Variant report

Variant	esv1824622
Chromosome Location	chr13:111319754-111343888
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:675)
CpG islands
(count:1040)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:675 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:111335600-111336012	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:111336891-111337374	HepG2	liver:	n/a	n/a
3	ATF2	chr13:111328300-111329671	GM12878	blood:	n/a	n/a
4	ATF2	chr13:111328388-111328778	GM12878	blood:	n/a	n/a
5	BATF	chr13:111328517-111328988	GM12878	blood:	n/a	n/a
6	BATF	chr13:111329690-111330085	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:111328428-111328936	GM12878	blood:	n/a	n/a
8	BCL11A	chr13:111329451-111330173	GM12878	blood:	n/a	n/a
9	BCL3	chr13:111328387-111328879	GM12878	blood:	n/a	n/a
10	BCLAF1	chr13:111328372-111329520	GM12878	blood:	n/a	n/a
11	BCLAF1	chr13:111328295-111329322	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:111328344-111329778	GM12878	blood:	n/a	chr13:111328790-111328806 chr13:111328782-111328798
13	BRCA1	chr13:111328583-111329166	GM12878	blood:	n/a	n/a
14	CEBPB	chr13:111336870-111336959	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:111335776-111336154	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:111335784-111336094	A549	lung:	n/a	n/a
17	CEBPB	chr13:111335778-111336129	K562	blood:	n/a	n/a
18	CHD1	chr13:111328530-111329169	GM12878	blood:	n/a	n/a
19	CHD2	chr13:111336887-111337087	HepG2	liver:	n/a	n/a
20	CHD2	chr13:111328434-111329393	GM12878	blood:	n/a	n/a
21	CREB1	chr13:111328407-111329638	GM12878	blood:	n/a	n/a
22	CTCF	chr13:111328480-111328630	GM06990	blood:	n/a	n/a
23	CTCF	chr13:111335605-111335858	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr13:111330240-111330390	AG09309	skin:	n/a	chr13:111330308-111330326
25	CTCF	chr13:111328960-111329110	GM12878	blood:	n/a	n/a
26	CTCF	chr13:111335720-111335870	GM06990	blood:	n/a	n/a
27	CTCF	chr13:111328730-111328732	GM12891	blood:	n/a	n/a
28	CTCF	chr13:111333011-111333709	A549	lung:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
29	CTCF	chr13:111328860-111329010	GM12873	blood:	n/a	n/a
30	CTCF	chr13:111333249-111333489	Gliobla	brain:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
31	CTCF	chr13:111335637-111335825	GM12878	blood:	n/a	n/a
32	CTCF	chr13:111335660-111335810	AG04450	lung:	n/a	n/a
33	CTCF	chr13:111333229-111333412	SK-N-SH_RA	brain:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
34	CTCF	chr13:111333300-111333450	GM12866	blood:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
35	CTCF	chr13:111335437-111336025	HCT-116	colon:	n/a	n/a
36	CTCF	chr13:111335627-111335803	GM12891	blood:	n/a	n/a
37	CTCF	chr13:111330294-111330378	H1-hESC	embryonic stem cell:	n/a	chr13:111330308-111330326
38	CTCF	chr13:111335702-111335787	GM20000	blood:	n/a	n/a
39	CTCF	chr13:111336800-111336950	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr13:111335680-111335830	HEK293	kidney:	n/a	n/a
41	CTCF	chr13:111335160-111335310	GM12871	blood:	n/a	n/a
42	CTCF	chr13:111333240-111333390	NHEK	skin:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
43	CTCF	chr13:111333300-111333450	HBMEC	blood vessel:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
44	CTCF	chr13:111333320-111333470	NB4	blood:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
45	CTCF	chr13:111333338-111333444	GM13976	blood:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379
46	CTCF	chr13:111335660-111335810	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr13:111335640-111335790	HRE	kidney:	n/a	n/a
48	CTCF	chr13:111333200-111333350	GM12878	blood:	n/a	n/a
49	CTCF	chr13:111335663-111335802	GM10266	blood:	n/a	n/a
50	CTCF	chr13:111333211-111333483	MCF-7	breast:	n/a	chr13:111333356-111333374 chr13:111333359-111333368 chr13:111333357-111333373 chr13:111333358-111333379

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111336430-111336480	HEEpiC	esophagus:	n/a
2	chr13:111340409-111340459	GM12891	blood:	n/a
3	chr13:111340250-111340300	HL-60	blood:	n/a
4	chr13:111336430-111336480	HEEpiC	esophagus:	n/a
5	chr13:111340409-111340459	GM12891	blood:	n/a
6	chr13:111340250-111340300	HL-60	blood:	n/a
7	chr13:111340159-111340209	HEK293	kidney:	embryo
8	chr13:111333333-111333383	A549	lung:	n/a
