Variant report

Variant	nsv1023767
Chromosome Location	chr7:104931143-105190662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4760)
CpG islands
(count:3482)
Chromatin interactive
region (count:311)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4760 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104976462-104976771	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:105042035-105042531	K562	blood:	n/a	n/a
3	ARID3A	chr7:104999888-105000102	K562	blood:	n/a	n/a
4	ARID3A	chr7:104994259-104994459	K562	blood:	n/a	n/a
5	ARID3A	chr7:104970982-104971041	K562	blood:	n/a	n/a
6	ARID3A	chr7:105172276-105172771	K562	blood:	n/a	n/a
7	ARID3A	chr7:105015076-105015149	K562	blood:	n/a	n/a
8	ARID3A	chr7:104976432-104976788	K562	blood:	n/a	n/a
9	ARID3A	chr7:104972080-104972123	K562	blood:	n/a	n/a
10	ARID3A	chr7:105042910-105043317	K562	blood:	n/a	n/a
11	ARID3A	chr7:104999465-104999651	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:105039651-105040180	K562	blood:	n/a	n/a
13	ARID3A	chr7:105162675-105163137	K562	blood:	n/a	n/a
14	ARID3A	chr7:105173865-105174045	HepG2	liver:	n/a	n/a
15	ARID3A	chr7:104944460-104945017	HepG2	liver:	n/a	n/a
16	ARID3A	chr7:105070152-105070549	K562	blood:	n/a	n/a
17	ARID3A	chr7:105006603-105006770	K562	blood:	n/a	n/a
18	ARID3A	chr7:105007981-105008379	HepG2	liver:	n/a	n/a
19	ARID3A	chr7:105080108-105080325	HepG2	liver:	n/a	n/a
20	ARID3A	chr7:105042094-105042482	HepG2	liver:	n/a	n/a
21	ARID3A	chr7:105008783-105009038	K562	blood:	n/a	n/a
22	ARID3A	chr7:105141763-105141769	K562	blood:	n/a	n/a
23	ARID3A	chr7:105128201-105128752	K562	blood:	n/a	n/a
24	ARID3A	chr7:104999428-104999583	K562	blood:	n/a	n/a
25	ARID3A	chr7:105028117-105028318	K562	blood:	n/a	n/a
26	ARID3A	chr7:105172230-105172894	HepG2	liver:	n/a	n/a
27	ARID3A	chr7:105162532-105162842	HepG2	liver:	n/a	n/a
28	ARID3A	chr7:105019839-105020013	K562	blood:	n/a	n/a
29	ARID3A	chr7:105039898-105040131	HepG2	liver:	n/a	n/a
30	ARID3A	chr7:105017364-105017690	K562	blood:	n/a	n/a
31	ARID3A	chr7:105029792-105030248	HepG2	liver:	n/a	n/a
32	ARID3A	chr7:105070221-105070610	HepG2	liver:	n/a	n/a
33	ATF1	chr7:105128345-105128752	K562	blood:	n/a	n/a
34	ATF1	chr7:105007289-105007410	K562	blood:	n/a	n/a
35	ATF1	chr7:105070205-105070516	K562	blood:	n/a	n/a
36	ATF2	chr7:104992448-104993159	GM12878	blood:	n/a	n/a
37	ATF2	chr7:105172329-105172807	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr7:105172257-105172894	GM12878	blood:	n/a	n/a
39	ATF2	chr7:105171988-105172822	GM12878	blood:	n/a	n/a
40	ATF2	chr7:105162441-105162701	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr7:104944617-104945385	GM12878	blood:	n/a	n/a
42	ATF3	chr7:105162419-105162922	K562	blood:	n/a	chr7:105162516-105162525
43	ATF3	chr7:104944489-104944823	HCT-116	colon:	n/a	n/a
44	ATF3	chr7:105162479-105162756	A549	lung:	n/a	chr7:105162516-105162525
45	ATF3	chr7:105172202-105172799	K562	blood:	n/a	n/a
46	BACH1	chr7:104952147-104952403	K562	blood:	n/a	n/a
47	BACH1	chr7:105172426-105172817	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr7:105162629-105162935	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr7:105172328-105172846	K562	blood:	n/a	n/a
50	BACH1	chr7:105103081-105103084	K562	blood:	n/a	n/a

