Variant report

Variant	nsv900078
Chromosome Location	chr13:51454896-51478716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:51466205-51467011	GM12878	blood:	n/a	n/a
2	ATF2	chr13:51467449-51468203	GM12878	blood:	n/a	n/a
3	BCLAF1	chr13:51467397-51468142	GM12878	blood:	n/a	chr13:51467850-51467859
4	BHLHE40	chr13:51474588-51474638	K562	blood:	n/a	n/a
5	BHLHE40	chr13:51467550-51468123	GM12878	blood:	n/a	n/a
6	CEBPB	chr13:51476512-51476765	K562	blood:	n/a	n/a
7	CEBPB	chr13:51470997-51471247	A549	lung:	n/a	n/a
8	CHD1	chr13:51467312-51468058	GM12878	blood:	n/a	n/a
9	CHD2	chr13:51466338-51466594	GM12878	blood:	n/a	n/a
10	CHD2	chr13:51461306-51461506	GM12878	blood:	n/a	n/a
11	CTCF	chr13:51465460-51465610	GM06990	blood:	n/a	n/a
12	CTCF	chr13:51463500-51463650	GM12872	blood:	n/a	n/a
13	CTCF	chr13:51471002-51471094	Lung_OC	lung:	n/a	n/a
14	CTCF	chr13:51468300-51468418	Lung_OC	lung:	n/a	n/a
15	CUX1	chr13:51466576-51466586	GM12878	blood:	n/a	n/a
16	CUX1	chr13:51461434-51461551	GM12878	blood:	n/a	n/a
17	E2F4	chr13:51459186-51459316	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr13:51475893-51476400	MCF10A-Er-Src	breast:	n/a	chr13:51476025-51476032 chr13:51476025-51476032 chr13:51476025-51476032 chr13:51476024-51476033
19	E2F4	chr13:51462053-51462270	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr13:51467675-51468083	GM12878	blood:	n/a	n/a
21	EBF1	chr13:51466318-51466644	GM12878	blood:	n/a	n/a
22	ELF1	chr13:51466324-51466553	GM12878	blood:	n/a	n/a
23	ELK1	chr13:51466425-51466595	GM12878	blood:	n/a	n/a
24	EP300	chr13:51467344-51468085	GM12878	blood:	n/a	chr13:51467427-51467437 chr13:51467850-51467864
25	EP300	chr13:51467342-51468051	SK-N-SH_RA	brain:	n/a	chr13:51467427-51467437 chr13:51467850-51467864
26	EP300	chr13:51461316-51461747	GM12878	blood:	n/a	n/a
27	EP300	chr13:51461474-51461537	GM12878	blood:	n/a	n/a
28	EP300	chr13:51466210-51468760	SK-N-SH	brain:	n/a	chr13:51466712-51466726 chr13:51467427-51467437 chr13:51466668-51466677 chr13:51467057-51467071 chr13:51466667-51466681 chr13:51467051-51467065 chr13:51467850-51467864 chr13:51467053-51467067
29	EP300	chr13:51466525-51466535	GM12878	blood:	n/a	n/a
30	EP300	chr13:51467335-51467964	SK-N-SH	brain:	n/a	chr13:51467427-51467437 chr13:51467850-51467864
31	EP300	chr13:51468327-51468410	GM12878	blood:	n/a	n/a
32	EP300	chr13:51466342-51466538	GM12878	blood:	n/a	n/a
33	EP300	chr13:51467572-51468086	GM12878	blood:	n/a	chr13:51467850-51467864
34	EP300	chr13:51467335-51468032	SK-N-SH_RA	brain:	n/a	chr13:51467427-51467437 chr13:51467850-51467864
35	EP300	chr13:51461297-51461621	GM12878	blood:	n/a	n/a
36	EP300	chr13:51467696-51468069	GM12878	blood:	n/a	chr13:51467850-51467864
37	FOS	chr13:51475941-51476358	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr13:51476194-51476337	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr13:51475885-51476362	MCF10A-Er-Src	breast:	n/a	n/a
40	FOXA1	chr13:51475920-51476124	T-47D	breast:	n/a	n/a
41	FOXM1	chr13:51467573-51468036	GM12878	blood:	n/a	n/a
42	FOXM1	chr13:51467506-51468200	GM12878	blood:	n/a	n/a
43	FOXP2	chr13:51467680-51468058	SK-N-MC	brain:	n/a	n/a
44	GATA2	chr13:51466062-51466613	SH-SY5Y	brain:	n/a	chr13:51466385-51466396
45	GATA2	chr13:51467323-51467887	SH-SY5Y	brain:	n/a	chr13:51467784-51467793
46	GATA3	chr13:51462434-51462771	SH-SY5Y	brain:	n/a	chr13:51462558-51462565
47	GATA3	chr13:51467230-51468046	SK-N-SH	brain:	n/a	chr13:51467784-51467793
48	GATA3	chr13:51467269-51468050	SH-SY5Y	brain:	n/a	chr13:51467784-51467793
49	GATA3	chr13:51467196-51468056	SK-N-SH	brain:	n/a	chr13:51467784-51467793
50	GATA3	chr13:51466171-51466601	SH-SY5Y	brain:	n/a	chr13:51466385-51466396

