Variant report

Variant	nsv1067379
Chromosome Location	chr20:25355484-25593240
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4361)
CpG islands
(count:3112)
Chromatin interactive
region (count:186)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4361 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:25387822-25388496	HepG2	liver:	n/a	chr20:25388309-25388317
3	ARID3A	chr20:25488240-25489133	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:25371552-25371951	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:25506350-25507074	HepG2	liver:	n/a	n/a
7	ARID3A	chr20:25358787-25359630	HepG2	liver:	n/a	n/a
8	ARID3A	chr20:25589872-25589910	K562	blood:	n/a	n/a
9	ARID3A	chr20:25557897-25557902	HepG2	liver:	n/a	n/a
10	ARID3A	chr20:25530308-25530796	HepG2	liver:	n/a	n/a
11	ARID3A	chr20:25388096-25388261	K562	blood:	n/a	n/a
12	ARID3A	chr20:25379639-25380138	HepG2	liver:	n/a	n/a
13	ARID3A	chr20:25519655-25520011	HepG2	liver:	n/a	n/a
14	ARID3A	chr20:25379777-25380076	K562	blood:	n/a	n/a
15	ARID3A	chr20:25583644-25583908	HepG2	liver:	n/a	n/a
16	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
17	ARID3A	chr20:25555145-25555336	HepG2	liver:	n/a	n/a
18	ARID3A	chr20:25559627-25559973	HepG2	liver:	n/a	n/a
19	ATF1	chr20:25397252-25397513	K562	blood:	n/a	n/a
20	ATF1	chr20:25587145-25587281	K562	blood:	n/a	n/a
21	ATF1	chr20:25450740-25450940	K562	blood:	n/a	n/a
22	ATF1	chr20:25524173-25524617	K562	blood:	n/a	n/a
23	ATF1	chr20:25520966-25521214	K562	blood:	n/a	n/a
24	ATF2	chr20:25520859-25521226	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr20:25388112-25388527	GM12878	blood:	n/a	n/a
26	ATF2	chr20:25371534-25371990	GM12878	blood:	n/a	n/a
27	ATF2	chr20:25387954-25388507	GM12878	blood:	n/a	n/a
28	ATF3	chr20:25387974-25388532	A549	lung:	n/a	chr20:25388194-25388203
29	ATF3	chr20:25488628-25489026	A549	lung:	n/a	n/a
30	ATF3	chr20:25388032-25388664	A549	lung:	n/a	chr20:25388194-25388203
31	ATF3	chr20:25523783-25524037	K562	blood:	n/a	n/a
32	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr20:25371722-25371849	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr20:25520911-25521321	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr20:25470160-25470452	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr20:25370649-25370864	H1-hESC	embryonic stem cell:	n/a	n/a
37	BATF	chr20:25399506-25399665	GM12878	blood:	n/a	chr20:25399587-25399598
38	BATF	chr20:25387943-25388438	GM12878	blood:	n/a	chr20:25388072-25388081
39	BATF	chr20:25499248-25499445	GM12878	blood:	n/a	n/a
40	BATF	chr20:25583645-25583879	GM12878	blood:	n/a	n/a
41	BCL3	chr20:25387945-25388694	A549	lung:	n/a	chr20:25388326-25388335
42	BCL3	chr20:25590098-25590301	GM12878	blood:	n/a	n/a
43	BCL3	chr20:25590100-25590330	GM12878	blood:	n/a	n/a
44	BCL3	chr20:25565131-25566237	A549	lung:	n/a	chr20:25565815-25565824 chr20:25565704-25565717 chr20:25565700-25565713 chr20:25565668-25565681 chr20:25565884-25565893 chr20:25565855-25565868 chr20:25565861-25565869
45	BCL3	chr20:25387957-25388925	A549	lung:	n/a	chr20:25388326-25388335
46	BCL3	chr20:25388706-25389225	GM12878	blood:	n/a	n/a
47	BCL3	chr20:25371548-25372060	A549	lung:	n/a	chr20:25371619-25371632
48	BCLAF1	chr20:25371157-25371962	GM12878	blood:	n/a	chr20:25371487-25371496 chr20:25371619-25371632
49	BCLAF1	chr20:25388018-25388559	GM12878	blood:	n/a	chr20:25388326-25388335
50	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378

