Variant report

Variant	esv34929
Chromosome Location	chr10:43116194-43329770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3060)
CpG islands
(count:3177)
Chromatin interactive
region (count:133)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43264291-43264671	K562	blood:	n/a	n/a
2	ARID3A	chr10:43137131-43137331	K562	blood:	n/a	n/a
3	ARID3A	chr10:43133235-43133242	K562	blood:	n/a	n/a
4	ARID3A	chr10:43141814-43141940	K562	blood:	n/a	n/a
5	ARID3A	chr10:43145651-43145857	K562	blood:	n/a	n/a
6	ARID3A	chr10:43142426-43142906	K562	blood:	n/a	n/a
7	ARID3A	chr10:43277876-43278461	K562	blood:	n/a	n/a
8	ARID3A	chr10:43175769-43175936	K562	blood:	n/a	n/a
9	ARID3A	chr10:43149257-43150354	K562	blood:	n/a	n/a
10	ARID3A	chr10:43148649-43148667	K562	blood:	n/a	n/a
11	ARID3A	chr10:43140563-43140930	K562	blood:	n/a	n/a
12	ARID3A	chr10:43134199-43134647	K562	blood:	n/a	n/a
13	ARID3A	chr10:43139678-43139682	K562	blood:	n/a	n/a
14	ARID3A	chr10:43137031-43137458	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:43133462-43134226	HepG2	liver:	n/a	n/a
16	ARID3A	chr10:43277794-43278837	HepG2	liver:	n/a	n/a
17	ATF1	chr10:43149998-43150327	K562	blood:	n/a	n/a
18	ATF1	chr10:43264252-43264654	K562	blood:	n/a	n/a
19	ATF1	chr10:43234242-43234371	K562	blood:	n/a	n/a
20	ATF1	chr10:43180091-43180303	K562	blood:	n/a	n/a
21	ATF1	chr10:43149120-43149317	K562	blood:	n/a	n/a
22	ATF1	chr10:43140556-43140958	K562	blood:	n/a	n/a
23	ATF1	chr10:43327236-43327383	K562	blood:	n/a	n/a
24	ATF1	chr10:43239265-43239373	K562	blood:	n/a	n/a
25	ATF1	chr10:43277837-43279020	K562	blood:	n/a	n/a
26	ATF1	chr10:43133442-43134439	K562	blood:	n/a	n/a
27	ATF1	chr10:43142344-43142887	K562	blood:	n/a	n/a
28	ATF2	chr10:43277895-43278451	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr10:43277906-43278566	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr10:43133605-43134047	GM12878	blood:	n/a	n/a
31	ATF2	chr10:43277935-43278664	GM12878	blood:	n/a	n/a
32	ATF2	chr10:43277891-43278637	GM12878	blood:	n/a	n/a
33	ATF2	chr10:43133365-43134480	GM12878	blood:	n/a	n/a
34	ATF2	chr10:43296575-43296964	GM12878	blood:	n/a	n/a
35	ATF3	chr10:43277721-43278499	A549	lung:	n/a	n/a
36	ATF3	chr10:43278350-43278642	K562	blood:	n/a	n/a
37	ATF3	chr10:43140517-43140863	K562	blood:	n/a	n/a
38	ATF3	chr10:43277853-43278406	A549	lung:	n/a	n/a
39	BACH1	chr10:43323789-43323995	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr10:43277956-43278287	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr10:43133731-43134405	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr10:43144172-43144293	K562	blood:	n/a	n/a
43	BACH1	chr10:43141933-43141976	K562	blood:	n/a	n/a
44	BACH1	chr10:43277990-43278352	K562	blood:	n/a	n/a
45	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr10:43140045-43140294	K562	blood:	n/a	n/a
47	BATF	chr10:43277973-43278382	GM12878	blood:	n/a	n/a
48	BATF	chr10:43218973-43219261	GM12878	blood:	n/a	n/a
49	BATF	chr10:43296561-43297027	GM12878	blood:	n/a	n/a
50	BCL11A	chr10:43277864-43278662	GM12878	blood:	n/a	n/a

(count:3177 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43250063-43250113	BE2_C	brain:	n/a
2	chr10:43252305-43252355	NHBE	bronchial:	n/a
3	chr10:43275316-43275366	U87	brain:	n/a
4	chr10:43187321-43187371	HRPEpiC	eye:	n/a
5	chr10:43133352-43133402	H1-hESC	embryonic stem cell:	embryo
6	chr10:43250063-43250113	BE2_C	brain:	n/a
7	chr10:43252305-43252355	NHBE	bronchial:	n/a
8	chr10:43275316-43275366	U87	brain:	n/a
9	chr10:43187321-43187371	HRPEpiC	eye:	n/a
10	chr10:43133352-43133402	H1-hESC	embryonic stem cell:	embryo
11	chr10:43278349-43278399	GM06990	blood:	n/a
12	chr10:43277745-43277795	GM12892	blood:	n/a
13	chr10:43277745-43277795	NH-A	brain:	n/a
14	chr10:43277941-43277991	PrEC	prostate:	n/a
15	chr10:43134038-43134088	NB4	blood:	n/a
16	chr10:43263580-43263630	NT2-D1	testis:	n/a
17	chr10:43277850-43277900	LNCaP	prostate:	n/a
18	chr10:43250063-43250113	HRCEpiC	kidney:	n/a
19	chr10:43187175-43187225	GM06990	blood:	n/a
20	chr10:43277913-43277963	LNCaP	prostate:	n/a
