Variant report

Variant	nsv1045854
Chromosome Location	chr11:75871240-75908910
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:1038)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:75877442-75877843	GM12878	blood:	n/a	n/a
2	ATF2	chr11:75877385-75877776	GM12878	blood:	n/a	n/a
3	BATF	chr11:75880537-75880793	GM12878	blood:	n/a	n/a
4	BATF	chr11:75880507-75880811	GM12878	blood:	n/a	n/a
5	BATF	chr11:75877503-75877745	GM12878	blood:	n/a	n/a
6	BATF	chr11:75877452-75877791	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:75877450-75877789	GM12878	blood:	n/a	chr11:75877743-75877752
8	BCL11A	chr11:75880481-75880847	GM12878	blood:	n/a	chr11:75880797-75880806
9	BCL11A	chr11:75877511-75877755	GM12878	blood:	n/a	chr11:75877743-75877752
10	BHLHE40	chr11:75879567-75879848	K562	blood:	n/a	n/a
11	BHLHE40	chr11:75874344-75874627	K562	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
12	BHLHE40	chr11:75874343-75874668	HepG2	liver:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
13	BHLHE40	chr11:75874450-75874566	GM12878	blood:	n/a	chr11:75874506-75874515 chr11:75874499-75874520 chr11:75874505-75874514 chr11:75874505-75874514 chr11:75874504-75874513
14	BHLHE40	chr11:75880588-75880997	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:75895960-75896047	K562	blood:	n/a	n/a
16	BHLHE40	chr11:75877454-75877762	GM12878	blood:	n/a	n/a
17	CBX3	chr11:75873978-75874336	K562	blood:	n/a	n/a
18	CCNT2	chr11:75872492-75872651	K562	blood:	n/a	n/a
19	CCNT2	chr11:75895841-75896045	K562	blood:	n/a	n/a
20	CEBPB	chr11:75901486-75901900	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:75895861-75896066	K562	blood:	n/a	n/a
22	CEBPD	chr11:75895671-75896175	K562	blood:	n/a	n/a
23	CHD2	chr11:75880552-75880866	GM12878	blood:	n/a	n/a
24	CHD2	chr11:75877442-75877713	GM12878	blood:	n/a	n/a
25	CTCF	chr11:75905988-75905993	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:75905984-75906019	GM12891	blood:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
27	CTCF	chr11:75905880-75906030	BJ	skin:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
28	CTCF	chr11:75886940-75887090	HepG2	liver:	n/a	chr11:75886958-75886971
29	CTCF	chr11:75886860-75887010	AG04449	skin:	n/a	chr11:75886958-75886971
30	CTCF	chr11:75893351-75893483	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr11:75886820-75886970	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr11:75873900-75874050	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr11:75892487-75892684	H1-hESC	embryonic stem cell:	n/a	chr11:75892629-75892637
34	CTCF	chr11:75875782-75875840	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr11:75893277-75893382	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr11:75900080-75900230	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr11:75892540-75892690	Caco-2	colon:	n/a	chr11:75892629-75892637
38	CTCF	chr11:75907160-75907310	HEK293	kidney:	n/a	n/a
39	CTCF	chr11:75905960-75905978	MCF-7	breast:	n/a	n/a
40	CTCF	chr11:75897220-75897370	BE2_C	brain:	n/a	n/a
41	CTCF	chr11:75897240-75897390	AG09319	gingival:	n/a	n/a
42	CTCF	chr11:75892580-75892730	WERI-Rb-1	eye:	n/a	chr11:75892629-75892637
43	CTCF	chr11:75893388-75893447	K562	blood:	n/a	n/a
44	CTCF	chr11:75900080-75900230	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr11:75905920-75906070	Hela-S3	cervix:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
46	CTCF	chr11:75892546-75892701	H1-hESC	embryonic stem cell:	n/a	chr11:75892629-75892637
47	CTCF	chr11:75905924-75906068	H1-hESC	embryonic stem cell:	n/a	chr11:75905992-75906010 chr11:75905995-75906004 chr11:75905994-75906015
48	CTCF	chr11:75893220-75893370	Caco-2	colon:	n/a	n/a
49	E2F6	chr11:75872539-75872756	K562	blood:	n/a	n/a
50	E2F6	chr11:75904357-75904504	K562	blood:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75873027-75873077	RPTEC	kidney:	n/a
2	chr11:75873027-75873077	RPTEC	kidney:	n/a
3	chr11:75898132-75898182	AG04450	lung:	fetal
4	chr11:75875926-75875976	GM19239	blood:	n/a
5	chr11:75898132-75898182	SK-N-SH	brain:	n/a
6	chr11:75875926-75875976	GM06990	blood:	n/a
7	chr11:75875926-75875976	HRCEpiC	kidney:	n/a
8	chr11:75876135-75876185	NB4	blood:	n/a
9	chr11:75902270-75902320	GM12892	blood:	n/a
10	chr11:75902270-75902320	HRE	kidney:	n/a
11	chr11:75876135-75876185	A549	lung:	n/a
12	chr11:75875926-75875976	HAEpiC	amniotic membrane:	n/a
13	chr11:75898132-75898182	NB4	blood:	n/a
