Variant report

Variant	nsv10330
Chromosome Location	chr3:137832799-137834598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:464)
CpG islands
(count:671)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:137833993-137834128	HepG2	liver:	n/a	n/a
2	BACH1	chr3:137833857-137834555	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr3:137833926-137834066	GM12878	blood:	n/a	chr3:137834021-137834037
4	BHLHE40	chr3:137833655-137834725	K562	blood:	n/a	chr3:137834021-137834037
5	BRCA1	chr3:137834414-137834756	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr3:137833713-137834448	K562	blood:	n/a	chr3:137834325-137834334
7	CEBPB	chr3:137834272-137834592	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr3:137834018-137834019	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:137833758-137835222	Hela-S3	cervix:	n/a	chr3:137835056-137835069
10	CHD1	chr3:137834359-137834749	H1-hESC	embryonic stem cell:	n/a	chr3:137834484-137834494
11	CHD2	chr3:137833903-137834802	Hela-S3	cervix:	n/a	chr3:137834484-137834494 chr3:137834016-137834026
12	CHD2	chr3:137834170-137834194	HepG2	liver:	n/a	n/a
13	CHD2	chr3:137833569-137834031	H1-hESC	embryonic stem cell:	n/a	chr3:137834016-137834026
14	CHD2	chr3:137834450-137834715	H1-hESC	embryonic stem cell:	n/a	chr3:137834484-137834494
15	CREB1	chr3:137833793-137834186	A549	lung:	n/a	n/a
16	CTBP2	chr3:137833340-137834761	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr3:137833720-137833870	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr3:137833660-137833810	HCT-116	colon:	n/a	chr3:137833678-137833691
19	CTCF	chr3:137833801-137834243	K562	blood:	n/a	n/a
20	CTCF	chr3:137833340-137833490	GM12872	blood:	n/a	n/a
21	CTCF	chr3:137833900-137834050	Caco-2	colon:	n/a	n/a
22	CTCF	chr3:137833880-137834030	GM12869	blood:	n/a	n/a
23	CTCF	chr3:137833880-137834030	RPTEC	kidney:	n/a	n/a
24	CTCF	chr3:137834360-137834510	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr3:137833560-137833710	HepG2	liver:	n/a	chr3:137833678-137833691
26	CTCF	chr3:137833860-137834010	GM12870	blood:	n/a	n/a
27	CTCF	chr3:137833560-137833710	GM12871	blood:	n/a	chr3:137833678-137833691
28	CTCF	chr3:137833913-137834037	Medullo	brain:	n/a	n/a
29	CTCF	chr3:137833380-137833530	BJ	skin:	n/a	n/a
30	CTCF	chr3:137833880-137834030	GM12870	blood:	n/a	n/a
31	CTCF	chr3:137833800-137833950	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr3:137833920-137834070	GM12864	blood:	n/a	n/a
33	CTCF	chr3:137834380-137834530	GM12865	blood:	n/a	n/a
34	CTCF	chr3:137833820-137833970	AG04450	lung:	n/a	n/a
35	CTCF	chr3:137833880-137834030	GM12872	blood:	n/a	n/a
36	CTCF	chr3:137833860-137834010	HCM	heart:	n/a	n/a
37	CTCF	chr3:137833860-137834010	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr3:137833960-137834110	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr3:137833660-137833810	RPTEC	kidney:	n/a	chr3:137833678-137833691
40	CTCF	chr3:137833940-137834090	GM12867	blood:	n/a	n/a
41	CTCF	chr3:137833880-137834030	GM12865	blood:	n/a	n/a
42	CTCF	chr3:137833846-137834103	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr3:137833862-137834109	GM10248	blood:	n/a	n/a
44	CTCF	chr3:137833860-137834010	AG04449	skin:	n/a	n/a
45	CTCF	chr3:137833860-137834010	HCT-116	colon:	n/a	n/a
46	CTCF	chr3:137833846-137834125	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:137833940-137834090	K562	blood:	n/a	n/a
48	CTCF	chr3:137833900-137834050	NB4	blood:	n/a	n/a
49	CTCF	chr3:137833460-137833610	AG04449	skin:	n/a	n/a
50	CTCF	chr3:137833900-137834050	GM12875	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:137833634-137833684	AG09309	skin:	n/a
2	chr3:137833494-137833544	HEEpiC	esophagus:	n/a
3	chr3:137834484-137834534	ProgFib	skin:	n/a
4	chr3:137834238-137834288	H1-hESC	embryonic stem cell:	embryo
5	chr3:137834571-137834621	H1-hESC	embryonic stem cell:	embryo
6	chr3:137833494-137833544	GM06990	blood:	n/a
7	chr3:137834591-137834641	SK-N-MC	brain:	n/a
8	chr3:137834489-137834539	HCM	heart:	n/a
9	chr3:137833634-137833684	HepG2	liver:	n/a
10	chr3:137833675-137833725	ProgFib	skin:	n/a
11	chr3:137834231-137834281	NH-A	brain:	n/a
12	chr3:137834238-137834288	HCPEpiC	choroid plexus:	n/a
13	chr3:137834238-137834288	ECC-1	luminal epithelium:	n/a
14	chr3:137833983-137834033	HL-60	blood:	n/a
15	chr3:137834582-137834632	NHDF-neo	bronchial:	n/a
16	chr3:137834231-137834281	AoSMC	blood vessel:	n/a
17	chr3:137834571-137834621	ovcar-3	ovarian:	n/a
18	chr3:137834238-137834288	Caco-2	colon:	n/a
19	chr3:137834591-137834641	NB4	blood:	n/a
20	chr3:137834591-137834641	LNCaP	prostate:	n/a
21	chr3:137834489-137834539	ovcar-3	ovarian:	n/a
22	chr3:137834231-137834281	PANC-1	pancreas:	n/a
23	chr3:137834489-137834539	H1-hESC	embryonic stem cell:	embryo
24	chr3:137834238-137834288	PANC-1	pancreas:	n/a
25	chr3:137833983-137834033	SK-N-SH_RA	brain:	n/a
