Variant report

Variant	nsv539050
Chromosome Location	chr7:105018374-105153618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2377)
CpG islands
(count:1222)
Chromatin interactive
region (count:152)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2377 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
2	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
3	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
5	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
7	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
8	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
11	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
12	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
13	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
14	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
15	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
16	BACH1	chr7:105029716-105030051	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:105028171-105028753	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:105042903-105043365	K562	blood:	n/a	n/a
19	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a
20	BACH1	chr7:105027844-105028042	K562	blood:	n/a	n/a
21	BACH1	chr7:105029014-105029308	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:105113662-105113870	K562	blood:	n/a	n/a
23	BACH1	chr7:105113653-105113991	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr7:105041762-105041974	GM12878	blood:	n/a	n/a
25	BATF	chr7:105084864-105085128	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:105029678-105029984	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:105029661-105030115	K562	blood:	n/a	chr7:105029666-105029682
28	BHLHE40	chr7:105042095-105042394	K562	blood:	n/a	n/a
29	BHLHE40	chr7:105128299-105128701	K562	blood:	n/a	n/a
30	BHLHE40	chr7:105029124-105029187	K562	blood:	n/a	n/a
31	BHLHE40	chr7:105028352-105028581	GM12878	blood:	n/a	chr7:105028425-105028441
32	BHLHE40	chr7:105028285-105028701	K562	blood:	n/a	chr7:105028425-105028441
33	BHLHE40	chr7:105088647-105088769	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:105039812-105040017	K562	blood:	n/a	n/a
35	BRCA1	chr7:105029780-105029800	GM12878	blood:	n/a	n/a
36	BRCA1	chr7:105029695-105029834	HepG2	liver:	n/a	n/a
37	CBX3	chr7:105034985-105035371	K562	blood:	n/a	n/a
38	CBX3	chr7:105042025-105042557	HCT-116	colon:	n/a	n/a
39	CBX3	chr7:105041976-105042503	K562	blood:	n/a	n/a
40	CCNT2	chr7:105028142-105029984	K562	blood:	n/a	chr7:105028594-105028603 chr7:105029564-105029573
41	CCNT2	chr7:105042201-105042473	K562	blood:	n/a	n/a
42	CCNT2	chr7:105128383-105128706	K562	blood:	n/a	chr7:105128481-105128501
43	CEBPB	chr7:105091342-105091701	A549	lung:	n/a	chr7:105091512-105091523
44	CEBPB	chr7:105091327-105091705	IMR90	lung:	n/a	chr7:105091512-105091523
45	CEBPB	chr7:105058039-105058281	K562	blood:	n/a	n/a
46	CEBPB	chr7:105134424-105134917	IMR90	lung:	n/a	chr7:105134761-105134778
47	CEBPB	chr7:105070146-105070591	MCF-7	breast:	n/a	chr7:105070571-105070583
48	CEBPB	chr7:105091412-105091705	MCF-7	breast:	n/a	chr7:105091512-105091523
49	CEBPB	chr7:105039451-105039665	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:105113654-105113964	A549	lung:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105029385-105029435	AG04450	lung:	fetal
2	chr7:105110948-105110998	HMEC	breast:	n/a
3	chr7:105029385-105029435	AG04450	lung:	fetal
4	chr7:105110948-105110998	HMEC	breast:	n/a
5	chr7:105029895-105029945	CMK	blood:	n/a
6	chr7:105029485-105029535	Hepatocyte	liver:	n/a
7	chr7:105028539-105028589	GM06990	blood:	n/a
8	chr7:105029385-105029435	Caco-2	colon:	n/a
9	chr7:105094993-105095043	BE2_C	brain:	n/a
10	chr7:105030752-105030802	Hela-S3	cervix:	n/a
11	chr7:105029499-105029549	T-47D	breast:	n/a
12	chr7:105110948-105110998	MCF10A-Er-Src	breast:	n/a
13	chr7:105029497-105029547	SK-N-MC	brain:	n/a
14	chr7:105137683-105137733	NH-A	brain:	n/a
15	chr7:105029895-105029945	SAEC	small airway:	n/a
16	chr7:105028539-105028589	ovcar-3	ovarian:	n/a
17	chr7:105128488-105128538	IMR90	lung:	fetal
18	chr7:105029497-105029547	AG09319	gingival:	n/a
19	chr7:105029492-105029542	PrEC	prostate:	n/a
20	chr7:105027541-105027591	MCF-7	breast:	n/a
21	chr7:105112740-105112790	CMK	blood:	n/a
22	chr7:105029492-105029542	NH-A	brain:	n/a
23	chr7:105026171-105026221	SKMC	muscle:	n/a
24	chr7:105128488-105128538	SK-N-SH	brain:	n/a
25	chr7:105097168-105097218	SK-N-SH_RA	brain:	n/a
26	chr7:105029485-105029535	HRCEpiC	kidney:	n/a
27	chr7:105029492-105029542	ovcar-3	ovarian:	n/a
28	chr7:105029125-105029175	HRCEpiC	kidney:	n/a
29	chr7:105029385-105029435	HCM	heart:	n/a
30	chr7:105029895-105029945	HNPCEpiC	eye:	n/a
31	chr7:105029497-105029547	Hela-S3	cervix:	n/a
32	chr7:105029385-105029435	NT2-D1	testis:	n/a
33	chr7:105030752-105030802	HAEpiC	amniotic membrane:	n/a
34	chr7:105079663-105079713	NH-A	brain:	n/a
35	chr7:105137683-105137733	GM12891	blood:	n/a
36	chr7:105110948-105110998	BJ	skin:	n/a
37	chr7:105029895-105029945	HMEC	breast:	n/a
38	chr7:105029895-105029945	HRPEpiC	eye:	n/a
39	chr7:105137683-105137733	GM06990	blood:	n/a
40	chr7:105110948-105110998	HCT-116	colon:	n/a
41	chr7:105137683-105137733	ECC-1	luminal epithelium:	n/a
42	chr7:105079663-105079713	PrEC	prostate:	n/a
43	chr7:105027541-105027591	HEK293	kidney:	embryo
44	chr7:105029485-105029535	NT2-D1	testis:	n/a
45	chr7:105029385-105029435	GM19239	blood:	n/a
46	chr7:105030752-105030802	HCF	heart:	n/a
47	chr7:105026171-105026221	CMK	blood:	n/a
48	chr7:105137683-105137733	HRE	kidney:	n/a
49	chr7:105029497-105029547	A549	lung:	n/a
50	chr7:105027541-105027591	BE2_C	brain:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:105083940..105087066-chr7:105087136..105090105,3	K562	blood:
2	chr7:105039769..105040575-chr7:105229933..105230493,2	MCF-7	breast:
3	chr7:105033753..105035269-chr7:105037769..105040166,2	K562	blood:
4	chr7:105039517..105040114-chr7:105128184..105128801,2	MCF-7	breast:
5	chr7:105135383..105138778-chr7:105145127..105148143,3	MCF-7	breast:
6	chr7:104981388..104983616-chr7:105078711..105081522,2	MCF-7	breast:
7	chr7:105115487..105117775-chr7:105123011..105125006,2	K562	blood:
8	chr7:105019911..105021910-chr7:105024677..105026313,2	K562	blood:
9	chr7:105143576..105146396-chr7:105147042..105149947,3	K562	blood:
10	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
11	chr7:105103194..105105383-chr7:105105621..105108054,3	K562	blood:
12	chr7:105111430..105113564-chr7:105117315..105119361,2	K562	blood:
13	chr7:105070328..105070998-chr7:105230063..105230628,2	K562	blood:
14	chr7:104793384..104794011-chr7:105128109..105129098,2	MCF-7	breast:
15	chr7:105012234..105014245-chr7:105022510..105026066,3	K562	blood:
16	chr7:105078097..105081437-chr7:105081895..105086252,7	MCF-7	breast:
17	chr7:105038386..105041784-chr7:105078829..105081619,3	MCF-7	breast:
18	chr7:105026975..105030937-chr7:105032940..105036440,7	K562	blood:
19	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
20	chr7:105116272..105117859-chr7:105118414..105120932,2	K562	blood:
21	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:
22	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
23	chr7:105128652..105130431-chr7:105155897..105157484,2	MCF-7	breast:
24	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
25	chr7:105093737..105097449-chr7:105099816..105103606,4	K562	blood:
26	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
27	chr7:105141175..105142796-chr7:105145360..105147513,2	MCF-7	breast:
28	chr7:105041648..105042543-chr7:105069609..105070839,7	MCF-7	breast:
29	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
30	chr7:104757007..104759673-chr7:105027481..105029991,2	MCF-7	breast:
31	chr7:104649601..104653676-chr7:105029497..105032094,4	K562	blood:
32	chr7:105069861..105070836-chr7:105128119..105128880,2	MCF-7	breast:
33	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
34	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
35	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
36	chr7:105029590..105031238-chr7:105038445..105041248,2	MCF-7	breast:
37	chr7:105012623..105015003-chr7:105017126..105018970,2	MCF-7	breast:
38	chr7:105069861..105070836-chr7:105128119..105128880,2	MCF-7	breast:
39	chr7:105041915..105043798-chr7:105045520..105047244,3	K562	blood:
40	chr7:105123891..105126807-chr7:105127065..105130619,3	K562	blood:
41	chr7:104653578..104656991-chr7:105040264..105042441,3	MCF-7	breast:
42	chr7:105038088..105039818-chr7:105043302..105044810,2	K562	blood:
43	chr7:105125271..105127106-chr7:105136833..105138910,2	K562	blood:
44	chr7:104621410..104622279-chr7:105069837..105070818,3	K562	blood:
45	chr7:105027932..105031943-chr7:105036648..105042469,7	K562	blood:
46	chr7:105129866..105132116-chr7:105135974..105138549,2	K562	blood:
47	chr7:105111430..105113380-chr7:105117315..105120062,2	K562	blood:
48	chr7:105039956..105042512-chr7:105104408..105106506,2	K562	blood:
49	chr7:105041786..105042328-chr7:105128303..105129103,3	MCF-7	breast:
50	chr7:105030763..105032789-chr7:105035167..105036681,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614
2	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PUS7	hsa-miR-32-5p	chr7:105098074-105098095
2	PUS7	hsa-miR-155-5p	chr7:105097684-105097705

Variant related genes	Relation type
PUS7	TF binding region
SRPK2	TF binding region
PUS7	CpG island
SRPK2	CpG island
ENSG00000091127	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000080298	chromatin interactions

Extended variants
information (count: 5188 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5188 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536808160	chr7:105018439-105018440	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs541147074	chr7:105018444-105018445	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs560940204	chr7:105018462-105018463	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs570008041	chr7:105018476-105018477	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs537490952	chr7:105018592-105018593	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs185628487	chr7:105018609-105018610	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs571041978	chr7:105018616-105018617	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs67678290	chr7:105018663-105018664	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372749025	chr7:105018664-105018665	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76975839	chr7:105018679-105018680	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs79863941	chr7:105018680-105018681	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs533374486	chr7:105018714-105018715	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs533665290	chr7:105018737-105018738	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs188892429	chr7:105018801-105018802	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs144635854	chr7:105018811-105018812	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531518399	chr7:105018830-105018831	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs193153038	chr7:105018835-105018836	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs551478063	chr7:105018853-105018854	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576383582	chr7:105018870-105018871	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs545454178	chr7:105018960-105018961	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs565297604	chr7:105018983-105018984	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570811697	chr7:105018994-105018995	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs549491643	chr7:105019006-105019007	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs185322140	chr7:105019012-105019013	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs368957567	chr7:105019031-105019032	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs139392031	chr7:105019039-105019040	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs571006447	chr7:105019047-105019048	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs538306505	