Variant report

Variant	nsv540625
Chromosome Location	chr10:52009869-52135542
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2332)
CpG islands
(count:244)
Chromatin interactive
region (count:113)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:2332 , 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	chr10:52076596-52077385	K562	blood:	n/a	n/a
2	ARID3A	chr10:52117735-52118515	K562	blood:	n/a	n/a
3	ARID3A	chr10:52091151-52092344	K562	blood:	n/a	n/a
4	ARID3A	chr10:52127535-52127844	K562	blood:	n/a	n/a
5	ARID3A	chr10:52099381-52099787	K562	blood:	n/a	n/a
6	ARID3A	chr10:52111590-52111825	K562	blood:	n/a	n/a
7	ARID3A	chr10:52063453-52063845	K562	blood:	n/a	n/a
8	ARID3A	chr10:52078573-52079065	K562	blood:	n/a	n/a
9	ARID3A	chr10:52096785-52097419	K562	blood:	n/a	n/a
10	ARID3A	chr10:52081241-52082196	K562	blood:	n/a	n/a
11	ARID3A	chr10:52011227-52011506	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:52055144-52055451	K562	blood:	n/a	n/a
13	ARID3A	chr10:52124449-52124686	K562	blood:	n/a	n/a
14	ARID3A	chr10:52035412-52035803	K562	blood:	n/a	n/a
15	ARID3A	chr10:52077960-52078184	K562	blood:	n/a	n/a
16	ARID3A	chr10:52020838-52021159	HepG2	liver:	n/a	n/a
17	ARID3A	chr10:52072531-52073538	K562	blood:	n/a	n/a
18	ARID3A	chr10:52051151-52051887	K562	blood:	n/a	chr10:52051843-52051859
19	ARID3A	chr10:52075129-52075588	K562	blood:	n/a	n/a
20	ARID3A	chr10:52120334-52120358	K562	blood:	n/a	n/a
21	ARID3A	chr10:52070534-52070946	K562	blood:	n/a	n/a
22	ARID3A	chr10:52084484-52089746	K562	blood:	n/a	chr10:52089059-52089075 chr10:52089058-52089074
23	ARID3A	chr10:52090227-52090559	K562	blood:	n/a	n/a
24	ARID3A	chr10:52132787-52132975	K562	blood:	n/a	n/a
25	ATF1	chr10:52020533-52020905	K562	blood:	n/a	n/a
26	ATF1	chr10:52085140-52085785	K562	blood:	n/a	n/a
27	ATF1	chr10:52086523-52087559	K562	blood:	n/a	n/a
28	ATF1	chr10:52072566-52073079	K562	blood:	n/a	n/a
29	ATF2	chr10:52020470-52020997	GM12878	blood:	n/a	n/a
30	ATF2	chr10:52122180-52122928	GM12878	blood:	n/a	n/a
31	ATF2	chr10:52134583-52135111	GM12878	blood:	n/a	n/a
32	ATF2	chr10:52106973-52107749	GM12878	blood:	n/a	n/a
33	ATF2	chr10:52107026-52107665	GM12878	blood:	n/a	n/a
34	ATF2	chr10:52020317-52021056	GM12878	blood:	n/a	n/a
35	ATF2	chr10:52122262-52123094	GM12878	blood:	n/a	n/a
36	ATF2	chr10:52085076-52085573	GM12878	blood:	n/a	n/a
37	ATF3	chr10:52086482-52087108	K562	blood:	n/a	n/a
38	ATF3	chr10:52085055-52085796	K562	blood:	n/a	n/a
39	BACH1	chr10:52092573-52092805	K562	blood:	n/a	n/a
40	BACH1	chr10:52125123-52125148	K562	blood:	n/a	n/a
41	BACH1	chr10:52042451-52042475	K562	blood:	n/a	n/a
42	BACH1	chr10:52079541-52079637	K562	blood:	n/a	n/a
43	BACH1	chr10:52076598-52077012	K562	blood:	n/a	n/a
44	BACH1	chr10:52086440-52087663	K562	blood:	n/a	n/a
45	BACH1	chr10:52100879-52101325	K562	blood:	n/a	n/a
46	BACH1	chr10:52039370-52039740	K562	blood:	n/a	chr10:52039520-52039534
47	BACH1	chr10:52035455-52035788	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr10:52035377-52035783	K562	blood:	n/a	n/a
49	BACH1	chr10:52073601-52073850	K562	blood:	n/a	n/a
50	BACH1	chr10:52091726-52092287	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52120283-52120333	HNPCEpiC	eye:	n/a
2	chr10:52120283-52120333	U87	brain:	n/a
3	chr10:52120283-52120333	NT2-D1	testis:	n/a
4	chr10:52115682-52115732	RPTEC	kidney:	n/a
5	chr10:52120283-52120333	ovcar-3	ovarian:	n/a
6	chr10:52115682-52115732	K562	blood:	n/a
7	chr10:52066867-52066917	NT2-D1	testis:	n/a
8	chr10:52120283-52120333	Hela-S3	cervix:	n/a
9	chr10:52120283-52120333	PFSK-1	brain:	n/a
10	chr10:52066867-52066917	HNPCEpiC	eye:	n/a
11	chr10:52115183-52115233	IMR90	lung:	fetal
