Variant report

Variant	nsv974564
Chromosome Location	chr15:43092730-43095751
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:166)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:166 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:43093350-43093482	SK-N-SH_RA	brain:	n/a	n/a
2	CTCF	chr15:43093360-43093510	HPAF	blood vessel:	n/a	n/a
3	CTCF	chr15:43093311-43093651	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr15:43093040-43093190	HEEpiC	esophagus:	n/a	n/a
5	CTCF	chr15:43093300-43093450	HCT-116	colon:	n/a	n/a
6	CTCF	chr15:43093320-43093470	AG09319	gingival:	n/a	n/a
7	CTCF	chr15:43093480-43093630	HCT-116	colon:	n/a	n/a
8	CTCF	chr15:43093372-43093522	GM19239	blood:	n/a	n/a
9	CTCF	chr15:43093300-43093450	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr15:43093377-43093523	Pancreas_OC	pancreas:	n/a	n/a
11	CTCF	chr15:43093300-43093450	GM12874	blood:	n/a	n/a
12	CTCF	chr15:43093320-43093470	GM12872	blood:	n/a	n/a
13	CTCF	chr15:43093346-43093556	GM12878	blood:	n/a	n/a
14	CTCF	chr15:43093060-43093210	GM12872	blood:	n/a	n/a
15	CTCF	chr15:43093340-43093490	A549	lung:	n/a	n/a
16	CTCF	chr15:43093334-43093563	A549	lung:	n/a	n/a
17	CTCF	chr15:43093360-43093510	AG09319	gingival:	n/a	n/a
18	CTCF	chr15:43093343-43093535	GM19240	blood:	n/a	n/a
19	CTCF	chr15:43093305-43093581	MCF-7	breast:	n/a	n/a
20	CTCF	chr15:43093349-43093576	NHEK	skin:	n/a	n/a
21	CTCF	chr15:43093232-43093624	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr15:43093340-43093490	HCT-116	colon:	n/a	n/a
23	CTCF	chr15:43093320-43093470	GM06990	blood:	n/a	n/a
24	CTCF	chr15:43093306-43093586	HepG2	liver:	n/a	n/a
25	CTCF	chr15:43093400-43093550	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr15:43093323-43093556	K562	blood:	n/a	n/a
27	CTCF	chr15:43093320-43093470	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr15:43093159-43093232	GM12891	blood:	n/a	n/a
29	CTCF	chr15:43093320-43093470	HepG2	liver:	n/a	n/a
30	CTCF	chr15:43093320-43093470	BJ	skin:	n/a	n/a
31	CTCF	chr15:43093324-43093586	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:43093380-43093530	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr15:43093339-43093559	GM13977	blood:	n/a	n/a
34	CTCF	chr15:43093145-43093185	MCF-7	breast:	n/a	n/a
35	CTCF	chr15:43093287-43093586	GM19238	blood:	n/a	n/a
36	CTCF	chr15:43093312-43093592	A549	lung:	n/a	n/a
37	CTCF	chr15:43093320-43093470	HEK293	kidney:	n/a	n/a
38	CTCF	chr15:43093360-43093510	GM12873	blood:	n/a	n/a
39	CTCF	chr15:43093340-43093490	HMF	breast:	n/a	n/a
40	CTCF	chr15:43093340-43093490	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr15:43093320-43093470	HCFaa	heart:	n/a	n/a
42	CTCF	chr15:43093380-43093530	AG04449	skin:	n/a	n/a
43	CTCF	chr15:43092920-43093070	GM12866	blood:	n/a	n/a
44	CTCF	chr15:43093360-43093510	K562	blood:	n/a	n/a
45	CTCF	chr15:43093340-43093490	GM12868	blood:	n/a	n/a
46	CTCF	chr15:43093380-43093530	GM12878	blood:	n/a	n/a
47	CTCF	chr15:43093300-43093450	K562	blood:	n/a	n/a
48	CTCF	chr15:43093380-43093530	GM12866	blood:	n/a	n/a
49	CTCF	chr15:43093720-43093870	HepG2	liver:	n/a	n/a
50	CTCF	chr15:43093520-43093670	HFF-Myc	foreskin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43094585-43094635	MCF10A-Er-Src	breast:	n/a
2	chr15:43094585-43094635	K562	blood:	n/a
3	chr15:43094585-43094635	SKMC	muscle:	n/a
4	chr15:43094585-43094635	SK-N-MC	brain:	n/a
5	chr15:43094585-43094635	ProgFib	skin:	n/a
6	chr15:43094585-43094635	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:43094585-43094635	HCF	heart:	n/a
8	chr15:43094585-43094635	GM06990	blood:	n/a
9	chr15:43094585-43094635	NB4	blood:	n/a
10	chr15:43094585-43094635	A549	lung:	n/a
11	chr15:43094585-43094635	HCM	heart:	n/a
12	chr15:43094585-43094635	SAEC	small airway:	n/a
13	chr15:43094585-43094635	ECC-1	luminal epithelium:	n/a
14	chr15:43094585-43094635	IMR90	lung:	fetal
15	chr15:43094585-43094635	HepG2	liver:	n/a
16	chr15:43094585-43094635	CMK	blood:	n/a
17	chr15:43094585-43094635	SK-N-SH	brain:	n/a
18	chr15:43094585-43094635	AG04450	lung:	fetal
19	chr15:43094585-43094635	PrEC	prostate:	n/a
20	chr15:43094585-43094635	SK-N-SH_RA	brain:	n/a
21	chr15:43094585-43094635	HCT-116	colon:	n/a
22	chr15:43094585-43094635	GM12891	blood:	n/a
23	chr15:43094585-43094635	PANC-1	pancreas:	n/a
24	chr15:43094585-43094635	U87	brain:	n/a
25	chr15:43094585-43094635	H1-hESC	embryonic stem cell:	embryo
26	chr15:43094585-43094635	GM12892	blood:	n/a
27	chr15:43094585-43094635	HRCEpiC	kidney:	n/a
28	chr15:43094585-43094635	BJ	skin:	n/a
29	chr15:43094585-43094635	AoSMC	blood vessel:	n/a
30	chr15:43094585-43094635	Hela-S3	cervix:	n/a
31	chr15:43094585-43094635	HEK293	kidney:	embryo
32	chr15:43094585-43094635	AG09309	skin:	n/a
