Variant report

Variant	nsv551832
Chromosome Location	chr10:89630424-89650759
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	chr10:89638569-89639130	K562	blood:	n/a	n/a
2	ATF1	chr10:89638697-89639079	K562	blood:	n/a	n/a
3	BCLAF1	chr10:89638664-89639157	K562	blood:	n/a	n/a
4	BHLHE40	chr10:89632799-89632804	K562	blood:	n/a	n/a
5	CBX3	chr10:89638705-89639172	K562	blood:	n/a	n/a
6	CBX3	chr10:89646389-89646880	HCT-116	colon:	n/a	n/a
7	CBX3	chr10:89638725-89639060	K562	blood:	n/a	n/a
8	CCNT2	chr10:89643089-89643289	K562	blood:	n/a	n/a
9	CCNT2	chr10:89638737-89639000	K562	blood:	n/a	chr10:89638935-89638955
10	CEBPB	chr10:89637645-89637830	H1-hESC	embryonic stem cell:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
11	CEBPB	chr10:89635970-89636287	IMR90	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
12	CEBPB	chr10:89635985-89636266	A549	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
13	CEBPB	chr10:89635944-89636282	K562	blood:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
14	CEBPB	chr10:89635936-89636307	Hela-S3	cervix:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
15	CEBPB	chr10:89637644-89637833	Hela-S3	cervix:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
16	CEBPB	chr10:89637658-89637806	HepG2	liver:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
17	CEBPB	chr10:89635900-89636337	A549	lung:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
18	CEBPB	chr10:89638751-89639193	K562	blood:	n/a	n/a
19	CEBPB	chr10:89644708-89644936	H1-hESC	embryonic stem cell:	n/a	chr10:89644783-89644794
20	CEBPB	chr10:89644634-89644939	A549	lung:	n/a	chr10:89644783-89644794
21	CEBPB	chr10:89637633-89637831	IMR90	lung:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
22	CEBPB	chr10:89638808-89639206	K562	blood:	n/a	n/a
23	CEBPB	chr10:89644635-89644971	HepG2	liver:	n/a	chr10:89644783-89644794
24	CEBPB	chr10:89644622-89644937	K562	blood:	n/a	chr10:89644783-89644794
25	CEBPB	chr10:89638870-89639070	K562	blood:	n/a	n/a
26	CEBPB	chr10:89637619-89637930	K562	blood:	n/a	chr10:89637754-89637767 chr10:89637754-89637767 chr10:89637755-89637766 chr10:89637754-89637765
27	CEBPB	chr10:89644644-89644954	IMR90	lung:	n/a	chr10:89644783-89644794
28	CEBPB	chr10:89635960-89636273	HepG2	liver:	n/a	chr10:89636111-89636122 chr10:89636113-89636122 chr10:89636166-89636178 chr10:89636112-89636123
29	CEBPB	chr10:89644695-89644955	Hela-S3	cervix:	n/a	chr10:89644783-89644794
30	CEBPD	chr10:89638647-89639113	K562	blood:	n/a	n/a
31	CTCF	chr10:89644753-89644865	Lung_OC	lung:	n/a	n/a
32	CTCF	chr10:89633200-89633350	SAEC	small airway:	n/a	n/a
33	CUX1	chr10:89638165-89638309	K562	blood:	n/a	n/a
34	EBF1	chr10:89630614-89630616	GM12878	blood:	n/a	n/a
35	EP300	chr10:89642117-89642896	SK-N-SH	brain:	n/a	chr10:89642458-89642472 chr10:89642588-89642602
36	EP300	chr10:89633096-89633126	GM12878	blood:	n/a	n/a
37	EP300	chr10:89638631-89639190	K562	blood:	n/a	n/a
38	EP300	chr10:89642233-89642606	SK-N-SH_RA	brain:	n/a	chr10:89642458-89642472 chr10:89642588-89642602
39	EP300	chr10:89638792-89639146	K562	blood:	n/a	n/a
40	FOS	chr10:89636048-89636288	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr10:89630724-89630917	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr10:89635979-89636288	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr10:89636088-89636262	MCF10A-Er-Src	breast:	n/a	n/a
44	FOXA1	chr10:89643178-89643524	T-47D	breast:	n/a	n/a
45	FOXA2	chr10:89643202-89643397	HepG2	liver:	n/a	n/a
46	GATA1	chr10:89638581-89639416	PBDE	blood:	n/a	chr10:89638938-89638955
47	GATA2	chr10:89638696-89639218	K562	blood:	n/a	chr10:89638938-89638955
48	GATA3	chr10:89630541-89630811	SH-SY5Y	brain:	n/a	chr10:89630679-89630696 chr10:89630678-89630687 chr10:89630678-89630687
49	GATA3	chr10:89636847-89636903	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr10:89642400-89642604	SH-SY5Y	brain:	n/a	chr10:89642451-89642462

