Variant report

Variant	nsv888974
Chromosome Location	chr7:110516659-110660055
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	ARID3A	chr7:110634723-110635192	K562	blood:	n/a	n/a
2	ATF1	chr7:110594853-110594948	K562	blood:	n/a	n/a
3	ATF1	chr7:110634674-110635014	K562	blood:	n/a	n/a
4	ATF2	chr7:110559170-110559447	GM12878	blood:	n/a	n/a
5	ATF3	chr7:110634636-110635037	K562	blood:	n/a	n/a
6	ATF3	chr7:110629178-110629445	K562	blood:	n/a	n/a
7	BACH1	chr7:110566972-110567002	K562	blood:	n/a	n/a
8	BACH1	chr7:110584962-110585666	H1-hESC	embryonic stem cell:	n/a	chr7:110585569-110585583
9	BATF	chr7:110653407-110653722	GM12878	blood:	n/a	n/a
10	BATF	chr7:110559152-110559518	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
11	BATF	chr7:110554297-110554621	GM12878	blood:	n/a	n/a
12	BATF	chr7:110653358-110653749	GM12878	blood:	n/a	n/a
13	BATF	chr7:110559184-110559475	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
14	BCL11A	chr7:110559197-110559496	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:110559122-110559539	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:110634646-110634901	K562	blood:	n/a	n/a
17	BHLHE40	chr7:110559153-110559472	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:110653412-110653737	GM12878	blood:	n/a	n/a
19	CBX3	chr7:110634597-110635044	K562	blood:	n/a	n/a
20	CCNT2	chr7:110634682-110634982	K562	blood:	n/a	chr7:110634847-110634867
21	CEBPB	chr7:110654201-110654470	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr7:110602043-110602084	K562	blood:	n/a	n/a
23	CEBPB	chr7:110652214-110652580	IMR90	lung:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
24	CEBPB	chr7:110654177-110654502	K562	blood:	n/a	n/a
25	CEBPB	chr7:110524419-110524763	HepG2	liver:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
26	CEBPB	chr7:110605295-110605582	IMR90	lung:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
27	CEBPB	chr7:110529398-110529581	K562	blood:	n/a	n/a
28	CEBPB	chr7:110562837-110563369	MCF-7	breast:	n/a	n/a
29	CEBPB	chr7:110654357-110654423	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:110562920-110563368	A549	lung:	n/a	n/a
31	CEBPB	chr7:110652257-110652608	MCF-7	breast:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
32	CEBPB	chr7:110654199-110654492	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:110634644-110635105	K562	blood:	n/a	n/a
34	CEBPB	chr7:110529337-110529519	A549	lung:	n/a	n/a
35	CEBPB	chr7:110586701-110586882	K562	blood:	n/a	n/a
36	CEBPB	chr7:110524427-110524734	K562	blood:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
37	CEBPB	chr7:110652239-110652574	A549	lung:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
38	CEBPB	chr7:110652118-110652667	A549	lung:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
39	CEBPB	chr7:110605295-110605603	HepG2	liver:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
40	CEBPB	chr7:110652276-110652491	HepG2	liver:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
41	CEBPB	chr7:110654223-110654498	K562	blood:	n/a	n/a
42	CEBPB	chr7:110652187-110652510	A549	lung:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
43	CEBPB	chr7:110524467-110524738	A549	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
44	CEBPB	chr7:110651925-110652603	Hela-S3	cervix:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
45	CEBPB	chr7:110652324-110652446	K562	blood:	n/a	chr7:110652381-110652392 chr7:110652425-110652436
46	CEBPB	chr7:110605335-110605583	A549	lung:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
47	CEBPB	chr7:110586732-110586873	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:110561985-110562300	IMR90	lung:	n/a	chr7:110562028-110562041
49	CEBPB	chr7:110605370-110605573	K562	blood:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
50	CEBPB	chr7:110524438-110524770	IMR90	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110562986-110563036	Jurkat	blood:	n/a
2	chr7:110562986-110563036	Jurkat	blood:	n/a
3	chr7:110562986-110563036	HRPEpiC	eye:	n/a
4	chr7:110547138-110547188	AG09309	skin:	n/a
5	chr7:110585140-110585190	A549	lung:	n/a
6	chr7:110547138-110547188	Caco-2	colon:	n/a
7	chr7:110585140-110585190	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:110658544-110658594	AG09319	gingival:	n/a
9	chr7:110547138-110547188	SK-N-SH	brain:	n/a
10	chr7:110562986-110563036	HEK293	kidney:	embryo
11	chr7:110547138-110547188	PFSK-1	brain:	n/a
12	chr7:110547138-110547188	AoSMC	blood vessel:	n/a
13	chr7:110562986-110563036	PrEC	prostate:	n/a
14	chr7:110585140-110585190	PrEC	prostate:	n/a
15	chr7:110547138-110547188	CMK	blood:	n/a
16	chr7:110562986-110563036	IMR90	lung:	fetal
17	chr7:110585140-110585190	PFSK-1	brain:	n/a
18	chr7:110547138-110547188	ECC-1	luminal epithelium:	n/a
19	chr7:110658544-110658594	SK-N-SH	brain:	n/a
20	chr7:110562986-110563036	MCF-7	breast:	n/a
21	chr7:110585140-110585190	GM19239	blood:	n/a
22	chr7:110658544-110658594	LNCaP	prostate:	n/a
23	chr7:110547138-110547188	ovcar-3	ovarian:	n/a
24	chr7:110585140-110585190	HAEpiC	amniotic membrane:	n/a
25	chr7:110658544-110658594	Caco-2	colon:	n/a
26	chr7:110585140-110585190	HRE	kidney:	n/a
27	chr7:110585140-110585190	AG04450	lung:	fetal
28	chr7:110658544-110658594	HRPEpiC	eye:	n/a
29	chr7:110585140-110585190	HEEpiC	esophagus:	n/a
30	chr7:110547138-110547188	MCF10A-Er-Src	breast:	n/a
31	chr7:110658544-110658594	SK-N-SH_RA	brain:	n/a
32	chr7:110658544-110658594	HAEpiC	amniotic membrane:	n/a
33	chr7:110562986-110563036	H1-hESC	embryonic stem cell:	embryo
34	chr7:110547138-110547188	T-47D	breast:	n/a
35	chr7:110658544-110658594	GM12891	blood:	n/a
36	chr7:110658544-110658594	AG04450	lung:	fetal
37	chr7:110547138-110547188	GM06990	blood:	n/a
38	chr7:110562986-110563036	A549	lung:	n/a
