Variant report

Variant	nsv900462
Chromosome Location	chr13:69545435-69598479
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	chr13:69584667-69584945	K562	blood:	n/a	n/a
2	CCNT2	chr13:69558900-69559144	K562	blood:	n/a	n/a
3	CTCF	chr13:69566652-69566736	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr13:69587095-69587140	ProgFib	skin:	n/a	n/a
5	CTCF	chr13:69575186-69575268	GM10248	blood:	n/a	n/a
6	E2F4	chr13:69598378-69598410	MCF10A-Er-Src	breast:	n/a	n/a
7	E2F4	chr13:69547675-69547808	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr13:69547144-69547250	MCF10A-Er-Src	breast:	n/a	n/a
9	E2F6	chr13:69558784-69559197	K562	blood:	n/a	chr13:69559076-69559088 chr13:69558955-69558965 chr13:69559034-69559044
10	E2F6	chr13:69558778-69559314	K562	blood:	n/a	chr13:69559076-69559088 chr13:69558955-69558965 chr13:69559034-69559044
11	E2F6	chr13:69558872-69559017	K562	blood:	n/a	chr13:69558955-69558965
12	EBF1	chr13:69591435-69591668	GM12878	blood:	n/a	chr13:69591524-69591535
13	EGR1	chr13:69558908-69559079	K562	blood:	n/a	chr13:69558991-69559004 chr13:69558994-69559004
14	FOS	chr13:69587162-69587390	MCF10A-Er-Src	breast:	n/a	chr13:69587313-69587323 chr13:69587314-69587322
15	FOS	chr13:69587222-69587458	MCF10A-Er-Src	breast:	n/a	chr13:69587313-69587323 chr13:69587314-69587322
16	FOS	chr13:69587193-69587422	MCF10A-Er-Src	breast:	n/a	chr13:69587313-69587323 chr13:69587314-69587322
17	HEY1	chr13:69559012-69559233	K562	blood:	n/a	n/a
18	JUN	chr13:69585367-69585538	H1-hESC	embryonic stem cell:	n/a	n/a
19	JUN	chr13:69589111-69589272	HepG2	liver:	n/a	chr13:69589233-69589246
20	JUND	chr13:69559054-69559254	K562	blood:	n/a	n/a
21	KAP1	chr13:69592436-69592722	HEK293	kidney:	n/a	n/a
22	KAP1	chr13:69557799-69557996	HEK293	kidney:	n/a	n/a
23	MAFF	chr13:69556565-69556790	HepG2	liver:	n/a	chr13:69556691-69556709
24	MAFK	chr13:69556580-69556785	IMR90	lung:	n/a	chr13:69556692-69556708 chr13:69556696-69556707 chr13:69556697-69556708 chr13:69556695-69556709 chr13:69556696-69556707 chr13:69556697-69556708
25	MAFK	chr13:69556553-69556853	HepG2	liver:	n/a	chr13:69556692-69556708 chr13:69556696-69556707 chr13:69556697-69556708 chr13:69556695-69556709 chr13:69556696-69556707 chr13:69556697-69556708
26	MAFK	chr13:69587781-69588013	HepG2	liver:	n/a	chr13:69587862-69587873
27	MAX	chr13:69558812-69559045	K562	blood:	n/a	chr13:69558994-69559004
28	MAX	chr13:69558792-69559082	K562	blood:	n/a	chr13:69558994-69559004
29	MAX	chr13:69558713-69559216	K562	blood:	n/a	chr13:69558994-69559004
30	MAZ	chr13:69558904-69559230	K562	blood:	n/a	chr13:69558994-69559004
31	MYC	chr13:69558801-69559157	K562	blood:	n/a	chr13:69558994-69559004
32	MYC	chr13:69546346-69546423	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr13:69558808-69559115	K562	blood:	n/a	chr13:69558994-69559004
34	MYC	chr13:69559158-69559248	MCF-7	breast:	n/a	n/a
35	NFYA	chr13:69573901-69574082	GM12878	blood:	n/a	n/a
36	NFYB	chr13:69557778-69558088	K562	blood:	n/a	n/a
37	NFYB	chr13:69569390-69569621	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr13:69572626-69572745	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr13:69559164-69559301	Gliobla	brain:	n/a	n/a
40	POLR2A	chr13:69583582-69583727	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr13:69548986-69549151	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr13:69558868-69559241	K562	blood:	n/a	n/a
43	POLR2A	chr13:69552602-69552801	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr13:69550159-69550586	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr13:69570505-69570644	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr13:69573605-69573757	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr13:69553787-69553856	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr13:69572962-69573032	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr13:69559117-69559143	MCF-7	breast:	n/a	n/a
50	POLR2A	chr13:69559150-69559292	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69557960-69558010	NT2-D1	testis:	n/a
2	chr13:69557960-69558010	NT2-D1	testis:	n/a
3	chr13:69559303-69559353	CMK	blood:	n/a
4	chr13:69559039-69559089	GM12878	blood:	n/a
5	chr13:69555907-69555957	Jurkat	blood:	n/a
6	chr13:69561352-69561402	HPAEpiC	pulmonary alveolar:	n/a
7	chr13:69555907-69555957	GM06990	blood:	n/a
8	chr13:69561352-69561402	MCF-7	breast:	n/a
9	chr13:69557960-69558010	SAEC	small airway:	n/a
10	chr13:69559039-69559089	ProgFib	skin:	n/a
11	chr13:69555907-69555957	AoSMC	blood vessel:	n/a
12	chr13:69559303-69559353	AG04449	skin:	fetal
13	chr13:69561352-69561402	AG09309	skin:	n/a
14	chr13:69558928-69558978	AG04450	lung:	fetal
15	chr13:69559194-69559244	AG04449	skin:	fetal
16	chr13:69558928-69558978	HEEpiC	esophagus:	n/a
17	chr13:69557960-69558010	HRE	kidney:	n/a
18	chr13:69559039-69559089	RPTEC	kidney:	n/a
19	chr13:69557960-69558010	AG10803	skin:	n/a
20	chr13:69555907-69555957	NHDF-neo	bronchial:	n/a
21	chr13:69587760-69587810	HUVEC	blood vessel:	n/a
22	chr13:69558928-69558978	PrEC	prostate:	n/a
23	chr13:69559303-69559353	HIPEpiC	eye:	n/a
24	chr13:69587760-69587810	HRPEpiC	eye:	n/a
25	chr13:69561352-69561402	T-47D	breast:	n/a
26	chr13:69587760-69587810	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:69559303-69559353	HCT-116	colon:	n/a
