Variant report

Variant	nsv875002
Chromosome Location	chr2:127412013-127420211
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	chr2:127415614-127415762	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:127414553-127416294	K562	blood:	n/a	n/a
3	ARID3A	chr2:127413564-127413800	K562	blood:	n/a	n/a
4	ARID3A	chr2:127412458-127413073	K562	blood:	n/a	n/a
5	ATF1	chr2:127414676-127415765	K562	blood:	n/a	n/a
6	ATF2	chr2:127416324-127417113	GM12878	blood:	n/a	n/a
7	ATF2	chr2:127415339-127415791	GM12878	blood:	n/a	n/a
8	ATF2	chr2:127414211-127415036	GM12878	blood:	n/a	n/a
9	ATF2	chr2:127413227-127413751	GM12878	blood:	n/a	n/a
10	ATF2	chr2:127415385-127415821	GM12878	blood:	n/a	n/a
11	ATF3	chr2:127415334-127415856	K562	blood:	n/a	chr2:127415837-127415846
12	ATF3	chr2:127414661-127415075	K562	blood:	n/a	chr2:127414862-127414873 chr2:127414862-127414873 chr2:127414671-127414680
13	ATF3	chr2:127415480-127415919	K562	blood:	n/a	chr2:127415837-127415846
14	ATF3	chr2:127416803-127417027	K562	blood:	n/a	n/a
15	BACH1	chr2:127413508-127414472	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr2:127415509-127415698	GM12878	blood:	n/a	n/a
17	BCL3	chr2:127419353-127419748	GM12878	blood:	n/a	n/a
18	BCL3	chr2:127419319-127419733	GM12878	blood:	n/a	n/a
19	BCLAF1	chr2:127413369-127413954	GM12878	blood:	n/a	n/a
20	BCLAF1	chr2:127415352-127415858	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:127412638-127416254	K562	blood:	n/a	chr2:127413932-127413948 chr2:127413940-127413956
22	BHLHE40	chr2:127416575-127417323	K562	blood:	n/a	n/a
23	BHLHE40	chr2:127416561-127417577	GM12878	blood:	n/a	n/a
24	BHLHE40	chr2:127414336-127415990	GM12878	blood:	n/a	n/a
25	BHLHE40	chr2:127419483-127419608	K562	blood:	n/a	n/a
26	BHLHE40	chr2:127413350-127413865	GM12878	blood:	n/a	n/a
27	BRCA1	chr2:127415519-127415952	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr2:127414763-127414979	GM12878	blood:	n/a	n/a
29	CBX3	chr2:127412716-127413774	K562	blood:	n/a	n/a
30	CBX3	chr2:127415307-127415760	K562	blood:	n/a	n/a
31	CBX3	chr2:127414569-127415956	K562	blood:	n/a	n/a
32	CCNT2	chr2:127414690-127415771	K562	blood:	n/a	n/a
33	CCNT2	chr2:127416762-127417057	K562	blood:	n/a	chr2:127416871-127416880
34	CCNT2	chr2:127413184-127414412	K562	blood:	n/a	chr2:127413687-127413696
35	CEBPB	chr2:127413186-127413873	IMR90	lung:	n/a	n/a
36	CEBPB	chr2:127415502-127416083	MCF-7	breast:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
37	CEBPB	chr2:127415374-127415987	H1-hESC	embryonic stem cell:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
38	CEBPB	chr2:127414448-127415234	K562	blood:	n/a	chr2:127414551-127414562 chr2:127414551-127414564
39	CEBPB	chr2:127415382-127416056	K562	blood:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
40	CEBPB	chr2:127413191-127413668	K562	blood:	n/a	n/a
41	CEBPB	chr2:127419006-127419093	K562	blood:	n/a	n/a
42	CEBPB	chr2:127413230-127413550	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:127416974-127417047	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:127414716-127415025	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:127414638-127415071	K562	blood:	n/a	n/a
46	CEBPB	chr2:127415231-127416110	HCT-116	colon:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
47	CEBPB	chr2:127415584-127416023	ECC-1	luminal epithelium:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
48	CEBPB	chr2:127415507-127416029	MCF-7	breast:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810
49	CEBPB	chr2:127414315-127416167	IMR90	lung:	n/a	chr2:127414551-127414562 chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810 chr2:127414551-127414564
50	CEBPB	chr2:127415687-127415938	K562	blood:	n/a	chr2:127415799-127415812 chr2:127415801-127415812 chr2:127415799-127415810

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127414802-127414852	PrEC	prostate:	n/a
2	chr2:127414827-127414877	HepG2	liver:	n/a
3	chr2:127413369-127413419	CMK	blood:	n/a
4	chr2:127414802-127414852	PrEC	prostate:	n/a
5	chr2:127414827-127414877	HepG2	liver:	n/a
6	chr2:127413369-127413419	CMK	blood:	n/a
7	chr2:127414802-127414852	PANC-1	pancreas:	n/a
8	chr2:127413530-127413580	H1-hESC	embryonic stem cell:	embryo
9	chr2:127414883-127414933	T-47D	breast:	n/a
10	chr2:127413936-127413986	HEEpiC	esophagus:	n/a
11	chr2:127415590-127415640	H1-hESC	embryonic stem cell:	embryo
12	chr2:127414455-127414505	SKMC	muscle:	n/a
13	chr2:127414802-127414852	Jurkat	blood:	n/a
14	chr2:127415590-127415640	HEK293	kidney:	embryo
15	chr2:127413831-127413881	A549	lung:	n/a
16	chr2:127413369-127413419	AG10803	skin:	n/a
17	chr2:127413831-127413881	HCM	heart:	n/a
18	chr2:127414883-127414933	HCPEpiC	choroid plexus:	n/a
19	chr2:127414108-127414158	GM12878	blood:	n/a
20	chr2:127413530-127413580	AG04450	lung:	fetal
21	chr2:127414802-127414852	HUVEC	blood vessel:	n/a
22	chr2:127414381-127414431	T-47D	breast:	n/a
23	chr2:127413936-127413986	T-47D	breast:	n/a
24	chr2:127414455-127414505	Hela-S3	cervix:	n/a
