Variant report

Variant	esv3432491
Chromosome Location	chr1:144981095-145095093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4473)
CpG islands
(count:3054)
Chromatin interactive
region (count:296)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4473 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145089768-145090509	K562	blood:	n/a	n/a
2	ARID3A	chr1:145091964-145092746	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:145027372-145031947	K562	blood:	n/a	n/a
4	ARID3A	chr1:145058588-145061058	K562	blood:	n/a	n/a
5	ARID3A	chr1:144997084-144999662	K562	blood:	n/a	n/a
6	ARID3A	chr1:144989106-144991213	K562	blood:	n/a	n/a
7	ARID3A	chr1:145039806-145040082	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:145007845-145011203	K562	blood:	n/a	n/a
9	ARID3A	chr1:144991522-144993662	K562	blood:	n/a	n/a
10	ARID3A	chr1:145005457-145007401	K562	blood:	n/a	n/a
11	ARID3A	chr1:145083440-145084471	K562	blood:	n/a	n/a
12	ARID3A	chr1:145061354-145062417	K562	blood:	n/a	n/a
13	ARID3A	chr1:145023275-145025964	K562	blood:	n/a	n/a
14	ARID3A	chr1:144988785-144990011	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:145000157-145004850	K562	blood:	n/a	chr1:145001553-145001569 chr1:145004748-145004764
16	ARID3A	chr1:145014466-145014972	HepG2	liver:	n/a	n/a
17	ARID3A	chr1:145012025-145018939	K562	blood:	n/a	chr1:145012568-145012584 chr1:145012567-145012583
18	ARID3A	chr1:145040051-145040226	K562	blood:	n/a	n/a
19	ARID3A	chr1:145040639-145043538	K562	blood:	n/a	n/a
20	ARID3A	chr1:144994237-144996744	K562	blood:	n/a	n/a
21	ARID3A	chr1:145054062-145056297	K562	blood:	n/a	chr1:145054435-145054451 chr1:145054273-145054289 chr1:145054272-145054288 chr1:145054436-145054452
22	ATF1	chr1:145070839-145072121	K562	blood:	n/a	n/a
23	ATF1	chr1:145074748-145075398	K562	blood:	n/a	n/a
24	ATF1	chr1:144991677-144992162	K562	blood:	n/a	n/a
25	ATF1	chr1:145058458-145062743	K562	blood:	n/a	n/a
26	ATF1	chr1:145029752-145031659	K562	blood:	n/a	n/a
27	ATF1	chr1:145090189-145090575	K562	blood:	n/a	n/a
28	ATF1	chr1:145054709-145055914	K562	blood:	n/a	n/a
29	ATF1	chr1:144997529-144998431	K562	blood:	n/a	n/a
30	ATF1	chr1:145018078-145018857	K562	blood:	n/a	n/a
31	ATF1	chr1:145069602-145070170	K562	blood:	n/a	n/a
32	ATF1	chr1:145080812-145081067	K562	blood:	n/a	n/a
33	ATF1	chr1:145078844-145078995	K562	blood:	n/a	n/a
34	ATF1	chr1:145001703-145004761	K562	blood:	n/a	n/a
35	ATF1	chr1:145068286-145068723	K562	blood:	n/a	n/a
36	ATF1	chr1:144988840-144990055	K562	blood:	n/a	n/a
37	ATF1	chr1:145032820-145034366	K562	blood:	n/a	n/a
38	ATF1	chr1:145077527-145078634	K562	blood:	n/a	n/a
39	ATF1	chr1:145027502-145029034	K562	blood:	n/a	n/a
40	ATF1	chr1:145082093-145082887	K562	blood:	n/a	n/a
41	ATF1	chr1:144998715-144999351	K562	blood:	n/a	n/a
42	ATF1	chr1:145014382-145016089	K562	blood:	n/a	n/a
43	ATF1	chr1:145073353-145074236	K562	blood:	n/a	n/a
44	ATF1	chr1:145008736-145009963	K562	blood:	n/a	n/a
45	ATF1	chr1:145083579-145084451	K562	blood:	n/a	n/a
46	ATF1	chr1:145086819-145087312	K562	blood:	n/a	n/a
47	ATF1	chr1:145012108-145014066	K562	blood:	n/a	n/a
48	ATF1	chr1:145023255-145025928	K562	blood:	n/a	n/a
49	ATF1	chr1:144994316-144996366	K562	blood:	n/a	n/a
50	ATF1	chr1:145020634-145021790	K562	blood:	n/a	n/a