(count:3482 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:105162859-105162909	CMK	blood:	n/a
2	chr7:105162470-105162520	ProgFib	skin:	n/a
3	chr7:104941821-104941871	Caco-2	colon:	n/a
4	chr7:105162941-105162991	HRE	kidney:	n/a
5	chr7:104939331-104939381	GM12878	blood:	n/a
6	chr7:105162859-105162909	CMK	blood:	n/a
7	chr7:105162470-105162520	ProgFib	skin:	n/a
8	chr7:104941821-104941871	Caco-2	colon:	n/a
9	chr7:105162941-105162991	HRE	kidney:	n/a
10	chr7:104939331-104939381	GM12878	blood:	n/a
11	chr7:105112740-105112790	HNPCEpiC	eye:	n/a
12	chr7:105094993-105095043	BE2_C	brain:	n/a
13	chr7:105172664-105172714	HEK293	kidney:	embryo
14	chr7:105030168-105030218	HRE	kidney:	n/a
15	chr7:104943515-104943565	HCT-116	colon:	n/a
16	chr7:105097168-105097218	HCF	heart:	n/a
17	chr7:105027541-105027591	GM12878	blood:	n/a
18	chr7:105128488-105128538	ECC-1	luminal epithelium:	n/a
19	chr7:105134734-105134784	NH-A	brain:	n/a
20	chr7:105172974-105173024	NHDF-neo	bronchial:	n/a
21	chr7:104945248-104945298	GM12891	blood:	n/a
22	chr7:105172403-105172453	AG09309	skin:	n/a
23	chr7:105134734-105134784	AG10803	skin:	n/a
24	chr7:105162941-105162991	AG09309	skin:	n/a
25	chr7:104941977-104942027	HNPCEpiC	eye:	n/a
26	chr7:105162600-105162650	HEEpiC	esophagus:	n/a
27	chr7:105110948-105110998	LNCaP	prostate:	n/a
28	chr7:105158109-105158159	HL-60	blood:	n/a
29	chr7:105018109-105018159	GM06990	blood:	n/a
30	chr7:105112740-105112790	SK-N-SH	brain:	n/a
31	chr7:105079663-105079713	HEEpiC	esophagus:	n/a
32	chr7:105134734-105134784	RPTEC	kidney:	n/a
33	chr7:105172820-105172870	CMK	blood:	n/a
34	chr7:105162735-105162785	PANC-1	pancreas:	n/a
35	chr7:105029492-105029542	NB4	blood:	n/a
36	chr7:105160482-105160532	MCF10A-Er-Src	breast:	n/a
37	chr7:105160482-105160532	NHDF-neo	bronchial:	n/a
38	chr7:105137683-105137733	HCT-116	colon:	n/a
39	chr7:104941898-104941948	ECC-1	luminal epithelium:	n/a
40	chr7:105029497-105029547	RPTEC	kidney:	n/a
41	chr7:105162470-105162520	GM12891	blood:	n/a
42	chr7:105162470-105162520	PrEC	prostate:	n/a
43	chr7:105030168-105030218	HCF	heart:	n/a
44	chr7:105162859-105162909	NH-A	brain:	n/a
45	chr7:105162878-105162928	PrEC	prostate:	n/a
46	chr7:105171843-105171893	PrEC	prostate:	n/a
47	chr7:105158109-105158159	SKMC	muscle:	n/a
48	chr7:105029895-105029945	HRPEpiC	eye:	n/a
49	chr7:105079663-105079713	RPTEC	kidney:	n/a
50	chr7:105172974-105173024	HEK293	kidney:	embryo

