Variant report

Variant	nsv874875
Chromosome Location	chr2:113038409-113070889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:113058801-113059089	IMR90	lung:	n/a	n/a
2	CEBPB	chr2:113058842-113059151	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr2:113039775-113039911	HepG2	liver:	n/a	chr2:113039881-113039892
4	CEBPB	chr2:113054220-113054447	K562	blood:	n/a	chr2:113054295-113054306
5	CEBPB	chr2:113054147-113054440	IMR90	lung:	n/a	chr2:113054295-113054306
6	CEBPB	chr2:113054273-113054381	H1-hESC	embryonic stem cell:	n/a	chr2:113054295-113054306
7	CEBPB	chr2:113054158-113054452	HepG2	liver:	n/a	chr2:113054295-113054306
8	CEBPB	chr2:113061078-113061157	K562	blood:	n/a	chr2:113061100-113061111
9	CEBPB	chr2:113044062-113044085	A549	lung:	n/a	n/a
10	CEBPB	chr2:113061081-113061116	HepG2	liver:	n/a	chr2:113061100-113061111
11	CHD2	chr2:113058763-113058906	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr2:113067341-113067352	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr2:113051165-113051259	GM10248	blood:	n/a	n/a
14	CTCF	chr2:113041930-113042054	GM10248	blood:	n/a	n/a
15	CTCF	chr2:113042119-113042155	Medullo	brain:	n/a	n/a
16	CTCF	chr2:113043020-113043059	GM10248	blood:	n/a	n/a
17	CTCF	chr2:113042167-113042197	Medullo	brain:	n/a	n/a
18	E2F4	chr2:113055716-113055908	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr2:113066781-113066964	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr2:113058601-113058845	GM12878	blood:	n/a	n/a
21	EP300	chr2:113058929-113059305	Hela-S3	cervix:	n/a	n/a
22	FOS	chr2:113058688-113059298	HUVEC	blood vessel:	n/a	n/a
23	FOS	chr2:113047644-113048174	HUVEC	blood vessel:	n/a	n/a
24	FOSL2	chr2:113039706-113039966	HepG2	liver:	n/a	n/a
25	FOXA2	chr2:113047778-113048013	HepG2	liver:	n/a	n/a
26	FOXA2	chr2:113040825-113041176	A549	lung:	n/a	chr2:113040882-113040894 chr2:113040995-113041007 chr2:113041043-113041055
27	GATA1	chr2:113067166-113067759	PBDE	blood:	n/a	chr2:113067317-113067327
28	GATA2	chr2:113047658-113048118	HUVEC	blood vessel:	n/a	n/a
29	GATA2	chr2:113040235-113040505	K562	blood:	n/a	n/a
30	GATA2	chr2:113058646-113059309	HUVEC	blood vessel:	n/a	chr2:113059127-113059134 chr2:113059122-113059138 chr2:113059127-113059134 chr2:113059127-113059134 chr2:113059165-113059176
31	GATA3	chr2:113058663-113059329	SK-N-SH	brain:	n/a	chr2:113059127-113059134 chr2:113059122-113059138 chr2:113059127-113059134 chr2:113059127-113059134 chr2:113059165-113059176
32	GATA3	chr2:113040303-113040609	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr2:113067105-113067608	SH-SY5Y	brain:	n/a	chr2:113067317-113067327
34	GATA3	chr2:113058639-113059350	SK-N-SH	brain:	n/a	chr2:113059127-113059134 chr2:113059122-113059138 chr2:113059127-113059134 chr2:113059127-113059134 chr2:113059165-113059176
35	GATA3	chr2:113056067-113056287	SH-SY5Y	brain:	n/a	n/a
36	GTF2F1	chr2:113058708-113058922	Hela-S3	cervix:	n/a	n/a
37	IRF1	chr2:113054323-113054329	K562	blood:	n/a	n/a
38	JUN	chr2:113063247-113063448	K562	blood:	n/a	n/a
39	JUN	chr2:113058528-113059321	Hela-S3	cervix:	n/a	n/a
40	MAFF	chr2:113054070-113054330	HepG2	liver:	n/a	chr2:113054178-113054196
41	MAFF	chr2:113051260-113051565	HepG2	liver:	n/a	chr2:113051408-113051426
42	MAFF	chr2:113069553-113069883	HepG2	liver:	n/a	chr2:113069696-113069714
43	MAFF	chr2:113069560-113069855	K562	blood:	n/a	chr2:113069696-113069714
44	MAFF	chr2:113054106-113054314	K562	blood:	n/a	chr2:113054178-113054196
45	MAFF	chr2:113051298-113051551	K562	blood:	n/a	chr2:113051408-113051426
46	MAFK	chr2:113067580-113067636	HepG2	liver:	n/a	n/a
47	MAFK	chr2:113054033-113054329	HepG2	liver:	n/a	n/a
48	MAFK	chr2:113051254-113051571	IMR90	lung:	n/a	n/a
49	MAFK	chr2:113069538-113069887	HepG2	liver:	n/a	chr2:113069698-113069713
50	MAFK	chr2:113063058-113063117	HepG2	liver:	n/a	chr2:113063067-113063078

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113058725-113058775	SKMC	muscle:	n/a
2	chr2:113058725-113058775	BE2_C	brain:	n/a
3	chr2:113058725-113058775	HEK293	kidney:	embryo
4	chr2:113058725-113058775	GM12891	blood:	n/a
5	chr2:113058725-113058775	IMR90	lung:	fetal
6	chr2:113058725-113058775	NH-A	brain:	n/a
7	chr2:113058725-113058775	T-47D	breast:	n/a
