Variant report

Variant	nsv1027447
Chromosome Location	chr8:108335387-108365566
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:183)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:108348924-108349468	K562	blood:	n/a	n/a
2	ARID3A	chr8:108346555-108347811	K562	blood:	n/a	n/a
3	ARID3A	chr8:108337533-108337702	K562	blood:	n/a	n/a
4	ARID3A	chr8:108356444-108357357	K562	blood:	n/a	n/a
5	ATF1	chr8:108356405-108356784	K562	blood:	n/a	n/a
6	ATF1	chr8:108343912-108344454	K562	blood:	n/a	n/a
7	ATF1	chr8:108336368-108336835	K562	blood:	n/a	n/a
8	BACH1	chr8:108361212-108361266	K562	blood:	n/a	n/a
9	BHLHE40	chr8:108347613-108347807	K562	blood:	n/a	n/a
10	BHLHE40	chr8:108344695-108344719	K562	blood:	n/a	n/a
11	BHLHE40	chr8:108343892-108344235	K562	blood:	n/a	n/a
12	CEBPB	chr8:108343836-108344675	K562	blood:	n/a	n/a
13	CEBPB	chr8:108348903-108349275	K562	blood:	n/a	n/a
14	CEBPB	chr8:108348847-108349202	K562	blood:	n/a	n/a
15	CEBPB	chr8:108347762-108347810	K562	blood:	n/a	n/a
16	CEBPB	chr8:108335139-108335467	K562	blood:	n/a	chr8:108335318-108335331
17	CEBPD	chr8:108361181-108361630	K562	blood:	n/a	n/a
18	CHD2	chr8:108356579-108356777	K562	blood:	n/a	n/a
19	CREB1	chr8:108348346-108348715	K562	blood:	n/a	n/a
20	CTCF	chr8:108344580-108344730	AG10803	skin:	n/a	n/a
21	CTCF	chr8:108344498-108344769	K562	blood:	n/a	n/a
22	CTCF	chr8:108344540-108344690	AG10803	skin:	n/a	n/a
23	CTCF	chr8:108359080-108359230	GM12871	blood:	n/a	n/a
24	CTCF	chr8:108344540-108344690	BJ	skin:	n/a	n/a
25	CTCF	chr8:108344580-108344730	AG04449	skin:	n/a	n/a
26	CTCF	chr8:108344540-108344690	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr8:108344540-108344690	AG09319	gingival:	n/a	n/a
28	CTCF	chr8:108344520-108344670	HFF	foreskin:	n/a	n/a
29	CTCF	chr8:108344600-108344750	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr8:108344600-108344750	AG04449	skin:	n/a	n/a
31	CTCF	chr8:108344580-108344730	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr8:108343714-108344231	K562	blood:	n/a	n/a
33	CTCF	chr8:108344580-108344730	AG09319	gingival:	n/a	n/a
34	CTCF	chr8:108344560-108344710	HCFaa	heart:	n/a	n/a
35	CTCF	chr8:108356566-108357011	K562	blood:	n/a	n/a
36	CUX1	chr8:108356452-108356806	K562	blood:	n/a	n/a
37	CUX1	chr8:108340422-108340532	K562	blood:	n/a	n/a
38	CUX1	chr8:108344668-108344678	K562	blood:	n/a	n/a
39	CUX1	chr8:108343978-108344464	K562	blood:	n/a	n/a
40	CUX1	chr8:108346960-108347957	K562	blood:	n/a	n/a
41	EP300	chr8:108348147-108348631	GM12878	blood:	n/a	n/a
42	EP300	chr8:108356367-108356818	K562	blood:	n/a	chr8:108356562-108356576 chr8:108356478-108356492
43	EP300	chr8:108343680-108344353	K562	blood:	n/a	n/a
44	EP300	chr8:108346363-108346466	K562	blood:	n/a	n/a
45	FAM48A	chr8:108337632-108337777	GM12878	blood:	n/a	n/a
46	FOS	chr8:108350729-108350815	MCF10A-Er-Src	breast:	n/a	chr8:108350754-108350763 chr8:108350755-108350763 chr8:108350755-108350762
47	FOS	chr8:108350680-108350840	MCF10A-Er-Src	breast:	n/a	chr8:108350754-108350763 chr8:108350755-108350763 chr8:108350755-108350762
48	FOS	chr8:108350633-108350859	MCF10A-Er-Src	breast:	n/a	chr8:108350754-108350763 chr8:108350755-108350763 chr8:108350755-108350762
49	FOXA1	chr8:108344517-108344845	T-47D	breast:	n/a	n/a
50	FOXA1	chr8:108344534-108344833	T-47D	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:108344200-108344250	NHDF-neo	bronchial:	n/a
2	chr8:108351562-108351612	HCT-116	colon:	n/a
3	chr8:108344200-108344250	HIPEpiC	eye:	n/a
4	chr8:108351562-108351612	AoSMC	blood vessel:	n/a
5	chr8:108344200-108344250	MCF-7	breast:	n/a
6	chr8:108359437-108359487	HEEpiC	esophagus:	n/a
7	chr8:108359437-108359487	GM12878	blood:	n/a
8	chr8:108359437-108359487	HIPEpiC	eye:	n/a
9	chr8:108344200-108344250	GM12878	blood:	n/a
10	chr8:108344200-108344250	HCF	heart:	n/a
11	chr8:108351562-108351612	T-47D	breast:	n/a
12	chr8:108351562-108351612	Jurkat	blood:	n/a
13	chr8:108359437-108359487	IMR90	lung:	fetal
14	chr8:108351562-108351612	HIPEpiC	eye:	n/a
15	chr8:108359437-108359487	Caco-2	colon:	n/a
