Variant report

Variant	nsv897648
Chromosome Location	chr11:63761169-63774370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:1160)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:63767064-63767328	GM12878	blood:	n/a	n/a
2	ATF2	chr11:63766903-63767235	GM12878	blood:	n/a	n/a
3	ATF2	chr11:63765834-63766357	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr11:63772005-63772436	K562	blood:	n/a	n/a
5	ATF3	chr11:63770902-63771103	K562	blood:	n/a	chr11:63771039-63771053
6	BACH1	chr11:63767436-63767607	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:63766437-63767186	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:63764721-63765243	K562	blood:	n/a	n/a
9	BCL3	chr11:63774182-63775698	A549	lung:	n/a	chr11:63774220-63774233
10	BCL3	chr11:63768826-63769206	A549	lung:	n/a	n/a
11	BCL3	chr11:63765401-63766255	K562	blood:	n/a	n/a
12	BCLAF1	chr11:63767874-63768219	GM12878	blood:	n/a	chr11:63767947-63767960 chr11:63767943-63767956 chr11:63767949-63767962 chr11:63767950-63767963 chr11:63768128-63768141
13	BHLHE40	chr11:63768018-63768154	GM12878	blood:	n/a	chr11:63768053-63768069
14	CBX3	chr11:63772036-63772445	K562	blood:	n/a	n/a
15	CCNT2	chr11:63766172-63766838	K562	blood:	n/a	n/a
16	CCNT2	chr11:63768203-63768343	K562	blood:	n/a	n/a
17	CCNT2	chr11:63767134-63767334	K562	blood:	n/a	n/a
18	CEBPB	chr11:63762671-63762784	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr11:63762675-63762804	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:63762673-63762842	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:63762605-63762787	K562	blood:	n/a	n/a
22	CEBPB	chr11:63762666-63762798	K562	blood:	n/a	n/a
23	CEBPB	chr11:63762633-63762842	IMR90	lung:	n/a	n/a
24	CHD1	chr11:63767806-63768260	IMR90	lung:	n/a	n/a
25	CHD1	chr11:63768022-63768091	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr11:63768043-63768260	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr11:63766549-63766749	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr11:63765944-63766326	H1-hESC	embryonic stem cell:	n/a	chr11:63766291-63766301
29	CREB1	chr11:63766459-63767457	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr11:63766581-63767524	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr11:63767940-63768090	HRE	kidney:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
32	CTCF	chr11:63766640-63766790	GM12871	blood:	n/a	n/a
33	CTCF	chr11:63767620-63767770	HBMEC	blood vessel:	n/a	chr11:63767672-63767685
34	CTCF	chr11:63767849-63768259	GM12878	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
35	CTCF	chr11:63767960-63768110	GM12875	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
36	CTCF	chr11:63766640-63766790	HMEC	breast:	n/a	n/a
37	CTCF	chr11:63767020-63767170	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr11:63767960-63768110	HMEC	breast:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
39	CTCF	chr11:63767897-63768210	H1-hESC	embryonic stem cell:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
40	CTCF	chr11:63766537-63766755	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr11:63767680-63767830	GM12872	blood:	n/a	n/a
42	CTCF	chr11:63767960-63768110	HFF-Myc	foreskin:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
43	CTCF	chr11:63768280-63768430	SAEC	small airway:	n/a	n/a
44	CTCF	chr11:63767239-63767245	GM19238	blood:	n/a	n/a
45	CTCF	chr11:63767940-63768090	NHEK	skin:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
46	CTCF	chr11:63767960-63768110	GM12872	blood:	n/a	chr11:63768050-63768066 chr11:63768052-63768065 chr11:63768049-63768067 chr11:63768052-63768065
47	CTCF	chr11:63764562-63764598	GM19239	blood:	n/a	n/a
48	CTCF	chr11:63767279-63767292	GM19238	blood:	n/a	n/a
49	CTCF	chr11:63766520-63766670	AG04449	skin:	n/a	n/a
50	CTCF	chr11:63766520-63766670	HUVEC	blood vessel:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63768032-63768082	Hepatocyte	liver:	n/a
2	chr11:63768032-63768082	Hepatocyte	liver:	n/a
3	chr11:63763834-63763884	NHDF-neo	bronchial:	n/a
4	chr11:63764925-63764975	MCF10A-Er-Src	breast:	n/a
5	chr11:63764602-63764652	LNCaP	prostate:	n/a
6	chr11:63764925-63764975	HCPEpiC	choroid plexus:	n/a
7	chr11:63763834-63763884	A549	lung:	n/a
8	chr11:63772824-63772874	HIPEpiC	eye:	n/a
