Variant report

Variant	esv2754281
Chromosome Location	chr2:210484777-210543711
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	BACH1	chr2:210526721-210526883	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr2:210494518-210494654	H1-hESC	embryonic stem cell:	n/a	chr2:210494580-210494594
3	BACH1	chr2:210536737-210536999	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:210507211-210507560	H1-hESC	embryonic stem cell:	n/a	chr2:210507379-210507393
5	BRCA1	chr2:210507193-210507606	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr2:210502938-210503425	HCT-116	colon:	n/a	n/a
7	CBX3	chr2:210502975-210503364	HCT-116	colon:	n/a	n/a
8	CEBPB	chr2:210510700-210510997	IMR90	lung:	n/a	chr2:210510870-210510881
9	CEBPB	chr2:210528460-210528762	A549	lung:	n/a	chr2:210528630-210528643 chr2:210528630-210528641 chr2:210528631-210528642
10	CEBPB	chr2:210510786-210510986	H1-hESC	embryonic stem cell:	n/a	chr2:210510870-210510881
11	CEBPB	chr2:210507143-210507746	Hela-S3	cervix:	n/a	chr2:210507732-210507745
12	CEBPB	chr2:210537528-210537565	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:210507086-210507504	HCT-116	colon:	n/a	n/a
14	CEBPB	chr2:210528454-210528792	HepG2	liver:	n/a	chr2:210528630-210528643 chr2:210528630-210528641 chr2:210528631-210528642
15	CEBPB	chr2:210507157-210507664	HCT-116	colon:	n/a	n/a
16	CEBPB	chr2:210510718-210511024	HepG2	liver:	n/a	chr2:210510870-210510881
17	CEBPB	chr2:210528478-210528795	IMR90	lung:	n/a	chr2:210528630-210528643 chr2:210528630-210528641 chr2:210528631-210528642
18	CEBPB	chr2:210513486-210513795	Hela-S3	cervix:	n/a	chr2:210513634-210513647
19	CEBPD	chr2:210502067-210502459	K562	blood:	n/a	n/a
20	CTCF	chr2:210509220-210509247	Lung_OC	lung:	n/a	n/a
21	CTCF	chr2:210511903-210511953	GM20000	blood:	n/a	n/a
22	CTCF	chr2:210488780-210488930	GM12868	blood:	n/a	n/a
23	CTCF	chr2:210526200-210526350	BE2_C	brain:	n/a	n/a
24	CTCF	chr2:210503360-210503510	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr2:210503420-210503570	HMF	breast:	n/a	n/a
26	E2F4	chr2:210507298-210507741	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr2:210503078-210503353	MCF10A-Er-Src	breast:	n/a	n/a
28	EP300	chr2:210502862-210503670	SK-N-SH	brain:	n/a	chr2:210503208-210503222 chr2:210503237-210503246 chr2:210503410-210503419 chr2:210503236-210503245
29	EP300	chr2:210502986-210503327	SK-N-SH_RA	brain:	n/a	chr2:210503208-210503222 chr2:210503237-210503246 chr2:210503236-210503245
30	EP300	chr2:210507160-210507584	SK-N-SH	brain:	n/a	chr2:210507382-210507391 chr2:210507381-210507390
31	EP300	chr2:210525653-210528975	SK-N-SH	brain:	n/a	chr2:210527917-210527931 chr2:210527566-210527580 chr2:210527561-210527575 chr2:210528149-210528158 chr2:210525863-210525877 chr2:210527563-210527577
32	EP300	chr2:210489096-210489776	SK-N-SH_RA	brain:	n/a	chr2:210489567-210489581
33	EP300	chr2:210527688-210528278	SK-N-SH_RA	brain:	n/a	chr2:210527917-210527931 chr2:210528149-210528158
34	EP300	chr2:210503049-210503643	SK-N-SH_RA	brain:	n/a	chr2:210503208-210503222 chr2:210503237-210503246 chr2:210503410-210503419 chr2:210503236-210503245
35	EP300	chr2:210527711-210528306	SK-N-SH_RA	brain:	n/a	chr2:210527917-210527931 chr2:210528149-210528158
36	EP300	chr2:210507198-210507549	Hela-S3	cervix:	n/a	chr2:210507382-210507391 chr2:210507381-210507390
37	EP300	chr2:210525996-210526222	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr2:210526034-210526338	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr2:210489165-210489721	SK-N-SH_RA	brain:	n/a	chr2:210489567-210489581
40	EP300	chr2:210497505-210498669	SK-N-SH	brain:	n/a	n/a
41	EP300	chr2:210497915-210498168	SK-N-SH_RA	brain:	n/a	n/a
42	FAM48A	chr2:210501404-210501503	GM12878	blood:	n/a	n/a
43	FOS	chr2:210505076-210505399	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr2:210494358-210494776	MCF10A-Er-Src	breast:	n/a	chr2:210494583-210494591 chr2:210494581-210494593 chr2:210494581-210494592 chr2:210494583-210494591 chr2:210494584-210494591 chr2:210494582-210494592
45	FOS	chr2:210505047-210505413	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr2:210526667-210526976	MCF10A-Er-Src	breast:	n/a	chr2:210526828-210526835 chr2:210526828-210526836
47	FOS	chr2:210494414-210494776	MCF10A-Er-Src	breast:	n/a	chr2:210494583-210494591 chr2:210494581-210494593 chr2:210494581-210494592 chr2:210494583-210494591 chr2:210494584-210494591 chr2:210494582-210494592
48	FOS	chr2:210494361-210494902	HUVEC	blood vessel:	n/a	chr2:210494583-210494591 chr2:210494581-210494593 chr2:210494581-210494592 chr2:210494583-210494591 chr2:210494584-210494591 chr2:210494582-210494592
49	FOS	chr2:210503018-210503558	MCF10A-Er-Src	breast:	n/a	chr2:210503237-210503244 chr2:210503410-210503418 chr2:210503237-210503245 chr2:210503410-210503418 chr2:210503410-210503417 chr2:210503238-210503249 chr2:210503237-210503246 chr2:210503235-210503246 chr2:210503236-210503245 chr2:210503408-210503420
50	FOS	chr2:210503003-210503482	MCF10A-Er-Src	breast:	n/a	chr2:210503237-210503244 chr2:210503410-210503418 chr2:210503237-210503245 chr2:210503410-210503418 chr2:210503410-210503417 chr2:210503238-210503249 chr2:210503237-210503246 chr2:210503235-210503246 chr2:210503236-210503245 chr2:210503408-210503420