(count:3112 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25368906-25368956	MCF10A-Er-Src	breast:	n/a
2	chr20:25368906-25368956	MCF10A-Er-Src	breast:	n/a
3	chr20:25371700-25371750	Hepatocyte	liver:	n/a
4	chr20:25371408-25371458	BE2_C	brain:	n/a
5	chr20:25388289-25388339	AG04449	skin:	fetal
6	chr20:25479848-25479898	MCF-7	breast:	n/a
7	chr20:25566470-25566520	SK-N-SH	brain:	n/a
8	chr20:25371439-25371489	MCF-7	breast:	n/a
9	chr20:25388369-25388419	HCT-116	colon:	n/a
10	chr20:25479848-25479898	U87	brain:	n/a
11	chr20:25581368-25581418	AG04449	skin:	fetal
12	chr20:25566470-25566520	HIPEpiC	eye:	n/a
13	chr20:25448861-25448911	AG09319	gingival:	n/a
14	chr20:25566470-25566520	ovcar-3	ovarian:	n/a
15	chr20:25387977-25388027	ECC-1	luminal epithelium:	n/a
16	chr20:25381464-25381514	HMEC	breast:	n/a
17	chr20:25388779-25388829	PANC-1	pancreas:	n/a
18	chr20:25371667-25371717	SK-N-MC	brain:	n/a
19	chr20:25371719-25371769	GM06990	blood:	n/a
20	chr20:25479848-25479898	SK-N-SH	brain:	n/a
21	chr20:25566513-25566563	NHDF-neo	bronchial:	n/a
22	chr20:25388289-25388339	HNPCEpiC	eye:	n/a
23	chr20:25388369-25388419	HEK293	kidney:	embryo
24	chr20:25382007-25382057	Caco-2	colon:	n/a
25	chr20:25386216-25386266	PANC-1	pancreas:	n/a
26	chr20:25387977-25388027	BJ	skin:	n/a
27	chr20:25371822-25371872	HL-60	blood:	n/a
28	chr20:25450839-25450889	SK-N-SH_RA	brain:	n/a
29	chr20:25427961-25428011	HCT-116	colon:	n/a
30	chr20:25583082-25583132	GM12878	blood:	n/a
31	chr20:25583324-25583374	U87	brain:	n/a
32	chr20:25388353-25388403	HEEpiC	esophagus:	n/a
33	chr20:25450839-25450889	PFSK-1	brain:	n/a
34	chr20:25388641-25388691	MCF-7	breast:	n/a
35	chr20:25371439-25371489	HRPEpiC	eye:	n/a
36	chr20:25565879-25565929	AG04449	skin:	fetal
37	chr20:25584456-25584506	GM12891	blood:	n/a
38	chr20:25433878-25433928	ProgFib	skin:	n/a
39	chr20:25371700-25371750	PFSK-1	brain:	n/a
40	chr20:25388278-25388328	SKMC	muscle:	n/a
41	chr20:25566180-25566230	HCPEpiC	choroid plexus:	n/a
42	chr20:25388369-25388419	HCM	heart:	n/a
43	chr20:25566180-25566230	AG04450	lung:	fetal
44	chr20:25374524-25374574	SK-N-SH_RA	brain:	n/a
45	chr20:25386216-25386266	U87	brain:	n/a
46	chr20:25388369-25388419	BJ	skin:	n/a
47	chr20:25371852-25371902	CMK	blood:	n/a
48	chr20:25371822-25371872	HRCEpiC	kidney:	n/a
49	chr20:25371852-25371902	AG10803	skin:	n/a
50	chr20:25433878-25433928	CMK	blood:	n/a