16	chr8:108359437-108359487	LNCaP	prostate:	n/a
17	chr8:108351562-108351612	HRE	kidney:	n/a
18	chr8:108351562-108351612	GM12891	blood:	n/a
19	chr8:108351562-108351612	NT2-D1	testis:	n/a
20	chr8:108344200-108344250	HCT-116	colon:	n/a
21	chr8:108344200-108344250	GM19239	blood:	n/a
22	chr8:108351562-108351612	HCPEpiC	choroid plexus:	n/a
23	chr8:108359437-108359487	RPTEC	kidney:	n/a
24	chr8:108359437-108359487	SKMC	muscle:	n/a
25	chr8:108351562-108351612	HepG2	liver:	n/a
26	chr8:108359437-108359487	SK-N-SH	brain:	n/a
27	chr8:108344200-108344250	HAEpiC	amniotic membrane:	n/a
28	chr8:108351562-108351612	NH-A	brain:	n/a
29	chr8:108359437-108359487	NT2-D1	testis:	n/a
30	chr8:108344200-108344250	AoSMC	blood vessel:	n/a
31	chr8:108359437-108359487	PANC-1	pancreas:	n/a
32	chr8:108351562-108351612	HRPEpiC	eye:	n/a
33	chr8:108351562-108351612	MCF-7	breast:	n/a
34	chr8:108359437-108359487	SK-N-MC	brain:	n/a
35	chr8:108344200-108344250	HCPEpiC	choroid plexus:	n/a
36	chr8:108351562-108351612	K562	blood:	n/a
37	chr8:108351562-108351612	BJ	skin:	n/a
38	chr8:108351562-108351612	HEK293	kidney:	embryo
39	chr8:108344200-108344250	HEK293	kidney:	embryo
40	chr8:108344200-108344250	AG04450	lung:	fetal
41	chr8:108359437-108359487	MCF10A-Er-Src	breast:	n/a
42	chr8:108359437-108359487	HCPEpiC	choroid plexus:	n/a
43	chr8:108344200-108344250	CMK	blood:	n/a
44	chr8:108344200-108344250	Jurkat	blood:	n/a
45	chr8:108344200-108344250	PrEC	prostate:	n/a
46	chr8:108344200-108344250	AG09309	skin:	n/a
47	chr8:108351562-108351612	NHBE	bronchial:	n/a
48	chr8:108351562-108351612	SK-N-MC	brain:	n/a
49	chr8:108351562-108351612	HAEpiC	amniotic membrane:	n/a
50	chr8:108359437-108359487	GM12891	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:108323328..108325135-chr8:108339439..108342402,2	MCF-7	breast:
2	chr8:108310092..108312826-chr8:108342773..108344986,2	K562	blood:
3	chr8:108320769..108323724-chr8:108344479..108346213,2	K562	blood:
4	chr8:108348181..108349692-chr8:108363485..108367458,3	K562	blood:
5	chr8:108323023..108324851-chr8:108334237..108336849,2	K562	blood:
6	chr8:108349228..108350761-chr8:108352462..108354445,2	K562	blood:
7	chr8:108364652..108367113-chr8:108367728..108369614,2	K562	blood:
8	chr8:108353442..108355542-chr8:108360326..108364497,3	K562	blood:
9	chr8:108338212..108341049-chr8:108453971..108455686,2	K562	blood:
10	chr8:108359440..108363202-chr8:108363264..108367284,4	K562	blood:
11	chr8:108349228..108350761-chr8:108352462..108354445,2	K562	blood:
12	chr8:108357325..108361446-chr8:108361724..108366195,5	K562	blood:
13	chr8:108327353..108329181-chr8:108342640..108344430,2	K562	blood:
14	chr8:108347496..108349858-chr8:108357880..108360055,2	K562	blood:
15	chr8:108349228..108351182-chr8:108352238..108354935,4	K562	blood:
16	chr8:108359440..108363202-chr8:108363264..108367284,4	K562	blood:
17	chr8:108349228..108351182-chr8:108352238..108354935,4	K562	blood:
18	chr8:108315162..108317666-chr8:108340503..108343303,2	K562	blood:
19	chr8:108346938..108349858-chr8:108355674..108360055,5	K562	blood:
20	chr8:108306316..108309008-chr8:108341130..108342850,2	K562	blood:
21	chr8:108357325..108361446-chr8:108361724..108366195,5	K562	blood:
22	chr8:108320003..108323467-chr8:108344820..108346729,3	K562	blood:
23	chr8:108332354..108335105-chr8:108336203..108338362,2	K562	blood:
24	chr8:108353442..108355542-chr8:108360326..108364497,3	K562	blood:

No data

Variant related genes	Relation type
ANGPT1	TF binding region
ANGPT1	CpG island
ENSG00000154188	chromatin interactions

Extended variants