8	chr2:113058725-113058775	HCPEpiC	choroid plexus:	n/a
9	chr2:113058725-113058775	SK-N-SH	brain:	n/a
10	chr2:113058725-113058775	HEEpiC	esophagus:	n/a
11	chr2:113058725-113058775	GM12878	blood:	n/a
12	chr2:113058725-113058775	HRPEpiC	eye:	n/a
13	chr2:113058725-113058775	NHBE	bronchial:	n/a
14	chr2:113058725-113058775	HCT-116	colon:	n/a
15	chr2:113058725-113058775	Caco-2	colon:	n/a
16	chr2:113058725-113058775	HRE	kidney:	n/a
17	chr2:113058725-113058775	HAEpiC	amniotic membrane:	n/a
18	chr2:113058725-113058775	GM12892	blood:	n/a
19	chr2:113058725-113058775	ProgFib	skin:	n/a
20	chr2:113058725-113058775	HNPCEpiC	eye:	n/a
21	chr2:113058725-113058775	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:113058725-113058775	NB4	blood:	n/a
23	chr2:113058725-113058775	K562	blood:	n/a
24	chr2:113058725-113058775	HL-60	blood:	n/a
25	chr2:113058725-113058775	AG10803	skin:	n/a
26	chr2:113058725-113058775	SAEC	small airway:	n/a
27	chr2:113058725-113058775	HCM	heart:	n/a
28	chr2:113058725-113058775	Hepatocyte	liver:	n/a
29	chr2:113058725-113058775	H1-hESC	embryonic stem cell:	embryo
30	chr2:113058725-113058775	BJ	skin:	n/a
31	chr2:113058725-113058775	HMEC	breast:	n/a
32	chr2:113058725-113058775	AG09319	gingival:	n/a
33	chr2:113058725-113058775	Jurkat	blood:	n/a
34	chr2:113058725-113058775	GM06990	blood:	n/a
35	chr2:113058725-113058775	HepG2	liver:	n/a
36	chr2:113058725-113058775	AG04449	skin:	fetal
37	chr2:113058725-113058775	HRCEpiC	kidney:	n/a
38	chr2:113058725-113058775	NT2-D1	testis:	n/a
39	chr2:113058725-113058775	HIPEpiC	eye:	n/a
40	chr2:113058725-113058775	HUVEC	blood vessel:	n/a
41	chr2:113058725-113058775	AG09309	skin:	n/a
42	chr2:113058725-113058775	MCF-7	breast:	n/a
43	chr2:113058725-113058775	AoSMC	blood vessel:	n/a
44	chr2:113058725-113058775	PANC-1	pancreas:	n/a
45	chr2:113058725-113058775	RPTEC	kidney:	n/a
46	chr2:113058725-113058775	HCF	heart:	n/a
47	chr2:113058725-113058775	NHDF-neo	bronchial:	n/a
48	chr2:113058725-113058775	PFSK-1	brain:	n/a
49	chr2:113058725-113058775	SK-N-MC	brain:	n/a
50	chr2:113058725-113058775	LNCaP	prostate:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113058676..113061409-chr2:113063002..113065958,2	K562	blood:
2	chr2:113059113..113060824-chr2:113069400..113071132,2	K562	blood:
3	chr2:113054203..113055924-chr2:113078046..113079641,2	K562	blood:
4	chr2:113059113..113060618-chr2:113068906..113071132,2	K562	blood:
5	chr2:113031293..113035273-chr2:113059413..113062262,3	MCF-7	breast:
6	chr2:113032119..113034119-chr2:113066343..113068200,2	MCF-7	breast:
7	chr2:113070638..113072405-chr2:113074120..113076541,2	MCF-7	breast:
8	chr2:113033709..113035506-chr2:113052735..113055582,2	K562	blood:
9	chr2:113033844..113035666-chr2:113048299..113050198,2	K562	blood:
10	chr2:113031383..113033830-chr2:113044346..113047264,3	MCF-7	breast:
11	chr2:113031311..113033993-chr2:113061525..113063078,2	K562	blood:
12	chr2:113059563..113061506-chr2:113099982..113102313,2	K562	blood:
13	chr2:113052733..113055599-chr2:113064270..113066173,2	MCF-7	breast:
14	chr2:113033406..113035209-chr2:113052659..113055582,2	K562	blood:
15	chr2:113052733..113055599-chr2:113064270..113066173,2	MCF-7	breast:
16	chr2:113058676..113061409-chr2:113063002..113065958,2	K562	blood:
17	chr2:113032184..113035804-chr2:113038196..113041130,4	MCF-7	breast:
18	chr2:113065168..113067342-chr2:113068406..113071056,2	K562	blood:
19	chr2:113070301..113072407-chr2:113075065..113076958,2	K562	blood:
20	chr2:113067314..113070627-chr2:113070650..113073571,3	MCF-7	breast:
21	chr2:113067314..113070627-chr2:113070650..113073571,3	MCF-7	breast:
22	chr2:113031677..113034717-chr2:113042895..113047019,4	K562	blood:
23	chr2:113065168..113067342-chr2:113068406..113071056,2	K562	blood:
24	chr2:113059113..113060618-chr2:113068906..113071132,2	K562	blood:
25	chr2:113033771..113036191-chr2:113057480..113059266,2	K562	blood:
26	chr2:113059113..113060824-chr2:113069400..113071132,2	K562	blood:
27	chr2:113032164..113034154-chr2:113058503..113060205,2	K562	blood:
28	chr2:113032383..113034533-chr2:113048360..113050723,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBLN7-4	chr2:113064844-113064928	NONHSAT073690
