Variant report

Variant	esv2755927
Chromosome Location	chr3:111794310-111834310
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1180)
CpG islands
(count:1222)
Chromatin interactive
region (count:46)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:111803955-111804105	HepG2	liver:	n/a	n/a
2	ATF1	chr3:111816224-111816602	K562	blood:	n/a	n/a
3	ATF2	chr3:111832269-111833259	GM12878	blood:	n/a	n/a
4	ATF2	chr3:111830559-111831225	GM12878	blood:	n/a	n/a
5	ATF2	chr3:111833318-111835941	GM12878	blood:	n/a	n/a
6	ATF2	chr3:111833452-111835530	GM12878	blood:	n/a	n/a
7	ATF2	chr3:111832076-111833278	GM12878	blood:	n/a	n/a
8	BACH1	chr3:111802338-111802344	K562	blood:	n/a	n/a
9	BACH1	chr3:111804969-111805633	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr3:111832554-111833114	GM12878	blood:	n/a	n/a
11	BATF	chr3:111833922-111834576	GM12878	blood:	n/a	n/a
12	BATF	chr3:111834072-111834535	GM12878	blood:	n/a	n/a
13	BATF	chr3:111832514-111833073	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:111832566-111833161	GM12878	blood:	n/a	chr3:111832743-111832752
15	BCL11A	chr3:111834017-111834442	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:111833987-111834537	GM12878	blood:	n/a	n/a
17	BCL3	chr3:111833793-111835349	GM12878	blood:	n/a	n/a
18	BCL3	chr3:111833926-111834513	GM12878	blood:	n/a	n/a
19	BCL3	chr3:111833419-111833772	GM12878	blood:	n/a	n/a
20	BCL3	chr3:111804801-111805488	A549	lung:	n/a	chr3:111805132-111805145
21	BCL3	chr3:111832536-111833082	GM12878	blood:	n/a	chr3:111832743-111832752
22	BCLAF1	chr3:111833422-111835417	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:111832470-111833277	GM12878	blood:	n/a	chr3:111832743-111832752
24	BCLAF1	chr3:111832529-111833288	GM12878	blood:	n/a	chr3:111832743-111832752
25	BCLAF1	chr3:111830576-111831105	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:111833457-111834638	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:111803737-111803747	K562	blood:	n/a	n/a
28	BHLHE40	chr3:111830739-111831010	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:111805111-111805377	K562	blood:	n/a	n/a
30	BHLHE40	chr3:111832672-111833166	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:111833501-111836145	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:111804396-111804471	K562	blood:	n/a	n/a
33	BRCA1	chr3:111804890-111804974	GM12878	blood:	n/a	n/a
34	BRCA1	chr3:111793465-111794383	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr3:111816140-111816615	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr3:111805324-111805339	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr3:111805114-111805584	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr3:111833991-111834518	GM12878	blood:	n/a	n/a
39	CBX3	chr3:111816145-111816708	HCT-116	colon:	n/a	n/a
40	CBX3	chr3:111793664-111794564	HCT-116	colon:	n/a	n/a
41	CBX3	chr3:111805019-111805450	K562	blood:	n/a	n/a
42	CCNT2	chr3:111805066-111805499	K562	blood:	n/a	n/a
43	CEBPB	chr3:111812026-111812324	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:111816033-111816731	HCT-116	colon:	n/a	n/a
45	CEBPB	chr3:111833414-111835497	GM12878	blood:	n/a	n/a
46	CEBPB	chr3:111815135-111815422	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:111816221-111816597	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:111815103-111815434	IMR90	lung:	n/a	n/a
49	CEBPB	chr3:111798050-111798323	MCF-7	breast:	n/a	n/a
50	CEBPB	chr3:111820792-111821297	IMR90	lung:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:111802305-111802355	K562	blood:	n/a
2	chr3:111802305-111802355	Caco-2	colon:	n/a
3	chr3:111802305-111802355	K562	blood:	n/a
4	chr3:111802305-111802355	Caco-2	colon:	n/a
5	chr3:111805385-111805435	Hela-S3	cervix:	n/a
6	chr3:111804830-111804880	GM12891	blood:	n/a
7	chr3:111805231-111805281	AG09319	gingival:	n/a
8	chr3:111804832-111804882	SK-N-SH	brain:	n/a
9	chr3:111805077-111805127	PANC-1	pancreas:	n/a
10	chr3:111804983-111805033	IMR90	lung:	fetal
11	chr3:111805385-111805435	SK-N-SH	brain:	n/a
12	chr3:111830803-111830853	CMK	blood:	n/a
13	chr3:111805005-111805055	AG10803	skin:	n/a
14	chr3:111821058-111821108	PrEC	prostate:	n/a
15	chr3:111804832-111804882	U87	brain:	n/a
16	chr3:111806031-111806081	HCT-116	colon:	n/a
17	chr3:111804983-111805033	AG09319	gingival:	n/a
18	chr3:111805077-111805127	NHBE	bronchial:	n/a
19	chr3:111830759-111830809	SK-N-SH_RA	brain:	n/a
20	chr3:111804981-111805031	ProgFib	skin:	n/a
21	chr3:111830759-111830809	HRPEpiC	eye:	n/a
22	chr3:111805385-111805435	ECC-1	luminal epithelium:	n/a
