Variant report

Variant	nsv888972
Chromosome Location	chr7:110470629-110635497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:708)
CpG islands
(count:488)
Chromatin interactive
region (count:52)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110634723-110635192	K562	blood:	n/a	n/a
2	ARID3A	chr7:110496770-110497154	HepG2	liver:	n/a	chr7:110496826-110496842
3	ARID3A	chr7:110496933-110497133	K562	blood:	n/a	n/a
4	ATF1	chr7:110594853-110594948	K562	blood:	n/a	n/a
5	ATF1	chr7:110480226-110480397	K562	blood:	n/a	n/a
6	ATF1	chr7:110634674-110635014	K562	blood:	n/a	n/a
7	ATF2	chr7:110559170-110559447	GM12878	blood:	n/a	n/a
8	ATF3	chr7:110629178-110629445	K562	blood:	n/a	n/a
9	ATF3	chr7:110634636-110635037	K562	blood:	n/a	n/a
10	BACH1	chr7:110496791-110497114	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:110584962-110585666	H1-hESC	embryonic stem cell:	n/a	chr7:110585569-110585583
12	BACH1	chr7:110566972-110567002	K562	blood:	n/a	n/a
13	BACH1	chr7:110490612-110490652	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr7:110559184-110559475	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
15	BATF	chr7:110559152-110559518	GM12878	blood:	n/a	chr7:110559283-110559292 chr7:110559329-110559340 chr7:110559453-110559461
16	BATF	chr7:110554297-110554621	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:110559122-110559539	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:110559197-110559496	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:110634646-110634901	K562	blood:	n/a	n/a
20	BHLHE40	chr7:110559153-110559472	GM12878	blood:	n/a	n/a
21	CBX3	chr7:110634597-110635044	K562	blood:	n/a	n/a
22	CCNT2	chr7:110511063-110511211	K562	blood:	n/a	n/a
23	CCNT2	chr7:110634682-110634982	K562	blood:	n/a	chr7:110634847-110634867
24	CEBPB	chr7:110529337-110529519	A549	lung:	n/a	n/a
25	CEBPB	chr7:110605295-110605582	IMR90	lung:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
26	CEBPB	chr7:110506409-110506739	H1-hESC	embryonic stem cell:	n/a	chr7:110506562-110506573
27	CEBPB	chr7:110563061-110563322	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:110475979-110476282	Hela-S3	cervix:	n/a	chr7:110476130-110476143
29	CEBPB	chr7:110562920-110563368	A549	lung:	n/a	n/a
30	CEBPB	chr7:110524438-110524770	IMR90	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
31	CEBPB	chr7:110524419-110524763	HepG2	liver:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
32	CEBPB	chr7:110506562-110506564	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:110562932-110563401	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:110634644-110635105	K562	blood:	n/a	n/a
35	CEBPB	chr7:110506417-110506734	HepG2	liver:	n/a	chr7:110506562-110506573
36	CEBPB	chr7:110501386-110501390	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr7:110501336-110501536	IMR90	lung:	n/a	chr7:110501390-110501401
38	CEBPB	chr7:110501259-110501500	A549	lung:	n/a	chr7:110501390-110501401
39	CEBPB	chr7:110501220-110501586	HepG2	liver:	n/a	chr7:110501390-110501401
40	CEBPB	chr7:110524427-110524734	K562	blood:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
41	CEBPB	chr7:110562837-110563369	MCF-7	breast:	n/a	n/a
42	CEBPB	chr7:110472128-110472426	HepG2	liver:	n/a	chr7:110472267-110472278
43	CEBPB	chr7:110605335-110605583	A549	lung:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
44	CEBPB	chr7:110605295-110605603	HepG2	liver:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
45	CEBPB	chr7:110586732-110586873	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr7:110602043-110602084	K562	blood:	n/a	n/a
47	CEBPB	chr7:110524467-110524738	A549	lung:	n/a	chr7:110524596-110524605 chr7:110524594-110524607 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524596-110524605 chr7:110524594-110524605 chr7:110524595-110524606
48	CEBPB	chr7:110605370-110605573	K562	blood:	n/a	chr7:110605435-110605448 chr7:110605435-110605446
49	CEBPB	chr7:110501269-110501507	Hela-S3	cervix:	n/a	chr7:110501390-110501401
50	CEBPB	chr7:110501231-110501585	HepG2	liver:	n/a	chr7:110501390-110501401

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110484554-110484604	H1-hESC	embryonic stem cell:	embryo
2	chr7:110482491-110482541	HEK293	kidney:	embryo
3	chr7:110506411-110506461	SAEC	small airway:	n/a
4	chr7:110562986-110563036	NHDF-neo	bronchial:	n/a
5	chr7:110496797-110496847	BE2_C	brain:	n/a
6	chr7:110511335-110511385	HMEC	breast:	n/a
7	chr7:110511335-110511385	CMK	blood:	n/a
8	chr7:110562986-110563036	H1-hESC	embryonic stem cell:	embryo
9	chr7:110484554-110484604	HMEC	breast:	n/a
10	chr7:110482491-110482541	ProgFib	skin:	n/a