No.	Distal block	Cell Line	Cell type
1	chr10:89576887..89579810-chr10:89632591..89635220,2	K562	blood:
2	chr10:89623575..89625821-chr10:89638981..89641950,2	K562	blood:
3	chr10:89642392..89644637-chr10:89652677..89655610,2	MCF-7	breast:
4	chr10:89627048..89629019-chr10:89631649..89634484,2	K562	blood:
5	chr10:89619679..89625889-chr10:89627245..89632129,8	K562	blood:
6	chr10:89649701..89651266-chr10:89669658..89672345,2	MCF-7	breast:
7	chr10:89628331..89631690-chr10:89632886..89636887,5	MCF-7	breast:
8	chr10:89630597..89633078-chr10:89635123..89637172,2	MCF-7	breast:
9	chr10:89621343..89626061-chr10:89634894..89638873,7	K562	blood:
10	chr10:89639033..89641731-chr10:89644524..89647018,2	K562	blood:
11	chr10:89632106..89634679-chr10:89635218..89637761,3	MCF-7	breast:
12	chr10:89622936..89626124-chr10:89632043..89636497,5	MCF-7	breast:
13	chr10:89638682..89641996-chr10:89653428..89657390,3	K562	blood:
14	chr10:89640838..89642681-chr10:89647239..89649894,3	K562	blood:
15	chr10:89640838..89642681-chr10:89647239..89649894,3	K562	blood:
16	chr10:89627960..89634049-chr10:89634179..89640530,8	K562	blood:
17	chr10:89619679..89625045-chr10:89627844..89633340,9	K562	blood:
18	chr10:89646944..89651726-chr10:89652897..89657139,4	MCF-7	breast:
19	chr10:89622085..89623655-chr10:89643936..89646220,2	MCF-7	breast:
20	chr10:89629893..89635065-chr10:89636010..89640351,6	K562	blood:
21	chr10:89632106..89634679-chr10:89635218..89637761,3	MCF-7	breast:
22	chr10:89628472..89630169-chr10:89642973..89645444,2	K562	blood:
23	chr10:89639384..89642070-chr10:89695863..89697662,2	K562	blood:
24	chr10:89620447..89623271-chr10:89637766..89641518,4	MCF-7	breast:
25	chr10:89628331..89631690-chr10:89632886..89636887,5	MCF-7	breast:
26	chr10:89631936..89633868-chr10:90147243..90149574,2	MCF-7	breast:
27	chr10:89641632..89644559-chr10:89685193..89686750,2	K562	blood:
28	chr10:89630597..89633078-chr10:89635123..89637172,2	MCF-7	breast:
29	chr10:89639033..89641731-chr10:89644524..89647018,2	K562	blood:
30	chr10:89630068..89631816-chr10:89794611..89796207,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPSS2-2	chr10:89639829-89639867	ENSG00000224745.1
2	lnc-PAPSS2-2	chr10:89638449-89638780	ENSG00000224745.1
3	lnc-PAPSS2-2	chr10:89640057-89640184	ENSG00000224745.1

Variant related genes	Relation type
ENSG00000224745	TF binding region
ENSG00000171862	chromatin interactions
ENSG00000224745	chromatin interactions
ENSG00000227268	chromatin interactions
ENSG00000223820	chromatin interactions
ENSG00000138138	chromatin interactions

