Variant report

Variant	nsv834627
Chromosome Location	chr3:20068115-20227975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2925)
CpG islands
(count:1896)
Chromatin interactive
region (count:188)
LncRNA
region (count:12)
Mature miRNA
region (count: 1)
miRNA target
sites (count:14)

(count:2925 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20227487-20228388	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:20227329-20228186	K562	blood:	n/a	n/a
3	ARID3A	chr3:20096000-20096345	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20082402-20082577	K562	blood:	n/a	n/a
5	ARID3A	chr3:20081499-20081651	K562	blood:	n/a	n/a
6	ARID3A	chr3:20102456-20102678	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:20079145-20079315	K562	blood:	n/a	n/a
8	ARID3A	chr3:20080060-20080685	K562	blood:	n/a	n/a
9	ARID3A	chr3:20083156-20083470	K562	blood:	n/a	n/a
10	ATF1	chr3:20145751-20146090	K562	blood:	n/a	n/a
11	ATF1	chr3:20226994-20228147	K562	blood:	n/a	n/a
12	ATF1	chr3:20092738-20093002	K562	blood:	n/a	n/a
13	ATF2	chr3:20082866-20083368	GM12878	blood:	n/a	n/a
14	ATF2	chr3:20227637-20228238	GM12878	blood:	n/a	n/a
15	ATF2	chr3:20167264-20167940	GM12878	blood:	n/a	n/a
16	ATF2	chr3:20145673-20146200	GM12878	blood:	n/a	n/a
17	ATF2	chr3:20081302-20081776	GM12878	blood:	n/a	n/a
18	ATF2	chr3:20145678-20146063	GM12878	blood:	n/a	n/a
19	ATF2	chr3:20167304-20167868	GM12878	blood:	n/a	n/a
20	ATF2	chr3:20227207-20228211	GM12878	blood:	n/a	n/a
21	ATF3	chr3:20092643-20092877	K562	blood:	n/a	chr3:20092813-20092828
22	ATF3	chr3:20227535-20227966	K562	blood:	n/a	n/a
23	ATF3	chr3:20227575-20227873	GM12878	blood:	n/a	n/a
24	ATF3	chr3:20227527-20228058	GM12878	blood:	n/a	n/a
25	ATF3	chr3:20095922-20096535	A549	lung:	n/a	n/a
26	ATF3	chr3:20227505-20227918	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr3:20227585-20227975	K562	blood:	n/a	n/a
28	ATF3	chr3:20227425-20228037	HepG2	liver:	n/a	n/a
29	ATF3	chr3:20095973-20096523	HCT-116	colon:	n/a	n/a
30	ATF3	chr3:20096028-20096490	A549	lung:	n/a	n/a
31	ATF3	chr3:20227448-20228043	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr3:20227605-20227903	HepG2	liver:	n/a	n/a
33	BACH1	chr3:20197358-20197428	K562	blood:	n/a	n/a
34	BATF	chr3:20090142-20090441	GM12878	blood:	n/a	n/a
35	BATF	chr3:20167475-20167827	GM12878	blood:	n/a	chr3:20167811-20167819
36	BATF	chr3:20098660-20098987	GM12878	blood:	n/a	chr3:20098865-20098876
37	BATF	chr3:20096097-20096464	GM12878	blood:	n/a	chr3:20096331-20096341 chr3:20096284-20096294
38	BATF	chr3:20167468-20167777	GM12878	blood:	n/a	n/a
39	BATF	chr3:20098688-20099122	GM12878	blood:	n/a	chr3:20098865-20098876
40	BCL11A	chr3:20167373-20167761	GM12878	blood:	n/a	n/a
41	BCL11A	chr3:20098689-20099052	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:20167426-20167745	GM12878	blood:	n/a	n/a
43	BCL3	chr3:20081163-20081784	GM12878	blood:	n/a	chr3:20081692-20081705 chr3:20081686-20081699 chr3:20081365-20081374 chr3:20081683-20081696 chr3:20081685-20081698 chr3:20081684-20081693 chr3:20081691-20081704
44	BCL3	chr3:20095916-20096563	A549	lung:	n/a	n/a
45	BCL3	chr3:20098725-20099099	GM12878	blood:	n/a	n/a
46	BCL3	chr3:20081817-20082483	GM12878	blood:	n/a	chr3:20081920-20081929 chr3:20081923-20081932 chr3:20081917-20081926 chr3:20081918-20081931 chr3:20082391-20082404 chr3:20081916-20081929
47	BCL3	chr3:20227304-20227885	A549	lung:	n/a	n/a
48	BCL3	chr3:20095806-20096557	A549	lung:	n/a	n/a
49	BCLAF1	chr3:20082061-20082647	GM12878	blood:	n/a	chr3:20082391-20082404
50	BCLAF1	chr3:20167291-20167861	GM12878	blood:	n/a	n/a

(count:1896 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20081516-20081566	K562	blood:	n/a
2	chr3:20081582-20081632	HCF	heart:	n/a
3	chr3:20227789-20227839	ovcar-3	ovarian:	n/a
4	chr3:20227663-20227713	K562	blood:	n/a
5	chr3:20227789-20227839	ProgFib	skin:	n/a
6	chr3:20081516-20081566	K562	blood:	n/a
7	chr3:20081582-20081632	HCF	heart:	n/a
