Variant report

Variant	nsv1036566
Chromosome Location	chr10:5037926-5261426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3221)
CpG islands
(count:1591)
Chromatin interactive
region (count:114)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3221 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5120586-5121209	K562	blood:	n/a	n/a
2	ARID3A	chr10:5113567-5114862	K562	blood:	n/a	n/a
3	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5136259-5137212	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5261272-5261624	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:5239083-5239264	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5077017-5077109	K562	blood:	n/a	n/a
8	ARID3A	chr10:5136891-5137133	K562	blood:	n/a	n/a
9	ARID3A	chr10:5081022-5081232	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:5061188-5061367	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:5147856-5147891	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:5051271-5051707	HepG2	liver:	n/a	n/a
13	ARID3A	chr10:5083803-5084201	HepG2	liver:	n/a	n/a
14	ARID3A	chr10:5112815-5114610	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
16	ARID3A	chr10:5110678-5110878	K562	blood:	n/a	n/a
17	ARID3A	chr10:5236523-5236713	HepG2	liver:	n/a	n/a
18	ARID3A	chr10:5062394-5062740	K562	blood:	n/a	n/a
19	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
20	ARID3A	chr10:5123254-5123638	HepG2	liver:	n/a	n/a
21	ARID3A	chr10:5089966-5091092	HepG2	liver:	n/a	chr10:5090324-5090340
22	ARID3A	chr10:5237741-5238762	HepG2	liver:	n/a	n/a
23	ARID3A	chr10:5044421-5044450	K562	blood:	n/a	n/a
24	ATF1	chr10:5044389-5044572	K562	blood:	n/a	n/a
25	ATF1	chr10:5113912-5114323	K562	blood:	n/a	n/a
26	ATF3	chr10:5113430-5114380	A549	lung:	n/a	n/a
27	ATF3	chr10:5113911-5114354	K562	blood:	n/a	n/a
28	ATF3	chr10:5043740-5045168	A549	lung:	n/a	n/a
29	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
30	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
31	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
32	ATF3	chr10:5112971-5114564	A549	lung:	n/a	n/a
33	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
34	ATF3	chr10:5051152-5051727	A549	lung:	n/a	n/a
35	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
36	ATF3	chr10:5207727-5207953	K562	blood:	n/a	n/a
37	ATF3	chr10:5051280-5051719	A549	lung:	n/a	n/a
38	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr10:5113506-5114634	K562	blood:	n/a	n/a
40	BACH1	chr10:5062492-5062763	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
42	BACH1	chr10:5075630-5075846	K562	blood:	n/a	chr10:5075716-5075730
43	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
44	BACH1	chr10:5062431-5062668	K562	blood:	n/a	n/a
45	BACH1	chr10:5054805-5055071	K562	blood:	n/a	n/a
46	BACH1	chr10:5113866-5114859	H1-hESC	embryonic stem cell:	n/a	n/a
47	BCL3	chr10:5045658-5046322	A549	lung:	n/a	n/a
48	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
49	BCL3	chr10:5050987-5051835	A549	lung:	n/a	n/a
50	BCL3	chr10:5043450-5044764	A549	lung:	n/a	chr10:5043544-5043553

(count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5228106-5228156	AoSMC	blood vessel:	n/a
2	chr10:5260740-5260790	A549	lung:	n/a
3	chr10:5227162-5227212	NT2-D1	testis:	n/a
4	chr10:5046097-5046147	NH-A	brain:	n/a
5	chr10:5044992-5045042	SKMC	muscle:	n/a
6	chr10:5228106-5228156	AoSMC	blood vessel:	n/a
7	chr10:5260740-5260790	A549	lung:	n/a
8	chr10:5227162-5227212	NT2-D1	testis:	n/a
9	chr10:5046097-5046147	NH-A	brain:	n/a
10	chr10:5044992-5045042	SKMC	muscle:	n/a
11	chr10:5113871-5113921	H1-hESC	embryonic stem cell:	embryo
12	chr10:5074993-5075043	SKMC	muscle:	n/a
13	chr10:5047487-5047537	HAEpiC	amniotic membrane:	n/a
14	chr10:5060291-5060341	A549	lung:	n/a
15	chr10:5227757-5227807	Hepatocyte	liver:	n/a
16	chr10:5228106-5228156	Caco-2	colon:	n/a
17	chr10:5113871-5113921	AG04450	lung:	fetal
18	chr10:5135453-5135503	HepG2	liver:	n/a
19	chr10:5046097-5046147	BJ	skin:	n/a
20	chr10:5227162-5227212	SK-N-SH	brain:	n/a
21	chr10:5047487-5047537	Caco-2	colon:	n/a
22	chr10:5260740-5260790	Hepatocyte	liver:	n/a
23	chr10:5060432-5060482	HRCEpiC	kidney:	n/a
24	chr10:5246625-5246675	AG10803	skin:	n/a
25	chr10:5237853-5237903	U87	brain:	n/a
26	chr10:5060566-5060616	AG09309	skin:	n/a
27	chr10:5046097-5046147	Jurkat	blood:	n/a
28	chr10:5260740-5260790	ProgFib	skin:	n/a
29	chr10:5227312-5227362	GM19239	blood:	n/a
30	chr10:5203419-5203469	AG09319	gingival:	n/a
31	chr10:5237853-5237903	BE2_C	brain:	n/a
32	chr10:5136782-5136832	HRCEpiC	kidney:	n/a
33	chr10:5042313-5042363	GM12891	blood:	n/a
34	chr10:5047487-5047537	ProgFib	skin:	n/a
35	chr10:5237881-5237931	AG09309	skin:	n/a
36	chr10:5238881-5238931	HCM	heart:	n/a
