Variant report

Variant	nsv524399
Chromosome Location	chr8:90627436-90635791
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	chr8:90629286-90629552	HepG2	liver:	n/a	n/a
2	BRCA1	chr8:90629299-90629540	Hela-S3	cervix:	n/a	n/a
3	CBX3	chr8:90629083-90629708	HCT-116	colon:	n/a	n/a
4	CEBPB	chr8:90627124-90627590	IMR90	lung:	n/a	chr8:90627187-90627200
5	CEBPB	chr8:90627282-90627592	HepG2	liver:	n/a	n/a
6	CEBPB	chr8:90627844-90628214	IMR90	lung:	n/a	n/a
7	CTCF	chr8:90629360-90629510	HMEC	breast:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
8	CTCF	chr8:90629341-90629555	GM12878	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
9	CTCF	chr8:90629420-90629570	GM12864	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
10	CTCF	chr8:90629301-90629649	H1-hESC	embryonic stem cell:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
11	CTCF	chr8:90629400-90629550	HL-60	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
12	CTCF	chr8:90629380-90629530	GM12873	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
13	CTCF	chr8:90629400-90629550	SK-N-SH_RA	brain:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
14	CTCF	chr8:90629360-90629510	GM12864	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
15	CTCF	chr8:90629400-90629550	HPAF	blood vessel:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
16	CTCF	chr8:90629460-90629610	BE2_C	brain:	n/a	n/a
17	CTCF	chr8:90629380-90629530	Caco-2	colon:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
18	CTCF	chr8:90629340-90629579	Pancreas_OC	pancreas:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
19	CTCF	chr8:90629860-90630010	AG10803	skin:	n/a	n/a
20	CTCF	chr8:90629380-90629530	AG04449	skin:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
21	CTCF	chr8:90629380-90629530	GM12866	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
22	CTCF	chr8:90629359-90629556	GM13977	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
23	CTCF	chr8:90629360-90629510	GM12801	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
24	CTCF	chr8:90629400-90629550	SAEC	small airway:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
25	CTCF	chr8:90629283-90629617	Medullo	brain:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
26	CTCF	chr8:90629320-90629470	HEK293	kidney:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
27	CTCF	chr8:90629340-90629490	AG09309	skin:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
28	CTCF	chr8:90629400-90629550	HPF	lung:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
29	CTCF	chr8:90629402-90629516	GM20000	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
30	CTCF	chr8:90629380-90629530	AG09309	skin:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
31	CTCF	chr8:90629340-90629490	GM12874	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
32	CTCF	chr8:90629420-90629570	GM12872	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
33	CTCF	chr8:90629126-90629834	SK-N-SH	brain:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
34	CTCF	chr8:90629360-90629510	RPTEC	kidney:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
35	CTCF	chr8:90629380-90629530	HMF	breast:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
36	CTCF	chr8:90629400-90629550	GM12865	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
37	CTCF	chr8:90629400-90629550	GM12872	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
38	CTCF	chr8:90629440-90629590	HCM	heart:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
39	CTCF	chr8:90629540-90629690	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:90629360-90629510	HVMF	connective:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
41	CTCF	chr8:90629400-90629550	GM12871	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
42	CTCF	chr8:90629360-90629510	GM12865	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
43	CTCF	chr8:90629360-90629510	AG04449	skin:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
44	CTCF	chr8:90629420-90629570	HRE	kidney:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
45	CTCF	chr8:90629314-90629595	HUVEC	blood vessel:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
46	CTCF	chr8:90629384-90629529	GM13976	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
47	CTCF	chr8:90629120-90629270	A549	lung:	n/a	n/a
48	CTCF	chr8:90629340-90629490	GM12870	blood:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
49	CTCF	chr8:90629360-90629510	HUVEC	blood vessel:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461
50	CTCF	chr8:90629420-90629570	WI-38	lung:	n/a	chr8:90629446-90629462 chr8:90629445-90629463 chr8:90629440-90629461

No.	Distal block	Cell Line	Cell type
1	chr8:90627324..90629190-chr8:90732562..90735490,2	MCF-7	breast:
2	chr8:90630071..90632374-chr8:90637298..90640018,2	K562	blood:
3	chr8:90270487..90271274-chr8:90627944..90628605,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
2	lnc-NBN-1	chr8:90629158-90629385	ENSG00000251136
3	lnc-NBN-1	chr8:90632912-90633104	ENSG00000251136
4	lnc-NBN-1	chr8:90629222-90629385	ENSG00000251136
5	lnc-NBN-1	chr8:90635314-90635433	ENSG00000251136
6	lnc-NBN-1	chr8:90629308-90629386	ENSG00000251136
7	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136
8	lnc-NBN-1	chr8:90627412-90627534	ENSG00000251136.4
9	lnc-RIPK2-2	chr8:90627189-90627723	NONHSAT127614
10	lnc-NBN-1	chr8:90627412-90627568	NONHSAT127613

