Variant report

Variant	nsv875765
Chromosome Location	chr2:210537660-210618203
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 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	chr2:210561560-210562437	GM12878	blood:	n/a	n/a
2	BATF	chr2:210561879-210562321	GM12878	blood:	n/a	n/a
3	BATF	chr2:210562123-210562326	GM12878	blood:	n/a	n/a
4	BATF	chr2:210561591-210561821	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:210561690-210562362	GM12878	blood:	n/a	n/a
6	BRCA1	chr2:210559306-210559317	GM12878	blood:	n/a	n/a
7	CEBPB	chr2:210617765-210618128	HepG2	liver:	n/a	chr2:210617945-210617956
8	CEBPB	chr2:210577229-210577377	A549	lung:	n/a	n/a
9	CEBPB	chr2:210575979-210576557	HepG2	liver:	n/a	chr2:210576423-210576434
10	CEBPB	chr2:210555600-210555864	A549	lung:	n/a	n/a
11	CEBPB	chr2:210560644-210560875	HepG2	liver:	n/a	chr2:210560761-210560772
12	CEBPB	chr2:210594256-210594501	A549	lung:	n/a	chr2:210594346-210594357 chr2:210594386-210594397
13	CEBPB	chr2:210555569-210555888	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:210617847-210618039	K562	blood:	n/a	chr2:210617945-210617956
15	CEBPB	chr2:210549572-210549682	A549	lung:	n/a	n/a
16	CEBPB	chr2:210617771-210618086	A549	lung:	n/a	chr2:210617945-210617956
17	CEBPB	chr2:210617771-210618092	IMR90	lung:	n/a	chr2:210617945-210617956
18	CEBPB	chr2:210594220-210594544	HepG2	liver:	n/a	chr2:210594346-210594357 chr2:210594386-210594397
19	CEBPB	chr2:210555645-210555863	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:210585969-210586291	HepG2	liver:	n/a	chr2:210586122-210586133
21	CEBPB	chr2:210576253-210576560	IMR90	lung:	n/a	chr2:210576423-210576434
22	CEBPB	chr2:210576347-210576414	A549	lung:	n/a	n/a
23	CEBPB	chr2:210576359-210576561	K562	blood:	n/a	chr2:210576423-210576434
24	CEBPB	chr2:210555562-210555880	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:210617852-210618033	H1-hESC	embryonic stem cell:	n/a	chr2:210617945-210617956
26	CTCF	chr2:210557620-210557770	HepG2	liver:	n/a	n/a
27	CTCF	chr2:210574739-210574803	GM20000	blood:	n/a	n/a
28	CTCF	chr2:210591256-210591289	Lung_OC	lung:	n/a	n/a
29	CTCF	chr2:210562591-210562623	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chr2:210544780-210544930	HCT-116	colon:	n/a	n/a
31	CTCF	chr2:210547174-210547209	Lung_OC	lung:	n/a	n/a
32	CTCF	chr2:210600660-210600810	GM12869	blood:	n/a	n/a
33	CTCF	chr2:210558120-210558270	GM12875	blood:	n/a	n/a
34	CUX1	chr2:210563082-210563270	GM12878	blood:	n/a	n/a
35	CUX1	chr2:210561801-210562415	GM12878	blood:	n/a	chr2:210562144-210562158
36	E2F4	chr2:210553208-210553570	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr2:210591098-210591340	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr2:210598066-210598515	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr2:210556998-210557297	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr2:210577059-210577276	MCF10A-Er-Src	breast:	n/a	n/a
41	EBF1	chr2:210561758-210562263	GM12878	blood:	n/a	n/a
42	EBF1	chr2:210560779-210561047	GM12878	blood:	n/a	chr2:210560949-210560960 chr2:210560931-210560942
43	EP300	chr2:210606362-210606631	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr2:210561749-210562341	GM12878	blood:	n/a	chr2:210562261-210562275 chr2:210562315-210562329
45	EP300	chr2:210566374-210566641	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr2:210566208-210566924	SK-N-SH	brain:	n/a	chr2:210566254-210566264
47	EP300	chr2:210606053-210607502	SK-N-SH	brain:	n/a	n/a
48	EP300	chr2:210586025-210586786	SK-N-SH	brain:	n/a	chr2:210586123-210586137 chr2:210586464-210586473
49	EP300	chr2:210567420-210567928	SK-N-SH_RA	brain:	n/a	chr2:210567526-210567540
50	EP300	chr2:210586020-210586844	SK-N-SH	brain:	n/a	chr2:210586123-210586137 chr2:210586464-210586473

