Variant report

Variant	nsv894796
Chromosome Location	chr10:5300976-5348491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1016)
CpG islands
(count:123)
Chromatin interactive
region (count:31)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1016 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	ATF1	chr10:5339509-5339711	K562	blood:	n/a	n/a
4	ATF1	chr10:5325479-5325806	K562	blood:	n/a	n/a
5	ATF1	chr10:5326291-5326744	K562	blood:	n/a	n/a
6	ATF1	chr10:5337658-5338224	K562	blood:	n/a	n/a
7	ATF1	chr10:5333613-5334043	K562	blood:	n/a	n/a
8	ATF3	chr10:5326289-5326817	K562	blood:	n/a	n/a
9	ATF3	chr10:5333465-5334182	A549	lung:	n/a	n/a
10	ATF3	chr10:5333223-5334296	A549	lung:	n/a	n/a
11	ATF3	chr10:5333695-5334079	K562	blood:	n/a	n/a
12	BACH1	chr10:5314040-5314410	K562	blood:	n/a	chr10:5314219-5314233
13	BACH1	chr10:5325193-5325762	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:5326467-5326786	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr10:5336196-5336356	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr10:5333705-5333941	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:5314029-5314452	H1-hESC	embryonic stem cell:	n/a	chr10:5314219-5314233
18	BACH1	chr10:5326454-5327033	K562	blood:	n/a	n/a
19	BCL3	chr10:5333309-5334562	A549	lung:	n/a	n/a
20	BCL3	chr10:5333183-5334316	A549	lung:	n/a	n/a
21	BCL3	chr10:5325157-5327103	A549	lung:	n/a	chr10:5326539-5326548
22	BCL3	chr10:5325009-5326832	A549	lung:	n/a	chr10:5326539-5326548
23	BHLHE40	chr10:5337719-5337915	K562	blood:	n/a	n/a
24	BHLHE40	chr10:5339529-5339545	K562	blood:	n/a	n/a
25	BHLHE40	chr10:5333619-5333920	K562	blood:	n/a	n/a
26	BHLHE40	chr10:5326335-5326780	K562	blood:	n/a	n/a
27	BRCA1	chr10:5336152-5336386	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr10:5333574-5334170	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr10:5336091-5336370	K562	blood:	n/a	n/a
30	CBX3	chr10:5326216-5326887	K562	blood:	n/a	n/a
31	CBX3	chr10:5336027-5336413	K562	blood:	n/a	n/a
32	CBX3	chr10:5333327-5334314	K562	blood:	n/a	n/a
33	CCNT2	chr10:5326424-5326723	K562	blood:	n/a	n/a
34	CEBPB	chr10:5326281-5326926	A549	lung:	n/a	n/a
35	CEBPB	chr10:5333464-5334124	K562	blood:	n/a	n/a
36	CEBPB	chr10:5326531-5326679	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:5326307-5326933	A549	lung:	n/a	n/a
38	CEBPB	chr10:5333471-5334125	MCF-7	breast:	n/a	n/a
39	CEBPB	chr10:5326351-5326856	A549	lung:	n/a	n/a
40	CEBPB	chr10:5333532-5333776	K562	blood:	n/a	n/a
41	CEBPB	chr10:5333444-5334060	HepG2	liver:	n/a	chr10:5333459-5333476
42	CEBPB	chr10:5333440-5334203	HCT-116	colon:	n/a	chr10:5333459-5333476
43	CEBPB	chr10:5333274-5334468	A549	lung:	n/a	chr10:5333459-5333476
44	CEBPB	chr10:5326460-5326723	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr10:5326435-5326793	K562	blood:	n/a	n/a
46	CEBPB	chr10:5326389-5326882	K562	blood:	n/a	n/a
47	CEBPB	chr10:5326460-5326848	K562	blood:	n/a	n/a
48	CEBPB	chr10:5324858-5325886	A549	lung:	n/a	chr10:5325630-5325642
49	CEBPB	chr10:5320571-5320633	A549	lung:	n/a	n/a
50	CEBPB	chr10:5333174-5334557	A549	lung:	n/a	chr10:5333459-5333476

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5333615-5333665	HCT-116	colon:	n/a
2	chr10:5333615-5333665	HCT-116	colon:	n/a
3	chr10:5302629-5302679	GM12891	blood:	n/a
4	chr10:5333615-5333665	NHDF-neo	bronchial:	n/a
5	chr10:5333615-5333665	PFSK-1	brain:	n/a
6	chr10:5333615-5333665	HCF	heart:	n/a
7	chr10:5333615-5333665	GM12878	blood:	n/a
8	chr10:5302629-5302679	HCPEpiC	choroid plexus:	n/a
9	chr10:5333615-5333665	NHBE	bronchial:	n/a
10	chr10:5333615-5333665	HCM	heart:	n/a
11	chr10:5333615-5333665	T-47D	breast:	n/a
12	chr10:5302629-5302679	SK-N-SH_RA	brain:	n/a
13	chr10:5302629-5302679	LNCaP	prostate:	n/a
14	chr10:5302629-5302679	T-47D	breast:	n/a
15	chr10:5302629-5302679	AG10803	skin:	n/a
16	chr10:5333615-5333665	HUVEC	blood vessel:	n/a
17	chr10:5302629-5302679	AG09309	skin:	n/a
18	chr10:5333615-5333665	HRPEpiC	eye:	n/a
19	chr10:5333615-5333665	LNCaP	prostate:	n/a
20	chr10:5333615-5333665	SKMC	muscle:	n/a
21	chr10:5302629-5302679	NHBE	bronchial:	n/a
22	chr10:5333615-5333665	GM12892	blood:	n/a
23	chr10:5302629-5302679	SAEC	small airway:	n/a
24	chr10:5333615-5333665	AG09309	skin:	n/a
25	chr10:5333615-5333665	PrEC	prostate:	n/a
26	chr10:5302629-5302679	NT2-D1	testis:	n/a
27	chr10:5302629-5302679	HRE	kidney:	n/a
28	chr10:5333615-5333665	AG09319	gingival:	n/a
