Variant report

Variant	esv3437356
Chromosome Location	chr2:233762908-233767406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:233764531-233764799	GM12878	blood:	n/a	n/a
2	BCL11A	chr2:233764191-233764835	GM12878	blood:	n/a	n/a
3	BCL11A	chr2:233764992-233765227	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:233765234-233765563	GM12878	blood:	n/a	n/a
5	BCL3	chr2:233765229-233765708	GM12878	blood:	n/a	n/a
6	BCL3	chr2:233764696-233765215	GM12878	blood:	n/a	n/a
7	BCL3	chr2:233763417-233765657	GM12878	blood:	n/a	n/a
8	BCL3	chr2:233763418-233764598	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:233766428-233767044	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr2:233766742-233766992	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:233766666-233767055	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:233766717-233767061	A549	lung:	n/a	n/a
13	CHD2	chr2:233766474-233767106	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:233763243-233763320	LNCaP	prostate:	n/a	n/a
15	CTCF	chr2:233766560-233766710	AG04449	skin:	n/a	n/a
16	CTCF	chr2:233766740-233766890	AG09319	gingival:	n/a	chr2:233766742-233766755
17	CTCF	chr2:233766800-233766950	HBMEC	blood vessel:	n/a	chr2:233766901-233766914
18	CTCF	chr2:233766740-233766890	HCPEpiC	choroid plexus:	n/a	chr2:233766742-233766755
19	CUX1	chr2:233763256-233763290	K562	blood:	n/a	n/a
20	ELK1	chr2:233766776-233767120	Hela-S3	cervix:	n/a	n/a
21	EP300	chr2:233766650-233767063	SK-N-SH_RA	brain:	n/a	chr2:233766828-233766844
22	EP300	chr2:233766668-233767012	SK-N-SH_RA	brain:	n/a	chr2:233766828-233766844
23	EP300	chr2:233766708-233767037	Hela-S3	cervix:	n/a	chr2:233766828-233766844
24	ETS1	chr2:233766676-233767081	A549	lung:	n/a	chr2:233766845-233766860
25	FOS	chr2:233766687-233767056	MCF10A-Er-Src	breast:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
26	FOS	chr2:233766681-233767051	MCF10A-Er-Src	breast:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
27	FOS	chr2:233766640-233767050	MCF10A-Er-Src	breast:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
28	FOS	chr2:233766659-233767263	MCF10A-Er-Src	breast:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
29	FOS	chr2:233766669-233767104	Hela-S3	cervix:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
30	FOS	chr2:233766288-233767253	HUVEC	blood vessel:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766866-233766877 chr2:233766868-233766875
31	FOSL1	chr2:233766744-233766977	K562	blood:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
32	FOSL1	chr2:233766181-233767251	HCT-116	colon:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
33	FOSL1	chr2:233766268-233767381	HCT-116	colon:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
34	FOSL2	chr2:233766650-233767079	A549	lung:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
35	FOSL2	chr2:233766613-233767146	MCF-7	breast:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
36	FOSL2	chr2:233766662-233766998	HepG2	liver:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
37	FOSL2	chr2:233766621-233767088	HepG2	liver:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
38	FOSL2	chr2:233766564-233767118	SK-N-SH	brain:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
39	FOSL2	chr2:233766258-233767212	SK-N-SH	brain:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
40	FOSL2	chr2:233766391-233767311	A549	lung:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766839-233766850 chr2:233766868-233766875
41	GABPA	chr2:233766766-233766984	A549	lung:	n/a	n/a
42	GABPA	chr2:233766628-233767090	A549	lung:	n/a	n/a
43	GTF2F1	chr2:233766552-233766989	Hela-S3	cervix:	n/a	n/a
44	JUN	chr2:233766636-233767066	HUVEC	blood vessel:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
45	JUN	chr2:233766466-233767184	K562	blood:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
46	JUN	chr2:233766700-233767053	Hela-S3	cervix:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
47	JUN	chr2:233766717-233767049	K562	blood:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
48	JUN	chr2:233766815-233766964	HepG2	liver:	n/a	chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
49	JUND	chr2:233766568-233767106	Hela-S3	cervix:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875
50	JUND	chr2:233766719-233766989	HepG2	liver:	n/a	chr2:233766840-233766851 chr2:233766868-233766876 chr2:233766867-233766877 chr2:233766868-233766875