information (count: 1035 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1035 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572374243	chr8:108335412-108335413	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs143587788	chr8:108335438-108335439	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs4451284	chr8:108335514-108335515	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs111646925	chr8:108335548-108335549	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs118091975	chr8:108335565-108335566	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563583043	chr8:108335693-108335694	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs557166038	chr8:108335701-108335702	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs73701085	chr8:108335722-108335723	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs542981881	chr8:108335733-108335734	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs561710027	chr8:108335734-108335735	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs527305522	chr8:108335737-108335738	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560832045	chr8:108335766-108335767	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547487784	chr8:108335836-108335837	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs577043458	chr8:108335924-108335925	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs115566705	chr8:108335933-108335934	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs148061196	chr8:108335961-108335962	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569796915	chr8:108335980-108335981	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs183154771	chr8:108336004-108336005	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs549039529	chr8:108336084-108336085	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs71524704	chr8:108336094-108336095	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534715623	chr8:108336108-108336109	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187448993	chr8:108336132-108336133	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10095329	chr8:108336152-108336153	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs564828194	chr8:108336153-108336154	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10095247	chr8:108336160-108336161	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557113710	chr8:108336209-108336210	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs113418679	chr8:108336210-108336211	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113105812	chr8:108336255-108336256	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191951446	chr8:108336258-108336259	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs62512846	chr8:108336259-108336260	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553412395	chr8:108336261-108336262	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554726532	chr8:108336287-108336288	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574918032	chr8:108336303-108336304	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115979078	chr8:108336324-108336325	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs532276715	chr8:108336328-108336329	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs17368715	chr8:108336337-108336338	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs533054937	chr8:108336362-108336363	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs540714083	chr8:108336365-108336366	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs79169900	chr8:108336388-108336389	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs532768850	chr8:108336392-108336393	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563480196	chr8:108336417-108336418	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs138529123	chr8:108336425-108336426	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201932664	chr8:108336431-108336432	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs200020859	chr8:108336433-108336434	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs67914604	chr8:108336434-108336435	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201196039	chr8:108336439-108336440	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201949786	chr8:108336443-108336444	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs60479338	chr8:108336444-108336445	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs71308721	chr8:108336463-108336464	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs529091695	chr8:108336503-108336504	Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	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
