Variant report

Variant	nsv1051636
Chromosome Location	chr10:50675292-50732280
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:664)
CpG islands
(count:244)
Chromatin interactive
region (count:59)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:50707271-50707668	K562	blood:	n/a	n/a
2	ATF1	chr10:50722611-50722644	K562	blood:	n/a	n/a
3	ATF1	chr10:50707420-50707711	K562	blood:	n/a	n/a
4	BHLHE40	chr10:50707446-50707646	K562	blood:	n/a	n/a
5	BHLHE40	chr10:50716461-50716866	GM12878	blood:	n/a	n/a
6	CEBPB	chr10:50718487-50718797	IMR90	lung:	n/a	chr10:50718636-50718647
7	CEBPB	chr10:50703982-50704028	K562	blood:	n/a	n/a
8	CEBPB	chr10:50718471-50718820	HepG2	liver:	n/a	chr10:50718636-50718647
9	CEBPB	chr10:50708485-50708825	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:50708508-50708774	K562	blood:	n/a	n/a
11	CEBPB	chr10:50707547-50707811	A549	lung:	n/a	chr10:50707687-50707700
12	CEBPB	chr10:50718491-50718786	A549	lung:	n/a	chr10:50718636-50718647
13	CEBPB	chr10:50709903-50710103	H1-hESC	embryonic stem cell:	n/a	chr10:50710069-50710077
14	CEBPB	chr10:50707483-50707875	K562	blood:	n/a	chr10:50707687-50707700
15	CEBPB	chr10:50708484-50708866	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr10:50692661-50693242	IMR90	lung:	n/a	n/a
17	CEBPB	chr10:50690938-50691134	A549	lung:	n/a	chr10:50691014-50691025 chr10:50691050-50691063
18	CEBPB	chr10:50708459-50708775	MCF-7	breast:	n/a	n/a
19	CEBPB	chr10:50700550-50700818	HepG2	liver:	n/a	chr10:50700627-50700638
20	CEBPB	chr10:50700619-50700869	IMR90	lung:	n/a	chr10:50700627-50700638
21	CEBPB	chr10:50708496-50708830	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:50691002-50691050	HepG2	liver:	n/a	chr10:50691014-50691025
23	CEBPB	chr10:50721958-50722235	IMR90	lung:	n/a	n/a
24	CHD2	chr10:50707560-50707564	K562	blood:	n/a	n/a
25	CTCF	chr10:50727115-50727345	HepG2	liver:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
26	CTCF	chr10:50720120-50720270	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr10:50720320-50720470	GM12865	blood:	n/a	n/a
28	CTCF	chr10:50727100-50727250	Hela-S3	cervix:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
29	CTCF	chr10:50720400-50720550	NHLF	lung:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
30	CTCF	chr10:50727140-50727290	HepG2	liver:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
31	CTCF	chr10:50727563-50727607	GM12892	blood:	n/a	n/a
32	CTCF	chr10:50720380-50720530	AG10803	skin:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
33	CTCF	chr10:50720400-50720550	HFF-Myc	foreskin:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
34	CTCF	chr10:50720351-50720546	SK-N-SH_RA	brain:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
35	CTCF	chr10:50727160-50727310	AoAF	blood vessel:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
36	CTCF	chr10:50727100-50727250	GM12869	blood:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
37	CTCF	chr10:50727200-50727350	HFF-Myc	foreskin:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
38	CTCF	chr10:50720380-50720530	AG09309	skin:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
39	CTCF	chr10:50727136-50727333	GM12892	blood:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
40	CTCF	chr10:50727160-50727310	HPAF	blood vessel:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
41	CTCF	chr10:50727080-50727230	GM12870	blood:	n/a	n/a
42	CTCF	chr10:50726260-50726410	GM12864	blood:	n/a	n/a
43	CTCF	chr10:50720267-50720595	A549	lung:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
44	CTCF	chr10:50727160-50727310	AG04450	lung:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
45	CTCF	chr10:50720400-50720550	MCF-7	breast:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
46	CTCF	chr10:50720229-50720663	K562	blood:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
47	CTCF	chr10:50727099-50727331	HepG2	liver:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
48	CTCF	chr10:50720388-50720532	Kidney_OC	kidney:	n/a	chr10:50720459-50720480 chr10:50720464-50720482 chr10:50720465-50720481
49	CTCF	chr10:50727070-50727382	SK-N-SH_RA	brain:	n/a	chr10:50727223-50727236 chr10:50727221-50727239
50	CTCF	chr10:50727121-50727297	SK-N-SH_RA	brain:	n/a	chr10:50727223-50727236 chr10:50727221-50727239

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50729975-50730025	HEK293	kidney:	embryo
2	chr10:50714434-50714484	NT2-D1	testis:	n/a
3	chr10:50724286-50724336	NHBE	bronchial:	n/a
4	chr10:50714434-50714484	HepG2	liver:	n/a
5	chr10:50729975-50730025	SK-N-MC	brain:	n/a
6	chr10:50729975-50730025	NT2-D1	testis:	n/a
7	chr10:50724286-50724336	HepG2	liver:	n/a
