Variant report

Variant	nsv464296
Chromosome Location	chr7:5792745-5850642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1146)
CpG islands
(count:1404)
Chromatin interactive
region (count:39)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1146 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5807434-5807806	HepG2	liver:	n/a	chr7:5807779-5807795
2	ARID3A	chr7:5821215-5821617	K562	blood:	n/a	n/a
3	ARID3A	chr7:5837477-5837688	K562	blood:	n/a	n/a
4	ARID3A	chr7:5813469-5813783	K562	blood:	n/a	n/a
5	ARID3A	chr7:5826122-5826510	K562	blood:	n/a	n/a
6	ARID3A	chr7:5795066-5795627	K562	blood:	n/a	n/a
7	ARID3A	chr7:5821223-5821516	HepG2	liver:	n/a	n/a
8	ATF1	chr7:5826182-5826466	K562	blood:	n/a	n/a
9	ATF1	chr7:5795291-5795600	K562	blood:	n/a	n/a
10	ATF1	chr7:5837427-5837729	K562	blood:	n/a	n/a
11	ATF1	chr7:5821130-5821587	K562	blood:	n/a	n/a
12	ATF2	chr7:5821065-5821572	GM12878	blood:	n/a	n/a
13	ATF2	chr7:5821109-5821583	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:5821082-5821515	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:5821109-5821676	A549	lung:	n/a	n/a
16	ATF3	chr7:5821176-5821637	A549	lung:	n/a	n/a
17	ATF3	chr7:5826145-5826345	K562	blood:	n/a	n/a
18	ATF3	chr7:5821100-5821451	K562	blood:	n/a	n/a
19	ATF3	chr7:5826108-5826365	K562	blood:	n/a	n/a
20	ATF3	chr7:5813323-5813726	K562	blood:	n/a	chr7:5813565-5813579
21	BACH1	chr7:5810847-5810938	K562	blood:	n/a	n/a
22	BACH1	chr7:5821155-5821414	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:5795215-5795679	K562	blood:	n/a	n/a
24	BACH1	chr7:5795391-5795591	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL3	chr7:5821185-5821680	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
26	BCL3	chr7:5821019-5821639	A549	lung:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
27	BCLAF1	chr7:5821091-5821689	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
28	BCLAF1	chr7:5821070-5821753	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
29	BCLAF1	chr7:5821069-5821672	K562	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
30	BCLAF1	chr7:5821040-5821673	GM12878	blood:	n/a	chr7:5821285-5821298 chr7:5821316-5821324
31	BHLHE40	chr7:5820771-5820774	K562	blood:	n/a	n/a
32	BHLHE40	chr7:5795306-5795596	K562	blood:	n/a	n/a
33	BHLHE40	chr7:5830403-5830547	A549	lung:	n/a	n/a
34	BHLHE40	chr7:5821157-5821452	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:5817625-5817897	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:5826102-5826422	K562	blood:	n/a	n/a
37	BHLHE40	chr7:5821124-5821604	K562	blood:	n/a	chr7:5821155-5821171
38	BHLHE40	chr7:5821108-5821597	GM12878	blood:	n/a	chr7:5821155-5821171
39	BRCA1	chr7:5813381-5813721	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr7:5820533-5820584	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr7:5821222-5821465	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr7:5821213-5821484	HepG2	liver:	n/a	n/a
43	CBX3	chr7:5821023-5821768	HCT-116	colon:	n/a	n/a
44	CBX3	chr7:5825939-5826501	K562	blood:	n/a	n/a
45	CBX3	chr7:5821114-5821700	K562	blood:	n/a	n/a
46	CBX3	chr7:5821041-5822095	K562	blood:	n/a	n/a
47	CBX3	chr7:5813239-5813778	K562	blood:	n/a	n/a
48	CBX3	chr7:5820938-5821793	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:5813109-5813866	HCT-116	colon:	n/a	n/a
50	CCNT2	chr7:5813501-5813508	K562	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5821313-5821363	HCF	heart:	n/a
2	chr7:5821313-5821363	HCF	heart:	n/a
3	chr7:5825437-5825487	ovcar-3	ovarian:	n/a
4	chr7:5812747-5812797	NT2-D1	testis:	n/a
5	chr7:5821305-5821355	HAEpiC	amniotic membrane:	n/a
6	chr7:5821305-5821355	AG10803	skin:	n/a
7	chr7:5821313-5821363	Hela-S3	cervix:	n/a
8	chr7:5819198-5819248	GM12891	blood:	n/a
9	chr7:5821320-5821370	HCF	heart:	n/a
10	chr7:5825437-5825487	HNPCEpiC	eye:	n/a
11	chr7:5819198-5819248	ECC-1	luminal epithelium:	n/a
12	chr7:5822206-5822256	SK-N-SH_RA	brain:	n/a
13	chr7:5821313-5821363	H1-hESC	embryonic stem cell:	embryo
14	chr7:5833275-5833325	HMEC	breast:	n/a
15	chr7:5834372-5834422	HCF	heart:	n/a
16	chr7:5816628-5816678	HUVEC	blood vessel:	n/a
17	chr7:5821099-5821149	Hepatocyte	liver:	n/a
18	chr7:5806497-5806547	SK-N-MC	brain:	n/a
19	chr7:5834292-5834342	AoSMC	blood vessel:	n/a
