Variant report

Variant	nsv961338
Chromosome Location	chr2:113657963-113691422
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	chr2:113685428-113685677	K562	blood:	n/a	n/a
2	ATF1	chr2:113662517-113662717	K562	blood:	n/a	n/a
3	ATF1	chr2:113678475-113678792	K562	blood:	n/a	n/a
4	BACH1	chr2:113681268-113681532	K562	blood:	n/a	n/a
5	BATF	chr2:113674183-113674484	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:113662608-113662734	K562	blood:	n/a	n/a
7	BHLHE40	chr2:113682108-113682201	K562	blood:	n/a	n/a
8	CBX3	chr2:113678342-113678908	HCT-116	colon:	n/a	n/a
9	CCNT2	chr2:113677966-113677977	K562	blood:	n/a	n/a
10	CCNT2	chr2:113662465-113662709	K562	blood:	n/a	chr2:113662634-113662654
11	CEBPB	chr2:113688781-113688803	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:113681359-113681873	K562	blood:	n/a	chr2:113681704-113681715
13	CEBPB	chr2:113681548-113681860	HepG2	liver:	n/a	chr2:113681704-113681715
14	CEBPB	chr2:113681553-113681794	H1-hESC	embryonic stem cell:	n/a	chr2:113681704-113681715
15	CEBPB	chr2:113681552-113681752	A549	lung:	n/a	chr2:113681704-113681715
16	CEBPB	chr2:113681513-113681893	K562	blood:	n/a	chr2:113681704-113681715
17	CEBPB	chr2:113681575-113681836	IMR90	lung:	n/a	chr2:113681704-113681715
18	CREB1	chr2:113678400-113678795	K562	blood:	n/a	n/a
19	CTCF	chr2:113678700-113678850	AG10803	skin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
20	CTCF	chr2:113680994-113681105	K562	blood:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
21	CTCF	chr2:113685500-113685650	NHEK	skin:	n/a	chr2:113685518-113685534
22	CTCF	chr2:113681000-113681150	HEEpiC	esophagus:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
23	CTCF	chr2:113681054-113681101	NHEK	skin:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
24	CTCF	chr2:113680980-113681130	HPAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
25	CTCF	chr2:113681060-113681210	HMF	breast:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
26	CTCF	chr2:113678700-113678850	HCPEpiC	choroid plexus:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
27	CTCF	chr2:113681042-113681197	K562	blood:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
28	CTCF	chr2:113678760-113678910	HBMEC	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
29	CTCF	chr2:113678760-113678910	HCT-116	colon:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
30	CTCF	chr2:113685451-113685660	K562	blood:	n/a	chr2:113685518-113685534
31	CTCF	chr2:113678761-113678832	NHEK	skin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
32	CTCF	chr2:113680980-113681130	NHEK	skin:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
33	CTCF	chr2:113680980-113681130	AoAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
34	CTCF	chr2:113678660-113678810	NHEK	skin:	n/a	n/a
35	CTCF	chr2:113681040-113681190	HAc	cerebellar:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
36	CTCF	chr2:113678760-113678910	HFF	foreskin:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
37	CTCF	chr2:113673580-113673730	GM12875	blood:	n/a	n/a
38	CTCF	chr2:113678760-113678910	HPAF	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
39	CTCF	chr2:113678730-113678743	K562	blood:	n/a	n/a
40	CTCF	chr2:113678700-113678850	HBMEC	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
41	CTCF	chr2:113680960-113681110	HBMEC	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
42	CTCF	chr2:113682140-113682290	GM12867	blood:	n/a	n/a
43	CTCF	chr2:113680980-113681130	HCFaa	heart:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
44	CTCF	chr2:113678720-113678870	HMF	breast:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
45	CTCF	chr2:113678700-113678850	HCM	heart:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
46	CTCF	chr2:113678760-113678910	HCFaa	heart:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
47	CTCF	chr2:113678720-113678870	HPAF	blood vessel:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
48	CTCF	chr2:113681000-113681150	HMEC	breast:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092
49	CTCF	chr2:113678760-113678910	HCPEpiC	choroid plexus:	n/a	chr2:113678802-113678811 chr2:113678791-113678812 chr2:113678798-113678811 chr2:113678796-113678814
50	CTCF	chr2:113680960-113681110	HPAF	blood vessel:	n/a	chr2:113681076-113681094 chr2:113681079-113681088 chr2:113681078-113681099 chr2:113681079-113681092

