Variant report

Variant	nsv967489
Chromosome Location	chr7:65445874-65469129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:918)
CpG islands
(count:977)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65447077-65447412	K562	blood:	n/a	n/a
2	ARID3A	chr7:65453282-65453411	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:65447151-65447400	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:65454435-65454695	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:65445966-65446151	K562	blood:	n/a	n/a
6	ATF1	chr7:65445769-65446159	K562	blood:	n/a	n/a
7	ATF1	chr7:65447060-65447460	K562	blood:	n/a	n/a
8	ATF1	chr7:65453324-65453356	K562	blood:	n/a	n/a
9	ATF2	chr7:65445713-65446255	GM12878	blood:	n/a	n/a
10	ATF2	chr7:65446932-65447474	GM12878	blood:	n/a	n/a
11	ATF2	chr7:65447034-65447435	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:65445705-65446301	GM12878	blood:	n/a	n/a
13	ATF2	chr7:65447052-65447518	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr7:65447033-65447445	GM12878	blood:	n/a	n/a
15	ATF3	chr7:65446985-65447520	HepG2	liver:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
16	ATF3	chr7:65447088-65447420	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
17	ATF3	chr7:65447078-65447417	HepG2	liver:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
18	ATF3	chr7:65447089-65447395	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
19	ATF3	chr7:65447012-65447430	H1-hESC	embryonic stem cell:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
20	ATF3	chr7:65446983-65447646	K562	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
21	ATF3	chr7:65446956-65447515	H1-hESC	embryonic stem cell:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
22	ATF3	chr7:65447011-65447482	GM12878	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
23	ATF3	chr7:65447143-65447363	GM12878	blood:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
24	ATF3	chr7:65446981-65447472	A549	lung:	n/a	chr7:65447245-65447265 chr7:65447240-65447260
25	BCL11A	chr7:65445804-65446185	GM12878	blood:	n/a	n/a
26	BCL3	chr7:65446964-65447481	A549	lung:	n/a	n/a
27	BCLAF1	chr7:65446977-65447523	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:65446982-65447503	K562	blood:	n/a	n/a
29	BCLAF1	chr7:65445700-65446344	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:65445743-65446248	GM12878	blood:	n/a	n/a
31	BHLHE40	chr7:65446938-65447667	GM12878	blood:	n/a	chr7:65447320-65447336
32	BHLHE40	chr7:65446962-65447716	K562	blood:	n/a	chr7:65447320-65447336
33	BHLHE40	chr7:65445579-65446242	K562	blood:	n/a	n/a
34	BHLHE40	chr7:65447115-65447406	A549	lung:	n/a	chr7:65447320-65447336
35	BHLHE40	chr7:65453207-65453397	K562	blood:	n/a	n/a
36	BHLHE40	chr7:65447033-65447638	HepG2	liver:	n/a	chr7:65447320-65447336
37	BRCA1	chr7:65447178-65447689	GM12878	blood:	n/a	n/a
38	BRCA1	chr7:65447137-65447387	HepG2	liver:	n/a	n/a
39	BRCA1	chr7:65446949-65447471	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr7:65447058-65447393	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr7:65449342-65449697	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr7:65447012-65447391	K562	blood:	n/a	n/a
43	CBX3	chr7:65445617-65446294	K562	blood:	n/a	n/a
44	CBX3	chr7:65446856-65447842	K562	blood:	n/a	n/a
45	CCNT2	chr7:65446794-65447554	K562	blood:	n/a	chr7:65447317-65447326
