Variant report

Variant	nsv832646
Chromosome Location	chr13:76300428-76483102
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2545)
CpG islands
(count:1956)
Chromatin interactive
region (count:27)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76444552-76444937	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76346001-76346202	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76450563-76450871	K562	blood:	n/a	n/a
4	ARID3A	chr13:76334296-76335488	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:76450475-76450923	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:76366535-76367382	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:76336178-76336848	HepG2	liver:	n/a	n/a
8	ARID3A	chr13:76365263-76365462	HepG2	liver:	n/a	n/a
9	ATF2	chr13:76336398-76337123	GM12878	blood:	n/a	n/a
10	ATF2	chr13:76336516-76337091	GM12878	blood:	n/a	n/a
11	ATF2	chr13:76377164-76377683	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr13:76313636-76314171	GM12878	blood:	n/a	n/a
13	ATF2	chr13:76335482-76335963	GM12878	blood:	n/a	n/a
14	ATF2	chr13:76313090-76314338	GM12878	blood:	n/a	n/a
15	BACH1	chr13:76399460-76399676	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:76463777-76463874	K562	blood:	n/a	n/a
17	BACH1	chr13:76463615-76464005	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr13:76336585-76337045	GM12878	blood:	n/a	n/a
19	BATF	chr13:76421762-76422001	GM12878	blood:	n/a	n/a
20	BATF	chr13:76335575-76335846	GM12878	blood:	n/a	n/a
21	BATF	chr13:76336647-76336971	GM12878	blood:	n/a	n/a
22	BATF	chr13:76372694-76373000	GM12878	blood:	n/a	chr13:76372915-76372925
23	BATF	chr13:76421703-76422063	GM12878	blood:	n/a	n/a
24	BCL11A	chr13:76377394-76377574	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr13:76336652-76336953	GM12878	blood:	n/a	n/a
26	BCL11A	chr13:76377334-76377612	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr13:76372781-76372993	GM12878	blood:	n/a	chr13:76372918-76372927
28	BCL11A	chr13:76335595-76335800	GM12878	blood:	n/a	chr13:76335725-76335734
29	BCL11A	chr13:76372678-76373069	GM12878	blood:	n/a	chr13:76372918-76372927
30	BCL11A	chr13:76336604-76336973	GM12878	blood:	n/a	n/a
31	BCL3	chr13:76313442-76313929	GM12878	blood:	n/a	n/a
32	BCL3	chr13:76336625-76337031	GM12878	blood:	n/a	n/a
33	BCL3	chr13:76335525-76335880	GM12878	blood:	n/a	chr13:76335725-76335734
34	BCLAF1	chr13:76336564-76337049	GM12878	blood:	n/a	n/a
35	BCLAF1	chr13:76336410-76337207	GM12878	blood:	n/a	n/a
36	BHLHE40	chr13:76336436-76337084	GM12878	blood:	n/a	n/a
37	BHLHE40	chr13:76335489-76335909	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:76450555-76450879	HepG2	liver:	n/a	n/a
39	BHLHE40	chr13:76438943-76439039	HepG2	liver:	n/a	n/a
40	BHLHE40	chr13:76361352-76361575	GM12878	blood:	n/a	n/a
41	BHLHE40	chr13:76444883-76444909	K562	blood:	n/a	n/a
42	BHLHE40	chr13:76334346-76335029	HepG2	liver:	n/a	n/a
