Variant report

Variant	nsv897724
Chromosome Location	chr11:65300252-65309514
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1088)
CpG islands
(count:795)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:65306340-65306689	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:65307632-65308275	GM12878	blood:	n/a	n/a
3	ATF2	chr11:65308245-65308723	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:65307666-65308170	GM12878	blood:	n/a	n/a
5	ATF3	chr11:65308217-65308671	A549	lung:	n/a	chr11:65308245-65308254 chr11:65308313-65308322 chr11:65308308-65308317
6	BACH1	chr11:65308280-65308573	K562	blood:	n/a	n/a
7	BACH1	chr11:65307823-65307979	K562	blood:	n/a	n/a
8	BACH1	chr11:65306552-65308642	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr11:65306484-65306830	GM12878	blood:	n/a	n/a
10	BCL3	chr11:65306972-65307292	GM12878	blood:	n/a	n/a
11	BCL3	chr11:65307673-65308736	A549	lung:	n/a	chr11:65308316-65308329 chr11:65308271-65308284 chr11:65307943-65307952
12	BCL3	chr11:65307636-65308628	A549	lung:	n/a	chr11:65308316-65308329 chr11:65308271-65308284 chr11:65307943-65307952
13	BCL3	chr11:65304726-65305378	A549	lung:	n/a	chr11:65304780-65304793
14	BCLAF1	chr11:65307706-65308230	GM12878	blood:	n/a	chr11:65307943-65307952
15	BCLAF1	chr11:65307656-65308685	GM12878	blood:	n/a	chr11:65308316-65308329 chr11:65308271-65308284 chr11:65307943-65307952
16	BHLHE40	chr11:65307621-65308613	GM12878	blood:	n/a	chr11:65308243-65308259 chr11:65308113-65308129
17	BHLHE40	chr11:65307688-65308646	K562	blood:	n/a	chr11:65308243-65308259 chr11:65308113-65308129
18	BRCA1	chr11:65308762-65308968	GM12878	blood:	n/a	n/a
19	BRCA1	chr11:65308398-65308596	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr11:65307672-65307813	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr11:65308292-65308535	GM12878	blood:	n/a	n/a
22	BRCA1	chr11:65307061-65307128	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr11:65307831-65308039	GM12878	blood:	n/a	n/a
24	BRCA1	chr11:65308399-65308573	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr11:65307648-65308699	K562	blood:	n/a	n/a
26	CCNT2	chr11:65307602-65308635	K562	blood:	n/a	chr11:65308191-65308200 chr11:65307673-65307682
27	CCNT2	chr11:65306096-65306126	K562	blood:	n/a	n/a
28	CEBPB	chr11:65308388-65308681	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:65308341-65308702	A549	lung:	n/a	n/a
30	CEBPB	chr11:65308341-65308701	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:65308255-65308601	K562	blood:	n/a	n/a
32	CEBPB	chr11:65307907-65308107	K562	blood:	n/a	n/a
33	CEBPB	chr11:65308342-65308685	IMR90	lung:	n/a	n/a
34	CEBPB	chr11:65308406-65308544	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:65308333-65308679	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:65308147-65308811	A549	lung:	n/a	n/a
37	CEBPB	chr11:65308332-65308718	K562	blood:	n/a	n/a
38	CEBPB	chr11:65307639-65308146	GM12878	blood:	n/a	n/a
39	CEBPB	chr11:65308220-65308770	MCF-7	breast:	n/a	n/a
40	CEBPB	chr11:65308326-65308703	Hela-S3	cervix:	n/a	n/a
41	CHD1	chr11:65307685-65308173	GM12878	blood:	n/a	n/a
42	CHD2	chr11:65307739-65308718	GM12878	blood:	n/a	chr11:65308309-65308319
43	CHD2	chr11:65307394-65307486	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr11:65307572-65308635	Hela-S3	cervix:	n/a	chr11:65308309-65308319
45	CHD2	chr11:65308408-65308531	HepG2	liver:	n/a	n/a
46	CHD2	chr11:65308306-65308499	H1-hESC	embryonic stem cell:	n/a	chr11:65308309-65308319
47	CREB1	chr11:65307821-65308392	A549	lung:	n/a	n/a
48	CREB1	chr11:65307109-65308664	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTBP2	chr11:65306801-65307540	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:65307720-65307870	AG09319	gingival:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65307006-65307056	AG09319	gingival:	n/a
2	chr11:65302203-65302253	HEEpiC	esophagus:	n/a
3	chr11:65307006-65307056	AG09319	gingival:	n/a
4	chr11:65302203-65302253	HEEpiC	esophagus:	n/a
5	chr11:65308501-65308551	U87	brain:	n/a
6	chr11:65307006-65307056	NHDF-neo	bronchial:	n/a
7	chr11:65308245-65308295	GM12891	blood:	n/a
8	chr11:65306186-65306236	K562	blood:	n/a
9	chr11:65302203-65302253	NH-A	brain:	n/a
10	chr11:65306116-65306166	HCT-116	colon:	n/a
11	chr11:65308423-65308473	LNCaP	prostate:	n/a
12	chr11:65307616-65307666	AoSMC	blood vessel:	n/a
