Variant report

Variant	nsv555641
Chromosome Location	chr11:85683554-85757589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:887)
CpG islands
(count:183)
Chromatin interactive
region (count:101)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:887 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:85745847-85746142	K562	blood:	n/a	chr11:85746093-85746109
2	ARID3A	chr11:85717835-85717853	K562	blood:	n/a	n/a
3	ARID3A	chr11:85752416-85752519	K562	blood:	n/a	n/a
4	ARID3A	chr11:85746984-85746991	K562	blood:	n/a	n/a
5	ARID3A	chr11:85755776-85755794	K562	blood:	n/a	n/a
6	ARID3A	chr11:85757105-85757526	K562	blood:	n/a	n/a
7	ARID3A	chr11:85732572-85732954	K562	blood:	n/a	n/a
8	ARID3A	chr11:85752889-85753338	K562	blood:	n/a	n/a
9	ARID3A	chr11:85726451-85726487	K562	blood:	n/a	n/a
10	ARID3A	chr11:85748985-85749017	K562	blood:	n/a	n/a
11	ARID3A	chr11:85752905-85753433	HepG2	liver:	n/a	n/a
12	ATF1	chr11:85732589-85732908	K562	blood:	n/a	n/a
13	ATF1	chr11:85752964-85753255	K562	blood:	n/a	n/a
14	ATF1	chr11:85719206-85719455	K562	blood:	n/a	n/a
15	ATF2	chr11:85752892-85753316	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr11:85732265-85732778	GM12878	blood:	n/a	n/a
17	BACH1	chr11:85747287-85747355	K562	blood:	n/a	n/a
18	BACH1	chr11:85732556-85732841	K562	blood:	n/a	n/a
19	BATF	chr11:85732438-85732846	GM12878	blood:	n/a	n/a
20	BATF	chr11:85699879-85700138	GM12878	blood:	n/a	n/a
21	BATF	chr11:85732499-85732822	GM12878	blood:	n/a	n/a
22	BCL11A	chr11:85732457-85732765	GM12878	blood:	n/a	n/a
23	BCLAF1	chr11:85752911-85753373	GM12878	blood:	n/a	n/a
24	BHLHE40	chr11:85732450-85732729	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:85748794-85748974	K562	blood:	n/a	n/a
26	BHLHE40	chr11:85755754-85755828	K562	blood:	n/a	n/a
27	BRCA1	chr11:85756981-85757015	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr11:85752941-85753289	Hela-S3	cervix:	n/a	n/a
29	CCNT2	chr11:85732550-85732800	K562	blood:	n/a	n/a
30	CCNT2	chr11:85753002-85753244	K562	blood:	n/a	n/a
31	CEBPB	chr11:85685190-85685947	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:85752913-85753705	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:85726613-85726614	K562	blood:	n/a	n/a
34	CEBPB	chr11:85713540-85713817	IMR90	lung:	n/a	n/a
35	CEBPB	chr11:85685649-85685972	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:85733966-85734064	K562	blood:	n/a	n/a
37	CEBPB	chr11:85713500-85713816	K562	blood:	n/a	n/a
38	CEBPB	chr11:85713519-85713841	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:85698265-85698327	A549	lung:	n/a	n/a
40	CEBPB	chr11:85738927-85738961	HepG2	liver:	n/a	chr11:85738944-85738955 chr11:85738946-85738957
41	CEBPB	chr11:85713624-85713677	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:85685646-85685975	A549	lung:	n/a	n/a
43	CEBPB	chr11:85700528-85700538	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:85692541-85692647	K562	blood:	n/a	n/a
45	CEBPB	chr11:85685223-85685949	K562	blood:	n/a	n/a
46	CEBPB	chr11:85713553-85713792	A549	lung:	n/a	n/a
47	CEBPB	chr11:85685198-85686001	IMR90	lung:	n/a	n/a
48	CHD1	chr11:85732399-85732624	GM12878	blood:	n/a	n/a
49	CHD2	chr11:85747263-85747309	K562	blood:	n/a	n/a
50	CREB1	chr11:85752908-85753358	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:85753082-85753132	NH-A	brain:	n/a
2	chr11:85755155-85755205	SAEC	small airway:	n/a
3	chr11:85753082-85753132	GM12891	blood:	n/a
4	chr11:85753082-85753132	NHBE	bronchial:	n/a
5	chr11:85755155-85755205	PrEC	prostate:	n/a
6	chr11:85744995-85745045	HNPCEpiC	eye:	n/a
7	chr11:85755155-85755205	AG10803	skin:	n/a
8	chr11:85753082-85753132	AG04449	skin:	fetal
9	chr11:85744995-85745045	MCF-7	breast:	n/a
10	chr11:85744995-85745045	ECC-1	luminal epithelium:	n/a
11	chr11:85755155-85755205	PFSK-1	brain:	n/a
12	chr11:85744995-85745045	SK-N-SH_RA	brain:	n/a
13	chr11:85753082-85753132	U87	brain:	n/a
14	chr11:85744995-85745045	SKMC	muscle:	n/a
15	chr11:85744995-85745045	GM12878	blood:	n/a
16	chr11:85755155-85755205	HEK293	kidney:	embryo
17	chr11:85744995-85745045	HIPEpiC	eye:	n/a
18	chr11:85753082-85753132	PFSK-1	brain:	n/a
19	chr11:85753082-85753132	SAEC	small airway:	n/a
20	chr11:85744995-85745045	HCM	heart:	n/a
21	chr11:85755155-85755205	BE2_C	brain:	n/a
22	chr11:85753082-85753132	HRCEpiC	kidney:	n/a
23	chr11:85753082-85753132	IMR90	lung:	fetal
24	chr11:85744995-85745045	Hepatocyte	liver:	n/a
25	chr11:85755155-85755205	MCF-7	breast:	n/a
26	chr11:85755155-85755205	AG04449	skin:	fetal