43	BRCA1	chr13:76359155-76359177	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr13:76461975-76461988	GM12878	blood:	n/a	n/a
45	BRCA1	chr13:76362667-76363375	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr13:76336566-76336924	GM12878	blood:	n/a	n/a
47	BRCA1	chr13:76335108-76335374	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr13:76298981-76300594	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr13:76334219-76334895	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr13:76344622-76345262	Hela-S3	cervix:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76313846-76313896	HRE	kidney:	n/a
2	chr13:76445055-76445105	SKMC	muscle:	n/a
3	chr13:76430665-76430715	HRPEpiC	eye:	n/a
4	chr13:76444850-76444900	AG04450	lung:	fetal
5	chr13:76313846-76313896	HRE	kidney:	n/a
6	chr13:76445055-76445105	SKMC	muscle:	n/a
7	chr13:76430665-76430715	HRPEpiC	eye:	n/a
8	chr13:76444850-76444900	AG04450	lung:	fetal
9	chr13:76313846-76313896	Caco-2	colon:	n/a
10	chr13:76387161-76387211	HIPEpiC	eye:	n/a
11	chr13:76333727-76333777	A549	lung:	n/a
12	chr13:76334866-76334916	BJ	skin:	n/a
13	chr13:76313846-76313896	HCPEpiC	choroid plexus:	n/a
14	chr13:76361354-76361404	A549	lung:	n/a
15	chr13:76313846-76313896	ovcar-3	ovarian:	n/a
16	chr13:76377366-76377416	SKMC	muscle:	n/a
17	chr13:76344333-76344383	HRPEpiC	eye:	n/a
18	chr13:76444293-76444343	BJ	skin:	n/a
19	chr13:76334707-76334757	MCF10A-Er-Src	breast:	n/a
20	chr13:76444850-76444900	HL-60	blood:	n/a
21	chr13:76430665-76430715	GM12891	blood:	n/a
22	chr13:76445108-76445158	HCF	heart:	n/a
23	chr13:76450676-76450726	MCF-7	breast:	n/a
24	chr13:76334039-76334089	PrEC	prostate:	n/a
25	chr13:76337398-76337448	ProgFib	skin:	n/a
26	chr13:76334583-76334633	ECC-1	luminal epithelium:	n/a
27	chr13:76392745-76392795	AG09319	gingival:	n/a
28	chr13:76444831-76444881	HCPEpiC	choroid plexus:	n/a
29	chr13:76445108-76445158	AG10803	skin:	n/a
30	chr13:76430722-76430772	SK-N-SH	brain:	n/a
31	chr13:76444823-76444873	HAEpiC	amniotic membrane:	n/a
32	chr13:76430665-76430715	HEEpiC	esophagus:	n/a
33	chr13:76400715-76400765	LNCaP	prostate:	n/a
34	chr13:76444293-76444343	GM12878	blood:	n/a
35	chr13:76450676-76450726	CMK	blood:	n/a
36	chr13:76361354-76361404	NHBE	bronchial:	n/a
37	chr13:76450676-76450726	GM06990	blood:	n/a
38	chr13:76333727-76333777	HRPEpiC	eye:	n/a
39	chr13:76361354-76361404	HPAEpiC	pulmonary alveolar:	n/a
40	chr13:76445055-76445105	AoSMC	blood vessel:	n/a
41	chr13:76333727-76333777	PFSK-1	brain:	n/a
42	chr13:76363851-76363901	HEEpiC	esophagus:	n/a
43	chr13:76334707-76334757	HRE	kidney:	n/a
44	chr13:76333727-76333777	HUVEC	blood vessel:	n/a
45	chr13:76430722-76430772	Jurkat	blood:	n/a
46	chr13:76444798-76444848	GM06990	blood:	n/a
47	chr13:76444293-76444343	ECC-1	luminal epithelium:	n/a
48	chr13:76445065-76445115	T-47D	breast:	n/a
49	chr13:76445065-76445115	HIPEpiC	eye:	n/a
50	chr13:76387161-76387211	HEK293	kidney:	embryo

