Variant report

Variant	nsv606339
Chromosome Location	chr7:16852808-17004301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1565)
CpG islands
(count:1282)
Chromatin interactive
region (count:122)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16886912-16887247	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:16954335-16954897	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:16967623-16968007	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:16998359-16998738	HepG2	liver:	n/a	n/a
5	ATF1	chr7:16920513-16920521	K562	blood:	n/a	n/a
6	ATF1	chr7:16938123-16938126	K562	blood:	n/a	n/a
7	ATF1	chr7:16955835-16955974	K562	blood:	n/a	n/a
8	ATF3	chr7:16886770-16887562	A549	lung:	n/a	n/a
9	ATF3	chr7:16955783-16956099	K562	blood:	n/a	n/a
10	ATF3	chr7:16886801-16887449	A549	lung:	n/a	n/a
11	ATF3	chr7:16944740-16945401	A549	lung:	n/a	n/a
12	BCL3	chr7:16944766-16945589	A549	lung:	n/a	n/a
13	BCL3	chr7:16886665-16887601	A549	lung:	n/a	n/a
14	BCL3	chr7:16886626-16887591	A549	lung:	n/a	n/a
15	BCL3	chr7:16944794-16945427	A549	lung:	n/a	n/a
16	BHLHE40	chr7:16955793-16956042	K562	blood:	n/a	n/a
17	BRCA1	chr7:16886387-16887480	Hela-S3	cervix:	n/a	chr7:16886665-16886672
18	BRCA1	chr7:17002614-17002970	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:16955847-16956041	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr7:16859128-16859157	GM12878	blood:	n/a	n/a
21	CBX3	chr7:16987785-16987980	K562	blood:	n/a	n/a
22	CEBPB	chr7:16986099-16986146	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:16954431-16954728	A549	lung:	n/a	chr7:16954714-16954722
24	CEBPB	chr7:16852900-16853100	K562	blood:	n/a	n/a
25	CEBPB	chr7:16960712-16961109	A549	lung:	n/a	n/a
26	CEBPB	chr7:16975016-16975338	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:16961496-16962032	MCF-7	breast:	n/a	n/a
28	CEBPB	chr7:16895188-16895415	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:16886971-16887172	K562	blood:	n/a	chr7:16887030-16887041
30	CEBPB	chr7:16939879-16940162	K562	blood:	n/a	chr7:16940012-16940023
31	CEBPB	chr7:16955017-16955459	MCF-7	breast:	n/a	chr7:16955093-16955110
32	CEBPB	chr7:16886566-16887551	A549	lung:	n/a	chr7:16887030-16887041
33	CEBPB	chr7:16886925-16887186	IMR90	lung:	n/a	chr7:16887030-16887041
34	CEBPB	chr7:17002622-17003009	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:16954349-16954765	HepG2	liver:	n/a	chr7:16954714-16954722
36	CEBPB	chr7:16852848-16853167	MCF-7	breast:	n/a	n/a
37	CEBPB	chr7:16886891-16887218	HepG2	liver:	n/a	chr7:16887030-16887041
38	CEBPB	chr7:16886195-16887591	Hela-S3	cervix:	n/a	chr7:16887030-16887041
39	CEBPB	chr7:16997229-16997330	IMR90	lung:	n/a	chr7:16997310-16997321
40	CEBPB	chr7:16966632-16967029	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr7:16954446-16954746	MCF-7	breast:	n/a	chr7:16954714-16954722
42	CEBPB	chr7:16939900-16940158	Hela-S3	cervix:	n/a	chr7:16940012-16940023
43	CEBPB	chr7:16939841-16940183	HepG2	liver:	n/a	chr7:16940012-16940023
44	CEBPB	chr7:16895239-16895386	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:16998429-16998711	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:16852829-16853135	A549	lung:	n/a	n/a
47	CEBPB	chr7:16954416-16954663	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:16948444-16948631	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:16934273-16934451	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:16886822-16887457	A549	lung:	n/a	chr7:16887030-16887041

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16890879-16890929	AG09309	skin:	n/a
2	chr7:16890879-16890929	AG09309	skin:	n/a
3	chr7:16945442-16945492	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:16922492-16922542	BJ	skin:	n/a
5	chr7:16913845-16913895	HCPEpiC	choroid plexus:	n/a
6	chr7:16921699-16921749	HPAEpiC	pulmonary alveolar:	n/a
7	chr7:16948307-16948357	HUVEC	blood vessel:	n/a
8	chr7:16891079-16891129	ECC-1	luminal epithelium:	n/a
9	chr7:16920271-16920321	SAEC	small airway:	n/a
10	chr7:16922492-16922542	Caco-2	colon:	n/a
11	chr7:16890775-16890825	SK-N-MC	brain:	n/a
12	chr7:16887412-16887462	Hela-S3	cervix:	n/a
13	chr7:16956550-16956600	HRCEpiC	kidney:	n/a
14	chr7:16890431-16890481	NHBE	bronchial:	n/a
15	chr7:16913845-16913895	AG09319	gingival:	n/a
16	chr7:16913845-16913895	SAEC	small airway:	n/a
17	chr7:16890769-16890819	HRE	kidney:	n/a
18	chr7:16922492-16922542	NHBE	bronchial:	n/a
19	chr7:16921699-16921749	GM19239	blood:	n/a
20	chr7:16922326-16922376	SK-N-SH	brain:	n/a
21	chr7:16887412-16887462	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:16966323-16966373	HL-60	blood:	n/a
