Variant report

Variant	esv3324945
Chromosome Location	chr8:124669371-124673969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:124670470-124670670	HepG2	liver:	n/a	n/a
2	CEBPB	chr8:124673959-124674903	MCF-7	breast:	n/a	chr8:124674688-124674701 chr8:124674463-124674472 chr8:124674463-124674472 chr8:124674461-124674472 chr8:124674463-124674474 chr8:124674463-124674472 chr8:124674611-124674624 chr8:124674463-124674472 chr8:124674461-124674474
3	CTCF	chr8:124670420-124670570	HCPEpiC	choroid plexus:	n/a	n/a
4	EGR1	chr8:124671277-124671506	K562	blood:	n/a	n/a
5	EP300	chr8:124670666-124671014	SK-N-SH_RA	brain:	n/a	n/a
6	EP300	chr8:124673935-124674855	T-47D	breast:	n/a	chr8:124674246-124674256 chr8:124674689-124674703 chr8:124674462-124674476
7	EP300	chr8:124670391-124670561	HepG2	liver:	n/a	n/a
8	EP300	chr8:124670704-124671007	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr8:124670494-124671146	SK-N-SH	brain:	n/a	n/a
10	FOSL2	chr8:124670492-124671181	SK-N-SH	brain:	n/a	chr8:124670919-124670928 chr8:124670915-124670926 chr8:124670735-124670744
11	FOXA1	chr8:124673965-124674689	T-47D	breast:	n/a	chr8:124674245-124674260
12	GATA3	chr8:124673922-124674954	T-47D	breast:	n/a	n/a
13	GATA3	chr8:124673969-124675014	T-47D	breast:	n/a	n/a
14	GATA3	chr8:124670477-124671287	SK-N-SH	brain:	n/a	chr8:124670917-124670926
15	GATA3	chr8:124670439-124671309	SK-N-SH	brain:	n/a	chr8:124670917-124670926
16	HNF4A	chr8:124670346-124670646	HepG2	liver:	n/a	chr8:124670508-124670523 chr8:124670510-124670522 chr8:124670508-124670523 chr8:124670556-124670564 chr8:124670508-124670523 chr8:124670508-124670523
17	HNF4A	chr8:124670361-124670672	HepG2	liver:	n/a	chr8:124670508-124670523 chr8:124670510-124670522 chr8:124670508-124670523 chr8:124670556-124670564 chr8:124670508-124670523 chr8:124670508-124670523
18	HNF4A	chr8:124670304-124670637	HepG2	liver:	n/a	chr8:124670508-124670523 chr8:124670510-124670522 chr8:124670508-124670523 chr8:124670556-124670564 chr8:124670508-124670523 chr8:124670508-124670523
19	HNF4G	chr8:124670310-124670729	HepG2	liver:	n/a	chr8:124670510-124670522 chr8:124670508-124670523 chr8:124670556-124670564 chr8:124670509-124670524 chr8:124670508-124670523 chr8:124670508-124670523
20	JUN	chr8:124670632-124670923	HepG2	liver:	n/a	chr8:124670731-124670744 chr8:124670735-124670744
21	JUN	chr8:124670650-124670707	K562	blood:	n/a	n/a
22	JUND	chr8:124670730-124670798	K562	blood:	n/a	chr8:124670735-124670744
23	JUND	chr8:124670422-124671172	SK-N-SH	brain:	n/a	chr8:124670919-124670928 chr8:124670915-124670926 chr8:124670735-124670744
24	JUND	chr8:124670559-124670913	HepG2	liver:	n/a	chr8:124670735-124670744
25	KAP1	chr8:124670621-124670938	U2OS	brain:	n/a	n/a
26	MAFK	chr8:124670690-124671089	IMR90	lung:	n/a	n/a
27	MAZ	chr8:124670464-124670694	HepG2	liver:	n/a	chr8:124670565-124670574
28	MXI1	chr8:124670254-124670709	HepG2	liver:	n/a	chr8:124670563-124670578 chr8:124670565-124670580
29	NFIC	chr8:124670450-124671198	SK-N-SH	brain:	n/a	n/a
30	NR3C1	chr8:124670691-124671143	A549	lung:	n/a	chr8:124670919-124670928 chr8:124670872-124670881 chr8:124670918-124670927
31	NR3C1	chr8:124670621-124671099	A549	lung:	n/a	chr8:124670919-124670928 chr8:124670872-124670881 chr8:124670918-124670927
32	NR3C1	chr8:124670714-124671081	A549	lung:	n/a	chr8:124670919-124670928 chr8:124670872-124670881 chr8:124670918-124670927
33	NR3C1	chr8:124673615-124674031	A549	lung:	n/a	n/a
34	PBX3	chr8:124670527-124671151	SK-N-SH	brain:	n/a	n/a
35	PBX3	chr8:124670418-124671207	SK-N-SH	brain:	n/a	n/a
36	POLR2A	chr8:124670557-124671033	SK-N-SH	brain:	n/a	n/a
37	POLR2A	chr8:124673936-124675131	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr8:124670524-124671092	U87	brain:	n/a	n/a
39	POLR2A	chr8:124670534-124671113	U87	brain:	n/a	n/a
40	POLR2A	chr8:124671333-124671456	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr8:124670749-124670766	HUVEC	blood vessel:	n/a	n/a
42	RAD21	chr8:124670630-124671003	SK-N-SH_RA	brain:	n/a	n/a
43	RAD21	chr8:124670656-124671089	IMR90	lung:	n/a	n/a
44	RAD21	chr8:124670721-124670967	SK-N-SH_RA	brain:	n/a	n/a
45	RCOR1	chr8:124670513-124670824	HepG2	liver:	n/a	n/a
46	RFX5	chr8:124670493-124670885	HepG2	liver:	n/a	chr8:124670564-124670579 chr8:124670564-124670579 chr8:124670563-124670580 chr8:124670564-124670579
47	RXRA	chr8:124670440-124671079	SK-N-SH	brain:	n/a	n/a
48	SMC3	chr8:124670494-124670714	HepG2	liver:	n/a	n/a
49	SP1	chr8:124670231-124670757	HepG2	liver:	n/a	n/a
