Variant report

Variant	nsv1037962
Chromosome Location	chr13:64254844-64370795
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:64262408-64262608	HepG2	liver:	n/a	chr13:64262502-64262513
2	CEBPB	chr13:64282619-64282952	IMR90	lung:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
3	CEBPB	chr13:64254753-64254953	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
5	CEBPB	chr13:64282710-64282910	H1-hESC	embryonic stem cell:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
6	CEBPB	chr13:64282631-64282951	HepG2	liver:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
7	CTCF	chr13:64334444-64334532	Spleen_OC	spleen:	n/a	n/a
8	CTCF	chr13:64324173-64324251	GM12878	blood:	n/a	n/a
9	CTCF	chr13:64324072-64324260	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr13:64324119-64324214	GM10248	blood:	n/a	n/a
11	CTCF	chr13:64362185-64362247	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr13:64324094-64324161	K562	blood:	n/a	n/a
13	CTCF	chr13:64324117-64324248	GM10266	blood:	n/a	n/a
14	CTCF	chr13:64261647-64261744	GM10248	blood:	n/a	n/a
15	CTCF	chr13:64324108-64324265	MCF-7	breast:	n/a	n/a
16	CTCF	chr13:64324040-64324265	HepG2	liver:	n/a	n/a
17	CTCF	chr13:64324133-64324244	ProgFib	skin:	n/a	n/a
18	CTCF	chr13:64324034-64324271	MCF-7	breast:	n/a	n/a
19	CTCF	chr13:64324125-64324255	Fibrobl	skin:	n/a	n/a
20	CTCF	chr13:64324183-64324225	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr13:64330314-64330384	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr13:64324128-64324253	GM19239	blood:	n/a	n/a
23	CTCF	chr13:64338203-64338280	GM13976	blood:	n/a	n/a
24	CTCF	chr13:64324050-64324261	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:64324028-64324296	A549	lung:	n/a	n/a
26	CTCF	chr13:64324080-64324269	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr13:64339091-64339163	Lung_OC	lung:	n/a	n/a
28	CTCF	chr13:64324146-64324249	GM19238	blood:	n/a	n/a
29	CTCF	chr13:64324042-64324308	LNCaP	prostate:	n/a	n/a
30	CTCF	chr13:64313949-64314007	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr13:64328827-64328856	LNCaP	prostate:	n/a	n/a
32	CTCF	chr13:64296335-64296399	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr13:64338496-64338540	ProgFib	skin:	n/a	n/a
34	CTCF	chr13:64297739-64297766	LNCaP	prostate:	n/a	n/a
35	CTCF	chr13:64281020-64281170	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr13:64312774-64312800	Spleen_OC	spleen:	n/a	n/a
37	CTCF	chr13:64324142-64324254	A549	lung:	n/a	n/a
38	CTCF	chr13:64292407-64292528	Lung_OC	lung:	n/a	n/a
39	CTCF	chr13:64324097-64324217	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr13:64330862-64330927	Medullo	brain:	n/a	n/a
41	CTCF	chr13:64324133-64324259	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:64324030-64324275	Gliobla	brain:	n/a	n/a
43	CTCF	chr13:64320948-64321033	LNCaP	prostate:	n/a	n/a
44	CTCF	chr13:64320841-64320933	LNCaP	prostate:	n/a	n/a
45	CTCF	chr13:64281060-64281210	HCT-116	colon:	n/a	n/a
46	CTCF	chr13:64324126-64324196	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr13:64324092-64324260	MCF-7	breast:	n/a	n/a
48	CTCF	chr13:64324024-64324308	K562	blood:	n/a	n/a
49	CTCF	chr13:64324079-64324211	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr13:64338485-64338489	ProgFib	skin:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64311397-64311447	HUVEC	blood vessel:	n/a
2	chr13:64311397-64311447	HUVEC	blood vessel:	n/a
3	chr13:64311397-64311447	BJ	skin:	n/a
