Variant report

Variant	esv3385057
Chromosome Location	chr2:73853505-73913858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:867)
CpG islands
(count:1098)
Chromatin interactive
region (count:16)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
3	ARID3A	chr2:73907372-73907682	HepG2	liver:	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	chr2:73907465-73907526	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:73857107-73857303	K562	blood:	n/a	n/a
10	BATF	chr2:73911582-73911820	GM12878	blood:	n/a	chr2:73911707-73911718
11	BATF	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
12	BATF	chr2:73901924-73902350	GM12878	blood:	n/a	n/a
13	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
14	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
15	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
17	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
18	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
20	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
22	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
24	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
28	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
29	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
30	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
31	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
34	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
35	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
36	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
37	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
38	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
39	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
40	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
41	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
42	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
43	CTCF	chr2:73907440-73907590	HBMEC	blood vessel:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
44	CTCF	chr2:73906900-73907050	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr2:73907440-73907590	GM12874	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
46	CTCF	chr2:73912260-73912410	HRE	kidney:	n/a	n/a
47	CTCF	chr2:73857837-73858127	Hela-S3	cervix:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006
48	CTCF	chr2:73879127-73879200	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:73858080-73858230	HVMF	connective:	n/a	n/a
50	CTCF	chr2:73912200-73912350	BE2_C	brain:	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	chr2:73870105-73870155	U87	brain:	n/a
2	chr2:73871915-73871965	SK-N-SH_RA	brain:	n/a
3	chr2:73871309-73871359	NH-A	brain:	n/a
4	chr2:73871942-73871992	HepG2	liver:	n/a
5	chr2:73869966-73870016	HEEpiC	esophagus:	n/a
6	chr2:73870653-73870703	ProgFib	skin:	n/a
7	chr2:73907327-73907377	Hela-S3	cervix:	n/a
8	chr2:73869666-73869716	AG04449	skin:	fetal
9	chr2:73871849-73871899	AG04449	skin:	fetal
10	chr2:73870105-73870155	HL-60	blood:	n/a
11	chr2:73868736-73868786	AG04450	lung:	fetal
12	chr2:73869966-73870016	MCF-7	breast:	n/a
13	chr2:73871855-73871905	HL-60	blood:	n/a
14	chr2:73871849-73871899	SK-N-SH	brain:	n/a
15	chr2:73868919-73868969	HRPEpiC	eye:	n/a
16	chr2:73870294-73870344	NB4	blood:	n/a
17	chr2:73871230-73871280	NB4	blood:	n/a
18	chr2:73871782-73871832	ECC-1	luminal epithelium:	n/a
19	chr2:73871309-73871359	HCM	heart:	n/a
20	chr2:73870653-73870703	U87	brain:	n/a
21	chr2:73871782-73871832	Caco-2	colon:	n/a
22	chr2:73868917-73868967	GM12892	blood:	n/a
23	chr2:73870294-73870344	ECC-1	luminal epithelium:	n/a
24	chr2:73871849-73871899	MCF10A-Er-Src	breast:	n/a
25	chr2:73870294-73870344	AG04449	skin:	fetal
26	chr2:73870653-73870703	NHDF-neo	bronchial:	n/a
27	chr2:73869666-73869716	MCF-7	breast:	n/a
28	chr2:73871782-73871832	ovcar-3	ovarian:	n/a
29	chr2:73870653-73870703	AG04450	lung:	fetal
30	chr2:73870294-73870344	HRCEpiC	kidney:	n/a
31	chr2:73907327-73907377	A549	lung:	n/a
32	chr2:73871782-73871832	HIPEpiC	eye:	n/a
33	chr2:73867196-73867246	NH-A	brain:	n/a
34	chr2:73870105-73870155	Jurkat	blood:	n/a
35	chr2:73869516-73869566	NHBE	bronchial:	n/a
36	chr2:73871309-73871359	HCF	heart:	n/a
37	chr2:73871782-73871832	HCF	heart:	n/a
38	chr2:73868736-73868786	HEEpiC	esophagus:	n/a
39	chr2:73871230-73871280	HCT-116	colon:	n/a
40	chr2:73907327-73907377	NH-A	brain:	n/a
41	chr2:73868919-73868969	HepG2	liver:	n/a
42	chr2:73871855-73871905	HIPEpiC	eye:	n/a
43	chr2:73868917-73868967	GM12891	blood:	n/a
44	chr2:73868919-73868969	GM12892	blood:	n/a
45	chr2:73870653-73870703	HAEpiC	amniotic membrane:	n/a
46	chr2:73867196-73867246	Caco-2	colon:	n/a
47	chr2:73867196-73867246	AG04449	skin:	fetal
48	chr2:73870294-73870344	MCF10A-Er-Src	breast:	n/a
49	chr2:73870653-73870703	ovcar-3	ovarian:	n/a
50	chr2:73871942-73871992	GM12892	blood:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
2	lnc-ALMS1-3	chr2:73912088-73912694	NR_003683
3	lnc-ALMS1-3	chr2:73899935-73900177	NR_003683
4	lnc-ALMS1-3	chr2:73901969-73902032	NR_003683
5	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
6	lnc-ALMS1-2	chr2:73868076-73868755	NONHSAT071625
7	lnc-ALMS1-3	chr2:73900940-73901123	NR_003683
8	lnc-ALMS1-3	chr2:73898207-73898277	NR_003683

