Variant report

Variant	nsv429942
Chromosome Location	chr8:130397818-130460011
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:0)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130432838-130433225	K562	blood:	n/a	n/a
2	ARID3A	chr8:130458766-130459136	K562	blood:	n/a	n/a
3	ATF1	chr8:130458833-130459202	K562	blood:	n/a	n/a
4	ATF1	chr8:130430061-130430286	K562	blood:	n/a	n/a
5	ATF1	chr8:130452326-130452592	K562	blood:	n/a	n/a
6	ATF1	chr8:130437723-130437776	K562	blood:	n/a	n/a
7	ATF1	chr8:130426847-130427166	K562	blood:	n/a	n/a
8	ATF1	chr8:130432735-130433139	K562	blood:	n/a	n/a
9	ATF2	chr8:130427610-130428253	GM12878	blood:	n/a	n/a
10	ATF3	chr8:130449150-130449463	K562	blood:	n/a	n/a
11	BACH1	chr8:130430708-130431054	K562	blood:	n/a	n/a
12	BACH1	chr8:130457886-130458107	H1-hESC	embryonic stem cell:	n/a	chr8:130458059-130458073
13	BACH1	chr8:130437927-130437931	K562	blood:	n/a	n/a
14	BATF	chr8:130400551-130400801	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:130427857-130428072	GM12878	blood:	n/a	n/a
16	BCL3	chr8:130427760-130428195	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:130458802-130459062	K562	blood:	n/a	n/a
18	BHLHE40	chr8:130427796-130428137	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:130433027-130433221	K562	blood:	n/a	n/a
20	BRCA1	chr8:130427937-130428111	GM12878	blood:	n/a	n/a
21	CBX3	chr8:130452293-130452793	K562	blood:	n/a	n/a
22	CBX3	chr8:130430772-130431220	K562	blood:	n/a	n/a
23	CBX3	chr8:130447482-130447864	K562	blood:	n/a	n/a
24	CBX3	chr8:130449011-130449459	K562	blood:	n/a	n/a
25	CCNT2	chr8:130432890-130433191	K562	blood:	n/a	n/a
26	CCNT2	chr8:130458771-130459225	K562	blood:	n/a	n/a
27	CCNT2	chr8:130426768-130426949	K562	blood:	n/a	n/a
28	CEBPB	chr8:130424574-130424823	HepG2	liver:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
29	CEBPB	chr8:130432684-130432985	K562	blood:	n/a	chr8:130432785-130432798
30	CEBPB	chr8:130452347-130452658	K562	blood:	n/a	chr8:130452617-130452634
31	CEBPB	chr8:130458841-130459121	K562	blood:	n/a	n/a
32	CEBPB	chr8:130449330-130449530	HepG2	liver:	n/a	chr8:130449427-130449438
33	CEBPB	chr8:130401299-130401584	K562	blood:	n/a	n/a
34	CEBPB	chr8:130424611-130424813	K562	blood:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
35	CEBPB	chr8:130449314-130449526	K562	blood:	n/a	chr8:130449427-130449438
36	CEBPB	chr8:130401310-130401551	IMR90	lung:	n/a	n/a
37	CEBPB	chr8:130458780-130459144	K562	blood:	n/a	n/a
38	CEBPB	chr8:130401316-130401616	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:130452429-130452670	K562	blood:	n/a	chr8:130452617-130452634
40	CEBPB	chr8:130424485-130424857	IMR90	lung:	n/a	chr8:130424665-130424676 chr8:130424665-130424678
41	CTCF	chr8:130458920-130459070	HL-60	blood:	n/a	n/a
42	CTCF	chr8:130406220-130406370	GM12865	blood:	n/a	n/a
43	CTCF	chr8:130406260-130406410	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr8:130406200-130406350	GM12873	blood:	n/a	n/a
45	CTCF	chr8:130441191-130441229	LNCaP	prostate:	n/a	n/a
46	CTCF	chr8:130409779-130409782	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:130435269-130435356	Fibrobl	skin:	n/a	n/a
48	CTCF	chr8:130406260-130406410	GM12875	blood:	n/a	n/a
49	CTCF	chr8:130406160-130406310	NB4	blood:	n/a	n/a
50	CTCF	chr8:130402079-130402143	GM20000	blood:	n/a	n/a

