Variant report

Variant	nsv900860
Chromosome Location	chr13:90008941-90259291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:814)
CpG islands
(count:488)
Chromatin interactive
region (count:9)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:814 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90166877-90167409	HepG2	liver:	n/a	n/a
2	ATF3	chr13:90166748-90167411	A549	lung:	n/a	n/a
3	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
6	BCL3	chr13:90166802-90167246	A549	lung:	n/a	n/a
7	BCL3	chr13:90166728-90167467	A549	lung:	n/a	n/a
8	BRCA1	chr13:90166960-90167339	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:90053390-90054036	A549	lung:	n/a	chr13:90053581-90053592
10	CEBPB	chr13:90010585-90010905	HepG2	liver:	n/a	chr13:90010757-90010768 chr13:90010755-90010766 chr13:90010755-90010768
11	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
12	CEBPB	chr13:90053490-90053648	K562	blood:	n/a	chr13:90053581-90053592
13	CEBPB	chr13:90032305-90032732	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr13:90120640-90120770	K562	blood:	n/a	chr13:90120722-90120733
15	CEBPB	chr13:90177917-90178057	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:90032305-90032917	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr13:90110164-90110667	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
19	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
20	CEBPB	chr13:90190489-90190619	K562	blood:	n/a	chr13:90190558-90190569
21	CEBPB	chr13:90209916-90210116	HepG2	liver:	n/a	n/a
22	CEBPB	chr13:90032530-90032817	A549	lung:	n/a	n/a
23	CEBPB	chr13:90053216-90053959	A549	lung:	n/a	chr13:90053581-90053592
24	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
25	CEBPB	chr13:90127840-90128138	A549	lung:	n/a	chr13:90128018-90128029
26	CEBPB	chr13:90076016-90076314	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:90120558-90120849	A549	lung:	n/a	chr13:90120722-90120733
28	CEBPB	chr13:90190414-90190730	A549	lung:	n/a	chr13:90190558-90190569
29	CEBPB	chr13:90166162-90166377	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:90224834-90224951	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:90030039-90030322	IMR90	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
32	CEBPB	chr13:90171065-90171290	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr13:90177810-90178090	A549	lung:	n/a	n/a
34	CEBPB	chr13:90110265-90110690	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr13:90190545-90190612	K562	blood:	n/a	chr13:90190558-90190569
36	CEBPB	chr13:90016763-90017043	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
38	CEBPB	chr13:90190408-90190739	K562	blood:	n/a	chr13:90190558-90190569
39	CEBPB	chr13:90166838-90167348	A549	lung:	n/a	n/a
40	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
41	CEBPB	chr13:90120562-90120885	HepG2	liver:	n/a	chr13:90120722-90120733
42	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
43	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
44	CEBPB	chr13:90242215-90242403	HepG2	liver:	n/a	chr13:90242323-90242334
45	CEBPB	chr13:90190494-90190716	HepG2	liver:	n/a	chr13:90190558-90190569
46	CEBPB	chr13:90166579-90167503	A549	lung:	n/a	n/a
47	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:90030123-90030303	A549	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
49	CEBPB	chr13:90190413-90190718	IMR90	lung:	n/a	chr13:90190558-90190569
50	CEBPB	chr13:90127859-90128113	Hela-S3	cervix:	n/a	chr13:90128018-90128029