50	STAT3	chr8:124672326-124672369	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:124656327..124658581-chr8:124667209..124669646,2	MCF-7	breast:
2	chr8:124662032..124665488-chr8:124668654..124670370,3	MCF-7	breast:
3	chr8:124673351..124678204-chr8:124678247..124683296,7	MCF-7	breast:
4	chr8:124668666..124670546-chr8:124672499..124675168,2	MCF-7	breast:
5	chr8:124668666..124670546-chr8:124672499..124675168,2	MCF-7	breast:
6	chr8:124661695..124666565-chr8:124667806..124672490,5	MCF-7	breast:
7	chr8:124668534..124670111-chr8:124695984..124698883,2	K562	blood:
8	chr8:124642600..124645867-chr8:124673711..124676775,3	MCF-7	breast:
9	chr8:124659242..124661407-chr8:124671915..124673705,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM91A1-1	chr8:124670489-124670810	ENSG00000253286.1

Variant related genes	Relation type
KLHL38	TF binding region
ENSG00000175946	chromatin interactions

Extended variants
information (count: 209 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:209 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555417502	chr8:124669437-124669438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs78839950	chr8:124669440-124669441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs544164340	chr8:124669472-124669473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs11996554	chr8:124669480-124669481	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532387998	chr8:124669517-124669518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs534476256	chr8:124669521-124669522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs141825281	chr8:124669528-124669529	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs190299050	chr8:124669547-124669548	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577694848	chr8:124669558-124669559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561065840	chr8:124669567-124669568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545520048	chr8:124669579-124669580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs72711245	chr8:124669624-124669625	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs540724592	chr8:124669636-124669637	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs549405639	chr8:124669670-124669671	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs530645514	chr8:124669672-124669673	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550549876	chr8:124669678-124669679	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs79620634	chr8:124669709-124669710	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562953591	chr8:124669749-124669750	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539463473	chr8:124669779-124669780	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs368760636	chr8:124669793-124669794	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546977930	chr8:124669800-124669801	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567178454	chr8:124669801-124669802	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181843627	chr8:124669812-124669813	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116304815	chr8:124669837-124669838	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552464938	chr8:124669845-124669846	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575305531	chr8:124669878-124669879	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs115531001	chr8:124669879-124669880	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542661092	chr8:124669888-124669889	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558090368	chr8:124669892-124669893	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561528073	chr8:124669897-124669898	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577948249	chr8:124669912-124669913	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75929859	chr8:124669919-124669920	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs114712886	chr8:124669965-124669966	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369278557	chr8:124670003-124670004	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115290106	chr8:124670011-124670012	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542019487	chr8:124670019-124670020	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528814285	chr8:124670046-124670047	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561869438	chr8:124670048-124670049	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs530582847	chr8:124670052-124670053	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142592731	chr8:124670082-124670083	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564256826	