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113672713-113672763	HCT-116	colon:	n/a
2	chr2:113672713-113672763	HCT-116	colon:	n/a
3	chr2:113672199-113672249	HRPEpiC	eye:	n/a
4	chr2:113670427-113670477	RPTEC	kidney:	n/a
5	chr2:113669835-113669885	AG09319	gingival:	n/a
6	chr2:113672713-113672763	Hepatocyte	liver:	n/a
7	chr2:113676413-113676463	PrEC	prostate:	n/a
8	chr2:113671813-113671863	MCF10A-Er-Src	breast:	n/a
9	chr2:113670427-113670477	HNPCEpiC	eye:	n/a
10	chr2:113676413-113676463	SK-N-SH_RA	brain:	n/a
11	chr2:113672758-113672808	HL-60	blood:	n/a
12	chr2:113672199-113672249	GM12892	blood:	n/a
13	chr2:113676235-113676285	A549	lung:	n/a
14	chr2:113669912-113669962	NHBE	bronchial:	n/a
15	chr2:113669419-113669469	SK-N-MC	brain:	n/a
16	chr2:113670427-113670477	T-47D	breast:	n/a
17	chr2:113669835-113669885	U87	brain:	n/a
18	chr2:113671813-113671863	HNPCEpiC	eye:	n/a
19	chr2:113671813-113671863	HRPEpiC	eye:	n/a
20	chr2:113672199-113672249	GM12891	blood:	n/a
21	chr2:113669912-113669962	RPTEC	kidney:	n/a
22	chr2:113669419-113669469	BJ	skin:	n/a
23	chr2:113669912-113669962	HCF	heart:	n/a
24	chr2:113669912-113669962	HMEC	breast:	n/a
25	chr2:113669912-113669962	ECC-1	luminal epithelium:	n/a
26	chr2:113672587-113672637	LNCaP	prostate:	n/a
27	chr2:113672587-113672637	HRPEpiC	eye:	n/a
28	chr2:113670427-113670477	GM19239	blood:	n/a
29	chr2:113672758-113672808	MCF-7	breast:	n/a
30	chr2:113669835-113669885	GM19239	blood:	n/a
31	chr2:113670427-113670477	ovcar-3	ovarian:	n/a
32	chr2:113670427-113670477	GM12892	blood:	n/a
33	chr2:113676235-113676285	ProgFib	skin:	n/a
34	chr2:113672587-113672637	HAEpiC	amniotic membrane:	n/a
35	chr2:113672758-113672808	A549	lung:	n/a
36	chr2:113672758-113672808	HPAEpiC	pulmonary alveolar:	n/a
37	chr2:113671813-113671863	Caco-2	colon:	n/a
38	chr2:113671356-113671406	SKMC	muscle:	n/a
39	chr2:113669835-113669885	PrEC	prostate:	n/a
40	chr2:113676235-113676285	HRCEpiC	kidney:	n/a
41	chr2:113669419-113669469	T-47D	breast:	n/a
42	chr2:113670582-113670632	HCT-116	colon:	n/a
43	chr2:113672587-113672637	GM19239	blood:	n/a
44	chr2:113676413-113676463	HAEpiC	amniotic membrane:	n/a
45	chr2:113676413-113676463	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:113672713-113672763	AG10803	skin:	n/a
47	chr2:113672758-113672808	SK-N-MC	brain:	n/a
48	chr2:113670427-113670477	AoSMC	blood vessel:	n/a
49	chr2:113672587-113672637	AG09309	skin:	n/a
50	chr2:113676413-113676463	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:113665026..113667362-chr2:113668191..113671168,3	K562	blood:
2	chr2:113340678..113342396-chr2:113662998..113664820,2	K562	blood:
3	chr2:113656283..113658369-chr2:113658759..113661477,2	MCF-7	breast:
4	chr2:113656283..113658369-chr2:113658759..113661477,2	MCF-7	breast:
5	chr2:113671840..113673562-chr2:113673585..113676227,2	K562	blood:
6	chr2:113488382..113489971-chr2:113681773..113683855,2	MCF-7	breast:
7	chr2:113665279..113667545-chr2:113668191..113672531,3	K562	blood:
8	chr2:113682507..113685123-chr2:113688848..113691185,2	K562	blood:
9	chr2:113674868..113678484-chr2:113678490..113681949,3	K562	blood:
10	chr2:113674868..113678484-chr2:113678490..113681949,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL37-2	chr2:113679974-113683444	ucscGeneNc_uc002tji_1
2	lnc-IL37-3	chr2:113690202-113690748	NONHSAT073735

Variant related genes	Relation type
IL37	TF binding region
ENSG00000227368	TF binding region
IL37	CpG island
ENSG00000227368	CpG island
ENSG00000125571	chromatin interactions
ENSG00000125611	chromatin interactions
ENSG00000227368	chromatin interactions

