Variant report

Variant	esv3376921
Chromosome Location	chr8:49289399-49293597
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	BACH1	chr8:49292560-49293076	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr8:49292125-49295009	IMR90	lung:	n/a	chr8:49293429-49293439
3	CHD2	chr8:49290404-49290482	Hela-S3	cervix:	n/a	n/a
4	CTBP2	chr8:49292630-49293601	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr8:49293340-49293490	AG04449	skin:	n/a	n/a
6	CTCF	chr8:49291616-49291621	GM19239	blood:	n/a	n/a
7	CTCF	chr8:49291446-49291611	GM19239	blood:	n/a	n/a
8	CTCF	chr8:49293460-49293610	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr8:49291424-49291639	MCF-7	breast:	n/a	n/a
10	E2F6	chr8:49292190-49293777	H1-hESC	embryonic stem cell:	n/a	chr8:49293002-49293011 chr8:49293580-49293587 chr8:49293227-49293237 chr8:49293579-49293588 chr8:49293408-49293417
11	E2F6	chr8:49292244-49292727	H1-hESC	embryonic stem cell:	n/a	n/a
12	E2F6	chr8:49293146-49293686	H1-hESC	embryonic stem cell:	n/a	chr8:49293580-49293587 chr8:49293227-49293237 chr8:49293579-49293588 chr8:49293408-49293417
13	EGR1	chr8:49293087-49293568	H1-hESC	embryonic stem cell:	n/a	chr8:49293248-49293259 chr8:49293192-49293205 chr8:49293197-49293207 chr8:49293414-49293424 chr8:49293411-49293424 chr8:49293411-49293424 chr8:49293248-49293258 chr8:49293302-49293315 chr8:49293411-49293424 chr8:49293411-49293424 chr8:49293414-49293423 chr8:49293247-49293260 chr8:49293407-49293429
14	EP300	chr8:49289669-49289925	SK-N-SH_RA	brain:	n/a	n/a
15	EP300	chr8:49292301-49292676	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr8:49288159-49290336	SK-N-SH	brain:	n/a	chr8:49288899-49288915
17	EP300	chr8:49292246-49292622	SK-N-SH_RA	brain:	n/a	chr8:49292250-49292259
18	EP300	chr8:49288600-49289466	SK-N-SH	brain:	n/a	chr8:49288899-49288915
19	EP300	chr8:49292869-49293767	SK-N-SH	brain:	n/a	n/a
20	FOSL2	chr8:49289585-49290293	SK-N-SH	brain:	n/a	chr8:49289703-49289714
21	FOXP2	chr8:49292322-49292825	SK-N-MC	brain:	n/a	n/a
22	FOXP2	chr8:49292333-49292610	SK-N-MC	brain:	n/a	n/a
23	GABPA	chr8:49293191-49293643	H1-hESC	embryonic stem cell:	n/a	chr8:49293218-49293227 chr8:49293197-49293206
24	GATA3	chr8:49288064-49290585	SK-N-SH	brain:	n/a	chr8:49289828-49289841 chr8:49289792-49289800 chr8:49290281-49290293 chr8:49290281-49290288 chr8:49289019-49289040 chr8:49290279-49290295
25	GATA3	chr8:49288221-49289571	SK-N-SH	brain:	n/a	chr8:49289019-49289040
26	GATA3	chr8:49292866-49293447	SK-N-SH	brain:	n/a	chr8:49293130-49293139
27	GATA3	chr8:49289607-49290524	SK-N-SH	brain:	n/a	chr8:49289828-49289841 chr8:49289792-49289800 chr8:49290281-49290293 chr8:49290281-49290288 chr8:49290279-49290295
28	JUN	chr8:49293224-49293263	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr8:49288734-49289405	SK-N-SH	brain:	n/a	n/a
30	JUND	chr8:49293263-49293324	H1-hESC	embryonic stem cell:	n/a	n/a
31	KAP1	chr8:49293017-49293776	HEK293	kidney:	n/a	n/a
32	MAX	chr8:49292881-49293764	SK-N-SH	brain:	n/a	chr8:49293197-49293207
33	MAX	chr8:49292344-49292769	SK-N-SH	brain:	n/a	n/a
34	MAX	chr8:49289760-49290253	SK-N-SH	brain:	n/a	n/a
35	MAX	chr8:49292842-49293844	SK-N-SH	brain:	n/a	chr8:49293197-49293207
36	MAX	chr8:49293179-49293625	H1-hESC	embryonic stem cell:	n/a	chr8:49293197-49293207
37	MAZ	chr8:49292889-49294404	IMR90	lung:	n/a	chr8:49293197-49293207
38	MXI1	chr8:49293342-49293349	H1-hESC	embryonic stem cell:	n/a	n/a
39	MYC	chr8:49291478-49291696	MCF-7	breast:	n/a	n/a
40	MYC	chr8:49291355-49291725	MCF-7	breast:	n/a	n/a
41	NFIC	chr8:49288643-49290311	SK-N-SH	brain:	n/a	n/a
42	PBX3	chr8:49288771-49289457	SK-N-SH	brain:	n/a	n/a
43	PBX3	chr8:49288707-49289511	SK-N-SH	brain:	n/a	n/a
44	PBX3	chr8:49289612-49290203	SK-N-SH	brain:	n/a	n/a
45	PBX3	chr8:49289582-49290296	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr8:49292691-49293552	ProgFib	skin:	n/a	n/a
47	POLR2A	chr8:49293559-49293564	ProgFib	skin:	n/a	n/a
48	POLR2A	chr8:49289762-49289983	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr8:49292230-49292743	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr8:49292972-49293363	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:49292851-49292901	HL-60	blood:	n/a
2	chr8:49292851-49292901	HMEC	breast:	n/a
3	chr8:49293546-49293596	HPAEpiC	pulmonary alveolar:	n/a
4	chr8:49292285-49292335	GM19239	blood:	n/a
5	chr8:49293546-49293596	BJ	skin:	n/a
6	chr8:49292486-49292536	HUVEC	blood vessel:	n/a
7	chr8:49293379-49293429	HCF	heart:	n/a
8	chr8:49293457-49293507	T-47D	breast:	n/a
9	chr8:49292950-49293000	SAEC	small airway:	n/a
10	chr8:49292950-49293000	HNPCEpiC	eye:	n/a
11	chr8:49293005-49293055	AoSMC	blood vessel:	n/a
12	chr8:49292685-49292735	ProgFib	skin:	n/a
13	chr8:49293546-49293596	GM06990	blood:	n/a
14	chr8:49292851-49292901	A549	lung:	n/a
15	chr8:49292486-49292536	PFSK-1	brain:	n/a
