Variant report

Variant	nsv1010475
Chromosome Location	chr3:118657382-118789714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:747)
CpG islands
(count:1345)
Chromatin interactive
region (count:18)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118703634-118704104	K562	blood:	n/a	n/a
2	ARID3A	chr3:118656861-118657834	K562	blood:	n/a	n/a
3	ARID3A	chr3:118664331-118664451	K562	blood:	n/a	n/a
4	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
5	ARID3A	chr3:118662403-118662823	K562	blood:	n/a	n/a
6	ARID3A	chr3:118679788-118679991	K562	blood:	n/a	n/a
7	ARID3A	chr3:118734227-118734231	HepG2	liver:	n/a	n/a
8	ATF1	chr3:118662434-118662770	K562	blood:	n/a	n/a
9	ATF1	chr3:118703609-118703888	K562	blood:	n/a	n/a
10	ATF1	chr3:118705608-118705894	K562	blood:	n/a	n/a
11	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
12	ATF1	chr3:118656994-118657817	K562	blood:	n/a	n/a
13	ATF3	chr3:118657196-118657890	K562	blood:	n/a	chr3:118657446-118657456
14	ATF3	chr3:118703574-118703992	K562	blood:	n/a	n/a
15	BACH1	chr3:118684191-118684212	K562	blood:	n/a	n/a
16	BACH1	chr3:118657669-118657869	K562	blood:	n/a	n/a
17	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr3:118703611-118703902	K562	blood:	n/a	chr3:118703784-118703805
19	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
20	BHLHE40	chr3:118679924-118680020	K562	blood:	n/a	n/a
21	BHLHE40	chr3:118657766-118657874	K562	blood:	n/a	n/a
22	BHLHE40	chr3:118688306-118688376	K562	blood:	n/a	n/a
23	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
24	CBX3	chr3:118661565-118661900	K562	blood:	n/a	n/a
25	CBX3	chr3:118657347-118657712	K562	blood:	n/a	n/a
26	CCNT2	chr3:118662443-118662860	K562	blood:	n/a	n/a
27	CCNT2	chr3:118657067-118657701	K562	blood:	n/a	n/a
28	CCNT2	chr3:118703639-118703962	K562	blood:	n/a	n/a
29	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
30	CEBPB	chr3:118708183-118708258	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
32	CEBPB	chr3:118662415-118662797	K562	blood:	n/a	n/a
33	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
34	CEBPB	chr3:118657322-118657749	K562	blood:	n/a	n/a
35	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
36	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
37	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
38	CEBPB	chr3:118657320-118657849	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
40	CEBPB	chr3:118662492-118662741	K562	blood:	n/a	n/a
41	CEBPB	chr3:118657204-118657855	K562	blood:	n/a	n/a
42	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
43	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
44	CEBPB	chr3:118662395-118662791	K562	blood:	n/a	n/a
45	CEBPB	chr3:118657213-118658003	A549	lung:	n/a	n/a
46	CEBPB	chr3:118657383-118657824	A549	lung:	n/a	n/a
47	CEBPD	chr3:118662310-118662768	K562	blood:	n/a	n/a
48	CEBPD	chr3:118662435-118662813	K562	blood:	n/a	n/a
49	CEBPD	chr3:118703581-118703942	K562	blood:	n/a	n/a
50	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118676357-118676407	LNCaP	prostate:	n/a
2	chr3:118753093-118753143	SKMC	muscle:	n/a
3	chr3:118754097-118754147	NHDF-neo	bronchial:	n/a
4	chr3:118676357-118676407	LNCaP	prostate:	n/a
5	chr3:118753093-118753143	SKMC	muscle:	n/a
6	chr3:118754097-118754147	NHDF-neo	bronchial:	n/a
7	chr3:118706648-118706698	SK-N-SH	brain:	n/a
8	chr3:118663697-118663747	HCM	heart:	n/a
9	chr3:118663642-118663692	Hepatocyte	liver:	n/a
10	chr3:118753660-118753710	AG09319	gingival:	n/a
11	chr3:118705126-118705176	HUVEC	blood vessel:	n/a
12	chr3:118663534-118663584	HCPEpiC	choroid plexus:	n/a
13	chr3:118754376-118754426	SK-N-SH	brain:	n/a
14	chr3:118753610-118753660	H1-hESC	embryonic stem cell:	embryo
15	chr3:118750463-118750513	BJ	skin:	n/a
16	chr3:118753705-118753755	BE2_C	brain:	n/a
17	chr3:118676357-118676407	RPTEC	kidney:	n/a
18	chr3:118753660-118753710	GM12891	blood:	n/a
19	chr3:118757898-118757948	NT2-D1	testis:	n/a
20	chr3:118663470-118663520	HUVEC	blood vessel:	n/a
21	chr3:118753707-118753757	SK-N-SH	brain:	n/a
22	chr3:118753093-118753143	HEK293	kidney:	embryo
23	chr3:118754376-118754426	AG09319	gingival:	n/a
24	chr3:118753660-118753710	HEK293	kidney:	embryo
25	chr3:118663534-118663584	GM12878	blood:	n/a
26	chr3:118757898-118757948	SAEC	small airway:	n/a
27	chr3:118686312-118686362	A549	lung:	n/a
28	chr3:118753093-118753143	SK-N-MC	brain:	n/a
29	chr3:118757898-118757948	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:118663642-118663692	ECC-1	luminal epithelium:	n/a
31	chr3:118663534-118663584	K562	blood:	n/a
32	chr3:118734756-118734806	CMK	blood:	n/a
33	chr3:118705126-118705176	IMR90	lung:	fetal
34	chr3:118753660-118753710	HNPCEpiC	eye:	n/a
35	chr3:118663697-118663747	HepG2	liver:	n/a
36	chr3:118663697-118663747	HCT-116	colon:	n/a
37	chr3:118753871-118753921	GM12891	blood:	n/a
38	chr3:118753714-118753764	HIPEpiC	eye:	n/a
39	chr3:118753707-118753757	AG04449	skin:	fetal
40	chr3:118757898-118757948	PANC-1	pancreas:	n/a
41	chr3:118757898-118757948	AG09319	gingival:	n/a
42	chr3:118734756-118734806	NB4	blood:	n/a
43	chr3:118663534-118663584	NHBE	bronchial:	n/a
44	chr3:118663470-118663520	HCT-116	colon:	n/a
45	chr3:118754376-118754426	HCM	heart:	n/a
46	chr3:118663697-118663747	NHBE	bronchial:	n/a
47	chr3:118734756-118734806	SKMC	muscle:	n/a
48	chr3:118753660-118753710	AoSMC	blood vessel:	n/a
49	chr3:118663642-118663692	HRE	kidney:	n/a
