Variant report

Variant	nsv540470
Chromosome Location	chr10:5120774-5261482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1704)
CpG islands
(count:854)
Chromatin interactive
region (count:68)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5261272-5261624	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5123254-5123638	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:5239083-5239264	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5136891-5137133	K562	blood:	n/a	n/a
8	ARID3A	chr10:5136259-5137212	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5236523-5236713	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:5147856-5147891	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:5120586-5121209	K562	blood:	n/a	n/a
12	ARID3A	chr10:5237741-5238762	HepG2	liver:	n/a	n/a
13	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
14	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
15	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
16	ATF3	chr10:5207727-5207953	K562	blood:	n/a	n/a
17	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
18	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
19	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
20	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
22	BCL3	chr10:5190290-5191005	A549	lung:	n/a	n/a
23	BCL3	chr10:5121933-5122486	A549	lung:	n/a	n/a
24	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
25	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
26	BCL3	chr10:5237721-5238466	A549	lung:	n/a	n/a
27	BCL3	chr10:5141308-5142213	A549	lung:	n/a	n/a
28	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
29	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
30	BCL3	chr10:5121775-5122553	A549	lung:	n/a	n/a
31	BCL3	chr10:5189111-5191215	A549	lung:	n/a	n/a
32	BCL3	chr10:5189224-5190092	A549	lung:	n/a	n/a
33	BHLHE40	chr10:5185410-5185563	HepG2	liver:	n/a	n/a
34	BHLHE40	chr10:5120759-5121300	K562	blood:	n/a	n/a
35	BHLHE40	chr10:5207857-5208008	K562	blood:	n/a	n/a
36	BHLHE40	chr10:5190346-5190928	HepG2	liver:	n/a	n/a
37	BRCA1	chr10:5136812-5137013	HepG2	liver:	n/a	n/a
38	BRCA1	chr10:5136453-5137624	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr10:5253743-5253974	K562	blood:	n/a	n/a
40	CBX3	chr10:5207666-5208060	K562	blood:	n/a	n/a
41	CBX3	chr10:5136392-5137166	K562	blood:	n/a	n/a
42	CBX3	chr10:5136765-5137213	HCT-116	colon:	n/a	n/a
43	CBX3	chr10:5178725-5179069	K562	blood:	n/a	n/a
44	CBX3	chr10:5178706-5179040	HCT-116	colon:	n/a	n/a
45	CBX3	chr10:5207656-5208172	HCT-116	colon:	n/a	n/a
46	CBX3	chr10:5136690-5137127	K562	blood:	n/a	n/a
47	CBX3	chr10:5178698-5179012	K562	blood:	n/a	n/a
48	CBX3	chr10:5120800-5121401	K562	blood:	n/a	n/a
49	CBX3	chr10:5207663-5208074	K562	blood:	n/a	n/a
50	CBX3	chr10:5252304-5252616	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5227757-5227807	PANC-1	pancreas:	n/a
2	chr10:5238881-5238931	AG10803	skin:	n/a
3	chr10:5135453-5135503	ECC-1	luminal epithelium:	n/a
4	chr10:5227162-5227212	SKMC	muscle:	n/a
5	chr10:5227162-5227212	GM12891	blood:	n/a
6	chr10:5149799-5149849	Hela-S3	cervix:	n/a
7	chr10:5238881-5238931	HMEC	breast:	n/a
8	chr10:5260740-5260790	HEEpiC	esophagus:	n/a
9	chr10:5260740-5260790	A549	lung:	n/a
10	chr10:5149799-5149849	K562	blood:	n/a
11	chr10:5227162-5227212	T-47D	breast:	n/a
12	chr10:5227162-5227212	HL-60	blood:	n/a
13	chr10:5149799-5149849	SAEC	small airway:	n/a
14	chr10:5135453-5135503	HUVEC	blood vessel:	n/a
15	chr10:5227162-5227212	K562	blood:	n/a
16	chr10:5260740-5260790	HRPEpiC	eye:	n/a
17	chr10:5227757-5227807	AG10803	skin:	n/a
18	chr10:5260740-5260790	T-47D	breast:	n/a
19	chr10:5135453-5135503	HCF	heart:	n/a
20	chr10:5203419-5203469	Hela-S3	cervix:	n/a
21	chr10:5237881-5237931	AG04450	lung:	fetal
22	chr10:5227312-5227362	K562	blood:	n/a
23	chr10:5227757-5227807	HepG2	liver:	n/a
24	chr10:5135453-5135503	NH-A	brain:	n/a
25	chr10:5238881-5238931	HUVEC	blood vessel:	n/a
26	chr10:5227757-5227807	T-47D	breast:	n/a
27	chr10:5135453-5135503	HCPEpiC	choroid plexus:	n/a
28	chr10:5203419-5203469	U87	brain:	n/a
29	chr10:5237881-5237931	HepG2	liver:	n/a
30	chr10:5227162-5227212	MCF10A-Er-Src	breast:	n/a
31	chr10:5136782-5136832	NHDF-neo	bronchial:	n/a
