Variant report

Variant	nsv550697
Chromosome Location	chr10:43721481-43849358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2343)
CpG islands
(count:3238)
Chromatin interactive
region (count:151)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2343 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43843997-43844253	HepG2	liver:	n/a	n/a
2	ATF1	chr10:43782794-43783112	K562	blood:	n/a	n/a
3	BACH1	chr10:43800080-43800440	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:43804602-43804617	K562	blood:	n/a	n/a
5	BACH1	chr10:43769765-43769851	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:43844047-43844300	K562	blood:	n/a	n/a
7	BACH1	chr10:43724255-43724899	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:43725811-43725979	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:43828364-43828380	K562	blood:	n/a	n/a
10	BATF	chr10:43829696-43830134	GM12878	blood:	n/a	chr10:43829882-43829893
11	BHLHE40	chr10:43751373-43751579	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:43810301-43810513	K562	blood:	n/a	n/a
13	BHLHE40	chr10:43843918-43844290	K562	blood:	n/a	n/a
14	BHLHE40	chr10:43751338-43751539	K562	blood:	n/a	n/a
15	BHLHE40	chr10:43843914-43844263	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:43808198-43808354	K562	blood:	n/a	n/a
17	BHLHE40	chr10:43791964-43792071	K562	blood:	n/a	n/a
18	BHLHE40	chr10:43800241-43800413	K562	blood:	n/a	chr10:43800372-43800388
19	BHLHE40	chr10:43805103-43805172	K562	blood:	n/a	n/a
20	BHLHE40	chr10:43788740-43788896	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:43782768-43783086	K562	blood:	n/a	n/a
22	BHLHE40	chr10:43788666-43789060	K562	blood:	n/a	chr10:43788989-43789005
23	BRCA1	chr10:43811217-43811226	HepG2	liver:	n/a	n/a
24	CBX3	chr10:43782709-43783165	K562	blood:	n/a	n/a
25	CBX3	chr10:43843811-43844299	K562	blood:	n/a	n/a
26	CCNT2	chr10:43800219-43800325	K562	blood:	n/a	n/a
27	CCNT2	chr10:43843970-43844213	K562	blood:	n/a	n/a
28	CCNT2	chr10:43844480-43844680	K562	blood:	n/a	n/a
29	CEBPB	chr10:43742646-43742953	IMR90	lung:	n/a	chr10:43742769-43742780
30	CEBPB	chr10:43742253-43742334	K562	blood:	n/a	n/a
31	CEBPB	chr10:43806377-43806655	Hela-S3	cervix:	n/a	chr10:43806507-43806524
32	CEBPB	chr10:43793647-43793803	K562	blood:	n/a	n/a
33	CEBPB	chr10:43742642-43742872	HepG2	liver:	n/a	chr10:43742769-43742780
34	CEBPB	chr10:43804499-43804773	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:43742639-43742903	K562	blood:	n/a	chr10:43742769-43742780
36	CEBPB	chr10:43812007-43812314	K562	blood:	n/a	n/a
37	CEBPB	chr10:43782785-43783407	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:43801285-43801494	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:43845512-43846084	MCF-7	breast:	n/a	n/a
40	CEBPB	chr10:43831401-43831447	K562	blood:	n/a	n/a
41	CEBPB	chr10:43783122-43783407	A549	lung:	n/a	n/a
42	CEBPB	chr10:43806356-43806707	HepG2	liver:	n/a	chr10:43806507-43806524
43	CEBPB	chr10:43806330-43806734	A549	lung:	n/a	chr10:43806507-43806524
44	CEBPB	chr10:43806331-43806705	IMR90	lung:	n/a	chr10:43806507-43806524
45	CEBPB	chr10:43806399-43806699	H1-hESC	embryonic stem cell:	n/a	chr10:43806507-43806524
46	CEBPB	chr10:43767821-43767970	HepG2	liver:	n/a	chr10:43767860-43767871
47	CEBPB	chr10:43801253-43801548	A549	lung:	n/a	n/a
48	CEBPB	chr10:43768487-43768677	A549	lung:	n/a	n/a
49	CEBPB	chr10:43807533-43807557	A549	lung:	n/a	n/a
50	CEBPB	chr10:43806389-43806748	K562	blood:	n/a	chr10:43806507-43806524

(count:3238 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43846281-43846331	AG04450	lung:	fetal
2	chr10:43820676-43820726	HepG2	liver:	n/a
3	chr10:43846574-43846624	HEK293	kidney:	embryo
4	chr10:43818365-43818415	Jurkat	blood:	n/a
5	chr10:43820676-43820726	Hepatocyte	liver:	n/a
6	chr10:43846281-43846331	AG04450	lung:	fetal
7	chr10:43820676-43820726	HepG2	liver:	n/a
8	chr10:43846574-43846624	HEK293	kidney:	embryo
9	chr10:43818365-43818415	Jurkat	blood:	n/a
10	chr10:43820676-43820726	Hepatocyte	liver:	n/a