29	chr10:5333615-5333665	HIPEpiC	eye:	n/a
30	chr10:5333615-5333665	H1-hESC	embryonic stem cell:	embryo
31	chr10:5302629-5302679	HEK293	kidney:	embryo
32	chr10:5333615-5333665	HNPCEpiC	eye:	n/a
33	chr10:5333615-5333665	AG04450	lung:	fetal
34	chr10:5302629-5302679	AG04450	lung:	fetal
35	chr10:5333615-5333665	SK-N-SH_RA	brain:	n/a
36	chr10:5302629-5302679	MCF10A-Er-Src	breast:	n/a
37	chr10:5302629-5302679	BJ	skin:	n/a
38	chr10:5302629-5302679	Hela-S3	cervix:	n/a
39	chr10:5302629-5302679	SK-N-SH	brain:	n/a
40	chr10:5302629-5302679	HIPEpiC	eye:	n/a
41	chr10:5333615-5333665	SK-N-MC	brain:	n/a
42	chr10:5302629-5302679	ECC-1	luminal epithelium:	n/a
43	chr10:5333615-5333665	ProgFib	skin:	n/a
44	chr10:5302629-5302679	HAEpiC	amniotic membrane:	n/a
45	chr10:5302629-5302679	PFSK-1	brain:	n/a
46	chr10:5302629-5302679	RPTEC	kidney:	n/a
47	chr10:5302629-5302679	HRPEpiC	eye:	n/a
48	chr10:5302629-5302679	AG09319	gingival:	n/a
49	chr10:5302629-5302679	SK-N-MC	brain:	n/a
50	chr10:5333615-5333665	MCF-7	breast:	n/a

(count:31 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 1971 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1971 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11597152	chr10:5300976-5300977	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553887621	chr10:5300999-5301000	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs71499631	chr10:5301012-5301013	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572989405	chr10:5301054-5301055	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181418165	chr10:5301055-5301056	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555617820	chr10:5301160-5301161	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573815848	chr10:5301170-5301171	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544542531	chr10:5301188-5301189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs184073602	chr10:5301256-5301257	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554343014	chr10:5301267-5301268	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs78605457	chr10:5301276-5301277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371801129	chr10:5301277-5301278	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140162279	chr10:5301306-5301307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545116586	chr10:5301329-5301330	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143906291	chr10:5301355-5301356	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577815094	chr10:5301356-5301357	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34713340	chr10:5301366-5301367	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370666078	chr10:5301383-5301384	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73609063	chr10:5301385-5301386	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs561547109	chr10:5301433-5301434	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566521349	chr10:5301466-5301467	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs182034836	chr10:5301499-5301500	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs113711783	chr10:5301539-5301540	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs386740338	chr10:5301583-5301584	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372470729	chr10:5301585-5301586	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192313673	chr10:5301663-5301664	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs11253067	chr10:5301698-5301699	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs7095117	chr10:5301704-5301705	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535182000	chr10:5301747-5301748	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558886613	chr10:5301777-5301778	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9423582	chr10:5301811-5301812	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs181760150	chr10:5301830-5301831	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185242362	chr10:5301832-5301833	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556540739	chr10:5301833-5301834	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577711409	chr10:5301844-5301845	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189699836	chr10:5301850-5301851	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114465553	chr10:5301859-5301860	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11253068	