13	chr11:65307006-65307056	RPTEC	kidney:	n/a
14	chr11:65308423-65308473	HNPCEpiC	eye:	n/a
15	chr11:65306186-65306236	A549	lung:	n/a
16	chr11:65306186-65306236	MCF10A-Er-Src	breast:	n/a
17	chr11:65306934-65306984	NH-A	brain:	n/a
18	chr11:65307006-65307056	HCM	heart:	n/a
19	chr11:65307616-65307666	AG09309	skin:	n/a
20	chr11:65302203-65302253	GM12891	blood:	n/a
21	chr11:65306934-65306984	H1-hESC	embryonic stem cell:	embryo
22	chr11:65308645-65308695	HEK293	kidney:	embryo
23	chr11:65306116-65306166	HUVEC	blood vessel:	n/a
24	chr11:65307791-65307841	Jurkat	blood:	n/a
25	chr11:65307791-65307841	LNCaP	prostate:	n/a
26	chr11:65306116-65306166	GM19239	blood:	n/a
27	chr11:65306186-65306236	HAEpiC	amniotic membrane:	n/a
28	chr11:65306116-65306166	HEK293	kidney:	embryo
29	chr11:65308245-65308295	BE2_C	brain:	n/a
30	chr11:65307791-65307841	SKMC	muscle:	n/a
31	chr11:65307791-65307841	NHBE	bronchial:	n/a
32	chr11:65308245-65308295	HAEpiC	amniotic membrane:	n/a
33	chr11:65308645-65308695	Hepatocyte	liver:	n/a
34	chr11:65307006-65307056	Hepatocyte	liver:	n/a
35	chr11:65307791-65307841	HMEC	breast:	n/a
36	chr11:65308423-65308473	HMEC	breast:	n/a
37	chr11:65306934-65306984	HAEpiC	amniotic membrane:	n/a
38	chr11:65306116-65306166	BJ	skin:	n/a
39	chr11:65306934-65306984	ECC-1	luminal epithelium:	n/a
40	chr11:65308423-65308473	SAEC	small airway:	n/a
41	chr11:65302203-65302253	SK-N-SH	brain:	n/a
42	chr11:65308245-65308295	SK-N-SH	brain:	n/a
43	chr11:65305575-65305625	H1-hESC	embryonic stem cell:	embryo
44	chr11:65308645-65308695	HAEpiC	amniotic membrane:	n/a
45	chr11:65302203-65302253	GM19239	blood:	n/a
46	chr11:65308501-65308551	HCPEpiC	choroid plexus:	n/a
47	chr11:65307791-65307841	HIPEpiC	eye:	n/a
48	chr11:65305575-65305625	BJ	skin:	n/a
49	chr11:65307791-65307841	PFSK-1	brain:	n/a
50	chr11:65306731-65306781	HepG2	liver:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65307697..65309026-chr3:64008900..64009738,3	MCF-7	breast:
2	chr11:65309008..65312326-chr11:65383111..65384790,3	K562	blood:
3	chr11:65307860..65308586-chr11:65319285..65320130,2	K562	blood:
4	chr11:65306856..65307488-chr17:73150357..73151051,2	Hela-S3	cervix:
5	chr11:65307252..65310035-chr11:65625535..65628177,3	K562	blood:
6	chr11:65189854..65192035-chr11:65305464..65309123,3	K562	blood:
7	chr11:65306623..65309907-chr11:65380382..65384254,6	MCF-7	breast:
8	chr11:65307310..65307872-chr11:65360978..65361533,2	MCF-7	breast:
9	chr11:65307871..65308546-chr11:65343015..65343628,2	K562	blood:
10	chr11:65189411..65192109-chr11:65300454..65301968,2	MCF-7	breast:
11	chr11:65307648..65308488-chr11:65318954..65319482,2	MCF-7	breast:
12	chr11:65307312..65308926-chr11:65339023..65340083,15	MCF-7	breast:
13	chr11:65307403..65309183-chr11:65336934..65338289,13	MCF-7	breast:
14	chr11:65187744..65191441-chr11:65307194..65309813,3	MCF-7	breast:
15	chr11:65307679..65310014-chr11:65429997..65432824,2	MCF-7	breast:
16	chr11:65307335..65308296-chr17:73775501..73776065,2	HCT-116	colon:
17	chr11:65302994..65303607-chr17:57784255..57785207,2	HCT-116	colon:
18	chr11:65306479..65309303-chr5:10247983..10249958,2	MCF-7	breast:
19	chr11:65308267..65308949-chr11:65339470..65340001,3	MCF-7	breast:
20	chr11:65307733..65308892-chr11:65339050..65340029,8	K562	blood:
21	chr11:65308291..65309442-chr11:65319131..65320116,6	MCF-7	breast:
22	chr11:65100032..65102632-chr11:65307572..65309259,3	MCF-7	breast:
23	chr11:65266245..65270118-chr11:65305867..65309860,5	MCF-7	breast:
24	chr11:65263261..65267812-chr11:65306192..65309215,4	MCF-7	breast:
25	chr11:65183635..65190622-chr11:65305653..65310980,8	MCF-7	breast:
26	chr11:65306570..65308318-chr11:65381821..65384190,3	K562	blood:
27	chr1:29063672..29064279-chr11:65307848..65308494,2	HCT-116	colon:
28	chr11:65308066..65308605-chr11:65337068..65337929,2	Hela-S3	cervix:
29	chr11:65307609..65308998-chr11:65336892..65338725,9	K562	blood:
30	chr11:65262833..65264423-chr11:65305627..65307751,2	K562	blood:

No data

Variant related genes	Relation type
LTBP3	TF binding region
SCYL1	TF binding region
LTBP3	CpG island
SCYL1	CpG island
ENSG00000173465	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000173442	chromatin interactions
ENSG00000189159	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000173327	chromatin interactions
