Variant report

Variant	nsv427805
Chromosome Location	chr7:126494789-126677843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:126646619-126646698	K562	blood:	n/a	n/a
2	ATF1	chr7:126586391-126586455	K562	blood:	n/a	n/a
3	ATF1	chr7:126509086-126509186	K562	blood:	n/a	n/a
4	BATF	chr7:126551713-126552013	GM12878	blood:	n/a	chr7:126551879-126551890
5	BCL11A	chr7:126522058-126522240	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:126496848-126496879	HepG2	liver:	n/a	n/a
7	CCNT2	chr7:126598491-126598668	K562	blood:	n/a	n/a
8	CEBPB	chr7:126512782-126513296	A549	lung:	n/a	chr7:126513180-126513191 chr7:126513051-126513062
9	CEBPB	chr7:126513084-126513338	HepG2	liver:	n/a	chr7:126513180-126513191
10	CEBPB	chr7:126524439-126524641	HepG2	liver:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
11	CEBPB	chr7:126650410-126650534	HepG2	liver:	n/a	chr7:126650447-126650458
12	CEBPB	chr7:126640722-126641110	K562	blood:	n/a	chr7:126640988-126640999
13	CEBPB	chr7:126619889-126620141	A549	lung:	n/a	chr7:126619992-126620003
14	CEBPB	chr7:126619872-126620171	HepG2	liver:	n/a	chr7:126619992-126620003
15	CEBPB	chr7:126640645-126641176	HepG2	liver:	n/a	chr7:126640988-126640999
16	CEBPB	chr7:126640794-126641172	A549	lung:	n/a	chr7:126640988-126640999
17	CEBPB	chr7:126611438-126611726	HepG2	liver:	n/a	chr7:126611572-126611583
18	CEBPB	chr7:126524451-126524692	Hela-S3	cervix:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
19	CEBPB	chr7:126640817-126641170	IMR90	lung:	n/a	chr7:126640988-126640999
20	CEBPB	chr7:126664292-126664492	HepG2	liver:	n/a	chr7:126664371-126664382
21	CEBPB	chr7:126675667-126675895	HepG2	liver:	n/a	chr7:126675790-126675801
22	CEBPB	chr7:126522805-126523396	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:126516526-126516933	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:126593940-126594250	HepG2	liver:	n/a	chr7:126594091-126594100 chr7:126594089-126594100 chr7:126594089-126594102
25	CEBPB	chr7:126651805-126652002	A549	lung:	n/a	n/a
26	CEBPB	chr7:126526182-126526382	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:126651754-126652063	H1-hESC	embryonic stem cell:	n/a	chr7:126652025-126652038
28	CEBPB	chr7:126524473-126524687	K562	blood:	n/a	chr7:126524616-126524628 chr7:126524579-126524592 chr7:126524579-126524590
29	CEBPB	chr7:126651787-126651946	IMR90	lung:	n/a	n/a
30	CTCF	chr7:126496840-126496990	AG04449	skin:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
31	CTCF	chr7:126540240-126540390	HCT-116	colon:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
32	CTCF	chr7:126496756-126497067	A549	lung:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
33	CTCF	chr7:126540180-126540330	GM12865	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
34	CTCF	chr7:126496820-126496970	GM12871	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
35	CTCF	chr7:126540260-126540410	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr7:126540240-126540390	WERI-Rb-1	eye:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
37	CTCF	chr7:126496860-126497010	HCFaa	heart:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
38	CTCF	chr7:126496880-126497030	GM12878	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
39	CTCF	chr7:126496793-126497048	LNCaP	prostate:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
40	CTCF	chr7:126605201-126605245	GM10248	blood:	n/a	n/a
41	CTCF	chr7:126540260-126540410	GM12878	blood:	n/a	n/a
42	CTCF	chr7:126540132-126540365	GM19240	blood:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
43	CTCF	chr7:126540260-126540410	HMEC	breast:	n/a	n/a
44	CTCF	chr7:126540180-126540330	SK-N-SH_RA	brain:	n/a	chr7:126540251-126540269 chr7:126540258-126540266 chr7:126540246-126540267 chr7:126540253-126540266
45	CTCF	chr7:126496840-126496990	HCT-116	colon:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
46	CTCF	chr7:126496820-126496970	GM12865	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
47	CTCF	chr7:126496860-126497010	HEEpiC	esophagus:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
48	CTCF	chr7:126496818-126497033	GM13977	blood:	n/a	chr7:126496914-126496932 chr7:126496916-126496937
49	CTCF	chr7:126522160-126522310	HEK293	kidney:	n/a	n/a
50	CTCF	chr7:126496820-126496970	HRPEpiC	eye:	n/a	chr7:126496914-126496932 chr7:126496916-126496937

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126675528-126675578	Jurkat	blood:	n/a
2	chr7:126675528-126675578	Jurkat	blood:	n/a
3	chr7:126675528-126675578	SKMC	muscle:	n/a
4	chr7:126615786-126615836	NT2-D1	testis:	n/a
