Variant report

Variant	esv1798496
Chromosome Location	chr11:45925495-45948304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1403)
CpG islands
(count:2076)
Chromatin interactive
region (count:32)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45939422-45939874	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:45939775-45940079	K562	blood:	n/a	n/a
3	ATF2	chr11:45939644-45939943	GM12878	blood:	n/a	n/a
4	ATF2	chr11:45939137-45939942	GM12878	blood:	n/a	n/a
5	ATF2	chr11:45944870-45945146	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:45939175-45939642	GM12878	blood:	n/a	n/a
7	ATF2	chr11:45939276-45939783	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:45939190-45939620	A549	lung:	n/a	chr11:45939582-45939590
9	ATF3	chr11:45939259-45939963	A549	lung:	n/a	chr11:45939582-45939590
10	BACH1	chr11:45943360-45944159	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:45929347-45929593	GM12878	blood:	n/a	n/a
12	BCL3	chr11:45939139-45940098	A549	lung:	n/a	n/a
13	BCL3	chr11:45939029-45939668	A549	lung:	n/a	n/a
14	BCLAF1	chr11:45939160-45940001	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:45940352-45940398	K562	blood:	n/a	n/a
16	BHLHE40	chr11:45938839-45939950	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:45926202-45926402	K562	blood:	n/a	n/a
18	BHLHE40	chr11:45938963-45940020	K562	blood:	n/a	n/a
19	BHLHE40	chr11:45944747-45945001	K562	blood:	n/a	chr11:45944938-45944954
20	BHLHE40	chr11:45934755-45934884	GM12878	blood:	n/a	n/a
21	BRCA1	chr11:45939990-45940329	HepG2	liver:	n/a	n/a
22	BRCA1	chr11:45939254-45940668	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:45939286-45939620	HepG2	liver:	n/a	n/a
24	CBX3	chr11:45939214-45939929	K562	blood:	n/a	n/a
25	CBX3	chr11:45925969-45926532	K562	blood:	n/a	n/a
26	CCNT2	chr11:45929515-45929778	K562	blood:	n/a	n/a
27	CCNT2	chr11:45926160-45926402	K562	blood:	n/a	n/a
28	CCNT2	chr11:45938994-45940528	K562	blood:	n/a	n/a
29	CCNT2	chr11:45943740-45944981	K562	blood:	n/a	chr11:45944138-45944147 chr11:45943905-45943914 chr11:45944108-45944117 chr11:45944015-45944024
30	CEBPB	chr11:45925553-45925797	K562	blood:	n/a	n/a
31	CEBPB	chr11:45939207-45940124	GM12878	blood:	n/a	n/a
32	CEBPB	chr11:45940340-45940385	K562	blood:	n/a	n/a
33	CEBPB	chr11:45939067-45940153	HCT-116	colon:	n/a	n/a
34	CEBPB	chr11:45925641-45925846	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:45939221-45939839	K562	blood:	n/a	n/a
36	CEBPB	chr11:45938966-45940565	Hela-S3	cervix:	n/a	chr11:45940408-45940416
37	CEBPB	chr11:45939219-45939741	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr11:45939298-45939540	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:45926108-45926209	K562	blood:	n/a	n/a
40	CEBPB	chr11:45939052-45939830	A549	lung:	n/a	n/a
41	CEBPB	chr11:45939274-45939890	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:45939231-45939633	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:45925537-45925758	HepG2	liver:	n/a	n/a
44	CEBPB	chr11:45939225-45939740	A549	lung:	n/a	n/a
45	CEBPB	chr11:45939323-45939515	GM12878	blood:	n/a	n/a
46	CEBPB	chr11:45938987-45939695	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr11:45939186-45939689	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:45939199-45939669	A549	lung:	n/a	n/a
49	CEBPB	chr11:45939176-45939858	MCF-7	breast:	n/a	n/a
50	CEBPB	chr11:45939174-45939735	MCF-7	breast:	n/a	n/a

(count:2076 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45942789-45942839	NHDF-neo	bronchial:	n/a
2	chr11:45944790-45944840	HAEpiC	amniotic membrane:	n/a
3	chr11:45942789-45942839	NHDF-neo	bronchial:	n/a
4	chr11:45944790-45944840	HAEpiC	amniotic membrane:	n/a
5	chr11:45940058-45940108	Jurkat	blood:	n/a
6	chr11:45944091-45944141	PFSK-1	brain:	n/a
7	chr11:45944076-45944126	HAEpiC	amniotic membrane:	n/a
8	chr11:45929519-45929569	NT2-D1	testis:	n/a
9	chr11:45929541-45929591	AG04449	skin:	fetal
10	chr11:45942176-45942226	AoSMC	blood vessel:	n/a
11	chr11:45944091-45944141	ProgFib	skin:	n/a
12	chr11:45929369-45929419	ovcar-3	ovarian:	n/a
13	chr11:45928988-45929038	GM06990	blood:	n/a
14	chr11:45944790-45944840	AG04449	skin:	fetal
15	chr11:45944076-45944126	GM19239	blood:	n/a
16	chr11:45937020-45937070	HIPEpiC	eye:	n/a