ENSG00000260233	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000197136	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000168056	chromatin interactions
ENSG00000173338	chromatin interactions
ENSG00000133884	chromatin interactions
ENSG00000198492	chromatin interactions
ENSG00000141378	chromatin interactions
ENSG00000173039	chromatin interactions
ENSG00000248968	chromatin interactions
ENSG00000132475	chromatin interactions

Extended variants
information (count: 407 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113328894	chr11:65300252-65300253	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs538419986	chr11:65300259-65300260	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs369356212	chr11:65300290-65300291	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs143625869	chr11:65300333-65300334	Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs578136317	chr11:65300421-65300422	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs370325278	chr11:65300422-65300423	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113783802	chr11:65300445-65300446	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs116905338	chr11:65300536-65300537	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11605810	chr11:65300619-65300620	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs140358806	chr11:65300621-65300622	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368324421	chr11:65300631-65300632	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576160170	chr11:65300731-65300732	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs185564787	chr11:65300760-65300761	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564887927	chr11:65300762-65300763	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527482697	chr11:65300763-65300764	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145549985	chr11:65300785-65300786	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs564660775	chr11:65300801-65300802	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs561276025	chr11:65300827-65300828	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529697083	chr11:65300842-65300843	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs549830670	chr11:65300988-65300989	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148072059	chr11:65301007-65301008	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs140655309	chr11:65301019-65301020	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117988461	chr11:65301107-65301108	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571704497	chr11:65301108-65301109	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs534452473	chr11:65301123-65301124	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150089651	chr11:65301143-65301144	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs540067754	chr11:65301157-65301158	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs138424178	chr11:65301206-65301207	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190226720	chr11:65301216-65301217	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576034514	chr11:65301279-65301280	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs371171519	chr11:65301282-65301283	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545050956	chr11:65301290-65301291	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142741689	chr11:65301319-65301320	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572136175	chr11:65301328-65301329	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372493507	chr11:65301343-65301344	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs1144928	chr11:65301410-65301411	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138471129	chr11:65301423-65301424	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529982224	chr11:65301428-65301429	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550121893	chr11:65301470-65301471	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563227727	chr11:65301474-65301475	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550252699	chr11:65301514-65301515	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs532153378	chr11:65301516-65301517	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs200456230	chr11:65301540-65301541	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551975135	