Variant report

Variant	nsv1019963
Chromosome Location	chr7:107033342-107188641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1032)
CpG islands
(count:244)
Chromatin interactive
region (count:149)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1032 , 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	chr7:107136091-107136277	K562	blood:	n/a	n/a
2	ARID3A	chr7:107135270-107135661	K562	blood:	n/a	n/a
3	ARID3A	chr7:107134973-107135199	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:107123148-107123204	K562	blood:	n/a	n/a
5	ARID3A	chr7:107142042-107142424	K562	blood:	n/a	n/a
6	ARID3A	chr7:107118303-107118312	K562	blood:	n/a	n/a
7	ARID3A	chr7:107121415-107121727	K562	blood:	n/a	n/a
8	ATF1	chr7:107142051-107142370	K562	blood:	n/a	n/a
9	ATF1	chr7:107121437-107121726	K562	blood:	n/a	n/a
10	ATF1	chr7:107134729-107135061	K562	blood:	n/a	n/a
11	BACH1	chr7:107103589-107104032	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:107087016-107087291	GM12878	blood:	n/a	chr7:107087175-107087186
13	BHLHE40	chr7:107103633-107103852	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:107121450-107121694	K562	blood:	n/a	n/a
15	BHLHE40	chr7:107103614-107103898	K562	blood:	n/a	n/a
16	BHLHE40	chr7:107142213-107142276	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:107135448-107135629	K562	blood:	n/a	n/a
18	BRCA1	chr7:107103728-107103991	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr7:107185678-107186055	HCT-116	colon:	n/a	n/a
20	CBX3	chr7:107185700-107186000	K562	blood:	n/a	n/a
21	CBX3	chr7:107185208-107186050	K562	blood:	n/a	n/a
22	CBX3	chr7:107135265-107135967	K562	blood:	n/a	n/a
23	CCNT2	chr7:107053859-107053901	K562	blood:	n/a	n/a
24	CCNT2	chr7:107135312-107135711	K562	blood:	n/a	n/a
25	CCNT2	chr7:107095460-107095764	K562	blood:	n/a	n/a
26	CCNT2	chr7:107121325-107121652	K562	blood:	n/a	n/a
27	CCNT2	chr7:107093876-107093890	K562	blood:	n/a	n/a
28	CEBPB	chr7:107062051-107062318	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr7:107136043-107136220	A549	lung:	n/a	n/a
30	CEBPB	chr7:107137227-107137437	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:107106576-107106861	HepG2	liver:	n/a	chr7:107106713-107106722 chr7:107106711-107106724 chr7:107106712-107106723
32	CEBPB	chr7:107137255-107137447	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:107125229-107125416	A549	lung:	n/a	n/a
34	CEBPB	chr7:107076870-107077071	K562	blood:	n/a	n/a
35	CEBPB	chr7:107137235-107137469	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:107137230-107137440	K562	blood:	n/a	n/a
37	CEBPB	chr7:107083795-107084022	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:107135998-107136198	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:107125236-107125424	K562	blood:	n/a	n/a
40	CEBPB	chr7:107146609-107146665	K562	blood:	n/a	n/a
41	CEBPB	chr7:107075334-107075519	HepG2	liver:	n/a	chr7:107075447-107075458
42	CEBPB	chr7:107079512-107079852	IMR90	lung:	n/a	chr7:107079696-107079707
43	CEBPB	chr7:107079613-107079794	Hela-S3	cervix:	n/a	chr7:107079696-107079707
44	CEBPB	chr7:107034841-107035155	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:107075432-107075547	A549	lung:	n/a	chr7:107075447-107075458
46	CEBPB	chr7:107135968-107136346	K562	blood:	n/a	n/a
47	CEBPB	chr7:107083759-107084051	K562	blood:	n/a	n/a
48	CEBPB	chr7:107079653-107079727	H1-hESC	embryonic stem cell:	n/a	chr7:107079696-107079707
49	CEBPB	chr7:107146426-107147478	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:107136002-107136354	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:107110551-107110601	MCF10A-Er-Src	breast:	n/a
2	chr7:107114615-107114665	HepG2	liver:	n/a
3	chr7:107103667-107103717	PFSK-1	brain:	n/a
4	chr7:107114615-107114665	HEEpiC	esophagus:	n/a
5	chr7:107148409-107148459	A549	lung:	n/a
6	chr7:107103667-107103717	BE2_C	brain:	n/a
7	chr7:107110551-107110601	GM06990	blood:	n/a
8	chr7:107110551-107110601	NH-A	brain:	n/a
9	chr7:107110551-107110601	AG09309	skin:	n/a
10	chr7:107148409-107148459	NB4	blood:	n/a
11	chr7:107103667-107103717	AG09309	skin:	n/a
12	chr7:107114615-107114665	NB4	blood:	n/a
13	chr7:107110551-107110601	CMK	blood:	n/a
14	chr7:107148409-107148459	GM06990	blood:	n/a
15	chr7:107103667-107103717	HCPEpiC	choroid plexus:	n/a
16	chr7:107148409-107148459	CMK	blood:	n/a
17	chr7:107114615-107114665	RPTEC	kidney:	n/a
18	chr7:107114615-107114665	HIPEpiC	eye:	n/a
19	chr7:107110551-107110601	ProgFib	skin:	n/a
20	chr7:107114615-107114665	BE2_C	brain:	n/a
21	chr7:107110551-107110601	Jurkat	blood:	n/a
22	chr7:107114615-107114665	ovcar-3	ovarian:	n/a
23	chr7:107148409-107148459	AG04449	skin:	fetal
24	chr7:107148409-107148459	HNPCEpiC	eye:	n/a