21	chr10:43215944-43215994	HIPEpiC	eye:	n/a
22	chr10:43136508-43136558	H1-hESC	embryonic stem cell:	embryo
23	chr10:43254088-43254138	H1-hESC	embryonic stem cell:	embryo
24	chr10:43187321-43187371	ovcar-3	ovarian:	n/a
25	chr10:43247938-43247988	A549	lung:	n/a
26	chr10:43187184-43187234	AG10803	skin:	n/a
27	chr10:43278700-43278750	PrEC	prostate:	n/a
28	chr10:43186810-43186860	A549	lung:	n/a
29	chr10:43134234-43134284	HL-60	blood:	n/a
30	chr10:43250063-43250113	ECC-1	luminal epithelium:	n/a
31	chr10:43209934-43209984	HCM	heart:	n/a
32	chr10:43249161-43249211	HEEpiC	esophagus:	n/a
33	chr10:43136508-43136558	Hepatocyte	liver:	n/a
34	chr10:43245080-43245130	CMK	blood:	n/a
35	chr10:43186868-43186918	HCT-116	colon:	n/a
36	chr10:43277534-43277584	GM12891	blood:	n/a
37	chr10:43186868-43186918	NT2-D1	testis:	n/a
38	chr10:43245080-43245130	Hepatocyte	liver:	n/a
39	chr10:43277757-43277807	MCF-7	breast:	n/a
40	chr10:43329092-43329142	NT2-D1	testis:	n/a
41	chr10:43275316-43275366	HepG2	liver:	n/a
42	chr10:43280976-43281026	AG09309	skin:	n/a
43	chr10:43209934-43209984	ECC-1	luminal epithelium:	n/a
44	chr10:43263649-43263699	AG10803	skin:	n/a
45	chr10:43277938-43277988	HMEC	breast:	n/a
46	chr10:43248870-43248920	U87	brain:	n/a
47	chr10:43186900-43186950	MCF-7	breast:	n/a
48	chr10:43187175-43187225	NT2-D1	testis:	n/a
49	chr10:43249161-43249211	HCPEpiC	choroid plexus:	n/a
50	chr10:43130877-43130927	ProgFib	skin:	n/a

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:43133575..43134141-chr10:43278109..43279018,2	MCF-7	breast:
2	chr10:43132682..43135189-chr10:43137259..43140017,4	MCF-7	breast:
3	chr10:43100572..43103779-chr10:43131525..43135101,4	MCF-7	breast:
4	chr10:43282048..43284162-chr10:43286079..43288954,3	K562	blood:
5	chr10:43275094..43277500-chr4:119200265..119202996,2	MCF-7	breast:
6	chr10:43130478..43132491-chr10:43132734..43134984,3	K562	blood:
7	chr10:43278278..43279935-chr10:43297692..43300575,2	K562	blood:
8	chr10:43141512..43143238-chr10:43157022..43158551,2	MCF-7	breast:
9	chr10:43133569..43135388-chr10:43147096..43149467,2	K562	blood:
10	chr10:43132537..43136859-chr10:43137751..43144882,8	MCF-7	breast:
11	chr10:43277103..43279687-chr10:43279795..43282779,2	MCF-7	breast:
12	chr10:43132863..43135217-chr10:43276470..43279459,4	K562	blood:
13	chr10:43270690..43272215-chr10:43274653..43276562,2	K562	blood:
14	chr10:43125083..43130093-chr10:43132029..43136060,7	K562	blood:
15	chr10:43258843..43262487-chr10:43264254..43267473,3	K562	blood:
16	chr10:43132954..43135205-chr10:43277445..43279937,2	K562	blood:
17	chr10:43285411..43287004-chr10:43291005..43292621,2	K562	blood:
18	chr10:43258843..43262487-chr10:43264254..43267473,3	K562	blood:
19	chr10:43132391..43135100-chr10:43189606..43191108,2	MCF-7	breast:
20	chr10:43291912..43294159-chr10:43296262..43298525,2	K562	blood:
21	chr10:43276494..43279738-chr10:43283503..43286419,4	MCF-7	breast:
22	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:
23	chr10:43046301..43049301-chr10:43278095..43279962,3	K562	blood:
24	chr10:43131361..43135006-chr10:43140847..43143635,4	MCF-7	breast:
25	chr10:43245352..43247530-chr10:43276802..43279739,2	K562	blood:
26	chr10:43179370..43182447-chr10:43184174..43186310,3	MCF-7	breast:
27	chr10:43277379..43280402-chr10:43288985..43292909,5	MCF-7	breast:
28	chr10:43228372..43230638-chr10:43276090..43278496,2	MCF-7	breast:
29	chr10:43132954..43135205-chr10:43277445..43279937,2	K562	blood:
30	chr10:43322775..43323340-chr10:43574006..43574597,2	MCF-7	breast:
31	chr10:43124209..43130093-chr10:43131977..43134761,6	K562	blood:
32	chr10:43132026..43134878-chr10:43134908..43136583,2	MCF-7	breast:
33	chr10:43250846..43253793-chr10:43254051..43256963,2	K562	blood:
34	chr10:43113714..43116283-chr10:43132528..43135183,2	MCF-7	breast:
35	chr10:43132101..43134395-chr10:43180123..43182624,3	K562	blood:
36	chr10:43285592..43290643-chr10:43292360..43294489,4	K562	blood:
37	chr10:43270031..43271737-chr10:43276984..43278616,2	K562	blood:
38	chr10:43137680..43139181-chr10:43140744..43142599,2	MCF-7	breast:
39	chr10:43253135..43254665-chr10:43264247..43266986,2	MCF-7	breast:
40	chr10:43280780..43283548-chr10:43285550..43289909,6	K562	blood:
41	chr10:43173150..43176514-chr10:43178445..43181832,3	K562	blood:
42	chr10:43125885..43127699-chr10:43129230..43130895,2	K562	blood:
43	chr10:43133575..43134141-chr10:43278109..43279018,2	MCF-7	breast:
44	chr10:43132703..43135183-chr10:43271199..43273394,2	K562	blood:
45	chr10:43272289..43273994-chr10:43276021..43278160,2	MCF-7	breast:
46	chr10:43285411..43287004-chr10:43291005..43292621,2	K562	blood:
47	chr10:43132526..43135261-chr10:43184647..43186574,3	MCF-7	breast:
48	chr10:43179370..43182447-chr10:43184174..43186310,3	MCF-7	breast:
49	chr10:43147543..43150157-chr10:43264028..43266927,2	K562	blood:
50	chr10:43133406..43134070-chr12:31476740..31477598,2	Hela-S3	cervix:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012922
2	lnc-ZNF33B-3	chr10:43127743-43127815	ENSG00000272373.1
3	lnc-BMS1-2	chr10:43191483-43191659	ENSG00000234864
4	lnc-ZNF33B-1	chr10:43186987-43187198	NONHSAT012922
5	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012924
6	lnc-ZNF33B-1	chr10:43169645-43169805	ENSG00000233515
7	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT139966
8	lnc-ZNF33B-3	chr10:43127377-43127472	ENSG00000272373.1
9	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012922
10	lnc-ZNF33B-1	chr10:43186181-43186249	NONHSAT139966
11	lnc-BMS1-4	chr10:43236053-43236103	NONHSAT012928
12	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012921
13	lnc-ZNF33B-1	chr10:43186983-43187171	ENSG00000233515
14	lnc-RET-4	chr10:43306923-43307499	l_299_chr10:43299976-43307499_brain
15	lnc-BMS1-2	chr10:43198870-43201901	ENSG00000234864
16	lnc-BMS1-4	chr10:43237124-43237260	NONHSAT012928
17	lnc-ZNF33B-5	chr10:43274740-43277953	NONHSAT012930
18	lnc-ZNF33B-1	chr10:43186983-43187198	NONHSAT012921
19	lnc-RET-4	chr10:43306826-43306918	l_299_chr10:43299976-43307499_brain
20	lnc-ZNF33B-1	chr10:43181399-43181464	ENSG00000233515
21	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT012921
22	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT139966
23	lnc-ZNF33B-1	chr10:43187438-43187527	NONHSAT012924
24	lnc-ZNF33B-1	chr10:43181399-43181464	NONHSAT012921
25	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT139966
26	lnc-BMS1-5	chr10:43156176-43157224	NONHSAT012919
27	lnc-ZNF33B-1	chr10:43169877-43169974	NONHSAT012924
28	lnc-BMS1-4	chr10:43236406-43236520	NONHSAT012928
29	lnc-ZNF33B-1	chr10:43178806-43178908	NONHSAT012924
30	lnc-ZNF33B-1	chr10:43178806-43178908	ENSG00000233515
31	lnc-ZNF33B-1	chr10:43169261-43169805	NONHSAT012922
32	lnc-BMS1-2	chr10:43196950-43197705	ENSG00000234864
33	lnc-RET-4	chr10:43299977-43300625	l_299_chr10:43299976-43307499_brain
34	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BMS1	hsa-miR-30a-5p	chr10:43327447-43327468

Variant related genes	Relation type
ENSG00000259869	TF binding region
ENSG00000234864	TF binding region
ENSG00000272373	TF binding region
ENSG00000232109	TF binding region
RNU6-885P	TF binding region
ENSG00000238732	TF binding region
ENSG00000233515	TF binding region
RSU1P1	TF binding region
DUXAP3	TF binding region
ZNF33B	TF binding region
BMS1	TF binding region
CUBNP1	TF binding region
ENSG00000259869	CpG island
ENSG00000234864	CpG island
ENSG00000272373	CpG island
ENSG00000232109	CpG island
RNU6-885P	CpG island
ENSG00000238732	CpG island
ENSG00000233515	CpG island
RSU1P1	CpG island
DUXAP3	CpG island
ZNF33B	CpG island
BMS1	CpG island
CUBNP1	CpG island
ENSG00000105372	chromatin interactions
ENSG00000179950	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000135847	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000269893	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000090661	chromatin interactions
ENSG00000106261	chromatin interactions
ENSG00000251783	chromatin interactions
ENSG00000185904	chromatin interactions
ENSG00000232109	chromatin interactions
ENSG00000234420	chromatin interactions
ENSG00000123358	chromatin interactions

Extended variants