2	lnc-FBLN7-4	chr2:113065544-113065987	NONHSAT073690
3	lnc-ZC3H8-1	chr2:113043634-113043999	NONHSAT073689

No data

Variant related genes	Relation type
ENSG00000235258	TF binding region
ZC3H6	TF binding region
ENSG00000235258	CpG island
ZC3H6	CpG island
ENSG00000188177	chromatin interactions

Extended variants
information (count: 1182 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10169797	chr2:113038409-113038410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs543166112	chr2:113038434-113038435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563231956	chr2:113038502-113038503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532145298	chr2:113038538-113038539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs111565441	chr2:113038561-113038562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552246316	chr2:113038592-113038593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs374986523	chr2:113038606-113038607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs367928391	chr2:113038667-113038668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528819255	chr2:113038724-113038725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548743895	chr2:113038731-113038732	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs372217464	chr2:113038776-113038777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs183500377	chr2:113038808-113038809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537518995	chr2:113038827-113038828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557046070	chr2:113038855-113038856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs187849451	chr2:113038909-113038910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192476197	chr2:113038952-113038953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183098937	chr2:113038983-113038984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375288625	chr2:113039094-113039095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs572281841	chr2:113039105-113039106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551484391	chr2:113039161-113039162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187983114	chr2:113039201-113039202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574553723	chr2:113039339-113039340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs571573749	chr2:113039368-113039369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543983679	chr2:113039384-113039385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563366392	chr2:113039542-113039543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs532283491	chr2:113039556-113039557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545803495	chr2:113039586-113039587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145807991	chr2:113039666-113039667	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191958255	chr2:113039679-113039680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184400281	chr2:113039755-113039756	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568600958	chr2:113039772-113039773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs531016295	chr2:113039932-113039933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537750295	chr2:113039944-113039945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114307261	chr2:113040025-113040026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs570596676	chr2:113040031-113040032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539573349	chr2:113040058-113040059	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs552920608	chr2:113040085-113040086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112414903	chr2:113040121-113040122	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534876282	chr2:113040132-113040133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557654519	chr2:113040137-113040138	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142849799	chr2:113040236-113040237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189083236	chr2:113040262-113040263	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs114207419	chr2:113040294-113040295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557230561	