chr8:124670083-124670084	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4871406	chr8:124670101-124670102	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs546606545	chr8:124670141-124670142	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs72711246	chr8:124670142-124670143	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150854434	chr8:124670172-124670173	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534256965	chr8:124670174-124670175	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549117976	chr8:124670230-124670231	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569653187	chr8:124670267-124670268	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186448640	chr8:124670308-124670309	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569116590	chr8:124670310-124670311	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	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
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:178 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124661200-124670000	Weak transcription	Duodenum Mucosa	Duodenum
2	chr8:124665000-124669400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:124666200-124669400	Weak transcription	HMEC	breast
4	chr8:124666200-124669600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:124666200-124674000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:124666400-124669600	Weak transcription	NH-A	brain
7	chr8:124666400-124669800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:124666400-124671200	Enhancers	Fetal Muscle Leg	muscle
9	chr8:124666600-124669800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:124666800-124670000	Weak transcription	HSMM	muscle
11	chr8:124666800-124678600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:124667000-124670000	Weak transcription	NHLF	lung
13	chr8:124667000-124670200	Weak transcription	Brain Anterior Caudate	brain
14	chr8:124667400-124669400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:124667400-124671400	Enhancers	Colon Smooth Muscle	Colon
16	chr8:124667600-124669600	Weak transcription	Fetal Intestine Small	intestine
17	chr8:124667600-124669600	Weak transcription	Right Atrium	heart
18	chr8:124667600-124670000	Weak transcription	HSMMtube	muscle
19	chr8:124667600-124670200	Weak transcription	Brain Angular Gyrus	brain
20	chr8:124667600-124670200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr8:124667600-124670200	Weak transcription	Fetal Brain Male	brain
22	chr8:124667600-124670800	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr8:124667800-124669600	Weak transcription	Aorta	Aorta
24	chr8:124667800-124669600	Weak transcription	HepG2	liver
25	chr8:124667800-124669800	Weak transcription	Placenta	Placenta
26	chr8:124667800-124670000	Weak transcription	NHDF-Ad	bronchial
27	chr8:124667800-124670200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:124668000-124669400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr8:124668000-124669600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:124668000-124669600	Enhancers	Stomach Smooth Muscle	stomach
31	chr8:124668000-124669800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:124668000-124670000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr8:124668200-124669400	Weak transcription	Osteobl	bone
34	chr8:124668200-124669800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:124668200-124669800	Weak transcription	Colonic Mucosa	Colon
36	chr8:124668200-124669800	Weak transcription	Lung	lung
37	chr8:124668200-124670000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:124668200-124671000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr8:124668200-124671200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr8:124668200-124673200	Weak transcription	Esophagus	oesophagus
41	chr8:124668200-124673600	Weak transcription	Pancreas	Pancrea
42	chr8:124668400-124669600	Weak transcription	Fetal Intestine Large	intestine
43	chr8:124668400-124669800	Weak transcription	Left Ventricle	heart
44	chr8:124668400-124670000	Weak transcription	Ovary	ovary
45	chr8:124668400-124680800	Weak transcription	Fetal Heart	heart
46	chr8:124668800-124669400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:124668800-124669600	Weak transcription	Psoas Muscle	Psoas
48	chr8:124669000-124669400	Weak transcription	Fetal Stomach	stomach
49	chr8:124669200-124669800	Enhancers	NHEK	skin
50	chr8:124669400-124669800	Enhancers	HMEC	breast

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