No data

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130419285..130421126-chr8:130422291..130424693,2	K562	blood:
2	chr8:130424297..130426458-chr8:130429983..130431740,3	K562	blood:
3	chr8:130424297..130426458-chr8:130429983..130431740,3	K562	blood:
4	chr8:130443086..130445932-chr8:130472163..130473857,2	MCF-7	breast:
5	chr8:130403263..130407136-chr8:130409731..130411798,3	K562	blood:
6	chr8:130448396..130450929-chr8:130509710..130511491,2	K562	blood:
7	chr8:130427156..130429100-chr8:130430204..130432175,2	K562	blood:
8	chr8:130446219..130448683-chr8:130450460..130453212,3	K562	blood:
9	chr11:62608631..62609567-chr8:130435702..130436693,2	NB4	blood:
10	chr8:130396550..130399217-chr8:130400172..130403294,3	K562	blood:
11	chr8:130433486..130436461-chr8:130437244..130438809,2	K562	blood:
12	chr8:130419752..130421541-chr8:130425916..130427776,2	K562	blood:
13	chr8:130406605..130408222-chr8:130415923..130417816,2	K562	blood:
14	chr8:130438946..130441544-chr8:130456592..130459697,3	K562	blood:
15	chr8:130402395..130404004-chr8:130404709..130406465,2	K562	blood:
16	chr8:130454492..130456593-chr8:130464974..130467695,2	K562	blood:
17	chr8:130409293..130412110-chr8:130418175..130420281,2	K562	blood:
18	chr8:130324110..130326533-chr8:130436449..130439248,2	K562	blood:
19	chr8:130444302..130447418-chr8:130460105..130463114,3	MCF-7	breast:
20	chr8:130433486..130436461-chr8:130437244..130438809,2	K562	blood:
21	chr8:130422480..130424858-chr8:130426519..130428589,2	K562	blood:
22	chr8:130403263..130407136-chr8:130409731..130411798,3	K562	blood:
23	chr8:130448325..130451235-chr8:130463069..130467328,3	K562	blood:
24	chr8:130459630..130462121-chr8:130462300..130464633,3	K562	blood:
25	chr8:130451014..130452708-chr8:130456649..130459238,2	K562	blood:
26	chr8:130394019..130396476-chr8:130408236..130409892,2	K562	blood:
27	chr8:130438946..130441544-chr8:130456592..130459697,3	K562	blood:
28	chr8:130432582..130435209-chr8:130544896..130547721,2	K562	blood:
29	chr8:130393992..130396529-chr8:130398581..130401379,2	K562	blood:
30	chr8:130402395..130404697-chr8:130404709..130406237,2	K562	blood:
31	chr8:130456549..130458693-chr8:130464674..130467504,3	MCF-7	breast:
32	chr3:98237384..98238009-chr8:130405189..130406045,2	MCF-7	breast:
33	chr8:130429538..130431900-chr8:130434547..130436688,2	MCF-7	breast:
34	chr8:130429538..130431900-chr8:130434547..130436688,2	MCF-7	breast:
35	chr8:130450871..130455095-chr8:130457353..130461574,6	MCF-7	breast:
36	chr8:130438496..130440259-chr8:130595633..130598498,2	K562	blood:
37	chr8:130402395..130404697-chr8:130404709..130406237,2	K562	blood:
38	chr8:130406605..130408222-chr8:130415923..130417816,2	K562	blood:
39	chr8:130446219..130448683-chr8:130450460..130453212,3	K562	blood:
40	chr8:130450871..130455095-chr8:130457353..130461574,6	MCF-7	breast:
41	chr8:130409293..130412110-chr8:130418175..130420281,2	K562	blood:
42	chr8:130451770..130455234-chr8:130460801..130462723,3	K562	blood:
43	chr8:130396550..130399217-chr8:130400172..130403294,3	K562	blood:
44	chr8:130419752..130421541-chr8:130425916..130427776,2	K562	blood:
45	chr8:130419285..130421126-chr8:130422291..130424693,2	K562	blood:
46	chr8:130402395..130404004-chr8:130404709..130406465,2	K562	blood:
47	chr8:130451014..130452708-chr8:130456649..130459238,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GSDMC-1	chr8:130411760-130411930	ENSG00000229140
2	lnc-MYC-3	chr8:130457499-130458098	NONHSAT129111
3	lnc-GSDMC-9	chr8:130433122-130434408	ucscGeneNc_uc003ysq_1

No data

Variant related genes	Relation type
ENSG00000253926	TF binding region
ENSG00000133316	chromatin interactions
ENSG00000266387	chromatin interactions
ENSG00000253926	chromatin interactions