23	chr3:111805312-111805362	NHDF-neo	bronchial:	n/a
24	chr3:111805005-111805055	HRPEpiC	eye:	n/a
25	chr3:111804832-111804882	A549	lung:	n/a
26	chr3:111804981-111805031	H1-hESC	embryonic stem cell:	embryo
27	chr3:111821058-111821108	SK-N-MC	brain:	n/a
28	chr3:111804830-111804880	HRCEpiC	kidney:	n/a
29	chr3:111805077-111805127	NHDF-neo	bronchial:	n/a
30	chr3:111830759-111830809	GM12891	blood:	n/a
31	chr3:111806031-111806081	CMK	blood:	n/a
32	chr3:111821058-111821108	CMK	blood:	n/a
33	chr3:111821058-111821108	HL-60	blood:	n/a
34	chr3:111830759-111830809	HEEpiC	esophagus:	n/a
35	chr3:111804981-111805031	GM12892	blood:	n/a
36	chr3:111804983-111805033	AoSMC	blood vessel:	n/a
37	chr3:111805225-111805275	HUVEC	blood vessel:	n/a
38	chr3:111830803-111830853	GM19239	blood:	n/a
39	chr3:111804983-111805033	HCM	heart:	n/a
40	chr3:111831279-111831329	A549	lung:	n/a
41	chr3:111805231-111805281	U87	brain:	n/a
42	chr3:111805408-111805458	PANC-1	pancreas:	n/a
43	chr3:111831279-111831329	NB4	blood:	n/a
44	chr3:111804343-111804393	HCT-116	colon:	n/a
45	chr3:111821058-111821108	SKMC	muscle:	n/a
46	chr3:111831279-111831329	K562	blood:	n/a
47	chr3:111805225-111805275	IMR90	lung:	fetal
48	chr3:111804832-111804882	HL-60	blood:	n/a
49	chr3:111805231-111805281	HRCEpiC	kidney:	n/a
50	chr3:111805231-111805281	SK-N-SH	brain:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:111803332..111805315-chr3:112279253..112281220,2	MCF-7	breast:
2	chr3:111818917..111821397-chr3:111825359..111828351,2	MCF-7	breast:
3	chr3:111794914..111797879-chr3:112278685..112280837,2	MCF-7	breast:
4	chr3:111792824..111796051-chr3:111796443..111799498,4	MCF-7	breast:
5	chr3:111803684..111806522-chr3:111810279..111813217,3	K562	blood:
6	chr3:111832694..111835578-chr3:112096846..112099201,2	MCF-7	breast:
7	chr3:111696629..111698580-chr3:111808489..111810447,2	MCF-7	breast:
8	chr3:111813403..111815465-chr3:112280077..112281630,2	K562	blood:
9	chr3:111804265..111807071-chr3:111815537..111817475,2	K562	blood:
10	chr3:111830456..111832040-chr3:112279153..112281688,2	K562	blood:
11	chr3:111799117..111801268-chr3:111802175..111804910,2	MCF-7	breast:
12	chr3:111803618..111805718-chr3:111824447..111826548,2	MCF-7	breast:
13	chr3:111815599..111817601-chr3:112708787..112711092,2	MCF-7	breast:
14	chr3:111792644..111794499-chr3:111797268..111798908,2	K562	blood:
15	chr3:111804469..111806477-chr3:111808239..111810533,4	MCF-7	breast:
16	chr3:111829764..111831902-chr3:111832844..111835474,2	MCF-7	breast:
17	chr3:111815832..111818403-chr3:112276886..112278586,2	MCF-7	breast:
18	chr3:111813838..111815744-chr3:111818709..111820600,2	K562	blood:
19	chr3:111830661..111831289-chr3:112238353..112238915,2	K562	blood:
20	chr3:111830414..111830964-chr3:112156344..112156927,2	MCF-7	breast:
21	chr12:50134972..50135639-chr3:111805318..111805831,2	Hela-S3	cervix:
22	chr3:111792657..111794523-chr3:111799735..111802519,2	MCF-7	breast:
23	chr3:111762244..111763263-chr3:111830391..111831101,4	MCF-7	breast:
24	chr3:111799117..111801268-chr3:111802175..111804910,2	MCF-7	breast:
25	chr3:111816694..111819684-chr3:111820082..111821696,2	MCF-7	breast:
26	chr3:111804970..111806559-chr3:111814043..111816179,2	MCF-7	breast:
27	chr3:111833809..111835627-chr3:111838661..111841118,2	K562	blood:
28	chr3:111794982..111796991-chr3:111800911..111803256,2	K562	blood:
29	chr3:111818917..111821397-chr3:111825359..111828351,2	MCF-7	breast:
30	chr15:59225042..59225969-chr3:111804939..111805795,2	Hela-S3	cervix:
31	chr3:111809767..111811797-chr3:111828280..111831117,2	MCF-7	breast:
32	chr3:111792657..111794523-chr3:111799735..111802519,2	MCF-7	breast:
33	chr3:111833855..111836501-chr3:111839924..111841508,2	MCF-7	breast:
34	chr3:111792824..111796051-chr3:111796443..111799498,4	MCF-7	breast:
35	chr3:111828383..111830236-chr3:111831483..111834219,2	MCF-7	breast:
36	chr1:26137085..26137948-chr3:111819284..111820031,2	MCF-7	breast:
37	chr3:111816694..111819684-chr3:111820082..111821696,2	MCF-7	breast:
38	chr3:111792401..111798775-chr3:111803596..111811380,13	MCF-7	breast:
39	chr3:111813838..111815744-chr3:111818709..111820600,2	K562	blood:
40	chr3:111794982..111796991-chr3:111800911..111803256,2	K562	blood:
41	chr3:111824816..111827651-chr3:111837771..111840373,2	K562	blood:
42	chr3:111830383..111831315-chr3:112250332..112250864,2	K562	blood:
43	chr3:111792644..111794499-chr3:111797268..111798908,2	K562	blood:
44	chr3:111803684..111807677-chr3:111807818..111813217,8	K562	blood:
45	chr3:111795641..111798787-chr3:111803858..111806431,4	MCF-7	breast:
46	chr3:111797278..111800126-chr3:111805062..111806679,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMPRSS7-2	chr3:111831811-111831865	NONHSAT091157
2	lnc-TMPRSS7-2	chr3:111830739-111830921	NONHSAT091157
3	lnc-TMPRSS7-2	chr3:111830299-111830627	NONHSAT091157

miRNA name	Chromosome Location	mirBase accession
hsa-miR-567	chr3:111831663-111831685	MIMAT0003231

No data

Variant related genes	Relation type
MIR567	TF binding region
C3orf52	TF binding region
MIR567	CpG island
C3orf52	CpG island
ENSG00000207940	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000144848	chromatin interactions
ENSG00000272844	chromatin interactions
ENSG00000163607	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000114529	chromatin interactions
ENSG00000144827	chromatin interactions

Extended variants
information (count: 1610 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574520652	chr3:111794327-111794328	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537379880	chr3:111794329-111794330	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs556961605	chr3:111794364-111794365	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1907639	chr3:111794365-111794366	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs7620996	chr3:111794391-111794392	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs559344406	chr3:111794399-111794400	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs563582475	chr3:111794476-111794477	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541911117	chr3:111794482-111794483	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs56008240	chr3:111794486-111794487	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs57907161	chr3:111794490-111794491	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs57851365	chr3:111794505-111794506	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs56060014	chr3:111794579-111794580	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs116073126	chr3:111794602-111794603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs558821740	chr3:111794615-111794616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35221662	chr3:111794652-111794653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs373814044	chr3:111794678-111794679	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181650953	chr3:111794798-111794799	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs73218005	chr3:111794816-111794817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs60562037	chr3:111794822-111794823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs368575518	chr3:111794825-111794826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs111251528	chr3:111794831-111794832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs16859145	chr3:111794835-111794836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs377090076	chr3:111794864-111794865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548255444	chr3:111794897-111794898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150602817	chr3:111794898-111794899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs56259975	chr3:111794900-111794901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557268693	chr3:111794912-111794913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs577064314	chr3:111794919-111794920	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs539703263	chr3:111794927-111794928	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs553018014	chr3:111795036-111795037	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs186847959	chr3:111795046-111795047	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs61250978	chr3:111795074-111795075	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139696480	chr3:111795094-111795095	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537676196	chr3:111795095-111795096	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs55955608	chr3:111795116-111795117	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs543661349	chr3:111795117-111795118	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563867421	chr3:111795152-111795153	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs577484952	chr3:111795184-111795185	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs111677685	chr3:111795194-111795195	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs146822926	chr3:111795232-111795233	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs34299361	chr3:111795243-111795244	