Variant report

Variant	esv1819001
Chromosome Location	chr7:6746810-6785602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1230)
CpG islands
(count:917)
Chromatin interactive
region (count:26)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1230 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6747987-6748210	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6769148-6769268	K562	blood:	n/a	n/a
3	ARID3A	chr7:6746508-6747088	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6769330-6769549	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:6746582-6746922	K562	blood:	n/a	n/a
6	ARID3A	chr7:6749446-6749789	HepG2	liver:	n/a	n/a
7	ATF2	chr7:6769041-6769427	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:6764577-6765116	GM12878	blood:	n/a	n/a
9	ATF2	chr7:6765435-6765872	GM12878	blood:	n/a	n/a
10	ATF2	chr7:6768932-6769576	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:6764660-6765106	GM12878	blood:	n/a	n/a
12	ATF3	chr7:6746344-6746860	A549	lung:	n/a	chr7:6746443-6746452
13	ATF3	chr7:6746338-6746843	A549	lung:	n/a	chr7:6746443-6746452
14	BATF	chr7:6764386-6765017	GM12878	blood:	n/a	n/a
15	BATF	chr7:6770212-6770532	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:6764490-6765004	GM12878	blood:	n/a	n/a
17	BCL3	chr7:6765434-6765865	GM12878	blood:	n/a	n/a
18	BCL3	chr7:6764602-6765093	GM12878	blood:	n/a	n/a
19	BCLAF1	chr7:6746183-6746931	GM12878	blood:	n/a	chr7:6746574-6746587 chr7:6746324-6746333 chr7:6746577-6746590 chr7:6746318-6746331 chr7:6746657-6746670
20	BCLAF1	chr7:6768933-6769605	GM12878	blood:	n/a	chr7:6768960-6768969
21	BCLAF1	chr7:6765486-6765849	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:6769053-6769626	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:6764543-6765036	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:6769211-6769538	K562	blood:	n/a	n/a
25	BHLHE40	chr7:6769947-6770143	K562	blood:	n/a	n/a
26	BHLHE40	chr7:6746430-6746875	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:6746435-6747008	K562	blood:	n/a	n/a
28	BHLHE40	chr7:6764639-6765044	GM12878	blood:	n/a	n/a
29	BHLHE40	chr7:6765444-6765862	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:6769137-6769602	GM12878	blood:	n/a	n/a
31	BRCA1	chr7:6746338-6747069	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:6746365-6746883	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr7:6769345-6769648	HepG2	liver:	n/a	n/a
34	BRCA1	chr7:6746551-6747053	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr7:6746299-6746907	HepG2	liver:	n/a	n/a
36	BRCA1	chr7:6769210-6769550	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr7:6768879-6769361	K562	blood:	n/a	n/a
38	CBX3	chr7:6749398-6749899	HCT-116	colon:	n/a	n/a
39	CBX3	chr7:6746593-6747092	K562	blood:	n/a	n/a
40	CBX3	chr7:6749453-6749879	K562	blood:	n/a	n/a
41	CBX3	chr7:6746385-6747206	K562	blood:	n/a	n/a
42	CBX3	chr7:6749454-6749792	K562	blood:	n/a	n/a
43	CBX3	chr7:6768880-6769635	K562	blood:	n/a	n/a
44	CBX3	chr7:6769851-6770383	K562	blood:	n/a	n/a
45	CCNT2	chr7:6769175-6769724	K562	blood:	n/a	n/a
46	CEBPB	chr7:6769943-6769977	HepG2	liver:	n/a	n/a
47	CHD1	chr7:6769255-6769940	GM12878	blood:	n/a	n/a
48	CHD1	chr7:6764785-6765290	GM12878	blood:	n/a	n/a
49	CHD2	chr7:6769061-6769581	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr7:6769097-6769650	GM12878	blood:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6774720-6774770	HNPCEpiC	eye:	n/a
2	chr7:6774169-6774219	HL-60	blood:	n/a
3	chr7:6774720-6774770	HNPCEpiC	eye:	n/a
4	chr7:6774169-6774219	HL-60	blood:	n/a
5	chr7:6773787-6773837	ECC-1	luminal epithelium:	n/a
6	chr7:6769406-6769456	AG10803	skin:	n/a
7	chr7:6766092-6766142	ovcar-3	ovarian:	n/a
8	chr7:6746977-6747027	GM12891	blood:	n/a
9	chr7:6769409-6769459	HCM	heart:	n/a
10	chr7:6746977-6747027	A549	lung:	n/a
11	chr7:6774720-6774770	HCF	heart:	n/a
12	chr7:6769322-6769372	A549	lung:	n/a
