Variant report

Variant	nsv3538
Chromosome Location	chr21:45267674-45297159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1243)
CpG islands
(count:367)
Chromatin interactive
region (count:69)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1243 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45287779-45288190	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45286059-45286524	K562	blood:	n/a	n/a
3	ARID3A	chr21:45277447-45277736	HepG2	liver:	n/a	n/a
4	ARID3A	chr21:45277647-45277656	K562	blood:	n/a	n/a
5	ARID3A	chr21:45274959-45275332	K562	blood:	n/a	n/a
6	ARID3A	chr21:45280762-45281019	K562	blood:	n/a	n/a
7	ARID3A	chr21:45286835-45287498	HepG2	liver:	n/a	n/a
8	ATF1	chr21:45275032-45275386	K562	blood:	n/a	n/a
9	ATF1	chr21:45277493-45277678	K562	blood:	n/a	n/a
10	ATF1	chr21:45279686-45279872	K562	blood:	n/a	n/a
11	ATF2	chr21:45286399-45287031	GM12878	blood:	n/a	n/a
12	ATF2	chr21:45274515-45275393	GM12878	blood:	n/a	n/a
13	ATF2	chr21:45274928-45275275	GM12878	blood:	n/a	n/a
14	ATF2	chr21:45286491-45286939	GM12878	blood:	n/a	n/a
15	BACH1	chr21:45284027-45284525	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr21:45284340-45284349	K562	blood:	n/a	n/a
17	BACH1	chr21:45285616-45285640	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr21:45279141-45279265	K562	blood:	n/a	n/a
19	BATF	chr21:45293619-45293823	GM12878	blood:	n/a	chr21:45293735-45293746
20	BATF	chr21:45286058-45286373	GM12878	blood:	n/a	n/a
21	BATF	chr21:45293627-45293871	GM12878	blood:	n/a	chr21:45293735-45293746
22	BCLAF1	chr21:45284000-45284450	GM12878	blood:	n/a	chr21:45284332-45284345 chr21:45284166-45284179 chr21:45284314-45284327 chr21:45284170-45284183
23	BCLAF1	chr21:45286489-45287012	GM12878	blood:	n/a	chr21:45286792-45286801
24	BCLAF1	chr21:45274787-45275371	GM12878	blood:	n/a	chr21:45275110-45275119
25	BHLHE40	chr21:45286465-45287173	GM12878	blood:	n/a	chr21:45286738-45286754
26	BHLHE40	chr21:45284193-45284534	HepG2	liver:	n/a	chr21:45284462-45284478
27	BHLHE40	chr21:45277401-45277739	HepG2	liver:	n/a	n/a
28	BHLHE40	chr21:45274700-45275277	GM12878	blood:	n/a	n/a
29	BHLHE40	chr21:45280627-45281128	K562	blood:	n/a	n/a
30	BHLHE40	chr21:45286695-45287347	HepG2	liver:	n/a	chr21:45286738-45286754
31	BHLHE40	chr21:45283542-45283626	GM12878	blood:	n/a	n/a
32	BHLHE40	chr21:45284071-45284585	K562	blood:	n/a	chr21:45284172-45284188 chr21:45284462-45284478 chr21:45284164-45284180
33	BHLHE40	chr21:45274714-45275378	K562	blood:	n/a	n/a
34	BHLHE40	chr21:45286876-45287206	K562	blood:	n/a	n/a
35	BHLHE40	chr21:45279270-45279523	HepG2	liver:	n/a	n/a
36	BHLHE40	chr21:45277428-45277724	K562	blood:	n/a	n/a
37	BHLHE40	chr21:45284068-45284585	GM12878	blood:	n/a	chr21:45284172-45284188 chr21:45284462-45284478 chr21:45284164-45284180
38	BRCA1	chr21:45284302-45284416	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr21:45280658-45281068	K562	blood:	n/a	n/a
40	CBX3	chr21:45280494-45281082	K562	blood:	n/a	n/a
41	CBX3	chr21:45270630-45271244	K562	blood:	n/a	n/a
42	CBX3	chr21:45279224-45279925	K562	blood:	n/a	n/a
43	CBX3	chr21:45270650-45271164	K562	blood:	n/a	n/a
44	CBX3	chr21:45268480-45268813	K562	blood:	n/a	n/a
45	CBX3	chr21:45273912-45275530	K562	blood:	n/a	n/a
46	CBX3	chr21:45295214-45295561	K562	blood:	n/a	n/a
47	CCNT2	chr21:45274800-45275386	K562	blood:	n/a	n/a
48	CCNT2	chr21:45284045-45284622	K562	blood:	n/a	chr21:45284353-45284362
49	CCNT2	chr21:45286676-45286979	K562	blood:	n/a	n/a
50	CCNT2	chr21:45285022-45285986	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45285836-45285886	HMEC	breast:	n/a
2	chr21:45285836-45285886	HMEC	breast:	n/a
3	chr21:45284425-45284475	GM12891	blood:	n/a
4	chr21:45285836-45285886	NHBE	bronchial:	n/a
5	chr21:45285448-45285498	SK-N-MC	brain:	n/a
6	chr21:45285898-45285948	NH-A	brain:	n/a
7	chr21:45285448-45285498	HCPEpiC	choroid plexus:	n/a
8	chr21:45284425-45284475	NHBE	bronchial:	n/a
9	chr21:45284362-45284412	HRE	kidney:	n/a
10	chr21:45285836-45285886	AG09319	gingival:	n/a
11	chr21:45284362-45284412	HEK293	kidney:	embryo
12	chr21:45285898-45285948	NB4	blood:	n/a
13	chr21:45284425-45284475	ProgFib	skin:	n/a
14	chr21:45284362-45284412	HRCEpiC	kidney:	n/a
15	chr21:45285836-45285886	NB4	blood:	n/a
16	chr21:45284362-45284412	SKMC	muscle:	n/a
17	chr21:45285448-45285498	SAEC	small airway:	n/a
18	chr21:45284425-45284475	HPAEpiC	pulmonary alveolar:	n/a
19	chr21:45284362-45284412	IMR90	lung:	fetal
20	chr21:45285448-45285498	GM19239	blood:	n/a
21	chr21:45285836-45285886	MCF-7	breast:	n/a
