Variant report

Variant	esv1010529
Chromosome Location	chr1:10476195-10478586
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:33)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:33 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr1:10478175-10478239	Lung_OC	lung:	n/a	n/a
2	POLR2A	chr1:10477444-10477545	K562	blood:	n/a	n/a
3	POLR2A	chr1:10477160-10478543	K562	blood:	n/a	n/a
4	POLR2A	chr1:10477300-10477758	A549	lung:	n/a	n/a
5	POLR2A	chr1:10478586-10478737	HepG2	liver:	n/a	n/a
6	POLR2A	chr1:10476775-10477516	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr1:10477145-10477166	HepG2	liver:	n/a	n/a
8	POLR2A	chr1:10476804-10476838	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:10477359-10477384	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr1:10477173-10478152	HepG2	liver:	n/a	n/a
11	POLR2A	chr1:10477440-10477715	A549	lung:	n/a	n/a
12	POLR2A	chr1:10477002-10477902	K562	blood:	n/a	n/a
13	POLR2A	chr1:10477426-10477535	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr1:10477405-10477755	A549	lung:	n/a	n/a
15	POLR2A	chr1:10476522-10476612	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr1:10476702-10476785	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr1:10477249-10477756	HepG2	liver:	n/a	n/a
18	POLR2A	chr1:10476794-10476974	K562	blood:	n/a	n/a
19	POLR2A	chr1:10476709-10476829	A549	lung:	n/a	n/a
20	POLR2A	chr1:10477148-10477284	A549	lung:	n/a	n/a
21	POLR2A	chr1:10477822-10477829	K562	blood:	n/a	n/a
22	POLR2A	chr1:10476979-10477653	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr1:10476621-10476671	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr1:10477639-10477683	MCF-7	breast:	n/a	n/a
25	POLR2A	chr1:10477138-10477270	A549	lung:	n/a	n/a
26	POLR2A	chr1:10476442-10476514	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr1:10476120-10476305	HepG2	liver:	n/a	n/a
28	POLR2A	chr1:10476145-10484723	A549	lung:	n/a	n/a
29	POLR2A	chr1:10477531-10477629	MCF-7	breast:	n/a	n/a
30	POLR2A	chr1:10477516-10477716	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr1:10477115-10477733	A549	lung:	n/a	n/a
32	POLR2A	chr1:10477120-10477769	HL-60	blood:	n/a	n/a
33	POLR2A	chr1:10477246-10477346	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10437214..10438077-chr1:10475535..10476340,2	MCF-7	breast:
2	chr1:10474109..10477987-chr1:10478782..10481616,9	K562	blood:
3	chr1:9969356..9971879-chr1:10474323..10477073,2	K562	blood:
4	chr1:10457797..10461098-chr1:10474071..10478087,9	K562	blood:
5	chr1:10477766..10478549-chr8:87566020..87566871,2	MCF-7	breast:
6	chr1:10437408..10438442-chr1:10475501..10476423,3	K562	blood:
7	chr1:10475618..10478486-chr1:10479191..10481866,2	MCF-7	breast:
8	chr1:10475480..10478071-chr1:10488933..10491824,2	K562	blood:
9	chr1:10474196..10477325-chr1:10477463..10484153,8	K562	blood:
10	chr1:10473791..10476777-chr1:10490511..10492354,2	K562	blood:
11	chr1:10474196..10477325-chr1:10477463..10484153,8	K562	blood:

No data

Variant related genes	Relation type
PGD	TF binding region
ENSG00000175279	chromatin interactions
ENSG00000142657	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000178585	chromatin interactions
ENSG00000251503	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61775986	chr1:10476196-10476197	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs555254941	chr1:10476218-10476219	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs61775987	chr1:10476229-10476230	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs576568639	chr1:10476264-10476265	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs199834291	chr1:10476308-10476309	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs185173776	chr1:10476325-10476326	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs569114883	chr1:10476339-10476340	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs536445948	chr1:10476397-10476398	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs189905809	chr1:10476413-10476414	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs576856332	chr1:10476472-10476473	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs368779837	chr1:10476489-10476490	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs34599736	chr1:10476584-10476585	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs11803409	chr1:10476585-10476586	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs554930728	chr1:10476603-10476604	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs558247200	chr1:10476612-10476613	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs3206335	chr1:10476618-10476619	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs57794695	chr1:10476643-10476644	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs530643626	chr1:10476665-10476666	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs139995241	chr1:10476689-10476690	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs565267608	chr1:10476697-10476698	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs573038685	chr1:10476761-10476762	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs372225736	chr1:10476762-10476763	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs113366145	chr1:10476771-10476772	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs188347857	chr1:10476776-10476777	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs375234390	chr1:10476792-10476793	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs145568297	chr1:10476822-10476823	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs180691829	chr1:10476837-10476838	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs536607599	chr1:10476850-10476851	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs548915009	chr1:10476853-10476854	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs570300895	chr1:10476929-10476930	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs186305705	chr1:10476940-10476941	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs575349436	chr1:10477012-10477013	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs373599760	chr1:10477055-10477056	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs149004719	chr1:10477092-10477093	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs576912506	chr1:10477111-10477112	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs151084742	chr1:10477132-10477133	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs201224678	chr1:10477140-10477141	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs200622919	chr1:10477155-10477156	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs199929432	chr1:10477157-10477158	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs373341638	chr1:10477197-10477198	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs376438081	chr1:10477210-10477211	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs370969316	chr1:10477214-10477215	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs2298569	chr1:10477234-10477235	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs202090685	chr1:10477287-10477288	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs61775988	chr1:10477295-10477296	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs541400253	chr1:10477301-10477302	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs563466177	chr1:10477313-10477314	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs575477432	chr1:10477340-10477341	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs545716904	chr1:10477375-10477376	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs564301694	chr1:10477377-10477378	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	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
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	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
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10460000-10490200	Weak transcription	Psoas Muscle	Psoas
2	chr1:10460600-10481200	Strong transcription	H1 Cell Line	embryonic stem cell
3	chr1:10460800-10480400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr1:10460800-10482000	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr1:10460800-10482400	Strong transcription	Fetal Stomach	stomach
6	chr1:10460800-10483400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:10461000-10476800	Weak transcription	Fetal Heart	heart
8	chr1:10461000-10482000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr1:10461200-10482000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:10461200-10482000	Strong transcription	Fetal Muscle Leg	muscle
11	chr1:10461200-10490000	Weak transcription	Right Atrium	heart
12	chr1:10461400-10483000	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:10461400-10483000	Strong transcription	Fetal Intestine Small	intestine
14	chr1:10461400-10483400	Strong transcription	Fetal Muscle Trunk	muscle
15	chr1:10461600-10481800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
16	chr1:10461600-10482800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:10461800-10482000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:10461800-10482000	Strong transcription	Dnd41	blood
19	chr1:10462000-10482000	Strong transcription	Fetal Intestine Large	intestine
20	chr1:10462000-10482200	Strong transcription	Brain Germinal Matrix	brain
21	chr1:10462000-10483000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:10462200-10481600	Strong transcription	Liver	Liver
23	chr1:10462200-10481600	Strong transcription	Skeletal Muscle Male	skeletal muscle
24	chr1:10462200-10482000	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr1:10462200-10483200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:10462600-10482000	Strong transcription	Duodenum Mucosa	Duodenum
27	chr1:10462800-10478200	Strong transcription	Fetal Lung	lung
28	chr1:10462800-10478400	Strong transcription	Brain Angular Gyrus	brain
29	chr1:10462800-10480400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr1:10462800-10481600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr1:10462800-10481600	Strong transcription	GM12878-XiMat	blood
32	chr1:10462800-10482200	Strong transcription	Thymus	Thymus
33	chr1:10462800-10482600	Strong transcription	Brain Anterior Caudate	brain
34	chr1:10462800-10483400	Strong transcription	Fetal Brain Female	brain
35	chr1:10463000-10478000	Strong transcription	Stomach Smooth Muscle	stomach
36	chr1:10463000-10480800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr1:10463000-10480800	Strong transcription	Left Ventricle	heart
38	chr1:10463000-10480800	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr1:10463000-10481000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr1:10463000-10481000	Strong transcription	Brain Inferior Temporal Lobe	brain
41	chr1:10463000-10482000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:10463000-10482200	Strong transcription	Fetal Thymus	thymus
43	chr1:10463200-10482000	Strong transcription	Brain Cingulate Gyrus	brain
44	chr1:10464200-10478400	Strong transcription	NHLF	lung
45	chr1:10464200-10482000	Strong transcription	Spleen	Spleen
46	chr1:10464400-10481800	Strong transcription	HSMMtube	muscle
47	chr1:10464400-10482200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:10464400-10482400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:10464400-10482800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:10466000-10478400	Strong transcription	Colon Smooth Muscle	Colon

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