Variant report

Variant	esv1836491
Chromosome Location	chr3:196051403-196078427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:651)
CpG islands
(count:734)
Chromatin interactive
region (count:69)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:196074051-196074658	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:196065223-196065568	K562	blood:	n/a	n/a
3	ARID3A	chr3:196066607-196067672	K562	blood:	n/a	n/a
4	ATF1	chr3:196066740-196066989	K562	blood:	n/a	n/a
5	ATF1	chr3:196064298-196064679	K562	blood:	n/a	n/a
6	ATF3	chr3:196065258-196065615	K562	blood:	n/a	n/a
7	ATF3	chr3:196066623-196067055	K562	blood:	n/a	n/a
8	ATF3	chr3:196066697-196066945	K562	blood:	n/a	n/a
9	ATF3	chr3:196064125-196064652	K562	blood:	n/a	n/a
10	ATF3	chr3:196065271-196065725	K562	blood:	n/a	n/a
11	BACH1	chr3:196052444-196052596	K562	blood:	n/a	n/a
12	BACH1	chr3:196067324-196067631	K562	blood:	n/a	n/a
13	BACH1	chr3:196066659-196066986	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr3:196066604-196067061	K562	blood:	n/a	n/a
15	BACH1	chr3:196064626-196065196	K562	blood:	n/a	n/a
16	BCL3	chr3:196071710-196072170	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:196066716-196067272	K562	blood:	n/a	n/a
18	BHLHE40	chr3:196074164-196074525	HepG2	liver:	n/a	n/a
19	BHLHE40	chr3:196075572-196075865	HepG2	liver:	n/a	n/a
20	BHLHE40	chr3:196066468-196067076	K562	blood:	n/a	n/a
21	BHLHE40	chr3:196074282-196074482	A549	lung:	n/a	n/a
22	BHLHE40	chr3:196074104-196074694	HepG2	liver:	n/a	n/a
23	BHLHE40	chr3:196063493-196063804	K562	blood:	n/a	n/a
24	BHLHE40	chr3:196064059-196065735	K562	blood:	n/a	n/a
25	BHLHE40	chr3:196074220-196074547	HepG2	liver:	n/a	n/a
26	BHLHE40	chr3:196067388-196067554	K562	blood:	n/a	n/a
27	BHLHE40	chr3:196065282-196065567	HepG2	liver:	n/a	n/a
28	BRCA1	chr3:196065333-196065678	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr3:196066503-196067045	K562	blood:	n/a	n/a
30	CBX3	chr3:196066465-196067185	K562	blood:	n/a	n/a
31	CBX3	chr3:196063948-196065779	K562	blood:	n/a	n/a
32	CBX3	chr3:196064013-196064926	K562	blood:	n/a	n/a
33	CCNT2	chr3:196066759-196066959	K562	blood:	n/a	n/a
34	CCNT2	chr3:196064394-196065660	K562	blood:	n/a	n/a
35	CEBPB	chr3:196064309-196064948	K562	blood:	n/a	n/a
36	CEBPB	chr3:196073998-196074538	MCF-7	breast:	n/a	n/a
37	CEBPB	chr3:196074153-196074406	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:196066681-196066995	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:196065313-196065714	K562	blood:	n/a	n/a
40	CEBPB	chr3:196066675-196066996	K562	blood:	n/a	n/a
41	CEBPB	chr3:196074101-196074508	A549	lung:	n/a	n/a
42	CEBPB	chr3:196066567-196067057	K562	blood:	n/a	n/a
43	CEBPB	chr3:196074134-196074512	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:196065389-196065664	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:196066690-196066987	IMR90	lung:	n/a	n/a
46	CEBPB	chr3:196074074-196074551	A549	lung:	n/a	n/a
47	CEBPB	chr3:196074107-196074482	HepG2	liver:	n/a	n/a
48	CEBPB	chr3:196064974-196065724	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr3:196066727-196066928	K562	blood:	n/a	n/a
50	CEBPB	chr3:196065302-196065701	A549	lung:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:196065289-196065339	AG04450	lung:	fetal
2	chr3:196065328-196065378	U87	brain:	n/a
3	chr3:196065289-196065339	AG04450	lung:	fetal
4	chr3:196065328-196065378	U87	brain:	n/a
5	chr3:196065328-196065378	GM19239	blood:	n/a
6	chr3:196065289-196065339	AG09319	gingival:	n/a
7	chr3:196065328-196065378	HIPEpiC	eye:	n/a
8	chr3:196065328-196065378	PFSK-1	brain:	n/a
9	chr3:196065688-196065738	U87	brain:	n/a
10	chr3:196065357-196065407	HIPEpiC	eye:	n/a
11	chr3:196065320-196065370	HIPEpiC	eye:	n/a
12	chr3:196065688-196065738	GM12891	blood:	n/a
13	chr3:196065320-196065370	RPTEC	kidney:	n/a
14	chr3:196065688-196065738	AoSMC	blood vessel:	n/a
15	chr3:196065357-196065407	GM19239	blood:	n/a
16	chr3:196065320-196065370	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:196065506-196065556	CMK	blood:	n/a
18	chr3:196065328-196065378	AG09319	gingival:	n/a
19	chr3:196065306-196065356	RPTEC	kidney:	n/a
20	chr3:196065688-196065738	T-47D	breast:	n/a
21	chr3:196065306-196065356	HepG2	liver:	n/a
22	chr3:196065688-196065738	HCF	heart:	n/a
23	chr3:196065318-196065368	HUVEC	blood vessel:	n/a
24	chr3:196065485-196065535	SK-N-SH	brain:	n/a
25	chr3:196065688-196065738	AG04450	lung:	fetal
26	chr3:196065320-196065370	BE2_C	brain:	n/a
27	chr3:196065306-196065356	SK-N-SH	brain:	n/a
28	chr3:196065106-196065156	HEEpiC	esophagus:	n/a
29	chr3:196065106-196065156	ovcar-3	ovarian:	n/a
30	chr3:196065357-196065407	Hela-S3	cervix:	n/a
31	chr3:196065318-196065368	Caco-2	colon:	n/a
32	chr3:196065485-196065535	ECC-1	luminal epithelium:	n/a
