Variant report

Variant	nsv549888
Chromosome Location	chr10:5285597-5348491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1167)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5326370-5326774	K562	blood:	n/a	n/a
2	ARID3A	chr10:5325483-5325825	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5285389-5285941	HepG2	liver:	n/a	n/a
4	ATF1	chr10:5337658-5338224	K562	blood:	n/a	n/a
5	ATF1	chr10:5326291-5326744	K562	blood:	n/a	n/a
6	ATF1	chr10:5339509-5339711	K562	blood:	n/a	n/a
7	ATF1	chr10:5300425-5300441	K562	blood:	n/a	n/a
8	ATF1	chr10:5333613-5334043	K562	blood:	n/a	n/a
9	ATF1	chr10:5325479-5325806	K562	blood:	n/a	n/a
10	ATF3	chr10:5333465-5334182	A549	lung:	n/a	n/a
11	ATF3	chr10:5333695-5334079	K562	blood:	n/a	n/a
12	ATF3	chr10:5333223-5334296	A549	lung:	n/a	n/a
13	ATF3	chr10:5326289-5326817	K562	blood:	n/a	n/a
14	BACH1	chr10:5333705-5333941	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr10:5326454-5327033	K562	blood:	n/a	n/a
16	BACH1	chr10:5336196-5336356	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:5314040-5314410	K562	blood:	n/a	chr10:5314219-5314233
18	BACH1	chr10:5314029-5314452	H1-hESC	embryonic stem cell:	n/a	chr10:5314219-5314233
19	BACH1	chr10:5325193-5325762	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:5326467-5326786	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr10:5333183-5334316	A549	lung:	n/a	n/a
22	BCL3	chr10:5325157-5327103	A549	lung:	n/a	chr10:5326539-5326548
23	BCL3	chr10:5333309-5334562	A549	lung:	n/a	n/a
24	BCL3	chr10:5325009-5326832	A549	lung:	n/a	chr10:5326539-5326548
25	BHLHE40	chr10:5326335-5326780	K562	blood:	n/a	n/a
26	BHLHE40	chr10:5333619-5333920	K562	blood:	n/a	n/a
27	BHLHE40	chr10:5337719-5337915	K562	blood:	n/a	n/a
28	BHLHE40	chr10:5339529-5339545	K562	blood:	n/a	n/a
29	BRCA1	chr10:5336152-5336386	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr10:5333574-5334170	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr10:5333327-5334314	K562	blood:	n/a	n/a
32	CBX3	chr10:5326216-5326887	K562	blood:	n/a	n/a
33	CBX3	chr10:5336091-5336370	K562	blood:	n/a	n/a
34	CBX3	chr10:5336027-5336413	K562	blood:	n/a	n/a
35	CCNT2	chr10:5326424-5326723	K562	blood:	n/a	n/a
36	CEBPB	chr10:5333440-5334203	HCT-116	colon:	n/a	chr10:5333459-5333476
37	CEBPB	chr10:5336136-5336428	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr10:5326281-5326926	A549	lung:	n/a	n/a
39	CEBPB	chr10:5333517-5334091	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:5326351-5326856	A549	lung:	n/a	n/a
41	CEBPB	chr10:5326460-5326723	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:5333174-5334557	A549	lung:	n/a	chr10:5333459-5333476
43	CEBPB	chr10:5285419-5285640	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:5333787-5334021	K562	blood:	n/a	n/a
45	CEBPB	chr10:5325100-5325739	A549	lung:	n/a	chr10:5325630-5325642
46	CEBPB	chr10:5324858-5325886	A549	lung:	n/a	chr10:5325630-5325642
47	CEBPB	chr10:5333418-5334399	Hela-S3	cervix:	n/a	chr10:5333459-5333476
48	CEBPB	chr10:5285358-5285791	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:5333332-5334222	A549	lung:	n/a	chr10:5333459-5333476
50	CEBPB	chr10:5333464-5334124	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5302629-5302679	HRE	kidney:	n/a
2	chr10:5302629-5302679	RPTEC	kidney:	n/a
3	chr10:5302629-5302679	LNCaP	prostate:	n/a
4	chr10:5302629-5302679	Hepatocyte	liver:	n/a
5	chr10:5302629-5302679	BE2_C	brain:	n/a
6	chr10:5333615-5333665	GM12891	blood:	n/a
7	chr10:5333615-5333665	GM12892	blood:	n/a
8	chr10:5302629-5302679	PrEC	prostate:	n/a
9	chr10:5333615-5333665	H1-hESC	embryonic stem cell:	embryo
10	chr10:5333615-5333665	MCF10A-Er-Src	breast:	n/a
11	chr10:5333615-5333665	HEK293	kidney:	embryo
12	chr10:5302629-5302679	HEEpiC	esophagus:	n/a
13	chr10:5333615-5333665	AG10803	skin:	n/a
14	chr10:5333615-5333665	HCF	heart:	n/a
15	chr10:5333615-5333665	HMEC	breast:	n/a
16	chr10:5333615-5333665	ovcar-3	ovarian:	n/a
17	chr10:5333615-5333665	CMK	blood:	n/a
18	chr10:5333615-5333665	HCPEpiC	choroid plexus:	n/a
19	chr10:5333615-5333665	GM19239	blood:	n/a