26	chr3:137834238-137834288	AG10803	skin:	n/a
27	chr3:137834231-137834281	GM12878	blood:	n/a
28	chr3:137834571-137834621	HRCEpiC	kidney:	n/a
29	chr3:137834582-137834632	MCF-7	breast:	n/a
30	chr3:137834484-137834534	Jurkat	blood:	n/a
31	chr3:137834484-137834534	HAEpiC	amniotic membrane:	n/a
32	chr3:137834571-137834621	RPTEC	kidney:	n/a
33	chr3:137833494-137833544	AG09309	skin:	n/a
34	chr3:137834571-137834621	HCT-116	colon:	n/a
35	chr3:137833675-137833725	MCF10A-Er-Src	breast:	n/a
36	chr3:137834489-137834539	Hela-S3	cervix:	n/a
37	chr3:137834571-137834621	MCF10A-Er-Src	breast:	n/a
38	chr3:137833634-137833684	PANC-1	pancreas:	n/a
39	chr3:137834571-137834621	SKMC	muscle:	n/a
40	chr3:137834231-137834281	HRE	kidney:	n/a
41	chr3:137833494-137833544	Hepatocyte	liver:	n/a
42	chr3:137833983-137834033	HAEpiC	amniotic membrane:	n/a
43	chr3:137834484-137834534	HMEC	breast:	n/a
44	chr3:137833494-137833544	ProgFib	skin:	n/a
45	chr3:137833494-137833544	HIPEpiC	eye:	n/a
46	chr3:137834238-137834288	A549	lung:	n/a
47	chr3:137833634-137833684	GM12892	blood:	n/a
48	chr3:137834231-137834281	MCF-7	breast:	n/a
49	chr3:137833983-137834033	PANC-1	pancreas:	n/a
50	chr3:137834591-137834641	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:137834045..137835023-chr5:180670513..180671496,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
DZIP1L	TF binding region
DZIP1L	CpG island
ENSG00000204628	chromatin interactions

Extended variants
information (count: 59 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:59 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540424527	chr3:137832804-137832805	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs553542963	chr3:137832806-137832807	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184078089	chr3:137832829-137832830	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs554449243	chr3:137832849-137832850	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542259560	chr3:137832871-137832872	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs571705396	chr3:137832981-137832982	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs561959355	chr3:137832993-137832994	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs113234498	chr3:137832994-137832995	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544610914	chr3:137833114-137833115	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144402722	chr3:137833143-137833144	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs374600737	chr3:137833184-137833185	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs375926140	chr3:137833222-137833223	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs533391968	chr3:137833229-137833230	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs188794790	chr3:137833241-137833242	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566679111	chr3:137833308-137833309	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs371524379	chr3:137833362-137833363	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs574428656	chr3:137833477-137833478	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148762032	chr3:137833522-137833523	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs547785984	chr3:137833523-137833524	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs142423810	chr3:137833534-137833535	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs567765950	chr3:137833552-137833553	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs537827293	chr3:137833579-137833580	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs13068449	chr3:137833592-137833593	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs375506775	chr3:137833674-137833675	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs571556850	chr3:137833730-137833731	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs541701738	chr3:137833737-137833738	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs559937651	chr3:137833764-137833765	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs558578760	chr3:137833772-137833773	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs181569066	chr3:137833791-137833792	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs386666278	chr3:137833800-137833801	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs36040436	chr3:137833840-137833841	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs573749699	chr3:137833859-137833860	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541972984	chr3:137833902-137833903	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs555812549	chr3:137833966-137833967	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs6781719	chr3:137834019-137834020	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs112687052	chr3:137834031-137834032	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs544193230	