(count:3054 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145075349-145075399	HEK293	kidney:	embryo
2	chr1:144995682-144995732	HUVEC	blood vessel:	n/a
3	chr1:145033094-145033144	MCF-7	breast:	n/a
4	chr1:144989624-144989674	NB4	blood:	n/a
5	chr1:145075349-145075399	HEK293	kidney:	embryo
6	chr1:144995682-144995732	HUVEC	blood vessel:	n/a
7	chr1:145033094-145033144	MCF-7	breast:	n/a
8	chr1:144989624-144989674	NB4	blood:	n/a
9	chr1:145021703-145021753	PFSK-1	brain:	n/a
10	chr1:145079447-145079497	HIPEpiC	eye:	n/a
11	chr1:145072507-145072557	GM12891	blood:	n/a
12	chr1:145035112-145035162	HEEpiC	esophagus:	n/a
13	chr1:144994715-144994765	PANC-1	pancreas:	n/a
14	chr1:145028465-145028515	SKMC	muscle:	n/a
15	chr1:145059467-145059517	HIPEpiC	eye:	n/a
16	chr1:145001340-145001390	A549	lung:	n/a
17	chr1:145036025-145036075	HepG2	liver:	n/a
18	chr1:145075538-145075588	SAEC	small airway:	n/a
19	chr1:145075831-145075881	SK-N-SH_RA	brain:	n/a
20	chr1:145054779-145054829	RPTEC	kidney:	n/a
21	chr1:145073743-145073793	SK-N-MC	brain:	n/a
22	chr1:145003040-145003090	HCPEpiC	choroid plexus:	n/a
23	chr1:145040886-145040936	HepG2	liver:	n/a
24	chr1:145040160-145040210	Jurkat	blood:	n/a
25	chr1:144989624-144989674	AG04449	skin:	fetal
26	chr1:145015987-145016037	AG04450	lung:	fetal
27	chr1:145028465-145028515	ovcar-3	ovarian:	n/a
28	chr1:144994542-144994592	AG09309	skin:	n/a
29	chr1:145077772-145077822	GM06990	blood:	n/a
30	chr1:145042811-145042861	HEEpiC	esophagus:	n/a
31	chr1:145004468-145004518	K562	blood:	n/a
32	chr1:145092485-145092535	GM12891	blood:	n/a
33	chr1:144994826-144994876	HAEpiC	amniotic membrane:	n/a
34	chr1:145021703-145021753	HCF	heart:	n/a
35	chr1:144995889-144995939	IMR90	lung:	fetal
36	chr1:145039741-145039791	HRE	kidney:	n/a
37	chr1:145075538-145075588	GM19239	blood:	n/a
38	chr1:145075538-145075588	HRPEpiC	eye:	n/a
39	chr1:145092576-145092626	NHBE	bronchial:	n/a
40	chr1:145075349-145075399	NB4	blood:	n/a
41	chr1:145042811-145042861	AoSMC	blood vessel:	n/a
42	chr1:144994715-144994765	Hela-S3	cervix:	n/a
43	chr1:145017064-145017114	AG10803	skin:	n/a
44	chr1:145039893-145039943	GM12891	blood:	n/a
45	chr1:145015987-145016037	NH-A	brain:	n/a
46	chr1:144994826-144994876	HCF	heart:	n/a
47	chr1:145054067-145054117	PANC-1	pancreas:	n/a
48	chr1:144995682-144995732	HCPEpiC	choroid plexus:	n/a
49	chr1:145039929-145039979	HCT-116	colon:	n/a
50	chr1:145017064-145017114	HEK293	kidney:	embryo