27	chr11:85744995-85745045	AG04450	lung:	fetal
28	chr11:85744995-85745045	PFSK-1	brain:	n/a
29	chr11:85744995-85745045	T-47D	breast:	n/a
30	chr11:85753082-85753132	HAEpiC	amniotic membrane:	n/a
31	chr11:85755155-85755205	ProgFib	skin:	n/a
32	chr11:85755155-85755205	AoSMC	blood vessel:	n/a
33	chr11:85744995-85745045	NHBE	bronchial:	n/a
34	chr11:85744995-85745045	SK-N-MC	brain:	n/a
35	chr11:85744995-85745045	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:85753082-85753132	Caco-2	colon:	n/a
37	chr11:85744995-85745045	GM19239	blood:	n/a
38	chr11:85744995-85745045	AG09309	skin:	n/a
39	chr11:85755155-85755205	NT2-D1	testis:	n/a
40	chr11:85753082-85753132	PANC-1	pancreas:	n/a
41	chr11:85755155-85755205	HMEC	breast:	n/a
42	chr11:85755155-85755205	K562	blood:	n/a
43	chr11:85744995-85745045	HL-60	blood:	n/a
44	chr11:85744995-85745045	CMK	blood:	n/a
45	chr11:85755155-85755205	HNPCEpiC	eye:	n/a
46	chr11:85755155-85755205	LNCaP	prostate:	n/a
47	chr11:85744995-85745045	AG04449	skin:	fetal
48	chr11:85744995-85745045	Hela-S3	cervix:	n/a
49	chr11:85744995-85745045	HepG2	liver:	n/a
50	chr11:85744995-85745045	HEK293	kidney:	embryo

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:85752045..85752748-chr11:85904571..85905268,2	MCF-7	breast:
2	chr11:85742480..85744643-chr11:85751587..85754338,2	K562	blood:
3	chr11:85708264..85711014-chr11:85715226..85717341,2	MCF-7	breast:
4	chr11:85752614..85753427-chr11:85904132..85904873,3	K562	blood:
5	chr11:85744986..85747847-chr11:85984634..85986736,2	K562	blood:
6	chr11:85705046..85706635-chr11:85716420..85718688,2	K562	blood:
7	chr11:85746383..85749282-chr11:85752081..85754619,3	K562	blood:
8	chr11:85750217..85751892-chr11:85925009..85927244,2	MCF-7	breast:
9	chr11:85752698..85753481-chr11:85904297..85904797,2	MCF-7	breast:
10	chr11:85726928..85728602-chr11:85729875..85731910,2	K562	blood:
11	chr11:85752985..85755269-chr11:85927440..85930207,2	MCF-7	breast:
12	chr11:85579605..85581387-chr11:85752967..85754863,2	MCF-7	breast:
13	chr11:85689777..85692184-chr11:85694082..85696432,2	K562	blood:
14	chr11:85752345..85755214-chr11:85762057..85763811,2	K562	blood:
15	chr11:85741019..85743980-chr11:85750116..85753197,4	K562	blood:
16	chr11:85733299..85737465-chr11:85737887..85740923,4	MCF-7	breast:
17	chr11:85687169..85689223-chr11:85690219..85693440,3	K562	blood:
18	chr11:85734003..85736029-chr11:85992603..85995155,2	K562	blood:
19	chr11:85566679..85569060-chr11:85698600..85700675,2	K562	blood:
20	chr11:85741083..85743215-chr11:85744719..85747264,4	K562	blood:
21	chr11:85693271..85695512-chr11:85698266..85700653,2	K562	blood:
22	chr11:85704658..85706834-chr11:85708165..85710507,4	K562	blood:
23	chr11:85700649..85702593-chr11:85712728..85715089,2	K562	blood:
24	chr11:85752681..85753613-chr11:85986298..85987019,2	K562	blood:
25	chr11:85741889..85743543-chr11:85978004..85980141,2	K562	blood:
26	chr11:85710067..85712653-chr11:85717011..85721337,4	K562	blood:
27	chr11:85754103..85756697-chr11:85903724..85906078,2	K562	blood:
28	chr11:85685478..85688187-chr11:85691942..85693675,2	K562	blood:
29	chr11:85750753..85754921-chr11:85777860..85781815,4	MCF-7	breast:
30	chr11:85685478..85688187-chr11:85691942..85693675,2	K562	blood:
31	chr11:85720851..85723422-chr11:85723803..85726700,2	K562	blood:
32	chr11:85740366..85741884-chr11:85743938..85745486,2	MCF-7	breast:
33	chr11:85685544..85689773-chr11:85693823..85697719,5	K562	blood:
34	chr11:85752653..85753611-chr11:85929070..85929776,5	K562	blood:
35	chr11:85687169..85689223-chr11:85690219..85693440,3	K562	blood:
36	chr11:85721705..85724500-chr11:85725494..85727078,2	MCF-7	breast:
37	chr11:85690198..85692699-chr11:85699878..85701452,2	K562	blood:
38	chr11:85702541..85705321-chr11:85738673..85740319,2	K562	blood:
39	chr11:85753274..85754881-chr11:85905097..85907303,2	MCF-7	breast:
40	chr11:85705046..85706635-chr11:85716420..85718688,2	K562	blood:
41	chr11:85682994..85684881-chr11:85691232..85694113,2	K562	blood:
42	chr11:85702541..85705321-chr11:85738673..85740319,2	K562	blood:
43	chr11:85725973..85728229-chr11:85733987..85735840,2	K562	blood:
44	chr11:85681676..85683901-chr11:85687173..85691157,4	K562	blood:
45	chr11:85730097..85732249-chr11:85732722..85734634,2	K562	blood:
46	chr11:85565205..85567430-chr11:85698598..85700468,2	MCF-7	breast:
47	chr11:85740366..85741884-chr11:85743938..85745486,2	MCF-7	breast:
48	chr11:85739615..85742133-chr11:85904906..85907542,2	K562	blood:
49	chr11:85756990..85760040-chr11:85954686..85957890,3	K562	blood:
50	chr11:85746383..85749282-chr11:85752081..85754619,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC83-1	chr11:85718321-85719570	ENSG00000247103
2	lnc-CCDC83-1	chr11:85723166-85725382	ENSG00000247103

No data

Variant related genes	Relation type
PICALM	TF binding region
PICALM	CpG island
ENSG00000215504	chromatin interactions
ENSG00000074266	chromatin interactions
ENSG00000146731	chromatin interactions
ENSG00000073921	chromatin interactions
ENSG00000254783	chromatin interactions
ENSG00000254502	chromatin interactions
ENSG00000150676	chromatin interactions
ENSG00000254699	chromatin interactions
LIN28B	miRNA target sites

Extended variants
information (count: 3167 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3167 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10501604	chr11:85683554-85683555	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563837265	chr11:85683649-85683650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190621997	chr11:85683656-85683657	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567613498	chr11:85683676-85683677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs140191517	chr11:85683686-85683687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550193905	chr11:85683701-85683702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571593170	chr11:85683721-85683722	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536041091	chr11:85683744-85683745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554082623	chr11:85683760-85683761	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375111751	chr11:85683779-85683780	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs367616082	chr11:85683840-85683841	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536019628	chr11:85683965-85683966	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs80133204	chr11:85683968-85683969	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs181452846	chr11:85684023-85684024	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543044217	chr11:85684060-85684061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558115938	chr11:85684072-85684073	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576393471	chr11:85684102-85684103	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545314532	chr11:85684118-85684119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560575438	chr11:85684174-85684175	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34260197	chr11:85684190-85684191	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186645187	chr11:85684205-85684206	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191036281	chr11:85684243-85684244	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542843013	chr11:85684264-85684265	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75617639	chr11:85684270-85684271	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182882969	chr11:85684309-85684310	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376323178	chr11:85684358-85684359	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144669234	chr11:85684429-85684430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564138673	chr11:85684459-85684460	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528324540	chr11:85684486-85684487	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571690624	chr11:85684508-85684509	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532503022	chr11:85684560-85684561	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77821050	chr11:85684668-85684669	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148515841	chr11:85684698-85684699	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372924016	chr11:85684712-85684713	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546537644	chr11:85684766-85684767	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536495969	chr11:85684780-85684781	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554449179	chr11:85684896-85684897	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs588380	chr11:85684935-85684936	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs200063775	chr11:85684949-85684950	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192519687	chr11:85684959-85684960	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs550381940	chr11:85684989-85684990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554442568	chr11:85685035-85685036	