Variant report

Variant	esv1798949
Chromosome Location	chr8:48960737-48976333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:48975614-48975808	K562	blood:	n/a	n/a
2	CTCF	chr8:48965220-48965370	HCPEpiC	choroid plexus:	n/a	n/a
3	CTCF	chr8:48967340-48967490	NHDF-neo	bronchial:	n/a	n/a
4	CTCF	chr8:48962960-48963110	A549	lung:	n/a	n/a
5	E2F4	chr8:48975437-48975577	MCF10A-Er-Src	breast:	n/a	n/a
6	FOXA1	chr8:48973807-48974179	T-47D	breast:	n/a	n/a
7	FOXP2	chr8:48975534-48975893	SK-N-MC	brain:	n/a	n/a
8	IRF1	chr8:48961938-48962069	K562	blood:	n/a	chr8:48961984-48961998 chr8:48961986-48961996
9	IRF1	chr8:48961212-48961263	K562	blood:	n/a	n/a
10	JUN	chr8:48968783-48968883	H1-hESC	embryonic stem cell:	n/a	n/a
11	KAP1	chr8:48960715-48961094	HEK293	kidney:	n/a	n/a
12	MAFK	chr8:48960630-48960916	H1-hESC	embryonic stem cell:	n/a	n/a
13	MYC	chr8:48970977-48971009	MCF-7	breast:	n/a	n/a
14	MYC	chr8:48971059-48971088	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr8:48970461-48970755	K562	blood:	n/a	n/a
16	POLR2A	chr8:48975073-48975107	K562	blood:	n/a	n/a
17	POLR2A	chr8:48975731-48975785	GM12878	blood:	n/a	n/a
18	POLR2A	chr8:48974960-48975177	K562	blood:	n/a	n/a
19	POLR2A	chr8:48975550-48975982	SK-N-MC	brain:	n/a	n/a
20	POLR2A	chr8:48975671-48975718	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr8:48962597-48962824	K562	blood:	n/a	n/a
22	POLR2A	chr8:48963629-48964697	K562	blood:	n/a	n/a
23	POLR2A	chr8:48974765-48975571	K562	blood:	n/a	n/a
24	POLR2A	chr8:48965556-48965642	MCF-7	breast:	n/a	n/a
25	POLR2A	chr8:48971000-48971008	MCF-7	breast:	n/a	n/a
26	POLR2A	chr8:48975577-48975786	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr8:48965463-48965579	HepG2	liver:	n/a	n/a
28	POLR2A	chr8:48962305-48962375	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr8:48965591-48965607	HepG2	liver:	n/a	n/a
30	POLR2A	chr8:48975666-48975807	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr8:48975317-48975917	K562	blood:	n/a	n/a
32	POLR2A	chr8:48973751-48974209	K562	blood:	n/a	n/a
33	POLR2A	chr8:48969116-48969167	GM12878	blood:	n/a	n/a
34	POLR2A	chr8:48969592-48969918	K562	blood:	n/a	n/a
35	POLR2A	chr8:48975347-48976253	K562	blood:	n/a	n/a
36	POLR2A	chr8:48975070-48975133	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr8:48975806-48975826	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr8:48975354-48975462	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr8:48965051-48965061	K562	blood:	n/a	n/a
40	POLR2A	chr8:48965416-48965454	HepG2	liver:	n/a	n/a
41	POLR2A	chr8:48975908-48976084	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr8:48963518-48963550	A549	lung:	n/a	n/a
43	POLR2A	chr8:48965371-48965518	K562	blood:	n/a	n/a
44	POLR2A	chr8:48969002-48969105	GM12878	blood:	n/a	n/a
45	POLR2A	chr8:48962158-48962244	K562	blood:	n/a	n/a
46	POLR2A	chr8:48975755-48975793	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr8:48975623-48975645	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr8:48975892-48975899	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr8:48971784-48973535	K562	blood:	n/a	n/a
50	POLR2A	chr8:48967583-48967606	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48973636-48973686	HCF	heart:	n/a
2	chr8:48973636-48973686	AG09309	skin:	n/a
3	chr8:48973636-48973686	Jurkat	blood:	n/a
4	chr8:48973636-48973686	K562	blood:	n/a
5	chr8:48973636-48973686	ECC-1	luminal epithelium:	n/a
6	chr8:48973636-48973686	AoSMC	blood vessel:	n/a
7	chr8:48973636-48973686	ProgFib	skin:	n/a
8	chr8:48973636-48973686	GM12892	blood:	n/a
9	chr8:48973636-48973686	BJ	skin:	n/a
10	chr8:48973636-48973686	PANC-1	pancreas:	n/a
11	chr8:48973636-48973686	HCM	heart:	n/a
12	chr8:48973636-48973686	HCPEpiC	choroid plexus:	n/a
13	chr8:48973636-48973686	Hela-S3	cervix:	n/a
14	chr8:48973636-48973686	BE2_C	brain:	n/a
15	chr8:48973636-48973686	CMK	blood:	n/a
16	chr8:48973636-48973686	SK-N-MC	brain:	n/a
17	chr8:48973636-48973686	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:48973636-48973686	HAEpiC	amniotic membrane:	n/a
19	chr8:48973636-48973686	HEEpiC	esophagus:	n/a
20	chr8:48973636-48973686	T-47D	breast:	n/a
21	chr8:48973636-48973686	SK-N-SH_RA	brain:	n/a
22	chr8:48973636-48973686	H1-hESC	embryonic stem cell:	embryo
23	chr8:48973636-48973686	A549	lung:	n/a
24	chr8:48973636-48973686	Caco-2	colon:	n/a
25	chr8:48973636-48973686	HIPEpiC	eye:	n/a
26	chr8:48973636-48973686	HepG2	liver:	n/a
27	chr8:48973636-48973686	AG09319	gingival:	n/a
28	chr8:48973636-48973686	AG10803	skin:	n/a
29	chr8:48973636-48973686	NH-A	brain:	n/a
30	chr8:48973636-48973686	MCF-7	breast:	n/a
31	chr8:48973636-48973686	HCT-116	colon:	n/a
32	chr8:48973636-48973686	HEK293	kidney:	embryo
33	chr8:48973636-48973686	HUVEC	blood vessel:	n/a
34	chr8:48973636-48973686	HMEC	breast:	n/a
