Variant report

Variant	nsv541822
Chromosome Location	chr13:67550756-67594021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:406)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
2	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
4	BACH1	chr13:67582435-67582446	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
6	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
7	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
8	CEBPB	chr13:67551323-67551595	IMR90	lung:	n/a	n/a
9	CEBPB	chr13:67568038-67568652	A549	lung:	n/a	n/a
10	CEBPB	chr13:67568217-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr13:67568953-67569159	A549	lung:	n/a	n/a
12	CEBPB	chr13:67558478-67558699	HepG2	liver:	n/a	chr13:67558552-67558563
13	CEBPB	chr13:67570660-67571082	A549	lung:	n/a	chr13:67570842-67570855
14	CEBPB	chr13:67566342-67567192	IMR90	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
15	CEBPB	chr13:67566236-67566719	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
16	CEBPB	chr13:67590501-67590687	K562	blood:	n/a	n/a
17	CEBPB	chr13:67558401-67558722	IMR90	lung:	n/a	chr13:67558552-67558563
18	CEBPB	chr13:67568307-67568516	K562	blood:	n/a	n/a
19	CEBPB	chr13:67566840-67567107	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:67566839-67567157	K562	blood:	n/a	n/a
21	CEBPB	chr13:67558407-67558682	A549	lung:	n/a	chr13:67558552-67558563
22	CEBPB	chr13:67566763-67567107	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr13:67566346-67566737	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
24	CEBPB	chr13:67568217-67568468	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:67566898-67567137	A549	lung:	n/a	n/a
26	CEBPB	chr13:67568192-67568523	A549	lung:	n/a	n/a
27	CEBPB	chr13:67568171-67568602	A549	lung:	n/a	n/a
28	CEBPB	chr13:67566342-67566648	A549	lung:	n/a	n/a
29	CEBPB	chr13:67566854-67567179	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr13:67569170-67569763	GM12878	blood:	n/a	n/a
31	CHD2	chr13:67568389-67568563	K562	blood:	n/a	n/a
32	CHD2	chr13:67568285-67568652	H1-hESC	embryonic stem cell:	n/a	n/a
33	CREB1	chr13:67568282-67568593	A549	lung:	n/a	n/a
34	CTCF	chr13:67566400-67566550	SAEC	small airway:	n/a	n/a
35	CTCF	chr13:67568480-67568630	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr13:67568140-67568290	HMF	breast:	n/a	n/a
37	CTCF	chr13:67566420-67566570	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr13:67568402-67568649	Medullo	brain:	n/a	n/a
39	CTCF	chr13:67568440-67568590	HPF	lung:	n/a	n/a
40	CTCF	chr13:67568440-67568590	RPTEC	kidney:	n/a	n/a
41	CTCF	chr13:67566360-67566510	HPF	lung:	n/a	n/a
42	CTCF	chr13:67568400-67568550	AG04450	lung:	n/a	n/a
43	CTCF	chr13:67568434-67568617	GM20000	blood:	n/a	n/a
44	CTCF	chr13:67568440-67568590	AG04450	lung:	n/a	n/a
45	CTCF	chr13:67568440-67568590	Caco-2	colon:	n/a	n/a
46	CTCF	chr13:67568440-67568590	AG04449	skin:	n/a	n/a
47	CTCF	chr13:67568460-67568610	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr13:67568460-67568611	LNCaP	prostate:	n/a	n/a
49	CTCF	chr13:67568380-67568530	HMEC	breast:	n/a	n/a
50	CTCF	chr13:67568700-67568850	AG09319	gingival:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67568518-67568568	Hepatocyte	liver:	n/a
2	chr13:67570127-67570177	Jurkat	blood:	n/a