8	chr3:20227789-20227839	ovcar-3	ovarian:	n/a
9	chr3:20227663-20227713	K562	blood:	n/a
10	chr3:20227789-20227839	ProgFib	skin:	n/a
11	chr3:20227925-20227975	NHDF-neo	bronchial:	n/a
12	chr3:20227809-20227859	RPTEC	kidney:	n/a
13	chr3:20227940-20227990	BE2_C	brain:	n/a
14	chr3:20227925-20227975	ECC-1	luminal epithelium:	n/a
15	chr3:20078165-20078215	HAEpiC	amniotic membrane:	n/a
16	chr3:20195067-20195117	NB4	blood:	n/a
17	chr3:20195067-20195117	HNPCEpiC	eye:	n/a
18	chr3:20078165-20078215	ECC-1	luminal epithelium:	n/a
19	chr3:20226994-20227044	ovcar-3	ovarian:	n/a
20	chr3:20227663-20227713	BE2_C	brain:	n/a
21	chr3:20082425-20082475	H1-hESC	embryonic stem cell:	embryo
22	chr3:20081582-20081632	BJ	skin:	n/a
23	chr3:20078165-20078215	U87	brain:	n/a
24	chr3:20227059-20227109	IMR90	lung:	fetal
25	chr3:20082285-20082335	Caco-2	colon:	n/a
26	chr3:20082285-20082335	AG10803	skin:	n/a
27	chr3:20202403-20202453	SK-N-SH_RA	brain:	n/a
28	chr3:20081516-20081566	SK-N-MC	brain:	n/a
29	chr3:20082916-20082966	HCM	heart:	n/a
30	chr3:20183665-20183715	SK-N-MC	brain:	n/a
31	chr3:20227801-20227851	A549	lung:	n/a
32	chr3:20082285-20082335	HEEpiC	esophagus:	n/a
33	chr3:20226964-20227014	ProgFib	skin:	n/a
34	chr3:20081518-20081568	MCF10A-Er-Src	breast:	n/a
35	chr3:20227789-20227839	GM12878	blood:	n/a
36	chr3:20081161-20081211	IMR90	lung:	fetal
37	chr3:20082916-20082966	H1-hESC	embryonic stem cell:	embryo
38	chr3:20081585-20081635	SK-N-MC	brain:	n/a
39	chr3:20226964-20227014	HRE	kidney:	n/a
40	chr3:20227670-20227720	HRPEpiC	eye:	n/a
41	chr3:20078165-20078215	SKMC	muscle:	n/a
42	chr3:20227809-20227859	GM12891	blood:	n/a
43	chr3:20081518-20081568	SK-N-SH	brain:	n/a
44	chr3:20223923-20223973	RPTEC	kidney:	n/a
45	chr3:20227397-20227447	PANC-1	pancreas:	n/a
46	chr3:20081582-20081632	SK-N-SH	brain:	n/a
47	chr3:20081585-20081635	HAEpiC	amniotic membrane:	n/a
48	chr3:20227789-20227839	ECC-1	luminal epithelium:	n/a
49	chr3:20081161-20081211	GM19239	blood:	n/a
50	chr3:20227516-20227566	HepG2	liver:	n/a

(count:188 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:20188934..20192869-chr3:20226143..20228338,3	MCF-7	breast:
2	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
3	chr3:20201533..20203572-chr3:20204589..20206739,2	K562	blood:
4	chr3:20151399..20153827-chr3:20159687..20162098,3	K562	blood:
5	chr3:20200366..20203372-chr3:20209857..20212107,3	K562	blood:
6	chr3:20213813..20216501-chr3:20227432..20229116,2	MCF-7	breast:
7	chr3:20063995..20066056-chr3:20077383..20080079,2	K562	blood:
8	chr3:20197560..20199783-chr3:20225608..20228182,2	MCF-7	breast:
9	chr3:20197127..20199080-chr3:20208900..20210840,2	MCF-7	breast:
10	chr3:20091766..20093511-chr3:20226250..20228474,2	K562	blood:
11	chr3:20080757..20082677-chr3:20192981..20195193,2	K562	blood:
12	chr3:20211282..20213997-chr3:20225429..20228054,3	MCF-7	breast:
13	chr3:20133592..20135375-chr3:20142503..20144573,2	K562	blood:
14	chr3:20212661..20217850-chr3:20224065..20229766,9	K562	blood:
15	chr3:20083177..20086049-chr3:20086105..20087867,2	MCF-7	breast:
16	chr3:20206092..20207782-chr3:20216460..20218892,2	K562	blood:
17	chr3:20160386..20162756-chr3:20172063..20173693,2	K562	blood:
18	chr3:20079279..20082964-chr3:20226299..20229620,6	K562	blood:
19	chr3:20191414..20193219-chr3:20194880..20197331,2	K562	blood:
20	chr3:19988644..19989202-chr3:20081357..20082279,2	MCF-7	breast:
21	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
22	chr3:20187588..20190106-chr3:20193535..20195392,3	K562	blood:
23	chr3:20092001..20094712-chr3:20096791..20098373,2	K562	blood:
24	chr3:20202636..20204189-chr3:20204811..20206613,2	MCF-7	breast:
25	chr13:113841278..113842020-chr3:20226671..20227468,2	Hela-S3	cervix:
26	chr3:19988765..19989271-chr3:20079780..20080698,2	NB4	blood:
27	chr3:20116266..20118891-chr3:20121268..20123312,2	MCF-7	breast:
28	chr3:20193485..20196421-chr3:20205590..20208525,2	K562	blood:
29	chr3:20096569..20098445-chr3:20104189..20106827,2	MCF-7	breast:
30	chr1:167582674..167583549-chr3:20205708..20206218,2	MCF-7	breast:
31	chr3:20209340..20212001-chr3:20214407..20216140,2	K562	blood:
32	chr3:20161536..20163874-chr3:20167611..20170613,5	K562	blood:
33	chr3:20092001..20094712-chr3:20096791..20098373,2	K562	blood:
34	chr3:20158113..20160465-chr3:20226227..20229427,3	K562	blood:
35	chr15:42565172..42565968-chr3:20227231..20227766,2	Hela-S3	cervix:
36	chr3:20227937..20230614-chr3:20238703..20240365,2	K562	blood:
37	chr3:20138475..20140475-chr3:20146667..20148276,2	K562	blood:
38	chr3:19987980..19990853-chr3:20225710..20227616,2	MCF-7	breast:
39	chr3:20188319..20191715-chr3:20218902..20221810,3	K562	blood:
40	chr3:20131147..20133455-chr3:20135064..20136948,2	K562	blood:
41	chr3:20069120..20070627-chr3:20076892..20079468,2	K562	blood:
42	chr3:20058205..20061001-chr3:20066769..20068692,2	K562	blood:
43	chr3:20071377..20073447-chr3:20074855..20077238,2	K562	blood:
44	chr3:20212661..20217850-chr3:20224065..20229766,9	K562	blood:
45	chr3:20185698..20188649-chr3:20188952..20191423,4	K562	blood:
46	chr3:20105530..20108149-chr3:20143893..20147714,3	MCF-7	breast:
47	chr3:20121220..20122803-chr3:20153116..20155641,2	MCF-7	breast:
48	chr3:20200366..20203372-chr3:20209857..20212107,3	K562	blood:
49	chr3:20161409..20163112-chr3:20165671..20167276,2	MCF-7	breast:
50	chr3:20096664..20098215-chr3:20134683..20136839,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PP2D1-2	chr3:20211553-20212307	NONHSAT088614
2	lnc-KAT2B-1	chr3:20218709-20218742	ENSG00000237485.1
3	lnc-KAT2B-5	chr3:20202876-20203154	l_2328_chr3:20202875-20210905_testes
4	lnc-KAT2B-1	chr3:20215736-20216017	ENSG00000237485.1
5	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
6	lnc-KAT2B-1	chr3:20215778-20216017	ENSG00000237485.1
7	lnc-PP2D1-2	chr3:20212535-20212759	NONHSAT088614
8	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
9	lnc-KAT2B-1	chr3:20227467-20227919	ENSG00000237485.1
10	lnc-KAT2B-1	chr3:20227726-20230848	NONHSAT088617
11	lnc-KAT2B-5	chr3:20210846-20210905	l_2328_chr3:20202875-20210905_testes
12	lnc-KAT2B-1	chr3:20227467-20227607	ENSG00000237485.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3135a	chr3:20179066-20179087	MIMAT0015001

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KAT2B	hsa-miR-92a-3p	chr3:20195765-20195772
2	KAT2B	hsa-miR-32-5p	chr3:20195750-20195772
3	KAT2B	hsa-miR-25-3p	chr3:20195765-20195772
4	KAT2B	hsa-miR-106b-5p	chr3:20194137-20194143
5	KAT2B	hsa-miR-32-5p	chr3:20195765-20195772
6	KAT2B	hsa-miR-92a-3p	chr3:20195750-20195772
7	KAT2B	hsa-miR-106b-5p	chr3:20195703-20195723
8	KAT2B	hsa-miR-181a-5p	chr3:20194367-20194390
9	KAT2B	hsa-miR-93-5p	chr3:20194137-20194143
10	KAT2B	hsa-miR-93-5p	chr3:20195701-20195723
11	KAT2B	hsa-miR-181b-5p	chr3:20194367-20194390
12	KAT2B	hsa-miR-25-3p	chr3:20195750-20195772
13	KAT2B	hsa-miR-106b-5p	chr3:20194123-20194144
14	KAT2B	hsa-miR-93-5p	chr3:20194121-20194144

Variant related genes	Relation type
KAT2B	TF binding region
MIR3135A	TF binding region
SGOL1-AS1	TF binding region
SGOL1	TF binding region
KAT2B	CpG island
MIR3135A	CpG island
SGOL1-AS1	CpG island
SGOL1	CpG island
ENSG00000266745	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000126226	chromatin interactions
ENSG00000117625	chromatin interactions
ENSG00000235194	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000201545	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000237485	chromatin interactions
ENSG00000234779	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000158158	chromatin interactions
ENSG00000252442	chromatin interactions
ENSG00000163576	chromatin interactions

Extended variants