11	chr10:43834363-43834413	AG10803	skin:	n/a
12	chr10:43824891-43824941	Hepatocyte	liver:	n/a
13	chr10:43725277-43725327	BE2_C	brain:	n/a
14	chr10:43811183-43811233	HEEpiC	esophagus:	n/a
15	chr10:43739117-43739167	IMR90	lung:	fetal
16	chr10:43846281-43846331	GM19239	blood:	n/a
17	chr10:43818603-43818653	BJ	skin:	n/a
18	chr10:43846539-43846589	AG09309	skin:	n/a
19	chr10:43746736-43746786	HUVEC	blood vessel:	n/a
20	chr10:43815780-43815830	HRE	kidney:	n/a
21	chr10:43817997-43818047	PFSK-1	brain:	n/a
22	chr10:43723859-43723909	AG10803	skin:	n/a
23	chr10:43725277-43725327	Hepatocyte	liver:	n/a
24	chr10:43818603-43818653	NH-A	brain:	n/a
25	chr10:43846539-43846589	ProgFib	skin:	n/a
26	chr10:43834363-43834413	HCPEpiC	choroid plexus:	n/a
27	chr10:43843492-43843542	GM06990	blood:	n/a
28	chr10:43724742-43724792	ovcar-3	ovarian:	n/a
29	chr10:43725376-43725426	MCF-7	breast:	n/a
30	chr10:43818881-43818931	MCF-7	breast:	n/a
31	chr10:43818911-43818961	AG10803	skin:	n/a
32	chr10:43846574-43846624	GM06990	blood:	n/a
33	chr10:43846376-43846426	K562	blood:	n/a
34	chr10:43725741-43725791	Hela-S3	cervix:	n/a
35	chr10:43725411-43725461	GM12891	blood:	n/a
36	chr10:43818603-43818653	NT2-D1	testis:	n/a
37	chr10:43725376-43725426	GM19239	blood:	n/a
38	chr10:43818911-43818961	IMR90	lung:	fetal
39	chr10:43788993-43789043	Hepatocyte	liver:	n/a
40	chr10:43817997-43818047	HCPEpiC	choroid plexus:	n/a
41	chr10:43824891-43824941	NT2-D1	testis:	n/a
42	chr10:43818695-43818745	SK-N-SH_RA	brain:	n/a
43	chr10:43840571-43840621	RPTEC	kidney:	n/a
44	chr10:43818365-43818415	HMEC	breast:	n/a
45	chr10:43818365-43818415	NB4	blood:	n/a
46	chr10:43728230-43728280	HNPCEpiC	eye:	n/a
47	chr10:43818881-43818931	SAEC	small airway:	n/a
48	chr10:43746736-43746786	NT2-D1	testis:	n/a
49	chr10:43817997-43818047	NHBE	bronchial:	n/a
50	chr10:43824891-43824941	ProgFib	skin:	n/a

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:43842351..43846324-chr10:43890114..43894453,4	MCF-7	breast:
2	chr10:43847056..43849483-chr10:43852032..43853812,3	MCF-7	breast:
3	chr10:43771161..43773089-chr10:43903979..43905991,2	MCF-7	breast:
4	chr10:43700335..43700885-chr10:43843806..43844502,2	MCF-7	breast:
5	chr10:43633619..43635410-chr10:43761017..43763266,2	MCF-7	breast:
6	chr10:43786873..43787506-chr10:43843726..43844460,2	MCF-7	breast:
7	chr10:43834919..43837712-chr10:43842377..43845170,3	MCF-7	breast:
8	chr10:43787979..43788967-chr10:43843516..43844636,5	K562	blood:
9	chr10:43726760..43729695-chr10:43750265..43752104,2	MCF-7	breast:
10	chr10:43788331..43789347-chr10:43843553..43844589,11	MCF-7	breast:
11	chr10:43847403..43853479-chr10:43888233..43893881,11	MCF-7	breast:
12	chr10:43749536..43751095-chr10:43809193..43811814,2	K562	blood:
13	chr10:43844277..43847779-chr10:43901946..43904076,3	MCF-7	breast:
14	chr10:43757038..43760449-chr10:43762640..43764974,3	K562	blood:
15	chr10:43726760..43729695-chr10:43750265..43752104,2	MCF-7	breast:
16	chr10:43750917..43751578-chr10:43813067..43813837,2	K562	blood:
17	chr10:43832614..43835578-chr10:43888340..43890232,2	MCF-7	breast:
18	chr10:43822305..43824647-chr10:43844072..43845599,2	K562	blood:
19	chr10:43716570..43717454-chr10:43751032..43752428,7	MCF-7	breast:
20	chr10:43788453..43789259-chr10:43957179..43957947,3	MCF-7	breast:
21	chr10:43812264..43813765-chr10:43817090..43818832,2	K562	blood:
22	chr10:43809902..43812557-chr10:43814429..43816002,2	K562	blood:
23	chr10:43845449..43848194-chr10:43889287..43891526,2	K562	blood:
24	chr10:43746969..43750119-chr10:43752543..43755778,3	K562	blood:
25	chr10:43772713..43774253-chr10:43775459..43778308,2	K562	blood:
26	chr10:43753888..43756103-chr10:43898148..43900430,2	K562	blood:
27	chr10:43837942..43841047-chr10:43842473..43845770,3	MCF-7	breast:
28	chr10:43815310..43817377-chr10:43891214..43892928,3	K562	blood:
29	chr10:43848475..43851407-chr10:43948589..43951104,3	MCF-7	breast:
30	chr10:43787979..43788967-chr10:43843516..43844636,5	K562	blood:
31	chr10:43624978..43626803-chr10:43789083..43792063,2	K562	blood:
32	chr10:43600712..43601532-chr10:43751532..43752231,2	K562	blood:
33	chr10:43812235..43813804-chr10:43859221..43860786,2	K562	blood:
34	chr10:43847068..43851484-chr10:43869685..43874039,8	MCF-7	breast:
35	chr10:43788412..43790350-chr10:43892794..43895604,2	K562	blood:
36	chr10:43844606..43847679-chr10:43848074..43851632,6	MCF-7	breast:
37	chr10:43787258..43789990-chr10:43857247..43859004,2	MCF-7	breast:
38	chr10:43842329..43845784-chr10:43890164..43894425,6	MCF-7	breast:
39	chr10:43847199..43849445-chr10:43952721..43955628,2	MCF-7	breast:
40	chr10:43748329..43751092-chr10:43758387..43762104,3	MCF-7	breast:
41	chr10:43704701..43705317-chr10:43751108..43751738,2	MCF-7	breast:
42	chr10:43629065..43631893-chr10:43754557..43757372,3	MCF-7	breast:
43	chr10:43791107..43791656-chr10:43844974..43845746,2	MCF-7	breast:
44	chr10:43844606..43847679-chr10:43848074..43851632,6	MCF-7	breast:
45	chr10:43721241..43722992-chr10:43727167..43730117,3	MCF-7	breast:
46	chr10:43700322..43701097-chr10:43750638..43751735,4	MCF-7	breast:
47	chr10:43788471..43789248-chr10:43956837..43957692,2	MCF-7	breast:
48	chr10:43845581..43847759-chr10:43871473..43872986,2	MCF-7	breast:
49	chr10:43771948..43774253-chr10:43775459..43778308,3	K562	blood:
50	chr10:43759900..43762026-chr10:43901535..43903337,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FXYD4-1	chr10:43822000-43822045	NONHSAT012949
2	lnc-CSGALNACT2-2	chr10:43727898-43727932	NONHSAT012946
3	lnc-FXYD4-3	chr10:43840353-43840576	NONHSAT012953
4	lnc-FXYD4-2	chr10:43845685-43847096	NONHSAT012954
5	lnc-CSGALNACT2-2	chr10:43754457-43755996	NONHSAT012948
6	lnc-CSGALNACT2-2	chr10:43758646-43758735	l_304_chr10:43724730-43729936_testes
7	lnc-CSGALNACT2-2	chr10:43759311-43759487	l_304_chr10:43724730-43729936_testes
8	lnc-CSGALNACT2-2	chr10:43729213-43729936	l_304_chr10:43724730-43729936_testes
9	lnc-CSGALNACT2-2	chr10:43727803-43727932	l_304_chr10:43724730-43729936_testes
10	lnc-HNRNPF-2	chr10:43729604-43729960	NONHSAT012947
11	lnc-FXYD4-5	chr10:43795908-43798196	l_305_chr10:43781931-43798196_testes
12	lnc-CSGALNACT2-2	chr10:43759816-43759920	NONHSAT012948
13	lnc-FXYD4-1	chr10:43823118-43823380	XLOC_008466
14	lnc-HNRNPF-3	chr10:43727747-43727797	l_303_chr10:43716824-43727797_testes
15	lnc-FXYD4-1	chr10:43822819-43823417	XLOC_008466
16	lnc-CSGALNACT2-2	chr10:43724731-43724847	l_304_chr10:43724730-43729936_testes
17	lnc-FXYD4-1	chr10:43819113-43819148	XLOC_008466
18	lnc-CSGALNACT2-2	chr10:43780837-43781139	l_304_chr10:43724730-43729936_testes
19	lnc-FXYD4-1	chr10:43818459-43819148	XLOC_008466
20	lnc-HNRNPF-3	chr10:43727747-43727780	NONHSAT012945
21	lnc-CSGALNACT2-2	chr10:43758646-43758735	NONHSAT012948
22	lnc-CSGALNACT2-2	chr10:43729213-43729690	NONHSAT012946
23	lnc-CSGALNACT2-2	chr10:43759311-43759445	NONHSAT012948
24	lnc-HNRNPF-2	chr10:43729353-43729460	NONHSAT012947
25	lnc-FXYD4-5	chr10:43781932-43782168	l_305_chr10:43781931-43798196_testes
26	lnc-FXYD4-1	chr10:43822819-43822910	XLOC_008466
27	lnc-FXYD4-1	chr10:43818459-43819148	NONHSAT012949
28	lnc-CSGALNACT2-2	chr10:43756176-43756431	NONHSAT012948
29	lnc-CSGALNACT2-2	chr10:43724848-43725231	l_304_chr10:43724730-43729936_testes

No data

Variant related genes	Relation type
RNU6ATAC11P	TF binding region
RASGEF1A	TF binding region
ENSG00000224265	TF binding region
RNU6ATAC11P	CpG island
RASGEF1A	CpG island
ENSG00000224265	CpG island
ENSG00000221468	chromatin interactions
ENSG00000150201	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000198915	chromatin interactions
ENSG00000243660	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000252532	chromatin interactions
RLF	miRNA target sites
RIOK3	miRNA target sites

Extended variants
