Variant report

Variant	nsv824245
Chromosome Location	chr7:101455132-101461951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:101461092-101462192	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:101461170-101462030	K562	blood:	n/a	n/a
3	ARID3A	chr7:101458733-101458746	K562	blood:	n/a	n/a
4	ARID3A	chr7:101459131-101459413	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:101457931-101458268	K562	blood:	n/a	n/a
6	ARID3A	chr7:101459122-101459322	K562	blood:	n/a	n/a
7	ARID3A	chr7:101457553-101457564	K562	blood:	n/a	n/a
8	ARID3A	chr7:101457908-101458208	HepG2	liver:	n/a	n/a
9	ATF2	chr7:101458101-101458498	GM12878	blood:	n/a	n/a
10	ATF3	chr7:101457418-101457586	GM12878	blood:	n/a	n/a
11	ATF3	chr7:101457363-101457672	K562	blood:	n/a	n/a
12	BACH1	chr7:101457199-101459068	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr7:101457603-101458687	K562	blood:	n/a	n/a
14	BCL3	chr7:101457516-101458463	A549	lung:	n/a	chr7:101457612-101457625 chr7:101457901-101457910 chr7:101457611-101457624
15	BCL3	chr7:101457787-101458519	A549	lung:	n/a	chr7:101457901-101457910
16	BCLAF1	chr7:101459102-101459390	GM12878	blood:	n/a	chr7:101459194-101459203 chr7:101459195-101459208 chr7:101459191-101459200 chr7:101459190-101459203 chr7:101459192-101459205 chr7:101459193-101459206
17	BCLAF1	chr7:101457355-101457766	GM12878	blood:	n/a	chr7:101457612-101457625 chr7:101457379-101457388 chr7:101457380-101457393 chr7:101457611-101457624
18	BCLAF1	chr7:101458272-101458826	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:101457373-101457700	HepG2	liver:	n/a	chr7:101457525-101457534 chr7:101457526-101457535 chr7:101457526-101457535
20	BHLHE40	chr7:101460385-101461244	GM12878	blood:	n/a	chr7:101460862-101460871 chr7:101460862-101460871 chr7:101460397-101460413
21	BHLHE40	chr7:101460711-101461216	A549	lung:	n/a	chr7:101460862-101460871 chr7:101460862-101460871
22	BHLHE40	chr7:101456922-101459373	GM12878	blood:	n/a	chr7:101457525-101457534 chr7:101459184-101459200 chr7:101459190-101459206 chr7:101457526-101457535 chr7:101457526-101457535
23	BHLHE40	chr7:101460410-101461301	K562	blood:	n/a	chr7:101460862-101460871 chr7:101460862-101460871
24	BHLHE40	chr7:101460395-101461320	HepG2	liver:	n/a	chr7:101460862-101460871 chr7:101460862-101460871 chr7:101460397-101460413
25	BHLHE40	chr7:101457382-101457624	HepG2	liver:	n/a	chr7:101457525-101457534 chr7:101457526-101457535 chr7:101457526-101457535
26	BHLHE40	chr7:101460741-101460945	HepG2	liver:	n/a	chr7:101460862-101460871 chr7:101460862-101460871
27	BHLHE40	chr7:101457090-101459369	K562	blood:	n/a	chr7:101457525-101457534 chr7:101459184-101459200 chr7:101459190-101459206 chr7:101457526-101457535 chr7:101457526-101457535
28	BHLHE40	chr7:101457327-101459370	HepG2	liver:	n/a	chr7:101457525-101457534 chr7:101459184-101459200 chr7:101459190-101459206 chr7:101457526-101457535 chr7:101457526-101457535
29	BHLHE40	chr7:101457347-101457733	A549	lung:	n/a	chr7:101457525-101457534 chr7:101457526-101457535 chr7:101457526-101457535
30	BRCA1	chr7:101461048-101461376	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr7:101456809-101458457	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr7:101459233-101459305	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr7:101460895-101461380	K562	blood:	n/a	n/a
34	CBX3	chr7:101457037-101457798	K562	blood:	n/a	n/a
35	CBX3	chr7:101457349-101457748	K562	blood:	n/a	n/a
36	CCNT2	chr7:101457374-101457839	K562	blood:	n/a	chr7:101457374-101457383
37	CCNT2	chr7:101459826-101461251	K562	blood:	n/a	n/a
38	CCNT2	chr7:101458354-101459570	K562	blood:	n/a	chr7:101459541-101459550 chr7:101458875-101458884 chr7:101458998-101459007
39	CEBPB	chr7:101461190-101461497	IMR90	lung:	n/a	n/a
40	CEBPB	chr7:101457801-101458438	K562	blood:	n/a	n/a
41	CEBPB	chr7:101459231-101459395	K562	blood:	n/a	n/a
42	CEBPB	chr7:101458017-101458543	GM12878	blood:	n/a	n/a
43	CEBPB	chr7:101460974-101461512	K562	blood:	n/a	n/a
44	CEBPB	chr7:101459164-101459413	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:101460951-101461499	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:101456838-101458561	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:101461019-101461526	K562	blood:	n/a	n/a
48	CEBPD	chr7:101458512-101458754	HepG2	liver:	n/a	n/a
49	CEBPD	chr7:101458792-101459017	HepG2	liver:	n/a	n/a
50	CEBPD	chr7:101457437-101457695	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:101459386-101459436	NT2-D1	testis:	n/a
2	chr7:101457812-101457862	AG04450	lung:	fetal
3	chr7:101459386-101459436	NT2-D1	testis:	n/a
4	chr7:101457812-101457862	AG04450	lung:	fetal
5	chr7:101458365-101458415	HEEpiC	esophagus:	n/a
6	chr7:101460955-101461005	PrEC	prostate:	n/a
