Variant report

Variant	esv3444895
Chromosome Location	chr11:58614102-58779384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1701)
CpG islands
(count:2319)
Chromatin interactive
region (count:18)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58693760-58694429	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58648155-58648546	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:58713222-58713481	HepG2	liver:	n/a	n/a
4	ATF1	chr11:58691061-58691064	K562	blood:	n/a	n/a
5	ATF2	chr11:58694851-58695251	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:58672951-58673767	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:58690792-58691378	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:58618422-58618712	GM12878	blood:	n/a	n/a
9	BATF	chr11:58634982-58635318	GM12878	blood:	n/a	n/a
10	BATF	chr11:58618228-58618642	GM12878	blood:	n/a	n/a
11	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
12	BHLHE40	chr11:58668343-58668597	K562	blood:	n/a	n/a
13	BHLHE40	chr11:58618456-58618676	K562	blood:	n/a	n/a
14	BHLHE40	chr11:58618487-58618534	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:58618380-58618658	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:58693810-58694128	HepG2	liver:	n/a	n/a
17	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
18	BHLHE40	chr11:58673515-58673655	K562	blood:	n/a	n/a
19	BRCA1	chr11:58673350-58673665	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr11:58684602-58685036	HCT-116	colon:	n/a	n/a
21	CBX3	chr11:58684635-58685102	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:58684666-58684899	K562	blood:	n/a	n/a
23	CEBPB	chr11:58713294-58713398	HepG2	liver:	n/a	chr11:58713351-58713364
24	CEBPB	chr11:58648118-58648482	HepG2	liver:	n/a	chr11:58648287-58648300
25	CEBPB	chr11:58656076-58656380	IMR90	lung:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
26	CEBPB	chr11:58719387-58719568	H1-hESC	embryonic stem cell:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
27	CEBPB	chr11:58767634-58767824	Hela-S3	cervix:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
28	CEBPB	chr11:58767565-58767768	HepG2	liver:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
29	CEBPB	chr11:58745428-58745609	A549	lung:	n/a	chr11:58745468-58745479
30	CEBPB	chr11:58693679-58694509	IMR90	lung:	n/a	chr11:58694316-58694329
31	CEBPB	chr11:58648024-58648392	HepG2	liver:	n/a	chr11:58648287-58648300
32	CEBPB	chr11:58719331-58719581	A549	lung:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
33	CEBPB	chr11:58648183-58648434	A549	lung:	n/a	chr11:58648287-58648300
34	CEBPB	chr11:58719356-58719620	HepG2	liver:	n/a	chr11:58719485-58719496 chr11:58719485-58719498 chr11:58719487-58719498 chr11:58719485-58719498
35	CEBPB	chr11:58779256-58779450	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr11:58656689-58656951	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:58767586-58767847	H1-hESC	embryonic stem cell:	n/a	chr11:58767688-58767699 chr11:58767686-58767697
38	CEBPB	chr11:58747741-58747864	Hela-S3	cervix:	n/a	chr11:58747813-58747824 chr11:58747811-58747824
39	CEBPB	chr11:58656053-58656436	HepG2	liver:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
40	CEBPB	chr11:58713691-58713878	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:58745445-58745663	HepG2	liver:	n/a	chr11:58745468-58745479
42	CEBPB	chr11:58656131-58656456	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
43	CEBPB	chr11:58656085-58656389	Hela-S3	cervix:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
44	CEBPB	chr11:58774084-58774291	HepG2	liver:	n/a	chr11:58774243-58774254
45	CEBPB	chr11:58747697-58747942	A549	lung:	n/a	chr11:58747813-58747824 chr11:58747811-58747824
46	CEBPB	chr11:58648139-58648384	HepG2	liver:	n/a	chr11:58648287-58648300
47	CEBPB	chr11:58627346-58627618	HepG2	liver:	n/a	chr11:58627487-58627498
48	CEBPB	chr11:58656150-58656434	MCF-7	breast:	n/a	chr11:58656264-58656275 chr11:58656231-58656242 chr11:58656213-58656224
49	CEBPB	chr11:58713178-58713528	HepG2	liver:	n/a	chr11:58713351-58713364
50	CEBPB	chr11:58767676-58767679	K562	blood:	n/a	n/a

(count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58710158-58710208	Hepatocyte	liver:	n/a
2	chr11:58710158-58710208	Hepatocyte	liver:	n/a
3	chr11:58673615-58673665	GM12891	blood:	n/a
4	chr11:58731433-58731483	SK-N-SH_RA	brain:	n/a
5	chr11:58709394-58709444	HCPEpiC	choroid plexus:	n/a
6	chr11:58724252-58724302	ProgFib	skin:	n/a
7	chr11:58672702-58672752	NH-A	brain:	n/a
8	chr11:58673577-58673627	GM06990	blood:	n/a
9	chr11:58735304-58735354	SK-N-MC	brain:	n/a