32	chr10:5246625-5246675	GM12892	blood:	n/a
33	chr10:5227757-5227807	H1-hESC	embryonic stem cell:	embryo
34	chr10:5237869-5237919	NH-A	brain:	n/a
35	chr10:5237869-5237919	H1-hESC	embryonic stem cell:	embryo
36	chr10:5246625-5246675	Caco-2	colon:	n/a
37	chr10:5203419-5203469	NT2-D1	testis:	n/a
38	chr10:5136782-5136832	HRE	kidney:	n/a
39	chr10:5227757-5227807	HRE	kidney:	n/a
40	chr10:5237853-5237903	Hepatocyte	liver:	n/a
41	chr10:5228106-5228156	BJ	skin:	n/a
42	chr10:5228106-5228156	U87	brain:	n/a
43	chr10:5135453-5135503	NB4	blood:	n/a
44	chr10:5135453-5135503	HPAEpiC	pulmonary alveolar:	n/a
45	chr10:5136782-5136832	GM12878	blood:	n/a
46	chr10:5203419-5203469	MCF10A-Er-Src	breast:	n/a
47	chr10:5149799-5149849	IMR90	lung:	fetal
48	chr10:5237869-5237919	HUVEC	blood vessel:	n/a
49	chr10:5238881-5238931	HCM	heart:	n/a
50	chr10:5228106-5228156	Caco-2	colon:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5225688..5227346-chr10:5233053..5235554,2	MCF-7	breast:
2	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
3	chr10:5228162..5230153-chr10:5232988..5235199,2	K562	blood:
4	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
5	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
6	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
7	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
8	chr10:5248069..5249924-chr10:5250712..5252871,2	K562	blood:
9	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
10	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
11	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
12	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
13	chr10:5136589..5138613-chr10:5158907..5161668,2	MCF-7	breast:
14	chr10:5241329..5242148-chr10:5325053..5325709,2	MCF-7	breast:
15	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
16	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
17	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
18	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
19	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
20	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
21	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
22	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
23	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
24	chr10:5231335..5234110-chr10:5249009..5251135,2	MCF-7	breast:
25	chr10:5250240..5252491-chr10:5252736..5256514,3	K562	blood:
26	chr10:5135013..5137947-chr10:5149855..5151840,2	MCF-7	breast:
27	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
28	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
29	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
30	chr10:5132364..5134075-chr10:5134147..5137113,2	MCF-7	breast:
31	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
32	chr10:5136517..5137515-chr10:5241491..5242054,2	MCF-7	breast:
33	chr10:5247043..5249924-chr10:5250707..5254146,4	K562	blood:
34	chr10:5158412..5160412-chr20:46095387..46097285,2	MCF-7	breast:
35	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
36	chr10:5060824..5061816-chr10:5136872..5137424,2	MCF-7	breast:
37	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
38	chr10:5118918..5120947-chr10:5130785..5133580,2	MCF-7	breast:
39	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
40	chr10:5228162..5230153-chr10:5232988..5235199,2	K562	blood:
41	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
42	chr10:5250240..5252491-chr10:5252736..5256514,3	K562	blood:
43	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
44	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
45	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
46	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
47	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
48	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
49	chr10:5198281..5200177-chr10:5228677..5230787,2	K562	blood:
50	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C4-2	chr10:5237425-5237538	NONHSAT011140
2	lnc-AKR1CL1-2	chr10:5186655-5187952	ucscGeneNc_uc009xhz_1
3	lnc-AKR1C4-2	chr10:5238192-5238885	NONHSAT011140
4	lnc-AKR1CL1-2	chr10:5189836-5190001	ucscGeneNc_uc009xhz_1
5	lnc-AKR1CL1-2	chr10:5192082-5192149	ucscGeneNc_uc009xhz_1
6	lnc-AKR1C3-5	chr10:5249132-5249705	NONHSAT011142

