Variant report

Variant	nsv895893
Chromosome Location	chr10:93747260-93875264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1292)
CpG islands
(count:1282)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:1292 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:93847505-93847972	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:93873809-93874362	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:93871347-93871734	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:93786949-93787212	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:93786971-93787212	K562	blood:	n/a	n/a
6	ARID3A	chr10:93771386-93771666	K562	blood:	n/a	n/a
7	ATF1	chr10:93861106-93861410	K562	blood:	n/a	n/a
8	ATF1	chr10:93786998-93787210	K562	blood:	n/a	n/a
9	ATF2	chr10:93851686-93852219	GM12878	blood:	n/a	n/a
10	ATF2	chr10:93851717-93852172	GM12878	blood:	n/a	n/a
11	ATF2	chr10:93861527-93862056	GM12878	blood:	n/a	n/a
12	ATF2	chr10:93860953-93861557	GM12878	blood:	n/a	n/a
13	ATF2	chr10:93860940-93861515	GM12878	blood:	n/a	n/a
14	ATF2	chr10:93861575-93862108	GM12878	blood:	n/a	n/a
15	ATF3	chr10:93861027-93861408	K562	blood:	n/a	n/a
16	ATF3	chr10:93771342-93771679	K562	blood:	n/a	n/a
17	BACH1	chr10:93771423-93771698	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr10:93771368-93771794	K562	blood:	n/a	n/a
19	BACH1	chr10:93860853-93861427	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:93861059-93861377	K562	blood:	n/a	n/a
21	BACH1	chr10:93847382-93847396	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr10:93851746-93852035	GM12878	blood:	n/a	n/a
23	BATF	chr10:93861566-93861983	GM12878	blood:	n/a	n/a
24	BATF	chr10:93860988-93861964	GM12878	blood:	n/a	chr10:93861337-93861346
25	BATF	chr10:93861025-93861458	GM12878	blood:	n/a	chr10:93861337-93861346
26	BCL11A	chr10:93874969-93875206	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:93861026-93861518	GM12878	blood:	n/a	n/a
28	BCL11A	chr10:93860982-93861976	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:93861608-93861970	GM12878	blood:	n/a	n/a
30	BCL3	chr10:93869831-93870202	GM12878	blood:	n/a	n/a
31	BCL3	chr10:93861044-93861524	GM12878	blood:	n/a	n/a
32	BCLAF1	chr10:93847430-93847967	GM12878	blood:	n/a	n/a
33	BCLAF1	chr10:93851718-93852190	GM12878	blood:	n/a	n/a
34	BCLAF1	chr10:93860937-93861517	GM12878	blood:	n/a	n/a
35	BCLAF1	chr10:93860822-93861440	GM12878	blood:	n/a	chr10:93860854-93860863
36	BHLHE40	chr10:93860805-93862119	GM12878	blood:	n/a	n/a
37	BHLHE40	chr10:93847515-93847911	K562	blood:	n/a	n/a
38	BHLHE40	chr10:93861075-93861424	K562	blood:	n/a	n/a
39	BHLHE40	chr10:93775380-93775442	A549	lung:	n/a	n/a
40	BHLHE40	chr10:93851643-93852172	GM12878	blood:	n/a	n/a
41	BHLHE40	chr10:93847516-93847843	GM12878	blood:	n/a	n/a
42	CBX3	chr10:93861121-93861441	K562	blood:	n/a	n/a
43	CCNT2	chr10:93786974-93787174	K562	blood:	n/a	n/a
44	CEBPB	chr10:93861075-93861863	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:93865640-93865781	A549	lung:	n/a	chr10:93865705-93865716
46	CEBPB	chr10:93807518-93807841	HepG2	liver:	n/a	chr10:93807636-93807644
47	CEBPB	chr10:93828706-93829039	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:93850387-93850601	A549	lung:	n/a	chr10:93850455-93850468 chr10:93850455-93850466
49	CEBPB	chr10:93747396-93747729	IMR90	lung:	n/a	chr10:93747567-93747580
50	CEBPB	chr10:93747428-93747646	K562	blood:	n/a	chr10:93747567-93747580

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:93804999-93805049	A549	lung:	n/a
2	chr10:93804999-93805049	A549	lung:	n/a
3	chr10:93811958-93812008	HRPEpiC	eye:	n/a
4	chr10:93804898-93804948	Hepatocyte	liver:	n/a
5	chr10:93811989-93812039	ECC-1	luminal epithelium:	n/a
6	chr10:93805441-93805491	NHDF-neo	bronchial:	n/a
7	chr10:93789797-93789847	SAEC	small airway:	n/a
8	chr10:93861824-93861874	AG10803	skin:	n/a
9	chr10:93805590-93805640	HCM	heart:	n/a
10	chr10:93793140-93793190	GM06990	blood:	n/a
11	chr10:93870321-93870371	HCF	heart:	n/a
12	chr10:93811989-93812039	SK-N-MC	brain:	n/a
13	chr10:93812043-93812093	H1-hESC	embryonic stem cell:	embryo
14	chr10:93793140-93793190	RPTEC	kidney:	n/a
15	chr10:93809328-93809378	HRPEpiC	eye:	n/a
16	chr10:93805870-93805920	ProgFib	skin:	n/a
17	chr10:93804976-93805026	RPTEC	kidney:	n/a
18	chr10:93872745-93872795	HCPEpiC	choroid plexus:	n/a
19	chr10:93861385-93861435	H1-hESC	embryonic stem cell:	embryo
20	chr10:93805590-93805640	U87	brain:	n/a
21	chr10:93861824-93861874	Caco-2	colon:	n/a
22	chr10:93804898-93804948	SKMC	muscle:	n/a
23	chr10:93805870-93805920	HCM	heart:	n/a
24	chr10:93809328-93809378	U87	brain:	n/a
25	chr10:93804898-93804948	NT2-D1	testis:	n/a
