Variant report

Variant	esv2756457
Chromosome Location	chr13:64244499-64497199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:1281)
Chromatin interactive
region (count:8)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:64429710-64430077	HepG2	liver:	n/a	n/a
2	CEBPB	chr13:64409212-64409411	IMR90	lung:	n/a	chr13:64409350-64409361
3	CEBPB	chr13:64262408-64262608	HepG2	liver:	n/a	chr13:64262502-64262513
4	CEBPB	chr13:64282710-64282910	H1-hESC	embryonic stem cell:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
5	CEBPB	chr13:64282619-64282952	IMR90	lung:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
6	CEBPB	chr13:64409210-64409420	A549	lung:	n/a	chr13:64409350-64409361
7	CEBPB	chr13:64461878-64462200	HepG2	liver:	n/a	chr13:64462014-64462025
8	CEBPB	chr13:64409209-64409369	HepG2	liver:	n/a	chr13:64409350-64409361
9	CEBPB	chr13:64438372-64438635	A549	lung:	n/a	n/a
10	CEBPB	chr13:64438348-64438617	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:64438331-64438697	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
13	CEBPB	chr13:64282631-64282951	HepG2	liver:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
14	CEBPB	chr13:64422818-64422949	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:64249235-64249452	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:64494229-64494429	HepG2	liver:	n/a	chr13:64494372-64494383
17	CEBPB	chr13:64438259-64438697	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr13:64429868-64430208	IMR90	lung:	n/a	n/a
19	CEBPB	chr13:64254753-64254953	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr13:64385983-64386021	K562	blood:	n/a	n/a
21	CTCF	chr13:64403936-64403999	Spleen_OC	spleen:	n/a	n/a
22	CTCF	chr13:64334444-64334532	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr13:64356700-64356850	HepG2	liver:	n/a	n/a
24	CTCF	chr13:64403878-64404020	GM13977	blood:	n/a	n/a
25	CTCF	chr13:64339091-64339163	Lung_OC	lung:	n/a	n/a
26	CTCF	chr13:64475860-64476010	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr13:64434437-64434500	Lung_OC	lung:	n/a	n/a
28	CTCF	chr13:64475890-64476072	HepG2	liver:	n/a	n/a
29	CTCF	chr13:64324097-64324217	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr13:64475911-64476006	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:64324092-64324260	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:64313949-64314007	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr13:64424253-64424277	LNCaP	prostate:	n/a	n/a
34	CTCF	chr13:64384593-64384675	Lung_OC	lung:	n/a	n/a
35	CTCF	chr13:64324173-64324251	GM12878	blood:	n/a	n/a
36	CTCF	chr13:64261647-64261744	GM10248	blood:	n/a	n/a
37	CTCF	chr13:64324146-64324249	GM19238	blood:	n/a	n/a
38	CTCF	chr13:64475960-64476110	BE2_C	brain:	n/a	n/a
39	CTCF	chr13:64403823-64404050	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:64247080-64247230	AG10803	skin:	n/a	n/a
41	CTCF	chr13:64320841-64320933	LNCaP	prostate:	n/a	n/a
42	CTCF	chr13:64475886-64476039	A549	lung:	n/a	n/a
43	CTCF	chr13:64475860-64476010	Caco-2	colon:	n/a	n/a
44	CTCF	chr13:64312154-64312170	GM20000	blood:	n/a	n/a
45	CTCF	chr13:64475880-64476030	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr13:64388012-64388076	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:64403790-64404080	Gliobla	brain:	n/a	n/a
48	CTCF	chr13:64403907-64404012	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr13:64403855-64404062	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr13:64403907-64403977	K562	blood:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64418279-64418329	SKMC	muscle:	n/a
2	chr13:64411884-64411934	HEEpiC	esophagus:	n/a
3	chr13:64388106-64388156	U87	brain:	n/a
4	chr13:64421835-64421885	SKMC	muscle:	n/a
5	chr13:64418345-64418395	BJ	skin:	n/a
6	chr13:64315383-64315433	H1-hESC	embryonic stem cell:	embryo
7	chr13:64416816-64416866	BJ	skin:	n/a
8	chr13:64388106-64388156	CMK	blood:	n/a
9	chr13:64311397-64311447	SKMC	muscle:	n/a
10	chr13:64415303-64415353	GM12892	blood:	n/a
11	chr13:64311397-64311447	AG09309	skin:	n/a
12	chr13:64418676-64418726	MCF10A-Er-Src	breast:	n/a
13	chr13:64408172-64408222	MCF10A-Er-Src	breast:	n/a
14	chr13:64415303-64415353	HMEC	breast:	n/a