(count:311 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr7:105155451..105157293-chr7:105221576..105223932,2	K562	blood:
2	chr7:104935027..104937759-chr7:104947845..104950749,2	K562	blood:
3	chr7:105140985..105143756-chr7:105161298..105163196,2	K562	blood:
4	chr7:104651944..104654760-chr7:105154090..105156667,3	K562	blood:
5	chr7:104957510..104959385-chr7:104965005..104966675,2	MCF-7	breast:
6	chr7:105083591..105086006-chr7:105160365..105162043,2	K562	blood:
7	chr7:105158727..105165017-chr7:105166972..105176993,56	K562	blood:
8	chr7:104649601..104653676-chr7:105029497..105032094,4	K562	blood:
9	chr7:104772977..104775390-chr7:105160456..105162601,2	K562	blood:
10	chr7:105094953..105097499-chr7:105172737..105175685,2	K562	blood:
11	chr7:105134519..105138273-chr7:105140684..105142940,4	K562	blood:
12	chr7:105028493..105030859-chr7:105041112..105043880,2	MCF-7	breast:
13	chr7:104948405..104951039-chr7:105028553..105030252,2	MCF-7	breast:
14	chr7:105039769..105040575-chr7:105229933..105230493,2	MCF-7	breast:
15	chr7:104837867..104839378-chr7:104977960..104980667,2	MCF-7	breast:
16	chr7:105078529..105081334-chr7:105089630..105092260,2	MCF-7	breast:
17	chr7:104652835..104655509-chr7:105083181..105085882,2	K562	blood:
18	chr7:105007315..105010553-chr7:105026431..105029268,4	MCF-7	breast:
19	chr7:105078097..105081437-chr7:105081895..105086252,7	MCF-7	breast:
20	chr7:104971088..104973665-chr7:105027778..105030280,2	K562	blood:
21	chr7:105065275..105067790-chr7:105068952..105071449,2	K562	blood:
22	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:
23	chr7:105077610..105079593-chr7:105277215..105278771,2	MCF-7	breast:
24	chr7:105028707..105032086-chr7:105067490..105070575,3	K562	blood:
25	chr7:104994593..104996936-chr7:105006253..105008097,2	K562	blood:
26	chr7:105110346..105111937-chr7:105127717..105129867,2	K562	blood:
27	chr7:104922381..104923956-chr7:104935072..104936834,2	MCF-7	breast:
28	chr14:20937110..20938110-chr7:105172278..105173069,2	Hela-S3	cervix:
29	chr7:104937663..104939344-chr7:105026759..105029557,2	MCF-7	breast:
30	chr7:104663218..104665844-chr7:104995701..104998605,2	K562	blood:
31	chr7:104651368..104653205-chr7:105026206..105027848,2	K562	blood:
32	chr7:104960628..104963813-chr7:104964024..104966847,3	MCF-7	breast:
33	chr7:105108727..105111208-chr7:105115281..105117815,3	K562	blood:
34	chr7:105143860..105147794-chr7:105158802..105162576,5	K562	blood:
35	chr7:105139514..105141337-chr7:105172365..105174838,2	K562	blood:
36	chr7:104924587..104925130-chr7:104938642..104939172,2	MCF-7	breast:
37	chr7:105126837..105131294-chr7:105131811..105135446,3	K562	blood:
38	chr7:104653151..104655503-chr7:105160083..105164345,7	K562	blood:
39	chr1:209957159..209957989-chr7:105162027..105162579,2	Hela-S3	cervix:
40	chr7:105165151..105169952-chr7:105171142..105174252,8	MCF-7	breast:
41	chr7:104621410..104622279-chr7:105069837..105070818,3	K562	blood:
42	chr7:104651722..104654258-chr7:104946708..104948409,2	K562	blood:
43	chr7:105162283..105162894-chr7:105172462..105173034,2	NB4	blood:
44	chr7:105039077..105041810-chr7:105045428..105047601,2	K562	blood:
45	chr7:105028215..105030486-chr7:105171271..105172847,2	K562	blood:
46	chr17:33914164..33914765-chr7:105161584..105162384,2	Hela-S3	cervix:
47	chr7:104930219..104933081-chr7:104934544..104936219,2	K562	blood:
48	chr7:105027206..105036314-chr7:105036751..105044757,13	K562	blood:
49	chr7:105026975..105030937-chr7:105032940..105036440,7	K562	blood:
50	chr7:104984088..104985686-chr7:105028114..105030701,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDHR3-5	chr7:105182048-105182302	NONHSAT122624
2	lnc-SRPK2-5	chr7:105029691-105029837	NONHSAT122614
3	lnc-MLL5-6	chr7:104941969-104942533	NONHSAT122616
4	lnc-RINT1-2	chr7:105170656-105171118	NONHSAT122622
5	lnc-MLL5-1	chr7:104944724-104944878	ENSG00000242154.1
6	lnc-MLL5-1	chr7:104946699-104947089	ENSG00000242154.1
7	lnc-CDHR3-5	chr7:105182855-105183003	NONHSAT122624
8	lnc-PUS7-1	chr7:105170677-105170904	NONHSAT122623
9	lnc-PUS7-1	chr7:105171944-105171973	NONHSAT122623
10	lnc-SRPK2-5	chr7:105029095-105029149	NONHSAT122614

No data

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

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

Variant related genes	Relation type
ENSG00000223886	TF binding region
PUS7	TF binding region
RINT1	TF binding region
RWDD4P1	TF binding region
RNU6-1322P	TF binding region
ENSG00000242154	TF binding region
SRPK2	TF binding region
ENSG00000223886	CpG island
PUS7	CpG island
RINT1	CpG island
RWDD4P1	CpG island
RNU6-1322P	CpG island
ENSG00000242154	CpG island
SRPK2	CpG island
ENSG00000162757	chromatin interactions
ENSG00000091127	chromatin interactions
ENSG00000146776	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000072210	chromatin interactions
ENSG00000135249	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000201179	chromatin interactions
ENSG00000230508	chromatin interactions
ENSG00000223886	chromatin interactions
ENSG00000014123	chromatin interactions
ENSG00000172244	chromatin interactions
ENSG00000005483	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000080298	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000239569	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000128536	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000099622	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000242154	chromatin interactions
ENSG00000135250	chromatin interactions
ENSG00000244490	chromatin interactions
ENSG00000272604	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000233797	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000185055	chromatin interactions
ENSG00000231167	chromatin interactions

Extended variants
information (count: 10309 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:10309 , 50 per page) page: 1 2 3 4 5 6 7 ... 207

