Variant report

Variant	nsv1043295
Chromosome Location	chr10:43552895-43599363
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	BACH1	chr10:43598601-43598610	K562	blood:	n/a	n/a
2	BHLHE40	chr10:43574377-43574555	HepG2	liver:	n/a	n/a
3	BHLHE40	chr10:43574476-43574611	K562	blood:	n/a	n/a
4	BRCA1	chr10:43574519-43574717	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr10:43571020-43571170	AG04449	skin:	n/a	n/a
6	CTCF	chr10:43574480-43574630	Hela-S3	cervix:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
7	CTCF	chr10:43574540-43574690	GM12868	blood:	n/a	n/a
8	CTCF	chr10:43574420-43574570	GM12870	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
9	CTCF	chr10:43571010-43571177	HepG2	liver:	n/a	n/a
10	CTCF	chr10:43571220-43571370	GM12872	blood:	n/a	n/a
11	CTCF	chr10:43574431-43574734	GM12891	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
12	CTCF	chr10:43574500-43574650	NHLF	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
13	CTCF	chr10:43574500-43574650	AG04450	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
14	CTCF	chr10:43571860-43572010	NHEK	skin:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
15	CTCF	chr10:43571060-43571201	GM12892	blood:	n/a	n/a
16	CTCF	chr10:43574480-43574630	NB4	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
17	CTCF	chr10:43581040-43581190	HEK293	kidney:	n/a	n/a
18	CTCF	chr10:43571040-43571190	HepG2	liver:	n/a	n/a
19	CTCF	chr10:43571060-43571210	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr10:43588980-43589130	SAEC	small airway:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
21	CTCF	chr10:43588907-43589147	NHEK	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
22	CTCF	chr10:43574346-43574733	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
23	CTCF	chr10:43574419-43574702	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
24	CTCF	chr10:43571020-43571170	HRE	kidney:	n/a	n/a
25	CTCF	chr10:43574463-43574613	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
26	CTCF	chr10:43588900-43589050	NHDF-neo	bronchial:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
27	CTCF	chr10:43571260-43571410	GM12872	blood:	n/a	n/a
28	CTCF	chr10:43588920-43589070	HPAF	blood vessel:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
29	CTCF	chr10:43574207-43574807	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
30	CTCF	chr10:43597420-43597570	GM12875	blood:	n/a	n/a
31	CTCF	chr10:43566160-43566310	HMEC	breast:	n/a	n/a
32	CTCF	chr10:43589020-43589170	HMEC	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
33	CTCF	chr10:43574500-43574650	RPTEC	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
34	CTCF	chr10:43574442-43574680	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
35	CTCF	chr10:43571063-43571180	GM19240	blood:	n/a	n/a
36	CTCF	chr10:43574460-43574610	HUVEC	blood vessel:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
37	CTCF	chr10:43588900-43589174	GM12878	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
38	CTCF	chr10:43574460-43574610	GM12864	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
39	CTCF	chr10:43566225-43566383	K562	blood:	n/a	n/a
40	CTCF	chr10:43574441-43574650	LNCaP	prostate:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
41	CTCF	chr10:43571080-43571230	GM12866	blood:	n/a	n/a
42	CTCF	chr10:43571200-43571350	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr10:43574366-43574735	GM12878	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
44	CTCF	chr10:43574431-43574670	LNCaP	prostate:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
45	CTCF	chr10:43572000-43572150	BE2_C	brain:	n/a	n/a
46	CTCF	chr10:43588914-43589149	Gliobla	brain:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
47	CTCF	chr10:43566500-43566650	NB4	blood:	n/a	n/a
48	CTCF	chr10:43589002-43589104	GM19240	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
49	CTCF	chr10:43574460-43574610	GM12874	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
50	CTCF	chr10:43571049-43571229	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43573195-43573245	SKMC	muscle:	n/a
2	chr10:43562813-43562863	SKMC	muscle:	n/a
3	chr10:43573195-43573245	SKMC	muscle:	n/a
4	chr10:43562813-43562863	SKMC	muscle:	n/a
5	chr10:43585188-43585238	K562	blood:	n/a
6	chr10:43577025-43577075	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:43572244-43572294	SK-N-SH_RA	brain:	n/a
8	chr10:43573319-43573369	Jurkat	blood:	n/a
9	chr10:43572621-43572671	AoSMC	blood vessel:	n/a
10	chr10:43573332-43573382	SK-N-SH_RA	brain:	n/a
11	chr10:43572244-43572294	BJ	skin:	n/a
