Variant report

Variant	nsv1013142
Chromosome Location	chr2:73854911-73911511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:696)
CpG islands
(count:1101)
Chromatin interactive
region (count:16)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
3	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
6	ATF2	chr2:73901924-73902346	GM12878	blood:	n/a	n/a
7	ATF3	chr2:73903390-73903706	K562	blood:	n/a	n/a
8	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
10	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
11	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
12	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
15	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
16	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
17	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
22	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
24	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
26	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
28	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
29	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
30	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
32	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
35	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
38	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
39	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
40	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
41	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
42	CTCF	chr2:73899297-73899322	GM10248	blood:	n/a	n/a
43	CTCF	chr2:73907220-73907370	HFF	foreskin:	n/a	n/a
44	CTCF	chr2:73858060-73858210	HFF	foreskin:	n/a	n/a
45	CTCF	chr2:73857792-73858146	A549	lung:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
46	CTCF	chr2:73907440-73907590	HVMF	connective:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
47	CTCF	chr2:73857840-73857990	GM12865	blood:	n/a	n/a
48	CTCF	chr2:73874915-73875002	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:73907354-73907634	Gliobla	brain:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
50	CTCF	chr2:73907440-73907590	NB4	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73870653-73870703	HRCEpiC	kidney:	n/a
2	chr2:73871782-73871832	AG09319	gingival:	n/a
3	chr2:73868919-73868969	BJ	skin:	n/a
4	chr2:73870653-73870703	HRCEpiC	kidney:	n/a
5	chr2:73871782-73871832	AG09319	gingival:	n/a
6	chr2:73868919-73868969	BJ	skin:	n/a
7	chr2:73869666-73869716	GM12892	blood:	n/a
8	chr2:73871942-73871992	HMEC	breast:	n/a
9	chr2:73869666-73869716	AG04450	lung:	fetal
10	chr2:73869666-73869716	CMK	blood:	n/a
11	chr2:73871855-73871905	HIPEpiC	eye:	n/a
12	chr2:73871915-73871965	MCF-7	breast:	n/a
13	chr2:73871309-73871359	AG09309	skin:	n/a
14	chr2:73869966-73870016	A549	lung:	n/a
15	chr2:73867196-73867246	AG09319	gingival:	n/a
16	chr2:73869516-73869566	AG10803	skin:	n/a
17	chr2:73871309-73871359	AG09319	gingival:	n/a
18	chr2:73871309-73871359	HL-60	blood:	n/a
19	chr2:73868736-73868786	HRCEpiC	kidney:	n/a
20	chr2:73870653-73870703	ECC-1	luminal epithelium:	n/a
21	chr2:73871782-73871832	HCT-116	colon:	n/a
22	chr2:73869966-73870016	NH-A	brain:	n/a
23	chr2:73871230-73871280	NHBE	bronchial:	n/a
24	chr2:73871230-73871280	LNCaP	prostate:	n/a
25	chr2:73867196-73867246	SK-N-MC	brain:	n/a
26	chr2:73869666-73869716	HRPEpiC	eye:	n/a
27	chr2:73871309-73871359	HepG2	liver:	n/a
28	chr2:73871849-73871899	RPTEC	kidney:	n/a
29	chr2:73869966-73870016	H1-hESC	embryonic stem cell:	embryo
30	chr2:73871230-73871280	Caco-2	colon:	n/a
31	chr2:73871309-73871359	NHBE	bronchial:	n/a
32	chr2:73907327-73907377	NT2-D1	testis:	n/a
33	chr2:73867196-73867246	HAEpiC	amniotic membrane:	n/a
34	chr2:73870294-73870344	PrEC	prostate:	n/a
35	chr2:73867196-73867246	Caco-2	colon:	n/a
36	chr2:73868919-73868969	HUVEC	blood vessel:	n/a
37	chr2:73868736-73868786	SK-N-MC	brain:	n/a
38	chr2:73870294-73870344	H1-hESC	embryonic stem cell:	embryo
39	chr2:73871855-73871905	PrEC	prostate:	n/a
40	chr2:73868919-73868969	SK-N-MC	brain:	n/a
41	chr2:73869516-73869566	GM19239	blood:	n/a
42	chr2:73871309-73871359	BJ	skin:	n/a
43	chr2:73871915-73871965	K562	blood:	n/a
44	chr2:73871855-73871905	HCPEpiC	choroid plexus:	n/a
45	chr2:73870653-73870703	Caco-2	colon:	n/a
46	chr2:73871915-73871965	BJ	skin:	n/a
47	chr2:73871782-73871832	SAEC	small airway:	n/a
48	chr2:73869516-73869566	HEK293	kidney:	embryo
49	chr2:73870105-73870155	HMEC	breast:	n/a
50	chr2:73869516-73869566	HCF	heart:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
2	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
3	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
4	chr2:73868945..73872912-chr2:73927731..73932752,4	MCF-7	breast:
5	chr2:73846839..73847625-chr2:73907303..73907990,2	MCF-7	breast:
6	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
7	chr2:73850004..73850829-chr2:73907369..73907993,2	K562	blood:
8	chr2:73907051..73907568-chr2:74006793..74007607,2	MCF-7	breast:
9	chr2:73846810..73847325-chr2:73907451..73907990,3	K562	blood:
10	chr2:73878117..73880708-chr2:73881565..73884435,2	K562	blood:
11	chr2:73906056..73907836-chr2:74356105..74358909,2	MCF-7	breast:
12	chr2:73907073..73907951-chr2:74066396..74067279,2	MCF-7	breast:
13	chr2:73863562..73865457-chr2:73866043..73867971,2	MCF-7	breast:
14	chr2:73888338..73891192-chr2:73900081..73901857,2	K562	blood:
15	chr2:73880223..73882700-chr2:73884731..73886778,2	K562	blood:
16	chr2:73857783..73858474-chr2:73917561..73918197,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
2	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
3	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
4	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
5	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
6	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
7	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625