12	chr10:52120283-52120333	HMEC	breast:	n/a
13	chr10:52115682-52115732	Caco-2	colon:	n/a
14	chr10:52066867-52066917	GM12891	blood:	n/a
15	chr10:52066867-52066917	AoSMC	blood vessel:	n/a
16	chr10:52066867-52066917	AG10803	skin:	n/a
17	chr10:52066867-52066917	HCPEpiC	choroid plexus:	n/a
18	chr10:52120283-52120333	SAEC	small airway:	n/a
19	chr10:52120283-52120333	Caco-2	colon:	n/a
20	chr10:52115183-52115233	GM12892	blood:	n/a
21	chr10:52066867-52066917	ProgFib	skin:	n/a
22	chr10:52115682-52115732	AG10803	skin:	n/a
23	chr10:52066867-52066917	HAEpiC	amniotic membrane:	n/a
24	chr10:52115183-52115233	SAEC	small airway:	n/a
25	chr10:52115682-52115732	NH-A	brain:	n/a
26	chr10:52120283-52120333	AG10803	skin:	n/a
27	chr10:52115682-52115732	HRE	kidney:	n/a
28	chr10:52115183-52115233	HAEpiC	amniotic membrane:	n/a
29	chr10:52066867-52066917	GM12878	blood:	n/a
30	chr10:52115183-52115233	T-47D	breast:	n/a
31	chr10:52115682-52115732	CMK	blood:	n/a
32	chr10:52115183-52115233	SK-N-MC	brain:	n/a
33	chr10:52115183-52115233	LNCaP	prostate:	n/a
34	chr10:52115183-52115233	NB4	blood:	n/a
35	chr10:52066867-52066917	Hela-S3	cervix:	n/a
36	chr10:52120283-52120333	HL-60	blood:	n/a
37	chr10:52066867-52066917	HEEpiC	esophagus:	n/a
38	chr10:52120283-52120333	AoSMC	blood vessel:	n/a
39	chr10:52115183-52115233	MCF-7	breast:	n/a
40	chr10:52120283-52120333	HIPEpiC	eye:	n/a
41	chr10:52120283-52120333	HepG2	liver:	n/a
42	chr10:52115682-52115732	AG04450	lung:	fetal
43	chr10:52115682-52115732	Hepatocyte	liver:	n/a
44	chr10:52115682-52115732	BE2_C	brain:	n/a
45	chr10:52115682-52115732	AG09309	skin:	n/a
46	chr10:52115682-52115732	AG04449	skin:	fetal
47	chr10:52115183-52115233	A549	lung:	n/a
48	chr10:52066867-52066917	T-47D	breast:	n/a
49	chr10:52120283-52120333	SK-N-SH	brain:	n/a
50	chr10:52115682-52115732	GM12878	blood:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:52127640..52130879-chr10:52134264..52136292,3	K562	blood:
2	chr10:52050788..52053473-chr10:52085482..52088054,2	K562	blood:
3	chr10:52011614..52013335-chr10:52018420..52020373,2	K562	blood:
4	chr10:52078609..52080735-chr10:52099175..52100683,2	MCF-7	breast:
5	chr10:52132102..52134129-chr10:52137496..52139624,2	K562	blood:
6	chr10:52103151..52105270-chr10:52383748..52386662,2	K562	blood:
7	chr10:52065089..52067181-chr10:52085442..52087556,2	K562	blood:
8	chr10:52087443..52089388-chr10:52116523..52119614,3	K562	blood:
9	chr10:52014263..52015864-chr10:52038453..52040858,2	K562	blood:
10	chr10:52040531..52043332-chr10:52062739..52065495,2	K562	blood:
11	chr10:52047341..52049235-chr10:52083279..52085507,2	K562	blood:
12	chr10:52038390..52041263-chr10:52085010..52087882,2	K562	blood:
13	chr10:52127262..52128152-chr10:52180974..52181673,2	K562	blood:
14	chr10:52105040..52107754-chr10:52130504..52132718,2	MCF-7	breast:
15	chr10:52039584..52041526-chr10:52044440..52046214,2	MCF-7	breast:
16	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
17	chr10:52128591..52131322-chr10:52132559..52135165,2	MCF-7	breast:
18	chr10:52115339..52118395-chr10:52119759..52122908,4	K562	blood:
19	chr10:52014263..52015864-chr10:52038453..52040858,2	K562	blood:
20	chr10:52034197..52036639-chr10:52176402..52178569,2	K562	blood:
21	chr10:52083101..52087112-chr10:52175005..52179754,6	K562	blood:
22	chr10:52064687..52067489-chr10:52072620..52075726,3	K562	blood:
23	chr10:52125875..52128899-chr10:52129822..52132966,4	K562	blood:
24	chr10:52009441..52011844-chr10:52036005..52038580,2	K562	blood:
25	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
26	chr10:52063071..52064625-chr10:52072402..52074193,2	MCF-7	breast:
27	chr10:52100945..52103388-chr10:52103997..52106988,2	MCF-7	breast:
28	chr10:52120330..52124092-chr10:52125493..52129232,4	K562	blood:
29	chr10:52046559..52050186-chr10:52057567..52060183,3	K562	blood:
30	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
31	chr10:52091344..52092956-chr10:52110761..52113396,2	MCF-7	breast:
32	chr10:52036642..52039011-chr10:52040195..52041719,2	K562	blood:
33	chr10:52097924..52101512-chr10:52122361..52124512,3	K562	blood:
34	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
35	chr10:52125875..52128899-chr10:52129822..52132966,4	K562	blood:
36	chr10:52029815..52033760-chr10:52034548..52037259,4	K562	blood:
37	chr10:52075208..52077138-chr10:52380386..52382972,2	K562	blood:
38	chr10:52118184..52120411-chr10:52292971..52295430,2	K562	blood:
39	chr10:52132819..52134741-chr10:52135257..52137397,2	K562	blood:
40	chr10:52115339..52118395-chr10:52119759..52122908,4	K562	blood:
41	chr10:52128591..52131322-chr10:52132559..52135165,2	MCF-7	breast:
42	chr10:52029815..52033760-chr10:52034548..52037259,4	K562	blood:
43	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
44	chr10:52084925..52086838-chr10:52120229..52123147,2	K562	blood:
45	chr10:52131941..52133571-chr10:52135239..52137791,2	MCF-7	breast:
46	chr10:52079847..52082788-chr10:52084797..52086833,2	MCF-7	breast:
47	chr10:52084222..52086810-chr10:52173871..52176505,2	K562	blood:
48	chr10:52058612..52061385-chr10:52062063..52064503,2	K562	blood:
49	chr10:52120330..52124092-chr10:52125493..52129232,4	K562	blood:
50	chr10:52033462..52036031-chr10:52039236..52041874,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM21A-2	chr10:52062175-52063940	l_311_chr10:52061403-52063940_testes
2	lnc-ASAH2-5	chr10:52104168-52104349	l_312_chr10:52096258-52104698_testes
3	lnc-ASAH2-5	chr10:52096259-52096435	l_312_chr10:52096258-52104698_testes
4	lnc-ASAH2-5	chr10:52104608-52104698	l_312_chr10:52096258-52104698_testes
5	lnc-ASAH2-6	chr10:52103896-52104105	NONHSAT013379
6	lnc-FAM21A-2	chr10:52061404-52061522	l_311_chr10:52061403-52063940_testes
7	lnc-ASAH2-5	chr10:52096448-52096864	l_312_chr10:52096258-52104698_testes
8	lnc-ASAH2-4	chr10:52102202-52102561	NONHSAT013378

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SGMS1	hsa-miR-130b-3p	chr10:52066046-52066067
2	SGMS1	hsa-miR-124-3p	chr10:52066157-52066151
3	SGMS1	hsa-miR-130b-3p	chr10:52065388-52065411
4	SGMS1	hsa-miR-130b-3p	chr10:52066686-52066707
5	SGMS1	hsa-miR-33a-5p	chr10:52066188-52066208
6	SGMS1	hsa-miR-130b-3p	chr10:52066406-52066429
7	SGMS1	hsa-miR-93-5p	chr10:52065386-52065408
8	SGMS1	hsa-miR-33a-5p	chr10:52065390-52065409
9	SGMS1	hsa-miR-124-3p	chr10:52066151-52066170

Variant related genes	Relation type
SGMS1	TF binding region
ENSG00000269165	TF binding region
DYNC1I2P1	TF binding region
ASAH2	TF binding region
SGMS1	CpG island
ENSG00000269165	CpG island
DYNC1I2P1	CpG island
ASAH2	CpG island
ENSG00000226200	chromatin interactions
ENSG00000269165	chromatin interactions
ENSG00000198964	chromatin interactions

Extended variants
information (count: 4462 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4462 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74539463	chr10:52009887-52009888	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs573494446	chr10:52009926-52009927	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs182247458	chr10:52009968-52009969	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559140376	chr10:52010022-52010023	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs187997062	chr10:52010065-52010066	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs115445835	chr10:52010151-52010152	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs545293206	