Variant report

Variant	nsv889189
Chromosome Location	chr7:126699088-126963028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1726)
CpG islands
(count:1895)
Chromatin interactive
region (count:83)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126930941-126931104	K562	blood:	n/a	n/a
2	ATF1	chr7:126911065-126911165	K562	blood:	n/a	n/a
3	BACH1	chr7:126893656-126894093	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:126891700-126892211	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:126891032-126891379	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr7:126747776-126748061	GM12878	blood:	n/a	chr7:126747977-126747986
7	BHLHE40	chr7:126893553-126894248	K562	blood:	n/a	chr7:126893815-126893831
8	BHLHE40	chr7:126747718-126748132	K562	blood:	n/a	n/a
9	BHLHE40	chr7:126898150-126898361	K562	blood:	n/a	n/a
10	BHLHE40	chr7:126893036-126893157	K562	blood:	n/a	chr7:126893111-126893127
11	CBX3	chr7:126893428-126893769	K562	blood:	n/a	n/a
12	CBX3	chr7:126747686-126748104	K562	blood:	n/a	n/a
13	CBX3	chr7:126747633-126748162	K562	blood:	n/a	n/a
14	CCNT2	chr7:126892999-126894318	K562	blood:	n/a	chr7:126893359-126893368 chr7:126893745-126893754
15	CCNT2	chr7:126811817-126812017	K562	blood:	n/a	n/a
16	CCNT2	chr7:126837048-126837211	K562	blood:	n/a	n/a
17	CEBPB	chr7:126942956-126942987	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:126893507-126893665	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:126891129-126891384	K562	blood:	n/a	chr7:126891313-126891326
20	CEBPB	chr7:126793003-126793247	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:126891143-126891590	A549	lung:	n/a	chr7:126891313-126891326
22	CEBPB	chr7:126957651-126958002	K562	blood:	n/a	chr7:126957826-126957837
23	CEBPB	chr7:126891174-126891459	H1-hESC	embryonic stem cell:	n/a	chr7:126891313-126891326
24	CEBPB	chr7:126714285-126714566	IMR90	lung:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
25	CEBPB	chr7:126826461-126826618	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:126723317-126723623	HepG2	liver:	n/a	chr7:126723476-126723487
27	CEBPB	chr7:126787274-126787579	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:126893965-126894183	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:126957655-126957976	HepG2	liver:	n/a	chr7:126957826-126957837
30	CEBPB	chr7:126957643-126958032	A549	lung:	n/a	chr7:126957826-126957837
31	CEBPB	chr7:126714292-126714568	A549	lung:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
32	CEBPB	chr7:126729684-126729737	K562	blood:	n/a	chr7:126729719-126729730
33	CEBPB	chr7:126891146-126891481	K562	blood:	n/a	chr7:126891313-126891326
34	CEBPB	chr7:126714252-126714589	HepG2	liver:	n/a	chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714417-126714428 chr7:126714417-126714428 chr7:126714417-126714430 chr7:126714417-126714430 chr7:126714419-126714428 chr7:126714419-126714428 chr7:126714418-126714429 chr7:126714417-126714430
35	CEBPB	chr7:126723318-126723628	A549	lung:	n/a	chr7:126723476-126723487
36	CEBPB	chr7:126942789-126943071	K562	blood:	n/a	n/a
37	CEBPB	chr7:126957668-126958066	Hela-S3	cervix:	n/a	chr7:126957826-126957837
38	CEBPB	chr7:126957641-126958005	IMR90	lung:	n/a	chr7:126957826-126957837
39	CEBPB	chr7:126864372-126864434	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:126729643-126729857	HepG2	liver:	n/a	chr7:126729719-126729730
41	CEBPB	chr7:126957667-126958002	H1-hESC	embryonic stem cell:	n/a	chr7:126957826-126957837
42	CHD1	chr7:126892486-126892487	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr7:126893514-126893559	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr7:126910187-126910196	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr7:126891362-126891516	HepG2	liver:	n/a	n/a
46	CHD2	chr7:126894007-126894283	K562	blood:	n/a	n/a
47	CHD2	chr7:126893579-126893719	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:126894114-126894157	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr7:126893648-126893693	HepG2	liver:	n/a	n/a
50	CHD2	chr7:126892728-126892855	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126829514-126829564	ovcar-3	ovarian:	n/a
2	chr7:126884276-126884326	GM12878	blood:	n/a
3	chr7:126894250-126894300	NB4	blood:	n/a
4	chr7:126890973-126891023	HAEpiC	amniotic membrane:	n/a
5	chr7:126829514-126829564	ovcar-3	ovarian:	n/a
6	chr7:126884276-126884326	GM12878	blood:	n/a
7	chr7:126894250-126894300	NB4	blood:	n/a
8	chr7:126890973-126891023	HAEpiC	amniotic membrane:	n/a
9	chr7:126893362-126893412	SK-N-MC	brain:	n/a
10	chr7:126893287-126893337	HAEpiC	amniotic membrane:	n/a
11	chr7:126893890-126893940	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:126893287-126893337	PFSK-1	brain:	n/a
13	chr7:126854672-126854722	SAEC	small airway:	n/a
14	chr7:126891621-126891671	AG09319	gingival:	n/a
15	chr7:126893304-126893354	HCT-116	colon:	n/a
16	chr7:126765549-126765599	PrEC	prostate:	n/a
17	chr7:126892578-126892628	GM12878	blood:	n/a
18	chr7:126892599-126892649	NHBE	bronchial:	n/a
19	chr7:126891197-126891247	SK-N-SH	brain:	n/a
20	chr7:126926730-126926780	AG04450	lung:	fetal