8	chr10:50714434-50714484	HNPCEpiC	eye:	n/a
9	chr10:50724286-50724336	CMK	blood:	n/a
10	chr10:50724286-50724336	PrEC	prostate:	n/a
11	chr10:50714434-50714484	AoSMC	blood vessel:	n/a
12	chr10:50724286-50724336	HNPCEpiC	eye:	n/a
13	chr10:50716478-50716528	HepG2	liver:	n/a
14	chr10:50724286-50724336	NT2-D1	testis:	n/a
15	chr10:50714434-50714484	MCF-7	breast:	n/a
16	chr10:50729975-50730025	HNPCEpiC	eye:	n/a
17	chr10:50716478-50716528	HRE	kidney:	n/a
18	chr10:50724286-50724336	RPTEC	kidney:	n/a
19	chr10:50724286-50724336	PANC-1	pancreas:	n/a
20	chr10:50716478-50716528	AG04450	lung:	fetal
21	chr10:50714434-50714484	HCPEpiC	choroid plexus:	n/a
22	chr10:50716478-50716528	HCM	heart:	n/a
23	chr10:50714434-50714484	AG04450	lung:	fetal
24	chr10:50729975-50730025	CMK	blood:	n/a
25	chr10:50724286-50724336	HUVEC	blood vessel:	n/a
26	chr10:50729975-50730025	HepG2	liver:	n/a
27	chr10:50716478-50716528	PrEC	prostate:	n/a
28	chr10:50724286-50724336	HCF	heart:	n/a
29	chr10:50724286-50724336	HEEpiC	esophagus:	n/a
30	chr10:50716478-50716528	AG04449	skin:	fetal
31	chr10:50729975-50730025	SKMC	muscle:	n/a
32	chr10:50729975-50730025	HL-60	blood:	n/a
33	chr10:50729975-50730025	AG09309	skin:	n/a
34	chr10:50716478-50716528	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:50714434-50714484	SK-N-SH	brain:	n/a
36	chr10:50714434-50714484	Jurkat	blood:	n/a
37	chr10:50716478-50716528	IMR90	lung:	fetal
38	chr10:50716478-50716528	HNPCEpiC	eye:	n/a
39	chr10:50716478-50716528	GM12892	blood:	n/a
40	chr10:50729975-50730025	GM19239	blood:	n/a
41	chr10:50724286-50724336	HRCEpiC	kidney:	n/a
42	chr10:50716478-50716528	HCT-116	colon:	n/a
43	chr10:50729975-50730025	ProgFib	skin:	n/a
44	chr10:50724286-50724336	ProgFib	skin:	n/a
45	chr10:50714434-50714484	AG10803	skin:	n/a
46	chr10:50724286-50724336	Hela-S3	cervix:	n/a
47	chr10:50724286-50724336	Caco-2	colon:	n/a
48	chr10:50729975-50730025	SK-N-SH_RA	brain:	n/a
49	chr10:50716478-50716528	GM19239	blood:	n/a
50	chr10:50716478-50716528	PANC-1	pancreas:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:50726159..50727907-chr10:50745055..50747037,2	MCF-7	breast:
2	chr10:50695638..50697710-chr10:50701601..50704243,2	K562	blood:
3	chr10:49866085..49866961-chr10:50720002..50720537,2	K562	blood:
4	chr10:50694526..50696414-chr10:50698639..50700547,2	MCF-7	breast:
5	chr10:50712711..50715456-chr10:50724740..50726788,2	K562	blood:
6	chr10:50719950..50720567-chr10:50801233..50801768,2	K562	blood:
7	chr10:50686326..50689045-chr10:50690550..50693258,2	K562	blood:
8	chr10:50698101..50700651-chr10:50705011..50706943,2	K562	blood:
9	chr10:50731383..50733326-chr10:50736507..50739448,3	K562	blood:
10	chr10:50615329..50616281-chr10:50719977..50720927,6	K562	blood:
11	chr10:50686326..50689045-chr10:50690550..50693258,2	K562	blood:
12	chr10:50726029..50728979-chr10:50731581..50735350,6	K562	blood:
13	chr10:50614876..50616264-chr10:50720008..50720823,3	MCF-7	breast:
14	chr10:50712711..50715456-chr10:50724740..50726788,2	K562	blood:
15	chr10:50184130..50184883-chr10:50720113..50720967,2	MCF-7	breast:
16	chr10:50695638..50697710-chr10:50701601..50704243,2	K562	blood:
17	chr10:50700902..50702826-chr10:50705116..50707314,2	K562	blood:
18	chr10:50724821..50729589-chr10:50731335..50734731,5	K562	blood:
19	chr10:50189578..50192203-chr10:50707466..50710047,2	K562	blood:
20	chr10:50717666..50720146-chr10:50727918..50729928,2	MCF-7	breast:
21	chr10:50615306..50616280-chr10:50726775..50727751,7	MCF-7	breast:
22	chr10:50694526..50696414-chr10:50698639..50700547,2	MCF-7	breast:
23	chr10:50617610..50618526-chr10:50720225..50721007,3	MCF-7	breast:
24	chr10:49866459..49866966-chr10:50720079..50720742,2	MCF-7	breast:
25	chr10:50189481..50189991-chr10:50720433..50720944,2	K562	blood:
26	chr10:50691160..50693919-chr10:50697549..50699397,2	K562	blood:
27	chr10:50684472..50687283-chr10:50689821..50691644,2	MCF-7	breast:
28	chr10:50698101..50700651-chr10:50705011..50706943,2	K562	blood:
29	chr10:50727908..50731629-chr10:50735183..50738136,3	MCF-7	breast:
30	chr10:50183988..50185069-chr10:50726829..50727783,3	K562	blood:
31	chr10:50713439..50715475-chr10:50717765..50720148,2	K562	blood:
32	chr10:50700902..50702826-chr10:50705116..50707314,2	K562	blood:
33	chr10:50715569..50718101-chr10:50726217..50728314,2	K562	blood:
34	chr10:50717666..50720146-chr10:50727918..50729928,2	MCF-7	breast:
35	chr10:50532596..50533234-chr10:50720810..50721429,2	MCF-7	breast:
36	chr10:50615493..50616931-chr10:50720236..50720959,5	MCF-7	breast:
37	chr10:50684472..50687283-chr10:50689821..50691644,2	MCF-7	breast:
38	chr10:50678585..50680371-chr10:50684775..50686552,2	K562	blood:
39	chr10:50715711..50718094-chr10:50726640..50728977,2	K562	blood:
40	chr10:50625768..50626670-chr10:50720019..50720792,2	MCF-7	breast:
41	chr10:50708831..50710894-chr10:50713188..50715760,2	K562	blood:
42	chr10:50715711..50718094-chr10:50726640..50728977,2	K562	blood:
43	chr10:50715569..50718101-chr10:50726217..50728314,2	K562	blood:
44	chr10:50724821..50729589-chr10:50731335..50734731,5	K562	blood:
45	chr10:50691160..50693919-chr10:50697549..50699397,2	K562	blood:
46	chr10:50710531..50713420-chr10:50731110..50733529,2	K562	blood:
47	chr10:49866375..49866922-chr10:50726828..50727744,2	K562	blood:
48	chr10:50722386..50724704-chr10:50727797..50729912,2	K562	blood:
49	chr10:50185149..50185671-chr10:50720018..50720966,2	MCF-7	breast:
50	chr10:50717195..50718876-chr10:50739121..50741065,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf71-1	chr10:50680749-50680949	ENSG00000235939.1
2	lnc-DRGX-3	chr10:50726991-50729600	NONHSAT013309

No data

Variant related genes	Relation type
ERCC6	TF binding region
PGBD3	TF binding region
ERCC6	CpG island
PGBD3	CpG island
ENSG00000243251	chromatin interactions
ENSG00000225830	chromatin interactions

Extended variants
information (count: 2270 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2270 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374960223	chr10:50675327-50675328	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs57460451	chr10:50675329-50675330	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566551107	chr10:50675333-50675334	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534061087	chr10:50675365-50675366	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558615487	chr10:50675387-50675388	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576949155	chr10:50675392-50675393	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537700009	chr10:50675402-50675403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556281653	chr10:50675411-50675412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374639643	chr10:50675422-50675423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574542172	chr10:50675457-50675458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576528024	chr10:50675482-50675483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117525685	chr10:50675568-50675569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28454254	chr10:50675598-50675599	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547996154	chr10:50675653-50675654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540904791	chr10:50675711-50675712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373742386	chr10:50675712-50675713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183015636	chr10:50675738-50675739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527446982	chr10:50675746-50675747	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187758327	chr10:50675772-50675773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562746072	chr10:50675776-50675777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560815159	chr10:50675777-50675778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149666343	chr10:50675820-50675821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190840145	chr10:50675844-50675845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529921980	chr10:50675854-50675855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566844971	chr10:50675857-50675858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs932735	chr10:50675924-50675925	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552445244	chr10:50675929-50675930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs570700505	chr10:50675939-50675940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183988801	chr10:50675963-50675964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377342567	chr10:50676021-50676022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145668431	chr10:50676084-50676085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568281946	chr10:50676086-50676087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114143901	chr10:50676161-50676162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73305562	chr10:50676165-50676166	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187999276	chr10:50676202-50676203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148905772	chr10:50676224-50676225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192139039	chr10:50676300-50676301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551944135	chr10:50676308-50676309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544526702	