Variant report

Variant	esv3355190
Chromosome Location	chr8:87186336-87190934
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	E2F4	chr8:87188803-87188979	MCF10A-Er-Src	breast:	n/a	n/a
2	EP300	chr8:87189025-87189384	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
3	EP300	chr8:87188997-87189386	SK-N-SH_RA	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
4	EP300	chr8:87189054-87189336	Hela-S3	cervix:	n/a	chr8:87189194-87189203
5	EP300	chr8:87188804-87189398	SK-N-SH	brain:	n/a	chr8:87189048-87189061 chr8:87189194-87189203
6	FOS	chr8:87188684-87189378	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
7	FOS	chr8:87188768-87189386	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
8	FOS	chr8:87188835-87189335	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
9	FOS	chr8:87188778-87189577	HUVEC	blood vessel:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
10	FOS	chr8:87187991-87188555	HUVEC	blood vessel:	n/a	n/a
11	FOS	chr8:87188908-87189343	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189192-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
12	FOS	chr8:87188217-87188290	MCF10A-Er-Src	breast:	n/a	n/a
13	FOSL1	chr8:87188728-87189476	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
14	FOSL1	chr8:87188598-87189574	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
15	FOSL2	chr8:87188913-87189377	SK-N-SH	brain:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
16	FOSL2	chr8:87186131-87186517	HepG2	liver:	n/a	n/a
17	FOSL2	chr8:87188664-87189453	A549	lung:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
18	FOSL2	chr8:87188926-87189439	MCF-7	breast:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
19	FOSL2	chr8:87188877-87189475	MCF-7	breast:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
20	FOSL2	chr8:87189033-87189353	A549	lung:	n/a	chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
21	FOSL2	chr8:87188740-87189499	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
22	FOXA1	chr8:87185990-87186489	HepG2	liver:	n/a	n/a
23	FOXA1	chr8:87188358-87188707	T-47D	breast:	n/a	n/a
24	FOXA1	chr8:87188321-87188674	T-47D	breast:	n/a	n/a
25	FOXA1	chr8:87186074-87186459	HepG2	liver:	n/a	n/a
26	FOXA1	chr8:87185969-87186511	HepG2	liver:	n/a	n/a
27	FOXA1	chr8:87185980-87186441	HepG2	liver:	n/a	n/a
28	FOXA2	chr8:87186072-87186400	A549	lung:	n/a	n/a
29	FOXA2	chr8:87186050-87186636	A549	lung:	n/a	n/a
30	FOXA2	chr8:87186103-87186444	HepG2	liver:	n/a	n/a
31	FOXA2	chr8:87185903-87186572	HepG2	liver:	n/a	n/a
32	GATA2	chr8:87188090-87188666	HUVEC	blood vessel:	n/a	n/a
33	GATA3	chr8:87187938-87189502	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr8:87188260-87188701	MCF-7	breast:	n/a	n/a
35	GATA3	chr8:87188000-87188740	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr8:87188196-87188678	T-47D	breast:	n/a	n/a
37	GATA3	chr8:87188177-87188715	T-47D	breast:	n/a	n/a
38	GATA3	chr8:87187934-87189005	MCF-7	breast:	n/a	n/a
39	GATA3	chr8:87188822-87189441	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr8:87188078-87188780	MCF-7	breast:	n/a	n/a
41	GATA3	chr8:87188257-87188651	MCF-7	breast:	n/a	n/a
42	JUND	chr8:87188732-87189501	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
43	JUND	chr8:87186192-87186431	HepG2	liver:	n/a	n/a
44	JUND	chr8:87188630-87189489	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
45	JUND	chr8:87188771-87189548	HCT-116	colon:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
46	JUND	chr8:87188826-87189503	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
47	JUND	chr8:87188865-87189477	SK-N-SH	brain:	n/a	chr8:87189434-87189446 chr8:87189194-87189202 chr8:87189193-87189203 chr8:87189194-87189201 chr8:87189192-87189204 chr8:87189194-87189202
48	MAFK	chr8:87189011-87189308	Hela-S3	cervix:	n/a	chr8:87189194-87189204
49	MAFK	chr8:87189156-87189283	K562	blood:	n/a	chr8:87189194-87189204
50	MYC	chr8:87189107-87189307	MCF10A-Er-Src	breast:	n/a	chr8:87189194-87189203

No.	Distal block	Cell Line	Cell type
1	chr8:87190469..87192191-chr8:87210663..87212770,3	MCF-7	breast:
2	chr8:87177733..87179455-chr8:87185682..87188485,3	MCF-7	breast:
3	chr8:87186174..87188770-chr8:87209763..87212500,2	MCF-7	breast:
4	chr8:87187097..87192513-chr8:87353340..87357451,6	MCF-7	breast:
5	chr8:87186847..87188623-chr8:87190111..87192908,2	MCF-7	breast:
6	chr8:87187218..87190589-chr8:87353304..87356196,4	MCF-7	breast:
7	chr8:87188610..87190453-chr8:87196607..87198359,2	MCF-7	breast:
8	chr8:87189537..87192109-chr8:87199086..87201093,2	MCF-7	breast:
9	chr8:87185465..87188007-chr8:87211775..87213428,2	MCF-7	breast:
10	chr8:87187644..87190858-chr8:87193352..87196070,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253699	TF binding region
ENSG00000123124	chromatin interactions
ENSG00000254231	chromatin interactions
ENSG00000253699	chromatin interactions

