Variant report

Variant	nsv1000865
Chromosome Location	chr3:141846105-142086659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3039)
CpG islands
(count:1403)
Chromatin interactive
region (count:145)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3039 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
2	ARID3A	chr3:142085451-142085580	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:142082266-142082975	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
5	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
7	ARID3A	chr3:141848736-141848803	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:141868086-141868286	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:142085359-142085586	K562	blood:	n/a	n/a
10	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
11	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
12	ARID3A	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
14	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
15	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
16	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
17	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
18	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
19	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
20	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
22	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
23	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
24	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
25	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
27	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
30	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
31	BATF	chr3:142074556-142074897	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
37	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
38	BHLHE40	chr3:141867704-141868571	HepG2	liver:	n/a	n/a
39	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
41	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
42	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
44	BRCA1	chr3:141867873-141868061	HepG2	liver:	n/a	n/a
45	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr3:141868168-141868537	K562	blood:	n/a	n/a
49	CBX3	chr3:142003802-142004433	K562	blood:	n/a	n/a
50	CBX3	chr3:142003887-142004274	K562	blood:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141944519-141944569	GM06990	blood:	n/a
2	chr3:141995701-141995751	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:141941279-141941329	SK-N-SH_RA	brain:	n/a
4	chr3:141867994-141868044	HRCEpiC	kidney:	n/a
5	chr3:141868409-141868459	SAEC	small airway:	n/a
6	chr3:141877942-141877992	IMR90	lung:	fetal
7	chr3:142027066-142027116	ProgFib	skin:	n/a
8	chr3:141944519-141944569	HepG2	liver:	n/a
9	chr3:142027066-142027116	HCF	heart:	n/a
10	chr3:141867862-141867912	HRE	kidney:	n/a
11	chr3:141945703-141945753	GM12892	blood:	n/a
12	chr3:141868459-141868509	HUVEC	blood vessel:	n/a
13	chr3:141867862-141867912	HCT-116	colon:	n/a
14	chr3:141944620-141944670	HCT-116	colon:	n/a
15	chr3:141867862-141867912	GM12891	blood:	n/a
16	chr3:141868997-141869047	HCF	heart:	n/a
17	chr3:141944516-141944566	SK-N-SH_RA	brain:	n/a
18	chr3:141944318-141944368	HCM	heart:	n/a
19	chr3:141943895-141943945	HCPEpiC	choroid plexus:	n/a
20	chr3:141944344-141944394	MCF10A-Er-Src	breast:	n/a
21	chr3:141867862-141867912	Hepatocyte	liver:	n/a
22	chr3:142027066-142027116	PrEC	prostate:	n/a
23	chr3:141945790-141945840	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:141867862-141867912	AoSMC	blood vessel:	n/a
25	chr3:142027066-142027116	HEEpiC	esophagus:	n/a
26	chr3:141944516-141944566	HepG2	liver:	n/a
27	chr3:141944077-141944127	HCT-116	colon:	n/a
28	chr3:141944516-141944566	AG10803	skin:	n/a
29	chr3:141877942-141877992	HCM	heart:	n/a
30	chr3:141944516-141944566	AG04450	lung:	fetal
31	chr3:141928789-141928839	AG04449	skin:	fetal
32	chr3:141945703-141945753	HCM	heart:	n/a
33	chr3:141944077-141944127	U87	brain:	n/a
34	chr3:141868612-141868662	AG10803	skin:	n/a
35	chr3:141868997-141869047	ProgFib	skin:	n/a
36	chr3:141944318-141944368	Hela-S3	cervix:	n/a
37	chr3:141945703-141945753	HCPEpiC	choroid plexus:	n/a
38	chr3:141944077-141944127	HRCEpiC	kidney:	n/a
39	chr3:141944519-141944569	ProgFib	skin:	n/a
40	chr3:141871386-141871436	AG04449	skin:	fetal
41	chr3:141868459-141868509	PrEC	prostate:	n/a
42	chr3:141941279-141941329	NT2-D1	testis:	n/a
43	chr3:141944077-141944127	HRPEpiC	eye:	n/a
44	chr3:141888226-141888276	HEEpiC	esophagus:	n/a
45	chr3:141945790-141945840	Hepatocyte	liver:	n/a
46	chr3:141941279-141941329	BE2_C	brain:	n/a
47	chr3:141888226-141888276	PANC-1	pancreas:	n/a
48	chr3:141944620-141944670	GM19239	blood:	n/a
49	chr3:141877942-141877992	HCPEpiC	choroid plexus:	n/a
50	chr3:141928789-141928839	HL-60	blood:	n/a

