Variant report

Variant	nsv455881
Chromosome Location	chr13:49134412-49169570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:719)
CpG islands
(count:245)
Chromatin interactive
region (count:15)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:49157738-49158332	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:49154483-49154514	K562	blood:	n/a	n/a
3	ARID3A	chr13:49165779-49166168	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:49137931-49138462	K562	blood:	n/a	n/a
5	ARID3A	chr13:49163757-49164122	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:49154380-49154733	HepG2	liver:	n/a	n/a
7	ATF2	chr13:49136260-49136920	GM12878	blood:	n/a	n/a
8	ATF2	chr13:49153159-49153854	GM12878	blood:	n/a	n/a
9	ATF2	chr13:49152608-49153895	GM12878	blood:	n/a	n/a
10	ATF2	chr13:49136294-49137061	GM12878	blood:	n/a	n/a
11	ATF3	chr13:49138155-49138461	K562	blood:	n/a	n/a
12	BATF	chr13:49136432-49136799	GM12878	blood:	n/a	n/a
13	BATF	chr13:49136430-49136783	GM12878	blood:	n/a	n/a
14	BATF	chr13:49153307-49153679	GM12878	blood:	n/a	n/a
15	BATF	chr13:49145822-49146009	GM12878	blood:	n/a	n/a
16	BATF	chr13:49168239-49168462	GM12878	blood:	n/a	chr13:49168382-49168393
17	BATF	chr13:49153243-49153666	GM12878	blood:	n/a	n/a
18	BCL11A	chr13:49153244-49153642	GM12878	blood:	n/a	chr13:49153493-49153502
19	BCL11A	chr13:49136485-49136819	GM12878	blood:	n/a	n/a
20	BCL11A	chr13:49165635-49165831	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:49153180-49153756	GM12878	blood:	n/a	chr13:49153493-49153502
22	BCL11A	chr13:49136399-49136919	GM12878	blood:	n/a	n/a
23	BCL3	chr13:49136456-49136844	GM12878	blood:	n/a	n/a
24	BCL3	chr13:49136411-49136871	GM12878	blood:	n/a	n/a
25	BCL3	chr13:49153211-49153698	GM12878	blood:	n/a	chr13:49153493-49153502
26	BCLAF1	chr13:49152984-49153657	GM12878	blood:	n/a	chr13:49153493-49153502
27	BCLAF1	chr13:49136264-49136919	GM12878	blood:	n/a	n/a
28	BCLAF1	chr13:49136388-49136919	GM12878	blood:	n/a	n/a
29	BCLAF1	chr13:49153049-49153812	GM12878	blood:	n/a	chr13:49153493-49153502
30	BHLHE40	chr13:49136270-49136928	GM12878	blood:	n/a	n/a
31	BHLHE40	chr13:49154405-49154636	GM12878	blood:	n/a	n/a
32	BHLHE40	chr13:49144371-49144571	K562	blood:	n/a	n/a
33	BHLHE40	chr13:49153027-49153799	GM12878	blood:	n/a	n/a
34	BRCA1	chr13:49154474-49154674	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr13:49154562-49154862	GM12878	blood:	n/a	n/a
36	CCNT2	chr13:49138287-49138792	K562	blood:	n/a	n/a
37	CEBPB	chr13:49136382-49136841	GM12878	blood:	n/a	n/a
38	CEBPB	chr13:49134390-49134568	A549	lung:	n/a	n/a
39	CEBPB	chr13:49141961-49142141	Hela-S3	cervix:	n/a	chr13:49142067-49142078 chr13:49142067-49142080 chr13:49142069-49142080
40	CEBPB	chr13:49139778-49139806	HepG2	liver:	n/a	n/a
41	CEBPB	chr13:49136275-49136935	GM12878	blood:	n/a	n/a
42	CEBPB	chr13:49142014-49142141	A549	lung:	n/a	chr13:49142067-49142078 chr13:49142067-49142080 chr13:49142069-49142080
43	CEBPB	chr13:49165698-49165952	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:49141880-49142217	HepG2	liver:	n/a	chr13:49142067-49142078 chr13:49142067-49142080 chr13:49142069-49142080
45	CEBPB	chr13:49153286-49153609	GM12878	blood:	n/a	n/a
46	CEBPB	chr13:49153139-49153809	GM12878	blood:	n/a	n/a
47	CEBPB	chr13:49142017-49142133	IMR90	lung:	n/a	chr13:49142067-49142078 chr13:49142067-49142080 chr13:49142069-49142080
48	CEBPD	chr13:49160710-49161186	K562	blood:	n/a	n/a
49	CHD1	chr13:49152889-49153743	GM12878	blood:	n/a	n/a
50	CHD2	chr13:49153085-49153708	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49168127-49168177	IMR90	lung:	fetal
2	chr13:49168127-49168177	IMR90	lung:	fetal
3	chr13:49147573-49147623	HPAEpiC	pulmonary alveolar:	n/a