chr10:50676313-50676314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183171071	chr10:50676341-50676342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530267021	chr10:50676374-50676375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541900352	chr10:50676394-50676395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560430232	chr10:50676422-50676423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527679768	chr10:50676432-50676433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145272065	chr10:50676481-50676482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371061152	chr10:50676564-50676565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187536268	chr10:50676568-50676569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192815443	chr10:50676596-50676597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147620907	chr10:50676664-50676665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550113815	chr10:50676665-50676666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Hypotonia	21948486	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50662200-50677800	Weak transcription	Fetal Heart	heart
2	chr10:50662200-50691600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr10:50662400-50690000	Weak transcription	Stomach Mucosa	stomach
4	chr10:50662400-50693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:50662600-50676600	Weak transcription	Small Intestine	intestine
6	chr10:50662600-50677600	Weak transcription	NHDF-Ad	bronchial
7	chr10:50662600-50691400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:50663000-50675800	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:50663200-50693800	Weak transcription	HepG2	liver
10	chr10:50664000-50677400	Weak transcription	Fetal Kidney	kidney
11	chr10:50664600-50678200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr10:50666600-50676400	Weak transcription	K562	blood
13	chr10:50666600-50684400	Weak transcription	NHLF	lung
14	chr10:50666800-50678200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr10:50667600-50675600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:50667800-50677600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr10:50667800-50707400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr10:50668000-50713400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr10:50668200-50675800	Weak transcription	Esophagus	oesophagus
20	chr10:50668200-50680200	Weak transcription	GM12878-XiMat	blood
21	chr10:50668400-50676400	Weak transcription	Hela-S3	cervix
22	chr10:50668400-50677600	Weak transcription	NH-A	brain
23	chr10:50668400-50677800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr10:50668400-50677800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr10:50668400-50678200	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr10:50668800-50677600	Weak transcription	Psoas Muscle	Psoas
27	chr10:50668800-50677800	Weak transcription	Fetal Thymus	thymus
28	chr10:50669000-50678200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:50669600-50675600	Weak transcription	Fetal Intestine Large	intestine
30	chr10:50669600-50675600	Weak transcription	Gastric	stomach
31	chr10:50669600-50675800	Weak transcription	Brain Anterior Caudate	brain
32	chr10:50669600-50675800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr10:50669600-50675800	Weak transcription	Spleen	Spleen
34	chr10:50669600-50676000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr10:50669600-50676000	Weak transcription	Brain Angular Gyrus	brain
36	chr10:50669600-50676000	Weak transcription	Brain Substantia Nigra	brain
37	chr10:50669600-50676000	Weak transcription	Fetal Brain Female	brain
38	chr10:50669600-50676000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr10:50669600-50676000	Weak transcription	Right Ventricle	heart
40	chr10:50669600-50676200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr10:50669600-50677800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr10:50670600-50691600	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr10:50671600-50686600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:50671800-50679400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr10:50671800-50693800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr10:50672000-50679600	Weak transcription	Dnd41	blood
47	chr10:50672000-50687200	Strong transcription	Fetal Muscle Leg	muscle
48	chr10:50672000-50691800	Strong transcription	Primary T cells from cord blood	blood
49	chr10:50672200-50676000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr10:50672200-50679400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

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