Variant report

Variant	esv2754234
Chromosome Location	chr13:64637596-64901664
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	chr13:64648424-64648624	K562	blood:	n/a	n/a
3	ARID3A	chr13:64647343-64648012	K562	blood:	n/a	n/a
4	ARID3A	chr13:64647471-64647547	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:64649942-64650348	HepG2	liver:	n/a	n/a
6	ATF1	chr13:64649727-64650392	K562	blood:	n/a	n/a
7	ATF3	chr13:64649966-64650442	HepG2	liver:	n/a	n/a
8	ATF3	chr13:64650004-64650247	K562	blood:	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	BACH1	chr13:64886036-64886448	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr13:64886118-64886453	K562	blood:	n/a	n/a
13	BHLHE40	chr13:64649695-64650426	K562	blood:	n/a	n/a
14	BHLHE40	chr13:64828941-64829013	A549	lung:	n/a	n/a
15	BHLHE40	chr13:64649668-64650427	HepG2	liver:	n/a	n/a
16	BRCA1	chr13:64650041-64650270	HepG2	liver:	n/a	n/a
17	CBX3	chr13:64649553-64650322	K562	blood:	n/a	n/a
18	CCNT2	chr13:64848559-64848900	K562	blood:	n/a	n/a
19	CCNT2	chr13:64649960-64650241	K562	blood:	n/a	n/a
20	CEBPB	chr13:64704673-64705102	HepG2	liver:	n/a	chr13:64704897-64704908
21	CEBPB	chr13:64754885-64755271	A549	lung:	n/a	chr13:64754887-64754898 chr13:64754888-64754900 chr13:64755080-64755091
22	CEBPB	chr13:64837294-64837537	IMR90	lung:	n/a	n/a
23	CEBPB	chr13:64754908-64755275	IMR90	lung:	n/a	chr13:64755080-64755091
24	CEBPB	chr13:64760695-64761006	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:64704763-64705044	IMR90	lung:	n/a	chr13:64704897-64704908
26	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
27	CEBPB	chr13:64823756-64824037	A549	lung:	n/a	chr13:64823911-64823922
28	CEBPB	chr13:64879410-64879737	IMR90	lung:	n/a	n/a
29	CEBPB	chr13:64848506-64848895	K562	blood:	n/a	n/a
30	CEBPB	chr13:64760710-64761000	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:64879398-64879782	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr13:64645538-64645794	HepG2	liver:	n/a	n/a
33	CEBPB	chr13:64867855-64868449	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:64754910-64755245	K562	blood:	n/a	chr13:64755080-64755091
35	CEBPB	chr13:64645492-64645866	K562	blood:	n/a	n/a
36	CEBPB	chr13:64859239-64859478	IMR90	lung:	n/a	chr13:64859327-64859338 chr13:64859327-64859340 chr13:64859327-64859340
37	CEBPB	chr13:64867811-64868543	MCF-7	breast:	n/a	chr13:64868449-64868460
38	CEBPB	chr13:64820751-64821175	IMR90	lung:	n/a	n/a
39	CEBPB	chr13:64848648-64848879	K562	blood:	n/a	n/a
40	CEBPB	chr13:64645645-64645840	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr13:64646287-64646619	HepG2	liver:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
42	CEBPB	chr13:64754905-64755176	MCF-7	breast:	n/a	chr13:64755080-64755091
43	CEBPB	chr13:64754989-64755204	H1-hESC	embryonic stem cell:	n/a	chr13:64755080-64755091
44	CEBPB	chr13:64754927-64755270	Hela-S3	cervix:	n/a	chr13:64755080-64755091
45	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
46	CEBPB	chr13:64702066-64702266	HepG2	liver:	n/a	n/a
47	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
48	CEBPB	chr13:64774126-64774382	HepG2	liver:	n/a	n/a
49	CEBPB	chr13:64646320-64646576	A549	lung:	n/a	chr13:64646454-64646467 chr13:64646455-64646466
50	CEBPB	chr13:64823772-64824053	Hela-S3	cervix:	n/a	chr13:64823911-64823922

