Variant report

Variant	esv2497164
Chromosome Location	chr2:73850717-73912022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:832)
CpG islands
(count:1099)
Chromatin interactive
region (count:17)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:832 , 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	chr2:73857942-73858125	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:73867690-73868035	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:73907394-73907641	K562	blood:	n/a	n/a
5	ARID3A	chr2:73869857-73870120	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	chr2:73855647-73855936	GM12878	blood:	n/a	n/a
13	BATF	chr2:73851315-73851489	GM12878	blood:	n/a	chr2:73851419-73851430
14	BATF	chr2:73851278-73851536	GM12878	blood:	n/a	chr2:73851419-73851430
15	BATF	chr2:73901777-73902343	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:73855638-73856013	GM12878	blood:	n/a	n/a
17	BCL11A	chr2:73901938-73902290	GM12878	blood:	n/a	chr2:73902211-73902220 chr2:73902210-73902219
18	BHLHE40	chr2:73871815-73871977	K562	blood:	n/a	n/a
19	CBX3	chr2:73865650-73865822	K562	blood:	n/a	n/a
20	CEBPB	chr2:73900871-73900878	A549	lung:	n/a	n/a
21	CEBPB	chr2:73903375-73903643	IMR90	lung:	n/a	chr2:73903539-73903550
22	CEBPB	chr2:73903414-73903663	A549	lung:	n/a	chr2:73903539-73903550
23	CEBPB	chr2:73903410-73903643	K562	blood:	n/a	chr2:73903539-73903550
24	CEBPB	chr2:73903357-73903734	K562	blood:	n/a	chr2:73903539-73903550
25	CEBPB	chr2:73903369-73903615	HepG2	liver:	n/a	chr2:73903539-73903550
26	CEBPB	chr2:73903437-73903637	H1-hESC	embryonic stem cell:	n/a	chr2:73903539-73903550
27	CEBPB	chr2:73877646-73878600	HepG2	liver:	n/a	chr2:73878449-73878460
28	CEBPB	chr2:73869492-73869669	HepG2	liver:	n/a	n/a
29	CEBPB	chr2:73903365-73903683	K562	blood:	n/a	chr2:73903539-73903550
30	CEBPB	chr2:73859061-73859298	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:73877660-73878170	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:73903402-73903602	Hela-S3	cervix:	n/a	chr2:73903539-73903550
33	CEBPB	chr2:73877993-73878055	K562	blood:	n/a	n/a
34	CEBPB	chr2:73877771-73878092	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr2:73900813-73900977	K562	blood:	n/a	chr2:73900873-73900886
36	CEBPB	chr2:73867669-73868041	HepG2	liver:	n/a	chr2:73867845-73867858
37	CEBPB	chr2:73869936-73870184	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:73867630-73868101	MCF-7	breast:	n/a	chr2:73867845-73867858
39	CEBPB	chr2:73865645-73865764	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr2:73867603-73868071	MCF-7	breast:	n/a	chr2:73867845-73867858
41	CEBPB	chr2:73877667-73878169	A549	lung:	n/a	n/a
42	CEBPB	chr2:73869472-73869730	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:73867840-73867965	A549	lung:	n/a	chr2:73867845-73867858
44	CHD2	chr2:73869804-73870074	HepG2	liver:	n/a	n/a
45	CTCF	chr2:73907300-73907708	H1-hESC	embryonic stem cell:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
46	CTCF	chr2:73907460-73907610	HAc	cerebellar:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
47	CTCF	chr2:73851920-73852070	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr2:73907440-73907590	GM12873	blood:	n/a	chr2:73907497-73907513 chr2:73907499-73907512 chr2:73907498-73907519 chr2:73907496-73907514
49	CTCF	chr2:73851880-73852030	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:73857787-73858233	HepG2	liver:	n/a	chr2:73857989-73858007 chr2:73857992-73858005 chr2:73857994-73858002 chr2:73857991-73858012 chr2:73857990-73858006

