Variant report

Variant	nsv907711
Chromosome Location	chr17:15978663-16092902
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:183)
Chromatin interactive
region (count:65)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:16009878-16010075	K562	blood:	n/a	n/a
2	ARID3A	chr17:16074975-16075244	HepG2	liver:	n/a	n/a
3	ATF1	chr17:16009815-16010155	K562	blood:	n/a	n/a
4	BACH1	chr17:15995090-15995456	K562	blood:	n/a	n/a
5	BACH1	chr17:15995089-15995466	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr17:16070087-16070406	GM12878	blood:	n/a	n/a
7	BATF	chr17:15990257-15990528	GM12878	blood:	n/a	n/a
8	BATF	chr17:16070087-16070463	GM12878	blood:	n/a	n/a
9	BHLHE40	chr17:15990365-15990449	GM12878	blood:	n/a	n/a
10	BHLHE40	chr17:16010701-16010761	K562	blood:	n/a	n/a
11	BHLHE40	chr17:16009819-16010168	K562	blood:	n/a	n/a
12	BRCA1	chr17:16065799-16065822	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr17:16025764-16025823	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr17:15995175-15995382	K562	blood:	n/a	n/a
15	CBX3	chr17:16018440-16018697	K562	blood:	n/a	n/a
16	CBX3	chr17:15984887-15985173	K562	blood:	n/a	n/a
17	CCNT2	chr17:15992643-15992843	K562	blood:	n/a	n/a
18	CCNT2	chr17:16020242-16020442	K562	blood:	n/a	n/a
19	CEBPB	chr17:16032207-16032525	A549	lung:	n/a	chr17:16032395-16032408 chr17:16032353-16032364
20	CEBPB	chr17:16053516-16054006	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr17:16044171-16044537	A549	lung:	n/a	chr17:16044346-16044357
22	CEBPB	chr17:16090858-16091421	A549	lung:	n/a	n/a
23	CEBPB	chr17:16044216-16044558	MCF-7	breast:	n/a	chr17:16044346-16044357
24	CEBPB	chr17:16044253-16044421	H1-hESC	embryonic stem cell:	n/a	chr17:16044346-16044357
25	CEBPB	chr17:16090992-16091274	K562	blood:	n/a	n/a
26	CEBPB	chr17:16032195-16032501	IMR90	lung:	n/a	chr17:16032395-16032408 chr17:16032353-16032364
27	CEBPB	chr17:16044159-16044526	A549	lung:	n/a	chr17:16044346-16044357
28	CEBPB	chr17:16044203-16044528	HepG2	liver:	n/a	chr17:16044346-16044357
29	CEBPB	chr17:15979148-15979711	A549	lung:	n/a	chr17:15979463-15979474
30	CEBPB	chr17:16091082-16091276	HepG2	liver:	n/a	n/a
31	CEBPB	chr17:15979290-15979645	Hela-S3	cervix:	n/a	chr17:15979463-15979474
32	CEBPB	chr17:15991998-15992145	A549	lung:	n/a	n/a
33	CEBPB	chr17:16044203-16044628	A549	lung:	n/a	chr17:16044346-16044357
34	CEBPB	chr17:16032224-16032527	HepG2	liver:	n/a	chr17:16032395-16032408 chr17:16032353-16032364
35	CEBPB	chr17:16053564-16053908	IMR90	lung:	n/a	n/a
36	CEBPB	chr17:15988407-15988944	IMR90	lung:	n/a	n/a
37	CEBPB	chr17:15979276-15979642	A549	lung:	n/a	chr17:15979463-15979474
38	CEBPB	chr17:15979288-15979647	IMR90	lung:	n/a	chr17:15979463-15979474
39	CEBPB	chr17:16091092-16091292	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr17:16091068-16091321	K562	blood:	n/a	n/a
41	CEBPB	chr17:16065146-16065239	K562	blood:	n/a	n/a
42	CEBPB	chr17:16041351-16041618	IMR90	lung:	n/a	chr17:16041485-16041496
43	CEBPB	chr17:16032313-16032565	K562	blood:	n/a	chr17:16032395-16032408 chr17:16032353-16032364
44	CEBPB	chr17:16044207-16044530	K562	blood:	n/a	chr17:16044346-16044357
45	CEBPB	chr17:16009839-16010093	K562	blood:	n/a	n/a
46	CEBPB	chr17:16053508-16053963	HCT-116	colon:	n/a	n/a
47	CEBPB	chr17:16065154-16065280	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr17:16059545-16059746	H1-hESC	embryonic stem cell:	n/a	chr17:16059700-16059711
49	CEBPB	chr17:15979293-15979632	H1-hESC	embryonic stem cell:	n/a	chr17:15979463-15979474
50	CEBPB	chr17:16044181-16044523	IMR90	lung:	n/a	chr17:16044346-16044357

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:16049075-16049125	Caco-2	colon:	n/a
2	chr17:16048275-16048325	SK-N-SH	brain:	n/a
3	chr17:16049075-16049125	A549	lung:	n/a
4	chr17:16048275-16048325	SAEC	small airway:	n/a
5	chr17:16048275-16048325	NH-A	brain:	n/a
6	chr17:16049075-16049125	CMK	blood:	n/a
7	chr17:16048275-16048325	HNPCEpiC	eye:	n/a
8	chr17:16049075-16049125	IMR90	lung:	fetal
9	chr17:16048275-16048325	Hepatocyte	liver:	n/a
10	chr17:16048275-16048325	HUVEC	blood vessel:	n/a
11	chr17:16048275-16048325	SK-N-MC	brain:	n/a
12	chr17:16048275-16048325	HRCEpiC	kidney:	n/a
13	chr17:16048275-16048325	HMEC	breast:	n/a
14	chr17:16049075-16049125	H1-hESC	embryonic stem cell:	embryo
15	chr17:16049075-16049125	GM06990	blood:	n/a
16	chr17:16049075-16049125	HEEpiC	esophagus:	n/a
17	chr17:16048731-16048781	Jurkat	blood:	n/a
18	chr17:16048731-16048781	HCF	heart:	n/a
19	chr17:16048731-16048781	AoSMC	blood vessel:	n/a
20	chr17:16048731-16048781	A549	lung:	n/a
21	chr17:16048275-16048325	PFSK-1	brain:	n/a