35	chr8:48973636-48973686	RPTEC	kidney:	n/a
36	chr8:48973636-48973686	NT2-D1	testis:	n/a
37	chr8:48973636-48973686	GM12878	blood:	n/a
38	chr8:48973636-48973686	AG04450	lung:	fetal
39	chr8:48973636-48973686	IMR90	lung:	fetal
40	chr8:48973636-48973686	ovcar-3	ovarian:	n/a
41	chr8:48973636-48973686	PFSK-1	brain:	n/a
42	chr8:48973636-48973686	Hepatocyte	liver:	n/a
43	chr8:48973636-48973686	SK-N-SH	brain:	n/a
44	chr8:48973636-48973686	GM06990	blood:	n/a
45	chr8:48973636-48973686	MCF10A-Er-Src	breast:	n/a
46	chr8:48973636-48973686	PrEC	prostate:	n/a
47	chr8:48973636-48973686	HRPEpiC	eye:	n/a
48	chr8:48973636-48973686	NHBE	bronchial:	n/a
49	chr8:48973636-48973686	HL-60	blood:	n/a
50	chr8:48973636-48973686	NB4	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:48953429..48954984-chr8:48960210..48961992,2	K562	blood:
2	chr8:48965207..48966957-chr8:48986549..48988912,2	K562	blood:
3	chr8:48955264..48957497-chr8:48959787..48961410,2	K562	blood:
4	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
5	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
6	chr8:48957775..48961134-chr8:48963246..48966717,4	K562	blood:
7	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:
8	chr8:48957775..48961134-chr8:48963246..48966621,3	K562	blood:
9	chr8:48970388..48974071-chr8:48975063..48978866,4	K562	blood:

No data

Variant related genes	Relation type
UBE2V2	TF binding region
UBE2V2	CpG island
ENSG00000169139	chromatin interactions

Extended variants
information (count: 502 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13280727	chr8:48960737-48960738	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564436475	chr8:48960770-48960771	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146888562	chr8:48960824-48960825	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs13261463	chr8:48960852-48960853	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543690918	chr8:48960880-48960881	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561857411	chr8:48960956-48960957	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs529418427	chr8:48961042-48961043	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs547825472	chr8:48961103-48961104	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139181636	chr8:48961250-48961251	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565964409	chr8:48961263-48961264	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547341968	chr8:48961292-48961293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144584904	chr8:48961306-48961307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs567147791	chr8:48961348-48961349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs551470034	chr8:48961380-48961381	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs80148994	chr8:48961399-48961400	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs537339745	chr8:48961408-48961409	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566835446	chr8:48961501-48961502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs192468317	chr8:48961532-48961533	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535194882	chr8:48961579-48961580	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553794575	chr8:48961617-48961618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559116525	chr8:48961620-48961621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs377317150	chr8:48961621-48961622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182092987	chr8:48961691-48961692	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539444770	chr8:48961692-48961693	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557462194	chr8:48961693-48961694	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576448737	chr8:48961715-48961716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138534610	chr8:48961716-48961717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185884926	chr8:48961773-48961774	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374936780	chr8:48961776-48961777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376156175	chr8:48961788-48961789	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372366060	chr8:48961789-48961790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573853647	chr8:48961808-48961809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541183332	chr8:48961835-48961836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs569304170	chr8:48961856-48961857	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559833939	chr8:48961872-48961873	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533246415	chr8:48961884-48961885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534329633	chr8:48961911-48961912	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529789736	chr8:48961913-48961914	