25	chr2:127413367-127413417	HIPEpiC	eye:	n/a
26	chr2:127413363-127413413	HCT-116	colon:	n/a
27	chr2:127413530-127413580	SAEC	small airway:	n/a
28	chr2:127414381-127414431	ovcar-3	ovarian:	n/a
29	chr2:127413369-127413419	BJ	skin:	n/a
30	chr2:127414802-127414852	U87	brain:	n/a
31	chr2:127414827-127414877	SK-N-MC	brain:	n/a
32	chr2:127414108-127414158	HepG2	liver:	n/a
33	chr2:127413367-127413417	PANC-1	pancreas:	n/a
34	chr2:127413367-127413417	Jurkat	blood:	n/a
35	chr2:127414883-127414933	AoSMC	blood vessel:	n/a
36	chr2:127416839-127416889	GM12878	blood:	n/a
37	chr2:127416839-127416889	GM06990	blood:	n/a
38	chr2:127413831-127413881	HRPEpiC	eye:	n/a
39	chr2:127414455-127414505	SK-N-MC	brain:	n/a
40	chr2:127414455-127414505	Hepatocyte	liver:	n/a
41	chr2:127413367-127413417	HCM	heart:	n/a
42	chr2:127414381-127414431	NHBE	bronchial:	n/a
43	chr2:127414827-127414877	ProgFib	skin:	n/a
44	chr2:127414108-127414158	HEEpiC	esophagus:	n/a
45	chr2:127413505-127413555	Caco-2	colon:	n/a
46	chr2:127413367-127413417	NHBE	bronchial:	n/a
47	chr2:127413367-127413417	IMR90	lung:	fetal
48	chr2:127414381-127414431	HUVEC	blood vessel:	n/a
49	chr2:127414381-127414431	Jurkat	blood:	n/a
50	chr2:127415590-127415640	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:127064260..127066484-chr2:127415621..127417230,2	K562	blood:
2	chr2:127414075..127416361-chr2:127822342..127824026,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114783.1.1-6	chr2:127413709-127413888	NONHSAT074132
2	lnc-AC114783.1.1-6	chr2:127413718-127413888	NONHSAT074133
3	lnc-AC114783.1.1-6	chr2:127415183-127415768	NONHSAT074132

Variant related genes	Relation type
GYPC	TF binding region
GYPC	CpG island
ENSG00000235774	chromatin interactions
ENSG00000136717	chromatin interactions

Extended variants
information (count: 349 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:349 , 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	rs28387074	chr2:127412013-127412014	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs540275384	chr2:127412048-127412049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559925026	chr2:127412080-127412081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532142029	chr2:127412098-127412099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193245631	chr2:127412099-127412100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568842054	chr2:127412115-127412116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531620273	chr2:127412124-127412125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550740667	chr2:127412153-127412154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs78672084	chr2:127412168-127412169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536353401	chr2:127412175-127412176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553465327	chr2:127412206-127412207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539618601	chr2:127412266-127412267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113931201	chr2:127412308-127412309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28387075	chr2:127412320-127412321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528375191	chr2:127412324-127412325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188479231	chr2:127412325-127412326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192947176	chr2:127412332-127412333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372962915	chr2:127412336-127412337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs551709719	chr2:127412357-127412358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138177042	chr2:127412404-127412405	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs28387076	chr2:127412405-127412406	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs28387077	chr2:127412407-127412408	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554269543	chr2:127412478-127412479	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28387078	chr2:127412495-127412496	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs539967833	chr2:127412517-127412518	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559788773	chr2:127412539-127412540	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs530603100	chr2:127412547-127412548	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs908640	chr2:127412558-127412559	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs184031556	chr2:127412624-127412625	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs188613491	chr2:127412628-127412629	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs28387079	chr2:127412633-127412634	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs531555645	chr2:127412690-127412691	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs142602138	chr2:127412696-127412697	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs561138631	chr2:127412702-127412703	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs115171907	chr2:127412715-127412716	