23	chr7:16922492-16922542	U87	brain:	n/a
24	chr7:16879330-16879380	HNPCEpiC	eye:	n/a
25	chr7:16879330-16879380	HL-60	blood:	n/a
26	chr7:16890431-16890481	HUVEC	blood vessel:	n/a
27	chr7:16948307-16948357	ECC-1	luminal epithelium:	n/a
28	chr7:16890769-16890819	NB4	blood:	n/a
29	chr7:16966323-16966373	HMEC	breast:	n/a
30	chr7:16922492-16922542	CMK	blood:	n/a
31	chr7:16920271-16920321	PrEC	prostate:	n/a
32	chr7:16966323-16966373	CMK	blood:	n/a
33	chr7:16922492-16922542	ECC-1	luminal epithelium:	n/a
34	chr7:16913845-16913895	PANC-1	pancreas:	n/a
35	chr7:16887412-16887462	HL-60	blood:	n/a
36	chr7:16879330-16879380	SKMC	muscle:	n/a
37	chr7:16890879-16890929	HCF	heart:	n/a
38	chr7:16921699-16921749	AG10803	skin:	n/a
39	chr7:16890431-16890481	HRCEpiC	kidney:	n/a
40	chr7:16890769-16890819	HIPEpiC	eye:	n/a
41	chr7:16890879-16890929	PFSK-1	brain:	n/a
42	chr7:16966323-16966373	H1-hESC	embryonic stem cell:	embryo
43	chr7:16890769-16890819	SK-N-SH_RA	brain:	n/a
44	chr7:16922421-16922471	Jurkat	blood:	n/a
45	chr7:16948307-16948357	LNCaP	prostate:	n/a
46	chr7:16887412-16887462	HCPEpiC	choroid plexus:	n/a
47	chr7:16890431-16890481	BE2_C	brain:	n/a
48	chr7:16890775-16890825	ECC-1	luminal epithelium:	n/a
49	chr7:16922492-16922542	HEK293	kidney:	embryo
50	chr7:16879330-16879380	NB4	blood:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:16843577..16845838-chr7:16892758..16894482,2	MCF-7	breast:
2	chr7:16895265..16896877-chr7:16900259..16902475,2	MCF-7	breast:
3	chr7:16927987..16930694-chr7:16959155..16960951,2	MCF-7	breast:
4	chr20:3453585..3454504-chr7:16965685..16966413,2	MCF-7	breast:
5	chr7:16961828..16963481-chr7:16965140..16966973,2	K562	blood:
6	chr7:16862568..16864717-chr7:16882217..16883862,2	MCF-7	breast:
7	chr7:16876778..16878697-chr7:16884099..16885965,2	MCF-7	breast:
8	chr7:16734967..16735996-chr7:16957631..16958558,3	K562	blood:
9	chr7:16973110..16976162-chr7:16977705..16980003,3	K562	blood:
10	chr7:16843687..16847356-chr7:16880969..16885089,4	MCF-7	breast:
11	chr7:16883300..16885078-chr7:16885250..16887314,2	K562	blood:
12	chr7:16960280..16962673-chr7:16969030..16970953,2	MCF-7	breast:
13	chr7:16846231..16849111-chr7:16853009..16855819,2	K562	blood:
14	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
15	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
16	chr7:16920618..16921311-chr8:99380929..99381723,2	MCF-7	breast:
17	chr7:16842139..16846678-chr7:16885089..16889372,16	MCF-7	breast:
18	chr7:16929547..16932168-chr7:17718216..17720768,2	MCF-7	breast:
19	chr7:16882221..16884477-chr7:16885403..16887201,3	MCF-7	breast:
20	chr7:16876778..16878697-chr7:16884099..16885965,2	MCF-7	breast:
21	chr7:16847748..16852819-chr7:16884544..16888713,8	MCF-7	breast:
22	chr7:16956640..16958922-chr7:17019855..17022543,2	MCF-7	breast:
23	chr7:16966017..16967722-chr7:16978514..16980998,2	MCF-7	breast:
24	chr7:16985473..16987561-chr7:16989843..16993604,3	MCF-7	breast:
25	chr7:16852860..16855364-chr7:16884704..16887275,2	MCF-7	breast:
26	chr7:16840041..16842170-chr7:16902969..16904527,2	MCF-7	breast:
27	chr7:16862568..16864717-chr7:16882217..16883862,2	MCF-7	breast:
28	chr7:16968832..16971770-chr7:16973554..16975101,2	MCF-7	breast:
29	chr7:16840685..16841439-chr7:16957586..16958283,2	MCF-7	breast:
30	chr7:16839003..16842522-chr7:16955974..16958585,3	MCF-7	breast:
31	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
32	chr7:16985473..16987561-chr7:16989843..16993604,3	MCF-7	breast:
33	chr7:16962023..16963912-chr7:16979161..16982109,2	K562	blood:
34	chr7:16895265..16896877-chr7:16900259..16902475,2	MCF-7	breast:
35	chr7:16843304..16845867-chr7:16878790..16881977,4	MCF-7	breast:
36	chr7:16853700..16855388-chr7:16865354..16867185,2	MCF-7	breast:
37	chr7:16973925..16976162-chr7:16977721..16980003,2	K562	blood:
38	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
39	chr7:16930305..16931804-chr7:16957626..16958588,7	MCF-7	breast:
40	chr7:16847748..16852819-chr7:16884544..16888713,8	MCF-7	breast:
41	chr7:16882638..16888125-chr7:16917806..16922749,7	MCF-7	breast:
42	chr7:16880852..16883494-chr7:16885535..16888915,3	MCF-7	breast:
43	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
44	chr7:16839543..16841251-chr7:16918984..16920555,2	MCF-7	breast:
45	chr7:16922993..16923881-chr9:94630482..94631276,2	MCF-7	breast:
46	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
47	chr7:16944622..16945221-chr7:16961355..16961992,2	MCF-7	breast:
48	chr7:16931815..16932543-chr7:16957591..16958753,3	MCF-7	breast:
49	chr7:16834464..16837381-chr7:16917250..16920233,2	MCF-7	breast:
50	chr7:16930864..16931608-chr7:16957731..16958689,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGR2-1	chr7:16921568-16921597	NONHSAT119307
2	lnc-AGR2-1	chr7:16918134-16918269	NONHSAT119307
3	lnc-AGR2-1	chr7:16913040-16913467	NONHSAT119307
4	lnc-TSPAN13-1	chr7:16928245-16928509	NONHSAT119308
5	lnc-TSPAN13-2	chr7:16977849-16978181	NONHSAT119309
6	lnc-AGR3-3	chr7:17004158-17004405	NONHSAT119310

No data

Variant related genes	Relation type
ENSG00000227965	TF binding region
AGR2	TF binding region
RAD17P1	TF binding region
ENSG00000270593	TF binding region
AGR3	TF binding region
ENSG00000223867	TF binding region
ENSG00000227965	CpG island
AGR2	CpG island
RAD17P1	CpG island
ENSG00000270593	CpG island
AGR3	CpG island
ENSG00000223867	CpG island
ENSG00000106537	chromatin interactions
ENSG00000229688	chromatin interactions
ENSG00000227965	chromatin interactions
ENSG00000173467	chromatin interactions
ENSG00000228675	chromatin interactions
ENSG00000232400	chromatin interactions
ENSG00000106541	chromatin interactions
ENSG00000106546	chromatin interactions
ENSG00000223867	chromatin interactions
ENSG00000237773	chromatin interactions

Extended variants
information (count: 7082 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7082 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17136694	chr7:16852808-16852809	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556220155	chr7:16852930-16852931	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547630678	chr7:16852943-16852944	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538807856	chr7:16852953-16852954	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553957809	chr7:16852974-16852975	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547543417	chr7:16852993-16852994	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572374733	chr7:16853004-16853005	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542890760	chr7:16853008-16853009	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570811304	chr7:16853107-16853108	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368493603	chr7:16853133-16853134	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs561468224	chr7:16853143-16853144	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576384013	chr7:16853156-16853157	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187231650	chr7:16853194-16853195	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567529255	chr7:16853197-16853198	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs565342395	chr7:16853253-16853254	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143096726	chr7:16853280-16853281	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190355295	chr7:16853284-16853285	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs138738989	chr7:16853313-16853314	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs527518107	chr7:16853403-16853404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376332565	chr7:16853413-16853414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs34938176	chr7:16853414-16853415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs549249719	chr7:16853441-16853442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567495437	chr7:16853442-16853443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537800971	chr7:16853451-16853452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549520709	chr7:16853471-16853472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536555580	chr7:16853505-16853506	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35121244	chr7:16853566-16853567	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181086106	chr7:16853592-16853593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533601756	chr7:16853618-16853619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142736425	chr7:16853652-16853653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575253435	chr7:16853673-16853674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34003339	chr7:16853674-16853675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553476824	chr7:16853696-16853697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572288192	chr7:16853706-16853707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536496433	chr7:16853762-16853763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147405578	chr7:16853814-16853815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370808055	chr7:16853816-16853817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543768307	