Variant report

Variant	nsv887810
Chromosome Location	chr7:18193589-18391557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1559)
CpG islands
(count:366)
Chromatin interactive
region (count:97)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:18230594-18230697	K562	blood:	n/a	n/a
2	ARID3A	chr7:18218013-18218198	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:18217852-18218274	K562	blood:	n/a	n/a
4	ARID3A	chr7:18303709-18303826	K562	blood:	n/a	n/a
5	ARID3A	chr7:18231163-18231437	K562	blood:	n/a	n/a
6	ARID3A	chr7:18216717-18217627	K562	blood:	n/a	n/a
7	ATF1	chr7:18360525-18360954	K562	blood:	n/a	n/a
8	ATF1	chr7:18355303-18355464	K562	blood:	n/a	n/a
9	ATF1	chr7:18214616-18214939	K562	blood:	n/a	n/a
10	ATF1	chr7:18329927-18330098	K562	blood:	n/a	n/a
11	ATF1	chr7:18301886-18302085	K562	blood:	n/a	n/a
12	ATF1	chr7:18216885-18217560	K562	blood:	n/a	n/a
13	ATF1	chr7:18217858-18218308	K562	blood:	n/a	n/a
14	ATF2	chr7:18217364-18218418	GM12878	blood:	n/a	n/a
15	ATF3	chr7:18217814-18218252	K562	blood:	n/a	n/a
16	BACH1	chr7:18385285-18385657	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:18360062-18360314	K562	blood:	n/a	n/a
18	BATF	chr7:18218797-18219127	GM12878	blood:	n/a	n/a
19	BATF	chr7:18217382-18217699	GM12878	blood:	n/a	n/a
20	BATF	chr7:18217858-18218265	GM12878	blood:	n/a	n/a
21	BATF	chr7:18217334-18217781	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:18217377-18217760	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:18217980-18218363	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:18219765-18219857	K562	blood:	n/a	n/a
25	BHLHE40	chr7:18217930-18218221	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:18229222-18229524	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:18217461-18217661	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:18216983-18218305	K562	blood:	n/a	n/a
29	BHLHE40	chr7:18335718-18335912	GM12878	blood:	n/a	chr7:18335758-18335779 chr7:18335763-18335772
30	BHLHE40	chr7:18214755-18214817	K562	blood:	n/a	n/a
31	BHLHE40	chr7:18357060-18357405	K562	blood:	n/a	n/a
32	BHLHE40	chr7:18357066-18357374	HepG2	liver:	n/a	n/a
33	BRCA1	chr7:18357054-18357425	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr7:18214377-18214940	K562	blood:	n/a	n/a
35	CBX3	chr7:18217004-18217346	K562	blood:	n/a	n/a
36	CBX3	chr7:18277838-18278216	K562	blood:	n/a	n/a
37	CBX3	chr7:18301694-18302044	HCT-116	colon:	n/a	n/a
38	CBX3	chr7:18216792-18218313	K562	blood:	n/a	n/a
39	CBX3	chr7:18214475-18214818	K562	blood:	n/a	n/a
40	CBX3	chr7:18301669-18302135	K562	blood:	n/a	n/a
41	CBX3	chr7:18301664-18302173	HCT-116	colon:	n/a	n/a
42	CBX3	chr7:18217740-18218263	K562	blood:	n/a	n/a
43	CBX3	chr7:18301668-18302097	K562	blood:	n/a	n/a
44	CBX3	chr7:18274143-18274460	K562	blood:	n/a	n/a
45	CCNT2	chr7:18215800-18216153	K562	blood:	n/a	n/a
46	CCNT2	chr7:18216722-18218280	K562	blood:	n/a	n/a
47	CCNT2	chr7:18360724-18360924	K562	blood:	n/a	n/a
48	CEBPB	chr7:18256134-18256364	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:18217958-18218185	K562	blood:	n/a	n/a
50	CEBPB	chr7:18215357-18215778	K562	blood:	n/a	chr7:18215482-18215493 chr7:18215482-18215493 chr7:18215480-18215493

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18329602-18329652	AG04450	lung:	fetal
2	chr7:18194528-18194578	ovcar-3	ovarian:	n/a
3	chr7:18329916-18329966	NB4	blood:	n/a
4	chr7:18330092-18330142	HUVEC	blood vessel:	n/a
5	chr7:18329562-18329612	PFSK-1	brain:	n/a
6	chr7:18330092-18330142	SK-N-MC	brain:	n/a
7	chr7:18357830-18357880	K562	blood:	n/a
8	chr7:18194528-18194578	SKMC	muscle:	n/a
9	chr7:18329602-18329652	Caco-2	colon:	n/a
10	chr7:18357830-18357880	SK-N-MC	brain:	n/a
11	chr7:18329916-18329966	H1-hESC	embryonic stem cell:	embryo
12	chr7:18329916-18329966	AG04450	lung:	fetal
13	chr7:18329602-18329652	SAEC	small airway:	n/a
14	chr7:18329562-18329612	MCF-7	breast:	n/a
15	chr7:18357830-18357880	AG04450	lung:	fetal
16	chr7:18357830-18357880	MCF-7	breast:	n/a
17	chr7:18329602-18329652	AG09309	skin:	n/a
18	chr7:18329602-18329652	PrEC	prostate:	n/a
19	chr7:18194528-18194578	AoSMC	blood vessel:	n/a
20	chr7:18330092-18330142	HEK293	kidney:	embryo
21	chr7:18329562-18329612	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:18330092-18330142	PFSK-1	brain:	n/a
23	chr7:18194528-18194578	HCT-116	colon:	n/a
