Variant report

Variant	nsv1064549
Chromosome Location	chr21:45446358-45493720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:0)
Chromatin interactive
region (count:79)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 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	chr21:45449544-45449770	K562	blood:	n/a	n/a
2	ARID3A	chr21:45445220-45446419	K562	blood:	n/a	chr21:45445311-45445327
3	ATF2	chr21:45485245-45485784	GM12878	blood:	n/a	n/a
4	BACH1	chr21:45449503-45449620	K562	blood:	n/a	n/a
5	BHLHE40	chr21:45463581-45463851	K562	blood:	n/a	n/a
6	BHLHE40	chr21:45449598-45449626	K562	blood:	n/a	n/a
7	CCNT2	chr21:45445661-45446365	K562	blood:	n/a	chr21:45446093-45446102
8	CEBPB	chr21:45476975-45477292	A549	lung:	n/a	chr21:45477123-45477134
9	CEBPB	chr21:45485418-45485637	IMR90	lung:	n/a	n/a
10	CEBPB	chr21:45477040-45477240	Hela-S3	cervix:	n/a	chr21:45477123-45477134
11	CEBPB	chr21:45476959-45477294	K562	blood:	n/a	chr21:45477123-45477134
12	CEBPB	chr21:45476956-45477305	IMR90	lung:	n/a	chr21:45477123-45477134
13	CEBPB	chr21:45476970-45477274	HepG2	liver:	n/a	chr21:45477123-45477134
14	CREB1	chr21:45485149-45485833	GM12878	blood:	n/a	n/a
15	CREB1	chr21:45485250-45485742	GM12878	blood:	n/a	n/a
16	CTCF	chr21:45487340-45487490	HEK293	kidney:	n/a	n/a
17	CTCF	chr21:45487471-45487580	A549	lung:	n/a	chr21:45487508-45487521
18	CTCF	chr21:45487425-45487646	MCF-7	breast:	n/a	chr21:45487508-45487521
19	CTCF	chr21:45487493-45487573	GM10266	blood:	n/a	chr21:45487508-45487521
20	CTCF	chr21:45491740-45491890	MCF-7	breast:	n/a	n/a
21	CTCF	chr21:45491740-45491890	GM12873	blood:	n/a	n/a
22	CTCF	chr21:45491685-45491947	K562	blood:	n/a	n/a
23	CTCF	chr21:45491773-45491902	MCF-7	breast:	n/a	n/a
24	CTCF	chr21:45463764-45463851	GM19239	blood:	n/a	n/a
25	CTCF	chr21:45487412-45487603	HepG2	liver:	n/a	chr21:45487508-45487521
26	CTCF	chr21:45480482-45480604	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr21:45487480-45487630	HepG2	liver:	n/a	chr21:45487508-45487521
28	CTCF	chr21:45471640-45471790	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr21:45487520-45487670	BE2_C	brain:	n/a	n/a
30	CTCF	chr21:45487460-45487610	HVMF	connective:	n/a	chr21:45487508-45487521
31	CTCF	chr21:45491765-45491922	MCF-7	breast:	n/a	n/a
32	CTCF	chr21:45491740-45491890	HRE	kidney:	n/a	n/a
33	CTCF	chr21:45487600-45487750	MCF-7	breast:	n/a	n/a
34	CTCF	chr21:45485406-45485440	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr21:45469200-45469350	HRPEpiC	eye:	n/a	chr21:45469296-45469304
36	CTCF	chr21:45463763-45463905	K562	blood:	n/a	n/a
37	CTCF	chr21:45479994-45480020	GM13976	blood:	n/a	n/a
38	CTCF	chr21:45491800-45491950	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr21:45469540-45469690	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr21:45491840-45491990	HFF	foreskin:	n/a	n/a
41	CTCF	chr21:45463772-45463822	MCF-7	breast:	n/a	n/a
42	CTCF	chr21:45469219-45469296	MCF-7	breast:	n/a	n/a
43	CTCF	chr21:45487360-45487510	RPTEC	kidney:	n/a	n/a
44	CTCF	chr21:45471460-45471610	HCM	heart:	n/a	n/a
45	CTCF	chr21:45487400-45487550	HepG2	liver:	n/a	chr21:45487508-45487521
46	CTCF	chr21:45487480-45487630	K562	blood:	n/a	chr21:45487508-45487521
47	CTCF	chr21:45463785-45463847	GM19240	blood:	n/a	n/a
48	CTCF	chr21:45469183-45469189	MCF-7	breast:	n/a	n/a
49	CTCF	chr21:45469158-45469291	MCF-7	breast:	n/a	n/a
50	CTCF	chr21:45491760-45491910	HCT-116	colon:	n/a	n/a

