Variant report

Variant	esv2763084
Chromosome Location	chr2:209237587-209247384
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	ARID3A	chr2:209238174-209238580	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:209238240-209238613	K562	blood:	n/a	n/a
3	CCNT2	chr2:209243607-209243784	K562	blood:	n/a	n/a
4	CEBPB	chr2:209238250-209238569	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr2:209238239-209238489	A549	lung:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
6	CTCF	chr2:209237955-209238815	SK-N-SH	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
7	CTCF	chr2:209238280-209238430	AoAF	blood vessel:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
8	CTCF	chr2:209238320-209238470	HUVEC	blood vessel:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
9	CTCF	chr2:209238271-209238499	A549	lung:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
10	CTCF	chr2:209238300-209238450	MCF-7	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
11	CTCF	chr2:209238237-209238460	HepG2	liver:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
12	CTCF	chr2:209238300-209238450	HFF	foreskin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
13	CTCF	chr2:209238320-209238470	HCT-116	colon:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
14	CTCF	chr2:209238320-209238470	Hela-S3	cervix:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
15	CTCF	chr2:209237780-209237930	HMF	breast:	n/a	n/a
16	CTCF	chr2:209238320-209238470	NB4	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
17	CTCF	chr2:209238520-209238670	A549	lung:	n/a	n/a
18	CTCF	chr2:209238258-209238514	GM13977	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
19	CTCF	chr2:209238340-209238490	WERI-Rb-1	eye:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
20	CTCF	chr2:209238340-209238490	SK-N-SH_RA	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
21	CTCF	chr2:209238251-209238505	LNCaP	prostate:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
22	CTCF	chr2:209238246-209238492	MCF-7	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
23	CTCF	chr2:209238300-209238450	AG04449	skin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
24	CTCF	chr2:209238280-209238430	GM12865	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
25	CTCF	chr2:209238340-209238490	SAEC	small airway:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
26	CTCF	chr2:209238207-209238528	Spleen_OC	spleen:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
27	CTCF	chr2:209238320-209238470	AG09319	gingival:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
28	CTCF	chr2:209238340-209238490	HEK293	kidney:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
29	CTCF	chr2:209238261-209238495	GM10248	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
30	CTCF	chr2:209238760-209238910	GM12873	blood:	n/a	n/a
31	CTCF	chr2:209238300-209238450	GM12869	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
32	CTCF	chr2:209238166-209238545	T-47D	breast:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
33	CTCF	chr2:209238236-209238491	K562	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
34	CTCF	chr2:209238320-209238470	HEEpiC	esophagus:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
35	CTCF	chr2:209238235-209238586	K562	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
36	CTCF	chr2:209238340-209238490	BE2_C	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
37	CTCF	chr2:209238300-209238450	BJ	skin:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
38	CTCF	chr2:209238260-209238410	GM12875	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
39	CTCF	chr2:209238340-209238490	Hela-S3	cervix:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
40	CTCF	chr2:209238230-209238527	H1-hESC	embryonic stem cell:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
41	CTCF	chr2:209238280-209238430	GM12872	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
42	CTCF	chr2:209238108-209238612	GM12878	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
43	CTCF	chr2:209238300-209238450	GM12878	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
44	CTCF	chr2:209238222-209238536	Medullo	brain:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
45	CTCF	chr2:209238280-209238430	GM12870	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
46	CTCF	chr2:209238291-209238460	GM13976	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
47	CTCF	chr2:209238320-209238470	HPAF	blood vessel:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
48	CTCF	chr2:209238280-209238430	GM12864	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
49	CTCF	chr2:209238273-209238481	GM19240	blood:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408
50	CTCF	chr2:209238320-209238470	HAc	cerebellar:	n/a	chr2:209238390-209238398 chr2:209238385-209238403 chr2:209238387-209238408

