Variant report

Variant	esv1814789
Chromosome Location	chr8:119627671-119672134
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:353)
CpG islands
(count:671)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:353 , 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	ATF2	chr8:119633656-119634326	GM12878	blood:	n/a	n/a
2	BACH1	chr8:119634004-119634261	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr8:119633423-119633753	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:119627790-119628026	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:119639827-119640142	GM12878	blood:	n/a	n/a
6	BATF	chr8:119650982-119651273	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:119639874-119640136	GM12878	blood:	n/a	n/a
8	BCLAF1	chr8:119632868-119633338	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:119633139-119634823	GM12878	blood:	n/a	chr8:119634206-119634222
10	BHLHE40	chr8:119639927-119640003	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:119640702-119641204	GM12878	blood:	n/a	n/a
12	CEBPB	chr8:119656845-119657122	IMR90	lung:	n/a	chr8:119656973-119656984 chr8:119656973-119656986
13	CEBPB	chr8:119669577-119669749	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:119663079-119663315	A549	lung:	n/a	n/a
15	CEBPB	chr8:119640822-119641003	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:119663073-119663370	IMR90	lung:	n/a	n/a
17	CEBPB	chr8:119633093-119633293	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr8:119660453-119660731	IMR90	lung:	n/a	n/a
19	CEBPB	chr8:119645690-119646009	HepG2	liver:	n/a	chr8:119645848-119645859
20	CEBPB	chr8:119656925-119657105	A549	lung:	n/a	chr8:119656973-119656984 chr8:119656973-119656986
21	CEBPB	chr8:119645778-119645976	H1-hESC	embryonic stem cell:	n/a	chr8:119645848-119645859
22	CHD1	chr8:119632933-119634351	GM12878	blood:	n/a	n/a
23	CHD1	chr8:119634554-119635171	GM12878	blood:	n/a	chr8:119634634-119634644
24	CHD1	chr8:119639970-119640010	GM12878	blood:	n/a	n/a
25	CHD2	chr8:119632938-119634983	GM12878	blood:	n/a	chr8:119634634-119634644
26	CHD2	chr8:119633648-119633911	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr8:119633834-119634978	Hela-S3	cervix:	n/a	chr8:119634634-119634644
28	CHD2	chr8:119634212-119634471	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr8:119634054-119634372	A549	lung:	n/a	n/a
30	CREB1	chr8:119633412-119634397	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr8:119640592-119641088	GM12878	blood:	n/a	n/a
32	CREB1	chr8:119632833-119633880	GM12878	blood:	n/a	n/a
33	CREB1	chr8:119633440-119634269	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr8:119634386-119634741	A549	lung:	n/a	n/a
35	CREB1	chr8:119640565-119641118	GM12878	blood:	n/a	n/a
36	CTCF	chr8:119633740-119633890	SAEC	small airway:	n/a	n/a
37	CTCF	chr8:119633884-119633923	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:119634136-119634201	GM12878	blood:	n/a	n/a
39	CTCF	chr8:119634750-119634835	Lung_OC	lung:	n/a	n/a
40	CTCF	chr8:119633580-119633730	GM12869	blood:	n/a	n/a
41	CTCF	chr8:119633600-119633750	GM12865	blood:	n/a	n/a
42	CTCF	chr8:119634539-119634638	GM19239	blood:	n/a	n/a
43	CTCF	chr8:119634568-119634709	GM12878	blood:	n/a	chr8:119634639-119634649