22	chr17:16048731-16048781	AG10803	skin:	n/a
23	chr17:16048275-16048325	HPAEpiC	pulmonary alveolar:	n/a
24	chr17:16048731-16048781	HAEpiC	amniotic membrane:	n/a
25	chr17:16048731-16048781	HEEpiC	esophagus:	n/a
26	chr17:16048731-16048781	NH-A	brain:	n/a
27	chr17:16048275-16048325	U87	brain:	n/a
28	chr17:16048731-16048781	HCM	heart:	n/a
29	chr17:16048731-16048781	HCT-116	colon:	n/a
30	chr17:16049075-16049125	GM12892	blood:	n/a
31	chr17:16048731-16048781	HepG2	liver:	n/a
32	chr17:16048731-16048781	GM06990	blood:	n/a
33	chr17:16048275-16048325	MCF-7	breast:	n/a
34	chr17:16048275-16048325	IMR90	lung:	fetal
35	chr17:16048731-16048781	Caco-2	colon:	n/a
36	chr17:16048275-16048325	Jurkat	blood:	n/a
37	chr17:16048275-16048325	HRE	kidney:	n/a
38	chr17:16049075-16049125	AG10803	skin:	n/a
39	chr17:16048731-16048781	GM12878	blood:	n/a
40	chr17:16048731-16048781	U87	brain:	n/a
41	chr17:16048731-16048781	PrEC	prostate:	n/a
42	chr17:16048275-16048325	GM12892	blood:	n/a
43	chr17:16048731-16048781	Hela-S3	cervix:	n/a
44	chr17:16048275-16048325	CMK	blood:	n/a
45	chr17:16048731-16048781	MCF-7	breast:	n/a
46	chr17:16048731-16048781	GM12892	blood:	n/a
47	chr17:16048731-16048781	BE2_C	brain:	n/a
48	chr17:16049075-16049125	HRCEpiC	kidney:	n/a
49	chr17:16049075-16049125	HepG2	liver:	n/a
50	chr17:16048731-16048781	HIPEpiC	eye:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:16039156..16040813-chr17:16042197..16044363,3	MCF-7	breast:
2	chr17:15987048..15989365-chr17:16117375..16120147,2	MCF-7	breast:
3	chr17:16019669..16022129-chr17:16022606..16024865,2	K562	blood:
4	chr17:16073606..16076574-chr17:16118247..16120387,2	MCF-7	breast:
5	chr17:16036451..16038520-chr17:16043203..16046091,2	MCF-7	breast:
6	chr17:16056577..16058620-chr17:16118032..16120275,2	MCF-7	breast:
7	chr17:16039156..16040813-chr17:16042197..16044363,3	MCF-7	breast:
8	chr17:16052098..16053790-chr17:16057449..16059169,2	K562	blood:
9	chr17:16060434..16062194-chr17:16065832..16068470,2	K562	blood:
10	chr17:16064418..16066551-chr17:16067921..16069430,2	K562	blood:
11	chr17:16015557..16017498-chr17:16021823..16023792,2	MCF-7	breast:
12	chr17:16044585..16047415-chr17:16047650..16050913,4	MCF-7	breast:
13	chr17:16052098..16053790-chr17:16057449..16059169,2	K562	blood:
14	chr17:16000342..16002762-chr17:16006571..16009952,3	K562	blood:
15	chr17:16089835..16092985-chr17:16117505..16120902,3	K562	blood:
16	chr17:16085958..16087608-chr17:16095092..16097243,2	MCF-7	breast:
17	chr17:16073671..16077871-chr17:16116736..16119410,7	MCF-7	breast:
18	chr17:16027095..16029014-chr17:16033144..16034993,2	MCF-7	breast:
19	chr17:16019669..16022129-chr17:16022606..16024865,2	K562	blood:
20	chr17:16092491..16094768-chr17:16118634..16120351,2	K562	blood:
21	chr17:16072733..16074732-chr17:16076435..16078700,2	MCF-7	breast:
22	chr17:16043759..16046370-chr17:16052427..16055741,4	K562	blood:
23	chr17:16058959..16060577-chr17:16340966..16343929,2	MCF-7	breast:
24	chr17:16019956..16022065-chr17:16032573..16034409,2	K562	blood:
25	chr17:16019117..16021633-chr17:16117621..16119392,2	MCF-7	breast:
26	chr17:16089561..16091475-chr17:16117842..16119372,2	MCF-7	breast:
27	chr17:16027095..16029014-chr17:16033144..16034993,2	MCF-7	breast:
28	chr17:16018918..16021715-chr17:16028326..16030856,2	K562	blood:
29	chr17:16057635..16060524-chr17:16061549..16064453,2	MCF-7	breast:
30	chr17:16055611..16057622-chr17:16062780..16064444,2	K562	blood:
31	chr17:16074285..16076009-chr17:16119526..16121977,2	MCF-7	breast:
32	chr17:16057635..16060524-chr17:16061549..16064453,2	MCF-7	breast:
33	chr17:16018918..16021715-chr17:16028326..16030856,2	K562	blood:
34	chr17:16056755..16059055-chr17:16074181..16076719,2	MCF-7	breast:
35	chr17:15976524..15978868-chr17:15991864..15993766,2	K562	blood:
36	chr13:21346241..21348378-chr17:16020761..16023781,3	MCF-7	breast:
37	chr17:16032848..16034524-chr17:16038986..16041500,2	K562	blood:
38	chr17:15972800..15974994-chr17:15979206..15981179,2	MCF-7	breast:
39	chr17:16025863..16027774-chr17:16028606..16031135,2	K562	blood:
40	chr17:16064418..16066551-chr17:16067921..16069430,2	K562	blood:
41	chr17:15963401..15966357-chr17:16012433..16014400,2	K562	blood:
42	chr17:16050219..16053553-chr17:16118923..16122033,3	MCF-7	breast:
43	chr17:15992643..15994988-chr17:16118980..16121101,2	MCF-7	breast:
44	chr17:16056755..16059055-chr17:16074181..16076719,2	MCF-7	breast:
45	chr17:15978459..15981234-chr17:15984249..15986179,2	K562	blood:
46	chr17:16044585..16047415-chr17:16047650..16050913,4	MCF-7	breast:
47	chr17:16043759..16046370-chr17:16052427..16055741,4	K562	blood:
48	chr17:16044141..16046370-chr17:16053985..16055741,2	K562	blood:
49	chr17:16033296..16035320-chr17:16118483..16120440,2	MCF-7	breast:
50	chr17:16055611..16057622-chr17:16062780..16064444,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC19-1	chr17:15987356-15987695	NONHSAT145891

No data

Variant related genes	Relation type
RN7SL442P	TF binding region
RNU6-314P	TF binding region
RNU6-862P	TF binding region
NCOR1	TF binding region
ENSG00000233979	TF binding region
RN7SL442P	CpG island
RNU6-314P	CpG island
RNU6-862P	CpG island
NCOR1	CpG island
ENSG00000233979	CpG island
ENSG00000252383	chromatin interactions
ENSG00000199674	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000108474	chromatin interactions
ENSG00000150456	chromatin interactions
ENSG00000239221	chromatin interactions
ENSG00000141027	chromatin interactions

Extended variants
information (count: 4666 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:4666 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3760295	chr17:15978663-15978664	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560348715	chr17:15978705-15978706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529197039	chr17:15978777-15978778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372485535	chr17:15978794-15978795	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139184991	chr17:15978832-15978833	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144012103	chr17:15978954-15978955	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs373883382	chr17:15978957-15978958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149864614	chr17:15979014-15979015	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531410993	chr17:15979019-15979020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs144892815	chr17:15979053-15979054	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148692349	chr17:15979064-15979065	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528873855	chr17:15979070-15979071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527242099	chr17:15979094-15979095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547078036	chr17:15979118-15979119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs576042904	chr17:15979139-15979140	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs567918207	chr17:15979163-15979164	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536580591	chr17:15979170-15979171	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs556319983	chr17:15979183-15979184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369485597	chr17:15979193-15979194	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142199961	chr17:15979235-15979236	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77267303	chr17:15979239-15979240	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs562200896	chr17:15979277-15979278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs151200720	chr17:15979296-15979297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs73981437	chr17:15979384-15979385	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554681617	chr17:15979386-15979387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573864494	chr17:15979435-15979436	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111546309	chr17:15979449-15979450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191968543	chr17:15979468-15979469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572644982	chr17:15979499-15979500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551524997	chr17:15979572-15979573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533559675	chr17:15979611-15979612	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531574944	chr17:15979645-15979646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373750190	chr17:15979696-15979697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531843950	chr17:15979710-15979711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146979139	chr17:15979748-15979749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547263484	chr17:15979755-15979756	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183112433	chr17:15979825-15979826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188136284	chr17:15979856-15979857	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547356957	chr17:15979937-15979938	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192667997	chr17:15980146-15980147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567181030	chr17:15980215-15980216	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs73981438	