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs72951246	chr11:85685071-85685072	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187437749	chr11:85685077-85685078	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554487128	chr11:85685078-85685079	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs572645682	chr11:85685098-85685099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375726538	chr11:85685101-85685102	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs637304	chr11:85685166-85685167	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs528277234	chr11:85685237-85685238	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs17817648	chr11:85685285-85685286	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2473 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85659400-85745800	Weak transcription	Stomach Mucosa	stomach
2	chr11:85663400-85692000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:85663800-85740200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:85664400-85687200	Strong transcription	Primary T cells from cord blood	blood
5	chr11:85664400-85693600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:85664400-85699800	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr11:85664400-85726800	Strong transcription	Liver	Liver
8	chr11:85664400-85729000	Strong transcription	Placenta	Placenta
9	chr11:85664600-85693200	Strong transcription	Fetal Thymus	thymus
10	chr11:85664600-85730800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:85664800-85689400	Strong transcription	Primary B cells from cord blood	blood
12	chr11:85664800-85733000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:85665200-85742600	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr11:85665200-85743000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:85665400-85699800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr11:85665600-85687800	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr11:85665800-85699600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr11:85665800-85701200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr11:85665800-85711400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:85666000-85735800	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:85666400-85693600	Strong transcription	Primary hematopoietic stem cells	blood
22	chr11:85667800-85701800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:85667800-85712000	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr11:85668000-85691400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:85669400-85686200	Strong transcription	Fetal Intestine Large	intestine
26	chr11:85670000-85715800	Weak transcription	Colonic Mucosa	Colon
27	chr11:85671800-85710600	Weak transcription	Psoas Muscle	Psoas
28	chr11:85672400-85685400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:85673200-85702800	Weak transcription	Small Intestine	intestine
30	chr11:85674000-85685000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr11:85674000-85695200	Strong transcription	HSMM	muscle
32	chr11:85674000-85708600	Strong transcription	K562	blood
33	chr11:85674200-85715400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr11:85675000-85693200	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr11:85675000-85742600	Strong transcription	Primary B cells from peripheral blood	blood
36	chr11:85675200-85700000	Strong transcription	GM12878-XiMat	blood
37	chr11:85675400-85683800	Strong transcription	HMEC	breast
38	chr11:85675400-85693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:85675600-85693000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:85676200-85684600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr11:85676800-85684400	Weak transcription	Brain Germinal Matrix	brain
42	chr11:85677800-85709600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:85678000-85690200	Weak transcription	Pancreas	Pancrea
44	chr11:85679000-85684200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr11:85679200-85685600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:85679400-85688600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr11:85679600-85687600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr11:85679800-85697000	Strong transcription	HUES64 Cell Line	embryonic stem cell
49	chr11:85680000-85693600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:85680200-85683800	Strong transcription	Fetal Kidney	kidney

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