No data

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr21:45468088..45470419-chr21:45470553..45472490,2	K562	blood:
2	chr21:45446322..45447906-chr21:45454983..45457512,2	K562	blood:
3	chr21:45483406..45486402-chr21:45486575..45488365,2	MCF-7	breast:
4	chr21:45430957..45434047-chr21:45458987..45462690,3	MCF-7	breast:
5	chr21:45454985..45459889-chr21:45463803..45466700,4	K562	blood:
6	chr21:45483073..45485151-chr21:45486951..45488826,2	K562	blood:
7	chr21:45449660..45451508-chr21:45454288..45457087,2	MCF-7	breast:
8	chr21:45430900..45434144-chr21:45470946..45474131,3	K562	blood:
9	chr21:45446065..45448233-chr21:45527740..45530031,2	K562	blood:
10	chr21:45489183..45491870-chr21:45524868..45527531,3	MCF-7	breast:
11	chr21:45432147..45436364-chr21:45445225..45446864,3	MCF-7	breast:
12	chr21:45454985..45457664-chr21:45464641..45466700,2	K562	blood:
13	chr21:45461046..45464052-chr21:45468043..45471887,4	K562	blood:
14	chr21:45449259..45451430-chr21:45484484..45487019,2	K562	blood:
15	chr21:45446322..45447906-chr21:45454983..45457512,2	K562	blood:
16	chr21:45429269..45431828-chr21:45486431..45488648,2	MCF-7	breast:
17	chr21:45485859..45488146-chr21:45491483..45493752,2	K562	blood:
18	chr21:45476652..45480295-chr21:45485072..45489102,4	MCF-7	breast:
19	chr21:45485665..45487359-chr21:45490550..45492983,2	K562	blood:
20	chr21:45483486..45486444-chr21:45498121..45500781,3	K562	blood:
21	chr21:45474928..45477593-chr21:45490413..45492194,2	K562	blood:
22	chr21:45483073..45484734-chr21:45486730..45488826,2	K562	blood:
23	chr21:45474928..45477593-chr21:45490413..45492194,2	K562	blood:
24	chr21:45462776..45465739-chr21:45484700..45487223,2	K562	blood:
25	chr21:45483073..45485151-chr21:45486951..45488826,2	K562	blood:
26	chr21:45461125..45462708-chr21:45462843..45464529,2	K562	blood:
27	chr21:45485859..45488146-chr21:45491483..45493752,2	K562	blood:
28	chr21:45454972..45457368-chr21:45476022..45478398,2	MCF-7	breast:
29	chr21:45230492..45230995-chr21:45487103..45487981,2	MCF-7	breast:
30	chr21:45488029..45489681-chr21:45562055..45564999,2	K562	blood:
31	chr21:45431046..45433017-chr21:45448957..45451202,3	MCF-7	breast:
32	chr21:45476652..45480295-chr21:45485072..45489102,4	MCF-7	breast:
33	chr21:45454985..45459889-chr21:45463803..45466700,4	K562	blood:
34	chr21:45473377..45479336-chr21:45481371..45487468,11	K562	blood:
35	chr21:45473377..45479336-chr21:45481371..45487468,11	K562	blood:
36	chr21:45358902..45359545-chr21:45487441..45487957,2	MCF-7	breast:
37	chr21:45431167..45434118-chr21:45483747..45486139,3	K562	blood:
38	chr21:45444934..45447565-chr21:45527496..45530031,3	K562	blood:
39	chr21:45486005..45488268-chr21:45490821..45492740,2	MCF-7	breast:
40	chr21:45432713..45434258-chr21:45470082..45471621,2	MCF-7	breast:
41	chr21:45486005..45488268-chr21:45490821..45492740,2	MCF-7	breast:
42	chr21:45430666..45432570-chr21:45474186..45475949,2	MCF-7	breast:
43	chr21:45453079..45455479-chr21:45471617..45474018,2	K562	blood:
44	chr21:45454985..45457664-chr21:45464641..45466700,2	K562	blood:
45	chr21:45461125..45462708-chr21:45462843..45464529,2	K562	blood:
46	chr21:45311589..45314501-chr21:45483569..45485379,2	MCF-7	breast:
47	chr21:45462400..45464509-chr21:45491982..45494825,2	MCF-7	breast:
48	chr21:45487715..45490221-chr21:45492098..45495083,2	K562	blood:
49	chr21:45462400..45464509-chr21:45491982..45494825,2	MCF-7	breast:
50	chr21:45108488..45111399-chr21:45445674..45447508,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ICOSLG-11	chr21:45466228-45466387	NONHSAT082470
2	lnc-ICOSLG-11	chr21:45466688-45466922	NONHSAT082470

No data

Variant related genes	Relation type
H2AFZP1	TF binding region
ENSG00000160218	chromatin interactions
ENSG00000160221	chromatin interactions
ENSG00000241945	chromatin interactions

