Variant report

Variant	esv2759950
Chromosome Location	chr13:76321610-76542003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2612)
CpG islands
(count:2014)
Chromatin interactive
region (count:31)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2612 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76334296-76335488	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76450475-76450923	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76450563-76450871	K562	blood:	n/a	n/a
4	ARID3A	chr13:76336178-76336848	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76346001-76346202	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:76444552-76444937	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:76522818-76522965	K562	blood:	n/a	n/a
8	ARID3A	chr13:76366535-76367382	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:76537499-76537752	K562	blood:	n/a	n/a
10	ARID3A	chr13:76365263-76365462	HepG2	liver:	n/a	n/a
11	ATF2	chr13:76335482-76335963	GM12878	blood:	n/a	n/a
12	ATF2	chr13:76534622-76535151	GM12878	blood:	n/a	n/a
13	ATF2	chr13:76534509-76535156	GM12878	blood:	n/a	n/a
14	ATF2	chr13:76336398-76337123	GM12878	blood:	n/a	n/a
15	ATF2	chr13:76336516-76337091	GM12878	blood:	n/a	n/a
16	ATF2	chr13:76377164-76377683	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:76537470-76537809	K562	blood:	n/a	n/a
18	BACH1	chr13:76463777-76463874	K562	blood:	n/a	n/a
19	BACH1	chr13:76537448-76537842	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr13:76399460-76399676	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr13:76463615-76464005	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr13:76421762-76422001	GM12878	blood:	n/a	n/a
23	BATF	chr13:76335575-76335846	GM12878	blood:	n/a	n/a
24	BATF	chr13:76372694-76373000	GM12878	blood:	n/a	chr13:76372915-76372925
25	BATF	chr13:76336585-76337045	GM12878	blood:	n/a	n/a
26	BATF	chr13:76534611-76535247	GM12878	blood:	n/a	n/a
27	BATF	chr13:76336647-76336971	GM12878	blood:	n/a	n/a
28	BATF	chr13:76534633-76534979	GM12878	blood:	n/a	n/a
29	BATF	chr13:76421703-76422063	GM12878	blood:	n/a	n/a
30	BCL11A	chr13:76534599-76535183	GM12878	blood:	n/a	n/a
31	BCL11A	chr13:76534761-76534990	GM12878	blood:	n/a	n/a
32	BCL11A	chr13:76372678-76373069	GM12878	blood:	n/a	chr13:76372918-76372927
33	BCL11A	chr13:76372781-76372993	GM12878	blood:	n/a	chr13:76372918-76372927
34	BCL11A	chr13:76335595-76335800	GM12878	blood:	n/a	chr13:76335725-76335734
35	BCL11A	chr13:76336652-76336953	GM12878	blood:	n/a	n/a
36	BCL11A	chr13:76336604-76336973	GM12878	blood:	n/a	n/a
37	BCL11A	chr13:76377334-76377612	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL11A	chr13:76377394-76377574	H1-hESC	embryonic stem cell:	n/a	n/a
39	BCL3	chr13:76336625-76337031	GM12878	blood:	n/a	n/a
40	BCL3	chr13:76335525-76335880	GM12878	blood:	n/a	chr13:76335725-76335734
41	BCLAF1	chr13:76336410-76337207	GM12878	blood:	n/a	n/a
42	BCLAF1	chr13:76336564-76337049	GM12878	blood:	n/a	n/a
43	BHLHE40	chr13:76444883-76444909	K562	blood:	n/a	n/a
44	BHLHE40	chr13:76334346-76335029	HepG2	liver:	n/a	n/a
45	BHLHE40	chr13:76335489-76335909	GM12878	blood:	n/a	n/a
46	BHLHE40	chr13:76536089-76536327	K562	blood:	n/a	n/a
47	BHLHE40	chr13:76537516-76537890	K562	blood:	n/a	n/a
48	BHLHE40	chr13:76361352-76361575	GM12878	blood:	n/a	n/a
49	BHLHE40	chr13:76336436-76337084	GM12878	blood:	n/a	n/a
50	BHLHE40	chr13:76450555-76450879	HepG2	liver:	n/a	n/a

(count:2014 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76462678-76462728	SK-N-MC	brain:	n/a
2	chr13:76462678-76462728	SK-N-MC	brain:	n/a
3	chr13:76508987-76509037	ECC-1	luminal epithelium:	n/a
4	chr13:76334583-76334633	ECC-1	luminal epithelium:	n/a
5	chr13:76430188-76430238	Caco-2	colon:	n/a
6	chr13:76444831-76444881	H1-hESC	embryonic stem cell:	embryo
7	chr13:76445065-76445115	HepG2	liver:	n/a
8	chr13:76536939-76536989	SK-N-SH	brain:	n/a
9	chr13:76445108-76445158	HRCEpiC	kidney:	n/a
10	chr13:76432094-76432144	ProgFib	skin:	n/a
11	chr13:76462678-76462728	ovcar-3	ovarian:	n/a
12	chr13:76444823-76444873	ovcar-3	ovarian:	n/a
13	chr13:76334583-76334633	CMK	blood:	n/a
14	chr13:76334583-76334633	HAEpiC	amniotic membrane:	n/a
15	chr13:76430665-76430715	HRE	kidney:	n/a
16	chr13:76508987-76509037	AG10803	skin:	n/a