chr3:137834038-137834039	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs329386	chr3:137834098-137834099	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs533451196	chr3:137834111-137834112	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370111756	chr3:137834126-137834127	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374343671	chr3:137834159-137834160	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs186066855	chr3:137834198-137834199	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548833100	chr3:137834230-137834231	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs112357741	chr3:137834257-137834258	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531248749	chr3:137834285-137834286	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556125462	chr3:137834295-137834296	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs551404227	chr3:137834323-137834324	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572214317	chr3:137834399-137834400	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs576182307	chr3:137834427-137834428	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs571214107	chr3:137834434-137834435	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:137781000-137833200	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:137801600-137833200	Weak transcription	Brain Cingulate Gyrus	brain
3	chr3:137803200-137833200	Weak transcription	Placenta	Placenta
4	chr3:137811800-137833400	Weak transcription	Fetal Brain Male	brain
5	chr3:137812600-137833200	Weak transcription	Brain Angular Gyrus	brain
6	chr3:137813800-137833000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:137814000-137833000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr3:137814000-137833600	Weak transcription	Liver	Liver
9	chr3:137814200-137833200	Weak transcription	HUVEC	blood vessel
10	chr3:137816800-137833000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:137821000-137833200	Weak transcription	Fetal Intestine Small	intestine
12	chr3:137821600-137833000	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr3:137822400-137833200	Weak transcription	Brain Anterior Caudate	brain
14	chr3:137822600-137833000	Weak transcription	HSMMtube	muscle
15	chr3:137822600-137833200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:137822800-137833000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr3:137822800-137833200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr3:137822800-137833200	Weak transcription	Fetal Brain Female	brain
19	chr3:137823000-137833200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr3:137823000-137833200	Weak transcription	Lung	lung
21	chr3:137823000-137833400	Weak transcription	Gastric	stomach
22	chr3:137823200-137833200	Weak transcription	Pancreas	Pancrea
23	chr3:137823200-137833200	Weak transcription	Spleen	Spleen
24	chr3:137823600-137833200	Weak transcription	Right Ventricle	heart
25	chr3:137830400-137833000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr3:137830400-137833000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr3:137831200-137833000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr3:137831200-137833000	Enhancers	NHLF	lung
29	chr3:137831200-137833400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:137831400-137833000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:137831400-137833200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:137831600-137833000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr3:137831600-137833000	Enhancers	HMEC	breast
34	chr3:137831600-137833200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:137831800-137833000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr3:137831800-137833000	Enhancers	Fetal Heart	heart
37	chr3:137831800-137833000	Enhancers	NHDF-Ad	bronchial
38	chr3:137832000-137832800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr3:137832000-137833000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:137832000-137833000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:137832000-137833000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr3:137832000-137833000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr3:137832000-137833000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:137832000-137833000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:137832000-137833200	Enhancers	H1 Cell Line	embryonic stem cell
46	chr3:137832000-137833200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:137832000-137833200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:137832000-137833200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr3:137832000-137833200	Enhancers	Brain Germinal Matrix	brain
50	chr3:137832000-137833200	Enhancers	Brain Hippocampus Middle	brain

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