33	chr3:196065289-196065339	HRCEpiC	kidney:	n/a
34	chr3:196065320-196065370	ECC-1	luminal epithelium:	n/a
35	chr3:196065506-196065556	AG04450	lung:	fetal
36	chr3:196065320-196065370	SAEC	small airway:	n/a
37	chr3:196065506-196065556	T-47D	breast:	n/a
38	chr3:196065688-196065738	SKMC	muscle:	n/a
39	chr3:196065569-196065619	HAEpiC	amniotic membrane:	n/a
40	chr3:196065328-196065378	HRE	kidney:	n/a
41	chr3:196065569-196065619	HNPCEpiC	eye:	n/a
42	chr3:196065189-196065239	H1-hESC	embryonic stem cell:	embryo
43	chr3:196065357-196065407	CMK	blood:	n/a
44	chr3:196065569-196065619	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:196065506-196065556	GM12892	blood:	n/a
46	chr3:196065569-196065619	A549	lung:	n/a
47	chr3:196065569-196065619	PANC-1	pancreas:	n/a
48	chr3:196065688-196065738	NT2-D1	testis:	n/a
49	chr3:196065320-196065370	Jurkat	blood:	n/a
50	chr3:196065318-196065368	GM12891	blood:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:196012352..196016755-chr3:196062622..196069148,9	K562	blood:
2	chr3:196053196..196055442-chr3:196068574..196070294,2	MCF-7	breast:
3	chr3:196048792..196050575-chr3:196065911..196067478,2	MCF-7	breast:
4	chr3:196069058..196070648-chr3:196099629..196101467,2	K562	blood:
5	chr3:196074463..196076751-chr3:196080961..196082599,3	MCF-7	breast:
6	chr3:196064730..196065664-chr9:114658516..114659454,2	Hela-S3	cervix:
7	chr3:196049252..196052766-chr3:196054178..196057150,4	K562	blood:
8	chr3:195807059..195809798-chr3:196063350..196066594,3	K562	blood:
9	chr3:196007615..196009378-chr3:196070070..196071650,2	MCF-7	breast:
10	chr3:196068688..196070476-chr3:196293348..196295714,2	MCF-7	breast:
11	chr3:196069432..196071670-chr3:196228598..196230533,2	MCF-7	breast:
12	chr3:196013231..196016156-chr3:196060060..196062117,2	MCF-7	breast:
13	chr3:196043015..196046706-chr3:196061951..196066451,7	K562	blood:
14	chr3:196050354..196051997-chr3:196069518..196071791,2	MCF-7	breast:
15	chr3:196062836..196066201-chr3:196157853..196162484,6	K562	blood:
16	chr3:196068348..196070158-chr3:196074928..196076712,3	MCF-7	breast:
17	chr3:196050651..196052787-chr3:196063529..196066112,3	K562	blood:
18	chr3:195976340..195978485-chr3:196049925..196051821,2	K562	blood:
19	chr3:196062616..196065996-chr3:196228027..196230994,3	K562	blood:
20	chr3:196071912..196074086-chr3:196075769..196077797,2	MCF-7	breast:
21	chr3:196013208..196015292-chr3:196071968..196073510,2	MCF-7	breast:
22	chr3:196047776..196049836-chr3:196051866..196054572,2	MCF-7	breast:
23	chr3:196064683..196067033-chr3:196229952..196232006,2	K562	blood:
24	chr3:196012576..196016636-chr3:196061383..196069148,11	K562	blood:
25	chr3:196048971..196051262-chr3:196068046..196070208,4	MCF-7	breast:
26	chr3:196078088..196079673-chr3:196083665..196086587,2	MCF-7	breast:
27	chr3:196044828..196047817-chr3:196050115..196053393,5	K562	blood:
28	chr3:196062778..196068235-chr3:196157235..196160927,9	K562	blood:
29	chr3:196043658..196046454-chr3:196052736..196055681,2	MCF-7	breast:
30	chr3:196065505..196067615-chr3:196082041..196085251,3	K562	blood:
31	chr3:196062380..196065036-chr3:196160453..196162910,2	MCF-7	breast:
32	chr3:196050279..196052047-chr3:196065186..196067594,2	MCF-7	breast:
33	chr3:196067298..196070005-chr3:196075365..196077810,2	K562	blood:
34	chr3:196065700..196067576-chr3:196094863..196096889,2	K562	blood:
35	chr3:196050279..196052047-chr3:196065186..196067594,2	MCF-7	breast:
36	chr3:196075208..196077147-chr3:196092835..196095668,2	MCF-7	breast:
37	chr3:196070139..196072879-chr3:196076090..196077663,2	K562	blood:
38	chr3:196072873..196076573-chr3:196158373..196161329,3	MCF-7	breast:
39	chr3:196043015..196047197-chr3:196061951..196068288,11	K562	blood:
40	chr3:196070078..196071619-chr3:196082742..196085208,2	MCF-7	breast:
41	chr3:196013962..196014815-chr3:196069786..196070661,4	MCF-7	breast:
42	chr3:196062135..196067019-chr3:196076390..196080576,5	K562	blood:
43	chr3:196074413..196075944-chr3:196157333..196159734,2	MCF-7	breast:
44	chr3:196068585..196071026-chr3:196125432..196127097,2	MCF-7	breast:
45	chr3:196075057..196077486-chr3:196084676..196086437,2	K562	blood:
46	chr3:196054797..196056651-chr3:196089177..196091738,2	K562	blood:
47	chr3:196043597..196046565-chr3:196058227..196060990,3	K562	blood:
48	chr19:2234775..2236762-chr3:196074276..196076794,2	MCF-7	breast:
49	chr3:196013398..196015851-chr3:196068583..196071493,3	MCF-7	breast:
50	chr3:196044943..196046563-chr3:196056014..196058811,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC069257.9.1-3	chr3:196051153-196051737	NONHSAT094327
2	lnc-AC069257.9.1-3	chr3:196052471-196052758	NONHSAT094327
3	lnc-AC069257.9.1-3	chr3:196050701-196052441	ENSG00000235897.1

