Variant report

Variant	nsv1002255
Chromosome Location	chr2:114120037-114236620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1709)
CpG islands
(count:611)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114181075-114181226	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:114147862-114148323	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:114147934-114148353	K562	blood:	n/a	n/a
4	ARID3A	chr2:114127759-114128394	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:114165283-114165660	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:114165284-114165610	K562	blood:	n/a	n/a
7	ATF1	chr2:114195252-114195468	K562	blood:	n/a	n/a
8	ATF2	chr2:114134096-114134875	GM12878	blood:	n/a	n/a
9	ATF2	chr2:114147524-114148275	GM12878	blood:	n/a	n/a
10	ATF2	chr2:114134165-114134981	GM12878	blood:	n/a	n/a
11	ATF3	chr2:114147873-114148254	GM12878	blood:	n/a	n/a
12	ATF3	chr2:114195215-114195323	K562	blood:	n/a	n/a
13	ATF3	chr2:114128032-114128470	A549	lung:	n/a	n/a
14	BATF	chr2:114123077-114123326	GM12878	blood:	n/a	n/a
15	BATF	chr2:114217254-114217816	GM12878	blood:	n/a	n/a
16	BATF	chr2:114188569-114188750	GM12878	blood:	n/a	n/a
17	BATF	chr2:114190256-114190764	GM12878	blood:	n/a	n/a
18	BATF	chr2:114194968-114195790	GM12878	blood:	n/a	chr2:114195333-114195346
19	BATF	chr2:114217280-114217821	GM12878	blood:	n/a	n/a
20	BATF	chr2:114188894-114189247	GM12878	blood:	n/a	n/a
21	BATF	chr2:114175312-114175602	GM12878	blood:	n/a	chr2:114175554-114175563
22	BATF	chr2:114179478-114179679	GM12878	blood:	n/a	n/a
23	BATF	chr2:114174348-114174775	GM12878	blood:	n/a	n/a
24	BATF	chr2:114190291-114190748	GM12878	blood:	n/a	n/a
25	BATF	chr2:114189261-114190171	GM12878	blood:	n/a	chr2:114189910-114189918
26	BATF	chr2:114206782-114207175	GM12878	blood:	n/a	n/a
27	BATF	chr2:114188216-114188558	GM12878	blood:	n/a	n/a
28	BATF	chr2:114147578-114148177	GM12878	blood:	n/a	n/a
29	BATF	chr2:114134468-114134876	GM12878	blood:	n/a	n/a
30	BATF	chr2:114196004-114196344	GM12878	blood:	n/a	n/a
31	BATF	chr2:114216587-114216848	GM12878	blood:	n/a	n/a
32	BATF	chr2:114122973-114123368	GM12878	blood:	n/a	n/a
33	BATF	chr2:114206835-114207033	GM12878	blood:	n/a	n/a
34	BATF	chr2:114147663-114148035	GM12878	blood:	n/a	n/a
35	BATF	chr2:114134508-114134842	GM12878	blood:	n/a	n/a
36	BATF	chr2:114188181-114188552	GM12878	blood:	n/a	n/a
37	BATF	chr2:114188935-114190118	GM12878	blood:	n/a	chr2:114189910-114189918
38	BATF	chr2:114196999-114197200	GM12878	blood:	n/a	n/a
39	BATF	chr2:114221639-114221843	GM12878	blood:	n/a	n/a
40	BATF	chr2:114209720-114209940	GM12878	blood:	n/a	n/a
41	BATF	chr2:114196059-114196346	GM12878	blood:	n/a	n/a
42	BATF	chr2:114217887-114218111	GM12878	blood:	n/a	n/a
43	BATF	chr2:114214368-114214841	GM12878	blood:	n/a	n/a
44	BATF	chr2:114194949-114195748	GM12878	blood:	n/a	chr2:114195333-114195346
45	BATF	chr2:114173977-114174745	GM12878	blood:	n/a	n/a
46	BCL11A	chr2:114195894-114196377	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:114188907-114190102	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:114220336-114220741	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:114216516-114216944	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:114217254-114217924	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114151353-114151403	HAEpiC	amniotic membrane:	n/a
2	chr2:114151353-114151403	HAEpiC	amniotic membrane:	n/a
3	chr2:114196058-114196108	Hela-S3	cervix:	n/a
4	chr2:114151353-114151403	IMR90	lung:	fetal
5	chr2:114196091-114196141	HNPCEpiC	eye:	n/a
6	chr2:114196058-114196108	CMK	blood:	n/a
7	chr2:114196091-114196141	SK-N-MC	brain:	n/a
8	chr2:114164343-114164393	HepG2	liver:	n/a
9	chr2:114194645-114194695	IMR90	lung:	fetal
10	chr2:114164343-114164393	PANC-1	pancreas:	n/a
11	chr2:114194645-114194695	RPTEC	kidney:	n/a
12	chr2:114194645-114194695	U87	brain:	n/a
13	chr2:114196058-114196108	HCT-116	colon:	n/a
14	chr2:114194645-114194695	HUVEC	blood vessel:	n/a
15	chr2:114196058-114196108	HMEC	breast:	n/a
16	chr2:114194541-114194591	SK-N-MC	brain:	n/a
17	chr2:114194645-114194695	GM12892	blood:	n/a
18	chr2:114197839-114197889	HUVEC	blood vessel:	n/a
19	chr2:114163184-114163234	SK-N-SH_RA	brain:	n/a
20	chr2:114163184-114163234	AG04450	lung:	fetal
21	chr2:114195528-114195578	HEEpiC	esophagus:	n/a
22	chr2:114196058-114196108	ovcar-3	ovarian:	n/a
23	chr2:114194645-114194695	HRCEpiC	kidney:	n/a
24	chr2:114206313-114206363	HRE	kidney:	n/a
25	chr2:114163184-114163234	HEK293	kidney:	embryo
26	chr2:114164343-114164393	HUVEC	blood vessel:	n/a
27	chr2:114163184-114163234	H1-hESC	embryonic stem cell:	embryo
28	chr2:114194541-114194591	PrEC	prostate:	n/a
29	chr2:114151353-114151403	HCF	heart:	n/a
30	chr2:114194645-114194695	HCT-116	colon:	n/a
