Variant report

Variant	nsv562094
Chromosome Location	chr13:66499490-66582000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:66506502-66506548	A549	lung:	n/a	chr13:66506505-66506516
2	CEBPB	chr13:66506381-66506581	HepG2	liver:	n/a	chr13:66506505-66506516
3	CEBPB	chr13:66559601-66560095	MCF-7	breast:	n/a	n/a
4	CEBPB	chr13:66574571-66574786	HepG2	liver:	n/a	chr13:66574676-66574685 chr13:66574675-66574686 chr13:66574674-66574685
5	CEBPB	chr13:66559705-66560073	MCF-7	breast:	n/a	n/a
6	CEBPB	chr13:66571439-66571773	IMR90	lung:	n/a	n/a
7	CEBPB	chr13:66569441-66569593	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:66539663-66539995	IMR90	lung:	n/a	n/a
9	CHD2	chr13:66500909-66501075	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr13:66541093-66541356	HepG2	liver:	n/a	n/a
11	CTCF	chr13:66503500-66503650	HCFaa	heart:	n/a	n/a
12	CTCF	chr13:66500970-66501252	MCF-7	breast:	n/a	n/a
13	CTCF	chr13:66541180-66541330	GM12866	blood:	n/a	n/a
14	CTCF	chr13:66500995-66501209	GM12891	blood:	n/a	n/a
15	CTCF	chr13:66501060-66501210	GM12869	blood:	n/a	n/a
16	CTCF	chr13:66559756-66560123	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr13:66543800-66543950	AG10803	skin:	n/a	n/a
18	CTCF	chr13:66559860-66560010	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr13:66501080-66501230	HCT-116	colon:	n/a	n/a
20	CTCF	chr13:66501020-66501170	HepG2	liver:	n/a	n/a
21	CTCF	chr13:66559941-66559944	NHEK	skin:	n/a	n/a
22	CTCF	chr13:66559920-66560070	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr13:66501021-66501231	K562	blood:	n/a	n/a
24	CTCF	chr13:66559900-66560050	RPTEC	kidney:	n/a	n/a
25	CTCF	chr13:66541180-66541330	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr13:66501040-66501190	K562	blood:	n/a	n/a
27	CTCF	chr13:66501000-66501150	AG09319	gingival:	n/a	n/a
28	CTCF	chr13:66541160-66541310	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr13:66500959-66501292	K562	blood:	n/a	n/a
30	CTCF	chr13:66500966-66501230	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:66541120-66541270	HFF	foreskin:	n/a	n/a
32	CTCF	chr13:66501020-66501170	HRE	kidney:	n/a	n/a
33	CTCF	chr13:66500843-66500968	A549	lung:	n/a	n/a
34	CTCF	chr13:66501080-66501230	SAEC	small airway:	n/a	n/a
35	CTCF	chr13:66541063-66541373	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr13:66541200-66541350	GM12874	blood:	n/a	n/a
37	CTCF	chr13:66541070-66541527	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:66501040-66501190	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr13:66541160-66541310	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr13:66540964-66541442	A549	lung:	n/a	n/a
41	CTCF	chr13:66501040-66501190	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr13:66541140-66541290	HPF	lung:	n/a	n/a
43	CTCF	chr13:66501060-66501210	HEK293	kidney:	n/a	n/a
44	CTCF	chr13:66541100-66541390	LNCaP	prostate:	n/a	n/a
45	CTCF	chr13:66501060-66501210	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr13:66501080-66501230	GM12872	blood:	n/a	n/a
47	CTCF	chr13:66541010-66541452	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr13:66541220-66541370	A549	lung:	n/a	n/a
