Variant report

Variant	nsv900337
Chromosome Location	chr13:64643485-64856866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:64649045-64649723	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:64647343-64648012	K562	blood:	n/a	n/a
3	ARID3A	chr13:64648424-64648624	K562	blood:	n/a	n/a
4	ARID3A	chr13:64649942-64650348	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:64647471-64647547	HepG2	liver:	n/a	n/a
6	ATF1	chr13:64649727-64650392	K562	blood:	n/a	n/a
7	ATF3	chr13:64650004-64650247	K562	blood:	n/a	n/a
8	ATF3	chr13:64649966-64650442	HepG2	liver:	n/a	n/a
9	ATF3	chr13:64649957-64650249	HepG2	liver:	n/a	n/a
10	BACH1	chr13:64841992-64842115	K562	blood:	n/a	n/a
11	BHLHE40	chr13:64828941-64829013	A549	lung:	n/a	n/a
12	BHLHE40	chr13:64649668-64650427	HepG2	liver:	n/a	n/a
13	BHLHE40	chr13:64649695-64650426	K562	blood:	n/a	n/a
14	BRCA1	chr13:64650041-64650270	HepG2	liver:	n/a	n/a
15	CBX3	chr13:64649553-64650322	K562	blood:	n/a	n/a
16	CCNT2	chr13:64649960-64650241	K562	blood:	n/a	n/a
17	CCNT2	chr13:64848559-64848900	K562	blood:	n/a	n/a
18	CEBPB	chr13:64675628-64675976	HepG2	liver:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
19	CEBPB	chr13:64704806-64705056	H1-hESC	embryonic stem cell:	n/a	chr13:64704897-64704908
20	CEBPB	chr13:64704763-64705044	IMR90	lung:	n/a	chr13:64704897-64704908
21	CEBPB	chr13:64645492-64645866	K562	blood:	n/a	n/a
22	CEBPB	chr13:64646318-64646667	K562	blood:	n/a	chr13:64646454-64646467 chr13:64646617-64646630 chr13:64646455-64646466
23	CEBPB	chr13:64754905-64755176	MCF-7	breast:	n/a	chr13:64755080-64755091
24	CEBPB	chr13:64675622-64675994	IMR90	lung:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
25	CEBPB	chr13:64823756-64824037	A549	lung:	n/a	chr13:64823911-64823922
26	CEBPB	chr13:64837378-64837493	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:64754885-64755271	A549	lung:	n/a	chr13:64754887-64754898 chr13:64754888-64754900 chr13:64755080-64755091
28	CEBPB	chr13:64820751-64821175	IMR90	lung:	n/a	n/a
29	CEBPB	chr13:64807421-64807694	IMR90	lung:	n/a	n/a
30	CEBPB	chr13:64704853-64704978	K562	blood:	n/a	chr13:64704897-64704908
31	CEBPB	chr13:64848571-64848950	K562	blood:	n/a	n/a
32	CEBPB	chr13:64835984-64836173	IMR90	lung:	n/a	n/a
33	CEBPB	chr13:64645645-64645840	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr13:64774126-64774382	HepG2	liver:	n/a	n/a
35	CEBPB	chr13:64760710-64761000	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr13:64675737-64675975	H1-hESC	embryonic stem cell:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
37	CEBPB	chr13:64646287-64646619	HepG2	liver:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
38	CEBPB	chr13:64646320-64646576	A549	lung:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
39	CEBPB	chr13:64754902-64755260	HepG2	liver:	n/a	chr13:64755080-64755091
40	CEBPB	chr13:64848506-64848895	K562	blood:	n/a	n/a
41	CEBPB	chr13:64754928-64755251	A549	lung:	n/a	chr13:64755080-64755091
42	CEBPB	chr13:64754910-64755245	K562	blood:	n/a	chr13:64755080-64755091
43	CEBPB	chr13:64754989-64755204	H1-hESC	embryonic stem cell:	n/a	chr13:64755080-64755091
44	CEBPB	chr13:64760695-64761006	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:64774063-64774245	A549	lung:	n/a	n/a
46	CEBPB	chr13:64675687-64675952	K562	blood:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
47	CEBPB	chr13:64675653-64675957	A549	lung:	n/a	chr13:64675800-64675813 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675800-64675813 chr13:64675802-64675811 chr13:64675802-64675811 chr13:64675802-64675813 chr13:64675800-64675811
48	CEBPB	chr13:64835973-64836132	A549	lung:	n/a	n/a
49	CEBPB	chr13:64704718-64705094	HepG2	liver:	n/a	chr13:64704897-64704908
50	CEBPB	chr13:64848648-64848879	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64650215-64650265	U87	brain:	n/a
2	chr13:64650188-64650238	Caco-2	colon:	n/a
3	chr13:64651269-64651319	SK-N-SH	brain:	n/a
4	chr13:64650183-64650233	GM12891	blood:	n/a
5	chr13:64650215-64650265	HCPEpiC	choroid plexus:	n/a
6	chr13:64650183-64650233	NH-A	brain:	n/a
7	chr13:64650183-64650233	HCM	heart:	n/a
8	chr13:64650183-64650233	ProgFib	skin:	n/a
9	chr13:64650188-64650238	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:64650183-64650233	HPAEpiC	pulmonary alveolar:	n/a
11	chr13:64651269-64651319	NB4	blood:	n/a
12	chr13:64650183-64650233	HRCEpiC	kidney:	n/a
13	chr13:64651269-64651319	HEEpiC	esophagus:	n/a
14	chr13:64650183-64650233	Caco-2	colon:	n/a
15	chr13:64650215-64650265	Hela-S3	cervix:	n/a
16	chr13:64650215-64650265	SK-N-MC	brain:	n/a
17	chr13:64650215-64650265	ovcar-3	ovarian:	n/a
18	chr13:64650188-64650238	GM12892	blood:	n/a
19	chr13:64650183-64650233	HEK293	kidney:	embryo
20	chr13:64651269-64651319	IMR90	lung:	fetal
21	chr13:64650215-64650265	ProgFib	skin:	n/a
22	chr13:64650188-64650238	AG04450	lung:	fetal
23	chr13:64650183-64650233	IMR90	lung:	fetal
24	chr13:64650188-64650238	H1-hESC	embryonic stem cell:	embryo
25	chr13:64651269-64651319	Caco-2	colon:	n/a
26	chr13:64650188-64650238	CMK	blood:	n/a
27	chr13:64650183-64650233	GM19239	blood:	n/a
28	chr13:64650215-64650265	HNPCEpiC	eye:	n/a
29	chr13:64650215-64650265	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:64650183-64650233	HEEpiC	esophagus:	n/a
