Variant report

Variant	nsv1053492
Chromosome Location	chr15:45152371-45275226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:643)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45271890-45272170	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:45181194-45181211	K562	blood:	n/a	n/a
3	ARID3A	chr15:45205265-45205621	HepG2	liver:	n/a	n/a
4	ATF1	chr15:45182020-45182040	K562	blood:	n/a	n/a
5	ATF1	chr15:45168202-45168273	K562	blood:	n/a	n/a
6	ATF2	chr15:45174666-45175297	GM12878	blood:	n/a	n/a
7	ATF2	chr15:45203414-45203775	GM12878	blood:	n/a	n/a
8	ATF2	chr15:45203385-45203780	GM12878	blood:	n/a	n/a
9	ATF2	chr15:45174555-45175594	GM12878	blood:	n/a	n/a
10	BATF	chr15:45174732-45175340	GM12878	blood:	n/a	n/a
11	BATF	chr15:45191947-45192347	GM12878	blood:	n/a	n/a
12	BATF	chr15:45272154-45272541	GM12878	blood:	n/a	chr15:45272467-45272476
13	BATF	chr15:45191999-45192251	GM12878	blood:	n/a	n/a
14	BATF	chr15:45203489-45203757	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
15	BATF	chr15:45204924-45205158	GM12878	blood:	n/a	chr15:45204943-45204952
16	BATF	chr15:45260122-45260297	GM12878	blood:	n/a	n/a
17	BATF	chr15:45174500-45176189	GM12878	blood:	n/a	n/a
18	BATF	chr15:45175615-45176106	GM12878	blood:	n/a	n/a
19	BATF	chr15:45272208-45272505	GM12878	blood:	n/a	chr15:45272467-45272476
20	BATF	chr15:45203408-45203799	GM12878	blood:	n/a	chr15:45203595-45203606 chr15:45203708-45203717
21	BATF	chr15:45214951-45215126	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:45191932-45192270	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:45272174-45272394	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:45174655-45175245	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:45174637-45175348	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:45175527-45176004	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:45272182-45272561	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:45203459-45203776	GM12878	blood:	n/a	chr15:45203595-45203604 chr15:45203594-45203603
29	BCL11A	chr15:45175417-45176211	GM12878	blood:	n/a	n/a
30	BCL3	chr15:45174662-45175296	GM12878	blood:	n/a	n/a
31	BCLAF1	chr15:45174481-45175331	GM12878	blood:	n/a	n/a
32	BCLAF1	chr15:45173453-45173866	GM12878	blood:	n/a	n/a
33	BCLAF1	chr15:45174315-45175214	GM12878	blood:	n/a	n/a
34	BHLHE40	chr15:45205254-45205588	HepG2	liver:	n/a	n/a
35	BHLHE40	chr15:45174566-45175326	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:45175681-45176068	GM12878	blood:	n/a	n/a
37	BRCA1	chr15:45197020-45197149	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr15:45153846-45154522	K562	blood:	n/a	n/a
39	CBX3	chr15:45170134-45170405	K562	blood:	n/a	n/a
40	CBX3	chr15:45154120-45154506	K562	blood:	n/a	n/a
41	CBX3	chr15:45170132-45170460	K562	blood:	n/a	n/a
42	CBX3	chr15:45248617-45248975	K562	blood:	n/a	n/a
43	CEBPB	chr15:45190198-45190318	A549	lung:	n/a	n/a
44	CEBPB	chr15:45231991-45232144	K562	blood:	n/a	chr15:45232041-45232054
45	CEBPB	chr15:45205205-45205543	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:45271798-45272173	HepG2	liver:	n/a	n/a
47	CEBPB	chr15:45190110-45190355	K562	blood:	n/a	n/a
48	CEBPB	chr15:45205208-45205573	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:45173553-45176123	GM12878	blood:	n/a	n/a
50	CEBPB	chr15:45208995-45209180	HepG2	liver:	n/a	chr15:45209032-45209043

