Variant report

Variant	nsv1007742
Chromosome Location	chr3:100326173-100441716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1808)
CpG islands
(count:1525)
Chromatin interactive
region (count:73)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100328325-100328363	K562	blood:	n/a	n/a
2	ARID3A	chr3:100332649-100333246	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
4	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
6	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
7	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
8	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
12	ATF1	chr3:100328075-100328453	K562	blood:	n/a	n/a
13	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
14	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
15	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
16	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
17	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
18	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
19	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
20	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
21	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
22	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
24	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
25	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
26	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
28	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
29	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
30	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
31	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
32	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
36	BCLAF1	chr3:100325837-100326298	GM12878	blood:	n/a	n/a
37	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
38	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
39	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
40	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
42	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
43	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
44	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
45	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
46	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
47	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
48	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
49	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
50	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100428033-100428083	AG04449	skin:	fetal
2	chr3:100424830-100424880	HNPCEpiC	eye:	n/a
3	chr3:100349374-100349424	H1-hESC	embryonic stem cell:	embryo
4	chr3:100428172-100428222	HNPCEpiC	eye:	n/a
5	chr3:100437347-100437397	SK-N-SH_RA	brain:	n/a
6	chr3:100428172-100428222	GM06990	blood:	n/a
7	chr3:100327897-100327947	ECC-1	luminal epithelium:	n/a
8	chr3:100428145-100428195	SKMC	muscle:	n/a
9	chr3:100401270-100401320	CMK	blood:	n/a
10	chr3:100428869-100428919	HCM	heart:	n/a
11	chr3:100430811-100430861	NT2-D1	testis:	n/a
12	chr3:100328265-100328315	HRCEpiC	kidney:	n/a
13	chr3:100424830-100424880	HEK293	kidney:	embryo
14	chr3:100428140-100428190	HRPEpiC	eye:	n/a
15	chr3:100428070-100428120	CMK	blood:	n/a
16	chr3:100427239-100427289	GM12878	blood:	n/a
17	chr3:100328186-100328236	LNCaP	prostate:	n/a
18	chr3:100428005-100428055	SAEC	small airway:	n/a
19	chr3:100428033-100428083	GM12891	blood:	n/a
20	chr3:100428070-100428120	T-47D	breast:	n/a
21	chr3:100428398-100428448	AG10803	skin:	n/a
22	chr3:100428033-100428083	NT2-D1	testis:	n/a
23	chr3:100428172-100428222	GM12891	blood:	n/a
24	chr3:100424830-100424880	A549	lung:	n/a
25	chr3:100328186-100328236	HIPEpiC	eye:	n/a
26	chr3:100430811-100430861	NH-A	brain:	n/a
27	chr3:100427239-100427289	MCF-7	breast:	n/a
28	chr3:100428005-100428055	H1-hESC	embryonic stem cell:	embryo
29	chr3:100328265-100328315	SAEC	small airway:	n/a
30	chr3:100327897-100327947	Hepatocyte	liver:	n/a
31	chr3:100428642-100428692	AG09309	skin:	n/a
32	chr3:100328713-100328763	AG04450	lung:	fetal
33	chr3:100328713-100328763	IMR90	lung:	fetal
34	chr3:100428005-100428055	GM12892	blood:	n/a
35	chr3:100428642-100428692	Hepatocyte	liver:	n/a
36	chr3:100430811-100430861	NHDF-neo	bronchial:	n/a
37	chr3:100328713-100328763	HCT-116	colon:	n/a
38	chr3:100328745-100328795	NHDF-neo	bronchial:	n/a
39	chr3:100428147-100428197	BJ	skin:	n/a
40	chr3:100427239-100427289	K562	blood:	n/a
41	chr3:100428033-100428083	A549	lung:	n/a
42	chr3:100428869-100428919	Hela-S3	cervix:	n/a
43	chr3:100327897-100327947	PANC-1	pancreas:	n/a
44	chr3:100328745-100328795	CMK	blood:	n/a
45	chr3:100428147-100428197	NT2-D1	testis:	n/a
46	chr3:100428642-100428692	PrEC	prostate:	n/a
47	chr3:100428398-100428448	PANC-1	pancreas:	n/a
48	chr3:100424830-100424880	NH-A	brain:	n/a
49	chr3:100428642-100428692	AG09319	gingival:	n/a
50	chr3:100424830-100424880	BE2_C	brain:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
2	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
3	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
4	chr3:100181696..100182432-chr3:100355242..100355805,2	MCF-7	breast:
5	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
6	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
7	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
8	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
9	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
10	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
11	chr11:59436077..59436715-chr3:100428082..100428818,2	Hela-S3	cervix:
12	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
13	chr12:56435446..56435990-chr3:100428103..100428866,2	Hela-S3	cervix:
14	chr3:100437193..100438903-chr3:100441910..100444444,2	K562	blood:
15	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
16	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
17	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
18	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
19	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
20	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
21	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
22	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
23	chr3:100427539..100430990-chr3:100441684..100444095,3	MCF-7	breast:
24	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
25	chr3:100423356..100425214-chr3:100428038..100429852,2	K562	blood:
26	chr3:100352243..100354477-chr3:100424707..100427239,2	MCF-7	breast:
27	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:
28	chr3:100428169..100430169-chr3:100436770..100441506,6	MCF-7	breast:
29	chr3:100434706..100436343-chr3:100445572..100447869,2	K562	blood:
30	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
31	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
32	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
33	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
34	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
35	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
36	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
37	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
38	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
39	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
40	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
41	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
42	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
43	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
44	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
45	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
46	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:
47	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
48	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
49	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
50	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874
2	lnc-TMEM45A-1	chr3:100356146-100356419	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
ENSG00000143367	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000184220	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000154174	chromatin interactions
ENSG00000257449	chromatin interactions

Extended variants