49	CTCF	chr13:66501060-66501210	GM12868	blood:	n/a	n/a
50	CTCF	chr13:66541180-66541330	WERI-Rb-1	eye:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66501111-66501161	HUVEC	blood vessel:	n/a
2	chr13:66501111-66501161	U87	brain:	n/a
3	chr13:66501111-66501161	NHDF-neo	bronchial:	n/a
4	chr13:66501111-66501161	IMR90	lung:	fetal
5	chr13:66501111-66501161	HEK293	kidney:	embryo
6	chr13:66501111-66501161	NT2-D1	testis:	n/a
7	chr13:66501111-66501161	AG04450	lung:	fetal
8	chr13:66501111-66501161	H1-hESC	embryonic stem cell:	embryo
9	chr13:66501111-66501161	SK-N-SH	brain:	n/a
10	chr13:66501111-66501161	GM12892	blood:	n/a
11	chr13:66501111-66501161	BE2_C	brain:	n/a
12	chr13:66501111-66501161	ECC-1	luminal epithelium:	n/a
13	chr13:66501111-66501161	RPTEC	kidney:	n/a
14	chr13:66501111-66501161	SK-N-MC	brain:	n/a
15	chr13:66501111-66501161	K562	blood:	n/a
16	chr13:66501111-66501161	Hela-S3	cervix:	n/a
17	chr13:66501111-66501161	SAEC	small airway:	n/a
18	chr13:66501111-66501161	NHBE	bronchial:	n/a
19	chr13:66501111-66501161	HCF	heart:	n/a
20	chr13:66501111-66501161	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:66501111-66501161	SKMC	muscle:	n/a
22	chr13:66501111-66501161	GM19239	blood:	n/a
23	chr13:66501111-66501161	Caco-2	colon:	n/a
24	chr13:66501111-66501161	AG09319	gingival:	n/a
25	chr13:66501111-66501161	ovcar-3	ovarian:	n/a
26	chr13:66501111-66501161	Jurkat	blood:	n/a
27	chr13:66501111-66501161	HRPEpiC	eye:	n/a
28	chr13:66501111-66501161	SK-N-SH_RA	brain:	n/a
29	chr13:66501111-66501161	HEEpiC	esophagus:	n/a
30	chr13:66501111-66501161	HRE	kidney:	n/a
31	chr13:66501111-66501161	HCPEpiC	choroid plexus:	n/a
32	chr13:66501111-66501161	BJ	skin:	n/a
33	chr13:66501111-66501161	T-47D	breast:	n/a
34	chr13:66501111-66501161	HCM	heart:	n/a
35	chr13:66501111-66501161	GM12878	blood:	n/a
36	chr13:66501111-66501161	NH-A	brain:	n/a
37	chr13:66501111-66501161	HAEpiC	amniotic membrane:	n/a
38	chr13:66501111-66501161	HepG2	liver:	n/a
39	chr13:66501111-66501161	AG10803	skin:	n/a
40	chr13:66501111-66501161	MCF-7	breast:	n/a
41	chr13:66501111-66501161	CMK	blood:	n/a
42	chr13:66501111-66501161	GM06990	blood:	n/a
43	chr13:66501111-66501161	HIPEpiC	eye:	n/a
44	chr13:66501111-66501161	GM12891	blood:	n/a
45	chr13:66501111-66501161	AG09309	skin:	n/a
46	chr13:66501111-66501161	Hepatocyte	liver:	n/a
47	chr13:66501111-66501161	PFSK-1	brain:	n/a
48	chr13:66501111-66501161	AoSMC	blood vessel:	n/a
49	chr13:66501111-66501161	A549	lung:	n/a
50	chr13:66501111-66501161	MCF10A-Er-Src	breast:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
2	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
3	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
4	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-10	chr13:66515195-66515334	XLOC_010415
2	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
3	lnc-AL445989.1-9	chr13:66510419-66510480	XLOC_010414
4	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
5	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
6	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548x-3p	chr13:66540484-66540503	MIMAT0015081

