Variant report

Variant	nsv1018586
Chromosome Location	chr7:108759240-109034145
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:108791252-108791262	K562	blood:	n/a	n/a
2	ATF2	chr7:108871620-108872037	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:108895203-108895218	K562	blood:	n/a	n/a
4	BACH1	chr7:108794812-108795142	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr7:108870647-108870922	HepG2	liver:	n/a	chr7:108870795-108870806 chr7:108870795-108870808 chr7:108870795-108870808 chr7:108870797-108870806 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870795-108870808 chr7:108870797-108870806
6	CEBPB	chr7:108911956-108912156	HepG2	liver:	n/a	chr7:108912038-108912049
7	CEBPB	chr7:108879342-108879561	IMR90	lung:	n/a	chr7:108879422-108879433
8	CEBPB	chr7:108910412-108910678	HepG2	liver:	n/a	chr7:108910539-108910550
9	CEBPB	chr7:109019192-109019432	Hela-S3	cervix:	n/a	chr7:109019302-109019313
10	CEBPB	chr7:108771245-108771544	HepG2	liver:	n/a	chr7:108771390-108771401
11	CEBPB	chr7:108870692-108870981	A549	lung:	n/a	chr7:108870795-108870806 chr7:108870795-108870808 chr7:108870795-108870808 chr7:108870797-108870806 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870795-108870808 chr7:108870797-108870806
12	CEBPB	chr7:108813772-108814018	HepG2	liver:	n/a	chr7:108813879-108813890
13	CEBPB	chr7:109033645-109034051	HepG2	liver:	n/a	n/a
14	CEBPB	chr7:108910428-108910645	A549	lung:	n/a	chr7:108910539-108910550
15	CEBPB	chr7:108777013-108777281	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr7:108910445-108910657	IMR90	lung:	n/a	chr7:108910539-108910550
17	CEBPB	chr7:109019170-109019448	HepG2	liver:	n/a	chr7:109019302-109019313
18	CEBPB	chr7:109019300-109019460	K562	blood:	n/a	chr7:109019302-109019313
19	CEBPB	chr7:108771231-108771529	A549	lung:	n/a	chr7:108771390-108771401
20	CEBPB	chr7:108819697-108819855	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:108776991-108777339	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:109017585-109017927	HepG2	liver:	n/a	chr7:109017757-109017768
23	CEBPB	chr7:108910394-108910624	K562	blood:	n/a	chr7:108910539-108910550
24	CEBPB	chr7:108777002-108777283	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:109019049-109019385	A549	lung:	n/a	chr7:109019302-109019313
26	CEBPB	chr7:108879312-108879556	A549	lung:	n/a	chr7:108879422-108879433
27	CEBPB	chr7:108776992-108777306	A549	lung:	n/a	n/a
28	CEBPB	chr7:108813798-108814024	MCF-7	breast:	n/a	chr7:108813879-108813890
29	CEBPB	chr7:108870685-108870955	K562	blood:	n/a	chr7:108870795-108870806 chr7:108870795-108870808 chr7:108870795-108870808 chr7:108870797-108870806 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870795-108870808 chr7:108870797-108870806
30	CEBPB	chr7:108931360-108931601	A549	lung:	n/a	chr7:108931471-108931480 chr7:108931471-108931480 chr7:108931469-108931480 chr7:108931471-108931480 chr7:108931469-108931482 chr7:108931471-108931480 chr7:108931471-108931482
31	CEBPB	chr7:108771305-108771519	H1-hESC	embryonic stem cell:	n/a	chr7:108771390-108771401
32	CEBPB	chr7:108983779-108984138	Hela-S3	cervix:	n/a	chr7:108983955-108983968 chr7:108983956-108983967 chr7:108983955-108983968 chr7:108983955-108983966 chr7:108983955-108983966
33	CEBPB	chr7:108879270-108879566	HepG2	liver:	n/a	chr7:108879422-108879433
34	CEBPB	chr7:108777008-108777396	MCF-7	breast:	n/a	n/a
35	CEBPB	chr7:108874096-108874294	A549	lung:	n/a	n/a
36	CEBPB	chr7:109017612-109017804	H1-hESC	embryonic stem cell:	n/a	chr7:109017757-109017768
37	CEBPB	chr7:108771250-108771518	Hela-S3	cervix:	n/a	chr7:108771390-108771401
38	CEBPB	chr7:108892779-108892938	A549	lung:	n/a	chr7:108892880-108892891
39	CEBPB	chr7:108870683-108870951	IMR90	lung:	n/a	chr7:108870795-108870806 chr7:108870795-108870808 chr7:108870795-108870808 chr7:108870797-108870806 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870797-108870806 chr7:108870797-108870808 chr7:108870795-108870808 chr7:108870797-108870806
40	CEBPB	chr7:108892778-108892882	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:108983843-108984061	A549	lung:	n/a	chr7:108983955-108983968 chr7:108983956-108983967 chr7:108983955-108983968 chr7:108983955-108983966 chr7:108983955-108983966
42	CEBPB	chr7:108777000-108777312	IMR90	lung:	n/a	n/a
43	CEBPB	chr7:108931312-108931584	HepG2	liver:	n/a	chr7:108931471-108931480 chr7:108931471-108931480 chr7:108931469-108931480 chr7:108931471-108931480 chr7:108931469-108931482 chr7:108931471-108931480 chr7:108931471-108931482
44	CEBPB	chr7:108771208-108771535	K562	blood:	n/a	chr7:108771390-108771401
45	CEBPB	chr7:108931321-108931616	K562	blood:	n/a	chr7:108931471-108931480 chr7:108931471-108931480 chr7:108931469-108931480 chr7:108931471-108931480 chr7:108931469-108931482 chr7:108931471-108931480 chr7:108931471-108931482