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs140630235	chr3:111795266-111795267	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs559350511	chr3:111795292-111795293	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs16859152	chr3:111795318-111795319	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548317617	chr3:111795347-111795348	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs568459114	chr3:111795349-111795350	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs188490797	chr3:111795357-111795358	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs550510393	chr3:111795359-111795360	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570589914	chr3:111795364-111795365	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs539764089	chr3:111795395-111795396	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
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
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111791600-111796600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr3:111791800-111794600	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr3:111792400-111794800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr3:111792600-111794600	Flanking Active TSS	Osteobl	bone
5	chr3:111792600-111795200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:111792800-111794400	Enhancers	HSMMtube	muscle
7	chr3:111792800-111794400	Enhancers	NHDF-Ad	bronchial
8	chr3:111792800-111794400	Enhancers	NHLF	lung
9	chr3:111792800-111794600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:111792800-111794600	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr3:111792800-111794600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr3:111792800-111794600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
13	chr3:111792800-111794800	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr3:111792800-111794800	Enhancers	HUVEC	blood vessel
15	chr3:111793000-111794400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:111793200-111794400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr3:111793200-111794400	Enhancers	Aorta	Aorta
18	chr3:111793200-111794600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr3:111793200-111794600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr3:111793200-111795000	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr3:111793200-111795400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:111793400-111794400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:111793400-111794600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr3:111793600-111794400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:111793600-111794400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr3:111793600-111794400	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr3:111793600-111794400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:111793600-111794400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:111793600-111794600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr3:111793600-111794600	Flanking Active TSS	Thymus	Thymus
31	chr3:111793600-111794600	Flanking Active TSS	A549	lung
32	chr3:111793600-111796000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr3:111793800-111794400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr3:111793800-111794400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:111793800-111794400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:111793800-111794400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr3:111793800-111794400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr3:111793800-111794400	Flanking Active TSS	Primary T cells from cord blood	blood
39	chr3:111793800-111794400	Flanking Active TSS	Duodenum Mucosa	Duodenum
40	chr3:111793800-111794400	Enhancers	Pancreas	Pancrea
41	chr3:111793800-111794400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
42	chr3:111793800-111794400	Enhancers	Right Ventricle	heart
43	chr3:111793800-111794400	Enhancers	GM12878-XiMat	blood
44	chr3:111793800-111794400	Flanking Active TSS	HepG2	liver
45	chr3:111793800-111794400	Flanking Active TSS	HSMM	muscle
46	chr3:111793800-111794600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr3:111793800-111794600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr3:111793800-111794600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr3:111793800-111794600	Flanking Active TSS	Hela-S3	cervix
50	chr3:111793800-111794800	Enhancers	Primary T cells fromperipheralblood	blood

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