11	chr7:110506411-110506461	LNCaP	prostate:	n/a
12	chr7:110484554-110484604	IMR90	lung:	fetal
13	chr7:110585140-110585190	HCPEpiC	choroid plexus:	n/a
14	chr7:110547138-110547188	AG09319	gingival:	n/a
15	chr7:110585140-110585190	HL-60	blood:	n/a
16	chr7:110562986-110563036	MCF10A-Er-Src	breast:	n/a
17	chr7:110484554-110484604	HAEpiC	amniotic membrane:	n/a
18	chr7:110484554-110484604	PFSK-1	brain:	n/a
19	chr7:110585140-110585190	RPTEC	kidney:	n/a
20	chr7:110506411-110506461	HEK293	kidney:	embryo
21	chr7:110511335-110511385	U87	brain:	n/a
22	chr7:110482491-110482541	AG04449	skin:	fetal
23	chr7:110506411-110506461	HMEC	breast:	n/a
24	chr7:110482491-110482541	Jurkat	blood:	n/a
25	chr7:110506411-110506461	IMR90	lung:	fetal
26	chr7:110562986-110563036	NB4	blood:	n/a
27	chr7:110496797-110496847	HRPEpiC	eye:	n/a
28	chr7:110547138-110547188	BE2_C	brain:	n/a
29	chr7:110547138-110547188	Hepatocyte	liver:	n/a
30	chr7:110496797-110496847	Hela-S3	cervix:	n/a
31	chr7:110585140-110585190	Jurkat	blood:	n/a
32	chr7:110496797-110496847	NH-A	brain:	n/a
33	chr7:110547138-110547188	GM12891	blood:	n/a
34	chr7:110482491-110482541	AG09319	gingival:	n/a
35	chr7:110482491-110482541	MCF10A-Er-Src	breast:	n/a
36	chr7:110506411-110506461	AG09309	skin:	n/a
37	chr7:110547138-110547188	BJ	skin:	n/a
38	chr7:110585140-110585190	HEEpiC	esophagus:	n/a
39	chr7:110562986-110563036	HMEC	breast:	n/a
40	chr7:110484554-110484604	NH-A	brain:	n/a
41	chr7:110585140-110585190	AG10803	skin:	n/a
42	chr7:110547138-110547188	SKMC	muscle:	n/a
43	chr7:110484554-110484604	Jurkat	blood:	n/a
44	chr7:110484554-110484604	NT2-D1	testis:	n/a
45	chr7:110496797-110496847	AG09309	skin:	n/a
46	chr7:110482491-110482541	PFSK-1	brain:	n/a
47	chr7:110482491-110482541	HCPEpiC	choroid plexus:	n/a
48	chr7:110496797-110496847	MCF-7	breast:	n/a
49	chr7:110562986-110563036	SKMC	muscle:	n/a
50	chr7:110562986-110563036	A549	lung:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:110505153..110508497-chr7:110509523..110512758,4	K562	blood:
2	chr7:110491238..110492962-chr7:110493024..110495999,2	MCF-7	breast:
3	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
4	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
5	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
6	chr7:110486220..110490301-chr7:110491105..110494112,5	K562	blood:
7	chr7:110569192..110573990-chr7:110577708..110581637,5	K562	blood:
8	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
9	chr7:110481885..110484031-chr7:110503607..110505454,2	K562	blood:
10	chr7:110494179..110496543-chr7:110498006..110500004,2	MCF-7	breast:
11	chr1:244816363..244816913-chr7:110550021..110550823,2	MCF-7	breast:
12	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
13	chr7:110506997..110509461-chr7:110511258..110513064,2	K562	blood:
14	chr7:110561201..110563985-chr7:110569951..110571783,2	K562	blood:
15	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
16	chr7:110586343..110587993-chr7:110588822..110590951,2	MCF-7	breast:
17	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:
18	chr7:110514426..110517089-chr7:110544753..110547740,2	K562	blood:
19	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
20	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
21	chr6:22768459..22769224-chr7:110535482..110536237,2	MCF-7	breast:
22	chr7:110497630..110499420-chr7:110504943..110507709,2	K562	blood:
23	chr7:110562762..110564605-chr7:110608157..110609660,2	K562	blood:
24	chr7:110506997..110509461-chr7:110511258..110513064,2	K562	blood:
25	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
26	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
27	chr7:110467805..110472166-chr7:110475358..110479910,4	K562	blood:
28	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
29	chr7:110467805..110472166-chr7:110475358..110479910,4	K562	blood:
30	chr7:110488051..110490301-chr7:110491279..110492842,2	K562	blood:
31	chr7:110528672..110530178-chr7:110533792..110535345,2	K562	blood:
32	chr7:110486220..110490301-chr7:110491105..110494112,5	K562	blood:
33	chr7:110601538..110603235-chr7:110611982..110613966,2	K562	blood:
34	chr7:110497630..110499420-chr7:110504943..110507709,2	K562	blood:
35	chr7:110505153..110508497-chr7:110509523..110512758,4	K562	blood:
36	chr7:110635157..110638146-chr7:111201987..111204497,2	K562	blood:
37	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
38	chr7:110630007..110632205-chr7:110633801..110636131,2	K562	blood:
39	chr7:110543756..110546433-chr7:110564740..110566931,2	MCF-7	breast:
40	chr7:110634034..110636972-chr7:110638479..110640199,3	K562	blood:
41	chr7:110488051..110490301-chr7:110491279..110492842,2	K562	blood:
42	chr7:110474759..110477642-chr7:110478690..110480944,3	K562	blood:
43	chr7:110524744..110527697-chr7:110528738..110530755,2	K562	blood:
44	chr7:110545807..110549093-chr7:110551950..110553990,3	K562	blood:
45	chr7:110566336..110568071-chr7:110568673..110570980,2	MCF-7	breast:
46	chr7:110494179..110496543-chr7:110498006..110500004,2	MCF-7	breast:
47	chr7:110562485..110565430-chr7:110569547..110571783,2	K562	blood:
48	chr7:110491238..110492962-chr7:110493024..110495999,2	MCF-7	breast:
49	chr7:110474759..110477642-chr7:110478690..110480944,3	K562	blood:
50	chr7:110551799..110553652-chr7:110557425..110559559,2	K562	blood:

No data

Variant related genes	Relation type
IMMP2L	TF binding region
ENSG00000221279	TF binding region
IMMP2L	CpG island
ENSG00000221279	CpG island
ENSG00000121644	chromatin interactions
ENSG00000184903	chromatin interactions

Extended variants
information (count: 5276 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5276 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1528035	chr7:110470629-110470630	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535927953	chr7:110470631-110470632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556128460	chr7:110470646-110470647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576001320	chr7:110470647-110470648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563132419	chr7:110470658-110470659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538619187	chr7:110470672-110470673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138345328	chr7:110470723-110470724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376795134	chr7:110470724-110470725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12673194	chr7:110470743-110470744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555034704	chr7:110470763-110470764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113667166	chr7:110470764-110470765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578242924	chr7:110470795-110470796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569193607	chr7:110470844-110470845	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181827890	chr7:110470869-110470870	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574080736	chr7:110470877-110470878	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576372582	chr7:110470920-110470921	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113540945	chr7:110470925-110470926	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542176412	chr7:110470952-110470953	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185183297	chr7:110470995-110470996	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562987737	chr7:110471023-110471024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531646257	chr7:110471035-110471036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188040527	chr7:110471050-110471051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376047613	chr7:110471053-110471054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181241603	chr7:110471078-110471079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575078561	chr7:110471079-110471080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547200154	chr7:110471123-110471124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112737760	chr7:110471136-110471137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs58926710	chr7:110471240-110471241	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs143428724	chr7:110471321-110471322	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569710380	chr7:110471369-110471370	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572333472	chr7:110471382-110471383	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs953146	chr7:110471397-110471398	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs558552206	chr7:110471420-110471421	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs953143	chr7:110471452-110471453	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147984201	chr7:110471484-110471485	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs57646158	chr7:110471547-110471548	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs953144	chr7:110471552-110471553	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73716459	chr7:110471557-110471558	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs543188781	chr7:110471577-110471578	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs112318546	