Variant report

Variant	nsv1047484
Chromosome Location	chr10:5076258-5261482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2225)
CpG islands
(count:916)
Chromatin interactive
region (count:91)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2225 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

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	chr10:5236523-5236713	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5136891-5137133	K562	blood:	n/a	n/a
4	ARID3A	chr10:5081022-5081232	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5136259-5137212	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5113567-5114862	K562	blood:	n/a	n/a
8	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5089966-5091092	HepG2	liver:	n/a	chr10:5090324-5090340
10	ARID3A	chr10:5237741-5238762	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:5112815-5114610	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:5147856-5147891	HepG2	liver:	n/a	n/a
13	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
14	ARID3A	chr10:5083803-5084201	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:5123254-5123638	HepG2	liver:	n/a	n/a
16	ARID3A	chr10:5077017-5077109	K562	blood:	n/a	n/a
17	ARID3A	chr10:5261272-5261624	HepG2	liver:	n/a	n/a
18	ARID3A	chr10:5239083-5239264	HepG2	liver:	n/a	n/a
19	ARID3A	chr10:5110678-5110878	K562	blood:	n/a	n/a
20	ATF1	chr10:5113912-5114323	K562	blood:	n/a	n/a
21	ATF3	chr10:5207727-5207953	K562	blood:	n/a	n/a
22	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
23	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
24	ATF3	chr10:5113430-5114380	A549	lung:	n/a	n/a
25	ATF3	chr10:5112971-5114564	A549	lung:	n/a	n/a
26	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
27	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
28	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
29	ATF3	chr10:5113911-5114354	K562	blood:	n/a	n/a
30	BACH1	chr10:5113506-5114634	K562	blood:	n/a	n/a
31	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
32	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
33	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr10:5113866-5114859	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL3	chr10:5121933-5122486	A549	lung:	n/a	n/a
36	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
37	BCL3	chr10:5189224-5190092	A549	lung:	n/a	n/a
38	BCL3	chr10:5141308-5142213	A549	lung:	n/a	n/a
39	BCL3	chr10:5189111-5191215	A549	lung:	n/a	n/a
40	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
41	BCL3	chr10:5237721-5238466	A549	lung:	n/a	n/a
42	BCL3	chr10:5121775-5122553	A549	lung:	n/a	n/a
43	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
44	BCL3	chr10:5112642-5114508	A549	lung:	n/a	n/a
45	BCL3	chr10:5190290-5191005	A549	lung:	n/a	n/a
46	BCL3	chr10:5112966-5115139	A549	lung:	n/a	n/a
47	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
48	BHLHE40	chr10:5120759-5121300	K562	blood:	n/a	n/a
49	BHLHE40	chr10:5113561-5114284	K562	blood:	n/a	n/a
50	BHLHE40	chr10:5207857-5208008	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5227162-5227212	MCF-7	breast:	n/a
2	chr10:5227162-5227212	MCF-7	breast:	n/a
3	chr10:5113871-5113921	IMR90	lung:	fetal
4	chr10:5237881-5237931	GM12878	blood:	n/a
5	chr10:5135453-5135503	HCT-116	colon:	n/a
6	chr10:5227312-5227362	IMR90	lung:	fetal
7	chr10:5246625-5246675	NB4	blood:	n/a
8	chr10:5237869-5237919	T-47D	breast:	n/a
9	chr10:5149799-5149849	PrEC	prostate:	n/a
10	chr10:5149799-5149849	HEK293	kidney:	embryo
11	chr10:5237853-5237903	NHBE	bronchial:	n/a
12	chr10:5227312-5227362	Caco-2	colon:	n/a
13	chr10:5113871-5113921	NB4	blood:	n/a
14	chr10:5260740-5260790	AG04450	lung:	fetal
15	chr10:5149799-5149849	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:5113871-5113921	H1-hESC	embryonic stem cell:	embryo
17	chr10:5237881-5237931	AG09309	skin:	n/a
18	chr10:5237881-5237931	GM12891	blood:	n/a
19	chr10:5237869-5237919	BE2_C	brain:	n/a
20	chr10:5149799-5149849	MCF10A-Er-Src	breast:	n/a
21	chr10:5227162-5227212	ECC-1	luminal epithelium:	n/a
22	chr10:5260740-5260790	AoSMC	blood vessel:	n/a
23	chr10:5149799-5149849	U87	brain:	n/a
24	chr10:5228106-5228156	NT2-D1	testis:	n/a
25	chr10:5136782-5136832	HepG2	liver:	n/a
26	chr10:5237869-5237919	HMEC	breast:	n/a
27	chr10:5237869-5237919	HRE	kidney:	n/a
28	chr10:5113871-5113921	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:5135453-5135503	GM06990	blood:	n/a
30	chr10:5227312-5227362	GM12892	blood:	n/a
31	chr10:5260740-5260790	GM12892	blood:	n/a
32	chr10:5227162-5227212	K562	blood:	n/a
33	chr10:5113871-5113921	HMEC	breast:	n/a
34	chr10:5237869-5237919	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:5113871-5113921	GM12891	blood:	n/a
36	chr10:5136782-5136832	ECC-1	luminal epithelium:	n/a
37	chr10:5260740-5260790	RPTEC	kidney:	n/a
38	chr10:5246625-5246675	MCF-7	breast:	n/a
39	chr10:5113871-5113921	NT2-D1	testis:	n/a
40	chr10:5237853-5237903	HEK293	kidney:	embryo
41	chr10:5227162-5227212	GM12878	blood:	n/a
42	chr10:5237881-5237931	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:5227162-5227212	LNCaP	prostate:	n/a
44	chr10:5260740-5260790	MCF10A-Er-Src	breast:	n/a
45	chr10:5136782-5136832	NB4	blood:	n/a
46	chr10:5237853-5237903	GM12892	blood:	n/a
47	chr10:5237869-5237919	PFSK-1	brain:	n/a
48	chr10:5228106-5228156	SKMC	muscle:	n/a
49	chr10:5149799-5149849	BJ	skin:	n/a
50	chr10:5227162-5227212	HepG2	liver:	n/a

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