44	CTCF	chr8:119627800-119627950	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:119659100-119659143	GM10248	blood:	n/a	n/a
46	CTCF	chr8:119633900-119634050	NHEK	skin:	n/a	n/a
47	CUX1	chr8:119633286-119633468	GM12878	blood:	n/a	n/a
48	CUX1	chr8:119634993-119635074	GM12878	blood:	n/a	n/a
49	E2F4	chr8:119634058-119634356	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr8:119657020-119657034	MCF10A-Er-Src	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119633844-119633894	MCF-7	breast:	n/a
2	chr8:119633844-119633894	NHBE	bronchial:	n/a
3	chr8:119634602-119634652	AG09319	gingival:	n/a
4	chr8:119634140-119634190	HepG2	liver:	n/a
5	chr8:119634294-119634344	GM12878	blood:	n/a
6	chr8:119634155-119634205	NH-A	brain:	n/a
7	chr8:119634294-119634344	SAEC	small airway:	n/a
8	chr8:119638289-119638339	U87	brain:	n/a
9	chr8:119634294-119634344	HCPEpiC	choroid plexus:	n/a
10	chr8:119634294-119634344	SK-N-MC	brain:	n/a
11	chr8:119634634-119634684	NB4	blood:	n/a
12	chr8:119633844-119633894	HRE	kidney:	n/a
13	chr8:119634283-119634333	SAEC	small airway:	n/a
14	chr8:119634294-119634344	HUVEC	blood vessel:	n/a
15	chr8:119634155-119634205	HEEpiC	esophagus:	n/a
16	chr8:119634302-119634352	BE2_C	brain:	n/a
17	chr8:119634294-119634344	K562	blood:	n/a
18	chr8:119634283-119634333	NH-A	brain:	n/a
19	chr8:119634612-119634662	NH-A	brain:	n/a
20	chr8:119634634-119634684	HRE	kidney:	n/a
21	chr8:119634602-119634652	NB4	blood:	n/a
22	chr8:119634140-119634190	NHDF-neo	bronchial:	n/a
23	chr8:119630154-119630204	NT2-D1	testis:	n/a
24	chr8:119634283-119634333	ECC-1	luminal epithelium:	n/a
25	chr8:119634634-119634684	T-47D	breast:	n/a
26	chr8:119630154-119630204	HL-60	blood:	n/a
27	chr8:119634283-119634333	HAEpiC	amniotic membrane:	n/a
28	chr8:119633844-119633894	GM06990	blood:	n/a
29	chr8:119638289-119638339	SK-N-SH	brain:	n/a
30	chr8:119634294-119634344	MCF-7	breast:	n/a
31	chr8:119634634-119634684	LNCaP	prostate:	n/a
32	chr8:119634634-119634684	K562	blood:	n/a
33	chr8:119634612-119634662	LNCaP	prostate:	n/a
34	chr8:119633844-119633894	HepG2	liver:	n/a
35	chr8:119634612-119634662	HUVEC	blood vessel:	n/a
36	chr8:119634634-119634684	CMK	blood:	n/a
37	chr8:119634155-119634205	U87	brain:	n/a
38	chr8:119634634-119634684	NT2-D1	testis:	n/a
39	chr8:119630154-119630204	HNPCEpiC	eye:	n/a
40	chr8:119638289-119638339	NHDF-neo	bronchial:	n/a
41	chr8:119634294-119634344	RPTEC	kidney:	n/a
42	chr8:119633844-119633894	BE2_C	brain:	n/a
43	chr8:119634283-119634333	NB4	blood:	n/a
44	chr8:119634602-119634652	AG04449	skin:	fetal
45	chr8:119634294-119634344	SKMC	muscle:	n/a
46	chr8:119634612-119634662	AG09319	gingival:	n/a
47	chr8:119634294-119634344	NH-A	brain:	n/a
48	chr8:119638289-119638339	HIPEpiC	eye:	n/a
49	chr8:119634294-119634344	ProgFib	skin:	n/a
50	chr8:119630154-119630204	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:119626648..119628226-chr8:119632877..119634473,2	MCF-7	breast:
2	chr8:119633762..119636095-chr8:119645506..119648099,2	MCF-7	breast:
3	chr8:119633322..119635580-chr8:119639291..119641315,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC023590.1.1-2	chr8:119633240-119633425	NONHSAT128412
2	lnc-AC023590.1.1-2	chr8:119633774-119633894	NONHSAT128412

