Variant report

Variant	nsv831376
Chromosome Location	chr8:85577422-85726311
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	CBX3	chr8:85664935-85665222	K562	blood:	n/a	n/a
2	CEBPB	chr8:85694854-85695145	Hela-S3	cervix:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
3	CEBPB	chr8:85637089-85637282	A549	lung:	n/a	n/a
4	CEBPB	chr8:85694836-85695160	A549	lung:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
5	CEBPB	chr8:85709248-85709533	HepG2	liver:	n/a	chr8:85709368-85709379
6	CEBPB	chr8:85694869-85695208	ECC-1	luminal epithelium:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
7	CEBPB	chr8:85694842-85695106	K562	blood:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
8	CEBPB	chr8:85582523-85582840	HepG2	liver:	n/a	chr8:85582680-85582691
9	CEBPB	chr8:85694825-85695177	ECC-1	luminal epithelium:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
10	CEBPB	chr8:85626448-85627231	IMR90	lung:	n/a	chr8:85627114-85627131 chr8:85626565-85626576 chr8:85627011-85627024 chr8:85627115-85627126
11	CEBPB	chr8:85694814-85695192	HepG2	liver:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
12	CEBPB	chr8:85626431-85627155	HepG2	liver:	n/a	chr8:85627114-85627131 chr8:85626565-85626576 chr8:85627011-85627024 chr8:85627115-85627126
13	CEBPB	chr8:85582525-85582816	A549	lung:	n/a	chr8:85582680-85582691
14	CEBPB	chr8:85709252-85709566	A549	lung:	n/a	chr8:85709368-85709379
15	CEBPB	chr8:85626564-85626593	H1-hESC	embryonic stem cell:	n/a	chr8:85626565-85626576
16	CEBPB	chr8:85588569-85588865	HepG2	liver:	n/a	chr8:85588668-85588679
17	CEBPB	chr8:85709329-85709424	H1-hESC	embryonic stem cell:	n/a	chr8:85709368-85709379
18	CEBPB	chr8:85601053-85601292	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:85626430-85627151	A549	lung:	n/a	chr8:85627114-85627131 chr8:85626565-85626576 chr8:85627011-85627024 chr8:85627115-85627126
20	CEBPB	chr8:85588098-85588856	A549	lung:	n/a	chr8:85588668-85588679
21	CEBPB	chr8:85626422-85626641	K562	blood:	n/a	chr8:85626565-85626576
22	CEBPB	chr8:85694816-85695188	H1-hESC	embryonic stem cell:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
23	CEBPB	chr8:85694767-85695161	MCF-7	breast:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
24	CEBPB	chr8:85694818-85695169	IMR90	lung:	n/a	chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004 chr8:85694995-85695004
25	CEBPB	chr8:85644090-85644235	HepG2	liver:	n/a	n/a
26	CTCF	chr8:85714700-85714850	GM12865	blood:	n/a	n/a
27	CTCF	chr8:85696260-85696408	HepG2	liver:	n/a	chr8:85696361-85696379
28	CTCF	chr8:85597420-85597570	HMEC	breast:	n/a	n/a
29	CTCF	chr8:85714713-85714808	LNCaP	prostate:	n/a	n/a
30	CTCF	chr8:85597468-85597690	H1-hESC	embryonic stem cell:	n/a	chr8:85597579-85597588 chr8:85597578-85597599
31	CTCF	chr8:85704524-85704641	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:85704500-85704650	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:85725500-85725650	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr8:85714730-85714781	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:85696180-85696330	HAc	cerebellar:	n/a	n/a
36	CTCF	chr8:85714620-85714770	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr8:85696400-85696550	GM12872	blood:	n/a	n/a
38	CTCF	chr8:85714680-85714830	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:85696346-85696404	H1-hESC	embryonic stem cell:	n/a	chr8:85696361-85696379
40	CTCF	chr8:85714660-85714810	GM06990	blood:	n/a	n/a
41	CTCF	chr8:85614096-85614129	Lung_OC	lung:	n/a	n/a
42	CTCF	chr8:85597524-85597653	LNCaP	prostate:	n/a	chr8:85597579-85597588 chr8:85597578-85597599
43	CTCF	chr8:85714600-85714750	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:85714700-85714850	Caco-2	colon:	n/a	n/a
45	CTCF	chr8:85704720-85704870	GM06990	blood:	n/a	n/a
46	CTCF	chr8:85597500-85597650	WERI-Rb-1	eye:	n/a	chr8:85597579-85597588 chr8:85597578-85597599
47	CTCF	chr8:85600958-85601014	GM20000	blood:	n/a	n/a
48	CTCF	chr8:85613900-85614050	GM12875	blood:	n/a	n/a
49	CTCF	chr8:85714732-85714792	HepG2	liver:	n/a	n/a
50	CTCF	chr8:85696320-85696470	NB4	blood:	n/a	chr8:85696361-85696379

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:85686184-85686234	H1-hESC	embryonic stem cell:	embryo
2	chr8:85686184-85686234	MCF10A-Er-Src	breast:	n/a
3	chr8:85618021-85618071	SK-N-SH	brain:	n/a
4	chr8:85686184-85686234	Hepatocyte	liver:	n/a
5	chr8:85618021-85618071	NB4	blood:	n/a
6	chr8:85711159-85711209	Jurkat	blood:	n/a
7	chr8:85686184-85686234	HCT-116	colon:	n/a
8	chr8:85711159-85711209	A549	lung:	n/a
9	chr8:85685344-85685394	GM19239	blood:	n/a
10	chr8:85618021-85618071	HCF	heart:	n/a
11	chr8:85686184-85686234	HRPEpiC	eye:	n/a
12	chr8:85711159-85711209	K562	blood:	n/a
13	chr8:85685344-85685394	PANC-1	pancreas:	n/a
14	chr8:85711159-85711209	HNPCEpiC	eye:	n/a
15	chr8:85618021-85618071	NH-A	brain:	n/a
16	chr8:85686184-85686234	PANC-1	pancreas:	n/a
17	chr8:85618021-85618071	BJ	skin:	n/a
18	chr8:85686184-85686234	SK-N-SH	brain:	n/a
19	chr8:85685344-85685394	GM12891	blood:	n/a