37	chr10:5227312-5227362	AG09309	skin:	n/a
38	chr10:5246625-5246675	H1-hESC	embryonic stem cell:	embryo
39	chr10:5060318-5060368	BJ	skin:	n/a
40	chr10:5246625-5246675	Hela-S3	cervix:	n/a
41	chr10:5046097-5046147	A549	lung:	n/a
42	chr10:5237881-5237931	HIPEpiC	eye:	n/a
43	chr10:5060318-5060368	IMR90	lung:	fetal
44	chr10:5061094-5061144	HRPEpiC	eye:	n/a
45	chr10:5061094-5061144	U87	brain:	n/a
46	chr10:5135453-5135503	Caco-2	colon:	n/a
47	chr10:5042313-5042363	HCT-116	colon:	n/a
48	chr10:5113871-5113921	AG09319	gingival:	n/a
49	chr10:5042313-5042363	Hepatocyte	liver:	n/a
50	chr10:5246625-5246675	GM12878	blood:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:4867516..4869900-chr10:5135201..5137283,2	K562	blood:
2	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
3	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
4	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
5	chr10:5225688..5227346-chr10:5233053..5235554,2	MCF-7	breast:
6	chr10:5110976..5115702-chr10:5115793..5122715,9	K562	blood:
7	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
8	chr10:5247043..5249924-chr10:5250707..5254146,4	K562	blood:
9	chr10:4891883..4892464-chr10:5057320..5057832,2	MCF-7	breast:
10	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
11	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
12	chr10:5086402..5088845-chr10:5091899..5093648,2	K562	blood:
13	chr10:5136517..5137515-chr10:5241491..5242054,2	MCF-7	breast:
14	chr10:5198281..5200177-chr10:5228677..5230787,2	K562	blood:
15	chr10:5112364..5115030-chr10:5137295..5139055,2	K562	blood:
16	chr10:5248069..5249924-chr10:5250712..5252871,2	K562	blood:
17	chr10:4997960..5000911-chr10:5049814..5051321,2	MCF-7	breast:
18	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
19	chr10:5078550..5080875-chr10:5082513..5084099,2	K562	blood:
20	chr10:5073664..5075237-chr10:5075576..5077420,2	MCF-7	breast:
21	chr10:5227828..5229662-chr10:5232988..5235057,2	K562	blood:
22	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
23	chr10:5040612..5043134-chr10:5043757..5046328,2	K562	blood:
24	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
25	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
26	chr10:5112556..5115410-chr10:5118342..5122673,4	K562	blood:
27	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
28	chr10:5012978..5016166-chr10:5111425..5114136,3	K562	blood:
29	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
30	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
31	chr10:5158412..5160412-chr20:46095387..46097285,2	MCF-7	breast:
32	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
33	chr10:5086986..5088845-chr10:5092148..5094003,2	K562	blood:
34	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
35	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
36	chr10:5074304..5076231-chr10:5473842..5475799,2	K562	blood:
37	chr10:5049047..5051331-chr10:5062456..5064553,2	MCF-7	breast:
38	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
39	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
40	chr10:5118918..5120947-chr10:5130785..5133580,2	MCF-7	breast:
41	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
42	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
43	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
44	chr10:5118736..5120512-chr10:5120642..5122422,2	MCF-7	breast:
45	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
46	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
47	chr10:5048912..5051298-chr10:5054151..5056215,2	MCF-7	breast:
48	chr10:5039943..5042485-chr10:5047433..5049901,2	MCF-7	breast:
49	chr10:5052203..5054008-chr10:5065761..5068228,2	MCF-7	breast:
50	chr10:5227828..5229662-chr10:5232988..5235057,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C2-6	chr10:5057095-5057426	NONHSAT011131
2	lnc-AKR1CL1-2	chr10:5192082-5192149	ucscGeneNc_uc009xhz_1
3	lnc-AKR1C1-2	chr10:5039432-5039572	ENSG00000224251.1
4	lnc-AKR1C2-6	chr10:5049599-5049698	NONHSAT011130
5	lnc-AKR1C2-6	chr10:5052536-5052845	NONHSAT011130
6	lnc-AKR1C2-6	chr10:5052536-5052845	NONHSAT011129
7	lnc-AKR1C3-5	chr10:5249132-5249705	NONHSAT011142
8	lnc-AKR1C1-2	chr10:5039432-5039569	ENSG00000224251.1
9	lnc-AKR1C2-6	chr10:5048187-5048244	NONHSAT011129
10	lnc-AKR1C2-6	chr10:5060092-5060126	NONHSAT011130
11	lnc-AKR1C1-2	chr10:5038045-5038338	ENSG00000224251.1
12	lnc-AKR1C2-6	chr10:5052655-5052845	NONHSAT011131
13	lnc-AKR1C4-2	chr10:5237425-5237538	NONHSAT011140
14	lnc-AKR1C2-6	chr10:5048654-5048784	NONHSAT011130
15	lnc-AKR1C4-2	chr10:5238192-5238885	NONHSAT011140
16	lnc-AKR1C2-6	chr10:5060092-5060223	NONHSAT011129
17	lnc-AKR1C1-2	chr10:5038229-5038338	ENSG00000224251.2