9	chr11:63764177-63764227	NHDF-neo	bronchial:	n/a
10	chr11:63767561-63767611	Jurkat	blood:	n/a
11	chr11:63772824-63772874	NH-A	brain:	n/a
12	chr11:63768032-63768082	LNCaP	prostate:	n/a
13	chr11:63767561-63767611	NH-A	brain:	n/a
14	chr11:63765561-63765611	HRE	kidney:	n/a
15	chr11:63772049-63772099	MCF10A-Er-Src	breast:	n/a
16	chr11:63764804-63764854	ProgFib	skin:	n/a
17	chr11:63768032-63768082	HNPCEpiC	eye:	n/a
18	chr11:63765561-63765611	IMR90	lung:	fetal
19	chr11:63766787-63766837	Jurkat	blood:	n/a
20	chr11:63766286-63766336	IMR90	lung:	fetal
21	chr11:63768665-63768715	HCPEpiC	choroid plexus:	n/a
22	chr11:63764217-63764267	RPTEC	kidney:	n/a
23	chr11:63768032-63768082	GM06990	blood:	n/a
24	chr11:63764925-63764975	SK-N-SH_RA	brain:	n/a
25	chr11:63764217-63764267	Jurkat	blood:	n/a
26	chr11:63764925-63764975	K562	blood:	n/a
27	chr11:63767561-63767611	GM12878	blood:	n/a
28	chr11:63768040-63768090	AG09309	skin:	n/a
29	chr11:63768412-63768462	GM06990	blood:	n/a
30	chr11:63768032-63768082	Jurkat	blood:	n/a
31	chr11:63763834-63763884	T-47D	breast:	n/a
32	chr11:63768794-63768844	AG10803	skin:	n/a
33	chr11:63768412-63768462	NT2-D1	testis:	n/a
34	chr11:63768412-63768462	NHBE	bronchial:	n/a
35	chr11:63764925-63764975	H1-hESC	embryonic stem cell:	embryo
36	chr11:63764602-63764652	NH-A	brain:	n/a
37	chr11:63768794-63768844	HRCEpiC	kidney:	n/a
38	chr11:63772049-63772099	HEEpiC	esophagus:	n/a
39	chr11:63766787-63766837	T-47D	breast:	n/a
40	chr11:63768794-63768844	HEK293	kidney:	embryo
41	chr11:63768794-63768844	LNCaP	prostate:	n/a
42	chr11:63767561-63767611	A549	lung:	n/a
43	chr11:63766787-63766837	HCPEpiC	choroid plexus:	n/a
44	chr11:63766546-63766596	PANC-1	pancreas:	n/a
45	chr11:63772824-63772874	SKMC	muscle:	n/a
46	chr11:63768665-63768715	ECC-1	luminal epithelium:	n/a
47	chr11:63768412-63768462	HCPEpiC	choroid plexus:	n/a
48	chr11:63766546-63766596	HL-60	blood:	n/a
49	chr11:63763834-63763884	HIPEpiC	eye:	n/a
50	chr11:63766546-63766596	Hela-S3	cervix:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63766936..63768720-chr11:63772081..63775398,3	K562	blood:
2	chr11:63763234..63766933-chr11:63772186..63775317,4	K562	blood:
3	chr11:63773041..63776570-chr11:63852588..63855753,3	K562	blood:
4	chr11:63760836..63762379-chr11:63771626..63773976,2	K562	blood:
5	chr11:63741871..63744034-chr11:63764319..63766020,2	MCF-7	breast:
6	chr11:63766001..63768236-chr11:63932252..63933831,2	MCF-7	breast:
7	chr11:63765613..63767970-chr11:63932144..63934171,3	MCF-7	breast:
8	chr11:63770454..63773392-chr11:63780828..63782649,3	K562	blood:
9	chr11:63741996..63743584-chr11:63770498..63773173,2	K562	blood:
10	chr11:63740468..63742451-chr11:63765485..63768295,3	K562	blood:
11	chr11:63608184..63610790-chr11:63772494..63774086,2	K562	blood:
12	chr11:63763212..63764799-chr11:63914863..63917321,2	MCF-7	breast:
13	chr11:63684070..63686718-chr11:63758305..63761285,3	MCF-7	breast:
14	chr11:63752288..63756029-chr11:63763681..63768717,11	MCF-7	breast:
15	chr11:63760836..63762379-chr11:63771626..63773976,2	K562	blood:
16	chr11:63752150..63755098-chr11:63772817..63775491,2	K562	blood:
17	chr11:63766704..63768642-chr11:63953085..63955113,2	MCF-7	breast:
18	chr11:63766346..63770572-chr11:63771597..63778027,8	MCF-7	breast:
19	chr11:63765241..63769899-chr11:63951624..63954334,5	MCF-7	breast:
20	chr11:63770570..63773392-chr11:63780661..63782649,3	K562	blood:
21	chr11:63741723..63745192-chr11:63773910..63776843,3	K562	blood:
22	chr11:63741878..63743584-chr11:63769928..63773173,3	K562	blood:
23	chr11:63765735..63770391-chr11:63772325..63777720,7	MCF-7	breast:
24	chr11:63771047..63773567-chr11:63779179..63781426,2	MCF-7	breast:
25	chr11:63767743..63768450-chr16:50186380..50187229,2	NB4	blood:
26	chr11:63718773..63720987-chr11:63762744..63764440,2	K562	blood:
27	chr11:63771593..63774373-chr11:63777234..63778755,2	MCF-7	breast:
28	chr11:63751963..63753694-chr11:63759818..63761321,2	K562	blood:
29	chr11:63762419..63763931-chr11:63767012..63769520,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX8A-2	chr11:63768587-63768992	NONHSAT021929
2	lnc-COX8A-2	chr11:63769188-63769239	NONHSAT021929

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OTUB1	hsa-miR-28-5p	chr11:63765840-63765846

