Variant report

Variant	esv3429298
Chromosome Location	chr21:40670131-40688774
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1129)
CpG islands
(count:613)
Chromatin interactive
region (count:80)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:40684160-40684495	K562	blood:	n/a	n/a
2	ARID3A	chr21:40684237-40684587	HepG2	liver:	n/a	n/a
3	ARID3A	chr21:40685459-40685944	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:40685486-40686045	K562	blood:	n/a	n/a
5	ATF1	chr21:40684204-40684554	K562	blood:	n/a	n/a
6	ATF2	chr21:40685445-40685848	GM12878	blood:	n/a	n/a
7	ATF2	chr21:40685478-40685788	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr21:40685801-40686058	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr21:40686129-40686473	GM12878	blood:	n/a	n/a
10	ATF2	chr21:40686170-40686911	GM12878	blood:	n/a	n/a
11	ATF3	chr21:40685702-40686024	K562	blood:	n/a	n/a
12	ATF3	chr21:40685537-40685975	A549	lung:	n/a	n/a
13	BACH1	chr21:40685672-40686138	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr21:40686590-40686830	K562	blood:	n/a	n/a
15	BACH1	chr21:40684507-40684547	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr21:40685595-40685978	K562	blood:	n/a	n/a
17	BACH1	chr21:40683959-40684349	K562	blood:	n/a	n/a
18	BATF	chr21:40686500-40686798	GM12878	blood:	n/a	n/a
19	BATF	chr21:40686512-40686785	GM12878	blood:	n/a	n/a
20	BCL3	chr21:40685633-40686059	GM12878	blood:	n/a	chr21:40685860-40685873 chr21:40685852-40685865
21	BCLAF1	chr21:40685340-40686135	GM12878	blood:	n/a	chr21:40685860-40685873 chr21:40685852-40685865
22	BCLAF1	chr21:40685291-40686106	GM12878	blood:	n/a	chr21:40685860-40685873 chr21:40685852-40685865
23	BHLHE40	chr21:40685487-40686202	HepG2	liver:	n/a	chr21:40685751-40685767 chr21:40685847-40685863
24	BHLHE40	chr21:40684135-40684760	K562	blood:	n/a	n/a
25	BHLHE40	chr21:40685454-40686741	GM12878	blood:	n/a	chr21:40685751-40685767 chr21:40685847-40685863
26	BHLHE40	chr21:40685118-40686771	K562	blood:	n/a	chr21:40685139-40685155 chr21:40685751-40685767 chr21:40685847-40685863
27	BHLHE40	chr21:40684117-40684584	GM12878	blood:	n/a	n/a
28	BRCA1	chr21:40684271-40684587	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr21:40685535-40685880	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr21:40685589-40685909	HepG2	liver:	n/a	n/a
31	BRCA1	chr21:40685426-40686178	GM12878	blood:	n/a	n/a
32	CBX3	chr21:40685309-40686130	HCT-116	colon:	n/a	n/a
33	CBX3	chr21:40684026-40684650	K562	blood:	n/a	n/a
34	CBX3	chr21:40686166-40686912	K562	blood:	n/a	n/a
35	CBX3	chr21:40685292-40686110	K562	blood:	n/a	n/a
36	CCNT2	chr21:40684281-40684672	K562	blood:	n/a	n/a
37	CCNT2	chr21:40684902-40686697	K562	blood:	n/a	chr21:40685051-40685060 chr21:40685265-40685274 chr21:40685765-40685774
38	CEBPB	chr21:40685845-40686035	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr21:40685578-40686039	K562	blood:	n/a	n/a
40	CEBPB	chr21:40684297-40684385	K562	blood:	n/a	chr21:40684309-40684322
41	CEBPB	chr21:40685352-40685969	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr21:40685891-40686125	HepG2	liver:	n/a	n/a
43	CEBPD	chr21:40685302-40686093	K562	blood:	n/a	n/a
44	CEBPD	chr21:40685339-40686011	HepG2	liver:	n/a	n/a
45	CEBPD	chr21:40685788-40685973	HepG2	liver:	n/a	n/a
46	CEBPD	chr21:40684297-40684684	HepG2	liver:	n/a	n/a
47	CEBPD	chr21:40686056-40686420	HepG2	liver:	n/a	n/a
48	CHD1	chr21:40685130-40686858	GM12878	blood:	n/a	chr21:40685430-40685440 chr21:40685423-40685433
49	CHD1	chr21:40685647-40686747	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr21:40685328-40685423	H1-hESC	embryonic stem cell:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:40684269-40684319	SK-N-SH_RA	brain:	n/a
2	chr21:40685342-40685392	HRE	kidney:	n/a
3	chr21:40686621-40686671	NHBE	bronchial:	n/a
4	chr21:40684269-40684319	SK-N-SH_RA	brain:	n/a
5	chr21:40685342-40685392	HRE	kidney:	n/a
