Variant report

Variant	nsv1020310
Chromosome Location	chr7:13839681-14015794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1218)
CpG islands
(count:305)
Chromatin interactive
region (count:81)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1218 , 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	chr7:13915440-13915557	K562	blood:	n/a	n/a
2	ARID3A	chr7:13889765-13890070	K562	blood:	n/a	n/a
3	ARID3A	chr7:13959750-13960140	K562	blood:	n/a	n/a
4	ATF1	chr7:13987729-13988052	K562	blood:	n/a	n/a
5	ATF1	chr7:13934044-13934292	K562	blood:	n/a	n/a
6	ATF1	chr7:13900658-13900844	K562	blood:	n/a	n/a
7	ATF1	chr7:13889729-13890161	K562	blood:	n/a	n/a
8	ATF1	chr7:13959834-13960225	K562	blood:	n/a	n/a
9	ATF1	chr7:13862322-13862554	K562	blood:	n/a	n/a
10	ATF3	chr7:13889705-13890029	K562	blood:	n/a	n/a
11	BACH1	chr7:13873923-13874075	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:13889847-13890003	H1-hESC	embryonic stem cell:	n/a	chr7:13889889-13889903
13	BACH1	chr7:13840793-13840928	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr7:13959838-13960065	K562	blood:	n/a	n/a
15	BHLHE40	chr7:13915327-13915479	K562	blood:	n/a	n/a
16	BHLHE40	chr7:13889782-13890158	K562	blood:	n/a	n/a
17	BHLHE40	chr7:13987491-13987899	K562	blood:	n/a	n/a
18	BHLHE40	chr7:13972912-13973017	K562	blood:	n/a	n/a
19	BRCA1	chr7:13959665-13960170	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr7:13889755-13890146	K562	blood:	n/a	n/a
21	CBX3	chr7:13889571-13890520	HCT-116	colon:	n/a	n/a
22	CBX3	chr7:13919485-13920390	HCT-116	colon:	n/a	n/a
23	CBX3	chr7:13889637-13890195	K562	blood:	n/a	n/a
24	CBX3	chr7:13959551-13960396	HCT-116	colon:	n/a	n/a
25	CBX3	chr7:13889630-13890509	HCT-116	colon:	n/a	n/a
26	CBX3	chr7:13948217-13948986	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:13919496-13920313	HCT-116	colon:	n/a	n/a
28	CBX3	chr7:13959648-13960390	HCT-116	colon:	n/a	n/a
29	CCNT2	chr7:13889753-13890143	K562	blood:	n/a	n/a
30	CCNT2	chr7:13945243-13945446	K562	blood:	n/a	n/a
31	CEBPB	chr7:13959668-13960221	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:13943701-13944070	K562	blood:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
33	CEBPB	chr7:13943707-13944054	A549	lung:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
34	CEBPB	chr7:13871986-13872328	K562	blood:	n/a	chr7:13872154-13872167 chr7:13872154-13872167 chr7:13872156-13872167
35	CEBPB	chr7:13880948-13881315	HepG2	liver:	n/a	chr7:13881124-13881135
36	CEBPB	chr7:13886140-13886336	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:13943706-13944047	HepG2	liver:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
38	CEBPB	chr7:13928758-13928975	IMR90	lung:	n/a	chr7:13928854-13928865
39	CEBPB	chr7:13866280-13866761	IMR90	lung:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
40	CEBPB	chr7:13943678-13944033	Hela-S3	cervix:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
41	CEBPB	chr7:13943530-13944071	IMR90	lung:	n/a	chr7:13943906-13943918 chr7:13943878-13943889 chr7:13943876-13943889 chr7:13943876-13943887 chr7:13943876-13943889 chr7:13943878-13943887 chr7:13943878-13943887 chr7:13943878-13943889 chr7:13943878-13943887 chr7:13943878-13943887
42	CEBPB	chr7:13932728-13932820	A549	lung:	n/a	n/a
43	CEBPB	chr7:13886123-13886339	K562	blood:	n/a	n/a
44	CEBPB	chr7:13900168-13900410	H1-hESC	embryonic stem cell:	n/a	chr7:13900271-13900282 chr7:13900271-13900284 chr7:13900271-13900284
45	CEBPB	chr7:13935047-13935258	HepG2	liver:	n/a	chr7:13935149-13935160
46	CEBPB	chr7:13923797-13923997	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:13866317-13866517	K562	blood:	n/a	chr7:13866439-13866450 chr7:13866439-13866452
48	CEBPB	chr7:13869718-13870004	HepG2	liver:	n/a	chr7:13869838-13869849
49	CEBPB	chr7:13948068-13949024	HCT-116	colon:	n/a	chr7:13948234-13948247
50	CEBPB	chr7:13928771-13928971	HepG2	liver:	n/a	chr7:13928854-13928865