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: 2219 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2219 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4241256	chr2:73853509-73853510	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557534942	chr2:73853513-73853514	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573181998	chr2:73853565-73853566	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs540562824	chr2:73853575-73853576	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150879050	chr2:73853590-73853591	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529491921	chr2:73853607-73853608	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544341199	chr2:73853626-73853627	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs59627701	chr2:73853641-73853642	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56012019	chr2:73853642-73853643	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563922899	chr2:73853653-73853654	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563017161	chr2:73853675-73853676	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533148681	chr2:73853677-73853678	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551733664	chr2:73853679-73853680	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543328031	chr2:73853736-73853737	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182997776	chr2:73853748-73853749	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139730630	chr2:73853763-73853764	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546964471	chr2:73853773-73853774	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370773792	chr2:73853784-73853785	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568216424	chr2:73853812-73853813	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62149809	chr2:73853830-73853831	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144036959	chr2:73853885-73853886	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568911816	chr2:73853894-73853895	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192635548	chr2:73853921-73853922	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557319834	chr2:73853979-73853980	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182987012	chr2:73853993-73853994	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540476868	chr2:73853994-73853995	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555651680	chr2:73853997-73853998	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34404189	chr2:73854069-73854070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527970234	chr2:73854070-73854071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574120110	chr2:73854096-73854097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544815244	chr2:73854097-73854098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13007306	chr2:73854133-73854134	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113165835	chr2:73854145-73854146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545560274	chr2:73854157-73854158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560489812	chr2:73854168-73854169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149672018	chr2:73854170-73854171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546880785	chr2:73854177-73854178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562036185	chr2:73854180-73854181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370482682	chr2:73854193-73854194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529201365	chr2:73854219-73854220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559585750	chr2:73854220-73854221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568995273	chr2:73854266-73854267	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374727122	chr2:73854276-73854277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187511330	chr2:73854282-73854283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551061993	chr2:73854307-73854308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566090109	chr2:73854309-73854310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs193257750	chr2:73854340-73854341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145598756	chr2:73854341-73854342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370964996	chr2:73854342-73854343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574255749	chr2:73854350-73854351	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:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73830600-73854800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:73844000-73854800	Weak transcription	Fetal Brain Female	brain
3	chr2:73852400-73854000	Enhancers	Liver	Liver
4	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr2:73852600-73853800	Enhancers	Ovary	ovary
6	chr2:73852600-73854000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr2:73852600-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr2:73852600-73854400	Enhancers	Primary hematopoietic stem cells	blood
9	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr2:73853000-73854000	Enhancers	GM12878-XiMat	blood
11	chr2:73853200-73853600	Enhancers	HepG2	liver
12	chr2:73853400-73853600	Enhancers	Fetal Intestine Large	intestine
13	chr2:73853800-73854000	Weak transcription	Ovary	ovary
14	chr2:73854000-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr2:73854000-73858000	Weak transcription	Liver	Liver
16	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
18	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
19	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
20	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
21	chr2:73857000-73857200	Active TSS	NHLF	lung
22	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
23	chr2:73857000-73857400	Active TSS	HSMM	muscle
24	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
25	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle
26	chr2:73859800-73860400	Enhancers	Ovary	ovary
27	chr2:73860400-73867000	Weak transcription	Ovary	ovary
28	chr2:73863600-73863800	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr2:73863800-73864600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr2:73864200-73867400	Enhancers	Liver	Liver
31	chr2:73864400-73865000	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr2:73864400-73865400	Enhancers	Duodenum Mucosa	Duodenum
33	chr2:73864600-73865400	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr2:73864600-73865600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr2:73865000-73865200	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr2:73865200-73865400	Enhancers	Stomach Smooth Muscle	stomach
37	chr2:73865200-73867600	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr2:73865400-73868000	Weak transcription	Duodenum Mucosa	Duodenum
39	chr2:73865400-73868000	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr2:73865600-73867200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr2:73866200-73867200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr2:73866200-73870600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:73866400-73866600	Enhancers	Fetal Muscle Trunk	muscle
44	chr2:73866400-73866600	Enhancers	Right Atrium	heart
45	chr2:73866400-73866800	ZNF genes & repeats	Spleen	Spleen
46	chr2:73866400-73868800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr2:73866400-73871200	Enhancers	Fetal Lung	lung
48	chr2:73866600-73867600	Enhancers	HepG2	liver
49	chr2:73866800-73867800	Weak transcription	Spleen	Spleen
50	chr2:73867000-73867400	Enhancers	Placenta	Placenta

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