6	chr21:40686621-40686671	NHBE	bronchial:	n/a
7	chr21:40686185-40686235	AG09319	gingival:	n/a
8	chr21:40686185-40686235	NHBE	bronchial:	n/a
9	chr21:40686621-40686671	ovcar-3	ovarian:	n/a
10	chr21:40685342-40685392	HNPCEpiC	eye:	n/a
11	chr21:40686053-40686103	AG10803	skin:	n/a
12	chr21:40686621-40686671	K562	blood:	n/a
13	chr21:40684751-40684801	HUVEC	blood vessel:	n/a
14	chr21:40685679-40685729	T-47D	breast:	n/a
15	chr21:40685679-40685729	HRPEpiC	eye:	n/a
16	chr21:40685208-40685258	NT2-D1	testis:	n/a
17	chr21:40686053-40686103	HPAEpiC	pulmonary alveolar:	n/a
18	chr21:40685342-40685392	HUVEC	blood vessel:	n/a
19	chr21:40685679-40685729	HCPEpiC	choroid plexus:	n/a
20	chr21:40684269-40684319	PANC-1	pancreas:	n/a
21	chr21:40685342-40685392	SK-N-SH_RA	brain:	n/a
22	chr21:40686185-40686235	AG04450	lung:	fetal
23	chr21:40686621-40686671	ProgFib	skin:	n/a
24	chr21:40686053-40686103	PANC-1	pancreas:	n/a
25	chr21:40685208-40685258	HUVEC	blood vessel:	n/a
26	chr21:40684269-40684319	HPAEpiC	pulmonary alveolar:	n/a
27	chr21:40686185-40686235	Caco-2	colon:	n/a
28	chr21:40685679-40685729	LNCaP	prostate:	n/a
29	chr21:40684269-40684319	MCF10A-Er-Src	breast:	n/a
30	chr21:40686053-40686103	Hepatocyte	liver:	n/a
31	chr21:40685208-40685258	IMR90	lung:	fetal
32	chr21:40685208-40685258	Caco-2	colon:	n/a
33	chr21:40685342-40685392	K562	blood:	n/a
34	chr21:40686621-40686671	LNCaP	prostate:	n/a
35	chr21:40685342-40685392	T-47D	breast:	n/a
36	chr21:40684751-40684801	HepG2	liver:	n/a
37	chr21:40685208-40685258	HCT-116	colon:	n/a
38	chr21:40684751-40684801	HEK293	kidney:	embryo
39	chr21:40686053-40686103	ECC-1	luminal epithelium:	n/a
40	chr21:40685679-40685729	HCT-116	colon:	n/a
41	chr21:40686053-40686103	NB4	blood:	n/a
42	chr21:40685342-40685392	Caco-2	colon:	n/a
43	chr21:40686053-40686103	HNPCEpiC	eye:	n/a
44	chr21:40684751-40684801	K562	blood:	n/a
45	chr21:40685679-40685729	HPAEpiC	pulmonary alveolar:	n/a
46	chr21:40686621-40686671	AG10803	skin:	n/a
47	chr21:40685679-40685729	U87	brain:	n/a
48	chr21:40684269-40684319	U87	brain:	n/a
49	chr21:40686621-40686671	NHDF-neo	bronchial:	n/a
50	chr21:40686621-40686671	SK-N-SH	brain:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:40683319..40690926-chr21:40755872..40762716,23	MCF-7	breast:
2	chr21:40685845..40686781-chr3:9438942..9439442,2	Hela-S3	cervix:
3	chr21:40671338..40675047-chr21:40676117..40679838,4	K562	blood:
4	chr21:40671338..40675047-chr21:40676117..40679838,4	K562	blood:
5	chr21:40645807..40648656-chr21:40680491..40682941,2	K562	blood:
6	chr21:40553454..40557456-chr21:40682892..40687176,12	K562	blood:
7	chr19:33863948..33864786-chr21:40685269..40686182,2	Hela-S3	cervix:
8	chr21:40684107..40685647-chr21:40816624..40819498,2	K562	blood:
9	chr21:40683876..40687631-chr21:40749667..40753921,6	K562	blood:
10	chr1:9064907..9065782-chr21:40687864..40688368,2	MCF-7	breast:
11	chr21:40660582..40664374-chr21:40667695..40671151,4	MCF-7	breast:
12	chr11:64545391..64546081-chr21:40685867..40686815,2	NB4	blood:
13	chr21:40682856..40693378-chr21:40754350..40765471,56	MCF-7	breast:
14	chr21:40670757..40673579-chr21:40719041..40722481,3	K562	blood:
15	chr21:40683717..40685708-chr21:40747929..40750593,3	MCF-7	breast:
16	chr21:40671195..40673748-chr21:40675125..40678603,4	K562	blood:
17	chr21:40672762..40675001-chr21:40682440..40684098,2	K562	blood:
18	21:40687235-40690033..21:40757151-40764378	K562	blood:
19	chr21:40550424..40553042-chr21:40683249..40686279,3	K562	blood:
20	chr20:50349937..50351852-chr21:40684525..40686487,2	MCF-7	breast:
21	chr21:40684138..40686385-chr9:131445458..131447217,2	MCF-7	breast:
22	chr19:2475923..2476512-chr21:40687961..40688912,2	Hela-S3	cervix:
23	chr21:40671488..40672356-chr21:40760178..40761118,2	MCF-7	breast:
24	chr21:40663279..40665811-chr21:40674696..40676596,2	K562	blood:
25	chr2:238392237..238394703-chr21:40685639..40687456,2	MCF-7	breast:
26	chr21:40675223..40677979-chr21:40720098..40723094,2	MCF-7	breast:
27	chr21:40555032..40557155-chr21:40684133..40685858,2	MCF-7	breast:
28	chr21:40683837..40687545-chr21:40816624..40819639,6	K562	blood:
29	chr21:40681596..40696529-chr21:40715399..40724266,46	K562	blood:
30	chr21:40683507..40684404-chr21:40721331..40722058,2	MCF-7	breast:
31	chr21:40687654..40692063-chr21:40815994..40821163,6	MCF-7	breast:
32	chr21:40675820..40678831-chr21:40721085..40724268,3	K562	blood:
33	chr21:40666937..40669991-chr21:40672116..40674107,3	MCF-7	breast:
34	chr21:40672849..40674870-chr21:40685560..40688525,2	K562	blood:
35	chr21:40684582..40688018-chr21:40762846..40766549,4	MCF-7	breast:
36	chr21:40671119..40673164-chr21:40679954..40681992,2	K562	blood:
37	chr21:40684648..40686149-chr3:63849352..63850917,2	MCF-7	breast:
38	21:40686083-40686932..21:40757151-40764378	K562	blood:
39	chr21:40645055..40648656-chr21:40680491..40684092,3	K562	blood:
40	chr21:40674900..40676993-chr21:40757962..40759771,2	MCF-7	breast:
41	21:40671591-40673895..21:40748850-40752541	Hela-S3	cervix:
42	chr21:40681416..40687854-chr21:40744378..40751195,8	K562	blood:
43	chr21:40685837..40686745-chr5:175875260..175875880,2	Hela-S3	cervix:
44	chr21:40664381..40666644-chr21:40671132..40672895,2	K562	blood:
45	chr21:40591760..40593585-chr21:40682186..40684474,2	K562	blood:
46	chr21:40684444..40687629-chr3:63848425..63851169,6	MCF-7	breast:
47	chr21:40684332..40690368-chr21:40756970..40764337,16	K562	blood:
48	chr21:40673370..40675883-chr21:40685458..40687060,2	K562	blood:
49	chr21:40554013..40557423-chr21:40684520..40688084,3	MCF-7	breast:
50	chr21:40581217..40582784-chr21:40687990..40689879,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRWD1-IT2-1	chr21:40685888-40686369	ENSG00000255568.2
2	lnc-BRWD1-IT2-1	chr21:40685887-40686886	ENSG00000255568.2
3	lnc-WRB-5	chr21:40676880-40677252	ucscGeneNc_uc002yyu_2
4	lnc-WRB-5	chr21:40678376-40679152	ucscGeneNc_uc002yyu_2
5	lnc-BRWD1-IT2-1	chr21:40685861-40686888	NONHSAT082161
6	lnc-WRB-2	chr21:40687633-40687741	XLOC_013942
7	lnc-WRB-2	chr21:40685704-40686091	XLOC_013942

No data

Variant related genes	Relation type
BRWD1	TF binding region
BRWD1-AS1	TF binding region
BRWD1-IT2	TF binding region
BRWD1	CpG island
BRWD1-AS1	CpG island
BRWD1-IT2	CpG island
ENSG00000227406	chromatin interactions
ENSG00000119335	chromatin interactions
ENSG00000185437	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000113194	chromatin interactions
ENSG00000255568	chromatin interactions
ENSG00000183527	chromatin interactions
ENSG00000232608	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000238141	chromatin interactions
ENSG00000272991	chromatin interactions
ENSG00000215444	chromatin interactions
ENSG00000252915	chromatin interactions
ENSG00000168137	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000238556	chromatin interactions
ENSG00000186432	chromatin interactions
ENSG00000185658	chromatin interactions
ENSG00000163634	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000158615	chromatin interactions
ENSG00000153879	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000163635	chromatin interactions
ENSG00000236830	chromatin interactions
ENSG00000115648	chromatin interactions
ENSG00000182093	chromatin interactions
ENSG00000205581	chromatin interactions
ENSG00000157578	chromatin interactions
EXOC5	miRNA target sites

Extended variants