33	chr15:43094585-43094635	AG09319	gingival:	n/a
34	chr15:43094585-43094635	BE2_C	brain:	n/a
35	chr15:43094585-43094635	NHBE	bronchial:	n/a
36	chr15:43094585-43094635	HCPEpiC	choroid plexus:	n/a
37	chr15:43094585-43094635	HIPEpiC	eye:	n/a
38	chr15:43094585-43094635	GM19239	blood:	n/a
39	chr15:43094585-43094635	Hepatocyte	liver:	n/a
40	chr15:43094585-43094635	NH-A	brain:	n/a
41	chr15:43094585-43094635	HRPEpiC	eye:	n/a
42	chr15:43094585-43094635	NHDF-neo	bronchial:	n/a
43	chr15:43094585-43094635	HRE	kidney:	n/a
44	chr15:43094585-43094635	HAEpiC	amniotic membrane:	n/a
45	chr15:43094585-43094635	RPTEC	kidney:	n/a
46	chr15:43094585-43094635	GM12878	blood:	n/a
47	chr15:43094585-43094635	HEEpiC	esophagus:	n/a
48	chr15:43094585-43094635	T-47D	breast:	n/a
49	chr15:43094585-43094635	HUVEC	blood vessel:	n/a
50	chr15:43094585-43094635	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:43094398..43098116-chr15:43199741..43201552,3	K562	blood:
2	chr15:43093067..43093836-chr15:43218523..43219050,2	MCF-7	breast:

No data

Variant related genes	Relation type
KRT8P50	TF binding region
KRT8P50	CpG island
ENSG00000128881	chromatin interactions

Extended variants
information (count: 157 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:157 , 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	rs74477607	chr15:43092774-43092775	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537387438	chr15:43092801-43092802	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556585716	chr15:43092805-43092806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141309927	chr15:43092823-43092824	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370942353	chr15:43092837-43092838	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35232898	chr15:43092878-43092879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540150356	chr15:43092891-43092892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535483363	chr15:43092921-43092922	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199708459	chr15:43092922-43092923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200816143	chr15:43092943-43092944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201597323	chr15:43092956-43092957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112019959	chr15:43092957-43092958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541636688	chr15:43092960-43092961	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76768143	chr15:43092972-43092973	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555802205	chr15:43092987-43092988	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572462928	chr15:43093010-43093011	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147893729	chr15:43093011-43093012	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564368083	chr15:43093014-43093015	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577914256	chr15:43093024-43093025	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368496631	chr15:43093040-43093041	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564963907	chr15:43093041-43093042	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563650112	chr15:43093069-43093070	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs554874572	chr15:43093088-43093089	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35602987	chr15:43093121-43093122	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs56367236	chr15:43093126-43093127	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374521919	chr15:43093127-43093128	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201561234	chr15:43093136-43093137	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199844995	chr15:43093154-43093155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370914431	chr15:43093169-43093170	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374345226	chr15:43093207-43093208	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200315636	chr15:43093208-43093209	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186858488	chr15:43093214-43093215	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs377714318	chr15:43093232-43093233	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191241739	chr15:43093243-43093244	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371877305	chr15:43093257-43093258	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528210657	chr15:43093301-43093302	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551583073	chr15:43093354-43093355	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141551647	chr15:43093369-43093370	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537250440	chr15:43093376-43093377	