Variant report

Variant	nsv1006559
Chromosome Location	chr3:100324275-100427937
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1296)
CpG islands
(count:733)
Chromatin interactive
region (count:54)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1296 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
2	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
3	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
4	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
6	ARID3A	chr3:100332649-100333246	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:100328325-100328363	K562	blood:	n/a	n/a
10	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
11	ATF1	chr3:100328075-100328453	K562	blood:	n/a	n/a
12	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
13	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
14	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
15	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
16	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
17	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
18	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
19	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
20	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
22	BACH1	chr3:100324408-100324438	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
24	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
25	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
26	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
27	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:100325837-100326298	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
34	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
38	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
39	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr3:100427818-100428510	K562	blood:	n/a	n/a
42	CBX3	chr3:100415727-100416040	K562	blood:	n/a	n/a
43	CCNT2	chr3:100328275-100328511	K562	blood:	n/a	n/a
44	CCNT2	chr3:100427839-100429006	K562	blood:	n/a	chr3:100428771-100428780 chr3:100428796-100428805
45	CCNT2	chr3:100348632-100349219	K562	blood:	n/a	n/a
46	CEBPB	chr3:100381321-100381668	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:100370210-100370426	A549	lung:	n/a	chr3:100370349-100370362
48	CEBPB	chr3:100373411-100373726	HepG2	liver:	n/a	chr3:100373575-100373586
49	CEBPB	chr3:100385592-100385797	K562	blood:	n/a	chr3:100385738-100385749
50	CEBPB	chr3:100370097-100370487	IMR90	lung:	n/a	chr3:100370349-100370362

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100328745-100328795	HNPCEpiC	eye:	n/a
2	chr3:100328745-100328795	HNPCEpiC	eye:	n/a
3	chr3:100401200-100401250	Hela-S3	cervix:	n/a
4	chr3:100424830-100424880	NHDF-neo	bronchial:	n/a
5	chr3:100328713-100328763	A549	lung:	n/a
6	chr3:100427096-100427146	HCM	heart:	n/a
7	chr3:100328186-100328236	NHBE	bronchial:	n/a
8	chr3:100401284-100401334	U87	brain:	n/a
9	chr3:100424830-100424880	Caco-2	colon:	n/a
10	chr3:100424830-100424880	NH-A	brain:	n/a
11	chr3:100328713-100328763	GM12878	blood:	n/a
12	chr3:100424830-100424880	LNCaP	prostate:	n/a
13	chr3:100328745-100328795	NHBE	bronchial:	n/a
14	chr3:100427239-100427289	HAEpiC	amniotic membrane:	n/a
15	chr3:100401270-100401320	ECC-1	luminal epithelium:	n/a
16	chr3:100427239-100427289	ECC-1	luminal epithelium:	n/a
17	chr3:100328186-100328236	NB4	blood:	n/a
18	chr3:100427239-100427289	Hela-S3	cervix:	n/a
19	chr3:100401200-100401250	AG04450	lung:	fetal
20	chr3:100349374-100349424	HRE	kidney:	n/a
21	chr3:100427239-100427289	AG04450	lung:	fetal
22	chr3:100328265-100328315	HAEpiC	amniotic membrane:	n/a
23	chr3:100328265-100328315	K562	blood:	n/a
24	chr3:100328713-100328763	HCM	heart:	n/a
25	chr3:100328265-100328315	AG10803	skin:	n/a
26	chr3:100349374-100349424	CMK	blood:	n/a
27	chr3:100427239-100427289	RPTEC	kidney:	n/a
28	chr3:100427239-100427289	BJ	skin:	n/a
29	chr3:100349374-100349424	RPTEC	kidney:	n/a
30	chr3:100327897-100327947	HCF	heart:	n/a
31	chr3:100328186-100328236	HL-60	blood:	n/a
32	chr3:100349374-100349424	HCPEpiC	choroid plexus:	n/a
33	chr3:100328186-100328236	AG04449	skin:	fetal
34	chr3:100349374-100349424	NH-A	brain:	n/a
35	chr3:100427239-100427289	NHBE	bronchial:	n/a
36	chr3:100349374-100349424	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:100327897-100327947	PANC-1	pancreas:	n/a
38	chr3:100401200-100401250	SKMC	muscle:	n/a
39	chr3:100328713-100328763	GM06990	blood:	n/a
40	chr3:100349374-100349424	AG04449	skin:	fetal
41	chr3:100401200-100401250	HRPEpiC	eye:	n/a
42	chr3:100327897-100327947	Hepatocyte	liver:	n/a
43	chr3:100349374-100349424	MCF10A-Er-Src	breast:	n/a
44	chr3:100427096-100427146	GM12892	blood:	n/a
45	chr3:100401284-100401334	GM06990	blood:	n/a
46	chr3:100328265-100328315	HUVEC	blood vessel:	n/a
47	chr3:100349374-100349424	SK-N-SH	brain:	n/a
48	chr3:100401270-100401320	MCF10A-Er-Src	breast:	n/a
49	chr3:100427096-100427146	AoSMC	blood vessel:	n/a
50	chr3:100328713-100328763	H1-hESC	embryonic stem cell:	embryo

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
2	chr3:100322209..100326377-chr3:100427335..100430667,5	MCF-7	breast:
3	chr3:100364940..100366707-chr3:100366782..100369483,3	K562	blood:
4	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
5	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
6	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
7	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
8	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
9	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
10	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
11	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
12	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
13	chr3:100118924..100121912-chr3:100362623..100364573,2	K562	blood:
14	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
15	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
16	chr3:100118375..100121332-chr3:100329278..100332064,2	K562	blood:
17	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
18	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
19	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
20	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
21	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
22	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
23	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
24	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
25	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
26	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
27	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
28	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
29	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
30	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
31	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
32	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
33	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
34	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
35	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
36	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
37	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
38	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
39	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
40	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
41	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
42	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
43	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
44	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
45	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
46	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
47	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
48	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
49	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
50	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:

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

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

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
ENSG00000188938	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000144820	chromatin interactions

Extended variants
information (count: 4186 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4186 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9867401	chr3:100324275-100324276	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562194169	chr3:100324281-100324282	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs1676335	chr3:100324342-100324343	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs137968419	chr3:100324348-100324349	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368330542	chr3:100324352-100324353	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs149461493	chr3:100324357-100324358	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188376191	chr3:100324376-100324377	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535483214	chr3:100324389-100324390	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537130245	chr3:100324390-100324391	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs193160037	chr3:100324423-100324424	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570549863	chr3:100324425-100324426	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs17280554	chr3:100324442-100324443	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs1718272	chr3:100324522-100324523	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs539629486	chr3:100324533-100324534	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs143011231	chr3:100324534-100324535	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535405482	chr3:100324545-100324546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374109547	chr3:100324572-100324573	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs9867888	chr3:100324640-100324641	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575129039	chr3:100324652-100324653	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573208981	chr3:100324662-100324663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142000741	chr3:100324666-100324667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs71620022	chr3:100324669-100324670	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2461499	chr3:100324670-100324671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12486537	chr3:100324674-100324675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
25	rs71620024	chr3:100324676-100324677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201797094	chr3:100324681-100324682	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs6441359	chr3:100324684-100324685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
28	rs540259867	chr3:100324685-100324686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184012158	chr3:100324696-100324697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs58942998	chr3:100324703-100324704	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562161790	chr3:100324712-100324713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377681499	chr3:100324723-100324724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs529591381	chr3:100324727-100324728	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551332553	chr3:100324737-100324738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563191664	chr3:100324741-100324742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs370428503	chr3:100324746-100324747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs373594593	chr3:100324750-100324751	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs202025100	chr3:100324754-100324755	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs377532011	chr3:100324756-100324757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200152100	chr3:100324758-100324759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371022791	chr3:100324760-100324761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62776961	chr3:100324762-100324763	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6783455	chr3:100324764-100324765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371186369	chr3:100324767-100324768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533538940	chr3:100324774-100324775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200183505	chr3:100324775-100324776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs544225096	chr3:100324776-100324777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570411092	chr3:100324779-100324780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563224989	chr3:100324782-100324783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534755885	chr3:100324795-100324796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	22037309	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:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100322800-100325600	Weak transcription	Stomach Mucosa	stomach
2	chr3:100322800-100327800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:100322800-100327800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr3:100322800-100328000	Weak transcription	Colonic Mucosa	Colon
5	chr3:100322800-100328000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:100322800-100328200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:100322800-100328200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:100322800-100330200	Weak transcription	HepG2	liver
9	chr3:100323000-100325200	Weak transcription	GM12878-XiMat	blood
10	chr3:100323000-100325800	Weak transcription	Primary B cells from peripheral blood	blood
11	chr3:100323000-100325800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr3:100323000-100325800	Weak transcription	Fetal Intestine Large	intestine
13	chr3:100323000-100325800	Weak transcription	Fetal Intestine Small	intestine
14	chr3:100323000-100327800	Weak transcription	Primary T cells from cord blood	blood
15	chr3:100323000-100328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:100323000-100328200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr3:100323000-100328200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:100323200-100324400	Weak transcription	Liver	Liver
19	chr3:100323200-100327800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:100323200-100328400	Weak transcription	HMEC	breast
21	chr3:100324000-100324400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:100324200-100324400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr3:100324200-100324400	Enhancers	Spleen	Spleen
24	chr3:100324200-100324600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:100324200-100324600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr3:100324200-100324600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:100324200-100324600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:100324400-100325200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:100325200-100325800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:100325200-100326600	Enhancers	GM12878-XiMat	blood
31	chr3:100325600-100326000	Enhancers	Stomach Mucosa	stomach
32	chr3:100325800-100326200	Enhancers	Primary B cells from peripheral blood	blood
33	chr3:100325800-100326200	Enhancers	Duodenum Mucosa	Duodenum
34	chr3:100325800-100326200	Enhancers	Fetal Intestine Small	intestine
35	chr3:100325800-100326400	Enhancers	Fetal Intestine Large	intestine
36	chr3:100325800-100326800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:100326000-100328400	Weak transcription	Stomach Mucosa	stomach
38	chr3:100326200-100327200	Weak transcription	Fetal Intestine Small	intestine
39	chr3:100326200-100327400	Weak transcription	Duodenum Mucosa	Duodenum
40	chr3:100326400-100326800	Weak transcription	Fetal Intestine Large	intestine
41	chr3:100326600-100327000	Flanking Active TSS	GM12878-XiMat	blood
42	chr3:100326800-100328000	Enhancers	Fetal Intestine Large	intestine
43	chr3:100327000-100327200	Enhancers	GM12878-XiMat	blood
44	chr3:100327200-100328400	Enhancers	Fetal Intestine Small	intestine
45	chr3:100327400-100327600	Enhancers	Duodenum Mucosa	Duodenum
46	chr3:100327600-100334200	Active TSS	Duodenum Mucosa	Duodenum
47	chr3:100327800-100328000	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr3:100327800-100328200	Enhancers	Fetal Thymus	thymus
49	chr3:100327800-100328600	Enhancers	Dnd41	blood
50	chr3:100327800-100328800	Enhancers	Primary T cells from cord blood	blood

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