Variant related genes	Relation type
OTUB1	TF binding region
MACROD1	TF binding region
OTUB1	CpG island
MACROD1	CpG island
ENSG00000256100	chromatin interactions
ENSG00000167771	chromatin interactions
ENSG00000168439	chromatin interactions
ENSG00000176340	chromatin interactions
ENSG00000121274	chromatin interactions
ENSG00000110583	chromatin interactions
ENSG00000167770	chromatin interactions
ENSG00000133315	chromatin interactions

Extended variants
information (count: 513 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11231671	chr11:63761169-63761170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10792424	chr11:63761207-63761208	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs527244612	chr11:63761269-63761270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540776523	chr11:63761289-63761290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560988208	chr11:63761297-63761298	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529747031	chr11:63761300-63761301	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549986190	chr11:63761364-63761365	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569493353	chr11:63761369-63761370	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549818303	chr11:63761386-63761387	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34143455	chr11:63761406-63761407	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36068502	chr11:63761414-63761415	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35279945	chr11:63761438-63761439	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35361996	chr11:63761443-63761444	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs36073815	chr11:63761445-63761446	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553872543	chr11:63761464-63761465	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532297859	chr11:63761547-63761548	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576741335	chr11:63761548-63761549	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558164466	chr11:63761604-63761605	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552020752	chr11:63761648-63761649	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571319321	chr11:63761680-63761681	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188485131	chr11:63761682-63761683	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34028180	chr11:63761727-63761728	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553877503	chr11:63761773-63761774	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555900708	chr11:63761789-63761790	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575503585	chr11:63761798-63761799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3019784	chr11:63761805-63761806	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs375215479	chr11:63761827-63761828	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536333242	chr11:63761847-63761848	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192879760	chr11:63761881-63761882	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544504432	chr11:63761951-63761952	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371383049	chr11:63761959-63761960	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139049388	chr11:63762024-63762025	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559251815	chr11:63762027-63762028	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571946528	chr11:63762060-63762061	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541066042	chr11:63762115-63762116	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201368063	chr11:63762195-63762196	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574729473	chr11:63762206-63762207	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560709375	chr11:63762273-63762274	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149341457	chr11:63762319-63762320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77459372	chr11:63762330-63762331	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563160367	chr11:63762372-63762373	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540324462	chr11:63762395-63762396	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76249827	chr11:63762489-63762490	