Variant report

Variant	esv2759819
Chromosome Location	chr11:35319320-35480522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3042)
CpG islands
(count:1774)
Chromatin interactive
region (count:225)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3042 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35373786-35374132	K562	blood:	n/a	n/a
2	ARID3A	chr11:35413647-35414051	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:35368897-35369267	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:35358871-35359010	K562	blood:	n/a	n/a
5	ARID3A	chr11:35358700-35359201	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:35364472-35365174	K562	blood:	n/a	n/a
7	ARID3A	chr11:35412510-35413014	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:35395224-35395527	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:35380723-35382236	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:35408993-35409542	HepG2	liver:	n/a	n/a
11	ATF1	chr11:35412695-35412905	K562	blood:	n/a	n/a
12	ATF1	chr11:35373724-35374140	K562	blood:	n/a	n/a
13	ATF1	chr11:35358795-35359139	K562	blood:	n/a	n/a
14	ATF1	chr11:35352559-35352767	K562	blood:	n/a	n/a
15	ATF1	chr11:35342700-35342937	K562	blood:	n/a	n/a
16	ATF1	chr11:35355965-35356213	K562	blood:	n/a	n/a
17	ATF1	chr11:35364484-35365206	K562	blood:	n/a	n/a
18	ATF1	chr11:35426167-35426388	K562	blood:	n/a	n/a
19	ATF2	chr11:35364427-35365005	GM12878	blood:	n/a	n/a
20	ATF2	chr11:35440059-35440289	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr11:35413379-35414144	GM12878	blood:	n/a	n/a
22	ATF2	chr11:35334605-35335580	GM12878	blood:	n/a	n/a
23	ATF2	chr11:35411508-35411976	GM12878	blood:	n/a	n/a
24	ATF2	chr11:35411575-35412075	GM12878	blood:	n/a	n/a
25	ATF2	chr11:35334536-35335496	GM12878	blood:	n/a	n/a
26	ATF2	chr11:35340409-35340908	GM12878	blood:	n/a	n/a
27	ATF2	chr11:35412320-35413222	GM12878	blood:	n/a	n/a
28	ATF2	chr11:35366728-35367161	GM12878	blood:	n/a	n/a
29	ATF2	chr11:35412413-35413040	GM12878	blood:	n/a	n/a
30	ATF3	chr11:35412537-35413221	A549	lung:	n/a	n/a
31	ATF3	chr11:35358753-35359166	K562	blood:	n/a	n/a
32	ATF3	chr11:35412658-35412940	K562	blood:	n/a	n/a
33	BACH1	chr11:35348200-35348246	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr11:35440397-35441572	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr11:35358840-35359002	K562	blood:	n/a	chr11:35358987-35359001
36	BATF	chr11:35358785-35359108	GM12878	blood:	n/a	chr11:35358990-35359001 chr11:35358961-35358972 chr11:35358962-35358972
37	BATF	chr11:35364477-35364841	GM12878	blood:	n/a	n/a
38	BATF	chr11:35334841-35335359	GM12878	blood:	n/a	n/a
39	BATF	chr11:35327319-35327604	GM12878	blood:	n/a	n/a
40	BATF	chr11:35411648-35411902	GM12878	blood:	n/a	n/a
41	BATF	chr11:35412550-35412992	GM12878	blood:	n/a	n/a
42	BATF	chr11:35412524-35413154	GM12878	blood:	n/a	n/a
43	BATF	chr11:35355930-35356203	GM12878	blood:	n/a	n/a
44	BATF	chr11:35358773-35359153	GM12878	blood:	n/a	chr11:35358990-35359001 chr11:35358961-35358972 chr11:35358962-35358972
45	BCL11A	chr11:35334793-35335421	GM12878	blood:	n/a	chr11:35335039-35335048
46	BCL11A	chr11:35412464-35413007	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:35364642-35364893	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:35334923-35335278	GM12878	blood:	n/a	chr11:35335039-35335048
49	BCL3	chr11:35412508-35412943	A549	lung:	n/a	n/a
50	BCL3	chr11:35358670-35359077	GM12878	blood:	n/a	chr11:35358989-35358998 chr11:35358990-35358999

(count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35441012-35441062	HEEpiC	esophagus:	n/a
2	chr11:35441881-35441931	AG09319	gingival:	n/a
3	chr11:35441900-35441950	AG09319	gingival:	n/a
4	chr11:35442225-35442275	HRE	kidney:	n/a
5	chr11:35441311-35441361	NH-A	brain:	n/a
6	chr11:35441012-35441062	HEEpiC	esophagus:	n/a
7	chr11:35441881-35441931	AG09319	gingival:	n/a
8	chr11:35441900-35441950	AG09319	gingival:	n/a
9	chr11:35442225-35442275	HRE	kidney:	n/a
10	chr11:35441311-35441361	NH-A	brain:	n/a
11	chr11:35343789-35343839	SK-N-SH	brain:	n/a
12	chr11:35439994-35440044	HepG2	liver:	n/a
13	chr11:35436672-35436722	GM06990	blood:	n/a
14	chr11:35441593-35441643	HEK293	kidney:	embryo
15	chr11:35441593-35441643	MCF10A-Er-Src	breast:	n/a
16	chr11:35366721-35366771	HepG2	liver:	n/a
17	chr11:35453590-35453640	Hepatocyte	liver:	n/a
18	chr11:35425551-35425601	U87	brain:	n/a
19	chr11:35441198-35441248	MCF-7	breast:	n/a
20	chr11:35442918-35442968	HAEpiC	amniotic membrane:	n/a
21	chr11:35441088-35441138	HIPEpiC	eye:	n/a
22	chr11:35440252-35440302	SKMC	muscle:	n/a
