Variant report

Variant	esv2763033
Chromosome Location	chr13:67853794-68042797
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	ARID3A	chr13:67857713-67858283	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:67957650-67957867	HepG2	liver:	n/a	n/a
3	ATF1	chr13:68014427-68014642	K562	blood:	n/a	n/a
4	ATF2	chr13:67990402-67990747	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr13:67981208-67981213	GM12878	blood:	n/a	n/a
6	BHLHE40	chr13:67940874-67940875	GM12878	blood:	n/a	n/a
7	BHLHE40	chr13:67914600-67914697	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:67957539-67957853	HepG2	liver:	n/a	n/a
9	BHLHE40	chr13:67877967-67878020	A549	lung:	n/a	n/a
10	BHLHE40	chr13:67914536-67914710	K562	blood:	n/a	n/a
11	BRCA1	chr13:67941712-67941854	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:67886478-67886759	IMR90	lung:	n/a	chr13:67886624-67886635
13	CEBPB	chr13:67957560-67957902	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:67886506-67886696	A549	lung:	n/a	chr13:67886624-67886635
15	CEBPB	chr13:67926095-67926421	HepG2	liver:	n/a	chr13:67926245-67926256
16	CEBPB	chr13:67925283-67925549	A549	lung:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
17	CEBPB	chr13:67933103-67933363	IMR90	lung:	n/a	chr13:67933196-67933205 chr13:67933194-67933205
18	CEBPB	chr13:67952124-67952426	Hela-S3	cervix:	n/a	chr13:67952260-67952271
19	CEBPB	chr13:67957573-67957884	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:67952103-67952421	HepG2	liver:	n/a	chr13:67952260-67952271
21	CEBPB	chr13:67917657-67917912	A549	lung:	n/a	chr13:67917760-67917771
22	CEBPB	chr13:68006413-68006613	A549	lung:	n/a	n/a
23	CEBPB	chr13:67952091-67952396	IMR90	lung:	n/a	chr13:67952260-67952271
24	CEBPB	chr13:67983010-67983379	HepG2	liver:	n/a	chr13:67983192-67983203
25	CEBPB	chr13:67982954-67983392	ECC-1	luminal epithelium:	n/a	chr13:67983192-67983203
26	CEBPB	chr13:67983018-67983330	HepG2	liver:	n/a	chr13:67983192-67983203
27	CEBPB	chr13:67926161-67926331	K562	blood:	n/a	chr13:67926245-67926256
28	CEBPB	chr13:67857728-67858180	HepG2	liver:	n/a	chr13:67857737-67857746
29	CEBPB	chr13:67917602-67917928	HepG2	liver:	n/a	chr13:67917760-67917771
30	CEBPB	chr13:67926113-67926355	Hela-S3	cervix:	n/a	chr13:67926245-67926256
31	CEBPB	chr13:67952150-67952336	A549	lung:	n/a	chr13:67952260-67952271
32	CEBPB	chr13:67886478-67886731	K562	blood:	n/a	chr13:67886624-67886635
33	CEBPB	chr13:67983079-67983282	HepG2	liver:	n/a	chr13:67983192-67983203
34	CEBPB	chr13:67957646-67957798	IMR90	lung:	n/a	n/a
35	CEBPB	chr13:67957575-67957884	A549	lung:	n/a	n/a
36	CEBPB	chr13:67941312-67941520	IMR90	lung:	n/a	chr13:67941396-67941409 chr13:67941398-67941409
37	CEBPB	chr13:67900201-67900450	A549	lung:	n/a	chr13:67900293-67900304
38	CEBPB	chr13:67925266-67925623	IMR90	lung:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
39	CEBPB	chr13:67925274-67925615	K562	blood:	n/a	chr13:67925441-67925450 chr13:67925439-67925450 chr13:67925441-67925450 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925441-67925450 chr13:67925439-67925452 chr13:67925377-67925388
40	CEBPB	chr13:67893074-67893347	Hela-S3	cervix:	n/a	chr13:67893126-67893139
41	CEBPB	chr13:67933072-67933331	A549	lung:	n/a	chr13:67933196-67933205 chr13:67933194-67933205
42	CEBPB	chr13:67933047-67933298	HepG2	liver:	n/a	chr13:67933196-67933205 chr13:67933194-67933205
43	CEBPB	chr13:67957598-67957798	K562	blood:	n/a	n/a
44	CEBPB	chr13:67917618-67917912	Hela-S3	cervix:	n/a	chr13:67917760-67917771
45	CEBPB	chr13:67987937-67987951	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:67952159-67952428	H1-hESC	embryonic stem cell:	n/a	chr13:67952260-67952271
47	CEBPB	chr13:67944123-67944438	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr13:67860708-67860903	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:67917699-67917847	K562	blood:	n/a	chr13:67917760-67917771
50	CEBPB	chr13:67873385-67873803	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67872416-67872466	NHBE	bronchial:	n/a
2	chr13:67872416-67872466	SK-N-MC	brain:	n/a
3	chr13:67872416-67872466	SKMC	muscle:	n/a
4	chr13:67872416-67872466	HRE	kidney:	n/a
5	chr13:67872416-67872466	Hela-S3	cervix:	n/a
6	chr13:67872416-67872466	Hepatocyte	liver:	n/a
7	chr13:67872416-67872466	BE2_C	brain:	n/a
8	chr13:67872416-67872466	GM12892	blood:	n/a
9	chr13:67872416-67872466	LNCaP	prostate:	n/a
10	chr13:67872416-67872466	GM12878	blood:	n/a
11	chr13:67872416-67872466	HAEpiC	amniotic membrane:	n/a
12	chr13:67872416-67872466	GM06990	blood:	n/a
13	chr13:67872416-67872466	HCT-116	colon:	n/a
14	chr13:67872416-67872466	PANC-1	pancreas:	n/a
15	chr13:67872416-67872466	SK-N-SH	brain:	n/a
16	chr13:67872416-67872466	AG04450	lung:	fetal
17	chr13:67872416-67872466	ECC-1	luminal epithelium:	n/a
18	chr13:67872416-67872466	Caco-2	colon:	n/a
19	chr13:67872416-67872466	HCM	heart:	n/a
20	chr13:67872416-67872466	SAEC	small airway:	n/a
21	chr13:67872416-67872466	SK-N-SH_RA	brain:	n/a
22	chr13:67872416-67872466	NH-A	brain:	n/a