24	chr7:18329562-18329612	PANC-1	pancreas:	n/a
25	chr7:18329602-18329652	NB4	blood:	n/a
26	chr7:18329916-18329966	HIPEpiC	eye:	n/a
27	chr7:18329562-18329612	HEK293	kidney:	embryo
28	chr7:18329602-18329652	HCPEpiC	choroid plexus:	n/a
29	chr7:18329602-18329652	BJ	skin:	n/a
30	chr7:18357830-18357880	HCPEpiC	choroid plexus:	n/a
31	chr7:18357830-18357880	PrEC	prostate:	n/a
32	chr7:18329562-18329612	NHBE	bronchial:	n/a
33	chr7:18330092-18330142	HL-60	blood:	n/a
34	chr7:18329916-18329966	HRCEpiC	kidney:	n/a
35	chr7:18194528-18194578	BJ	skin:	n/a
36	chr7:18329602-18329652	HEEpiC	esophagus:	n/a
37	chr7:18329562-18329612	HEEpiC	esophagus:	n/a
38	chr7:18329916-18329966	BJ	skin:	n/a
39	chr7:18357830-18357880	AG09319	gingival:	n/a
40	chr7:18329562-18329612	NT2-D1	testis:	n/a
41	chr7:18194528-18194578	K562	blood:	n/a
42	chr7:18329916-18329966	HRPEpiC	eye:	n/a
43	chr7:18329562-18329612	HAEpiC	amniotic membrane:	n/a
44	chr7:18357830-18357880	RPTEC	kidney:	n/a
45	chr7:18330092-18330142	H1-hESC	embryonic stem cell:	embryo
46	chr7:18357830-18357880	U87	brain:	n/a
47	chr7:18194528-18194578	HRE	kidney:	n/a
48	chr7:18329602-18329652	SK-N-SH	brain:	n/a
49	chr7:18329916-18329966	AG10803	skin:	n/a
50	chr7:18329562-18329612	MCF10A-Er-Src	breast:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:18236690..18239423-chr7:18240922..18243186,4	K562	blood:
2	chr7:18246359..18249174-chr7:18251023..18252849,2	K562	blood:
3	chr7:17977337..17980448-chr7:18216760..18219646,3	K562	blood:
4	chr7:18192988..18195732-chr7:18197133..18198734,2	K562	blood:
5	chr7:18224613..18227615-chr7:18227879..18232094,3	K562	blood:
6	chr7:18217240..18219162-chr7:18248697..18251214,2	MCF-7	breast:
7	chr7:18217795..18220211-chr7:18222403..18225204,2	MCF-7	breast:
8	chr7:17977338..17980907-chr7:18216760..18220938,4	K562	blood:
9	chr7:18251666..18253931-chr7:18265138..18267912,2	K562	blood:
10	chr7:18219431..18222297-chr7:18224982..18227511,2	K562	blood:
11	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
12	chr7:18218078..18219602-chr7:18220654..18223400,2	K562	blood:
13	chr7:16685782..16688238-chr7:18215892..18218697,2	K562	blood:
14	chr7:18206006..18208720-chr7:18214404..18217269,2	K562	blood:
15	chr7:18255155..18255694-chr7:18360726..18361262,2	MCF-7	breast:
16	chr7:18222330..18224720-chr7:18264492..18267054,2	K562	blood:
17	chr7:18205313..18207419-chr7:18215960..18218809,2	K562	blood:
18	chr7:18250651..18253317-chr7:18302876..18305651,2	K562	blood:
19	chr7:18216226..18218726-chr7:18250746..18252267,2	K562	blood:
20	chr7:18192988..18195732-chr7:18197133..18198734,2	K562	blood:
21	chr7:18254922..18255723-chr7:18360545..18361137,3	MCF-7	breast:
22	chr7:18219431..18222297-chr7:18224982..18227511,2	K562	blood:
23	chr7:18246359..18249174-chr7:18251023..18252849,2	K562	blood:
24	chr7:17809174..17809741-chr7:18384978..18385956,3	MCF-7	breast:
25	chr7:18217795..18220211-chr7:18222403..18225204,2	MCF-7	breast:
26	chr7:18310468..18313091-chr7:18314736..18317253,2	K562	blood:
27	chr7:18218078..18219602-chr7:18220654..18223400,2	K562	blood:
28	chr7:18254427..18256952-chr7:18257278..18259018,2	K562	blood:
29	chr7:18338973..18341007-chr7:18351398..18353885,2	K562	blood:
30	chr7:18215961..18218185-chr7:18229835..18233297,4	K562	blood:
31	chr7:18240899..18246753-chr7:18248807..18254845,6	K562	blood:
32	chr7:18354053..18356213-chr7:18358057..18360963,3	K562	blood:
33	chr7:18285766..18287431-chr7:18290399..18292754,2	MCF-7	breast:
34	chr7:18237325..18238963-chr7:18240694..18242384,2	MCF-7	breast:
35	chr7:18237325..18238963-chr7:18240694..18242384,2	MCF-7	breast:
36	chr7:18162840..18165489-chr7:18245304..18246939,2	K562	blood:
37	chr7:18250651..18253317-chr7:18302876..18305651,2	K562	blood:
38	chr7:18240899..18244580-chr7:18250175..18254118,3	K562	blood:
39	chr7:17745871..17747109-chr7:18385010..18385969,4	MCF-7	breast:
40	chr7:18233266..18236170-chr7:18243676..18245578,2	K562	blood:
41	chr7:18255155..18255694-chr7:18360726..18361262,2	MCF-7	breast:
42	chr7:18254427..18256952-chr7:18257278..18259018,2	K562	blood:
43	chr7:18010695..18011460-chr7:18360393..18361102,3	MCF-7	breast:
44	chr7:18325772..18327455-chr7:18347556..18349575,2	K562	blood:
45	chr7:18255243..18258028-chr7:18260325..18261899,2	MCF-7	breast:
46	chr7:18373835..18376264-chr7:18376406..18378512,2	K562	blood:
47	chr7:18236690..18239423-chr7:18240922..18243186,4	K562	blood:
48	chr7:18103570..18104553-chr7:18385072..18385885,2	MCF-7	breast:
49	chr7:18321787..18324563-chr7:18327488..18329360,2	K562	blood:
50	chr7:18217240..18219162-chr7:18248697..18251214,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHR-8	chr7:18329811-18329970	NONHSAT119359
2	lnc-AHR-8	chr7:18367072-18367381	NONHSAT119359
3	lnc-AHR-8	chr7:18330064-18330138	NONHSAT119359
4	lnc-AHR-8	chr7:18201852-18202251	NONHSAT119356
5	lnc-AHR-8	chr7:18201852-18201972	NONHSAT119358
6	lnc-AHR-8	chr7:18365135-18365215	NONHSAT119358
7	lnc-AHR-8	chr7:18367072-18367235	NONHSAT119358
8	lnc-AHR-8	chr7:18365135-18365215	NONHSAT119359
9	lnc-AHR-8	chr7:18330073-18330138	NONHSAT119360

No data

Variant related genes	Relation type
ENSG00000223030	TF binding region
HDAC9	TF binding region
ENSG00000223030	CpG island
HDAC9	CpG island
ENSG00000071189	chromatin interactions
ENSG00000136261	chromatin interactions

Extended variants
information (count: 6331 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:6331 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12171593	chr7:18193589-18193590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138199256	chr7:18193680-18193681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548565111	chr7:18193697-18193698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570337045	chr7:18193699-18193700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11981992	chr7:18193712-18193713	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs552145925	chr7:18193718-18193719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6971014	chr7:18193719-18193720	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368390130	chr7:18193731-18193732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191923945	chr7:18193755-18193756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs571059177	chr7:18193771-18193772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545825473	chr7:18193775-18193776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553132671	chr7:18193855-18193856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574658636	chr7:18193869-18193870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535656340	chr7:18193940-18193941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556937334	chr7:18193965-18193966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142812457	chr7:18193974-18193975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545829085	chr7:18194001-18194002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568799433	chr7:18194044-18194045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576851650	chr7:18194050-18194051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372602805	chr7:18194116-18194117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541095982	chr7:18194250-18194251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377264855	chr7:18194251-18194252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369048164	chr7:18194276-18194277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559434985	chr7:18194292-18194293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150690402	chr7:18194296-18194297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182970871	chr7:18194311-18194312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139995528	chr7:18194313-18194314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186786179	chr7:18194314-18194315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149391116	chr7:18194339-18194340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144796704	chr7:18194356-18194357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191916716	chr7:18194381-18194382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546685200	chr7:18194405-18194406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568172277	chr7:18194409-18194410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1950040	chr7:18194414-18194415	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs116314648	chr7:18194422-18194423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs17138689	chr7:18194469-18194470	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539696010	chr7:18194477-18194478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58495781	chr7:18194528-18194529	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572789787	