Variant report

Variant	esv3361173
Chromosome Location	chr15:42445160-42449558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:490)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr15:42446942-42447787	GM12878	blood:	n/a	n/a
2	BCL3	chr15:42446975-42447700	GM12878	blood:	n/a	n/a
3	CEBPB	chr15:42448766-42448895	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr15:42448796-42448803	HepG2	liver:	n/a	n/a
5	CHD2	chr15:42447101-42447122	GM12878	blood:	n/a	n/a
6	CTCF	chr15:42449050-42449134	LNCaP	prostate:	n/a	chr15:42449074-42449095
7	CTCF	chr15:42448720-42448870	HEEpiC	esophagus:	n/a	n/a
8	CTCF	chr15:42449020-42449170	HBMEC	blood vessel:	n/a	chr15:42449074-42449095
9	CTCF	chr15:42448980-42449130	MCF-7	breast:	n/a	chr15:42449074-42449095
10	CTCF	chr15:42448940-42449090	HCT-116	colon:	n/a	n/a
11	CTCF	chr15:42448960-42449110	HCPEpiC	choroid plexus:	n/a	chr15:42449074-42449095
12	CTCF	chr15:42449060-42449210	HRPEpiC	eye:	n/a	chr15:42449074-42449095
13	CTCF	chr15:42448980-42449130	RPTEC	kidney:	n/a	chr15:42449074-42449095
14	CTCF	chr15:42449020-42449170	SAEC	small airway:	n/a	chr15:42449074-42449095
15	CTCF	chr15:42449000-42449150	HEEpiC	esophagus:	n/a	chr15:42449074-42449095
16	CTCF	chr15:42449080-42449230	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr15:42449046-42449132	Hela-S3	cervix:	n/a	chr15:42449074-42449095
18	CTCF	chr15:42448820-42448970	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr15:42448900-42449050	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr15:42448780-42448930	BE2_C	brain:	n/a	n/a
21	CTCF	chr15:42449000-42449150	HCFaa	heart:	n/a	chr15:42449074-42449095
22	CTCF	chr15:42448940-42449090	HepG2	liver:	n/a	n/a
23	CTCF	chr15:42448880-42449030	GM12871	blood:	n/a	n/a
24	CTCF	chr15:42449072-42449161	H1-hESC	embryonic stem cell:	n/a	chr15:42449074-42449095
25	CTCF	chr15:42449060-42449210	HFF	foreskin:	n/a	chr15:42449074-42449095
26	CTCF	chr15:42448980-42449130	GM12866	blood:	n/a	chr15:42449074-42449095
27	CTCF	chr15:42449000-42449150	HMEC	breast:	n/a	chr15:42449074-42449095
28	CTCF	chr15:42449020-42449170	NHEK	skin:	n/a	chr15:42449074-42449095
29	CTCF	chr15:42448560-42448710	GM12871	blood:	n/a	n/a
30	CTCF	chr15:42448940-42449090	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:42449099-42449100	LNCaP	prostate:	n/a	n/a
32	CTCF	chr15:42448980-42449130	HRE	kidney:	n/a	chr15:42449074-42449095
33	CTCF	chr15:42449056-42449131	NHEK	skin:	n/a	chr15:42449074-42449095
34	CTCF	chr15:42448940-42449090	SAEC	small airway:	n/a	n/a
35	CTCF	chr15:42448940-42449090	RPTEC	kidney:	n/a	n/a
36	E2F6	chr15:42448157-42448438	K562	blood:	n/a	n/a
37	ELF1	chr15:42448762-42449040	K562	blood:	n/a	chr15:42448908-42448921
38	ELF1	chr15:42448036-42448536	MCF-7	breast:	n/a	n/a
39	ELF1	chr15:42447982-42449265	MCF-7	breast:	n/a	chr15:42448908-42448921
40	EP300	chr15:42448122-42448492	T-47D	breast:	n/a	n/a
41	FOS	chr15:42448644-42448653	MCF10A-Er-Src	breast:	n/a	n/a
42	FOXA1	chr15:42448678-42448974	T-47D	breast:	n/a	n/a
43	GATA2	chr15:42448098-42448524	SH-SY5Y	brain:	n/a	chr15:42448301-42448322
44	GATA3	chr15:42447981-42448643	SK-N-SH	brain:	n/a	chr15:42448301-42448322
45	GATA3	chr15:42447857-42449035	MCF-7	breast:	n/a	chr15:42448301-42448322
46	GATA3	chr15:42448109-42448523	SH-SY5Y	brain:	n/a	chr15:42448301-42448322
47	GATA3	chr15:42447932-42448661	SK-N-SH	brain:	n/a	chr15:42448301-42448322
48	GATA3	chr15:42448019-42448464	T-47D	breast:	n/a	chr15:42448301-42448322
49	GATA3	chr15:42447993-42448548	MCF-7	breast:	n/a	chr15:42448301-42448322
50	GATA3	chr15:42448624-42448892	T-47D	breast:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42448786-42448836	Caco-2	colon:	n/a
2	chr15:42447989-42448039	K562	blood:	n/a
3	chr15:42448786-42448836	Caco-2	colon:	n/a
4	chr15:42447989-42448039	K562	blood:	n/a
5	chr15:42448760-42448810	GM12892	blood:	n/a
6	chr15:42448786-42448836	H1-hESC	embryonic stem cell:	embryo
7	chr15:42448786-42448836	HNPCEpiC	eye:	n/a
8	chr15:42448079-42448129	U87	brain:	n/a
9	chr15:42447840-42447890	NT2-D1	testis:	n/a
10	chr15:42448234-42448284	IMR90	lung:	fetal
11	chr15:42448079-42448129	T-47D	breast:	n/a
12	chr15:42448259-42448309	AoSMC	blood vessel:	n/a
13	chr15:42448079-42448129	Jurkat	blood:	n/a
14	chr15:42448259-42448309	RPTEC	kidney:	n/a
15	chr15:42448079-42448129	GM06990	blood:	n/a
16	chr15:42447989-42448039	NT2-D1	testis:	n/a
17	chr15:42448786-42448836	GM19239	blood:	n/a
18	chr15:42449015-42449065	HCPEpiC	choroid plexus:	n/a
19	chr15:42448760-42448810	BE2_C	brain:	n/a
20	chr15:42448079-42448129	AG04449	skin:	fetal
21	chr15:42449015-42449065	AG10803	skin:	n/a
22	chr15:42448786-42448836	HepG2	liver:	n/a
23	chr15:42448234-42448284	HRE	kidney:	n/a
24	chr15:42448234-42448284	SK-N-MC	brain:	n/a
25	chr15:42448786-42448836	A549	lung:	n/a
26	chr15:42447840-42447890	CMK	blood:	n/a
27	chr15:42448259-42448309	Caco-2	colon:	n/a