information (count: 7702 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7702 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6593439	chr10:43116207-43116208	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557472797	chr10:43116251-43116252	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146572950	chr10:43116318-43116319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs209383	chr10:43116381-43116382	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs116785037	chr10:43116385-43116386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191760192	chr10:43116392-43116393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534292195	chr10:43116425-43116426	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs11239706	chr10:43116434-43116435	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs118106337	chr10:43116471-43116472	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs111869081	chr10:43116478-43116479	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs563443331	chr10:43116502-43116503	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs560867795	chr10:43116510-43116511	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs574267428	chr10:43116573-43116574	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs575298118	chr10:43116591-43116592	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs71014278	chr10:43116608-43116609	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs397845268	chr10:43116609-43116610	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs542851510	chr10:43116618-43116619	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs398013290	chr10:43116624-43116625	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs555258498	chr10:43116647-43116648	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs561130280	chr10:43116655-43116656	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs112588289	chr10:43116666-43116667	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs546942086	chr10:43116672-43116673	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs565128984	chr10:43116673-43116674	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs532588227	chr10:43116707-43116708	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs112913511	chr10:43116727-43116728	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs374479968	chr10:43116737-43116738	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs183324979	chr10:43116769-43116770	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs142897968	chr10:43116778-43116779	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs187437141	chr10:43116825-43116826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543244384	chr10:43116826-43116827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374907158	chr10:43116858-43116859	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs158376	chr10:43116859-43116860	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs556955237	chr10:43116891-43116892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566751657	chr10:43116899-43116900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534206577	chr10:43116919-43116920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559242102	chr10:43116940-43116941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190740054	chr10:43116946-43116947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183249137	chr10:43116967-43116968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556738952	chr10:43116991-43116992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116174796	chr10:43116992-43116993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60215790	chr10:43117002-43117003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140584214	chr10:43117007-43117008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186642504	chr10:43117009-43117010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573118116	chr10:43117022-43117023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540533598	chr10:43117065-43117066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565189981	