Variant report

Variant	nsv540467
Chromosome Location	chr10:5114577-5225365
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1389)
CpG islands
(count:244)
Chromatin interactive
region (count:57)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5113567-5114862	K562	blood:	n/a	n/a
2	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5136891-5137133	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	chr10:5112815-5114610	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5147856-5147891	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:5120586-5121209	K562	blood:	n/a	n/a
11	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
12	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
13	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
14	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
15	ATF3	chr10:5207727-5207953	K562	blood:	n/a	n/a
16	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
17	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
18	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:5113506-5114634	K562	blood:	n/a	n/a
20	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
21	BACH1	chr10:5113866-5114859	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr10:5141308-5142213	A549	lung:	n/a	n/a
23	BCL3	chr10:5121933-5122486	A549	lung:	n/a	n/a
24	BCL3	chr10:5121775-5122553	A549	lung:	n/a	n/a
25	BCL3	chr10:5189224-5190092	A549	lung:	n/a	n/a
26	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
27	BCL3	chr10:5189111-5191215	A549	lung:	n/a	n/a
28	BCL3	chr10:5190290-5191005	A549	lung:	n/a	n/a
29	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
30	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
31	BCL3	chr10:5112966-5115139	A549	lung:	n/a	n/a
32	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
33	BHLHE40	chr10:5185410-5185563	HepG2	liver:	n/a	n/a
34	BHLHE40	chr10:5190346-5190928	HepG2	liver:	n/a	n/a
35	BHLHE40	chr10:5207857-5208008	K562	blood:	n/a	n/a
36	BHLHE40	chr10:5120759-5121300	K562	blood:	n/a	n/a
37	BRCA1	chr10:5136453-5137624	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr10:5136812-5137013	HepG2	liver:	n/a	n/a
39	CBX3	chr10:5136690-5137127	K562	blood:	n/a	n/a
40	CBX3	chr10:5136765-5137213	HCT-116	colon:	n/a	n/a
41	CBX3	chr10:5207656-5208172	HCT-116	colon:	n/a	n/a
42	CBX3	chr10:5178706-5179040	HCT-116	colon:	n/a	n/a
43	CBX3	chr10:5207666-5208060	K562	blood:	n/a	n/a
44	CBX3	chr10:5207589-5208043	HCT-116	colon:	n/a	n/a
45	CBX3	chr10:5207663-5208074	K562	blood:	n/a	n/a
46	CBX3	chr10:5136392-5137166	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	chr10:5178725-5179069	K562	blood:	n/a	n/a
50	CEBPB	chr10:5189144-5189943	A549	lung:	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	chr10:5149799-5149849	ECC-1	luminal epithelium:	n/a
2	chr10:5203419-5203469	HL-60	blood:	n/a
3	chr10:5136782-5136832	ProgFib	skin:	n/a
4	chr10:5203419-5203469	HPAEpiC	pulmonary alveolar:	n/a
5	chr10:5149799-5149849	HUVEC	blood vessel:	n/a
6	chr10:5136782-5136832	Hepatocyte	liver:	n/a
7	chr10:5149799-5149849	HL-60	blood:	n/a
8	chr10:5136782-5136832	SK-N-SH	brain:	n/a
9	chr10:5149799-5149849	SK-N-SH	brain:	n/a
10	chr10:5203419-5203469	AG09309	skin:	n/a
11	chr10:5203419-5203469	A549	lung:	n/a
12	chr10:5203419-5203469	HCF	heart:	n/a
13	chr10:5149799-5149849	HMEC	breast:	n/a
14	chr10:5203419-5203469	SK-N-SH_RA	brain:	n/a
15	chr10:5136782-5136832	MCF-7	breast:	n/a
16	chr10:5203419-5203469	AG10803	skin:	n/a
17	chr10:5149799-5149849	HAEpiC	amniotic membrane:	n/a
18	chr10:5203419-5203469	NHDF-neo	bronchial:	n/a
19	chr10:5149799-5149849	HIPEpiC	eye:	n/a
20	chr10:5203419-5203469	PANC-1	pancreas:	n/a
21	chr10:5135453-5135503	HAEpiC	amniotic membrane:	n/a
22	chr10:5136782-5136832	CMK	blood:	n/a
23	chr10:5149799-5149849	HRCEpiC	kidney:	n/a
24	chr10:5135453-5135503	HNPCEpiC	eye:	n/a
25	chr10:5149799-5149849	HepG2	liver:	n/a
26	chr10:5135453-5135503	HRE	kidney:	n/a
27	chr10:5136782-5136832	HEK293	kidney:	embryo
28	chr10:5149799-5149849	MCF10A-Er-Src	breast:	n/a
29	chr10:5203419-5203469	NHBE	bronchial:	n/a
30	chr10:5149799-5149849	GM06990	blood:	n/a
31	chr10:5149799-5149849	IMR90	lung:	fetal
32	chr10:5135453-5135503	H1-hESC	embryonic stem cell:	embryo
33	chr10:5135453-5135503	NHDF-neo	bronchial:	n/a
34	chr10:5203419-5203469	HNPCEpiC	eye:	n/a
35	chr10:5149799-5149849	HCF	heart:	n/a
36	chr10:5135453-5135503	HRPEpiC	eye:	n/a
37	chr10:5203419-5203469	AoSMC	blood vessel:	n/a
38	chr10:5203419-5203469	BJ	skin:	n/a
39	chr10:5203419-5203469	CMK	blood:	n/a
40	chr10:5203419-5203469	H1-hESC	embryonic stem cell:	embryo
41	chr10:5203419-5203469	HIPEpiC	eye:	n/a
42	chr10:5135453-5135503	HEEpiC	esophagus:	n/a
43	chr10:5136782-5136832	HNPCEpiC	eye:	n/a
44	chr10:5135453-5135503	Hepatocyte	liver:	n/a
45	chr10:5135453-5135503	Jurkat	blood:	n/a
46	chr10:5203419-5203469	Hela-S3	cervix:	n/a
47	chr10:5149799-5149849	NH-A	brain:	n/a
48	chr10:5136782-5136832	A549	lung:	n/a
49	chr10:5135453-5135503	GM12891	blood:	n/a
50	chr10:5149799-5149849	NHDF-neo	bronchial:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
2	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
3	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
4	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