28	chr15:42448234-42448284	GM12891	blood:	n/a
29	chr15:42449015-42449065	Caco-2	colon:	n/a
30	chr15:42448786-42448836	GM12892	blood:	n/a
31	chr15:42448079-42448129	HAEpiC	amniotic membrane:	n/a
32	chr15:42448259-42448309	HMEC	breast:	n/a
33	chr15:42448259-42448309	SKMC	muscle:	n/a
34	chr15:42448079-42448129	NB4	blood:	n/a
35	chr15:42448760-42448810	GM06990	blood:	n/a
36	chr15:42448786-42448836	HCPEpiC	choroid plexus:	n/a
37	chr15:42449015-42449065	HAEpiC	amniotic membrane:	n/a
38	chr15:42448259-42448309	NB4	blood:	n/a
39	chr15:42448786-42448836	NH-A	brain:	n/a
40	chr15:42447840-42447890	HRCEpiC	kidney:	n/a
41	chr15:42447840-42447890	HMEC	breast:	n/a
42	chr15:42448079-42448129	SK-N-SH	brain:	n/a
43	chr15:42448234-42448284	AoSMC	blood vessel:	n/a
44	chr15:42448259-42448309	HNPCEpiC	eye:	n/a
45	chr15:42448079-42448129	AG04450	lung:	fetal
46	chr15:42448760-42448810	HCT-116	colon:	n/a
47	chr15:42447989-42448039	AoSMC	blood vessel:	n/a
48	chr15:42448234-42448284	GM06990	blood:	n/a
49	chr15:42448079-42448129	AG09309	skin:	n/a
50	chr15:42447840-42447890	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:42444314..42447262-chr15:42447408..42450681,4	K562	blood:
2	chr15:42448110..42450231-chr15:42456166..42458018,2	MCF-7	breast:
3	chr15:42445910..42447999-chr15:42452272..42454986,2	K562	blood:
4	chr15:42440587..42442217-chr15:42443778..42446321,2	K562	blood:
5	chr15:42444865..42447535-chr15:42448992..42450632,2	K562	blood:
6	chr15:42375390..42378323-chr15:42449253..42451439,2	K562	blood:
7	chr15:42429960..42432547-chr15:42445427..42447652,2	MCF-7	breast:
8	chr15:42444865..42447535-chr15:42448992..42450632,2	K562	blood:

No data

Variant related genes	Relation type
PLA2G4F	TF binding region
PLA2G4F	CpG island
ENSG00000159337	chromatin interactions
ENSG00000168907	chromatin interactions
ENSG00000166887	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564468970	chr15:42445178-42445179	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs368848524	chr15:42445226-42445227	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532344990	chr15:42445284-42445285	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546038588	chr15:42445305-42445306	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562545766	chr15:42445346-42445347	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372900178	chr15:42445389-42445390	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201932217	chr15:42445441-42445442	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367612077	chr15:42445452-42445453	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371552729	chr15:42445454-42445455	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375970891	chr15:42445455-42445456	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs370070222	chr15:42445460-42445461	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200401032	chr15:42445473-42445474	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531508290	chr15:42445474-42445475	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201701552	chr15:42445484-42445485	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs373285044	chr15:42445515-42445516	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10220859	chr15:42445554-42445555	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs201218709	chr15:42445573-42445574	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114912604	chr15:42445575-42445576	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138404001	chr15:42445585-42445586	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570383489	chr15:42445593-42445594	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112858254	chr15:42445621-42445622	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1703754	chr15:42445654-42445655	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs570169225	chr15:42445662-42445663	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs681029	chr15:42445679-42445680	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs377755144	chr15:42445695-42445696	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs624841	chr15:42445724-42445725	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs373028006	chr15:42445771-42445772	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371489882	chr15:42445779-42445780	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374304057	chr15:42445793-42445794	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115750855	chr15:42445797-42445798	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200114279	chr15:42445806-42445807	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140734223	chr15:42445827-42445828	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534770676	chr15:42445835-42445836	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577924021	chr15:42445839-42445840	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375021460	