14	chr11:75898203-75898253	PrEC	prostate:	n/a
15	chr11:75873027-75873077	SAEC	small airway:	n/a
16	chr11:75876135-75876185	GM12892	blood:	n/a
17	chr11:75879348-75879398	HepG2	liver:	n/a
18	chr11:75905850-75905900	A549	lung:	n/a
19	chr11:75905718-75905768	NB4	blood:	n/a
20	chr11:75878127-75878177	HNPCEpiC	eye:	n/a
21	chr11:75905850-75905900	HEEpiC	esophagus:	n/a
22	chr11:75905850-75905900	HMEC	breast:	n/a
23	chr11:75898132-75898182	MCF10A-Er-Src	breast:	n/a
24	chr11:75898203-75898253	AG04450	lung:	fetal
25	chr11:75878127-75878177	NT2-D1	testis:	n/a
26	chr11:75904184-75904234	HCF	heart:	n/a
27	chr11:75897427-75897477	HCT-116	colon:	n/a
28	chr11:75898132-75898182	AG09309	skin:	n/a
29	chr11:75876135-75876185	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:75904184-75904234	MCF-7	breast:	n/a
31	chr11:75876135-75876185	SK-N-SH_RA	brain:	n/a
32	chr11:75904184-75904234	ProgFib	skin:	n/a
33	chr11:75898132-75898182	NHBE	bronchial:	n/a
34	chr11:75905718-75905768	SKMC	muscle:	n/a
35	chr11:75876135-75876185	HAEpiC	amniotic membrane:	n/a
36	chr11:75878127-75878177	HAEpiC	amniotic membrane:	n/a
37	chr11:75905850-75905900	Hepatocyte	liver:	n/a
38	chr11:75898132-75898182	GM19239	blood:	n/a
39	chr11:75897427-75897477	HEEpiC	esophagus:	n/a
40	chr11:75876419-75876469	AG09319	gingival:	n/a
41	chr11:75905718-75905768	Jurkat	blood:	n/a
42	chr11:75875926-75875976	HUVEC	blood vessel:	n/a
43	chr11:75905850-75905900	GM12878	blood:	n/a
44	chr11:75905718-75905768	SK-N-SH	brain:	n/a
45	chr11:75896332-75896382	H1-hESC	embryonic stem cell:	embryo
46	chr11:75905917-75905967	GM12891	blood:	n/a
47	chr11:75902270-75902320	CMK	blood:	n/a
48	chr11:75905850-75905900	SKMC	muscle:	n/a
49	chr11:75905850-75905900	NHDF-neo	bronchial:	n/a
50	chr11:75898132-75898182	HPAEpiC	pulmonary alveolar:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:75895025..75897686-chr11:75910991..75913944,2	K562	blood:
2	chr11:75864698..75867155-chr11:75871013..75872936,2	MCF-7	breast:
3	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
4	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
5	chr11:75902153..75903768-chr11:75945033..75947723,2	K562	blood:
6	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
7	chr11:75864528..75867031-chr11:75871798..75873454,2	K562	blood:
8	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
9	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
10	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
11	chr11:75901629..75903680-chr11:75921082..75923446,2	K562	blood:
12	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
13	chr11:75879470..75881382-chr11:75903439..75906024,2	MCF-7	breast:
14	chr11:75908327..75910235-chr11:75911530..75913999,2	K562	blood:
15	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
16	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:
17	chr11:75679088..75681419-chr11:75870768..75873220,2	K562	blood:
18	chr11:75896186..75898075-chr11:75909574..75912491,2	K562	blood:
19	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
20	chr11:75887769..75890550-chr11:75903812..75906303,2	K562	blood:
21	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
22	chr11:75892849..75895480-chr11:75897932..75899434,2	K562	blood:
23	chr11:75904809..75906919-chr11:75917526..75920230,2	K562	blood:
24	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
25	chr11:75907463..75909415-chr11:75917684..75920104,2	MCF-7	breast:
26	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
27	chr11:75886513..75888497-chr11:75907057..75909283,2	MCF-7	breast:
28	chr11:75877596..75879712-chr11:75888366..75889930,2	K562	blood:
29	chr11:75867883..75870652-chr11:75871506..75874252,2	MCF-7	breast:
30	chr11:75908679..75911274-chr11:75914998..75917762,2	K562	blood:
31	chr11:75526830..75528448-chr11:75885826..75888721,2	K562	blood:
32	chr11:75907802..75910235-chr11:75912499..75914692,2	K562	blood:
33	chr11:75901884..75904848-chr11:76015737..76018383,2	MCF-7	breast:
34	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
35	chr11:75879470..75881382-chr11:75903439..75906024,2	MCF-7	breast:
36	chr11:75871119..75872885-chr11:75874380..75876840,2	MCF-7	breast:
37	chr11:75881616..75884148-chr11:75897760..75900480,2	MCF-7	breast:
38	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
39	chr11:75891012..75893171-chr11:75895940..75897806,2	K562	blood:
40	chr11:75865596..75868388-chr11:75876534..75879243,2	K562	blood:
41	chr11:75898285..75900069-chr11:75902238..75904019,2	K562	blood:
42	chr11:75895372..75898295-chr11:75906346..75908229,2	K562	blood:
43	chr11:75886596..75888940-chr11:75889618..75892110,2	MCF-7	breast:
44	chr11:75888382..75891358-chr11:75893738..75896231,2	MCF-7	breast:
45	chr11:75892849..75895759-chr11:75897789..75899434,2	K562	blood:
46	chr11:75878808..75880535-chr11:75885544..75887523,2	K562	blood:
47	chr11:75872410..75875308-chr11:75879381..75883436,3	K562	blood:
48	chr11:75874099..75876373-chr11:75881253..75883763,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UVRAG-2	chr11:75905685-75906115	ENSG00000254933.1
2	lnc-UVRAG-2	chr11:75901769-75901950	ENSG00000254933.1

No data

Variant related genes	Relation type
ENSG00000254933	TF binding region
ENSG00000254933	CpG island
ENSG00000085741	chromatin interactions

Extended variants
information (count: 1748 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1748 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10899166	chr11:75871240-75871241	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140213467	chr11:75871289-75871290	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs7952005	chr11:75871290-75871291	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs183892925	chr11:75871301-75871302	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs372860167	chr11:75871314-75871315	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs377223857	chr11:75871389-75871390	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs145260496	chr11:75871397-75871398	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs188760780	chr11:75871409-75871410	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs536058903	chr11:75871422-75871423	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs552622572	chr11:75871427-75871428	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs7120552	chr11:75871453-75871454	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs34751412	chr11:75871454-75871455	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs544589799	chr11:75871484-75871485	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs11236635	chr11:75871516-75871517	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs575134048	chr11:75871524-75871525	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs10793140	chr11:75871535-75871536	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs193292680	chr11:75871597-75871598	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs547956769	chr11:75871600-75871601	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs371277577	chr11:75871608-75871609	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs374707179	chr11:75871632-75871633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs10793141	chr11:75871642-75871643	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs185585531	chr11:75871643-75871644	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs149054052	chr11:75871651-75871652	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs77130395	chr11:75871660-75871661	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs569188028	chr11:75871748-75871749	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs7925119	chr11:75871771-75871772	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs368113415	chr11:75871772-75871773	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs79512754	chr11:75871786-75871787	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs143098920	chr11:75871825-75871826	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs77097974	chr11:75871847-75871848	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs148244896	chr11:75871848-75871849	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs538300173	chr11:75871865-75871866	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs576467686	chr11:75871922-75871923	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs537447820	chr11:75871927-75871928	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs112888184	chr11:75871928-75871929	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs141294718	chr11:75871963-75871964	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs75390697	chr11:75871981-75871982	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs577174148	chr11:75871982-75871983	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs575063403	chr11:75871985-75871986	