12	chr10:43585188-43585238	Jurkat	blood:	n/a
13	chr10:43573319-43573369	HRPEpiC	eye:	n/a
14	chr10:43569045-43569095	HIPEpiC	eye:	n/a
15	chr10:43596996-43597046	GM12878	blood:	n/a
16	chr10:43572621-43572671	ProgFib	skin:	n/a
17	chr10:43572359-43572409	AG04450	lung:	fetal
18	chr10:43598772-43598822	HAEpiC	amniotic membrane:	n/a
19	chr10:43562544-43562594	HEK293	kidney:	embryo
20	chr10:43572424-43572474	MCF10A-Er-Src	breast:	n/a
21	chr10:43562544-43562594	T-47D	breast:	n/a
22	chr10:43572359-43572409	HEEpiC	esophagus:	n/a
23	chr10:43569045-43569095	HEEpiC	esophagus:	n/a
24	chr10:43572621-43572671	RPTEC	kidney:	n/a
25	chr10:43572359-43572409	HEK293	kidney:	embryo
26	chr10:43572467-43572517	Hepatocyte	liver:	n/a
27	chr10:43573332-43573382	AG04449	skin:	fetal
28	chr10:43571169-43571219	HCM	heart:	n/a
29	chr10:43585188-43585238	ovcar-3	ovarian:	n/a
30	chr10:43573195-43573245	PrEC	prostate:	n/a
31	chr10:43577025-43577075	SK-N-SH_RA	brain:	n/a
32	chr10:43572467-43572517	SKMC	muscle:	n/a
33	chr10:43575142-43575192	HNPCEpiC	eye:	n/a
34	chr10:43585188-43585238	HUVEC	blood vessel:	n/a
35	chr10:43571169-43571219	Jurkat	blood:	n/a
36	chr10:43577025-43577075	GM12892	blood:	n/a
37	chr10:43572065-43572115	ovcar-3	ovarian:	n/a
38	chr10:43596996-43597046	HCF	heart:	n/a
39	chr10:43562544-43562594	SAEC	small airway:	n/a
40	chr10:43572065-43572115	MCF10A-Er-Src	breast:	n/a
41	chr10:43562813-43562863	MCF10A-Er-Src	breast:	n/a
42	chr10:43572467-43572517	HCPEpiC	choroid plexus:	n/a
43	chr10:43572413-43572463	HMEC	breast:	n/a
44	chr10:43577025-43577075	HMEC	breast:	n/a
45	chr10:43572065-43572115	GM12892	blood:	n/a
46	chr10:43562544-43562594	ovcar-3	ovarian:	n/a
47	chr10:43572359-43572409	SAEC	small airway:	n/a
48	chr10:43575142-43575192	HCF	heart:	n/a
49	chr10:43575142-43575192	H1-hESC	embryonic stem cell:	embryo
50	chr10:43572244-43572294	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43564728..43567195-chr10:43570638..43572674,3	MCF-7	breast:
2	chr10:43521534..43522099-chr10:43595175..43595724,2	MCF-7	breast:
3	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
4	chr10:43555354..43557716-chr10:43558344..43560863,2	K562	blood:
5	chr10:43556494..43558733-chr10:43559960..43563613,3	MCF-7	breast:
6	chr10:43551076..43553051-chr10:43554800..43557668,3	MCF-7	breast:
7	chr10:43522999..43525382-chr10:43554403..43557112,2	MCF-7	breast:
8	chr10:43521855..43522376-chr10:43577254..43578134,2	MCF-7	breast:
9	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
10	chr10:43594982..43596781-chr10:43603444..43605896,2	MCF-7	breast:
11	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
12	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
13	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
14	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
15	chr10:43556705..43558416-chr10:43560624..43562176,2	MCF-7	breast:
16	chr10:43557710..43559940-chr10:43561579..43563313,2	K562	blood:
17	chr10:43520346..43523029-chr10:43587909..43590894,3	MCF-7	breast:
18	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
19	chr10:43557710..43559940-chr10:43561579..43563313,2	K562	blood:
20	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
21	chr10:43516622..43519495-chr10:43560494..43562660,2	MCF-7	breast:
22	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
23	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
24	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:
25	chr10:43571954..43575948-chr10:43588456..43593172,4	MCF-7	breast:
26	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
27	chr10:43539794..43541332-chr10:43557128..43559148,2	MCF-7	breast:
28	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
29	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
30	chr10:43476676..43477639-chr10:43581673..43582410,2	MCF-7	breast:
31	chr10:43544147..43547451-chr10:43554029..43556833,3	MCF-7	breast:
32	chr10:43597660..43599265-chr10:43602367..43604242,2	K562	blood:
33	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
34	chr10:43571533..43575007-chr10:43595685..43599211,4	MCF-7	breast:
35	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
36	chr10:43562048..43563046-chr17:73389829..73390578,3	MCF-7	breast:
37	chr10:43521503..43524600-chr10:43558785..43561738,3	MCF-7	breast:
38	chr10:43523482..43525302-chr10:43587306..43589145,2	MCF-7	breast:
39	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
40	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
41	chr10:43567330..43568843-chr10:43570636..43572926,2	MCF-7	breast:
42	chr10:43549704..43551367-chr10:43558936..43561777,2	MCF-7	breast:
43	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
44	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
45	chr10:43581616..43582507-chr10:43605989..43606921,3	MCF-7	breast:
46	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:
47	chr10:43574755..43578524-chr10:43632183..43633949,3	MCF-7	breast:
48	chr10:43556494..43558733-chr10:43559960..43563613,3	MCF-7	breast:
49	chr10:43476076..43477138-chr10:43577286..43578259,3	MCF-7	breast:
50	chr10:43540474..43542331-chr10:43555929..43558160,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGEF1A-3	chr10:43593022-43593304	l_302_chr10:43593021-43594323_testes
2	lnc-RASGEF1A-3	chr10:43594036-43594080	NONHSAT012942
3	lnc-RASGEF1A-3	chr10:43593016-43593304	NONHSAT012941
4	lnc-RASGEF1A-3	chr10:43593016-43593304	NONHSAT012942
5	lnc-RASGEF1A-3	chr10:43594036-43594323	l_302_chr10:43593021-43594323_testes
6	lnc-RASGEF1A-3	chr10:43594161-43594279	NONHSAT012941

Variant related genes	Relation type
RET	TF binding region
RET	CpG island
ENSG00000273008	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000177885	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000265342	chromatin interactions
ENSG00000234944	chromatin interactions

Extended variants
information (count: 1850 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7069590	chr10:43552895-43552896	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7092603	chr10:43552931-43552932	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs207470830	chr10:43552941-43552942	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs183665938	chr10:43552953-43552954	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs10082477	chr10:43552963-43552964	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs386743161	chr10:43552984-43552985	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs188423213	chr10:43552998-43552999	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs530593505	chr10:43552999-43553000	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs377316022	chr10:43553015-43553016	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs181219957	chr10:43553019-43553020	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs559381586	chr10:43553074-43553075	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs186523451	chr10:43553091-43553092	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs555530340	chr10:43553132-43553133	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs76700918	chr10:43553139-43553140	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs369487416	chr10:43553143-43553144	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs541088537	chr10:43553196-43553197	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs559294578	chr10:43553204-43553205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs72779402	chr10:43553230-43553231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545013819	chr10:43553231-43553232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563227046	chr10:43553232-43553233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140987784	chr10:43553308-43553309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541622945	chr10:43553362-43553363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542631292	chr10:43553392-43553393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181500398	chr10:43553408-43553409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528584857	chr10:43553457-43553458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547023783	chr10:43553519-43553520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11412561	chr10:43553537-43553538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs33913998	chr10:43553538-43553539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571795905	chr10:43553558-43553559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112793182	chr10:43553559-43553560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79964517	chr10:43553596-43553597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541603983	chr10:43553634-43553635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568808107	chr10:43553650-43553651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76864336	chr10:43553662-43553663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12414147	chr10:43553693-43553694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536917855	chr10:43553705-43553706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185876758	