18	lnc-AKR1C1-2	chr10:5038229-5038338	ENSG00000224251.1
19	lnc-AKR1CL1-2	chr10:5186655-5187952	ucscGeneNc_uc009xhz_1
20	lnc-AKR1C1-2	chr10:5039432-5039566	ENSG00000224251.2
21	lnc-AKR1CL1-2	chr10:5189836-5190001	ucscGeneNc_uc009xhz_1
22	lnc-AKR1C1-2	chr10:5038074-5038124	ENSG00000224251.1
23	lnc-AKR1C2-6	chr10:5049599-5049698	NONHSAT011129
24	lnc-AKR1C2-6	chr10:5058029-5058084	NONHSAT011131

No data

Variant related genes	Relation type
AKR1C3	TF binding region
ENSG00000251909	TF binding region
AKR1C2	TF binding region
AKR1C4	TF binding region
ENSG00000239148	TF binding region
ENSG00000251740	TF binding region
AKR1C5P	TF binding region
AKR1CL1	TF binding region
ENSG00000237831	TF binding region
ENSG00000224251	TF binding region
ENSG00000239142	TF binding region
ENSG00000228291	TF binding region
AKR1C3	CpG island
ENSG00000251909	CpG island
AKR1C2	CpG island
AKR1C4	CpG island
ENSG00000239148	CpG island
ENSG00000251740	CpG island
AKR1C5P	CpG island
AKR1CL1	CpG island
ENSG00000237831	CpG island
ENSG00000224251	CpG island
ENSG00000239142	CpG island
ENSG00000228291	CpG island
ENSG00000196326	chromatin interactions
ENSG00000151632	chromatin interactions
ENSG00000228291	chromatin interactions
ENSG00000239142	chromatin interactions
ENSG00000165568	chromatin interactions
ENSG00000196139	chromatin interactions
ENSG00000225418	chromatin interactions

Extended variants
information (count: 11235 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:11235 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550209837	chr10:5037936-5037937	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs374253499	chr10:5037962-5037963	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200650974	chr10:5037977-5037978	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571588082	chr10:5037980-5037981	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs138437499	chr10:5038000-5038001	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs149560142	chr10:5038011-5038012	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566167986	chr10:5038019-5038020	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111932774	chr10:5038022-5038023	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536442138	chr10:5038032-5038033	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555081842	chr10:5038100-5038101	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs111999542	chr10:5038105-5038106	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs573408906	chr10:5038111-5038112	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs543860135	chr10:5038116-5038117	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs2518034	chr10:5038149-5038150	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs577535131	chr10:5038158-5038159	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs548057107	chr10:5038179-5038180	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs560375110	chr10:5038186-5038187	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs572316911	chr10:5038261-5038262	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs189362843	chr10:5038295-5038296	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs180751645	chr10:5038296-5038297	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs531863949	chr10:5038300-5038301	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs369014332	chr10:5038307-5038308	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs201933166	chr10:5038309-5038310	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs565169026	chr10:5038314-5038315	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs532515117	chr10:5038370-5038371	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116519120	chr10:5038420-5038421	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566020813	chr10:5038432-5038433	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536506322	chr10:5038449-5038450	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs117952235	chr10:5038464-5038465	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569889481	chr10:5038473-5038474	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs78379963	chr10:5038481-5038482	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs200462318	chr10:5038492-5038493	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs145300678	chr10:5038515-5038516	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577597857	chr10:5038533-5038534	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184937102	chr10:5038540-5038541	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs538625349	chr10:5038551-5038552	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575018401	chr10:5038670-5038671	