15	chr13:64412172-64412222	Hela-S3	cervix:	n/a
16	chr13:64311555-64311605	PANC-1	pancreas:	n/a
17	chr13:64418678-64418728	HMEC	breast:	n/a
18	chr13:64418345-64418395	U87	brain:	n/a
19	chr13:64412172-64412222	HCM	heart:	n/a
20	chr13:64311397-64311447	GM12891	blood:	n/a
21	chr13:64408172-64408222	SK-N-SH_RA	brain:	n/a
22	chr13:64416816-64416866	ProgFib	skin:	n/a
23	chr13:64418337-64418387	ECC-1	luminal epithelium:	n/a
24	chr13:64412172-64412222	GM19239	blood:	n/a
25	chr13:64388106-64388156	BJ	skin:	n/a
26	chr13:64411884-64411934	NH-A	brain:	n/a
27	chr13:64418678-64418728	AG09319	gingival:	n/a
28	chr13:64411884-64411934	Hepatocyte	liver:	n/a
29	chr13:64411884-64411934	HCT-116	colon:	n/a
30	chr13:64385881-64385931	A549	lung:	n/a
31	chr13:64411884-64411934	AG09309	skin:	n/a
32	chr13:64418337-64418387	IMR90	lung:	fetal
33	chr13:64412172-64412222	AoSMC	blood vessel:	n/a
34	chr13:64384119-64384169	AoSMC	blood vessel:	n/a
35	chr13:64385720-64385770	NHDF-neo	bronchial:	n/a
36	chr13:64386020-64386070	SK-N-SH	brain:	n/a
37	chr13:64311555-64311605	NH-A	brain:	n/a
38	chr13:64382075-64382125	HCF	heart:	n/a
39	chr13:64315383-64315433	GM19239	blood:	n/a
40	chr13:64388106-64388156	HEEpiC	esophagus:	n/a
41	chr13:64418678-64418728	GM06990	blood:	n/a
42	chr13:64388106-64388156	HepG2	liver:	n/a
43	chr13:64416816-64416866	T-47D	breast:	n/a
44	chr13:64415303-64415353	HNPCEpiC	eye:	n/a
45	chr13:64315383-64315433	SK-N-MC	brain:	n/a
46	chr13:64415303-64415353	PrEC	prostate:	n/a
47	chr13:64315383-64315433	BE2_C	brain:	n/a
48	chr13:64382075-64382125	IMR90	lung:	fetal
49	chr13:64418279-64418329	HRE	kidney:	n/a
50	chr13:64311555-64311605	HUVEC	blood vessel:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:64478683..64481675-chr13:64487598..64489103,2	MCF-7	breast:
2	chr13:64478683..64481675-chr13:64487598..64489103,2	MCF-7	breast:
3	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
4	chr13:64461452..64464035-chr13:64465171..64467980,2	K562	blood:
5	chr13:64475617..64476410-chr13:64728809..64729366,2	MCF-7	breast:
6	chr11:1968235..1969201-chr13:64430713..64431213,2	NB4	blood:
7	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
8	chr13:64461452..64464035-chr13:64465171..64467980,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-10	chr13:64413882-64414219	NONHSAT034181
2	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173
3	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
4	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
5	lnc-PCDH20-10	chr13:64405587-64405660	NONHSAT034181
6	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
7	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
8	lnc-PCDH20-10	chr13:64405587-64405985	ENSG00000219926.6
9	lnc-PCDH20-10	chr13:64413203-64413330	NONHSAT034187
10	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
11	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
12	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
13	lnc-PCDH20-10	chr13:64412250-64412371	NONHSAT034187
14	lnc-PCDH20-10	chr13:64411124-64411575	NONHSAT034185
15	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
16	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175
17	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
18	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
19	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
20	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
21	lnc-PCDH20-10	chr13:64412293-64412877	NONHSAT034185
22	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
23	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
24	lnc-PCDH20-10	chr13:64405587-64405985	NONHSAT034184
25	lnc-PCDH20-10	chr13:64402902-64403292	ENSG00000219926.3
26	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
27	lnc-PCDH20-10	chr13:64402973-64403285	ENSG00000219926.6
28	lnc-PCDH20-10	chr13:64403127-64403285	NONHSAT034184
29	lnc-PCDH20-9	chr13:64261535-64261688	XLOC_010643
30	lnc-PCDH20-10	chr13:64405587-64405985	ENSG00000219926.3
31	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
32	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
33	lnc-AL445989.1-21	chr13:64411166-64411589	NONHSAT034186
34	lnc-PCDH20-10	chr13:64402967-64403285	NONHSAT034181