50	chr3:118753714-118753764	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
2	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
3	chr3:118683148..118684956-chr3:118685063..118686921,2	K562	blood:
4	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
5	chr3:118648830..118650762-chr3:118659707..118662135,2	K562	blood:
6	chr3:118661298..118663595-chr3:118665722..118667353,2	K562	blood:
7	chr3:118655482..118657417-chr3:118667049..118669730,2	K562	blood:
8	chr3:118683148..118684956-chr3:118685063..118686921,2	K562	blood:
9	chr3:118650890..118655376-chr3:118655958..118658547,6	K562	blood:
10	chr3:118651043..118653014-chr3:118655958..118658566,3	K562	blood:
11	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
12	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
13	chr3:118675897..118678259-chr3:118679117..118681449,2	MCF-7	breast:
14	chr3:118675897..118678259-chr3:118679117..118681449,2	MCF-7	breast:
15	chr3:118656387..118657894-chr3:118659835..118662017,2	K562	blood:
16	chr3:118654131..118656982-chr3:118667151..118670304,3	K562	blood:
17	chr3:118655482..118657417-chr3:118667049..118669730,2	K562	blood:
18	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf30-1	chr3:118664715-118664882	NR_046230
2	lnc-C3orf30-1	chr3:118661920-118662033	ENSG00000239877.2
3	lnc-C3orf30-1	chr3:118663709-118663837	ENSG00000239877.2
4	lnc-C3orf30-1	chr3:118663709-118663837	NR_046230
5	lnc-C3orf30-1	chr3:118664715-118664882	ENSG00000239877.1
6	lnc-C3orf30-1	chr3:118664715-118664882	ENSG00000239877.2
7	lnc-C3orf30-1	chr3:118663709-118663837	ENSG00000239877.1
8	lnc-C3orf30-1	chr3:118665896-118667071	ENSG00000239877.1
9	lnc-C3orf30-1	chr3:118665896-118667088	ENSG00000239877.2
10	lnc-C3orf30-1	chr3:118661920-118662033	ENSG00000239877.1
11	lnc-B4GALT4-2	chr3:118667167-118667231	NONHSAT091373
12	lnc-C3orf30-1	chr3:118665896-118667088	NR_046230
13	lnc-C3orf30-1	chr3:118663709-118663837	NONHSAT091372
14	lnc-C3orf30-1	chr3:118661923-118662033	NR_046230
15	lnc-C3orf30-1	chr3:118661926-118662058	NONHSAT091372
16	lnc-C3orf30-1	chr3:118664715-118664882	NONHSAT091372
17	lnc-C3orf30-1	chr3:118665896-118667088	NONHSAT091372
18	lnc-B4GALT4-2	chr3:118668076-118668165	NONHSAT091373

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11-AS1	TF binding region
IGSF11	CpG island
IGSF11-AS1	CpG island
ENSG00000232429	chromatin interactions
ENSG00000144847	chromatin interactions
ENSG00000239877	chromatin interactions

Extended variants
information (count: 4038 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4038 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549287795	chr3:118657423-118657424	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs76704813	chr3:118657458-118657459	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146519289	chr3:118657497-118657498	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs376499330	chr3:118657610-118657611	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs573798294	chr3:118657624-118657625	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142010076	chr3:118657690-118657691	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540032921	chr3:118657712-118657713	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs558295390	chr3:118657713-118657714	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576747487	chr3:118657716-118657717	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs112366580	chr3:118657769-118657770	Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs144181697	chr3:118657804-118657805	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529644538	chr3:118657815-118657816	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541951960	chr3:118657846-118657847	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150656589	chr3:118657870-118657871	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs528716036	chr3:118657906-118657907	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547234213	chr3:118657942-118657943	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571844994	chr3:118657943-118657944	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs192935703	chr3:118657973-118657974	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs551255134	chr3:118657984-118657985	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4687961	chr3:118658003-118658004	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs116791376	chr3:118658014-118658015	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536249323	chr3:118658027-118658028	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555074864	chr3:118658048-118658049	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs184944535	chr3:118658056-118658057	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs534000272	chr3:118658057-118658058	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558334143	chr3:118658060-118658061	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs188256346	chr3:118658087-118658088	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs532593167	chr3:118658089-118658090	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs9814712	chr3:118658095-118658096	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574399422	chr3:118658140-118658141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541444154	chr3:118658148-118658149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560061614	