17	chr11:45944091-45944141	AG10803	skin:	n/a
18	chr11:45942789-45942839	HAEpiC	amniotic membrane:	n/a
19	chr11:45942027-45942077	A549	lung:	n/a
20	chr11:45943237-45943287	SK-N-MC	brain:	n/a
21	chr11:45938923-45938973	HL-60	blood:	n/a
22	chr11:45939619-45939669	ProgFib	skin:	n/a
23	chr11:45937020-45937070	MCF-7	breast:	n/a
24	chr11:45943130-45943180	MCF10A-Er-Src	breast:	n/a
25	chr11:45928848-45928898	H1-hESC	embryonic stem cell:	embryo
26	chr11:45944076-45944126	BJ	skin:	n/a
27	chr11:45928854-45928904	HCF	heart:	n/a
28	chr11:45926170-45926220	HepG2	liver:	n/a
29	chr11:45942176-45942226	Jurkat	blood:	n/a
30	chr11:45928841-45928891	HRPEpiC	eye:	n/a
31	chr11:45944920-45944970	BJ	skin:	n/a
32	chr11:45938923-45938973	T-47D	breast:	n/a
33	chr11:45942027-45942077	GM19239	blood:	n/a
34	chr11:45929519-45929569	ProgFib	skin:	n/a
35	chr11:45927645-45927695	HCPEpiC	choroid plexus:	n/a
36	chr11:45943237-45943287	HL-60	blood:	n/a
37	chr11:45928848-45928898	GM12878	blood:	n/a
38	chr11:45942176-45942226	HCM	heart:	n/a
39	chr11:45944790-45944840	HMEC	breast:	n/a
40	chr11:45944076-45944126	CMK	blood:	n/a
41	chr11:45944091-45944141	HMEC	breast:	n/a
42	chr11:45939723-45939773	GM12891	blood:	n/a
43	chr11:45928370-45928420	K562	blood:	n/a
44	chr11:45939458-45939508	HCPEpiC	choroid plexus:	n/a
45	chr11:45928898-45928948	CMK	blood:	n/a
46	chr11:45928937-45928987	HCT-116	colon:	n/a
47	chr11:45927645-45927695	HCM	heart:	n/a
48	chr11:45944091-45944141	SK-N-SH_RA	brain:	n/a
49	chr11:45944790-45944840	AoSMC	blood vessel:	n/a
50	chr11:45942027-45942077	HEK293	kidney:	embryo

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:45904585..45907305-chr11:45939491..45941669,2	K562	blood:
2	chr11:45939411..45941074-chr11:46142423..46143961,2	MCF-7	breast:
3	chr11:45825326..45828118-chr11:45934084..45936499,2	K562	blood:
4	chr11:45937934..45940310-chr17:56708373..56710113,2	MCF-7	breast:
5	chr11:45942684..45944705-chr11:46141351..46143147,2	K562	blood:
6	chr11:45943430..45944211-chr5:39074478..39074986,2	HCT-116	colon:
7	chr11:45904999..45908778-chr11:45926674..45929138,4	MCF-7	breast:
8	chr11:45906755..45908288-chr11:45937921..45939853,2	MCF-7	breast:
9	chr11:45867151..45870859-chr11:45942545..45946514,4	K562	blood:
10	chr11:45880127..45882891-chr11:45927875..45929936,2	K562	blood:
11	chr11:45890873..45893526-chr11:45930539..45932384,2	K562	blood:
12	chr11:45939172..45939872-chr2:113032560..113033279,2	HCT-116	colon:
13	chr11:45928634..45930948-chr12:122237013..122238884,2	MCF-7	breast:
14	chr11:45948094..45950923-chr11:45957515..45959352,2	K562	blood:
15	chr11:45944787..45946706-chr11:45959461..45962306,2	K562	blood:
16	chr11:45938612..45941036-chr11:46368136..46369719,2	K562	blood:
17	chr11:45944749..45946540-chr11:45946715..45948340,2	K562	blood:
18	chr11:45925111..45927750-chr11:45943585..45946023,2	K562	blood:
19	chr11:45944749..45946540-chr11:45946715..45948340,2	K562	blood:
20	chr11:45879680..45881437-chr11:45942342..45944046,2	MCF-7	breast:
21	chr11:45924750..45927395-chr11:45942360..45945085,3	K562	blood:
22	chr11:45942020..45943576-chr11:46141975..46144467,2	MCF-7	breast:
23	chr11:45826170..45827093-chr11:45939119..45939790,2	NB4	blood:
24	chr11:45824638..45826704-chr11:45938955..45940480,2	MCF-7	breast:
25	chr11:45868914..45870628-chr11:45938803..45941080,3	MCF-7	breast:
26	chr11:45867027..45870378-chr11:45924400..45927960,4	K562	blood:
27	chr11:45868765..45870683-chr11:45944601..45946304,2	MCF-7	breast:
28	chr11:45939300..45941780-chr11:46259462..46260979,2	K562	blood:
29	chr11:45921817..45923409-chr11:45925394..45927956,2	K562	blood:
30	chr11:45937002..45939512-chr11:45985947..45988260,2	MCF-7	breast:
31	chr11:45868894..45870500-chr11:45937119..45938981,2	K562	blood:
32	chr11:45907546..45909448-chr11:45934193..45936568,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf94-1	chr11:45927960-45928012	ENSG00000255498.1
2	lnc-C11orf94-2	chr11:45926604-45926823	expReg_chr11_3331_-
3	lnc-C11orf94-1	chr11:45927492-45927847	ENSG00000255498.1

No data

Variant related genes	Relation type
ENSG00000255498	TF binding region
GYLTL1B	TF binding region
PEX16	TF binding region
C11orf94	TF binding region