25	chr7:107103667-107103717	NB4	blood:	n/a
26	chr7:107103667-107103717	Jurkat	blood:	n/a
27	chr7:107148409-107148459	HCF	heart:	n/a
28	chr7:107114615-107114665	NT2-D1	testis:	n/a
29	chr7:107148409-107148459	Caco-2	colon:	n/a
30	chr7:107148409-107148459	HEEpiC	esophagus:	n/a
31	chr7:107148409-107148459	AG10803	skin:	n/a
32	chr7:107114615-107114665	Hepatocyte	liver:	n/a
33	chr7:107110551-107110601	SKMC	muscle:	n/a
34	chr7:107114615-107114665	HCPEpiC	choroid plexus:	n/a
35	chr7:107110551-107110601	HepG2	liver:	n/a
36	chr7:107148409-107148459	K562	blood:	n/a
37	chr7:107103667-107103717	Hepatocyte	liver:	n/a
38	chr7:107114615-107114665	HEK293	kidney:	embryo
39	chr7:107110551-107110601	BE2_C	brain:	n/a
40	chr7:107103667-107103717	HCM	heart:	n/a
41	chr7:107148409-107148459	HIPEpiC	eye:	n/a
42	chr7:107114615-107114665	HCF	heart:	n/a
43	chr7:107148409-107148459	SKMC	muscle:	n/a
44	chr7:107103667-107103717	SKMC	muscle:	n/a
45	chr7:107114615-107114665	NHDF-neo	bronchial:	n/a
46	chr7:107103667-107103717	HEEpiC	esophagus:	n/a
47	chr7:107110551-107110601	ovcar-3	ovarian:	n/a
48	chr7:107110551-107110601	AG04449	skin:	fetal
49	chr7:107110551-107110601	A549	lung:	n/a
50	chr7:107148409-107148459	GM12891	blood:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:107132036..107135481-chr7:107143415..107147537,5	K562	blood:
2	chr7:107105274..107109720-chr7:107110378..107116920,7	K562	blood:
3	chr7:107170354..107171870-chr7:107238486..107240172,2	K562	blood:
4	chr7:107129283..107132125-chr7:107690846..107692465,2	K562	blood:
5	chr7:107165516..107168282-chr7:107172051..107174509,2	MCF-7	breast:
6	chr7:107156199..107157888-chr7:107162043..107164824,2	K562	blood:
7	chr7:107061830..107063741-chr7:107065312..107067099,2	K562	blood:
8	chr7:107028942..107031560-chr7:107035315..107037970,2	K562	blood:
9	chr7:107126043..107128116-chr7:107129532..107131728,2	K562	blood:
10	chr7:107040494..107042085-chr7:107043869..107046355,2	K562	blood:
11	chr7:107135926..107138327-chr7:107219311..107220923,2	MCF-7	breast:
12	chr7:107038136..107039966-chr7:107054259..107057095,2	K562	blood:
13	chr7:107094353..107098308-chr7:107101232..107104487,5	K562	blood:
14	chr7:107042878..107044924-chr7:107048140..107050111,2	MCF-7	breast:
15	chr7:107136181..107138698-chr7:107141821..107143834,2	MCF-7	breast:
16	chr7:107078024..107080245-chr7:107082230..107084596,2	K562	blood:
17	chr7:107045595..107047319-chr7:107047624..107049995,2	MCF-7	breast:
18	chr7:107109371..107111739-chr7:107112489..107114985,2	K562	blood:
19	chr7:107053101..107055652-chr7:107062376..107064538,2	MCF-7	breast:
20	chr7:107165516..107168282-chr7:107172051..107174509,2	MCF-7	breast:
21	chr7:107084181..107086566-chr7:107109898..107112666,2	K562	blood:
22	chr7:107103257..107104298-chr7:107365292..107366426,11	MCF-7	breast:
23	chr7:107055009..107056631-chr7:107059832..107062299,2	MCF-7	breast:
24	chr7:107134560..107137629-chr7:107140496..107142146,3	K562	blood:
25	chr7:107123396..107125120-chr7:107128160..107130150,2	K562	blood:
26	chr7:107181589..107184372-chr7:107196670..107198393,2	K562	blood:
27	chr7:106845720..106848557-chr7:107077031..107079776,2	K562	blood:
28	chr7:107165422..107167408-chr7:107219933..107221750,2	K562	blood:
29	chr7:107080847..107083435-chr7:107084345..107087287,2	K562	blood:
30	chr7:107042056..107044075-chr7:107048262..107050371,2	K562	blood:
31	chr7:107183753..107186619-chr7:107203811..107206645,3	K562	blood:
32	chr7:107055009..107056631-chr7:107059832..107062299,2	MCF-7	breast:
33	chr7:107166785..107169332-chr7:107203065..107207052,3	MCF-7	breast:
34	chr7:107092382..107094170-chr7:107096108..107097678,2	K562	blood:
35	chr7:107162501..107165341-chr7:107166519..107168432,2	K562	blood:
36	chr7:107126321..107127891-chr7:107219171..107222115,2	K562	blood:
37	chr1:175935286..175935786-chr7:107104571..107105072,2	NB4	blood:
38	chr7:107120115..107121857-chr7:107137628..107139612,2	K562	blood:
39	chr7:107166936..107168955-chr7:107170505..107173136,2	MCF-7	breast:
40	chr7:107095839..107098568-chr7:107102987..107104881,2	K562	blood:
41	chr7:107027220..107028831-chr7:107032404..107035234,2	MCF-7	breast:
42	chr7:107111916..107113727-chr7:107113763..107116184,2	MCF-7	breast:
43	chr7:107182738..107185543-chr7:107201971..107204570,2	MCF-7	breast:
44	chr7:107026679..107030350-chr7:107031871..107033708,4	K562	blood:
45	chr7:107162501..107165341-chr7:107166519..107168432,2	K562	blood:
46	chr7:106842005..106842978-chr7:107141533..107142664,4	K562	blood:
47	chr7:107103704..107104222-chr7:107141765..107142480,2	K562	blood:
48	chr7:107143924..107148910-chr7:107218443..107222194,8	MCF-7	breast:
49	chr7:107103338..107104124-chr7:107515047..107515601,2	MCF-7	breast:
50	chr7:107103371..107104126-chr7:107365303..107366034,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC26A3-2	chr7:107084197-107087887	refGeneNc_3039_NR_028137
2	lnc-SLC26A3-2	chr7:107089283-107089479	refGeneNc_3039_NR_028137
3	lnc-GPR22-1	chr7:107110463-107110494	NONHSAT122680
4	lnc-GPR22-1	chr7:107111817-107111994	NONHSAT122680
5	lnc-GPR22-1	chr7:107110641-107110890	NONHSAT122680
6	lnc-SLC26A3-3	chr7:107188443-107188625	NONHSAT122681
7	lnc-GPR22-2	chr7:107090528-107090807	NONHSAT122679

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GPR22	hsa-miR-26b-5p	chr7:107115962-107115982

Variant related genes	Relation type
GPR22	TF binding region
COG5	TF binding region
ENSG00000228341	TF binding region
GPR22	CpG island
COG5	CpG island
ENSG00000228341	CpG island
ENSG00000105856	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000272854	chromatin interactions
ENSG00000172209	chromatin interactions
ENSG00000164597	chromatin interactions
ENSG00000105865	chromatin interactions

Extended variants
information (count: 6019 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6019 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538918115	chr7:107033372-107033373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369589269	chr7:107033374-107033375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575347323	chr7:107033396-107033397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs537905176	chr7:107033425-107033426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80131081	chr7:107033448-107033449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547089063	chr7:107033452-107033453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373880252	chr7:107033459-107033460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs534785042	chr7:107033498-107033499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185806576	chr7:107033564-107033565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553322392	chr7:107033588-107033589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560226111	chr7:107033601-107033602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79607134	chr7:107033619-107033620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543391600	chr7:107033653-107033654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190336341	chr7:107033685-107033686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531824540	chr7:107033743-107033744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551821642	chr7:107033746-107033747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78970447	chr7:107033757-107033758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77024766	chr7:107033758-107033759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371722372	chr7:107033782-107033783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538261564	chr7:107033797-107033798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556965053	chr7:107033812-107033813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145943985	chr7:107033813-107033814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114018371	chr7:107033819-107033820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374931198	chr7:107033821-107033822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs139849881	chr7:107033852-107033853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114418584	chr7:107033856-107033857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537666997	chr7:107033863-107033864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74525825	chr7:107033878-107033879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372238938	chr7:107033884-107033885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76266570	chr7:107033952-107033953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182556125	chr7:107033958-107033959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143268939	chr7:107033987-107033988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575123585	chr7:107034003-107034004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573684814	chr7:107034064-107034065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146351371	chr7:107034100-107034101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556596674	chr7:107034109-107034110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187628265	chr7:107034142-107034143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576699225	chr7:107034166-107034167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554222714	chr7:107034201-107034202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545253895	