chr15:42445854-42445855	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545802488	chr15:42445856-42445857	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150082965	chr15:42445860-42445861	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562769081	chr15:42445868-42445869	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531488177	chr15:42445869-42445870	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs369203056	chr15:42445878-42445879	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561544535	chr15:42445887-42445888	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527391396	chr15:42445904-42445905	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547040207	chr15:42445917-42445918	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200036658	chr15:42445931-42445932	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561683579	chr15:42445970-42445971	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139967658	chr15:42445980-42445981	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs1624183	chr15:42445987-42445988	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570354542	chr15:42446015-42446016	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536152073	chr15:42446029-42446030	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76841924	chr15:42446034-42446035	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42436000-42452000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:42439400-42451200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr15:42439400-42451800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr15:42439600-42448600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr15:42441200-42450600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr15:42441600-42446200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr15:42441800-42451000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr15:42442600-42447000	Enhancers	Esophagus	oesophagus
9	chr15:42442600-42447400	Weak transcription	Spleen	Spleen
10	chr15:42442800-42445400	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:42443000-42445600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:42443400-42445200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr15:42443400-42445400	Enhancers	Fetal Muscle Trunk	muscle
14	chr15:42443400-42447600	Enhancers	Gastric	stomach
15	chr15:42443600-42445800	Enhancers	Left Ventricle	heart
16	chr15:42443600-42445800	Enhancers	Lung	lung
17	chr15:42443600-42445800	Enhancers	Psoas Muscle	Psoas
18	chr15:42443600-42447000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr15:42443600-42447600	Enhancers	Colonic Mucosa	Colon
20	chr15:42443800-42446400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr15:42443800-42448000	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr15:42444000-42451600	Weak transcription	HUVEC	blood vessel
23	chr15:42444200-42445400	Enhancers	Right Atrium	heart
24	chr15:42444200-42445800	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr15:42444400-42446400	Strong transcription	Fetal Intestine Small	intestine
26	chr15:42444400-42446600	Weak transcription	Fetal Thymus	thymus
27	chr15:42444400-42447000	Weak transcription	Fetal Kidney	kidney
28	chr15:42444400-42450400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr15:42444600-42445200	Bivalent Enhancer	Stomach Mucosa	stomach
30	chr15:42444600-42445600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:42444600-42448200	Weak transcription	HSMMtube	muscle
32	chr15:42444600-42450200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr15:42444800-42446600	Weak transcription	Fetal Muscle Leg	muscle
34	chr15:42444800-42447000	Weak transcription	Fetal Lung	lung
35	chr15:42444800-42449800	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr15:42444800-42450200	Weak transcription	Brain Substantia Nigra	brain
37	chr15:42444800-42450200	Weak transcription	HSMM	muscle
38	chr15:42444800-42450600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:42444800-42450600	Weak transcription	Brain Germinal Matrix	brain
40	chr15:42444800-42451000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:42444800-42451000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr15:42444800-42451200	Weak transcription	Aorta	Aorta
43	chr15:42445000-42445200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr15:42445000-42446000	Weak transcription	Right Ventricle	heart
45	chr15:42445000-42446400	Weak transcription	HMEC	breast
46	chr15:42445000-42446600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:42445000-42446600	Weak transcription	Fetal Heart	heart
48	chr15:42445000-42446600	Weak transcription	NHEK	skin
49	chr15:42445000-42449800	Weak transcription	Brain Anterior Caudate	brain
50	chr15:42445000-42450000	Weak transcription	Brain Cingulate Gyrus	brain

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