Variant report

Variant	esv1792086
Chromosome Location	chr1:85644478-85667608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:636)
CpG islands
(count:793)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:85646564-85646790	K562	blood:	n/a	n/a
2	ARID3A	chr1:85664678-85664931	K562	blood:	n/a	n/a
3	ARID3A	chr1:85666651-85666847	HepG2	liver:	n/a	n/a
4	ATF2	chr1:85666959-85667677	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:85667272-85667840	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:85666008-85666112	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr1:85654922-85655137	GM12878	blood:	n/a	n/a
8	BATF	chr1:85654918-85655143	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:85666301-85666915	GM12878	blood:	n/a	chr1:85666767-85666780 chr1:85666802-85666811 chr1:85666748-85666757
10	BHLHE40	chr1:85666096-85667957	K562	blood:	n/a	chr1:85667358-85667374 chr1:85667142-85667158 chr1:85667177-85667193 chr1:85667163-85667179 chr1:85667107-85667120 chr1:85667171-85667187 chr1:85666769-85666785
11	BHLHE40	chr1:85667537-85667910	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:85666683-85667794	HepG2	liver:	n/a	chr1:85667358-85667374 chr1:85667142-85667158 chr1:85667177-85667193 chr1:85667163-85667179 chr1:85667107-85667120 chr1:85667171-85667187 chr1:85666769-85666785
13	BHLHE40	chr1:85666906-85667278	GM12878	blood:	n/a	chr1:85667142-85667158 chr1:85667177-85667193 chr1:85667163-85667179 chr1:85667107-85667120 chr1:85667171-85667187
14	BRCA1	chr1:85666679-85667166	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:85665981-85666181	GM12878	blood:	n/a	n/a
16	CBX3	chr1:85666284-85666990	K562	blood:	n/a	n/a
17	CBX3	chr1:85665803-85666281	K562	blood:	n/a	n/a
18	CBX3	chr1:85667497-85667984	K562	blood:	n/a	n/a
19	CCNT2	chr1:85665858-85667849	K562	blood:	n/a	n/a
20	CEBPB	chr1:85666651-85666892	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr1:85662387-85662612	HepG2	liver:	n/a	chr1:85662449-85662460 chr1:85662448-85662459
22	CEBPB	chr1:85667235-85668507	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:85662416-85662457	A549	lung:	n/a	n/a
24	CEBPB	chr1:85661482-85661774	HepG2	liver:	n/a	chr1:85661750-85661763
25	CEBPB	chr1:85662299-85662619	K562	blood:	n/a	chr1:85662449-85662460 chr1:85662448-85662459
26	CEBPB	chr1:85666599-85666869	K562	blood:	n/a	n/a
27	CEBPB	chr1:85667329-85667653	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:85647440-85647649	K562	blood:	n/a	n/a
29	CEBPD	chr1:85666589-85667069	K562	blood:	n/a	n/a
30	CEBPD	chr1:85666469-85667004	HepG2	liver:	n/a	n/a
31	CEBPD	chr1:85667275-85667610	HepG2	liver:	n/a	n/a
32	CHD1	chr1:85666994-85668342	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr1:85666229-85666647	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:85667229-85667929	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:85667220-85667403	GM12878	blood:	n/a	n/a
36	CHD2	chr1:85667275-85667528	HepG2	liver:	n/a	n/a
37	CHD2	chr1:85666028-85667837	K562	blood:	n/a	n/a
38	CHD2	chr1:85666228-85667831	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:85666107-85666147	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr1:85666612-85666944	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:85666705-85666857	HepG2	liver:	n/a	n/a
42	CREB1	chr1:85666551-85667296	GM12878	blood:	n/a	n/a
43	CREB1	chr1:85665782-85666337	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr1:85666458-85667346	K562	blood:	n/a	n/a
45	CREB1	chr1:85666067-85667848	HepG2	liver:	n/a	n/a
46	CREB1	chr1:85666564-85667071	A549	lung:	n/a	n/a
47	CTBP2	chr1:85665918-85667824	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:85666720-85666870	AG04449	skin:	n/a	chr1:85666765-85666778 chr1:85666755-85666768
49	CTCF	chr1:85666291-85666397	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:85667120-85667270	GM12866	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85665883-85665933	HMEC	breast:	n/a
2	chr1:85666720-85666770	H1-hESC	embryonic stem cell:	embryo
3	chr1:85666720-85666770	Hepatocyte	liver:	n/a
4	chr1:85666741-85666791	SKMC	muscle:	n/a
5	chr1:85666741-85666791	RPTEC	kidney:	n/a
6	chr1:85663719-85663769	HCPEpiC	choroid plexus:	n/a