20	chr7:5821294-5821344	AG10803	skin:	n/a
21	chr7:5833444-5833494	NB4	blood:	n/a
22	chr7:5821307-5821357	HUVEC	blood vessel:	n/a
23	chr7:5821294-5821344	AoSMC	blood vessel:	n/a
24	chr7:5821227-5821277	HepG2	liver:	n/a
25	chr7:5822206-5822256	HCM	heart:	n/a
26	chr7:5821294-5821344	K562	blood:	n/a
27	chr7:5825437-5825487	ProgFib	skin:	n/a
28	chr7:5833444-5833494	MCF-7	breast:	n/a
29	chr7:5821294-5821344	BE2_C	brain:	n/a
30	chr7:5833275-5833325	NB4	blood:	n/a
31	chr7:5822206-5822256	MCF10A-Er-Src	breast:	n/a
32	chr7:5806497-5806547	AG09319	gingival:	n/a
33	chr7:5821305-5821355	T-47D	breast:	n/a
34	chr7:5833383-5833433	HCM	heart:	n/a
35	chr7:5806497-5806547	HCT-116	colon:	n/a
36	chr7:5820542-5820592	NHDF-neo	bronchial:	n/a
37	chr7:5806497-5806547	MCF10A-Er-Src	breast:	n/a
38	chr7:5833275-5833325	HNPCEpiC	eye:	n/a
39	chr7:5833383-5833433	U87	brain:	n/a
40	chr7:5821596-5821646	HNPCEpiC	eye:	n/a
41	chr7:5821320-5821370	SKMC	muscle:	n/a
42	chr7:5822206-5822256	AG04450	lung:	fetal
43	chr7:5833275-5833325	HepG2	liver:	n/a
44	chr7:5821099-5821149	AG10803	skin:	n/a
45	chr7:5834372-5834422	AG09309	skin:	n/a
46	chr7:5834292-5834342	HL-60	blood:	n/a
47	chr7:5812747-5812797	A549	lung:	n/a
48	chr7:5821297-5821347	SK-N-SH	brain:	n/a
49	chr7:5821313-5821363	Caco-2	colon:	n/a
50	chr7:5820542-5820592	ProgFib	skin:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5813104..5816450-chr7:5816759..5819412,5	MCF-7	breast:
2	chr7:5195253..5196797-chr7:5849975..5851503,2	MCF-7	breast:
3	chr7:5804467..5808977-chr7:5818984..5822702,6	MCF-7	breast:
4	chr7:5813104..5816450-chr7:5816759..5819412,5	MCF-7	breast:
5	chr7:5012931..5013720-chr7:5820910..5821674,3	MCF-7	breast:
6	chr7:5794825..5797015-chr7:5812858..5815077,2	K562	blood:
7	chr7:5782625..5785209-chr7:5794939..5796627,2	K562	blood:
8	chr7:5012217..5014206-chr7:5819722..5821650,2	MCF-7	breast:
9	chr7:5798985..5801479-chr7:5819651..5822590,2	MCF-7	breast:
10	chr7:5012944..5014466-chr7:5819776..5821589,2	MCF-7	breast:
11	chr7:5802352..5803887-chr7:5805406..5807643,2	MCF-7	breast:
12	chr7:5805043..5806822-chr7:5811285..5813063,2	MCF-7	breast:
13	chr7:5810649..5812378-chr7:5816522..5818185,2	K562	blood:
14	chr7:5810649..5812378-chr7:5816522..5818185,2	K562	blood:
15	chr7:5198471..5200829-chr7:5846767..5848341,2	MCF-7	breast:
16	chr7:5798985..5801479-chr7:5819651..5822590,2	MCF-7	breast:
17	chr7:5012284..5014483-chr7:5819277..5821280,2	K562	blood:
18	chr7:5814291..5819419-chr7:5819714..5822624,8	MCF-7	breast:
19	chr6:74233083..74233652-chr7:5820678..5821633,2	Hela-S3	cervix:
20	chr7:5816356..5819327-chr7:5819768..5821296,2	MCF-7	breast:
21	chr7:5012695..5014428-chr7:5820890..5822170,10	MCF-7	breast:
22	chr7:5013565..5014445-chr7:5820432..5821785,4	K562	blood:
23	chr7:5812370..5815650-chr7:5819494..5823462,5	K562	blood:
24	chr7:5792453..5794631-chr7:5795297..5797484,2	K562	blood:
25	chr7:5013249..5014674-chr7:5819932..5821408,8	Hela-S3	cervix:
26	chr7:5802352..5803887-chr7:5805406..5807643,2	MCF-7	breast:
27	chr7:5805613..5808202-chr7:5813571..5816146,2	K562	blood:
28	chr7:5792453..5794631-chr7:5795297..5797484,2	K562	blood:
29	chr7:5805613..5808202-chr7:5812244..5816146,3	K562	blood:
30	chr7:5794825..5797015-chr7:5812858..5815077,2	K562	blood:
31	chr7:5790125..5792090-chr7:5812066..5813881,3	K562	blood:
32	chr7:5569817..5572389-chr7:5795762..5797317,2	K562	blood:
33	chr7:5805613..5808202-chr7:5812244..5816146,3	K562	blood:
34	chr7:5012983..5015694-chr7:5819277..5821133,2	K562	blood:
35	chr7:5795115..5796838-chr7:5800518..5802402,2	K562	blood:
36	chr7:5013311..5013911-chr7:5820908..5821412,3	HCT-116	colon:
37	chr7:5805613..5808202-chr7:5813571..5816146,2	K562	blood:
38	chr7:5805043..5806822-chr7:5811285..5813063,2	MCF-7	breast:
39	chr7:5811498..5815650-chr7:5819399..5823462,6	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
2	lnc-OCM-1	chr7:5834112-5834518	NONHSAT118937
3	lnc-OCM-1	chr7:5850593-5850617	NONHSAT118937
4	lnc-RSPH10B-2	chr7:5817157-5817259	NONHSAT118936
5	lnc-RSPH10B-2	chr7:5806526-5806570	NONHSAT118935
6	lnc-RSPH10B-2	chr7:5800719-5800769	NONHSAT118935
7	lnc-RSPH10B-2	chr7:5819616-5819923	NONHSAT118935
8	lnc-OCM-1	chr7:5850594-5850617	XLOC_005976
