Variant report

Variant	nsv237800
Chromosome Location	chr3:133178030-133185521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:278)
CpG islands
(count:123)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:133185291-133186134	GM12878	blood:	n/a	n/a
2	BATF	chr3:133183505-133183734	GM12878	blood:	n/a	n/a
3	BCLAF1	chr3:133183407-133183825	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:133185370-133185738	GM12878	blood:	n/a	n/a
5	CEBPB	chr3:133182281-133182765	MCF-7	breast:	n/a	n/a
6	CEBPB	chr3:133180018-133180708	MCF-7	breast:	n/a	n/a
7	CEBPB	chr3:133181289-133181524	HepG2	liver:	n/a	chr3:133181406-133181417
8	CEBPB	chr3:133180044-133180474	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:133182556-133182558	K562	blood:	n/a	n/a
10	CEBPB	chr3:133180147-133180507	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr3:133180124-133180496	HepG2	liver:	n/a	n/a
12	CEBPZ	chr3:133178468-133178491	HepG2	liver:	n/a	n/a
13	CTCF	chr3:133183520-133183670	HPF	lung:	n/a	n/a
14	CTCF	chr3:133183540-133183690	HAc	cerebellar:	n/a	n/a
15	CTCF	chr3:133183580-133183730	HCM	heart:	n/a	n/a
16	CTCF	chr3:133183391-133183764	IMR90	lung:	n/a	n/a
17	CTCF	chr3:133183540-133183690	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr3:133183500-133183650	GM12871	blood:	n/a	n/a
19	CTCF	chr3:133183480-133183630	A549	lung:	n/a	n/a
20	CTCF	chr3:133183500-133183650	GM12869	blood:	n/a	n/a
21	CTCF	chr3:133183520-133183670	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr3:133183520-133183670	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr3:133183500-133183650	GM12866	blood:	n/a	n/a
24	CTCF	chr3:133183606-133183654	NHEK	skin:	n/a	n/a
25	CTCF	chr3:133183540-133183690	GM12873	blood:	n/a	n/a
26	CTCF	chr3:133183500-133183650	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr3:133183480-133183630	HPF	lung:	n/a	n/a
28	CTCF	chr3:133183292-133183856	A549	lung:	n/a	n/a
29	CTCF	chr3:133183560-133183710	HVMF	connective:	n/a	n/a
30	CTCF	chr3:133183520-133183670	GM12874	blood:	n/a	n/a
31	CTCF	chr3:133183540-133183690	HRE	kidney:	n/a	n/a
32	CTCF	chr3:133183500-133183650	GM12870	blood:	n/a	n/a
33	CTCF	chr3:133183507-133183674	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:133183500-133183650	HCT-116	colon:	n/a	n/a
35	CTCF	chr3:133183494-133183679	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr3:133183488-133183665	GM13977	blood:	n/a	n/a
37	CTCF	chr3:133183475-133183679	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr3:133183552-133183603	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr3:133183490-133183588	HepG2	liver:	n/a	n/a
40	CTCF	chr3:133183500-133183650	AG09319	gingival:	n/a	n/a
41	CTCF	chr3:133183563-133183592	K562	blood:	n/a	n/a
42	CTCF	chr3:133183480-133183630	GM12864	blood:	n/a	n/a
43	CTCF	chr3:133183499-133183654	GM13976	blood:	n/a	n/a
44	CTCF	chr3:133183442-133183639	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr3:133183361-133183941	SK-N-SH	brain:	n/a	n/a
46	CTCF	chr3:133183560-133183710	GM06990	blood:	n/a	n/a
47	CTCF	chr3:133183464-133183656	GM10266	blood:	n/a	n/a
48	CTCF	chr3:133183520-133183670	AG04449	skin:	n/a	n/a
49	CTCF	chr3:133183510-133183642	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:133183520-133183670	AG09319	gingival:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133180261-133180311	Hela-S3	cervix:	n/a
2	chr3:133180261-133180311	Hela-S3	cervix:	n/a
3	chr3:133182835-133182885	HepG2	liver:	n/a
4	chr3:133182835-133182885	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:133180261-133180311	T-47D	breast:	n/a
6	chr3:133182835-133182885	HL-60	blood:	n/a
7	chr3:133182835-133182885	HUVEC	blood vessel:	n/a
8	chr3:133182835-133182885	GM12892	blood:	n/a
9	chr3:133182835-133182885	NHDF-neo	bronchial:	n/a
10	chr3:133180261-133180311	GM12892	blood:	n/a
11	chr3:133180261-133180311	GM06990	blood:	n/a
12	chr3:133182835-133182885	HRE	kidney:	n/a
13	chr3:133182835-133182885	HCF	heart:	n/a
14	chr3:133182835-133182885	ovcar-3	ovarian:	n/a
15	chr3:133182835-133182885	SK-N-MC	brain:	n/a
16	chr3:133182835-133182885	Caco-2	colon:	n/a
17	chr3:133180261-133180311	SK-N-SH	brain:	n/a
18	chr3:133180261-133180311	AG04449	skin:	fetal
19	chr3:133182835-133182885	PANC-1	pancreas:	n/a
20	chr3:133182835-133182885	HCM	heart:	n/a
21	chr3:133182835-133182885	A549	lung:	n/a
22	chr3:133182835-133182885	K562	blood:	n/a
23	chr3:133182835-133182885	RPTEC	kidney:	n/a
24	chr3:133180261-133180311	H1-hESC	embryonic stem cell:	embryo
25	chr3:133180261-133180311	LNCaP	prostate:	n/a
26	chr3:133182835-133182885	NH-A	brain:	n/a
27	chr3:133182835-133182885	SKMC	muscle:	n/a
28	chr3:133182835-133182885	GM06990	blood:	n/a
29	chr3:133180261-133180311	SAEC	small airway:	n/a
30	chr3:133180261-133180311	ovcar-3	ovarian:	n/a
31	chr3:133180261-133180311	AG04450	lung:	fetal
32	chr3:133180261-133180311	HPAEpiC	pulmonary alveolar:	n/a
33	chr3:133182835-133182885	Jurkat	blood:	n/a
34	chr3:133182835-133182885	T-47D	breast:	n/a
35	chr3:133180261-133180311	HAEpiC	amniotic membrane:	n/a
36	chr3:133180261-133180311	GM12878	blood:	n/a
37	chr3:133180261-133180311	HIPEpiC	eye:	n/a