9	chr13:111334467-111334517	HepG2	liver:	n/a
10	chr13:111328783-111328833	HPAEpiC	pulmonary alveolar:	n/a
11	chr13:111331104-111331154	SK-N-MC	brain:	n/a
12	chr13:111340409-111340459	HRCEpiC	kidney:	n/a
13	chr13:111322081-111322131	SK-N-SH	brain:	n/a
14	chr13:111322081-111322131	Hela-S3	cervix:	n/a
15	chr13:111330802-111330852	HEEpiC	esophagus:	n/a
16	chr13:111340409-111340459	MCF-7	breast:	n/a
17	chr13:111322081-111322131	GM06990	blood:	n/a
18	chr13:111329221-111329271	HNPCEpiC	eye:	n/a
19	chr13:111329221-111329271	AG10803	skin:	n/a
20	chr13:111340191-111340241	H1-hESC	embryonic stem cell:	embryo
21	chr13:111340250-111340300	ProgFib	skin:	n/a
22	chr13:111328783-111328833	NH-A	brain:	n/a
23	chr13:111340350-111340400	HCPEpiC	choroid plexus:	n/a
24	chr13:111331255-111331305	PrEC	prostate:	n/a
25	chr13:111329221-111329271	LNCaP	prostate:	n/a
26	chr13:111331324-111331374	Hela-S3	cervix:	n/a
27	chr13:111331255-111331305	HPAEpiC	pulmonary alveolar:	n/a
28	chr13:111331324-111331374	H1-hESC	embryonic stem cell:	embryo
29	chr13:111334467-111334517	NHDF-neo	bronchial:	n/a
30	chr13:111322081-111322131	AoSMC	blood vessel:	n/a
31	chr13:111340409-111340459	PrEC	prostate:	n/a
32	chr13:111336430-111336480	GM12878	blood:	n/a
33	chr13:111340191-111340241	HEK293	kidney:	embryo
34	chr13:111333333-111333383	HUVEC	blood vessel:	n/a
35	chr13:111330699-111330749	AG04449	skin:	fetal
36	chr13:111331324-111331374	HNPCEpiC	eye:	n/a
37	chr13:111340409-111340459	SK-N-MC	brain:	n/a
38	chr13:111340350-111340400	NHDF-neo	bronchial:	n/a
39	chr13:111340409-111340459	HPAEpiC	pulmonary alveolar:	n/a
40	chr13:111331255-111331305	Hepatocyte	liver:	n/a
41	chr13:111322081-111322131	BE2_C	brain:	n/a
42	chr13:111329221-111329271	HAEpiC	amniotic membrane:	n/a
43	chr13:111340159-111340209	IMR90	lung:	fetal
44	chr13:111333333-111333383	ECC-1	luminal epithelium:	n/a
45	chr13:111330699-111330749	HPAEpiC	pulmonary alveolar:	n/a
46	chr13:111333333-111333383	MCF10A-Er-Src	breast:	n/a
47	chr13:111331324-111331374	GM19239	blood:	n/a
48	chr13:111331324-111331374	MCF-7	breast:	n/a
49	chr13:111329221-111329271	BE2_C	brain:	n/a
50	chr13:111333333-111333383	HIPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:111330512..111332280-chr13:111367075..111369007,2	K562	blood:
2	chr13:111335027..111337821-chr13:111366043..111367943,3	K562	blood:
3	chr13:111333021..111335304-chr13:111366011..111368539,3	K562	blood:
4	chr13:111320304..111323011-chr13:111365996..111367898,2	K562	blood:
5	chr13:111341286..111343605-chr13:111352948..111355342,2	K562	blood:
6	chr13:111336321..111339230-chr13:111365853..111367619,2	K562	blood:
7	chr13:111334321..111336628-chr13:111364897..111367415,3	MCF-7	breast:
8	chr13:111319875..111322001-chr13:111366343..111369154,2	MCF-7	breast:
9	chr13:111335534..111341041-chr13:111341252..111346282,8	K562	blood:
10	chr13:111332795..111333429-chr13:111365730..111366453,2	K562	blood:
11	chr13:111328800..111332502-chr13:111363272..111367932,6	K562	blood:
12	chr13:111334523..111337110-chr13:111337713..111340706,3	K562	blood:
13	chr13:111339867..111342003-chr13:111356640..111358659,2	MCF-7	breast:
14	chr13:111335461..111337308-chr13:111363462..111365716,2	MCF-7	breast:
15	chr13:111331878..111333857-chr13:111363101..111365113,2	MCF-7	breast:
16	chr13:111340529..111343866-chr13:111358060..111360020,4	K562	blood:
17	chr13:111340758..111343844-chr13:111351055..111354448,3	K562	blood:
18	chr13:111341464..111343204-chr13:111366168..111368327,2	MCF-7	breast:
19	chr13:111332786..111335109-chr13:111356617..111359801,4	MCF-7	breast:
20	chr13:111339852..111341870-chr13:111364379..111365979,2	K562	blood:
21	chr13:111314783..111317177-chr13:111319064..111320921,2	K562	blood:
22	chr13:111338558..111340999-chr13:111366379..111367908,2	MCF-7	breast:
23	chr13:111335534..111341041-chr13:111341252..111346282,8	K562	blood:
24	chr13:111339506..111342066-chr13:111350294..111353169,2	MCF-7	breast:
25	chr13:111331059..111333327-chr13:111365310..111368139,4	MCF-7	breast:
26	chr13:111328800..111330834-chr13:111364440..111366788,2	K562	blood:

No data

Variant related genes	Relation type
CARS2	TF binding region
CARS2	CpG island
ENSG00000134905	chromatin interactions
ENSG00000153487	chromatin interactions

Extended variants
