Variant report

Variant	nsv965167
Chromosome Location	chr3:51702892-51707059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:906)
CpG islands
(count:734)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:51705901-51705928	HepG2	liver:	n/a	n/a
2	ATF2	chr3:51703245-51703708	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:51703302-51703723	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:51703381-51703643	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:51704893-51705980	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:51705056-51705226	K562	blood:	n/a	n/a
7	BCL3	chr3:51704904-51705663	GM12878	blood:	n/a	chr3:51705410-51705423
8	BCL3	chr3:51704839-51705260	A549	lung:	n/a	n/a
9	BCLAF1	chr3:51704830-51705664	GM12878	blood:	n/a	chr3:51705410-51705423
10	BCLAF1	chr3:51705789-51706158	GM12878	blood:	n/a	chr3:51705850-51705863 chr3:51705852-51705861 chr3:51705849-51705858
11	BHLHE40	chr3:51704865-51706208	GM12878	blood:	n/a	chr3:51705859-51705872 chr3:51705525-51705541 chr3:51705996-51706012
12	BHLHE40	chr3:51703329-51703641	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:51704853-51706235	K562	blood:	n/a	chr3:51705859-51705872 chr3:51705525-51705541 chr3:51705996-51706012
14	BHLHE40	chr3:51705713-51706041	A549	lung:	n/a	chr3:51705859-51705872 chr3:51705996-51706012
15	BHLHE40	chr3:51705650-51705960	HepG2	liver:	n/a	chr3:51705859-51705872
16	BHLHE40	chr3:51703286-51703735	K562	blood:	n/a	n/a
17	BHLHE40	chr3:51704957-51706193	HepG2	liver:	n/a	chr3:51705859-51705872 chr3:51705525-51705541 chr3:51705996-51706012
18	BHLHE40	chr3:51706420-51706544	GM12878	blood:	n/a	n/a
19	BRCA1	chr3:51703298-51703590	HepG2	liver:	n/a	n/a
20	BRCA1	chr3:51704910-51705674	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr3:51704714-51704918	GM12878	blood:	n/a	n/a
22	BRCA1	chr3:51705220-51705275	HepG2	liver:	n/a	n/a
23	CCNT2	chr3:51704931-51706071	K562	blood:	n/a	n/a
24	CCNT2	chr3:51703327-51703731	K562	blood:	n/a	chr3:51703341-51703361
25	CEBPB	chr3:51704644-51705335	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:51703249-51703707	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:51704644-51705164	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:51704927-51705146	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:51704924-51705173	K562	blood:	n/a	n/a
30	CEBPB	chr3:51704898-51705088	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:51704876-51705218	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:51704818-51705139	A549	lung:	n/a	n/a
33	CEBPB	chr3:51703287-51703620	A549	lung:	n/a	n/a
34	CEBPB	chr3:51703210-51703593	MCF-7	breast:	n/a	n/a
35	CEBPB	chr3:51704919-51705121	MCF-7	breast:	n/a	n/a
36	CEBPB	chr3:51703273-51703574	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:51703206-51703571	K562	blood:	n/a	n/a
38	CEBPB	chr3:51703242-51703627	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:51703252-51703580	K562	blood:	n/a	n/a
40	CEBPD	chr3:51705071-51705427	HepG2	liver:	n/a	n/a
41	CEBPD	chr3:51705700-51706043	HepG2	liver:	n/a	n/a
42	CEBPD	chr3:51703223-51703557	K562	blood:	n/a	n/a
43	CHD1	chr3:51703357-51703569	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:51704883-51706507	GM12878	blood:	n/a	n/a
45	CHD2	chr3:51705811-51705980	HepG2	liver:	n/a	n/a
46	CHD2	chr3:51704860-51706118	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr3:51703314-51703582	GM12878	blood:	n/a	n/a
48	CHD2	chr3:51705233-51705553	HepG2	liver:	n/a	n/a
49	CHD2	chr3:51703303-51703557	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr3:51703265-51703635	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51705063-51705113	NB4	blood:	n/a
2	chr3:51705150-51705200	NB4	blood:	n/a
3	chr3:51705063-51705113	NB4	blood:	n/a
4	chr3:51705150-51705200	NB4	blood:	n/a
5	chr3:51705912-51705962	HRPEpiC	eye:	n/a
6	chr3:51704960-51705010	MCF10A-Er-Src	breast:	n/a
7	chr3:51705097-51705147	LNCaP	prostate:	n/a
8	chr3:51705045-51705095	Hepatocyte	liver:	n/a
9	chr3:51705045-51705095	HPAEpiC	pulmonary alveolar:	n/a
10	chr3:51705912-51705962	NB4	blood:	n/a
11	chr3:51704351-51704401	Caco-2	colon:	n/a
12	chr3:51705912-51705962	AG09319	gingival:	n/a
13	chr3:51705680-51705730	AG09319	gingival:	n/a
14	chr3:51704351-51704401	AG09319	gingival:	n/a
15	chr3:51704351-51704401	HAEpiC	amniotic membrane:	n/a
16	chr3:51705097-51705147	Caco-2	colon:	n/a
17	chr3:51706056-51706106	MCF10A-Er-Src	breast:	n/a
18	chr3:51705680-51705730	SAEC	small airway:	n/a
19	chr3:51705680-51705730	HCT-116	colon:	n/a
20	chr3:51705097-51705147	MCF-7	breast:	n/a
21	chr3:51705097-51705147	BJ	skin:	n/a
22	chr3:51705150-51705200	GM12891	blood:	n/a
23	chr3:51705912-51705962	SK-N-MC	brain:	n/a
24	chr3:51705912-51705962	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:51704960-51705010	ovcar-3	ovarian:	n/a
26	chr3:51703814-51703864	AG09309	skin:	n/a
27	chr3:51705063-51705113	K562	blood:	n/a
28	chr3:51705912-51705962	AG04449	skin:	fetal
29	chr3:51706056-51706106	HMEC	breast:	n/a
30	chr3:51705045-51705095	RPTEC	kidney:	n/a
31	chr3:51705097-51705147	GM19239	blood:	n/a
32	chr3:51706056-51706106	HEEpiC	esophagus:	n/a
33	chr3:51705097-51705147	SK-N-SH_RA	brain:	n/a