31	chr2:114164343-114164393	HCF	heart:	n/a
32	chr2:114151353-114151403	SK-N-SH	brain:	n/a
33	chr2:114197839-114197889	PrEC	prostate:	n/a
34	chr2:114206313-114206363	Jurkat	blood:	n/a
35	chr2:114194645-114194695	HEEpiC	esophagus:	n/a
36	chr2:114196091-114196141	AG09309	skin:	n/a
37	chr2:114194541-114194591	Hepatocyte	liver:	n/a
38	chr2:114197839-114197889	AG09319	gingival:	n/a
39	chr2:114196091-114196141	Hela-S3	cervix:	n/a
40	chr2:114151353-114151403	AoSMC	blood vessel:	n/a
41	chr2:114195528-114195578	AoSMC	blood vessel:	n/a
42	chr2:114194645-114194695	Jurkat	blood:	n/a
43	chr2:114164343-114164393	HIPEpiC	eye:	n/a
44	chr2:114206313-114206363	HRCEpiC	kidney:	n/a
45	chr2:114194645-114194695	GM06990	blood:	n/a
46	chr2:114151353-114151403	SK-N-MC	brain:	n/a
47	chr2:114197839-114197889	AG04450	lung:	fetal
48	chr2:114194645-114194695	HEK293	kidney:	embryo
49	chr2:114151353-114151403	AG10803	skin:	n/a
50	chr2:114163184-114163234	HL-60	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:97777932..97778642-chr2:114147602..114148330,3	MCF-7	breast:
2	chr2:114006491..114007402-chr2:114127850..114128740,6	MCF-7	breast:
3	chr2:113961603..113962131-chr2:114147652..114148320,2	K562	blood:
4	chr2:114006433..114007490-chr2:114127813..114128753,6	MCF-7	breast:
5	chr2:113958498..113959276-chr2:114147736..114148311,2	K562	blood:
6	chr2:113837374..113837912-chr2:114127892..114128718,2	K562	blood:
7	chr2:96406055..96406842-chr2:114139694..114140465,2	MCF-7	breast:
8	chr2:113895658..113897096-chr2:114147534..114148565,6	K562	blood:
9	chr2:113837351..113838104-chr2:114147540..114148341,3	K562	blood:
10	chr2:114140085..114141972-chr2:114145675..114147776,2	K562	blood:
11	chr2:113894600..113895171-chr2:114147816..114148753,2	MCF-7	breast:
12	chr2:114127277..114131238-chr2:114131557..114134448,3	K562	blood:
13	chr2:114040686..114041186-chr2:114127813..114128575,2	MCF-7	breast:
14	chr2:113961183..113962044-chr2:114147703..114148314,2	MCF-7	breast:
15	chr2:114006461..114007910-chr2:114147631..114148371,4	K562	blood:
16	chr2:114010394..114011259-chr2:114127840..114128840,2	MCF-7	breast:
17	chr2:113961213..113962188-chr2:114127876..114128919,5	K562	blood:
18	chr2:114006796..114007421-chr2:114127816..114128725,5	K562	blood:
19	chr2:114159767..114162349-chr2:114163621..114165460,2	MCF-7	breast:
20	chr2:113961230..113961845-chr2:114127857..114128433,2	MCF-7	breast:
21	chr2:97778139..97778659-chr2:114147598..114148210,2	K562	blood:
22	chr2:114012941..114014608-chr2:114128232..114129740,2	MCF-7	breast:
23	chr2:114085306..114088063-chr2:114124693..114126212,2	MCF-7	breast:
24	chr2:97778136..97778658-chr2:114147633..114148424,9	MCF-7	breast:
25	chr12:808962..809943-chr2:114147779..114148497,2	MCF-7	breast:
26	chr2:114127277..114131238-chr2:114131557..114134448,3	K562	blood:
27	chr2:113952635..113954838-chr2:114132062..114134620,2	K562	blood:
28	chr2:113962501..113963279-chr2:114127874..114128718,2	K562	blood:
29	chr2:114140085..114141972-chr2:114145675..114147776,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC016745.1-4	chr2:114186646-114186941	expReg_chr2_8628_-
2	lnc-CBWD2-2	chr2:114190177-114193619	ENSG00000272563.1
3	lnc-AC016745.1-5	chr2:114184831-114185141	expReg_chr2_8625_-
4	lnc-CBWD2-1	chr2:114182475-114182901	ENSG00000234997.1
5	lnc-CBWD2-1	chr2:114182072-114182152	ENSG00000234997.1
6	lnc-AC016745.1-3	chr2:114189481-114189719	expReg_chr2_8632_-

No data

Variant related genes	Relation type
ENSG00000238091	TF binding region
CBWD2	TF binding region
ENSG00000272563	TF binding region
ENSG00000234997	TF binding region
IGKV1OR2-108	TF binding region
ENSG00000238091	CpG island
CBWD2	CpG island
ENSG00000272563	CpG island
ENSG00000234997	CpG island
IGKV1OR2-108	CpG island
ENSG00000125637	chromatin interactions
ENSG00000189223	chromatin interactions
ENSG00000231292	chromatin interactions

Extended variants
information (count: 3369 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3369 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4849200	chr2:114120037-114120038	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561420429	chr2:114120080-114120081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530261847	chr2:114120084-114120085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184729916	chr2:114120148-114120149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12470761	chr2:114120160-114120161	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572928461	chr2:114120238-114120239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372465425	chr2:114120272-114120273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72958619	chr2:114120400-114120401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs200592632	