31	chr13:64650188-64650238	NT2-D1	testis:	n/a
32	chr13:64650183-64650233	PANC-1	pancreas:	n/a
33	chr13:64651269-64651319	HCM	heart:	n/a
34	chr13:64650215-64650265	BE2_C	brain:	n/a
35	chr13:64651269-64651319	PANC-1	pancreas:	n/a
36	chr13:64650215-64650265	MCF-7	breast:	n/a
37	chr13:64650215-64650265	HMEC	breast:	n/a
38	chr13:64650183-64650233	HCPEpiC	choroid plexus:	n/a
39	chr13:64651269-64651319	BJ	skin:	n/a
40	chr13:64650215-64650265	SKMC	muscle:	n/a
41	chr13:64650215-64650265	Jurkat	blood:	n/a
42	chr13:64651269-64651319	HAEpiC	amniotic membrane:	n/a
43	chr13:64651269-64651319	LNCaP	prostate:	n/a
44	chr13:64650188-64650238	HEK293	kidney:	embryo
45	chr13:64650188-64650238	HCPEpiC	choroid plexus:	n/a
46	chr13:64650215-64650265	NH-A	brain:	n/a
47	chr13:64651269-64651319	NHBE	bronchial:	n/a
48	chr13:64651269-64651319	HIPEpiC	eye:	n/a
49	chr13:64651269-64651319	PrEC	prostate:	n/a
50	chr13:64650183-64650233	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:64753621..64755784-chr13:64760416..64762529,2	K562	blood:
2	chr13:64629925..64632065-chr13:64645172..64647089,2	K562	blood:
3	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
4	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
5	chr13:64645390..64648132-chr13:64648675..64650217,2	K562	blood:
6	chr13:64753621..64755784-chr13:64760416..64762529,2	K562	blood:
7	chr13:64648914..64651680-chr13:64658514..64661246,2	K562	blood:
8	chr13:64733418..64735180-chr13:64740431..64742208,2	MCF-7	breast:
9	chr13:64651720..64653220-chr20:35806448..35807989,2	K562	blood:
10	chr13:64642482..64644473-chr13:64648903..64651732,2	K562	blood:
11	chr13:64650229..64650817-chr15:52311651..52312545,2	Hela-S3	cervix:
12	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
13	chr13:64733418..64735180-chr13:64740431..64742208,2	MCF-7	breast:
14	chr13:64637404..64639561-chr13:64642021..64643825,2	K562	blood:
15	chr13:64475617..64476410-chr13:64728809..64729366,2	MCF-7	breast:
16	chr13:64792758..64793744-chr7:131539225..131540176,2	MCF-7	breast:
17	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
18	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:
19	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:

Variant related genes	Relation type
LINC00355	TF binding region
LINC00355	CpG island
ENSG00000069956	chromatin interactions
ENSG00000227674	chromatin interactions
ENSG00000118705	chromatin interactions
ENSG00000101353	chromatin interactions

Extended variants
information (count: 2657 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2657 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs269623	chr13:64643485-64643486	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182634475	chr13:64643505-64643506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs565922046	chr13:64643506-64643507	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545792338	chr13:64643523-64643524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557901531	chr13:64643559-64643560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs187624960	chr13:64643654-64643655	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578039813	chr13:64643673-64643674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142415190	chr13:64643674-64643675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs146300289	chr13:64643725-64643726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568613031	chr13:64643771-64643772	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555492223	chr13:64643778-64643779	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141804784	chr13:64643780-64643781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540979688	chr13:64643795-64643796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34112677	chr13:64643846-64643847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550728418	chr13:64643865-64643866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192078131	chr13:64643867-64643868	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527949544	chr13:64643880-64643881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs78681868	chr13:64643989-64643990	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184434573	chr13:64643991-64643992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189128104	chr13:64644065-64644066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs193026805	chr13:64644079-64644080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568214938	chr13:64644093-64644094	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529351647	chr13:64644175-64644176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570633270	chr13:64644214-64644215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369042090	chr13:64644248-64644249	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565956677	chr13:64644272-64644273	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373233534	chr13:64644292-64644293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376554490	chr13:64644295-64644296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372708489	chr13:64644382-64644383	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs539525998	