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577617227	chr7:104931167-104931168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181568670	chr7:104931179-104931180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560263343	chr7:104931206-104931207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567455868	chr7:104931213-104931214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112243483	chr7:104931245-104931246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529199054	chr7:104931252-104931253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549326198	chr7:104931258-104931259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs55898317	chr7:104931276-104931277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531780983	chr7:104931282-104931283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142442077	chr7:104931313-104931314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571658411	chr7:104931314-104931315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534263237	chr7:104931320-104931321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10247799	chr7:104931338-104931339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370740609	chr7:104931342-104931343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373239014	chr7:104931345-104931346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370183124	chr7:104931378-104931379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576323294	chr7:104931408-104931409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537448536	chr7:104931433-104931434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545017939	chr7:104931491-104931492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs60337781	chr7:104931512-104931513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs367899824	chr7:104931513-104931514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189273155	chr7:104931534-104931535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7790653	chr7:104931545-104931546	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs116657462	chr7:104931548-104931549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540297772	chr7:104931660-104931661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376039103	chr7:104931672-104931673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559972667	chr7:104931683-104931684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573915549	chr7:104931703-104931704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542835056	chr7:104931802-104931803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562819379	chr7:104931896-104931897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531591039	chr7:104931917-104931918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563305096	chr7:104931937-104931938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551814365	chr7:104931946-104931947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565253020	chr7:104931948-104931949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530543715	chr7:104932006-104932007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527663272	chr7:104932022-104932023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547903097	chr7:104932033-104932034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567642315	chr7:104932046-104932047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180950810	chr7:104932050-104932051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549913265	chr7:104932057-104932058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186117632	chr7:104932107-104932108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6958609	chr7:104932114-104932115	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567575971	chr7:104932142-104932143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557492949	chr7:104932164-104932165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542482867	chr7:104932168-104932169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76575273	chr7:104932175-104932176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191024058	chr7:104932209-104932210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs117827531	chr7:104932244-104932245	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373599090	chr7:104932247-104932248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182807330	chr7:104932273-104932274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Bladder cancer	21909424	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
Melanoma	20877625	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD

Chromatin state (count:5857 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104910200-104935000	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:104910800-104934400	Weak transcription	Primary T cells from cord blood	blood
3	chr7:104910800-104946000	Weak transcription	Primary B cells from cord blood	blood
4	chr7:104911400-104934800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr7:104912200-104939200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:104913200-104936200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr7:104917200-104944600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr7:104918200-104939000	Weak transcription	Primary B cells from peripheral blood	blood
9	chr7:104919200-104939000	Weak transcription	Pancreas	Pancrea
10	chr7:104919800-104939000	Weak transcription	Thymus	Thymus
11	chr7:104919800-104939200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:104920400-104939200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:104920600-104937200	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr7:104920600-104959600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr7:104923200-104944200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:104924800-104939000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr7:104924800-104939200	Weak transcription	Left Ventricle	heart
18	chr7:104925000-104936200	Weak transcription	HepG2	liver
19	chr7:104925000-104944200	Weak transcription	A549	lung
20	chr7:104926200-104934200	Weak transcription	K562	blood
21	chr7:104926400-104944600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:104927200-104934400	Weak transcription	Brain Cingulate Gyrus	brain
23	chr7:104929000-104939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:104929200-104931800	Enhancers	Dnd41	blood
25	chr7:104929400-104944600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr7:104929600-104938800	Weak transcription	Fetal Thymus	thymus
27	chr7:104929800-104944000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:104930400-104934400	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr7:104930600-104934200	Weak transcription	Brain Angular Gyrus	brain
30	chr7:104930600-104934200	Weak transcription	Brain Substantia Nigra	brain
31	chr7:104930600-104934400	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:104930600-104936600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr7:104930800-104935800	Weak transcription	GM12878-XiMat	blood
34	chr7:104930800-104936200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr7:104930800-104937200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:104931600-104931800	Enhancers	Rectal Smooth Muscle	rectum
37	chr7:104931800-104934400	Weak transcription	Dnd41	blood
38	chr7:104931800-104936200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr7:104931800-104936200	Weak transcription	Rectal Smooth Muscle	rectum
40	chr7:104934200-104934600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr7:104934200-104934600	Enhancers	Brain Substantia Nigra	brain
42	chr7:104934200-104934600	Enhancers	K562	blood
43	chr7:104934200-104934800	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr7:104934200-104935200	Enhancers	Brain Angular Gyrus	brain
45	chr7:104934400-104934600	Enhancers	Psoas Muscle	Psoas
46	chr7:104934400-104934800	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr7:104934400-104934800	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr7:104934400-104935000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr7:104934400-104935000	Enhancers	Brain Cingulate Gyrus	brain
50	chr7:104934400-104935000	Enhancers	Brain Hippocampus Middle	brain

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