13	chr7:6749638-6749688	ECC-1	luminal epithelium:	n/a
14	chr7:6774169-6774219	AG10803	skin:	n/a
15	chr7:6746799-6746849	H1-hESC	embryonic stem cell:	embryo
16	chr7:6770940-6770990	SK-N-SH_RA	brain:	n/a
17	chr7:6750462-6750512	AG10803	skin:	n/a
18	chr7:6774720-6774770	HEK293	kidney:	embryo
19	chr7:6766092-6766142	HCT-116	colon:	n/a
20	chr7:6746977-6747027	AoSMC	blood vessel:	n/a
21	chr7:6772985-6773035	Hepatocyte	liver:	n/a
22	chr7:6746799-6746849	HCF	heart:	n/a
23	chr7:6774169-6774219	PANC-1	pancreas:	n/a
24	chr7:6749638-6749688	HL-60	blood:	n/a
25	chr7:6746977-6747027	HRPEpiC	eye:	n/a
26	chr7:6774720-6774770	PANC-1	pancreas:	n/a
27	chr7:6746799-6746849	NT2-D1	testis:	n/a
28	chr7:6746977-6747027	HUVEC	blood vessel:	n/a
29	chr7:6746837-6746887	AoSMC	blood vessel:	n/a
30	chr7:6746837-6746887	HEK293	kidney:	embryo
31	chr7:6769406-6769456	HRPEpiC	eye:	n/a
32	chr7:6772985-6773035	Jurkat	blood:	n/a
33	chr7:6766092-6766142	SKMC	muscle:	n/a
34	chr7:6750462-6750512	SK-N-MC	brain:	n/a
35	chr7:6746799-6746849	Hela-S3	cervix:	n/a
36	chr7:6772985-6773035	SK-N-SH	brain:	n/a
37	chr7:6769322-6769372	AG09309	skin:	n/a
38	chr7:6749638-6749688	SK-N-MC	brain:	n/a
39	chr7:6746977-6747027	PrEC	prostate:	n/a
40	chr7:6750462-6750512	GM06990	blood:	n/a
41	chr7:6746799-6746849	AG09319	gingival:	n/a
42	chr7:6769322-6769372	ovcar-3	ovarian:	n/a
43	chr7:6769322-6769372	SAEC	small airway:	n/a
44	chr7:6772985-6773035	SAEC	small airway:	n/a
45	chr7:6749638-6749688	HUVEC	blood vessel:	n/a
46	chr7:6769322-6769372	HNPCEpiC	eye:	n/a
47	chr7:6746837-6746887	HCF	heart:	n/a
48	chr7:6774720-6774770	NHDF-neo	bronchial:	n/a
49	chr7:6774720-6774770	GM12878	blood:	n/a
50	chr7:6769409-6769459	HCT-116	colon:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6048395..6048947-chr7:6768981..6769924,2	NB4	blood:
2	chr17:59484738..59486572-chr7:6745021..6746847,2	MCF-7	breast:
3	chr7:6745040..6747820-chr7:6753016..6755979,2	K562	blood:
4	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:
5	chr2:179315296..179317868-chr7:6745682..6748008,2	MCF-7	breast:
6	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
7	chr7:6755281..6757989-chr7:6768169..6769805,2	K562	blood:
8	chr7:6761698..6764136-chr7:6769053..6770920,2	MCF-7	breast:
9	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
10	chr7:6681243..6682856-chr7:6746246..6748831,2	K562	blood:
11	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
12	chr7:6616941..6618678-chr7:6767339..6769412,2	MCF-7	breast:
13	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
14	chr7:6729955..6731866-chr7:6746781..6748682,2	MCF-7	breast:
15	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
16	chr7:6675529..6677980-chr7:6768487..6770695,2	K562	blood:
17	chr2:85554880..85555877-chr7:6769205..6770035,2	Hela-S3	cervix:
18	chr7:6746161..6747688-chr7:6768318..6771249,2	MCF-7	breast:
19	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
20	chr7:6767588..6769922-chr7:6774691..6777140,2	MCF-7	breast:
21	chr7:6744871..6747873-chr7:6767656..6771321,4	K562	blood:
22	chr7:6768428..6771621-chr7:6773707..6775724,3	MCF-7	breast:
23	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
24	chr7:6745105..6747702-chr7:6760857..6762901,2	MCF-7	breast:
25	chr7:6745224..6747442-chr7:6767898..6770902,3	MCF-7	breast:
26	chr7:6745463..6748475-chr7:6767656..6769994,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6751010-6751093	NONHSAT119062
2	lnc-AC073343.1-1	chr7:6747932-6748026	ENSG00000228010.1
3	lnc-AC073343.1-1	chr7:6751010-6751133	NONHSAT119061
4	lnc-RSPH10B2-1	chr7:6749757-6749869	NONHSAT119063
5	lnc-RSPH10B2-1	chr7:6771528-6771586	NONHSAT119063
6	lnc-AC073343.1-1	chr7:6748199-6748532	ENSG00000228010.1
7	lnc-AC073343.1-1	chr7:6748310-6748670	NONHSAT119062
8	lnc-AC073343.1-1	chr7:6750381-6750402	NONHSAT119061
9	lnc-AC073343.1-1	chr7:6746704-6748672	NONHSAT119061

