Variant report

Variant	esv3523301
Chromosome Location	chr15:41626760-41629083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41626673-41627190	K562	blood:	n/a	n/a
2	BHLHE40	chr15:41626886-41626908	K562	blood:	n/a	n/a
3	BHLHE40	chr15:41628842-41629191	K562	blood:	n/a	n/a
4	BHLHE40	chr15:41628614-41629153	GM12878	blood:	n/a	n/a
5	CCNT2	chr15:41626520-41627036	K562	blood:	n/a	n/a
6	CEBPB	chr15:41626653-41627268	K562	blood:	n/a	n/a
7	CEBPB	chr15:41626931-41626997	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:41626817-41627062	K562	blood:	n/a	n/a
9	CEBPD	chr15:41626657-41627183	K562	blood:	n/a	n/a
10	CEBPD	chr15:41626559-41627130	K562	blood:	n/a	n/a
11	CTCF	chr15:41628780-41628930	GM12878	blood:	n/a	n/a
12	CUX1	chr15:41628749-41628754	GM12878	blood:	n/a	n/a
13	CUX1	chr15:41626710-41626832	K562	blood:	n/a	n/a
14	ELK1	chr15:41628754-41628766	GM12878	blood:	n/a	n/a
15	EP300	chr15:41626690-41627054	K562	blood:	n/a	n/a
16	EP300	chr15:41628986-41629185	K562	blood:	n/a	n/a
17	EP300	chr15:41626907-41626968	K562	blood:	n/a	n/a
18	FOS	chr15:41628954-41628969	MCF10A-Er-Src	breast:	n/a	n/a
19	GATA1	chr15:41628687-41629166	PBDE	blood:	n/a	n/a
20	GATA1	chr15:41626542-41627297	PBDE	blood:	n/a	chr15:41626884-41626895
21	GATA2	chr15:41626579-41627103	K562	blood:	n/a	chr15:41626884-41626895
22	GATA2	chr15:41628846-41629006	SH-SY5Y	brain:	n/a	n/a
23	GTF3C2	chr15:41625093-41627178	Hela-S3	cervix:	n/a	n/a
24	HEY1	chr15:41626501-41626919	K562	blood:	n/a	n/a
25	IKZF1	chr15:41628877-41629141	GM12878	blood:	n/a	n/a
26	IRF1	chr15:41626704-41627238	K562	blood:	n/a	n/a
27	JUN	chr15:41626765-41627165	K562	blood:	n/a	n/a
28	JUND	chr15:41626788-41627026	K562	blood:	n/a	n/a
29	KAP1	chr15:41626194-41627237	HEK293	kidney:	n/a	n/a
30	MAFF	chr15:41626662-41626897	K562	blood:	n/a	n/a
31	MAX	chr15:41626837-41627117	K562	blood:	n/a	n/a
32	MAX	chr15:41626994-41626997	Hela-S3	cervix:	n/a	n/a
33	MAZ	chr15:41626878-41626994	K562	blood:	n/a	n/a
34	MAZ	chr15:41629057-41629058	GM12878	blood:	n/a	n/a
35	MXI1	chr15:41626708-41626801	K562	blood:	n/a	n/a
36	MYC	chr15:41626774-41627031	K562	blood:	n/a	n/a
37	MYC	chr15:41626668-41626888	K562	blood:	n/a	n/a
38	NR2F2	chr15:41626605-41627092	K562	blood:	n/a	n/a
39	NR2F2	chr15:41626415-41627198	K562	blood:	n/a	n/a
40	PAX5	chr15:41628759-41629034	GM12878	blood:	n/a	n/a
41	PML	chr15:41626563-41627115	K562	blood:	n/a	n/a
42	POLR2A	chr15:41626641-41627098	K562	blood:	n/a	n/a
43	POLR2A	chr15:41626561-41627147	GM12878	blood:	n/a	n/a
44	POLR2A	chr15:41626621-41627097	K562	blood:	n/a	n/a
45	POLR2A	chr15:41626542-41627048	K562	blood:	n/a	n/a
46	POLR2A	chr15:41626744-41627010	HepG2	liver:	n/a	n/a
47	RCOR1	chr15:41626994-41627011	Hela-S3	cervix:	n/a	n/a
48	RCOR1	chr15:41626577-41627070	K562	blood:	n/a	n/a
49	RCOR1	chr15:41628973-41629181	K562	blood:	n/a	n/a
50	RCOR1	chr15:41626708-41626917	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41628806-41628856	RPTEC	kidney:	n/a
2	chr15:41628806-41628856	AG09309	skin:	n/a
3	chr15:41628806-41628856	SK-N-MC	brain:	n/a
4	chr15:41628806-41628856	MCF-7	breast:	n/a
5	chr15:41628806-41628856	NHBE	bronchial:	n/a
6	chr15:41628806-41628856	HRPEpiC	eye:	n/a
7	chr15:41628806-41628856	HIPEpiC	eye:	n/a
8	chr15:41628806-41628856	BE2_C	brain:	n/a
9	chr15:41628806-41628856	T-47D	breast:	n/a
10	chr15:41628806-41628856	MCF10A-Er-Src	breast:	n/a
11	chr15:41628806-41628856	GM12891	blood:	n/a
12	chr15:41628806-41628856	Hela-S3	cervix:	n/a
13	chr15:41628806-41628856	A549	lung:	n/a
14	chr15:41628806-41628856	SK-N-SH	brain:	n/a
15	chr15:41628806-41628856	AoSMC	blood vessel:	n/a
16	chr15:41628806-41628856	ProgFib	skin:	n/a
17	chr15:41628806-41628856	HCPEpiC	choroid plexus:	n/a
18	chr15:41628806-41628856	HCM	heart:	n/a
19	chr15:41628806-41628856	CMK	blood:	n/a
20	chr15:41628806-41628856	H1-hESC	embryonic stem cell:	embryo
21	chr15:41628806-41628856	Caco-2	colon:	n/a
22	chr15:41628806-41628856	HRCEpiC	kidney:	n/a
23	chr15:41628806-41628856	AG04449	skin:	fetal
24	chr15:41628806-41628856	GM19239	blood:	n/a
25	chr15:41628806-41628856	HEEpiC	esophagus:	n/a
26	chr15:41628806-41628856	HCF	heart:	n/a
27	chr15:41628806-41628856	GM12878	blood:	n/a
28	chr15:41628806-41628856	HMEC	breast:	n/a
29	chr15:41628806-41628856	HEK293	kidney:	embryo
30	chr15:41628806-41628856	Jurkat	blood:	n/a
31	chr15:41628806-41628856	AG04450	lung:	fetal
32	chr15:41628806-41628856	ovcar-3	ovarian:	n/a
33	chr15:41628806-41628856	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:41628806-41628856	HL-60	blood:	n/a
35	chr15:41628806-41628856	GM12892	blood:	n/a
36	chr15:41628806-41628856	GM06990	blood:	n/a
37	chr15:41628806-41628856	NT2-D1	testis:	n/a
38	chr15:41628806-41628856	NH-A	brain:	n/a