20	chr10:5333615-5333665	SKMC	muscle:	n/a
21	chr10:5333615-5333665	SK-N-SH	brain:	n/a
22	chr10:5302629-5302679	NHDF-neo	bronchial:	n/a
23	chr10:5333615-5333665	PFSK-1	brain:	n/a
24	chr10:5302629-5302679	GM06990	blood:	n/a
25	chr10:5302629-5302679	AG10803	skin:	n/a
26	chr10:5302629-5302679	HAEpiC	amniotic membrane:	n/a
27	chr10:5333615-5333665	AoSMC	blood vessel:	n/a
28	chr10:5302629-5302679	IMR90	lung:	fetal
29	chr10:5333615-5333665	ProgFib	skin:	n/a
30	chr10:5333615-5333665	Hepatocyte	liver:	n/a
31	chr10:5333615-5333665	AG09319	gingival:	n/a
32	chr10:5333615-5333665	HepG2	liver:	n/a
33	chr10:5302629-5302679	HCF	heart:	n/a
34	chr10:5302629-5302679	HRPEpiC	eye:	n/a
35	chr10:5302629-5302679	NB4	blood:	n/a
36	chr10:5333615-5333665	BE2_C	brain:	n/a
37	chr10:5333615-5333665	PANC-1	pancreas:	n/a
38	chr10:5302629-5302679	BJ	skin:	n/a
39	chr10:5302629-5302679	PFSK-1	brain:	n/a
40	chr10:5302629-5302679	PANC-1	pancreas:	n/a
41	chr10:5302629-5302679	A549	lung:	n/a
42	chr10:5302629-5302679	ovcar-3	ovarian:	n/a
43	chr10:5333615-5333665	LNCaP	prostate:	n/a
44	chr10:5302629-5302679	HCPEpiC	choroid plexus:	n/a
45	chr10:5302629-5302679	SAEC	small airway:	n/a
46	chr10:5333615-5333665	HCT-116	colon:	n/a
47	chr10:5302629-5302679	SK-N-SH	brain:	n/a
48	chr10:5302629-5302679	GM12892	blood:	n/a
49	chr10:5333615-5333665	U87	brain:	n/a
50	chr10:5333615-5333665	HAEpiC	amniotic membrane:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5024232..5024860-chr10:5325292..5325936,2	K562	blood:
2	chr10:5314790..5316685-chr10:5325493..5327295,2	K562	blood:
3	chr10:5325782..5327303-chr10:5331354..5334117,2	K562	blood:
4	chr10:5082340..5083456-chr10:5325202..5326034,4	MCF-7	breast:
5	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
6	chr10:5343873..5346040-chr10:5352452..5353968,2	MCF-7	breast:
7	chr10:5335891..5336750-chr10:5390020..5390722,2	MCF-7	breast:
8	chr10:5056816..5057785-chr10:5335747..5336705,2	MCF-7	breast:
9	chr10:4891547..4892555-chr10:5325301..5326118,4	MCF-7	breast:
10	chr10:5338258..5343485-chr10:5345968..5350797,5	K562	blood:
11	chr10:5308367..5310948-chr10:5323905..5325582,2	K562	blood:
12	chr10:5061036..5061618-chr10:5325622..5326440,2	MCF-7	breast:
13	chr10:5344285..5346013-chr10:5348255..5349922,2	K562	blood:
14	chr10:5336010..5336717-chr10:5425689..5426611,2	MCF-7	breast:
15	chr10:4891638..4892533-chr10:5325193..5326077,4	MCF-7	breast:
16	chr10:5325782..5327303-chr10:5331354..5334117,2	K562	blood:
17	chr10:5308367..5310948-chr10:5323905..5325582,2	K562	blood:
18	chr10:5336048..5336657-chr10:5385291..5386158,2	MCF-7	breast:
19	chr10:4857887..4858608-chr10:5325585..5326522,2	K562	blood:
20	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
21	chr10:5327837..5330329-chr10:5330922..5333846,2	K562	blood:
22	chr10:4869978..4871994-chr10:5334140..5336719,2	K562	blood:
23	chr10:5300898..5303251-chr10:5486479..5488838,2	K562	blood:
24	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
25	chr10:4856147..4859117-chr10:5323721..5326556,2	K562	blood:
26	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
27	chr10:5344285..5346013-chr10:5348255..5349922,2	K562	blood:
28	chr10:5347252..5349655-chr10:5350748..5353704,2	K562	blood:
29	chr10:5241329..5242148-chr10:5325053..5325709,2	MCF-7	breast:
30	chr10:5314790..5316685-chr10:5325493..5327295,2	K562	blood:
31	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
32	chr10:5309166..5310938-chr10:5312604..5314202,2	K562	blood:
33	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
34	chr10:5210740..5212996-chr10:5319959..5322251,2	MCF-7	breast:
35	chr10:5333712..5336149-chr10:5487099..5489733,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1CL1-1	chr10:5313161-5313199	XLOC_008706
2	lnc-AKR1CL1-3	chr10:5303161-5303199	NONHSAT011146
3	lnc-TUBAL3-1	chr10:5346394-5346828	NONHSAT011148
4	lnc-AKR1C4-1	chr10:5304924-5305165	XLOC_008363
5	lnc-AKR1C4-3	chr10:5294924-5295165	NONHSAT011143
6	lnc-AKR1C4-1	chr10:5304928-5305371	ENSG00000231039.2
7	lnc-AKR1CL1-3	chr10:5297996-5298648	NONHSAT011146
