Variant report

Variant	esv3312195
Chromosome Location	chr15:41868660-41873158
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:41873116-41873682	A549	lung:	n/a	chr15:41873437-41873450
2	CTCF	chr15:41870340-41870399	GM19239	blood:	n/a	n/a
3	CTCF	chr15:41870380-41870530	GM12874	blood:	n/a	n/a
4	CTCF	chr15:41873106-41873723	SK-N-SH	brain:	n/a	chr15:41873437-41873450 chr15:41873677-41873685
5	MYC	chr15:41870308-41870377	MCF-7	breast:	n/a	n/a
6	PBX3	chr15:41868751-41868892	GM12878	blood:	n/a	n/a
7	POLR2A	chr15:41870239-41870595	MCF-7	breast:	n/a	n/a
8	POLR2A	chr15:41870458-41870492	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr15:41870695-41870959	MCF-7	breast:	n/a	n/a
10	POLR2A	chr15:41870517-41870539	MCF-7	breast:	n/a	n/a
11	POLR2A	chr15:41870250-41870459	MCF-7	breast:	n/a	n/a
12	POLR2A	chr15:41869632-41869717	HepG2	liver:	n/a	n/a
13	POLR2A	chr15:41870705-41871005	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr15:41872230-41872316	K562	blood:	n/a	n/a
15	POLR2A	chr15:41870965-41871236	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr15:41870286-41870398	MCF-7	breast:	n/a	n/a
17	POLR2A	chr15:41872855-41873586	HepG2	liver:	n/a	n/a
18	POLR2A	chr15:41870818-41870822	K562	blood:	n/a	n/a
19	POLR2A	chr15:41870937-41870978	K562	blood:	n/a	n/a
20	POLR2A	chr15:41870427-41871087	K562	blood:	n/a	n/a
21	POLR2A	chr15:41871641-41871694	K562	blood:	n/a	n/a
22	POLR2A	chr15:41870557-41870569	MCF-7	breast:	n/a	n/a
23	POLR2A	chr15:41871314-41871412	K562	blood:	n/a	n/a
24	POLR2A	chr15:41872014-41872031	K562	blood:	n/a	n/a
25	POLR2A	chr15:41870687-41870697	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr15:41870262-41870434	Gliobla	brain:	n/a	n/a
27	POLR2A	chr15:41872427-41872675	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr15:41870515-41870516	MCF-7	breast:	n/a	n/a
29	POLR2A	chr15:41870527-41870550	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr15:41872386-41872448	K562	blood:	n/a	n/a
31	POLR2A	chr15:41871009-41871019	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr15:41871042-41871135	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr15:41870637-41870955	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr15:41870573-41870780	K562	blood:	n/a	n/a
35	POLR2A	chr15:41870343-41870589	K562	blood:	n/a	n/a
36	POLR2A	chr15:41870342-41870366	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr15:41871139-41871185	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr15:41872327-41872351	K562	blood:	n/a	n/a
39	POLR2A	chr15:41870225-41870461	HepG2	liver:	n/a	n/a
40	POLR2A	chr15:41870188-41870439	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr15:41871669-41871775	HepG2	liver:	n/a	n/a
42	POLR2A	chr15:41872465-41872680	HepG2	liver:	n/a	n/a
43	POLR2A	chr15:41869846-41869877	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr15:41872991-41872996	K562	blood:	n/a	n/a
45	POLR2A	chr15:41870731-41871723	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr15:41872287-41872428	K562	blood:	n/a	n/a
