Variant report

Variant	nsv1053818
Chromosome Location	chr13:39512274-39533011
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	BACH1	chr13:39532129-39532286	H1-hESC	embryonic stem cell:	n/a	n/a
2	CCNT2	chr13:39531978-39532426	K562	blood:	n/a	n/a
3	CEBPB	chr13:39515627-39515922	A549	lung:	n/a	chr13:39515798-39515809
4	CEBPB	chr13:39519504-39519727	A549	lung:	n/a	chr13:39519591-39519602
5	CEBPB	chr13:39515677-39515849	HepG2	liver:	n/a	chr13:39515798-39515809
6	CEBPB	chr13:39526988-39527174	A549	lung:	n/a	chr13:39527105-39527116
7	CEBPB	chr13:39515682-39515887	K562	blood:	n/a	chr13:39515798-39515809
8	CEBPB	chr13:39519432-39519696	IMR90	lung:	n/a	chr13:39519591-39519602
9	CEBPB	chr13:39526890-39527287	MCF-7	breast:	n/a	chr13:39527105-39527116
10	CEBPB	chr13:39519492-39519730	HepG2	liver:	n/a	chr13:39519591-39519602
11	CEBPB	chr13:39515513-39516144	Hela-S3	cervix:	n/a	chr13:39515798-39515809
12	CEBPB	chr13:39525676-39525990	Hela-S3	cervix:	n/a	chr13:39525826-39525839
13	CEBPB	chr13:39526949-39527226	HepG2	liver:	n/a	chr13:39527105-39527116
14	CEBPB	chr13:39526918-39527265	MCF-7	breast:	n/a	chr13:39527105-39527116
15	CTCF	chr13:39522160-39522310	HEK293	kidney:	n/a	chr13:39522217-39522226
16	CTCF	chr13:39523200-39523203	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr13:39529885-39529931	GM10266	blood:	n/a	n/a
18	CTCF	chr13:39522196-39522254	H1-hESC	embryonic stem cell:	n/a	chr13:39522217-39522226
19	CTCF	chr13:39522500-39522650	GM12869	blood:	n/a	n/a
20	CTCF	chr13:39522180-39522330	HepG2	liver:	n/a	chr13:39522217-39522226
21	CTCF	chr13:39523137-39523141	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr13:39523146-39523195	H1-hESC	embryonic stem cell:	n/a	n/a
23	E2F4	chr13:39525403-39525647	MCF10A-Er-Src	breast:	n/a	chr13:39525546-39525555
24	E2F4	chr13:39526957-39527369	MCF10A-Er-Src	breast:	n/a	n/a
25	EP300	chr13:39515562-39515827	Hela-S3	cervix:	n/a	n/a
26	FOS	chr13:39522848-39523048	MCF10A-Er-Src	breast:	n/a	chr13:39523029-39523038 chr13:39523030-39523039 chr13:39523029-39523039
27	FOS	chr13:39521326-39521390	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:39521369-39521488	MCF10A-Er-Src	breast:	n/a	chr13:39521388-39521396 chr13:39521387-39521397 chr13:39521387-39521397 chr13:39521386-39521398
29	FOS	chr13:39528454-39528782	HUVEC	blood vessel:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528617-39528628 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
30	FOS	chr13:39526690-39527386	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:39528130-39528816	MCF10A-Er-Src	breast:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528617-39528628 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
32	FOS	chr13:39525819-39526011	MCF10A-Er-Src	breast:	n/a	chr13:39525896-39525905
33	FOS	chr13:39528181-39529053	MCF10A-Er-Src	breast:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528617-39528628 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
34	FOS	chr13:39522926-39523106	MCF10A-Er-Src	breast:	n/a	chr13:39523029-39523038 chr13:39523030-39523039 chr13:39523029-39523039
35	FOS	chr13:39528055-39528816	MCF10A-Er-Src	breast:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528617-39528628 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
36	FOS	chr13:39526857-39527643	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr13:39525692-39526092	MCF10A-Er-Src	breast:	n/a	chr13:39525896-39525905
38	FOS	chr13:39521381-39521515	MCF10A-Er-Src	breast:	n/a	chr13:39521388-39521396 chr13:39521387-39521397 chr13:39521387-39521397 chr13:39521386-39521398
39	FOS	chr13:39525794-39526021	HUVEC	blood vessel:	n/a	chr13:39525896-39525905
40	FOS	chr13:39526957-39527392	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr13:39522944-39523188	MCF10A-Er-Src	breast:	n/a	chr13:39523029-39523038 chr13:39523030-39523039 chr13:39523029-39523039 chr13:39523105-39523113
42	FOS	chr13:39522941-39522969	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:39525736-39526047	MCF10A-Er-Src	breast:	n/a	chr13:39525896-39525905
44	FOS	chr13:39528468-39528824	MCF10A-Er-Src	breast:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528617-39528628 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
45	FOS	chr13:39526862-39527771	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL1	chr13:39528425-39528758	HCT-116	colon:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
47	FOSL2	chr13:39526897-39527324	MCF-7	breast:	n/a	n/a
48	FOSL2	chr13:39528448-39528719	HepG2	liver:	n/a	chr13:39528619-39528627 chr13:39528618-39528627 chr13:39528619-39528628 chr13:39528617-39528629 chr13:39528620-39528627 chr13:39528618-39528628
49	FOSL2	chr13:39527022-39527402	MCF-7	breast:	n/a	n/a
50	GATA1	chr13:39525498-39526399	PBDE	blood:	n/a	chr13:39525914-39525924

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:39526272-39526322	HL-60	blood:	n/a
2	chr13:39526272-39526322	PFSK-1	brain:	n/a
3	chr13:39526272-39526322	NH-A	brain:	n/a
4	chr13:39526272-39526322	MCF-7	breast:	n/a
5	chr13:39526272-39526322	Caco-2	colon:	n/a
6	chr13:39526272-39526322	HNPCEpiC	eye:	n/a
7	chr13:39526272-39526322	NHBE	bronchial:	n/a