21	chr7:126883640-126883690	HIPEpiC	eye:	n/a
22	chr7:126866923-126866973	GM12892	blood:	n/a
23	chr7:126897376-126897426	HEK293	kidney:	embryo
24	chr7:126890973-126891023	Hepatocyte	liver:	n/a
25	chr7:126894250-126894300	AG09319	gingival:	n/a
26	chr7:126889015-126889065	K562	blood:	n/a
27	chr7:126889015-126889065	BE2_C	brain:	n/a
28	chr7:126893237-126893287	HCPEpiC	choroid plexus:	n/a
29	chr7:126893237-126893287	SK-N-MC	brain:	n/a
30	chr7:126889555-126889605	MCF-7	breast:	n/a
31	chr7:126889015-126889065	MCF-7	breast:	n/a
32	chr7:126866923-126866973	GM19239	blood:	n/a
33	chr7:126883137-126883187	PFSK-1	brain:	n/a
34	chr7:126866923-126866973	BJ	skin:	n/a
35	chr7:126883137-126883187	HCF	heart:	n/a
36	chr7:126897376-126897426	HCPEpiC	choroid plexus:	n/a
37	chr7:126897376-126897426	SK-N-SH	brain:	n/a
38	chr7:126892599-126892649	NH-A	brain:	n/a
39	chr7:126893304-126893354	Jurkat	blood:	n/a
40	chr7:126891621-126891671	SAEC	small airway:	n/a
41	chr7:126890973-126891023	HCM	heart:	n/a
42	chr7:126890512-126890562	HIPEpiC	eye:	n/a
43	chr7:126893007-126893057	HCF	heart:	n/a
44	chr7:126889555-126889605	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:126889555-126889605	LNCaP	prostate:	n/a
46	chr7:126894250-126894300	K562	blood:	n/a
47	chr7:126893007-126893057	HEK293	kidney:	embryo
48	chr7:126893287-126893337	GM12878	blood:	n/a
49	chr7:126894250-126894300	HCPEpiC	choroid plexus:	n/a
50	chr7:126893007-126893057	PFSK-1	brain:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:126744151..126746757-chr7:126749061..126750994,2	K562	blood:
2	chr7:126747288..126748236-chr7:126893729..126894723,2	K562	blood:
3	chr7:126892205..126895115-chr7:127030974..127032697,2	MCF-7	breast:
4	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
5	chr7:126748685..126750706-chr7:126758876..126761407,2	K562	blood:
6	chr7:126892951..126894660-chr7:127031651..127034423,2	MCF-7	breast:
7	chr7:126884819..126886507-chr7:126900468..126902207,2	K562	blood:
8	chr7:126795668..126798128-chr7:126799668..126802365,2	K562	blood:
9	chr7:126884819..126886507-chr7:126900468..126902207,2	K562	blood:
10	chr7:126875739..126881778-chr7:126881781..126887011,8	K562	blood:
11	chr7:126928309..126929229-chr9:85704406..85705155,2	MCF-7	breast:
12	chr7:126925615..126928461-chr7:126932611..126935289,2	K562	blood:
13	chr7:126920847..126923556-chr7:127113482..127116443,2	K562	blood:
14	chr12:52235461..52236089-chr7:126903724..126904354,2	MCF-7	breast:
15	chr7:126855088..126856692-chr7:126866803..126869023,2	K562	blood:
16	chr7:126784108..126786629-chr7:126806406..126809235,2	K562	blood:
17	chr7:126719826..126721988-chr7:126731679..126734281,2	K562	blood:
18	chr7:126784108..126786629-chr7:126806406..126809235,2	K562	blood:
19	chr7:126954427..126956826-chr7:126958992..126960680,2	MCF-7	breast:
20	chr7:126812464..126813971-chr7:126814116..126815770,2	K562	blood:
21	chr7:126959954..126961544-chr7:126962863..126965065,3	K562	blood:
22	chr7:126844024..126846766-chr7:126858329..126861025,2	K562	blood:
23	chr7:126900301..126902703-chr7:127030705..127032341,2	MCF-7	breast:
24	chr7:126842484..126844799-chr7:126846564..126849446,2	K562	blood:
25	chr7:126747301..126748195-chr7:127154353..127155146,2	MCF-7	breast:
26	chr7:126719826..126721988-chr7:126731679..126734281,2	K562	blood:
27	7:126085913-126088095..7:126960843-126968648	GM12878	blood:
28	chr7:126714682..126717546-chr7:126724506..126726256,2	K562	blood:
29	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
30	chr7:126891429..126894759-chr7:127030328..127033331,3	K562	blood:
31	chr7:126857935..126859467-chr7:126862307..126865217,2	K562	blood:
32	chr7:126931393..126934392-chr7:126943666..126946573,2	K562	blood:
33	7:126085913-126088095..7:126815147-126825227	GM12878	blood:
34	chr7:126883585..126886396-chr7:126892877..126894797,2	K562	blood:
35	chr7:126844024..126846766-chr7:126858329..126861025,2	K562	blood:
36	chr7:126828890..126831389-chr7:126845053..126847311,2	K562	blood:
37	chr1:164509263..164509920-chr7:126837817..126838611,2	MCF-7	breast:
38	chr7:126841412..126842988-chr7:126847997..126850796,2	K562	blood:
39	chr7:126718359..126720333-chr7:126729809..126731677,2	K562	blood:
40	chr7:126894392..126896260-chr7:126987799..126989472,2	K562	blood:
41	chr7:126748685..126750706-chr7:126758876..126761407,2	K562	blood:
42	chr7:126747293..126748237-chr7:126893164..126894608,6	MCF-7	breast:
43	chr7:126714682..126717546-chr7:126724506..126726256,2	K562	blood:
44	chr7:126795668..126798128-chr7:126799668..126802365,2	K562	blood:
45	chr7:126825377..126827148-chr7:126829233..126831138,2	K562	blood:
46	chr7:126893732..126895403-chr7:127004899..127007535,2	K562	blood:
47	chr7:126709768..126712072-chr7:126713094..126716180,3	K562	blood:
48	chr7:126857935..126859467-chr7:126862307..126865217,2	K562	blood:
49	chr7:126959954..126961544-chr7:126962863..126965065,3	K562	blood:
50	chr7:126942985..126945660-chr7:127029803..127032756,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-13	chr7:126904173-126904259	NONHSAT123133