chr10:52010202-52010203	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs565093885	chr10:52010204-52010205	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs368456965	chr10:52010218-52010219	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs538132633	chr10:52010222-52010223	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs557513336	chr10:52010224-52010225	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145180298	chr10:52010293-52010294	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs138700021	chr10:52010297-52010298	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567394026	chr10:52010357-52010358	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192421422	chr10:52010360-52010361	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368151162	chr10:52010374-52010375	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs149356259	chr10:52010394-52010395	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs144711266	chr10:52010405-52010406	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs10508920	chr10:52010410-52010411	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559211169	chr10:52010445-52010446	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs571144483	chr10:52010513-52010514	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs116031597	chr10:52010549-52010550	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556625082	chr10:52010550-52010551	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs573370531	chr10:52010555-52010556	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs185222065	chr10:52010584-52010585	Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs552704451	chr10:52010623-52010624	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs116324108	chr10:52010641-52010642	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544966708	chr10:52010674-52010675	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs565230439	chr10:52010696-52010697	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs10508921	chr10:52010708-52010709	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
31	rs544650908	chr10:52010824-52010825	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs561283144	chr10:52010918-52010919	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs530187693	chr10:52010963-52010964	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs1865747	chr10:52010964-52010965	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs114508519	chr10:52010978-52010979	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs10508922	chr10:52010979-52010980	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148535058	chr10:52010985-52010986	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs569560004	chr10:52011011-52011012	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs34555591	chr10:52011016-52011017	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs190071595	chr10:52011017-52011018	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs556513789	chr10:52011049-52011050	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs566929186	chr10:52011062-52011063	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs76397798	chr10:52011075-52011076	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs201605661	chr10:52011077-52011078	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs79576617	chr10:52011086-52011087	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs572950596	chr10:52011098-52011099	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs538855649	chr10:52011142-52011143	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558558219	chr10:52011184-52011185	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs575461068	chr10:52011219-52011220	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs192712253	chr10:52011235-52011236	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52007400-52010000	Enhancers	HepG2	liver
