Variant report

Variant	nsv831442
Chromosome Location	chr8:119181675-119390122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1072)
CpG islands
(count:549)
Chromatin interactive
region (count:41)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:119260387-119260391	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:119356049-119356587	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:119358963-119359088	HepG2	liver:	n/a	n/a
4	ATF2	chr8:119293955-119294652	GM12878	blood:	n/a	n/a
5	ATF2	chr8:119291573-119292171	GM12878	blood:	n/a	n/a
6	ATF2	chr8:119271005-119271525	GM12878	blood:	n/a	n/a
7	ATF2	chr8:119290755-119292196	GM12878	blood:	n/a	n/a
8	ATF2	chr8:119293971-119294645	GM12878	blood:	n/a	n/a
9	ATF2	chr8:119208086-119208496	GM12878	blood:	n/a	n/a
10	ATF3	chr8:119356054-119356627	A549	lung:	n/a	n/a
11	ATF3	chr8:119356109-119356594	A549	lung:	n/a	n/a
12	BATF	chr8:119291646-119291984	GM12878	blood:	n/a	n/a
13	BATF	chr8:119271124-119271491	GM12878	blood:	n/a	n/a
14	BATF	chr8:119208134-119208514	GM12878	blood:	n/a	chr8:119208320-119208331 chr8:119208336-119208347
15	BATF	chr8:119294110-119294449	GM12878	blood:	n/a	n/a
16	BATF	chr8:119344507-119344804	GM12878	blood:	n/a	chr8:119344696-119344706 chr8:119344695-119344706
17	BATF	chr8:119208218-119208444	GM12878	blood:	n/a	chr8:119208320-119208331 chr8:119208336-119208347
18	BATF	chr8:119291657-119292065	GM12878	blood:	n/a	n/a
19	BATF	chr8:119271098-119271518	GM12878	blood:	n/a	n/a
20	BATF	chr8:119294097-119294448	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:119294051-119294494	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:119291688-119291964	GM12878	blood:	n/a	chr8:119291861-119291870
23	BCL11A	chr8:119294067-119294534	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:119291618-119292116	GM12878	blood:	n/a	chr8:119291861-119291870
25	BCL3	chr8:119356130-119356707	A549	lung:	n/a	n/a
26	BCL3	chr8:119356023-119356727	A549	lung:	n/a	n/a
27	BCL3	chr8:119260653-119260886	GM12878	blood:	n/a	n/a
28	BCL3	chr8:119337004-119337403	GM12878	blood:	n/a	n/a
29	BCL3	chr8:119344491-119344829	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:119291581-119292125	GM12878	blood:	n/a	chr8:119291861-119291870
31	BCLAF1	chr8:119294016-119294660	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:119271140-119271438	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:119291615-119292330	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:119356184-119356616	HepG2	liver:	n/a	n/a
35	BHLHE40	chr8:119294058-119294639	GM12878	blood:	n/a	n/a
36	CBX3	chr8:119207935-119208712	HCT-116	colon:	n/a	n/a
37	CEBPB	chr8:119189765-119189973	HepG2	liver:	n/a	chr8:119189872-119189883
38	CEBPB	chr8:119355947-119356766	A549	lung:	n/a	n/a
39	CEBPB	chr8:119199994-119200356	IMR90	lung:	n/a	chr8:119200182-119200193
40	CEBPB	chr8:119200028-119200440	MCF-7	breast:	n/a	chr8:119200182-119200193
41	CEBPB	chr8:119216830-119217116	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:119282230-119282581	IMR90	lung:	n/a	chr8:119282405-119282416 chr8:119282403-119282414 chr8:119282403-119282416
43	CEBPB	chr8:119327654-119327968	IMR90	lung:	n/a	n/a
44	CEBPB	chr8:119208133-119208565	IMR90	lung:	n/a	n/a
45	CEBPB	chr8:119282260-119282545	A549	lung:	n/a	chr8:119282405-119282416 chr8:119282403-119282414 chr8:119282403-119282416
46	CEBPB	chr8:119307924-119308183	A549	lung:	n/a	n/a
47	CEBPB	chr8:119297674-119297937	K562	blood:	n/a	chr8:119297800-119297809 chr8:119297799-119297810
48	CEBPB	chr8:119225524-119225799	A549	lung:	n/a	n/a
49	CEBPB	chr8:119189800-119189925	IMR90	lung:	n/a	chr8:119189872-119189883
50	CEBPB	chr8:119297729-119297881	Hela-S3	cervix:	n/a	chr8:119297800-119297809 chr8:119297799-119297810

