Variant report

Variant	nsv1028695
Chromosome Location	chr8:112036331-112117490
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
2	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
3	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
4	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
5	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
6	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
7	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
8	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
9	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
10	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
11	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
12	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
13	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
14	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
15	CCNT2	chr8:112098454-112098654	K562	blood:	n/a	n/a
16	CEBPB	chr8:112044174-112044499	HepG2	liver:	n/a	chr8:112044333-112044344
17	CEBPB	chr8:112054718-112055073	A549	lung:	n/a	n/a
18	CEBPB	chr8:112054727-112055059	HepG2	liver:	n/a	n/a
19	CEBPB	chr8:112057976-112058248	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:112072418-112072646	HepG2	liver:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
21	CEBPB	chr8:112101790-112102112	HepG2	liver:	n/a	chr8:112101947-112101958
22	CEBPB	chr8:112072478-112072685	IMR90	lung:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
23	CEBPB	chr8:112044195-112044491	K562	blood:	n/a	chr8:112044333-112044344
24	CEBPB	chr8:112054708-112055042	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:112101702-112102116	A549	lung:	n/a	chr8:112101947-112101958
26	CEBPB	chr8:112054880-112054909	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:112058029-112058214	K562	blood:	n/a	n/a
28	CEBPB	chr8:112054705-112055080	K562	blood:	n/a	n/a
29	CEBPB	chr8:112101875-112101968	K562	blood:	n/a	chr8:112101947-112101958
30	CEBPB	chr8:112101778-112102105	H1-hESC	embryonic stem cell:	n/a	chr8:112101947-112101958
31	CEBPD	chr8:112052015-112052671	K562	blood:	n/a	n/a
32	CEBPD	chr8:112052444-112052807	K562	blood:	n/a	n/a
33	CHD2	chr8:112044601-112045061	K562	blood:	n/a	n/a
34	CHD2	chr8:112052288-112052845	K562	blood:	n/a	n/a
35	CTCF	chr8:112112846-112113096	LNCaP	prostate:	n/a	n/a
36	CTCF	chr8:112112860-112113010	HMEC	breast:	n/a	n/a
37	CTCF	chr8:112112880-112113030	GM12871	blood:	n/a	n/a
38	CTCF	chr8:112112860-112113010	GM12865	blood:	n/a	n/a
39	CTCF	chr8:112112860-112113010	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr8:112112800-112112950	HAc	cerebellar:	n/a	n/a
41	CTCF	chr8:112112860-112113010	GM12864	blood:	n/a	n/a
42	CTCF	chr8:112112903-112113005	GM10266	blood:	n/a	n/a
43	CTCF	chr8:112112880-112113030	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr8:112112848-112113073	HepG2	liver:	n/a	n/a
45	CTCF	chr8:112112840-112112990	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr8:112112840-112112990	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr8:112112860-112113010	HVMF	connective:	n/a	n/a
48	CTCF	chr8:112112854-112113075	GM19240	blood:	n/a	n/a
49	CTCF	chr8:112112862-112113086	GM12878	blood:	n/a	n/a
50	CTCF	chr8:112112881-112113050	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112052376-112052426	SK-N-SH	brain:	n/a
2	chr8:112053139-112053189	AG09319	gingival:	n/a
3	chr8:112053139-112053189	SKMC	muscle:	n/a
4	chr8:112052376-112052426	PFSK-1	brain:	n/a
5	chr8:112052376-112052426	HRE	kidney:	n/a
6	chr8:112053139-112053189	NHDF-neo	bronchial:	n/a
7	chr8:112053356-112053406	T-47D	breast:	n/a
8	chr8:112053356-112053406	Hepatocyte	liver:	n/a
9	chr8:112053139-112053189	PANC-1	pancreas:	n/a
10	chr8:112053356-112053406	HRPEpiC	eye:	n/a
11	chr8:112053356-112053406	HEEpiC	esophagus:	n/a
12	chr8:112052376-112052426	HCM	heart:	n/a
13	chr8:112052376-112052426	GM12891	blood:	n/a
14	chr8:112053139-112053189	NB4	blood:	n/a
15	chr8:112053356-112053406	BJ	skin:	n/a
16	chr8:112052376-112052426	AG09309	skin:	n/a
17	chr8:112052376-112052426	HCPEpiC	choroid plexus:	n/a
18	chr8:112052376-112052426	HepG2	liver:	n/a
19	chr8:112052376-112052426	HEK293	kidney:	embryo
20	chr8:112052376-112052426	T-47D	breast:	n/a
21	chr8:112053139-112053189	U87	brain:	n/a
22	chr8:112053356-112053406	HCT-116	colon:	n/a