information (count: 1013 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1013 , 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	rs4628819	chr13:111319754-111319755	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372086632	chr13:111319799-111319800	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs374623780	chr13:111319831-111319832	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548625666	chr13:111319836-111319837	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368114798	chr13:111319862-111319863	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201019544	chr13:111319865-111319866	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs9521884	chr13:111319884-111319885	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs149548457	chr13:111319895-111319896	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs113454684	chr13:111319921-111319922	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76243178	chr13:111319945-111319946	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538096627	chr13:111319992-111319993	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs556322220	chr13:111320021-111320022	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531862002	chr13:111320022-111320023	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs9521885	chr13:111320078-111320079	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs559492444	chr13:111320221-111320222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528580501	chr13:111320289-111320290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554157381	chr13:111320316-111320317	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs572705570	chr13:111320332-111320333	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540222479	chr13:111320353-111320354	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185245140	chr13:111320371-111320372	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs532221248	chr13:111320382-111320383	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544448292	chr13:111320411-111320412	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs530231828	chr13:111320414-111320415	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75580228	chr13:111320420-111320421	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs530033164	chr13:111320472-111320473	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551885774	chr13:111320516-111320517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548464976	chr13:111320545-111320546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs190122861	chr13:111320558-111320559	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs527730124	chr13:111320574-111320575	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182293285	chr13:111320577-111320578	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570890633	chr13:111320613-111320614	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs386774763	chr13:111320616-111320617	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112522215	chr13:111320617-111320618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs72661682	chr13:111320618-111320619	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs187299621	chr13:111320651-111320652	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs554093887	chr13:111320665-111320666	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs375157518	chr13:111320666-111320667	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs367786037	chr13:111320675-111320676	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs138328518	chr13:111320746-111320747	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs143850046	chr13:111320748-111320749	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs576887753	chr13:111320753-111320754	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs540785631	chr13:111320758-111320759	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562683514	chr13:111320784-111320785	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs376266548	chr13:111320820-111320821	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs367796965	chr13:111320821-111320822	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560227550	chr13:111320844-111320845	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs35206921	chr13:111320867-111320868	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs9521886	chr13:111320868-111320869	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs570795456	chr13:111320884-111320885	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs11370567	chr13:111320888-111320889	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Cancer	20164919	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