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119222516-119222566	HRPEpiC	eye:	n/a
2	chr8:119372894-119372944	SK-N-MC	brain:	n/a
3	chr8:119220574-119220624	HRE	kidney:	n/a
4	chr8:119372894-119372944	SAEC	small airway:	n/a
5	chr8:119268828-119268878	PFSK-1	brain:	n/a
6	chr8:119302728-119302778	BJ	skin:	n/a
7	chr8:119222516-119222566	HEEpiC	esophagus:	n/a
8	chr8:119302728-119302778	MCF-7	breast:	n/a
9	chr8:119372894-119372944	HIPEpiC	eye:	n/a
10	chr8:119268828-119268878	BE2_C	brain:	n/a
11	chr8:119302728-119302778	NT2-D1	testis:	n/a
12	chr8:119268828-119268878	H1-hESC	embryonic stem cell:	embryo
13	chr8:119372894-119372944	HUVEC	blood vessel:	n/a
14	chr8:119302728-119302778	AG04449	skin:	fetal
15	chr8:119344904-119344954	Hepatocyte	liver:	n/a
16	chr8:119358052-119358102	RPTEC	kidney:	n/a
17	chr8:119220574-119220624	ProgFib	skin:	n/a
18	chr8:119208486-119208536	H1-hESC	embryonic stem cell:	embryo
19	chr8:119372894-119372944	HRE	kidney:	n/a
20	chr8:119358052-119358102	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:119220574-119220624	LNCaP	prostate:	n/a
22	chr8:119208486-119208536	SK-N-SH_RA	brain:	n/a
23	chr8:119208486-119208536	SK-N-MC	brain:	n/a
24	chr8:119344904-119344954	HRE	kidney:	n/a
25	chr8:119344904-119344954	HNPCEpiC	eye:	n/a
26	chr8:119302728-119302778	H1-hESC	embryonic stem cell:	embryo
27	chr8:119344904-119344954	SKMC	muscle:	n/a
28	chr8:119344904-119344954	AG10803	skin:	n/a
29	chr8:119372894-119372944	ovcar-3	ovarian:	n/a
30	chr8:119220574-119220624	GM06990	blood:	n/a
31	chr8:119208486-119208536	Hepatocyte	liver:	n/a
32	chr8:119208486-119208536	HRE	kidney:	n/a
33	chr8:119208486-119208536	PrEC	prostate:	n/a
34	chr8:119291748-119291798	PANC-1	pancreas:	n/a
35	chr8:119222516-119222566	HEK293	kidney:	embryo
36	chr8:119222516-119222566	HCF	heart:	n/a
37	chr8:119344904-119344954	AG04449	skin:	fetal
38	chr8:119358052-119358102	H1-hESC	embryonic stem cell:	embryo
39	chr8:119358052-119358102	T-47D	breast:	n/a
40	chr8:119358052-119358102	HL-60	blood:	n/a
41	chr8:119220574-119220624	Hela-S3	cervix:	n/a
42	chr8:119358052-119358102	BE2_C	brain:	n/a
43	chr8:119268828-119268878	SKMC	muscle:	n/a
44	chr8:119291748-119291798	GM19239	blood:	n/a
45	chr8:119302728-119302778	HL-60	blood:	n/a
46	chr8:119220574-119220624	HCF	heart:	n/a
47	chr8:119291748-119291798	Caco-2	colon:	n/a
48	chr8:119358052-119358102	GM19239	blood:	n/a
49	chr8:119302728-119302778	AG10803	skin:	n/a
50	chr8:119372894-119372944	HRCEpiC	kidney:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:119237839..119239918-chr8:119250046..119252760,2	K562	blood:
2	chr8:119257831..119260580-chr8:119263913..119265980,2	MCF-7	breast:
3	chr8:119313185..119314685-chr8:119324258..119326116,2	MCF-7	breast:
4	chr8:119122724..119124967-chr8:119284674..119287665,2	MCF-7	breast:
5	chr8:119344779..119346281-chr8:119346898..119348552,2	K562	blood:
6	chr8:119341376..119343834-chr8:119345796..119348597,3	MCF-7	breast:
7	chr8:118875478..118876394-chr8:119340079..119340635,2	MCF-7	breast:
8	chr8:119226355..119229018-chr8:119253039..119255314,2	K562	blood:
9	chr8:119363913..119366502-chr8:119371713..119373996,2	MCF-7	breast:
10	chr8:119220054..119222499-chr8:119225215..119227233,2	MCF-7	breast:
11	8:118911988-118922970..8:119208477-119211356	GM12878	blood:
12	8:118988958-118993290..8:119208477-119211356	H1-hESC	embryonic stem cell:	embryo
13	chr8:119226355..119229018-chr8:119253039..119255314,2	K562	blood:
14	chr8:119227641..119229899-chr8:119231537..119234268,2	K562	blood:
15	8:119208477-119211356..8:119221082-119223921	K562	blood:
16	chr8:119237839..119239918-chr8:119250046..119252760,2	K562	blood:
17	chr8:119356234..119358532-chr8:119360102..119363000,2	MCF-7	breast:
18	chr8:119347457..119349643-chr8:119350580..119352155,2	MCF-7	breast:
19	chr8:119309293..119311281-chr8:119320840..119322590,2	MCF-7	breast:
20	chr8:119356234..119358532-chr8:119360102..119363000,2	MCF-7	breast:
21	chr8:119347457..119349643-chr8:119350580..119352155,2	MCF-7	breast:
22	8:119208477-119211356..8:119221082-119223921	K562	blood:
23	chr8:119264517..119266750-chr8:119270051..119271645,2	MCF-7	breast:
24	chr8:119313185..119314685-chr8:119324258..119326116,2	MCF-7	breast:
25	chr8:119122977..119125363-chr8:119249195..119251345,2	MCF-7	breast:
26	chr8:119363913..119366502-chr8:119371713..119373996,2	MCF-7	breast:
27	chr8:119341376..119343834-chr8:119345796..119348597,3	MCF-7	breast:
28	chr8:119123155..119125790-chr8:119234202..119237087,2	MCF-7	breast:
29	chr8:119209093..119211365-chr8:119212463..119213987,2	K562	blood:
30	chr8:119227641..119229899-chr8:119231537..119234268,2	K562	blood:
31	chr8:119122948..119125565-chr8:119354805..119357689,2	MCF-7	breast:
32	8:118847934-118851389..8:119208477-119211356	H1-hESC	embryonic stem cell:	embryo
33	chr8:119209093..119211365-chr8:119212463..119213987,2	K562	blood:
34	chr8:119344779..119346281-chr8:119346898..119348552,2	K562	blood:
35	8:118831545-118831953..8:119208477-119211356	H1-hESC	embryonic stem cell:	embryo
36	8:118823602-118831545..8:119208477-119211356	H1-hESC	embryonic stem cell:	embryo
37	chr8:119264517..119266750-chr8:119270051..119271645,2	MCF-7	breast:
38	chr8:119309293..119311281-chr8:119320840..119322590,2	MCF-7	breast:
39	chr8:119220054..119222499-chr8:119225215..119227233,2	MCF-7	breast:
40	chr8:119257831..119260580-chr8:119263913..119265980,2	MCF-7	breast:
41	chr8:119132540..119133242-chr8:119361404..119362055,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC023590.1.1-1	chr8:119307914-119307933	NONHSAT128408
2	lnc-AC023590.1.1-1	chr8:119307914-119307932	NONHSAT128407
3	lnc-EXT1-6	chr8:119273043-119274046	NONHSAT128406
4	lnc-AC023590.1.1-1	chr8:119303452-119303585	NONHSAT128408
5	lnc-EXT1-7	chr8:119387940-119388095	NONHSAT128410
6	lnc-AC023590.1.1-1	chr8:119294378-119294399	NONHSAT128407
7	lnc-AC023590.1.1-1	chr8:119300478-119300555	NONHSAT128408
8	lnc-EXT1-6	chr8:119271563-119272945	NONHSAT128406
9	lnc-AC023590.1.1-1	chr8:119296535-119296660	NONHSAT128408
10	lnc-AC023590.1.1-1	chr8:119303452-119303585	NONHSAT128407
11	lnc-AC023590.1.1-1	chr8:119303447-119303585	NONHSAT128409
12	lnc-AC023590.1.1-1	chr8:119300478-119300555	NONHSAT128407
13	lnc-AC023590.1.1-1	chr8:119296753-119296825	NONHSAT128408
14	lnc-AC023590.1.1-1	chr8:119296511-119296660	NONHSAT128407

