Variant report

Variant	nsv470133
Chromosome Location	chr7:16269632-16312056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:489)
CpG islands
(count:0)
Chromatin interactive
region (count:37)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16299684-16300431	K562	blood:	n/a	n/a
2	ARID3A	chr7:16307063-16308041	K562	blood:	n/a	n/a
3	ARID3A	chr7:16302411-16302607	K562	blood:	n/a	n/a
4	ARID3A	chr7:16299083-16299409	K562	blood:	n/a	n/a
5	ARID3A	chr7:16300636-16301991	K562	blood:	n/a	n/a
6	ARID3A	chr7:16308350-16309290	K562	blood:	n/a	n/a
7	ARID3A	chr7:16304739-16305925	K562	blood:	n/a	n/a
8	ATF1	chr7:16300049-16300351	K562	blood:	n/a	n/a
9	ATF1	chr7:16308377-16309311	K562	blood:	n/a	n/a
10	ATF1	chr7:16304760-16305221	K562	blood:	n/a	n/a
11	ATF1	chr7:16301437-16301703	K562	blood:	n/a	n/a
12	ATF3	chr7:16308269-16309108	K562	blood:	n/a	n/a
13	BCL3	chr7:16308310-16309048	K562	blood:	n/a	n/a
14	BCLAF1	chr7:16301267-16301844	K562	blood:	n/a	n/a
15	BCLAF1	chr7:16305341-16306186	K562	blood:	n/a	n/a
16	BCLAF1	chr7:16308244-16309056	K562	blood:	n/a	n/a
17	BCLAF1	chr7:16308322-16309035	K562	blood:	n/a	n/a
18	BHLHE40	chr7:16304830-16305615	K562	blood:	n/a	n/a
19	BHLHE40	chr7:16303074-16303109	K562	blood:	n/a	n/a
20	BHLHE40	chr7:16306312-16306532	K562	blood:	n/a	n/a
21	BHLHE40	chr7:16297424-16297442	K562	blood:	n/a	n/a
22	BHLHE40	chr7:16308296-16309332	K562	blood:	n/a	n/a
23	CBX3	chr7:16269828-16270194	K562	blood:	n/a	n/a
24	CBX3	chr7:16308325-16309283	K562	blood:	n/a	n/a
25	CBX3	chr7:16271850-16272277	K562	blood:	n/a	n/a
26	CBX3	chr7:16295561-16295958	K562	blood:	n/a	n/a
27	CBX3	chr7:16269898-16270150	K562	blood:	n/a	n/a
28	CBX3	chr7:16308343-16309472	K562	blood:	n/a	n/a
29	CCNT2	chr7:16301397-16301732	K562	blood:	n/a	n/a
30	CCNT2	chr7:16310417-16310723	K562	blood:	n/a	n/a
31	CCNT2	chr7:16304676-16305206	K562	blood:	n/a	n/a
32	CCNT2	chr7:16308074-16309185	K562	blood:	n/a	n/a
33	CCNT2	chr7:16299875-16300334	K562	blood:	n/a	n/a
34	CEBPB	chr7:16308212-16309353	K562	blood:	n/a	n/a
35	CEBPB	chr7:16308351-16308943	K562	blood:	n/a	n/a
36	CEBPB	chr7:16305889-16305921	K562	blood:	n/a	n/a
37	CEBPB	chr7:16308357-16309029	IMR90	lung:	n/a	n/a
38	CEBPB	chr7:16274104-16274388	K562	blood:	n/a	n/a
39	CEBPB	chr7:16308306-16309211	K562	blood:	n/a	n/a
40	CEBPB	chr7:16304794-16305678	K562	blood:	n/a	n/a
41	CEBPB	chr7:16299062-16299191	K562	blood:	n/a	n/a
42	CEBPB	chr7:16279656-16279856	HepG2	liver:	n/a	chr7:16279790-16279801
43	CEBPB	chr7:16304910-16305502	K562	blood:	n/a	n/a
44	CEBPB	chr7:16301287-16301995	K562	blood:	n/a	n/a
45	CEBPB	chr7:16299779-16300445	K562	blood:	n/a	n/a
46	CEBPB	chr7:16285457-16285721	HepG2	liver:	n/a	chr7:16285552-16285563
47	CEBPB	chr7:16304474-16304690	K562	blood:	n/a	n/a
48	CEBPD	chr7:16308218-16309234	K562	blood:	n/a	n/a
49	CEBPD	chr7:16308288-16309202	K562	blood:	n/a	n/a
50	CEBPD	chr7:16304751-16305266	K562	blood:	n/a	n/a

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16302428..16304569-chr7:16686662..16689057,2	K562	blood:
2	chr7:16285409..16288180-chr7:16295653..16298089,2	K562	blood:
3	chr7:16302626..16306339-chr7:16456665..16460333,5	K562	blood:
4	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
5	chr7:16301506..16303412-chr7:20253971..20256529,2	K562	blood:
6	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
7	chr7:16275733..16277560-chr7:16684679..16686192,2	K562	blood:
8	chr7:16285409..16288180-chr7:16295653..16298089,2	K562	blood:
9	chr7:16271837..16274588-chr7:16275186..16279473,3	K562	blood:
10	chr7:16307417..16309237-chr7:16685352..16687215,2	K562	blood:
11	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
12	chr7:12753228..12755385-chr7:16301600..16303385,2	K562	blood:
13	chr7:16301478..16303849-chr7:16518183..16519712,2	K562	blood:
14	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
15	chr7:16307891..16309646-chr7:16460887..16462647,2	K562	blood:
16	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:
17	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
18	chr7:16221967..16224628-chr7:16306153..16308389,2	K562	blood:
19	chr7:16307737..16311020-chr7:16684818..16687152,3	K562	blood:
20	chr7:16271772..16276074-chr7:16279630..16282231,4	K562	blood:
21	chr7:16302978..16309646-chr7:16456908..16462647,13	K562	blood:
22	chr7:16274806..16276431-chr7:16298235..16300903,2	K562	blood:
23	chr7:16272248..16274869-chr7:16305157..16307096,2	K562	blood:
24	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
25	chr7:16272248..16275452-chr7:16305157..16308165,4	K562	blood:
26	chr7:16263097..16266771-chr7:16270720..16274586,3	K562	blood:
27	chr7:16303209..16307181-chr7:16682528..16687363,4	K562	blood:
28	chr7:16277063..16278861-chr7:16280781..16282424,2	K562	blood:
29	chr7:16309917..16312167-chr7:16461370..16463570,2	K562	blood:
30	chr7:16297813..16300771-chr7:16597599..16599779,2	K562	blood:
31	chr7:16304631..16307990-chr7:16437547..16440554,3	K562	blood:
32	chr7:16262958..16265861-chr7:16270760..16273242,2	K562	blood:
33	chr7:16300347..16301994-chr7:16462021..16464400,2	K562	blood:
34	chr7:16304973..16307091-chr7:16435445..16437043,2	K562	blood:
35	chr7:16301403..16303759-chr7:16503630..16506930,3	K562	blood:
36	chr7:16165242..16168046-chr7:16300329..16302056,2	K562	blood:
37	chr7:16277063..16278675-chr7:16280781..16282945,2	K562	blood:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119292
2	lnc-AC006035.2-1	chr7:16310142-16310229	ENSG00000241044
3	lnc-AC006035.2-1	chr7:16276934-16277035	NONHSAT119295
4	lnc-AC006035.2-1	chr7:16272377-16272461	ucscGeneNc_uc003stf_2
5	lnc-AC006035.2-1	chr7:16276934-16277035	ENSG00000229688.3
6	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119293
7	lnc-AC006035.2-1	chr7:16288360-16288362	NONHSAT119294
8	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119296
9	lnc-AC006035.2-1	chr7:16308482-16310229	ENSG00000229688
10	lnc-AC006035.2-1	chr7:16310630-16310643	NONHSAT119294
11	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119294
12	lnc-AC006035.2-1	chr7:16276934-16276977	NONHSAT119292
13	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119293
14	lnc-AC006035.2-1	chr7:16301524-16301721	ENSG00000229688
15	lnc-AC006035.2-1	chr7:16308482-16308872	ENSG00000229688
16	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119294
17	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119295
18	lnc-AC006035.2-1	chr7:16301527-16301721	NONHSAT119294
19	lnc-AC006035.2-1	chr7:16276934-16277038	NONHSAT119293
20	lnc-AC006035.2-1	chr7:16308482-16309502	NONHSAT119295
21	lnc-AC006035.2-1	chr7:16275007-16276752	ucscGeneNc_uc003stf_2
22	lnc-AC006035.2-1	chr7:16308874-16309215	ENSG00000241044
23	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
24	lnc-AC006035.2-1	chr7:16275527-16275604	ENSG00000229688
25	lnc-AC006035.2-1	chr7:16308482-16310229	NONHSAT119294
26	lnc-AC006035.2-1	chr7:16305852-16305936	ENSG00000229688
27	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119296
28	lnc-AC006035.2-1	chr7:16276934-16277031	ENSG00000229688.3
29	lnc-AC006035.2-1	chr7:16301524-16301721	NONHSAT119293
30	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119292
31	lnc-AC006035.2-1	chr7:16305852-16305936	NONHSAT119295
32	lnc-AC006035.2-1	chr7:16276934-16276977	ENSG00000229688
33	lnc-AC006035.2-1	chr7:16275527-16275604	NONHSAT119292
34	lnc-AC006035.2-1	chr7:16287510-16287714	ENSG00000229688.3
35	lnc-AC006035.2-1	chr7:16276934-16277038	ENSG00000229688

No data

Variant related genes	Relation type
ISPD-AS1	TF binding region
ENSG00000136261	chromatin interactions
ENSG00000106524	chromatin interactions
ENSG00000214960	chromatin interactions
ENSG00000171243	chromatin interactions
TTC8	miRNA target sites
LMLN	miRNA target sites
DIS3L	miRNA target sites
GLTP	miRNA target sites
RSRC2	miRNA target sites
CDKN1B	miRNA target sites
SEC63	miRNA target sites
HAS3	miRNA target sites