chr10:43117113-43117114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192486154	chr10:43117139-43117140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550969006	chr10:43117147-43117148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184804801	chr10:43117148-43117149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530112839	chr10:43117165-43117166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:3858 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43089600-43123600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr10:43089800-43126000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:43089800-43133000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:43089800-43133000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr10:43089800-43133000	Weak transcription	Right Ventricle	heart
6	chr10:43090000-43119200	Weak transcription	Brain Anterior Caudate	brain
7	chr10:43090000-43119200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr10:43090400-43118600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr10:43090800-43133000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr10:43091000-43123800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr10:43091200-43123600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr10:43091200-43126000	Weak transcription	Small Intestine	intestine
13	chr10:43091200-43132800	Weak transcription	Colon Smooth Muscle	Colon
14	chr10:43091400-43119600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr10:43091400-43132400	Weak transcription	HMEC	breast
16	chr10:43091400-43132800	Weak transcription	Colonic Mucosa	Colon
17	chr10:43094000-43119400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr10:43094000-43119400	Weak transcription	Spleen	Spleen
19	chr10:43094200-43119400	Weak transcription	Right Atrium	heart
20	chr10:43094400-43133200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:43095400-43126000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr10:43095600-43125800	Weak transcription	HUVEC	blood vessel
23	chr10:43096800-43119400	Weak transcription	NHEK	skin
24	chr10:43097600-43118400	Weak transcription	Esophagus	oesophagus
25	chr10:43100400-43118400	Weak transcription	Pancreas	Pancrea
26	chr10:43101000-43133000	Weak transcription	NH-A	brain
27	chr10:43102000-43119400	Weak transcription	Gastric	stomach
28	chr10:43102000-43126200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:43102000-43132000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr10:43105800-43119400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr10:43106200-43132600	Weak transcription	Fetal Heart	heart
32	chr10:43107000-43133000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr10:43107400-43129000	Strong transcription	HUES64 Cell Line	embryonic stem cell
34	chr10:43107800-43119400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr10:43108000-43133200	Weak transcription	Psoas Muscle	Psoas
36	chr10:43108600-43116400	Weak transcription	HepG2	liver
37	chr10:43108800-43119400	Weak transcription	Left Ventricle	heart
38	chr10:43109000-43133200	Weak transcription	Aorta	Aorta
39	chr10:43109200-43117200	Weak transcription	Adipose Nuclei	Adipose
40	chr10:43109400-43119000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr10:43109600-43118000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:43109600-43118600	Weak transcription	Stomach Smooth Muscle	stomach
43	chr10:43109600-43118800	Weak transcription	Brain Germinal Matrix	brain
44	chr10:43109600-43119200	Weak transcription	Fetal Kidney	kidney
45	chr10:43109600-43119400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr10:43109600-43119400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr10:43109600-43119400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:43109600-43119400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:43109600-43119400	Weak transcription	Fetal Stomach	stomach
50	chr10:43109800-43116400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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