Variant report

Variant	nsv1026481
Chromosome Location	chr7:103813522-103890770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:549)
Chromatin interactive
region (count:78)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:103815344-103815600	K562	blood:	n/a	n/a
2	ARID3A	chr7:103847939-103848441	K562	blood:	n/a	n/a
3	ARID3A	chr7:103846505-103846671	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:103871982-103872175	HepG2	liver:	n/a	n/a
5	ATF1	chr7:103848018-103848733	K562	blood:	n/a	n/a
6	ATF2	chr7:103848068-103848919	GM12878	blood:	n/a	n/a
7	ATF3	chr7:103864757-103865170	K562	blood:	n/a	n/a
8	ATF3	chr7:103864889-103865078	K562	blood:	n/a	n/a
9	ATF3	chr7:103848070-103848638	A549	lung:	n/a	chr7:103848499-103848512
10	BACH1	chr7:103864786-103865120	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:103848242-103848683	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:103864836-103865036	K562	blood:	n/a	n/a
13	BCL3	chr7:103848157-103848739	A549	lung:	n/a	chr7:103848488-103848501
14	BCLAF1	chr7:103848209-103848904	GM12878	blood:	n/a	chr7:103848488-103848501
15	BCLAF1	chr7:103848130-103848774	GM12878	blood:	n/a	chr7:103848488-103848501
16	BHLHE40	chr7:103846992-103847195	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:103848180-103848729	K562	blood:	n/a	n/a
18	BHLHE40	chr7:103848253-103848821	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:103847075-103847327	K562	blood:	n/a	n/a
20	BHLHE40	chr7:103815189-103815625	K562	blood:	n/a	n/a
21	BRCA1	chr7:103848249-103848661	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:103848084-103848661	GM12878	blood:	n/a	n/a
23	BRCA1	chr7:103842955-103842976	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr7:103864702-103865262	HCT-116	colon:	n/a	n/a
25	CBX3	chr7:103847789-103849355	K562	blood:	n/a	n/a
26	CBX3	chr7:103848213-103848707	K562	blood:	n/a	n/a
27	CBX3	chr7:103864720-103865228	K562	blood:	n/a	n/a
28	CBX3	chr7:103839285-103839705	K562	blood:	n/a	n/a
29	CBX3	chr7:103839082-103839761	K562	blood:	n/a	n/a
30	CBX3	chr7:103815102-103815647	K562	blood:	n/a	n/a
31	CBX3	chr7:103860649-103860996	K562	blood:	n/a	n/a
32	CBX3	chr7:103863482-103863741	K562	blood:	n/a	n/a
33	CBX3	chr7:103860565-103860913	HCT-116	colon:	n/a	n/a
34	CBX3	chr7:103829097-103829441	K562	blood:	n/a	n/a
35	CCNT2	chr7:103815423-103815623	K562	blood:	n/a	n/a
36	CCNT2	chr7:103848272-103848686	K562	blood:	n/a	n/a
37	CEBPB	chr7:103864968-103865272	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:103868816-103869262	MCF-7	breast:	n/a	n/a
39	CEBPB	chr7:103848240-103848477	K562	blood:	n/a	n/a
40	CEBPB	chr7:103846382-103846625	HepG2	liver:	n/a	chr7:103846530-103846541
41	CEBPB	chr7:103848266-103848501	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:103847971-103848651	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:103847924-103848602	IMR90	lung:	n/a	n/a
44	CEBPB	chr7:103868750-103869248	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:103847908-103848771	K562	blood:	n/a	n/a
46	CEBPB	chr7:103845855-103846035	K562	blood:	n/a	chr7:103845879-103845892 chr7:103845879-103845890 chr7:103845879-103845892
47	CEBPB	chr7:103847886-103848630	A549	lung:	n/a	n/a
48	CEBPB	chr7:103847884-103848755	K562	blood:	n/a	n/a
49	CEBPB	chr7:103864915-103865268	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:103848273-103848563	H1-hESC	embryonic stem cell:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:103848368-103848418	NB4	blood:	n/a
2	chr7:103849187-103849237	RPTEC	kidney:	n/a
3	chr7:103848368-103848418	HRPEpiC	eye:	n/a
4	chr7:103848802-103848852	HRE	kidney:	n/a
5	chr7:103848112-103848162	NHBE	bronchial:	n/a
6	chr7:103848319-103848369	HepG2	liver:	n/a
7	chr7:103815074-103815124	SK-N-SH	brain:	n/a
8	chr7:103849187-103849237	K562	blood:	n/a
9	chr7:103849187-103849237	Caco-2	colon:	n/a
10	chr7:103848112-103848162	ProgFib	skin:	n/a
11	chr7:103848079-103848129	PrEC	prostate:	n/a
12	chr7:103848368-103848418	SAEC	small airway:	n/a
13	chr7:103848752-103848802	GM06990	blood:	n/a
14	chr7:103871917-103871967	NT2-D1	testis:	n/a
15	chr7:103849187-103849237	SK-N-MC	brain:	n/a
16	chr7:103848752-103848802	HL-60	blood:	n/a
17	chr7:103848079-103848129	AG09309	skin:	n/a
18	chr7:103848802-103848852	ovcar-3	ovarian:	n/a
19	chr7:103848112-103848162	HAEpiC	amniotic membrane:	n/a
20	chr7:103848752-103848802	HRCEpiC	kidney:	n/a
21	chr7:103849187-103849237	ProgFib	skin:	n/a