28	chr13:69559303-69559353	PrEC	prostate:	n/a
29	chr13:69559039-69559089	HCM	heart:	n/a
30	chr13:69559194-69559244	ECC-1	luminal epithelium:	n/a
31	chr13:69559303-69559353	IMR90	lung:	fetal
32	chr13:69559039-69559089	AG09309	skin:	n/a
33	chr13:69559039-69559089	HEEpiC	esophagus:	n/a
34	chr13:69557960-69558010	HepG2	liver:	n/a
35	chr13:69557960-69558010	PANC-1	pancreas:	n/a
36	chr13:69558928-69558978	HCM	heart:	n/a
37	chr13:69555907-69555957	ProgFib	skin:	n/a
38	chr13:69555907-69555957	Hepatocyte	liver:	n/a
39	chr13:69559194-69559244	A549	lung:	n/a
40	chr13:69555907-69555957	PANC-1	pancreas:	n/a
41	chr13:69587760-69587810	PrEC	prostate:	n/a
42	chr13:69559039-69559089	SK-N-MC	brain:	n/a
43	chr13:69558928-69558978	GM12892	blood:	n/a
44	chr13:69561352-69561402	H1-hESC	embryonic stem cell:	embryo
45	chr13:69559039-69559089	NB4	blood:	n/a
46	chr13:69587760-69587810	ECC-1	luminal epithelium:	n/a
47	chr13:69561352-69561402	MCF10A-Er-Src	breast:	n/a
48	chr13:69558928-69558978	NB4	blood:	n/a
49	chr13:69559039-69559089	H1-hESC	embryonic stem cell:	embryo
50	chr13:69558928-69558978	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:52026657..52027294-chr13:69594051..69594992,2	Hela-S3	cervix:
2	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
3	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
4	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:
5	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
6	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
7	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
8	chr13:69557613..69560490-chr13:69560641..69563029,2	K562	blood:
9	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
10	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
11	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
12	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
13	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
14	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-25	chr13:69559190-69560196	NONHSAT034239

Variant related genes	Relation type
ZDHHC20P4	TF binding region
ZDHHC20P4	CpG island
ENSG00000232380	chromatin interactions
ENSG00000102786	chromatin interactions

Extended variants
information (count: 1030 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1030 , 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	rs9572063	chr13:69545435-69545436	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529953171	chr13:69545491-69545492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546587756	chr13:69545623-69545624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541812714	chr13:69545642-69545643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538422952	chr13:69545646-69545647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375028419	chr13:69545714-69545715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74089905	chr13:69545728-69545729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368170736	chr13:69545791-69545792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375726479	chr13:69545840-69545841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533756981	chr13:69545863-69545864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183686524	chr13:69545867-69545868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73519914	chr13:69545873-69545874	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547235524	chr13:69545937-69545938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567558618	chr13:69545950-69545951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571877137	chr13:69545991-69545992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76142089	chr13:69546001-69546002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553385859	chr13:69546002-69546003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573510330	chr13:69546042-69546043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139983900	chr13:69546062-69546063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558757602	chr13:69546087-69546088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559212941	chr13:69546215-69546216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78300462	chr13:69546231-69546232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188007347	chr13:69546241-69546242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561600324	chr13:69546251-69546252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570532049	chr13:69546256-69546257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181899533	chr13:69546286-69546287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540271104	chr13:69546324-69546325	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143449436	chr13:69546334-69546335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185497282	chr13:69546335-69546336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532288378	chr13:69546338-69546339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77082807	chr13:69546348-69546349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115930489	chr13:69546376-69546377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530869821	chr13:69546377-69546378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190172743	