chr7:18194564-18194565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535324416	chr7:18194566-18194567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535467459	chr7:18194567-18194568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140362714	chr7:18194585-18194586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193169457	chr7:18194607-18194608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185102294	chr7:18194624-18194625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190747406	chr7:18194667-18194668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144287605	chr7:18194673-18194674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561602650	chr7:18194696-18194697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs34168137	chr7:18194699-18194700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76783086	chr7:18194717-18194718	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373149531	chr7:18194719-18194720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18188200-18202800	Weak transcription	Aorta	Aorta
2	chr7:18190000-18194800	Enhancers	Fetal Heart	heart
3	chr7:18192200-18200600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:18192200-18207400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr7:18193000-18201800	Weak transcription	Left Ventricle	heart
6	chr7:18193000-18201800	Weak transcription	Spleen	Spleen
7	chr7:18194200-18195000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:18194800-18195000	Flanking Active TSS	Fetal Heart	heart
9	chr7:18195000-18195400	Enhancers	Fetal Heart	heart
10	chr7:18195400-18195800	Flanking Active TSS	Fetal Heart	heart
11	chr7:18195800-18197400	Enhancers	Fetal Heart	heart
12	chr7:18200600-18202200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:18201200-18202600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:18201200-18203000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:18201400-18201800	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:18201800-18202600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:18201800-18202600	Enhancers	Adipose Nuclei	Adipose
18	chr7:18201800-18203000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:18201800-18203000	Enhancers	Left Ventricle	heart
20	chr7:18201800-18203000	Enhancers	Right Atrium	heart
21	chr7:18201800-18203000	Enhancers	Spleen	Spleen
22	chr7:18202200-18202600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:18202600-18203000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:18202600-18206600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:18202800-18203000	Enhancers	Aorta	Aorta
26	chr7:18202800-18203000	Enhancers	NHDF-Ad	bronchial
27	chr7:18203000-18203400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr7:18203000-18214800	Weak transcription	Left Ventricle	heart
29	chr7:18203400-18207200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:18206600-18207400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr7:18207200-18207600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:18207400-18207600	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:18207600-18208400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr7:18214400-18214600	Enhancers	Right Atrium	heart
35	chr7:18214400-18215000	Enhancers	K562	blood
36	chr7:18214400-18215200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr7:18214400-18215200	Enhancers	Primary B cells from peripheral blood	blood
38	chr7:18214400-18215200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:18214600-18215000	Enhancers	Spleen	Spleen
40	chr7:18214800-18215000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:18214800-18215200	Enhancers	Placenta	Placenta
42	chr7:18214800-18215200	Enhancers	Left Ventricle	heart
43	chr7:18214800-18216200	Enhancers	HepG2	liver
44	chr7:18215000-18215200	Flanking Active TSS	K562	blood
45	chr7:18215000-18216000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr7:18215000-18216200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:18215000-18217200	Weak transcription	Spleen	Spleen
48	chr7:18215200-18215400	Enhancers	K562	blood
49	chr7:18215200-18217000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:18215200-18217000	Weak transcription	Primary B cells from peripheral blood	blood

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