chr7:110471649-110471650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556413492	chr7:110471651-110471652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576456670	chr7:110471672-110471673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs953145	chr7:110471687-110471688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191582439	chr7:110471693-110471694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200112057	chr7:110471700-110471701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs527584569	chr7:110471710-110471711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540975318	chr7:110471713-110471714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532917137	chr7:110471759-110471760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561227176	chr7:110471788-110471789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183840120	chr7:110471804-110471805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
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
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:569 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110470200-110470800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:110470200-110471200	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr7:110470200-110472800	Enhancers	Adipose Nuclei	Adipose
4	chr7:110470800-110471000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:110470800-110471200	Enhancers	Colonic Mucosa	Colon
6	chr7:110470800-110471200	Enhancers	Fetal Intestine Large	intestine
7	chr7:110470800-110471200	Enhancers	Fetal Intestine Small	intestine
8	chr7:110470800-110471200	Enhancers	Fetal Muscle Leg	muscle
9	chr7:110470800-110471200	Enhancers	Right Atrium	heart
10	chr7:110470800-110471400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr7:110470800-110471800	Enhancers	Fetal Heart	heart
12	chr7:110470800-110472600	Enhancers	HepG2	liver
13	chr7:110471000-110471200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:110471000-110471200	Enhancers	Aorta	Aorta
15	chr7:110471000-110471400	Enhancers	Right Ventricle	heart
16	chr7:110471200-110471600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:110471200-110471600	Weak transcription	Aorta	Aorta
18	chr7:110471200-110473800	Weak transcription	Fetal Intestine Large	intestine
19	chr7:110471200-110474200	Weak transcription	Fetal Intestine Small	intestine
20	chr7:110471200-110475000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr7:110471400-110475000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr7:110471600-110472800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:110471800-110472000	Enhancers	Small Intestine	intestine
24	chr7:110472000-110472200	Enhancers	Aorta	Aorta
25	chr7:110472600-110475600	Weak transcription	HepG2	liver
26	chr7:110473800-110474000	Enhancers	Fetal Intestine Large	intestine
27	chr7:110473800-110474000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr7:110474000-110474400	Weak transcription	Fetal Intestine Large	intestine
29	chr7:110474000-110474600	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr7:110474200-110476400	Enhancers	Fetal Intestine Small	intestine
31	chr7:110474400-110475200	Enhancers	Small Intestine	intestine
32	chr7:110474400-110475600	Enhancers	Primary T cells from cord blood	blood
33	chr7:110474400-110476600	Enhancers	Fetal Intestine Large	intestine
34	chr7:110474600-110475400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr7:110474600-110475600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr7:110474800-110475200	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr7:110474800-110475800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr7:110474800-110475800	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:110474800-110476000	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr7:110474800-110476200	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr7:110475000-110475400	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr7:110475000-110475400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr7:110475000-110475600	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr7:110475000-110475600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:110475000-110475800	Enhancers	Dnd41	blood
46	chr7:110475200-110475600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:110475200-110476400	Enhancers	Hela-S3	cervix
48	chr7:110475200-110480000	Weak transcription	Small Intestine	intestine
49	chr7:110475400-110476000	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr7:110475600-110476400	Enhancers	HepG2	liver

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