Variant report

Variant	nsv899067
Chromosome Location	chr12:49329695-49344508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:433)
CpG islands
(count:306)
Chromatin interactive
region (count:52)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:49330253-49330453	HepG2	liver:	n/a	n/a
2	BRCA1	chr12:49330238-49330408	HepG2	liver:	n/a	n/a
3	CEBPB	chr12:49341603-49341816	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr12:49341709-49341780	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:49341123-49341195	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr12:49331100-49331295	MCF-7	breast:	n/a	n/a
7	CTCF	chr12:49330260-49330410	GM12878	blood:	n/a	n/a
8	CTCF	chr12:49331180-49331330	K562	blood:	n/a	n/a
9	CTCF	chr12:49330234-49330492	MCF-7	breast:	n/a	n/a
10	CTCF	chr12:49331170-49331317	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr12:49329700-49329990	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr12:49330980-49331130	HFF	foreskin:	n/a	n/a
13	CTCF	chr12:49330807-49330881	GM19239	blood:	n/a	n/a
14	CTCF	chr12:49330074-49330743	HCT-116	colon:	n/a	n/a
15	CTCF	chr12:49330209-49330510	GM19240	blood:	n/a	n/a
16	CTCF	chr12:49330240-49330390	HMEC	breast:	n/a	n/a
17	CTCF	chr12:49330230-49330482	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:49330080-49330230	A549	lung:	n/a	n/a
19	CTCF	chr12:49331120-49331270	HMF	breast:	n/a	n/a
20	CTCF	chr12:49331520-49331670	HEK293	kidney:	n/a	n/a
21	CTCF	chr12:49330280-49330430	GM12867	blood:	n/a	n/a
22	CTCF	chr12:49330230-49330519	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr12:49330594-49330719	GM10266	blood:	n/a	n/a
24	CTCF	chr12:49331202-49331282	GM13977	blood:	n/a	n/a
25	CTCF	chr12:49331080-49331230	HAc	cerebellar:	n/a	n/a
26	CTCF	chr12:49331229-49331273	LNCaP	prostate:	n/a	n/a
27	CTCF	chr12:49330280-49330430	AG10803	skin:	n/a	n/a
28	CTCF	chr12:49331140-49331290	HEK293	kidney:	n/a	n/a
29	CTCF	chr12:49330280-49330430	NHEK	skin:	n/a	n/a
30	CTCF	chr12:49329620-49329770	GM12868	blood:	n/a	n/a
31	CTCF	chr12:49330213-49330517	GM12878	blood:	n/a	n/a
32	CTCF	chr12:49330300-49330450	GM12875	blood:	n/a	n/a
33	CTCF	chr12:49330280-49330430	GM06990	blood:	n/a	n/a
34	CTCF	chr12:49330860-49331010	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr12:49331120-49331270	GM12867	blood:	n/a	n/a
36	CTCF	chr12:49331078-49331318	HepG2	liver:	n/a	n/a
37	CTCF	chr12:49330260-49330410	GM12870	blood:	n/a	n/a
38	CTCF	chr12:49331200-49331350	AG09319	gingival:	n/a	n/a
39	CTCF	chr12:49330880-49331030	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr12:49331180-49331330	HFF	foreskin:	n/a	n/a
41	CTCF	chr12:49331080-49331230	GM12870	blood:	n/a	n/a
42	CTCF	chr12:49331123-49331349	K562	blood:	n/a	n/a
43	CTCF	chr12:49331080-49331230	A549	lung:	n/a	n/a
44	CTCF	chr12:49330280-49330430	GM12868	blood:	n/a	n/a
45	CTCF	chr12:49330888-49330929	K562	blood:	n/a	n/a
46	CTCF	chr12:49331160-49331310	HepG2	liver:	n/a	n/a
47	CTCF	chr12:49331023-49331467	K562	blood:	n/a	n/a
48	CTCF	chr12:49331158-49331289	GM12878	blood:	n/a	n/a
49	CTCF	chr12:49330214-49330484	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr12:49337080-49337230	HMEC	breast:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49340730-49340780	HRPEpiC	eye:	n/a
2	chr12:49340730-49340780	HRPEpiC	eye:	n/a
3	chr12:49332783-49332833	AoSMC	blood vessel:	n/a
4	chr12:49334797-49334847	PrEC	prostate:	n/a
5	chr12:49330158-49330208	AG09309	skin:	n/a
6	chr12:49333479-49333529	NHBE	bronchial:	n/a
7	chr12:49334797-49334847	HMEC	breast:	n/a
8	chr12:49334797-49334847	HCT-116	colon:	n/a
9	chr12:49332783-49332833	HEK293	kidney:	embryo
10	chr12:49340730-49340780	GM12891	blood:	n/a
11	chr12:49330158-49330208	SK-N-MC	brain:	n/a
12	chr12:49340730-49340780	AoSMC	blood vessel:	n/a
13	chr12:49330158-49330208	Hela-S3	cervix:	n/a
14	chr12:49333479-49333529	HMEC	breast:	n/a
15	chr12:49330158-49330208	SK-N-SH_RA	brain:	n/a
16	chr12:49334797-49334847	HepG2	liver:	n/a
17	chr12:49333479-49333529	NT2-D1	testis:	n/a
18	chr12:49334797-49334847	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:49330158-49330208	SK-N-SH	brain:	n/a
20	chr12:49330158-49330208	NB4	blood:	n/a
21	chr12:49330158-49330208	NHDF-neo	bronchial:	n/a
22	chr12:49330158-49330208	AG10803	skin:	n/a
23	chr12:49332783-49332833	BE2_C	brain:	n/a
24	chr12:49340730-49340780	AG10803	skin:	n/a
25	chr12:49332783-49332833	ECC-1	luminal epithelium:	n/a
26	chr12:49332783-49332833	HRCEpiC	kidney:	n/a
27	chr12:49330158-49330208	H1-hESC	embryonic stem cell:	embryo
28	chr12:49330158-49330208	GM19239	blood:	n/a
29	chr12:49340730-49340780	HRCEpiC	kidney:	n/a