chr10:43553715-43553716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567213167	chr10:43553749-43553750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370873407	chr10:43553750-43553751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530723537	chr10:43553766-43553767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553022594	chr10:43553809-43553810	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116867180	chr10:43553832-43553833	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544783157	chr10:43553857-43553858	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556706899	chr10:43553868-43553869	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569974204	chr10:43553883-43553884	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12219378	chr10:43553949-43553950	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528412511	chr10:43554032-43554033	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150252155	chr10:43554045-43554046	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561126745	chr10:43554113-43554114	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111672249	chr10:43554129-43554130	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43540200-43556600	Weak transcription	Spleen	Spleen
2	chr10:43542400-43553600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:43549000-43553400	Enhancers	Liver	Liver
4	chr10:43551200-43553200	Enhancers	Right Ventricle	heart
5	chr10:43551400-43553200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr10:43551800-43553200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr10:43552400-43555600	Weak transcription	Pancreas	Pancrea
8	chr10:43552600-43555400	Weak transcription	Left Ventricle	heart
9	chr10:43552800-43553000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
10	chr10:43553200-43555400	Weak transcription	Right Ventricle	heart
11	chr10:43553400-43554800	Weak transcription	Liver	Liver
12	chr10:43553600-43553800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:43553800-43554200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:43554200-43555000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr10:43554400-43554600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr10:43554400-43572000	Weak transcription	Right Atrium	heart
17	chr10:43554600-43555000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr10:43554800-43557800	Enhancers	Liver	Liver
19	chr10:43555000-43555600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:43555000-43560400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:43555200-43556200	Enhancers	Duodenum Mucosa	Duodenum
22	chr10:43555200-43556200	Enhancers	Fetal Heart	heart
23	chr10:43555200-43556400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr10:43555400-43556200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr10:43555400-43556200	Enhancers	Left Ventricle	heart
26	chr10:43555400-43556200	Enhancers	Right Ventricle	heart
27	chr10:43555600-43556200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:43555600-43556200	Enhancers	Gastric	stomach
29	chr10:43555600-43556200	Enhancers	Pancreas	Pancrea
30	chr10:43555800-43556200	Enhancers	HMEC	breast
31	chr10:43556200-43559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:43556200-43559600	Weak transcription	Left Ventricle	heart
33	chr10:43556600-43556800	Enhancers	Spleen	Spleen
34	chr10:43556800-43563200	Weak transcription	Spleen	Spleen
35	chr10:43557600-43558000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:43557800-43558000	Enhancers	Right Ventricle	heart
37	chr10:43558000-43563400	Weak transcription	Right Ventricle	heart
38	chr10:43558800-43559000	Enhancers	Esophagus	oesophagus
39	chr10:43559000-43561400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:43559000-43562600	Weak transcription	Esophagus	oesophagus
41	chr10:43559400-43560600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr10:43559600-43560000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:43559600-43560000	Enhancers	Left Ventricle	heart
44	chr10:43559600-43560600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr10:43559600-43560600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr10:43560000-43560400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr10:43560000-43564400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr10:43560400-43560800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:43560400-43561600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:43560800-43570800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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