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SAMD12	hsa-miR-93-5p	chr8:119209420-119209441
2	SAMD12	hsa-miR-93-5p	chr8:119209426-119209419
3	SAMD12	hsa-miR-340-5p	chr8:119209423-119209417

Variant related genes	Relation type
ENSG00000225885	TF binding region
ENSG00000225885	CpG island
ENSG00000182197	chromatin interactions

Extended variants
information (count: 7776 )
Associated
traits (count: 155 )

Variant overlapped rSNPs/rCNVs (count:7776 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562310091	chr8:119187435-119187436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs548134118	chr8:119187439-119187440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145286522	chr8:119187481-119187482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534615487	chr8:119187483-119187484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs139660487	chr8:119187488-119187489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1457199	chr8:119187514-119187515	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs565239279	chr8:119187526-119187527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1457200	chr8:119187549-119187550	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs554412843	chr8:119187553-119187554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113322593	chr8:119187554-119187555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147418273	chr8:119187572-119187573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183040572	chr8:119187608-119187609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575143850	chr8:119187666-119187667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186730308	chr8:119187672-119187673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557042414	chr8:119187731-119187732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375288709	chr8:119187734-119187735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574366019	chr8:119187762-119187763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575165194	chr8:119187768-119187769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4609224	chr8:119187774-119187775	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs564184774	chr8:119187785-119187786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572972914	chr8:119187801-119187802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191572551	chr8:119187808-119187809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs118188427	chr8:119187839-119187840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531702797	chr8:119187869-119187870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17478099	chr8:119187927-119187928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550454161	chr8:119188028-119188029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545216993	chr8:119188041-119188042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530912246	chr8:119188058-119188059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552414273	chr8:119188082-119188083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570891179	chr8:119188120-119188121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113071541	chr8:119188130-119188131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534914661	chr8:119188132-119188133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565368695	chr8:119188174-119188175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527799799	chr8:119188175-119188176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537283398	chr8:119188213-119188214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568666921	chr8:119188217-119188218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs28737768	chr8:119188266-119188267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs17480662	chr8:119188267-119188268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs113458456	chr8:119188284-119188285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182983154	chr8:119188292-119188293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557582117	chr8:119188293-119188294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572851170	chr8:119188311-119188312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539938511	chr8:119188333-119188334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148949345	chr8:119188336-119188337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573488157	chr8:119188354-119188355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142940339	chr8:119188412-119188413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527717620	chr8:119188413-119188414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562774868	chr8:119188417-119188418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28737769	chr8:119188422-119188423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs17478106	chr8:119188451-119188452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:155)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	17268525	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	19204574	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	18698023	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung adenocarcinoma	21935476	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1541 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119187400-119187800	Enhancers	Thymus	Thymus
2	chr8:119187800-119188800	Weak transcription	Thymus	Thymus
3	chr8:119188600-119190800	Enhancers	Dnd41	blood
4	chr8:119188800-119189600	Enhancers	Thymus	Thymus
5	chr8:119188800-119190600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr8:119189000-119190000	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:119189000-119190200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:119189000-119190800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:119189200-119189600	Enhancers	Fetal Thymus	thymus
10	chr8:119189600-119190000	Flanking Active TSS	Fetal Thymus	thymus
11	chr8:119189600-119190000	Flanking Active TSS	Thymus	Thymus
12	chr8:119190000-119190200	Enhancers	Thymus	Thymus
13	chr8:119190000-119190400	Enhancers	GM12878-XiMat	blood
14	chr8:119190000-119193200	Enhancers	Fetal Thymus	thymus
15	chr8:119190200-119190400	Flanking Active TSS	Thymus	Thymus
16	chr8:119190400-119192000	Enhancers	Thymus	Thymus
17	chr8:119192000-119192400	Enhancers	NHEK	skin
18	chr8:119192400-119192800	Weak transcription	NHEK	skin
19	chr8:119192600-119193000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:119192800-119193400	Enhancers	NHEK	skin
21	chr8:119193000-119193800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:119193000-119194000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:119193000-119194000	Enhancers	Aorta	Aorta
24	chr8:119193000-119194000	Enhancers	Osteobl	bone
25	chr8:119193600-119194000	Enhancers	Esophagus	oesophagus
26	chr8:119193600-119194200	Enhancers	Rectal Smooth Muscle	rectum
27	chr8:119193600-119194600	Enhancers	Colon Smooth Muscle	Colon
28	chr8:119193800-119202200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:119194000-119198000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:119194000-119198200	Weak transcription	Osteobl	bone
31	chr8:119194000-119202600	Weak transcription	Aorta	Aorta
32	chr8:119198000-119199000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:119198200-119199000	Enhancers	Osteobl	bone
34	chr8:119198200-119200000	Enhancers	HSMM	muscle
35	chr8:119198400-119200400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr8:119198600-119198800	Enhancers	NHDF-Ad	bronchial
37	chr8:119198600-119199200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr8:119198600-119199600	Enhancers	HSMMtube	muscle
39	chr8:119198600-119200200	Enhancers	HMEC	breast
40	chr8:119198600-119200400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:119198800-119199200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:119198800-119202400	Weak transcription	NHDF-Ad	bronchial
43	chr8:119199000-119199400	Enhancers	NH-A	brain
44	chr8:119199000-119199400	Flanking Active TSS	Osteobl	bone
45	chr8:119199000-119199600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:119199000-119199800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr8:119199000-119203800	Enhancers	Primary T cells from cord blood	blood
48	chr8:119199200-119199400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:119199200-119200800	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr8:119199200-119206800	Enhancers	Thymus	Thymus

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