22	chr7:103871917-103871967	AG09309	skin:	n/a
23	chr7:103848319-103848369	SK-N-SH_RA	brain:	n/a
24	chr7:103848079-103848129	HAEpiC	amniotic membrane:	n/a
25	chr7:103848752-103848802	RPTEC	kidney:	n/a
26	chr7:103848368-103848418	BJ	skin:	n/a
27	chr7:103848112-103848162	ECC-1	luminal epithelium:	n/a
28	chr7:103848112-103848162	SK-N-MC	brain:	n/a
29	chr7:103849187-103849237	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:103848368-103848418	AoSMC	blood vessel:	n/a
31	chr7:103848802-103848852	NB4	blood:	n/a
32	chr7:103849187-103849237	HCPEpiC	choroid plexus:	n/a
33	chr7:103848079-103848129	T-47D	breast:	n/a
34	chr7:103815074-103815124	HepG2	liver:	n/a
35	chr7:103848112-103848162	HCT-116	colon:	n/a
36	chr7:103848112-103848162	AG04450	lung:	fetal
37	chr7:103848752-103848802	HMEC	breast:	n/a
38	chr7:103849187-103849237	SK-N-SH	brain:	n/a
39	chr7:103871917-103871967	ovcar-3	ovarian:	n/a
40	chr7:103848752-103848802	T-47D	breast:	n/a
41	chr7:103848368-103848418	K562	blood:	n/a
42	chr7:103815074-103815124	SK-N-SH_RA	brain:	n/a
43	chr7:103815074-103815124	ovcar-3	ovarian:	n/a
44	chr7:103848112-103848162	GM19239	blood:	n/a
45	chr7:103848112-103848162	GM12878	blood:	n/a
46	chr7:103848368-103848418	NH-A	brain:	n/a
47	chr7:103849187-103849237	A549	lung:	n/a
48	chr7:103848112-103848162	AG10803	skin:	n/a
49	chr7:103848079-103848129	U87	brain:	n/a
50	chr7:103848112-103848162	SKMC	muscle:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:103839985..103843508-chr7:103846553..103850027,4	MCF-7	breast:
2	chr7:103864521..103866383-chr7:103867413..103869166,2	MCF-7	breast:
3	chr7:103815431..103817815-chr7:103822435..103824014,2	K562	blood:
4	chr1:174992554..174993204-chr7:103848517..103849356,2	Hela-S3	cervix:
5	chr7:103832288..103834707-chr7:103835398..103837117,2	MCF-7	breast:
6	chr7:103855618..103859131-chr7:103859954..103863291,3	MCF-7	breast:
7	chr7:103826365..103828969-chr7:103829886..103833367,4	K562	blood:
8	chr7:103832288..103834707-chr7:103835398..103837117,2	MCF-7	breast:
9	chr7:103814607..103816187-chr7:103821734..103824304,2	K562	blood:
10	chr7:103871547..103872530-chr7:104558465..104559716,7	K562	blood:
11	chr7:103831421..103833734-chr7:103840628..103842889,2	MCF-7	breast:
12	chr7:103839347..103842114-chr7:103842519..103845580,4	K562	blood:
13	chr7:103820850..103822660-chr7:103828536..103831512,3	K562	blood:
14	chr7:103826303..103828394-chr7:103832799..103835414,2	K562	blood:
15	chr7:103871788..103872679-chr7:103892569..103893462,4	MCF-7	breast:
16	chr7:103858966..103863231-chr7:103865702..103869473,3	K562	blood:
17	chr7:103835421..103837340-chr7:103844960..103847432,2	K562	blood:
18	chr7:103825941..103829096-chr7:103846030..103849198,3	MCF-7	breast:
19	chr7:103846497..103848385-chr7:103909952..103912269,2	MCF-7	breast:
20	chr7:103831421..103833734-chr7:103840628..103842889,2	MCF-7	breast:
21	chr7:103814625..103817852-chr7:103818209..103821544,4	K562	blood:
22	chr7:103826587..103829336-chr7:103841216..103843346,2	K562	blood:
23	chr7:103846910..103851184-chr7:103856864..103861366,6	MCF-7	breast:
24	chr7:103858966..103860906-chr7:103867973..103872038,3	K562	blood:
25	chr7:103858966..103863231-chr7:103865702..103869473,3	K562	blood:
26	chr7:103833753..103835540-chr7:103846175..103847854,2	K562	blood:
27	chr7:103831029..103833821-chr7:103834047..103836928,2	K562	blood:
28	chr7:103855618..103859131-chr7:103859954..103863291,3	MCF-7	breast:
29	chr7:103879381..103883166-chr7:103888951..103893508,5	MCF-7	breast:
30	chr7:103846992..103849875-chr7:103861564..103863128,2	K562	blood:
31	chr7:103865736..103867349-chr7:104538878..104541224,2	MCF-7	breast:
32	chr7:103844120..103846835-chr7:103848105..103849807,2	MCF-7	breast:
33	chr7:103890321..103892926-chr7:103895199..103897765,2	K562	blood:
34	chr7:103820510..103823425-chr7:103831806..103833927,2	MCF-7	breast:
35	chr7:103815431..103817815-chr7:103822435..103824014,2	K562	blood:
36	chr7:103814607..103816187-chr7:103821734..103824304,2	K562	blood:
37	chr11:111797157..111798115-chr7:103848389..103849351,2	NB4	blood:
38	chr7:103820510..103823425-chr7:103831806..103833927,2	MCF-7	breast:
39	chr7:103826365..103828969-chr7:103829886..103833367,4	K562	blood:
40	chr7:103858966..103860906-chr7:103867973..103872038,3	K562	blood:
41	chr7:103846683..103848713-chr7:103864388..103866402,2	K562	blood:
42	chr16:3930315..3931064-chr7:103847985..103848730,2	HCT-116	colon:
43	chr7:103847842..103850053-chr7:103878233..103880195,2	MCF-7	breast:
44	chr7:103809096..103810934-chr7:103815107..103817801,2	K562	blood:
45	chr7:103628555..103630772-chr7:103847007..103849982,2	K562	blood:
46	chr7:103882149..103884182-chr7:103888404..103891368,2	K562	blood:
47	chr7:103814625..103817852-chr7:103818209..103821544,4	K562	blood:
48	chr7:103820850..103822660-chr7:103828536..103831512,3	K562	blood:
49	chr7:103833476..103836240-chr7:103847903..103849703,2	K562	blood:
50	chr7:103848404..103850130-chr7:104653038..104655393,2	MCF-7	breast:

No data

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

Extended variants
information (count: 2645 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2645 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7804535	chr7:103813522-103813523	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567027751	chr7:103813530-103813531	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551835006	chr7:103813535-103813536	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76501964	chr7:103813539-103813540	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555792354	chr7:103813540-103813541	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113363908	chr7:103813547-103813548	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538236415	chr7:103813583-103813584	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556621829	chr7:103813602-103813603	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs181591765	chr7:103813633-103813634	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs577985796	chr7:103813738-103813739	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs183748863	chr7:103813825-103813826	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553801919	chr7:103813850-103813851	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188299918	chr7:103813866-103813867	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181835551	chr7:103813868-103813869	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572158179	chr7:103813938-103813939	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542466275	chr7:103813949-103813950	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10275484	chr7:103813984-103813985	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537494137	chr7:103813999-103814000	Strong transcription Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570360173	chr7:103814015-103814016	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12705181	chr7:103814044-103814045	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs373257134	chr7:103814047-103814048	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549707322	chr7:103814091-103814092	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564507179	chr7:103814107-103814108	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532034360	chr7:103814118-103814119	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552006189	chr7:103814125-103814126	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567063431	chr7:103814157-103814158	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527879497	chr7:103814168-103814169	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149212795	chr7:103814175-103814176	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567738297	chr7:103814184-103814185	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538373439	chr7:103814190-103814191	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558678610	chr7:103814200-103814201	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571588015	chr7:103814233-103814234	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577897546	chr7:103814248-103814249	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56821345	chr7:103814264-103814265	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs186489341	chr7:103814276-103814277	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374824655	chr7:103814287-103814288	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565005850	chr7:103814293-103814294	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59535311	chr7:103814301-103814302	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71154394	chr7:103814310-103814311	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12705183	chr7:103814315-103814316	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12705184	chr7:103814332-103814333	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs543087312	chr7:103814353-103814354	