5	chr7:126615786-126615836	BE2_C	brain:	n/a
6	chr7:126615786-126615836	Hela-S3	cervix:	n/a
7	chr7:126675358-126675408	HCPEpiC	choroid plexus:	n/a
8	chr7:126675528-126675578	HAEpiC	amniotic membrane:	n/a
9	chr7:126615786-126615836	HIPEpiC	eye:	n/a
10	chr7:126675358-126675408	SK-N-SH_RA	brain:	n/a
11	chr7:126615786-126615836	HepG2	liver:	n/a
12	chr7:126675358-126675408	GM12892	blood:	n/a
13	chr7:126675358-126675408	PFSK-1	brain:	n/a
14	chr7:126615786-126615836	CMK	blood:	n/a
15	chr7:126675358-126675408	SKMC	muscle:	n/a
16	chr7:126675358-126675408	HNPCEpiC	eye:	n/a
17	chr7:126675528-126675578	HRCEpiC	kidney:	n/a
18	chr7:126675528-126675578	HCT-116	colon:	n/a
19	chr7:126675358-126675408	Hela-S3	cervix:	n/a
20	chr7:126615786-126615836	Caco-2	colon:	n/a
21	chr7:126615786-126615836	HEEpiC	esophagus:	n/a
22	chr7:126675358-126675408	A549	lung:	n/a
23	chr7:126615786-126615836	HNPCEpiC	eye:	n/a
24	chr7:126615786-126615836	SKMC	muscle:	n/a
25	chr7:126615786-126615836	T-47D	breast:	n/a
26	chr7:126675358-126675408	SK-N-SH	brain:	n/a
27	chr7:126675528-126675578	BE2_C	brain:	n/a
28	chr7:126615786-126615836	ovcar-3	ovarian:	n/a
29	chr7:126675358-126675408	AoSMC	blood vessel:	n/a
30	chr7:126675528-126675578	PrEC	prostate:	n/a
31	chr7:126675528-126675578	HL-60	blood:	n/a
32	chr7:126675528-126675578	BJ	skin:	n/a
33	chr7:126675528-126675578	HEK293	kidney:	embryo
34	chr7:126675358-126675408	T-47D	breast:	n/a
35	chr7:126675358-126675408	HRPEpiC	eye:	n/a
36	chr7:126615786-126615836	HAEpiC	amniotic membrane:	n/a
37	chr7:126675358-126675408	RPTEC	kidney:	n/a
38	chr7:126675528-126675578	SK-N-SH_RA	brain:	n/a
39	chr7:126615786-126615836	GM12892	blood:	n/a
40	chr7:126675528-126675578	GM12892	blood:	n/a
41	chr7:126675358-126675408	HIPEpiC	eye:	n/a
42	chr7:126615786-126615836	SK-N-SH_RA	brain:	n/a
43	chr7:126675528-126675578	ECC-1	luminal epithelium:	n/a
44	chr7:126615786-126615836	SK-N-SH	brain:	n/a
45	chr7:126615786-126615836	GM12891	blood:	n/a
46	chr7:126675358-126675408	SK-N-MC	brain:	n/a
47	chr7:126675528-126675578	HMEC	breast:	n/a
48	chr7:126615786-126615836	H1-hESC	embryonic stem cell:	embryo
49	chr7:126675358-126675408	U87	brain:	n/a
50	chr7:126675358-126675408	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:126612202..126614471-chr7:126617154..126618998,2	K562	blood:
2	chr7:126443207..126444075-chr7:126540061..126540769,2	MCF-7	breast:
3	7:126085913-126088095..7:126492401-126497300	GM12878	blood:
4	chr7:126634749..126637802-chr7:126647798..126650684,3	K562	blood:
5	7:126593467-126596179..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
6	chr7:126586006..126588015-chr7:126594826..126596374,2	MCF-7	breast:
7	7:126587367-126589276..7:126880504-126885902	H1-hESC	embryonic stem cell:	embryo
8	chr7:126634749..126636430-chr7:126647798..126650007,2	K562	blood:
9	chr7:126483492..126485257-chr7:126496192..126497874,2	K562	blood:
10	7:126085913-126088095..7:126639464-126642359	K562	blood:
11	chr7:126580578..126583397-chr7:126589821..126591578,2	MCF-7	breast:
12	chr7:126643620..126647077-chr7:126648157..126650582,3	K562	blood:
13	chr7:126577088..126579543-chr7:126581963..126584921,2	K562	blood:
14	7:126085913-126088095..7:126587367-126589276	H1-hESC	embryonic stem cell:	embryo
15	7:126085913-126088095..7:126662926-126671620	K562	blood:
16	7:126085913-126088095..7:126537894-126544517	GM12878	blood:
17	7:126085913-126088095..7:126563918-126569249	K562	blood:
18	7:126651745-126656082..7:126756671-126761022	H1-hESC	embryonic stem cell:	embryo
19	chr7:126580578..126583397-chr7:126589821..126591578,2	MCF-7	breast:
20	chr7:126492682..126494185-chr7:126494985..126497035,2	K562	blood:
21	chr7:126634749..126637802-chr7:126647798..126650684,3	K562	blood:
22	7:126587367-126589276..7:126733290-126737485	H1-hESC	embryonic stem cell:	embryo
23	chr7:126643620..126647077-chr7:126648157..126650582,3	K562	blood:
24	chr7:126612202..126614471-chr7:126617154..126618998,2	K562	blood:
25	chr7:126586006..126588015-chr7:126594826..126596374,2	MCF-7	breast:
26	7:126587367-126589276..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
27	7:126584558-126585048..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
28	chr10:97065210..97065763-chr7:126649354..126650093,2	MCF-7	breast:
29	7:126587367-126589276..7:126756671-126761022	H1-hESC	embryonic stem cell:	embryo
30	chr7:126577088..126579543-chr7:126581963..126584921,2	K562	blood:
31	chr7:126496786..126498746-chr7:126500529..126502173,2	MCF-7	breast:
32	7:126651745-126656082..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo
33	chr7:126634749..126636430-chr7:126647798..126650007,2	K562	blood:
34	chr7:126496786..126498746-chr7:126500529..126502173,2	MCF-7	breast:
35	7:126537894-126544517..7:126890676-126899918	H1-hESC	embryonic stem cell:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-15	chr7:126655663-126657210	ucscGeneNc_uc003vlv_2
2	lnc-ZNF800-7	chr7:126508821-126510586	NONHSAT123122
3	lnc-ARF5-15	chr7:126642417-126642543	ucscGeneNc_uc003vlv_2
4	lnc-ARF5-15	chr7:126646757-126646992	ucscGeneNc_uc003vlv_2

Variant related genes	Relation type
ENSG00000230820	TF binding region
ENSG00000224981	TF binding region
ENSG00000230820	CpG island
ENSG00000224981	CpG island
ENSG00000179603	chromatin interactions

Extended variants
information (count: 2953 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2953 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73723512	chr7:126494810-126494811	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530610837	chr7:126494931-126494932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539439254	chr7:126495026-126495027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150521720	chr7:126495038-126495039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs564063403	chr7:126495050-126495051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528387036	chr7:126495074-126495075	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs546956490	chr7:126495084-126495085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs193090881	chr7:126495108-126495109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529132280	chr7:126495124-126495125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs550782737	chr7:126495169-126495170	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569269408	chr7:126495210-126495211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183047774	chr7:126495238-126495239	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs114419875	chr7:126495258-126495259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566816334	chr7:126495340-126495341	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188080236	chr7:126495353-126495354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs28539218	chr7:126495382-126495383	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555684836	chr7:126495453-126495454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191338858	chr7:126495474-126495475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11428822	chr7:126495526-126495527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542243276	chr7:126495527-126495528	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs76883489	chr7:126495541-126495542	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs77503380	chr7:126495542-126495543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs538084252	chr7:126495556-126495557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568315226	chr7:126495593-126495594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556682713	chr7:126495680-126495681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183739616	chr7:126495706-126495707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545844895	chr7:126495728-126495729	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs4731333	chr7:126495742-126495743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564017517	chr7:126495756-126495757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs1204512	chr7:126495767-126495768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540213959	chr7:126495775-126495776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139456699	chr7:126495776-126495777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs529170112	chr7:126495787-126495788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550818953	chr7:126495828-126495829	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562653574	chr7:126495845-126495846	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533273934	chr7:126495914-126495915	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs551887833	chr7:126495925-126495926	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566845797	chr7:126495956-126495957	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs149753779	chr7:126496010-126496011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548950235	chr7:126496072-126496073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs7808572	chr7:126496138-126496139	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186580211	chr7:126496149-126496150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139177715	