Variant report

Variant	nsv891413
Chromosome Location	chr8:119607281-119679668
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:556)
CpG islands
(count:795)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:119674779-119674950	HepG2	liver:	n/a	n/a
2	ATF2	chr8:119633656-119634326	GM12878	blood:	n/a	n/a
3	BACH1	chr8:119634004-119634261	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:119633423-119633753	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:119627790-119628026	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:119639827-119640142	GM12878	blood:	n/a	n/a
7	BATF	chr8:119650982-119651273	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:119639874-119640136	GM12878	blood:	n/a	n/a
9	BCL3	chr8:119610903-119611240	GM12878	blood:	n/a	n/a
10	BCL3	chr8:119624796-119625072	GM12878	blood:	n/a	n/a
11	BCLAF1	chr8:119632868-119633338	GM12878	blood:	n/a	n/a
12	BHLHE40	chr8:119640702-119641204	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:119639927-119640003	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:119633139-119634823	GM12878	blood:	n/a	chr8:119634206-119634222
15	CEBPB	chr8:119663079-119663315	A549	lung:	n/a	n/a
16	CEBPB	chr8:119656845-119657122	IMR90	lung:	n/a	chr8:119656973-119656984 chr8:119656973-119656986
17	CEBPB	chr8:119677573-119677634	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:119633093-119633293	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:119663073-119663370	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:119660453-119660731	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:119640822-119641003	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr8:119645778-119645976	H1-hESC	embryonic stem cell:	n/a	chr8:119645848-119645859
23	CEBPB	chr8:119645690-119646009	HepG2	liver:	n/a	chr8:119645848-119645859
24	CEBPB	chr8:119669577-119669749	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:119656925-119657105	A549	lung:	n/a	chr8:119656973-119656984 chr8:119656973-119656986
26	CHD1	chr8:119634554-119635171	GM12878	blood:	n/a	chr8:119634634-119634644
27	CHD1	chr8:119632933-119634351	GM12878	blood:	n/a	n/a
28	CHD1	chr8:119639970-119640010	GM12878	blood:	n/a	n/a
29	CHD2	chr8:119633834-119634978	Hela-S3	cervix:	n/a	chr8:119634634-119634644
30	CHD2	chr8:119634212-119634471	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr8:119633648-119633911	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr8:119632938-119634983	GM12878	blood:	n/a	chr8:119634634-119634644
33	CREB1	chr8:119633440-119634269	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr8:119640592-119641088	GM12878	blood:	n/a	n/a
35	CREB1	chr8:119633412-119634397	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr8:119634054-119634372	A549	lung:	n/a	n/a
37	CREB1	chr8:119634386-119634741	A549	lung:	n/a	n/a
38	CREB1	chr8:119640565-119641118	GM12878	blood:	n/a	n/a
39	CREB1	chr8:119632833-119633880	GM12878	blood:	n/a	n/a
40	CTCF	chr8:119674680-119674830	GM12864	blood:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
41	CTCF	chr8:119674820-119674970	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:119674720-119674870	GM12872	blood:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
43	CTCF	chr8:119674714-119674901	Gliobla	brain:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
44	CTCF	chr8:119674720-119674870	GM12864	blood:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
45	CTCF	chr8:119674660-119674810	HCFaa	heart:	n/a	n/a
46	CTCF	chr8:119674720-119674870	GM12865	blood:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