5	chr10:5118736..5120512-chr10:5120642..5122422,2	MCF-7	breast:
6	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
7	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
8	chr10:5119351..5122041-chr10:5135538..5138283,2	MCF-7	breast:
9	chr10:5198281..5200177-chr10:5228677..5230787,2	K562	blood:
10	chr10:5118918..5120947-chr10:5130785..5133580,2	MCF-7	breast:
11	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
12	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
13	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
14	chr10:4891149..4892494-chr10:5136639..5137645,6	MCF-7	breast:
15	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
16	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
17	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
18	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
19	chr10:5136589..5138613-chr10:5158907..5161668,2	MCF-7	breast:
20	chr10:5114807..5118123-chr10:5118660..5122292,3	MCF-7	breast:
21	chr10:5135730..5138479-chr10:5140412..5142462,2	K562	blood:
22	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
23	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
24	chr10:5112364..5115030-chr10:5137295..5139055,2	K562	blood:
25	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
26	chr10:5135013..5137947-chr10:5149855..5151840,2	MCF-7	breast:
27	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
28	chr10:4973639..4975791-chr10:5115008..5116577,2	K562	blood:
29	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
30	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
31	chr10:5140565..5143325-chr10:5148088..5150883,2	MCF-7	breast:
32	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:
33	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
34	chr10:5210740..5212996-chr10:5319959..5322251,2	MCF-7	breast:
35	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
36	chr10:5110976..5115702-chr10:5115793..5122715,9	K562	blood:
37	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
38	chr10:4867516..4869900-chr10:5135201..5137283,2	K562	blood:
39	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
40	chr10:5158412..5160412-chr20:46095387..46097285,2	MCF-7	breast:
41	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
42	chr10:5113654..5115809-chr10:5119275..5121684,2	MCF-7	breast:
43	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:
44	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
45	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
46	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
47	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
48	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
49	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
50	chr10:5124077..5126424-chr10:5132088..5134931,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 5622 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:5622 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527508979	chr10:5114603-5114604	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548976152	chr10:5114613-5114614	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567569120	chr10:5114652-5114653	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1937908	chr10:5114693-5114694	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs549756525	chr10:5114768-5114769	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571313763	chr10:5114774-5114775	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538727950	chr10:5114791-5114792	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs186743984	chr10:5114808-5114809	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190058662	chr10:5114835-5114836	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181646849	chr10:5114837-5114838	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs553766879	chr10:5114845-5114846	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554922858	chr10:5114890-5114891	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576676596	chr10:5114900-5114901	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs544764209	chr10:5114909-5114910	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543808056	chr10:5114919-5114920	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs368179511	chr10:5114941-5114942	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs185775654	chr10:5114952-5114953	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576857668	chr10:5114975-5114976	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542410155	chr10:5114980-5114981	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs117352425	chr10:5115032-5115033	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559440983	chr10:5115124-5115125	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7078343	chr10:5115159-5115160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549172154	chr10:5115173-5115174	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs79920620	chr10:5115199-5115200	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs148274131	chr10:5115241-5115242	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs190386737	chr10:5115242-5115243	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564264037	chr10:5115272-5115273	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141237173	chr10:5115302-5115303	