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233765616-233765666	MCF10A-Er-Src	breast:	n/a
2	chr2:233765616-233765666	A549	lung:	n/a
3	chr2:233766002-233766052	SAEC	small airway:	n/a
4	chr2:233765616-233765666	HRPEpiC	eye:	n/a
5	chr2:233764831-233764881	Hela-S3	cervix:	n/a
6	chr2:233766002-233766052	HIPEpiC	eye:	n/a
7	chr2:233766658-233766708	HCF	heart:	n/a
8	chr2:233766118-233766168	IMR90	lung:	fetal
9	chr2:233766658-233766708	HL-60	blood:	n/a
10	chr2:233766118-233766168	SKMC	muscle:	n/a
11	chr2:233766118-233766168	H1-hESC	embryonic stem cell:	embryo
12	chr2:233766002-233766052	NHBE	bronchial:	n/a
13	chr2:233765616-233765666	SKMC	muscle:	n/a
14	chr2:233765872-233765922	ovcar-3	ovarian:	n/a
15	chr2:233766118-233766168	GM12892	blood:	n/a
16	chr2:233765616-233765666	T-47D	breast:	n/a
17	chr2:233765616-233765666	CMK	blood:	n/a
18	chr2:233765616-233765666	HCM	heart:	n/a
19	chr2:233764831-233764881	ovcar-3	ovarian:	n/a
20	chr2:233766002-233766052	CMK	blood:	n/a
21	chr2:233764831-233764881	NHBE	bronchial:	n/a
22	chr2:233766658-233766708	MCF10A-Er-Src	breast:	n/a
23	chr2:233764831-233764881	ProgFib	skin:	n/a
24	chr2:233766118-233766168	Caco-2	colon:	n/a
25	chr2:233765616-233765666	HNPCEpiC	eye:	n/a
26	chr2:233765616-233765666	HRE	kidney:	n/a
27	chr2:233766118-233766168	ProgFib	skin:	n/a
28	chr2:233765872-233765922	HUVEC	blood vessel:	n/a
29	chr2:233766002-233766052	AG10803	skin:	n/a
30	chr2:233765616-233765666	SK-N-SH	brain:	n/a
31	chr2:233766002-233766052	HCF	heart:	n/a
32	chr2:233765872-233765922	HL-60	blood:	n/a
33	chr2:233765872-233765922	K562	blood:	n/a
34	chr2:233766118-233766168	K562	blood:	n/a
35	chr2:233765872-233765922	HCM	heart:	n/a
36	chr2:233766658-233766708	HCT-116	colon:	n/a
37	chr2:233766118-233766168	T-47D	breast:	n/a
38	chr2:233766118-233766168	HAEpiC	amniotic membrane:	n/a
39	chr2:233766002-233766052	PrEC	prostate:	n/a
40	chr2:233766118-233766168	AoSMC	blood vessel:	n/a
41	chr2:233766002-233766052	T-47D	breast:	n/a
42	chr2:233765616-233765666	GM06990	blood:	n/a
43	chr2:233766118-233766168	HNPCEpiC	eye:	n/a
44	chr2:233766002-233766052	AG04450	lung:	fetal
45	chr2:233766002-233766052	HepG2	liver:	n/a
46	chr2:233765616-233765666	NB4	blood:	n/a
47	chr2:233766658-233766708	HRPEpiC	eye:	n/a
48	chr2:233766658-233766708	RPTEC	kidney:	n/a
49	chr2:233766002-233766052	Hela-S3	cervix:	n/a
50	chr2:233766002-233766052	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:233755071..233758000-chr2:233760102..233763754,5	MCF-7	breast:
2	chr2:233766884..233768683-chr2:233770434..233772099,2	K562	blood:

Variant related genes	Relation type
NGEF	TF binding region
NGEF	CpG island
ENSG00000066248	chromatin interactions

