Variant report

Variant	nsv967615
Chromosome Location	chr8:90424836-90429374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:132)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:132 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:90425760-90425857	HepG2	liver:	n/a	n/a
2	CTCF	chr8:90425074-90425166	ProgFib	skin:	n/a	n/a
3	CTCF	chr8:90425020-90425170	GM12865	blood:	n/a	n/a
4	CTCF	chr8:90425067-90425195	GM19240	blood:	n/a	n/a
5	CTCF	chr8:90425660-90425810	GM12874	blood:	n/a	n/a
6	CTCF	chr8:90425025-90425257	MCF-7	breast:	n/a	n/a
7	CTCF	chr8:90425040-90425190	AG04449	skin:	n/a	n/a
8	CTCF	chr8:90425040-90425190	HCM	heart:	n/a	n/a
9	CTCF	chr8:90425000-90425150	GM12873	blood:	n/a	n/a
10	CTCF	chr8:90425043-90425249	Fibrobl	skin:	n/a	n/a
11	CTCF	chr8:90425120-90425270	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr8:90425080-90425230	GM12864	blood:	n/a	n/a
13	CTCF	chr8:90425020-90425170	GM12870	blood:	n/a	n/a
14	CTCF	chr8:90425050-90425220	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr8:90425020-90425170	SAEC	small airway:	n/a	n/a
16	CTCF	chr8:90425700-90425850	Caco-2	colon:	n/a	n/a
17	CTCF	chr8:90425080-90425230	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr8:90425034-90425233	MCF-7	breast:	n/a	n/a
19	CTCF	chr8:90425020-90425170	HCT-116	colon:	n/a	n/a
20	CTCF	chr8:90425747-90425819	GM19238	blood:	n/a	n/a
21	CTCF	chr8:90425000-90425150	GM12875	blood:	n/a	n/a
22	CTCF	chr8:90425020-90425170	GM12878	blood:	n/a	n/a
23	CTCF	chr8:90425672-90425848	HepG2	liver:	n/a	n/a
24	CTCF	chr8:90425737-90425813	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:90424940-90425090	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr8:90425085-90425183	Gliobla	brain:	n/a	n/a
27	CTCF	chr8:90425043-90425182	HepG2	liver:	n/a	n/a
28	CTCF	chr8:90424940-90425090	GM12874	blood:	n/a	n/a
29	CTCF	chr8:90426915-90426947	Lung_OC	lung:	n/a	n/a
30	CTCF	chr8:90425060-90425210	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr8:90425080-90425230	SAEC	small airway:	n/a	n/a
32	CTCF	chr8:90425680-90425830	HepG2	liver:	n/a	n/a
33	CTCF	chr8:90425060-90425210	NHEK	skin:	n/a	n/a
34	CTCF	chr8:90424960-90425110	GM12872	blood:	n/a	n/a
35	CTCF	chr8:90425040-90425190	A549	lung:	n/a	n/a
36	CTCF	chr8:90425020-90425170	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr8:90427740-90427890	HMEC	breast:	n/a	n/a
38	CTCF	chr8:90425039-90425206	GM12892	blood:	n/a	n/a
39	CTCF	chr8:90425086-90425189	GM12878	blood:	n/a	n/a
40	CTCF	chr8:90425040-90425190	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr8:90425300-90425450	A549	lung:	n/a	n/a
42	CTCF	chr8:90425005-90425278	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:90425020-90425170	GM12869	blood:	n/a	n/a
44	CTCF	chr8:90425678-90425982	HepG2	liver:	n/a	n/a
45	CTCF	chr8:90425040-90425190	NHEK	skin:	n/a	n/a
46	CTCF	chr8:90425725-90425891	HepG2	liver:	n/a	n/a
47	CTCF	chr8:90425026-90425221	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:90425660-90425810	GM06990	blood:	n/a	n/a
49	CTCF	chr8:90425736-90425843	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:90425000-90425150	HMF	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90427508-90427558	U87	brain:	n/a
2	chr8:90427508-90427558	MCF10A-Er-Src	breast:	n/a
3	chr8:90427508-90427558	Jurkat	blood:	n/a
4	chr8:90427508-90427558	HRCEpiC	kidney:	n/a
5	chr8:90427508-90427558	Hepatocyte	liver:	n/a
6	chr8:90427508-90427558	HAEpiC	amniotic membrane:	n/a
7	chr8:90427508-90427558	H1-hESC	embryonic stem cell:	embryo
8	chr8:90427508-90427558	NHBE	bronchial:	n/a
9	chr8:90427508-90427558	HEK293	kidney:	embryo
10	chr8:90427508-90427558	HIPEpiC	eye:	n/a
11	chr8:90427508-90427558	HRE	kidney:	n/a
12	chr8:90427508-90427558	GM12892	blood:	n/a
13	chr8:90427508-90427558	LNCaP	prostate:	n/a
14	chr8:90427508-90427558	RPTEC	kidney:	n/a
15	chr8:90427508-90427558	SK-N-MC	brain:	n/a
16	chr8:90427508-90427558	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:90427508-90427558	CMK	blood:	n/a
18	chr8:90427508-90427558	AG09319	gingival:	n/a
19	chr8:90427508-90427558	HCM	heart:	n/a
20	chr8:90427508-90427558	AoSMC	blood vessel:	n/a
21	chr8:90427508-90427558	AG04450	lung:	fetal
22	chr8:90427508-90427558	GM12878	blood:	n/a
23	chr8:90427508-90427558	ProgFib	skin:	n/a
24	chr8:90427508-90427558	BJ	skin:	n/a
25	chr8:90427508-90427558	AG10803	skin:	n/a
26	chr8:90427508-90427558	K562	blood:	n/a
27	chr8:90427508-90427558	GM19239	blood:	n/a
28	chr8:90427508-90427558	HNPCEpiC	eye:	n/a
29	chr8:90427508-90427558	HRPEpiC	eye:	n/a
30	chr8:90427508-90427558	HMEC	breast:	n/a
31	chr8:90427508-90427558	HEEpiC	esophagus:	n/a
32	chr8:90427508-90427558	SAEC	small airway:	n/a
33	chr8:90427508-90427558	PANC-1	pancreas:	n/a
34	chr8:90427508-90427558	NH-A	brain:	n/a
35	chr8:90427508-90427558	AG09309	skin:	n/a
36	chr8:90427508-90427558	IMR90	lung:	fetal
37	chr8:90427508-90427558	Caco-2	colon:	n/a
38	chr8:90427508-90427558	SK-N-SH_RA	brain:	n/a
39	chr8:90427508-90427558	T-47D	breast:	n/a
40	chr8:90427508-90427558	HCF	heart:	n/a
41	chr8:90427508-90427558	NHDF-neo	bronchial:	n/a
42	chr8:90427508-90427558	HCPEpiC	choroid plexus:	n/a
43	chr8:90427508-90427558	ovcar-3	ovarian:	n/a
44	chr8:90427508-90427558	BE2_C	brain:	n/a
45	chr8:90427508-90427558	PrEC	prostate:	n/a
46	chr8:90427508-90427558	HCT-116	colon:	n/a
47	chr8:90427508-90427558	SK-N-SH	brain:	n/a
48	chr8:90427508-90427558	ECC-1	luminal epithelium:	n/a
49	chr8:90427508-90427558	MCF-7	breast:	n/a
50	chr8:90427508-90427558	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:90424990..90426276-chr8:90629028..90629951,3	MCF-7	breast:
2	chr8:90427557..90429111-chr8:90431047..90432856,2	MCF-7	breast:

No data

Variant related genes	Relation type
KRT8P4	TF binding region
KRT8P4	CpG island
ENSG00000251136	chromatin interactions

Extended variants
information (count: 186 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:186 , 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	rs554488103	chr8:90424850-90424851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576139613	chr8:90424868-90424869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147092535	chr8:90424889-90424890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565020909	chr8:90424891-90424892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190426271	chr8:90424894-90424895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541063391	chr8:90424895-90424896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559359183	chr8:90424948-90424949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530352361	chr8:90424956-90424957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548818222	chr8:90425003-90425004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs570791386	chr8:90425023-90425024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138257089	chr8:90425025-90425026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs569029065	chr8:90425042-90425043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531172855	chr8:90425059-90425060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs552347637	chr8:90425061-90425062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570637125	chr8:90425072-90425073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534776562	chr8:90425098-90425099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552963968	chr8:90425134-90425135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114969755	chr8:90425179-90425180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149596042	chr8:90425201-90425202	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144278028	chr8:90425266-90425267	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576254810	chr8:90425279-90425280	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs148727933	chr8:90425282-90425283	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183585428	chr8:90425288-90425289	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552801631	chr8:90425301-90425302	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577030642	chr8:90425306-90425307	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs141953819	chr8:90425321-90425322	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112425048	chr8:90425325-90425326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146288565	chr8:90425329-90425330	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73696309	chr8:90425371-90425372	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189023887	chr8:90425372-90425373	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534964069	chr8:90425466-90425467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375853566	chr8:90425492-90425493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139418138	chr8:90425493-90425494	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531086078	chr8:90425517-90425518	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552386215	chr8:90425540-90425541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564305401	chr8:90425558-90425559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541761150	chr8:90425571-90425572	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs528584725	chr8:90425594-90425595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371578435	chr8:90425595-90425596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374826685	chr8:90425643-90425644	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368689452	chr8:90425647-90425648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568370638	chr8:90425648-90425649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs144129961	chr8:90425674-90425675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150988798	chr8:90425676-90425677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs193150971	chr8:90425706-90425707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs75338651	chr8:90425735-90425736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556719370	chr8:90425738-90425739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537309124	chr8:90425745-90425746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs558812152	chr8:90425759-90425760	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs59693881	chr8:90425762-90425763	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:106)

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
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90415600-90427200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:90421600-90427000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:90421600-90430600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:90421800-90427400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr8:90422200-90427400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:90422400-90425800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:90422400-90427200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:90422600-90425200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:90424400-90435200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:90424800-90426600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:90425000-90426400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:90425200-90425400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr8:90425200-90425600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr8:90425400-90425600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:90425400-90427800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr8:90425800-90427000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:90426800-90427000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr8:90427000-90427400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:90427000-90428200	Enhancers	H9 Cell Line	embryonic stem cell
20	chr8:90427200-90428200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr8:90427200-90428400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:90427200-90428400	Enhancers	HMEC	breast
23	chr8:90427200-90428800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:90427200-90429000	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:90427400-90427800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:90427400-90427800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr8:90427400-90428200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr8:90427400-90428200	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr8:90427600-90428000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:90427600-90428200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr8:90427600-90428200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:90427600-90428200	Enhancers	NHEK	skin
33	chr8:90427600-90428400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:90427800-90428000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr8:90427800-90428400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr8:90428000-90428400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr8:90428200-90429000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr8:90428400-90428800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr8:90428400-90439000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr8:90428800-90434400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr8:90429000-90429200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:90429200-90430600	Weak transcription	H9 Cell Line	embryonic stem cell

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