10	chr11:58709394-58709444	HAEpiC	amniotic membrane:	n/a
11	chr11:58673087-58673137	HEK293	kidney:	embryo
12	chr11:58731634-58731684	SK-N-SH_RA	brain:	n/a
13	chr11:58731357-58731407	HL-60	blood:	n/a
14	chr11:58694219-58694269	PFSK-1	brain:	n/a
15	chr11:58673615-58673665	HCF	heart:	n/a
16	chr11:58673453-58673503	K562	blood:	n/a
17	chr11:58672888-58672938	SKMC	muscle:	n/a
18	chr11:58668345-58668395	HCPEpiC	choroid plexus:	n/a
19	chr11:58651984-58652034	HAEpiC	amniotic membrane:	n/a
20	chr11:58731104-58731154	HepG2	liver:	n/a
21	chr11:58668488-58668538	HepG2	liver:	n/a
22	chr11:58672702-58672752	MCF-7	breast:	n/a
23	chr11:58668977-58669027	AG04450	lung:	fetal
24	chr11:58736104-58736154	ProgFib	skin:	n/a
25	chr11:58673453-58673503	NH-A	brain:	n/a
26	chr11:58736081-58736131	GM19239	blood:	n/a
27	chr11:58667960-58668010	Jurkat	blood:	n/a
28	chr11:58651984-58652034	MCF10A-Er-Src	breast:	n/a
29	chr11:58673087-58673137	SAEC	small airway:	n/a
30	chr11:58731505-58731555	HAEpiC	amniotic membrane:	n/a
31	chr11:58673577-58673627	U87	brain:	n/a
32	chr11:58673615-58673665	GM06990	blood:	n/a
33	chr11:58736104-58736154	HL-60	blood:	n/a
34	chr11:58709394-58709444	AoSMC	blood vessel:	n/a
35	chr11:58667960-58668010	MCF-7	breast:	n/a
36	chr11:58694950-58695000	HepG2	liver:	n/a
37	chr11:58731357-58731407	MCF10A-Er-Src	breast:	n/a
38	chr11:58696069-58696119	AG09309	skin:	n/a
39	chr11:58673087-58673137	HAEpiC	amniotic membrane:	n/a
40	chr11:58735304-58735354	HMEC	breast:	n/a
41	chr11:58673453-58673503	HCPEpiC	choroid plexus:	n/a
42	chr11:58673087-58673137	ovcar-3	ovarian:	n/a
43	chr11:58673477-58673527	Hepatocyte	liver:	n/a
44	chr11:58672702-58672752	AG04449	skin:	fetal
45	chr11:58694950-58695000	HIPEpiC	eye:	n/a
46	chr11:58724252-58724302	GM06990	blood:	n/a
47	chr11:58673167-58673217	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:58672768-58672818	SK-N-SH	brain:	n/a
49	chr11:58696069-58696119	HAEpiC	amniotic membrane:	n/a
50	chr11:58668977-58669027	SKMC	muscle:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
2	chr11:58421165..58421796-chr11:58687413..58688096,2	MCF-7	breast:
3	chr11:58729566..58731391-chr11:58732930..58735906,2	K562	blood:
4	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:
5	chr11:58671775..58674615-chr11:58675003..58676520,2	K562	blood:
6	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
7	chr11:58677524..58679024-chr6:58777164..58778728,2	K562	blood:
8	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
9	chr11:58345930..58347450-chr11:58657978..58660327,2	K562	blood:
10	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
11	chr11:58661995..58664743-chr11:58668611..58670936,2	K562	blood:
12	chr11:58678524..58679504-chr6:58777166..58777745,2	MCF-7	breast:
13	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
14	chr11:58346639..58348965-chr11:58654113..58656554,2	K562	blood:
15	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
16	chr11:58678524..58679504-chr6:58776958..58777672,3	MCF-7	breast:
17	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
18	chr11:58669175..58672165-chr11:58677460..58679347,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL1-2	chr11:58714519-58714948	NONHSAT021491
2	lnc-GLYATL1-1	chr11:58660135-58660445	ENSG00000254717
3	lnc-GLYAT-1	chr11:58656261-58656370	l_477_chr11:58656260-58660325_ovary
4	lnc-GLYAT-1	chr11:58659760-58660337	l_477_chr11:58656260-58660325_ovary
5	lnc-GLYATL1-2	chr11:58711016-58711139	NONHSAT021491
6	lnc-GLYATL1-1	chr11:58652379-58652497	ENSG00000254717
7	lnc-GLYATL2-1	chr11:58684488-58684757	ENSG00000255523.1
8	lnc-GLYATL2-2	chr11:58725690-58726293	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853
10	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
11	lnc-GLYATL1-2	chr11:58714519-58714734	NONHSAT021492
12	lnc-GLYATL2-2	chr11:58701116-58703171	NR_033853
13	lnc-GLYATL1-1	chr11:58660135-58660266	NONHSAT021485
14	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
15	lnc-GLYATL1-1	chr11:58652424-58652497	NONHSAT021485
16	lnc-GLYATL2-1	chr11:58695790-58696162	ENSG00000255523.1
17	lnc-GLYATL1-3	chr11:58672343-58672709	NONHSAT021486
18	lnc-GLYATL2-2	chr11:58736426-58736546	ENSG00000255240.1
19	lnc-GLYAT-1	chr11:58657761-58659741	l_477_chr11:58656260-58660325_ovary
20	lnc-GLYATL1-2	chr11:58710789-58711139	NONHSAT021492
21	lnc-GLYAT-1	chr11:58664013-58664214	l_477_chr11:58656260-58660325_ovary
22	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
23	lnc-GLYATL1-1	chr11:58645775-58645854	ENSG00000254717
24	lnc-GLYATL1-2	chr11:58710760-58710795	NONHSAT021491