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532261606	chr15:43093382-43093383	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550845568	chr15:43093384-43093385	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367993590	chr15:43093394-43093395	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183043570	chr15:43093422-43093423	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188439392	chr15:43093448-43093449	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73413003	chr15:43093449-43093450	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs375725326	chr15:43093466-43093467	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369970930	chr15:43093475-43093476	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572480149	chr15:43093476-43093477	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374374932	chr15:43093490-43093491	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377208670	chr15:43093498-43093499	Weak transcription Enhancers Strong transcription Genic enhancers	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:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43030000-43093600	Weak transcription	Colonic Mucosa	Colon
2	chr15:43053600-43112200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:43054800-43146000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr15:43056800-43116800	Weak transcription	HepG2	liver
5	chr15:43057600-43107000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:43060800-43122200	Weak transcription	GM12878-XiMat	blood
7	chr15:43063000-43093000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:43063400-43093600	Weak transcription	Esophagus	oesophagus
9	chr15:43063400-43136200	Weak transcription	Psoas Muscle	Psoas
10	chr15:43064000-43114200	Weak transcription	Fetal Kidney	kidney
11	chr15:43064800-43150800	Weak transcription	HSMM	muscle
12	chr15:43066400-43095600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:43066600-43097600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr15:43067400-43147200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr15:43067600-43092800	Weak transcription	Brain Germinal Matrix	brain
16	chr15:43067800-43093000	Weak transcription	Fetal Brain Female	brain
17	chr15:43067800-43095200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr15:43068000-43093000	Weak transcription	Spleen	Spleen
19	chr15:43068400-43093000	Weak transcription	Aorta	Aorta
20	chr15:43068400-43093600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr15:43069000-43092800	Weak transcription	Fetal Muscle Trunk	muscle
22	chr15:43069000-43093400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr15:43075200-43093600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr15:43075200-43143800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:43075400-43135800	Weak transcription	HSMMtube	muscle
26	chr15:43075600-43093000	Weak transcription	Brain Cingulate Gyrus	brain
27	chr15:43075600-43093400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:43075600-43093600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:43075600-43093600	Weak transcription	Fetal Lung	lung
30	chr15:43075600-43093600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr15:43075600-43150800	Weak transcription	Colon Smooth Muscle	Colon
32	chr15:43075800-43093000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr15:43075800-43093000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr15:43075800-43093000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr15:43075800-43093000	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr15:43075800-43093000	Weak transcription	Left Ventricle	heart
37	chr15:43075800-43093000	Weak transcription	Lung	lung
38	chr15:43075800-43093000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr15:43075800-43093200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:43075800-43093200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr15:43075800-43093200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr15:43075800-43093200	Weak transcription	Right Ventricle	heart
43	chr15:43075800-43093200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr15:43075800-43093400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:43075800-43093400	Weak transcription	Ovary	ovary
46	chr15:43075800-43093600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:43075800-43093600	Weak transcription	Brain Substantia Nigra	brain
48	chr15:43075800-43094400	Weak transcription	Fetal Thymus	thymus
49	chr15:43075800-43117200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:43075800-43119200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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