Variant report

Variant	nsv540463
Chromosome Location	chr10:5090313-5196900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1620)
CpG islands
(count:245)
Chromatin interactive
region (count:58)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5110678-5110878	K562	blood:	n/a	n/a
2	ARID3A	chr10:5089966-5091092	HepG2	liver:	n/a	chr10:5090324-5090340
3	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5113567-5114862	K562	blood:	n/a	n/a
5	ARID3A	chr10:5120586-5121209	K562	blood:	n/a	n/a
6	ARID3A	chr10:5136259-5137212	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5123254-5123638	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:5136891-5137133	K562	blood:	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	ATF1	chr10:5113912-5114323	K562	blood:	n/a	n/a
14	ATF3	chr10:5113430-5114380	A549	lung:	n/a	n/a
15	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
16	ATF3	chr10:5113911-5114354	K562	blood:	n/a	n/a
17	ATF3	chr10:5112971-5114564	A549	lung:	n/a	n/a
18	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
19	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
20	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
21	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
22	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
23	BACH1	chr10:5113506-5114634	K562	blood:	n/a	n/a
24	BACH1	chr10:5113866-5114859	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
27	BCL3	chr10:5112642-5114508	A549	lung:	n/a	n/a
28	BCL3	chr10:5190290-5191005	A549	lung:	n/a	n/a
29	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
30	BCL3	chr10:5121775-5122553	A549	lung:	n/a	n/a
31	BCL3	chr10:5121933-5122486	A549	lung:	n/a	n/a
32	BCL3	chr10:5189224-5190092	A549	lung:	n/a	n/a
33	BCL3	chr10:5189111-5191215	A549	lung:	n/a	n/a
34	BCL3	chr10:5112966-5115139	A549	lung:	n/a	n/a
35	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
36	BCL3	chr10:5141308-5142213	A549	lung:	n/a	n/a
37	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
38	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
39	BHLHE40	chr10:5113561-5114284	K562	blood:	n/a	n/a
40	BHLHE40	chr10:5185410-5185563	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:5190346-5190928	HepG2	liver:	n/a	n/a
42	BHLHE40	chr10:5120759-5121300	K562	blood:	n/a	n/a
43	BHLHE40	chr10:5113493-5114242	HepG2	liver:	n/a	n/a
44	BRCA1	chr10:5136812-5137013	HepG2	liver:	n/a	n/a
45	BRCA1	chr10:5113573-5114550	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr10:5136453-5137624	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr10:5111352-5111692	K562	blood:	n/a	n/a
48	CBX3	chr10:5136690-5137127	K562	blood:	n/a	n/a
49	CBX3	chr10:5178706-5179040	HCT-116	colon:	n/a	n/a
50	CBX3	chr10:5178725-5179069	K562	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5136782-5136832	PFSK-1	brain:	n/a
2	chr10:5136782-5136832	PFSK-1	brain:	n/a
3	chr10:5113871-5113921	ECC-1	luminal epithelium:	n/a
4	chr10:5113871-5113921	NHBE	bronchial:	n/a
5	chr10:5149799-5149849	AG10803	skin:	n/a
6	chr10:5113871-5113921	CMK	blood:	n/a
7	chr10:5113871-5113921	HepG2	liver:	n/a
8	chr10:5149799-5149849	NH-A	brain:	n/a
9	chr10:5113871-5113921	RPTEC	kidney:	n/a
10	chr10:5113871-5113921	PFSK-1	brain:	n/a
11	chr10:5136782-5136832	SK-N-SH_RA	brain:	n/a
12	chr10:5149799-5149849	Jurkat	blood:	n/a
13	chr10:5149799-5149849	HRE	kidney:	n/a
14	chr10:5113871-5113921	NT2-D1	testis:	n/a
15	chr10:5136782-5136832	AoSMC	blood vessel:	n/a
16	chr10:5135453-5135503	HRCEpiC	kidney:	n/a
17	chr10:5136782-5136832	ovcar-3	ovarian:	n/a
18	chr10:5149799-5149849	U87	brain:	n/a
19	chr10:5149799-5149849	GM06990	blood:	n/a
20	chr10:5113871-5113921	NB4	blood:	n/a
21	chr10:5135453-5135503	ProgFib	skin:	n/a
22	chr10:5136782-5136832	HCPEpiC	choroid plexus:	n/a
23	chr10:5113871-5113921	MCF-7	breast:	n/a
24	chr10:5136782-5136832	HIPEpiC	eye:	n/a
25	chr10:5136782-5136832	AG09309	skin:	n/a
26	chr10:5113871-5113921	SAEC	small airway:	n/a
27	chr10:5135453-5135503	HL-60	blood:	n/a
28	chr10:5136782-5136832	ECC-1	luminal epithelium:	n/a
29	chr10:5136782-5136832	GM12878	blood:	n/a