39	chr15:41628806-41628856	SKMC	muscle:	n/a
40	chr15:41628806-41628856	HNPCEpiC	eye:	n/a
41	chr15:41628806-41628856	HCT-116	colon:	n/a
42	chr15:41628806-41628856	SK-N-SH_RA	brain:	n/a
43	chr15:41628806-41628856	AG10803	skin:	n/a
44	chr15:41628806-41628856	AG09319	gingival:	n/a
45	chr15:41628806-41628856	HRE	kidney:	n/a
46	chr15:41628806-41628856	PrEC	prostate:	n/a
47	chr15:41628806-41628856	HAEpiC	amniotic membrane:	n/a
48	chr15:41628806-41628856	PFSK-1	brain:	n/a
49	chr15:41628806-41628856	IMR90	lung:	fetal
50	chr15:41628806-41628856	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:41624254..41626833-chr15:41952098..41954867,2	K562	blood:
2	chr15:41573497..41577986-chr15:41624362..41627823,9	K562	blood:
3	chr15:41625051..41627000-chr15:41692954..41695637,2	K562	blood:
4	chr15:41575029..41577348-chr15:41624329..41626974,5	K562	blood:
5	chr15:41506769..41509087-chr15:41627220..41629152,2	K562	blood:
6	chr15:41623109..41624716-chr15:41626647..41628687,2	K562	blood:
7	chr15:41623039..41626480-chr15:41628933..41631074,3	MCF-7	breast:
8	chr15:41575115..41577125-chr15:41624466..41626801,3	MCF-7	breast:

No data

Variant related genes	Relation type
OIP5	TF binding region
OIP5	CpG island
ENSG00000137804	chromatin interactions
ENSG00000247556	chromatin interactions
ENSG00000137806	chromatin interactions
ENSG00000104147	chromatin interactions
ENSG00000174197	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539315016	chr15:41626892-41626893	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs558122085	chr15:41626895-41626896	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs3034611	chr15:41626903-41626904	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs59299220	chr15:41626904-41626905	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs397835722	chr15:41626917-41626918	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs398026994	chr15:41626918-41626919	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs577630769	chr15:41626953-41626954	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs543444617	chr15:41626982-41626983	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs191031658	chr15:41626993-41626994	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs73404972	chr15:41626997-41626998	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs144614671	chr15:41627035-41627036	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549518377	chr15:41627076-41627077	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs540403804	chr15:41627133-41627134	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs554526205	chr15:41627161-41627162	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs561927167	chr15:41627191-41627192	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs181664537	chr15:41627256-41627257	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs10635011	chr15:41627470-41627471	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs34842886	chr15:41627471-41627472	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs59107612	chr15:41627473-41627474	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs56053993	chr15:41627474-41627475	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112758208	chr15:41627484-41627485	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs547688352	chr15:41627487-41627488	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536260229	chr15:41627517-41627518	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs59972234	chr15:41627559-41627560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs112696782	chr15:41627603-41627604	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs11631396	chr15:41627609-41627610	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs36091573	chr15:41627646-41627647	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs148445385	chr15:41627680-41627681	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs533251473	chr15:41627720-41627721	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs549832804	chr15:41627725-41627726	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs546755787	chr15:41627743-41627744	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs557063813	chr15:41627774-41627775	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs185900477	chr15:41627871-41627872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs142623873	chr15:41627911-41627912	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372678158	chr15:41627919-41627920	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111400362	chr15:41627922-41627923	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs548763496	chr15:41627934-41627935	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566267423	