25	lnc-GLYATL2-4	chr11:58735069-58735764	NONHSAT021495
26	lnc-GLYATL2-2	chr11:58736415-58736546	ENSG00000255240.1
27	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
28	lnc-GLYAT-1	chr11:58656394-58657698	l_477_chr11:58656260-58660325_ovary
29	lnc-GLYATL2-2	chr11:58701116-58703171	ENSG00000255240.1

No data

Variant related genes	Relation type
ENSG00000224130	TF binding region
ENSG00000254786	TF binding region
GLYATL1	TF binding region
GLYATL1P2	TF binding region
GLYATL1P1	TF binding region
ENSG00000255240	TF binding region
ENSG00000254877	TF binding region
GLYATL2	TF binding region
ENSG00000255523	TF binding region
ENSG00000224130	CpG island
ENSG00000254786	CpG island
GLYATL1	CpG island
GLYATL1P2	CpG island
GLYATL1P1	CpG island
ENSG00000255240	CpG island
ENSG00000254877	CpG island
GLYATL2	CpG island
ENSG00000255523	CpG island
ENSG00000166840	chromatin interactions
ENSG00000255240	chromatin interactions
ENSG00000255073	chromatin interactions
ENSG00000156689	chromatin interactions
ENSG00000186660	chromatin interactions
ENSG00000224130	chromatin interactions
ENSG00000254877	chromatin interactions

Extended variants
information (count: 6138 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:6138 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116967972	chr11:58614126-58614127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559572270	chr11:58614127-58614128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530373726	chr11:58614178-58614179	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs116351517	chr11:58614217-58614218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148900228	chr11:58614219-58614220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531011436	chr11:58614220-58614221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552361380	chr11:58614246-58614247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570936351	chr11:58614294-58614295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72913216	chr11:58614303-58614304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564145989	chr11:58614341-58614342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143620700	chr11:58614415-58614416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148028250	chr11:58614442-58614443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556973748	chr11:58614481-58614482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535784118	chr11:58614500-58614501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577598227	chr11:58614512-58614513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1943286	chr11:58614564-58614565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs529522692	chr11:58614594-58614595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575105536	chr11:58614613-58614614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141746211	chr11:58614623-58614624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs1943287	chr11:58614660-58614661	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1943288	chr11:58614666-58614667	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541223652	chr11:58614719-58614720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75597539	chr11:58614759-58614760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1943289	chr11:58614804-58614805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542186113	chr11:58614806-58614807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528249782	chr11:58614859-58614860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530571073	chr11:58614874-58614875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs112023868	chr11:58614892-58614893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146080459	chr11:58614893-58614894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1943290	chr11:58614945-58614946	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs78254416	chr11:58614969-58614970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184651062	chr11:58615004-58615005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553267258	chr11:58615007-58615008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1943291	chr11:58615090-58615091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs568292104	chr11:58615108-58615109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189519022	chr11:58615119-58615120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550569719	chr11:58615135-58615136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569142179	chr11:58615155-58615156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539018345	