(count:27 , 50 per page) page: 1

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

(count:5 , 50 per page) page: 1

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

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	chr13:76432682-76432703
2	LMO7	hsa-miR-16-5p	chr13:76432114-76432135

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

Extended variants
information (count: 7243 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:7243 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554169350	chr13:76300436-76300437	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs565835047	chr13:76300437-76300438	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs186749241	chr13:76300454-76300455	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs536489157	chr13:76300457-76300458	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs559236391	chr13:76300492-76300493	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554243494	chr13:76300499-76300500	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs577690409	chr13:76300548-76300549	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs575761671	chr13:76300558-76300559	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs80306381	chr13:76300565-76300566	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs564507121	chr13:76300566-76300567	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs565440093	chr13:76300579-76300580	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs541275025	chr13:76300630-76300631	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs189075072	chr13:76300662-76300663	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs634002	chr13:76300682-76300683	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113006523	chr13:76300691-76300692	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140543193	chr13:76300755-76300756	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs531804083	chr13:76300770-76300771	Weak transcription Genic enhancers Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs113701656	chr13:76300807-76300808	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112295119	chr13:76300808-76300809	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35248472	chr13:76300809-76300810	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531212937	chr13:76300837-76300838	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs509450	chr13:76300864-76300865	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34603691	chr13:76300877-76300878	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531044869	chr13:76300880-76300881	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs508596	chr13:76300942-76300943	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs549745683	chr13:76300944-76300945	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538662560	chr13:76300953-76300954	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548063045	chr13:76300955-76300956	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566292450	chr13:76300962-76300963	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145637683	chr13:76300979-76300980	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs635307	chr13:76300984-76300985	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs368609853	chr13:76300993-76300994	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576245903	chr13:76301049-76301050	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138499595	chr13:76301087-76301088	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558234419	chr13:76301089-76301090	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114238530	chr13:76301101-76301102	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540716180	chr13:76301129-76301130	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369115712	chr13:76301141-76301142	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs73536580	chr13:76301189-76301190	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140368500	chr13:76301190-76301191	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145642799	chr13:76301193-76301194	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138203445	chr13:76301229-76301230	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201245586	chr13:76301254-76301255	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200412226	chr13:76301258-76301259	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375045231	chr13:76301260-76301261	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374236242	chr13:76301261-76301262	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377001128	chr13:76301277-76301278	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532536244	chr13:76301279-76301280	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375445168	chr13:76301280-76301281	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547504547	chr13:76301282-76301283	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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

Chromatin state (count:3927 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76279400-76308000	Weak transcription	Left Ventricle	heart
2	chr13:76283600-76308000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:76294800-76321800	Weak transcription	NH-A	brain
4	chr13:76297000-76300800	Enhancers	Hela-S3	cervix
5	chr13:76297800-76301400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr13:76297800-76301400	Enhancers	Muscle Satellite Cultured Cells	--
7	chr13:76298000-76301400	Enhancers	Stomach Mucosa	stomach
8	chr13:76298200-76300600	Enhancers	A549	lung
9	chr13:76298200-76301000	Enhancers	HUVEC	blood vessel
10	chr13:76298400-76301200	Enhancers	Fetal Lung	lung
11	chr13:76298600-76309200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr13:76298600-76313000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:76298600-76318800	Weak transcription	Gastric	stomach
14	chr13:76299200-76301000	Enhancers	Fetal Heart	heart
15	chr13:76299200-76307800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr13:76299200-76308000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr13:76299400-76307800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr13:76299600-76300600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:76299600-76300800	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr13:76299600-76310400	Weak transcription	NHLF	lung
21	chr13:76299800-76300800	Weak transcription	Fetal Intestine Small	intestine
22	chr13:76299800-76313000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr13:76300000-76300800	Weak transcription	Osteobl	bone
24	chr13:76300000-76301400	Weak transcription	Fetal Intestine Large	intestine
25	chr13:76300200-76300600	Flanking Active TSS	Fetal Kidney	kidney
26	chr13:76300200-76300800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr13:76300200-76301200	Enhancers	HSMMtube	muscle
28	chr13:76300200-76309200	Weak transcription	NHDF-Ad	bronchial
29	chr13:76300200-76313000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr13:76300400-76301000	Weak transcription	HSMM	muscle
31	chr13:76300400-76301400	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:76300400-76301400	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr13:76300600-76301400	Enhancers	Fetal Kidney	kidney
34	chr13:76300800-76301200	Enhancers	Fetal Intestine Small	intestine
35	chr13:76300800-76301200	Flanking Active TSS	Hela-S3	cervix
36	chr13:76300800-76301400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr13:76300800-76301400	Strong transcription	Osteobl	bone
38	chr13:76301000-76301200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr13:76301000-76301400	Genic enhancers	HSMM	muscle
40	chr13:76301200-76301400	Enhancers	Hela-S3	cervix
41	chr13:76301200-76310400	Weak transcription	HSMMtube	muscle
42	chr13:76301400-76306400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr13:76301400-76307600	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr13:76301400-76307800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr13:76301400-76307800	Weak transcription	HSMM	muscle
46	chr13:76301400-76307800	Weak transcription	Osteobl	bone
47	chr13:76301400-76308000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:76301400-76310800	Weak transcription	Fetal Kidney	kidney
49	chr13:76304200-76307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:76304600-76310800	Weak transcription	Fetal Intestine Large	intestine

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