16	chr8:49292950-49293000	GM12892	blood:	n/a
17	chr8:49292685-49292735	HCPEpiC	choroid plexus:	n/a
18	chr8:49293546-49293596	SAEC	small airway:	n/a
19	chr8:49292851-49292901	HCF	heart:	n/a
20	chr8:49292851-49292901	SK-N-SH_RA	brain:	n/a
21	chr8:49293379-49293429	HepG2	liver:	n/a
22	chr8:49292950-49293000	HUVEC	blood vessel:	n/a
23	chr8:49292851-49292901	RPTEC	kidney:	n/a
24	chr8:49293457-49293507	Hepatocyte	liver:	n/a
25	chr8:49293379-49293429	CMK	blood:	n/a
26	chr8:49293546-49293596	GM12892	blood:	n/a
27	chr8:49293457-49293507	GM12892	blood:	n/a
28	chr8:49292486-49292536	RPTEC	kidney:	n/a
29	chr8:49292685-49292735	GM12891	blood:	n/a
30	chr8:49292685-49292735	HEEpiC	esophagus:	n/a
31	chr8:49292685-49292735	U87	brain:	n/a
32	chr8:49293379-49293429	BE2_C	brain:	n/a
33	chr8:49293457-49293507	AG04449	skin:	fetal
34	chr8:49293457-49293507	GM19239	blood:	n/a
35	chr8:49293379-49293429	PrEC	prostate:	n/a
36	chr8:49293379-49293429	SKMC	muscle:	n/a
37	chr8:49293546-49293596	HAEpiC	amniotic membrane:	n/a
38	chr8:49292486-49292536	SK-N-MC	brain:	n/a
39	chr8:49292486-49292536	U87	brain:	n/a
40	chr8:49292486-49292536	LNCaP	prostate:	n/a
41	chr8:49293546-49293596	NHDF-neo	bronchial:	n/a
42	chr8:49293546-49293596	HCF	heart:	n/a
43	chr8:49293546-49293596	AG04450	lung:	fetal
44	chr8:49293379-49293429	HCPEpiC	choroid plexus:	n/a
45	chr8:49292486-49292536	AG09319	gingival:	n/a
46	chr8:49292685-49292735	PANC-1	pancreas:	n/a
47	chr8:49292685-49292735	HCM	heart:	n/a
48	chr8:49293457-49293507	LNCaP	prostate:	n/a
49	chr8:49293546-49293596	NT2-D1	testis:	n/a
50	chr8:49293379-49293429	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:49286935..49290413-chr8:49291309..49294157,4	MCF-7	breast:
2	chr8:49286935..49290413-chr8:49291309..49294157,4	MCF-7	breast:

Variant related genes	Relation type
RPL29P19	TF binding region
RPL29P19	CpG island

Extended variants
information (count: 144 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:144 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73678276	chr8:49289417-49289418	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554818086	chr8:49289456-49289457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543563969	chr8:49289513-49289514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542578096	chr8:49289515-49289516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540180208	chr8:49289521-49289522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558117829	chr8:49289525-49289526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576463037	chr8:49289579-49289580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113044435	chr8:49289605-49289606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562465213	chr8:49289606-49289607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530278169	chr8:49289667-49289668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542067237	chr8:49289671-49289672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369488099	chr8:49289672-49289673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527988682	chr8:49289698-49289699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552946170	chr8:49289711-49289712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564459299	chr8:49289742-49289743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531768085	chr8:49289780-49289781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530753400	chr8:49289799-49289800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550778852	chr8:49289801-49289802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138797055	chr8:49289841-49289842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568479601	chr8:49289854-49289855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536408954	chr8:49289865-49289866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562669898	chr8:49289938-49289939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548088522	chr8:49289939-49289940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566367821	chr8:49289980-49289981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533818918	chr8:49290024-49290025	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558450585	chr8:49290057-49290058	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs528130572	chr8:49290080-49290081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs576400451	chr8:49290132-49290133	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs537457140	chr8:49290137-49290138	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs112195675	chr8:49290174-49290175	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs574451250	chr8:49290189-49290190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs541955821	chr8:49290208-49290209	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560510904	chr8:49290234-49290235	