Variant report

Variant	nsv1019477
Chromosome Location	chr8:86468856-86557401
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:399)
CpG islands
(count:610)
Chromatin interactive
region (count:18)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
2	BACH1	chr8:86469052-86469363	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:86477700-86478018	K562	blood:	n/a	n/a
4	BACH1	chr8:86477707-86478028	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:86556713-86557155	GM12878	blood:	n/a	n/a
6	BATF	chr8:86557171-86557645	GM12878	blood:	n/a	n/a
7	BATF	chr8:86556634-86557157	GM12878	blood:	n/a	n/a
8	BATF	chr8:86557168-86557577	GM12878	blood:	n/a	n/a
9	BCL11A	chr8:86556317-86556493	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:86556627-86557168	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:86557171-86557821	GM12878	blood:	n/a	chr8:86557185-86557194
12	BCL11A	chr8:86556646-86557544	GM12878	blood:	n/a	chr8:86557185-86557194 chr8:86557162-86557171
13	BHLHE40	chr8:86530061-86530136	K562	blood:	n/a	n/a
14	BHLHE40	chr8:86557188-86557731	HepG2	liver:	n/a	n/a
15	BHLHE40	chr8:86556653-86557165	HepG2	liver:	n/a	n/a
16	CEBPB	chr8:86506060-86506371	IMR90	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
17	CEBPB	chr8:86526617-86526827	K562	blood:	n/a	chr8:86526677-86526688
18	CEBPB	chr8:86526501-86526858	HepG2	liver:	n/a	chr8:86526677-86526688
19	CEBPB	chr8:86541828-86542028	HepG2	liver:	n/a	chr8:86541944-86541955
20	CEBPB	chr8:86526496-86526857	IMR90	lung:	n/a	chr8:86526677-86526688
21	CEBPB	chr8:86506021-86506349	H1-hESC	embryonic stem cell:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
22	CEBPB	chr8:86526551-86526947	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
23	CEBPB	chr8:86506026-86506381	A549	lung:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
24	CEBPB	chr8:86526484-86526818	ECC-1	luminal epithelium:	n/a	chr8:86526677-86526688
25	CEBPB	chr8:86483060-86483308	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:86526425-86526941	MCF-7	breast:	n/a	chr8:86526677-86526688
27	CEBPB	chr8:86548074-86548266	HepG2	liver:	n/a	chr8:86548177-86548194
28	CEBPB	chr8:86475730-86475860	HepG2	liver:	n/a	chr8:86475757-86475770
29	CEBPB	chr8:86506081-86506340	K562	blood:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
30	CEBPB	chr8:86506027-86506610	HepG2	liver:	n/a	chr8:86506202-86506211 chr8:86506581-86506598 chr8:86506488-86506500 chr8:86506200-86506211
31	CEBPB	chr8:86505964-86506372	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
32	CEBPB	chr8:86506011-86506339	MCF-7	breast:	n/a	chr8:86506202-86506211 chr8:86506200-86506211
33	CEBPB	chr8:86526519-86526866	A549	lung:	n/a	chr8:86526677-86526688
34	CHD2	chr8:86509594-86509815	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr8:86482894-86483257	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr8:86544750-86544836	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr8:86488840-86488915	GM19240	blood:	n/a	n/a
38	CTCF	chr8:86541400-86541550	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr8:86488811-86488916	A549	lung:	n/a	n/a
40	CTCF	chr8:86488799-86488917	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:86488825-86488916	GM12891	blood:	n/a	n/a
42	CTCF	chr8:86488793-86488916	ProgFib	skin:	n/a	n/a
43	CTCF	chr8:86488826-86488917	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:86500740-86500890	HCT-116	colon:	n/a	n/a
45	CTCF	chr8:86515129-86515167	GM20000	blood:	n/a	n/a
46	CTCF	chr8:86488813-86488918	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:86494371-86494488	GM12878	blood:	n/a	n/a
48	CTCF	chr8:86488877-86488897	GM19238	blood:	n/a	n/a
49	CTCF	chr8:86480580-86480730	HRE	kidney:	n/a	n/a
50	CTCF	chr8:86488806-86488916	MCF-7	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86556749-86556799	AG04449	skin:	fetal
2	chr8:86556164-86556214	HRCEpiC	kidney:	n/a
3	chr8:86551492-86551542	ECC-1	luminal epithelium:	n/a
4	chr8:86504072-86504122	GM12878	blood:	n/a
5	chr8:86486097-86486147	NH-A	brain:	n/a
6	chr8:86556164-86556214	LNCaP	prostate:	n/a
7	chr8:86504072-86504122	GM12892	blood:	n/a
8	chr8:86556176-86556226	SK-N-MC	brain:	n/a
9	chr8:86556176-86556226	HEK293	kidney:	embryo
10	chr8:86554026-86554076	SK-N-SH_RA	brain:	n/a
11	chr8:86554888-86554938	GM12891	blood:	n/a
12	chr8:86554888-86554938	AG04449	skin:	fetal
13	chr8:86554888-86554938	NB4	blood:	n/a
14	chr8:86556903-86556953	GM12878	blood:	n/a
15	chr8:86556903-86556953	HCPEpiC	choroid plexus:	n/a
16	chr8:86556176-86556226	K562	blood:	n/a
17	chr8:86556176-86556226	ECC-1	luminal epithelium:	n/a
18	chr8:86556171-86556221	T-47D	breast:	n/a
19	chr8:86551492-86551542	AG04450	lung:	fetal
20	chr8:86556164-86556214	SAEC	small airway:	n/a
21	chr8:86556749-86556799	AG09309	skin:	n/a
22	chr8:86486097-86486147	AG09319	gingival:	n/a
23	chr8:86556171-86556221	BE2_C	brain:	n/a
24	chr8:86551492-86551542	SAEC	small airway:	n/a
25	chr8:86554888-86554938	Caco-2	colon:	n/a
26	chr8:86556749-86556799	SKMC	muscle:	n/a
27	chr8:86556749-86556799	GM12892	blood:	n/a
28	chr8:86554888-86554938	MCF10A-Er-Src	breast:	n/a
29	chr8:86554888-86554938	HRE	kidney:	n/a
30	chr8:86556171-86556221	AoSMC	blood vessel:	n/a
31	chr8:86556171-86556221	MCF10A-Er-Src	breast:	n/a