8	chr13:39526272-39526322	T-47D	breast:	n/a
9	chr13:39526272-39526322	IMR90	lung:	fetal
10	chr13:39526272-39526322	AG09309	skin:	n/a
11	chr13:39526272-39526322	GM19239	blood:	n/a
12	chr13:39526272-39526322	HRE	kidney:	n/a
13	chr13:39526272-39526322	HUVEC	blood vessel:	n/a
14	chr13:39526272-39526322	U87	brain:	n/a
15	chr13:39526272-39526322	SK-N-MC	brain:	n/a
16	chr13:39526272-39526322	BJ	skin:	n/a
17	chr13:39526272-39526322	HCPEpiC	choroid plexus:	n/a
18	chr13:39526272-39526322	HIPEpiC	eye:	n/a
19	chr13:39526272-39526322	HAEpiC	amniotic membrane:	n/a
20	chr13:39526272-39526322	PrEC	prostate:	n/a
21	chr13:39526272-39526322	ProgFib	skin:	n/a
22	chr13:39526272-39526322	GM12878	blood:	n/a
23	chr13:39526272-39526322	HPAEpiC	pulmonary alveolar:	n/a
24	chr13:39526272-39526322	HRCEpiC	kidney:	n/a
25	chr13:39526272-39526322	AG09319	gingival:	n/a
26	chr13:39526272-39526322	Jurkat	blood:	n/a
27	chr13:39526272-39526322	Hepatocyte	liver:	n/a
28	chr13:39526272-39526322	K562	blood:	n/a
29	chr13:39526272-39526322	A549	lung:	n/a
30	chr13:39526272-39526322	SKMC	muscle:	n/a
31	chr13:39526272-39526322	NT2-D1	testis:	n/a
32	chr13:39526272-39526322	RPTEC	kidney:	n/a
33	chr13:39526272-39526322	AG10803	skin:	n/a
34	chr13:39526272-39526322	PANC-1	pancreas:	n/a
35	chr13:39526272-39526322	MCF10A-Er-Src	breast:	n/a
36	chr13:39526272-39526322	HCT-116	colon:	n/a
37	chr13:39526272-39526322	AoSMC	blood vessel:	n/a
38	chr13:39526272-39526322	GM12892	blood:	n/a
39	chr13:39526272-39526322	LNCaP	prostate:	n/a
40	chr13:39526272-39526322	HEK293	kidney:	embryo
41	chr13:39526272-39526322	CMK	blood:	n/a
42	chr13:39526272-39526322	SK-N-SH	brain:	n/a
43	chr13:39526272-39526322	AG04449	skin:	fetal
44	chr13:39526272-39526322	SK-N-SH_RA	brain:	n/a
45	chr13:39526272-39526322	AG04450	lung:	fetal
46	chr13:39526272-39526322	HRPEpiC	eye:	n/a
47	chr13:39526272-39526322	NHDF-neo	bronchial:	n/a
48	chr13:39526272-39526322	ovcar-3	ovarian:	n/a
49	chr13:39526272-39526322	SAEC	small airway:	n/a
50	chr13:39526272-39526322	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:39520213..39521754-chr13:39613104..39615261,2	MCF-7	breast:
2	chr13:39521347..39523381-chr13:39525181..39526841,2	MCF-7	breast:
3	chr13:39531190..39533683-chr13:39627978..39630971,2	K562	blood:
4	chr13:39521347..39523381-chr13:39525181..39526841,2	MCF-7	breast:

Variant related genes	Relation type
ANKRD26P2	TF binding region
ANKRD26P2	CpG island

Extended variants
information (count: 976 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368325784	chr13:39514803-39514804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73449935	chr13:39514825-39514826	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs141320667	chr13:39514836-39514837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73449938	chr13:39514845-39514846	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563196013	chr13:39514848-39514849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532044038	chr13:39514850-39514851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73169404	chr13:39514852-39514853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548561055	chr13:39514863-39514864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568478089	chr13:39514868-39514869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534255570	chr13:39514887-39514888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547847516	chr13:39514925-39514926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570890762	chr13:39514934-39514935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534584884	chr13:39514954-39514955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538816663	chr13:39514992-39514993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9548552	chr13:39515006-39515007	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs575456785	chr13:39515012-39515013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150305226	chr13:39515031-39515032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11839539	chr13:39515037-39515038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183300258	chr13:39515051-39515052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539878721	chr13:39515071-39515072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9603482	chr13:39515082-39515083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs201746333	chr13:39515116-39515117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9603483	chr13:39515121-39515122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs57042899	chr13:39515125-39515126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs397973367	chr13:39515132-39515133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192184668	chr13:39515137-39515138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182930105	chr13:39515171-39515172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372789322	chr13:39515177-39515178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7321477	chr13:39515185-39515186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533409226	chr13:39515239-39515240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187790399	