30	chr12:49333479-49333529	SK-N-SH	brain:	n/a
31	chr12:49333479-49333529	Jurkat	blood:	n/a
32	chr12:49334797-49334847	GM19239	blood:	n/a
33	chr12:49334797-49334847	SAEC	small airway:	n/a
34	chr12:49340730-49340780	H1-hESC	embryonic stem cell:	embryo
35	chr12:49340730-49340780	AG04449	skin:	fetal
36	chr12:49340730-49340780	SK-N-MC	brain:	n/a
37	chr12:49332783-49332833	ProgFib	skin:	n/a
38	chr12:49332783-49332833	GM12892	blood:	n/a
39	chr12:49333479-49333529	GM12892	blood:	n/a
40	chr12:49332783-49332833	HL-60	blood:	n/a
41	chr12:49332783-49332833	GM19239	blood:	n/a
42	chr12:49330158-49330208	HCT-116	colon:	n/a
43	chr12:49332783-49332833	A549	lung:	n/a
44	chr12:49334797-49334847	HRPEpiC	eye:	n/a
45	chr12:49333479-49333529	A549	lung:	n/a
46	chr12:49332783-49332833	AG09309	skin:	n/a
47	chr12:49333479-49333529	HNPCEpiC	eye:	n/a
48	chr12:49334797-49334847	GM12892	blood:	n/a
49	chr12:49330158-49330208	HRPEpiC	eye:	n/a
50	chr12:49333479-49333529	HRE	kidney:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:49328293..49330504-chr12:49369546..49372334,2	K562	blood:
2	chr12:49333826..49338604-chr12:49339041..49343164,6	K562	blood:
3	chr12:49207436..49209924-chr12:49334897..49337810,2	K562	blood:
4	chr12:49322489..49325005-chr12:49330130..49332105,2	K562	blood:
5	chr12:49259749..49262409-chr12:49343841..49346815,2	MCF-7	breast:
6	chr12:49335548..49339838-chr12:49342673..49348492,5	K562	blood:
7	chr12:49074839..49076756-chr12:49341494..49343312,2	K562	blood:
8	chr12:49331313..49331816-chr12:49374581..49375319,2	K562	blood:
9	chr12:49328781..49333204-chr12:49334192..49337825,5	MCF-7	breast:
10	chr12:49327847..49329795-chr12:49334116..49336401,2	K562	blood:
11	chr12:49146911..49147822-chr12:49329907..49330804,2	K562	blood:
12	chr12:49216823..49218627-chr12:49340038..49341601,2	K562	blood:
13	chr12:49329077..49331051-chr12:49365390..49368274,2	K562	blood:
14	chr12:49335913..49337732-chr12:49340843..49342555,2	K562	blood:
15	chr12:49257751..49259570-chr12:49343720..49346615,2	MCF-7	breast:
16	chr12:49331421..49333688-chr12:49334182..49336584,2	K562	blood:
17	chr12:49344320..49348348-chr12:49348662..49352888,9	MCF-7	breast:
18	chr12:49335548..49339838-chr12:49342673..49348492,5	K562	blood:
19	chr12:49329355..49335445-chr12:49337368..49342700,9	MCF-7	breast:
20	chr12:49335061..49337813-chr12:49345711..49348492,2	K562	blood:
21	chr12:49316284..49318083-chr12:49329408..49331659,2	MCF-7	breast:
22	chr12:49333826..49338604-chr12:49339041..49343164,6	K562	blood:
23	chr12:49335338..49338102-chr12:49363046..49364930,2	MCF-7	breast:
24	chr12:49338699..49342027-chr12:49368577..49371110,3	MCF-7	breast:
25	chr12:49246371..49248199-chr12:49329739..49331713,10	K562	blood:
26	chr12:49258244..49260897-chr12:49333538..49336282,2	MCF-7	breast:
27	chr12:49148849..49150468-chr12:49329197..49331509,2	K562	blood:
28	chr12:49331273..49332162-chr3:52007627..52008354,2	HCT-116	colon:
29	chr12:49329635..49330325-chr12:49389189..49389770,2	MCF-7	breast:
30	chr12:49329708..49332921-chr12:49334561..49338029,3	K562	blood:
31	chr12:49244567..49247079-chr12:49330960..49332494,2	MCF-7	breast:
32	chr12:49332994..49335617-chr12:49335721..49338299,3	K562	blood:
33	chr12:49327847..49329795-chr12:49334116..49336401,2	K562	blood:
34	chr12:49338507..49340328-chr12:49351124..49352649,2	MCF-7	breast:
35	chr12:49326822..49334011-chr12:49345841..49353556,12	MCF-7	breast:
36	chr12:49244774..49246621-chr12:49330050..49332795,2	K562	blood:
37	chr12:49330325..49332788-chr12:49411249..49413822,2	MCF-7	breast:
38	chr12:49331003..49333458-chr20:47661511..47663292,2	MCF-7	breast:
39	chr12:49330699..49331279-chr12:49388862..49389822,2	MCF-7	breast:
40	chr12:49327870..49331449-chr12:49331583..49333328,3	MCF-7	breast:
41	chr12:49334719..49339630-chr12:49347637..49352407,8	MCF-7	breast:
42	chr12:49329708..49332921-chr12:49334561..49338029,3	K562	blood:
43	chr12:49328781..49333204-chr12:49334192..49337825,5	MCF-7	breast:
44	chr12:49323463..49325005-chr12:49330605..49333416,2	K562	blood:
45	chr12:49327870..49331449-chr12:49331583..49333328,3	MCF-7	breast:
46	chr12:49330046..49330703-chr12:49381732..49382240,2	MCF-7	breast:
47	chr12:49339279..49342706-chr12:49347580..49351500,3	K562	blood:
48	chr12:49324577..49326698-chr12:49333742..49335694,2	K562	blood:
49	chr12:49326274..49328572-chr12:49329967..49332828,2	K562	blood:
50	chr12:49208469..49208981-chr12:49330141..49331083,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073610.5.1-1	chr12:49332204-49332630	NONHSAT028050
2	lnc-AC073610.5.1-1	chr12:49334907-49334971	NONHSAT028052