No data

Variant related genes	Relation type
ENSG00000273331	TF binding region
RNU6-910P	TF binding region
TM4SF19	TF binding region
ENSG00000273331	CpG island
RNU6-910P	CpG island
TM4SF19	CpG island
ENSG00000185798	chromatin interactions
ENSG00000213123	chromatin interactions
ENSG00000145107	chromatin interactions
ENSG00000161217	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000272741	chromatin interactions
ENSG00000104886	chromatin interactions
ENSG00000235897	chromatin interactions
ENSG00000148154	chromatin interactions
ENSG00000273331	chromatin interactions
ENSG00000104897	chromatin interactions
ENSG00000228028	chromatin interactions
ENSG00000225822	chromatin interactions
ENSG00000130749	chromatin interactions
ENSG00000174013	chromatin interactions
ENSG00000163960	chromatin interactions
ENSG00000072274	chromatin interactions
ENSG00000243339	chromatin interactions
ENSG00000212146	chromatin interactions
ENSG00000163961	chromatin interactions

Extended variants
information (count: 1113 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1113 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2280526	chr3:196051403-196051404	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569625438	chr3:196051422-196051423	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
3	rs536990271	chr3:196051463-196051464	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
4	rs555140949	chr3:196051464-196051465	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
5	rs367817072	chr3:196051476-196051477	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
6	rs567380450	chr3:196051509-196051510	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
7	rs534704054	chr3:196051515-196051516	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
8	rs148975929	chr3:196051549-196051550	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
9	rs66942309	chr3:196051564-196051565	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs544686381	chr3:196051580-196051581	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
11	rs377594314	chr3:196051606-196051607	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
12	rs188640826	chr3:196051632-196051633	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
13	rs543367461	chr3:196051643-196051644	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
14	rs561451244	chr3:196051663-196051664	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
15	rs192735706	chr3:196051677-196051678	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
16	rs540693051	chr3:196051695-196051696	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
17	rs565236936	chr3:196051765-196051766	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
18	rs530433844	chr3:196051775-196051776	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
19	rs532498112	chr3:196051780-196051781	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
20	rs142994745	chr3:196051817-196051818	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
21	rs562590816	chr3:196051827-196051828	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
22	rs374406121	chr3:196051915-196051916	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
23	rs548903277	chr3:196052015-196052016	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
24	rs545645744	chr3:196052058-196052059	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
25	rs371258533	chr3:196052080-196052081	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
26	rs141938706	chr3:196052081-196052082	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
27	rs534540304	chr3:196052084-196052085	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
28	rs546631185	chr3:196052085-196052086	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
29	rs571243377	chr3:196052086-196052087	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
30	rs538782193	chr3:196052092-196052093	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
31	rs556971773	chr3:196052130-196052131	Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
32	rs575346023	chr3:196052132-196052133	Weak transcription	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
33	rs151115119	chr3:196052222-196052223	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
34	rs376020587	chr3:196052238-196052239	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
35	rs114978848	chr3:196052287-196052288	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
36	rs62409181	chr3:196052346-196052347	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
37	rs546657836	chr3:196052353-196052354	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
38	rs146372503	chr3:196052361-196052362	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	mRNA abundance