2	lnc-ZNF800-1	chr7:126722158-126722228	ENSG00000230206.1
3	lnc-ARF5-3	chr7:126855181-126855307	ENSG00000236340.1
4	lnc-ARF5-13	chr7:126912402-126913094	NONHSAT123133
5	lnc-ARF5-13	chr7:126906423-126906527	NONHSAT123133
6	lnc-ARF5-3	chr7:126855181-126855307	ENSG00000236340.1
7	lnc-ZNF800-4	chr7:126789744-126789976	expReg_chr7_8988_-
8	lnc-ZNF800-5	chr7:126778502-126778855	expReg_chr7_8972_-
9	lnc-ZNF800-6	chr7:126777123-126777583	NONHSAT123128
10	lnc-ARF5-3	chr7:126868427-126869087	ENSG00000236340.1
11	lnc-ZNF800-1	chr7:126735719-126735864	NONHSAT123126
12	lnc-ARF5-3	chr7:126859521-126859756	ENSG00000236340.1
13	lnc-ARF5-3	chr7:126868427-126869975	NR_110195
14	lnc-ARF5-14	chr7:126778688-126778813	NONHSAT123129
15	lnc-ZNF800-4	chr7:126787075-126792049	NONHSAT123130
16	lnc-ZNF800-1	chr7:126724745-126724843	NONHSAT123126
17	lnc-ZNF800-3	chr7:126800086-126800564	expReg_chr7_9032_-
18	lnc-ARF5-13	chr7:126904887-126904958	NONHSAT123133
19	lnc-ARF5-3	chr7:126868427-126869975	ENSG00000236340.1
20	lnc-ZNF800-1	chr7:126724343-126724469	NONHSAT123126
21	lnc-ZNF800-1	chr7:126724745-126724843	ENSG00000230206.1
22	lnc-ARF5-3	chr7:126855181-126855307	NR_110195
23	lnc-ZNF800-1	chr7:126730963-126730972	ENSG00000230206.1
24	lnc-ZNF800-1	chr7:126720747-126720931	ENSG00000230206.1
25	lnc-ARF5-14	chr7:126777418-126777807	NONHSAT123129
26	lnc-ZNF800-1	chr7:126730963-126731067	NONHSAT123126

No data

Variant related genes	Relation type
ENSG00000236340	TF binding region
MIR592	TF binding region
ENSG00000236105	TF binding region
GRM8	TF binding region
ENSG00000236340	CpG island
MIR592	CpG island
ENSG00000236105	CpG island
GRM8	CpG island
ENSG00000124171	chromatin interactions
ENSG00000048405	chromatin interactions
ENSG00000236340	chromatin interactions
ENSG00000179603	chromatin interactions
ENSG00000179562	chromatin interactions

Extended variants
information (count: 4052 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4052 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112085725	chr7:126701365-126701366	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs10268335	chr7:126701367-126701368	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs541449912	chr7:126701368-126701369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559713651	chr7:126701403-126701404	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143532164	chr7:126701411-126701412	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs372991066	chr7:126701412-126701413	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs75934403	chr7:126701415-126701416	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200093781	chr7:126701416-126701417	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs530275685	chr7:126701457-126701458	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs548810208	chr7:126701476-126701477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs17865085	chr7:126701477-126701478	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191563435	chr7:126701509-126701510	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs565821658	chr7:126708636-126708637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1419444	chr7:126708654-126708655	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs543233799	chr7:126708661-126708662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17865563	chr7:126708692-126708693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151127202	chr7:126708715-126708716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189032194	chr7:126708803-126708804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141094830	chr7:126708812-126708813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559194850	chr7:126708846-126708847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530379599	chr7:126708860-126708861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577410573	chr7:126708886-126708887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201093905	chr7:126708916-126708917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541591074	chr7:126708940-126708941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143055041	chr7:126718365-126718366	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569389858	chr7:126718370-126718371	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536758653	chr7:126718371-126718372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs188162688	chr7:126718383-126718384	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570161439	chr7:126718387-126718388	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs375073370	chr7:126718394-126718395	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147451736	chr7:126718395-126718396	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552881972	chr7:126718408-126718409	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138579845	chr7:126718442-126718443	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533770866	chr7:126718450-126718451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2237786	chr7:126718480-126718481	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs556880201	