No data

Variant related genes	Relation type
AKR1C3	TF binding region
ENSG00000251909	TF binding region
AKR1C4	TF binding region
AKR1C5P	TF binding region
AKR1CL1	TF binding region
ENSG00000239142	TF binding region
ENSG00000228291	TF binding region
AKR1C3	CpG island
ENSG00000251909	CpG island
AKR1C4	CpG island
AKR1C5P	CpG island
AKR1CL1	CpG island
ENSG00000239142	CpG island
ENSG00000228291	CpG island
ENSG00000239142	chromatin interactions
ENSG00000225418	chromatin interactions
ENSG00000228291	chromatin interactions
ENSG00000196139	chromatin interactions
ENSG00000165568	chromatin interactions
ENSG00000196326	chromatin interactions

Extended variants
information (count: 7000 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7000 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78132167	chr10:5120800-5120801	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs537393052	chr10:5120838-5120839	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs558519135	chr10:5120904-5120905	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576859641	chr10:5120927-5120928	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs142576098	chr10:5120939-5120940	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs75371034	chr10:5120963-5120964	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs74710128	chr10:5121007-5121008	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs17304691	chr10:5121021-5121022	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs115778922	chr10:5121037-5121038	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs561190737	chr10:5121065-5121066	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs77168456	chr10:5121073-5121074	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs370075317	chr10:5121080-5121081	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs543783166	chr10:5121144-5121145	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs111537719	chr10:5121145-5121146	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76526379	chr10:5121166-5121167	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7898263	chr10:5121206-5121207	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs180701763	chr10:5121244-5121245	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376493440	chr10:5121291-5121292	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183997085	chr10:5121327-5121328	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs371002166	chr10:5121341-5121342	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548491355	chr10:5121354-5121355	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569954663	chr10:5121384-5121385	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537332031	chr10:5121414-5121415	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs570690854	chr10:5121416-5121417	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs189560543	chr10:5121424-5121425	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570484337	chr10:5121450-5121451	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534725960	chr10:5121481-5121482	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs553392615	chr10:5121492-5121493	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs143316813	chr10:5121561-5121562	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574840979	chr10:5121629-5121630	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs535992487	chr10:5121637-5121638	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534804919	chr10:5121639-5121640	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs554796930	chr10:5121703-5121704	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs12570303	chr10:5121745-5121746	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs543720455	chr10:5121770-5121771	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565201920	chr10:5121808-5121809	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73599928	chr10:5121823-5121824	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373401799	chr10:5121836-5121837	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs4881397	chr10:5121872-5121873	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182157816	chr10:5121880-5121881	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs535960122	chr10:5121892-5121893	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148113963	chr10:5121916-5121917	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs186692328	chr10:5121925-5121926	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563519806	chr10:5121987-5121988	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11252924	chr10:5122033-5122034	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141818488	chr10:5122092-5122093	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150612332	chr10:5122096-5122097	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139720724	chr10:5122103-5122104	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539476445	chr10:5122104-5122105	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568485012	chr10:5122138-5122139	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5095400-5120800	Weak transcription	Right Atrium	heart
2	chr10:5113200-5121000	Weak transcription	Gastric	stomach
3	chr10:5114600-5121000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:5114600-5121400	Weak transcription	Fetal Kidney	kidney
5	chr10:5116000-5120800	Weak transcription	Fetal Intestine Small	intestine
6	chr10:5116200-5121000	Weak transcription	Fetal Intestine Large	intestine
7	chr10:5116200-5121200	Weak transcription	Small Intestine	intestine
8	chr10:5119000-5122600	Weak transcription	Adipose Nuclei	Adipose
9	chr10:5119800-5121600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:5119800-5124000	Weak transcription	NHDF-Ad	bronchial
11	chr10:5119800-5124400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr10:5120000-5121000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:5120400-5121000	Enhancers	K562	blood
14	chr10:5120400-5124800	Enhancers	Stomach Mucosa	stomach
15	chr10:5120600-5121600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:5120600-5122000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr10:5120600-5122000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr10:5120600-5122600	Flanking Active TSS	A549	lung
19	chr10:5120600-5124600	Enhancers	HepG2	liver
20	chr10:5120800-5121600	Enhancers	Hela-S3	cervix
21	chr10:5120800-5121800	Enhancers	HMEC	breast
22	chr10:5120800-5123600	Enhancers	Fetal Intestine Small	intestine
23	chr10:5121000-5121200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr10:5121000-5121400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr10:5121000-5121400	Enhancers	Gastric	stomach
26	chr10:5121000-5121600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr10:5121000-5121600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:5121000-5121600	Flanking Active TSS	K562	blood
29	chr10:5121000-5121800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr10:5121000-5121800	Enhancers	Pancreas	Pancrea
31	chr10:5121000-5122000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:5121000-5122000	Enhancers	NHEK	skin
33	chr10:5121000-5122200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr10:5121000-5122400	Enhancers	Duodenum Mucosa	Duodenum
35	chr10:5121000-5123400	Enhancers	Fetal Intestine Large	intestine
36	chr10:5121200-5121600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr10:5121200-5122000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:5121200-5122200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr10:5121200-5122400	Enhancers	Small Intestine	intestine
40	chr10:5121400-5121600	Enhancers	Fetal Kidney	kidney
41	chr10:5121400-5121800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr10:5121400-5121800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr10:5121600-5122200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:5121600-5123000	Enhancers	K562	blood
45	chr10:5121800-5124000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:5122000-5132200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr10:5122200-5124400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:5122400-5122800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr10:5122400-5123000	Weak transcription	Small Intestine	intestine
50	chr10:5122600-5123000	Enhancers	Adipose Nuclei	Adipose

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