2	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
3	chr10:5078550..5080875-chr10:5082513..5084099,2	K562	blood:
4	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
5	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
6	chr10:5023921..5025963-chr10:5094008..5095926,2	MCF-7	breast:
7	chr10:5112556..5115410-chr10:5118342..5122673,4	K562	blood:
8	chr10:5073664..5075237-chr10:5075576..5077420,2	MCF-7	breast:
9	chr10:5227828..5229662-chr10:5232988..5235057,2	K562	blood:
10	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
11	chr10:4973639..4975791-chr10:5115008..5116577,2	K562	blood:
12	chr10:5118736..5120512-chr10:5120642..5122422,2	MCF-7	breast:
13	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
14	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
15	chr10:5082340..5083456-chr10:5325202..5326034,4	MCF-7	breast:
16	chr10:5248069..5249924-chr10:5250712..5252871,2	K562	blood:
17	chr10:5250240..5252491-chr10:5252736..5256514,3	K562	blood:
18	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
19	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
20	chr10:5112364..5115030-chr10:5137295..5139055,2	K562	blood:
21	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
22	chr10:5078550..5080875-chr10:5082513..5084099,2	K562	blood:
23	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
24	chr10:4891149..4892494-chr10:5136639..5137645,6	MCF-7	breast:
25	chr10:5135013..5137947-chr10:5149855..5151840,2	MCF-7	breast:
26	chr10:5067000..5068647-chr10:5074072..5076812,2	MCF-7	breast:
27	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
28	chr10:5247043..5249924-chr10:5250707..5254146,4	K562	blood:
29	chr10:5250240..5252491-chr10:5252736..5256514,3	K562	blood:
30	chr10:5060824..5061816-chr10:5136872..5137424,2	MCF-7	breast:
31	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
32	chr10:5113654..5115809-chr10:5119275..5121684,2	MCF-7	breast:
33	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
34	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
35	chr10:5077326..5079910-chr10:5080689..5083376,2	K562	blood:
36	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
37	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
38	chr10:5118918..5120947-chr10:5130785..5133580,2	MCF-7	breast:
39	chr10:5136589..5138613-chr10:5158907..5161668,2	MCF-7	breast:
40	chr10:5086986..5088845-chr10:5092148..5094003,2	K562	blood:
41	chr10:5086402..5088845-chr10:5091899..5093648,2	K562	blood:
42	chr10:5110976..5115702-chr10:5115793..5122715,9	K562	blood:
43	chr10:5228162..5230153-chr10:5232988..5235199,2	K562	blood:
44	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
45	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
46	chr10:4867516..4869900-chr10:5135201..5137283,2	K562	blood:
47	chr10:5135730..5138479-chr10:5140412..5142462,2	K562	blood:
48	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
49	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
50	chr10:5225688..5227346-chr10:5233053..5235554,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 9179 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:9179 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543900890	chr10:5076280-5076281	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs558741836	chr10:5076313-5076314	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs371153189	chr10:5076354-5076355	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs12416161	chr10:5076367-5076368	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs544258876	chr10:5076368-5076369	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs59774735	chr10:5076400-5076401	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs578181680	chr10:5076443-5076444	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs75785373	chr10:5076445-5076446	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs72772114	chr10:5076450-5076451	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs527904702	chr10:5076454-5076455	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs145881523	chr10:5076496-5076497	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs371288133	chr10:5076511-5076512	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs61301840	chr10:5076533-5076534	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs72772115	chr10:5076585-5076586	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs186734769	chr10:5076629-5076630	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs532005368	chr10:5076654-5076655	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138487032	chr10:5076685-5076686	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529028074	chr10:5076775-5076776	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7081787	chr10:5076866-5076867	Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190359108	chr10:5076878-5076879	Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548141464	chr10:5076915-5076916	Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs68192167	chr10:5076937-5076938	Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs7081949	chr10:5076992-5076993	Enhancers ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs183099884	chr10:5077001-5077002	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs199991051	chr10:5077069-5077070	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201109785	chr10:5077070-5077071	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200777914	chr10:5077071-5077072	