Variant report

Variant	nsv946000
Chromosome Location	chr1:76208402-76210101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:57)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:57 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:76208612-76208659	Lung_OC	lung:	n/a	n/a
2	POLR2A	chr1:76208097-76209453	GM12878	blood:	n/a	n/a
3	POLR2A	chr1:76208607-76208720	HepG2	liver:	n/a	n/a
4	POLR2A	chr1:76209119-76209303	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr1:76208783-76209284	GM12892	blood:	n/a	n/a
6	POLR2A	chr1:76208102-76208599	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr1:76208384-76208694	A549	lung:	n/a	n/a
8	POLR2A	chr1:76209069-76210252	GM12891	blood:	n/a	n/a
9	POLR2A	chr1:76208306-76208561	K562	blood:	n/a	n/a
10	POLR2A	chr1:76208837-76209128	K562	blood:	n/a	n/a
11	POLR2A	chr1:76208913-76209249	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr1:76209969-76209992	K562	blood:	n/a	n/a
13	POLR2A	chr1:76209732-76209814	K562	blood:	n/a	n/a
14	POLR2A	chr1:76209201-76209477	HepG2	liver:	n/a	n/a
15	POLR2A	chr1:76209896-76210157	HepG2	liver:	n/a	n/a
16	POLR2A	chr1:76209085-76209310	GM12878	blood:	n/a	n/a
17	POLR2A	chr1:76208878-76209065	GM12878	blood:	n/a	n/a
18	POLR2A	chr1:76209015-76209021	A549	lung:	n/a	n/a
19	POLR2A	chr1:76209606-76209650	K562	blood:	n/a	n/a
20	POLR2A	chr1:76209882-76209911	K562	blood:	n/a	n/a
21	POLR2A	chr1:76209893-76210067	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr1:76208875-76209077	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr1:76209105-76209400	HepG2	liver:	n/a	n/a
24	POLR2A	chr1:76208129-76208663	K562	blood:	n/a	n/a
25	POLR2A	chr1:76209849-76209860	K562	blood:	n/a	n/a
26	POLR2A	chr1:76209254-76209305	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr1:76209962-76209988	Gliobla	brain:	n/a	n/a
28	POLR2A	chr1:76209481-76209517	K562	blood:	n/a	n/a
29	POLR2A	chr1:76209890-76209978	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr1:76209837-76210097	GM12878	blood:	n/a	n/a
31	POLR2A	chr1:76208281-76208572	GM12878	blood:	n/a	n/a
32	POLR2A	chr1:76208245-76209496	GM12878	blood:	n/a	n/a
33	POLR2A	chr1:76210064-76210285	K562	blood:	n/a	n/a
34	POLR2A	chr1:76209939-76209943	Gliobla	brain:	n/a	n/a
35	POLR2A	chr1:76208867-76209298	GM12878	blood:	n/a	n/a
36	POLR2A	chr1:76208010-76211534	K562	blood:	n/a	n/a
37	POLR2A	chr1:76208224-76208585	GM12891	blood:	n/a	n/a
38	POLR2A	chr1:76208773-76208831	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr1:76208812-76209158	K562	blood:	n/a	n/a
40	POLR2A	chr1:76208476-76208611	GM12878	blood:	n/a	n/a
41	POLR2A	chr1:76208442-76208679	K562	blood:	n/a	n/a
42	POLR2A	chr1:76208936-76209268	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr1:76209631-76210064	K562	blood:	n/a	n/a
44	POLR2A	chr1:76208138-76209244	K562	blood:	n/a	n/a
45	POLR2A	chr1:76209504-76210361	GM12878	blood:	n/a	n/a
46	POLR2A	chr1:76208080-76208681	K562	blood:	n/a	n/a
47	POLR2A	chr1:76209189-76209480	K562	blood:	n/a	n/a
48	POLR2A	chr1:76209094-76209128	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr1:76208482-76208655	HepG2	liver:	n/a	n/a
50	POLR2A	chr1:76208588-76208698	Hela-S3	cervix:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76208288..76210222-chr1:76210745..76212663,2	K562	blood:
2	chr1:76197560..76200556-chr1:76208948..76211290,2	K562	blood:
3	chr1:76208992..76212319-chr1:76261590..76264096,3	K562	blood:
4	chr1:76205678..76212783-chr1:76212896..76217702,9	K562	blood:
5	chr1:76208509..76211228-chr1:76250454..76252141,2	K562	blood:
6	chr1:76189028..76194220-chr1:76209012..76215464,6	K562	blood:

No data

Variant related genes	Relation type
ACADM	TF binding region
ENSG00000057468	chromatin interactions
ENSG00000117054	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000137955	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561015373	chr1:76208447-76208448	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558768732	chr1:76208483-76208484	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1146578	chr1:76208488-76208489	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs538173364	chr1:76208596-76208597	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs185512895	chr1:76208597-76208598	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532044700	chr1:76208603-76208604	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs386632515	chr1:76208604-76208605	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs372334337	chr1:76208606-76208607	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs188841516	chr1:76208645-76208646	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs554088451	chr1:76208729-76208730	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs572457001	chr1:76208759-76208760	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs546309007	chr1:76208761-76208762	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs139225427	chr1:76208771-76208772	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372760986	chr1:76208848-76208849	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs201683611	chr1:76208851-76208852	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs577097806	chr1:76208853-76208854	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs111906303	chr1:76208860-76208861	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs34053323	chr1:76208861-76208862	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs397707598	chr1:76208869-76208870	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs544389007	chr1:76208870-76208871	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs562662553	chr1:76208902-76208903	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs191886432	chr1:76208907-76208908	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs547888209	chr1:76208928-76208929	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs560085740	chr1:76208931-76208932	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs149945460	chr1:76208933-76208934	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs551831493	chr1:76208934-76208935	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs570744382	chr1:76208945-76208946	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs117828807	chr1:76208956-76208957	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs114494552	chr1:76208969-76208970	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs566877486	chr1:76208975-76208976	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11578480	chr1:76208989-76208990	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs184021327	chr1:76208993-76208994	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs146489094	chr1:76208994-76208995	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs188436738	chr1:76209032-76209033	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs539974962	chr1:76209095-76209096	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs558300989	chr1:76209105-76209106	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs140971682	chr1:76209139-76209140	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs375875108	chr1:76209156-76209157	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs562665536	chr1:76209177-76209178	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs181108266	chr1:76209201-76209202	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs540090732	chr1:76209214-76209215	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs559923606	chr1:76209238-76209239	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs527275527	chr1:76209248-76209249	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs114256378	chr1:76209287-76209288	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs375715811	chr1:76209296-76209297	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs563858154	chr1:76209396-76209397	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs531257353	chr1:76209399-76209400	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs550116467	chr1:76209401-76209402	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs184614488	chr1:76209402-76209403	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs575775584	chr1:76209413-76209414	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:162 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76191200-76219600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:76191800-76209400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:76192000-76210200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:76192000-76220400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:76192000-76220600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:76192000-76227800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:76192200-76217800	Weak transcription	Fetal Brain Male	brain
8	chr1:76192200-76222000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:76193600-76220200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:76193800-76208600	Weak transcription	Small Intestine	intestine
11	chr1:76193800-76220200	Weak transcription	Fetal Heart	heart
12	chr1:76195600-76219600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:76195800-76213800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:76196000-76210800	Strong transcription	Primary B cells from peripheral blood	blood
15	chr1:76196000-76222000	Strong transcription	Liver	Liver
16	chr1:76196200-76212600	Strong transcription	Fetal Thymus	thymus
17	chr1:76196400-76210800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr1:76196400-76213000	Strong transcription	Dnd41	blood
19	chr1:76197600-76209600	Strong transcription	Primary monocytes fromperipheralblood	blood
20	chr1:76197600-76211400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr1:76197600-76212000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:76197600-76219400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr1:76197800-76210600	Strong transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:76198000-76210400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr1:76198200-76209800	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr1:76198200-76210400	Strong transcription	Adipose Nuclei	Adipose
27	chr1:76198200-76210600	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr1:76198400-76210400	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr1:76198600-76210200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:76198600-76210400	Strong transcription	Duodenum Mucosa	Duodenum
31	chr1:76198600-76211600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:76198600-76212000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr1:76198800-76209400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:76198800-76210600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:76198800-76210800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr1:76199000-76210200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:76199600-76218600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr1:76199600-76220400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:76201600-76217800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr1:76202000-76225000	Weak transcription	Stomach Mucosa	stomach
41	chr1:76202600-76210400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr1:76203400-76230800	Weak transcription	NHDF-Ad	bronchial
43	chr1:76203600-76208800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr1:76203800-76211200	Strong transcription	Primary T cells fromperipheralblood	blood
45	chr1:76204200-76209600	Strong transcription	Primary T helper cells PMA-I stimulated	--
46	chr1:76204200-76210600	Strong transcription	Stomach Smooth Muscle	stomach
47	chr1:76204200-76212000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr1:76204200-76212000	Strong transcription	K562	blood
49	chr1:76204400-76208800	Strong transcription	NHEK	skin
50	chr1:76204400-76209400	Strong transcription	Primary neutrophils fromperipheralblood	blood

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