23	chr11:35436672-35436722	HRE	kidney:	n/a
24	chr11:35413951-35414001	T-47D	breast:	n/a
25	chr11:35360531-35360581	HL-60	blood:	n/a
26	chr11:35441107-35441157	NT2-D1	testis:	n/a
27	chr11:35343789-35343839	PrEC	prostate:	n/a
28	chr11:35441088-35441138	IMR90	lung:	fetal
29	chr11:35439994-35440044	HEK293	kidney:	embryo
30	chr11:35436672-35436722	U87	brain:	n/a
31	chr11:35441900-35441950	NT2-D1	testis:	n/a
32	chr11:35441311-35441361	SKMC	muscle:	n/a
33	chr11:35441593-35441643	MCF-7	breast:	n/a
34	chr11:35440136-35440186	SKMC	muscle:	n/a
35	chr11:35441558-35441608	PANC-1	pancreas:	n/a
36	chr11:35385435-35385485	HCM	heart:	n/a
37	chr11:35441777-35441827	HCPEpiC	choroid plexus:	n/a
38	chr11:35425551-35425601	HCPEpiC	choroid plexus:	n/a
39	chr11:35440062-35440112	Jurkat	blood:	n/a
40	chr11:35441900-35441950	SK-N-SH	brain:	n/a
41	chr11:35441107-35441157	HL-60	blood:	n/a
42	chr11:35440252-35440302	NB4	blood:	n/a
43	chr11:35441088-35441138	HAEpiC	amniotic membrane:	n/a
44	chr11:35441260-35441310	HepG2	liver:	n/a
45	chr11:35441198-35441248	AoSMC	blood vessel:	n/a
46	chr11:35366721-35366771	HRPEpiC	eye:	n/a
47	chr11:35385435-35385485	NH-A	brain:	n/a
48	chr11:35441881-35441931	HMEC	breast:	n/a
49	chr11:35385435-35385485	AG04449	skin:	fetal
50	chr11:35442918-35442968	GM06990	blood:	n/a

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr11:35386181..35389087-chr11:35424824..35428139,4	MCF-7	breast:
2	chr11:35343264..35345981-chr11:35357333..35358972,2	MCF-7	breast:
3	chr11:35360058..35364651-chr11:35365186..35370074,5	K562	blood:
4	chr11:35448881..35450556-chr11:35461534..35464155,2	MCF-7	breast:
5	chr11:35359115..35360850-chr11:35385171..35387976,3	MCF-7	breast:
6	chr11:35325412..35330750-chr11:35411649..35414159,5	MCF-7	breast:
7	chr11:35344560..35346248-chr11:35411918..35413925,2	MCF-7	breast:
8	chr11:34936665..34939175-chr11:35400592..35403537,3	K562	blood:
9	chr11:35347909..35350349-chr11:35386183..35388809,2	MCF-7	breast:
10	chr11:35295544..35300568-chr11:35411012..35415613,12	MCF-7	breast:
11	chr11:35343264..35345981-chr11:35357333..35358972,2	MCF-7	breast:
12	chr11:35358486..35360321-chr11:35376414..35377943,2	MCF-7	breast:
13	chr11:35281817..35285244-chr11:35384315..35387489,3	MCF-7	breast:
14	chr11:35330316..35333880-chr11:35383154..35386545,4	MCF-7	breast:
15	chr11:35296807..35297598-chr11:35383959..35384853,2	MCF-7	breast:
16	chr11:35397672..35399931-chr11:35409140..35411675,2	MCF-7	breast:
17	chr11:35407289..35409789-chr11:35410338..35413893,3	MCF-7	breast:
18	chr11:35387150..35387754-chr11:35411229..35411733,2	MCF-7	breast:
19	chr11:35282903..35283518-chr11:35327015..35328007,3	MCF-7	breast:
20	chr11:35315763..35317448-chr11:35338066..35339856,2	MCF-7	breast:
21	chr11:35310052..35313543-chr11:35317974..35319677,3	MCF-7	breast:
22	chr11:35083507..35086389-chr11:35411165..35412873,2	MCF-7	breast:
23	chr11:35327935..35328765-chr4:72769646..72770565,2	MCF-7	breast:
24	chr11:35370125..35373303-chr11:35374872..35377145,3	MCF-7	breast:
25	chr11:35425781..35426726-chr11:35506944..35507719,2	K562	blood:
26	chr11:35410859..35414389-chr11:35422710..35426072,4	MCF-7	breast:
27	chr11:35400990..35408348-chr11:35409888..35413137,13	MCF-7	breast:
28	chr11:35344560..35346248-chr11:35411918..35413925,2	MCF-7	breast:
29	chr11:35406611..35409466-chr11:35417708..35419228,2	MCF-7	breast:
30	chr11:35377674..35381317-chr11:35383998..35385696,3	MCF-7	breast:
31	chr11:35285135..35288083-chr11:35386749..35388761,2	MCF-7	breast:
32	chr11:35409190..35411863-chr11:35413358..35416120,2	MCF-7	breast:
33	chr11:35367320..35368822-chr11:35387386..35389201,2	MCF-7	breast:
34	chr11:35393897..35397897-chr11:35401211..35403993,3	MCF-7	breast:
35	chr11:35334087..35336895-chr11:35384207..35386170,2	MCF-7	breast:
36	chr11:35334087..35336895-chr11:35384207..35386170,2	MCF-7	breast:
37	chr11:35387393..35390278-chr11:35400406..35402784,2	K562	blood:
38	chr11:35479245..35483851-chr11:35487174..35489833,4	K562	blood:
39	chr11:35285333..35287124-chr11:35412297..35413804,2	MCF-7	breast:
40	chr11:35400075..35401806-chr11:35403404..35405754,2	K562	blood:
41	chr11:35370125..35373303-chr11:35374872..35377145,3	MCF-7	breast:
42	chr11:35323596..35326224-chr11:35411777..35414366,2	MCF-7	breast:
43	chr11:35327322..35328895-chr11:35375252..35377771,2	MCF-7	breast:
44	chr11:35316339..35320306-chr11:35324557..35327417,4	MCF-7	breast:
45	chr11:35323422..35325913-chr11:35358470..35360620,2	MCF-7	breast:
46	chr11:35427207..35428920-chr11:35441702..35443377,2	K562	blood:
47	chr11:35432842..35435212-chr11:35436167..35439122,4	K562	blood:
48	chr11:35370405..35374305-chr11:35384183..35385741,3	MCF-7	breast:
49	chr11:35362046..35363846-chr11:35365711..35367318,2	MCF-7	breast:
50	chr11:35344472..35346445-chr11:35423970..35426429,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD44-2	chr11:35440604-35440654	ENSG00000255542.1
2	lnc-CD44-6	chr11:35395812-35396021	NONHSAT018790
3	lnc-CD44-2	chr11:35442083-35442549	ENSG00000255542.1

No data

Variant related genes	Relation type
SLC1A2	TF binding region
ENSG00000255542	TF binding region
ENSG00000215380	TF binding region
PAMR1	TF binding region
SLC1A2	CpG island
ENSG00000255542	CpG island
ENSG00000215380	CpG island
PAMR1	CpG island
ENSG00000149089	chromatin interactions
ENSG00000135374	chromatin interactions
ENSG00000110436	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000255542	chromatin interactions
ENSG00000215380	chromatin interactions
ENSG00000255004	chromatin interactions
ENSG00000026508	chromatin interactions
ENSG00000110435	chromatin interactions

Extended variants
information (count: 6178 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6178 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7114260	chr11:35319353-35319354	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140215966	chr11:35319368-35319369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531276451	chr11:35319382-35319383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551275613	chr11:35319415-35319416	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570993010	chr11:35319492-35319493	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144051519	chr11:35319527-35319528	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11033062	chr11:35319545-35319546	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539992822	chr11:35319740-35319741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532157393	chr11:35319746-35319747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551835247	chr11:35319819-35319820	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566910677	chr11:35319825-35319826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147142269	chr11:35319838-35319839	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543831735	chr11:35319979-35319980	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs555384675	chr11:35319985-35319986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs190059693	chr11:35320012-35320013	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542377101	chr11:35320040-35320041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs377442362	chr11:35320069-35320070	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs140336616	chr11:35320070-35320071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs371157907	chr11:35320073-35320074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs4756208	chr11:35320084-35320085	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs559189756	chr11:35320130-35320131	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572726230	chr11:35320149-35320150	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149665168	chr11:35320157-35320158	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541940158	chr11:35320179-35320180	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564361623	chr11:35320226-35320227	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181784898	chr11:35320248-35320249	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529783525	chr11:35320279-35320280	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185351176	chr11:35320284-35320285	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2901536	chr11:35320302-35320303	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551010060	chr11:35320332-35320333	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564775616	chr11:35320387-35320388	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75712526	chr11:35320411-35320412	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547131593	chr11:35320420-35320421	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs566714942	chr11:35320423-35320424	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs376113540	chr11:35320450-35320451	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs567566653	chr11:35320476-35320477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs370537095	chr11:35320486-35320487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs535602044	chr11:35320494-35320495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144508941	chr11:35320498-35320499	