chr11:58615175-58615176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557782425	chr11:58615178-58615179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192973357	chr11:58615209-58615210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567872681	chr11:58615226-58615227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368512910	chr11:58615272-58615273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560709763	chr11:58615298-58615299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61889909	chr11:58615313-58615314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553127515	chr11:58615325-58615326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574664169	chr11:58615369-58615370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553699222	chr11:58615374-58615375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1943292	chr11:58615397-58615398	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs575894555	chr11:58615403-58615404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	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
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58610800-58614200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:58610800-58614600	Enhancers	Primary hematopoietic stem cells	blood
3	chr11:58613000-58618000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:58613200-58614200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:58614000-58615000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:58617600-58618000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:58618000-58618600	Active TSS	Liver	Liver
8	chr11:58618000-58618800	Enhancers	Primary B cells from peripheral blood	blood
9	chr11:58619800-58620000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr11:58620000-58623800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr11:58623800-58624800	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr11:58631000-58631400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:58631000-58631400	ZNF genes & repeats	Thymus	Thymus
14	chr11:58631200-58631400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr11:58631400-58635000	Enhancers	Thymus	Thymus
16	chr11:58631600-58632400	Enhancers	Fetal Thymus	thymus
17	chr11:58632400-58632800	Weak transcription	Fetal Thymus	thymus
18	chr11:58632800-58634600	Enhancers	Fetal Thymus	thymus
19	chr11:58633800-58634000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:58634000-58634800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:58634000-58635800	Enhancers	NHEK	skin
22	chr11:58634200-58634600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:58634200-58635600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:58634400-58635000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:58634400-58635600	Enhancers	HMEC	breast
26	chr11:58634800-58635400	Enhancers	NHDF-Ad	bronchial
27	chr11:58634800-58635600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:58635000-58635600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr11:58635000-58636000	Weak transcription	Thymus	Thymus
30	chr11:58635000-58668000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr11:58635600-58637600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:58636000-58636200	Enhancers	Thymus	Thymus
33	chr11:58637600-58638200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr11:58638200-58638400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:58643600-58644800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr11:58645400-58645600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr11:58645400-58646400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
38	chr11:58645600-58652400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr11:58647600-58649000	Enhancers	Liver	Liver
40	chr11:58647600-58649000	Enhancers	HepG2	liver
41	chr11:58647800-58648000	Enhancers	Fetal Intestine Small	intestine
42	chr11:58648000-58654400	Weak transcription	Fetal Lung	lung
43	chr11:58648000-58655000	Weak transcription	Fetal Intestine Small	intestine
44	chr11:58651000-58671200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:58651400-58660200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:58652400-58653200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr11:58652600-58653400	ZNF genes & repeats	Fetal Stomach	stomach
48	chr11:58653200-58661400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr11:58654400-58654800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:58658000-58667600	Weak transcription	Brain Germinal Matrix	brain

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