Variant report

Variant	nsv1015269
Chromosome Location	chr7:140412464-140458821
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	ARID3A	chr7:140441286-140441486	K562	blood:	n/a	n/a
2	ARID3A	chr7:140443757-140444069	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:140424401-140424425	K562	blood:	n/a	n/a
4	CEBPB	chr7:140452473-140452652	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
5	CEBPB	chr7:140422165-140422344	Hela-S3	cervix:	n/a	chr7:140422214-140422225
6	CEBPB	chr7:140428271-140428323	K562	blood:	n/a	n/a
7	CEBPB	chr7:140428147-140428649	IMR90	lung:	n/a	chr7:140428533-140428550
8	CEBPB	chr7:140452355-140452759	K562	blood:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
9	CEBPB	chr7:140452380-140452750	H1-hESC	embryonic stem cell:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
10	CEBPB	chr7:140452379-140452752	IMR90	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
11	CEBPB	chr7:140452362-140452751	ECC-1	luminal epithelium:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
12	CEBPB	chr7:140449718-140450079	HepG2	liver:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
13	CEBPB	chr7:140452370-140452755	ECC-1	luminal epithelium:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
14	CEBPB	chr7:140452370-140452718	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
15	CEBPB	chr7:140452194-140452743	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
16	CEBPB	chr7:140452392-140452752	Hela-S3	cervix:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
17	CEBPB	chr7:140422119-140422389	HepG2	liver:	n/a	chr7:140422214-140422225
18	CEBPB	chr7:140452286-140452756	A549	lung:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
19	CEBPB	chr7:140422179-140422436	K562	blood:	n/a	chr7:140422214-140422225
20	CEBPB	chr7:140452434-140452680	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
21	CEBPB	chr7:140452417-140452668	K562	blood:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
22	CEBPB	chr7:140449722-140450116	A549	lung:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
23	CEBPB	chr7:140452187-140452766	K562	blood:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
24	CEBPB	chr7:140449761-140450074	K562	blood:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
25	CEBPB	chr7:140452069-140452762	HepG2	liver:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
26	CEBPB	chr7:140452373-140452748	MCF-7	breast:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
27	CEBPB	chr7:140422034-140422410	ECC-1	luminal epithelium:	n/a	chr7:140422214-140422225
28	CEBPB	chr7:140452352-140452824	MCF-7	breast:	n/a	chr7:140452566-140452579 chr7:140452566-140452577
29	CEBPB	chr7:140422048-140422367	IMR90	lung:	n/a	chr7:140422214-140422225
30	CEBPB	chr7:140449735-140450037	A549	lung:	n/a	chr7:140449899-140449912 chr7:140449899-140449912 chr7:140449901-140449910 chr7:140449901-140449912 chr7:140449901-140449910 chr7:140449899-140449910 chr7:140449901-140449910 chr7:140449901-140449910
31	CEBPD	chr7:140441161-140441652	K562	blood:	n/a	n/a
32	CTCF	chr7:140426160-140426310	GM12875	blood:	n/a	n/a
33	CTCF	chr7:140426189-140426394	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr7:140426240-140426390	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr7:140440638-140440818	K562	blood:	n/a	chr7:140440717-140440738 chr7:140440723-140440739
36	CTCF	chr7:140433980-140434130	HPF	lung:	n/a	n/a
37	CTCF	chr7:140426260-140426410	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:140426200-140426350	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr7:140426240-140426390	AG04449	skin:	n/a	n/a
40	CTCF	chr7:140426260-140426410	HAc	cerebellar:	n/a	n/a
41	CTCF	chr7:140426200-140426350	GM12874	blood:	n/a	n/a
42	CTCF	chr7:140426240-140426390	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr7:140426240-140426390	GM12878	blood:	n/a	n/a
44	CTCF	chr7:140426200-140426350	SAEC	small airway:	n/a	n/a
45	CTCF	chr7:140426219-140426418	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr7:140426200-140426350	Caco-2	colon:	n/a	n/a
47	CTCF	chr7:140426240-140426390	GM12873	blood:	n/a	n/a
48	CTCF	chr7:140426180-140426330	GM12871	blood:	n/a	n/a
49	CTCF	chr7:140426280-140426430	HMEC	breast:	n/a	n/a
50	CTCF	chr7:140426029-140426575	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140454740-140454790	Jurkat	blood:	n/a
2	chr7:140452281-140452331	Hela-S3	cervix:	n/a
3	chr7:140454740-140454790	A549	lung:	n/a
4	chr7:140454740-140454790	AG10803	skin:	n/a
5	chr7:140452281-140452331	HCF	heart:	n/a
6	chr7:140454740-140454790	BE2_C	brain:	n/a
7	chr7:140452281-140452331	GM12892	blood:	n/a
8	chr7:140454740-140454790	MCF-7	breast:	n/a
9	chr7:140452281-140452331	SK-N-SH_RA	brain:	n/a
10	chr7:140452281-140452331	SK-N-SH	brain:	n/a