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
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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Multiple myeloma	16461302	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Breast cancer	21364760	CNVD
Gastric cancer	22539939	CNVD
Non-small cell lung cancer	19010865	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:108323000-108349000	Weak transcription	HSMM	muscle
2	chr8:108327400-108340800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:108328000-108336000	Enhancers	Primary hematopoietic stem cells	blood
4	chr8:108328200-108342600	Weak transcription	Osteobl	bone
5	chr8:108328200-108344000	Weak transcription	Aorta	Aorta
6	chr8:108328400-108341800	Weak transcription	NHDF-Ad	bronchial
7	chr8:108328400-108342200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:108328400-108344000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:108329400-108342000	Weak transcription	NHLF	lung
10	chr8:108329600-108342200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:108330600-108342200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:108331600-108335800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr8:108333600-108338400	Weak transcription	Fetal Lung	lung
14	chr8:108333600-108368800	Weak transcription	Fetal Kidney	kidney
15	chr8:108334400-108335800	Weak transcription	K562	blood
16	chr8:108335200-108336000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:108335200-108336000	Enhancers	Rectal Smooth Muscle	rectum
18	chr8:108335400-108335800	Enhancers	Colon Smooth Muscle	Colon
19	chr8:108335800-108336000	Genic enhancers	K562	blood
20	chr8:108335800-108340400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr8:108335800-108342000	Weak transcription	Colon Smooth Muscle	Colon
22	chr8:108336000-108336400	Weak transcription	K562	blood
23	chr8:108336000-108336600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr8:108336000-108337600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr8:108336000-108339600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr8:108336400-108340600	Genic enhancers	K562	blood
27	chr8:108336600-108336800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:108336600-108337000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:108336600-108337800	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr8:108336800-108339600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:108337000-108344600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:108337600-108338800	Enhancers	Primary hematopoietic stem cells	blood
33	chr8:108337800-108360200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr8:108338400-108339200	Enhancers	Fetal Lung	lung
35	chr8:108338800-108339600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr8:108339200-108342000	Weak transcription	Fetal Lung	lung
37	chr8:108339600-108340000	Enhancers	Rectal Smooth Muscle	rectum
38	chr8:108339600-108340200	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr8:108339600-108340200	Enhancers	Stomach Smooth Muscle	stomach
40	chr8:108339600-108340400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:108339600-108340600	Enhancers	Primary hematopoietic stem cells	blood
42	chr8:108339800-108340000	Enhancers	Ovary	ovary
43	chr8:108340000-108340400	Enhancers	Fetal Heart	heart
44	chr8:108340000-108343800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr8:108340000-108344600	Weak transcription	Ovary	ovary
46	chr8:108340200-108342200	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr8:108340200-108343800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr8:108340400-108340600	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr8:108340400-108341000	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr8:108340400-108342400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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