4	chr13:49145436-49145486	HNPCEpiC	eye:	n/a
5	chr13:49159767-49159817	MCF10A-Er-Src	breast:	n/a
6	chr13:49168127-49168177	GM19239	blood:	n/a
7	chr13:49147573-49147623	HRCEpiC	kidney:	n/a
8	chr13:49147573-49147623	HNPCEpiC	eye:	n/a
9	chr13:49145436-49145486	HRPEpiC	eye:	n/a
10	chr13:49168127-49168177	T-47D	breast:	n/a
11	chr13:49159767-49159817	HCPEpiC	choroid plexus:	n/a
12	chr13:49147573-49147623	SAEC	small airway:	n/a
13	chr13:49147573-49147623	Hepatocyte	liver:	n/a
14	chr13:49168127-49168177	NHBE	bronchial:	n/a
15	chr13:49168127-49168177	HRCEpiC	kidney:	n/a
16	chr13:49159767-49159817	K562	blood:	n/a
17	chr13:49147573-49147623	HCPEpiC	choroid plexus:	n/a
18	chr13:49147573-49147623	AG09319	gingival:	n/a
19	chr13:49159767-49159817	AG09319	gingival:	n/a
20	chr13:49159767-49159817	RPTEC	kidney:	n/a
21	chr13:49159767-49159817	GM12878	blood:	n/a
22	chr13:49145436-49145486	ProgFib	skin:	n/a
23	chr13:49147573-49147623	CMK	blood:	n/a
24	chr13:49147573-49147623	HL-60	blood:	n/a
25	chr13:49147573-49147623	T-47D	breast:	n/a
26	chr13:49159767-49159817	ovcar-3	ovarian:	n/a
27	chr13:49159767-49159817	LNCaP	prostate:	n/a
28	chr13:49147573-49147623	PANC-1	pancreas:	n/a
29	chr13:49147573-49147623	BE2_C	brain:	n/a
30	chr13:49145436-49145486	MCF10A-Er-Src	breast:	n/a
31	chr13:49159767-49159817	T-47D	breast:	n/a
32	chr13:49168127-49168177	HCT-116	colon:	n/a
33	chr13:49159767-49159817	NHBE	bronchial:	n/a
34	chr13:49159767-49159817	AG04449	skin:	fetal
35	chr13:49147573-49147623	HMEC	breast:	n/a
36	chr13:49145436-49145486	RPTEC	kidney:	n/a
37	chr13:49159767-49159817	GM19239	blood:	n/a
38	chr13:49147573-49147623	GM06990	blood:	n/a
39	chr13:49159767-49159817	SK-N-SH_RA	brain:	n/a
40	chr13:49168127-49168177	BE2_C	brain:	n/a
41	chr13:49168127-49168177	NH-A	brain:	n/a
42	chr13:49168127-49168177	HNPCEpiC	eye:	n/a
43	chr13:49159767-49159817	HRE	kidney:	n/a
44	chr13:49145436-49145486	HIPEpiC	eye:	n/a
45	chr13:49159767-49159817	A549	lung:	n/a
46	chr13:49168127-49168177	U87	brain:	n/a
47	chr13:49168127-49168177	HepG2	liver:	n/a
48	chr13:49168127-49168177	HCM	heart:	n/a
49	chr13:49145436-49145486	A549	lung:	n/a
50	chr13:49168127-49168177	SK-N-MC	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:49145648..49148059-chr13:49151703..49153220,2	K562	blood:
2	chr13:49169482..49170418-chr13:49342940..49343870,6	K562	blood:
3	chr13:49106089..49108573-chr13:49138293..49140212,2	MCF-7	breast:
4	chr13:49106056..49107969-chr13:49140390..49142172,2	MCF-7	breast:
5	chr13:48806307..48808548-chr13:49152200..49154470,2	MCF-7	breast:
6	chr13:49141688..49143234-chr13:49148647..49150198,2	MCF-7	breast:
7	chr13:49141688..49143234-chr13:49148647..49150198,2	MCF-7	breast:
8	chr13:49145648..49148059-chr13:49151703..49153220,2	K562	blood:
9	chr13:49169501..49170445-chr13:49342944..49343864,14	MCF-7	breast:
10	chr13:49143466..49145650-chr13:49355908..49357695,2	MCF-7	breast:
11	chr13:49169295..49170510-chr13:49305795..49306796,15	MCF-7	breast:
12	chr13:49115025..49117372-chr13:49140241..49143183,2	MCF-7	breast:
13	chr13:49142248..49144143-chr13:49147250..49149323,2	K562	blood:
14	chr13:49169339..49170769-chr13:49342414..49344167,53	MCF-7	breast:
15	chr13:48908843..48909363-chr13:49153698..49154640,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCBTB2-3	chr13:49152149-49152224	NONHSAT033722
2	lnc-RCBTB2-2	chr13:49147244-49147453	XLOC_010606
3	lnc-RCBTB2-1	chr13:49143977-49144083	XLOC_010605
4	lnc-RCBTB2-3	chr13:49154977-49155037	NONHSAT033722
5	lnc-RCBTB2-1	chr13:49142298-49142483	XLOC_010605
6	lnc-RCBTB2-3	chr13:49151110-49151995	NONHSAT033722
7	lnc-RCBTB2-1	chr13:49144444-49144479	XLOC_010605
8	lnc-RCBTB2-2	chr13:49144775-49144977	XLOC_010606