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:141873069..141875142-chr3:141877650..141879337,2	K562	blood:
2	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
3	chr3:141866172..141869567-chr3:141870149..141874954,7	MCF-7	breast:
4	chr17:62222919..62223709-chr3:141944062..141944934,2	HCT-116	colon:
5	chr3:141844475..141845747-chr3:141998357..141999102,5	K562	blood:
6	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
7	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:
8	chr3:142071094..142074933-chr3:142076608..142079513,3	MCF-7	breast:
9	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
10	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
11	chr3:141866471..141869350-chr3:141942355..141944493,2	K562	blood:
12	chr3:141745328..141748975-chr3:142003993..142005586,3	K562	blood:
13	chr3:141681160..141682062-chr3:141998578..141999511,3	K562	blood:
14	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
15	chr3:141866276..141868412-chr3:141942932..141945800,2	MCF-7	breast:
16	chr3:141746412..141748907-chr3:141928677..141931000,3	K562	blood:
17	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
18	chr3:141918309..141919900-chr3:141924207..141926926,2	MCF-7	breast:
19	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
20	chr3:142048008..142050372-chr3:142051605..142054312,2	K562	blood:
21	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
22	chr3:141865638..141868267-chr3:141942930..141945180,2	MCF-7	breast:
23	chr3:142034226..142036473-chr3:142044742..142046537,2	K562	blood:
24	chr3:141866047..141867912-chr3:141873721..141875434,2	K562	blood:
25	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
26	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
27	chr3:141932221..141937955-chr3:141938851..141945696,9	K562	blood:
28	chr3:141942954..141945885-chr3:141988032..141991755,3	MCF-7	breast:
29	chr3:141941642..141944817-chr3:141944838..141947150,3	K562	blood:
30	chr3:141888192..141890414-chr3:141943053..141945967,2	MCF-7	breast:
31	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
32	chr3:141681241..141682037-chr3:141894141..141895360,3	MCF-7	breast:
33	chr3:141998539..142000204-chr3:142002540..142004917,2	K562	blood:
34	chr3:141844885..141845509-chr3:141998474..141999186,2	MCF-7	breast:
35	chr3:142025469..142027957-chr3:142037548..142040461,2	K562	blood:
36	chr3:142031696..142033287-chr3:142037661..142039925,2	MCF-7	breast:
37	chr3:141883292..141885881-chr3:141942350..141944457,2	K562	blood:
38	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
39	chr3:141943937..141944882-chr5:32585069..32586043,2	Hela-S3	cervix:
40	chr3:142071094..142074933-chr3:142076608..142079513,3	MCF-7	breast:
41	chr3:141940937..141945863-chr3:141947298..141949257,5	K562	blood:
42	chr3:141873069..141875142-chr3:141877650..141879337,2	K562	blood:
43	chr3:141942905..141947103-chr3:141949028..141953369,8	MCF-7	breast:
44	chr3:141866424..141868170-chr3:141875148..141877149,2	MCF-7	breast:
45	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
46	chr3:141740878..141741732-chr3:141899625..141900228,2	MCF-7	breast:
47	chr3:141919047..141920973-chr3:141943572..141945964,2	MCF-7	breast:
48	chr3:141944032..141945017-chr8:143808717..143809376,2	Hela-S3	cervix:
49	chr1:45284275..45285951-chr3:141939370..141941710,2	K562	blood:
50	chr3:141866276..141868412-chr3:141942932..141945800,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-7	chr3:141876369-141880820	ENSG00000272565.1

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GK5	hsa-miR-340-5p	chr3:141878164-141878157
2	XRN1	hsa-miR-10a-5p	chr3:142029586-142029608
3	XRN1	hsa-let-7b-5p	chr3:142030132-142030126
4	GK5	hsa-miR-124-3p	chr3:141883855-141883849
5	XRN1	hsa-miR-10a-5p	chr3:142029592-142029585
6	XRN1	hsa-miR-335-5p	chr3:142025482-142025506

Variant related genes	Relation type
GK5	TF binding region
XRN1	TF binding region
RNU6-425P	TF binding region
ENSG00000272565	TF binding region
TFDP2	TF binding region
GK5	CpG island
XRN1	CpG island
RNU6-425P	CpG island
ENSG00000272565	CpG island
TFDP2	CpG island
ENSG00000206604	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000272565	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000130193	chromatin interactions