(count:1099 , 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	AG10803	skin:	n/a
2	chr2:73871230-73871280	AG10803	skin:	n/a
3	chr2:73868919-73868969	SK-N-SH_RA	brain:	n/a
4	chr2:73869516-73869566	HCT-116	colon:	n/a
5	chr2:73871915-73871965	Caco-2	colon:	n/a
6	chr2:73871230-73871280	GM12891	blood:	n/a
7	chr2:73869516-73869566	HNPCEpiC	eye:	n/a
8	chr2:73871309-73871359	HepG2	liver:	n/a
9	chr2:73870653-73870703	SK-N-MC	brain:	n/a
10	chr2:73869966-73870016	NT2-D1	testis:	n/a
11	chr2:73871230-73871280	PFSK-1	brain:	n/a
12	chr2:73871782-73871832	PANC-1	pancreas:	n/a
13	chr2:73869966-73870016	MCF-7	breast:	n/a
14	chr2:73867196-73867246	RPTEC	kidney:	n/a
15	chr2:73869516-73869566	AG09309	skin:	n/a
16	chr2:73868736-73868786	NHDF-neo	bronchial:	n/a
17	chr2:73868919-73868969	HRPEpiC	eye:	n/a
18	chr2:73869516-73869566	T-47D	breast:	n/a
19	chr2:73870294-73870344	AG04450	lung:	fetal
20	chr2:73871942-73871992	HCF	heart:	n/a
21	chr2:73868917-73868967	T-47D	breast:	n/a
22	chr2:73871855-73871905	AG04449	skin:	fetal
23	chr2:73871309-73871359	SKMC	muscle:	n/a
24	chr2:73871942-73871992	SKMC	muscle:	n/a
25	chr2:73869516-73869566	Hepatocyte	liver:	n/a
26	chr2:73871942-73871992	Hela-S3	cervix:	n/a
27	chr2:73868919-73868969	NT2-D1	testis:	n/a
28	chr2:73870294-73870344	H1-hESC	embryonic stem cell:	embryo
29	chr2:73871782-73871832	AG10803	skin:	n/a
30	chr2:73869666-73869716	HAEpiC	amniotic membrane:	n/a
31	chr2:73869666-73869716	SK-N-SH	brain:	n/a
32	chr2:73868919-73868969	GM12891	blood:	n/a
33	chr2:73871782-73871832	HCM	heart:	n/a
34	chr2:73871942-73871992	HRCEpiC	kidney:	n/a
35	chr2:73870653-73870703	SAEC	small airway:	n/a
36	chr2:73868917-73868967	NHBE	bronchial:	n/a
37	chr2:73871855-73871905	HUVEC	blood vessel:	n/a
38	chr2:73867196-73867246	HMEC	breast:	n/a
39	chr2:73869516-73869566	PANC-1	pancreas:	n/a
40	chr2:73869516-73869566	ECC-1	luminal epithelium:	n/a
41	chr2:73868919-73868969	BJ	skin:	n/a
42	chr2:73870653-73870703	AG04449	skin:	fetal
43	chr2:73869966-73870016	HCT-116	colon:	n/a
44	chr2:73868736-73868786	NT2-D1	testis:	n/a
45	chr2:73871782-73871832	AG04449	skin:	fetal
46	chr2:73869966-73870016	BJ	skin:	n/a
47	chr2:73868919-73868969	AG09319	gingival:	n/a
48	chr2:73871230-73871280	Jurkat	blood:	n/a
49	chr2:73869966-73870016	RPTEC	kidney:	n/a
50	chr2:73871849-73871899	GM12891	blood:	n/a

(count:17 , 50 per page) page: 1

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

(count:7 , 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	chr2:73900940-73901123	NR_003683
3	lnc-ALMS1-3	chr2:73899436-73899622	NR_003683
4	lnc-ALMS1-3	chr2:73872046-73872281	NR_003683
5	lnc-ALMS1-3	chr2:73898207-73898277	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
ENSG00000204872	chromatin interactions
ENSG00000144048	chromatin interactions