chr13:64644413-64644414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569967527	chr13:64644431-64644432	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537240117	chr13:64644452-64644453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111987871	chr13:64644453-64644454	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184490606	chr13:64644455-64644456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114276965	chr13:64644515-64644516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs269624	chr13:64644553-64644554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552903783	chr13:64644600-64644601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189162812	chr13:64644761-64644762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553127788	chr13:64644824-64644825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545019818	chr13:64644898-64644899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564618967	chr13:64644930-64644931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74487275	chr13:64644939-64644940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543565001	chr13:64644966-64644967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561956001	chr13:64644972-64644973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75840676	chr13:64645030-64645031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566851009	chr13:64645037-64645038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371904647	chr13:64645039-64645040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148447926	chr13:64645071-64645072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs559826057	chr13:64645096-64645097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191853848	chr13:64645114-64645115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	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	15273396	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64632000-64646200	Weak transcription	HepG2	liver
2	chr13:64644800-64645200	Enhancers	K562	blood
3	chr13:64645200-64645400	Weak transcription	K562	blood
4	chr13:64645400-64645800	Enhancers	K562	blood
5	chr13:64645800-64646200	Weak transcription	K562	blood
6	chr13:64646200-64647400	Enhancers	HepG2	liver
7	chr13:64646200-64651400	Active TSS	K562	blood
8	chr13:64647400-64649000	Active TSS	HepG2	liver
9	chr13:64648200-64654200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr13:64648600-64651600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr13:64649000-64650200	Bivalent/Poised TSS	HepG2	liver
12	chr13:64649000-64650600	Active TSS	Hela-S3	cervix
13	chr13:64649200-64650200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:64650200-64650600	Active TSS	HepG2	liver
15	chr13:64650200-64652600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:64650600-64651000	Flanking Active TSS	HepG2	liver
17	chr13:64650800-64651800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr13:64651000-64653400	Active TSS	HepG2	liver
19	chr13:64652600-64653200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr13:64654200-64654400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr13:64674000-64674800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:64682800-64683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:64683000-64683600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:64695000-64695800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:64695600-64695800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:64695800-64706200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:64697200-64698400	Enhancers	Muscle Satellite Cultured Cells	--
28	chr13:64701800-64702400	Enhancers	HUVEC	blood vessel
29	chr13:64704400-64706000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr13:64704600-64705000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:64704600-64705000	Enhancers	Fetal Muscle Trunk	muscle
32	chr13:64704600-64705000	Enhancers	HSMM	muscle
33	chr13:64704600-64705400	Enhancers	Adipose Nuclei	Adipose
34	chr13:64704600-64705600	Enhancers	Fetal Muscle Leg	muscle
35	chr13:64705000-64705600	Enhancers	HSMMtube	muscle
36	chr13:64705600-64706800	Weak transcription	Fetal Muscle Leg	muscle
37	chr13:64706200-64706400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:64730200-64730800	Enhancers	HUVEC	blood vessel
39	chr13:64730800-64732600	Weak transcription	HUVEC	blood vessel
40	chr13:64732400-64732600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr13:64732600-64733000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr13:64732600-64734000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr13:64732600-64734000	Enhancers	HUVEC	blood vessel
44	chr13:64733000-64733600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr13:64738600-64738800	Enhancers	Gastric	stomach
46	chr13:64743800-64745800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr13:64745800-64747000	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr13:64747000-64747400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr13:64760600-64761200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr13:64764600-64765000	Enhancers	Primary T helper naive cells from peripheral blood	blood

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