7	chr7:101457447-101457497	HIPEpiC	eye:	n/a
8	chr7:101457359-101457409	A549	lung:	n/a
9	chr7:101459954-101460004	PANC-1	pancreas:	n/a
10	chr7:101459024-101459074	RPTEC	kidney:	n/a
11	chr7:101459386-101459436	GM12891	blood:	n/a
12	chr7:101460955-101461005	AG09319	gingival:	n/a
13	chr7:101459330-101459380	GM12892	blood:	n/a
14	chr7:101459292-101459342	U87	brain:	n/a
15	chr7:101457447-101457497	HNPCEpiC	eye:	n/a
16	chr7:101459283-101459333	BJ	skin:	n/a
17	chr7:101457812-101457862	GM12878	blood:	n/a
18	chr7:101458740-101458790	SKMC	muscle:	n/a
19	chr7:101458740-101458790	NHDF-neo	bronchial:	n/a
20	chr7:101458365-101458415	HAEpiC	amniotic membrane:	n/a
21	chr7:101459024-101459074	HIPEpiC	eye:	n/a
22	chr7:101459283-101459333	A549	lung:	n/a
23	chr7:101457175-101457225	GM06990	blood:	n/a
24	chr7:101457175-101457225	HNPCEpiC	eye:	n/a
25	chr7:101461823-101461873	GM12891	blood:	n/a
26	chr7:101457812-101457862	H1-hESC	embryonic stem cell:	embryo
27	chr7:101459386-101459436	PFSK-1	brain:	n/a
28	chr7:101460955-101461005	IMR90	lung:	fetal
29	chr7:101458740-101458790	SK-N-SH_RA	brain:	n/a
30	chr7:101457647-101457697	HL-60	blood:	n/a
31	chr7:101459024-101459074	NHBE	bronchial:	n/a
32	chr7:101459386-101459436	RPTEC	kidney:	n/a
33	chr7:101459954-101460004	H1-hESC	embryonic stem cell:	embryo
34	chr7:101458433-101458483	GM19239	blood:	n/a
35	chr7:101458365-101458415	AoSMC	blood vessel:	n/a
36	chr7:101457647-101457697	T-47D	breast:	n/a
37	chr7:101457812-101457862	AG10803	skin:	n/a
38	chr7:101458433-101458483	HIPEpiC	eye:	n/a
39	chr7:101459024-101459074	SK-N-SH	brain:	n/a
40	chr7:101458365-101458415	HCM	heart:	n/a
41	chr7:101459292-101459342	Caco-2	colon:	n/a
42	chr7:101459954-101460004	T-47D	breast:	n/a
43	chr7:101458365-101458415	Hela-S3	cervix:	n/a
44	chr7:101457447-101457497	Hela-S3	cervix:	n/a
45	chr7:101458365-101458415	BJ	skin:	n/a
46	chr7:101458433-101458483	PrEC	prostate:	n/a
47	chr7:101460955-101461005	AG09309	skin:	n/a
48	chr7:101459330-101459380	HRPEpiC	eye:	n/a
49	chr7:101459283-101459333	AG04449	skin:	fetal
50	chr7:101458740-101458790	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:101456128..101458480-chr7:101471279..101473363,2	K562	blood:
2	chr20:39764220..39767002-chr7:101458142..101460292,2	MCF-7	breast:
3	chr7:101456865..101462678-chr7:101466062..101470276,9	MCF-7	breast:
4	chr7:101331319..101332632-chr7:101457135..101458012,7	MCF-7	breast:
5	chr7:101195035..101196752-chr7:101457071..101459067,2	MCF-7	breast:
6	chr1:149222882..149224744-chr7:101459055..101461575,2	MCF-7	breast:
7	chr1:156084197..156084939-chr7:101457529..101458250,2	Hela-S3	cervix:
8	chr7:101331355..101332298-chr7:101457115..101458094,12	MCF-7	breast:
9	chr1:201682650..201683305-chr7:101457575..101458388,2	Hela-S3	cervix:
10	chr7:101456296..101461488-chr7:101913983..101918398,7	MCF-7	breast:
11	chr1:28836517..28839239-chr7:101457794..101459450,2	MCF-7	breast:
12	chr13:48611688..48613332-chr7:101457559..101460225,2	MCF-7	breast:
13	chr10:126849675..126850175-chr7:101459356..101459877,2	Hela-S3	cervix:
14	chr16:2818449..2821278-chr7:101459206..101460777,2	MCF-7	breast:
15	chr15:52469891..52472535-chr7:101457623..101459859,2	MCF-7	breast:
16	chr7:101185071..101186578-chr7:101457268..101458103,4	MCF-7	breast:
17	chr12:125398918..125401326-chr7:101458032..101459768,2	K562	blood:
18	chr3:127394387..127395170-chr7:101458070..101458842,2	Hela-S3	cervix:
19	chr7:101331265..101332297-chr7:101457072..101458122,8	K562	blood:
20	chr12:53297960..53298460-chr7:101458053..101458556,2	Hela-S3	cervix:
21	chr7:101448496..101448999-chr7:101457160..101457885,2	MCF-7	breast:
22	chr7:101245522..101246394-chr7:101457419..101458061,2	K562	blood:
23	chr7:101245091..101246357-chr7:101457101..101458459,9	MCF-7	breast:
24	chr7:101338626..101341236-chr7:101455601..101457433,2	K562	blood:
25	chr1:6267970..6270950-chr7:101455402..101457329,2	K562	blood:
26	chr7:101271948..101273835-chr7:101457651..101460196,2	MCF-7	breast:
27	chr1:6268950..6269450-chr7:101457184..101457840,2	MCF-7	breast:
28	chr12:56572158..56573016-chr7:101457560..101458297,2	Hela-S3	cervix:
29	chr7:101454557..101456902-chr9:132258528..132261469,2	MCF-7	breast:
30	chr2:207024339..207026427-chr7:101458417..101459962,2	MCF-7	breast:
31	chr7:101457570..101460867-chr7:101928374..101931760,6	MCF-7	breast:
32	chr7:101455693..101458203-chr7:101915599..101917150,2	MCF-7	breast:
33	chr7:101451313..101452903-chr7:101455577..101457484,2	K562	blood:
34	chr7:101330663..101332938-chr7:101456021..101458863,3	K562	blood:
35	chr7:101454521..101456839-chr7:101502808..101505104,2	K562	blood:
36	chr7:101457026..101461124-chr7:101554455..101559051,6	MCF-7	breast:
37	chr11:134527652..134528152-chr7:101457119..101458073,2	K562	blood:
38	chr7:101330300..101332201-chr7:101453903..101456304,2	MCF-7	breast:

Variant related genes	Relation type
CUX1	TF binding region
CUX1	CpG island
ENSG00000167978	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000124181	chromatin interactions
ENSG00000158286	chromatin interactions
ENSG00000139613	chromatin interactions
ENSG00000265864	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000259294	chromatin interactions
ENSG00000226648	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000160963	chromatin interactions
ENSG00000259577	chromatin interactions
ENSG00000114942	chromatin interactions
ENSG00000175029	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000150991	chromatin interactions
ENSG00000160789	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000160999	chromatin interactions
ENSG00000114626	chromatin interactions
ENSG00000106436	chromatin interactions
ENSG00000257923	chromatin interactions
ENSG00000265345	chromatin interactions
ENSG00000116251	chromatin interactions

Extended variants
information (count: 193 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:193 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144544017	chr7:101455134-101455135	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs553719642	chr7:101455316-101455317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147855621	chr7:101455336-101455337	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532531636	chr7:101455355-101455356	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541850097	chr7:101455358-101455359	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs187307284	chr7:101455374-101455375	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs71559429	chr7:101455384-101455385	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530561320	chr7:101455438-101455439	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs141295558	chr7:101455452-101455453	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs545867436	chr7:101455462-101455463	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs200865510	chr7:101455473-101455474	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs36090391	chr7:101455474-101455475	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs192685517	chr7:101455487-101455488	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs528291478	chr7:101455522-101455523	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs546353438	chr7:101455653-101455654	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs568021415	chr7:101455655-101455656	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs529102376	chr7:101455693-101455694	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs551276565	chr7:101455815-101455816	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs548336860	chr7:101455827-101455828	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs570019616	chr7:101455829-101455830	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs562991897	chr7:101455866-101455867	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs537180294	chr7:101455887-101455888	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs529700706	chr7:101455907-101455908	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs80031117	chr7:101455908-101455909	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs143554496	chr7:101455972-101455973	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs533733301	chr7:101456029-101456030	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs185477870	chr7:101456068-101456069	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs374589815	chr7:101456097-101456098	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs189808741	chr7:101456110-101456111	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs575258285	chr7:101456124-101456125	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs193262895	chr7:101456169-101456170	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs184578293	chr7:101456184-101456185	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs547867441	chr7:101456192-101456193	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs189236922	chr7:101456253-101456254	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs545451808	chr7:101456270-101456271	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs376184059	chr7:101456281-101456282	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs73712552	chr7:101456318-101456319	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs180967757	chr7:101456335-101456336	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs201076283	chr7:101456345-101456346	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs35873051	