47	POLR2A	chr15:41870496-41870503	H1-hESC	embryonic stem cell:	n/a	n/a
48	RAD21	chr15:41873121-41873728	H1-hESC	embryonic stem cell:	n/a	n/a
49	RAD21	chr15:41873117-41873746	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41871084-41871134	IMR90	lung:	fetal
2	chr15:41871084-41871134	GM12891	blood:	n/a
3	chr15:41871084-41871134	HMEC	breast:	n/a
4	chr15:41871084-41871134	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:41871084-41871134	MCF-7	breast:	n/a
6	chr15:41871084-41871134	RPTEC	kidney:	n/a
7	chr15:41871084-41871134	SK-N-MC	brain:	n/a
8	chr15:41871084-41871134	PrEC	prostate:	n/a
9	chr15:41871084-41871134	AoSMC	blood vessel:	n/a
10	chr15:41871084-41871134	SK-N-SH_RA	brain:	n/a
11	chr15:41871084-41871134	BE2_C	brain:	n/a
12	chr15:41871084-41871134	AG04449	skin:	fetal
13	chr15:41871084-41871134	HEK293	kidney:	embryo
14	chr15:41871084-41871134	HRCEpiC	kidney:	n/a
15	chr15:41871084-41871134	HRPEpiC	eye:	n/a
16	chr15:41871084-41871134	NT2-D1	testis:	n/a
17	chr15:41871084-41871134	HNPCEpiC	eye:	n/a
18	chr15:41871084-41871134	HUVEC	blood vessel:	n/a
19	chr15:41871084-41871134	NHBE	bronchial:	n/a
20	chr15:41871084-41871134	A549	lung:	n/a
21	chr15:41871084-41871134	HEEpiC	esophagus:	n/a
22	chr15:41871084-41871134	SKMC	muscle:	n/a
23	chr15:41871084-41871134	SAEC	small airway:	n/a
24	chr15:41871084-41871134	MCF10A-Er-Src	breast:	n/a
25	chr15:41871084-41871134	K562	blood:	n/a
26	chr15:41871084-41871134	GM19239	blood:	n/a
27	chr15:41871084-41871134	HCM	heart:	n/a
28	chr15:41871084-41871134	ECC-1	luminal epithelium:	n/a
29	chr15:41871084-41871134	HepG2	liver:	n/a
30	chr15:41871084-41871134	HCF	heart:	n/a
31	chr15:41871084-41871134	T-47D	breast:	n/a
32	chr15:41871084-41871134	GM12878	blood:	n/a
33	chr15:41871084-41871134	HL-60	blood:	n/a
34	chr15:41871084-41871134	NB4	blood:	n/a
35	chr15:41871084-41871134	AG09309	skin:	n/a
36	chr15:41871084-41871134	NH-A	brain:	n/a
37	chr15:41871084-41871134	NHDF-neo	bronchial:	n/a
38	chr15:41871084-41871134	H1-hESC	embryonic stem cell:	embryo
39	chr15:41871084-41871134	Hela-S3	cervix:	n/a
40	chr15:41871084-41871134	Jurkat	blood:	n/a
41	chr15:41871084-41871134	HRE	kidney:	n/a
42	chr15:41871084-41871134	GM12892	blood:	n/a
43	chr15:41871084-41871134	HCPEpiC	choroid plexus:	n/a
44	chr15:41871084-41871134	ProgFib	skin:	n/a
45	chr15:41871084-41871134	HIPEpiC	eye:	n/a
46	chr15:41871084-41871134	SK-N-SH	brain:	n/a
47	chr15:41871084-41871134	Hepatocyte	liver:	n/a
48	chr15:41871084-41871134	AG09319	gingival:	n/a
49	chr15:41871084-41871134	ovcar-3	ovarian:	n/a
50	chr15:41871084-41871134	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr15:41870467..41873632-chr15:41874350..41878118,3	K562	blood:
2	chr15:41870694..41874947-chr15:41876174..41878118,3	K562	blood:
3	chr15:41836227..41837993-chr15:41866817..41868834,2	K562	blood:
4	chr15:41861308..41862926-chr15:41869698..41872291,2	K562	blood:

No data

Variant related genes	Relation type
TYRO3	TF binding region
TYRO3	CpG island
ENSG00000103932	chromatin interactions
ENSG00000092445	chromatin interactions

Extended variants
information (count: 170 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:170 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557735578	chr15:41868697-41868698	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541198887	chr15:41868722-41868723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551494514	chr15:41868768-41868769	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571582139	chr15:41868779-41868780	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537168339	chr15:41868795-41868796	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs551070471	chr15:41868804-41868805	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569899200	chr15:41868833-41868834	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs141088050	chr15:41868834-41868835	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs8039228	chr15:41868867-41868868	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs57151483	chr15:41868868-41868869	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs59152322	chr15:41868869-41868870	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs77314087	chr15:41868876-41868877	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs76821374	chr15:41868878-41868879	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs80253138	chr15:41868879-41868880	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs74432857	chr15:41868880-41868881	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561849224	chr15:41868911-41868912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555556963	chr15:41869006-41869007	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146932714	chr15:41869018-41869019	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35102460	chr15:41869031-41869032	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550769865	chr15:41869051-41869052	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534887126	chr15:41869059-41869060	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2588325	chr15:41869097-41869098	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs28657602	chr15:41869162-41869163	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs543188152	chr15:41869188-41869189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563036875	chr15:41869228-41869229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551301272	chr15:41869230-41869231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570506903	chr15:41869279-41869280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147628350	chr15:41869388-41869389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28508151	chr15:41869423-41869424	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs368545497	chr15:41869517-41869518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142313007	chr15:41869519-41869520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1200342	chr15:41869545-41869546	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565161252	chr15:41869580-41869581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1200343	chr15:41869583-41869584	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs551133903	chr15:41869584-41869585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149304196	chr15:41869600-41869601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535644413	chr15:41869624-41869625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530178870	chr15:41869764-41869765	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549215850	chr15:41869775-41869776	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565841682	chr15:41869776-41869777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs534640324	chr15:41869777-41869778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs558016741	chr15:41869789-41869790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143273304	chr15:41869858-41869859	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557591433	chr15:41869909-41869910	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556491262	chr15:41869930-41869931	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533323226	chr15:41869931-41869932	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575967641	chr15:41869935-41869936	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540277049	chr15:41869947-41869948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573361014	chr15:41869953-41869954	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201903073	chr15:41870009-41870010	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41852200-41877400	Weak transcription	Aorta	Aorta
2	chr15:41852400-41877200	Weak transcription	Colon Smooth Muscle	Colon
3	chr15:41852600-41877400	Weak transcription	HMEC	breast
4	chr15:41852800-41877400	Weak transcription	NHEK	skin
5	chr15:41853200-41872600	Weak transcription	Hela-S3	cervix
6	chr15:41853400-41870600	Weak transcription	Stomach Mucosa	stomach
7	chr15:41854000-41871400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:41854200-41877000	Weak transcription	Fetal Brain Male	brain
9	chr15:41855400-41877000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr15:41855400-41877200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:41859000-41869000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:41860800-41871800	Strong transcription	Brain Germinal Matrix	brain
13	chr15:41861000-41877200	Weak transcription	HUVEC	blood vessel
14	chr15:41861200-41870000	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr15:41861200-41870000	Weak transcription	HSMMtube	muscle
16	chr15:41861200-41871200	Weak transcription	Small Intestine	intestine
17	chr15:41861200-41877000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr15:41861400-41870000	Strong transcription	Fetal Muscle Leg	muscle
19	chr15:41861400-41870400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr15:41861400-41870400	Strong transcription	Fetal Stomach	stomach
21	chr15:41861400-41870600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr15:41861400-41870600	Strong transcription	Fetal Muscle Trunk	muscle
23	chr15:41861400-41870800	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr15:41861400-41871000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:41861400-41871400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr15:41861400-41871400	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr15:41861400-41873200	Weak transcription	K562	blood
28	chr15:41861600-41871400	Strong transcription	H9 Cell Line	embryonic stem cell
29	chr15:41861600-41871400	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:41861800-41870000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:41861800-41870200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr15:41861800-41870200	Strong transcription	Spleen	Spleen
33	chr15:41861800-41871000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:41861800-41871000	Strong transcription	Fetal Intestine Large	intestine
35	chr15:41862000-41870400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:41862000-41870600	Strong transcription	H1 Cell Line	embryonic stem cell
37	chr15:41862000-41870800	Strong transcription	Fetal Intestine Small	intestine
38	chr15:41862000-41871200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:41862200-41870800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr15:41862400-41870600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr15:41863000-41871400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr15:41863200-41869000	Strong transcription	Ovary	ovary
43	chr15:41863200-41871200	Strong transcription	Fetal Brain Female	brain
44	chr15:41863800-41873000	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr15:41864200-41877000	Weak transcription	Fetal Kidney	kidney
46	chr15:41864800-41870000	Strong transcription	Brain Angular Gyrus	brain
47	chr15:41865800-41877000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr15:41865800-41877000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr15:41865800-41877200	Weak transcription	NHLF	lung
50	chr15:41866800-41870800	Weak transcription	Fetal Lung	lung

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