17	chr13:76444831-76444881	HCF	heart:	n/a
18	chr13:76432094-76432144	GM12891	blood:	n/a
19	chr13:76334866-76334916	ovcar-3	ovarian:	n/a
20	chr13:76323667-76323717	SK-N-SH	brain:	n/a
21	chr13:76377366-76377416	NB4	blood:	n/a
22	chr13:76445108-76445158	HEK293	kidney:	embryo
23	chr13:76334039-76334089	HUVEC	blood vessel:	n/a
24	chr13:76444798-76444848	GM12891	blood:	n/a
25	chr13:76445108-76445158	GM19239	blood:	n/a
26	chr13:76462678-76462728	BE2_C	brain:	n/a
27	chr13:76334583-76334633	Hela-S3	cervix:	n/a
28	chr13:76334583-76334633	Hepatocyte	liver:	n/a
29	chr13:76444293-76444343	HEK293	kidney:	embryo
30	chr13:76430665-76430715	HUVEC	blood vessel:	n/a
31	chr13:76361354-76361404	NHDF-neo	bronchial:	n/a
32	chr13:76334039-76334089	MCF-7	breast:	n/a
33	chr13:76444850-76444900	AoSMC	blood vessel:	n/a
34	chr13:76445108-76445158	NHDF-neo	bronchial:	n/a
35	chr13:76344333-76344383	PANC-1	pancreas:	n/a
36	chr13:76323667-76323717	T-47D	breast:	n/a
37	chr13:76334039-76334089	SK-N-SH	brain:	n/a
38	chr13:76444823-76444873	SK-N-SH_RA	brain:	n/a
39	chr13:76344333-76344383	Hepatocyte	liver:	n/a
40	chr13:76430665-76430715	Hepatocyte	liver:	n/a
41	chr13:76432094-76432144	HNPCEpiC	eye:	n/a
42	chr13:76462678-76462728	HEK293	kidney:	embryo
43	chr13:76334039-76334089	HEK293	kidney:	embryo
44	chr13:76430188-76430238	SK-N-SH_RA	brain:	n/a
45	chr13:76445108-76445158	PrEC	prostate:	n/a
46	chr13:76337398-76337448	HCPEpiC	choroid plexus:	n/a
47	chr13:76430722-76430772	RPTEC	kidney:	n/a
48	chr13:76462678-76462728	BJ	skin:	n/a
49	chr13:76400715-76400765	U87	brain:	n/a
50	chr13:76445055-76445105	Caco-2	colon:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76450136..76450986-chr13:77047347..77048254,3	K562	blood:
2	chr13:76450288..76451169-chr13:77047376..77048381,7	MCF-7	breast:
3	chr13:76340127..76340627-chr17:18161935..18162436,2	Hela-S3	cervix:
4	chr13:76269710..76270622-chr13:76374395..76375242,4	MCF-7	breast:
5	chr13:76444326..76445057-chr13:77047425..77048326,2	K562	blood:
6	chr13:76334345..76334921-chr5:1633791..1634398,2	Hela-S3	cervix:
7	chr13:76278980..76279662-chr13:76374280..76374967,2	MCF-7	breast:
8	chr13:76515246..76517813-chr7:2394882..2397172,2	MCF-7	breast:
9	chr13:76438174..76440869-chr13:76485798..76487391,2	K562	blood:
10	chr13:76438174..76440869-chr13:76485798..76487391,2	K562	blood:
11	chr13:76269693..76270610-chr13:76444514..76445100,2	MCF-7	breast:
12	chr13:76417193..76419149-chr13:76428786..76430734,2	K562	blood:
13	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:
14	chr13:76540838..76542386-chr13:76542518..76545047,2	MCF-7	breast:
15	chr13:76450462..76451207-chr13:76591002..76591569,2	MCF-7	breast:
16	chr13:76450119..76450751-chr13:76590749..76591620,4	MCF-7	breast:
17	chr13:76401876..76403467-chr13:76404663..76406392,2	K562	blood:
18	chr13:76444133..76445077-chr13:77047746..77048410,4	MCF-7	breast:
19	chr13:76261020..76261898-chr13:76374424..76375313,3	MCF-7	breast:
20	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:
21	chr13:76330862..76332459-chr13:76334740..76336321,2	MCF-7	breast:
22	chr13:76334419..76334975-chr13:76374390..76375255,2	MCF-7	breast:
23	chr13:76444149..76445101-chr13:76593232..76594146,4	MCF-7	breast:
24	chr13:76334449..76335189-chr15:65588194..65588821,2	Hela-S3	cervix:
25	chr13:76317185..76320050-chr13:76322503..76324953,2	K562	blood:
26	chr13:76386406..76389041-chr13:76432929..76434756,2	MCF-7	breast:
27	chr13:76450221..76451145-chr13:76590691..76591575,2	K562	blood:
28	chr13:76401876..76403467-chr13:76404663..76406392,2	K562	blood:
29	chr13:76334673..76336320-chr13:76344020..76346194,2	MCF-7	breast:
30	chr13:76425109..76426616-chr13:76428342..76430833,2	K562	blood:
31	chr13:76386406..76389041-chr13:76432929..76434756,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL359392.1-1	chr13:76445174-76445379	XLOC_010433
2	lnc-COMMD6-10	chr13:76434594-76435511	NONHSAT034374
3	lnc-AL359392.1-1	chr13:76447793-76447870	XLOC_010433
4	lnc-AL359392.1-1	chr13:76457186-76457947	XLOC_010433
5	lnc-COMMD6-3	chr13:76506531-76509268	ENSG00000261206.1
6	lnc-AL359392.1-1	chr13:76447988-76448108	XLOC_010433

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LMO7	hsa-miR-16-5p	chr13:76432114-76432135