ENSG00000255498	CpG island
GYLTL1B	CpG island
PEX16	CpG island
C11orf94	CpG island
ENSG00000139725	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000188177	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000121653	chromatin interactions
ENSG00000181830	chromatin interactions
ENSG00000164327	chromatin interactions

Extended variants
information (count: 1073 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1073 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376192530	chr11:45925496-45925497	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs367722310	chr11:45925500-45925501	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs542880986	chr11:45925510-45925511	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370124285	chr11:45925526-45925527	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559632365	chr11:45925555-45925556	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs144563506	chr11:45925561-45925562	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138531749	chr11:45925585-45925586	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551950802	chr11:45925606-45925607	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141186128	chr11:45925653-45925654	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374856732	chr11:45925675-45925676	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs150751406	chr11:45925682-45925683	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533033002	chr11:45925699-45925700	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs138879867	chr11:45925700-45925701	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs549930864	chr11:45925717-45925718	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs148381852	chr11:45925755-45925756	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112012761	chr11:45925775-45925776	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs112993823	chr11:45925811-45925812	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs111694968	chr11:45925825-45925826	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs534650251	chr11:45925835-45925836	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs367664113	chr11:45925884-45925885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557916080	chr11:45925904-45925905	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577788977	chr11:45925915-45925916	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537116711	chr11:45925939-45925940	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs77705826	chr11:45925962-45925963	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372041578	chr11:45925964-45925965	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573661250	chr11:45925993-45925994	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375621107	chr11:45926048-45926049	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs17847257	chr11:45926079-45926080	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559537569	chr11:45926091-45926092	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs41275172	chr11:45926094-45926095	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573473409	chr11:45926171-45926172	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200110741	chr11:45926224-45926225	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs17847258	chr11:45926235-45926236	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201278305	chr11:45926263-45926264	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144836273	chr11:45926307-45926308	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368947533	chr11:45926311-45926312	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs55963197	chr11:45926334-45926335	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531150800	chr11:45926338-45926339	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs540169892	chr11:45926339-45926340	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375813364	chr11:45926344-45926345	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549861347	chr11:45926356-45926357	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs145667143	chr11:45926364-45926365	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200861362	chr11:45926404-45926405	