Extended variants
information (count: 187 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:187 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7825985	chr8:87186356-87186357	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530400136	chr8:87186359-87186360	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs7837075	chr8:87186360-87186361	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs35844270	chr8:87186373-87186374	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs539149890	chr8:87186399-87186400	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs554359171	chr8:87186405-87186406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552600304	chr8:87186409-87186410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs57851767	chr8:87186428-87186429	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs538278766	chr8:87186490-87186491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572526829	chr8:87186499-87186500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372539337	chr8:87186509-87186510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554651079	chr8:87186535-87186536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35978872	chr8:87186546-87186547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs533809556	chr8:87186580-87186581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs386727430	chr8:87186583-87186584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576590676	chr8:87186584-87186585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12541468	chr8:87186586-87186587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4076882	chr8:87186589-87186590	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs12548440	chr8:87186599-87186600	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs75560671	chr8:87186618-87186619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370453171	chr8:87186627-87186628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12541480	chr8:87186678-87186679	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561644494	chr8:87186702-87186703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189693107	chr8:87186728-87186729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs191347402	chr8:87186740-87186741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12541499	chr8:87186771-87186772	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs115692034	chr8:87186803-87186804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78332179	chr8:87186822-87186823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144383887	chr8:87186849-87186850	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183526827	chr8:87186862-87186863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188070583	chr8:87186872-87186873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182008616	chr8:87186888-87186889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12541053	chr8:87186940-87186941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs533846684	chr8:87186950-87186951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531784109	chr8:87186958-87186959	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140196751	chr8:87186999-87187000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570413475	chr8:87187026-87187027	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539656567	chr8:87187031-87187032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556066208	chr8:87187043-87187044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs6470428	chr8:87187050-87187051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs13272356	chr8:87187077-87187078	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs554489515	chr8:87187086-87187087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143784598	chr8:87187095-87187096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13272593	chr8:87187113-87187114	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs371453945	chr8:87187151-87187152	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs540930879	chr8:87187155-87187156	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs187370694	chr8:87187161-87187162	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs532679344	chr8:87187191-87187192	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs4076881	chr8:87187195-87187196	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs56199972	chr8:87187274-87187275	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87180000-87187400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:87186000-87186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:87186000-87186400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr8:87186000-87186400	Enhancers	Gastric	stomach
5	chr8:87186000-87186600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:87186000-87186800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr8:87186200-87186400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
8	chr8:87186200-87188400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:87186200-87189200	Enhancers	HepG2	liver
10	chr8:87186400-87186600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:87186400-87187400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr8:87186600-87186800	Enhancers	A549	lung
13	chr8:87186600-87187200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:87186600-87188400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:87186800-87187800	Weak transcription	A549	lung
16	chr8:87186800-87188400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr8:87187000-87189800	Enhancers	Hela-S3	cervix
18	chr8:87187200-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:87187400-87187600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:87187400-87188000	Enhancers	HUVEC	blood vessel
21	chr8:87187400-87188200	Enhancers	HMEC	breast
22	chr8:87187400-87188400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr8:87187600-87188200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr8:87187600-87188200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:87187600-87188200	Enhancers	NHEK	skin
26	chr8:87187600-87189000	Enhancers	Fetal Lung	lung
27	chr8:87187600-87189800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr8:87187800-87188000	Enhancers	A549	lung
29	chr8:87187800-87188000	Enhancers	HSMMtube	muscle
30	chr8:87187800-87188000	Enhancers	NH-A	brain
31	chr8:87187800-87188200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr8:87187800-87188400	Enhancers	HSMM	muscle
33	chr8:87187800-87189400	Enhancers	Osteobl	bone
34	chr8:87187800-87190000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:87188000-87188200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:87188000-87188400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:87188000-87188400	Flanking Active TSS	HSMMtube	muscle
38	chr8:87188000-87188600	Enhancers	Fetal Brain Female	brain
39	chr8:87188000-87189000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr8:87188000-87189200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:87188000-87189200	Flanking Active TSS	A549	lung
42	chr8:87188000-87189200	Flanking Active TSS	NH-A	brain
43	chr8:87188000-87189400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr8:87188000-87189400	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr8:87188000-87189400	Flanking Active TSS	HUVEC	blood vessel
46	chr8:87188200-87188400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:87188200-87188600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr8:87188200-87188600	Enhancers	Adipose Nuclei	Adipose
49	chr8:87188200-87188800	Enhancers	Colon Smooth Muscle	Colon
50	chr8:87188200-87189000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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