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568925089	chr11:35320502-35320503	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs3847604	chr11:35320561-35320562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs148425072	chr11:35320578-35320579	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs577024039	chr11:35320615-35320616	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539341340	chr11:35320622-35320623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190212801	chr11:35320647-35320648	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111587636	chr11:35320654-35320655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs3847605	chr11:35320661-35320662	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146478162	chr11:35320742-35320743	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561733775	chr11:35320757-35320758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2901535	chr11:35320763-35320764	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:2996 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35298200-35326000	Weak transcription	Brain Substantia Nigra	brain
2	chr11:35299000-35326600	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:35299800-35328600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr11:35302400-35327000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:35302600-35329000	Weak transcription	Brain Angular Gyrus	brain
6	chr11:35304000-35324800	Weak transcription	Liver	Liver
7	chr11:35304600-35326600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:35308000-35324000	Weak transcription	HepG2	liver
9	chr11:35308600-35325800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:35308600-35326400	Weak transcription	Brain Anterior Caudate	brain
11	chr11:35310000-35325800	Weak transcription	Brain Germinal Matrix	brain
12	chr11:35312000-35324000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:35312600-35324000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr11:35312800-35324000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:35313400-35321800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr11:35313600-35320200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:35314200-35329200	Weak transcription	Fetal Brain Male	brain
18	chr11:35314800-35327000	Weak transcription	Fetal Stomach	stomach
19	chr11:35315200-35324800	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr11:35315800-35319800	Enhancers	Placenta	Placenta
21	chr11:35317600-35326800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr11:35317600-35327600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr11:35318400-35324200	Weak transcription	Pancreas	Pancrea
24	chr11:35318600-35321400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:35318800-35319400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr11:35318800-35319400	Strong transcription	NHDF-Ad	bronchial
27	chr11:35318800-35319600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr11:35318800-35325400	Weak transcription	Fetal Brain Female	brain
29	chr11:35319400-35319600	Genic enhancers	NHDF-Ad	bronchial
30	chr11:35319400-35324000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr11:35319600-35324000	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr11:35319600-35324000	Weak transcription	NHDF-Ad	bronchial
33	chr11:35319800-35320200	Weak transcription	Placenta	Placenta
34	chr11:35320200-35320400	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:35320200-35320400	Enhancers	Placenta	Placenta
36	chr11:35320200-35320400	Enhancers	NHLF	lung
37	chr11:35320400-35322000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr11:35320400-35324000	Weak transcription	NHLF	lung
39	chr11:35320400-35325600	Weak transcription	Placenta	Placenta
40	chr11:35321400-35323200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:35321800-35323200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr11:35322000-35322800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:35322000-35327000	Weak transcription	Aorta	Aorta
44	chr11:35322600-35325000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr11:35322600-35327400	Enhancers	Adipose Nuclei	Adipose
46	chr11:35322800-35323200	Enhancers	Colon Smooth Muscle	Colon
47	chr11:35322800-35326600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr11:35323000-35323400	Enhancers	Fetal Muscle Leg	muscle
49	chr11:35323000-35323600	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:35323200-35325200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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