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210616647-210616697	HEEpiC	esophagus:	n/a
2	chr2:210557706-210557756	Jurkat	blood:	n/a
3	chr2:210557706-210557756	HRCEpiC	kidney:	n/a
4	chr2:210557706-210557756	GM12892	blood:	n/a
5	chr2:210597871-210597921	AG04450	lung:	fetal
6	chr2:210597871-210597921	HRCEpiC	kidney:	n/a
7	chr2:210597871-210597921	HCPEpiC	choroid plexus:	n/a
8	chr2:210616647-210616697	U87	brain:	n/a
9	chr2:210597871-210597921	SAEC	small airway:	n/a
10	chr2:210616647-210616697	GM12891	blood:	n/a
11	chr2:210597871-210597921	Jurkat	blood:	n/a
12	chr2:210597871-210597921	ovcar-3	ovarian:	n/a
13	chr2:210557706-210557756	Hepatocyte	liver:	n/a
14	chr2:210616647-210616697	AG04449	skin:	fetal
15	chr2:210616647-210616697	PFSK-1	brain:	n/a
16	chr2:210557706-210557756	HEK293	kidney:	embryo
17	chr2:210557706-210557756	HL-60	blood:	n/a
18	chr2:210597871-210597921	BJ	skin:	n/a
19	chr2:210616647-210616697	SKMC	muscle:	n/a
20	chr2:210616647-210616697	GM12878	blood:	n/a
21	chr2:210597871-210597921	GM12892	blood:	n/a
22	chr2:210597871-210597921	Hela-S3	cervix:	n/a
23	chr2:210557706-210557756	IMR90	lung:	fetal
24	chr2:210597871-210597921	AG10803	skin:	n/a
25	chr2:210597871-210597921	GM12878	blood:	n/a
26	chr2:210597871-210597921	GM12891	blood:	n/a
27	chr2:210557706-210557756	AG09319	gingival:	n/a
28	chr2:210557706-210557756	LNCaP	prostate:	n/a
29	chr2:210616647-210616697	LNCaP	prostate:	n/a
30	chr2:210557706-210557756	AG04450	lung:	fetal
31	chr2:210557706-210557756	Hela-S3	cervix:	n/a
32	chr2:210557706-210557756	HMEC	breast:	n/a
33	chr2:210597871-210597921	SK-N-SH_RA	brain:	n/a
34	chr2:210616647-210616697	SK-N-SH	brain:	n/a
35	chr2:210597871-210597921	HIPEpiC	eye:	n/a
36	chr2:210616647-210616697	ECC-1	luminal epithelium:	n/a
37	chr2:210557706-210557756	ovcar-3	ovarian:	n/a
38	chr2:210616647-210616697	NB4	blood:	n/a
39	chr2:210597871-210597921	NHDF-neo	bronchial:	n/a
40	chr2:210597871-210597921	Caco-2	colon:	n/a
41	chr2:210557706-210557756	NHDF-neo	bronchial:	n/a
42	chr2:210557706-210557756	GM12878	blood:	n/a
43	chr2:210597871-210597921	AoSMC	blood vessel:	n/a
44	chr2:210616647-210616697	Hela-S3	cervix:	n/a
45	chr2:210557706-210557756	HUVEC	blood vessel:	n/a
46	chr2:210557706-210557756	MCF-7	breast:	n/a
47	chr2:210616647-210616697	HNPCEpiC	eye:	n/a
48	chr2:210597871-210597921	MCF10A-Er-Src	breast:	n/a
49	chr2:210557706-210557756	SK-N-MC	brain:	n/a
50	chr2:210597871-210597921	AG04449	skin:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:210583521..210585486-chr2:210593240..210596147,2	MCF-7	breast:
2	chr2:210538640..210540966-chr2:210544100..210546598,2	K562	blood:
3	chr2:210552164..210552796-chr6:157542121..157542793,2	HCT-116	colon:
4	chr2:210565316..210567066-chr2:210695462..210698010,2	K562	blood:
5	chr1:117887756..117888531-chr2:210557968..210558828,2	MCF-7	breast:
6	chr2:210538640..210540966-chr2:210544100..210546598,2	K562	blood:
7	chr2:210538146..210538666-chr20:1193654..1194280,2	K562	blood:
8	chr2:210583521..210585486-chr2:210593240..210596147,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC80-1	chr2:210595376-210597491	ncRnaDb_ncrna_FR060983_1

No data

Variant related genes	Relation type
RNA5SP118	TF binding region
MAP2	TF binding region
RNA5SP118	CpG island
MAP2	CpG island

