Variant report

Variant	nsv870589
Chromosome Location	chr1:10840905-10901994
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1139)
CpG islands
(count:2504)
Chromatin interactive
region (count:116)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1139 , 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	chr1:10856617-10856959	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10856711-10856837	K562	blood:	n/a	n/a
3	ATF1	chr1:10892500-10892630	K562	blood:	n/a	n/a
4	ATF2	chr1:10856584-10856977	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:10856521-10856938	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr1:10856547-10856918	A549	lung:	n/a	n/a
7	ATF3	chr1:10853238-10853505	K562	blood:	n/a	n/a
8	BACH1	chr1:10853903-10854532	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:10848905-10848939	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:10899649-10899712	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:10895531-10896453	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr1:10856646-10856973	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr1:10871791-10872058	GM12878	blood:	n/a	n/a
14	BCL3	chr1:10856552-10857000	A549	lung:	n/a	chr1:10856780-10856793 chr1:10856690-10856703 chr1:10856590-10856599 chr1:10856585-10856598 chr1:10856593-10856602
15	BHLHE40	chr1:10854031-10854127	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:10853971-10854236	K562	blood:	n/a	n/a
17	BHLHE40	chr1:10854020-10854171	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:10853978-10854020	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr1:10895940-10896274	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr1:10893936-10894419	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr1:10856661-10856883	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr1:10856755-10856873	HepG2	liver:	n/a	n/a
23	CBX3	chr1:10856631-10856918	K562	blood:	n/a	n/a
24	CCNT2	chr1:10856670-10856938	K562	blood:	n/a	n/a
25	CCNT2	chr1:10853919-10854201	K562	blood:	n/a	chr1:10853946-10853955
26	CCNT2	chr1:10895926-10896187	K562	blood:	n/a	chr1:10896161-10896170
27	CEBPB	chr1:10856568-10857024	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr1:10853229-10853488	IMR90	lung:	n/a	chr1:10853340-10853351
29	CEBPB	chr1:10853180-10853538	Hela-S3	cervix:	n/a	chr1:10853340-10853351
30	CEBPB	chr1:10900367-10900646	HepG2	liver:	n/a	chr1:10900546-10900559 chr1:10900490-10900501
31	CEBPB	chr1:10871939-10872009	HepG2	liver:	n/a	chr1:10871985-10871996
32	CEBPB	chr1:10853195-10853505	K562	blood:	n/a	chr1:10853340-10853351
33	CEBPB	chr1:10857222-10857252	H1-hESC	embryonic stem cell:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
34	CEBPB	chr1:10859370-10859447	K562	blood:	n/a	chr1:10859417-10859426 chr1:10859417-10859426
35	CEBPB	chr1:10891037-10891376	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:10900431-10900615	H1-hESC	embryonic stem cell:	n/a	chr1:10900546-10900559 chr1:10900490-10900501
37	CEBPB	chr1:10859305-10859480	Hela-S3	cervix:	n/a	chr1:10859417-10859426 chr1:10859417-10859426
38	CEBPB	chr1:10857145-10857399	K562	blood:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
39	CEBPB	chr1:10900336-10900627	A549	lung:	n/a	chr1:10900546-10900559 chr1:10900490-10900501
40	CEBPB	chr1:10851826-10852074	MCF-7	breast:	n/a	n/a
41	CEBPB	chr1:10900438-10900567	K562	blood:	n/a	chr1:10900546-10900559 chr1:10900490-10900501
42	CEBPB	chr1:10853154-10853570	H1-hESC	embryonic stem cell:	n/a	chr1:10853340-10853351
43	CEBPB	chr1:10853820-10854164	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr1:10851855-10851973	K562	blood:	n/a	n/a
45	CEBPB	chr1:10890992-10891486	MCF-7	breast:	n/a	n/a
46	CEBPB	chr1:10853217-10853510	HepG2	liver:	n/a	chr1:10853340-10853351
47	CEBPB	chr1:10895966-10896166	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:10875181-10875385	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:10856646-10856864	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr1:10851767-10852015	Hela-S3	cervix:	n/a	n/a