chr7:105019053-105019054	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs189099997	chr7:105019073-105019074	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs532649898	chr7:105019142-105019143	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs144120312	chr7:105019156-105019157	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112615342	chr7:105019159-105019160	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs533733970	chr7:105019185-105019186	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs553594397	chr7:105019200-105019201	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs181079041	chr7:105019204-105019205	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs35549009	chr7:105019208-105019209	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs111661001	chr7:105019209-105019210	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs536085876	chr7:105019226-105019227	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs75833619	chr7:105019279-105019280	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs556379118	chr7:105019287-105019288	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs576271796	chr7:105019309-105019310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs545345688	chr7:105019320-105019321	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs558846309	chr7:105019341-105019342	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs7357199	chr7:105019355-105019356	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541409090	chr7:105019421-105019422	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs184266989	chr7:105019423-105019424	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs117825161	chr7:105019424-105019425	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs530185760	chr7:105019505-105019506	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570118216	chr7:105019519-105019520	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs543640247	chr7:105019525-105019526	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
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
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16573809	CNVD
Myxofibrosarcoma	20639860	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2336 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104995200-105028200	Weak transcription	Esophagus	oesophagus
2	chr7:104995400-105028000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:104995600-105027200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:104995800-105027200	Weak transcription	Primary T cells from cord blood	blood
5	chr7:104997400-105026800	Weak transcription	Primary B cells from cord blood	blood
6	chr7:105000000-105021800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr7:105000000-105028200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:105000200-105025800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:105003200-105027600	Weak transcription	Fetal Intestine Small	intestine
10	chr7:105003600-105025200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:105005000-105021200	Weak transcription	Fetal Stomach	stomach
12	chr7:105006200-105027600	Weak transcription	Hela-S3	cervix
13	chr7:105006400-105021400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr7:105006400-105027400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:105008200-105028200	Weak transcription	Pancreas	Pancrea
16	chr7:105009200-105018600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:105009200-105027200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:105009200-105028000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr7:105009200-105028000	Weak transcription	Psoas Muscle	Psoas
20	chr7:105010000-105027400	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr7:105015800-105018800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:105016200-105025800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:105016200-105026200	Weak transcription	Dnd41	blood
24	chr7:105016400-105027000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr7:105016400-105027200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr7:105017400-105018400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr7:105017400-105018400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:105017400-105018600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:105017400-105018600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr7:105017400-105018600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr7:105017400-105018600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:105017400-105018600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:105017400-105018600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr7:105017400-105018600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:105017400-105018800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:105017600-105018800	Enhancers	Gastric	stomach
37	chr7:105017600-105018800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr7:105017600-105027200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr7:105017800-105018400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr7:105017800-105018400	Weak transcription	Spleen	Spleen
41	chr7:105017800-105018600	Enhancers	Primary T cells fromperipheralblood	blood
42	chr7:105017800-105018600	Enhancers	Right Atrium	heart
43	chr7:105017800-105018800	Enhancers	K562	blood
44	chr7:105017800-105022200	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr7:105017800-105027200	Weak transcription	Primary B cells from peripheral blood	blood
46	chr7:105017800-105027400	Weak transcription	Fetal Muscle Leg	muscle
47	chr7:105017800-105027400	Weak transcription	A549	lung
48	chr7:105018000-105018400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr7:105018000-105018600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr7:105018000-105018800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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