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ARF3	hsa-miR-30c-5p	chr12:49330885-49330909
2	ARF3	hsa-miR-125b-5p	chr12:49332191-49332185
3	ARF3	hsa-miR-320a	chr12:49330177-49330198
4	ARF3	hsa-miR-1	chr12:49330287-49330307
5	ARF3	hsa-miR-1	chr12:49332517-49332511

Variant related genes	Relation type
ENSG00000255863	TF binding region
ENSG00000255863	CpG island
ENSG00000139620	chromatin interactions
ENSG00000172602	chromatin interactions
ENSG00000200303	chromatin interactions
ENSG00000258283	chromatin interactions
ENSG00000167535	chromatin interactions
ENSG00000227431	chromatin interactions
ENSG00000174243	chromatin interactions
ENSG00000169884	chromatin interactions
ENSG00000134287	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000272822	chromatin interactions
ENSG00000124207	chromatin interactions
ENSG00000181929	chromatin interactions
ENSG00000272762	chromatin interactions
ENSG00000248487	chromatin interactions
ENSG00000255863	chromatin interactions

Extended variants
information (count: 539 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2272311	chr12:49329695-49329696	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570229727	chr12:49329752-49329753	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs554660580	chr12:49329783-49329784	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs529388441	chr12:49329789-49329790	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs549024098	chr12:49329886-49329887	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs565739096	chr12:49329901-49329902	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs79523799	chr12:49329907-49329908	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs57728708	chr12:49329954-49329955	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs1054760	chr12:49330069-49330070	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs567709511	chr12:49330076-49330077	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs570686715	chr12:49330122-49330123	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs186845876	chr12:49330124-49330125	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs556129454	chr12:49330150-49330151	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs41291973	chr12:49330151-49330152	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs1064060	chr12:49330177-49330178	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region miRNA target site	6 gene(s)	Overlapped CNVs	n/a
16	rs3209224	chr12:49330204-49330205	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs535549770	chr12:49330221-49330222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs1803045	chr12:49330252-49330253	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs11547438	chr12:49330308-49330309	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs78440727	chr12:49330354-49330355	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs76068497	chr12:49330372-49330373	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs1803050	chr12:49330430-49330431	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs541065503	chr12:49330434-49330435	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs145190582	chr12:49330493-49330494	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs182969770	chr12:49330510-49330511	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs376098319	chr12:49330529-49330530	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs578221731	chr12:49330653-49330654	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs41291975	chr12:49330659-49330660	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs147693959	chr12:49330726-49330727	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs148209110	chr12:49330774-49330775	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs187995169	chr12:49330777-49330778	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs75520473	chr12:49330778-49330779	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs528578500	chr12:49330782-49330783	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs76251264	chr12:49330785-49330786	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs78588974	chr12:49330798-49330799	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs79768729	chr12:49330804-49330805	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs76640300	chr12:49330805-49330806	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs75984804	chr12:49330810-49330811	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs79908244	chr12:49330811-49330812	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs529398656	chr12:49330826-49330827	