606749	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs537229652	chr7:39606783-39606784	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39604600-39606600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr7:39605000-39606600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:39605000-39606600	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr7:39605000-39606800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:39605000-39606800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:39605000-39606800	Active TSS	Aorta	Aorta
7	chr7:39605000-39606800	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr7:39605000-39606800	Active TSS	GM12878-XiMat	blood
9	chr7:39605000-39606800	Active TSS	HMEC	breast
10	chr7:39605000-39606800	Active TSS	K562	blood
11	chr7:39605000-39607000	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr7:39605000-39607000	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr7:39605000-39607000	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr7:39605000-39607000	Active TSS	Fetal Kidney	kidney
15	chr7:39605000-39607000	Active TSS	NHDF-Ad	bronchial
16	chr7:39605000-39607200	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr7:39605000-39607200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:39605000-39607200	Active TSS	Rectal Smooth Muscle	rectum
19	chr7:39605000-39607400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr7:39605000-39607600	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr7:39605000-39607600	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr7:39605000-39607600	Active TSS	A549	lung
23	chr7:39605000-39607600	Active TSS	NHLF	lung
24	chr7:39605200-39606400	Active TSS	Brain Anterior Caudate	brain
25	chr7:39605200-39606400	Active TSS	Brain Substantia Nigra	brain
26	chr7:39605200-39606400	Active TSS	Duodenum Mucosa	Duodenum
27	chr7:39605200-39606400	Active TSS	Placenta	Placenta
28	chr7:39605200-39606600	Active TSS	Brain Cingulate Gyrus	brain
29	chr7:39605200-39606600	Active TSS	Colonic Mucosa	Colon
30	chr7:39605200-39606600	Active TSS	Colon Smooth Muscle	Colon
31	chr7:39605200-39606600	Active TSS	Duodenum Smooth Muscle	Duodenum
32	chr7:39605200-39606600	Active TSS	Fetal Heart	heart
33	chr7:39605200-39606600	Active TSS	Sigmoid Colon	Sigmoid Colon
34	chr7:39605200-39606600	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr7:39605200-39606800	Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr7:39605200-39606800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:39605200-39606800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:39605200-39606800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:39605200-39606800	Active TSS	Brain Hippocampus Middle	brain
40	chr7:39605200-39606800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr7:39605200-39606800	ZNF genes & repeats	Fetal Brain Male	brain
42	chr7:39605200-39606800	Active TSS	Fetal Muscle Leg	muscle
43	chr7:39605200-39606800	Active TSS	Fetal Stomach	stomach
44	chr7:39605200-39606800	Active TSS	Fetal Thymus	thymus
45	chr7:39605200-39606800	Active TSS	Stomach Mucosa	stomach
46	chr7:39605200-39606800	Active TSS	Thymus	Thymus
47	chr7:39605200-39607000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr7:39605200-39607000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:39605200-39607000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:39605200-39607000	Active TSS	Fetal Intestine Large	intestine

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