No data

Variant related genes	Relation type
LINC01077	TF binding region
LINC00462	TF binding region
LINC01077	CpG island
LINC00462	CpG island
ENSG00000233456	chromatin interactions
ENSG00000136161	chromatin interactions
ENSG00000233610	chromatin interactions
ENSG00000136156	chromatin interactions
RNF182	miRNA target sites
RNF145	miRNA target sites

Extended variants
information (count: 1331 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9591177	chr13:49134412-49134413	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556348045	chr13:49134465-49134466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147025872	chr13:49134474-49134475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548519180	chr13:49134574-49134575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561617669	chr13:49134576-49134577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73489012	chr13:49134604-49134605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557561274	chr13:49134607-49134608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530715461	chr13:49134623-49134624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138398385	chr13:49134644-49134645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386770812	chr13:49134649-49134650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9591178	chr13:49134650-49134651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs199634530	chr13:49134764-49134765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574726626	chr13:49134799-49134800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541866965	chr13:49134866-49134867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564118532	chr13:49134882-49134883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563973208	chr13:49134886-49134887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575869128	chr13:49134946-49134947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76194270	chr13:49134957-49134958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564711602	chr13:49134965-49134966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111706626	chr13:49134997-49134998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187872203	chr13:49135019-49135020	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs546358724	chr13:49135042-49135043	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs143913111	chr13:49135043-49135044	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs566596688	chr13:49135088-49135089	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs192748095	chr13:49135156-49135157	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs550330548	chr13:49135158-49135159	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs569113428	chr13:49135208-49135209	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs146856553	chr13:49135211-49135212	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs56179737	chr13:49135221-49135222	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs189429737	chr13:49135247-49135248	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs533737667	chr13:49135256-49135257	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs60646582	chr13:49135261-49135262	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs115533505	chr13:49135265-49135266	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs569526226	chr13:49135276-49135277	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs74768400	chr13:49135289-49135290	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs557104205	chr13:49135294-49135295	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575878049	chr13:49135327-49135328	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs74074955	chr13:49135395-49135396	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs558493880	chr13:49135404-49135405	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs558533666	chr13:49135468-49135469	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs149439161	chr13:49135483-49135484	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540846701	chr13:49135498-49135499	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs73489016	chr13:49135529-49135530	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35990381	chr13:49135551-49135552	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs529009117	chr13:49135556-49135557	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs373659557	chr13:49135640-49135641	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs192477655	chr13:49135662-49135663	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs562387964	chr13:49135675-49135676	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533249962	chr13:49135676-49135677	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs551211673	chr13:49135686-49135687	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49132200-49135000	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr13:49132200-49135000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr13:49133200-49134800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:49133400-49135600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:49133600-49134600	Enhancers	K562	blood
6	chr13:49133600-49134600	Enhancers	Osteobl	bone
7	chr13:49133600-49135000	Enhancers	Dnd41	blood
8	chr13:49133600-49135000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr13:49133600-49136000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr13:49133800-49134600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:49133800-49134600	Enhancers	NH-A	brain
12	chr13:49133800-49135800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr13:49134000-49135600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr13:49134200-49136200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr13:49134200-49136200	Weak transcription	HSMM	muscle
16	chr13:49134200-49137400	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr13:49134400-49135600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr13:49134400-49136200	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr13:49134400-49136200	Weak transcription	HMEC	breast
20	chr13:49134400-49137600	Enhancers	Primary T cells fromperipheralblood	blood
21	chr13:49134600-49135600	Weak transcription	K562	blood
22	chr13:49134600-49136400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr13:49134600-49138000	Weak transcription	Osteobl	bone
24	chr13:49134800-49137800	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr13:49135000-49135200	Enhancers	Placenta	Placenta
26	chr13:49135000-49135200	Enhancers	GM12878-XiMat	blood
27	chr13:49135000-49135800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr13:49135000-49135800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr13:49135000-49135800	Enhancers	Fetal Thymus	thymus
30	chr13:49135000-49136000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr13:49135000-49136200	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr13:49135000-49136200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr13:49135000-49136400	Flanking Active TSS	Dnd41	blood
34	chr13:49135000-49136800	Enhancers	HepG2	liver
35	chr13:49135000-49137200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr13:49135000-49137200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr13:49135000-49137800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr13:49135000-49138600	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr13:49135000-49140000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr13:49135000-49155000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr13:49135200-49135400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr13:49135200-49135600	Bivalent Enhancer	Primary T cells from cord blood	blood
43	chr13:49135200-49136000	Bivalent Enhancer	Primary B cells from cord blood	blood
44	chr13:49135200-49137200	Flanking Active TSS	GM12878-XiMat	blood
45	chr13:49135200-49141800	Weak transcription	Placenta	Placenta
46	chr13:49135400-49135800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
47	chr13:49135400-49136400	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr13:49135400-49136800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr13:49135400-49137200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr13:49135600-49135800	Flanking Active TSS	Primary T cells from cord blood	blood

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