chr7:126496174-126496175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546930358	chr7:126496175-126496176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563536505	chr7:126496185-126496186	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377530066	chr7:126496186-126496187	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192689427	chr7:126496226-126496227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs555196717	chr7:126496279-126496280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139384158	chr7:126496281-126496282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538855046	chr7:126496311-126496312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Attention deficit hyperactivity disorder	22138692	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Malignant melanoma	17260012	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126493200-126495000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr7:126494200-126496600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:126495800-126496000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:126496600-126497000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:126496600-126497400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr7:126496600-126497400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr7:126496600-126497400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr7:126496800-126497400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:126496800-126498600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:126497000-126497400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr7:126497000-126497400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr7:126497000-126497400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr7:126497000-126497800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr7:126497400-126498400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:126497400-126498600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:126497400-126498600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:126497400-126498600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:126498600-126498800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr7:126498600-126498800	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr7:126498800-126499000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:126498800-126499000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:126498800-126499000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:126508200-126508400	Enhancers	Pancreas	Pancrea
24	chr7:126513600-126513800	Enhancers	Small Intestine	intestine
25	chr7:126516200-126517000	Enhancers	Hela-S3	cervix
26	chr7:126517000-126521400	Weak transcription	Hela-S3	cervix
27	chr7:126521400-126521600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr7:126521400-126521800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:126521400-126521800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr7:126521400-126521800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr7:126521400-126521800	Enhancers	Lung	lung
32	chr7:126521400-126521800	Enhancers	Hela-S3	cervix
33	chr7:126521600-126521800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:126521800-126523000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr7:126521800-126523000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr7:126521800-126523000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr7:126521800-126523200	Weak transcription	Hela-S3	cervix
38	chr7:126521800-126523400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:126521800-126523400	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr7:126522600-126523200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr7:126523000-126523200	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:126523000-126523200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:126523000-126523400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:126523000-126524000	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr7:126523200-126524000	Enhancers	Hela-S3	cervix
46	chr7:126523200-126527600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr7:126523400-126523800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr7:126523400-126524400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:126525000-126525400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:126525400-126527000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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