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111280800-111328600	Weak transcription	Psoas Muscle	Psoas
2	chr13:111297800-111336400	Weak transcription	Small Intestine	intestine
3	chr13:111298000-111320400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:111301200-111322800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr13:111301600-111322800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:111301600-111324400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:111302000-111322800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr13:111302200-111351400	Weak transcription	Stomach Mucosa	stomach
9	chr13:111303400-111327800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr13:111307600-111322800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr13:111308000-111322800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr13:111309600-111321800	Strong transcription	Osteobl	bone
13	chr13:111309800-111322400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:111310400-111321800	Strong transcription	NHEK	skin
15	chr13:111310600-111322800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr13:111310800-111352200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr13:111311400-111320800	Strong transcription	Liver	Liver
18	chr13:111311400-111321800	Strong transcription	HSMM	muscle
19	chr13:111311400-111322000	Strong transcription	NHDF-Ad	bronchial
20	chr13:111311400-111322200	Strong transcription	Ovary	ovary
21	chr13:111311400-111322400	Strong transcription	Stomach Smooth Muscle	stomach
22	chr13:111311400-111322600	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr13:111311600-111320400	Strong transcription	Muscle Satellite Cultured Cells	--
24	chr13:111311600-111321000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr13:111311600-111321400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:111311600-111322600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr13:111311600-111352000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr13:111311800-111324200	Strong transcription	Duodenum Mucosa	Duodenum
29	chr13:111312000-111320000	Strong transcription	Primary T cells from cord blood	blood
30	chr13:111312000-111322400	Strong transcription	Adipose Nuclei	Adipose
31	chr13:111312800-111357400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr13:111313000-111323000	Strong transcription	Fetal Muscle Trunk	muscle
33	chr13:111313200-111322800	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr13:111313400-111320600	Genic enhancers	Primary B cells from peripheral blood	blood
35	chr13:111313400-111320600	Strong transcription	Placenta	Placenta
36	chr13:111313400-111321800	Strong transcription	HMEC	breast
37	chr13:111313400-111322400	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr13:111313400-111322400	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr13:111313400-111322800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr13:111313400-111323400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr13:111313600-111319800	Strong transcription	Brain Anterior Caudate	brain
42	chr13:111313600-111319800	Strong transcription	HepG2	liver
43	chr13:111313600-111320200	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr13:111313600-111320400	Strong transcription	Brain Inferior Temporal Lobe	brain
45	chr13:111313600-111321800	Strong transcription	Primary T helper cells fromperipheralblood	blood
46	chr13:111313800-111319800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr13:111313800-111321800	Strong transcription	Hela-S3	cervix
48	chr13:111313800-111322600	Strong transcription	Skeletal Muscle Male	skeletal muscle
49	chr13:111313800-111322800	Strong transcription	Sigmoid Colon	Sigmoid Colon
50	chr13:111314000-111320000	Strong transcription	Lung	lung

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