Variant report

Variant	nsv1005065
Chromosome Location	chr3:100353809-100442478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1652)
CpG islands
(count:1164)
Chromatin interactive
region (count:63)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1652 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
2	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
3	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
6	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
8	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
9	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
10	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
11	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
12	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
13	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
14	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
15	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
16	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
17	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
20	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
21	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
22	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
23	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
24	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
25	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
29	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
30	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
31	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
32	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
33	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
35	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
36	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
39	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
40	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
41	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
42	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
44	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
46	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
47	CBX3	chr3:100429573-100429981	K562	blood:	n/a	n/a
48	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
49	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
50	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805

(count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100428869-100428919	NHBE	bronchial:	n/a
2	chr3:100437347-100437397	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:100428033-100428083	K562	blood:	n/a
4	chr3:100428005-100428055	PANC-1	pancreas:	n/a
5	chr3:100427239-100427289	SK-N-SH_RA	brain:	n/a
6	chr3:100428869-100428919	NHBE	bronchial:	n/a
7	chr3:100437347-100437397	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:100428033-100428083	K562	blood:	n/a
9	chr3:100428005-100428055	PANC-1	pancreas:	n/a
10	chr3:100427239-100427289	SK-N-SH_RA	brain:	n/a
11	chr3:100428398-100428448	ovcar-3	ovarian:	n/a
12	chr3:100428172-100428222	HIPEpiC	eye:	n/a
13	chr3:100428642-100428692	HRPEpiC	eye:	n/a
14	chr3:100428070-100428120	HRPEpiC	eye:	n/a
15	chr3:100428147-100428197	HUVEC	blood vessel:	n/a
16	chr3:100401270-100401320	GM12891	blood:	n/a
17	chr3:100427096-100427146	BE2_C	brain:	n/a
18	chr3:100427096-100427146	K562	blood:	n/a
19	chr3:100428869-100428919	Hepatocyte	liver:	n/a
20	chr3:100428033-100428083	HCPEpiC	choroid plexus:	n/a
21	chr3:100428869-100428919	HRCEpiC	kidney:	n/a
22	chr3:100427096-100427146	GM12878	blood:	n/a
23	chr3:100401200-100401250	AG09309	skin:	n/a
24	chr3:100437347-100437397	AG04449	skin:	fetal
25	chr3:100429064-100429114	HL-60	blood:	n/a
26	chr3:100430811-100430861	SAEC	small airway:	n/a
27	chr3:100427096-100427146	H1-hESC	embryonic stem cell:	embryo
28	chr3:100401284-100401334	GM19239	blood:	n/a
29	chr3:100424830-100424880	HEEpiC	esophagus:	n/a
30	chr3:100424830-100424880	AG10803	skin:	n/a
31	chr3:100401284-100401334	HL-60	blood:	n/a
32	chr3:100437347-100437397	SKMC	muscle:	n/a
33	chr3:100428005-100428055	ECC-1	luminal epithelium:	n/a
34	chr3:100428172-100428222	GM19239	blood:	n/a
35	chr3:100428140-100428190	SKMC	muscle:	n/a
36	chr3:100428070-100428120	HNPCEpiC	eye:	n/a
37	chr3:100428145-100428195	NB4	blood:	n/a
38	chr3:100427096-100427146	T-47D	breast:	n/a
39	chr3:100428033-100428083	HCF	heart:	n/a
40	chr3:100401270-100401320	AG09319	gingival:	n/a
41	chr3:100437347-100437397	HCPEpiC	choroid plexus:	n/a
42	chr3:100424830-100424880	SK-N-SH	brain:	n/a
43	chr3:100428147-100428197	NT2-D1	testis:	n/a
44	chr3:100428140-100428190	HMEC	breast:	n/a
45	chr3:100429064-100429114	MCF-7	breast:	n/a
46	chr3:100428145-100428195	PFSK-1	brain:	n/a
47	chr3:100437347-100437397	PrEC	prostate:	n/a
48	chr3:100401200-100401250	GM06990	blood:	n/a
49	chr3:100428145-100428195	U87	brain:	n/a
50	chr3:100427096-100427146	AG10803	skin:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
2	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
3	chr3:100363955..100366251-chr3:100430276..100432024,2	K562	blood:
4	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
5	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
6	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
7	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
8	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
9	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
10	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
11	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
12	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
13	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
14	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
15	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
16	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
17	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
18	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
19	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
20	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
21	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
22	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
23	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
24	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
25	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
26	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
27	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
28	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
29	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
30	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
31	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
32	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
33	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
34	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
35	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
36	chr3:100441058..100442704-chr3:100448594..100450149,2	K562	blood:
37	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
38	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
39	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
40	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
41	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
42	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
43	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
44	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
45	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
46	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
47	chr3:100120411..100122999-chr3:100364924..100367578,2	K562	blood:
48	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
49	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
50	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI3BP-1	chr3:100383894-100384320	NONHSAT090876
2	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874
3	lnc-TMEM45A-1	chr3:100356146-100356419	NONHSAT090874

No data

Variant related genes	Relation type
TFG	TF binding region
GPR128	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
TFG	CpG island
GPR128	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000143367	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000184220	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000199004	chromatin interactions