Extended variants
information (count: 314 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113718721	chr2:233762912-233762913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577648010	chr2:233762947-233762948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546540035	chr2:233763051-233763052	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563128053	chr2:233763052-233763053	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs142231021	chr2:233763054-233763055	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372948048	chr2:233763062-233763063	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2592114	chr2:233763064-233763065	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561081616	chr2:233763069-233763070	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs529729243	chr2:233763087-233763088	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546421139	chr2:233763089-233763090	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566343399	chr2:233763266-233763267	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs538420640	chr2:233763273-233763274	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115915053	chr2:233763326-233763327	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189693086	chr2:233763342-233763343	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12477794	chr2:233763362-233763363	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs554663326	chr2:233763386-233763387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574905590	chr2:233763479-233763480	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374225519	chr2:233763496-233763497	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs534022353	chr2:233763561-233763562	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554275134	chr2:233763570-233763571	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372968417	chr2:233763655-233763656	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546376490	chr2:233763680-233763681	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556409169	chr2:233763682-233763683	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563213327	chr2:233763683-233763684	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372205693	chr2:233763693-233763694	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532506706	chr2:233763694-233763695	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201092968	chr2:233763717-233763718	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141119753	chr2:233763752-233763753	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181292451	chr2:233763800-233763801	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs140345101	chr2:233763825-233763826	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs544222286	chr2:233763832-233763833	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs541444190	chr2:233763846-233763847	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs200265328	chr2:233763855-233763856	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs142804753	chr2:233763857-233763858	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs369452011	chr2:233763860-233763861	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs560705454	chr2:233763887-233763888	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs529657367	chr2:233763907-233763908	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs199824333	chr2:233763913-233763914	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs151240038	chr2:233763921-233763922	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539963090	chr2:233763925-233763926	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs115397492	chr2:233763937-233763938	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574946908	chr2:233763946-233763947	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs532185107	chr2:233763962-233763963	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs551945142	chr2:233763965-233763966	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs569182495	chr2:233763966-233763967	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs10580077	chr2:233763981-233763982	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs398061181	chr2:233763987-233763988	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs531487146	chr2:233763999-233764000	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs540838925	chr2:233764002-233764003	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs548600760	chr2:233764022-233764023	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233749400-233766000	Weak transcription	A549	lung
2	chr2:233751000-233766000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:233756200-233763600	Weak transcription	NHLF	lung
4	chr2:233756400-233763800	Weak transcription	Right Atrium	heart
5	chr2:233756600-233763400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr2:233756600-233766400	Weak transcription	Brain Substantia Nigra	brain
7	chr2:233756800-233765400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:233757000-233765400	Weak transcription	Pancreas	Pancrea
9	chr2:233757000-233766200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:233757000-233766200	Weak transcription	Fetal Brain Female	brain
11	chr2:233757000-233766400	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:233757200-233763400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr2:233757400-233776600	Weak transcription	Brain Angular Gyrus	brain
14	chr2:233757600-233763400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr2:233757800-233763400	Weak transcription	Gastric	stomach
16	chr2:233758200-233768800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr2:233759000-233763200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr2:233759200-233784400	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr2:233759400-233763400	Weak transcription	Fetal Intestine Small	intestine
20	chr2:233759400-233765800	Weak transcription	Esophagus	oesophagus
21	chr2:233759800-233763200	Weak transcription	Liver	Liver
22	chr2:233759800-233763400	Weak transcription	Spleen	Spleen
23	chr2:233759800-233766000	Weak transcription	Colonic Mucosa	Colon
24	chr2:233759800-233766400	Weak transcription	HepG2	liver
25	chr2:233761000-233765800	Weak transcription	Brain Anterior Caudate	brain
26	chr2:233761800-233763600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr2:233762800-233764000	Strong transcription	Duodenum Mucosa	Duodenum
28	chr2:233763200-233764000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:233763200-233764200	Strong transcription	Liver	Liver
30	chr2:233763200-233766200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr2:233763400-233763600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr2:233763400-233763600	Strong transcription	Fetal Intestine Small	intestine
33	chr2:233763400-233763600	Genic enhancers	Gastric	stomach
34	chr2:233763400-233763600	Enhancers	Stomach Mucosa	stomach
35	chr2:233763400-233764000	Genic enhancers	Brain Cingulate Gyrus	brain
36	chr2:233763400-233764000	Strong transcription	Rectal Mucosa Donor 31	rectum
37	chr2:233763400-233764200	Genic enhancers	Spleen	Spleen
38	chr2:233763600-233763800	Bivalent Enhancer	Fetal Heart	heart
39	chr2:233763600-233763800	Enhancers	Fetal Kidney	kidney
40	chr2:233763600-233763800	Active TSS	Fetal Lung	lung
41	chr2:233763600-233763800	Flanking Active TSS	Right Ventricle	heart
42	chr2:233763600-233764000	Strong transcription	Gastric	stomach
43	chr2:233763600-233764200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:233763600-233764200	Enhancers	NHLF	lung
45	chr2:233763600-233764400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr2:233763600-233765600	Weak transcription	Fetal Intestine Small	intestine
47	chr2:233763600-233766000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr2:233763800-233764000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:233763800-233764000	Flanking Active TSS	Fetal Lung	lung
50	chr2:233763800-233764000	Enhancers	Right Atrium	heart

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