11	chr7:140454740-140454790	HepG2	liver:	n/a
12	chr7:140454740-140454790	U87	brain:	n/a
13	chr7:140454740-140454790	Hela-S3	cervix:	n/a
14	chr7:140452281-140452331	GM12878	blood:	n/a
15	chr7:140454740-140454790	SAEC	small airway:	n/a
16	chr7:140452281-140452331	A549	lung:	n/a
17	chr7:140452281-140452331	AoSMC	blood vessel:	n/a
18	chr7:140452281-140452331	ovcar-3	ovarian:	n/a
19	chr7:140454740-140454790	NHDF-neo	bronchial:	n/a
20	chr7:140454740-140454790	HCF	heart:	n/a
21	chr7:140452281-140452331	T-47D	breast:	n/a
22	chr7:140454740-140454790	NB4	blood:	n/a
23	chr7:140454740-140454790	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:140454740-140454790	IMR90	lung:	fetal
25	chr7:140452281-140452331	HCPEpiC	choroid plexus:	n/a
26	chr7:140454740-140454790	HRCEpiC	kidney:	n/a
27	chr7:140454740-140454790	HNPCEpiC	eye:	n/a
28	chr7:140452281-140452331	HNPCEpiC	eye:	n/a
29	chr7:140452281-140452331	ProgFib	skin:	n/a
30	chr7:140452281-140452331	BJ	skin:	n/a
31	chr7:140452281-140452331	U87	brain:	n/a
32	chr7:140454740-140454790	AG09309	skin:	n/a
33	chr7:140452281-140452331	HAEpiC	amniotic membrane:	n/a
34	chr7:140454740-140454790	PFSK-1	brain:	n/a
35	chr7:140452281-140452331	HL-60	blood:	n/a
36	chr7:140454740-140454790	AoSMC	blood vessel:	n/a
37	chr7:140454740-140454790	K562	blood:	n/a
38	chr7:140454740-140454790	PANC-1	pancreas:	n/a
39	chr7:140452281-140452331	SAEC	small airway:	n/a
40	chr7:140454740-140454790	AG04449	skin:	fetal
41	chr7:140452281-140452331	HRCEpiC	kidney:	n/a
42	chr7:140452281-140452331	BE2_C	brain:	n/a
43	chr7:140452281-140452331	Hepatocyte	liver:	n/a
44	chr7:140454740-140454790	HCPEpiC	choroid plexus:	n/a
45	chr7:140454740-140454790	Hepatocyte	liver:	n/a
46	chr7:140454740-140454790	HIPEpiC	eye:	n/a
47	chr7:140454740-140454790	NHBE	bronchial:	n/a
48	chr7:140454740-140454790	SK-N-SH_RA	brain:	n/a
49	chr7:140452281-140452331	H1-hESC	embryonic stem cell:	embryo
50	chr7:140452281-140452331	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:140443946..140445790-chr7:140457847..140460570,2	K562	blood:
2	chr7:140416340..140419154-chr7:140424735..140426861,2	MCF-7	breast:
3	chr7:140371637..140374196-chr7:140414800..140417349,2	MCF-7	breast:
4	chr7:140397557..140400522-chr7:140416030..140418868,2	K562	blood:
5	chr7:140394191..140397016-chr7:140424090..140426297,2	MCF-7	breast:
6	chr7:140371233..140372859-chr7:140417535..140420248,2	MCF-7	breast:
7	chr7:140434733..140440913-chr7:140443989..140447709,5	K562	blood:
8	chr7:140434733..140440913-chr7:140443989..140447709,5	K562	blood:
9	chr7:140427973..140429882-chr7:140713219..140714769,2	MCF-7	breast:
10	chr7:140416340..140419154-chr7:140424735..140426861,2	MCF-7	breast:
11	chr7:140394913..140398367-chr7:140415393..140417213,3	MCF-7	breast:
12	chr7:140442723..140444606-chr7:140448955..140450528,2	K562	blood:
13	chr7:140442723..140444606-chr7:140448955..140450528,2	K562	blood:
14	chr7:140396522..140398034-chr7:140415917..140417633,2	MCF-7	breast:
15	chr7:140425901..140426656-chr7:140683716..140684230,2	MCF-7	breast:
16	chr7:140421606..140424129-chr7:140426224..140428173,2	MCF-7	breast:
17	chr7:140421606..140424129-chr7:140426224..140428173,2	MCF-7	breast:
18	chr7:140449958..140452334-chr7:140454838..140457503,3	K562	blood:
19	chr7:140425877..140426809-chr7:140711477..140712513,4	MCF-7	breast:
20	chr7:140448573..140452334-chr7:140454838..140458113,4	K562	blood:
21	chr7:140416316..140418989-chr7:140421406..140423687,2	K562	blood:
22	chr7:140425976..140426774-chr7:140510803..140511321,2	MCF-7	breast:
23	chr7:140447067..140448647-chr7:140714489..140716015,2	MCF-7	breast:
24	chr7:140414826..140417259-chr7:140419669..140421264,2	K562	blood:
25	chr7:140442457..140444329-chr7:140447305..140448913,2	K562	blood:
26	chr7:140448573..140452334-chr7:140454838..140458113,4	K562	blood:
27	chr7:140424087..140425930-chr7:140432654..140434237,2	K562	blood:
28	chr7:140458046..140459583-chr7:140475705..140477212,2	K562	blood:
29	chr7:140423472..140425930-chr7:140432737..140435210,2	K562	blood:
30	chr7:140442457..140444329-chr7:140447305..140448913,2	K562	blood:
31	chr7:140395317..140397215-chr7:140414761..140416702,2	K562	blood:
32	chr7:140396319..140397970-chr7:140423059..140425912,3	K562	blood:
33	chr7:140423472..140425930-chr7:140432737..140435210,2	K562	blood:
34	chr7:140400483..140403338-chr7:140425369..140427117,2	K562	blood:
35	chr7:140429621..140431191-chr7:140448921..140450687,2	K562	blood:
36	chr7:140443740..140445240-chr7:140449142..140451877,2	MCF-7	breast:
37	chr7:140443946..140445790-chr7:140457847..140460570,2	K562	blood:
38	chr7:140449958..140452334-chr7:140454838..140457503,3	K562	blood:
39	chr7:140414826..140417259-chr7:140419669..140421264,2	K562	blood:
40	chr7:140425846..140426811-chr7:140711662..140712678,3	MCF-7	breast:
41	chr7:140414826..140417394-chr7:140419160..140421169,2	K562	blood:
42	chr7:140402003..140403554-chr7:140431273..140432954,2	MCF-7	breast:
43	chr7:140424087..140425930-chr7:140432654..140434237,2	K562	blood:
44	chr7:140443740..140445240-chr7:140449142..140451877,2	MCF-7	breast:
45	chr7:140396427..140399298-chr7:140424412..140427398,2	K562	blood:
46	chr7:140416316..140418989-chr7:140421406..140423687,2	K562	blood:
47	chr7:140414826..140417394-chr7:140419160..140421169,2	K562	blood:
48	chr7:140429621..140431191-chr7:140448921..140450687,2	K562	blood:
49	chr7:140395873..140397806-chr7:140448733..140451318,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRAF-1	chr7:140419138-140421887	NONHSAT123692
2	lnc-BRAF-1	chr7:140422072-140423908	NONHSAT123693
3	lnc-BRAF-1	chr7:140419593-140421126	NONHSAT123693
4	lnc-BRAF-1	chr7:140425329-140426316	NONHSAT123693
5	lnc-BRAF-1	chr7:140419138-140421228	NONHSAT123691

Variant related genes	Relation type
BRAF	TF binding region
BRAF	CpG island
ENSG00000240889	chromatin interactions
ENSG00000090263	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000146966	chromatin interactions
ENSG00000133597	chromatin interactions

Extended variants
information (count: 1634 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553655579	chr7:140412509-140412510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs578200429	chr7:140412530-140412531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10275183	chr7:140412536-140412537	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376034091	chr7:140412546-140412547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563737118	chr7:140412657-140412658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575432931	chr7:140412688-140412689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543154217	chr7:140412692-140412693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112530413	chr7:140412720-140412721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142918118	chr7:140412793-140412794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528886181	chr7:140412794-140412795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547100544	chr7:140412808-140412809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559266456	chr7:140412849-140412850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533084849	chr7:140412867-140412868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111939618	chr7:140412906-140412907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370838386	chr7:140412944-140412945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569912913	chr7:140413019-140413020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2907949	chr7:140413056-140413057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs549531433	chr7:140413105-140413106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564093840	chr7:140413109-140413110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567738432	chr7:140413119-140413120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528409415	chr7:140413162-140413163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367964563	chr7:140413191-140413192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371053001	chr7:140413198-140413199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184091835	chr7:140413199-140413200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553103330	chr7:140413201-140413202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577924327	chr7:140413225-140413226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375653619	chr7:140413226-140413227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539012617	chr7:140413239-140413240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368638940	chr7:140413240-140413241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557623827	chr7:140413257-140413258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575468064	chr7:140413298-140413299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200870828	chr7:140413301-140413302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144845695	chr7:140413307-140413308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561118909	chr7:140413345-140413346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573416952	chr7:140413351-140413352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372598032	chr7:140413354-140413355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559089572	chr7:140413372-140413373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187575427	chr7:140413374-140413375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545013534	chr7:140413403-140413404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192813533	