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs200937821	chr11:75871987-75871988	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs146998791	chr11:75872003-75872004	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560711254	chr11:75872029-75872030	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs138212935	chr11:75872040-75872041	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs142967297	chr11:75872047-75872048	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs202196231	chr11:75872048-75872049	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73500042	chr11:75872108-75872109	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs531703721	chr11:75872109-75872110	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs548321535	chr11:75872206-75872207	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs561220984	chr11:75872227-75872228	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs75333165	chr11:75872279-75872280	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75833400-75872800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:75864400-75871800	Weak transcription	Right Atrium	heart
3	chr11:75864600-75872600	Weak transcription	Fetal Intestine Large	intestine
4	chr11:75865000-75876000	Weak transcription	Spleen	Spleen
5	chr11:75867800-75875200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr11:75869200-75871600	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr11:75869200-75874400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr11:75869400-75871600	Weak transcription	Fetal Heart	heart
9	chr11:75869400-75871600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr11:75869400-75872600	Weak transcription	Adipose Nuclei	Adipose
11	chr11:75869600-75872600	Enhancers	Pancreas	Pancrea
12	chr11:75869600-75873000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:75870200-75871800	Weak transcription	Placenta	Placenta
14	chr11:75870400-75874400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:75870400-75874600	Enhancers	Fetal Muscle Leg	muscle
16	chr11:75870600-75873800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr11:75870800-75871400	Weak transcription	Fetal Lung	lung
18	chr11:75871000-75873600	Enhancers	Fetal Brain Male	brain
19	chr11:75871200-75871800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr11:75871200-75872000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr11:75871200-75872600	Enhancers	Brain Germinal Matrix	brain
22	chr11:75871200-75872600	Enhancers	Fetal Brain Female	brain
23	chr11:75871400-75871800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:75871400-75873400	Enhancers	Fetal Lung	lung
25	chr11:75871600-75871800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr11:75871600-75872000	Bivalent Enhancer	HepG2	liver
27	chr11:75871600-75872600	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr11:75871600-75872600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr11:75871600-75873800	Enhancers	Fetal Heart	heart
30	chr11:75871800-75872000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:75871800-75872400	Enhancers	Right Atrium	heart
32	chr11:75871800-75873000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr11:75871800-75874400	Enhancers	Placenta	Placenta
34	chr11:75872000-75872200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr11:75872000-75872400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr11:75872000-75872400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr11:75872000-75872400	Bivalent Enhancer	Fetal Stomach	stomach
38	chr11:75872000-75872400	Enhancers	Right Ventricle	heart
39	chr11:75872000-75872400	Enhancers	K562	blood
40	chr11:75872000-75872600	Bivalent/Poised TSS	HepG2	liver
41	chr11:75872000-75873800	Enhancers	Left Ventricle	heart
42	chr11:75872200-75873200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr11:75872400-75872600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:75872400-75872600	Active TSS	Stomach Smooth Muscle	stomach
45	chr11:75872400-75872800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr11:75872400-75872800	Active TSS	Ovary	ovary
47	chr11:75872400-75872800	Flanking Active TSS	Right Atrium	heart
48	chr11:75872400-75872800	Active TSS	Right Ventricle	heart
49	chr11:75872400-75872800	Weak transcription	K562	blood
50	chr11:75872400-75873200	Enhancers	Cortex derived primary cultured neurospheres	brain

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