(count:186 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr20:25476823..25479458-chr20:25499157..25501846,2	MCF-7	breast:
2	chr14:64971494..64972452-chr20:25388243..25388799,2	Hela-S3	cervix:
3	chr20:25360614..25362965-chr20:25368758..25370561,4	K562	blood:
4	chr20:25360394..25363180-chr20:25371562..25374296,2	MCF-7	breast:
5	chr20:25392116..25394910-chr20:25395209..25398004,3	K562	blood:
6	chr20:25512408..25515336-chr20:25515482..25519858,3	MCF-7	breast:
7	chr20:25578107..25581222-chr20:25601982..25605095,3	MCF-7	breast:
8	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
9	chr20:25590781..25592605-chr20:25602144..25606440,3	MCF-7	breast:
10	chr20:25274830..25275740-chr20:25378372..25379283,2	MCF-7	breast:
11	chr20:25387920..25388819-chr7:6048429..6049127,2	NB4	blood:
12	chr20:25589103..25590623-chr3:128880296..128881849,2	K562	blood:
13	chr20:25589936..25592096-chr20:25592501..25595194,2	MCF-7	breast:
14	chr20:25289881..25292169-chr20:25388744..25391503,2	MCF-7	breast:
15	chr20:25528846..25530545-chr20:25675898..25678279,2	MCF-7	breast:
16	chr20:25491958..25494931-chr20:25496004..25498993,2	MCF-7	breast:
17	chr20:25388650..25390177-chr20:25402470..25404637,3	MCF-7	breast:
18	chr20:25290481..25292963-chr20:25369877..25371974,2	MCF-7	breast:
19	chr20:25397786..25400078-chr20:25402229..25405600,3	MCF-7	breast:
20	chr20:25277010..25279912-chr20:25462998..25464763,2	K562	blood:
21	chr20:25579638..25582269-chr20:25599435..25601779,2	K562	blood:
22	chr20:25564944..25567747-chr20:25571041..25572866,2	MCF-7	breast:
23	chr17:59433764..59435297-chr20:25448424..25451207,2	MCF-7	breast:
24	chr20:25588843..25590699-chr20:25604414..25605941,2	MCF-7	breast:
25	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
26	chr20:25387859..25390842-chr20:25397411..25399483,2	MCF-7	breast:
27	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
28	chr20:25341755..25344650-chr20:25359957..25362246,2	MCF-7	breast:
29	chr20:25367909..25369647-chr20:25375596..25377784,2	MCF-7	breast:
30	chr20:25487824..25490513-chr20:25503941..25506270,3	MCF-7	breast:
31	chr20:25228496..25230155-chr20:25552419..25555224,2	MCF-7	breast:
32	chr20:25535541..25538221-chr20:25603940..25606059,2	MCF-7	breast:
33	chr20:25551184..25554457-chr20:25563697..25566263,4	MCF-7	breast:
34	chr20:25503491..25506421-chr20:25552111..25554965,2	MCF-7	breast:
35	chr20:25508566..25510611-chr20:25564676..25566360,2	MCF-7	breast:
36	chr20:25481164..25483105-chr20:25484955..25487000,2	K562	blood:
37	chr20:25324909..25327111-chr20:25375106..25376972,2	MCF-7	breast:
38	chr20:25550297..25552120-chr20:25553741..25555593,3	MCF-7	breast:
39	chr20:25274847..25275686-chr20:25555235..25555796,2	K562	blood:
40	chr20:25316897..25317523-chr20:25554784..25555668,2	MCF-7	breast:
41	chr20:25521309..25522938-chr20:25526944..25528978,2	MCF-7	breast:
42	chr20:25474956..25477524-chr20:25604184..25606432,2	MCF-7	breast:
43	chr20:25318544..25319155-chr20:25379499..25380008,2	MCF-7	breast:
44	chr20:25316916..25317821-chr20:25379512..25380380,4	MCF-7	breast:
45	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
46	chr20:25356181..25358893-chr20:25361208..25363554,2	MCF-7	breast:
47	chr20:25370702..25372613-chr20:25374796..25376547,2	MCF-7	breast:
48	chr20:25563758..25567670-chr20:25600746..25606260,10	MCF-7	breast:
49	chr20:25573368..25577137-chr20:25602924..25606486,3	MCF-7	breast:
50	chr20:25369196..25373772-chr20:25386901..25390344,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GINS1-4	chr20:25513663-25514148	NONHSAT079162

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GINS1	hsa-miR-7-5p	chr20:25428910-25428929

Variant related genes	Relation type
ABHD12	TF binding region
RNU6ATAC17P	TF binding region
NINL	TF binding region
GINS1	TF binding region
ABHD12	CpG island
RNU6ATAC17P	CpG island
NINL	CpG island
GINS1	CpG island
ENSG00000251883	chromatin interactions
ENSG00000197586	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000233325	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000261796	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000150456	chromatin interactions
ENSG00000162409	chromatin interactions
ENSG00000075790	chromatin interactions
ENSG00000101474	chromatin interactions
ENSG00000166262	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000240682	chromatin interactions
ENSG00000104047	chromatin interactions
ENSG00000236542	chromatin interactions
ENSG00000227379	chromatin interactions
ENSG00000130684	chromatin interactions
ENSG00000162407	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000213742	chromatin interactions

Extended variants
information (count: 9834 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:9834 , 50 per page) page: 1 2 3 4 5 6 7 ... 197

