Variant report

Variant	nsv1015553
Chromosome Location	chr7:7053923-7201291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1398)
CpG islands
(count:1591)
Chromatin interactive
region (count:59)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1398 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7139212-7139608	K562	blood:	n/a	n/a
2	ARID3A	chr7:7082264-7082356	K562	blood:	n/a	n/a
3	ARID3A	chr7:7154338-7154908	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:7057749-7057838	K562	blood:	n/a	n/a
5	ARID3A	chr7:7165620-7166057	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:7139264-7139512	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:7142979-7143350	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:7149678-7149724	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:7143853-7144462	K562	blood:	n/a	n/a
10	ARID3A	chr7:7158402-7159467	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:7142948-7143370	K562	blood:	n/a	n/a
12	ARID3A	chr7:7176371-7177083	HepG2	liver:	n/a	chr7:7176873-7176889
13	ARID3A	chr7:7176140-7176500	K562	blood:	n/a	n/a
14	ARID3A	chr7:7188780-7189277	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:7167688-7167736	K562	blood:	n/a	n/a
16	ATF1	chr7:7176120-7176411	K562	blood:	n/a	n/a
17	ATF1	chr7:7188492-7188856	K562	blood:	n/a	n/a
18	ATF1	chr7:7139100-7140550	K562	blood:	n/a	n/a
19	ATF1	chr7:7144752-7145210	K562	blood:	n/a	n/a
20	ATF1	chr7:7142975-7143263	K562	blood:	n/a	n/a
21	ATF1	chr7:7082150-7082478	K562	blood:	n/a	n/a
22	ATF1	chr7:7087921-7088178	K562	blood:	n/a	n/a
23	ATF2	chr7:7139110-7139663	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr7:7139074-7139654	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr7:7139135-7139440	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr7:7139062-7139623	K562	blood:	n/a	n/a
27	ATF3	chr7:7139200-7139443	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr7:7143920-7144344	K562	blood:	n/a	n/a
29	BACH1	chr7:7138953-7140610	K562	blood:	n/a	n/a
30	BACH1	chr7:7133484-7133598	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr7:7139023-7140417	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr7:7115198-7115562	GM12878	blood:	n/a	n/a
33	BCL3	chr7:7113441-7113781	GM12878	blood:	n/a	n/a
34	BCL3	chr7:7115189-7115529	GM12878	blood:	n/a	n/a
35	BCL3	chr7:7108235-7108611	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:7082156-7082340	K562	blood:	n/a	n/a
37	BHLHE40	chr7:7158410-7158801	HepG2	liver:	n/a	n/a
38	BHLHE40	chr7:7154449-7154760	HepG2	liver:	n/a	n/a
39	BHLHE40	chr7:7143943-7144257	K562	blood:	n/a	n/a
40	BHLHE40	chr7:7139269-7139613	K562	blood:	n/a	n/a
41	BHLHE40	chr7:7139856-7140450	K562	blood:	n/a	n/a
42	BHLHE40	chr7:7154504-7154564	A549	lung:	n/a	n/a
43	BHLHE40	chr7:7154375-7154885	HepG2	liver:	n/a	n/a
44	BHLHE40	chr7:7139013-7139020	K562	blood:	n/a	n/a
45	BRCA1	chr7:7142971-7143222	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr7:7166595-7166645	GM12878	blood:	n/a	n/a
47	BRCA1	chr7:7139261-7139507	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr7:7148380-7148918	K562	blood:	n/a	n/a
49	CBX3	chr7:7142969-7143329	K562	blood:	n/a	n/a
50	CBX3	chr7:7139811-7140560	K562	blood:	n/a	n/a