4	chr13:64311397-64311447	HNPCEpiC	eye:	n/a
5	chr13:64311555-64311605	RPTEC	kidney:	n/a
6	chr13:64311555-64311605	Caco-2	colon:	n/a
7	chr13:64311555-64311605	IMR90	lung:	fetal
8	chr13:64311397-64311447	GM19239	blood:	n/a
9	chr13:64315383-64315433	NHDF-neo	bronchial:	n/a
10	chr13:64315383-64315433	HAEpiC	amniotic membrane:	n/a
11	chr13:64311397-64311447	NHDF-neo	bronchial:	n/a
12	chr13:64311555-64311605	HNPCEpiC	eye:	n/a
13	chr13:64311397-64311447	SK-N-SH_RA	brain:	n/a
14	chr13:64315383-64315433	NT2-D1	testis:	n/a
15	chr13:64315383-64315433	IMR90	lung:	fetal
16	chr13:64315383-64315433	HRCEpiC	kidney:	n/a
17	chr13:64311555-64311605	MCF10A-Er-Src	breast:	n/a
18	chr13:64315383-64315433	AG10803	skin:	n/a
19	chr13:64315383-64315433	PFSK-1	brain:	n/a
20	chr13:64311555-64311605	H1-hESC	embryonic stem cell:	embryo
21	chr13:64315383-64315433	CMK	blood:	n/a
22	chr13:64315383-64315433	GM12878	blood:	n/a
23	chr13:64315383-64315433	HRPEpiC	eye:	n/a
24	chr13:64315383-64315433	Hepatocyte	liver:	n/a
25	chr13:64315383-64315433	T-47D	breast:	n/a
26	chr13:64311397-64311447	H1-hESC	embryonic stem cell:	embryo
27	chr13:64315383-64315433	SK-N-MC	brain:	n/a
28	chr13:64311555-64311605	SK-N-MC	brain:	n/a
29	chr13:64311555-64311605	A549	lung:	n/a
30	chr13:64311555-64311605	ovcar-3	ovarian:	n/a
31	chr13:64311397-64311447	HCM	heart:	n/a
32	chr13:64311555-64311605	CMK	blood:	n/a
33	chr13:64315383-64315433	HRE	kidney:	n/a
34	chr13:64311397-64311447	SKMC	muscle:	n/a
35	chr13:64311555-64311605	ECC-1	luminal epithelium:	n/a
36	chr13:64311555-64311605	ProgFib	skin:	n/a
37	chr13:64311555-64311605	AG04450	lung:	fetal
38	chr13:64311397-64311447	ovcar-3	ovarian:	n/a
39	chr13:64311555-64311605	AG09319	gingival:	n/a
40	chr13:64311555-64311605	HCF	heart:	n/a
41	chr13:64311555-64311605	SK-N-SH_RA	brain:	n/a
42	chr13:64311397-64311447	GM12878	blood:	n/a
43	chr13:64315383-64315433	HEK293	kidney:	embryo
44	chr13:64311397-64311447	SK-N-SH	brain:	n/a
45	chr13:64311397-64311447	HEEpiC	esophagus:	n/a
46	chr13:64315383-64315433	PANC-1	pancreas:	n/a
47	chr13:64315383-64315433	HUVEC	blood vessel:	n/a
48	chr13:64311397-64311447	U87	brain:	n/a
49	chr13:64311397-64311447	K562	blood:	n/a
50	chr13:64311555-64311605	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
2	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
2	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
3	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
4	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173
5	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
6	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
7	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
8	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
9	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
10	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
11	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
12	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
13	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
14	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
15	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
16	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
17	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
18	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175
19	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
20	lnc-PCDH20-9	chr13:64261535-64261688	XLOC_010643