46	CCNT2	chr7:65445729-65446235	K562	blood:	n/a	n/a
47	CEBPB	chr7:65447074-65447384	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:65447065-65447553	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:65454001-65454668	HepG2	liver:	n/a	chr7:65454484-65454495
50	CEBPB	chr7:65454062-65454209	H1-hESC	embryonic stem cell:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65447328-65447378	ovcar-3	ovarian:	n/a
2	chr7:65447328-65447378	ovcar-3	ovarian:	n/a
3	chr7:65447418-65447468	HL-60	blood:	n/a
4	chr7:65447622-65447672	HEK293	kidney:	embryo
5	chr7:65447384-65447434	HNPCEpiC	eye:	n/a
6	chr7:65447069-65447119	NHBE	bronchial:	n/a
7	chr7:65447384-65447434	AG04450	lung:	fetal
8	chr7:65447622-65447672	AG04449	skin:	fetal
9	chr7:65449491-65449541	MCF-7	breast:	n/a
10	chr7:65447489-65447539	GM12891	blood:	n/a
11	chr7:65447249-65447299	ProgFib	skin:	n/a
12	chr7:65447565-65447615	AG04449	skin:	fetal
13	chr7:65447069-65447119	ovcar-3	ovarian:	n/a
14	chr7:65447069-65447119	HRCEpiC	kidney:	n/a
15	chr7:65447418-65447468	BJ	skin:	n/a
16	chr7:65447322-65447372	NT2-D1	testis:	n/a
17	chr7:65447249-65447299	HCT-116	colon:	n/a
18	chr7:65447249-65447299	Caco-2	colon:	n/a
19	chr7:65447489-65447539	HCF	heart:	n/a
20	chr7:65447339-65447389	GM12891	blood:	n/a
21	chr7:65447565-65447615	HCPEpiC	choroid plexus:	n/a
22	chr7:65447069-65447119	A549	lung:	n/a
23	chr7:65447489-65447539	HCM	heart:	n/a
24	chr7:65447322-65447372	Hela-S3	cervix:	n/a
25	chr7:65447339-65447389	Hepatocyte	liver:	n/a
26	chr7:65447339-65447389	HL-60	blood:	n/a
27	chr7:65447242-65447292	H1-hESC	embryonic stem cell:	embryo
28	chr7:65447249-65447299	PrEC	prostate:	n/a
29	chr7:65447622-65447672	MCF10A-Er-Src	breast:	n/a
30	chr7:65447489-65447539	PFSK-1	brain:	n/a
31	chr7:65447451-65447501	GM12878	blood:	n/a
32	chr7:65447451-65447501	HepG2	liver:	n/a
33	chr7:65447328-65447378	SK-N-SH	brain:	n/a
34	chr7:65447332-65447382	AoSMC	blood vessel:	n/a
35	chr7:65447565-65447615	MCF10A-Er-Src	breast:	n/a
36	chr7:65449491-65449541	GM12891	blood:	n/a
37	chr7:65447138-65447188	T-47D	breast:	n/a
38	chr7:65447384-65447434	PFSK-1	brain:	n/a
39	chr7:65447622-65447672	GM12878	blood:	n/a
40	chr7:65447328-65447378	RPTEC	kidney:	n/a
41	chr7:65447332-65447382	HMEC	breast:	n/a
42	chr7:65447113-65447163	AG04450	lung:	fetal
43	chr7:65447242-65447292	Caco-2	colon:	n/a
44	chr7:65447622-65447672	NHDF-neo	bronchial:	n/a
45	chr7:65447069-65447119	HRE	kidney:	n/a
46	chr7:65447332-65447382	AG10803	skin:	n/a
47	chr7:65447339-65447389	HCT-116	colon:	n/a
48	chr7:65447138-65447188	IMR90	lung:	fetal
49	chr7:65447069-65447119	U87	brain:	n/a
50	chr7:65447113-65447163	NB4	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65431377..65432977-chr7:65445764..65448122,2	K562	blood:
2	chr7:65438802..65441733-chr7:65444240..65447107,3	MCF-7	breast:
3	chr7:65446738..65449065-chr7:65452732..65454803,2	K562	blood:
4	chr7:65445709..65448649-chr7:65579782..65581390,2	K562	blood:
5	chr7:65444977..65446741-chr7:65453126..65455205,2	K562	blood:
6	chr11:10829765..10830505-chr7:65446635..65447376,2	Hela-S3	cervix:
7	chr7:65419413..65421834-chr7:65450885..65452622,2	K562	blood:
8	chr12:57039358..57039922-chr7:65446744..65447549,2	Hela-S3	cervix:
9	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:

No data

Variant related genes	Relation type
GUSB	TF binding region
ENSG00000224365	TF binding region
GUSB	CpG island
ENSG00000224365	CpG island
ENSG00000241258	chromatin interactions
ENSG00000196715	chromatin interactions
ENSG00000169919	chromatin interactions
ENSG00000110955	chromatin interactions
ENSG00000110321	chromatin interactions

Extended variants
information (count: 823 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546117603	chr7:65445930-65445931	Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs113280671	chr7:65445963-65445964	Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs181497670	chr7:65445978-65445979	Flanking Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs541628089	chr7:65446037-65446038	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs561941113	chr7:65446045-65446046	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs527349927	chr7:65446058-65446059	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs547130670	chr7:65446070-65446071	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs139032620	chr7:65446079-65446080	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs73150009	chr7:65446082-65446083	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs550919882	chr7:65446097-65446098	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs574375317	chr7:65446102-65446103	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs532791912	chr7:65446120-65446121	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs184260361	chr7:65446122-65446123	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs569978543	chr7:65446149-65446150	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs374269696	chr7:65446157-65446158	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs555631844	chr7:65446176-65446177	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs7801713	chr7:65446187-65446188	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs374713676	chr7:65446206-65446207	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs139960341	chr7:65446220-65446221	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs546603873	chr7:65446221-65446222	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs71051326	chr7:65446233-65446234	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs188494920	chr7:65446245-65446246	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs534801652	chr7:65446277-65446278	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs558331546	chr7:65446395-65446396	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs578057296	chr7:65446424-65446425	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs537478601	chr7:65446439-65446440	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs557407904	chr7:65446458-65446459	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs543096263	chr7:65446469-65446470	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs1723276	chr7:65446470-65446471	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs1701764	chr7:65446471-65446472	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs542111321	chr7:65446501-65446502	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs200262205	chr7:65446526-65446527	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs561692592	chr7:65446569-65446570	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs113706592	chr7:65446579-65446580	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs540701047	chr7:65446589-65446590	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs563872660	chr7:65446603-65446604	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs76375516	chr7:65446626-65446627	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs562336295	chr7:65446672-65446673	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs180910743	chr7:65446684-65446685	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs533096468	chr7:65446715-65446716	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs549334852	chr7:65446737-65446738	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs563296056	chr7:65446749-65446750	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs529518331	chr7:65446773-65446774	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs549693410	chr7:65446787-65446788	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs551143349	chr7:65446864-65446865	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs373155959	chr7:65446918-65446919	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs375779624	chr7:65446939-65446940	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs377626207	chr7:65446941-65446942	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs551892631	chr7:65446970-65446971	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs571736757	chr7:65446986-65446987	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Chronic myeloid leukemia	18641042	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65418800-65446000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:65438400-65446000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:65439600-65446200	Weak transcription	Psoas Muscle	Psoas
4	chr7:65444000-65446000	Transcr. at gene 5' and 3'	Dnd41	blood
5	chr7:65444400-65446400	Weak transcription	Aorta	Aorta
6	chr7:65444800-65446000	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
7	chr7:65445200-65446000	Enhancers	Primary hematopoietic stem cells	blood
8	chr7:65445200-65446000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr7:65445200-65446000	Genic enhancers	Fetal Muscle Trunk	muscle
10	chr7:65445200-65446000	Enhancers	Left Ventricle	heart
11	chr7:65445200-65446200	Enhancers	Primary B cells from peripheral blood	blood
12	chr7:65445200-65446600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr7:65445400-65446000	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:65445400-65446000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:65445400-65446000	Transcr. at gene 5' and 3'	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:65445400-65446000	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr7:65445400-65446000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:65445400-65446000	Enhancers	Placenta	Placenta
19	chr7:65445400-65446000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
20	chr7:65445400-65446000	Flanking Active TSS	GM12878-XiMat	blood
21	chr7:65445400-65446200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:65445400-65446200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:65445400-65446200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
24	chr7:65445400-65446200	Flanking Active TSS	Colon Smooth Muscle	Colon
25	chr7:65445400-65446200	Enhancers	Fetal Brain Male	brain
26	chr7:65445400-65446200	Transcr. at gene 5' and 3'	Thymus	Thymus
27	chr7:65445400-65446200	Flanking Active TSS	Hela-S3	cervix
28	chr7:65445400-65446400	Flanking Active TSS	Liver	Liver
29	chr7:65445400-65446400	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr7:65445400-65446400	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr7:65445400-65446400	Flanking Active TSS	HepG2	liver
32	chr7:65445400-65446600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr7:65445400-65446600	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr7:65445400-65446600	Flanking Active TSS	Duodenum Mucosa	Duodenum
35	chr7:65445400-65446800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr7:65445400-65446800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr7:65445400-65446800	Enhancers	Fetal Heart	heart
38	chr7:65445400-65447600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
39	chr7:65445600-65446000	Transcr. at gene 5' and 3'	HUES48 Cell Line	embryonic stem cell
40	chr7:65445600-65446000	Transcr. at gene 5' and 3'	iPS-18 Cell Line	embryonic stem cell
41	chr7:65445600-65446000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr7:65445600-65446000	Flanking Active TSS	Esophagus	oesophagus
43	chr7:65445600-65446000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
44	chr7:65445600-65446000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
45	chr7:65445600-65446000	Enhancers	Ovary	ovary
46	chr7:65445600-65446000	Transcr. at gene 5' and 3'	K562	blood
47	chr7:65445600-65446000	Enhancers	NHEK	skin
48	chr7:65445600-65446200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
49	chr7:65445600-65446200	Transcr. at gene 5' and 3'	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:65445600-65446200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell

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