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564643312	chr7:103814355-103814356	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576734228	chr7:103814368-103814369	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540714092	chr7:103814381-103814382	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10233580	chr7:103814400-103814401	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549580644	chr7:103814444-103814445	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538616963	chr7:103814449-103814450	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561431600	chr7:103814453-103814454	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373870214	chr7:103814482-103814483	Weak transcription ZNF genes & repeats 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:1884 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103763800-103815000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:103764000-103829800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:103764400-103820200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr7:103765600-103815000	Weak transcription	Brain Angular Gyrus	brain
5	chr7:103765600-103840200	Weak transcription	Small Intestine	intestine
6	chr7:103766200-103816000	Weak transcription	Brain Substantia Nigra	brain
7	chr7:103766200-103823600	Weak transcription	Esophagus	oesophagus
8	chr7:103766200-103838400	Weak transcription	Spleen	Spleen
9	chr7:103766400-103822600	Weak transcription	Colon Smooth Muscle	Colon
10	chr7:103767200-103829200	Weak transcription	Gastric	stomach
11	chr7:103767200-103843600	Weak transcription	Right Ventricle	heart
12	chr7:103767600-103820200	Weak transcription	Brain Germinal Matrix	brain
13	chr7:103769200-103822600	Weak transcription	Fetal Kidney	kidney
14	chr7:103771800-103820000	Weak transcription	NHEK	skin
15	chr7:103773200-103822800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr7:103775200-103829200	Weak transcription	Lung	lung
17	chr7:103776800-103820200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr7:103776800-103822800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:103777000-103819600	Weak transcription	Fetal Brain Female	brain
20	chr7:103777200-103819400	Weak transcription	GM12878-XiMat	blood
21	chr7:103777400-103819800	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr7:103779200-103815000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:103779200-103815000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:103781600-103822800	Weak transcription	HSMMtube	muscle
25	chr7:103781800-103822400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr7:103791200-103822800	Weak transcription	Brain Anterior Caudate	brain
27	chr7:103791800-103819200	Weak transcription	HepG2	liver
28	chr7:103792800-103815000	Weak transcription	Aorta	Aorta
29	chr7:103796400-103843600	Weak transcription	Fetal Brain Male	brain
30	chr7:103797200-103847000	Weak transcription	Fetal Heart	heart
31	chr7:103797400-103822600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:103797600-103817000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr7:103798400-103815000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:103798400-103829600	Weak transcription	Rectal Smooth Muscle	rectum
35	chr7:103798600-103819600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr7:103800000-103822200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr7:103800200-103815000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:103800800-103829600	Weak transcription	NHLF	lung
39	chr7:103801800-103818000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:103802200-103838600	Weak transcription	Psoas Muscle	Psoas
41	chr7:103802400-103822600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:103804200-103823000	Weak transcription	Thymus	Thymus
43	chr7:103804200-103824800	Weak transcription	Pancreas	Pancrea
44	chr7:103804800-103813800	Weak transcription	Ovary	ovary
45	chr7:103804800-103820200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:103805000-103819600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:103805000-103821800	Weak transcription	Fetal Stomach	stomach
48	chr7:103805000-103822600	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:103805200-103815000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:103805200-103816000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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