(count:2504 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10853793-10853843	BJ	skin:	n/a
2	chr1:10887875-10887925	HCT-116	colon:	n/a
3	chr1:10856707-10856757	SAEC	small airway:	n/a
4	chr1:10853793-10853843	BJ	skin:	n/a
5	chr1:10887875-10887925	HCT-116	colon:	n/a
6	chr1:10856707-10856757	SAEC	small airway:	n/a
7	chr1:10855062-10855112	PFSK-1	brain:	n/a
8	chr1:10855226-10855276	GM19239	blood:	n/a
9	chr1:10895950-10896000	ovcar-3	ovarian:	n/a
10	chr1:10855062-10855112	AG09309	skin:	n/a
11	chr1:10895978-10896028	HepG2	liver:	n/a
12	chr1:10853793-10853843	AG10803	skin:	n/a
13	chr1:10891531-10891581	Jurkat	blood:	n/a
14	chr1:10856657-10856707	IMR90	lung:	fetal
15	chr1:10846092-10846142	GM12878	blood:	n/a
16	chr1:10846092-10846142	IMR90	lung:	fetal
17	chr1:10854307-10854357	IMR90	lung:	fetal
18	chr1:10847541-10847591	HL-60	blood:	n/a
19	chr1:10856739-10856789	MCF10A-Er-Src	breast:	n/a
20	chr1:10896004-10896054	AG09319	gingival:	n/a
21	chr1:10857436-10857486	GM06990	blood:	n/a
22	chr1:10854445-10854495	SAEC	small airway:	n/a
23	chr1:10856707-10856757	U87	brain:	n/a
24	chr1:10843154-10843204	SAEC	small airway:	n/a
25	chr1:10856739-10856789	AG10803	skin:	n/a
26	chr1:10855806-10855856	AG09319	gingival:	n/a
27	chr1:10855226-10855276	Hela-S3	cervix:	n/a
28	chr1:10888566-10888616	AG09309	skin:	n/a
29	chr1:10875522-10875572	RPTEC	kidney:	n/a
30	chr1:10851647-10851697	PANC-1	pancreas:	n/a
31	chr1:10854307-10854357	NHDF-neo	bronchial:	n/a
32	chr1:10851647-10851697	Jurkat	blood:	n/a
33	chr1:10896343-10896393	HRCEpiC	kidney:	n/a
34	chr1:10853918-10853968	Jurkat	blood:	n/a
35	chr1:10847594-10847644	HL-60	blood:	n/a
36	chr1:10857110-10857160	CMK	blood:	n/a
37	chr1:10856657-10856707	GM12891	blood:	n/a
38	chr1:10893824-10893874	SAEC	small airway:	n/a
39	chr1:10857091-10857141	PrEC	prostate:	n/a
40	chr1:10853793-10853843	MCF10A-Er-Src	breast:	n/a
41	chr1:10857436-10857486	NHDF-neo	bronchial:	n/a
42	chr1:10895950-10896000	Caco-2	colon:	n/a
43	chr1:10854307-10854357	HCPEpiC	choroid plexus:	n/a
44	chr1:10856943-10856993	MCF10A-Er-Src	breast:	n/a
45	chr1:10856943-10856993	HMEC	breast:	n/a
46	chr1:10874315-10874365	NH-A	brain:	n/a
47	chr1:10856657-10856707	Hepatocyte	liver:	n/a
48	chr1:10853918-10853968	LNCaP	prostate:	n/a
49	chr1:10896004-10896054	AG10803	skin:	n/a
50	chr1:10856466-10856516	ECC-1	luminal epithelium:	n/a