23	chr13:67872416-67872466	AG09319	gingival:	n/a
24	chr13:67872416-67872466	HEK293	kidney:	embryo
25	chr13:67872416-67872466	HNPCEpiC	eye:	n/a
26	chr13:67872416-67872466	RPTEC	kidney:	n/a
27	chr13:67872416-67872466	MCF-7	breast:	n/a
28	chr13:67872416-67872466	HIPEpiC	eye:	n/a
29	chr13:67872416-67872466	HL-60	blood:	n/a
30	chr13:67872416-67872466	CMK	blood:	n/a
31	chr13:67872416-67872466	HMEC	breast:	n/a
32	chr13:67872416-67872466	H1-hESC	embryonic stem cell:	embryo
33	chr13:67872416-67872466	T-47D	breast:	n/a
34	chr13:67872416-67872466	GM19239	blood:	n/a
35	chr13:67872416-67872466	HEEpiC	esophagus:	n/a
36	chr13:67872416-67872466	K562	blood:	n/a
37	chr13:67872416-67872466	PrEC	prostate:	n/a
38	chr13:67872416-67872466	AG10803	skin:	n/a
39	chr13:67872416-67872466	AG09309	skin:	n/a
40	chr13:67872416-67872466	NHDF-neo	bronchial:	n/a
41	chr13:67872416-67872466	PFSK-1	brain:	n/a
42	chr13:67872416-67872466	HCPEpiC	choroid plexus:	n/a
43	chr13:67872416-67872466	MCF10A-Er-Src	breast:	n/a
44	chr13:67872416-67872466	HRCEpiC	kidney:	n/a
45	chr13:67872416-67872466	HepG2	liver:	n/a
46	chr13:67872416-67872466	A549	lung:	n/a
47	chr13:67872416-67872466	ovcar-3	ovarian:	n/a
48	chr13:67872416-67872466	HCF	heart:	n/a
49	chr13:67872416-67872466	BJ	skin:	n/a
50	chr13:67872416-67872466	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:113839422..113840262-chr13:68011903..68012677,2	MCF-7	breast:
2	chr13:67919389..67921263-chr13:67925624..67927193,2	MCF-7	breast:
3	chr13:67844700..67846615-chr13:67859322..67861875,2	K562	blood:
4	chr13:67896040..67897805-chr13:67907096..67909108,2	K562	blood:
5	chr13:67839825..67842452-chr13:67857701..67859414,2	MCF-7	breast:
6	chr13:67649311..67650094-chr13:67990535..67991084,2	MCF-7	breast:
7	chr13:67919389..67921263-chr13:67925624..67927193,2	MCF-7	breast:
8	chr13:67896040..67897805-chr13:67907096..67909108,2	K562	blood:

Variant related genes	Relation type
LINC00364	TF binding region
LINC00364	CpG island
ENSG00000214263	chromatin interactions

Extended variants
information (count: 2762 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2762 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9529214	chr13:67853794-67853795	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145475419	chr13:67853856-67853857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192343652	chr13:67853978-67853979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533654195	chr13:67853983-67853984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs377486373	chr13:67854011-67854012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145335120	chr13:67854114-67854115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536972823	chr13:67854132-67854133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139412897	chr13:67854134-67854135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77547640	chr13:67854154-67854155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184561786	chr13:67854196-67854197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9541050	chr13:67854267-67854268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528600517	chr13:67854291-67854292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9541051	chr13:67854326-67854327	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs200095916	chr13:67854332-67854333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374856156	chr13:67854333-67854334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189392668	chr13:67854343-67854344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573877006	chr13:67854378-67854379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77289244	chr13:67854382-67854383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs569790141	chr13:67854388-67854389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556092336	chr13:67854402-67854403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1325680	chr13:67854436-67854437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs555648977	chr13:67854437-67854438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1325681	chr13:67854447-67854448	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142456872	chr13:67854471-67854472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541161877	chr13:67854473-67854474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557767385	chr13:67854474-67854475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577737729	chr13:67854532-67854533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs35818869	chr13:67854545-67854546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544062096	chr13:67854610-67854611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563838434	chr13:67854612-67854613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1334229	chr13:67854662-67854663	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs151327647	chr13:67854685-67854686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559553497	chr13:67854728-67854729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140212151	