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:13960140-13960190	NHDF-neo	bronchial:	n/a
2	chr7:13935467-13935517	Caco-2	colon:	n/a
3	chr7:13935467-13935517	H1-hESC	embryonic stem cell:	embryo
4	chr7:13960140-13960190	PrEC	prostate:	n/a
5	chr7:13889871-13889921	AG09309	skin:	n/a
6	chr7:13985664-13985714	NB4	blood:	n/a
7	chr7:13935467-13935517	A549	lung:	n/a
8	chr7:13960140-13960190	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:13889871-13889921	SK-N-MC	brain:	n/a
10	chr7:13935467-13935517	HAEpiC	amniotic membrane:	n/a
11	chr7:13889871-13889921	RPTEC	kidney:	n/a
12	chr7:13960140-13960190	MCF10A-Er-Src	breast:	n/a
13	chr7:13842752-13842802	HMEC	breast:	n/a
14	chr7:13935467-13935517	SK-N-SH	brain:	n/a
15	chr7:13842752-13842802	HCM	heart:	n/a
16	chr7:13985664-13985714	HUVEC	blood vessel:	n/a
17	chr7:13985664-13985714	HMEC	breast:	n/a
18	chr7:13960140-13960190	H1-hESC	embryonic stem cell:	embryo
19	chr7:13935467-13935517	NH-A	brain:	n/a
20	chr7:13935467-13935517	NB4	blood:	n/a
21	chr7:13842752-13842802	ovcar-3	ovarian:	n/a
22	chr7:13935467-13935517	GM12878	blood:	n/a
23	chr7:13985664-13985714	AoSMC	blood vessel:	n/a
24	chr7:13842752-13842802	AG09319	gingival:	n/a
25	chr7:13935467-13935517	PrEC	prostate:	n/a
26	chr7:13842752-13842802	HEEpiC	esophagus:	n/a
27	chr7:13985664-13985714	AG09309	skin:	n/a
28	chr7:13960140-13960190	Caco-2	colon:	n/a
29	chr7:13960140-13960190	AoSMC	blood vessel:	n/a
30	chr7:13960140-13960190	MCF-7	breast:	n/a
31	chr7:13889871-13889921	HepG2	liver:	n/a
32	chr7:13960140-13960190	Hela-S3	cervix:	n/a
33	chr7:13960140-13960190	GM06990	blood:	n/a
34	chr7:13960140-13960190	GM12878	blood:	n/a
35	chr7:13889871-13889921	AG10803	skin:	n/a
36	chr7:13889871-13889921	HCPEpiC	choroid plexus:	n/a
37	chr7:13985664-13985714	HNPCEpiC	eye:	n/a
38	chr7:13935467-13935517	NHDF-neo	bronchial:	n/a
39	chr7:13935467-13935517	PFSK-1	brain:	n/a
40	chr7:13842752-13842802	AG04450	lung:	fetal
41	chr7:13935467-13935517	HEEpiC	esophagus:	n/a
42	chr7:13985664-13985714	HAEpiC	amniotic membrane:	n/a
43	chr7:13889871-13889921	ProgFib	skin:	n/a
44	chr7:13842752-13842802	GM12892	blood:	n/a
45	chr7:13889871-13889921	GM12891	blood:	n/a
46	chr7:13985664-13985714	GM06990	blood:	n/a
47	chr7:13889871-13889921	Caco-2	colon:	n/a
48	chr7:13935467-13935517	HCM	heart:	n/a
49	chr7:13985664-13985714	RPTEC	kidney:	n/a
50	chr7:13960140-13960190	U87	brain:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:13997095..13998598-chr7:14011763..14014097,2	K562	blood:
2	chr7:13980622..13983188-chr7:14022030..14023536,2	K562	blood:
3	chr7:13999444..14001578-chr7:14011983..14013986,2	K562	blood:
4	chr7:13940952..13942572-chr7:13946206..13948609,2	K562	blood:
5	chr7:13989943..13991716-chr7:13993587..13996241,2	K562	blood:
6	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
7	chr7:13859282..13862271-chr7:13864269..13866964,2	K562	blood:
8	chr7:14008558..14010409-chr7:14028328..14031106,2	K562	blood:
9	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
10	chr7:13989697..13991875-chr7:13998508..14000403,2	K562	blood:
11	chr7:13994487..13997447-chr7:13998861..14001557,3	K562	blood:
12	chr7:13929008..13930898-chr7:13949066..13950636,2	K562	blood:
13	chr7:13989697..13992273-chr7:13998903..14000492,2	K562	blood:
14	chr7:13937992..13940139-chr7:13941426..13943158,2	K562	blood:
15	chr7:14006832..14009874-chr7:14010267..14013655,4	K562	blood:
16	chr7:13991446..13994404-chr7:14016165..14019066,2	K562	blood:
17	chr7:13985844..13987492-chr7:14019235..14021498,3	K562	blood:
18	chr7:14011992..14014933-chr7:14015921..14017592,2	K562	blood:
19	chr7:13940952..13942572-chr7:13946206..13948609,2	K562	blood:
20	chr7:13997566..14001513-chr7:14018273..14020813,4	K562	blood:
21	chr7:13888536..13892464-chr7:13896702..13899784,3	K562	blood:
22	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
23	chr7:13929540..13931526-chr7:13932770..13934783,2	K562	blood:
24	chr7:13888923..13892464-chr7:13896702..13899775,3	K562	blood:
25	chr7:13934709..13935267-chr7:14497324..14498029,2	MCF-7	breast:
26	chr7:13883716..13885561-chr7:13890341..13892357,2	K562	blood:
27	chr7:13989697..13991875-chr7:13998508..14000403,2	K562	blood:
28	chr7:13997007..14000342-chr7:14017723..14020427,3	K562	blood:
29	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
30	chr7:13973434..13976076-chr7:13978028..13980321,2	K562	blood:
31	chr7:13964325..13967217-chr7:14020611..14022495,2	K562	blood:
32	chr7:13859282..13862271-chr7:13864269..13866964,2	K562	blood:
33	chr7:13996982..14001014-chr7:14002058..14006442,5	K562	blood:
34	chr7:14000124..14001645-chr7:14029158..14031129,2	K562	blood:
35	chr7:13998712..14001529-chr7:14011348..14014089,2	K562	blood:
36	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
37	chr7:14008374..14010454-chr7:14010741..14014267,3	K562	blood:
38	chr7:13898559..13901034-chr7:13906643..13908176,2	K562	blood:
39	chr7:14006507..14011484-chr7:14016197..14021172,5	K562	blood:
40	chr7:13980412..13983231-chr7:14027961..14030275,2	K562	blood:
41	chr7:13946657..13948257-chr7:13950013..13952270,2	K562	blood:
42	chr7:14006642..14008318-chr7:14033077..14034662,2	K562	blood:
43	chr7:13996982..13998734-chr7:14003556..14005276,2	K562	blood:
44	chr7:13887425..13891202-chr7:13891537..13895717,6	K562	blood:
45	chr7:13869026..13872125-chr7:13876719..13879737,3	K562	blood:
46	chr7:13921967..13924964-chr7:13941231..13943091,2	K562	blood:
47	chr7:13931063..13934018-chr7:13935773..13937430,2	K562	blood:
48	chr7:13894294..13896373-chr7:13930641..13933578,2	K562	blood:
49	chr7:13993113..13994903-chr7:14003071..14005104,2	K562	blood:
50	chr7:14014823..14017219-chr7:14018906..14020830,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ETV1-1	chr7:13898560-13898650	XLOC_006359
2	lnc-ETV1-3	chr7:13865085-13865175	NONHSAT119257
3	lnc-ARL4A-8	chr7:13934333-13934794	NONHSAT119259
4	lnc-ETV1-1	chr7:13893980-13894247	XLOC_006359
5	lnc-ETV1-3	chr7:13860505-13860772	NONHSAT119257