38	chr3:133182835-133182885	HMEC	breast:	n/a
39	chr3:133182835-133182885	AG04449	skin:	fetal
40	chr3:133180261-133180311	NH-A	brain:	n/a
41	chr3:133180261-133180311	HCT-116	colon:	n/a
42	chr3:133182835-133182885	HEEpiC	esophagus:	n/a
43	chr3:133180261-133180311	ECC-1	luminal epithelium:	n/a
44	chr3:133182835-133182885	AG09309	skin:	n/a
45	chr3:133182835-133182885	NT2-D1	testis:	n/a
46	chr3:133182835-133182885	HNPCEpiC	eye:	n/a
47	chr3:133180261-133180311	MCF10A-Er-Src	breast:	n/a
48	chr3:133180261-133180311	AG10803	skin:	n/a
49	chr3:133180261-133180311	BE2_C	brain:	n/a
50	chr3:133182835-133182885	Hepatocyte	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:133180499..133182281-chr3:133188502..133190705,2	MCF-7	breast:
2	chr3:133161498..133163430-chr3:133177580..133180492,2	MCF-7	breast:
3	chr3:133169398..133190840-chr3:133288286..133298861,41	MCF-7	breast:
4	chr3:133180154..133181710-chr3:133287523..133290190,2	MCF-7	breast:
5	chr3:133182317..133184120-chr3:133296724..133299109,2	MCF-7	breast:
6	chr3:133166486..133169051-chr3:133181517..133184490,2	MCF-7	breast:
7	chr3:133153374..133155623-chr3:133178756..133181568,2	MCF-7	breast:
8	chr3:133175597..133178522-chr3:133290456..133293347,3	MCF-7	breast:
9	chr3:133180327..133181853-chr3:133181928..133184881,2	MCF-7	breast:
10	chr3:133182617..133183639-chr3:133297124..133298374,5	MCF-7	breast:
11	chr3:133179282..133181210-chr3:133205623..133208031,2	MCF-7	breast:
12	chr3:133173610..133177245-chr3:133178784..133182075,5	MCF-7	breast:
13	chr3:133179034..133181660-chr3:133249507..133251496,2	MCF-7	breast:
14	chr3:133180327..133181853-chr3:133181928..133184881,2	MCF-7	breast:
15	chr3:133179746..133182359-chr3:133292415..133294343,2	K562	blood:
16	chr3:133167608..133169678-chr3:133177159..133179764,2	MCF-7	breast:
17	chr3:133179819..133183044-chr3:133290517..133294355,4	MCF-7	breast:
18	chr3:133182278..133184590-chr3:133188280..133190685,2	MCF-7	breast:
19	chr3:133182951..133184510-chr3:133300267..133301904,2	K562	blood:
20	chr3:133178497..133180168-chr3:133538134..133540708,2	MCF-7	breast:

No data

Variant related genes	Relation type
BFSP2-AS1	TF binding region
BFSP2-AS1	CpG island
ENSG00000249993	chromatin interactions
ENSG00000091527	chromatin interactions
ENSG00000170819	chromatin interactions

Extended variants
information (count: 289 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190127123	chr3:133178059-133178060	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs35207395	chr3:133178075-133178076	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs563621524	chr3:133178078-133178079	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs532539833	chr3:133178098-133178099	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs552503648	chr3:133178102-133178103	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs565944250	chr3:133178107-133178108	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs528559360	chr3:133178119-133178120	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs548408877	chr3:133178120-133178121	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs568301249	chr3:133178123-133178124	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs181288080	chr3:133178125-133178126	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11715830	chr3:133178148-133178149	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549073843	chr3:133178230-133178231	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs111569943	chr3:133178271-133178272	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs539756403	chr3:133178346-133178347	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs371685282	chr3:133178426-133178427	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs1317554	chr3:133178432-133178433	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541102869	chr3:133178436-133178437	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs372873084	chr3:133178463-133178464	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554731231	chr3:133178469-133178470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs114824634	chr3:133178500-133178501	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs185883635	chr3:133178514-133178515	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs563481736	chr3:133178522-133178523	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs532401771	chr3:133178541-133178542	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs548234816	chr3:133178556-133178557	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs567986330	chr3:133178567-133178568	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs77424388	chr3:133178585-133178586	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs150550290	chr3:133178629-133178630	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs561895686	chr3:133178641-133178642	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs112064980	chr3:133178676-133178677	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs138586838	chr3:133178704-133178705	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs372433501	chr3:133178814-133178815	