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138655141	chr20:25355499-25355500	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189716544	chr20:25355552-25355553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567174393	chr20:25355616-25355617	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs527422136	chr20:25355623-25355624	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535322912	chr20:25355628-25355629	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs67069812	chr20:25355678-25355679	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs533652428	chr20:25355722-25355723	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556004340	chr20:25355750-25355751	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574331982	chr20:25355795-25355796	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs532948362	chr20:25355809-25355810	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182068630	chr20:25355891-25355892	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs34670114	chr20:25355898-25355899	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7353468	chr20:25355924-25355925	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs569633749	chr20:25355965-25355966	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117357168	chr20:25355977-25355978	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73347078	chr20:25355986-25355987	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs66501707	chr20:25355999-25356000	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs187911716	chr20:25356005-25356006	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141271057	chr20:25356006-25356007	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs192277747	chr20:25356118-25356119	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35411172	chr20:25356130-25356131	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs116771498	chr20:25356139-25356140	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556258072	chr20:25356180-25356181	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576840969	chr20:25356197-25356198	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs542530352	chr20:25356215-25356216	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183552903	chr20:25356222-25356223	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572680703	chr20:25356285-25356286	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs113285845	chr20:25356300-25356301	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147994457	chr20:25356315-25356316	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs386813582	chr20:25356331-25356332	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141745068	chr20:25356365-25356366	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188600985	chr20:25356378-25356379	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6107032	chr20:25356410-25356411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192835359	chr20:25356494-25356495	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2500401	chr20:25356497-25356498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs565594638	chr20:25356531-25356532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534827280	chr20:25356588-25356589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138778186	chr20:25356632-25356633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs570948191	chr20:25356654-25356655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184261493	chr20:25356747-25356748	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374119522	chr20:25356761-25356762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553307022	chr20:25356772-25356773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576500669	chr20:25356794-25356795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs186994682	chr20:25356799-25356800	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs6037099	chr20:25356876-25356877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs572740474	chr20:25356896-25356897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541630994	chr20:25356941-25356942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564498564	chr20:25356949-25356950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577700276	chr20:25356963-25356964	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543144455	chr20:25357002-25357003	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:6392 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25327400-25361400	Weak transcription	Primary T cells from cord blood	blood
2	chr20:25334600-25357600	Weak transcription	Fetal Muscle Leg	muscle
3	chr20:25334800-25362600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr20:25337000-25370000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr20:25337400-25355600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr20:25337600-25362800	Weak transcription	Spleen	Spleen
7	chr20:25338000-25369400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr20:25338200-25359000	Weak transcription	Fetal Intestine Large	intestine
9	chr20:25339400-25359600	Weak transcription	Lung	lung
10	chr20:25341800-25357600	Weak transcription	Ovary	ovary
11	chr20:25342200-25361800	Weak transcription	Primary B cells from cord blood	blood
12	chr20:25342200-25362600	Weak transcription	Primary B cells from peripheral blood	blood
13	chr20:25342200-25370000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr20:25342400-25355600	Weak transcription	A549	lung
15	chr20:25342400-25357600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr20:25343800-25370000	Weak transcription	Small Intestine	intestine
17	chr20:25345200-25369800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr20:25345800-25357600	Weak transcription	Right Atrium	heart
19	chr20:25345800-25359400	Weak transcription	Left Ventricle	heart
20	chr20:25345800-25359600	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr20:25345800-25361600	Weak transcription	K562	blood
22	chr20:25345800-25363200	Weak transcription	Esophagus	oesophagus
23	chr20:25345800-25369800	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr20:25345800-25370000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr20:25345800-25370000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr20:25346200-25357600	Weak transcription	HepG2	liver
27	chr20:25346200-25362800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr20:25347600-25357600	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr20:25350600-25357000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr20:25351400-25357000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr20:25351400-25359800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr20:25351400-25369600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr20:25351800-25370000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr20:25352000-25356000	Weak transcription	Pancreas	Pancrea
35	chr20:25352000-25356800	Weak transcription	Brain Angular Gyrus	brain
36	chr20:25352000-25357200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr20:25352000-25359600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr20:25352000-25359600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr20:25352000-25362600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr20:25352400-25355600	Weak transcription	Brain Substantia Nigra	brain
41	chr20:25352400-25357000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr20:25352600-25356000	Weak transcription	Brain Hippocampus Middle	brain
43	chr20:25352600-25356200	Weak transcription	Brain Anterior Caudate	brain
44	chr20:25353000-25370000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr20:25353800-25359800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr20:25353800-25361200	Weak transcription	Aorta	Aorta
47	chr20:25353800-25365200	Weak transcription	Fetal Lung	lung
48	chr20:25353800-25368800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr20:25353800-25370000	Weak transcription	Adipose Nuclei	Adipose
50	chr20:25353800-25370000	Weak transcription	HSMM	muscle

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