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7106149-7106199	GM19239	blood:	n/a
2	chr7:7101641-7101691	ovcar-3	ovarian:	n/a
3	chr7:7105916-7105966	Hepatocyte	liver:	n/a
4	chr7:7189008-7189058	LNCaP	prostate:	n/a
5	chr7:7189008-7189058	HCPEpiC	choroid plexus:	n/a
6	chr7:7106149-7106199	GM19239	blood:	n/a
7	chr7:7101641-7101691	ovcar-3	ovarian:	n/a
8	chr7:7105916-7105966	Hepatocyte	liver:	n/a
9	chr7:7189008-7189058	LNCaP	prostate:	n/a
10	chr7:7189008-7189058	HCPEpiC	choroid plexus:	n/a
11	chr7:7099843-7099893	GM12891	blood:	n/a
12	chr7:7139271-7139321	A549	lung:	n/a
13	chr7:7097910-7097960	Jurkat	blood:	n/a
14	chr7:7110876-7110926	SK-N-MC	brain:	n/a
15	chr7:7099843-7099893	AG10803	skin:	n/a
16	chr7:7099843-7099893	H1-hESC	embryonic stem cell:	embryo
17	chr7:7109903-7109953	HRPEpiC	eye:	n/a
18	chr7:7110790-7110840	AG04449	skin:	fetal
19	chr7:7101738-7101788	AG10803	skin:	n/a
20	chr7:7111071-7111121	Jurkat	blood:	n/a
21	chr7:7110876-7110926	SK-N-SH	brain:	n/a
22	chr7:7099858-7099908	HepG2	liver:	n/a
23	chr7:7105916-7105966	PFSK-1	brain:	n/a
24	chr7:7099858-7099908	PANC-1	pancreas:	n/a
25	chr7:7139271-7139321	SK-N-MC	brain:	n/a
26	chr7:7099843-7099893	T-47D	breast:	n/a
27	chr7:7111826-7111876	HepG2	liver:	n/a
28	chr7:7189008-7189058	ovcar-3	ovarian:	n/a
29	chr7:7110722-7110772	PANC-1	pancreas:	n/a
30	chr7:7109903-7109953	PANC-1	pancreas:	n/a
31	chr7:7110876-7110926	AG09309	skin:	n/a
32	chr7:7105809-7105859	HCF	heart:	n/a
33	chr7:7101641-7101691	T-47D	breast:	n/a
34	chr7:7110876-7110926	RPTEC	kidney:	n/a
35	chr7:7106149-7106199	HRPEpiC	eye:	n/a
36	chr7:7097910-7097960	ECC-1	luminal epithelium:	n/a
37	chr7:7111071-7111121	HNPCEpiC	eye:	n/a
38	chr7:7106214-7106264	BE2_C	brain:	n/a
39	chr7:7098182-7098232	HRCEpiC	kidney:	n/a
40	chr7:7097910-7097960	HCT-116	colon:	n/a
41	chr7:7189008-7189058	HEEpiC	esophagus:	n/a
42	chr7:7189008-7189058	GM12892	blood:	n/a
43	chr7:7106149-7106199	HEEpiC	esophagus:	n/a
44	chr7:7111870-7111920	ECC-1	luminal epithelium:	n/a
45	chr7:7111213-7111263	HIPEpiC	eye:	n/a
46	chr7:7097910-7097960	NH-A	brain:	n/a
47	chr7:7106306-7106356	AG10803	skin:	n/a
48	chr7:7106214-7106264	HCT-116	colon:	n/a
49	chr7:7099858-7099908	PFSK-1	brain:	n/a
50	chr7:7101738-7101788	HEK293	kidney:	embryo