47	CTCF	chr8:119674740-119674890	SK-N-SH_RA	brain:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
48	CTCF	chr8:119674770-119674853	GM19240	blood:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
49	CTCF	chr8:119674740-119674890	HBMEC	blood vessel:	n/a	chr8:119674798-119674811 chr8:119674796-119674812
50	CTCF	chr8:119674820-119674970	NHLF	lung:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119638289-119638339	AG04450	lung:	fetal
2	chr8:119626989-119627039	CMK	blood:	n/a
3	chr8:119638289-119638339	AG04450	lung:	fetal
4	chr8:119626989-119627039	CMK	blood:	n/a
5	chr8:119608979-119609029	HRPEpiC	eye:	n/a
6	chr8:119638289-119638339	HAEpiC	amniotic membrane:	n/a
7	chr8:119634283-119634333	PANC-1	pancreas:	n/a
8	chr8:119634140-119634190	SKMC	muscle:	n/a
9	chr8:119634140-119634190	CMK	blood:	n/a
10	chr8:119634612-119634662	HEK293	kidney:	embryo
11	chr8:119633844-119633894	BJ	skin:	n/a
12	chr8:119634602-119634652	MCF-7	breast:	n/a
13	chr8:119634612-119634662	T-47D	breast:	n/a
14	chr8:119634302-119634352	HL-60	blood:	n/a
15	chr8:119630154-119630204	CMK	blood:	n/a
16	chr8:119608979-119609029	GM19239	blood:	n/a
17	chr8:119634283-119634333	HMEC	breast:	n/a
18	chr8:119634283-119634333	GM12891	blood:	n/a
19	chr8:119634294-119634344	RPTEC	kidney:	n/a
20	chr8:119626989-119627039	MCF-7	breast:	n/a
21	chr8:119626989-119627039	NHBE	bronchial:	n/a
22	chr8:119608979-119609029	HUVEC	blood vessel:	n/a
23	chr8:119634155-119634205	Hela-S3	cervix:	n/a
24	chr8:119634140-119634190	Hela-S3	cervix:	n/a
25	chr8:119634283-119634333	HEEpiC	esophagus:	n/a
26	chr8:119634612-119634662	PANC-1	pancreas:	n/a
27	chr8:119638289-119638339	GM12878	blood:	n/a
28	chr8:119634302-119634352	HUVEC	blood vessel:	n/a
29	chr8:119633844-119633894	K562	blood:	n/a
30	chr8:119634302-119634352	HRPEpiC	eye:	n/a
31	chr8:119630154-119630204	BE2_C	brain:	n/a
32	chr8:119634155-119634205	HNPCEpiC	eye:	n/a
33	chr8:119634294-119634344	HEEpiC	esophagus:	n/a
34	chr8:119634283-119634333	NHDF-neo	bronchial:	n/a
35	chr8:119634140-119634190	SK-N-SH_RA	brain:	n/a
36	chr8:119634302-119634352	CMK	blood:	n/a
37	chr8:119634294-119634344	IMR90	lung:	fetal
38	chr8:119608979-119609029	HepG2	liver:	n/a
39	chr8:119638289-119638339	NB4	blood:	n/a
40	chr8:119608979-119609029	U87	brain:	n/a
41	chr8:119634602-119634652	AG09309	skin:	n/a
42	chr8:119634283-119634333	K562	blood:	n/a
43	chr8:119626989-119627039	PFSK-1	brain:	n/a
44	chr8:119634140-119634190	SAEC	small airway:	n/a
45	chr8:119608979-119609029	AG04449	skin:	fetal
46	chr8:119634283-119634333	RPTEC	kidney:	n/a
47	chr8:119634602-119634652	CMK	blood:	n/a
48	chr8:119634602-119634652	U87	brain:	n/a
49	chr8:119634634-119634684	HNPCEpiC	eye:	n/a
50	chr8:119608979-119609029	GM12878	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:119633762..119636095-chr8:119645506..119648099,2	MCF-7	breast:
2	chr8:119607906..119610373-chr8:119611996..119614737,2	MCF-7	breast:
3	chr8:119607906..119610373-chr8:119611996..119614737,2	MCF-7	breast:
4	chr8:119617998..119620916-chr8:119621606..119623559,2	K562	blood:
5	chr8:119633322..119635580-chr8:119639291..119641315,2	MCF-7	breast:
6	chr8:119674640..119675239-chr8:120082658..120083255,2	MCF-7	breast:
7	chr8:119674405..119675238-chr8:119724363..119725275,3	MCF-7	breast:
8	chr8:119593350..119595391-chr8:119606701..119608716,2	MCF-7	breast:
9	chr8:119617998..119620916-chr8:119621606..119623559,2	K562	blood:
10	chr8:119626648..119628226-chr8:119632877..119634473,2	MCF-7	breast:
11	chr8:119674415..119675263-chr8:120082432..120082985,2	MCF-7	breast:

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

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

No data

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

Extended variants
information (count: 2353 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:2353 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10505340	chr8:119607281-119607282	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534662983	chr8:119607303-119607304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs16891236	chr8:119607315-119607316	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376997608	chr8:119607322-119607323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574984253	chr8:119607336-119607337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542506489	chr8:119607347-119607348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562693909	chr8:119607352-119607353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370115926	chr8:119607354-119607355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575777310	chr8:119607359-119607360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531498845	chr8:119607374-119607375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs16891238	chr8:119607379-119607380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548411414	chr8:119607400-119607401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564137616	chr8:119607401-119607402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs187914687	chr8:119607448-119607449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs55829046	chr8:119607468-119607469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs561722299	chr8:119607506-119607507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9643131	chr8:119607597-119607598	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs72678175	chr8:119607607-119607608	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs550678756	chr8:119607624-119607625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570909818	chr8:119607688-119607689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78796184	chr8:119607693-119607694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539594392	chr8:119607766-119607767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551174301	chr8:119607797-119607798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377491142	chr8:119607830-119607831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534794191	chr8:119607885-119607886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs553094810	chr8:119607904-119607905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370318925	chr8:119607924-119607925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192583595	chr8:119608032-119608033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182755154	chr8:119608083-119608084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557611194	chr8:119608127-119608128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187283010	chr8:119608128-119608129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78615846	chr8:119608132-119608133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558388547	chr8:119608174-119608175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192100494	chr8:119608208-119608209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376039118	chr8:119608213-119608214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561668172	chr8:119608240-119608241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs184686267	chr8:119608244-119608245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75467492	chr8:119608326-119608327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7002279	chr8:119608342-119608343	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs117178826	chr8:119608353-119608354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139635323	chr8:119608380-119608381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566325368	chr8:119608388-119608389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567513667	chr8:119608470-119608471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527523087	chr8:119608490-119608491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547054162	chr8:119608498-119608499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553331287	chr8:119608579-119608580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568489338	chr8:119608589-119608590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535812652	chr8:119608593-119608594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546590797	chr8:119608610-119608611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557087984	chr8:119608668-119608669	Enhancers Weak transcription	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:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119600200-119610600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:119600600-119622600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:119605600-119610400	Weak transcription	GM12878-XiMat	blood
4	chr8:119605600-119613200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr8:119605800-119631800	Weak transcription	Fetal Intestine Small	intestine
6	chr8:119607000-119609200	Weak transcription	Brain Angular Gyrus	brain
7	chr8:119607200-119608400	Enhancers	Fetal Brain Female	brain
8	chr8:119607200-119609400	Weak transcription	Brain Substantia Nigra	brain
9	chr8:119607200-119610600	Enhancers	Fetal Brain Male	brain
10	chr8:119607600-119607800	Enhancers	Brain Cingulate Gyrus	brain
11	chr8:119607800-119609400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr8:119608000-119610400	Enhancers	Brain Hippocampus Middle	brain
13	chr8:119608200-119608400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr8:119608200-119608800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:119608400-119609800	Weak transcription	Fetal Brain Female	brain
16	chr8:119608400-119614000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:119608600-119610600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr8:119609000-119610600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr8:119609200-119609400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:119609200-119610000	Enhancers	Lung	lung
21	chr8:119609200-119610600	Enhancers	Brain Angular Gyrus	brain
22	chr8:119609200-119633000	Weak transcription	Gastric	stomach
23	chr8:119609400-119610200	Enhancers	Brain Substantia Nigra	brain
24	chr8:119609400-119610200	Enhancers	HSMMtube	muscle
25	chr8:119609400-119610600	Enhancers	Brain Cingulate Gyrus	brain
26	chr8:119609400-119633600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:119609800-119610400	Enhancers	Brain Anterior Caudate	brain
28	chr8:119609800-119610600	Enhancers	Fetal Brain Female	brain
29	chr8:119610000-119622000	Weak transcription	Lung	lung
30	chr8:119610200-119613800	Weak transcription	Brain Substantia Nigra	brain
31	chr8:119610400-119613200	Weak transcription	Brain Hippocampus Middle	brain
32	chr8:119610400-119626600	Weak transcription	Brain Anterior Caudate	brain
33	chr8:119610600-119611400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:119610600-119613200	Weak transcription	Brain Angular Gyrus	brain
35	chr8:119610600-119613200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr8:119610600-119613800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr8:119611400-119618800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr8:119613200-119614600	Enhancers	Brain Angular Gyrus	brain
39	chr8:119613200-119614600	Enhancers	Brain Hippocampus Middle	brain
40	chr8:119613200-119614600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr8:119613800-119614000	Enhancers	Aorta	Aorta
42	chr8:119613800-119614200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:119613800-119614400	Enhancers	Brain Cingulate Gyrus	brain
44	chr8:119613800-119614400	Enhancers	Brain Substantia Nigra	brain
45	chr8:119614000-119614200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr8:119614000-119614600	Enhancers	Right Atrium	heart
47	chr8:119614400-119618600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr8:119614400-119621400	Weak transcription	Brain Substantia Nigra	brain
49	chr8:119614600-119618800	Weak transcription	Brain Hippocampus Middle	brain
50	chr8:119614600-119619000	Weak transcription	Brain Angular Gyrus	brain

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