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79957745	chr2:127412716-127412717	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs191869720	chr2:127412721-127412722	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs539123360	chr2:127412728-127412729	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs552850220	chr2:127412793-127412794	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569385208	chr2:127412794-127412795	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536413467	chr2:127412847-127412848	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs538164782	chr2:127412920-127412921	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs146909678	chr2:127413028-127413029	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs28387080	chr2:127413056-127413057	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs28387081	chr2:127413101-127413102	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553337779	chr2:127413114-127413115	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs3811541	chr2:127413135-127413136	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs141438116	chr2:127413145-127413146	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs183765634	chr2:127413147-127413148	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs189328377	chr2:127413168-127413169	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:901 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127406400-127412400	Weak transcription	Fetal Muscle Leg	muscle
2	chr2:127408000-127413000	Weak transcription	Aorta	Aorta
3	chr2:127410400-127412600	Enhancers	K562	blood
4	chr2:127410800-127412600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:127410800-127412800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:127410800-127414200	Weak transcription	Hela-S3	cervix
7	chr2:127411000-127412400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr2:127411000-127412400	Weak transcription	Left Ventricle	heart
9	chr2:127411000-127412600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:127411000-127412800	Weak transcription	Ovary	ovary
11	chr2:127411200-127412400	Weak transcription	Fetal Heart	heart
12	chr2:127411400-127412600	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr2:127411400-127412600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr2:127411600-127412200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:127411600-127412800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:127411800-127412200	Weak transcription	Primary T cells from cord blood	blood
17	chr2:127411800-127412400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:127411800-127412400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr2:127411800-127412800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:127411800-127412800	Enhancers	Fetal Lung	lung
21	chr2:127411800-127413000	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:127412000-127412800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr2:127412000-127413000	Enhancers	Fetal Muscle Trunk	muscle
24	chr2:127412200-127413000	Enhancers	Primary T cells from cord blood	blood
25	chr2:127412200-127413000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr2:127412400-127412600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:127412400-127412600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:127412400-127412600	Enhancers	Adipose Nuclei	Adipose
29	chr2:127412400-127412600	Enhancers	Stomach Smooth Muscle	stomach
30	chr2:127412400-127412800	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:127412400-127412800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr2:127412400-127413000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:127412400-127413000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr2:127412400-127413000	Enhancers	Fetal Heart	heart
35	chr2:127412400-127413000	Enhancers	Fetal Muscle Leg	muscle
36	chr2:127412400-127413000	Enhancers	Fetal Stomach	stomach
37	chr2:127412400-127413000	Enhancers	Left Ventricle	heart
38	chr2:127412400-127413200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:127412400-127413200	Enhancers	Fetal Thymus	thymus
40	chr2:127412400-127413600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:127412600-127412800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr2:127412600-127412800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr2:127412600-127412800	Enhancers	Colon Smooth Muscle	Colon
44	chr2:127412600-127412800	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr2:127412600-127412800	Enhancers	Lung	lung
46	chr2:127412600-127413000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr2:127412600-127413000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr2:127412600-127413000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr2:127412600-127413000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:127412600-127413000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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