32	chr8:86551492-86551542	Hepatocyte	liver:	n/a
33	chr8:86556176-86556226	GM06990	blood:	n/a
34	chr8:86554026-86554076	H1-hESC	embryonic stem cell:	embryo
35	chr8:86556176-86556226	Hela-S3	cervix:	n/a
36	chr8:86556164-86556214	MCF10A-Er-Src	breast:	n/a
37	chr8:86551492-86551542	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:86486097-86486147	GM12891	blood:	n/a
39	chr8:86504072-86504122	BJ	skin:	n/a
40	chr8:86556176-86556226	HepG2	liver:	n/a
41	chr8:86556749-86556799	AG10803	skin:	n/a
42	chr8:86556171-86556221	HCT-116	colon:	n/a
43	chr8:86556171-86556221	AG04450	lung:	fetal
44	chr8:86556176-86556226	HCM	heart:	n/a
45	chr8:86556176-86556226	GM12891	blood:	n/a
46	chr8:86556164-86556214	AoSMC	blood vessel:	n/a
47	chr8:86551492-86551542	HEEpiC	esophagus:	n/a
48	chr8:86504072-86504122	LNCaP	prostate:	n/a
49	chr8:86554026-86554076	IMR90	lung:	fetal
50	chr8:86504072-86504122	NH-A	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
2	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
3	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
4	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
5	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
6	chr8:86439507..86442336-chr8:86514176..86515935,2	MCF-7	breast:
7	chr8:86468837..86470919-chr8:86472571..86475543,2	MCF-7	breast:
8	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
9	chr8:86468837..86470919-chr8:86472571..86475543,2	MCF-7	breast:
10	chr22:21257752..21260264-chr8:86546631..86548915,2	MCF-7	breast:
11	chr8:86374283..86376503-chr8:86538225..86540669,2	MCF-7	breast:
12	chr8:43092411..43092911-chr8:86471290..86472121,2	MCF-7	breast:
13	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
14	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
15	chr8:86482210..86485611-chr8:86487040..86489200,3	MCF-7	breast:
16	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
17	chr8:86375239..86377397-chr8:86481535..86484020,2	MCF-7	breast:
18	chr8:86375424..86377352-chr8:86545353..86547430,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537
2	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537

No data

Variant related genes	Relation type
ENSG00000253680	TF binding region
REXO1L8P	TF binding region
ENSG00000253680	CpG island
REXO1L8P	CpG island
ENSG00000253549	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 2448 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2448 , 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	rs540117964	chr8:86468901-86468902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559753970	chr8:86468969-86468970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576425018	chr8:86469012-86469013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545428554	chr8:86469020-86469021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528972044	chr8:86469053-86469054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs562610634	chr8:86469239-86469240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531273270	chr8:86469273-86469274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146188667	chr8:86469282-86469283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs137898881	chr8:86469307-86469308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530452173	chr8:86469334-86469335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183401954	chr8:86469554-86469555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs359529	chr8:86469610-86469611	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs539028184	chr8:86469611-86469612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552250729	chr8:86469655-86469656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569351114	chr8:86469675-86469676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187698436	chr8:86469696-86469697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550790301	chr8:86469697-86469698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116436301	chr8:86469725-86469726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80210052	chr8:86469757-86469758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574279859	chr8:86469771-86469772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533878324	chr8:86469780-86469781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142230530	chr8:86469804-86469805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150915822	chr8:86469806-86469807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139357421	chr8:86469831-86469832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555857628	chr8:86469885-86469886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576115197	chr8:86469894-86469895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541931658	chr8:86469914-86469915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561507518	chr8:86470072-86470073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530315581	chr8:86470087-86470088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540783829	chr8:86470122-86470123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560778527	chr8:86470160-86470161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs359528	chr8:86470188-86470189	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7014618	chr8:86470231-86470232	