26	chr10:93870321-93870371	HEK293	kidney:	embryo
27	chr10:93828960-93829010	PANC-1	pancreas:	n/a
28	chr10:93861385-93861435	RPTEC	kidney:	n/a
29	chr10:93870321-93870371	SKMC	muscle:	n/a
30	chr10:93872745-93872795	NHBE	bronchial:	n/a
31	chr10:93812043-93812093	ProgFib	skin:	n/a
32	chr10:93804898-93804948	HRCEpiC	kidney:	n/a
33	chr10:93805844-93805894	GM06990	blood:	n/a
34	chr10:93805844-93805894	H1-hESC	embryonic stem cell:	embryo
35	chr10:93809328-93809378	GM12878	blood:	n/a
36	chr10:93804976-93805026	LNCaP	prostate:	n/a
37	chr10:93793140-93793190	AG09309	skin:	n/a
38	chr10:93872745-93872795	HUVEC	blood vessel:	n/a
39	chr10:93870321-93870371	Hepatocyte	liver:	n/a
40	chr10:93811989-93812039	SK-N-SH_RA	brain:	n/a
41	chr10:93805441-93805491	SAEC	small airway:	n/a
42	chr10:93872745-93872795	SK-N-SH	brain:	n/a
43	chr10:93872745-93872795	AG09309	skin:	n/a
44	chr10:93804999-93805049	GM12892	blood:	n/a
45	chr10:93793140-93793190	K562	blood:	n/a
46	chr10:93789797-93789847	MCF10A-Er-Src	breast:	n/a
47	chr10:93805441-93805491	LNCaP	prostate:	n/a
48	chr10:93861824-93861874	ProgFib	skin:	n/a
49	chr10:93861824-93861874	HCM	heart:	n/a
50	chr10:93804999-93805049	U87	brain:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:93794777..93796964-chr10:93801927..93804598,2	K562	blood:
2	chr10:93843200..93844774-chr10:93846231..93849117,2	MCF-7	breast:
3	chr10:93842541..93844667-chr10:94333754..94335512,2	K562	blood:
4	chr10:93745728..93747622-chr10:93786870..93789108,2	MCF-7	breast:
5	chr10:93765227..93769197-chr10:93769906..93772761,3	K562	blood:
6	chr10:93832600..93835291-chr10:93841541..93844058,2	K562	blood:
7	chr10:93870349..93872149-chr10:93874074..93876039,2	K562	blood:
8	chr10:93775489..93777686-chr10:93780974..93783915,2	MCF-7	breast:
9	chr10:93787212..93789291-chr10:93808674..93810691,2	K562	blood:
10	chr10:93847286..93847823-chr10:93976420..93976923,2	MCF-7	breast:
11	chr10:93789370..93791558-chr10:93805147..93807749,2	MCF-7	breast:
12	chr10:93806774..93809379-chr14:90548303..90550699,2	MCF-7	breast:
13	chr10:93838081..93839704-chr10:93849974..93852116,2	K562	blood:
14	chr10:93775489..93777686-chr10:93780974..93783915,2	MCF-7	breast:
15	chr10:93847221..93848633-chr10:94050307..94052486,7	MCF-7	breast:
16	chr10:93798638..93801510-chr10:93804838..93807467,2	K562	blood:
17	chr10:93794777..93796964-chr10:93801927..93804598,2	K562	blood:
18	chr10:93802984..93807030-chr10:93808304..93810729,3	K562	blood:
19	chr10:93847596..93848128-chr10:94194513..94195033,2	K562	blood:
20	chr10:93866014..93868686-chr10:93868973..93871759,2	K562	blood:
21	chr10:93847240..93848138-chr10:94194463..94195433,3	MCF-7	breast:
22	chr10:93809868..93812362-chr10:93812392..93814570,2	MCF-7	breast:
23	chr10:93765227..93769197-chr10:93769906..93772761,3	K562	blood:
24	chr10:93764003..93765937-chr10:93769485..93771662,2	MCF-7	breast:
25	chr10:93768343..93770359-chr10:93773791..93775387,2	K562	blood:
26	chr10:93767539..93770503-chr10:93771684..93774422,2	MCF-7	breast:
27	chr10:93838081..93839704-chr10:93849974..93852116,2	K562	blood:
28	chr10:93764003..93765937-chr10:93769485..93771662,2	MCF-7	breast:
29	chr10:93866014..93868686-chr10:93868973..93871759,2	K562	blood:
30	chr10:93751005..93753979-chr10:93756542..93758224,3	MCF-7	breast:
31	chr10:93802984..93807030-chr10:93808304..93810729,3	K562	blood:
32	chr10:93751005..93753979-chr10:93756542..93758224,3	MCF-7	breast:
33	chr10:93751650..93753642-chr10:93774282..93776982,2	MCF-7	breast:
34	chr10:93759429..93762295-chr10:93766132..93769049,2	K562	blood:
35	chr10:93847007..93848850-chr10:93883133..93885140,2	MCF-7	breast:
36	chr10:93767539..93770503-chr10:93771684..93774422,2	MCF-7	breast:
37	chr10:93759429..93762295-chr10:93766132..93769049,2	K562	blood:
38	chr10:93870349..93872149-chr10:93874074..93876039,2	K562	blood:
39	chr10:93832600..93835291-chr10:93841541..93844058,2	K562	blood:
40	chr10:93787212..93789291-chr10:93808674..93810691,2	K562	blood:
41	chr10:93768343..93770359-chr10:93773791..93775387,2	K562	blood:
42	chr10:93744030..93746572-chr10:93747290..93749067,2	MCF-7	breast:
43	chr10:93846195..93847705-chr10:94049440..94051742,2	K562	blood:
44	chr10:93847257..93847877-chr10:94051559..94052425,3	MCF-7	breast:
45	chr10:93798638..93801510-chr10:93804838..93807467,2	K562	blood:
46	chr10:93745728..93747622-chr10:93786870..93789108,2	MCF-7	breast:
47	chr10:93809868..93812362-chr10:93812392..93814570,2	MCF-7	breast:
48	chr10:93682820..93685768-chr10:93751546..93754267,2	MCF-7	breast:
49	chr10:93751650..93753642-chr10:93774282..93776982,2	MCF-7	breast:
50	chr10:93789370..93791558-chr10:93805147..93807749,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	CPEB3	hsa-miR-196a-5p	chr10:93809568-93809589
2	BTAF1	hsa-miR-15b-5p	chr10:93788714-93788721
3	CPEB3	hsa-miR-320a	chr10:93809614-93809635
4	CPEB3	hsa-miR-21-5p	chr10:93811007-93811029
5	CPEB3	hsa-miR-29a-3p	chr10:93809405-93809399
6	CPEB3	hsa-miR-26a-5p	chr10:93809076-93809070
7	CPEB3	hsa-miR-21-5p	chr10:93811013-93811006
8	BTAF1	hsa-miR-16-5p	chr10:93788700-93788721
9	BTAF1	hsa-miR-16-5p	chr10:93788714-93788721
10	CPEB3	hsa-miR-320a	chr10:93808519-93808513
11	CPEB3	hsa-miR-21-5p	chr10:93811375-93811396
12	BTAF1	hsa-miR-15b-5p	chr10:93788702-93788721
13	CPEB3	hsa-miR-29a-3p	chr10:93808616-93808635
14	CPEB3	hsa-miR-29a-3p	chr10:93809399-93809420

Variant related genes	Relation type
BTAF1	TF binding region
ENSG00000252993	TF binding region
SDHCP2	TF binding region
BTAF1	CpG island
ENSG00000252993	CpG island
SDHCP2	CpG island
ENSG00000119912	chromatin interactions
ENSG00000095564	chromatin interactions
ENSG00000107864	chromatin interactions
ENSG00000198060	chromatin interactions

Extended variants
information (count: 4337 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4337 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2792026	chr10:93747260-93747261	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142471484	chr10:93747316-93747317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189048108	chr10:93747346-93747347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181990669	chr10:93747536-93747537	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552907095	chr10:93747551-93747552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572976842	chr10:93747573-93747574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535412149	chr10:93747574-93747575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555697465	chr10:93747653-93747654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575353074	chr10:93747700-93747701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544238384	chr10:93747728-93747729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564025566	chr10:93747762-93747763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187469374	chr10:93747833-93747834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72825305	chr10:93747839-93747840	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540291556	chr10:93747850-93747851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144655728	chr10:93747908-93747909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376665082	chr10:93747927-93747928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529483462	chr10:93747976-93747977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549450974	chr10:93748024-93748025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552270119	chr10:93748119-93748120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74149346	chr10:93748120-93748121	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568922328	chr10:93748157-93748158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531838350	chr10:93748198-93748199	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551383027	chr10:93748218-93748219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571273266	chr10:93748234-93748235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72825306	chr10:93748263-93748264	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs547847849	chr10:93748272-93748273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566596470	chr10:93748277-93748278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371266276	chr10:93748285-93748286	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535631088	chr10:93748289-93748290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555561221	chr10:93748298-93748299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190629431	chr10:93748314-93748315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538110804	chr10:93748362-93748363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557805854	chr10:93748364-93748365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180919931	chr10:93748367-93748368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185506885	chr10:93748422-93748423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539998111	chr10:93748452-93748453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548056095	chr10:93748475-93748476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553819055	chr10:93748495-93748496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35153631	chr10:93748522-93748523	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573612343	