chr13:69546379-69546380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567791729	chr13:69546441-69546442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181792341	chr13:69546536-69546537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553368119	chr13:69546538-69546539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567021022	chr13:69546624-69546625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539365158	chr13:69546664-69546665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536698736	chr13:69546680-69546681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1340730	chr13:69546717-69546718	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs140912968	chr13:69546809-69546810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548474904	chr13:69546815-69546816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115441380	chr13:69546876-69546877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs574508086	chr13:69546912-69546913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs539811596	chr13:69546913-69546914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186478998	chr13:69546921-69546922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532224819	chr13:69546948-69546949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74089908	chr13:69546966-69546967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9541662	chr13:69547033-69547034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
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
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	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69543800-69545600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr13:69543800-69545800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:69543800-69546200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr13:69543800-69546400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:69544000-69545800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr13:69544000-69546000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr13:69544200-69545600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr13:69544200-69545800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:69545400-69547400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:69547600-69547800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:69554000-69554400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:69557200-69557600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr13:69557200-69558000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:69557600-69558000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:69558000-69559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:69558000-69570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:69558800-69559000	Enhancers	Placenta	Placenta
18	chr13:69559000-69559400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr13:69559000-69559400	Flanking Active TSS	Placenta	Placenta
20	chr13:69559000-69559400	Active TSS	K562	blood
21	chr13:69559200-69559400	ZNF genes & repeats	Pancreas	Pancrea
22	chr13:69559400-69562400	Weak transcription	Pancreas	Pancrea
23	chr13:69563600-69563800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr13:69563800-69569800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr13:69564000-69564200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr13:69564200-69569400	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr13:69567400-69567600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr13:69569400-69571200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr13:69569400-69571800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:69569600-69571800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr13:69569800-69570200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr13:69569800-69571200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr13:69570200-69570400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr13:69570200-69570600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr13:69570200-69570600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:69570200-69571200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:69570400-69571000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr13:69570400-69571000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr13:69570600-69571000	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr13:69570600-69571200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr13:69571000-69571200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr13:69583600-69585800	Active TSS	K562	blood
43	chr13:69584400-69584600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:69584600-69587600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr13:69587600-69588400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr13:69587600-69590200	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr13:69587800-69588800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr13:69588000-69588400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr13:69590200-69590400	Enhancers	H9 Cell Line	embryonic stem cell

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