chr7:140413424-140413425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375905742	chr7:140413425-140413426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549219533	chr7:140413439-140413440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183908005	chr7:140413440-140413441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6953568	chr7:140413459-140413460	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs547070571	chr7:140413481-140413482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571595687	chr7:140413523-140413524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539008032	chr7:140413551-140413552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10441168	chr7:140413569-140413570	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529291210	chr7:140413604-140413605	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569232560	chr7:140413620-140413621	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	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
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140398000-140419400	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:140398000-140466600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:140398200-140473800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr7:140398200-140492600	Weak transcription	Colonic Mucosa	Colon
5	chr7:140398400-140422000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:140398400-140432200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr7:140398600-140414800	Weak transcription	Small Intestine	intestine
8	chr7:140398600-140459400	Weak transcription	Brain Germinal Matrix	brain
9	chr7:140398600-140491800	Weak transcription	Fetal Brain Male	brain
10	chr7:140399400-140414200	Weak transcription	Gastric	stomach
11	chr7:140399400-140468200	Weak transcription	Right Ventricle	heart
12	chr7:140399600-140443800	Weak transcription	Fetal Heart	heart
13	chr7:140400000-140474000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:140404400-140452400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:140404800-140414200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr7:140404800-140419600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:140404800-140427600	Weak transcription	HSMMtube	muscle
18	chr7:140404800-140489000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr7:140404800-140517000	Weak transcription	Psoas Muscle	Psoas
20	chr7:140405200-140470800	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:140405600-140472200	Weak transcription	Brain Substantia Nigra	brain
22	chr7:140406000-140414200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:140406200-140418800	Weak transcription	Fetal Kidney	kidney
24	chr7:140406600-140414000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:140406600-140472800	Weak transcription	Hela-S3	cervix
26	chr7:140407000-140413800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr7:140407000-140414200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr7:140407000-140425600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:140407000-140425600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:140407000-140427400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr7:140407000-140427600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:140407000-140428800	Weak transcription	NHLF	lung
33	chr7:140407000-140454200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr7:140407000-140466800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:140407200-140413600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr7:140407200-140413800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr7:140407200-140413800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:140407200-140413800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:140407200-140413800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:140407200-140413800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr7:140407200-140413800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr7:140407200-140413800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr7:140407200-140413800	Weak transcription	Fetal Muscle Leg	muscle
44	chr7:140407200-140413800	Weak transcription	Fetal Stomach	stomach
45	chr7:140407200-140413800	Weak transcription	Thymus	Thymus
46	chr7:140407200-140414000	Weak transcription	Primary B cells from cord blood	blood
47	chr7:140407200-140414000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:140407200-140414000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:140407200-140414000	Weak transcription	Fetal Muscle Trunk	muscle
50	chr7:140407200-140414200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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