information (count: 5206 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:5206 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7915431	chr10:43721481-43721482	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138791244	chr10:43721489-43721490	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115343025	chr10:43721552-43721553	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577682230	chr10:43721705-43721706	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs544664536	chr10:43721747-43721748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs182222756	chr10:43721812-43721813	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs534504501	chr10:43721824-43721825	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs75277515	chr10:43721909-43721910	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs75729584	chr10:43721910-43721911	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs77287957	chr10:43721951-43721952	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs542984335	chr10:43721957-43721958	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs186911520	chr10:43721992-43721993	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs141751787	chr10:43722013-43722014	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs150566829	chr10:43722071-43722072	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs138573201	chr10:43722091-43722092	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs79009967	chr10:43722099-43722100	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs111655680	chr10:43722138-43722139	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs571321205	chr10:43722159-43722160	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs527441053	chr10:43722183-43722184	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs569144892	chr10:43722225-43722226	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs536442002	chr10:43722264-43722265	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs371242699	chr10:43722315-43722316	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs566830002	chr10:43722372-43722373	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs11238482	chr10:43722382-43722383	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552953163	chr10:43722392-43722393	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs117657945	chr10:43722411-43722412	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs117414926	chr10:43722421-43722422	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs527543421	chr10:43722429-43722430	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs556771627	chr10:43722435-43722436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs372486709	chr10:43722446-43722447	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs375737006	chr10:43722502-43722503	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs575556915	chr10:43722521-43722522	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs554699761	chr10:43722616-43722617	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs115420526	chr10:43722617-43722618	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs569475104	chr10:43722626-43722627	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs528411963	chr10:43722714-43722715	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs574553442	chr10:43722719-43722720	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs540129075	chr10:43722741-43722742	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs538453443	chr10:43722747-43722748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs191754367	chr10:43722773-43722774	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs183605981	chr10:43722781-43722782	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs369757941	chr10:43722796-43722797	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs59141258	chr10:43722840-43722841	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs397955978	chr10:43722845-43722846	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs373452518	chr10:43722860-43722861	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs75465756	chr10:43722901-43722902	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs79089853	chr10:43722913-43722914	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs548386774	chr10:43723018-43723019	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76532295	chr10:43723050-43723051	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537112827	chr10:43723089-43723090	Weak transcription Bivalent Enhancer Enhancers	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2595 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43698000-43722800	Weak transcription	Gastric	stomach