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45248744-45248794	K562	blood:	n/a
2	chr15:45248932-45248982	NB4	blood:	n/a
3	chr15:45248463-45248513	CMK	blood:	n/a
4	chr15:45248463-45248513	NHBE	bronchial:	n/a
5	chr15:45248463-45248513	AG09319	gingival:	n/a
6	chr15:45247870-45247920	NB4	blood:	n/a
7	chr15:45248806-45248856	HAEpiC	amniotic membrane:	n/a
8	chr15:45248744-45248794	AG09309	skin:	n/a
9	chr15:45247870-45247920	HAEpiC	amniotic membrane:	n/a
10	chr15:45248806-45248856	HCM	heart:	n/a
11	chr15:45248806-45248856	HNPCEpiC	eye:	n/a
12	chr15:45248932-45248982	HEK293	kidney:	embryo
13	chr15:45248463-45248513	HEK293	kidney:	embryo
14	chr15:45248806-45248856	SK-N-SH	brain:	n/a
15	chr15:45248932-45248982	HCM	heart:	n/a
16	chr15:45248878-45248928	HEK293	kidney:	embryo
17	chr15:45247870-45247920	HL-60	blood:	n/a
18	chr15:45248878-45248928	HCF	heart:	n/a
19	chr15:45248932-45248982	GM12892	blood:	n/a
20	chr15:45248744-45248794	MCF-7	breast:	n/a
21	chr15:45248744-45248794	NHBE	bronchial:	n/a
22	chr15:45248932-45248982	H1-hESC	embryonic stem cell:	embryo
23	chr15:45248806-45248856	NB4	blood:	n/a
24	chr15:45248744-45248794	HRPEpiC	eye:	n/a
25	chr15:45248932-45248982	GM19239	blood:	n/a
26	chr15:45248806-45248856	Hela-S3	cervix:	n/a
27	chr15:45248744-45248794	AG09319	gingival:	n/a
28	chr15:45247870-45247920	BE2_C	brain:	n/a
29	chr15:45248878-45248928	ProgFib	skin:	n/a
30	chr15:45247870-45247920	PANC-1	pancreas:	n/a
31	chr15:45248878-45248928	AG04449	skin:	fetal
32	chr15:45248744-45248794	HEK293	kidney:	embryo
33	chr15:45247870-45247920	Jurkat	blood:	n/a
34	chr15:45248932-45248982	SAEC	small airway:	n/a
35	chr15:45248744-45248794	NT2-D1	testis:	n/a
36	chr15:45248806-45248856	NHDF-neo	bronchial:	n/a
37	chr15:45248463-45248513	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:45248806-45248856	HEEpiC	esophagus:	n/a
39	chr15:45248744-45248794	A549	lung:	n/a
40	chr15:45248463-45248513	HMEC	breast:	n/a
41	chr15:45248744-45248794	H1-hESC	embryonic stem cell:	embryo
42	chr15:45247870-45247920	NHDF-neo	bronchial:	n/a
43	chr15:45248878-45248928	GM12892	blood:	n/a
44	chr15:45248878-45248928	GM12878	blood:	n/a
45	chr15:45248463-45248513	K562	blood:	n/a
46	chr15:45248744-45248794	LNCaP	prostate:	n/a
47	chr15:45247870-45247920	AG04450	lung:	fetal
48	chr15:45247870-45247920	AG10803	skin:	n/a
49	chr15:45248463-45248513	A549	lung:	n/a
50	chr15:45248463-45248513	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr15:45264164..45266093-chr15:45270183..45271983,2	K562	blood:
2	chr15:45003163..45005190-chr15:45225441..45227864,2	K562	blood:
3	chr15:45153661..45154310-chr15:45315073..45315837,2	NB4	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf43-1	chr15:45212156-45213018	NONHSAT042202
2	lnc-DUOX2-4	chr15:45262233-45263376	NONHSAT042205
3	lnc-C15orf43-2	chr15:45174295-45174981	NONHSAT042199
4	lnc-C15orf43-1	chr15:45211574-45211851	NONHSAT042202

No data

Variant related genes	Relation type
ENSG00000259479	TF binding region
RNU6-966P	TF binding region
C15orf43	TF binding region
RNU6-1332P	TF binding region
RNU1-119P	TF binding region
ENSG00000259742	TF binding region
ENSG00000259304	TF binding region
RNU6-1108P	TF binding region
ENSG00000259231	TF binding region
ENSG00000259479	CpG island
RNU6-966P	CpG island
C15orf43	CpG island
RNU6-1332P	CpG island
RNU1-119P	CpG island
ENSG00000259742	CpG island
ENSG00000259304	CpG island
RNU6-1108P	CpG island
ENSG00000259231	CpG island
ENSG00000166710	chromatin interactions
ENSG00000252288	chromatin interactions
ENSG00000140263	chromatin interactions
ENSG00000229474	chromatin interactions

