Variant report

Variant	nsv608258
Chromosome Location	chr7:117342771-117393516
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:61)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:117390714-117390984	K562	blood:	n/a	n/a
2	ATF1	chr7:117393431-117393483	K562	blood:	n/a	n/a
3	ATF1	chr7:117390651-117390850	K562	blood:	n/a	n/a
4	ATF1	chr7:117345754-117345961	K562	blood:	n/a	n/a
5	ATF1	chr7:117371587-117371970	K562	blood:	n/a	n/a
6	ATF2	chr7:117371502-117371937	GM12878	blood:	n/a	n/a
7	BATF	chr7:117371519-117371976	GM12878	blood:	n/a	chr7:117371727-117371738
8	BATF	chr7:117369022-117369250	GM12878	blood:	n/a	n/a
9	BATF	chr7:117368960-117369256	GM12878	blood:	n/a	n/a
10	BATF	chr7:117371523-117371939	GM12878	blood:	n/a	chr7:117371727-117371738
11	BCL11A	chr7:117371557-117371913	GM12878	blood:	n/a	chr7:117371805-117371814
12	BCL11A	chr7:117371608-117371892	GM12878	blood:	n/a	chr7:117371805-117371814
13	BCLAF1	chr7:117355912-117356148	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:117371567-117371987	GM12878	blood:	n/a	chr7:117371805-117371814
15	BCLAF1	chr7:117371428-117371966	GM12878	blood:	n/a	chr7:117371805-117371814
16	BHLHE40	chr7:117343373-117343379	K562	blood:	n/a	n/a
17	BHLHE40	chr7:117368936-117369195	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:117371559-117371927	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:117355838-117356201	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:117355776-117355809	GM12878	blood:	n/a	n/a
21	BRCA1	chr7:117371726-117371859	GM12878	blood:	n/a	n/a
22	CCNT2	chr7:117366619-117366697	K562	blood:	n/a	n/a
23	CCNT2	chr7:117371534-117371867	K562	blood:	n/a	n/a
24	CEBPB	chr7:117346347-117346706	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:117357472-117357731	A549	lung:	n/a	chr7:117357590-117357601
26	CEBPB	chr7:117388557-117388654	Hela-S3	cervix:	n/a	chr7:117388591-117388602
27	CEBPB	chr7:117357448-117357764	IMR90	lung:	n/a	chr7:117357590-117357601
28	CEBPB	chr7:117388449-117388753	K562	blood:	n/a	chr7:117388591-117388602
29	CEBPB	chr7:117357494-117357736	Hela-S3	cervix:	n/a	chr7:117357590-117357601
30	CEBPB	chr7:117388473-117388748	IMR90	lung:	n/a	chr7:117388591-117388602
31	CEBPB	chr7:117381994-117382382	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:117355427-117356136	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:117357569-117357603	HepG2	liver:	n/a	chr7:117357590-117357601
34	CEBPB	chr7:117388459-117388750	HepG2	liver:	n/a	chr7:117388591-117388602
35	CEBPB	chr7:117344099-117344506	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr7:117355506-117355706	A549	lung:	n/a	n/a
37	CEBPB	chr7:117357582-117357615	K562	blood:	n/a	chr7:117357590-117357601
38	CHD1	chr7:117371645-117371830	GM12878	blood:	n/a	n/a
39	CHD2	chr7:117371549-117371930	GM12878	blood:	n/a	n/a
40	CTCF	chr7:117387560-117387605	LNCaP	prostate:	n/a	n/a
41	CTCF	chr7:117355941-117356147	GM19238	blood:	n/a	chr7:117356037-117356053 chr7:117356031-117356052 chr7:117356036-117356054
42	CTCF	chr7:117355960-117356110	MCF-7	breast:	n/a	chr7:117356037-117356053 chr7:117356031-117356052 chr7:117356036-117356054
43	CTCF	chr7:117356000-117356150	HAc	cerebellar:	n/a	chr7:117356037-117356053 chr7:117356031-117356052 chr7:117356036-117356054
44	CTCF	chr7:117354835-117354943	A549	lung:	n/a	n/a
45	CTCF	chr7:117390760-117390910	AG04449	skin:	n/a	chr7:117390843-117390856 chr7:117390840-117390858 chr7:117390842-117390863
46	CTCF	chr7:117356404-117356415	GM10248	blood:	n/a	n/a
47	CTCF	chr7:117355946-117356131	GM19239	blood:	n/a	chr7:117356037-117356053 chr7:117356031-117356052 chr7:117356036-117356054
48	CTCF	chr7:117390780-117390930	HCM	heart:	n/a	chr7:117390843-117390856 chr7:117390840-117390858 chr7:117390842-117390863
49	CTCF	chr7:117390800-117390950	WI-38	lung:	n/a	chr7:117390843-117390856 chr7:117390840-117390858 chr7:117390842-117390863
50	CTCF	chr7:117391060-117391210	AG10803	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117356490-117356540	GM06990	blood:	n/a
2	chr7:117356490-117356540	HIPEpiC	eye:	n/a
3	chr7:117356490-117356540	RPTEC	kidney:	n/a
4	chr7:117356490-117356540	HCM	heart:	n/a
5	chr7:117356490-117356540	PFSK-1	brain:	n/a
6	chr7:117356490-117356540	Jurkat	blood:	n/a
7	chr7:117356490-117356540	AoSMC	blood vessel:	n/a
8	chr7:117356490-117356540	CMK	blood:	n/a
9	chr7:117356490-117356540	HCT-116	colon:	n/a
10	chr7:117356490-117356540	MCF-7	breast:	n/a
11	chr7:117356490-117356540	HL-60	blood:	n/a
12	chr7:117356490-117356540	HepG2	liver:	n/a
13	chr7:117356490-117356540	HCPEpiC	choroid plexus:	n/a
14	chr7:117356490-117356540	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:117356490-117356540	Caco-2	colon:	n/a