2	LMO7	hsa-miR-16-5p	chr13:76432682-76432703

Variant related genes	Relation type
ENSG00000223458	TF binding region
LINC00561	TF binding region
C13orf45	TF binding region
LMO7	TF binding region
ENSG00000223458	CpG island
LINC00561	CpG island
C13orf45	CpG island
LMO7	CpG island
ENSG00000177731	chromatin interactions
ENSG00000136153	chromatin interactions
ENSG00000188002	chromatin interactions
ENSG00000199568	chromatin interactions
LBR	miRNA target sites
LCLAT1	miRNA target sites

Extended variants
information (count: 7593 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:7593 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532949553	chr13:76321637-76321638	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545749385	chr13:76321720-76321721	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544760851	chr13:76321751-76321752	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368356759	chr13:76321888-76321889	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145389726	chr13:76321932-76321933	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537995271	chr13:76321974-76321975	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147248447	chr13:76321990-76321991	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75539369	chr13:76322029-76322030	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115703950	chr13:76322030-76322031	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183169712	chr13:76322039-76322040	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552030	chr13:76322065-76322066	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs116311568	chr13:76322067-76322068	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567070263	chr13:76322069-76322070	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533634991	chr13:76322077-76322078	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555466560	chr13:76322092-76322093	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543162441	chr13:76322139-76322140	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573296911	chr13:76322145-76322146	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537486706	chr13:76322172-76322173	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561452679	chr13:76322180-76322181	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371501218	chr13:76322183-76322184	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187901191	chr13:76322202-76322203	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116703096	chr13:76322210-76322211	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114348050	chr13:76322212-76322213	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528943626	chr13:76322238-76322239	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560077307	chr13:76322241-76322242	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572235631	chr13:76322270-76322271	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191956280	chr13:76322273-76322274	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185256660	chr13:76322308-76322309	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529416649	chr13:76322312-76322313	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs151317359	chr13:76322381-76322382	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562892112	chr13:76322448-76322449	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533630863	chr13:76322471-76322472	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188078475	chr13:76322496-76322497	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566928482	chr13:76322528-76322529	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376632448	chr13:76322549-76322550	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369909849	chr13:76322571-76322572	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192729975	chr13:76322652-76322653	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185052008	chr13:76322656-76322657	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34793255	chr13:76322725-76322726	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372521103	chr13:76322729-76322730	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs9600546	chr13:76322793-76322794	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555709443	chr13:76322807-76322808	