Variant report

Variant	esv2763096
Chromosome Location	chr15:42989603-43009399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:297)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43000560-43000618	K562	blood:	n/a	n/a
2	ARID3A	chr15:43008561-43008586	HepG2	liver:	n/a	n/a
3	BACH1	chr15:42999321-42999521	K562	blood:	n/a	n/a
4	CEBPB	chr15:43006909-43007151	IMR90	lung:	n/a	chr15:43007037-43007048
5	CEBPB	chr15:42991266-42991507	A549	lung:	n/a	chr15:42991439-42991450
6	CEBPB	chr15:43006914-43007205	HepG2	liver:	n/a	chr15:43007037-43007048
7	CEBPB	chr15:42996684-42996880	A549	lung:	n/a	n/a
8	CEBPB	chr15:42991253-42991568	IMR90	lung:	n/a	chr15:42991439-42991450
9	CEBPB	chr15:42991282-42991562	HepG2	liver:	n/a	chr15:42991439-42991450
10	CEBPB	chr15:42991244-42991562	K562	blood:	n/a	chr15:42991439-42991450
11	CEBPB	chr15:42991299-42991445	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr15:42996680-42996830	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr15:42996720-42996870	GM12875	blood:	n/a	n/a
14	CTCF	chr15:42996700-42996850	HPF	lung:	n/a	n/a
15	CTCF	chr15:42997060-42997210	HMEC	breast:	n/a	n/a
16	CTCF	chr15:42996634-42996935	GM12878	blood:	n/a	n/a
17	CTCF	chr15:42996680-42996830	GM12878	blood:	n/a	n/a
18	CTCF	chr15:42996680-42996830	BJ	skin:	n/a	n/a
19	CTCF	chr15:42996700-42996850	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr15:42996656-42996909	MCF-7	breast:	n/a	n/a
21	CTCF	chr15:42996680-42996830	HAc	cerebellar:	n/a	n/a
22	CTCF	chr15:42996680-42996902	GM19239	blood:	n/a	n/a
23	CTCF	chr15:42996617-42996955	A549	lung:	n/a	n/a
24	CTCF	chr15:42996680-42996830	HL-60	blood:	n/a	n/a
25	CTCF	chr15:42996660-42996930	GM19238	blood:	n/a	n/a
26	CTCF	chr15:42996580-42996980	HepG2	liver:	n/a	n/a
27	CTCF	chr15:42996659-42996869	A549	lung:	n/a	n/a
28	CTCF	chr15:42996487-42997009	HCT-116	colon:	n/a	n/a
29	CTCF	chr15:42996680-42996830	RPTEC	kidney:	n/a	n/a
30	CTCF	chr15:42996680-42996830	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr15:42997120-42997270	GM12872	blood:	n/a	n/a
32	CTCF	chr15:42996645-42996899	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr15:42996700-42996850	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr15:42996700-42996850	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr15:42996700-42996850	GM12873	blood:	n/a	n/a
36	CTCF	chr15:42996720-42996870	HMEC	breast:	n/a	n/a
37	CTCF	chr15:42996700-42996850	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr15:42996720-42996870	NHLF	lung:	n/a	n/a
39	CTCF	chr15:42996700-42996850	AG09319	gingival:	n/a	n/a
40	CTCF	chr15:42996700-42996850	GM12875	blood:	n/a	n/a
41	CTCF	chr15:42996651-42996923	A549	lung:	n/a	n/a
42	CTCF	chr15:42996650-42996890	GM10266	blood:	n/a	n/a
43	CTCF	chr15:42996634-42996940	MCF-7	breast:	n/a	n/a
44	CTCF	chr15:42996631-42996924	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr15:42996570-42997033	K562	blood:	n/a	n/a
46	CTCF	chr15:42996660-42996810	HAc	cerebellar:	n/a	n/a
47	CTCF	chr15:42996700-42996850	NHEK	skin:	n/a	n/a
48	CTCF	chr15:42996643-42996881	ECC-1	luminal epithelium:	n/a	n/a
49	CTCF	chr15:42996597-42996950	K562	blood:	n/a	n/a
50	CTCF	chr15:42996683-42996912	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43008690-43008740	Caco-2	colon:	n/a
2	chr15:43008690-43008740	PANC-1	pancreas:	n/a
3	chr15:43008690-43008740	AG09319	gingival:	n/a
4	chr15:43008690-43008740	RPTEC	kidney:	n/a
5	chr15:43008690-43008740	NB4	blood:	n/a
6	chr15:43008690-43008740	AoSMC	blood vessel:	n/a
7	chr15:43008690-43008740	ECC-1	luminal epithelium:	n/a
8	chr15:43008690-43008740	PFSK-1	brain:	n/a
9	chr15:43008690-43008740	HepG2	liver:	n/a
10	chr15:43008690-43008740	HCF	heart:	n/a
11	chr15:43008690-43008740	MCF10A-Er-Src	breast:	n/a
12	chr15:43008690-43008740	NHBE	bronchial:	n/a
13	chr15:43008690-43008740	AG04449	skin:	fetal
14	chr15:43008690-43008740	HNPCEpiC	eye:	n/a
15	chr15:43008690-43008740	Jurkat	blood:	n/a
16	chr15:43008690-43008740	NHDF-neo	bronchial:	n/a
17	chr15:43008690-43008740	BE2_C	brain:	n/a
18	chr15:43008690-43008740	ovcar-3	ovarian:	n/a
19	chr15:43008690-43008740	SK-N-SH_RA	brain:	n/a
20	chr15:43008690-43008740	HMEC	breast:	n/a
21	chr15:43008690-43008740	HEK293	kidney:	embryo
22	chr15:43008690-43008740	H1-hESC	embryonic stem cell:	embryo
23	chr15:43008690-43008740	GM12878	blood:	n/a
24	chr15:43008690-43008740	HCT-116	colon:	n/a
25	chr15:43008690-43008740	GM12892	blood:	n/a
26	chr15:43008690-43008740	GM06990	blood:	n/a
27	chr15:43008690-43008740	U87	brain:	n/a
28	chr15:43008690-43008740	SAEC	small airway:	n/a
29	chr15:43008690-43008740	AG10803	skin:	n/a
30	chr15:43008690-43008740	HRPEpiC	eye:	n/a
31	chr15:43008690-43008740	HAEpiC	amniotic membrane:	n/a
32	chr15:43008690-43008740	CMK	blood:	n/a
33	chr15:43008690-43008740	GM12891	blood:	n/a
34	chr15:43008690-43008740	A549	lung:	n/a
35	chr15:43008690-43008740	ProgFib	skin:	n/a
36	chr15:43008690-43008740	HEEpiC	esophagus:	n/a
37	chr15:43008690-43008740	IMR90	lung:	fetal