Extended variants
information (count: 1871 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1871 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139066768	chr21:45446373-45446374	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552577536	chr21:45446377-45446378	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs116779617	chr21:45446386-45446387	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564353361	chr21:45446459-45446460	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148157613	chr21:45446464-45446465	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2276531	chr21:45446487-45446488	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2256392	chr21:45446504-45446505	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs17262187	chr21:45446514-45446515	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2256441	chr21:45446589-45446590	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs114487281	chr21:45446594-45446595	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528069309	chr21:45446604-45446605	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs17004621	chr21:45446623-45446624	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564891679	chr21:45446628-45446629	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375649851	chr21:45446646-45446647	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532204962	chr21:45446647-45446648	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550699401	chr21:45446652-45446653	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs569432688	chr21:45446716-45446717	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187790377	chr21:45446762-45446763	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535232130	chr21:45446796-45446797	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548840632	chr21:45446829-45446830	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547204189	chr21:45446885-45446886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs137896682	chr21:45446975-45446976	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534237115	chr21:45446999-45447000	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565407765	chr21:45447002-45447003	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs373092574	chr21:45447010-45447011	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs539172913	chr21:45447035-45447036	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs558480889	chr21:45447094-45447095	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs570513009	chr21:45447129-45447130	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs149470289	chr21:45447190-45447191	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs556421539	chr21:45447207-45447208	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192925482	chr21:45447221-45447222	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142512649	chr21:45447224-45447225	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185122231	chr21:45447246-45447247	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373924438	chr21:45447347-45447348	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113944673	chr21:45447393-45447394	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187538021	chr21:45447451-45447452	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573022561	chr21:45447455-45447456	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs12627141	chr21:45447522-45447523	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs79133589	chr21:45447534-45447535	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147154247	chr21:45447543-45447544	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192419805	chr21:45447548-45447549	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs367714981	chr21:45447559-45447560	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78293273	chr21:45447562-45447563	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538525491	chr21:45447564-45447565	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79512727	chr21:45447580-45447581	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554459002	chr21:45447581-45447582	Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529817048	chr21:45447608-45447609	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs578210024	chr21:45447623-45447624	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138733136	chr21:45447646-45447647	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184826437	chr21:45447673-45447674	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
small cell lung cancer	17426248	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1856 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45433200-45452600	Weak transcription	Aorta	Aorta
2	chr21:45433800-45448000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr21:45434200-45448800	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr21:45434200-45450800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr21:45434400-45446800	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr21:45434400-45451000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr21:45434800-45447200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr21:45434800-45447400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr21:45435000-45450200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr21:45436800-45446800	Enhancers	Primary T cells fromperipheralblood	blood
11	chr21:45438200-45451400	Weak transcription	Hela-S3	cervix
12	chr21:45440600-45446800	Enhancers	Primary B cells from peripheral blood	blood
13	chr21:45440800-45451400	Weak transcription	Dnd41	blood
14	chr21:45441200-45447600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr21:45441800-45452400	Weak transcription	Fetal Brain Female	brain
16	chr21:45442600-45447000	Enhancers	Skeletal Muscle Male	skeletal muscle
17	chr21:45443200-45446800	Enhancers	Brain Anterior Caudate	brain
18	chr21:45443200-45447000	Enhancers	Brain Substantia Nigra	brain
19	chr21:45443400-45446800	Enhancers	Brain Cingulate Gyrus	brain
20	chr21:45443600-45446400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr21:45443600-45447000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr21:45443800-45448600	Enhancers	Left Ventricle	heart
23	chr21:45444000-45446400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr21:45444000-45446400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr21:45444000-45446400	Enhancers	Primary T cells from cord blood	blood
26	chr21:45444000-45446800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr21:45444000-45447000	Enhancers	Spleen	Spleen
28	chr21:45444000-45448400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr21:45444200-45446400	Enhancers	Fetal Kidney	kidney
30	chr21:45444200-45446400	Enhancers	NHDF-Ad	bronchial
31	chr21:45444200-45446400	Enhancers	Osteobl	bone
32	chr21:45444200-45446800	Enhancers	Brain Angular Gyrus	brain
33	chr21:45444200-45446800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr21:45444200-45447800	Enhancers	Psoas Muscle	Psoas
35	chr21:45444400-45448000	Enhancers	Primary hematopoietic stem cells	blood
36	chr21:45444400-45452400	Weak transcription	Fetal Intestine Small	intestine
37	chr21:45444600-45446400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr21:45444600-45446400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr21:45444600-45446400	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr21:45444600-45446400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr21:45444600-45446600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr21:45444600-45446600	Enhancers	NH-A	brain
43	chr21:45444800-45446400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr21:45444800-45446400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr21:45444800-45446400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr21:45444800-45446400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr21:45444800-45446400	Enhancers	Primary B cells from cord blood	blood
48	chr21:45444800-45446400	Enhancers	Fetal Heart	heart
49	chr21:45444800-45446400	Enhancers	Thymus	Thymus
50	chr21:45444800-45446600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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