Extended variants
information (count: 1354 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375952261	chr2:113658007-113658008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs11690539	chr2:113658015-113658016	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2723154	chr2:113658075-113658076	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs532159832	chr2:113658191-113658192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186371451	chr2:113658223-113658224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190927693	chr2:113658284-113658285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200887698	chr2:113658376-113658377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568609718	chr2:113658438-113658439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531126239	chr2:113658441-113658442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183440487	chr2:113658442-113658443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544553688	chr2:113658472-113658473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539460714	chr2:113658488-113658489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs552984119	chr2:113658494-113658495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566505464	chr2:113658516-113658517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556797466	chr2:113658562-113658563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534646762	chr2:113658574-113658575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573069890	chr2:113658588-113658589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185787718	chr2:113658617-113658618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191039587	chr2:113658663-113658664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543557462	chr2:113658668-113658669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs4591347	chr2:113658705-113658706	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs113465881	chr2:113658710-113658711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143937016	chr2:113658716-113658717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2954819	chr2:113658724-113658725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs528093175	chr2:113658768-113658769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542587684	chr2:113658865-113658866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554934555	chr2:113658902-113658903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562358511	chr2:113658903-113658904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182971460	chr2:113658904-113658905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551117856	chr2:113658908-113658909	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570937895	chr2:113658909-113658910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs80115953	chr2:113658935-113658936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75186371	chr2:113658938-113658939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs57356116	chr2:113658945-113658946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78758796	chr2:113658951-113658952	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs5833470	chr2:113658954-113658955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368616889	chr2:113658955-113658956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541575819	chr2:113659033-113659034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369243799	chr2:113659097-113659098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146527042	chr2:113659120-113659121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546684874	chr2:113659139-113659140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188415089	chr2:113659236-113659237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192017726	chr2:113659391-113659392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554571907	chr2:113659491-113659492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34343857	chr2:113659508-113659509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568317396	chr2:113659522-113659523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536868381	chr2:113659556-113659557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557154156	chr2:113659608-113659609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576944323	chr2:113659614-113659615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2723153	chr2:113659632-113659633	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:78)

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
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113655200-113659800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:113657400-113660600	Enhancers	Fetal Intestine Large	intestine
3	chr2:113657400-113660800	Enhancers	Fetal Intestine Small	intestine
4	chr2:113658400-113658600	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr2:113658600-113659600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr2:113659200-113660000	Enhancers	HepG2	liver
7	chr2:113659600-113659800	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr2:113659600-113660000	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr2:113659800-113660000	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr2:113660000-113660400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr2:113660400-113660800	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr2:113660600-113663200	Weak transcription	Fetal Intestine Large	intestine
13	chr2:113661200-113663800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr2:113662200-113663400	Enhancers	K562	blood
15	chr2:113662400-113663600	Enhancers	Fetal Heart	heart
16	chr2:113662800-113663000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr2:113663000-113663600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:113663200-113663400	Enhancers	Fetal Intestine Large	intestine
19	chr2:113663200-113663400	Enhancers	Spleen	Spleen
20	chr2:113663400-113664000	Weak transcription	Fetal Intestine Large	intestine
21	chr2:113663400-113665000	Enhancers	HMEC	breast
22	chr2:113663600-113664800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr2:113663600-113665600	Weak transcription	Fetal Heart	heart
24	chr2:113663800-113664400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr2:113663800-113664800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr2:113664000-113664200	Enhancers	Fetal Intestine Large	intestine
27	chr2:113664000-113664200	Enhancers	Spleen	Spleen
28	chr2:113664000-113664600	Enhancers	NHEK	skin
29	chr2:113664200-113664600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr2:113664400-113665200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:113664600-113668400	Weak transcription	NHEK	skin
32	chr2:113664800-113668200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:113664800-113678000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:113665000-113668400	Weak transcription	HMEC	breast
35	chr2:113665600-113666200	Enhancers	Fetal Heart	heart
36	chr2:113667000-113667200	Enhancers	K562	blood
37	chr2:113667000-113667400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr2:113667000-113668400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr2:113667200-113668600	Enhancers	HepG2	liver
40	chr2:113667600-113668400	Enhancers	Brain Germinal Matrix	brain
41	chr2:113668200-113668600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr2:113668400-113668600	Enhancers	HMEC	breast
43	chr2:113668400-113669000	Enhancers	NHEK	skin
44	chr2:113671400-113671600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:113671600-113674400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr2:113671600-113674800	Enhancers	Primary T cells fromperipheralblood	blood
47	chr2:113671600-113683000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:113671800-113674600	Enhancers	Fetal Thymus	thymus
49	chr2:113671800-113675000	Enhancers	Thymus	Thymus
50	chr2:113672000-113672200	Enhancers	Spleen	Spleen

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