Extended variants
information (count: 1809 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1809 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4719461	chr7:16269632-16269633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79531512	chr7:16269690-16269691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376669920	chr7:16269694-16269695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569018241	chr7:16269699-16269700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1113569	chr7:16269711-16269712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs61640204	chr7:16269712-16269713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566480803	chr7:16269715-16269716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147104089	chr7:16269726-16269727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555652496	chr7:16269743-16269744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373888643	chr7:16269766-16269767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185426586	chr7:16269830-16269831	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10243886	chr7:16269861-16269862	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs576514254	chr7:16269878-16269879	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78526106	chr7:16269908-16269909	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542290952	chr7:16269915-16269916	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555789630	chr7:16269917-16269918	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545101684	chr7:16269923-16269924	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190285594	chr7:16269924-16269925	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150334239	chr7:16269956-16269957	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114172729	chr7:16269971-16269972	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375969211	chr7:16270029-16270030	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113871500	chr7:16270032-16270033	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561652050	chr7:16270071-16270072	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367810952	chr7:16270073-16270074	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs375810126	chr7:16270098-16270099	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541494846	chr7:16270112-16270113	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs55924345	chr7:16270230-16270231	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114713467	chr7:16270249-16270250	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182533734	chr7:16270251-16270252	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185703282	chr7:16270270-16270271	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370114960	chr7:16270290-16270291	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577313422	chr7:16270291-16270292	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532301660	chr7:16270328-16270329	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6956986	chr7:16270332-16270333	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs562399005	chr7:16270340-16270341	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368762892	chr7:16270350-16270351	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566442651	chr7:16270385-16270386	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs7790551	chr7:16270388-16270389	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs137974307	chr7:16270399-16270400	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567599144	chr7:16270444-16270445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537636106	chr7:16270465-16270466	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149517279	chr7:16270468-16270469	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547820487	chr7:16270475-16270476	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571130742	chr7:16270477-16270478	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191937742	chr7:16270504-16270505	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553882087	chr7:16270512-16270513	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375226219	chr7:16270547-16270548	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536695604	chr7:16270552-16270553	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144060628	chr7:16270615-16270616	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138641482	chr7:16270657-16270658	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	19805367	CNVD