23	chr8:112053356-112053406	PFSK-1	brain:	n/a
24	chr8:112053139-112053189	H1-hESC	embryonic stem cell:	embryo
25	chr8:112053356-112053406	ECC-1	luminal epithelium:	n/a
26	chr8:112053139-112053189	HCPEpiC	choroid plexus:	n/a
27	chr8:112053139-112053189	HEK293	kidney:	embryo
28	chr8:112052376-112052426	HEEpiC	esophagus:	n/a
29	chr8:112053356-112053406	NHDF-neo	bronchial:	n/a
30	chr8:112053139-112053189	NT2-D1	testis:	n/a
31	chr8:112053356-112053406	GM19239	blood:	n/a
32	chr8:112053356-112053406	SK-N-SH_RA	brain:	n/a
33	chr8:112053356-112053406	GM12892	blood:	n/a
34	chr8:112053139-112053189	MCF10A-Er-Src	breast:	n/a
35	chr8:112053139-112053189	PFSK-1	brain:	n/a
36	chr8:112052376-112052426	HAEpiC	amniotic membrane:	n/a
37	chr8:112053356-112053406	LNCaP	prostate:	n/a
38	chr8:112052376-112052426	HCT-116	colon:	n/a
39	chr8:112052376-112052426	H1-hESC	embryonic stem cell:	embryo
40	chr8:112053356-112053406	GM12878	blood:	n/a
41	chr8:112053356-112053406	H1-hESC	embryonic stem cell:	embryo
42	chr8:112053139-112053189	MCF-7	breast:	n/a
43	chr8:112052376-112052426	GM06990	blood:	n/a
44	chr8:112053139-112053189	HMEC	breast:	n/a
45	chr8:112052376-112052426	Jurkat	blood:	n/a
46	chr8:112053356-112053406	PANC-1	pancreas:	n/a
47	chr8:112053356-112053406	HCF	heart:	n/a
48	chr8:112053356-112053406	HRCEpiC	kidney:	n/a
49	chr8:112052376-112052426	A549	lung:	n/a
50	chr8:112052376-112052426	K562	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
2	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
3	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
4	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:
5	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
6	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
7	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
8	chr5:159495628..159496384-chr8:112067763..112068421,2	MCF-7	breast:
9	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
10	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
11	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
12	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
13	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
14	chr8:112044268..112046186-chr8:112050654..112052583,2	K562	blood:
15	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
16	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
17	chr8:112113576..112114171-chr8:112248201..112249138,2	MCF-7	breast:
18	chr8:112112573..112113471-chr8:121617637..121618420,2	MCF-7	breast:
19	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
20	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
21	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
22	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
23	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
24	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
25	chr8:112112155..112113418-chr8:112247960..112249178,7	MCF-7	breast:
26	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
27	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
28	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
29	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
30	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
31	chr8:111905363..111907255-chr8:112045592..112048412,2	K562	blood:
32	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
33	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
34	chr8:112044268..112046186-chr8:112050654..112052583,2	K562	blood:
35	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
36	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
37	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
38	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
39	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
2	lnc-CSMD3-3	chr8:112111190-112111368	ENSG00000253103
3	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
4	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182
5	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
6	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain
7	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
8	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain
9	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877
10	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
11	lnc-KCNV1-7	chr8:112108711-112108928	l_3667_chr8:112084787-112108928_brain