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547487997	chr10:5115331-5115332	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565789209	chr10:5115345-5115346	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs61856141	chr10:5115357-5115358	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368003332	chr10:5115375-5115376	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576599299	chr10:5115396-5115397	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs537731332	chr10:5115397-5115398	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs61856142	chr10:5115401-5115402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558848037	chr10:5115419-5115420	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34280922	chr10:5115440-5115441	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532388243	chr10:5115452-5115453	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541040672	chr10:5115512-5115513	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559382461	chr10:5115524-5115525	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs56166478	chr10:5115529-5115530	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542007789	chr10:5115537-5115538	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142014886	chr10:5115574-5115575	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs75093619	chr10:5115659-5115660	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530423190	chr10:5115665-5115666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548761926	chr10:5115672-5115673	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565201559	chr10:5115676-5115677	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532112373	chr10:5115701-5115702	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs80261696	chr10:5115735-5115736	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs565726277	chr10:5115764-5115765	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:790 , 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	chr10:5111800-5116200	Enhancers	Fetal Intestine Large	intestine
3	chr10:5112000-5115200	Enhancers	Adipose Nuclei	Adipose
4	chr10:5112800-5114600	Enhancers	HMEC	breast
5	chr10:5112800-5115000	Enhancers	Stomach Mucosa	stomach
6	chr10:5113000-5114600	Enhancers	Fetal Kidney	kidney
7	chr10:5113000-5114600	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr10:5113000-5114600	Enhancers	NHEK	skin
9	chr10:5113000-5114800	Enhancers	Colon Smooth Muscle	Colon
10	chr10:5113000-5114800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr10:5113000-5115000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr10:5113000-5115200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr10:5113200-5114600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr10:5113200-5114600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr10:5113200-5114600	Enhancers	Rectal Smooth Muscle	rectum
16	chr10:5113200-5114800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr10:5113200-5115000	Enhancers	Brain Anterior Caudate	brain
18	chr10:5113200-5121000	Weak transcription	Gastric	stomach
19	chr10:5113400-5114600	Enhancers	Brain Angular Gyrus	brain
20	chr10:5113400-5114600	Enhancers	Brain Substantia Nigra	brain
21	chr10:5113400-5114600	Enhancers	Fetal Lung	lung
22	chr10:5113400-5114800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr10:5113400-5114800	Weak transcription	Small Intestine	intestine
24	chr10:5113400-5115000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr10:5113400-5115000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr10:5113400-5115000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr10:5113600-5114600	Enhancers	Right Ventricle	heart
28	chr10:5113600-5114800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr10:5113600-5115000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr10:5113600-5115000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr10:5113800-5114600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:5113800-5114600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr10:5113800-5114600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr10:5113800-5114600	Flanking Active TSS	K562	blood
35	chr10:5113800-5114600	Enhancers	NH-A	brain
36	chr10:5113800-5115000	Enhancers	HSMMtube	muscle
37	chr10:5113800-5115000	Enhancers	NHLF	lung
38	chr10:5113800-5115200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:5113800-5116000	Enhancers	NHDF-Ad	bronchial
40	chr10:5114000-5114600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr10:5114000-5115000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr10:5114000-5115200	Weak transcription	Ovary	ovary
43	chr10:5114000-5116000	Enhancers	Fetal Intestine Small	intestine
44	chr10:5114000-5116000	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr10:5114200-5114600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:5114200-5114600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr10:5114200-5114600	Enhancers	Stomach Smooth Muscle	stomach
48	chr10:5114200-5115000	Enhancers	Muscle Satellite Cultured Cells	--
49	chr10:5114200-5115000	Flanking Active TSS	A549	lung
50	chr10:5114400-5114600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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