chr13:39515289-39515290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73449941	chr13:39515301-39515302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527670281	chr13:39515328-39515329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs547515302	chr13:39515346-39515347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570919817	chr13:39515381-39515382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147166267	chr13:39515404-39515405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7322050	chr13:39515444-39515445	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs568735164	chr13:39515509-39515510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537678539	chr13:39515510-39515511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs375522361	chr13:39515547-39515548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191726579	chr13:39515565-39515566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533542308	chr13:39515611-39515612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140349077	chr13:39515630-39515631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6563652	chr13:39515642-39515643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs79531518	chr13:39515650-39515651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4643179	chr13:39515667-39515668	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs80121384	chr13:39515680-39515681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542476817	chr13:39515684-39515685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7338854	chr13:39515708-39515709	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs7317892	chr13:39515713-39515714	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Monoclonal gammopathy of undetermined significance	19135901	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39514800-39524200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:39515200-39515600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:39515200-39515800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr13:39515200-39516200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr13:39520000-39520200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:39520200-39541600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:39521200-39521600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:39521200-39521600	Enhancers	Colon Smooth Muscle	Colon
9	chr13:39521200-39523400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:39521400-39521800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:39521800-39526200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr13:39525000-39525600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr13:39525200-39525400	Enhancers	Pancreas	Pancrea
14	chr13:39525400-39526400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr13:39525400-39526800	Weak transcription	Pancreas	Pancrea
16	chr13:39525600-39525800	Enhancers	HUVEC	blood vessel
17	chr13:39525800-39526400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr13:39525800-39526400	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr13:39525800-39526400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr13:39525800-39526400	Flanking Active TSS	HUVEC	blood vessel
21	chr13:39525800-39526600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr13:39526000-39526200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr13:39526000-39526200	Active TSS	Adipose Nuclei	Adipose
24	chr13:39526000-39526200	Active TSS	Duodenum Mucosa	Duodenum
25	chr13:39526000-39526400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr13:39526000-39526400	Active TSS	Right Atrium	heart
27	chr13:39526200-39526400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr13:39526200-39526400	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr13:39526200-39526600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:39526200-39526600	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr13:39526200-39526600	Flanking Active TSS	Duodenum Mucosa	Duodenum
32	chr13:39526200-39526600	Enhancers	Fetal Intestine Small	intestine
33	chr13:39526200-39527000	Enhancers	HMEC	breast
34	chr13:39526200-39529200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr13:39526400-39526600	Enhancers	HUVEC	blood vessel
36	chr13:39526400-39526800	Enhancers	Brain Cingulate Gyrus	brain
37	chr13:39526600-39528000	Enhancers	NHEK	skin
38	chr13:39526600-39528200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:39526800-39527000	Enhancers	Pancreas	Pancrea
40	chr13:39526800-39527200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr13:39527000-39527800	Weak transcription	Pancreas	Pancrea
42	chr13:39527000-39528200	Weak transcription	HMEC	breast
43	chr13:39527800-39528000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr13:39527800-39528000	Enhancers	Pancreas	Pancrea
45	chr13:39528000-39532000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr13:39528200-39529200	Enhancers	HMEC	breast
47	chr13:39528600-39528800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr13:39532000-39532200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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