46	CEBPB	chr7:108813805-108814010	A549	lung:	n/a	chr7:108813879-108813890
47	CEBPB	chr7:108765141-108765245	A549	lung:	n/a	n/a
48	CEBPB	chr7:108777009-108777342	K562	blood:	n/a	n/a
49	CEBPB	chr7:109017627-109017859	MCF-7	breast:	n/a	chr7:109017757-109017768
50	CEBPB	chr7:108983855-108984082	MCF-7	breast:	n/a	chr7:108983955-108983968 chr7:108983956-108983967 chr7:108983955-108983968 chr7:108983955-108983966 chr7:108983955-108983966

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:108845010-108845060	SK-N-SH_RA	brain:	n/a
2	chr7:108767676-108767726	PFSK-1	brain:	n/a
3	chr7:108767676-108767726	HNPCEpiC	eye:	n/a
4	chr7:108899319-108899369	HRPEpiC	eye:	n/a
5	chr7:108899319-108899369	HEK293	kidney:	embryo
6	chr7:108899319-108899369	HRE	kidney:	n/a
7	chr7:108767676-108767726	HepG2	liver:	n/a
8	chr7:108899319-108899369	Hepatocyte	liver:	n/a
9	chr7:108899319-108899369	A549	lung:	n/a
10	chr7:108899319-108899369	NB4	blood:	n/a
11	chr7:108767676-108767726	AoSMC	blood vessel:	n/a
12	chr7:108767676-108767726	HUVEC	blood vessel:	n/a
13	chr7:108767676-108767726	HEK293	kidney:	embryo
14	chr7:108767676-108767726	GM06990	blood:	n/a
15	chr7:108899319-108899369	SK-N-MC	brain:	n/a
16	chr7:108899319-108899369	BE2_C	brain:	n/a
17	chr7:108845010-108845060	Caco-2	colon:	n/a
18	chr7:108845010-108845060	HNPCEpiC	eye:	n/a
19	chr7:108845010-108845060	NH-A	brain:	n/a
20	chr7:108767676-108767726	RPTEC	kidney:	n/a
21	chr7:108899319-108899369	HRCEpiC	kidney:	n/a
22	chr7:108767676-108767726	U87	brain:	n/a
23	chr7:108845010-108845060	GM12891	blood:	n/a
24	chr7:108899319-108899369	IMR90	lung:	fetal
25	chr7:108899319-108899369	BJ	skin:	n/a
26	chr7:108767676-108767726	SK-N-MC	brain:	n/a
27	chr7:108899319-108899369	HCM	heart:	n/a
28	chr7:108767676-108767726	H1-hESC	embryonic stem cell:	embryo
29	chr7:108767676-108767726	ovcar-3	ovarian:	n/a
30	chr7:108845010-108845060	HL-60	blood:	n/a
31	chr7:108899319-108899369	MCF-7	breast:	n/a
32	chr7:108899319-108899369	HCF	heart:	n/a
33	chr7:108767676-108767726	K562	blood:	n/a
34	chr7:108767676-108767726	GM12891	blood:	n/a
35	chr7:108767676-108767726	Jurkat	blood:	n/a
36	chr7:108845010-108845060	AG04449	skin:	fetal
37	chr7:108767676-108767726	HCT-116	colon:	n/a
38	chr7:108845010-108845060	HRE	kidney:	n/a
39	chr7:108845010-108845060	MCF-7	breast:	n/a
40	chr7:108899319-108899369	GM12892	blood:	n/a
41	chr7:108767676-108767726	AG10803	skin:	n/a
42	chr7:108845010-108845060	BE2_C	brain:	n/a
43	chr7:108767676-108767726	SK-N-SH_RA	brain:	n/a
44	chr7:108899319-108899369	SAEC	small airway:	n/a
45	chr7:108845010-108845060	GM06990	blood:	n/a
46	chr7:108767676-108767726	HL-60	blood:	n/a
47	chr7:108767676-108767726	HCM	heart:	n/a
48	chr7:108767676-108767726	ProgFib	skin:	n/a
49	chr7:108845010-108845060	HepG2	liver:	n/a
50	chr7:108899319-108899369	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:108930299..108932601-chr7:108936912..108938938,2	K562	blood:
2	chr7:108987373..108988897-chr7:109004557..109006154,2	K562	blood:
3	chr7:108864624..108866381-chr7:108866624..108869588,2	MCF-7	breast:
4	chr7:108829756..108831722-chr9:116036249..116037826,2	MCF-7	breast:
5	chr7:108800063..108802230-chr7:108802806..108804951,2	K562	blood:
6	chr7:108972641..108975247-chr7:108976692..108978678,2	K562	blood:
7	chr7:108987373..108988897-chr7:109004557..109006154,2	K562	blood:
8	chr7:109007974..109010890-chr7:109012511..109014699,2	K562	blood:
9	chr7:108832801..108835363-chr7:108836904..108839577,2	K562	blood:
10	chr7:108832801..108835363-chr7:108836904..108839577,2	K562	blood:
11	chr7:108890203..108893066-chr7:108896329..108898326,2	K562	blood:
12	chr7:109007974..109010890-chr7:109012511..109014699,2	K562	blood:
13	chr15:85523640..85524561-chr7:108854830..108855472,2	MCF-7	breast:
14	chr7:108840265..108842020-chr7:108843538..108846052,2	K562	blood:
15	chr7:108900168..108902978-chr7:108903344..108906087,2	MCF-7	breast:
16	chr6:101816226..101817017-chr7:108978282..108979156,2	MCF-7	breast:
17	chr7:108835627..108837336-chr7:108841998..108844540,2	K562	blood:
18	chr7:108972641..108975247-chr7:108976692..108978678,2	K562	blood:
19	chr7:108783473..108786187-chr7:108837145..108838988,2	K562	blood:
20	chr7:109003272..109005677-chr7:109013003..109015248,2	MCF-7	breast:
21	chr7:108783473..108786187-chr7:108837145..108838988,2	K562	blood:
22	chr6:125963245..125963978-chr7:108992120..108992898,2	MCF-7	breast:
23	chr7:108890203..108893066-chr7:108896329..108898326,2	K562	blood:
24	chr7:108926418..108928901-chr7:108931710..108934777,3	K562	blood:
25	chr7:108926418..108928901-chr7:108931710..108934777,3	K562	blood:
26	chr7:108900168..108902978-chr7:108903344..108906087,2	MCF-7	breast:
27	chr7:108800063..108802230-chr7:108802806..108804951,2	K562	blood:
28	chr7:109004368..109006710-chr7:109007454..109009368,2	MCF-7	breast:
29	chr7:109004368..109006710-chr7:109007454..109009368,2	MCF-7	breast:
30	chr7:108860832..108863154-chr7:108863395..108865934,2	K562	blood:
31	chr7:108930299..108932601-chr7:108936912..108938938,2	K562	blood:
32	chr7:108860832..108863154-chr7:108863395..108865934,2	K562	blood:
33	chr7:108835627..108837336-chr7:108841998..108844540,2	K562	blood:
34	chr7:108864624..108866381-chr7:108866624..108869588,2	MCF-7	breast:
35	chr7:109003272..109005677-chr7:109013003..109015248,2	MCF-7	breast:
36	chr7:108840265..108842020-chr7:108843538..108846052,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf66-1	chr7:108966269-108966372	XLOC_006559
2	lnc-C7orf66-1	chr7:108962377-108962670	XLOC_006559

Variant related genes	Relation type
ENSG00000230941	TF binding region
ENSG00000230941	CpG island
ENSG00000136875	chromatin interactions
ENSG00000073417	chromatin interactions
PLAG1	miRNA target sites

Extended variants
information (count: 2407 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2407 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7782995	chr7:108759240-108759241	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540554010	chr7:108759253-108759254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558270979	chr7:108759263-108759264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116219020	chr7:108759271-108759272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140736181	chr7:108759302-108759303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189636694	chr7:108759303-108759304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113780031	chr7:108759321-108759322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192671876	chr7:108759356-108759357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530914229	chr7:108759382-108759383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550734507	chr7:108759392-108759393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570528847	chr7:108759395-108759396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533418794	chr7:108759396-108759397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112175427	chr7:108759417-108759418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150086816	chr7:108759419-108759420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114970038	chr7:108759464-108759465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535721969	chr7:108759476-108759477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145532876	chr7:108759630-108759631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2030739	chr7:108759641-108759642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78430779	chr7:108759683-108759684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565317280	chr7:108759703-108759704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114470419	chr7:108759725-108759726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184916569	chr7:108759755-108759756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148839149	chr7:108759869-108759870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368027386	chr7:108759884-108759885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188750556	chr7:108759910-108759911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573880094	chr7:108759911-108759912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542486756	chr7:108759952-108759953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73713377	chr7:108759975-108759976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs145797143	chr7:108759988-108759989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2030738	chr7:108760031-108760032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181605681	chr7:108760034-108760035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540070134	chr7:108760056-108760057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533165537	chr7:108760064-108760065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186121608	chr7:108760107-108760108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566852094	chr7:108760116-108760117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73713379	chr7:108760169-108760170	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs1525037	chr7:108760184-108760185	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs189240671	chr7:108760190-108760191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529186086	chr7:108760208-108760209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117103029	chr7:108760218-108760219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182592823	