information (count: 933 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180781034	chr21:40670147-40670148	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185203534	chr21:40670151-40670152	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2836979	chr21:40670167-40670168	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs138191164	chr21:40670193-40670194	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189315619	chr21:40670221-40670222	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181735124	chr21:40670225-40670226	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548296436	chr21:40670227-40670228	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568180305	chr21:40670237-40670238	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374712682	chr21:40670274-40670275	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369766127	chr21:40670293-40670294	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373956782	chr21:40670298-40670299	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs367551925	chr21:40670420-40670421	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566493773	chr21:40670451-40670452	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199917402	chr21:40670456-40670457	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148989363	chr21:40670457-40670458	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2056844	chr21:40670460-40670461	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs201946650	chr21:40670491-40670492	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35418992	chr21:40670524-40670525	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560906405	chr21:40670542-40670543	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142781843	chr21:40670548-40670549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76577873	chr21:40670573-40670574	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs146072612	chr21:40670590-40670591	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535692467	chr21:40670629-40670630	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555506231	chr21:40670640-40670641	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575344654	chr21:40670641-40670642	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139611733	chr21:40670660-40670661	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537843974	chr21:40670668-40670669	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564189966	chr21:40670728-40670729	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577607817	chr21:40670780-40670781	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116667048	chr21:40670839-40670840	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559368433	chr21:40670883-40670884	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149757843	chr21:40670934-40670935	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548096491	chr21:40670983-40670984	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190366789	chr21:40671075-40671076	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530624191	chr21:40671091-40671092	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs111962333	chr21:40671096-40671097	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372817529	chr21:40671104-40671105	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539047115	chr21:40671136-40671137	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148457782	chr21:40671138-40671139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183766666	chr21:40671139-40671140	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186277283	chr21:40671151-40671152	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145082630	chr21:40671157-40671158	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34445556	chr21:40671174-40671175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575431047	chr21:40671181-40671182	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537991845	chr21:40671183-40671184	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs28459078	chr21:40671185-40671186	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573390980	chr21:40671186-40671187	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112066443	chr21:40671187-40671188	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540294313	chr21:40671189-40671190	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560501452	chr21:40671237-40671238	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Down syndrome	20877625	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21147910	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40641400-40683800	Strong transcription	Placenta	Placenta