No data

Variant related genes	Relation type
ALMS1P	TF binding region
NAT8	TF binding region
ALMS1P	CpG island
NAT8	CpG island
ENSG00000144048	chromatin interactions
ENSG00000204872	chromatin interactions

Extended variants
information (count: 2032 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2032 , 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	rs545941930	chr2:73854915-73854916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142206035	chr2:73854916-73854917	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368649983	chr2:73854964-73854965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs539256107	chr2:73854965-73854966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554432493	chr2:73854991-73854992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62149810	chr2:73854999-73855000	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs116217516	chr2:73855018-73855019	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111662976	chr2:73855068-73855069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112463845	chr2:73855074-73855075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184270331	chr2:73855089-73855090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189993921	chr2:73855140-73855141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532935095	chr2:73855151-73855152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11680056	chr2:73855176-73855177	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs559949818	chr2:73855177-73855178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181140260	chr2:73855217-73855218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186162129	chr2:73855240-73855241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548855153	chr2:73855267-73855268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147057320	chr2:73855284-73855285	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188977127	chr2:73855360-73855361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2947860	chr2:73855386-73855387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs571946802	chr2:73855400-73855401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539373216	chr2:73855417-73855418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs202164668	chr2:73855420-73855421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138412830	chr2:73855423-73855424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566323825	chr2:73855479-73855480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10178409	chr2:73855507-73855508	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs554773850	chr2:73855544-73855545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569537077	chr2:73855579-73855580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543475837	chr2:73855604-73855605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558939397	chr2:73855640-73855641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536874900	chr2:73855668-73855669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs386647346	chr2:73855683-73855684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374658328	chr2:73855684-73855685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149430357	chr2:73855685-73855686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527488610	chr2:73855744-73855745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555360119	chr2:73855761-73855762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199691634	chr2:73855777-73855778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542668745	chr2:73855795-73855796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527368139	chr2:73855809-73855810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560837712	chr2:73855844-73855845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531461569	chr2:73855848-73855849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549494087	chr2:73855859-73855860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571301723	chr2:73855878-73855879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78319290	chr2:73855884-73855885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs398090400	chr2:73855885-73855886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368674630	chr2:73855886-73855887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548112751	chr2:73855896-73855897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs566235963	chr2:73855900-73855901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536460617	chr2:73855914-73855915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145154220	chr2:73855967-73855968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
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
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr2:73854000-73858000	Weak transcription	Liver	Liver
4	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
5	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
6	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
7	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
8	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
9	chr2:73857000-73857200	Active TSS	NHLF	lung
10	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
11	chr2:73857000-73857400	Active TSS	HSMM	muscle
12	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
13	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle
14	chr2:73859800-73860400	Enhancers	Ovary	ovary
15	chr2:73860400-73867000	Weak transcription	Ovary	ovary
16	chr2:73863600-73863800	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr2:73863800-73864600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr2:73864200-73867400	Enhancers	Liver	Liver
19	chr2:73864400-73865000	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr2:73864400-73865400	Enhancers	Duodenum Mucosa	Duodenum
21	chr2:73864600-73865400	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr2:73864600-73865600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr2:73865000-73865200	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr2:73865200-73865400	Enhancers	Stomach Smooth Muscle	stomach
25	chr2:73865200-73867600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr2:73865400-73868000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr2:73865400-73868000	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr2:73865600-73867200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr2:73866200-73867200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:73866200-73870600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:73866400-73866600	Enhancers	Fetal Muscle Trunk	muscle
32	chr2:73866400-73866600	Enhancers	Right Atrium	heart
33	chr2:73866400-73866800	ZNF genes & repeats	Spleen	Spleen
34	chr2:73866400-73868800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:73866400-73871200	Enhancers	Fetal Lung	lung
36	chr2:73866600-73867600	Enhancers	HepG2	liver
37	chr2:73866800-73867800	Weak transcription	Spleen	Spleen
38	chr2:73867000-73867400	Enhancers	Placenta	Placenta
39	chr2:73867000-73868200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:73867000-73868600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr2:73867000-73872200	Enhancers	Ovary	ovary
42	chr2:73867200-73869000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr2:73867200-73869800	Enhancers	Colonic Mucosa	Colon
44	chr2:73867400-73867800	Weak transcription	Placenta	Placenta
45	chr2:73867400-73868400	Enhancers	Brain Hippocampus Middle	brain
46	chr2:73867400-73868600	Enhancers	Adipose Nuclei	Adipose
47	chr2:73867400-73868600	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:73867400-73869800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr2:73867400-73870200	Flanking Active TSS	Liver	Liver
50	chr2:73867400-73870200	Enhancers	Fetal Intestine Large	intestine

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