(count:116 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:10674874..10677843-chr1:10895529..10897337,2	K562	blood:
2	chr1:10876492..10878024-chr1:10879047..10880771,2	K562	blood:
3	chr1:10882954..10889403-chr1:10891369..10897064,9	MCF-7	breast:
4	chr1:10892514..10895346-chr1:10924391..10927017,2	K562	blood:
5	chr1:10813375..10816020-chr1:10863170..10865862,2	MCF-7	breast:
6	chr1:10872908..10874910-chr1:10877344..10879444,2	K562	blood:
7	chr1:10895780..10898598-chr1:10906718..10908430,2	K562	blood:
8	chr1:10863738..10865854-chr1:10872019..10875037,3	MCF-7	breast:
9	chr1:10874108..10876222-chr1:10881051..10883171,3	K562	blood:
10	chr1:10837835..10840476-chr1:10895758..10897278,2	MCF-7	breast:
11	chr1:10859862..10862247-chr1:10862997..10864599,2	MCF-7	breast:
12	chr1:10859730..10862103-chr1:10872540..10874271,2	K562	blood:
13	chr1:10888572..10890725-chr1:10893676..10896099,3	K562	blood:
14	chr1:10854264..10855791-chr1:10891105..10892781,2	MCF-7	breast:
15	chr1:10841137..10843114-chr1:10851742..10854578,2	MCF-7	breast:
16	chr1:10888572..10890725-chr1:10893676..10896099,3	K562	blood:
17	chr1:10813459..10815846-chr1:10840414..10843318,2	MCF-7	breast:
18	chr1:10873474..10875148-chr1:10878520..10880387,2	MCF-7	breast:
19	chr1:10868648..10871546-chr1:10878409..10880098,2	K562	blood:
20	chr1:10887422..10891418-chr1:10892933..10896099,4	K562	blood:
21	chr1:10876866..10879184-chr1:10889466..10891905,3	K562	blood:
22	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
23	chr1:10859862..10862247-chr1:10862997..10864599,2	MCF-7	breast:
24	chr1:10842014..10843891-chr1:10851096..10853809,2	K562	blood:
25	chr1:10717765..10719511-chr1:10863932..10866703,2	K562	blood:
26	chr1:10864191..10865741-chr1:10869374..10870963,2	MCF-7	breast:
27	chr1:10859540..10861856-chr1:11072997..11074622,2	MCF-7	breast:
28	chr1:10850430..10851341-chr19:18956907..18957709,2	MCF-7	breast:
29	chr1:10886250..10887868-chr1:10894690..10896395,2	MCF-7	breast:
30	chr1:10855453..10857266-chr1:10883652..10886481,2	MCF-7	breast:
31	chr1:10862380..10865168-chr1:10872409..10876550,4	K562	blood:
32	chr1:10872908..10874910-chr1:10877344..10879444,2	K562	blood:
33	chr1:10854336..10856933-chr1:10871680..10874443,2	MCF-7	breast:
34	chr1:10835909..10837640-chr1:10847012..10848890,2	MCF-7	breast:
35	chr1:10854966..10857805-chr1:10877688..10880210,2	K562	blood:
36	chr1:10614584..10616162-chr1:10883183..10885480,2	K562	blood:
37	chr1:10694140..10696229-chr1:10885047..10887221,2	MCF-7	breast:
38	chr1:10899594..10902862-chr1:10958489..10961568,3	MCF-7	breast:
39	chr1:10854264..10855791-chr1:10891105..10892781,2	MCF-7	breast:
40	chr1:10864191..10865741-chr1:10869374..10870963,2	MCF-7	breast:
41	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
42	chr1:10854648..10857123-chr1:10863461..10865008,2	K562	blood:
43	chr1:10892296..10895253-chr1:10897751..10901247,3	K562	blood:
44	chr1:10890948..10893091-chr1:10894513..10897214,2	MCF-7	breast:
45	chr1:10789630..10791683-chr1:10843060..10845092,2	MCF-7	breast:
46	chr1:10868718..10870802-chr1:10872433..10874614,2	MCF-7	breast:
47	chr1:10893753..10896374-chr1:10897751..10899906,2	K562	blood:
48	chr1:10845553..10848125-chr1:10850138..10852600,3	K562	blood:
49	chr1:10876866..10879184-chr1:10889466..10891905,3	K562	blood:
50	chr1:10873474..10875148-chr1:10878520..10880387,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASZ1-3	chr1:10888161-10888435	uc_10_-
2	lnc-PEX14-9	chr1:10847997-10848198	uc_9_+
3	lnc-TARDBP-10	chr1:10888161-10888435	uc_10_+
4	lnc-C1orf127-1	chr1:10847997-10848198	uc_9_-

No data

Variant related genes	Relation type
CASZ1	TF binding region
CASZ1	CpG island
ENSG00000243267	chromatin interactions
ENSG00000130940	chromatin interactions
ENSG00000120948	chromatin interactions