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577771903	chr13:76322817-76322818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373343901	chr13:76322819-76322820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577255997	chr13:76322830-76322831	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538538206	chr13:76322915-76322916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111332093	chr13:76322931-76322932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201734132	chr13:76322947-76322948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554084379	chr13:76322950-76322951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376720178	chr13:76322951-76322952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3830 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76294800-76321800	Weak transcription	NH-A	brain
2	chr13:76306200-76330600	Weak transcription	Thymus	Thymus
3	chr13:76308200-76324800	Weak transcription	Left Ventricle	heart
4	chr13:76308200-76345200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:76313600-76324800	Weak transcription	Psoas Muscle	Psoas
6	chr13:76313800-76323600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:76314000-76323600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr13:76314000-76323800	Weak transcription	Fetal Heart	heart
9	chr13:76314200-76323200	Weak transcription	NHLF	lung
10	chr13:76314600-76321800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr13:76314600-76321800	Weak transcription	HSMMtube	muscle
12	chr13:76316600-76322600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr13:76319000-76323600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:76319000-76323600	Weak transcription	NHEK	skin
15	chr13:76319200-76323000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr13:76320400-76321800	Weak transcription	HSMM	muscle
17	chr13:76321200-76323400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr13:76321200-76324600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr13:76321400-76322200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr13:76321400-76322200	Genic enhancers	NHDF-Ad	bronchial
21	chr13:76321400-76322800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr13:76321400-76322800	Genic enhancers	Osteobl	bone
23	chr13:76321600-76322200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:76321600-76322200	Strong transcription	Muscle Satellite Cultured Cells	--
25	chr13:76321800-76322400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr13:76321800-76322400	Strong transcription	HSMMtube	muscle
27	chr13:76321800-76322600	Strong transcription	NH-A	brain
28	chr13:76321800-76322800	Strong transcription	HSMM	muscle
29	chr13:76322200-76323000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr13:76322200-76323200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr13:76322200-76324000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr13:76322200-76324800	Enhancers	NHDF-Ad	bronchial
33	chr13:76322400-76323400	Weak transcription	HSMMtube	muscle
34	chr13:76322400-76334800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr13:76322600-76322800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:76322600-76323600	Weak transcription	NH-A	brain
37	chr13:76322800-76323200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:76322800-76323400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:76322800-76323800	Enhancers	Osteobl	bone
40	chr13:76322800-76324600	Weak transcription	HSMM	muscle
41	chr13:76323000-76324000	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr13:76323000-76325200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr13:76323200-76323600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr13:76323200-76323600	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr13:76323200-76324000	Enhancers	NHLF	lung
46	chr13:76323200-76325800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr13:76323400-76323600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr13:76323400-76323600	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr13:76323400-76323800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr13:76323400-76323800	Enhancers	HSMMtube	muscle

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