chr10:93748580-93748581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371423175	chr10:93748700-93748701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547751594	chr10:93748776-93748777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113155608	chr10:93748792-93748793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561316546	chr10:93748801-93748802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562713265	chr10:93748821-93748822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190219216	chr10:93748847-93748848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545281212	chr10:93748872-93748873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200102417	chr10:93748896-93748897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76236373	chr10:93748911-93748912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149243426	chr10:93748917-93748918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2623 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93697800-93748800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr10:93699600-93750600	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr10:93704800-93807400	Weak transcription	Gastric	stomach
4	chr10:93709000-93771800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:93710000-93750200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:93714600-93768000	Weak transcription	Right Ventricle	heart
7	chr10:93718400-93774000	Weak transcription	Spleen	Spleen
8	chr10:93719400-93761000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr10:93720000-93757400	Weak transcription	Small Intestine	intestine
10	chr10:93720400-93757400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:93723800-93786600	Weak transcription	Colonic Mucosa	Colon
12	chr10:93724200-93748200	Weak transcription	Psoas Muscle	Psoas
13	chr10:93728000-93757400	Weak transcription	Fetal Brain Male	brain
14	chr10:93728600-93751600	Weak transcription	K562	blood
15	chr10:93729800-93765600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:93730400-93750200	Weak transcription	Fetal Intestine Small	intestine
17	chr10:93734600-93750200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:93734800-93763400	Strong transcription	Dnd41	blood
19	chr10:93735400-93750200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr10:93735800-93750600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:93736200-93749200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr10:93736200-93755400	Weak transcription	Esophagus	oesophagus
23	chr10:93736200-93784400	Weak transcription	Pancreas	Pancrea
24	chr10:93737400-93750800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:93738800-93750200	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr10:93739400-93750200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
27	chr10:93739800-93750000	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr10:93739800-93750000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr10:93740000-93749800	Strong transcription	Primary B cells from cord blood	blood
30	chr10:93740000-93750000	Strong transcription	Primary T cells from cord blood	blood
31	chr10:93740000-93750200	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr10:93740000-93750200	Strong transcription	Liver	Liver
33	chr10:93740000-93750800	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr10:93740200-93749600	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr10:93740200-93750000	Strong transcription	Primary hematopoietic stem cells	blood
36	chr10:93740200-93750000	Strong transcription	HSMM	muscle
37	chr10:93740200-93750200	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr10:93740200-93750200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:93740200-93750400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr10:93740200-93750400	Strong transcription	NH-A	brain
41	chr10:93740200-93766200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr10:93740400-93750600	Strong transcription	Duodenum Mucosa	Duodenum
43	chr10:93740400-93761000	Strong transcription	Primary B cells from peripheral blood	blood
44	chr10:93740400-93764400	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr10:93740400-93770800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr10:93741000-93750400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr10:93741200-93748000	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr10:93741200-93750400	Strong transcription	Adipose Nuclei	Adipose
49	chr10:93741400-93749800	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr10:93741400-93750000	Strong transcription	Rectal Mucosa Donor 29	rectum

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