2	chr21:40643800-40684200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr21:40646600-40683400	Weak transcription	Fetal Brain Male	brain
4	chr21:40650200-40671600	Weak transcription	Aorta	Aorta
5	chr21:40651400-40671600	Weak transcription	Pancreas	Pancrea
6	chr21:40655000-40676800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr21:40655000-40683000	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr21:40655400-40683200	Strong transcription	Dnd41	blood
9	chr21:40655600-40671800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr21:40655800-40671800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr21:40655800-40672200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr21:40655800-40672800	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr21:40655800-40673800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr21:40655800-40677400	Strong transcription	Duodenum Mucosa	Duodenum
15	chr21:40655800-40677400	Strong transcription	Fetal Thymus	thymus
16	chr21:40656200-40672400	Strong transcription	Liver	Liver
17	chr21:40656200-40672600	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr21:40656200-40674200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr21:40656400-40670200	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr21:40656400-40675400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr21:40656400-40676600	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr21:40656400-40676800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr21:40656400-40683800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr21:40656600-40671600	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr21:40658800-40670600	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr21:40658800-40672000	Strong transcription	Primary B cells from peripheral blood	blood
27	chr21:40658800-40672000	Strong transcription	Adipose Nuclei	Adipose
28	chr21:40659000-40673600	Strong transcription	Hela-S3	cervix
29	chr21:40659200-40674600	Strong transcription	K562	blood
30	chr21:40659600-40670800	Strong transcription	HepG2	liver
31	chr21:40659600-40671800	Strong transcription	Fetal Muscle Leg	muscle
32	chr21:40659600-40676800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr21:40659600-40676800	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr21:40659800-40672800	Strong transcription	NH-A	brain
35	chr21:40661800-40683400	Weak transcription	Stomach Mucosa	stomach
36	chr21:40662000-40672200	Strong transcription	Fetal Muscle Trunk	muscle
37	chr21:40662400-40675400	Strong transcription	Osteobl	bone
38	chr21:40662600-40671400	Strong transcription	HMEC	breast
39	chr21:40662600-40673800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr21:40663000-40670400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr21:40663000-40672600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr21:40663000-40672800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr21:40663200-40672000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr21:40663600-40683400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr21:40663800-40670800	Strong transcription	Primary hematopoietic stem cells	blood
46	chr21:40663800-40671200	Weak transcription	Fetal Heart	heart
47	chr21:40663800-40671600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr21:40663800-40672000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr21:40663800-40672000	Weak transcription	Right Ventricle	heart
50	chr21:40663800-40672600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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