9	lnc-RSPH10B-2	chr7:5819616-5819899	NONHSAT118936
10	lnc-OCM-1	chr7:5834113-5834518	XLOC_005976
11	lnc-RSPH10B-2	chr7:5817118-5817259	NONHSAT118935

No data

Variant related genes	Relation type
RNF216	TF binding region
RNF216	CpG island
ENSG00000156508	chromatin interactions
ENSG00000196204	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000011275	chromatin interactions
NR3C1	miRNA target sites

Extended variants
information (count: 3255 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3255 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6463513	chr7:5792745-5792746	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115221976	chr7:5792747-5792748	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190715149	chr7:5792750-5792751	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148357415	chr7:5792752-5792753	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141532178	chr7:5792757-5792758	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540636071	chr7:5792767-5792768	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73048704	chr7:5792776-5792777	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532841279	chr7:5792814-5792815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544498064	chr7:5792818-5792819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544930468	chr7:5792888-5792889	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138332803	chr7:5792890-5792891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11980653	chr7:5792896-5792897	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548699951	chr7:5792913-5792914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370178502	chr7:5792955-5792956	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548086181	chr7:5792967-5792968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567379073	chr7:5793013-5793014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374050276	chr7:5793061-5793062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182903392	chr7:5793072-5793073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571110576	chr7:5793074-5793075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538982143	chr7:5793084-5793085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs59608453	chr7:5793088-5793089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562174889	chr7:5793191-5793192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569100493	chr7:5793277-5793278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529450428	chr7:5793301-5793302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536472120	chr7:5793344-5793345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554432850	chr7:5793349-5793350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557176754	chr7:5793366-5793367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540319329	chr7:5793397-5793398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117354018	chr7:5793438-5793439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558453410	chr7:5793453-5793454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577156237	chr7:5793454-5793455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544541074	chr7:5793482-5793483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149550027	chr7:5793498-5793499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533044300	chr7:5793514-5793515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542036891	chr7:5793523-5793524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560442072	chr7:5793543-5793544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528194593	chr7:5793562-5793563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147257676	chr7:5793565-5793566	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7789481	chr7:5793570-5793571	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs532122733	chr7:5793621-5793622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550566376	chr7:5793625-5793626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569188672	chr7:5793632-5793633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569503181	chr7:5793659-5793660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552995765	chr7:5793664-5793665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111618510	chr7:5793670-5793671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117636845	chr7:5793687-5793688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554750622	chr7:5793750-5793751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374104480	chr7:5793751-5793752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs398047576	chr7:5793752-5793753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs59052517	chr7:5793790-5793791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Multiple myeloma	17550852	CNVD