38	chr15:43008690-43008740	HCPEpiC	choroid plexus:	n/a
39	chr15:43008690-43008740	HRE	kidney:	n/a
40	chr15:43008690-43008740	SKMC	muscle:	n/a
41	chr15:43008690-43008740	HRCEpiC	kidney:	n/a
42	chr15:43008690-43008740	HPAEpiC	pulmonary alveolar:	n/a
43	chr15:43008690-43008740	HL-60	blood:	n/a
44	chr15:43008690-43008740	SK-N-SH	brain:	n/a
45	chr15:43008690-43008740	PrEC	prostate:	n/a
46	chr15:43008690-43008740	MCF-7	breast:	n/a
47	chr15:43008690-43008740	AG04450	lung:	fetal
48	chr15:43008690-43008740	K562	blood:	n/a
49	chr15:43008690-43008740	Hela-S3	cervix:	n/a
50	chr15:43008690-43008740	T-47D	breast:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:42996644..42997222-chr15:43014554..43015613,3	MCF-7	breast:
2	chr15:43004420..43008133-chr15:43008696..43011545,3	K562	blood:
3	chr15:42996634..42997289-chr15:43496048..43497151,3	MCF-7	breast:
4	chr15:43002992..43005620-chr15:43005783..43008129,2	K562	blood:
5	chr15:43002992..43005620-chr15:43005783..43008129,2	K562	blood:
6	chr15:42996049..42999040-chr15:43025539..43027255,2	K562	blood:
7	chr15:43007397..43009798-chr15:43011681..43013458,2	MCF-7	breast:
8	chr15:43004420..43008133-chr15:43008696..43011545,3	K562	blood:
9	chr15:42996313..42997182-chr15:43218578..43219161,2	MCF-7	breast:
10	chr15:42996508..42997091-chr15:43015306..43015832,2	MCF-7	breast:
11	chr15:43007694..43010580-chr15:43015984..43019053,4	K562	blood:
12	chr15:43005044..43007388-chr15:43020446..43022660,2	K562	blood:
13	chr15:42983549..42985784-chr15:42989459..42991340,2	K562	blood:
14	chr15:42996321..42997267-chr15:43577508..43578431,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000239025	TF binding region
ENSG00000239025	CpG island
ENSG00000140326	chromatin interactions

Extended variants
information (count: 791 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548289854	chr15:42989625-42989626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554569698	chr15:42989645-42989646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557732887	chr15:42989655-42989656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182392365	chr15:42989697-42989698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543548830	chr15:42989717-42989718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563535732	chr15:42989764-42989765	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574177594	chr15:42989794-42989795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543287618	chr15:42989830-42989831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185430926	chr15:42989839-42989840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528787521	chr15:42989849-42989850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551357404	chr15:42989884-42989885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1877136	chr15:42989885-42989886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190287691	chr15:42989886-42989887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563110880	chr15:42989890-42989891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs151023573	chr15:42989908-42989909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567440386	chr15:42989909-42989910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116318862	chr15:42989917-42989918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182475636	chr15:42989988-42989989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566602526	chr15:42990005-42990006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34029692	chr15:42990006-42990007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35841211	chr15:42990022-42990023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76506589	chr15:42990064-42990065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557720612	chr15:42990077-42990078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78081991	chr15:42990078-42990079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537124746	chr15:42990081-42990082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563878953	chr15:42990098-42990099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528267195	chr15:42990112-42990113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543084498	chr15:42990117-42990118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557206444	chr15:42990153-42990154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574092882	chr15:42990168-42990169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542810182	chr15:42990200-42990201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559908416	chr15:42990228-42990229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78278998	chr15:42990231-42990232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78831432	chr15:42990232-42990233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573451268	chr15:42990243-42990244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113077367	chr15:42990258-42990259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545764721	