Extended variants
information (count: 717 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:717 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35161364	chr10:89630424-89630425	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192655554	chr10:89630437-89630438	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs559879058	chr10:89630481-89630482	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs367799770	chr10:89630483-89630484	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs574887412	chr10:89630520-89630521	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184313731	chr10:89630526-89630527	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139554020	chr10:89630536-89630537	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs60706946	chr10:89630537-89630538	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115656016	chr10:89630550-89630551	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs376409281	chr10:89630566-89630567	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs574492533	chr10:89630582-89630583	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs7085328	chr10:89630650-89630651	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs564069698	chr10:89630721-89630722	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs528071471	chr10:89630728-89630729	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs370114925	chr10:89630729-89630730	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs546228864	chr10:89630840-89630841	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs192836744	chr10:89630881-89630882	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148593767	chr10:89630916-89630917	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs200750915	chr10:89630921-89630922	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs142921964	chr10:89630933-89630934	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553935180	chr10:89630963-89630964	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs548462510	chr10:89630994-89630995	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150677631	chr10:89631003-89631004	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs537674113	chr10:89631006-89631007	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs184849931	chr10:89631034-89631035	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs139495295	chr10:89631057-89631058	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534977270	chr10:89631088-89631089	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs553337440	chr10:89631137-89631138	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs143274601	chr10:89631142-89631143	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs542324849	chr10:89631154-89631155	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs201241484	chr10:89631212-89631213	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs542314704	chr10:89631218-89631219	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs369222252	chr10:89631291-89631292	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs557208798	chr10:89631320-89631321	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs563592390	chr10:89631337-89631338	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs545641643	chr10:89631366-89631367	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs146654290	chr10:89631395-89631396	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs140225996	chr10:89631401-89631402	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs539795499	chr10:89631402-89631403	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113098012	chr10:89631425-89631426	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs74566162	chr10:89631427-89631428	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551930900	chr10:89631445-89631446	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs34958728	chr10:89631451-89631452	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs189354630	chr10:89631461-89631462	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs550633412	chr10:89631474-89631475	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs568885898	chr10:89631476-89631477	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs531123025	chr10:89631478-89631479	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs180787853	chr10:89631493-89631494	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554858136	chr10:89631513-89631514	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571113023	chr10:89631529-89631530	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Glioblastoma multiforme	19115005	CNVD
Prostate cancer	21147910	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	20020426	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22065749	CNVD
Cancer	22000013	CNVD
Colon cancer	22065749	CNVD
Endometrial cancer	22065749	CNVD
Lung cancer	20668451	CNVD
Breast cancer	17634833	CNVD
Cancer	20215515	CNVD
Glioblastoma multiforme	21727940	CNVD
Prostate cancer	19363497	CNVD
Prostate cancer	17700571	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20964600	CNVD
Endometrial cancer	19261849	CNVD
Central neurocytomas	17123091	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89621200-89630800	Active TSS	Aorta	Aorta
2	chr10:89621800-89630600	Active TSS	NHLF	lung
3	chr10:89621800-89632400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr10:89621800-89632400	Active TSS	GM12878-XiMat	blood
5	chr10:89624200-89631800	Transcr. at gene 5' and 3'	Dnd41	blood
6	chr10:89624400-89646400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:89624800-89631200	Weak transcription	Spleen	Spleen
8	chr10:89625600-89663000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:89625800-89632400	Weak transcription	Small Intestine	intestine
10	chr10:89627200-89630600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:89627200-89645800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr10:89627400-89630800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr10:89627400-89631600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr10:89627400-89638200	Weak transcription	Placenta	Placenta
15	chr10:89627600-89645600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr10:89628000-89635200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr10:89628200-89635800	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr10:89628200-89646200	Weak transcription	Fetal Muscle Leg	muscle
19	chr10:89628200-89646600	Weak transcription	Colonic Mucosa	Colon
20	chr10:89628400-89633800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr10:89628400-89637800	Weak transcription	Fetal Intestine Small	intestine
22	chr10:89628400-89662000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr10:89628600-89630600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr10:89628600-89630800	Weak transcription	Brain Substantia Nigra	brain
25	chr10:89628600-89631200	Enhancers	Colon Smooth Muscle	Colon
26	chr10:89628600-89631200	Enhancers	HepG2	liver
27	chr10:89628600-89631400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr10:89628600-89631400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr10:89628600-89631800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr10:89628600-89632400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr10:89628600-89632800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr10:89628600-89632800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr10:89628600-89633600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr10:89628600-89635000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:89628600-89636400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr10:89628600-89638200	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr10:89628600-89645800	Weak transcription	HSMMtube	muscle
38	chr10:89628800-89630600	Enhancers	Fetal Intestine Large	intestine
39	chr10:89628800-89630600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr10:89628800-89630800	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:89628800-89631000	Enhancers	Brain Angular Gyrus	brain
42	chr10:89628800-89631200	Enhancers	Brain Anterior Caudate	brain
43	chr10:89628800-89631400	Enhancers	Liver	Liver
44	chr10:89628800-89631800	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr10:89628800-89633200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr10:89628800-89638400	Weak transcription	K562	blood
47	chr10:89628800-89645600	Weak transcription	Fetal Kidney	kidney
48	chr10:89628800-89647000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr10:89629000-89631000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:89629000-89631000	Enhancers	Fetal Brain Female	brain

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