No data

Variant related genes	Relation type
MIR548X2	TF binding region
MIR548X2	CpG island
INO80D	miRNA target sites

Extended variants
information (count: 1781 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1781 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201988102	chr13:66499490-66499491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558708843	chr13:66499529-66499530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561639228	chr13:66499553-66499554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569204054	chr13:66499569-66499570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538166801	chr13:66499611-66499612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148086723	chr13:66499650-66499651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141861736	chr13:66499680-66499681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534163230	chr13:66499758-66499759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143750490	chr13:66499796-66499797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73506855	chr13:66499835-66499836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572633774	chr13:66499873-66499874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73506858	chr13:66499876-66499877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs370085334	chr13:66499887-66499888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564745700	chr13:66499898-66499899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575134577	chr13:66499944-66499945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544179763	chr13:66499948-66499949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77905888	chr13:66499957-66499958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577992001	chr13:66500003-66500004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546850343	chr13:66500096-66500097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs560366254	chr13:66500150-66500151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532674458	chr13:66500153-66500154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs9564290	chr13:66500235-66500236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569162918	chr13:66500241-66500242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543402765	chr13:66500291-66500292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192064275	chr13:66500316-66500317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568452574	chr13:66500357-66500358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182944183	chr13:66500377-66500378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575540040	chr13:66500380-66500381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553969857	chr13:66500417-66500418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150215138	chr13:66500422-66500423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188293118	chr13:66500468-66500469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558573175	chr13:66500481-66500482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12862969	chr13:66500486-66500487	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs544232420	chr13:66500536-66500537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138834939	chr13:66500547-66500548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73506860	chr13:66500550-66500551	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs192142222	chr13:66500557-66500558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560403009	chr13:66500576-66500577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115630148	chr13:66500608-66500609	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552085180	chr13:66500638-66500639	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563039767	chr13:66500654-66500655	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12865385	chr13:66500742-66500743	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs80050795	chr13:66500783-66500784	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531696166	chr13:66500824-66500825	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73506863	chr13:66500825-66500826	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs76426667	chr13:66500835-66500836	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77324337	chr13:66500836-66500837	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534239378	chr13:66500838-66500839	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547508986	chr13:66500843-66500844	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547647141	chr13:66500860-66500861	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66497000-66501200	Weak transcription	Osteobl	bone
2	chr13:66500400-66500800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:66500600-66500800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:66500600-66501000	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr13:66500800-66501000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr13:66500800-66501000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr13:66500800-66501000	Enhancers	Fetal Muscle Trunk	muscle
8	chr13:66500800-66501200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr13:66500800-66501200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr13:66500800-66501200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr13:66500800-66501200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:66500800-66501200	Enhancers	Liver	Liver
13	chr13:66500800-66501200	Enhancers	HMEC	breast
14	chr13:66500800-66501400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:66500800-66501400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr13:66500800-66501400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr13:66500800-66501400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr13:66500800-66501400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr13:66500800-66501400	Enhancers	Right Atrium	heart
20	chr13:66500800-66501600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr13:66500800-66501600	Enhancers	Fetal Lung	lung
22	chr13:66500800-66501600	Enhancers	Left Ventricle	heart
23	chr13:66500800-66501600	Enhancers	Pancreas	Pancrea
24	chr13:66501000-66501200	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr13:66501000-66501200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr13:66501000-66501200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr13:66501000-66501400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr13:66501000-66501400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr13:66501200-66501400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:66501200-66501400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr13:66501200-66501400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr13:66501200-66501600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr13:66501200-66501600	Enhancers	Brain Cingulate Gyrus	brain
34	chr13:66501200-66501800	Enhancers	Psoas Muscle	Psoas
35	chr13:66501400-66501600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr13:66501800-66513400	Weak transcription	Psoas Muscle	Psoas
37	chr13:66506800-66507200	Enhancers	Muscle Satellite Cultured Cells	--
38	chr13:66506800-66507200	Enhancers	Colon Smooth Muscle	Colon
39	chr13:66506800-66507200	Enhancers	NHDF-Ad	bronchial
40	chr13:66506800-66507400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr13:66506800-66507400	Enhancers	Osteobl	bone
42	chr13:66507000-66507400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr13:66507000-66507400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr13:66507200-66511200	Weak transcription	Colon Smooth Muscle	Colon
45	chr13:66510200-66512400	Enhancers	Brain Germinal Matrix	brain
46	chr13:66511200-66511600	Enhancers	Colon Smooth Muscle	Colon
47	chr13:66511600-66513200	Weak transcription	Colon Smooth Muscle	Colon
48	chr13:66512400-66514400	Weak transcription	Brain Germinal Matrix	brain
49	chr13:66513200-66514600	Enhancers	Colon Smooth Muscle	Colon
50	chr13:66513400-66513600	Enhancers	Psoas Muscle	Psoas

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