8	lnc-AKR1CL1-1	chr10:5307996-5308648	XLOC_008706

No data

Variant related genes	Relation type
ENSG00000224034	TF binding region
AKR1C7P	TF binding region
ENSG00000223987	TF binding region
ENSG00000224034	CpG island
AKR1C7P	CpG island
ENSG00000223987	CpG island
ENSG00000224034	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000223987	chromatin interactions
ENSG00000151632	chromatin interactions
ENSG00000215267	chromatin interactions
OLIG3	miRNA target sites
LRP1B	miRNA target sites

Extended variants
information (count: 2581 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2581 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1931676	chr10:5285597-5285598	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375006943	chr10:5285620-5285621	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529294118	chr10:5285640-5285641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139217273	chr10:5285678-5285679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1931677	chr10:5285696-5285697	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs149930834	chr10:5285703-5285704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79924114	chr10:5285746-5285747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551867393	chr10:5285752-5285753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144083364	chr10:5285756-5285757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565544689	chr10:5285765-5285766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528300285	chr10:5285791-5285792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546482134	chr10:5285833-5285834	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541586218	chr10:5285839-5285840	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568061329	chr10:5285856-5285857	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114922649	chr10:5285869-5285870	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377061725	chr10:5285876-5285877	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556576903	chr10:5285889-5285890	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534915898	chr10:5285890-5285891	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs56107516	chr10:5285892-5285893	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs185829945	chr10:5285893-5285894	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530909651	chr10:5285945-5285946	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117725200	chr10:5286007-5286008	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573314782	chr10:5286019-5286020	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540867397	chr10:5286025-5286026	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12777723	chr10:5286076-5286077	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs1931678	chr10:5286098-5286099	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556749941	chr10:5286105-5286106	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528505653	chr10:5286148-5286149	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373095770	chr10:5286161-5286162	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9423393	chr10:5286162-5286163	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs188849644	chr10:5286179-5286180	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533384595	chr10:5286244-5286245	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs386740337	chr10:5286261-5286262	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35314085	chr10:5286262-5286263	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528272577	chr10:5286270-5286271	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192438168	chr10:5286351-5286352	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112392612	chr10:5286395-5286396	Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561633752	chr10:5286472-5286473	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183787202	chr10:5286489-5286490	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148524008	chr10:5286494-5286495	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34521172	