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr1:144999924..145002233-chr6:21588409..21590209,2	MCF-7	breast:
2	chr1:144929480..144934765-chr1:145057603..145063573,9	MCF-7	breast:
3	chr1:145058445..145059351-chr12:58299064..58299785,2	MCF-7	breast:
4	chr1:144925446..144929176-chr1:145057629..145060761,3	MCF-7	breast:
5	chr1:145070476..145072137-chr10:116063962..116066541,2	MCF-7	breast:
6	chr1:144532050..144536421-chr1:145006819..145011373,9	K562	blood:
7	chr1:145012040..145014419-chr1:145052808..145055801,2	K562	blood:
8	chr1:144932167..144933314-chr1:145058712..145059472,5	MCF-7	breast:
9	chr1:145056819..145059219-chr1:145060207..145063114,3	K562	blood:
10	chr1:144931701..144934508-chr1:145029528..145032354,3	MCF-7	breast:
11	chr1:145023266..145026073-chr1:145059016..145061272,2	MCF-7	breast:
12	chr1:145013143..145015357-chr1:145059234..145060924,2	K562	blood:
13	chr1:144992633..144993235-chr1:145029941..145030565,2	MCF-7	breast:
14	chr1:144992586..144994194-chr1:145030165..145032446,2	MCF-7	breast:
15	chr1:145087779..145091493-chr1:145381530..145384517,3	MCF-7	breast:
16	chr1:145012787..145014315-chr11:46834339..46836400,2	MCF-7	breast:
17	chr1:145006816..145009107-chr1:145057701..145060152,2	K562	blood:
18	chr1:145038465..145040335-chr1:145073529..145077328,4	MCF-7	breast:
19	chr1:145052529..145054250-chr1:145070398..145073752,3	K562	blood:
20	chr1:144917701..144918598-chr1:145059017..145059574,2	MCF-7	breast:
21	chr1:145045315..145047510-chr1:145064968..145067113,2	K562	blood:
22	chr1:145061658..145065193-chr1:145068421..145071280,4	MCF-7	breast:
23	chr1:120428584..120429097-chr1:145061707..145062386,2	MCF-7	breast:
24	chr1:144530904..144535858-chr1:144986921..144991934,7	K562	blood:
25	chr1:145052557..145054250-chr1:145070398..145072943,2	K562	blood:
26	chr1:145000528..145004410-chr1:145059527..145062479,4	K562	blood:
27	chr1:145061540..145065119-chr1:145065155..145068193,4	MCF-7	breast:
28	chr1:145014334..145015129-chr1:145055872..145056456,2	MCF-7	breast:
29	chr1:144534036..144535735-chr1:145018265..145020000,2	K562	blood:
30	chr1:144934215..144935781-chr1:144986460..144988163,2	MCF-7	breast:
31	chr1:144923562..144926497-chr1:145006728..145009314,2	MCF-7	breast:
32	chr1:145069959..145072647-chr1:145097335..145099798,3	K562	blood:
33	chr1:144995840..144996760-chr1:145055377..145055895,2	K562	blood:
34	chr1:145013488..145015671-chr1:145056479..145059269,3	MCF-7	breast:
35	chr1:144533700..144535665-chr1:145063411..145067268,4	K562	blood:
36	chr1:144930835..144932990-chr1:145009036..145011761,2	MCF-7	breast:
37	chr1:145012523..145015160-chr1:145055357..145057301,2	K562	blood:
38	chr1:144888141..144890870-chr1:145070504..145072082,2	K562	blood:
39	chr1:145052947..145056723-chr1:145060283..145063800,4	K562	blood:
40	chr1:144993668..144997286-chr1:145038559..145041171,3	MCF-7	breast:
41	chr1:144532567..144534443-chr1:145045258..145048893,3	K562	blood:
42	chr1:145036987..145043387-chr1:145051088..145058255,9	MCF-7	breast:
43	chr1:145069551..145072010-chr1:145087296..145089112,2	K562	blood:
44	chr1:144931078..144932841-chr1:145013046..145015215,2	MCF-7	breast:
45	chr1:145014159..145015000-chr1:145060710..145062762,6	MCF-7	breast:
46	chr1:144532674..144534262-chr1:145089036..145091259,2	K562	blood:
47	chr1:145005888..145007907-chr1:145011945..145014640,3	MCF-7	breast:
48	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
49	chr1:145006961..145008693-chr1:145104666..145107384,2	K562	blood:
50	chr1:144534213..144536284-chr1:145054889..145056789,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR3GL-6	chr1:145021112-145021167	NONHSAT005872
2	lnc-NBPF9-3	chr1:145004781-145005286	NONHSAT005869
3	lnc-POLR3GL-6	chr1:145039590-145039851	NONHSAT005872
4	lnc-POLR3GL-6	chr1:145017881-145017999	NONHSAT005872
5	lnc-NBPF9-4	chr1:145016388-145016968	NONHSAT005870
6	lnc-NOTCH2NL-4	chr1:145044651-145044900	NONHSAT005873
7	lnc-NBPF9-4	chr1:145013726-145013828	NONHSAT005870
8	lnc-NBPF9-5	chr1:145018395-145018959	ENSG00000272755.1
9	lnc-POLR3GL-6	chr1:145015873-145016011	NONHSAT005872
10	lnc-PDE4DIP-5	chr1:145088039-145088567	NONHSAT005874

No data

Variant related genes	Relation type
SEC22B	TF binding region
RN7SKP88	TF binding region
ENSG00000272755	TF binding region
PDE4DIP	TF binding region
ENSG00000271546	TF binding region
ENSG00000268172	TF binding region
SEC22B	CpG island
RN7SKP88	CpG island
ENSG00000272755	CpG island
PDE4DIP	CpG island
ENSG00000271546	CpG island
ENSG00000268172	CpG island
ENSG00000184260	chromatin interactions
ENSG00000180370	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000160972	chromatin interactions
ENSG00000079335	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000226446	chromatin interactions
ENSG00000271546	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000203843	chromatin interactions
ENSG00000188486	chromatin interactions
ENSG00000169129	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000223491	chromatin interactions
ENSG00000255182	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000252656	chromatin interactions
ENSG00000261139	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000174827	chromatin interactions
ENSG00000125347	chromatin interactions