Cancer	17440070	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1549 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5753200-5794400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:5762000-5820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:5768800-5798200	Weak transcription	Colonic Mucosa	Colon
4	chr7:5774200-5800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:5781400-5799600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:5781400-5816800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:5782800-5794400	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr7:5783600-5798200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:5784000-5819600	Weak transcription	Fetal Heart	heart
10	chr7:5784200-5792800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:5784200-5792800	Strong transcription	Primary T helper cells PMA-I stimulated	--
12	chr7:5784200-5798000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:5784400-5792800	Strong transcription	Primary T cells from cord blood	blood
14	chr7:5784800-5792800	Strong transcription	Dnd41	blood
15	chr7:5785000-5792800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr7:5785000-5795400	Strong transcription	Fetal Muscle Trunk	muscle
17	chr7:5785200-5807000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:5785400-5793000	Strong transcription	Primary B cells from peripheral blood	blood
19	chr7:5785600-5794200	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr7:5785800-5793000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:5786000-5792800	Strong transcription	K562	blood
22	chr7:5786000-5798000	Weak transcription	Fetal Brain Male	brain
23	chr7:5786200-5795000	Weak transcription	HUVEC	blood vessel
24	chr7:5787600-5794000	Weak transcription	Stomach Mucosa	stomach
25	chr7:5787800-5794600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr7:5788600-5792800	Strong transcription	Osteobl	bone
27	chr7:5789000-5792800	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr7:5789000-5794200	Strong transcription	Fetal Thymus	thymus
29	chr7:5789200-5792800	Strong transcription	HSMM	muscle
30	chr7:5789200-5793000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr7:5789200-5793200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr7:5789400-5792800	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr7:5789400-5792800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr7:5789400-5793000	Strong transcription	Primary hematopoietic stem cells	blood
35	chr7:5789400-5793000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:5789600-5792800	Strong transcription	Primary T cells fromperipheralblood	blood
37	chr7:5789800-5792800	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr7:5789800-5792800	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:5789800-5792800	Strong transcription	Muscle Satellite Cultured Cells	--
40	chr7:5789800-5792800	Strong transcription	Liver	Liver
41	chr7:5789800-5792800	Strong transcription	Duodenum Mucosa	Duodenum
42	chr7:5789800-5792800	Strong transcription	Fetal Muscle Leg	muscle
43	chr7:5789800-5792800	Strong transcription	Placenta	Placenta
44	chr7:5789800-5792800	Strong transcription	GM12878-XiMat	blood
45	chr7:5789800-5792800	Strong transcription	NHEK	skin
46	chr7:5789800-5794400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr7:5790000-5792800	Strong transcription	Adipose Nuclei	Adipose
48	chr7:5790000-5792800	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr7:5790000-5795000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr7:5790200-5792800	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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