39	chr7:110585140-110585190	HRPEpiC	eye:	n/a
40	chr7:110658544-110658594	GM12878	blood:	n/a
41	chr7:110547138-110547188	HCM	heart:	n/a
42	chr7:110547138-110547188	RPTEC	kidney:	n/a
43	chr7:110562986-110563036	MCF10A-Er-Src	breast:	n/a
44	chr7:110585140-110585190	Caco-2	colon:	n/a
45	chr7:110658544-110658594	Hela-S3	cervix:	n/a
46	chr7:110585140-110585190	SK-N-MC	brain:	n/a
47	chr7:110547138-110547188	HEEpiC	esophagus:	n/a
48	chr7:110658544-110658594	HNPCEpiC	eye:	n/a
49	chr7:110547138-110547188	HIPEpiC	eye:	n/a
50	chr7:110585140-110585190	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
2	chr7:110650313..110653197-chr7:110655896..110658694,2	K562	blood:
3	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
4	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
5	chr7:110650313..110653197-chr7:110655896..110658694,2	K562	blood:
6	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
7	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
8	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
9	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
10	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
11	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
12	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
13	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
14	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
15	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
16	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
17	chr7:110645729..110647636-chr7:110649973..110652991,3	K562	blood:
18	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
19	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
20	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
21	chr7:110642788..110644757-chr7:111200772..111203526,2	K562	blood:
22	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
23	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
24	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
25	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
26	chr7:110644466..110647207-chr7:110661227..110663752,2	MCF-7	breast:
27	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
28	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
29	chr7:110641915..110646048-chr7:110658516..110661977,3	K562	blood:
30	chr7:110641707..110643850-chr7:110679248..110680877,2	K562	blood:
31	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
32	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
33	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
34	chr1:244816363..244816913-chr7:110550021..110550823,2	MCF-7	breast:
35	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
36	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
37	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
38	chr7:110635157..110638146-chr7:111201987..111204497,2	K562	blood:
39	chr6:22768459..22769224-chr7:110535482..110536237,2	MCF-7	breast:
40	chr7:110641915..110646048-chr7:110658516..110661977,3	K562	blood:
41	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
42	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
43	chr7:110654683..110656937-chr7:110658000..110660146,2	K562	blood:
44	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:

Variant related genes	Relation type
IMMP2L	TF binding region
ENSG00000221279	TF binding region
IMMP2L	CpG island
ENSG00000221279	CpG island
ENSG00000184903	chromatin interactions
ENSG00000121644	chromatin interactions

Extended variants
information (count: 4498 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4498 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10258933	chr7:110516659-110516660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373976691	chr7:110516738-110516739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184581603	chr7:110516765-110516766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112541688	chr7:110516787-110516788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190256979	chr7:110516839-110516840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575923991	chr7:110516879-110516880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544565912	chr7:110516899-110516900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181757686	chr7:110516913-110516914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10259286	chr7:110516918-110516919	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs186057476	chr7:110516919-110516920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62464044	chr7:110516933-110516934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75314346	chr7:110516957-110516958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189603453	chr7:110516958-110516959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548115838	chr7:110516967-110516968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181868436	chr7:110516968-110516969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549403290	chr7:110516979-110516980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs145202574	chr7:110516983-110516984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150987471	chr7:110517039-110517040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77499654	chr7:110517118-110517119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560543554	chr7:110517126-110517127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370989208	chr7:110517209-110517210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555096601	chr7:110517252-110517253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567338174	chr7:110517350-110517351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567416640	chr7:110517435-110517436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537962068	chr7:110517549-110517550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556161048	