Extended variants
information (count: 2250 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2250 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530102696	chr2:210537661-210537662	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75968051	chr2:210537804-210537805	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182974319	chr2:210537834-210537835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114850581	chr2:210537843-210537844	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs3768823	chr2:210537908-210537909	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs386654671	chr2:210538006-210538007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3768821	chr2:210538007-210538008	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548173258	chr2:210538018-210538019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187529428	chr2:210538034-210538035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371988061	chr2:210538038-210538039	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533903409	chr2:210538058-210538059	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150215172	chr2:210538078-210538079	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570596429	chr2:210538084-210538085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539580217	chr2:210538156-210538157	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556188857	chr2:210538190-210538191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373732136	chr2:210538260-210538261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575904837	chr2:210538271-210538272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544217104	chr2:210538287-210538288	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377055771	chr2:210538288-210538289	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554580597	chr2:210538299-210538300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574486522	chr2:210538349-210538350	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193274625	chr2:210538428-210538429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560591903	chr2:210538451-210538452	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532599257	chr2:210538557-210538558	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3768820	chr2:210538610-210538611	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs563054458	chr2:210538664-210538665	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs568160546	chr2:210538752-210538753	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138892289	chr2:210538759-210538760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185418238	chr2:210538791-210538792	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187539360	chr2:210538825-210538826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72999560	chr2:210538828-210538829	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527270008	chr2:210538905-210538906	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370650188	chr2:210538918-210538919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547186348	chr2:210538938-210538939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570482753	chr2:210538952-210538953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539279166	chr2:210538979-210538980	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76776683	chr2:210538997-210538998	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191973219	chr2:210539007-210539008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141920716	chr2:210539075-210539076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536529977	chr2:210539215-210539216	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77199316	chr2:210539250-210539251	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537357148	chr2:210539257-210539258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541161149	chr2:210539289-210539290	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550565549	chr2:210539307-210539308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150597155	chr2:210539345-210539346	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559498220	chr2:210539346-210539347	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184525760	chr2:210539349-210539350	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148034692	chr2:210539353-210539354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540572098	chr2:210539355-210539356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs58681596	chr2:210539385-210539386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	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
Prostate cancer	18632612	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
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Developmental delay	21147756	CNVD
Mantle cell lymphoma	21518781	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210518200-210543200	Weak transcription	Aorta	Aorta
2	chr2:210528600-210550200	Weak transcription	Brain Substantia Nigra	brain
3	chr2:210528800-210550200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:210531400-210587800	Weak transcription	Brain Angular Gyrus	brain
5	chr2:210536400-210544800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:210536600-210539400	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr2:210536600-210545400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:210536600-210552200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:210536800-210537800	Enhancers	Fetal Brain Female	brain
10	chr2:210537000-210541800	Weak transcription	Brain Anterior Caudate	brain
11	chr2:210537000-210543200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr2:210537000-210545800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:210537000-210550400	Weak transcription	Brain Hippocampus Middle	brain
14	chr2:210537000-210596800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:210537200-210543800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:210537600-210547000	Weak transcription	Brain Germinal Matrix	brain
17	chr2:210537600-210550200	Weak transcription	Fetal Brain Male	brain
18	chr2:210537800-210545000	Weak transcription	Fetal Brain Female	brain
19	chr2:210539400-210543000	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr2:210540200-210552200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr2:210540400-210543200	Weak transcription	Ovary	ovary
22	chr2:210541600-210543400	Weak transcription	Left Ventricle	heart
23	chr2:210541600-210550600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr2:210541800-210542400	Enhancers	Brain Anterior Caudate	brain
25	chr2:210541800-210551600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:210541800-210596400	Weak transcription	Gastric	stomach
27	chr2:210542000-210555400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr2:210542200-210542400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:210542400-210543400	Weak transcription	Brain Anterior Caudate	brain
30	chr2:210542400-210546000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr2:210543000-210543800	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr2:210543200-210544000	Strong transcription	Aorta	Aorta
33	chr2:210543200-210544000	Strong transcription	Ovary	ovary
34	chr2:210543200-210549000	Strong transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:210543400-210544000	Genic enhancers	Brain Anterior Caudate	brain
36	chr2:210543400-210544200	Strong transcription	Left Ventricle	heart
37	chr2:210543600-210552200	Weak transcription	Pancreas	Pancrea
38	chr2:210543800-210548000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:210543800-210550200	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr2:210544000-210547400	Weak transcription	Aorta	Aorta
41	chr2:210544000-210550200	Weak transcription	Brain Anterior Caudate	brain
42	chr2:210544000-210596600	Weak transcription	Ovary	ovary
43	chr2:210544200-210555200	Weak transcription	Left Ventricle	heart
44	chr2:210544400-210598600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr2:210544800-210546800	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:210545000-210546000	Strong transcription	Fetal Brain Female	brain
47	chr2:210545200-210546400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:210545400-210546400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr2:210545800-210546200	Enhancers	NHEK	skin
50	chr2:210545800-210546400	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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