No data

Variant related genes	Relation type
ENSG00000226974	TF binding region
RNU6-81P	TF binding region
LINC00395	TF binding region
ENSG00000237378	TF binding region
OR7E156P	TF binding region
ENSG00000226974	CpG island
RNU6-81P	CpG island
LINC00395	CpG island
ENSG00000237378	CpG island
OR7E156P	CpG island
DUSP3	miRNA target sites
DUSP2	miRNA target sites

Extended variants
information (count: 1154 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146356760	chr13:64254848-64254849	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs148535412	chr13:64254913-64254914	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs546490264	chr13:64254949-64254950	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570916679	chr13:64255077-64255078	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs538219484	chr13:64255154-64255155	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142850894	chr13:64255178-64255179	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs575270049	chr13:64255240-64255241	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113365601	chr13:64255259-64255260	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368022556	chr13:64255301-64255302	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs137927326	chr13:64255309-64255310	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs58091041	chr13:64255310-64255311	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2810867	chr13:64255340-64255341	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376541632	chr13:64255369-64255370	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370338047	chr13:64255389-64255390	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185116607	chr13:64255401-64255402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138018820	chr13:64255402-64255403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2810868	chr13:64255406-64255407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs376892996	chr13:64255407-64255408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181149693	chr13:64255417-64255418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530942852	chr13:64255433-64255434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187062581	chr13:64255457-64255458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373581489	chr13:64255458-64255459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116254634	chr13:64255490-64255491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115340035	chr13:64255515-64255516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs374498370	chr13:64255516-64255517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191709072	chr13:64255518-64255519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546500883	chr13:64255577-64255578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371569485	chr13:64255646-64255647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs151060975	chr13:64255721-64255722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547939620	chr13:64255776-64255777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576914194	chr13:64255797-64255798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375404046	chr13:64255800-64255801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532410530	chr13:64255844-64255845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183604720	chr13:64255891-64255892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139722745	chr13:64255903-64255904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537829711	chr13:64255965-64255966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536007377	chr13:64255974-64255975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs116671625	chr13:64256005-64256006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2590926	chr13:64256073-64256074	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556106194	chr13:64256077-64256078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553725495	chr13:64256091-64256092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147650542	chr13:64256096-64256097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545669275	chr13:64256100-64256101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187387268	chr13:64256109-64256110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575593466	chr13:64256200-64256201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574359782	chr13:64256252-64256253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373284090	chr13:64256327-64256328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567748332	chr13:64256338-64256339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190881531	chr13:64256341-64256342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77926930	chr13:64256354-64256355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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	19036926	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64253800-64255000	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:64254200-64256200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr13:64254600-64255000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr13:64254600-64255400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr13:64254600-64255400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr13:64254800-64255200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr13:64254800-64255200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:64254800-64255200	Enhancers	Fetal Lung	lung
9	chr13:64254800-64255400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr13:64254800-64256000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:64255000-64255200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr13:64255000-64255200	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr13:64255000-64255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:64255000-64255400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr13:64255000-64255400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:64255000-64255400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr13:64255200-64255400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr13:64255200-64259000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr13:64255400-64256000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr13:64255400-64256000	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr13:64255400-64256200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:64255400-64256200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr13:64255400-64256400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:64256000-64256200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr13:64256000-64256200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr13:64259000-64259800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr13:64259000-64259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr13:64259200-64259600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr13:64262800-64263600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:64274200-64275000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr13:64274400-64274800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr13:64274400-64275000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr13:64274600-64275200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr13:64279200-64279600	Enhancers	Fetal Brain Male	brain
35	chr13:64302400-64302800	Enhancers	Fetal Intestine Small	intestine
36	chr13:64302400-64303200	Enhancers	Fetal Intestine Large	intestine
37	chr13:64302800-64303800	Weak transcription	Fetal Intestine Small	intestine
38	chr13:64303200-64303600	Weak transcription	Fetal Intestine Large	intestine
39	chr13:64303600-64303800	Enhancers	Fetal Intestine Large	intestine
40	chr13:64303800-64304400	Enhancers	Fetal Intestine Small	intestine
41	chr13:64303800-64305800	Weak transcription	Fetal Intestine Large	intestine
42	chr13:64304400-64305800	Weak transcription	Fetal Intestine Small	intestine
43	chr13:64305600-64306000	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr13:64305800-64306200	Enhancers	HepG2	liver
45	chr13:64305800-64306600	Enhancers	Fetal Intestine Large	intestine
46	chr13:64305800-64306600	Enhancers	Stomach Mucosa	stomach
47	chr13:64305800-64307200	Enhancers	Fetal Intestine Small	intestine
48	chr13:64306000-64307800	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr13:64306200-64307000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:64307800-64308200	Enhancers	Pancreatic Islets	Pancreatic Islet

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