7	chr1:85666720-85666770	RPTEC	kidney:	n/a
8	chr1:85665883-85665933	NHDF-neo	bronchial:	n/a
9	chr1:85667233-85667283	NHDF-neo	bronchial:	n/a
10	chr1:85665444-85665494	MCF10A-Er-Src	breast:	n/a
11	chr1:85665444-85665494	AG09309	skin:	n/a
12	chr1:85665444-85665494	HUVEC	blood vessel:	n/a
13	chr1:85667454-85667504	K562	blood:	n/a
14	chr1:85667454-85667504	PANC-1	pancreas:	n/a
15	chr1:85665883-85665933	PFSK-1	brain:	n/a
16	chr1:85666874-85666924	GM06990	blood:	n/a
17	chr1:85666741-85666791	PANC-1	pancreas:	n/a
18	chr1:85666159-85666209	Caco-2	colon:	n/a
19	chr1:85665902-85665952	HRCEpiC	kidney:	n/a
20	chr1:85666970-85667020	PANC-1	pancreas:	n/a
21	chr1:85665883-85665933	AG09319	gingival:	n/a
22	chr1:85665902-85665952	HCT-116	colon:	n/a
23	chr1:85663719-85663769	HRE	kidney:	n/a
24	chr1:85666720-85666770	Jurkat	blood:	n/a
25	chr1:85665444-85665494	HEK293	kidney:	embryo
26	chr1:85666720-85666770	HUVEC	blood vessel:	n/a
27	chr1:85666673-85666723	Jurkat	blood:	n/a
28	chr1:85665902-85665952	HL-60	blood:	n/a
29	chr1:85667454-85667504	SK-N-SH_RA	brain:	n/a
30	chr1:85663719-85663769	AG04449	skin:	fetal
31	chr1:85665444-85665494	Hepatocyte	liver:	n/a
32	chr1:85666708-85666758	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:85667233-85667283	NB4	blood:	n/a
34	chr1:85666970-85667020	BE2_C	brain:	n/a
35	chr1:85666874-85666924	HCPEpiC	choroid plexus:	n/a
36	chr1:85666159-85666209	Jurkat	blood:	n/a
37	chr1:85663719-85663769	Hela-S3	cervix:	n/a
38	chr1:85663719-85663769	NB4	blood:	n/a
39	chr1:85665444-85665494	GM19239	blood:	n/a
40	chr1:85665902-85665952	HAEpiC	amniotic membrane:	n/a
41	chr1:85666708-85666758	ProgFib	skin:	n/a
42	chr1:85665902-85665952	PrEC	prostate:	n/a
43	chr1:85667233-85667283	PFSK-1	brain:	n/a
44	chr1:85666673-85666723	SK-N-SH	brain:	n/a
45	chr1:85667454-85667504	GM19239	blood:	n/a
46	chr1:85666741-85666791	GM12891	blood:	n/a
47	chr1:85666970-85667020	GM06990	blood:	n/a
48	chr1:85667233-85667283	HCF	heart:	n/a
49	chr1:85667454-85667504	NHDF-neo	bronchial:	n/a
50	chr1:85665444-85665494	SK-N-MC	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:85597874..85599552-chr1:85665218..85666801,2	MCF-7	breast:
2	chr1:85665631..85669772-chr1:85739485..85744059,5	K562	blood:
3	chr1:85665227..85667257-chr1:85740935..85743875,2	K562	blood:
4	chr1:85642382..85644917-chr1:85665862..85668186,3	K562	blood:
5	chr1:85665913..85668656-chr1:85741362..85743092,3	MCF-7	breast:
6	chr1:85660899..85662912-chr1:86045569..86048259,2	K562	blood:
7	chr1:85648216..85651053-chr1:85665650..85668630,4	K562	blood:
8	chr1:85649149..85651128-chr1:85658455..85661384,2	K562	blood:
9	chr1:85654589..85657084-chr1:85709286..85710971,2	K562	blood:
10	chr1:85648785..85651613-chr1:85652965..85656068,3	K562	blood:
11	chr1:85638349..85640691-chr1:85643382..85648074,4	K562	blood:
12	chr1:85666179..85667836-chr1:85723614..85725791,2	K562	blood:
13	chr1:85667494..85671075-chr1:85689483..85691213,3	K562	blood:
14	chr1:85653773..85655948-chr1:85662257..85664650,2	MCF-7	breast:
15	chr1:85649149..85651128-chr1:85658455..85661384,2	K562	blood:
16	chr1:85642542..85645439-chr1:85647337..85651293,4	K562	blood:
17	chr1:85624154..85626625-chr1:85666842..85668443,2	MCF-7	breast:
18	chr1:85658898..85664597-chr1:85664894..85668250,7	MCF-7	breast:
19	chr1:85648785..85651613-chr1:85652965..85656068,3	K562	blood:
20	chr1:85660381..85662955-chr1:85716611..85718297,2	K562	blood:
21	chr1:85665831..85667640-chr1:86041122..86042846,2	MCF-7	breast:
22	chr1:85666946..85668694-chr1:85686380..85689036,2	K562	blood:
23	chr1:85642542..85645439-chr1:85647337..85651293,4	K562	blood:
24	chr1:85666785..85669663-chr1:85715100..85717431,2	K562	blood:
25	chr1:85664620..85668785-chr1:85722586..85726821,6	MCF-7	breast:
26	chr1:85653773..85655948-chr1:85662257..85664650,2	MCF-7	breast:
27	chr1:85641887..85644190-chr1:85657826..85660116,2	K562	blood:
28	chr1:85663638..85666684-chr1:85666937..85669926,3	MCF-7	breast:
29	chr1:85642419..85645228-chr1:85665862..85667979,2	K562	blood:
30	chr1:85644133..85647252-chr1:85665806..85669037,3	MCF-7	breast:
31	chr1:85654751..85658445-chr1:85665571..85669140,5	MCF-7	breast:
32	chr1:85666758..85667459-chr11:107879642..107880312,2	NB4	blood:
33	chr1:85641812..85644016-chr1:85661347..85664205,2	K562	blood:

No data

Variant related genes	Relation type
SYDE2	TF binding region
SYDE2	CpG island
ENSG00000266110	chromatin interactions
ENSG00000153904	chromatin interactions
ENSG00000162642	chromatin interactions
ENSG00000223653	chromatin interactions
ENSG00000097096	chromatin interactions
ENSG00000166266	chromatin interactions
ENSG00000142867	chromatin interactions
ENSG00000142871	chromatin interactions

Extended variants
information (count: 832 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10493762	chr1:85644478-85644479	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548885424	chr1:85644482-85644483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561898861	chr1:85644513-85644514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs527690009	chr1:85644544-85644545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181256458	chr1:85644549-85644550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186189830	chr1:85644588-85644589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs817442	chr1:85644590-85644591	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs549544845	chr1:85644605-85644606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569538965	chr1:85644651-85644652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs535355776	chr1:85644671-85644672	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555646539	chr1:85644711-85644712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558078141	chr1:85644764-85644765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571897413	chr1:85644768-85644769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534606057	chr1:85644773-85644774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557826298	chr1:85644804-85644805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189098650	chr1:85644872-85644873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181910690	chr1:85644953-85644954	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35846581	chr1:85644954-85644955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376888575	chr1:85645119-85645120	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186083395	chr1:85645145-85645146	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2994490	chr1:85645165-85645166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs574757613	chr1:85645256-85645257	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542116443	chr1:85645305-85645306	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543490484	chr1:85645311-85645312	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs139801579	chr1:85645341-85645342	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528015452	chr1:85645407-85645408	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375912632	chr1:85645448-85645449	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs59976187	chr1:85645515-85645516	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs398102975	chr1:85645517-85645518	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs201140568	chr1:85645520-85645521	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547372882	chr1:85645525-85645526	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545297084	chr1:85645527-85645528	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571529052	chr1:85645578-85645579	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs564703111	chr1:85645615-85645616	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11342287	chr1:85645632-85645633	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs398074128	chr1:85645633-85645634	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533227303	chr1:85645676-85645677	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs111280159	chr1:85645709-85645710	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs147205175	chr1:85645732-85645733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs569713484	chr1:85645742-85645743	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535643647	chr1:85645748-85645749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs114520424	chr1:85645844-85645845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565953156	