Variant report

Variant	nsv829460
Chromosome Location	chr2:73856145-73913711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:828)
CpG islands
(count:1098)
Chromatin interactive
region (count:16)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:828 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73907372-73907682	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
4	ARID3A	chr2:73869857-73870120	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:73857942-73858125	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	chr2:73857107-73857303	K562	blood:	n/a	n/a
9	BACH1	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
11	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
12	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
14	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
15	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
16	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
17	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
18	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
19	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
20	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
21	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
23	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
24	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
25	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
29	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
32	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
34	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
36	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
38	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
39	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
40	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
41	CTCF	chr2:73858080-73858230	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr2:73907440-73907590	Hela-S3	cervix:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
43	CTCF	chr2:73907440-73907590	GM12873	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73907740-73907890	GM12869	blood:	n/a	n/a
45	CTCF	chr2:73912148-73912383	HepG2	liver:	n/a	n/a
46	CTCF	chr2:73912260-73912410	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr2:73907435-73907622	MCF-7	breast:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
48	CTCF	chr2:73907440-73907590	SAEC	small airway:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73857818-73858163	Medullo	brain:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
50	CTCF	chr2:73907180-73907330	AG10803	skin:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:73871230-73871280	AG09309	skin:	n/a
2	chr2:73870653-73870703	PANC-1	pancreas:	n/a
3	chr2:73867196-73867246	HPAEpiC	pulmonary alveolar:	n/a
4	chr2:73868736-73868786	AG04449	skin:	fetal
5	chr2:73907327-73907377	HRCEpiC	kidney:	n/a
6	chr2:73871855-73871905	HEK293	kidney:	embryo
7	chr2:73869966-73870016	NHDF-neo	bronchial:	n/a
8	chr2:73868919-73868969	HEK293	kidney:	embryo
9	chr2:73869966-73870016	HMEC	breast:	n/a
10	chr2:73871230-73871280	NHBE	bronchial:	n/a
11	chr2:73871230-73871280	HepG2	liver:	n/a
12	chr2:73870653-73870703	MCF10A-Er-Src	breast:	n/a
13	chr2:73870294-73870344	Jurkat	blood:	n/a
14	chr2:73871230-73871280	PFSK-1	brain:	n/a
15	chr2:73870105-73870155	LNCaP	prostate:	n/a
16	chr2:73907327-73907377	HEK293	kidney:	embryo
17	chr2:73868919-73868969	AG10803	skin:	n/a
18	chr2:73869966-73870016	HRCEpiC	kidney:	n/a
19	chr2:73871230-73871280	K562	blood:	n/a
20	chr2:73871782-73871832	NT2-D1	testis:	n/a
21	chr2:73871309-73871359	U87	brain:	n/a
22	chr2:73868919-73868969	HNPCEpiC	eye:	n/a
23	chr2:73869966-73870016	PANC-1	pancreas:	n/a
24	chr2:73871942-73871992	SK-N-SH	brain:	n/a
25	chr2:73869666-73869716	AG09319	gingival:	n/a
26	chr2:73871915-73871965	AG09309	skin:	n/a
27	chr2:73907327-73907377	HepG2	liver:	n/a
28	chr2:73869516-73869566	MCF-7	breast:	n/a
29	chr2:73869666-73869716	HRCEpiC	kidney:	n/a
30	chr2:73868736-73868786	HEK293	kidney:	embryo
31	chr2:73871849-73871899	ProgFib	skin:	n/a
32	chr2:73871230-73871280	HRPEpiC	eye:	n/a
33	chr2:73871915-73871965	U87	brain:	n/a
34	chr2:73871915-73871965	PrEC	prostate:	n/a
35	chr2:73871309-73871359	MCF10A-Er-Src	breast:	n/a
36	chr2:73869966-73870016	GM12891	blood:	n/a
37	chr2:73868736-73868786	HIPEpiC	eye:	n/a
38	chr2:73871782-73871832	ECC-1	luminal epithelium:	n/a
39	chr2:73871782-73871832	GM06990	blood:	n/a
40	chr2:73871309-73871359	SAEC	small airway:	n/a
41	chr2:73871230-73871280	HEK293	kidney:	embryo
42	chr2:73871849-73871899	Hepatocyte	liver:	n/a
43	chr2:73868919-73868969	H1-hESC	embryonic stem cell:	embryo
44	chr2:73871849-73871899	LNCaP	prostate:	n/a
45	chr2:73871309-73871359	GM19239	blood:	n/a
46	chr2:73871915-73871965	Jurkat	blood:	n/a
47	chr2:73869516-73869566	GM19239	blood:	n/a
48	chr2:73869666-73869716	K562	blood:	n/a
49	chr2:73869966-73870016	NHBE	bronchial:	n/a
50	chr2:73869966-73870016	HIPEpiC	eye:	n/a

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

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

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
2	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
3	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683
4	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
5	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
6	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
7	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
8	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: 2081 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571877358	chr2:73856145-73856146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542480622	chr2:73856152-73856153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116695224	chr2:73856205-73856206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576045135	chr2:73856225-73856226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs543548941	chr2:73856243-73856244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564821765	chr2:73856253-73856254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532153463	chr2:73856260-73856261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548074499	chr2:73856267-73856268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560109652	chr2:73856280-73856281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2947859	chr2:73856289-73856290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34570629	chr2:73856320-73856321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs530453745	chr2:73856325-73856326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114973039	chr2:73856356-73856357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186560137	chr2:73856366-73856367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191021051	chr2:73856414-73856415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539010586	chr2:73856422-73856423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552259530	chr2:73856464-73856465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6713651	chr2:73856490-73856491	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs78636755	chr2:73856500-73856501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35103131	chr2:73856501-73856502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186032767	chr2:73856513-73856514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543277758	chr2:73856515-73856516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536588035	chr2:73856521-73856522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191510670	chr2:73856533-73856534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570659043	chr2:73856542-73856543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543110549	chr2:73856590-73856591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564988027	chr2:73856619-73856620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576879077	chr2:73856719-73856720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182789097	chr2:73856731-73856732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73947821	chr2:73856744-73856745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4852939	chr2:73856769-73856770	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs142985646	chr2:73856810-73856811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187906223	chr2:73856815-73856816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531148120	chr2:73856834-73856835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552220990	chr2:73856896-73856897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192491254	chr2:73856904-73856905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182200004	chr2:73856921-73856922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547030990	chr2:73856942-73856943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187875713	chr2:73856968-73856969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546578409	chr2:73856972-73856973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368926271	chr2:73856974-73856975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534751279	chr2:73856977-73856978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568486986	chr2:73856983-73856984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192441247	chr2:73857000-73857001	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4852940	chr2:73857002-73857003	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs201602504	chr2:73857066-73857067	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576122137	chr2:73857075-73857076	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57809531	chr2:73857092-73857093	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs150010907	chr2:73857094-73857095	ZNF genes & repeats Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376048599	chr2:73857105-73857106	ZNF genes & repeats Enhancers Active TSS 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:220 , 50 per page) page: 1 2 3 4 5

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

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