39	rs182363473	chr3:196052366-196052367	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
40	rs562529681	chr3:196052392-196052393	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs370845650	chr3:196052430-196052431	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs145155981	chr3:196052464-196052465	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs4916484	chr3:196052521-196052522	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs548839372	chr3:196052541-196052542	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
45	rs4916485	chr3:196052557-196052558	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs560150577	chr3:196052600-196052601	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
47	rs12633502	chr3:196052616-196052617	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs546473106	chr3:196052714-196052715	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs571445452	chr3:196052716-196052717	Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs529268423	chr3:196052771-196052772	Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:546 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:196045600-196053800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:196045600-196054000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:196045600-196054000	Weak transcription	Pancreas	Pancrea
4	chr3:196045600-196054200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:196045600-196054200	Weak transcription	Ovary	ovary
6	chr3:196045800-196052400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr3:196045800-196052800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr3:196045800-196053000	Weak transcription	Fetal Intestine Small	intestine
9	chr3:196045800-196054200	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr3:196046000-196053600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr3:196046000-196054400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr3:196046200-196054200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:196047200-196054600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:196047400-196053800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:196047400-196054200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:196047600-196053800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr3:196047600-196053800	Weak transcription	HMEC	breast
18	chr3:196047600-196054400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr3:196047600-196063600	Weak transcription	NHEK	skin
20	chr3:196048800-196052000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:196049000-196053600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr3:196049600-196052200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr3:196050200-196052000	Enhancers	Fetal Muscle Leg	muscle
24	chr3:196050600-196051600	Enhancers	HSMMtube	muscle
25	chr3:196050600-196051800	Enhancers	Fetal Muscle Trunk	muscle
26	chr3:196050800-196051800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:196051000-196057200	Weak transcription	Hela-S3	cervix
28	chr3:196051200-196051800	Enhancers	Fetal Thymus	thymus
29	chr3:196051200-196053200	Weak transcription	K562	blood
30	chr3:196051200-196054000	Weak transcription	Fetal Stomach	stomach
31	chr3:196051400-196063600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:196051600-196054200	Weak transcription	HSMMtube	muscle
33	chr3:196051800-196054800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr3:196052000-196062600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:196053200-196054800	Strong transcription	K562	blood
36	chr3:196053600-196054800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:196053800-196054000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:196053800-196054000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr3:196053800-196054600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr3:196053800-196054800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr3:196054000-196054200	Enhancers	Fetal Stomach	stomach
42	chr3:196054000-196054400	Enhancers	Pancreas	Pancrea
43	chr3:196054000-196054400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr3:196054000-196054600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr3:196054000-196054600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:196054000-196054600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr3:196054000-196055600	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr3:196054200-196054400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr3:196054200-196054400	Bivalent Enhancer	Fetal Stomach	stomach
50	chr3:196054200-196054400	Active TSS	Osteobl	bone

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