Extended variants
information (count: 2280 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:2280 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16904062	chr8:130397821-130397822	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185403378	chr8:130397822-130397823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562774654	chr8:130397842-130397843	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529686899	chr8:130397920-130397921	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541823137	chr8:130397922-130397923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190114374	chr8:130397941-130397942	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73389105	chr8:130397957-130397958	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs552492689	chr8:130397967-130397968	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570748660	chr8:130398042-130398043	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531794813	chr8:130398070-130398071	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181389800	chr8:130398101-130398102	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568434378	chr8:130398134-130398135	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186019000	chr8:130398175-130398176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367894464	chr8:130398177-130398178	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554168118	chr8:130398233-130398234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113691981	chr8:130398242-130398243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566040681	chr8:130398302-130398303	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150477368	chr8:130398338-130398339	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138353479	chr8:130398407-130398408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577066980	chr8:130398436-130398437	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538061499	chr8:130398484-130398485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149189139	chr8:130398528-130398529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574818325	chr8:130398563-130398564	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555282814	chr8:130398583-130398584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201837076	chr8:130398614-130398615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541438206	chr8:130398633-130398634	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371929439	chr8:130398675-130398676	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560140205	chr8:130398681-130398682	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192087413	chr8:130398693-130398694	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545840771	chr8:130398734-130398735	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563839699	chr8:130398771-130398772	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531760441	chr8:130398819-130398820	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549976467	chr8:130398832-130398833	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145114126	chr8:130398850-130398851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567307618	chr8:130398853-130398854	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183815747	chr8:130398866-130398867	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113237716	chr8:130398879-130398880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115002953	chr8:130398911-130398912	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116684395	chr8:130398940-130398941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551880332	chr8:130398995-130398996	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28463195	chr8:130398996-130398997	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188884541	chr8:130399015-130399016	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs976437	chr8:130399041-130399042	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs574639342	chr8:130399110-130399111	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142061802	chr8:130399116-130399117	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553791555	chr8:130399168-130399169	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145620386	chr8:130399171-130399172	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191968907	chr8:130399180-130399181	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545711627	chr8:130399232-130399233	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545502272	chr8:130399245-130399246	Weak transcription Flanking Active TSS Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

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
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
Acute myeloid leukemia	20729466	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
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
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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	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
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130394600-130399000	Enhancers	Dnd41	blood
2	chr8:130394600-130401000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:130394800-130399200	Enhancers	Fetal Thymus	thymus
4	chr8:130394800-130411800	Strong transcription	K562	blood
5	chr8:130395600-130399400	Enhancers	Thymus	Thymus
6	chr8:130397800-130401000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:130398200-130401200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr8:130399000-130399400	Flanking Active TSS	Dnd41	blood
9	chr8:130399200-130399600	Flanking Active TSS	Fetal Thymus	thymus
10	chr8:130399400-130400600	Weak transcription	Thymus	Thymus
11	chr8:130399400-130400600	Enhancers	Dnd41	blood
12	chr8:130399600-130400600	Active TSS	Fetal Thymus	thymus
13	chr8:130400600-130400800	Flanking Active TSS	Fetal Thymus	thymus
14	chr8:130400600-130400800	Genic enhancers	Dnd41	blood
15	chr8:130400600-130401400	Enhancers	Fetal Muscle Trunk	muscle
16	chr8:130400600-130401400	Enhancers	Right Atrium	heart
17	chr8:130400600-130401600	Enhancers	Fetal Muscle Leg	muscle
18	chr8:130400600-130401600	Enhancers	Thymus	Thymus
19	chr8:130400600-130402000	Enhancers	Brain Hippocampus Middle	brain
20	chr8:130400600-130403200	Enhancers	Brain Germinal Matrix	brain
21	chr8:130400800-130401200	Enhancers	Fetal Brain Female	brain
22	chr8:130400800-130401200	Enhancers	Dnd41	blood
23	chr8:130400800-130401600	Enhancers	Fetal Thymus	thymus
24	chr8:130400800-130402400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr8:130400800-130402400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:130401000-130401400	Enhancers	Brain Cingulate Gyrus	brain
27	chr8:130401000-130401400	Enhancers	Fetal Stomach	stomach
28	chr8:130401000-130401400	Enhancers	Left Ventricle	heart
29	chr8:130401000-130401600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr8:130401000-130401600	Enhancers	Adipose Nuclei	Adipose
31	chr8:130401000-130401600	Enhancers	Brain Angular Gyrus	brain
32	chr8:130401000-130401600	Enhancers	Brain Anterior Caudate	brain
33	chr8:130401000-130401600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr8:130401000-130401600	Bivalent Enhancer	Brain Substantia Nigra	brain
35	chr8:130401000-130401600	Enhancers	Colon Smooth Muscle	Colon
36	chr8:130401000-130401800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:130401000-130401800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:130401000-130402000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:130401200-130401400	Genic enhancers	Dnd41	blood
40	chr8:130401200-130401800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr8:130401400-130402600	Enhancers	Dnd41	blood
42	chr8:130401800-130402800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr8:130401800-130405600	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr8:130401800-130405800	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr8:130402600-130406600	Weak transcription	Dnd41	blood
46	chr8:130405600-130406000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr8:130405800-130406400	Enhancers	Primary B cells from cord blood	blood
48	chr8:130405800-130407400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr8:130405800-130407400	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:130406000-130406800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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