3	chr13:67568473-67568523	PANC-1	pancreas:	n/a
4	chr13:67568518-67568568	BJ	skin:	n/a
5	chr13:67568518-67568568	HEEpiC	esophagus:	n/a
6	chr13:67570127-67570177	PANC-1	pancreas:	n/a
7	chr13:67568473-67568523	GM12891	blood:	n/a
8	chr13:67568473-67568523	HEK293	kidney:	embryo
9	chr13:67570127-67570177	RPTEC	kidney:	n/a
10	chr13:67570127-67570177	HCF	heart:	n/a
11	chr13:67568518-67568568	SK-N-MC	brain:	n/a
12	chr13:67568518-67568568	ECC-1	luminal epithelium:	n/a
13	chr13:67568518-67568568	IMR90	lung:	fetal
14	chr13:67570127-67570177	AG09319	gingival:	n/a
15	chr13:67568473-67568523	SKMC	muscle:	n/a
16	chr13:67568473-67568523	RPTEC	kidney:	n/a
17	chr13:67568518-67568568	PANC-1	pancreas:	n/a
18	chr13:67570127-67570177	NT2-D1	testis:	n/a
19	chr13:67570127-67570177	HepG2	liver:	n/a
20	chr13:67568473-67568523	HRCEpiC	kidney:	n/a
21	chr13:67568473-67568523	SAEC	small airway:	n/a
22	chr13:67568518-67568568	ovcar-3	ovarian:	n/a
23	chr13:67568518-67568568	SK-N-SH_RA	brain:	n/a
24	chr13:67570127-67570177	GM12892	blood:	n/a
25	chr13:67570127-67570177	SK-N-MC	brain:	n/a
26	chr13:67568473-67568523	BE2_C	brain:	n/a
27	chr13:67570127-67570177	NH-A	brain:	n/a
28	chr13:67568518-67568568	NHBE	bronchial:	n/a
29	chr13:67568518-67568568	SK-N-SH	brain:	n/a
30	chr13:67568518-67568568	NB4	blood:	n/a
31	chr13:67568473-67568523	PFSK-1	brain:	n/a
32	chr13:67568518-67568568	AG04450	lung:	fetal
33	chr13:67570127-67570177	CMK	blood:	n/a
34	chr13:67568518-67568568	T-47D	breast:	n/a
35	chr13:67568518-67568568	HL-60	blood:	n/a
36	chr13:67570127-67570177	AoSMC	blood vessel:	n/a
37	chr13:67570127-67570177	AG04449	skin:	fetal
38	chr13:67568473-67568523	Hepatocyte	liver:	n/a
39	chr13:67570127-67570177	NHBE	bronchial:	n/a
40	chr13:67568518-67568568	NH-A	brain:	n/a
41	chr13:67570127-67570177	IMR90	lung:	fetal
42	chr13:67568473-67568523	A549	lung:	n/a
43	chr13:67568473-67568523	AG10803	skin:	n/a
44	chr13:67570127-67570177	ECC-1	luminal epithelium:	n/a
45	chr13:67570127-67570177	HRE	kidney:	n/a
46	chr13:67568518-67568568	HCM	heart:	n/a
47	chr13:67568518-67568568	AoSMC	blood vessel:	n/a
48	chr13:67570127-67570177	H1-hESC	embryonic stem cell:	embryo
49	chr13:67570127-67570177	SK-N-SH_RA	brain:	n/a
50	chr13:67568473-67568523	NB4	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
2	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:
3	chr13:67579094..67581367-chr13:67581814..67584582,2	K562	blood:
4	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
5	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
6	chr13:67584111..67586911-chr13:67593760..67595933,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
2	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
3	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
4	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637
5	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
6	lnc-AL445989.1-16	chr13:67575978-67576139	ENSG00000233840.1
7	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
8	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
9	lnc-AL445989.1-16	chr13:67575978-67576132	NR_046637
10	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
11	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
12	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215