chr10:5286496-5286497	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550485535	chr10:5286498-5286499	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568715290	chr10:5286502-5286503	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551191715	chr10:5286514-5286515	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34212531	chr10:5286515-5286516	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541521138	chr10:5286520-5286521	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569510147	chr10:5286532-5286533	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188133343	chr10:5286533-5286534	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147660438	chr10:5286549-5286550	Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7895816	chr10:5286600-5286601	Enhancers Active TSS Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	23223014	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5284200-5287200	Enhancers	HepG2	liver
2	chr10:5284600-5286200	Weak transcription	A549	lung
3	chr10:5285200-5285600	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr10:5285200-5285800	Enhancers	Liver	Liver
5	chr10:5285800-5286400	Flanking Active TSS	Liver	Liver
6	chr10:5286200-5286600	Strong transcription	A549	lung
7	chr10:5286200-5287000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr10:5286400-5287200	Active TSS	Liver	Liver
9	chr10:5286600-5293800	Weak transcription	A549	lung
10	chr10:5287000-5287200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr10:5287000-5287400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr10:5287200-5287400	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr10:5293800-5294400	Enhancers	A549	lung
14	chr10:5293800-5295000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr10:5293800-5295000	Enhancers	HepG2	liver
16	chr10:5294200-5294600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr10:5294200-5294600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr10:5294200-5294600	Enhancers	Esophagus	oesophagus
19	chr10:5294200-5294600	Enhancers	Placenta	Placenta
20	chr10:5294200-5294600	Bivalent Enhancer	Left Ventricle	heart
21	chr10:5294200-5294600	Enhancers	Stomach Mucosa	stomach
22	chr10:5294200-5294600	Enhancers	HMEC	breast
23	chr10:5294200-5294800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr10:5294200-5294800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:5294200-5294800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr10:5294400-5294600	Flanking Active TSS	A549	lung
27	chr10:5294400-5294800	Enhancers	Muscle Satellite Cultured Cells	--
28	chr10:5294600-5295200	Enhancers	A549	lung
29	chr10:5294600-5296000	Weak transcription	Esophagus	oesophagus
30	chr10:5294600-5296400	Weak transcription	Stomach Mucosa	stomach
31	chr10:5295000-5300600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr10:5295000-5301400	Weak transcription	HepG2	liver
33	chr10:5295200-5301400	Weak transcription	A549	lung
34	chr10:5296000-5296400	Enhancers	Esophagus	oesophagus
35	chr10:5296000-5296600	Enhancers	Colonic Mucosa	Colon
36	chr10:5296200-5296600	Enhancers	Duodenum Mucosa	Duodenum
37	chr10:5296200-5296600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr10:5296200-5296600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr10:5296200-5296600	Enhancers	NHEK	skin
40	chr10:5296400-5296800	Enhancers	Stomach Mucosa	stomach
41	chr10:5300600-5302000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr10:5300800-5303200	Enhancers	Liver	Liver
43	chr10:5301200-5301600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:5301400-5302400	Enhancers	HepG2	liver
45	chr10:5301400-5303400	Strong transcription	A549	lung
46	chr10:5302200-5302600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr10:5302400-5304400	Weak transcription	HepG2	liver
48	chr10:5302600-5303000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:5302800-5303600	Enhancers	H1 Cell Line	embryonic stem cell
50	chr10:5303200-5305000	Weak transcription	Liver	Liver

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