2	chr10:52007400-52010200	Enhancers	Liver	Liver
3	chr10:52009000-52010000	Enhancers	Duodenum Mucosa	Duodenum
4	chr10:52009400-52010200	Flanking Active TSS	Fetal Intestine Small	intestine
5	chr10:52009600-52010000	Flanking Active TSS	Fetal Intestine Large	intestine
6	chr10:52010000-52010200	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr10:52010000-52010400	Active TSS	Fetal Intestine Large	intestine
8	chr10:52010000-52011600	Flanking Active TSS	HepG2	liver
9	chr10:52010200-52010400	Active TSS	Fetal Intestine Small	intestine
10	chr10:52010200-52010600	Flanking Active TSS	Liver	Liver
11	chr10:52010200-52010600	Active TSS	Duodenum Mucosa	Duodenum
12	chr10:52010200-52011400	Enhancers	K562	blood
13	chr10:52010400-52010600	Flanking Active TSS	Fetal Intestine Small	intestine
14	chr10:52010400-52011400	Flanking Active TSS	Fetal Intestine Large	intestine
15	chr10:52010600-52010800	Active TSS	Fetal Intestine Small	intestine
16	chr10:52010600-52011400	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr10:52010600-52011800	Enhancers	Liver	Liver
18	chr10:52010800-52011200	Flanking Active TSS	Fetal Intestine Small	intestine
19	chr10:52011000-52011200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr10:52011000-52011400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr10:52011200-52011400	Active TSS	Fetal Intestine Small	intestine
22	chr10:52011400-52011800	Enhancers	Duodenum Mucosa	Duodenum
23	chr10:52011400-52012000	Weak transcription	Fetal Intestine Small	intestine
24	chr10:52011400-52012200	Enhancers	Fetal Intestine Large	intestine
25	chr10:52011600-52011800	Enhancers	HepG2	liver
26	chr10:52011800-52014600	Weak transcription	HepG2	liver
27	chr10:52011800-52020200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr10:52012000-52012200	Enhancers	Fetal Intestine Small	intestine
29	chr10:52012200-52015600	Weak transcription	Pancreas	Pancrea
30	chr10:52012200-52019400	Weak transcription	Fetal Intestine Large	intestine
31	chr10:52014400-52014600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr10:52014600-52014800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr10:52014600-52015000	Enhancers	HepG2	liver
34	chr10:52014800-52016400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr10:52015000-52017400	Weak transcription	HepG2	liver
36	chr10:52015600-52015800	ZNF genes & repeats	Pancreas	Pancrea
37	chr10:52015800-52016200	Weak transcription	Pancreas	Pancrea
38	chr10:52016400-52016600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr10:52016400-52016800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr10:52017400-52018200	Enhancers	HepG2	liver
41	chr10:52017400-52018400	Enhancers	Fetal Intestine Small	intestine
42	chr10:52017600-52018000	Bivalent Enhancer	Small Intestine	intestine
43	chr10:52017800-52018200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr10:52018200-52020400	Weak transcription	HepG2	liver
45	chr10:52018400-52019400	Weak transcription	Fetal Intestine Small	intestine
46	chr10:52019400-52022200	Enhancers	Fetal Intestine Small	intestine
47	chr10:52019400-52022400	Enhancers	K562	blood
48	chr10:52019400-52022600	Enhancers	Fetal Intestine Large	intestine
49	chr10:52019600-52019800	Enhancers	Small Intestine	intestine
50	chr10:52019600-52020200	Enhancers	GM12878-XiMat	blood

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