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64651269-64651319	HEK293	kidney:	embryo
2	chr13:64650183-64650233	SK-N-SH_RA	brain:	n/a
3	chr13:64651269-64651319	NB4	blood:	n/a
4	chr13:64651269-64651319	SAEC	small airway:	n/a
5	chr13:64650183-64650233	GM12891	blood:	n/a
6	chr13:64650183-64650233	SAEC	small airway:	n/a
7	chr13:64650188-64650238	MCF10A-Er-Src	breast:	n/a
8	chr13:64651269-64651319	ProgFib	skin:	n/a
9	chr13:64650188-64650238	AG09309	skin:	n/a
10	chr13:64650183-64650233	SKMC	muscle:	n/a
11	chr13:64651269-64651319	GM06990	blood:	n/a
12	chr13:64650188-64650238	HPAEpiC	pulmonary alveolar:	n/a
13	chr13:64650215-64650265	NH-A	brain:	n/a
14	chr13:64651269-64651319	BE2_C	brain:	n/a
15	chr13:64651269-64651319	H1-hESC	embryonic stem cell:	embryo
16	chr13:64650215-64650265	NHBE	bronchial:	n/a
17	chr13:64650183-64650233	BJ	skin:	n/a
18	chr13:64651269-64651319	HL-60	blood:	n/a
19	chr13:64651269-64651319	Hela-S3	cervix:	n/a
20	chr13:64650188-64650238	NHBE	bronchial:	n/a
21	chr13:64650215-64650265	HCF	heart:	n/a
22	chr13:64650183-64650233	PANC-1	pancreas:	n/a
23	chr13:64650215-64650265	GM06990	blood:	n/a
24	chr13:64651269-64651319	HUVEC	blood vessel:	n/a
25	chr13:64650215-64650265	SKMC	muscle:	n/a
26	chr13:64650188-64650238	HRPEpiC	eye:	n/a
27	chr13:64650215-64650265	Hepatocyte	liver:	n/a
28	chr13:64651269-64651319	AG09309	skin:	n/a
29	chr13:64651269-64651319	BJ	skin:	n/a
30	chr13:64651269-64651319	NHBE	bronchial:	n/a
31	chr13:64650183-64650233	NB4	blood:	n/a
32	chr13:64650188-64650238	SKMC	muscle:	n/a
33	chr13:64650183-64650233	U87	brain:	n/a
34	chr13:64651269-64651319	HCM	heart:	n/a
35	chr13:64650188-64650238	AG04450	lung:	fetal
36	chr13:64651269-64651319	ECC-1	luminal epithelium:	n/a
37	chr13:64651269-64651319	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:64650188-64650238	Hela-S3	cervix:	n/a
39	chr13:64651269-64651319	GM12878	blood:	n/a
40	chr13:64650215-64650265	SAEC	small airway:	n/a
41	chr13:64651269-64651319	MCF10A-Er-Src	breast:	n/a
42	chr13:64650215-64650265	HPAEpiC	pulmonary alveolar:	n/a
43	chr13:64650215-64650265	GM12891	blood:	n/a
44	chr13:64650215-64650265	MCF-7	breast:	n/a
45	chr13:64650183-64650233	HUVEC	blood vessel:	n/a
46	chr13:64650215-64650265	U87	brain:	n/a
47	chr13:64650188-64650238	BE2_C	brain:	n/a
48	chr13:64650215-64650265	GM19239	blood:	n/a
49	chr13:64650183-64650233	H1-hESC	embryonic stem cell:	embryo
50	chr13:64651269-64651319	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:64648914..64651680-chr13:64658514..64661246,2	K562	blood:
2	chr13:64629925..64632065-chr13:64645172..64647089,2	K562	blood:
3	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:
4	chr13:64733418..64735180-chr13:64740431..64742208,2	MCF-7	breast:
5	chr13:64475617..64476410-chr13:64728809..64729366,2	MCF-7	breast:
6	chr13:64650229..64650817-chr15:52311651..52312545,2	Hela-S3	cervix:
7	chr13:64733418..64735180-chr13:64740431..64742208,2	MCF-7	breast:
8	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
9	chr13:64637404..64639561-chr13:64642021..64643825,2	K562	blood:
10	chr13:64858043..64860843-chr13:64861855..64863663,2	K562	blood:
11	chr13:64637718..64641008-chr13:64648657..64651427,4	K562	blood:
12	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
13	chr13:64792758..64793744-chr7:131539225..131540176,2	MCF-7	breast:
14	chr13:64651720..64653220-chr20:35806448..35807989,2	K562	blood:
15	chr13:64637404..64639561-chr13:64642021..64643825,2	K562	blood:
16	chr13:64858043..64860843-chr13:64861855..64863663,2	K562	blood:
17	chr13:64645390..64648132-chr13:64648675..64650217,2	K562	blood:
18	chr13:64753621..64755784-chr13:64760416..64762529,2	K562	blood:
19	chr13:64753621..64755784-chr13:64760416..64762529,2	K562	blood:
20	chr13:64862774..64864824-chr13:64866758..64868899,2	MCF-7	breast:
21	chr13:64642973..64645650-chr13:64650232..64651765,2	K562	blood:
22	chr13:64652193..64655150-chr13:64666356..64668232,2	K562	blood:
23	chr13:64663876..64666807-chr13:64668849..64670966,2	MCF-7	breast:
24	chr13:64642482..64644473-chr13:64648903..64651732,2	K562	blood:
25	chr13:64862774..64864824-chr13:64866758..64868899,2	MCF-7	breast:

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

Extended variants
information (count: 3036 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3036 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs166622	chr13:64637596-64637597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs386771752	chr13:64637630-64637631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542634106	chr13:64637638-64637639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12585880	chr13:64637651-64637652	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181420628	chr13:64637662-64637663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186431771	chr13:64637688-64637689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs79628072	chr13:64637710-64637711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12585874	chr13:64637713-64637714	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs551607886	chr13:64637725-64637726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563833465	chr13:64637786-64637787	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191077026	chr13:64637822-64637823	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549400950	chr13:64637824-64637825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147087705	chr13:64637856-64637857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs532305566	chr13:64637916-64637917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545682398	chr13:64637931-64637932	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534921439	chr13:64637939-64637940	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546774503	chr13:64637952-64637953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562469511	chr13:64637960-64637961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138432274	chr13:64637972-64637973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs76146581	chr13:64637975-64637976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556757337	chr13:64637999-64638000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs575331218	chr13:64638013-64638014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs269613	chr13:64638017-64638018	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs528276862	chr13:64638024-64638025	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149578038	chr13:64638122-64638123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545244819	chr13:64638166-64638167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs377335367	chr13:64638203-64638204	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573949371	chr13:64638239-64638240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527466470	chr13:64638246-64638247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182053314	chr13:64638299-64638300	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371314012	chr13:64638336-64638337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541341593	chr13:64638370-64638371	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185706954	chr13:64638375-64638376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190906571	chr13:64638385-64638386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183228600	chr13:64638413-64638414	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs144236043	chr13:64638441-64638442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531082779	chr13:64638446-64638447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549354355	chr13:64638522-64638523	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561279274	chr13:64638528-64638529	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376014960	chr13:64638535-64638536	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs377711630	chr13:64638540-64638541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs269614	chr13:64638579-64638580	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs34066905	chr13:64638591-64638592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199878621	chr13:64638618-64638619	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs9571099	chr13:64638629-64638630	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538438118	chr13:64638635-64638636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs269615	chr13:64638665-64638666	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs568855538	chr13:64638702-64638703	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs145456287	chr13:64638762-64638763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374707463	chr13:64638763-64638764	Weak transcription	Chromatin interactive region	1 gene(s)	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:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64632000-64646200	Weak transcription	HepG2	liver
2	chr13:64636200-64640600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr13:64640600-64641000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr13:64640600-64642200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr13:64640800-64642000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:64641200-64641600	Enhancers	Primary hematopoietic stem cells	blood
7	chr13:64644800-64645200	Enhancers	K562	blood
8	chr13:64645200-64645400	Weak transcription	K562	blood
9	chr13:64645400-64645800	Enhancers	K562	blood
10	chr13:64645800-64646200	Weak transcription	K562	blood
11	chr13:64646200-64647400	Enhancers	HepG2	liver
12	chr13:64646200-64651400	Active TSS	K562	blood
13	chr13:64647400-64649000	Active TSS	HepG2	liver
14	chr13:64648200-64654200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:64648600-64651600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr13:64649000-64650200	Bivalent/Poised TSS	HepG2	liver
17	chr13:64649000-64650600	Active TSS	Hela-S3	cervix
18	chr13:64649200-64650200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr13:64650200-64650600	Active TSS	HepG2	liver
20	chr13:64650200-64652600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr13:64650600-64651000	Flanking Active TSS	HepG2	liver
22	chr13:64650800-64651800	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr13:64651000-64653400	Active TSS	HepG2	liver
24	chr13:64652600-64653200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr13:64654200-64654400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:64674000-64674800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:64682800-64683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr13:64683000-64683600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr13:64695000-64695800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:64695600-64695800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr13:64695800-64706200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr13:64697200-64698400	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:64701800-64702400	Enhancers	HUVEC	blood vessel
34	chr13:64704400-64706000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr13:64704600-64705000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:64704600-64705000	Enhancers	Fetal Muscle Trunk	muscle
37	chr13:64704600-64705000	Enhancers	HSMM	muscle
38	chr13:64704600-64705400	Enhancers	Adipose Nuclei	Adipose
39	chr13:64704600-64705600	Enhancers	Fetal Muscle Leg	muscle
40	chr13:64705000-64705600	Enhancers	HSMMtube	muscle
41	chr13:64705600-64706800	Weak transcription	Fetal Muscle Leg	muscle
42	chr13:64706200-64706400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr13:64730200-64730800	Enhancers	HUVEC	blood vessel
44	chr13:64730800-64732600	Weak transcription	HUVEC	blood vessel
45	chr13:64732400-64732600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr13:64732600-64733000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr13:64732600-64734000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr13:64732600-64734000	Enhancers	HUVEC	blood vessel
49	chr13:64733000-64733600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr13:64738600-64738800	Enhancers	Gastric	stomach

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