2	chr10:43699400-43724600	Weak transcription	Right Atrium	heart
3	chr10:43714800-43722000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:43717000-43724000	Weak transcription	A549	lung
5	chr10:43717600-43724000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:43720400-43721800	Enhancers	Brain Anterior Caudate	brain
7	chr10:43720400-43722200	Enhancers	Primary T cells fromperipheralblood	blood
8	chr10:43720400-43722200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:43720400-43722200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr10:43720600-43724400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr10:43720800-43721800	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr10:43720800-43721800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr10:43720800-43724000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr10:43720800-43724200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr10:43720800-43724600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr10:43721000-43721600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr10:43721000-43721600	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr10:43721000-43722200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr10:43721000-43724200	Weak transcription	Pancreas	Pancrea
20	chr10:43721000-43724600	Enhancers	Spleen	Spleen
21	chr10:43721200-43721600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:43721200-43721600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:43721200-43721600	Bivalent Enhancer	Placenta	Placenta
24	chr10:43721200-43722000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:43721400-43721800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr10:43721600-43722000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:43721600-43722400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr10:43721600-43723800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr10:43721800-43722200	Weak transcription	Brain Anterior Caudate	brain
30	chr10:43721800-43722400	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr10:43721800-43724000	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr10:43722000-43722200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:43722000-43722200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr10:43722000-43722400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr10:43722200-43722400	Enhancers	Brain Anterior Caudate	brain
36	chr10:43722200-43723800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr10:43722200-43724000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr10:43722400-43722600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr10:43722400-43723000	Weak transcription	Brain Anterior Caudate	brain
40	chr10:43722400-43724000	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr10:43722600-43722800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr10:43722800-43723000	Bivalent Enhancer	Placenta	Placenta
43	chr10:43722800-43723000	Enhancers	Gastric	stomach
44	chr10:43723000-43724000	Weak transcription	Gastric	stomach
45	chr10:43723000-43724200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:43723000-43724200	Enhancers	Brain Anterior Caudate	brain
47	chr10:43723400-43723600	Enhancers	Brain Hippocampus Middle	brain
48	chr10:43723400-43723800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr10:43723400-43724200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:43723600-43724200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--

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