34	chr3:51705150-51705200	MCF10A-Er-Src	breast:	n/a
35	chr3:51705088-51705138	K562	blood:	n/a
36	chr3:51705150-51705200	AG10803	skin:	n/a
37	chr3:51705085-51705135	HMEC	breast:	n/a
38	chr3:51705085-51705135	GM12892	blood:	n/a
39	chr3:51704960-51705010	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:51705150-51705200	Hela-S3	cervix:	n/a
41	chr3:51705045-51705095	MCF10A-Er-Src	breast:	n/a
42	chr3:51705085-51705135	HAEpiC	amniotic membrane:	n/a
43	chr3:51705912-51705962	GM12892	blood:	n/a
44	chr3:51705063-51705113	H1-hESC	embryonic stem cell:	embryo
45	chr3:51705097-51705147	GM12878	blood:	n/a
46	chr3:51703814-51703864	AG09319	gingival:	n/a
47	chr3:51705063-51705113	HEEpiC	esophagus:	n/a
48	chr3:51705097-51705147	CMK	blood:	n/a
49	chr3:51705150-51705200	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:51705085-51705135	HCT-116	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51689639..51691996-chr3:51702378..51704180,2	K562	blood:
2	chr3:51705086..51705705-chr9:86536186..86536829,2	HCT-116	colon:
3	chr3:51694128..51695719-chr3:51702275..51704283,2	K562	blood:
4	chr3:51533144..51535964-chr3:51704671..51707377,2	MCF-7	breast:
5	chr3:51703488..51706346-chr3:51714334..51716919,2	MCF-7	breast:
6	chr11:16759738..16760372-chr3:51705251..51705984,2	HCT-116	colon:
7	chr3:51535785..51536669-chr3:51703108..51703917,3	MCF-7	breast:
8	chr3:51699216..51703004-chr3:51704481..51706948,3	MCF-7	breast:
9	chr3:51532457..51535099-chr3:51703667..51706623,4	MCF-7	breast:
10	chr3:51675829..51676718-chr3:51702251..51702905,2	MCF-7	breast:
11	chr3:51692768..51695628-chr3:51701276..51703775,2	K562	blood:
12	chr3:51702918..51706936-chr3:51707889..51711767,6	MCF-7	breast:
13	chr3:51704201..51711015-chr3:51712254..51717093,7	K562	blood:
14	chr3:51532560..51534895-chr3:51704003..51706915,3	K562	blood:
15	chr3:51706347..51708181-chr3:51714827..51717093,2	K562	blood:
16	chr3:51704425..51707228-chr3:51714036..51717789,3	MCF-7	breast:
17	chr3:51532096..51536424-chr3:51702408..51707498,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IQCF6-2	chr3:51704665-51704909	NONHSAT089874
2	lnc-IQCF6-2	chr3:51700250-51703672	NONHSAT089874

No data

Variant related genes	Relation type
TEX264	TF binding region
TEX264	CpG island
ENSG00000164081	chromatin interactions
ENSG00000110693	chromatin interactions
ENSG00000165115	chromatin interactions
ENSG00000110696	chromatin interactions
ENSG00000145041	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147412207	chr3:51702950-51702951	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs571655360	chr3:51702974-51702975	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs538850799	chr3:51702977-51702978	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs554303367	chr3:51703003-51703004	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs566147662	chr3:51703004-51703005	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs9824779	chr3:51703025-51703026	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555132372	chr3:51703046-51703047	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs6775666	chr3:51703064-51703065	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs531410418	chr3:51703136-51703137	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs78145702	chr3:51703178-51703179	Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs374036277	chr3:51703320-51703321	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs192246333	chr3:51703364-51703365	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs577024473	chr3:51703395-51703396	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs138190949	chr3:51703456-51703457	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs559471231	chr3:51703467-51703468	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs574561754	chr3:51703480-51703481	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs541508804	chr3:51703498-51703499	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs904144	chr3:51703510-51703511	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530423908	chr3:51703784-51703785	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs184734604	chr3:51703866-51703867	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561488184	chr3:51703870-51703871	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs149546860	chr3:51703878-51703879	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs547799204	chr3:51703999-51704000	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs370487674	chr3:51704016-51704017	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs71297370	chr3:51704073-51704074	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566233743	chr3:51704075-51704076	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs561336629	chr3:51704175-51704176	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs536470862	chr3:51704182-51704183	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs373627491	chr3:51704288-51704289	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs190349635	chr3:51704302-51704303	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs537550069	chr3:51704322-51704323	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs182592901	