30	chr10:5113871-5113921	Jurkat	blood:	n/a
31	chr10:5149799-5149849	Hela-S3	cervix:	n/a
32	chr10:5113871-5113921	AG09319	gingival:	n/a
33	chr10:5135453-5135503	HCT-116	colon:	n/a
34	chr10:5135453-5135503	HCM	heart:	n/a
35	chr10:5136782-5136832	BE2_C	brain:	n/a
36	chr10:5135453-5135503	PrEC	prostate:	n/a
37	chr10:5149799-5149849	HCF	heart:	n/a
38	chr10:5135453-5135503	HMEC	breast:	n/a
39	chr10:5113871-5113921	BJ	skin:	n/a
40	chr10:5149799-5149849	IMR90	lung:	fetal
41	chr10:5136782-5136832	RPTEC	kidney:	n/a
42	chr10:5113871-5113921	IMR90	lung:	fetal
43	chr10:5149799-5149849	PrEC	prostate:	n/a
44	chr10:5135453-5135503	SK-N-SH	brain:	n/a
45	chr10:5113871-5113921	SK-N-MC	brain:	n/a
46	chr10:5136782-5136832	SK-N-SH	brain:	n/a
47	chr10:5136782-5136832	HCM	heart:	n/a
48	chr10:5136782-5136832	A549	lung:	n/a
49	chr10:5136782-5136832	NHBE	bronchial:	n/a
50	chr10:5113871-5113921	HIPEpiC	eye:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5136589..5138613-chr10:5158907..5161668,2	MCF-7	breast:
2	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
3	chr10:4891149..4892494-chr10:5136639..5137645,6	MCF-7	breast:
4	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
5	chr10:5118736..5120512-chr10:5120642..5122422,2	MCF-7	breast:
6	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
7	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
8	chr10:4973639..4975791-chr10:5115008..5116577,2	K562	blood:
9	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
10	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
11	chr10:5132364..5134075-chr10:5134147..5137113,2	MCF-7	breast:
12	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
13	chr10:5112364..5115030-chr10:5137295..5139055,2	K562	blood:
14	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
15	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
16	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
17	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
18	chr10:5114807..5118123-chr10:5118660..5122292,3	MCF-7	breast:
19	chr10:4867516..4869900-chr10:5135201..5137283,2	K562	blood:
20	chr10:5135730..5138479-chr10:5140412..5142462,2	K562	blood:
21	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
22	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
23	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
24	chr10:5110976..5115702-chr10:5115793..5122715,9	K562	blood:
25	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
26	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
27	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
28	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
29	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
30	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
31	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
32	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
33	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
34	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
35	chr10:5012978..5016166-chr10:5111425..5114136,3	K562	blood:
36	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
37	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
38	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
39	chr10:5086402..5088845-chr10:5091899..5093648,2	K562	blood:
40	chr10:5118918..5120947-chr10:5130785..5133580,2	MCF-7	breast:
41	chr10:5113654..5115809-chr10:5119275..5121684,2	MCF-7	breast:
42	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
43	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
44	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
45	chr10:5023921..5025963-chr10:5094008..5095926,2	MCF-7	breast:
46	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
47	chr10:5158412..5160412-chr20:46095387..46097285,2	MCF-7	breast:
48	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
49	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
50	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1CL1-2	chr10:5189836-5190001	ucscGeneNc_uc009xhz_1
2	lnc-AKR1CL1-2	chr10:5186655-5187952	ucscGeneNc_uc009xhz_1
3	lnc-AKR1CL1-2	chr10:5192082-5192149	ucscGeneNc_uc009xhz_1

