Variant report

Variant	nsv526062
Chromosome Location	chr7:103817597-103891085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1036)
CpG islands
(count:488)
Chromatin interactive
region (count:76)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103846505-103846671	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:103871982-103872175	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:103847939-103848441	K562	blood:	n/a	n/a
4	ATF1	chr7:103848018-103848733	K562	blood:	n/a	n/a
5	ATF2	chr7:103848068-103848919	GM12878	blood:	n/a	n/a
6	ATF3	chr7:103864757-103865170	K562	blood:	n/a	n/a
7	ATF3	chr7:103848070-103848638	A549	lung:	n/a	chr7:103848499-103848512
8	ATF3	chr7:103864889-103865078	K562	blood:	n/a	n/a
9	BACH1	chr7:103848242-103848683	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:103864786-103865120	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:103864836-103865036	K562	blood:	n/a	n/a
12	BCL3	chr7:103848157-103848739	A549	lung:	n/a	chr7:103848488-103848501
13	BCLAF1	chr7:103848130-103848774	GM12878	blood:	n/a	chr7:103848488-103848501
14	BCLAF1	chr7:103848209-103848904	GM12878	blood:	n/a	chr7:103848488-103848501
15	BHLHE40	chr7:103848180-103848729	K562	blood:	n/a	n/a
16	BHLHE40	chr7:103848253-103848821	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:103847075-103847327	K562	blood:	n/a	n/a
18	BHLHE40	chr7:103846992-103847195	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:103848084-103848661	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:103848249-103848661	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr7:103842955-103842976	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr7:103863482-103863741	K562	blood:	n/a	n/a
23	CBX3	chr7:103829097-103829441	K562	blood:	n/a	n/a
24	CBX3	chr7:103839285-103839705	K562	blood:	n/a	n/a
25	CBX3	chr7:103864702-103865262	HCT-116	colon:	n/a	n/a
26	CBX3	chr7:103860565-103860913	HCT-116	colon:	n/a	n/a
27	CBX3	chr7:103864720-103865228	K562	blood:	n/a	n/a
28	CBX3	chr7:103839082-103839761	K562	blood:	n/a	n/a
29	CBX3	chr7:103848213-103848707	K562	blood:	n/a	n/a
30	CBX3	chr7:103860649-103860996	K562	blood:	n/a	n/a
31	CBX3	chr7:103847789-103849355	K562	blood:	n/a	n/a
32	CCNT2	chr7:103848272-103848686	K562	blood:	n/a	n/a
33	CEBPB	chr7:103848273-103848563	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:103865027-103865192	A549	lung:	n/a	n/a
35	CEBPB	chr7:103848266-103848501	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:103847908-103848771	K562	blood:	n/a	n/a
37	CEBPB	chr7:103847882-103849114	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:103848240-103848477	K562	blood:	n/a	n/a
39	CEBPB	chr7:103847886-103848630	A549	lung:	n/a	n/a
40	CEBPB	chr7:103823526-103823546	HepG2	liver:	n/a	chr7:103823533-103823544
41	CEBPB	chr7:103847884-103848755	K562	blood:	n/a	n/a
42	CEBPB	chr7:103845855-103846035	K562	blood:	n/a	chr7:103845879-103845892 chr7:103845879-103845890 chr7:103845879-103845892
43	CEBPB	chr7:103864915-103865268	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:103865062-103865252	K562	blood:	n/a	n/a
45	CEBPB	chr7:103868750-103869248	MCF-7	breast:	n/a	n/a
46	CEBPB	chr7:103868816-103869262	MCF-7	breast:	n/a	n/a
47	CEBPB	chr7:103846382-103846625	HepG2	liver:	n/a	chr7:103846530-103846541
48	CEBPB	chr7:103847924-103848602	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:103847881-103848591	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:103847971-103848651	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103849187-103849237	AoSMC	blood vessel:	n/a
2	chr7:103871917-103871967	SAEC	small airway:	n/a
3	chr7:103848112-103848162	HIPEpiC	eye:	n/a
4	chr7:103849187-103849237	PrEC	prostate:	n/a
5	chr7:103848368-103848418	HRCEpiC	kidney:	n/a
6	chr7:103871917-103871967	K562	blood:	n/a
7	chr7:103848079-103848129	HRCEpiC	kidney:	n/a
8	chr7:103848368-103848418	HEK293	kidney:	embryo
9	chr7:103848802-103848852	AG10803	skin:	n/a
10	chr7:103871917-103871967	SK-N-MC	brain:	n/a
11	chr7:103848079-103848129	Jurkat	blood:	n/a
12	chr7:103848752-103848802	MCF10A-Er-Src	breast:	n/a
13	chr7:103848079-103848129	NB4	blood:	n/a
14	chr7:103848112-103848162	A549	lung:	n/a
15	chr7:103848802-103848852	NT2-D1	testis:	n/a
16	chr7:103848079-103848129	HIPEpiC	eye:	n/a
17	chr7:103848319-103848369	GM06990	blood:	n/a
18	chr7:103848752-103848802	Hela-S3	cervix:	n/a
19	chr7:103848112-103848162	HCM	heart:	n/a
20	chr7:103849187-103849237	HRCEpiC	kidney:	n/a
21	chr7:103848112-103848162	SK-N-SH_RA	brain:	n/a
22	chr7:103848319-103848369	HEK293	kidney:	embryo