chr7:126718493-126718494	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs575354863	chr7:126718551-126718552	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs563076253	chr7:126718613-126718614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs17865293	chr7:126718694-126718695	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564567906	chr7:126718695-126718696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372652671	chr7:126718702-126718703	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573310328	chr7:126718727-126718728	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192821626	chr7:126718778-126718779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs144116025	chr7:126718788-126718789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150686250	chr7:126718810-126718811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6942923	chr7:126718835-126718836	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs139887731	chr7:126718840-126718841	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533347163	chr7:126718866-126718867	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566824808	chr7:126718874-126718875	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371609062	chr7:126718888-126718889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Autism	20808228	CNVD
Prostate cancer	22341455	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126708600-126709000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:126720200-126721600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:126720400-126721400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr7:126721200-126721400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:126721600-126722000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:126721800-126722000	Enhancers	Brain Anterior Caudate	brain
7	chr7:126734400-126734800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr7:126734600-126735200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:126735200-126742400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:126742400-126742600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:126745000-126745600	Enhancers	Brain Germinal Matrix	brain
12	chr7:126753400-126755400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:126754000-126755200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr7:126754200-126755400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:126754400-126755200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr7:126754400-126755200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:126754400-126755200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr7:126754400-126755400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr7:126754400-126755400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr7:126755000-126755200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr7:126755000-126755400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:126755800-126756000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:126763000-126764000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:126763000-126764400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:126763000-126764400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr7:126786800-126787600	Enhancers	HepG2	liver
27	chr7:126792200-126792800	Enhancers	Liver	Liver
28	chr7:126792400-126793200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:126806800-126807200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr7:126826600-126827800	Enhancers	Thymus	Thymus
31	chr7:126827400-126828400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr7:126827600-126827800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr7:126828200-126830400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:126828600-126829200	Enhancers	Brain Hippocampus Middle	brain
35	chr7:126828600-126830400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:126828800-126829200	Enhancers	Brain Cingulate Gyrus	brain
37	chr7:126828800-126829200	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:126828800-126829200	Enhancers	Brain Substantia Nigra	brain
39	chr7:126828800-126830200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:126828800-126830400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr7:126828800-126830600	Enhancers	Brain Angular Gyrus	brain
42	chr7:126829000-126829600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr7:126829000-126829600	Active TSS	Brain Anterior Caudate	brain
44	chr7:126829000-126830200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:126829000-126830200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:126829000-126830400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr7:126829000-126830400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:126829200-126829400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr7:126829200-126829400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr7:126829200-126829600	Active TSS	Brain Substantia Nigra	brain

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