Extended variants
information (count: 4708 )
Associated
traits (count: 181 )

Variant overlapped rSNPs/rCNVs (count:4708 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587711072	chr1:144981145-144981146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587776220	chr1:144981170-144981171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587666255	chr1:144981214-144981215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs59004385	chr1:144981238-144981239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587692417	chr1:144981248-144981249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201633700	chr1:144981270-144981271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140960113	chr1:144981303-144981304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587744450	chr1:144981338-144981339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs58159184	chr1:144981339-144981340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587648619	chr1:144981438-144981439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587699646	chr1:144981586-144981587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587608021	chr1:144981608-144981609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs71226069	chr1:144981635-144981636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587638823	chr1:144981638-144981639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs587720685	chr1:144981666-144981667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587599708	chr1:144981672-144981673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587657789	chr1:144981685-144981686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587743452	chr1:144981693-144981694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371862256	chr1:144981727-144981728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72701820	chr1:144981735-144981736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587598559	chr1:144981737-144981738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547806332	chr1:144981748-144981749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587676167	chr1:144981754-144981755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143796731	chr1:144981755-144981756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs150181268	chr1:144981762-144981763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138733441	chr1:144981764-144981765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57845050	chr1:144981773-144981774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587756497	chr1:144982029-144982030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141438254	chr1:144982104-144982105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587653846	chr1:144982310-144982311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs587713169	chr1:144982312-144982313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587769540	chr1:144982370-144982371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150824545	chr1:144982371-144982372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201919844	chr1:144982378-144982379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587687267	chr1:144982416-144982417	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs200005475	chr1:144982476-144982477	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs139426961	chr1:144982497-144982498	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs587751066	chr1:144982559-144982560	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs1778586	chr1:144982598-144982599	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs1663996	chr1:144982610-144982611	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587641509	chr1:144982612-144982613	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140891766	chr1:144982621-144982622	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587685767	chr1:144982630-144982631	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71664026	chr1:144982643-144982644	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs587765900	chr1:144982645-144982646	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587640995	chr1:144982649-144982650	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587720579	chr1:144982653-144982654	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71664027	chr1:144982659-144982660	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587769103	chr1:144982676-144982677	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12239862	chr1:144982751-144982752	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:181)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:5421 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144951000-144982400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:144965000-144982400	Weak transcription	Fetal Intestine Large	intestine
3	chr1:144966400-144982400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:144966400-144982400	Weak transcription	Brain Angular Gyrus	brain
5	chr1:144966600-144982400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr1:144966600-144982400	Weak transcription	K562	blood
7	chr1:144967400-144982400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:144967600-144982400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:144968000-144982400	Weak transcription	Brain Hippocampus Middle	brain
10	chr1:144968000-144982400	Weak transcription	HSMM	muscle
11	chr1:144968200-144982400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:144968200-144982600	Weak transcription	Osteobl	bone
13	chr1:144968600-144982400	Weak transcription	Primary B cells from peripheral blood	blood
14	chr1:144970800-144982600	Weak transcription	Placenta	Placenta
15	chr1:144973000-144982400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:144973000-144982600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:144973200-144982400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr1:144973200-144982600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:144973200-144986000	Weak transcription	Right Atrium	heart
20	chr1:144974000-144982600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr1:144976400-144982000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:144976400-144982400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr1:144976400-144982400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr1:144976400-144982400	Weak transcription	Fetal Muscle Leg	muscle
25	chr1:144976400-144982400	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr1:144976400-144982600	Weak transcription	Left Ventricle	heart
27	chr1:144976600-144982400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr1:144977400-144982400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr1:144978200-144982400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:144978200-144987800	Weak transcription	Primary B cells from cord blood	blood
31	chr1:144978600-144981200	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr1:144981200-144981400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr1:144981200-144982600	Weak transcription	Psoas Muscle	Psoas
34	chr1:144981400-144982400	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr1:144981800-144982400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:144982000-144982800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr1:144982000-144982800	Enhancers	Fetal Kidney	kidney
38	chr1:144982000-144983000	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr1:144982400-144982600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:144982400-144982600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:144982400-144982600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr1:144982400-144982600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr1:144982400-144982600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr1:144982400-144982600	Enhancers	Liver	Liver
45	chr1:144982400-144982600	Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr1:144982400-144982600	Enhancers	Stomach Smooth Muscle	stomach
47	chr1:144982400-144982600	Enhancers	HMEC	breast
48	chr1:144982400-144982600	Enhancers	HSMM	muscle
49	chr1:144982400-144982600	Enhancers	K562	blood
50	chr1:144982400-144982600	Enhancers	NHEK	skin

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