Extended variants
information (count: 7740 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7740 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192437399	chr3:141846112-141846113	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs577782671	chr3:141846193-141846194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565353247	chr3:141846237-141846238	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs9869592	chr3:141846293-141846294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563595197	chr3:141846298-141846299	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs116432292	chr3:141846352-141846353	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs543048859	chr3:141846357-141846358	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138164657	chr3:141846365-141846366	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561124393	chr3:141846380-141846381	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs73236016	chr3:141846470-141846471	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs140313725	chr3:141846473-141846474	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs182341141	chr3:141846474-141846475	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs115832188	chr3:141846506-141846507	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs551703774	chr3:141846528-141846529	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs574044702	chr3:141846577-141846578	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs114268299	chr3:141846760-141846761	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs187591174	chr3:141846780-141846781	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144073349	chr3:141846827-141846828	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs534732881	chr3:141846908-141846909	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs116228027	chr3:141846957-141846958	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs146488890	chr3:141846958-141846959	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs141079203	chr3:141846972-141846973	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192925174	chr3:141846979-141846980	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143197918	chr3:141846983-141846984	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575942180	chr3:141847025-141847026	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542930825	chr3:141847054-141847055	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs561367245	chr3:141847114-141847115	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs148281099	chr3:141847115-141847116	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs540751121	chr3:141847127-141847128	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184594941	chr3:141847146-141847147	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533168522	chr3:141847200-141847201	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140438928	chr3:141847222-141847223	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs372615965	chr3:141847259-141847260	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115163871	chr3:141847268-141847269	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150414056	chr3:141847323-141847324	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs375891565	chr3:141847346-141847347	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs567278183	chr3:141847379-141847380	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs74692112	chr3:141847405-141847406	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558171075	chr3:141847415-141847416	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190292757	chr3:141847425-141847426	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547889514	chr3:141847433-141847434	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs57901013	chr3:141847437-141847438	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538343294	chr3:141847458-141847459	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6785705	chr3:141847460-141847461	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557162520	chr3:141847496-141847497	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530881127	chr3:141847528-141847529	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs371298659	chr3:141847533-141847534	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs533755101	chr3:141847556-141847557	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192032473	chr3:141847673-141847674	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs554935252	chr3:141847675-141847676	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:4872 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141836400-141866200	Weak transcription	Primary T cells from cord blood	blood
2	chr3:141836600-141847200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:141837200-141847200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr3:141838200-141866200	Weak transcription	Adipose Nuclei	Adipose
5	chr3:141838600-141850600	Weak transcription	Fetal Intestine Small	intestine
6	chr3:141840200-141865400	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:141840200-141866000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:141842800-141858400	Weak transcription	Fetal Intestine Large	intestine
9	chr3:141844800-141859600	Weak transcription	Fetal Stomach	stomach
10	chr3:141845000-141863600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:141845200-141846400	Enhancers	Fetal Thymus	thymus
12	chr3:141845200-141847400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:141845400-141867200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr3:141845600-141859000	Weak transcription	Thymus	Thymus
15	chr3:141846000-141846400	Weak transcription	Dnd41	blood
16	chr3:141846000-141846600	Weak transcription	Brain Germinal Matrix	brain
17	chr3:141846000-141848600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:141846400-141847600	Genic enhancers	Fetal Thymus	thymus
19	chr3:141846400-141849600	Enhancers	Dnd41	blood
20	chr3:141846600-141847200	Enhancers	Brain Germinal Matrix	brain
21	chr3:141846600-141848200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr3:141846800-141847000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:141846800-141847800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:141846800-141848200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr3:141846800-141848200	Enhancers	Liver	Liver
26	chr3:141847000-141847200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:141847000-141848000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:141847000-141859400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr3:141847200-141847400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:141847200-141847400	Enhancers	Fetal Brain Female	brain
31	chr3:141847200-141847600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr3:141847200-141847600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:141847200-141848000	Weak transcription	Brain Germinal Matrix	brain
34	chr3:141847200-141848200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:141847200-141848200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:141847200-141848400	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr3:141847400-141848200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr3:141847400-141857800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr3:141847400-141859600	Weak transcription	Fetal Brain Female	brain
40	chr3:141847600-141848600	Enhancers	Fetal Thymus	thymus
41	chr3:141848000-141848200	Enhancers	Primary hematopoietic stem cells	blood
42	chr3:141848000-141848200	Enhancers	Brain Germinal Matrix	brain
43	chr3:141848000-141866200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr3:141848200-141859000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr3:141848200-141859600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr3:141848200-141859600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr3:141848200-141866400	Weak transcription	Liver	Liver
48	chr3:141848400-141856400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr3:141848600-141848800	Weak transcription	Fetal Thymus	thymus
50	chr3:141848600-141852200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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