chr3:118658186-118658187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527418521	chr3:118658244-118658245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545870481	chr3:118658280-118658281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374658444	chr3:118658301-118658302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565491457	chr3:118658398-118658399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192961266	chr3:118658414-118658415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567172195	chr3:118658421-118658422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372537315	chr3:118658422-118658423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569510213	chr3:118658424-118658425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34558286	chr3:118658435-118658436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185225252	chr3:118658445-118658446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530144357	chr3:118658473-118658474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548313176	chr3:118658479-118658480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189386299	chr3:118658494-118658495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151149942	chr3:118658495-118658496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60660207	chr3:118658498-118658499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367728079	chr3:118658512-118658513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12492855	chr3:118658518-118658519	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs181730449	chr3:118658525-118658526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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	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
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118620200-118663200	Weak transcription	Pancreas	Pancrea
2	chr3:118645200-118661600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:118645800-118661600	Weak transcription	Left Ventricle	heart
4	chr3:118647600-118661000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:118651800-118661200	Weak transcription	Right Atrium	heart
6	chr3:118653000-118660600	Weak transcription	Brain Angular Gyrus	brain
7	chr3:118653800-118661200	Weak transcription	Psoas Muscle	Psoas
8	chr3:118655400-118657800	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr3:118655800-118661000	Weak transcription	Brain Cingulate Gyrus	brain
10	chr3:118656000-118660800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr3:118656000-118661200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr3:118656200-118657400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:118656800-118657800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr3:118657000-118657600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr3:118657000-118657800	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr3:118657000-118657800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr3:118657000-118657800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr3:118657000-118657800	Enhancers	Hela-S3	cervix
19	chr3:118657200-118657400	Enhancers	Small Intestine	intestine
20	chr3:118657200-118657600	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:118657200-118657600	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr3:118657200-118657600	Enhancers	HUVEC	blood vessel
23	chr3:118657200-118657600	Enhancers	NHEK	skin
24	chr3:118657200-118657800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr3:118657200-118657800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr3:118657200-118657800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:118657200-118657800	Enhancers	HMEC	breast
28	chr3:118657200-118657800	Flanking Active TSS	K562	blood
29	chr3:118657200-118658000	Enhancers	Brain Anterior Caudate	brain
30	chr3:118657200-118658000	Flanking Active TSS	A549	lung
31	chr3:118657400-118657600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:118657600-118661200	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr3:118657800-118658800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:118657800-118660200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr3:118657800-118660200	Weak transcription	K562	blood
36	chr3:118657800-118660400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr3:118657800-118660600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr3:118657800-118661200	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr3:118658000-118668400	Weak transcription	A549	lung
40	chr3:118658800-118659000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr3:118659000-118661000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:118660200-118660800	Enhancers	K562	blood
43	chr3:118660200-118661200	Enhancers	Primary T cells from cord blood	blood
44	chr3:118660200-118662800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr3:118660400-118662200	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr3:118660600-118661000	Enhancers	Fetal Heart	heart
47	chr3:118660600-118662000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr3:118660600-118662000	Enhancers	Brain Angular Gyrus	brain
49	chr3:118660600-118662200	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr3:118660600-118662200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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