information (count: 6203 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:6203 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539521249	chr3:20068192-20068193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551831778	chr3:20068205-20068206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141531951	chr3:20068253-20068254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368968781	chr3:20068282-20068283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147024946	chr3:20068308-20068309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372856082	chr3:20068363-20068364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573951034	chr3:20068364-20068365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74379246	chr3:20068388-20068389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556449296	chr3:20068440-20068441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs578105520	chr3:20068463-20068464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138087369	chr3:20068471-20068472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541260544	chr3:20068484-20068485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs180828343	chr3:20068494-20068495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185094270	chr3:20068559-20068560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543481199	chr3:20068584-20068585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540186942	chr3:20068610-20068611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561675039	chr3:20068661-20068662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556325159	chr3:20068675-20068676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529167996	chr3:20068697-20068698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375864910	chr3:20068714-20068715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544517348	chr3:20068786-20068787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562668715	chr3:20068843-20068844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs570545765	chr3:20068894-20068895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557968649	chr3:20068921-20068922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551329016	chr3:20068940-20068941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566623051	chr3:20068964-20068965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527785261	chr3:20069099-20069100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201824537	chr3:20069169-20069170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs57793586	chr3:20069171-20069172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200331002	chr3:20069172-20069173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78603075	chr3:20069185-20069186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs546699270	chr3:20069194-20069195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149529890	chr3:20069199-20069200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538123952	chr3:20069207-20069208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374356199	chr3:20069233-20069234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189693830	chr3:20069237-20069238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371442741	chr3:20069238-20069239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571885088	chr3:20069239-20069240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543734914	chr3:20069253-20069254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539217086	chr3:20069267-20069268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554073386	chr3:20069278-20069279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572933655	chr3:20069279-20069280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181337272	chr3:20069289-20069290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562114526	chr3:20069330-20069331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114988550	chr3:20069360-20069361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573658098	chr3:20069364-20069365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202215209	chr3:20069421-20069422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543902813	chr3:20069431-20069432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs397988888	chr3:20069438-20069439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562793289	chr3:20069446-20069447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Prostate cancer	19363497	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD

Chromatin state (count:4807 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20056600-20080000	Weak transcription	Right Atrium	heart
2	chr3:20065800-20068600	Weak transcription	Stomach Mucosa	stomach
3	chr3:20065800-20070200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:20065800-20070200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:20066000-20068800	Weak transcription	HUVEC	blood vessel
6	chr3:20067000-20068400	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr3:20067200-20068800	Weak transcription	Adipose Nuclei	Adipose
8	chr3:20067400-20076000	Weak transcription	K562	blood
9	chr3:20067800-20068400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:20067800-20068600	Enhancers	Lung	lung
11	chr3:20067800-20069000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr3:20067800-20070600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:20068400-20078800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:20068600-20069200	Enhancers	Stomach Mucosa	stomach
15	chr3:20068800-20069200	Enhancers	Adipose Nuclei	Adipose
16	chr3:20068800-20069200	Enhancers	Fetal Lung	lung
17	chr3:20068800-20069400	Enhancers	HUVEC	blood vessel
18	chr3:20069000-20070200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:20070200-20070400	Active TSS	Brain Cingulate Gyrus	brain
20	chr3:20070200-20070800	Active TSS	Brain Anterior Caudate	brain
21	chr3:20070200-20071000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:20070200-20071000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr3:20070400-20070600	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr3:20070400-20070600	Active TSS	Brain Substantia Nigra	brain
25	chr3:20070400-20070800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:20070400-20071000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr3:20070400-20071000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:20070400-20071200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:20070600-20070800	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr3:20070600-20071000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr3:20070600-20071000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:20070600-20071000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:20070600-20071000	Enhancers	Brain Germinal Matrix	brain
34	chr3:20070600-20071200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr3:20070600-20071200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:20070800-20071000	Enhancers	Brain Anterior Caudate	brain
37	chr3:20070800-20071400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:20076000-20076800	Enhancers	K562	blood
39	chr3:20076200-20076400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:20076200-20077200	Enhancers	Liver	Liver
41	chr3:20076800-20078800	Weak transcription	K562	blood
42	chr3:20077000-20077200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:20077000-20077200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr3:20077200-20079800	Weak transcription	Liver	Liver
45	chr3:20077200-20080000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr3:20077600-20078800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr3:20078600-20078800	Bivalent Enhancer	HepG2	liver
48	chr3:20078800-20080000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:20078800-20080000	Enhancers	K562	blood
50	chr3:20078800-20080200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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