No data

Variant related genes	Relation type
ENSG00000253877	TF binding region
ENSG00000253877	CpG island
ENSG00000253103	chromatin interactions
TFRC	miRNA target sites

Extended variants
information (count: 1027 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1027 , 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	rs374027636	chr8:112036363-112036364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73316628	chr8:112036417-112036418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530300161	chr8:112036425-112036426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs546979992	chr8:112036474-112036475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189660676	chr8:112036480-112036481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141661420	chr8:112036505-112036506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552243897	chr8:112036506-112036507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181136988	chr8:112036522-112036523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573515960	chr8:112036564-112036565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114230666	chr8:112036566-112036567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568267516	chr8:112036580-112036581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534053836	chr8:112036615-112036616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577335143	chr8:112036658-112036659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186289490	chr8:112036721-112036722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573187366	chr8:112036743-112036744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545100663	chr8:112036749-112036750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558610559	chr8:112036786-112036787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542135428	chr8:112036827-112036828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3134525	chr8:112036870-112036871	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs190347190	chr8:112036880-112036881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1834738	chr8:112036902-112036903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1834737	chr8:112036908-112036909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540910709	chr8:112036940-112036941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560666667	chr8:112036952-112036953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143870545	chr8:112036965-112036966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551917740	chr8:112036988-112036989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs111412917	chr8:112037005-112037006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376984638	chr8:112037009-112037010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568895876	chr8:112037026-112037027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564216665	chr8:112037028-112037029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200560839	chr8:112037029-112037030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548316470	chr8:112037061-112037062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1834736	chr8:112037092-112037093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs77149481	chr8:112037120-112037121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112968544	chr8:112037161-112037162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376141624	chr8:112037206-112037207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35615970	chr8:112037216-112037217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529712297	chr8:112037235-112037236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541552061	chr8:112037246-112037247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374330446	chr8:112037253-112037254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372128011	chr8:112037254-112037255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199782860	chr8:112037257-112037258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61617543	chr8:112037290-112037291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554012909	chr8:112037332-112037333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561789908	chr8:112037375-112037376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144887904	chr8:112037398-112037399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186421993	chr8:112037406-112037407	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs558499670	chr8:112037433-112037434	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs114795832	chr8:112037493-112037494	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544258198	chr8:112037502-112037503	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	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
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
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	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
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112023200-112039000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:112025000-112047800	Weak transcription	K562	blood
3	chr8:112035000-112037400	Weak transcription	Brain Hippocampus Middle	brain
4	chr8:112035000-112037400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:112035800-112037400	Weak transcription	Brain Angular Gyrus	brain
6	chr8:112035800-112038800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:112036000-112037400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:112036000-112037400	Weak transcription	Fetal Heart	heart
9	chr8:112037400-112037800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr8:112037400-112037800	Active TSS	Brain Substantia Nigra	brain
11	chr8:112037400-112037800	Enhancers	Fetal Heart	heart
12	chr8:112037400-112038000	Active TSS	Brain Hippocampus Middle	brain
13	chr8:112037400-112040000	Active TSS	Brain Angular Gyrus	brain
14	chr8:112037400-112040000	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr8:112037400-112040400	Active TSS	Brain Anterior Caudate	brain
16	chr8:112037800-112038800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:112037800-112039000	Weak transcription	Brain Substantia Nigra	brain
18	chr8:112038000-112038800	Weak transcription	Brain Hippocampus Middle	brain
19	chr8:112038800-112039400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr8:112038800-112039800	Active TSS	Brain Cingulate Gyrus	brain
21	chr8:112038800-112040000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:112038800-112040000	Active TSS	Brain Hippocampus Middle	brain
23	chr8:112039000-112040000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr8:112039000-112040000	Active TSS	Brain Substantia Nigra	brain
25	chr8:112039600-112040000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:112039800-112041200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr8:112040000-112040200	Flanking Active TSS	Brain Substantia Nigra	brain
28	chr8:112040000-112040600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr8:112040000-112041600	Weak transcription	Brain Angular Gyrus	brain
30	chr8:112040000-112042800	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr8:112040200-112040400	Enhancers	Brain Substantia Nigra	brain
32	chr8:112040600-112041000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:112041000-112041400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:112041200-112041400	Enhancers	Brain Cingulate Gyrus	brain
35	chr8:112041400-112041800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr8:112041600-112042200	Active TSS	Brain Angular Gyrus	brain
37	chr8:112041800-112042200	Enhancers	Brain Cingulate Gyrus	brain
38	chr8:112042800-112043000	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr8:112043600-112044000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:112047800-112048000	Active TSS	K562	blood
41	chr8:112048000-112048600	Enhancers	K562	blood
42	chr8:112048600-112052600	Active TSS	K562	blood
43	chr8:112052600-112053600	Weak transcription	K562	blood
44	chr8:112053600-112054400	Active TSS	K562	blood
45	chr8:112054400-112055400	Weak transcription	K562	blood
46	chr8:112055400-112055600	Enhancers	K562	blood
47	chr8:112055800-112056000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr8:112056000-112056200	Active TSS	Brain Hippocampus Middle	brain
49	chr8:112056000-112056200	Active TSS	Brain Substantia Nigra	brain
50	chr8:112056000-112056400	Enhancers	Brain Angular Gyrus	brain

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