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370242494	chr8:48962012-48962013	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs555474175	chr8:48962018-48962019	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs531112770	chr8:48962031-48962032	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549236609	chr8:48962066-48962067	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs45558936	chr8:48962084-48962085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534920428	chr8:48962102-48962103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149260100	chr8:48962183-48962184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546853489	chr8:48962218-48962219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565812733	chr8:48962312-48962313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182589761	chr8:48962323-48962324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557747631	chr8:48962324-48962325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576062517	chr8:48962327-48962328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48921800-48966800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:48922400-48975400	Weak transcription	Fetal Brain Male	brain
3	chr8:48935200-48963000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr8:48949800-48963200	Weak transcription	Brain Substantia Nigra	brain
5	chr8:48953200-48983400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:48953800-48974800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr8:48954200-48965800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:48954400-48961000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:48954400-48967000	Strong transcription	Placenta	Placenta
10	chr8:48954600-48966000	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:48954600-48975200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:48954600-48975600	Weak transcription	Pancreas	Pancrea
13	chr8:48954800-48966000	Strong transcription	Primary B cells from peripheral blood	blood
14	chr8:48954800-48971800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:48954800-48975800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr8:48955000-48965800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr8:48955000-48975000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:48955200-48964400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr8:48955200-48965800	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr8:48955400-48969600	Strong transcription	Dnd41	blood
21	chr8:48955600-48961600	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr8:48955600-48961800	Strong transcription	Primary T cells from cord blood	blood
23	chr8:48955600-48965800	Strong transcription	Fetal Thymus	thymus
24	chr8:48955600-48966200	Strong transcription	Primary neutrophils fromperipheralblood	blood
25	chr8:48955600-48967000	Strong transcription	Adipose Nuclei	Adipose
26	chr8:48955800-48960800	Strong transcription	Fetal Muscle Trunk	muscle
27	chr8:48955800-48960800	Strong transcription	Fetal Muscle Leg	muscle
28	chr8:48955800-48961200	Strong transcription	Fetal Brain Female	brain
29	chr8:48955800-48961400	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr8:48955800-48962200	Strong transcription	NH-A	brain
31	chr8:48955800-48965800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr8:48955800-48975000	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr8:48956000-48960800	Strong transcription	Fetal Intestine Large	intestine
34	chr8:48956000-48961400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr8:48956000-48962600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:48956000-48965800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr8:48956000-48967000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr8:48956000-48974800	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr8:48956200-48965400	Strong transcription	Osteobl	bone
40	chr8:48956400-48965800	Strong transcription	Fetal Lung	lung
41	chr8:48956600-48960800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr8:48956600-48960800	Strong transcription	Fetal Stomach	stomach
43	chr8:48956800-48962800	Weak transcription	Right Ventricle	heart
44	chr8:48956800-48965800	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr8:48956800-48973200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr8:48957000-48961000	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr8:48957200-48965200	Weak transcription	Psoas Muscle	Psoas
48	chr8:48957200-48975400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr8:48957400-48961000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:48957600-48974400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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