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51466941-51466991	GM12878	blood:	n/a
2	chr13:51466941-51466991	AG04450	lung:	fetal
3	chr13:51466941-51466991	HCT-116	colon:	n/a
4	chr13:51466941-51466991	SK-N-SH_RA	brain:	n/a
5	chr13:51466941-51466991	SKMC	muscle:	n/a
6	chr13:51466941-51466991	NB4	blood:	n/a
7	chr13:51466941-51466991	PANC-1	pancreas:	n/a
8	chr13:51466941-51466991	MCF10A-Er-Src	breast:	n/a
9	chr13:51466941-51466991	HEK293	kidney:	embryo
10	chr13:51466941-51466991	NT2-D1	testis:	n/a
11	chr13:51466941-51466991	HCPEpiC	choroid plexus:	n/a
12	chr13:51466941-51466991	HRCEpiC	kidney:	n/a
13	chr13:51466941-51466991	HRE	kidney:	n/a
14	chr13:51466941-51466991	HRPEpiC	eye:	n/a
15	chr13:51466941-51466991	NH-A	brain:	n/a
16	chr13:51466941-51466991	HepG2	liver:	n/a
17	chr13:51466941-51466991	BE2_C	brain:	n/a
18	chr13:51466941-51466991	SK-N-MC	brain:	n/a
19	chr13:51466941-51466991	Caco-2	colon:	n/a
20	chr13:51466941-51466991	CMK	blood:	n/a
21	chr13:51466941-51466991	ECC-1	luminal epithelium:	n/a
22	chr13:51466941-51466991	AG04449	skin:	fetal
23	chr13:51466941-51466991	Jurkat	blood:	n/a
24	chr13:51466941-51466991	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:51466941-51466991	Hepatocyte	liver:	n/a
26	chr13:51466941-51466991	U87	brain:	n/a
27	chr13:51466941-51466991	AG09319	gingival:	n/a
28	chr13:51466941-51466991	PrEC	prostate:	n/a
29	chr13:51466941-51466991	SAEC	small airway:	n/a
30	chr13:51466941-51466991	HL-60	blood:	n/a
31	chr13:51466941-51466991	IMR90	lung:	fetal
32	chr13:51466941-51466991	HCF	heart:	n/a
33	chr13:51466941-51466991	HMEC	breast:	n/a
34	chr13:51466941-51466991	BJ	skin:	n/a
35	chr13:51466941-51466991	HCM	heart:	n/a
36	chr13:51466941-51466991	AG10803	skin:	n/a
37	chr13:51466941-51466991	GM12892	blood:	n/a
38	chr13:51466941-51466991	PFSK-1	brain:	n/a
39	chr13:51466941-51466991	NHBE	bronchial:	n/a
40	chr13:51466941-51466991	ovcar-3	ovarian:	n/a
41	chr13:51466941-51466991	GM19239	blood:	n/a
42	chr13:51466941-51466991	A549	lung:	n/a
43	chr13:51466941-51466991	AoSMC	blood vessel:	n/a
44	chr13:51466941-51466991	LNCaP	prostate:	n/a
45	chr13:51466941-51466991	HEEpiC	esophagus:	n/a
46	chr13:51466941-51466991	HIPEpiC	eye:	n/a
47	chr13:51466941-51466991	GM06990	blood:	n/a
48	chr13:51466941-51466991	GM12891	blood:	n/a
49	chr13:51466941-51466991	RPTEC	kidney:	n/a
50	chr13:51466941-51466991	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:51473891..51476765-chr13:51478767..51481533,2	MCF-7	breast:
2	chr13:51472736..51474284-chr13:51482598..51484808,2	MCF-7	breast:
3	chr13:51462818..51465395-chr13:51482325..51483926,2	K562	blood:
4	chr13:51473931..51480255-chr13:51481989..51485518,9	MCF-7	breast:
5	chr13:51452163..51454609-chr13:51458977..51461439,2	MCF-7	breast:
6	chr13:51464884..51467381-chr13:51471388..51473638,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
2	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
3	lnc-DLEU7-1	chr13:51463745-51463871	NR_046552
4	lnc-DLEU7-1	chr13:51456534-51456779	ENSG00000233672.2
5	lnc-DLEU7-1	chr13:51456515-51456781	NR_046552
6	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
7	lnc-DLEU7-1	chr13:51456600-51456781	ENSG00000233672.2
8	lnc-DLEU7-1	chr13:51456514-51456781	ENSG00000233672.1
9	lnc-DLEU7-1	chr13:51456688-51456781	ENSG00000233672.2
10	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
11	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.1
12	lnc-DLEU7-1	chr13:51456647-51456781	ENSG00000233672.2
13	lnc-DLEU7-1	chr13:51465440-51465640	ENSG00000233672.2
14	lnc-DLEU7-1	chr13:51456745-51456781	ENSG00000233672.2
15	lnc-DLEU7-1	chr13:51463745-51463871	ENSG00000233672.2
16	lnc-DLEU7-1	chr13:51465440-51465778	ENSG00000233672.2