chr7:108760246-108760247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540718035	chr7:108760260-108760261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571251754	chr7:108760261-108760262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533820346	chr7:108760289-108760290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185920972	chr7:108760311-108760312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565404051	chr7:108760331-108760332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532517841	chr7:108760370-108760371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374600270	chr7:108760415-108760416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536565395	chr7:108760463-108760464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59301351	chr7:108760465-108760466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	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
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108752600-108766800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:108759600-108760000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:108760000-108760200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:108760200-108764200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:108760800-108761000	Bivalent Enhancer	Fetal Lung	lung
6	chr7:108760800-108761400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:108760800-108763200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr7:108761000-108761200	Enhancers	Fetal Lung	lung
9	chr7:108761000-108762600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr7:108761200-108762400	Weak transcription	Fetal Lung	lung
11	chr7:108761400-108762200	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:108761400-108765400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:108762000-108762400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr7:108762000-108762400	Enhancers	Placenta Amnion	Placenta Amnion
15	chr7:108762000-108762600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr7:108762200-108762600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:108762200-108766000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr7:108762400-108763200	Enhancers	Fetal Lung	lung
19	chr7:108762400-108763600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:108762400-108769400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr7:108762600-108765800	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr7:108762600-108766400	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr7:108762600-108766800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:108763200-108765200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr7:108763600-108764800	Enhancers	Placenta Amnion	Placenta Amnion
26	chr7:108764200-108764400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:108764400-108764800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:108764800-108765800	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr7:108764800-108768200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:108765200-108767600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:108765200-108769800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:108765400-108767800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:108765400-108768200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr7:108765800-108767600	Enhancers	Placenta Amnion	Placenta Amnion
35	chr7:108765800-108769800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr7:108766000-108769600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:108766000-108769800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:108766200-108767800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr7:108766400-108767200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr7:108766400-108767200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:108766400-108768200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:108766800-108767000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:108766800-108767000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:108766800-108767200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:108766800-108767400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr7:108766800-108767600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr7:108766800-108768000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr7:108767000-108769000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:108767200-108768200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:108767200-108769000	Weak transcription	H1 Cell Line	embryonic stem cell

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