22	chr21:45284362-45284412	CMK	blood:	n/a
23	chr21:45284425-45284475	HRPEpiC	eye:	n/a
24	chr21:45284362-45284412	HCF	heart:	n/a
25	chr21:45285898-45285948	BJ	skin:	n/a
26	chr21:45285898-45285948	PANC-1	pancreas:	n/a
27	chr21:45284362-45284412	NT2-D1	testis:	n/a
28	chr21:45285448-45285498	AG04450	lung:	fetal
29	chr21:45285898-45285948	ECC-1	luminal epithelium:	n/a
30	chr21:45284362-45284412	AoSMC	blood vessel:	n/a
31	chr21:45285448-45285498	Hela-S3	cervix:	n/a
32	chr21:45285448-45285498	NHBE	bronchial:	n/a
33	chr21:45284425-45284475	HCT-116	colon:	n/a
34	chr21:45284344-45284394	NH-A	brain:	n/a
35	chr21:45284344-45284394	CMK	blood:	n/a
36	chr21:45284425-45284475	HCF	heart:	n/a
37	chr21:45284425-45284475	GM06990	blood:	n/a
38	chr21:45285898-45285948	SK-N-SH	brain:	n/a
39	chr21:45285836-45285886	GM12878	blood:	n/a
40	chr21:45285836-45285886	HUVEC	blood vessel:	n/a
41	chr21:45284362-45284412	BJ	skin:	n/a
42	chr21:45285836-45285886	LNCaP	prostate:	n/a
43	chr21:45285898-45285948	GM12878	blood:	n/a
44	chr21:45284362-45284412	PFSK-1	brain:	n/a
45	chr21:45284362-45284412	AG09309	skin:	n/a
46	chr21:45285448-45285498	HL-60	blood:	n/a
47	chr21:45284344-45284394	HEK293	kidney:	embryo
48	chr21:45284425-45284475	HNPCEpiC	eye:	n/a
49	chr21:45285448-45285498	U87	brain:	n/a
50	chr21:45284344-45284394	MCF-7	breast:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45294255..45295837-chr21:45318630..45320184,2	K562	blood:
2	chr21:45265753..45268307-chr21:45273441..45275141,2	K562	blood:
3	chr21:45295214..45297565-chr21:45298526..45301419,2	MCF-7	breast:
4	chr21:45282965..45285916-chr21:45430237..45433854,8	MCF-7	breast:
5	chr21:45285418..45288376-chr21:45321880..45324021,2	K562	blood:
6	chr21:45266653..45268520-chr21:45298545..45300170,2	K562	blood:
7	chr21:45209348..45212282-chr21:45284427..45288210,4	K562	blood:
8	chr21:45274532..45276467-chr21:45276902..45278896,2	MCF-7	breast:
9	chr21:45265753..45268307-chr21:45273441..45275141,2	K562	blood:
10	chr21:45252796..45255240-chr21:45273373..45275874,2	K562	blood:
11	chr21:45284985..45287311-chr21:45344207..45345768,2	K562	blood:
12	chr21:45288583..45290615-chr21:45331081..45332792,2	K562	blood:
13	chr21:45282912..45284880-chr21:45350407..45352499,2	K562	blood:
14	chr21:45279077..45280867-chr21:45358882..45361761,2	K562	blood:
15	chr21:45280145..45280762-chr21:45359058..45359617,2	MCF-7	breast:
16	chr21:45287059..45290436-chr21:45298345..45302746,3	MCF-7	breast:
17	chr21:45289974..45292578-chr21:45344758..45347739,2	K562	blood:
18	chr21:45282600..45286741-chr21:45429139..45433009,5	MCF-7	breast:
19	chr21:45283298..45287513-chr21:45338855..45343382,5	K562	blood:
20	chr21:45280312..45282784-chr21:45340621..45342718,2	K562	blood:
21	chr21:45281251..45288408-chr21:45292401..45302111,14	MCF-7	breast:
22	chr10:106911664..106912164-chr21:45274314..45274854,2	MCF-7	breast:
23	chr21:45227701..45229997-chr21:45280310..45283557,3	K562	blood:
24	chr21:45273597..45276751-chr21:45277053..45279889,4	K562	blood:
25	chr21:45228592..45232844-chr21:45283509..45286625,5	MCF-7	breast:
26	chr21:45288734..45291186-chr21:45298713..45301345,2	MCF-7	breast:
27	chr21:45277545..45281812-chr21:45337639..45343236,6	K562	blood:
28	chr21:45282912..45284880-chr21:45350407..45353939,3	K562	blood:
29	chr21:45272908..45275476-chr21:45277355..45279131,2	MCF-7	breast:
30	chr21:45261247..45264738-chr21:45270160..45273538,3	K562	blood:
31	chr21:45283616..45286882-chr21:45299913..45305661,6	MCF-7	breast:
32	chr19:2543070..2544057-chr21:45284224..45284926,2	Hela-S3	cervix:
33	chr21:45283392..45285849-chr21:45288020..45292209,4	MCF-7	breast:
34	chr21:45187250..45190053-chr21:45278541..45281497,2	K562	blood:
35	chr21:45279531..45281837-chr21:45307494..45310179,2	K562	blood:
36	chr21:45282036..45289054-chr21:45334704..45338842,9	K562	blood:
37	chr1:9692688..9694194-chr21:45288971..45291909,2	K562	blood:
38	chr21:45209429..45212325-chr21:45284308..45286024,2	MCF-7	breast:
39	chr21:45289119..45291947-chr21:45336176..45338497,2	K562	blood:
40	chr21:45279182..45280924-chr21:45283571..45285160,2	MCF-7	breast:
41	chr21:45233535..45235177-chr21:45269820..45272571,2	MCF-7	breast:
42	chr21:45274087..45276071-chr21:45284216..45286034,2	MCF-7	breast:
43	chr21:45291069..45293875-chr21:45339586..45342577,2	K562	blood:
44	chr21:45272908..45275476-chr21:45277355..45279131,2	MCF-7	breast:
45	chr21:45226367..45233141-chr21:45284145..45288607,11	K562	blood:
46	chr21:45278596..45280417-chr21:45324857..45327468,2	K562	blood:
47	chr21:45250176..45252507-chr21:45266082..45267987,2	MCF-7	breast:
48	chr21:45249455..45252079-chr21:45279419..45281351,2	K562	blood:
49	chr21:45283737..45286588-chr21:45430466..45433524,3	K562	blood:
50	chr21:45272094..45273764-chr21:45283911..45285574,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRP1-3	chr21:45287558-45287627	NONHSAT082463
2	lnc-RRP1-3	chr21:45287020-45287227	NONHSAT082463
3	lnc-RRP1-3	chr21:45286500-45286546	NONHSAT082463
4	lnc-RRP1-3	chr21:45287374-45287475	NONHSAT082463

No data

Variant related genes	Relation type
MYL6P1	TF binding region
AGPAT3	TF binding region
MYL6P1	CpG island
AGPAT3	CpG island
ENSG00000199598	chromatin interactions
ENSG00000160218	chromatin interactions
ENSG00000215458	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000160216	chromatin interactions
ENSG00000226543	chromatin interactions

Extended variants
information (count: 1256 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2838423	chr21:45267697-45267698	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576582213	chr21:45267715-45267716	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs151269276	chr21:45267755-45267756	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186728324	chr21:45267772-45267773	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557391523	chr21:45267789-45267790	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141698459	chr21:45267790-45267791	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147086291	chr21:45267791-45267792	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537429046	chr21:45267795-45267796	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556154819	chr21:45267820-45267821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567788941	chr21:45267833-45267834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545516113	chr21:45267835-45267836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113619014	chr21:45267840-45267841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370204761	chr21:45267870-45267871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575555832	chr21:45267880-45267881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs118167506	chr21:45267881-45267882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138485154	chr21:45267894-45267895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565125019	chr21:45267897-45267898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs13052284	chr21:45267899-45267900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560873950	chr21:45267902-45267903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115314322	chr21:45267919-45267920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9979747	chr21:45267929-45267930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142592168	chr21:45267938-45267939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117177643	chr21:45267956-45267957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73369349	chr21:45267997-45267998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2838424	chr21:45268009-45268010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115372388	chr21:45268015-45268016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559930457	chr21:45268023-45268024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13050382	chr21:45268046-45268047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191488474	chr21:45268097-45268098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150277155	chr21:45268119-45268120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570636193	chr21:45268136-45268137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561704158	chr21:45268137-45268138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs13052562	chr21:45268138-45268139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13052655	chr21:45268166-45268167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs3042084	chr21:45268170-45268171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13052658	chr21:45268172-45268173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs397866664	chr21:45268173-45268174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs55681300	chr21:45268176-45268177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184019242	chr21:45268180-45268181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs137870349	chr21:45268181-45268182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113303970	