16	chr7:117356490-117356540	NT2-D1	testis:	n/a
17	chr7:117356490-117356540	HRCEpiC	kidney:	n/a
18	chr7:117356490-117356540	AG09319	gingival:	n/a
19	chr7:117356490-117356540	SK-N-MC	brain:	n/a
20	chr7:117356490-117356540	LNCaP	prostate:	n/a
21	chr7:117356490-117356540	A549	lung:	n/a
22	chr7:117356490-117356540	ProgFib	skin:	n/a
23	chr7:117356490-117356540	GM12892	blood:	n/a
24	chr7:117356490-117356540	NHBE	bronchial:	n/a
25	chr7:117356490-117356540	Hepatocyte	liver:	n/a
26	chr7:117356490-117356540	AG09309	skin:	n/a
27	chr7:117356490-117356540	HUVEC	blood vessel:	n/a
28	chr7:117356490-117356540	GM12891	blood:	n/a
29	chr7:117356490-117356540	NHDF-neo	bronchial:	n/a
30	chr7:117356490-117356540	MCF10A-Er-Src	breast:	n/a
31	chr7:117356490-117356540	HAEpiC	amniotic membrane:	n/a
32	chr7:117356490-117356540	IMR90	lung:	fetal
33	chr7:117356490-117356540	T-47D	breast:	n/a
34	chr7:117356490-117356540	HEEpiC	esophagus:	n/a
35	chr7:117356490-117356540	HNPCEpiC	eye:	n/a
36	chr7:117356490-117356540	HEK293	kidney:	embryo
37	chr7:117356490-117356540	SK-N-SH	brain:	n/a
38	chr7:117356490-117356540	Hela-S3	cervix:	n/a
39	chr7:117356490-117356540	ovcar-3	ovarian:	n/a
40	chr7:117356490-117356540	AG04449	skin:	fetal
41	chr7:117356490-117356540	NB4	blood:	n/a
42	chr7:117356490-117356540	SAEC	small airway:	n/a
43	chr7:117356490-117356540	HMEC	breast:	n/a
44	chr7:117356490-117356540	SK-N-SH_RA	brain:	n/a
45	chr7:117356490-117356540	NH-A	brain:	n/a
46	chr7:117356490-117356540	GM12878	blood:	n/a
47	chr7:117356490-117356540	PANC-1	pancreas:	n/a
48	chr7:117356490-117356540	AG10803	skin:	n/a
49	chr7:117356490-117356540	U87	brain:	n/a
50	chr7:117356490-117356540	HRPEpiC	eye:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:117390392..117391300-chr7:117793147..117794278,5	MCF-7	breast:
2	chr7:117356959..117359693-chr7:117361540..117364405,2	K562	blood:
3	chr7:117355545..117356437-chr7:117793373..117793993,2	MCF-7	breast:
4	chr7:117349947..117351508-chr7:117351795..117354069,2	MCF-7	breast:
5	chr7:117392046..117394565-chr7:117395082..117398662,3	K562	blood:
6	chr7:117359274..117361366-chr7:117364889..117367642,2	K562	blood:
7	chr7:117390270..117390904-chr7:117744533..117745270,2	MCF-7	breast:
8	chr7:117101401..117103711-chr7:117353443..117355432,2	MCF-7	breast:
9	chr7:117373911..117375838-chr7:117379678..117382405,2	MCF-7	breast:
10	chr7:117342771..117345481-chr7:117345795..117348003,2	K562	blood:
11	chr7:117390818..117391522-chr7:117589429..117589982,2	MCF-7	breast:
12	chr7:117356959..117359693-chr7:117361540..117364405,2	K562	blood:
13	7:116728195-116740907..7:117341506-117356953	Hela-S3	cervix:
14	7:115847372-115857098..7:117371344-117373403	H1-hESC	embryonic stem cell:	embryo
15	chr7:117389243..117392160-chr7:117392467..117394936,2	K562	blood:
16	7:117100350-117112126..7:117341506-117356953	GM12878	blood:
17	7:115861595-115870968..7:117356953-117362271	GM12878	blood:
18	chr7:117388690..117390929-chr7:117821238..117823244,2	MCF-7	breast:
19	7:115890993-115892266..7:117356953-117362271	GM12878	blood:
20	chr7:117342771..117345481-chr7:117345795..117348003,2	K562	blood:
21	chr7:117338716..117341307-chr7:117344379..117346864,2	MCF-7	breast:
22	chr7:117390378..117390892-chr7:117835674..117836196,2	MCF-7	breast:
23	chr7:117358870..117360774-chr7:117364748..117367642,2	K562	blood:
24	7:116604327-116608063..7:117373403-117375287	H1-hESC	embryonic stem cell:	embryo
25	chr7:117389243..117392160-chr7:117392467..117394936,2	K562	blood:
26	7:117251668-117255413..7:117341506-117356953	Hela-S3	cervix:
27	chr7:117370170..117372103-chr7:117379526..117381745,2	MCF-7	breast:
28	chr7:117358870..117360774-chr7:117364748..117367642,2	K562	blood:
29	chr7:117370526..117372524-chr7:117372686..117375672,2	K562	blood:
30	7:116849860-116864942..7:117390750-117397080	Hela-S3	cervix:
31	7:115847372-115857098..7:117341506-117356953	Hela-S3	cervix:
32	7:117065049-117068137..7:117341506-117356953	H1-hESC	embryonic stem cell:	embryo
33	7:116754962-116765597..7:117341506-117356953	Hela-S3	cervix:
34	7:116307511-116321259..7:117341506-117356953	Hela-S3	cervix:
35	7:116651084-116657331..7:117341506-117356953	Hela-S3	cervix:
36	chr1:248764235..248764876-chr7:117353363..117354001,2	MCF-7	breast:
37	chr7:117340357..117343008-chr7:117343379..117345686,2	K562	blood:
38	chr7:117359274..117361366-chr7:117364889..117367642,2	K562	blood:
39	7:115890993-115892266..7:117387122-117390750	H1-hESC	embryonic stem cell:	embryo
40	7:116604327-116608063..7:117341506-117356953	H1-hESC	embryonic stem cell:	embryo
41	chr7:117390553..117391098-chr7:117421386..117421983,2	MCF-7	breast:
42	chr7:117373911..117375838-chr7:117379678..117382405,2	MCF-7	breast:
43	chr7:117340357..117343008-chr7:117343379..117345686,2	K562	blood:
44	chr7:117098786..117100223-chr7:117355606..117356387,7	MCF-7	breast:
45	7:115861595-115870968..7:117341506-117356953	Hela-S3	cervix:
46	7:116604327-116608063..7:117390750-117397080	Hela-S3	cervix:
47	chr7:117039966..117040781-chr7:117355514..117356581,4	MCF-7	breast:
48	chr7:117390803..117391431-chr7:118815895..118816706,2	MCF-7	breast:
49	7:116434729-116454408..7:117341506-117356953	Hela-S3	cervix:
50	7:115890993-115892266..7:117386109-117387122	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CFTR-1	chr7:117355812-117356025	ENSG00000227601.1

No data

Variant related genes	Relation type
CFTR	TF binding region
CTTNBP2	TF binding region
CFTR	CpG island
CTTNBP2	CpG island
ENSG00000228368	chromatin interactions
ENSG00000105976	chromatin interactions
ENSG00000271701	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000077063	chromatin interactions
ENSG00000154438	chromatin interactions
ENSG00000226367	chromatin interactions
ENSG00000198898	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000135269	chromatin interactions

Extended variants
information (count: 1939 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1939 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6977789	chr7:117342771-117342772	Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147514700	chr7:117342777-117342778	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs34805169	chr7:117342792-117342793	Weak transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs569652827	chr7:117342801-117342802	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs112743368	chr7:117342805-117342806	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs188405180	chr7:117342861-117342862	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs573663674	chr7:117342870-117342871	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs548992621	chr7:117342873-117342874	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs567320671	chr7:117342911-117342912	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs542396926	chr7:117342915-117342916	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs559297131	chr7:117342928-117342929	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs536137332	chr7:117342950-117342951	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs554540675	chr7:117342994-117342995	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs566229933	chr7:117343033-117343034	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs539667752	chr7:117343117-117343118	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs558186310	chr7:117343130-117343131	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs576448069	chr7:117343152-117343153	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs371016009	chr7:117343157-117343158	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs180819141	chr7:117343191-117343192	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs555319516	chr7:117343197-117343198	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs573731033	chr7:117343200-117343201	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs540889502	chr7:117343225-117343226	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs28403532	chr7:117343261-117343262	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185184463	chr7:117343297-117343298	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs544883824	chr7:117343312-117343313	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs374278896	chr7:117343399-117343400	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs148568929	chr7:117343415-117343416	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs371394756	chr7:117343427-117343428	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs28460732	chr7:117343439-117343440	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77896993	chr7:117343480-117343481	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs144552464	chr7:117343489-117343490	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs565142912	chr7:117343504-117343505	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs573164142	chr7:117343603-117343604	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs530848886	chr7:117343727-117343728	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs528109608	chr7:117343730-117343731	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs377735164	chr7:117343746-117343747	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs548082609	chr7:117343836-117343837	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs192392063	