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs193173793	chr8:86470234-86470235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185023647	chr8:86470282-86470283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188590408	chr8:86470293-86470294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73265413	chr8:86470313-86470314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192756771	chr8:86470323-86470324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183963785	chr8:86470378-86470379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374193863	chr8:86470415-86470416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112770001	chr8:86470484-86470485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188200759	chr8:86470495-86470496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539331635	chr8:86470525-86470526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556158837	chr8:86470559-86470560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575938086	chr8:86470571-86470572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541993187	chr8:86470596-86470597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7010491	chr8:86470645-86470646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544913838	chr8:86470724-86470725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144266476	chr8:86470728-86470729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180693093	chr8:86470744-86470745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Colorectal cancer	21645411	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86462800-86469200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:86463800-86469000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:86463800-86469000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:86464000-86469000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr8:86464200-86469000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:86464400-86469000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:86464600-86469000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr8:86464600-86469000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:86468000-86470200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr8:86468600-86469000	Enhancers	Brain Substantia Nigra	brain
11	chr8:86468600-86469600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr8:86468600-86470200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr8:86468800-86469000	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr8:86468800-86469400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:86468800-86469400	Enhancers	Brain Anterior Caudate	brain
16	chr8:86468800-86469400	Enhancers	Fetal Intestine Small	intestine
17	chr8:86468800-86469600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:86468800-86469800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:86468800-86469800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:86469000-86469200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:86469000-86469200	Weak transcription	Brain Hippocampus Middle	brain
22	chr8:86469000-86469400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr8:86469000-86469400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr8:86469000-86469400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr8:86469000-86469400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr8:86469000-86469400	Enhancers	HMEC	breast
27	chr8:86469000-86469600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:86469000-86469600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:86469000-86469600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr8:86469200-86469800	Weak transcription	Brain Substantia Nigra	brain
31	chr8:86469200-86470000	Enhancers	Brain Hippocampus Middle	brain
32	chr8:86469200-86470200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr8:86469200-86472000	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr8:86469400-86469600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:86469400-86471600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr8:86469400-86471600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr8:86469400-86474600	Weak transcription	Fetal Intestine Small	intestine
38	chr8:86469400-86475000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr8:86469400-86475000	Weak transcription	Brain Anterior Caudate	brain
40	chr8:86469600-86472600	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr8:86469800-86474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:86470000-86475400	Weak transcription	Brain Hippocampus Middle	brain
43	chr8:86470200-86471600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr8:86470200-86471800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:86470200-86474800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr8:86471600-86472200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:86471600-86472200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:86471600-86472200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr8:86471800-86472200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:86472000-86472200	Enhancers	H9 Cell Line	embryonic stem cell

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