chr1:85645970-85645971	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560691519	chr1:85645998-85645999	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373569764	chr1:85646003-85646004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs557762946	chr1:85646008-85646009	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577732701	chr1:85646039-85646040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537107857	chr1:85646092-85646093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557101742	chr1:85646093-85646094	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190547401	chr1:85646100-85646101	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85608600-85655200	Weak transcription	Aorta	Aorta
2	chr1:85610400-85647800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:85615400-85647600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:85615400-85655200	Weak transcription	Lung	lung
5	chr1:85615600-85654000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:85615800-85665800	Weak transcription	Esophagus	oesophagus
7	chr1:85617800-85648000	Weak transcription	Liver	Liver
8	chr1:85619000-85655000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:85619200-85647400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:85619800-85646800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:85621000-85645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:85624400-85647600	Weak transcription	HSMM	muscle
13	chr1:85625600-85654600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:85626800-85655600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr1:85627200-85657400	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr1:85627400-85654200	Weak transcription	Gastric	stomach
17	chr1:85627400-85655800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr1:85627400-85663000	Weak transcription	NHEK	skin
19	chr1:85627600-85648000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr1:85627800-85655800	Weak transcription	NHDF-Ad	bronchial
21	chr1:85627800-85664400	Weak transcription	Osteobl	bone
22	chr1:85628400-85647400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:85628600-85648000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr1:85629000-85645200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr1:85629800-85653600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:85630600-85647600	Weak transcription	Adipose Nuclei	Adipose
27	chr1:85630800-85647800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr1:85630800-85647800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr1:85631200-85654000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:85631400-85654200	Weak transcription	HepG2	liver
31	chr1:85632000-85648400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:85632600-85647800	Weak transcription	Stomach Smooth Muscle	stomach
33	chr1:85632800-85647800	Weak transcription	Fetal Lung	lung
34	chr1:85633400-85655000	Weak transcription	Fetal Intestine Small	intestine
35	chr1:85633600-85654200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:85634000-85655200	Weak transcription	Fetal Stomach	stomach
37	chr1:85634200-85645200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:85638400-85654800	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr1:85638600-85647400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:85638600-85655200	Weak transcription	Left Ventricle	heart
41	chr1:85638800-85647600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:85639000-85647600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:85639000-85647800	Weak transcription	Fetal Intestine Large	intestine
44	chr1:85639000-85665400	Weak transcription	Placenta	Placenta
45	chr1:85640200-85645200	Weak transcription	Fetal Heart	heart
46	chr1:85640800-85647200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:85641400-85647400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:85642000-85655800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:85643200-85658800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr1:85643400-85647800	Weak transcription	K562	blood

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