chr15:41627952-41627953	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs534870949	chr15:41627963-41627964	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558314874	chr15:41627966-41627967	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571634770	chr15:41627967-41627968	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537344035	chr15:41627998-41627999	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556974698	chr15:41628011-41628012	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146807557	chr15:41628022-41628023	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs543108132	chr15:41628073-41628074	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs553160660	chr15:41628236-41628237	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572223574	chr15:41628275-41628276	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540905204	chr15:41628300-41628301	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs111533086	chr15:41628319-41628320	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533313818	chr15:41628322-41628323	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	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
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41623000-41626800	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr15:41623000-41627200	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr15:41623000-41627200	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr15:41623000-41627200	Active TSS	A549	lung
5	chr15:41623000-41627400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:41623400-41627000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:41623400-41627200	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr15:41623400-41627200	Active TSS	H1 Cell Line	embryonic stem cell
9	chr15:41623400-41627400	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr15:41623600-41626800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr15:41623600-41626800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:41623600-41626800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr15:41623600-41627000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr15:41623600-41627000	Active TSS	H9 Cell Line	embryonic stem cell
15	chr15:41623600-41627200	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr15:41623600-41627200	Active TSS	Thymus	Thymus
17	chr15:41623600-41627200	Active TSS	Hela-S3	cervix
18	chr15:41623800-41626800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:41623800-41627200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:41623800-41627200	Active TSS	NHDF-Ad	bronchial
21	chr15:41623800-41627400	Active TSS	GM12878-XiMat	blood
22	chr15:41623800-41627400	Active TSS	K562	blood
23	chr15:41624000-41626800	Active TSS	Fetal Intestine Small	intestine
24	chr15:41624000-41627200	Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr15:41624000-41627400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr15:41624200-41626800	Active TSS	Fetal Kidney	kidney
27	chr15:41624200-41626800	Active TSS	NHLF	lung
28	chr15:41624200-41627000	Active TSS	Fetal Lung	lung
29	chr15:41624200-41627200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr15:41624200-41627200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:41624200-41627200	Active TSS	HSMM	muscle
32	chr15:41624200-41627400	Active TSS	Muscle Satellite Cultured Cells	--
33	chr15:41624400-41626800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:41624400-41626800	Active TSS	Rectal Smooth Muscle	rectum
35	chr15:41624400-41627000	Active TSS	Fetal Brain Female	brain
36	chr15:41624400-41627000	Active TSS	NH-A	brain
37	chr15:41625200-41627000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr15:41625400-41626800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr15:41625400-41670200	Weak transcription	Gastric	stomach
40	chr15:41625600-41626800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr15:41625600-41627200	Active TSS	Brain Germinal Matrix	brain
42	chr15:41625600-41659200	Weak transcription	Lung	lung
43	chr15:41625800-41627000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr15:41625800-41665800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr15:41625800-41694200	Weak transcription	Small Intestine	intestine
46	chr15:41626000-41626800	Weak transcription	Psoas Muscle	Psoas
47	chr15:41626000-41627200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr15:41626000-41642000	Weak transcription	Ovary	ovary
49	chr15:41626000-41665200	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr15:41626200-41626800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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