chr7:117343862-117343863	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs572263985	chr7:117343863-117343864	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs551678507	chr7:117343892-117343893	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs542813232	chr7:117343907-117343908	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs537132865	chr7:117343939-117343940	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs550774615	chr7:117343950-117343951	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs183653341	chr7:117344009-117344010	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs573667663	chr7:117344012-117344013	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs371664551	chr7:117344018-117344019	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs553190161	chr7:117344023-117344024	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs112972258	chr7:117344109-117344110	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs545336347	chr7:117344144-117344145	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs563320051	chr7:117344197-117344198	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117327000-117376400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:117338800-117343200	Weak transcription	Hela-S3	cervix
3	chr7:117343200-117345000	Enhancers	Hela-S3	cervix
4	chr7:117343800-117344000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:117344200-117344400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr7:117344200-117344400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:117344400-117350000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:117344400-117364400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:117345000-117345400	Weak transcription	Hela-S3	cervix
10	chr7:117345400-117347600	Enhancers	Hela-S3	cervix
11	chr7:117346400-117347800	Enhancers	Dnd41	blood
12	chr7:117346600-117373400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:117346800-117347400	Enhancers	A549	lung
14	chr7:117347000-117347800	Enhancers	Fetal Heart	heart
15	chr7:117347000-117358000	Weak transcription	Fetal Brain Male	brain
16	chr7:117347400-117347600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr7:117347400-117347600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:117347400-117347800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:117347600-117350000	Weak transcription	Hela-S3	cervix
20	chr7:117347600-117356800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:117347600-117366600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr7:117347800-117348800	Weak transcription	Dnd41	blood
23	chr7:117347800-117351000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:117347800-117363000	Weak transcription	Fetal Heart	heart
25	chr7:117348400-117348600	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
26	chr7:117348400-117357000	Weak transcription	Fetal Lung	lung
27	chr7:117348600-117354200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr7:117348800-117351000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr7:117348800-117351800	Enhancers	Dnd41	blood
30	chr7:117349000-117359000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:117349200-117354600	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:117349600-117350800	Enhancers	Primary T cells from cord blood	blood
33	chr7:117349600-117385000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr7:117350000-117350600	Enhancers	Hela-S3	cervix
35	chr7:117350000-117352400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:117350000-117357400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr7:117350200-117356800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr7:117350200-117356800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr7:117350200-117373800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr7:117350400-117364600	Weak transcription	NHLF	lung
41	chr7:117350600-117355000	Weak transcription	Hela-S3	cervix
42	chr7:117350600-117357000	Weak transcription	Stomach Smooth Muscle	stomach
43	chr7:117350800-117357200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:117351000-117351800	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr7:117351000-117353200	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr7:117351400-117354000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:117351600-117354000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:117351600-117364600	Weak transcription	Fetal Stomach	stomach
49	chr7:117351800-117352000	Enhancers	Fetal Thymus	thymus
50	chr7:117351800-117352600	Flanking Active TSS	Dnd41	blood

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