23	chr7:103871917-103871967	ovcar-3	ovarian:	n/a
24	chr7:103849187-103849237	ProgFib	skin:	n/a
25	chr7:103848112-103848162	SK-N-SH	brain:	n/a
26	chr7:103849187-103849237	AG04450	lung:	fetal
27	chr7:103849187-103849237	GM12891	blood:	n/a
28	chr7:103871917-103871967	U87	brain:	n/a
29	chr7:103849187-103849237	HepG2	liver:	n/a
30	chr7:103848752-103848802	AoSMC	blood vessel:	n/a
31	chr7:103848752-103848802	LNCaP	prostate:	n/a
32	chr7:103848802-103848852	Jurkat	blood:	n/a
33	chr7:103848079-103848129	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:103848752-103848802	HEK293	kidney:	embryo
35	chr7:103848752-103848802	GM06990	blood:	n/a
36	chr7:103849187-103849237	HCT-116	colon:	n/a
37	chr7:103848752-103848802	A549	lung:	n/a
38	chr7:103848802-103848852	H1-hESC	embryonic stem cell:	embryo
39	chr7:103848802-103848852	PFSK-1	brain:	n/a
40	chr7:103848112-103848162	HMEC	breast:	n/a
41	chr7:103848319-103848369	PANC-1	pancreas:	n/a
42	chr7:103848368-103848418	SK-N-SH_RA	brain:	n/a
43	chr7:103871917-103871967	HCT-116	colon:	n/a
44	chr7:103848802-103848852	AG04450	lung:	fetal
45	chr7:103849187-103849237	Hepatocyte	liver:	n/a
46	chr7:103848112-103848162	AG10803	skin:	n/a
47	chr7:103871917-103871967	HepG2	liver:	n/a
48	chr7:103871917-103871967	LNCaP	prostate:	n/a
49	chr7:103848079-103848129	HEK293	kidney:	embryo
50	chr7:103848802-103848852	AG09309	skin:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:103814607..103816187-chr7:103821734..103824304,2	K562	blood:
2	chr7:103820510..103823425-chr7:103831806..103833927,2	MCF-7	breast:
3	chr7:103820510..103823425-chr7:103831806..103833927,2	MCF-7	breast:
4	chr7:103811783..103814415-chr7:103819771..103821551,2	K562	blood:
5	chr7:103826303..103828394-chr7:103832799..103835414,2	K562	blood:
6	chr7:103810117..103812021-chr7:103825452..103828315,2	K562	blood:
7	chr7:103826587..103829336-chr7:103841216..103843346,2	K562	blood:
8	chr7:103846124..103848372-chr7:103861589..103863576,2	MCF-7	breast:
9	chr7:103835421..103837340-chr7:103844960..103847432,2	K562	blood:
10	chr7:103839265..103844326-chr7:103845849..103850093,7	K562	blood:
11	chr7:103833753..103835540-chr7:103846175..103847854,2	K562	blood:
12	chr7:103825084..103829055-chr7:103846776..103849865,4	MCF-7	breast:
13	chr1:205600489..205601100-chr7:103847992..103848705,2	MCF-7	breast:
14	chr7:103814625..103817852-chr7:103818209..103821544,4	K562	blood:
15	chr7:103855618..103859131-chr7:103859954..103863291,3	MCF-7	breast:
16	chr7:103847842..103850053-chr7:103878233..103880195,2	MCF-7	breast:
17	chr7:103820850..103822660-chr7:103828536..103831512,3	K562	blood:
18	chr7:103847113..103849971-chr7:103857214..103859263,3	MCF-7	breast:
19	chr7:103835421..103837340-chr7:103844960..103847432,2	K562	blood:
20	chr7:103882149..103884182-chr7:103888404..103891368,2	K562	blood:
21	chr7:103858966..103863231-chr7:103865702..103869473,3	K562	blood:
22	chr7:103820850..103822660-chr7:103828536..103831512,3	K562	blood:
23	chr11:62608947..62609703-chr7:103847857..103848492,2	HCT-116	colon:
24	chr7:103815431..103817815-chr7:103822435..103824014,2	K562	blood:
25	chr7:103844120..103846835-chr7:103848105..103849807,2	MCF-7	breast:
26	chr7:103858966..103860906-chr7:103867973..103872038,3	K562	blood:
27	chr7:103831421..103833734-chr7:103840628..103842889,2	MCF-7	breast:
28	chr7:103815431..103817815-chr7:103822435..103824014,2	K562	blood:
29	chr7:103839985..103843508-chr7:103846553..103850027,4	MCF-7	breast:
30	chr7:103879381..103883166-chr7:103888951..103893508,5	MCF-7	breast:
31	chr7:103833753..103835540-chr7:103846175..103847854,2	K562	blood:
32	chr7:103825941..103829096-chr7:103846030..103849198,3	MCF-7	breast:
33	chr7:103882149..103884182-chr7:103888404..103891368,2	K562	blood:
34	chr7:103846534..103850528-chr7:103863639..103871951,9	MCF-7	breast:
35	chr7:103846683..103848713-chr7:103864388..103866402,2	K562	blood:
36	chr7:103871818..103872475-chr7:103907890..103908480,2	MCF-7	breast:
37	chr7:103855618..103859131-chr7:103859954..103863291,3	MCF-7	breast:
38	chr7:103879381..103883166-chr7:103888951..103893508,5	MCF-7	breast:
39	chr7:103628555..103630772-chr7:103847007..103849982,2	K562	blood:
40	chr7:103826587..103829336-chr7:103841216..103843346,2	K562	blood:
41	chr7:103831029..103833821-chr7:103834047..103836928,2	K562	blood:
42	chr7:103864521..103866383-chr7:103867413..103869166,2	MCF-7	breast:
43	chr7:103814625..103817852-chr7:103818209..103821544,4	K562	blood:
44	chr7:103809096..103810934-chr7:103815107..103817801,2	K562	blood:
45	chr1:174992554..174993204-chr7:103848517..103849356,2	Hela-S3	cervix:
46	chr7:103848404..103850130-chr7:104653038..104655393,2	MCF-7	breast:
47	chr7:103839347..103842114-chr7:103842519..103845580,4	K562	blood:
48	chr7:103871788..103872679-chr7:103892569..103893462,4	MCF-7	breast:
49	chr7:103833476..103836240-chr7:103847903..103849703,2	K562	blood:
50	chr7:103846992..103849875-chr7:103861564..103863128,2	K562	blood:

No data

Variant related genes	Relation type
ORC5	TF binding region
ORC5	CpG island
ENSG00000228393	chromatin interactions
ENSG00000197993	chromatin interactions
ENSG00000120333	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000005339	chromatin interactions
ENSG00000150764	chromatin interactions
ENSG00000164815	chromatin interactions
ENSG00000189056	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000113739	chromatin interactions
ENSG00000158711	chromatin interactions
ENSG00000130164	chromatin interactions

Extended variants
information (count: 2477 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2477 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6975834	chr7:103817597-103817598	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571038068	chr7:103817711-103817712	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs146012767	chr7:103817747-103817748	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs367791614	chr7:103817800-103817801	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372794427	chr7:103817832-103817833	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553276419	chr7:103817850-103817851	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574647981	chr7:103817855-103817856	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554826557	chr7:103817874-103817875	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535664243	chr7:103817880-103817881	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79475156	chr7:103817975-103817976	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575741971	chr7:103817999-103818000	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545857606	chr7:103818019-103818020	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564539843	chr7:103818056-103818057	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573090156	chr7:103818057-103818058	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375775918	chr7:103818078-103818079	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182122028	chr7:103818141-103818142	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60200486	chr7:103818153-103818154	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188046335	chr7:103818182-103818183	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143708622	chr7:103818184-103818185	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146806918	chr7:103818242-103818243	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562420134	chr7:103818256-103818257	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148514131	chr7:103818261-103818262	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551200361	chr7:103818262-103818263	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191932676	chr7:103818288-103818289	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533558976	chr7:103818290-103818291	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373187843	chr7:103818300-103818301	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564883639	chr7:103818333-103818334	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184090380	chr7:103818359-103818360	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188265658	chr7:103818418-103818419	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77971319	chr7:103818461-103818462	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192223967	chr7:103818480-103818481	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183159221	chr7:103818523-103818524	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531301299	chr7:103818556-103818557	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557974012	chr7:103818558-103818559	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187088126	chr7:103818574-103818575	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540669857	chr7:103818583-103818584	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555695582	chr7:103818649-103818650	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574010226	chr7:103818656-103818657	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151032573	chr7:103818658-103818659	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191948986	chr7:103818678-103818679	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115345599	