chr13:67854808-67854809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181449047	chr13:67854887-67854888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7139681	chr13:67854924-67854925	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs530818237	chr13:67855136-67855137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9571747	chr13:67855145-67855146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569849800	chr13:67855173-67855174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs115434895	chr13:67855221-67855222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555585721	chr13:67855238-67855239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565912717	chr13:67855241-67855242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534681258	chr13:67855303-67855304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557904225	chr13:67855310-67855311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372064614	chr13:67855316-67855317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574888841	chr13:67855367-67855368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs78076954	chr13:67855374-67855375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143997777	chr13:67855441-67855442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114476993	chr13:67855486-67855487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199546072	chr13:67855514-67855515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Myelofibrosis	22110671	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67851600-67853800	Enhancers	HSMM	muscle
2	chr13:67851600-67854000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr13:67853000-67857800	Weak transcription	NH-A	brain
4	chr13:67853200-67855600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:67853400-67855600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:67853600-67853800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:67853800-67855200	Weak transcription	HSMM	muscle
8	chr13:67854000-67855800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr13:67854400-67856400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr13:67854400-67856600	Enhancers	Brain Germinal Matrix	brain
11	chr13:67855200-67855800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr13:67855200-67856000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:67855200-67856200	Enhancers	HSMM	muscle
14	chr13:67855400-67855800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr13:67855400-67856000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr13:67855400-67856000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr13:67855600-67855800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr13:67855600-67856000	Enhancers	H1 Cell Line	embryonic stem cell
19	chr13:67855600-67856000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr13:67855600-67856000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:67855600-67856000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr13:67855600-67856000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr13:67855600-67856600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr13:67855800-67856200	Enhancers	Muscle Satellite Cultured Cells	--
25	chr13:67855800-67858000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr13:67856000-67857600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr13:67856200-67857600	Weak transcription	HSMM	muscle
28	chr13:67857400-67858600	Enhancers	HepG2	liver
29	chr13:67857800-67858000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:67857800-67858000	Enhancers	HSMM	muscle
31	chr13:67857800-67858000	Enhancers	NH-A	brain
32	chr13:67857800-67858200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr13:67858000-67858400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr13:67860000-67860400	Enhancers	Fetal Heart	heart
35	chr13:67866200-67867600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr13:67866600-67867400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr13:67866800-67867200	Enhancers	Primary hematopoietic stem cells	blood
38	chr13:67867000-67867400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr13:67870600-67873200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr13:67870800-67871000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr13:67870800-67871000	Enhancers	Osteobl	bone
42	chr13:67870800-67874600	Enhancers	HSMM	muscle
43	chr13:67871000-67873800	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr13:67871200-67872400	Active TSS	Brain Hippocampus Middle	brain
45	chr13:67871200-67872400	Active TSS	Brain Substantia Nigra	brain
46	chr13:67871400-67872000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr13:67871400-67872000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr13:67871400-67872600	Active TSS	Brain Cingulate Gyrus	brain
49	chr13:67871400-67873400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr13:67871600-67872200	Active TSS	Brain Angular Gyrus	brain

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