chr15:42990318-42990319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187995678	chr15:42990326-42990327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530556614	chr15:42990344-42990345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546341416	chr15:42990351-42990352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193028695	chr15:42990352-42990353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560794370	chr15:42990372-42990373	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2136899	chr15:42990386-42990387	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs535352166	chr15:42990423-42990424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145878659	chr15:42990441-42990442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34560601	chr15:42990471-42990472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566698378	chr15:42990488-42990489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368106199	chr15:42990555-42990556	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35759000	chr15:42990569-42990570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538541542	chr15:42990575-42990576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Renal cell carcinoma	18765545	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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42908800-43015000	Weak transcription	Fetal Kidney	kidney
2	chr15:42949800-42999200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr15:42950400-42990200	Strong transcription	Fetal Stomach	stomach
4	chr15:42951000-42995000	Strong transcription	Fetal Muscle Trunk	muscle
5	chr15:42952600-42995600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:42952800-42996000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr15:42953400-42992200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:42955000-42990200	Strong transcription	Fetal Muscle Leg	muscle
9	chr15:42961400-42990800	Strong transcription	Colon Smooth Muscle	Colon
10	chr15:42966000-42992800	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:42968400-42992200	Weak transcription	Fetal Brain Male	brain
12	chr15:42968600-42996800	Weak transcription	Liver	Liver
13	chr15:42968600-42999000	Weak transcription	HUVEC	blood vessel
14	chr15:42970600-42990200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:42971400-42992600	Strong transcription	Adipose Nuclei	Adipose
16	chr15:42971600-42992400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:42973200-42991200	Strong transcription	Brain Germinal Matrix	brain
18	chr15:42973600-42992600	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr15:42975600-43011400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:42976600-42990400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr15:42976600-42992200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr15:42976600-42996800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr15:42976600-43015200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr15:42977000-42999400	Weak transcription	HepG2	liver
25	chr15:42977000-43011600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr15:42977000-43016600	Weak transcription	Hela-S3	cervix
27	chr15:42978200-42989800	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr15:42978200-42996800	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr15:42978200-43010400	Weak transcription	Thymus	Thymus
30	chr15:42978400-42991000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr15:42978600-42992400	Weak transcription	Small Intestine	intestine
32	chr15:42978800-43012000	Weak transcription	NH-A	brain
33	chr15:42979000-42992600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:42979200-42992400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr15:42979200-43011000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr15:42979600-43010000	Weak transcription	GM12878-XiMat	blood
37	chr15:42979800-43010600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr15:42980200-43002800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr15:42980400-43010400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr15:42980800-42992400	Weak transcription	Fetal Heart	heart
41	chr15:42981400-42999400	Weak transcription	HMEC	breast
42	chr15:42981400-43015000	Weak transcription	HSMM	muscle
43	chr15:42981600-42999400	Weak transcription	NHEK	skin
44	chr15:42981600-43009800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr15:42981600-43011000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr15:42981800-43010000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr15:42982000-42999400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr15:42983600-42989800	Strong transcription	Right Ventricle	heart
49	chr15:42983800-42990400	Strong transcription	Fetal Brain Female	brain
50	chr15:42984000-42995800	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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