No data

Variant related genes	Relation type
ZNF12	TF binding region
PMS2CL	TF binding region
ZNF12	CpG island
PMS2CL	CpG island
ENSG00000265245	chromatin interactions
ENSG00000204311	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000180228	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000152291	chromatin interactions

Extended variants
information (count: 1927 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1927 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147577390	chr7:6746826-6746827	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
2	rs370000763	chr7:6746845-6746846	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
3	rs558993807	chr7:6746859-6746860	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
4	rs570987387	chr7:6746894-6746895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
5	rs373755470	chr7:6746906-6746907	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
6	rs538075022	chr7:6746915-6746916	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
7	rs183324772	chr7:6746918-6746919	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
8	rs111573332	chr7:6746955-6746956	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
9	rs541963464	chr7:6746994-6746995	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
10	rs562952243	chr7:6747000-6747001	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
11	rs545775052	chr7:6747046-6747047	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
12	rs188686633	chr7:6747057-6747058	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
13	rs192253711	chr7:6747058-6747059	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
14	rs59433350	chr7:6747130-6747131	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs532307998	chr7:6747131-6747132	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
16	rs544060922	chr7:6747153-6747154	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
17	rs184683324	chr7:6747165-6747166	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
18	rs142947464	chr7:6747177-6747178	Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
19	rs7786706	chr7:6747267-6747268	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566432267	chr7:6747285-6747286	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs116685881	chr7:6747301-6747302	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs189423916	chr7:6747316-6747317	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs571033617	chr7:6747410-6747411	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs548024602	chr7:6747416-6747417	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs151087224	chr7:6747420-6747421	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs566060041	chr7:6747435-6747436	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs556330508	chr7:6747454-6747455	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs4370442	chr7:6747494-6747495	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs539347570	chr7:6747525-6747526	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs112985551	chr7:6747526-6747527	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs138291739	chr7:6747527-6747528	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs535512538	chr7:6747536-6747537	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs184536687	chr7:6747538-6747539	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs572371923	chr7:6747549-6747550	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs376049964	chr7:6747566-6747567	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs545900836	chr7:6747573-6747574	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs117877761	chr7:6747585-6747586	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs577052018	chr7:6747586-6747587	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs544563002	chr7:6747602-6747603	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs6463576	chr7:6747606-6747607	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs141115595	chr7:6747617-6747618	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs201881908	chr7:6747692-6747693	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs189453021	chr7:6747707-6747708	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs578090183	chr7:6747715-6747716	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
45	rs376578965	chr7:6747746-6747747	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs560309073	chr7:6747755-6747756	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs200734226	chr7:6747760-6747761	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs527406805	chr7:6747772-6747773	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs551873191	chr7:6747790-6747791	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs548907987	chr7:6747802-6747803	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6744600-6747200	Active TSS	Right Ventricle	heart
2	chr7:6744800-6747200	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr7:6745000-6747000	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr7:6745000-6747000	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr7:6745000-6747000	Active TSS	Fetal Intestine Large	intestine
6	chr7:6745000-6747000	Active TSS	Stomach Smooth Muscle	stomach
7	chr7:6745000-6747200	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr7:6745000-6747200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:6745000-6747200	Active TSS	Colonic Mucosa	Colon
10	chr7:6745000-6747200	Active TSS	Fetal Kidney	kidney
11	chr7:6745000-6747200	Active TSS	Ovary	ovary
12	chr7:6745000-6747200	Active TSS	Right Atrium	heart
13	chr7:6745000-6747400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:6745000-6747600	Active TSS	Rectal Mucosa Donor 29	rectum
15	chr7:6745200-6747000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:6745200-6747000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:6745200-6747000	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr7:6745200-6747000	Active TSS	A549	lung
19	chr7:6745200-6747200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr7:6745200-6747200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr7:6745200-6747200	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr7:6745200-6747200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr7:6745200-6747200	Active TSS	Left Ventricle	heart
24	chr7:6745200-6747200	Active TSS	Psoas Muscle	Psoas
25	chr7:6745200-6747200	Active TSS	NHDF-Ad	bronchial
26	chr7:6745200-6747400	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr7:6745200-6747400	Flanking Active TSS	Primary hematopoietic stem cells	blood
28	chr7:6745200-6747400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr7:6745400-6747000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:6745400-6747000	Active TSS	H9 Cell Line	embryonic stem cell
31	chr7:6745400-6747000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:6745400-6747000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:6745400-6747000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:6745400-6747200	Active TSS	Fetal Muscle Trunk	muscle
35	chr7:6745400-6747200	Active TSS	NHLF	lung
36	chr7:6745400-6747600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:6745600-6747000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr7:6745600-6747000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr7:6745600-6747000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr7:6745600-6747000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:6745600-6747000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
42	chr7:6745600-6747000	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr7:6745600-6747000	Active TSS	Fetal Brain Female	brain
44	chr7:6745600-6747000	Active TSS	Small Intestine	intestine
45	chr7:6745600-6747200	Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr7:6745600-6747200	Active TSS	Muscle Satellite Cultured Cells	--
47	chr7:6745600-6747200	Active TSS	Aorta	Aorta
48	chr7:6745600-6747400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:6745600-6747400	Active TSS	Colon Smooth Muscle	Colon
50	chr7:6745800-6747000	Active TSS	Primary T helper naive cells from peripheral blood	blood

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