chr10:5301882-5301883	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572011341	chr10:5301886-5301887	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79275509	chr10:5301894-5301895	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539735366	chr10:5301895-5301896	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531825929	chr10:5301925-5301926	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182633661	chr10:5301965-5301966	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188204140	chr10:5302015-5302016	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs191048611	chr10:5302033-5302034	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183689031	chr10:5302041-5302042	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150044842	chr10:5302054-5302055	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535626051	chr10:5302082-5302083	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530094207	chr10:5302084-5302085	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371395404	chr10:5302143-5302144	Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	23223014	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5295000-5301400	Weak transcription	HepG2	liver
2	chr10:5295200-5301400	Weak transcription	A549	lung
3	chr10:5300600-5302000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:5300800-5303200	Enhancers	Liver	Liver
5	chr10:5301200-5301600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:5301400-5302400	Enhancers	HepG2	liver
7	chr10:5301400-5303400	Strong transcription	A549	lung
8	chr10:5302200-5302600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr10:5302400-5304400	Weak transcription	HepG2	liver
10	chr10:5302600-5303000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr10:5302800-5303600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr10:5303200-5305000	Weak transcription	Liver	Liver
13	chr10:5303400-5307400	Weak transcription	A549	lung
14	chr10:5304400-5305200	Enhancers	HepG2	liver
15	chr10:5305000-5305200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr10:5305400-5306600	Weak transcription	Liver	Liver
17	chr10:5306400-5306600	Enhancers	Fetal Intestine Small	intestine
18	chr10:5306400-5325600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr10:5306600-5307400	Enhancers	Liver	Liver
20	chr10:5306600-5307400	Weak transcription	Fetal Intestine Small	intestine
21	chr10:5306800-5325400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr10:5307200-5308600	Enhancers	HepG2	liver
23	chr10:5307400-5307600	Flanking Active TSS	Liver	Liver
24	chr10:5307400-5308200	Enhancers	Fetal Intestine Small	intestine
25	chr10:5307400-5308200	Strong transcription	A549	lung
26	chr10:5307600-5307800	Enhancers	Liver	Liver
27	chr10:5307800-5308600	ZNF genes & repeats	Liver	Liver
28	chr10:5308200-5310200	ZNF genes & repeats	A549	lung
29	chr10:5308400-5308600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
30	chr10:5308600-5313600	Weak transcription	HepG2	liver
31	chr10:5308600-5325400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr10:5310000-5310800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr10:5310200-5312200	Genic enhancers	A549	lung
34	chr10:5312000-5312800	Enhancers	Fetal Lung	lung
35	chr10:5312200-5314000	Strong transcription	A549	lung
36	chr10:5313600-5314600	Enhancers	HepG2	liver
37	chr10:5313800-5315000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr10:5314000-5314600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr10:5314000-5314600	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr10:5314000-5314800	Genic enhancers	A549	lung
41	chr10:5314000-5315200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr10:5314200-5314400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr10:5314200-5314600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr10:5314200-5314800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr10:5314400-5324200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr10:5314600-5325200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr10:5314600-5325400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr10:5314800-5316400	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr10:5314800-5321000	Strong transcription	A549	lung
50	chr10:5315200-5318800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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