chr3:51704372-51704373	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs528307254	chr3:51704400-51704401	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs143870596	chr3:51704427-51704428	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs184230715	chr3:51704441-51704442	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs553025862	chr3:51704450-51704451	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13317936	chr3:51704481-51704482	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs375026461	chr3:51704487-51704488	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs114393721	chr3:51704497-51704498	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs115271353	chr3:51704501-51704502	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148612032	chr3:51704510-51704511	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs142091836	chr3:51704578-51704579	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs34867766	chr3:51704620-51704621	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs13321674	chr3:51704721-51704722	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs547106464	chr3:51704745-51704746	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs564083746	chr3:51704884-51704885	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs146216931	chr3:51704946-51704947	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs548045262	chr3:51704991-51704992	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs559838948	chr3:51705002-51705003	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs111421640	chr3:51705085-51705086	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51681600-51703200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr3:51682200-51704400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:51689800-51703000	Weak transcription	Fetal Heart	heart
4	chr3:51690400-51703000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr3:51690800-51704400	Weak transcription	HUVEC	blood vessel
6	chr3:51694200-51704800	Weak transcription	Psoas Muscle	Psoas
7	chr3:51694400-51704400	Weak transcription	Fetal Brain Male	brain
8	chr3:51694400-51704600	Weak transcription	NHDF-Ad	bronchial
9	chr3:51695800-51703000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr3:51696200-51704400	Weak transcription	Fetal Kidney	kidney
11	chr3:51696600-51704200	Weak transcription	Small Intestine	intestine
12	chr3:51697200-51703200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr3:51697200-51704600	Weak transcription	Brain Substantia Nigra	brain
14	chr3:51697400-51703000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr3:51697400-51703000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr3:51697400-51703000	Weak transcription	A549	lung
17	chr3:51697400-51703200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr3:51697400-51703400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr3:51697400-51703600	Weak transcription	GM12878-XiMat	blood
20	chr3:51697400-51704400	Weak transcription	Brain Angular Gyrus	brain
21	chr3:51697400-51704400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr3:51697400-51704600	Weak transcription	Left Ventricle	heart
23	chr3:51697400-51704800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:51697400-51704800	Weak transcription	Aorta	Aorta
25	chr3:51697600-51703000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr3:51697600-51703000	Weak transcription	Pancreas	Pancrea
27	chr3:51697600-51703200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:51697600-51704400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr3:51697800-51703000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:51697800-51703000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr3:51697800-51703000	Weak transcription	Colonic Mucosa	Colon
32	chr3:51697800-51703000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr3:51697800-51703000	Weak transcription	HepG2	liver
34	chr3:51697800-51703200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr3:51697800-51703200	Weak transcription	NHLF	lung
36	chr3:51697800-51704400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:51697800-51704600	Weak transcription	HSMM	muscle
38	chr3:51698000-51703200	Weak transcription	Thymus	Thymus
39	chr3:51698000-51703400	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr3:51698000-51703400	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr3:51698000-51703600	Weak transcription	Gastric	stomach
42	chr3:51698000-51704800	Weak transcription	Ovary	ovary
43	chr3:51698200-51703000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:51698200-51703000	Weak transcription	Primary B cells from cord blood	blood
45	chr3:51698200-51703200	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr3:51698200-51704600	Weak transcription	NH-A	brain
47	chr3:51698400-51703000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr3:51698400-51703000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:51698400-51703000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr3:51698400-51703000	Weak transcription	Esophagus	oesophagus

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