Extended variants
information (count: 2235 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2235 , 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	rs143177686	chr2:73850726-73850727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188759713	chr2:73850731-73850732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148280205	chr2:73850747-73850748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577130639	chr2:73850752-73850753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541083051	chr2:73850780-73850781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571988320	chr2:73850789-73850790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542553083	chr2:73850790-73850791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72811960	chr2:73850799-73850800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs561757545	chr2:73850803-73850804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6711001	chr2:73850820-73850821	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs376992845	chr2:73850871-73850872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115124629	chr2:73850876-73850877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140267525	chr2:73850891-73850892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547392454	chr2:73850893-73850894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181235217	chr2:73850935-73850936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530410220	chr2:73850999-73851000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548947896	chr2:73851003-73851004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs56658499	chr2:73851024-73851025	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs537260076	chr2:73851056-73851057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138762147	chr2:73851064-73851065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs3980696	chr2:73851086-73851087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs34057786	chr2:73851161-73851162	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs559827547	chr2:73851178-73851179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112833082	chr2:73851205-73851206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6714331	chr2:73851207-73851208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3076414	chr2:73851225-73851226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552046018	chr2:73851231-73851232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560451716	chr2:73851263-73851264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574537900	chr2:73851296-73851297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs201918228	chr2:73851305-73851306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554451969	chr2:73851327-73851328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2947856	chr2:73851409-73851410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2969608	chr2:73851416-73851417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2947855	chr2:73851422-73851423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2947854	chr2:73851423-73851424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116599886	chr2:73851440-73851441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2969607	chr2:73851456-73851457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368654445	chr2:73851463-73851464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565114239	chr2:73851540-73851541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532091575	chr2:73851575-73851576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541165918	chr2:73851686-73851687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371768230	chr2:73851757-73851758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374787058	chr2:73851761-73851762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369156942	chr2:73851768-73851769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559389303	chr2:73851810-73851811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529719288	chr2:73851844-73851845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548862566	chr2:73851849-73851850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570271360	chr2:73851940-73851941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531107101	chr2:73851954-73851955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371614120	chr2:73851972-73851973	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:233 , 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	chr2:73836400-73852600	Weak transcription	Ovary	ovary
3	chr2:73838400-73852600	Weak transcription	Right Ventricle	heart
4	chr2:73838600-73852600	Weak transcription	Pancreas	Pancrea
5	chr2:73842600-73852600	Weak transcription	Left Ventricle	heart
6	chr2:73844000-73854800	Weak transcription	Fetal Brain Female	brain
7	chr2:73850200-73852400	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr2:73850800-73851400	Enhancers	GM12878-XiMat	blood
9	chr2:73851400-73853000	Weak transcription	GM12878-XiMat	blood
10	chr2:73852000-73852600	Enhancers	HepG2	liver
11	chr2:73852400-73852600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:73852400-73854000	Enhancers	Liver	Liver
13	chr2:73852400-73857400	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr2:73852600-73852800	Enhancers	Fetal Intestine Large	intestine
15	chr2:73852600-73852800	Enhancers	Left Ventricle	heart
16	chr2:73852600-73852800	Flanking Active TSS	HepG2	liver
17	chr2:73852600-73853000	Enhancers	Colonic Mucosa	Colon
18	chr2:73852600-73853200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:73852600-73853200	Enhancers	Duodenum Mucosa	Duodenum
20	chr2:73852600-73853200	Enhancers	Pancreas	Pancrea
21	chr2:73852600-73853200	Enhancers	Right Ventricle	heart
22	chr2:73852600-73853800	Enhancers	Ovary	ovary
23	chr2:73852600-73854000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr2:73852600-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:73852600-73854400	Enhancers	Primary hematopoietic stem cells	blood
26	chr2:73852600-73855000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr2:73852800-73853000	Enhancers	HepG2	liver
28	chr2:73852800-73853200	Enhancers	A549	lung
29	chr2:73852800-73853200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr2:73853000-73853200	Flanking Active TSS	HepG2	liver
31	chr2:73853000-73853400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr2:73853000-73854000	Enhancers	GM12878-XiMat	blood
33	chr2:73853200-73853600	Enhancers	HepG2	liver
34	chr2:73853400-73853600	Enhancers	Fetal Intestine Large	intestine
35	chr2:73853800-73854000	Weak transcription	Ovary	ovary
36	chr2:73854000-73854200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr2:73854000-73858000	Weak transcription	Liver	Liver
38	chr2:73854800-73855000	Enhancers	Sigmoid Colon	Sigmoid Colon
39	chr2:73855600-73857000	Enhancers	GM12878-XiMat	blood
40	chr2:73856600-73857000	Weak transcription	HSMMtube	muscle
41	chr2:73857000-73857200	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
42	chr2:73857000-73857200	Active TSS	Primary B cells from cord blood	blood
43	chr2:73857000-73857200	Active TSS	NHLF	lung
44	chr2:73857000-73857400	Active TSS	GM12878-XiMat	blood
45	chr2:73857000-73857400	Active TSS	HSMM	muscle
46	chr2:73857000-73857400	ZNF genes & repeats	HSMMtube	muscle
47	chr2:73857400-73858800	Weak transcription	HSMMtube	muscle
48	chr2:73859800-73860400	Enhancers	Ovary	ovary
49	chr2:73860400-73867000	Weak transcription	Ovary	ovary
50	chr2:73863600-73863800	Enhancers	Sigmoid Colon	Sigmoid Colon

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