No data

Variant related genes	Relation type
ENSG00000224330	TF binding region
ETV1	TF binding region
ENSG00000213875	TF binding region
ENSG00000224330	CpG island
ETV1	CpG island
ENSG00000213875	CpG island
ENSG00000224330	chromatin interactions
ENSG00000006468	chromatin interactions

Extended variants
information (count: 7070 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7070 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535121919	chr7:13839710-13839711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs10277842	chr7:13839748-13839749	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572037608	chr7:13839754-13839755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143485537	chr7:13839767-13839768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs6978401	chr7:13839791-13839792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182485466	chr7:13839803-13839804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543557119	chr7:13839816-13839817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185246619	chr7:13839819-13839820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115256715	chr7:13839866-13839867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112080811	chr7:13839875-13839876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542276542	chr7:13839892-13839893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189622946	chr7:13839909-13839910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184033067	chr7:13839939-13839940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572679515	chr7:13839973-13839974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528034897	chr7:13840018-13840019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141731381	chr7:13840034-13840035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571081638	chr7:13840046-13840047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74737374	chr7:13840073-13840074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2158802	chr7:13840077-13840078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs569687670	chr7:13840093-13840094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535157100	chr7:13840109-13840110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554992410	chr7:13840126-13840127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565327509	chr7:13840153-13840154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534280063	chr7:13840157-13840158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564540523	chr7:13840168-13840169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368279799	chr7:13840212-13840213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557632831	chr7:13840214-13840215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146014545	chr7:13840218-13840219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577840770	chr7:13840232-13840233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138729961	chr7:13840240-13840241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189112075	chr7:13840244-13840245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193042777	chr7:13840261-13840262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141862258	chr7:13840281-13840282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562103291	chr7:13840282-13840283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545330015	chr7:13840297-13840298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73269516	chr7:13840304-13840305	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs578102798	chr7:13840328-13840329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183690560	chr7:13840331-13840332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76378542	chr7:13840338-13840339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550136776	chr7:13840395-13840396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563904225	chr7:13840480-13840481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570022579	chr7:13840519-13840520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528996501	chr7:13840520-13840521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187380778	chr7:13840526-13840527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565388897	chr7:13840581-13840582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545498825	chr7:13840594-13840595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73269518	chr7:13840598-13840599	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146292276	chr7:13840620-13840621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73269519	chr7:13840652-13840653	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs537328525	chr7:13840655-13840656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	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
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	21298110	CNVD
Glioblastoma multiforme	22122801	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Prostate cancer	17079440	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	19805367	CNVD
Glioblastoma multiforme	18628472	CNVD

Chromatin state (count:1538 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:13821800-13840400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:13837400-13840600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr7:13837600-13840400	Weak transcription	HUVEC	blood vessel
4	chr7:13837600-13845000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr7:13837800-13840400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr7:13837800-13840600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr7:13837800-13840600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:13837800-13840600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:13837800-13840600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:13837800-13840800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:13838000-13840200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr7:13839600-13841200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:13839600-13841400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr7:13839600-13841600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:13839800-13840600	Enhancers	Fetal Brain Female	brain
16	chr7:13840000-13841600	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr7:13840200-13841400	Enhancers	Osteobl	bone
18	chr7:13840200-13841600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr7:13840200-13841600	Enhancers	NH-A	brain
20	chr7:13840200-13843000	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr7:13840400-13840800	Enhancers	HMEC	breast
22	chr7:13840400-13841000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:13840400-13841200	Enhancers	HUVEC	blood vessel
24	chr7:13840400-13841600	Enhancers	NHDF-Ad	bronchial
25	chr7:13840400-13841800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:13840600-13840800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr7:13840600-13841000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr7:13840600-13841600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:13840600-13843400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr7:13840600-13844200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:13840800-13841200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr7:13840800-13843000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr7:13841000-13841400	Enhancers	Fetal Brain Male	brain
34	chr7:13841000-13841400	Enhancers	HMEC	breast
35	chr7:13841000-13842800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:13841000-13845000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr7:13841200-13841800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr7:13841600-13845000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr7:13841600-13845200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr7:13841800-13844800	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr7:13841800-13845600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr7:13842400-13843000	Enhancers	K562	blood
43	chr7:13842800-13843000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:13842800-13843000	Enhancers	HMEC	breast
45	chr7:13842800-13843200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr7:13842800-13843800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:13843000-13843600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:13843000-13843800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:13843000-13845000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr7:13843000-13845000	Weak transcription	H9 Cell Line	embryonic stem cell

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