No data

Variant related genes	Relation type
SAMD12	TF binding region
SAMD12	CpG island
ENSG00000177570	chromatin interactions

Extended variants
information (count: 1511 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1511 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17750541	chr8:119627671-119627672	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
2	rs531093654	chr8:119627689-119627690	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530714726	chr8:119627764-119627765	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs2460967	chr8:119627892-119627893	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs150526079	chr8:119627907-119627908	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528316926	chr8:119627942-119627943	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs115981061	chr8:119627955-119627956	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113308728	chr8:119628005-119628006	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545962892	chr8:119628109-119628110	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs35753077	chr8:119628137-119628138	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2460968	chr8:119628230-119628231	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs548174114	chr8:119628328-119628329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375441986	chr8:119628331-119628332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs368577071	chr8:119628338-119628339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs189261399	chr8:119628354-119628355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369708272	chr8:119628408-119628409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537325350	chr8:119628446-119628447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559227771	chr8:119628462-119628463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577337215	chr8:119628466-119628467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528190787	chr8:119628529-119628530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181010946	chr8:119628544-119628545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185418956	chr8:119628563-119628564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs386729179	chr8:119628586-119628587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535245003	chr8:119628593-119628594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9632827	chr8:119628611-119628612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188715643	chr8:119628622-119628623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114922139	chr8:119628671-119628672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181551546	chr8:119628768-119628769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185885209	chr8:119628779-119628780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575230464	chr8:119628781-119628782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555394446	chr8:119628840-119628841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545757796	chr8:119628842-119628843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149705695	chr8:119628850-119628851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528237741	chr8:119628909-119628910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115584704	chr8:119628959-119628960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561594064	chr8:119628995-119628996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369748969	chr8:119628996-119628997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2460969	chr8:119629006-119629007	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs145457235	chr8:119629016-119629017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371167266	chr8:119629018-119629019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73319402	chr8:119629021-119629022	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192117023	chr8:119629032-119629033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183935182	chr8:119629039-119629040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2514596	chr8:119629086-119629087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs575127316	chr8:119629094-119629095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs117341877	chr8:119629110-119629111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78650473	chr8:119629137-119629138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575105457	chr8:119629144-119629145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185961414	chr8:119629149-119629150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557729701	chr8:119629280-119629281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	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
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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119605800-119631800	Weak transcription	Fetal Intestine Small	intestine
2	chr8:119609200-119633000	Weak transcription	Gastric	stomach
3	chr8:119609400-119633600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:119619400-119632200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:119623200-119632200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:119623800-119632800	Weak transcription	Fetal Lung	lung
7	chr8:119624200-119632800	Weak transcription	Pancreas	Pancrea
8	chr8:119624400-119628600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:119625200-119632000	Weak transcription	Fetal Intestine Large	intestine
10	chr8:119626400-119627800	Enhancers	Right Atrium	heart
11	chr8:119626400-119628200	Enhancers	HSMMtube	muscle
12	chr8:119626400-119630600	Enhancers	Brain Angular Gyrus	brain
13	chr8:119626600-119627800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:119626600-119627800	Enhancers	Fetal Muscle Leg	muscle
15	chr8:119626600-119627800	Enhancers	Left Ventricle	heart
16	chr8:119626600-119628000	Enhancers	Esophagus	oesophagus
17	chr8:119626600-119628000	Enhancers	Lung	lung
18	chr8:119626600-119628200	Enhancers	HSMM	muscle
19	chr8:119626600-119629000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:119626600-119629000	Enhancers	Brain Anterior Caudate	brain
21	chr8:119626600-119630600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr8:119626800-119630800	Enhancers	Brain Hippocampus Middle	brain
23	chr8:119627000-119628000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:119627000-119628800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:119627000-119632000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr8:119627000-119632200	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr8:119627000-119632400	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr8:119627200-119628000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr8:119627200-119628000	Weak transcription	Right Ventricle	heart
30	chr8:119627200-119633200	Weak transcription	Aorta	Aorta
31	chr8:119627400-119628000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:119627400-119628600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:119627400-119628600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:119627600-119627800	Flanking Active TSS	Brain Cingulate Gyrus	brain
35	chr8:119627600-119627800	Enhancers	Colonic Mucosa	Colon
36	chr8:119627600-119627800	Enhancers	Spleen	Spleen
37	chr8:119627600-119627800	Genic enhancers	GM12878-XiMat	blood
38	chr8:119627600-119627800	Enhancers	NH-A	brain
39	chr8:119627600-119628600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:119627600-119629200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr8:119627600-119630600	Enhancers	Brain Substantia Nigra	brain
42	chr8:119627600-119632800	Weak transcription	NHEK	skin
43	chr8:119627600-119633600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:119627800-119628200	Flanking Active TSS	NH-A	brain
45	chr8:119627800-119630000	Enhancers	Brain Cingulate Gyrus	brain
46	chr8:119627800-119632000	Weak transcription	GM12878-XiMat	blood
47	chr8:119627800-119632400	Weak transcription	Left Ventricle	heart
48	chr8:119627800-119632400	Weak transcription	Right Atrium	heart
49	chr8:119627800-119632800	Weak transcription	Colonic Mucosa	Colon
50	chr8:119627800-119632800	Weak transcription	Spleen	Spleen

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