Extended variants
information (count: 1963 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1963 , 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	rs735480	chr15:45152371-45152372	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565713822	chr15:45152379-45152380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144196508	chr15:45152388-45152389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190099116	chr15:45152398-45152399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577790111	chr15:45152399-45152400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181855838	chr15:45152435-45152436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559346464	chr15:45152453-45152454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574607520	chr15:45152497-45152498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186421248	chr15:45152569-45152570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576673625	chr15:45152606-45152607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542463526	chr15:45152760-45152761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562242029	chr15:45152761-45152762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527727032	chr15:45152769-45152770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541013852	chr15:45152791-45152792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541913577	chr15:45152855-45152856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533227448	chr15:45152887-45152888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549583611	chr15:45152903-45152904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563447569	chr15:45152917-45152918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7174869	chr15:45152954-45152955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529073269	chr15:45152957-45152958	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549297056	chr15:45152962-45152963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565818699	chr15:45152984-45152985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150369672	chr15:45153051-45153052	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551367326	chr15:45153052-45153053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138044071	chr15:45153101-45153102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537102029	chr15:45153131-45153132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556799634	chr15:45153139-45153140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540608865	chr15:45153169-45153170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535663465	chr15:45153199-45153200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556061036	chr15:45153204-45153205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191367354	chr15:45153213-45153214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182260802	chr15:45153219-45153220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79028197	chr15:45153232-45153233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs532642775	chr15:45153269-45153270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149082216	chr15:45153275-45153276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543552926	chr15:45153345-45153346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185127304	chr15:45153369-45153370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145723355	chr15:45153376-45153377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548890342	chr15:45153382-45153383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12595073	chr15:45153405-45153406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs2470907	chr15:45153410-45153411	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs376489945	chr15:45153483-45153484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551400092	chr15:45153511-45153512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571221530	chr15:45153514-45153515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142806435	chr15:45153590-45153591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550696577	chr15:45153599-45153600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs564218217	chr15:45153613-45153614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567226034	chr15:45153617-45153618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112674995	chr15:45153683-45153684	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536078849	chr15:45153691-45153692	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45146000-45153200	Weak transcription	K562	blood
2	chr15:45151600-45152800	Weak transcription	Liver	Liver
3	chr15:45152800-45154000	Enhancers	Liver	Liver
4	chr15:45153200-45153800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr15:45153200-45154400	Enhancers	K562	blood
6	chr15:45153800-45154000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
7	chr15:45153800-45154400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:45154400-45155200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:45155200-45155400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr15:45158000-45158600	Enhancers	HepG2	liver
11	chr15:45167800-45172600	ZNF genes & repeats	GM12878-XiMat	blood
12	chr15:45172600-45172800	Weak transcription	GM12878-XiMat	blood
13	chr15:45172800-45174400	Active TSS	GM12878-XiMat	blood
14	chr15:45173600-45177200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:45174200-45176000	Enhancers	HMEC	breast
16	chr15:45174400-45174600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr15:45174400-45175000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr15:45174400-45175000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr15:45174400-45175000	Flanking Active TSS	GM12878-XiMat	blood
20	chr15:45174400-45175400	Enhancers	NHEK	skin
21	chr15:45174400-45175800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr15:45174600-45175000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr15:45174600-45175000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr15:45174600-45175000	Bivalent Enhancer	HepG2	liver
25	chr15:45174600-45175400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:45174600-45176000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr15:45174800-45177800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:45175000-45175400	Active TSS	GM12878-XiMat	blood
29	chr15:45175000-45176000	Enhancers	HepG2	liver
30	chr15:45175000-45176200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr15:45175400-45176400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr15:45175400-45176400	Flanking Active TSS	GM12878-XiMat	blood
33	chr15:45175800-45185200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:45176400-45177000	Enhancers	GM12878-XiMat	blood
35	chr15:45180200-45182000	Enhancers	K562	blood
36	chr15:45187800-45188800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr15:45187800-45189000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr15:45187800-45189000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:45188000-45189400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
40	chr15:45188200-45188600	Enhancers	Primary T cells fromperipheralblood	blood
41	chr15:45188200-45188800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr15:45188400-45188800	Enhancers	Primary B cells from peripheral blood	blood
43	chr15:45188600-45188800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr15:45188600-45188800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr15:45188600-45188800	Enhancers	Gastric	stomach
46	chr15:45188600-45189000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
47	chr15:45188600-45189000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr15:45195400-45196000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr15:45195800-45197000	Enhancers	Hela-S3	cervix
50	chr15:45196000-45197000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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