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90053523-90053573	BJ	skin:	n/a
2	chr13:90015774-90015824	BE2_C	brain:	n/a
3	chr13:90045847-90045897	HIPEpiC	eye:	n/a
4	chr13:90014513-90014563	GM12878	blood:	n/a
5	chr13:90015774-90015824	ovcar-3	ovarian:	n/a
6	chr13:90015774-90015824	SK-N-SH	brain:	n/a
7	chr13:90045847-90045897	HCM	heart:	n/a
8	chr13:90014813-90014863	HCM	heart:	n/a
9	chr13:90053523-90053573	MCF10A-Er-Src	breast:	n/a
10	chr13:90015774-90015824	BJ	skin:	n/a
11	chr13:90053523-90053573	NH-A	brain:	n/a
12	chr13:90045847-90045897	AG10803	skin:	n/a
13	chr13:90015912-90015962	ovcar-3	ovarian:	n/a
14	chr13:90015518-90015568	AG10803	skin:	n/a
15	chr13:90015774-90015824	PrEC	prostate:	n/a
16	chr13:90014513-90014563	A549	lung:	n/a
17	chr13:90015774-90015824	H1-hESC	embryonic stem cell:	embryo
18	chr13:90045847-90045897	PrEC	prostate:	n/a
19	chr13:90015774-90015824	ECC-1	luminal epithelium:	n/a
20	chr13:90015518-90015568	AG09319	gingival:	n/a
21	chr13:90014513-90014563	SK-N-SH	brain:	n/a
22	chr13:90015912-90015962	NB4	blood:	n/a
23	chr13:90015912-90015962	HUVEC	blood vessel:	n/a
24	chr13:90015774-90015824	IMR90	lung:	fetal
25	chr13:90015518-90015568	AoSMC	blood vessel:	n/a
26	chr13:90014813-90014863	GM12891	blood:	n/a
27	chr13:90014813-90014863	HRCEpiC	kidney:	n/a
28	chr13:90045847-90045897	AG09309	skin:	n/a
29	chr13:90014813-90014863	HIPEpiC	eye:	n/a
30	chr13:90015912-90015962	ProgFib	skin:	n/a
31	chr13:90015774-90015824	HNPCEpiC	eye:	n/a
32	chr13:90015633-90015683	GM19239	blood:	n/a
33	chr13:90014513-90014563	SKMC	muscle:	n/a
34	chr13:90014513-90014563	NT2-D1	testis:	n/a
35	chr13:90014813-90014863	MCF10A-Er-Src	breast:	n/a
36	chr13:90015518-90015568	ovcar-3	ovarian:	n/a
37	chr13:90045847-90045897	HCF	heart:	n/a
38	chr13:90015912-90015962	CMK	blood:	n/a
39	chr13:90014813-90014863	HL-60	blood:	n/a
40	chr13:90045847-90045897	H1-hESC	embryonic stem cell:	embryo
41	chr13:90053523-90053573	AG10803	skin:	n/a
42	chr13:90015774-90015824	NHBE	bronchial:	n/a
43	chr13:90014813-90014863	MCF-7	breast:	n/a
44	chr13:90014513-90014563	SK-N-SH_RA	brain:	n/a
45	chr13:90053523-90053573	IMR90	lung:	fetal
46	chr13:90045847-90045897	GM19239	blood:	n/a
47	chr13:90045847-90045897	GM06990	blood:	n/a
48	chr13:90045847-90045897	HCPEpiC	choroid plexus:	n/a
49	chr13:90015774-90015824	PFSK-1	brain:	n/a
50	chr13:90015774-90015824	MCF-7	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
2	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
3	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
4	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
5	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:
6	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
7	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
8	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
9	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-12	chr13:90205985-90206058	XLOC_010686
2	lnc-SLITRK6-12	chr13:90200945-90201465	XLOC_010686
3	lnc-SLITRK6-12	chr13:90204359-90204643	XLOC_010686
4	lnc-SLITRK6-12	chr13:90203455-90203544	XLOC_010686
5	lnc-SLITRK6-12	chr13:90203487-90203531	XLOC_010686
6	lnc-GPC5-4	chr13:90203487-90203531	ENSG00000271395.1
7	lnc-GPC5-4	chr13:90204359-90204643	ENSG00000271395.1
8	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685
9	lnc-SLITRK5-28	chr13:90186444-90186646	NONHSAT034630
10	lnc-SLITRK6-12	chr13:90203455-90203544	NONHSAT034632
11	lnc-SLITRK6-12	chr13:90201048-90201465	NONHSAT034632
12	lnc-SLITRK6-12	chr13:90216586-90216667	NONHSAT034632
13	lnc-SLITRK6-12	chr13:90205985-90206049	NONHSAT034632
14	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
15	lnc-SLITRK5-28	chr13:90186815-90187120	NONHSAT034630
16	lnc-GPC5-4	chr13:90204359-90204606	XLOC_010468
17	lnc-GPC5-4	chr13:90203039-90203531	XLOC_010468

No data

Variant related genes	Relation type
SP3P	TF binding region
LINC01040	TF binding region
LINC00353	TF binding region
ENSG00000271395	TF binding region
SP3P	CpG island
LINC01040	CpG island
LINC00353	CpG island
ENSG00000271395	CpG island
ENSG00000225530	chromatin interactions
HSP90B1	miRNA target sites
MBNL1	miRNA target sites