chr17:15980223-15980224	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114512423	chr17:15980233-15980234	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570024484	chr17:15980261-15980262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs115127943	chr17:15980275-15980276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7222645	chr17:15980290-15980291	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556361692	chr17:15980298-15980299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558748369	chr17:15980315-15980316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185005423	chr17:15980378-15980379	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34851903	chr17:15980391-15980392	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:3768 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15905200-15986400	Strong transcription	Primary T helper cells fromperipheralblood	blood
2	chr17:15913800-15990800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr17:15915400-15998000	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr17:15921000-15991000	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr17:15921000-15991200	Strong transcription	Primary B cells from peripheral blood	blood
6	chr17:15923800-15998000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:15926800-15985400	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr17:15926800-15987600	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr17:15927800-15987800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr17:15931800-15988800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr17:15940000-15980600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr17:15942000-15985000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr17:15944800-15991000	Strong transcription	Fetal Intestine Large	intestine
14	chr17:15948200-15978800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr17:15953800-15988400	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr17:15954000-15986000	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr17:15954200-15985400	Strong transcription	Duodenum Mucosa	Duodenum
18	chr17:15955800-15982200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:15955800-15985400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr17:15955800-15985400	Strong transcription	Primary B cells from cord blood	blood
21	chr17:15955800-15985600	Strong transcription	Dnd41	blood
22	chr17:15955800-15990600	Strong transcription	Fetal Thymus	thymus
23	chr17:15956200-15985400	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr17:15956400-15984000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr17:15956400-15985600	Strong transcription	Adipose Nuclei	Adipose
26	chr17:15956400-15990800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr17:15956800-15979600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr17:15957000-15985400	Strong transcription	Liver	Liver
29	chr17:15957400-15988200	Strong transcription	Primary T cells from cord blood	blood
30	chr17:15957400-15990600	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr17:15957600-15979200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr17:15957600-15980600	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr17:15957600-15986400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr17:15957600-15988400	Strong transcription	A549	lung
35	chr17:15958000-15984000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr17:15958000-15991000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr17:15958200-15988000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr17:15958400-15985000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr17:15958400-15985600	Strong transcription	GM12878-XiMat	blood
40	chr17:15958800-15985800	Strong transcription	Osteobl	bone
41	chr17:15959200-15981400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr17:15959200-15984800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr17:15960000-15985400	Strong transcription	NH-A	brain
44	chr17:15960200-15979400	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr17:15961600-15995000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr17:15962800-15984000	Strong transcription	HepG2	liver
47	chr17:15963000-15985200	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr17:15963000-15985400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr17:15964200-15984000	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr17:15964400-15984000	Strong transcription	H1 Cell Line	embryonic stem cell

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