chr7:103818679-103818680	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545044212	chr7:103818735-103818736	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12705185	chr7:103818780-103818781	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184321690	chr7:103818794-103818795	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10266337	chr7:103818822-103818823	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs146876114	chr7:103818823-103818824	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375888120	chr7:103818857-103818858	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529577500	chr7:103818859-103818860	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372751845	chr7:103818870-103818871	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189503690	chr7:103818883-103818884	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Basal cell lymphoma	17053054	CNVD

Chromatin state (count:1758 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103764000-103829800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:103764400-103820200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr7:103765600-103840200	Weak transcription	Small Intestine	intestine
4	chr7:103766200-103823600	Weak transcription	Esophagus	oesophagus
5	chr7:103766200-103838400	Weak transcription	Spleen	Spleen
6	chr7:103766400-103822600	Weak transcription	Colon Smooth Muscle	Colon
7	chr7:103767200-103829200	Weak transcription	Gastric	stomach
8	chr7:103767200-103843600	Weak transcription	Right Ventricle	heart
9	chr7:103767600-103820200	Weak transcription	Brain Germinal Matrix	brain
10	chr7:103769200-103822600	Weak transcription	Fetal Kidney	kidney
11	chr7:103771800-103820000	Weak transcription	NHEK	skin
12	chr7:103773200-103822800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr7:103775200-103829200	Weak transcription	Lung	lung
14	chr7:103776800-103820200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:103776800-103822800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr7:103777000-103819600	Weak transcription	Fetal Brain Female	brain
17	chr7:103777200-103819400	Weak transcription	GM12878-XiMat	blood
18	chr7:103777400-103819800	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr7:103781600-103822800	Weak transcription	HSMMtube	muscle
20	chr7:103781800-103822400	Weak transcription	Fetal Muscle Trunk	muscle
21	chr7:103791200-103822800	Weak transcription	Brain Anterior Caudate	brain
22	chr7:103791800-103819200	Weak transcription	HepG2	liver
23	chr7:103796400-103843600	Weak transcription	Fetal Brain Male	brain
24	chr7:103797200-103847000	Weak transcription	Fetal Heart	heart
25	chr7:103797400-103822600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:103798400-103829600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr7:103798600-103819600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:103800000-103822200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr7:103800800-103829600	Weak transcription	NHLF	lung
30	chr7:103801800-103818000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:103802200-103838600	Weak transcription	Psoas Muscle	Psoas
32	chr7:103802400-103822600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr7:103804200-103823000	Weak transcription	Thymus	Thymus
34	chr7:103804200-103824800	Weak transcription	Pancreas	Pancrea
35	chr7:103804800-103820200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr7:103805000-103819600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:103805000-103821800	Weak transcription	Fetal Stomach	stomach
38	chr7:103805000-103822600	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr7:103805200-103818800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr7:103805200-103819600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr7:103805200-103819600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr7:103805600-103819400	Weak transcription	Hela-S3	cervix
43	chr7:103805600-103820400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr7:103805600-103820400	Weak transcription	Fetal Intestine Large	intestine
45	chr7:103806000-103819600	Weak transcription	Osteobl	bone
46	chr7:103806000-103820200	Weak transcription	HMEC	breast
47	chr7:103806400-103820200	Weak transcription	Left Ventricle	heart
48	chr7:103806800-103820000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr7:103808000-103818800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr7:103808000-103820200	Weak transcription	NH-A	brain

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