Autism	20808228	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16250200-16275800	Weak transcription	Pancreas	Pancrea
2	chr7:16269800-16271200	ZNF genes & repeats	Liver	Liver
3	chr7:16270000-16271200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr7:16270200-16271200	ZNF genes & repeats	Fetal Lung	lung
5	chr7:16270400-16270600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:16270400-16270800	ZNF genes & repeats	Left Ventricle	heart
7	chr7:16270400-16272200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
8	chr7:16270400-16272200	ZNF genes & repeats	Ovary	ovary
9	chr7:16270400-16272200	ZNF genes & repeats	Psoas Muscle	Psoas
10	chr7:16270800-16273400	ZNF genes & repeats	K562	blood
11	chr7:16271200-16273200	Weak transcription	Fetal Lung	lung
12	chr7:16271600-16272200	ZNF genes & repeats	Liver	Liver
13	chr7:16272000-16272200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
14	chr7:16272200-16272800	Weak transcription	Ovary	ovary
15	chr7:16272200-16272800	Weak transcription	Psoas Muscle	Psoas
16	chr7:16272200-16276600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr7:16272200-16276800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr7:16272800-16273000	Enhancers	Primary T cells from cord blood	blood
19	chr7:16273000-16274200	Weak transcription	Primary T cells from cord blood	blood
20	chr7:16273200-16273400	Enhancers	Fetal Lung	lung
21	chr7:16273400-16274200	Weak transcription	Fetal Lung	lung
22	chr7:16273400-16274200	Weak transcription	K562	blood
23	chr7:16274200-16274800	Enhancers	Primary T cells from cord blood	blood
24	chr7:16274200-16274800	Enhancers	NHEK	skin
25	chr7:16274200-16275000	Enhancers	Fetal Lung	lung
26	chr7:16274200-16275600	Enhancers	Fetal Heart	heart
27	chr7:16274200-16275600	Enhancers	K562	blood
28	chr7:16274400-16275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:16275000-16304400	Weak transcription	Fetal Lung	lung
30	chr7:16275200-16275800	Enhancers	Fetal Brain Female	brain
31	chr7:16276400-16276800	Enhancers	Fetal Brain Male	brain
32	chr7:16276800-16277200	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr7:16277200-16278400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:16278600-16278800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr7:16280200-16289400	Weak transcription	Left Ventricle	heart
36	chr7:16284800-16287600	Weak transcription	Ovary	ovary
37	chr7:16286200-16287600	Enhancers	Brain Substantia Nigra	brain
38	chr7:16286400-16288600	Weak transcription	Fetal Stomach	stomach
39	chr7:16286600-16287000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:16286600-16287200	Enhancers	Brain Cingulate Gyrus	brain
41	chr7:16286800-16287400	Enhancers	Brain Hippocampus Middle	brain
42	chr7:16286800-16295800	Weak transcription	Stomach Smooth Muscle	stomach
43	chr7:16287600-16287800	ZNF genes & repeats	Ovary	ovary
44	chr7:16287800-16288000	Weak transcription	Ovary	ovary
45	chr7:16287800-16289200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:16288000-16291800	Weak transcription	Gastric	stomach
47	chr7:16288600-16289200	ZNF genes & repeats	Fetal Stomach	stomach
48	chr7:16289200-16296600	Weak transcription	Fetal Stomach	stomach
49	chr7:16291200-16293800	Weak transcription	Fetal Kidney	kidney
50	chr7:16295600-16296600	Weak transcription	K562	blood

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