No data

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS3	CpG island
ENSG00000233840	chromatin interactions

Extended variants
information (count: 1494 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558255983	chr13:67550764-67550765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs578127877	chr13:67550771-67550772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181854542	chr13:67550809-67550810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529927272	chr13:67550816-67550817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576303745	chr13:67550861-67550862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542058158	chr13:67550869-67550870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17195217	chr13:67550894-67550895	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs375750267	chr13:67550912-67550913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1359191	chr13:67550996-67550997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs373693248	chr13:67551005-67551006	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184879781	chr13:67551043-67551044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562201353	chr13:67551044-67551045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563868692	chr13:67551103-67551104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144093861	chr13:67551119-67551120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146489645	chr13:67551151-67551152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570229894	chr13:67551157-67551158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375003259	chr13:67551165-67551166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149103710	chr13:67551166-67551167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188717483	chr13:67551175-67551176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1323924	chr13:67551262-67551263	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs535046924	chr13:67551292-67551293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181240801	chr13:67551293-67551294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76229903	chr13:67551377-67551378	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537537702	chr13:67551382-67551383	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs574293256	chr13:67551417-67551418	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs541978146	chr13:67551423-67551424	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576143766	chr13:67551469-67551470	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs541770887	chr13:67551474-67551475	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs555609991	chr13:67551519-67551520	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571990208	chr13:67551524-67551525	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs540661982	chr13:67551535-67551536	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs368254742	chr13:67551545-67551546	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs560202253	chr13:67551623-67551624	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs563731878	chr13:67551629-67551630	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs527443610	chr13:67551630-67551631	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs184892886	chr13:67551634-67551635	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs543068641	chr13:67551639-67551640	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs563741046	chr13:67551716-67551717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529456084	chr13:67551731-67551732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549288400	chr13:67551732-67551733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372560945	chr13:67551738-67551739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116243099	chr13:67551753-67551754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs57353902	chr13:67551779-67551780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142227592	chr13:67551806-67551807	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77822782	chr13:67551866-67551867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571620665	chr13:67551869-67551870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537549855	chr13:67551884-67551885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557389278	chr13:67551994-67551995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374888075	chr13:67552006-67552007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571621641	chr13:67552008-67552009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Schizophrenia	23813976	CNVD
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67545400-67551000	Weak transcription	Brain Angular Gyrus	brain
2	chr13:67545400-67551400	Weak transcription	Brain Hippocampus Middle	brain
3	chr13:67545400-67551400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr13:67545600-67551400	Weak transcription	Brain Substantia Nigra	brain
5	chr13:67545800-67551400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr13:67551000-67552400	Enhancers	Brain Angular Gyrus	brain
7	chr13:67551400-67551800	Enhancers	Brain Cingulate Gyrus	brain
8	chr13:67551400-67551800	Enhancers	Brain Hippocampus Middle	brain
9	chr13:67551400-67552000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr13:67551400-67552200	Enhancers	Brain Substantia Nigra	brain
11	chr13:67551400-67552600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr13:67551800-67566200	Weak transcription	Brain Hippocampus Middle	brain
13	chr13:67552200-67557000	Weak transcription	Brain Substantia Nigra	brain
14	chr13:67557000-67558800	Enhancers	Brain Substantia Nigra	brain
15	chr13:67558400-67558600	Enhancers	Brain Cingulate Gyrus	brain
16	chr13:67558600-67566200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr13:67558800-67565800	Weak transcription	Brain Substantia Nigra	brain
18	chr13:67565200-67566800	Enhancers	A549	lung
19	chr13:67565800-67567800	Enhancers	Brain Substantia Nigra	brain
20	chr13:67566200-67566400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:67566200-67566600	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr13:67566200-67567000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr13:67566200-67567000	Enhancers	HUVEC	blood vessel
24	chr13:67566200-67567600	Enhancers	Brain Hippocampus Middle	brain
25	chr13:67566200-67568000	Enhancers	Brain Angular Gyrus	brain
26	chr13:67566400-67566600	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr13:67566400-67566600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr13:67566400-67566600	Active TSS	Brain Anterior Caudate	brain
29	chr13:67566400-67566600	Enhancers	Gastric	stomach
30	chr13:67566400-67567000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:67566400-67567000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr13:67566400-67567000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr13:67566400-67567000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr13:67566400-67567200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr13:67566400-67567200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr13:67566400-67567200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr13:67566400-67568000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:67566400-67568200	Enhancers	HMEC	breast
39	chr13:67566400-67568400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr13:67566600-67566800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr13:67566600-67567000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr13:67566600-67567000	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr13:67566600-67567000	Enhancers	Brain Cingulate Gyrus	brain
44	chr13:67566600-67568200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr13:67566600-67568200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr13:67566600-67571400	Weak transcription	Gastric	stomach
47	chr13:67566800-67567000	Flanking Active TSS	A549	lung
48	chr13:67566800-67567600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr13:67566800-67568400	Enhancers	Primary B cells from cord blood	blood
50	chr13:67567000-67567200	Enhancers	A549	lung

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