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567581307	chr8:49290311-49290312	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs546499050	chr8:49290505-49290506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34156363	chr8:49290548-49290549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs16936623	chr8:49290573-49290574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs531705176	chr8:49290617-49290618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549919681	chr8:49290767-49290768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185687321	chr8:49290782-49290783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372081104	chr8:49290786-49290787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529357113	chr8:49290794-49290795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543228906	chr8:49290799-49290800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141958967	chr8:49290816-49290817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566307027	chr8:49290828-49290829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190006824	chr8:49290832-49290833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552018702	chr8:49290836-49290837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375871455	chr8:49290843-49290844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150839891	chr8:49290845-49290846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537801040	chr8:49290847-49290848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49284200-49291000	Weak transcription	Fetal Intestine Small	intestine
2	chr8:49284200-49291400	Weak transcription	Fetal Kidney	kidney
3	chr8:49285000-49289800	Weak transcription	Fetal Lung	lung
4	chr8:49285600-49290000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:49285600-49292400	Enhancers	NHDF-Ad	bronchial
6	chr8:49286400-49289600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:49286600-49292400	Weak transcription	Spleen	Spleen
8	chr8:49288000-49289800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:49288000-49289800	Enhancers	Fetal Muscle Trunk	muscle
10	chr8:49288000-49289800	Enhancers	NHLF	lung
11	chr8:49288000-49290400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr8:49288000-49290600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:49288000-49290600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:49288000-49290600	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr8:49288000-49290600	Enhancers	Fetal Muscle Leg	muscle
16	chr8:49288000-49290600	Enhancers	Osteobl	bone
17	chr8:49288000-49292400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:49288000-49292400	Enhancers	Placenta Amnion	Placenta Amnion
19	chr8:49288200-49292600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr8:49288600-49290400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:49288600-49290400	Enhancers	NH-A	brain
22	chr8:49288600-49290600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr8:49288600-49290600	Enhancers	Placenta	Placenta
24	chr8:49288800-49289800	Weak transcription	Gastric	stomach
25	chr8:49288800-49290600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr8:49289000-49289600	Weak transcription	Stomach Mucosa	stomach
27	chr8:49289000-49290200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:49289000-49290400	Enhancers	HSMM	muscle
29	chr8:49289000-49292000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr8:49289200-49289400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:49289200-49290600	Enhancers	Fetal Stomach	stomach
32	chr8:49289200-49290600	Enhancers	Fetal Thymus	thymus
33	chr8:49289200-49290600	Enhancers	HSMMtube	muscle
34	chr8:49289400-49290000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr8:49289400-49291400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:49289600-49290600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr8:49289600-49290600	Enhancers	Stomach Mucosa	stomach
38	chr8:49289800-49290600	Enhancers	Fetal Lung	lung
39	chr8:49289800-49290600	Enhancers	Gastric	stomach
40	chr8:49289800-49291400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:49289800-49291800	Weak transcription	NHLF	lung
42	chr8:49290000-49290400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:49290400-49291800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:49290400-49292200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:49290400-49292200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr8:49290400-49292200	Weak transcription	NH-A	brain
47	chr8:49290400-49292400	Weak transcription	HSMM	muscle
48	chr8:49290600-49291400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr8:49290600-49291400	Weak transcription	Fetal Lung	lung
50	chr8:49290600-49291800	Weak transcription	Fetal Stomach	stomach

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