Variant related genes	Relation type
ENSG00000251136	TF binding region
ENSG00000251136	chromatin interactions
EIF2C1	miRNA target sites
NCOA3	miRNA target sites
HIPK3	miRNA target sites
HNF4A	miRNA target sites
NAPEPLD	miRNA target sites
CLN6	miRNA target sites
HNRNPD	miRNA target sites

Extended variants
information (count: 269 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:269 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2644012	chr8:90627436-90627437	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs572549720	chr8:90627507-90627508	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs539818877	chr8:90627542-90627543	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs192518115	chr8:90627650-90627651	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs574266918	chr8:90627660-90627661	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs201639697	chr8:90627667-90627668	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs544862230	chr8:90627735-90627736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs562950238	chr8:90627754-90627755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111805648	chr8:90627762-90627763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575847180	chr8:90627794-90627795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552554139	chr8:90627798-90627799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184498808	chr8:90627860-90627861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12155879	chr8:90627866-90627867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560547867	chr8:90627875-90627876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141281331	chr8:90627889-90627890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs17696834	chr8:90628008-90628009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs34784931	chr8:90628095-90628096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567639199	chr8:90628117-90628118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28433004	chr8:90628134-90628135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs115496475	chr8:90628144-90628145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188387621	chr8:90628195-90628196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181251227	chr8:90628196-90628197	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551088311	chr8:90628239-90628240	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541237162	chr8:90628246-90628247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185759535	chr8:90628271-90628272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189052398	chr8:90628276-90628277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554964850	chr8:90628282-90628283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182352083	chr8:90628298-90628299	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187407232	chr8:90628302-90628303	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556813748	chr8:90628304-90628305	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146958194	chr8:90628311-90628312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545603538	chr8:90628400-90628401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560637751	chr8:90628430-90628431	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572596932	chr8:90628455-90628456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192304384	chr8:90628498-90628499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369501725	chr8:90628517-90628518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs147996996	chr8:90628537-90628538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs182386279	chr8:90628542-90628543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550645537	chr8:90628586-90628587	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562778903	chr8:90628600-90628601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185363435	chr8:90628610-90628611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs216981	chr8:90628648-90628649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566302779	chr8:90628669-90628670	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533644489	chr8:90628700-90628701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190122439	chr8:90628707-90628708	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141638490	chr8:90628713-90628714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537824845	chr8:90628728-90628729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566866174	chr8:90628738-90628739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs160420	chr8:90628742-90628743	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs13254821	chr8:90628766-90628767	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
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
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
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90599600-90650800	Weak transcription	Left Ventricle	heart
2	chr8:90616000-90630000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr8:90616000-90652600	Weak transcription	Ovary	ovary
4	chr8:90621200-90637600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:90622400-90630800	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:90623600-90628000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:90624000-90629400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:90624000-90629400	Enhancers	NHEK	skin
9	chr8:90624200-90629400	Enhancers	HMEC	breast
10	chr8:90624400-90640400	Weak transcription	Aorta	Aorta
11	chr8:90624600-90628000	Weak transcription	NHLF	lung
12	chr8:90624600-90628200	Weak transcription	HSMM	muscle
13	chr8:90624600-90630200	Weak transcription	HSMMtube	muscle
14	chr8:90624600-90642800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr8:90625000-90628000	Weak transcription	NH-A	brain
16	chr8:90625400-90629400	Weak transcription	Fetal Lung	lung
17	chr8:90625600-90628000	Weak transcription	A549	lung
18	chr8:90625800-90628000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:90626000-90649200	Weak transcription	Brain Angular Gyrus	brain
20	chr8:90626600-90629400	Enhancers	NHDF-Ad	bronchial
21	chr8:90626800-90628800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr8:90626800-90629400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr8:90627000-90628800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr8:90627000-90629000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:90627000-90629400	Enhancers	Osteobl	bone
26	chr8:90627200-90628400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr8:90627400-90627600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr8:90627400-90627800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:90627400-90628800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:90627400-90629400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:90627800-90629400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:90628000-90628200	Enhancers	NHLF	lung
33	chr8:90628000-90628400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr8:90628000-90628600	Enhancers	Placenta	Placenta
35	chr8:90628000-90628600	Enhancers	A549	lung
36	chr8:90628000-90628800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:90628000-90629400	Enhancers	NH-A	brain
38	chr8:90628200-90628800	Enhancers	HSMM	muscle
39	chr8:90628400-90629200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr8:90629000-90630600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:90629200-90629400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:90629200-90629400	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr8:90629400-90644600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:90629400-90659000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:90630200-90631200	Enhancers	HSMMtube	muscle
46	chr8:90630400-90631000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr8:90630600-90631000	Enhancers	Brain Cingulate Gyrus	brain
48	chr8:90630600-90631000	Enhancers	Fetal Brain Female	brain
49	chr8:90630800-90631000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:90630800-90631000	Enhancers	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links