No data

Variant related genes	Relation type
AKR1C3	TF binding region
ENSG00000251740	TF binding region
AKR1C5P	TF binding region
ENSG00000237831	TF binding region
ENSG00000239142	TF binding region
AKR1C3	CpG island
ENSG00000251740	CpG island
AKR1C5P	CpG island
ENSG00000237831	CpG island
ENSG00000239142	CpG island
ENSG00000225418	chromatin interactions
ENSG00000196139	chromatin interactions
ENSG00000239142	chromatin interactions
ENSG00000165568	chromatin interactions

Extended variants
information (count: 5373 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5373 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557825573	chr10:5090313-5090314	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs77223032	chr10:5090328-5090329	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs71859378	chr10:5090329-5090330	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs72507158	chr10:5090331-5090332	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs10644075	chr10:5090332-5090333	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs530482028	chr10:5090393-5090394	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs112271064	chr10:5090401-5090402	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
8	rs570085789	chr10:5090404-5090405	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs77956500	chr10:5090409-5090410	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs546608338	chr10:5090427-5090428	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs151174077	chr10:5090434-5090435	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs76842064	chr10:5090445-5090446	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs185477226	chr10:5090473-5090474	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
14	rs78816991	chr10:5090482-5090483	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
15	rs568253019	chr10:5090486-5090487	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
16	rs190096915	chr10:5090550-5090551	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
17	rs183029847	chr10:5090566-5090567	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs59826042	chr10:5090567-5090568	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs369276335	chr10:5090594-5090595	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
20	rs59966207	chr10:5090602-5090603	Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369054018	chr10:5090611-5090612	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
22	rs568273730	chr10:5090639-5090640	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
23	rs535703535	chr10:5090646-5090647	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
24	rs7913122	chr10:5090667-5090668	Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs569216459	chr10:5090687-5090688	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
26	rs575301834	chr10:5090747-5090748	Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
27	rs10904402	chr10:5090790-5090791	Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs75712855	chr10:5090805-5090806	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
29	rs11815509	chr10:5090890-5090891	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11816834	chr10:5090915-5090916	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs111834570	chr10:5090933-5090934	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
32	rs573411363	chr10:5090977-5090978	Enhancers Flanking Active TSS	TF binding region	3 gene(s)	Overlapped CNVs	n/a
33	rs540259585	chr10:5091004-5091005	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs555779924	chr10:5091025-5091026	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185807038	chr10:5091047-5091048	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs140062662	chr10:5091076-5091077	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs578210910	chr10:5091090-5091091	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs545361304	chr10:5091091-5091092	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs60296137	chr10:5091120-5091121	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527746153	chr10:5091157-5091158	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs150297572	chr10:5091174-5091175	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs58845800	chr10:5091178-5091179	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs529091442	chr10:5091185-5091186	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs10736995	chr10:5091201-5091202	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs569111629	chr10:5091222-5091223	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs539374167	chr10:5091228-5091229	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs79629670	chr10:5091256-5091257	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs10736996	chr10:5091259-5091260	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs138085727	chr10:5091273-5091274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555040023	chr10:5091300-5091301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5088800-5091400	Enhancers	Duodenum Mucosa	Duodenum
2	chr10:5089000-5091000	Enhancers	Stomach Mucosa	stomach
3	chr10:5089200-5091600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:5089400-5091600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:5089800-5090800	Enhancers	NHDF-Ad	bronchial
6	chr10:5089800-5091200	Enhancers	Liver	Liver
7	chr10:5089800-5091800	Enhancers	HepG2	liver
8	chr10:5090000-5091000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:5090000-5091200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr10:5090000-5091200	Enhancers	NHEK	skin
11	chr10:5090000-5091200	Enhancers	Osteobl	bone
12	chr10:5090200-5090400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:5090200-5090400	Enhancers	NHLF	lung
14	chr10:5090200-5090600	Flanking Active TSS	A549	lung
15	chr10:5090200-5091200	Enhancers	HMEC	breast
16	chr10:5090200-5091200	Enhancers	HSMM	muscle
17	chr10:5090600-5092600	Enhancers	A549	lung
18	chr10:5090800-5091200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:5090800-5091200	Flanking Active TSS	NHDF-Ad	bronchial
20	chr10:5091000-5091200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:5091000-5091200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr10:5091000-5091200	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr10:5091000-5091200	Enhancers	NHLF	lung
24	chr10:5091000-5091400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr10:5091000-5097000	Weak transcription	Stomach Mucosa	stomach
26	chr10:5091200-5092200	Enhancers	NHDF-Ad	bronchial
27	chr10:5091200-5095400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr10:5091400-5092200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:5091800-5092400	Weak transcription	HepG2	liver
30	chr10:5092200-5092400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr10:5092400-5092600	Enhancers	HepG2	liver
32	chr10:5092400-5098600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr10:5093800-5094200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr10:5095200-5096000	Enhancers	Esophagus	oesophagus
35	chr10:5095400-5095800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:5095400-5095800	Enhancers	Gastric	stomach
37	chr10:5095400-5096000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr10:5095400-5096000	Enhancers	Lung	lung
39	chr10:5095400-5120800	Weak transcription	Right Atrium	heart
40	chr10:5095600-5095800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr10:5095600-5096000	Enhancers	Colonic Mucosa	Colon
42	chr10:5095800-5096200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr10:5096200-5096400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr10:5097000-5097600	Enhancers	Stomach Mucosa	stomach
45	chr10:5103000-5103400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:5103600-5104200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:5104600-5104800	Enhancers	Adipose Nuclei	Adipose
48	chr10:5104800-5105600	Weak transcription	Adipose Nuclei	Adipose
49	chr10:5105400-5105800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr10:5105600-5105800	Enhancers	Adipose Nuclei	Adipose

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