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs12248104	chr10:5077072-5077073	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs528408074	chr10:5077073-5077074	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs11458751	chr10:5077083-5077084	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs147266422	chr10:5077084-5077085	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs535057865	chr10:5077121-5077122	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551720420	chr10:5077126-5077127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs55933224	chr10:5077188-5077189	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs574838633	chr10:5077196-5077197	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12570555	chr10:5077244-5077245	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs542546165	chr10:5077283-5077284	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs548700630	chr10:5077320-5077321	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs533959996	chr10:5077380-5077381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs373363021	chr10:5077391-5077392	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs575814728	chr10:5077394-5077395	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs188132647	chr10:5077409-5077410	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs565027974	chr10:5077467-5077468	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs532071004	chr10:5077481-5077482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201580533	chr10:5077483-5077484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35198121	chr10:5077493-5077494	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs547040078	chr10:5077518-5077519	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs558930091	chr10:5077524-5077525	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs529603757	chr10:5077530-5077531	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs548481221	chr10:5077540-5077541	Enhancers Weak transcription	TF binding 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:1219 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5068000-5076800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:5074000-5078800	Weak transcription	Stomach Mucosa	stomach
3	chr10:5074800-5076600	Enhancers	Hela-S3	cervix
4	chr10:5075000-5076400	Enhancers	HMEC	breast
5	chr10:5075000-5076800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:5075000-5076800	Enhancers	Muscle Satellite Cultured Cells	--
7	chr10:5075200-5076600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr10:5075200-5076600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:5075200-5076600	Enhancers	NH-A	brain
10	chr10:5075200-5077000	ZNF genes & repeats	Adipose Nuclei	Adipose
11	chr10:5075600-5076800	Enhancers	Osteobl	bone
12	chr10:5076000-5076800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:5076200-5077400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:5076200-5080800	Weak transcription	NHDF-Ad	bronchial
15	chr10:5076400-5076600	ZNF genes & repeats	A549	lung
16	chr10:5076600-5077000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:5076800-5077000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:5077000-5078000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr10:5077400-5077600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr10:5077400-5077800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr10:5077600-5078600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr10:5077600-5078600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr10:5077600-5083000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:5077800-5078200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:5078400-5078600	Enhancers	Rectal Mucosa Donor 29	rectum
26	chr10:5078400-5078800	Enhancers	Fetal Intestine Large	intestine
27	chr10:5078400-5079200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr10:5078600-5079200	Enhancers	Duodenum Mucosa	Duodenum
29	chr10:5078600-5080200	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr10:5078600-5081000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr10:5078800-5081400	Enhancers	Stomach Mucosa	stomach
32	chr10:5079200-5079400	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr10:5079200-5080400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr10:5079400-5084600	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr10:5080000-5080200	Enhancers	Small Intestine	intestine
36	chr10:5080200-5080600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr10:5080200-5083200	Weak transcription	Small Intestine	intestine
38	chr10:5080400-5080800	Enhancers	Duodenum Mucosa	Duodenum
39	chr10:5080600-5083000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr10:5080800-5081400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:5080800-5081600	Enhancers	NHDF-Ad	bronchial
42	chr10:5080800-5083600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr10:5081000-5081600	Enhancers	HepG2	liver
44	chr10:5081000-5083600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr10:5081200-5081400	Enhancers	Adipose Nuclei	Adipose
46	chr10:5081200-5081400	Enhancers	Liver	Liver
47	chr10:5081400-5082600	Weak transcription	Adipose Nuclei	Adipose
48	chr10:5081400-5082800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:5081400-5083400	Weak transcription	Stomach Mucosa	stomach
50	chr10:5081600-5082800	Weak transcription	Liver	Liver

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