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189419944	chr10:5038673-5038674	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs553822241	chr10:5038693-5038694	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs181616930	chr10:5038737-5038738	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371538926	chr10:5038739-5038740	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377061764	chr10:5038740-5038741	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200451297	chr10:5038753-5038754	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs373454885	chr10:5038754-5038755	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557578968	chr10:5038767-5038768	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs61856064	chr10:5038829-5038830	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs76906176	chr10:5038831-5038832	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576288342	chr10:5038838-5038839	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543496759	chr10:5038880-5038881	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs186090261	chr10:5038900-5038901	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	21781307	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:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5005800-5045800	Weak transcription	HSMMtube	muscle
2	chr10:5008200-5044000	Weak transcription	Fetal Brain Male	brain
3	chr10:5011600-5044200	Weak transcription	Fetal Brain Female	brain
4	chr10:5011800-5043800	Weak transcription	Psoas Muscle	Psoas
5	chr10:5019400-5044600	Weak transcription	Brain Germinal Matrix	brain
6	chr10:5021800-5044400	Weak transcription	NHDF-Ad	bronchial
7	chr10:5024400-5039400	Weak transcription	Ovary	ovary
8	chr10:5024400-5040400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr10:5024400-5040600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:5024400-5056800	Weak transcription	Esophagus	oesophagus
11	chr10:5024800-5044400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:5024800-5051400	Weak transcription	Fetal Intestine Small	intestine
13	chr10:5025000-5045800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr10:5025200-5044200	Weak transcription	K562	blood
15	chr10:5027400-5042400	Weak transcription	Gastric	stomach
16	chr10:5027600-5045000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr10:5027800-5038600	Weak transcription	Left Ventricle	heart
18	chr10:5027800-5043200	Weak transcription	HepG2	liver
19	chr10:5027800-5045800	Weak transcription	Fetal Stomach	stomach
20	chr10:5027800-5045800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr10:5027800-5050600	Weak transcription	Pancreas	Pancrea
22	chr10:5028000-5045800	Weak transcription	Fetal Muscle Leg	muscle
23	chr10:5030200-5042200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:5030400-5039200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:5033800-5039800	Weak transcription	Liver	Liver
26	chr10:5033800-5040000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:5033800-5040000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr10:5033800-5040200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr10:5033800-5044600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr10:5034000-5040000	Weak transcription	Adipose Nuclei	Adipose
31	chr10:5034800-5042800	Weak transcription	Fetal Intestine Large	intestine
32	chr10:5036800-5043200	Weak transcription	Right Atrium	heart
33	chr10:5037800-5040000	Active TSS	A549	lung
34	chr10:5039200-5041200	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr10:5039800-5041800	Strong transcription	Liver	Liver
36	chr10:5040000-5041200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:5040000-5041200	Genic enhancers	Adipose Nuclei	Adipose
38	chr10:5040000-5041600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr10:5040000-5045200	Transcr. at gene 5' and 3'	A549	lung
40	chr10:5040000-5045600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr10:5040200-5041200	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr10:5040400-5041200	Strong transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:5040600-5041000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:5041000-5044600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:5041200-5042200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:5041200-5042200	Strong transcription	Adipose Nuclei	Adipose
47	chr10:5041200-5043800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr10:5041200-5044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:5041200-5044200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr10:5041600-5045800	Weak transcription	HMEC	breast

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