chr21:45268189-45268190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372890004	chr21:45268202-45268203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553448258	chr21:45268242-45268243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2329581	chr21:45268312-45268313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539624030	chr21:45268329-45268330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558350459	chr21:45268359-45268360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs8127150	chr21:45268381-45268382	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs544102711	chr21:45268451-45268452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145459976	chr21:45268460-45268461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188895071	chr21:45268470-45268471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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 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
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45263800-45269600	Weak transcription	Spleen	Spleen
2	chr21:45267400-45267800	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr21:45267600-45280400	Weak transcription	Gastric	stomach
4	chr21:45267800-45269600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr21:45268800-45269400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr21:45269200-45270600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr21:45269400-45269600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr21:45269400-45270000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:45269400-45270000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr21:45269600-45270000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr21:45269600-45270000	Enhancers	Adipose Nuclei	Adipose
12	chr21:45269600-45270000	Enhancers	Esophagus	oesophagus
13	chr21:45269600-45270000	Enhancers	Left Ventricle	heart
14	chr21:45269600-45270000	Enhancers	Right Ventricle	heart
15	chr21:45269600-45270000	Enhancers	Spleen	Spleen
16	chr21:45269600-45270000	Enhancers	Hela-S3	cervix
17	chr21:45269600-45270200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr21:45269600-45270200	Enhancers	Stomach Mucosa	stomach
19	chr21:45269600-45270400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr21:45269800-45270200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr21:45269800-45270200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr21:45269800-45270200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr21:45270000-45271200	Weak transcription	Right Ventricle	heart
24	chr21:45270000-45273400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr21:45270000-45274800	Weak transcription	Spleen	Spleen
26	chr21:45270400-45271200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr21:45270600-45272000	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
28	chr21:45271200-45271400	Enhancers	Right Ventricle	heart
29	chr21:45271200-45272000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr21:45271400-45271800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr21:45272000-45273600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr21:45273400-45273800	Enhancers	Brain Anterior Caudate	brain
33	chr21:45273400-45274200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr21:45273400-45275000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr21:45273600-45274800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr21:45273800-45274000	Bivalent Enhancer	HepG2	liver
37	chr21:45273800-45274400	ZNF genes & repeats	K562	blood
38	chr21:45274000-45274400	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr21:45274200-45274400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr21:45274200-45274800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr21:45274200-45274800	Enhancers	GM12878-XiMat	blood
42	chr21:45274200-45275200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:45274200-45275200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr21:45274200-45276000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr21:45274200-45276000	Enhancers	Placenta	Placenta
46	chr21:45274200-45276200	Enhancers	Primary hematopoietic stem cells	blood
47	chr21:45274200-45276200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr21:45274400-45274600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr21:45274400-45274800	Bivalent Enhancer	HepG2	liver
50	chr21:45274400-45275200	Flanking Active TSS	K562	blood

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