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:209240193-209240243	HUVEC	blood vessel:	n/a
2	chr2:209242596-209242646	AG04449	skin:	fetal
3	chr2:209242596-209242646	GM19239	blood:	n/a
4	chr2:209242596-209242646	HEEpiC	esophagus:	n/a
5	chr2:209240193-209240243	H1-hESC	embryonic stem cell:	embryo
6	chr2:209242596-209242646	Hepatocyte	liver:	n/a
7	chr2:209242596-209242646	SKMC	muscle:	n/a
8	chr2:209242596-209242646	AoSMC	blood vessel:	n/a
9	chr2:209240193-209240243	SK-N-SH	brain:	n/a
10	chr2:209240193-209240243	GM19239	blood:	n/a
11	chr2:209240193-209240243	SK-N-SH_RA	brain:	n/a
12	chr2:209240193-209240243	AG04449	skin:	fetal
13	chr2:209242596-209242646	HRPEpiC	eye:	n/a
14	chr2:209240193-209240243	AG10803	skin:	n/a
15	chr2:209242596-209242646	PrEC	prostate:	n/a
16	chr2:209242596-209242646	AG09309	skin:	n/a
17	chr2:209242596-209242646	ovcar-3	ovarian:	n/a
18	chr2:209240193-209240243	A549	lung:	n/a
19	chr2:209240193-209240243	BE2_C	brain:	n/a
20	chr2:209242596-209242646	HAEpiC	amniotic membrane:	n/a
21	chr2:209240193-209240243	RPTEC	kidney:	n/a
22	chr2:209240193-209240243	BJ	skin:	n/a
23	chr2:209240193-209240243	NHBE	bronchial:	n/a
24	chr2:209242596-209242646	NT2-D1	testis:	n/a
25	chr2:209242596-209242646	MCF-7	breast:	n/a
26	chr2:209242596-209242646	PANC-1	pancreas:	n/a
27	chr2:209242596-209242646	HUVEC	blood vessel:	n/a
28	chr2:209242596-209242646	AG04450	lung:	fetal
29	chr2:209242596-209242646	NH-A	brain:	n/a
30	chr2:209242596-209242646	MCF10A-Er-Src	breast:	n/a
31	chr2:209242596-209242646	HNPCEpiC	eye:	n/a
32	chr2:209240193-209240243	ECC-1	luminal epithelium:	n/a
33	chr2:209242596-209242646	SK-N-SH	brain:	n/a
34	chr2:209240193-209240243	HEK293	kidney:	embryo
35	chr2:209242596-209242646	AG09319	gingival:	n/a
36	chr2:209240193-209240243	GM12878	blood:	n/a
37	chr2:209242596-209242646	NHDF-neo	bronchial:	n/a
38	chr2:209240193-209240243	AG04450	lung:	fetal
39	chr2:209240193-209240243	PFSK-1	brain:	n/a
40	chr2:209240193-209240243	HAEpiC	amniotic membrane:	n/a
41	chr2:209242596-209242646	HRE	kidney:	n/a
42	chr2:209240193-209240243	HCF	heart:	n/a
43	chr2:209242596-209242646	T-47D	breast:	n/a
44	chr2:209242596-209242646	GM12878	blood:	n/a
45	chr2:209240193-209240243	LNCaP	prostate:	n/a
46	chr2:209240193-209240243	HEEpiC	esophagus:	n/a
47	chr2:209242596-209242646	HCF	heart:	n/a
48	chr2:209242596-209242646	NB4	blood:	n/a
49	chr2:209240193-209240243	AG09309	skin:	n/a
50	chr2:209242596-209242646	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:209244985..209246550-chr2:209250823..209252697,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000265454	TF binding region
ENSG00000265454	CpG island

Extended variants
information (count: 347 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:347 , 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	rs535801388	chr2:209237602-209237603	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs6711995	chr2:209237627-209237628	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs578066260	chr2:209237637-209237638	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs572546919	chr2:209237672-209237673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12617089	chr2:209237712-209237713	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs6757231	chr2:209237736-209237737	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs530647965	chr2:209237741-209237742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116268879	chr2:209237757-209237758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35466463	chr2:209237766-209237767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544492426	chr2:209237802-209237803	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561405842	chr2:209237805-209237806	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs6728530	chr2:209237839-209237840	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs540590962	chr2:209237916-209237917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184558224	chr2:209237996-209237997	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs201563172	chr2:209238034-209238035	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs532580391	chr2:209238067-209238068	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs34283482	chr2:209238077-209238078	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142253090	chr2:209238092-209238093	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs571466739	chr2:209238201-209238202	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs188482306	chr2:209238203-209238204	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs181425464	chr2:209238235-209238236	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs67608809	chr2:209238266-209238267	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573565234	chr2:209238303-209238304	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs535934828	chr2:209238308-209238309	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs552699956	chr2:209238329-209238330	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs11893137	chr2:209238331-209238332	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371242582	chr2:209238400-209238401	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs146104298	chr2:209238402-209238403	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs185916282	chr2:209238406-209238407	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs191157988	chr2:209238458-209238459	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs182002766	chr2:209238460-209238461	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs528837523	chr2:209238464-209238465	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs187245536	chr2:209238523-209238524	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs115632079	chr2:209238524-209238525	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs575125278	chr2:209238672-209238673	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs540726329	chr2:209238675-209238676	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs560602957	chr2:209238681-209238682	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532515843	chr2:209238690-209238691	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs112551273	chr2:209238749-209238750	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538238935	chr2:209238807-209238808	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs199917630	chr2:209238841-209238842	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs138312238	chr2:209238861-209238862	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs565141753	chr2:209238900-209238901	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs530726533	chr2:209239034-209239035	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191997917	chr2:209239049-209239050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs182722897	chr2:209239098-209239099	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550288483	chr2:209239187-209239188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140909109	chr2:209239203-209239204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546271717	chr2:209239225-209239226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187531870	chr2:209239245-209239246	Weak transcription Enhancers	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
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209233000-209240200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:209236000-209240200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:209238600-209238800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:209238800-209240000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:209239000-209241600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:209239800-209241600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:209240000-209240400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr2:209240000-209241000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:209240000-209241200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:209240000-209241400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:209240000-209241400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:209240000-209241600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:209240200-209240800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr2:209240200-209241000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr2:209240200-209241000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:209240200-209241000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr2:209240200-209241000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr2:209240400-209240800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:209240400-209241200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr2:209240400-209241400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr2:209241200-209243200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr2:209241600-209243000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr2:209242800-209243400	Weak transcription	Pancreas	Pancrea
24	chr2:209243200-209243800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
25	chr2:209243400-209243600	Enhancers	Pancreas	Pancrea
26	chr2:209243600-209243800	Enhancers	Liver	Liver
27	chr2:209243600-209245200	Weak transcription	Pancreas	Pancrea
28	chr2:209245200-209245600	Enhancers	Pancreas	Pancrea
29	chr2:209245400-209245600	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:209245600-209249400	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links