chr7:110517604-110517605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73425039	chr7:110517622-110517623	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538555913	chr7:110517629-110517630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558118281	chr7:110517641-110517642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577823714	chr7:110517651-110517652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140754959	chr7:110517675-110517676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534015874	chr7:110517715-110517716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560309715	chr7:110517726-110517727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573822524	chr7:110517735-110517736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542738670	chr7:110517752-110517753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74973629	chr7:110517754-110517755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531561338	chr7:110517769-110517770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551663931	chr7:110517847-110517848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565220021	chr7:110517848-110517849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527581613	chr7:110517909-110517910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150114024	chr7:110517927-110517928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112437434	chr7:110517959-110517960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569099628	chr7:110517975-110517976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536364155	chr7:110517983-110517984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558422360	chr7:110517988-110517989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549586021	chr7:110518039-110518040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556349037	chr7:110518050-110518051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78528301	chr7:110518061-110518062	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558117967	chr7:110518133-110518134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571653067	chr7:110518139-110518140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110511800-110517200	Weak transcription	Primary T cells from cord blood	blood
2	chr7:110515000-110522000	Weak transcription	Adipose Nuclei	Adipose
3	chr7:110515400-110517200	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr7:110515600-110517200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:110516400-110517600	Enhancers	Fetal Stomach	stomach
6	chr7:110516600-110517000	Enhancers	Fetal Lung	lung
7	chr7:110517000-110518200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:110517200-110517600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:110517200-110517600	Enhancers	Fetal Lung	lung
10	chr7:110517200-110517800	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr7:110517600-110521600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr7:110518200-110519400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:110519200-110519400	Enhancers	Spleen	Spleen
14	chr7:110519400-110522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:110521600-110522200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:110522000-110522400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:110522000-110522400	Enhancers	Adipose Nuclei	Adipose
18	chr7:110528000-110529000	Enhancers	Fetal Lung	lung
19	chr7:110528200-110528600	Enhancers	Brain Germinal Matrix	brain
20	chr7:110529600-110529800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:110529800-110530400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:110530200-110530800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr7:110530200-110531000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr7:110530400-110530800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr7:110530400-110531000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:110531000-110531600	Enhancers	Dnd41	blood
27	chr7:110540400-110540800	Enhancers	HSMMtube	muscle
28	chr7:110541000-110541400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:110542800-110545600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr7:110544800-110546000	Enhancers	Primary T cells from cord blood	blood
31	chr7:110545400-110546400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr7:110545600-110546000	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr7:110545600-110546600	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr7:110545800-110546600	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr7:110546000-110546400	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr7:110546000-110546600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr7:110546000-110546600	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr7:110546400-110546600	Enhancers	Primary T cells from cord blood	blood
39	chr7:110549000-110549200	Enhancers	A549	lung
40	chr7:110549000-110549400	Enhancers	Liver	Liver
41	chr7:110549000-110549400	Enhancers	HepG2	liver
42	chr7:110549000-110550200	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr7:110549800-110550200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:110550000-110550200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr7:110550200-110562000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr7:110552800-110553000	Enhancers	Esophagus	oesophagus
47	chr7:110556000-110561200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:110556600-110557000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:110557000-110557400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr7:110557000-110557600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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