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:187538048..187541049-chr7:7133355..7136702,3	MCF-7	breast:
2	chr7:7082115..7084689-chr7:7085988..7087819,2	K562	blood:
3	chr7:7149260..7151579-chr7:7161509..7164124,2	K562	blood:
4	chr1:176176383..176176965-chr7:7135101..7135756,2	Hela-S3	cervix:
5	chr7:7170022..7172068-chr7:7175923..7178427,2	MCF-7	breast:
6	chr7:7166750..7169151-chr7:7173134..7175146,2	K562	blood:
7	chr7:7154082..7156860-chr7:7158140..7160593,3	MCF-7	breast:
8	chr7:7139222..7141450-chr7:7606351..7608422,2	K562	blood:
9	chr7:7053634..7055657-chr7:7056741..7058413,2	MCF-7	breast:
10	chr7:7074008..7077103-chr7:7078870..7082330,3	K562	blood:
11	chr7:7152616..7154632-chr7:7156604..7158282,2	K562	blood:
12	chr7:7138712..7144572-chr7:7219459..7223789,7	K562	blood:
13	chr7:7176048..7178096-chr7:7220537..7222866,2	K562	blood:
14	chr7:7176669..7179632-chr7:7195588..7197284,2	MCF-7	breast:
15	chr7:7170022..7172068-chr7:7175923..7178427,2	MCF-7	breast:
16	chr7:7143123..7143712-chr7:7389680..7390354,2	MCF-7	breast:
17	chr7:7139063..7141673-chr7:7144287..7145917,3	K562	blood:
18	chr7:7138954..7142167-chr7:7147742..7150390,3	K562	blood:
19	chr7:7189739..7192550-chr7:7197850..7200790,2	K562	blood:
20	chr7:7199593..7201382-chr7:7207230..7208864,2	K562	blood:
21	chr7:7133633..7139012-chr7:7139035..7144614,7	K562	blood:
22	chr7:7074211..7076243-chr7:7083711..7086454,2	K562	blood:
23	chr7:7170206..7172107-chr7:7175182..7178064,2	K562	blood:
24	chr7:7187067..7192401-chr7:7219251..7224244,6	K562	blood:
25	chr7:7186780..7188942-chr7:7203710..7206617,3	K562	blood:
26	chr7:7074211..7076243-chr7:7083711..7086454,2	K562	blood:
27	chr7:7134412..7137246-chr7:7225961..7227712,2	K562	blood:
28	chr7:7138294..7142693-chr7:7219176..7223789,9	K562	blood:
29	chr7:7142758..7143661-chr7:7580812..7581638,2	MCF-7	breast:
30	chr7:7170206..7172107-chr7:7175182..7178064,2	K562	blood:
31	chr7:7084346..7086372-chr7:7102099..7103966,2	K562	blood:
32	chr7:7189739..7192550-chr7:7197850..7200790,2	K562	blood:
33	chr7:7154454..7157037-chr7:7221900..7223676,2	K562	blood:
34	chr7:7152128..7153936-chr7:7218003..7219590,2	MCF-7	breast:
35	chr7:7075155..7077103-chr7:7078870..7080838,2	K562	blood:
36	chr7:7154082..7156860-chr7:7158140..7160593,3	MCF-7	breast:
37	chr7:7170209..7171969-chr7:7172174..7174978,2	K562	blood:
38	chr7:7075155..7077103-chr7:7078870..7080838,2	K562	blood:
39	chr7:7074008..7077103-chr7:7078870..7082330,3	K562	blood:
40	chr7:7139063..7141673-chr7:7144287..7145917,3	K562	blood:
41	chr7:7149260..7151579-chr7:7161509..7164124,2	K562	blood:
42	chr7:7170209..7171969-chr7:7172174..7174978,2	K562	blood:
43	chr7:7133060..7138358-chr7:7139035..7145054,9	K562	blood:
44	chr7:7081880..7084410-chr7:7088797..7091542,2	K562	blood:
45	chr7:7165873..7168273-chr7:7221674..7223249,2	K562	blood:
46	chr7:7142761..7143623-chr7:7463315..7464213,2	MCF-7	breast:
47	chr7:7053634..7055657-chr7:7056741..7058413,2	MCF-7	breast:
48	chr7:7084346..7086372-chr7:7102099..7103966,2	K562	blood:
49	chr7:7071081..7073048-chr7:7074220..7077008,2	K562	blood:
50	chr7:7081880..7084410-chr7:7088797..7091542,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCZ1B-6	chr7:7117926-7118888	NONHSAT119098
2	lnc-CCZ1B-6	chr7:7136332-7136350	NONHSAT119099
3	lnc-CCZ1B-6	chr7:7129663-7129687	NONHSAT119099
4	lnc-CCZ1B-6	chr7:7142758-7143163	NONHSAT119099
5	lnc-CCZ1B-6	chr7:7119855-7120286	NONHSAT119099
6	lnc-C1GALT1-2	chr7:7189403-7189621	expReg_chr7_628_+
7	lnc-CCZ1B-6	chr7:7136382-7136779	NONHSAT119099
8	lnc-CCZ1B-6	chr7:7150642-7150906	NONHSAT119099
9	lnc-CCZ1B-6	chr7:7152259-7153318	NONHSAT119099

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3683	chr7:7106641-7106662	MIMAT0018111

No data

Variant related genes	Relation type
ENSG00000263504	TF binding region
ENSG00000201218	TF binding region
ENSG00000266121	TF binding region
C1GALT1	TF binding region
MIR3683	TF binding region
ENSG00000265155	TF binding region
ENSG00000239696	TF binding region
ENSG00000264679	TF binding region
ENSG00000266409	TF binding region
ENSG00000263504	CpG island
ENSG00000201218	CpG island
ENSG00000266121	CpG island
C1GALT1	CpG island
MIR3683	CpG island
ENSG00000265155	CpG island
ENSG00000239696	CpG island
ENSG00000264679	CpG island
ENSG00000266409	CpG island
ENSG00000164654	chromatin interactions
ENSG00000201218	chromatin interactions
ENSG00000106392	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000143207	chromatin interactions
ENSG00000236021	chromatin interactions