chr7:107034220-107034221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117182582	chr7:107034229-107034230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117577748	chr7:107034235-107034236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541128687	chr7:107034264-107034265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116191547	chr7:107034284-107034285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs111826845	chr7:107034295-107034296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530050676	chr7:107034303-107034304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559628227	chr7:107034306-107034307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139728496	chr7:107034307-107034308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs568436810	chr7:107034318-107034319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545373224	chr7:107034327-107034328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1827 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107001400-107037600	Weak transcription	Spleen	Spleen
2	chr7:107001400-107053600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr7:107003600-107045000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:107003800-107038800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr7:107003800-107048400	Weak transcription	Dnd41	blood
6	chr7:107003800-107050200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr7:107008400-107048200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr7:107013200-107038600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:107022200-107053000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr7:107024600-107038200	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr7:107024600-107045000	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:107025000-107038800	Weak transcription	Lung	lung
13	chr7:107025000-107039800	Weak transcription	Fetal Intestine Small	intestine
14	chr7:107025800-107039600	Weak transcription	Primary T cells from cord blood	blood
15	chr7:107027400-107035000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr7:107027400-107045800	Weak transcription	Right Atrium	heart
17	chr7:107027400-107053400	Weak transcription	Gastric	stomach
18	chr7:107027800-107047200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr7:107027800-107050200	Weak transcription	Primary B cells from peripheral blood	blood
20	chr7:107027800-107086800	Weak transcription	Aorta	Aorta
21	chr7:107028000-107038800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr7:107028000-107038800	Weak transcription	Psoas Muscle	Psoas
23	chr7:107028000-107044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:107028000-107052800	Weak transcription	Fetal Muscle Leg	muscle
25	chr7:107028000-107054400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:107028200-107039800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr7:107028200-107053000	Weak transcription	Fetal Stomach	stomach
28	chr7:107028200-107082400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr7:107028200-107103800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:107028800-107033400	Weak transcription	NHDF-Ad	bronchial
31	chr7:107028800-107033600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:107028800-107035800	Weak transcription	HUVEC	blood vessel
33	chr7:107028800-107053000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr7:107028800-107053200	Weak transcription	K562	blood
35	chr7:107029000-107034800	Weak transcription	Osteobl	bone
36	chr7:107029000-107035600	Weak transcription	NHLF	lung
37	chr7:107029400-107039800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr7:107029400-107050400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:107030200-107049000	Weak transcription	Right Ventricle	heart
40	chr7:107031600-107069600	Weak transcription	Fetal Kidney	kidney
41	chr7:107031800-107037400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr7:107031800-107050200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:107032000-107037600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:107032000-107050200	Weak transcription	Fetal Intestine Large	intestine
45	chr7:107032200-107040600	Weak transcription	Fetal Thymus	thymus
46	chr7:107032200-107045200	Weak transcription	HepG2	liver
47	chr7:107032400-107068000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr7:107032600-107034600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:107033000-107034000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:107033200-107033600	Enhancers	Adipose Nuclei	Adipose

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