Extended variants
information (count: 3610 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3610 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10936276	chr3:100353809-100353810	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142620077	chr3:100353844-100353845	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs71991216	chr3:100353845-100353846	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs386397408	chr3:100353854-100353855	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs10684141	chr3:100353873-100353874	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200316127	chr3:100353874-100353875	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs185886699	chr3:100353878-100353879	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532982180	chr3:100353889-100353890	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs530320101	chr3:100353890-100353891	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs75053796	chr3:100353891-100353892	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561005834	chr3:100353915-100353916	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111528085	chr3:100353933-100353934	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs377541760	chr3:100353934-100353935	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111599339	chr3:100353935-100353936	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs191185697	chr3:100353956-100353957	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs527863837	chr3:100353998-100353999	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs142708641	chr3:100354012-100354013	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556302167	chr3:100354033-100354034	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs138888122	chr3:100354038-100354039	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs34209095	chr3:100354067-100354068	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs150033193	chr3:100354074-100354075	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs10662752	chr3:100354075-100354076	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138969110	chr3:100354076-100354077	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs143971487	chr3:100354077-100354078	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs144476647	chr3:100354079-100354080	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs73145111	chr3:100354091-100354092	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs565492185	chr3:100354099-100354100	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs376850096	chr3:100354114-100354115	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181776979	chr3:100354169-100354170	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs10755119	chr3:100354170-100354171	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs554635591	chr3:100354172-100354173	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550109365	chr3:100354190-100354191	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs148385053	chr3:100354205-100354206	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs537433033	chr3:100354218-100354219	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs558717077	chr3:100354222-100354223	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs577188869	chr3:100354257-100354258	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs367607104	chr3:100354307-100354308	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566987111	chr3:100354351-100354352	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs541315407	chr3:100354354-100354355	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs186470835	chr3:100354385-100354386	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs575076675	chr3:100354386-100354387	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs141841819	chr3:100354496-100354497	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs141569776	chr3:100354508-100354509	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs1144122	chr3:100354524-100354525	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs375688473	chr3:100354533-100354534	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs370569749	chr3:100354558-100354559	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs373966742	chr3:100354599-100354600	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs199704593	chr3:100354612-100354613	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs190503505	chr3:100354621-100354622	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs142118691	chr3:100354622-100354623	Weak transcription Flanking Active TSS Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	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
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:100350600-100354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:100352600-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:100352800-100354000	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr3:100352800-100354800	Enhancers	Fetal Intestine Small	intestine
6	chr3:100353200-100354000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr3:100353400-100354000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr3:100353400-100354000	Enhancers	Primary hematopoietic stem cells	blood
9	chr3:100353400-100354000	Enhancers	HSMMtube	muscle
10	chr3:100353400-100354400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr3:100353400-100354600	Enhancers	Stomach Mucosa	stomach
12	chr3:100353600-100354000	Enhancers	Fetal Brain Male	brain
13	chr3:100353600-100354400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr3:100353600-100354400	Enhancers	HMEC	breast
15	chr3:100353600-100354400	Enhancers	K562	blood
16	chr3:100353800-100354000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:100353800-100354000	Flanking Active TSS	Duodenum Mucosa	Duodenum
18	chr3:100353800-100354400	Enhancers	Pancreas	Pancrea
19	chr3:100353800-100354400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr3:100353800-100354400	Flanking Active TSS	HepG2	liver
21	chr3:100353800-100354600	Active TSS	Liver	Liver
22	chr3:100353800-100355200	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr3:100353800-100356200	Enhancers	Fetal Intestine Large	intestine
24	chr3:100354000-100354200	Enhancers	Duodenum Mucosa	Duodenum
25	chr3:100354000-100354400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:100354000-100354600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:100354000-100357800	Weak transcription	Fetal Brain Male	brain
28	chr3:100354200-100354400	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr3:100354200-100354600	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr3:100354400-100354600	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr3:100354400-100355200	Enhancers	HepG2	liver
32	chr3:100354400-100356800	Weak transcription	Pancreas	Pancrea
33	chr3:100354400-100359000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr3:100354400-100360000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr3:100354600-100355400	Flanking Active TSS	Liver	Liver
36	chr3:100354600-100355600	Weak transcription	Duodenum Mucosa	Duodenum
37	chr3:100354600-100359600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:100354800-100355000	Enhancers	Small Intestine	intestine
39	chr3:100354800-100357600	Genic enhancers	Fetal Intestine Small	intestine
40	chr3:100355000-100359800	Weak transcription	Small Intestine	intestine
41	chr3:100355200-100357000	Strong transcription	Primary neutrophils fromperipheralblood	blood
42	chr3:100355200-100359000	Weak transcription	HepG2	liver
43	chr3:100355400-100355800	Active TSS	Liver	Liver
44	chr3:100355600-100357600	Strong transcription	Duodenum Mucosa	Duodenum
45	chr3:100355800-100356400	Flanking Active TSS	Liver	Liver
46	chr3:100355800-100356600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:100356000-100356600	Bivalent Enhancer	NHDF-Ad	bronchial
48	chr3:100356200-100356600	Bivalent Enhancer	Osteobl	bone
49	chr3:100356200-100359200	Genic enhancers	Fetal Intestine Large	intestine
50	chr3:100356400-100356600	Transcr. at gene 5' and 3'	Liver	Liver

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