chr7:101456346-101456347	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs397728853	chr7:101456361-101456362	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs540039004	chr7:101456364-101456365	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs533856678	chr7:101456410-101456411	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs552268635	chr7:101456449-101456450	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs566157560	chr7:101456456-101456457	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs561538582	chr7:101456465-101456466	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs185038719	chr7:101456489-101456490	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs529187536	chr7:101456569-101456570	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs550832067	chr7:101456582-101456583	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs569030369	chr7:101456594-101456595	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
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
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	19907438	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:101436800-101457400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:101448400-101456800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:101452600-101457000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:101453200-101456800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:101453600-101456200	Weak transcription	Hela-S3	cervix
6	chr7:101453600-101456800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:101453600-101456800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:101453600-101456800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:101453600-101457000	Weak transcription	HMEC	breast
10	chr7:101453800-101456800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr7:101456000-101457000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:101456200-101456800	Enhancers	A549	lung
13	chr7:101456200-101456800	Enhancers	Hela-S3	cervix
14	chr7:101456400-101456600	Enhancers	Thymus	Thymus
15	chr7:101456400-101456800	Enhancers	K562	blood
16	chr7:101456400-101457400	Enhancers	Small Intestine	intestine
17	chr7:101456600-101456800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:101456600-101457000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
19	chr7:101456600-101457200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr7:101456600-101457400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:101456600-101457600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:101456800-101457000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
23	chr7:101456800-101457000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:101456800-101457000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:101456800-101457000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
26	chr7:101456800-101457000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:101456800-101457000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:101456800-101457000	Enhancers	Primary B cells from cord blood	blood
29	chr7:101456800-101457000	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr7:101456800-101457000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
31	chr7:101456800-101457000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
32	chr7:101456800-101457000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:101456800-101457000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:101456800-101457000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:101456800-101457000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:101456800-101457000	Enhancers	Brain Angular Gyrus	brain
37	chr7:101456800-101457000	Enhancers	Colon Smooth Muscle	Colon
38	chr7:101456800-101457000	Enhancers	Ovary	ovary
39	chr7:101456800-101457000	Enhancers	Stomach Smooth Muscle	stomach
40	chr7:101456800-101457000	Bivalent Enhancer	Dnd41	blood
41	chr7:101456800-101457000	Flanking Active TSS	Hela-S3	cervix
42	chr7:101456800-101457000	Enhancers	NHEK	skin
43	chr7:101456800-101457200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:101456800-101457200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr7:101456800-101457200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:101456800-101457200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr7:101456800-101457200	Enhancers	Brain Hippocampus Middle	brain
48	chr7:101456800-101457200	Enhancers	Fetal Intestine Small	intestine
49	chr7:101456800-101457200	Enhancers	Fetal Stomach	stomach
50	chr7:101456800-101457200	Flanking Active TSS	A549	lung

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