Extended variants
information (count: 5134 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5134 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192202898	chr7:7053935-7053936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75804469	chr7:7053949-7053950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560246462	chr7:7053962-7053963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564889271	chr7:7053975-7053976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114633591	chr7:7053982-7053983	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77826340	chr7:7053992-7053993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569529621	chr7:7054001-7054002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11979022	chr7:7054012-7054013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548741970	chr7:7054017-7054018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs566697423	chr7:7054021-7054022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183191583	chr7:7054036-7054037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4724913	chr7:7054045-7054046	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs570254408	chr7:7054052-7054053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576833021	chr7:7054062-7054063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115096302	chr7:7054095-7054096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374221697	chr7:7054111-7054112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557012735	chr7:7054114-7054115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549789780	chr7:7054128-7054129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377529973	chr7:7054129-7054130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141784000	chr7:7054137-7054138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12671158	chr7:7054164-7054165	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs374770764	chr7:7054214-7054215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573039355	chr7:7054240-7054241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540339838	chr7:7054242-7054243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564925916	chr7:7054274-7054275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs150512815	chr7:7054296-7054297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139438410	chr7:7054316-7054317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs117552012	chr7:7054354-7054355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112978344	chr7:7054407-7054408	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs548567277	chr7:7054409-7054410	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566735073	chr7:7054421-7054422	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs10556618	chr7:7054426-7054427	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs551688814	chr7:7054438-7054439	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs527835725	chr7:7054445-7054446	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs201848658	chr7:7054456-7054457	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs552302521	chr7:7054468-7054469	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs570605159	chr7:7054510-7054511	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537883723	chr7:7054544-7054545	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs187927373	chr7:7054597-7054598	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs113372953	chr7:7054598-7054599	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs566054751	chr7:7054624-7054625	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74296224	chr7:7054625-7054626	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35795353	chr7:7054626-7054627	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554862196	chr7:7054651-7054652	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558270671	chr7:7054672-7054673	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191279053	chr7:7054674-7054675	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540424402	chr7:7054683-7054684	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76099260	chr7:7054699-7054700	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149277183	chr7:7054711-7054712	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543945435	chr7:7054722-7054723	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Melanoma	17363583	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7052400-7060600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:7052600-7054200	Weak transcription	Fetal Intestine Small	intestine
3	chr7:7052600-7058200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:7052800-7055000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:7053400-7055600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr7:7053600-7055000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:7053800-7055000	Enhancers	Brain Germinal Matrix	brain
8	chr7:7054000-7054400	Enhancers	Fetal Brain Female	brain
9	chr7:7054000-7054800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr7:7054200-7054400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:7054400-7054800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:7054400-7054800	Active TSS	Fetal Brain Female	brain
13	chr7:7054400-7055200	Enhancers	Fetal Brain Male	brain
14	chr7:7054600-7054800	Active TSS	Brain Anterior Caudate	brain
15	chr7:7054600-7055000	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr7:7054600-7055000	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr7:7054800-7055000	Flanking Active TSS	Brain Anterior Caudate	brain
18	chr7:7054800-7055000	Flanking Active TSS	Fetal Brain Female	brain
19	chr7:7054800-7055200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:7057200-7058400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:7057200-7058400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:7057400-7058400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:7065000-7065400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:7065400-7067000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:7067000-7069800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:7069800-7072000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:7075600-7075800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr7:7076800-7081800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr7:7080000-7081400	Enhancers	K562	blood
30	chr7:7081400-7082200	Flanking Active TSS	K562	blood
31	chr7:7081600-7082000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
32	chr7:7081600-7083000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr7:7081800-7082200	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:7081800-7082600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:7081800-7082800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr7:7081800-7083000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:7082000-7082600	Enhancers	Stomach Mucosa	stomach
38	chr7:7082000-7082800	Enhancers	Primary T cells fromperipheralblood	blood
39	chr7:7082200-7084200	Enhancers	K562	blood
40	chr7:7082400-7082800	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr7:7084200-7087200	Weak transcription	K562	blood
42	chr7:7084400-7084800	Enhancers	Placenta	Placenta
43	chr7:7086600-7087200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr7:7087000-7087800	Enhancers	HSMMtube	muscle
45	chr7:7087200-7088200	Enhancers	K562	blood
46	chr7:7087200-7090800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr7:7087800-7090800	Weak transcription	HSMMtube	muscle
48	chr7:7088200-7091000	Weak transcription	K562	blood
49	chr7:7090400-7091400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr7:7090600-7091000	Enhancers	Rectal Mucosa Donor 29	rectum

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