chr11:65301551-65301552	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565812920	chr11:65301559-65301560	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs139060080	chr11:65301603-65301604	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs192261399	chr11:65301627-65301628	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs183923231	chr11:65301628-65301629	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567532805	chr11:65301650-65301651	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188658992	chr11:65301659-65301660	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:892 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65293600-65305600	Weak transcription	Right Atrium	heart
2	chr11:65293600-65307600	Weak transcription	Small Intestine	intestine
3	chr11:65293800-65302800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:65294000-65300600	Strong transcription	HSMM	muscle
5	chr11:65294000-65300800	Strong transcription	Colonic Mucosa	Colon
6	chr11:65294000-65301400	Strong transcription	Esophagus	oesophagus
7	chr11:65294000-65305800	Strong transcription	Fetal Brain Female	brain
8	chr11:65294000-65305800	Strong transcription	Fetal Intestine Large	intestine
9	chr11:65294000-65306400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr11:65294000-65306400	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr11:65294000-65306400	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr11:65294000-65306600	Weak transcription	Fetal Heart	heart
13	chr11:65294000-65306800	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:65294000-65307000	Strong transcription	Lung	lung
15	chr11:65294000-65307200	Strong transcription	Brain Cingulate Gyrus	brain
16	chr11:65294200-65300400	Strong transcription	Muscle Satellite Cultured Cells	--
17	chr11:65294200-65300400	Strong transcription	GM12878-XiMat	blood
18	chr11:65294200-65301000	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr11:65294200-65301200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:65294200-65301200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr11:65294200-65301200	Strong transcription	NHEK	skin
22	chr11:65294200-65304800	Strong transcription	Fetal Muscle Leg	muscle
23	chr11:65294200-65306200	Strong transcription	Brain Hippocampus Middle	brain
24	chr11:65294200-65306200	Weak transcription	Fetal Brain Male	brain
25	chr11:65294200-65306200	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr11:65294200-65306400	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr11:65294200-65306800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:65294200-65307200	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr11:65294400-65301200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr11:65294400-65301200	Strong transcription	Duodenum Mucosa	Duodenum
31	chr11:65294400-65302400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:65294400-65306000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:65294400-65306200	Strong transcription	Fetal Intestine Small	intestine
34	chr11:65294400-65306400	Strong transcription	Brain Germinal Matrix	brain
35	chr11:65294400-65306400	Strong transcription	Brain Substantia Nigra	brain
36	chr11:65294400-65306600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:65294400-65307000	Strong transcription	Fetal Stomach	stomach
38	chr11:65294400-65307200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:65294400-65307400	Strong transcription	NHLF	lung
40	chr11:65294600-65301200	Strong transcription	Gastric	stomach
41	chr11:65294600-65304600	Strong transcription	Fetal Muscle Trunk	muscle
42	chr11:65294600-65306000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:65294600-65306400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:65294600-65306400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr11:65294600-65307000	Strong transcription	Adipose Nuclei	Adipose
46	chr11:65294600-65307200	Strong transcription	Placenta	Placenta
47	chr11:65294800-65302000	Strong transcription	Stomach Smooth Muscle	stomach
48	chr11:65294800-65304600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:65294800-65306400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:65294800-65306600	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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