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs549087199	chr12:49330828-49330829	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs550957705	chr12:49330829-49330830	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs559386605	chr12:49330838-49330839	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs546660336	chr12:49330876-49330877	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs551510759	chr12:49330919-49330920	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs149163510	chr12:49330993-49330994	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs539390475	chr12:49331006-49331007	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs550004870	chr12:49331014-49331015	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs11168796	chr12:49331069-49331070	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs35188035	chr12:49331099-49331100	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49314400-49338000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:49314400-49338600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:49319200-49349800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:49319400-49337800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:49319600-49331800	Weak transcription	Psoas Muscle	Psoas
6	chr12:49319600-49332800	Weak transcription	Small Intestine	intestine
7	chr12:49319600-49334600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:49319800-49331400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr12:49319800-49333200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:49319800-49349400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr12:49320800-49329800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:49320800-49333400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:49320800-49333600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr12:49320800-49335800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:49320800-49336000	Strong transcription	A549	lung
16	chr12:49320800-49338600	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr12:49321000-49330200	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:49321000-49332200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr12:49321000-49333400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:49321000-49334200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:49321000-49335000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:49321000-49335600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr12:49321000-49335800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr12:49321000-49336400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:49321000-49336800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:49321000-49338200	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr12:49321200-49332200	Strong transcription	Muscle Satellite Cultured Cells	--
28	chr12:49321400-49334200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr12:49321600-49334600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:49321800-49337800	Strong transcription	Fetal Intestine Small	intestine
31	chr12:49322800-49335200	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr12:49322800-49337600	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr12:49322800-49338600	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:49323000-49329800	Strong transcription	Colon Smooth Muscle	Colon
35	chr12:49323000-49330000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:49323000-49330200	Strong transcription	H9 Cell Line	embryonic stem cell
37	chr12:49323000-49330400	Strong transcription	HSMM	muscle
38	chr12:49323000-49334600	Strong transcription	Fetal Muscle Leg	muscle
39	chr12:49323000-49335200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr12:49323000-49335400	Strong transcription	Lung	lung
41	chr12:49323000-49335800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:49323000-49335800	Strong transcription	Adipose Nuclei	Adipose
43	chr12:49323000-49335800	Strong transcription	Fetal Brain Female	brain
44	chr12:49323000-49336400	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr12:49323000-49337800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr12:49323000-49338600	Strong transcription	GM12878-XiMat	blood
47	chr12:49323200-49332400	Strong transcription	Brain Anterior Caudate	brain
48	chr12:49323200-49332400	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:49323200-49334000	Strong transcription	Osteobl	bone
50	chr12:49323200-49335800	Strong transcription	Brain Germinal Matrix	brain

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