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs550724360	chr3:133178885-133178886	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149334582	chr3:133178889-133178890	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540088874	chr3:133178919-133178920	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs554267393	chr3:133178953-133178954	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs4557153	chr3:133179056-133179057	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs4521226	chr3:133179057-133179058	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs547010395	chr3:133179137-133179138	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs4283572	chr3:133179143-133179144	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs530498479	chr3:133179177-133179178	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs534367455	chr3:133179194-133179195	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs4571241	chr3:133179200-133179201	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs370875195	chr3:133179204-133179205	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs188099301	chr3:133179240-133179241	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs115948875	chr3:133179247-133179248	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs144592504	chr3:133179252-133179253	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs576979876	chr3:133179258-133179259	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs139485625	chr3:133179312-133179313	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs144998769	chr3:133179325-133179326	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs553728278	chr3:133179341-133179342	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133161000-133191000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:133165400-133178600	Weak transcription	Aorta	Aorta
3	chr3:133168200-133178800	Weak transcription	Fetal Kidney	kidney
4	chr3:133169800-133179400	Weak transcription	GM12878-XiMat	blood
5	chr3:133172400-133178400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:133172400-133178400	Weak transcription	Stomach Mucosa	stomach
7	chr3:133173000-133178400	Weak transcription	HepG2	liver
8	chr3:133173400-133178200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:133175000-133178800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:133175000-133179600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:133175400-133178200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr3:133176200-133178400	Weak transcription	Placenta	Placenta
13	chr3:133176200-133178600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr3:133177200-133185800	Enhancers	Fetal Thymus	thymus
15	chr3:133177400-133180600	Enhancers	Thymus	Thymus
16	chr3:133177600-133181600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:133177800-133178600	Enhancers	A549	lung
18	chr3:133177800-133179000	Enhancers	Liver	Liver
19	chr3:133177800-133179200	Enhancers	Colon Smooth Muscle	Colon
20	chr3:133177800-133179600	Enhancers	Esophagus	oesophagus
21	chr3:133177800-133180000	Enhancers	Fetal Stomach	stomach
22	chr3:133178000-133178400	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr3:133178000-133179000	Enhancers	Stomach Smooth Muscle	stomach
24	chr3:133178000-133180800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr3:133178200-133178400	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr3:133178200-133178600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:133178200-133178600	Enhancers	Fetal Muscle Trunk	muscle
28	chr3:133178200-133178600	Enhancers	Left Ventricle	heart
29	chr3:133178200-133178600	Enhancers	Ovary	ovary
30	chr3:133178200-133178600	Enhancers	Right Ventricle	heart
31	chr3:133178200-133179000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr3:133178200-133179000	Enhancers	Fetal Lung	lung
33	chr3:133178200-133179600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr3:133178200-133180000	Enhancers	Adipose Nuclei	Adipose
35	chr3:133178200-133180000	Enhancers	Psoas Muscle	Psoas
36	chr3:133178200-133180000	Enhancers	Right Atrium	heart
37	chr3:133178200-133180400	Enhancers	Fetal Muscle Leg	muscle
38	chr3:133178200-133180600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr3:133178200-133181000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr3:133178200-133181400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr3:133178400-133178600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr3:133178400-133178600	Bivalent Enhancer	NHLF	lung
43	chr3:133178400-133178800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr3:133178400-133178800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:133178400-133178800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr3:133178400-133178800	Enhancers	Brain Hippocampus Middle	brain
47	chr3:133178400-133178800	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr3:133178400-133178800	Enhancers	HepG2	liver
49	chr3:133178400-133179400	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:133178400-133180000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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