20	chr8:85685344-85685394	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:85686184-85686234	HEEpiC	esophagus:	n/a
22	chr8:85686184-85686234	PrEC	prostate:	n/a
23	chr8:85618021-85618071	SKMC	muscle:	n/a
24	chr8:85618021-85618071	HPAEpiC	pulmonary alveolar:	n/a
25	chr8:85618021-85618071	AG09319	gingival:	n/a
26	chr8:85686184-85686234	HCM	heart:	n/a
27	chr8:85711159-85711209	IMR90	lung:	fetal
28	chr8:85618021-85618071	Jurkat	blood:	n/a
29	chr8:85686184-85686234	GM12878	blood:	n/a
30	chr8:85685344-85685394	SAEC	small airway:	n/a
31	chr8:85685344-85685394	NHBE	bronchial:	n/a
32	chr8:85686184-85686234	GM19239	blood:	n/a
33	chr8:85686184-85686234	K562	blood:	n/a
34	chr8:85686184-85686234	SAEC	small airway:	n/a
35	chr8:85686184-85686234	GM12892	blood:	n/a
36	chr8:85618021-85618071	PFSK-1	brain:	n/a
37	chr8:85618021-85618071	AG09309	skin:	n/a
38	chr8:85618021-85618071	NT2-D1	testis:	n/a
39	chr8:85711159-85711209	CMK	blood:	n/a
40	chr8:85685344-85685394	AG04450	lung:	fetal
41	chr8:85711159-85711209	ECC-1	luminal epithelium:	n/a
42	chr8:85686184-85686234	T-47D	breast:	n/a
43	chr8:85686184-85686234	GM12891	blood:	n/a
44	chr8:85711159-85711209	NT2-D1	testis:	n/a
45	chr8:85711159-85711209	AG09309	skin:	n/a
46	chr8:85686184-85686234	HIPEpiC	eye:	n/a
47	chr8:85711159-85711209	GM12878	blood:	n/a
48	chr8:85685344-85685394	GM12892	blood:	n/a
49	chr8:85711159-85711209	AoSMC	blood vessel:	n/a
50	chr8:85618021-85618071	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:47395381..47396938-chr8:85644635..85646246,2	MCF-7	breast:
2	chr8:85637881..85639538-chr8:85676216..85677896,2	K562	blood:
3	chr8:85707935..85709870-chr8:85714528..85717320,2	K562	blood:
4	chr8:85637881..85639538-chr8:85676216..85677896,2	K562	blood:
5	chr1:121483928..121486918-chr8:85710303..85711824,2	K562	blood:
6	chr8:85707935..85709870-chr8:85714528..85717320,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRCC1-3	chr8:85591033-85592077	NONHSAT127504

Variant related genes	Relation type
ENSG00000253137	TF binding region
RALYL	TF binding region
RNU6-1040P	TF binding region
ENSG00000253137	CpG island
RALYL	CpG island
RNU6-1040P	CpG island

Extended variants
information (count: 2424 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2424 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368641477	chr8:85578714-85578715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs561179347	chr8:85578732-85578733	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs574753842	chr8:85578760-85578761	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs565070533	chr8:85578790-85578791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371912741	chr8:85578791-85578792	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540459937	chr8:85578798-85578799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs184870391	chr8:85578855-85578856	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115650788	chr8:85578857-85578858	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs75478721	chr8:85578861-85578862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs552464243	chr8:85579867-85579868	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs116718115	chr8:85579868-85579869	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549912308	chr8:85579883-85579884	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537922776	chr8:85579918-85579919	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554643639	chr8:85579958-85579959	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577029642	chr8:85580111-85580112	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs181936621	chr8:85580194-85580195	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs17794302	chr8:85580217-85580218	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148602487	chr8:85580251-85580252	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs77717305	chr8:85580252-85580253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs560997038	chr8:85580288-85580289	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141154944	chr8:85580346-85580347	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540197836	chr8:85580350-85580351	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs184375365	chr8:85580359-85580360	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs532670815	chr8:85580401-85580402	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs189130666	chr8:85580407-85580408	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs146138782	chr8:85580463-85580464	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs531479712	chr8:85580530-85580531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs140180102	chr8:85580618-85580619	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs568121487	chr8:85580629-85580630	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs368370619	chr8:85580653-85580654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs564287507	chr8:85580708-85580709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs533786233	chr8:85580730-85580731	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs568695738	