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2271847	chr11:45926445-45926446	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs186571372	chr11:45926446-45926447	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs576471268	chr11:45926471-45926472	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369375057	chr11:45926491-45926492	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373345172	chr11:45926492-45926493	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs377680043	chr11:45926493-45926494	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534893367	chr11:45926516-45926517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45921400-45933000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr11:45921600-45931400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr11:45922200-45931800	Weak transcription	Primary B cells from cord blood	blood
4	chr11:45922400-45934800	Weak transcription	A549	lung
5	chr11:45922600-45925800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:45922600-45929400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:45922600-45930600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:45922600-45930800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:45922600-45931400	Weak transcription	Aorta	Aorta
10	chr11:45922600-45932400	Weak transcription	Hela-S3	cervix
11	chr11:45922600-45932400	Weak transcription	Osteobl	bone
12	chr11:45922600-45934400	Weak transcription	HMEC	breast
13	chr11:45922600-45938400	Weak transcription	Fetal Kidney	kidney
14	chr11:45922800-45926000	Weak transcription	NHLF	lung
15	chr11:45922800-45928600	Weak transcription	Esophagus	oesophagus
16	chr11:45922800-45930000	Weak transcription	Left Ventricle	heart
17	chr11:45922800-45930400	Weak transcription	Liver	Liver
18	chr11:45923000-45927600	Weak transcription	Colonic Mucosa	Colon
19	chr11:45923000-45930600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:45923000-45938000	Weak transcription	NHDF-Ad	bronchial
21	chr11:45923000-45938400	Weak transcription	Right Atrium	heart
22	chr11:45923200-45925600	Weak transcription	K562	blood
23	chr11:45923200-45927800	Strong transcription	Ovary	ovary
24	chr11:45923200-45931200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr11:45923200-45932200	Weak transcription	HSMM	muscle
26	chr11:45923200-45935600	Weak transcription	NH-A	brain
27	chr11:45923400-45927400	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr11:45923400-45929200	Strong transcription	Fetal Stomach	stomach
29	chr11:45923400-45929600	Weak transcription	Colon Smooth Muscle	Colon
30	chr11:45923400-45931600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr11:45923400-45932000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr11:45923400-45932400	Weak transcription	HepG2	liver
33	chr11:45923400-45934800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:45923600-45925800	Transcr. at gene 5' and 3'	Brain Hippocampus Middle	brain
35	chr11:45923600-45927200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr11:45923600-45927400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
37	chr11:45923600-45928600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr11:45923600-45928800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr11:45923600-45929600	Weak transcription	Fetal Brain Male	brain
40	chr11:45923600-45936600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr11:45923800-45927000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr11:45923800-45927200	Strong transcription	H9 Cell Line	embryonic stem cell
43	chr11:45923800-45927200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:45923800-45928400	Strong transcription	Fetal Muscle Leg	muscle
45	chr11:45923800-45928800	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:45923800-45929600	Strong transcription	Brain Germinal Matrix	brain
47	chr11:45924000-45926200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr11:45924000-45927000	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr11:45924000-45927600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:45924000-45928200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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