chr7:16853828-16853829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs13237401	chr7:16853866-16853867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577338948	chr7:16853881-16853882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7783269	chr7:16853882-16853883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs139624166	chr7:16853907-16853908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141809326	chr7:16853928-16853929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs114961848	chr7:16853955-16853956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561195078	chr7:16853965-16853966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572533217	chr7:16853983-16853984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150588591	chr7:16853993-16853994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs77050822	chr7:16853994-16853995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570886096	chr7:16854033-16854034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532012670	chr7:16854052-16854053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16844600-16854800	Weak transcription	Small Intestine	intestine
2	chr7:16848000-16858200	Enhancers	Stomach Mucosa	stomach
3	chr7:16849400-16853400	Enhancers	Fetal Intestine Large	intestine
4	chr7:16849400-16853400	Enhancers	Fetal Intestine Small	intestine
5	chr7:16849400-16857600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:16850800-16854600	Weak transcription	HMEC	breast
7	chr7:16851400-16854400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr7:16851600-16853400	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr7:16851600-16853400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr7:16851800-16853400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr7:16851800-16856200	Weak transcription	Hela-S3	cervix
12	chr7:16851800-16856400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:16851800-16857200	Weak transcription	NH-A	brain
14	chr7:16851800-16858200	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr7:16852200-16853200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr7:16852400-16853400	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr7:16852400-16854000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:16852800-16853000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:16852800-16853000	Flanking Active TSS	Osteobl	bone
20	chr7:16852800-16853200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr7:16852800-16853200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:16852800-16853200	Enhancers	Colonic Mucosa	Colon
23	chr7:16852800-16853200	Flanking Active TSS	A549	lung
24	chr7:16853000-16853200	Enhancers	Osteobl	bone
25	chr7:16853000-16853400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:16853200-16853400	Enhancers	Pancreas	Pancrea
27	chr7:16853200-16853400	Flanking Active TSS	Osteobl	bone
28	chr7:16853200-16854400	Weak transcription	Colonic Mucosa	Colon
29	chr7:16853200-16854800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr7:16853200-16857200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:16853200-16857800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:16853200-16858600	Enhancers	A549	lung
33	chr7:16853400-16854400	Weak transcription	Fetal Intestine Large	intestine
34	chr7:16853400-16854400	Weak transcription	Fetal Intestine Small	intestine
35	chr7:16853400-16854400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr7:16853400-16854800	Weak transcription	Pancreas	Pancrea
37	chr7:16853400-16855400	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr7:16853400-16855400	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr7:16853400-16856800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:16853400-16857000	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr7:16853400-16857400	Weak transcription	Osteobl	bone
42	chr7:16854000-16854600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:16854400-16854600	Enhancers	Colonic Mucosa	Colon
44	chr7:16854400-16855000	Enhancers	Fetal Intestine Large	intestine
45	chr7:16854400-16855600	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:16854400-16856000	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr7:16854400-16858000	Enhancers	Fetal Intestine Small	intestine
48	chr7:16854600-16855000	Weak transcription	Colonic Mucosa	Colon
49	chr7:16854600-16855000	Enhancers	HMEC	breast
50	chr7:16854600-16857200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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