information (count: 4606 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:4606 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538671383	chr3:100326194-100326195	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs554417478	chr3:100326239-100326240	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs141342086	chr3:100326259-100326260	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs9811156	chr3:100326263-100326264	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543164747	chr3:100326279-100326280	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561184153	chr3:100326281-100326282	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573396519	chr3:100326322-100326323	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543939968	chr3:100326335-100326336	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540128280	chr3:100326347-100326348	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs532915739	chr3:100326389-100326390	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551094094	chr3:100326396-100326397	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560356761	chr3:100326428-100326429	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs191226131	chr3:100326430-100326431	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs183657735	chr3:100326444-100326445	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1718273	chr3:100326455-100326456	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs79063208	chr3:100326458-100326459	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189100401	chr3:100326505-100326506	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534171742	chr3:100326548-100326549	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538326265	chr3:100326712-100326713	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs570671714	chr3:100326772-100326773	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114824188	chr3:100326778-100326779	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs571670587	chr3:100326789-100326790	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs34085401	chr3:100326790-100326791	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371949695	chr3:100326796-100326797	Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs538974998	chr3:100326819-100326820	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs553887095	chr3:100326869-100326870	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192838351	chr3:100326876-100326877	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146974410	chr3:100326885-100326886	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147594144	chr3:100326886-100326887	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576199245	chr3:100326896-100326897	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543632135	chr3:100326941-100326942	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs370571750	chr3:100326942-100326943	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs386663881	chr3:100326953-100326954	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73143168	chr3:100326954-100326955	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs74616154	chr3:100326990-100326991	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559939895	chr3:100327027-100327028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs527561979	chr3:100327036-100327037	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs183103678	chr3:100327051-100327052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561183086	chr3:100327165-100327166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150096903	chr3:100327190-100327191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs187603314	chr3:100327222-100327223	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371338572	chr3:100327244-100327245	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs138380834	chr3:100327274-100327275	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538794970	chr3:100327315-100327316	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547763525	chr3:100327340-100327341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374463023	chr3:100327403-100327404	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs1676339	chr3:100327409-100327410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536264937	chr3:100327439-100327440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554817597	chr3:100327472-100327473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75448707	chr3:100327481-100327482	Weak transcription Enhancers	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:1838 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100322800-100327800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr3:100322800-100327800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:100322800-100328000	Weak transcription	Colonic Mucosa	Colon
4	chr3:100322800-100328000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:100322800-100328200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr3:100322800-100328200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr3:100322800-100330200	Weak transcription	HepG2	liver
8	chr3:100323000-100327800	Weak transcription	Primary T cells from cord blood	blood
9	chr3:100323000-100328000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:100323000-100328200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr3:100323000-100328200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:100323200-100327800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr3:100323200-100328400	Weak transcription	HMEC	breast
14	chr3:100325200-100326600	Enhancers	GM12878-XiMat	blood
15	chr3:100325800-100326200	Enhancers	Primary B cells from peripheral blood	blood
16	chr3:100325800-100326200	Enhancers	Duodenum Mucosa	Duodenum
17	chr3:100325800-100326200	Enhancers	Fetal Intestine Small	intestine
18	chr3:100325800-100326400	Enhancers	Fetal Intestine Large	intestine
19	chr3:100325800-100326800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:100326000-100328400	Weak transcription	Stomach Mucosa	stomach
21	chr3:100326200-100327200	Weak transcription	Fetal Intestine Small	intestine
22	chr3:100326200-100327400	Weak transcription	Duodenum Mucosa	Duodenum
23	chr3:100326400-100326800	Weak transcription	Fetal Intestine Large	intestine
24	chr3:100326600-100327000	Flanking Active TSS	GM12878-XiMat	blood
25	chr3:100326800-100328000	Enhancers	Fetal Intestine Large	intestine
26	chr3:100327000-100327200	Enhancers	GM12878-XiMat	blood
27	chr3:100327200-100328400	Enhancers	Fetal Intestine Small	intestine
28	chr3:100327400-100327600	Enhancers	Duodenum Mucosa	Duodenum
29	chr3:100327600-100334200	Active TSS	Duodenum Mucosa	Duodenum
30	chr3:100327800-100328000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr3:100327800-100328200	Enhancers	Fetal Thymus	thymus
32	chr3:100327800-100328600	Enhancers	Dnd41	blood
33	chr3:100327800-100328800	Enhancers	Primary T cells from cord blood	blood
34	chr3:100327800-100329000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr3:100327800-100329000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:100327800-100330200	Weak transcription	Liver	Liver
37	chr3:100328000-100328200	Enhancers	Colonic Mucosa	Colon
38	chr3:100328000-100328400	Flanking Active TSS	Fetal Intestine Large	intestine
39	chr3:100328000-100328400	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr3:100328000-100328600	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr3:100328000-100328600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr3:100328000-100328800	Enhancers	Primary hematopoietic stem cells	blood
43	chr3:100328000-100328800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:100328200-100328800	Enhancers	K562	blood
45	chr3:100328200-100329000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr3:100328200-100329000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr3:100328200-100329600	Weak transcription	Colonic Mucosa	Colon
48	chr3:100328200-100329800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:100328200-100329800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr3:100328400-100328600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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