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565684563	chr11:63762537-63762538	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528366649	chr11:63762573-63762574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547803817	chr11:63762617-63762618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376826996	chr11:63762631-63762632	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549163066	chr11:63762662-63762663	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184447143	chr11:63762669-63762670	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566075845	chr11:63762677-63762678	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63754800-63767600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:63755000-63766600	Weak transcription	Right Atrium	heart
3	chr11:63755000-63769000	Weak transcription	Fetal Kidney	kidney
4	chr11:63755200-63761200	Weak transcription	HUVEC	blood vessel
5	chr11:63755200-63762000	Weak transcription	Small Intestine	intestine
6	chr11:63755200-63766600	Weak transcription	Stomach Mucosa	stomach
7	chr11:63755200-63775200	Weak transcription	Psoas Muscle	Psoas
8	chr11:63755400-63762400	Weak transcription	Brain Substantia Nigra	brain
9	chr11:63755400-63765400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:63755400-63765400	Strong transcription	Fetal Stomach	stomach
11	chr11:63755400-63765600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr11:63755400-63766200	Strong transcription	Fetal Muscle Leg	muscle
13	chr11:63755400-63766200	Strong transcription	Fetal Thymus	thymus
14	chr11:63755400-63766400	Strong transcription	NHLF	lung
15	chr11:63755400-63766600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:63755600-63764800	Weak transcription	Fetal Brain Male	brain
17	chr11:63755600-63765800	Strong transcription	NHEK	skin
18	chr11:63755600-63766000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr11:63755600-63766400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr11:63755800-63762200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:63755800-63764800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:63755800-63765000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:63755800-63766200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:63756000-63762000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:63756000-63762200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:63756000-63764400	Strong transcription	Thymus	Thymus
27	chr11:63756000-63764600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:63756000-63765400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:63756000-63765600	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:63756000-63765800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:63756000-63766000	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr11:63756000-63766000	Strong transcription	Fetal Brain Female	brain
33	chr11:63756000-63766000	Strong transcription	Stomach Smooth Muscle	stomach
34	chr11:63756000-63766400	Weak transcription	Fetal Heart	heart
35	chr11:63756200-63765600	Strong transcription	Fetal Muscle Trunk	muscle
36	chr11:63756200-63766200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr11:63756200-63766800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:63756200-63769200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:63756400-63761400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:63756400-63764200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:63756400-63764200	Strong transcription	Lung	lung
42	chr11:63756400-63766200	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr11:63756400-63766400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:63756400-63766400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr11:63757600-63762400	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr11:63757600-63762600	Strong transcription	GM12878-XiMat	blood
47	chr11:63758000-63765000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:63758400-63764200	Weak transcription	HSMM	muscle
49	chr11:63758400-63766200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:63758600-63766600	Strong transcription	Fetal Intestine Small	intestine

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