No data

Variant related genes	Relation type
RNASEH2B-AS1	TF binding region
RNASEH2B-AS1	CpG island
ENSG00000136104	chromatin interactions
ENSG00000233672	chromatin interactions

Extended variants
information (count: 733 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7985661	chr13:51454896-51454897	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146774752	chr13:51454914-51454915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530034407	chr13:51454956-51454957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549881172	chr13:51454961-51454962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563360618	chr13:51455023-51455024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532431307	chr13:51455054-51455055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373041974	chr13:51455102-51455103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73186354	chr13:51455200-51455201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191699398	chr13:51455216-51455217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548797794	chr13:51455332-51455333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12875693	chr13:51455334-51455335	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs537770270	chr13:51455335-51455336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556161500	chr13:51455337-51455338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76418129	chr13:51455352-51455353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140526906	chr13:51455388-51455389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558681206	chr13:51455398-51455399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572210457	chr13:51455426-51455427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540849999	chr13:51455451-51455452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554775146	chr13:51455452-51455453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574612977	chr13:51455508-51455509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543713520	chr13:51455523-51455524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563297425	chr13:51455561-51455562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532369036	chr13:51455573-51455574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369962914	chr13:51455581-51455582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs1462033	chr13:51455660-51455661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34091910	chr13:51455665-51455666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545834497	chr13:51455677-51455678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559406304	chr13:51455687-51455688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372659283	chr13:51455746-51455747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs5803540	chr13:51455792-51455793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397796864	chr13:51455793-51455794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78531176	chr13:51455794-51455795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528614731	chr13:51455827-51455828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147130657	chr13:51455843-51455844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184047080	chr13:51455856-51455857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1462032	chr13:51455873-51455874	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs531069547	chr13:51455878-51455879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373325998	chr13:51455909-51455910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551297987	chr13:51455927-51455928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571206136	chr13:51456010-51456011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538626764	chr13:51456083-51456084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573677309	chr13:51456204-51456205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531108615	chr13:51456216-51456217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565615383	chr13:51456219-51456220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534733070	chr13:51456231-51456232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554430674	chr13:51456305-51456306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10590194	chr13:51456378-51456379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200496399	chr13:51456380-51456381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574579744	chr13:51456412-51456413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145872188	chr13:51456422-51456423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
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
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Melanoma	18172304	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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51454600-51455800	Enhancers	Fetal Thymus	thymus
2	chr13:51454800-51455600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr13:51454800-51455600	Enhancers	Thymus	Thymus
4	chr13:51455000-51455400	Enhancers	Primary B cells from peripheral blood	blood
5	chr13:51455000-51455600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr13:51455600-51456800	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr13:51455600-51456800	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr13:51455800-51458000	Weak transcription	Fetal Thymus	thymus
9	chr13:51456000-51456200	Weak transcription	Aorta	Aorta
10	chr13:51456800-51457000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr13:51456800-51457200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr13:51456800-51457400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
13	chr13:51457000-51457200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr13:51457000-51457400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr13:51457000-51458800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr13:51457200-51457600	Active TSS	Monocytes-CD14+_RO01746	blood
17	chr13:51457200-51464600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr13:51457400-51458200	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr13:51457400-51459200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr13:51457600-51458600	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr13:51457600-51459000	Enhancers	Primary hematopoietic stem cells	blood
22	chr13:51457600-51459200	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr13:51458000-51458600	Enhancers	Dnd41	blood
24	chr13:51458000-51458800	Enhancers	Fetal Thymus	thymus
25	chr13:51458200-51458600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr13:51458600-51459400	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr13:51458600-51461200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr13:51458800-51461000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr13:51458800-51463400	Weak transcription	Fetal Thymus	thymus
30	chr13:51459000-51461000	Weak transcription	Primary hematopoietic stem cells	blood
31	chr13:51459200-51461000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr13:51459200-51461200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr13:51459400-51461200	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr13:51461000-51461800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:51461000-51462000	Enhancers	Primary hematopoietic stem cells	blood
36	chr13:51461000-51462000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr13:51461000-51462200	Enhancers	Primary B cells from cord blood	blood
38	chr13:51461000-51462600	Weak transcription	Dnd41	blood
39	chr13:51461200-51461600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr13:51461200-51462000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr13:51461200-51462000	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr13:51461200-51462000	Enhancers	Primary B cells from peripheral blood	blood
43	chr13:51461200-51465200	Weak transcription	Aorta	Aorta
44	chr13:51461200-51465400	Enhancers	GM12878-XiMat	blood
45	chr13:51461600-51464200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr13:51461800-51464400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr13:51462000-51463400	Weak transcription	Primary B cells from peripheral blood	blood
48	chr13:51462000-51463600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr13:51462000-51464400	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr13:51462000-51464600	Weak transcription	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links