chr2:113040387-113040388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576993175	chr2:113040406-113040407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536820828	chr2:113040460-113040461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs72943935	chr2:113040477-113040478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs34251989	chr2:113040528-113040529	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559268664	chr2:113040533-113040534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111729053	chr2:113040563-113040564	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113034200-113058200	Weak transcription	Ovary	ovary
2	chr2:113034400-113047800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr2:113034400-113051400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr2:113034400-113097000	Weak transcription	Psoas Muscle	Psoas
5	chr2:113034600-113039600	Weak transcription	Fetal Heart	heart
6	chr2:113034800-113039600	Weak transcription	HepG2	liver
7	chr2:113034800-113041400	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr2:113035000-113046000	Weak transcription	Fetal Kidney	kidney
9	chr2:113035000-113057800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr2:113035000-113057800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:113035000-113057800	Weak transcription	Fetal Intestine Small	intestine
12	chr2:113035200-113040200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:113035400-113040600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr2:113035400-113047600	Weak transcription	Osteobl	bone
15	chr2:113035600-113040400	Weak transcription	Brain Anterior Caudate	brain
16	chr2:113035600-113041200	Weak transcription	K562	blood
17	chr2:113035600-113047600	Weak transcription	NHDF-Ad	bronchial
18	chr2:113035600-113058200	Weak transcription	Primary B cells from cord blood	blood
19	chr2:113035800-113040200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr2:113035800-113058000	Weak transcription	Primary T cells from cord blood	blood
21	chr2:113035800-113060400	Weak transcription	Fetal Thymus	thymus
22	chr2:113035800-113067400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr2:113036000-113040000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:113036000-113040000	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr2:113036000-113040600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr2:113036200-113041200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr2:113036600-113040000	Weak transcription	Liver	Liver
28	chr2:113036600-113058000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr2:113037000-113040000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr2:113037000-113054200	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr2:113038000-113038600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr2:113038600-113040000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:113039600-113040600	Enhancers	HepG2	liver
34	chr2:113039600-113041200	Enhancers	Fetal Heart	heart
35	chr2:113040000-113040200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr2:113040000-113040600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr2:113040000-113040800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr2:113040000-113041800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:113040000-113041800	Enhancers	Liver	Liver
40	chr2:113040000-113081800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:113040200-113040400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr2:113040200-113041200	Enhancers	Colon Smooth Muscle	Colon
43	chr2:113040200-113041800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr2:113040400-113040800	Enhancers	Brain Anterior Caudate	brain
45	chr2:113040600-113041400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:113040600-113041400	Enhancers	A549	lung
47	chr2:113040600-113041600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr2:113040600-113054400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr2:113041200-113041400	Enhancers	K562	blood
50	chr2:113041200-113041800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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