Extended variants
information (count: 2727 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17035713	chr1:10840905-10840906	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147003013	chr1:10840949-10840950	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs533418076	chr1:10840982-10840983	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs576543381	chr1:10840991-10840992	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs34910022	chr1:10841120-10841121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531646881	chr1:10841127-10841128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138186591	chr1:10841131-10841132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571074037	chr1:10841133-10841134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532240529	chr1:10841175-10841176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374446678	chr1:10841220-10841221	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs377075476	chr1:10841223-10841224	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs547649680	chr1:10841232-10841233	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs565882604	chr1:10841236-10841237	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs536234814	chr1:10841242-10841243	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs149545580	chr1:10841260-10841261	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs569674525	chr1:10841283-10841284	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs144032069	chr1:10841298-10841299	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs558703629	chr1:10841312-10841313	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs578105821	chr1:10841324-10841325	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs710135	chr1:10841333-10841334	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs554434097	chr1:10841334-10841335	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs572608124	chr1:10841345-10841346	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs117224327	chr1:10841420-10841421	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs560918931	chr1:10841465-10841466	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs576042622	chr1:10841474-10841475	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs34845269	chr1:10841484-10841485	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs543495280	chr1:10841487-10841488	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565265379	chr1:10841529-10841530	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs532333327	chr1:10841545-10841546	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs148259749	chr1:10841579-10841580	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs141869071	chr1:10841590-10841591	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs529902858	chr1:10841608-10841609	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548528322	chr1:10841633-10841634	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs569636950	chr1:10841640-10841641	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs61775155	chr1:10841676-10841677	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs537079960	chr1:10841678-10841679	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs552296719	chr1:10841679-10841680	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs710136	chr1:10841703-10841704	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76858928	chr1:10841713-10841714	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs186030831	chr1:10841727-10841728	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs150643994	chr1:10841767-10841768	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs190356627	chr1:10841790-10841791	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs534722450	chr1:10841791-10841792	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs140008979	chr1:10841806-10841807	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs572622732	chr1:10841832-10841833	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs536512844	chr1:10841833-10841834	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs554875105	chr1:10841841-10841842	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs60314749	chr1:10841886-10841887	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs182747222	chr1:10841994-10841995	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs187038615	chr1:10841997-10841998	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10832600-10853400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:10837200-10841000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr1:10837400-10841200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:10838000-10841200	Weak transcription	Gastric	stomach
5	chr1:10838200-10841800	Enhancers	Psoas Muscle	Psoas
6	chr1:10838400-10841000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:10838600-10841000	Enhancers	Fetal Intestine Small	intestine
8	chr1:10838600-10842200	Weak transcription	Fetal Kidney	kidney
9	chr1:10838600-10843200	Enhancers	Left Ventricle	heart
10	chr1:10838600-10852400	Enhancers	Fetal Heart	heart
11	chr1:10838800-10841600	Enhancers	Lung	lung
12	chr1:10838800-10843600	Enhancers	Stomach Mucosa	stomach
13	chr1:10839200-10841600	Weak transcription	Small Intestine	intestine
14	chr1:10839200-10843000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr1:10839400-10841600	Enhancers	Pancreas	Pancrea
16	chr1:10839600-10842000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:10840000-10841400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr1:10840000-10842000	Enhancers	Esophagus	oesophagus
19	chr1:10840200-10841200	Weak transcription	Right Atrium	heart
20	chr1:10840200-10841600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:10840200-10843400	Enhancers	Stomach Smooth Muscle	stomach
22	chr1:10840400-10841600	Enhancers	Fetal Muscle Leg	muscle
23	chr1:10840400-10841800	Enhancers	Colonic Mucosa	Colon
24	chr1:10840400-10842400	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:10840400-10842800	Enhancers	Right Ventricle	heart
26	chr1:10840400-10843600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr1:10840400-10845400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:10840400-10845600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:10840400-10846200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:10840400-10848600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:10840600-10841000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr1:10840600-10841200	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:10840600-10842000	Weak transcription	Fetal Intestine Large	intestine
34	chr1:10840600-10842600	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr1:10840600-10844600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr1:10840800-10841000	Bivalent Enhancer	Fetal Stomach	stomach
37	chr1:10840800-10841000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr1:10841000-10841200	Enhancers	Fetal Muscle Trunk	muscle
39	chr1:10841000-10841400	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr1:10841000-10841600	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr1:10841000-10843000	Weak transcription	Fetal Intestine Small	intestine
42	chr1:10841200-10841600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:10841200-10841800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:10841200-10842200	Enhancers	Right Atrium	heart
45	chr1:10841200-10842400	Enhancers	Gastric	stomach
46	chr1:10841200-10842600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr1:10841200-10843600	Enhancers	Colon Smooth Muscle	Colon
48	chr1:10841400-10841600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr1:10841400-10841800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr1:10841600-10842000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon

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