No data

Variant related genes	Relation type
LINC00395	TF binding region
ENSG00000226974	TF binding region
ENSG00000219926	TF binding region
PPP1R2P10	TF binding region
ENSG00000237378	TF binding region
RNU6-81P	TF binding region
OR7E104P	TF binding region
OR7E156P	TF binding region
ENSG00000272299	TF binding region
LINC00395	CpG island
ENSG00000226974	CpG island
ENSG00000219926	CpG island
PPP1R2P10	CpG island
ENSG00000237378	CpG island
RNU6-81P	CpG island
OR7E104P	CpG island
OR7E156P	CpG island
ENSG00000272299	CpG island
ENSG00000214026	chromatin interactions
DUSP2	miRNA target sites
DUSP3	miRNA target sites

Extended variants
information (count: 2912 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2912 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184383387	chr13:64245206-64245207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79160639	chr13:64245228-64245229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143475372	chr13:64245268-64245269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114116251	chr13:64245280-64245281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532472985	chr13:64245282-64245283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373326296	chr13:64245294-64245295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553420647	chr13:64245322-64245323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188822675	chr13:64245341-64245342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561969041	chr13:64245372-64245373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376755363	chr13:64245381-64245382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550467776	chr13:64245492-64245493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573563693	chr13:64245540-64245541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147143079	chr13:64245593-64245594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566811302	chr13:64245707-64245708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs1530407	chr13:64245708-64245709	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs532893994	chr13:64245750-64245751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529128189	chr13:64245769-64245770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181458309	chr13:64245796-64245797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548884553	chr13:64245851-64245852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140340550	chr13:64245883-64245884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531786441	chr13:64245910-64245911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550212344	chr13:64245911-64245912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568701950	chr13:64245930-64245931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535502002	chr13:64245939-64245940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547797615	chr13:64245994-64245995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373116813	chr13:64245996-64245997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566063008	chr13:64246029-64246030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575390583	chr13:64246040-64246041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539977020	chr13:64246045-64246046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186404639	chr13:64246047-64246048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371286992	chr13:64246096-64246097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576305217	chr13:64246098-64246099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191934701	chr13:64246108-64246109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549077152	chr13:64246115-64246116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567463855	chr13:64246143-64246144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568077380	chr13:64246166-64246167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573854341	chr13:64246182-64246183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181074689	chr13:64246189-64246190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558960903	chr13:64246194-64246195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185792956	chr13:64246252-64246253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558226865	chr13:64246303-64246304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577979327	chr13:64246320-64246321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs150912511	chr13:64246341-64246342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562998820	chr13:64246352-64246353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191486027	chr13:64246357-64246358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34398055	chr13:64246378-64246379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543967420	chr13:64246389-64246390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139401966	chr13:64246436-64246437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529626289	chr13:64246479-64246480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540605356	chr13:64246484-64246485	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Melanoma	20688739	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64245200-64247400	Enhancers	Fetal Lung	lung
2	chr13:64251800-64252000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr13:64252000-64253200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr13:64253000-64253200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:64253200-64253400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr13:64253200-64254200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr13:64253200-64254800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr13:64253400-64254600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr13:64253600-64254600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:64253800-64255000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:64254200-64254400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr13:64254200-64254600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr13:64254200-64256200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr13:64254600-64254800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr13:64254600-64255000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr13:64254600-64255400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr13:64254600-64255400	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr13:64254800-64255200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr13:64254800-64255200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr13:64254800-64255200	Enhancers	Fetal Lung	lung
21	chr13:64254800-64255400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
22	chr13:64254800-64256000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr13:64255000-64255200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr13:64255000-64255200	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr13:64255000-64255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr13:64255000-64255400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr13:64255000-64255400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:64255000-64255400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr13:64255200-64255400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr13:64255200-64259000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr13:64255400-64256000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr13:64255400-64256000	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr13:64255400-64256200	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr13:64255400-64256200	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr13:64255400-64256400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr13:64256000-64256200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr13:64256000-64256200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr13:64259000-64259800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr13:64259000-64259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:64259200-64259600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr13:64262800-64263600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr13:64274200-64275000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr13:64274400-64274800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:64274400-64275000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr13:64274600-64275200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr13:64279200-64279600	Enhancers	Fetal Brain Male	brain
47	chr13:64302400-64302800	Enhancers	Fetal Intestine Small	intestine
48	chr13:64302400-64303200	Enhancers	Fetal Intestine Large	intestine
49	chr13:64302800-64303800	Weak transcription	Fetal Intestine Small	intestine
50	chr13:64303200-64303600	Weak transcription	Fetal Intestine Large	intestine

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