chr8:85580734-85580735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373789879	chr8:85580776-85580777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532534765	chr8:85580807-85580808	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs547049706	chr8:85580833-85580834	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs181175271	chr8:85580853-85580854	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200725189	chr8:85580867-85580868	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs369438144	chr8:85580869-85580870	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186478860	chr8:85580874-85580875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556364232	chr8:85580878-85580879	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535774393	chr8:85580886-85580887	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs575831382	chr8:85580948-85580949	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535228051	chr8:85580966-85580967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190961170	chr8:85580967-85580968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541480816	chr8:85581010-85581011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369221763	chr8:85581021-85581022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11989935	chr8:85581033-85581034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574560332	chr8:85581118-85581119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143942369	chr8:85581129-85581130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85580800-85583400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr8:85583400-85583600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
3	chr8:85583400-85584000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:85588600-85589000	Enhancers	Adipose Nuclei	Adipose
5	chr8:85588800-85589000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:85589400-85590000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr8:85590000-85590200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:85590400-85590600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:85591200-85591400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:85596000-85596400	Active TSS	Placenta	Placenta
11	chr8:85597200-85597600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:85597200-85597800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:85597800-85598200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:85598200-85598600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:85612800-85613400	Enhancers	Fetal Heart	heart
16	chr8:85614000-85614200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:85614200-85615800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:85617000-85617600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:85617200-85618200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:85617400-85617600	Enhancers	Left Ventricle	heart
21	chr8:85617600-85619600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:85617800-85618000	Enhancers	Fetal Brain Female	brain
23	chr8:85617800-85618400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr8:85618000-85618200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:85618000-85619600	Active TSS	Fetal Brain Female	brain
26	chr8:85618200-85618600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr8:85618200-85618800	Active TSS	Fetal Brain Male	brain
28	chr8:85618200-85619000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:85618200-85619000	Active TSS	Brain Hippocampus Middle	brain
30	chr8:85618200-85619600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:85618200-85621200	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr8:85618400-85618800	Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr8:85618400-85619200	Enhancers	Brain Germinal Matrix	brain
34	chr8:85618400-85619600	Active TSS	Brain Inferior Temporal Lobe	brain
35	chr8:85618600-85619000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:85618800-85619000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
37	chr8:85618800-85619200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:85618800-85619200	Active TSS	Fetal Kidney	kidney
39	chr8:85619000-85619200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:85619000-85619400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:85619600-85619800	Enhancers	Fetal Brain Male	brain
42	chr8:85619600-85620000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr8:85620000-85620800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:85620400-85620600	Enhancers	Fetal Brain Female	brain
45	chr8:85620800-85621400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:85621200-85624600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr8:85621400-85624200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr8:85624200-85624600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:85624600-85625000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr8:85625000-85627000	Weak transcription	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links