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210493473-210493523	GM12891	blood:	n/a
2	chr2:210493473-210493523	HRE	kidney:	n/a
3	chr2:210516795-210516845	AG09309	skin:	n/a
4	chr2:210517441-210517491	NH-A	brain:	n/a
5	chr2:210517441-210517491	ovcar-3	ovarian:	n/a
6	chr2:210493473-210493523	HRCEpiC	kidney:	n/a
7	chr2:210516795-210516845	GM12878	blood:	n/a
8	chr2:210516795-210516845	HCF	heart:	n/a
9	chr2:210517441-210517491	GM19239	blood:	n/a
10	chr2:210517441-210517491	MCF-7	breast:	n/a
11	chr2:210493473-210493523	HNPCEpiC	eye:	n/a
12	chr2:210517441-210517491	HEEpiC	esophagus:	n/a
13	chr2:210517441-210517491	AG10803	skin:	n/a
14	chr2:210493473-210493523	BE2_C	brain:	n/a
15	chr2:210516795-210516845	PANC-1	pancreas:	n/a
16	chr2:210516795-210516845	NHBE	bronchial:	n/a
17	chr2:210516795-210516845	GM12891	blood:	n/a
18	chr2:210517441-210517491	AG04449	skin:	fetal
19	chr2:210516795-210516845	ProgFib	skin:	n/a
20	chr2:210493473-210493523	GM19239	blood:	n/a
21	chr2:210493473-210493523	SK-N-MC	brain:	n/a
22	chr2:210516795-210516845	HUVEC	blood vessel:	n/a
23	chr2:210493473-210493523	SK-N-SH_RA	brain:	n/a
24	chr2:210517441-210517491	BJ	skin:	n/a
25	chr2:210493473-210493523	HAEpiC	amniotic membrane:	n/a
26	chr2:210493473-210493523	AG10803	skin:	n/a
27	chr2:210516795-210516845	AG04449	skin:	fetal
28	chr2:210516795-210516845	NHDF-neo	bronchial:	n/a
29	chr2:210517441-210517491	SK-N-SH	brain:	n/a
30	chr2:210516795-210516845	HPAEpiC	pulmonary alveolar:	n/a
31	chr2:210493473-210493523	RPTEC	kidney:	n/a
32	chr2:210493473-210493523	AG09319	gingival:	n/a
33	chr2:210493473-210493523	MCF-7	breast:	n/a
34	chr2:210493473-210493523	A549	lung:	n/a
35	chr2:210517441-210517491	SK-N-SH_RA	brain:	n/a
36	chr2:210516795-210516845	GM12892	blood:	n/a
37	chr2:210517441-210517491	HIPEpiC	eye:	n/a
38	chr2:210493473-210493523	HEEpiC	esophagus:	n/a
39	chr2:210516795-210516845	GM19239	blood:	n/a
40	chr2:210516795-210516845	LNCaP	prostate:	n/a
41	chr2:210493473-210493523	BJ	skin:	n/a
42	chr2:210493473-210493523	GM06990	blood:	n/a
43	chr2:210517441-210517491	MCF10A-Er-Src	breast:	n/a
44	chr2:210493473-210493523	AG04449	skin:	fetal
45	chr2:210517441-210517491	HUVEC	blood vessel:	n/a
46	chr2:210516795-210516845	HEK293	kidney:	embryo
47	chr2:210516795-210516845	SK-N-SH_RA	brain:	n/a
48	chr2:210517441-210517491	AG04450	lung:	fetal
49	chr2:210516795-210516845	HIPEpiC	eye:	n/a
50	chr2:210516795-210516845	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:210491764..210493575-chr2:210496638..210498677,2	MCF-7	breast:
2	chr2:210491764..210493575-chr2:210496638..210498677,2	MCF-7	breast:
3	chr2:210514066..210516944-chr2:210516970..210520269,3	MCF-7	breast:
4	chr2:210538146..210538666-chr20:1193654..1194280,2	K562	blood:
5	chr2:210538640..210540966-chr2:210544100..210546598,2	K562	blood:

Variant related genes	Relation type
MAP2	TF binding region
MAP2	CpG island
ENSG00000078018	chromatin interactions

Extended variants
information (count: 2010 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2010 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16843257	chr2:210484777-210484778	Enhancers Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115540519	chr2:210484838-210484839	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367715529	chr2:210484976-210484977	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534298804	chr2:210485005-210485006	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181955116	chr2:210485015-210485016	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376318586	chr2:210485106-210485107	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116462659	chr2:210485151-210485152	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545105273	chr2:210485186-210485187	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564865596	chr2:210485328-210485329	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186123743	chr2:210485405-210485406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs190540734	chr2:210485418-210485419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560738904	chr2:210485425-210485426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529946500	chr2:210485456-210485457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546441559	chr2:210485458-210485459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183048603	chr2:210485459-210485460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375689842	chr2:210485494-210485495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547615403	chr2:210485539-210485540	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551733975	chr2:210485550-210485551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75439139	chr2:210485558-210485559	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139733827	chr2:210485595-210485596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557601471	chr2:210485604-210485605	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559448581	chr2:210485685-210485686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567815223	chr2:210485690-210485691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536969110	chr2:210485754-210485755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553670473	chr2:210485769-210485770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372925989	chr2:210485780-210485781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113363823	chr2:210485791-210485792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544707188	chr2:210485847-210485848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558522260	chr2:210485851-210485852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186929312	chr2:210485867-210485868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372083516	chr2:210485873-210485874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144505102	chr2:210485875-210485876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560750629	chr2:210485876-210485877	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529810446	chr2:210485905-210485906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539896630	chr2:210485923-210485924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540151783	chr2:210485978-210485979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560221346	chr2:210486024-210486025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551327375	chr2:210486028-210486029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532412305	chr2:210486052-210486053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191315733	chr2:210486078-210486079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs12996265	chr2:210486167-210486168	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571603546	chr2:210486175-210486176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376555063	chr2:210486228-210486229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531032370	chr2:210486238-210486239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551068698	chr2:210486246-210486247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183181513	chr2:210486275-210486276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12694187	chr2:210486280-210486281	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs553583729	chr2:210486337-210486338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13412699	chr2:210486396-210486397	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs539310315	chr2:210486413-210486414	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:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210476600-210493600	Weak transcription	Aorta	Aorta
2	chr2:210480000-210493200	Weak transcription	Brain Germinal Matrix	brain
3	chr2:210481000-210486400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:210481000-210493400	Weak transcription	Pancreas	Pancrea
5	chr2:210481000-210500400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:210481400-210493600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:210481600-210487800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:210483800-210485000	Enhancers	HUVEC	blood vessel
9	chr2:210484400-210484800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:210484400-210484800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:210484400-210484800	Enhancers	NHEK	skin
12	chr2:210484400-210485000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:210484400-210485200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
14	chr2:210484400-210486800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:210484600-210484800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:210484600-210484800	Enhancers	Fetal Brain Male	brain
17	chr2:210484600-210485000	Enhancers	Primary B cells from peripheral blood	blood
18	chr2:210484600-210485000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr2:210484600-210485200	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:210484600-210485200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:210484600-210485200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr2:210484600-210497200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:210484800-210485000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr2:210484800-210485400	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr2:210484800-210492800	Weak transcription	Fetal Brain Male	brain
26	chr2:210484800-210496000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:210485000-210485200	Weak transcription	Fetal Brain Female	brain
28	chr2:210485000-210489000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr2:210485200-210485400	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr2:210485200-210485400	Enhancers	Fetal Brain Female	brain
31	chr2:210485200-210487000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:210485400-210486400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr2:210485400-210486400	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr2:210485400-210494400	Weak transcription	Fetal Brain Female	brain
35	chr2:210486400-210486600	Enhancers	Brain Angular Gyrus	brain
36	chr2:210486400-210487000	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr2:210486400-210488000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:210486400-210489200	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr2:210486600-210487200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr2:210486600-210487200	Enhancers	Fetal Kidney	kidney
41	chr2:210486600-210493400	Weak transcription	Brain Angular Gyrus	brain
42	chr2:210486800-210488600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:210487000-210488600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr2:210487200-210494200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr2:210487800-210488000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr2:210488000-210489600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:210488600-210489400	Enhancers	Liver	Liver
48	chr2:210488600-210489600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr2:210488600-210490000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:210488800-210489000	Enhancers	Fetal Kidney	kidney

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