Extended variants
information (count: 5206 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:5206 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9583679	chr13:90008941-90008942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72630561	chr13:90008985-90008986	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs542304459	chr13:90009012-90009013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374540730	chr13:90009016-90009017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs560115440	chr13:90009026-90009027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111706087	chr13:90009028-90009029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201684225	chr13:90009047-90009048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183578858	chr13:90009063-90009064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188118574	chr13:90009125-90009126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192942530	chr13:90009132-90009133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147455599	chr13:90009242-90009243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550140826	chr13:90009274-90009275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568627131	chr13:90009276-90009277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535203646	chr13:90009283-90009284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184047240	chr13:90009312-90009313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547477446	chr13:90009313-90009314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543363921	chr13:90009325-90009326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536429131	chr13:90009342-90009343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188297932	chr13:90009420-90009421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563625721	chr13:90009431-90009432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565697941	chr13:90009502-90009503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539414750	chr13:90009651-90009652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557765226	chr13:90009693-90009694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576439334	chr13:90009694-90009695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537344861	chr13:90009717-90009718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72630562	chr13:90009738-90009739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs566566745	chr13:90009752-90009753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561877872	chr13:90009786-90009787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528729133	chr13:90009790-90009791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374734849	chr13:90009814-90009815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541966904	chr13:90009840-90009841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191262714	chr13:90009846-90009847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs79457752	chr13:90009912-90009913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545819799	chr13:90009924-90009925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564121067	chr13:90009928-90009929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147289651	chr13:90009931-90009932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145428825	chr13:90009945-90009946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370835483	chr13:90009956-90009957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566209793	chr13:90010025-90010026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147305573	chr13:90010026-90010027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112425563	chr13:90010041-90010042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547539149	chr13:90010050-90010051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs117704215	chr13:90010070-90010071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140886006	chr13:90010129-90010130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528655594	chr13:90010194-90010195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551437130	chr13:90010226-90010227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116850281	chr13:90010256-90010257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72630563	chr13:90010259-90010260	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555595320	chr13:90010293-90010294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372171867	chr13:90010296-90010297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90005000-90010600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:90010600-90010800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:90014800-90015600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:90015200-90015800	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr13:90015600-90015800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:90015800-90016000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:90015800-90017000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr13:90016600-90017200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr13:90016600-90017600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:90016800-90017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:90016800-90017400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:90017000-90017200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr13:90017000-90017400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:90017000-90017400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr13:90017000-90017400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr13:90023400-90023800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
17	chr13:90023800-90025400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:90027400-90028200	Enhancers	Fetal Muscle Leg	muscle
19	chr13:90027600-90028800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr13:90027600-90028800	Enhancers	HUVEC	blood vessel
21	chr13:90027600-90029000	Enhancers	Fetal Lung	lung
22	chr13:90027800-90028200	Enhancers	Adipose Nuclei	Adipose
23	chr13:90027800-90028400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:90027800-90028600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr13:90027800-90028600	Enhancers	Fetal Heart	heart
26	chr13:90027800-90028600	Enhancers	Fetal Stomach	stomach
27	chr13:90027800-90028800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:90027800-90028800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr13:90027800-90028800	Enhancers	Stomach Mucosa	stomach
30	chr13:90028000-90028400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr13:90028000-90028400	Enhancers	Fetal Brain Male	brain
32	chr13:90028000-90028600	Enhancers	Colon Smooth Muscle	Colon
33	chr13:90028200-90028800	Enhancers	NHEK	skin
34	chr13:90028400-90032200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr13:90028400-90032600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr13:90028800-90029800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr13:90028800-90030000	Weak transcription	Stomach Mucosa	stomach
38	chr13:90028800-90032200	Weak transcription	NHEK	skin
39	chr13:90030000-90030200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr13:90030000-90030200	Enhancers	Stomach Mucosa	stomach
41	chr13:90030200-90031000	Weak transcription	Stomach Mucosa	stomach
42	chr13:90030400-90031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr13:90030400-90032800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr13:90031000-90031200	Enhancers	Stomach Mucosa	stomach
45	chr13:90031000-90031800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr13:90031200-90031600	Enhancers	Gastric	stomach
47	chr13:90031200-90032400	Weak transcription	Stomach Mucosa	stomach
48	chr13:90031600-90032600	Weak transcription	Gastric	stomach
49	chr13:90032200-90033000	Enhancers	NHEK	skin
50	chr13:90032200-90033200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links