chr2:114120414-114120415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145896040	chr2:114120429-114120430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187992416	chr2:114120482-114120483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558590420	chr2:114120494-114120495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113682157	chr2:114120496-114120497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543604074	chr2:114120531-114120532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs72958621	chr2:114120566-114120567	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs536752735	chr2:114120572-114120573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111335571	chr2:114120578-114120579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556698572	chr2:114120599-114120600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576644379	chr2:114120633-114120634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113133954	chr2:114120636-114120637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553212546	chr2:114120637-114120638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113474385	chr2:114120639-114120640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541409135	chr2:114120652-114120653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559707063	chr2:114120661-114120662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112668772	chr2:114120680-114120681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72958622	chr2:114120755-114120756	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs13424459	chr2:114120785-114120786	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs142018247	chr2:114120803-114120804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532729222	chr2:114120855-114120856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552529556	chr2:114120883-114120884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530509371	chr2:114120938-114120939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72958623	chr2:114120942-114120943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528784470	chr2:114120969-114120970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548165425	chr2:114120973-114120974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567757931	chr2:114120974-114120975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs13424703	chr2:114120992-114120993	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550288545	chr2:114121025-114121026	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570232916	chr2:114121029-114121030	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530396342	chr2:114121073-114121074	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181058085	chr2:114121083-114121084	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552898860	chr2:114121092-114121093	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573044327	chr2:114121112-114121113	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535426621	chr2:114121122-114121123	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546947494	chr2:114121152-114121153	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75749601	chr2:114121229-114121230	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373208703	chr2:114121240-114121241	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112332610	chr2:114121264-114121265	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72960743	chr2:114121329-114121330	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563739681	chr2:114121337-114121338	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72960744	chr2:114121375-114121376	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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	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
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
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:664 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114106800-114129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:114110600-114124600	Weak transcription	A549	lung
3	chr2:114114400-114122600	Weak transcription	Fetal Intestine Small	intestine
4	chr2:114116800-114121000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:114116800-114126200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr2:114117000-114126600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:114117400-114126600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:114117400-114126600	Weak transcription	NHEK	skin
9	chr2:114117600-114124400	Weak transcription	HMEC	breast
10	chr2:114118400-114122600	Weak transcription	HSMMtube	muscle
11	chr2:114119200-114122000	Enhancers	Fetal Muscle Leg	muscle
12	chr2:114120000-114124400	Weak transcription	Lung	lung
13	chr2:114120800-114121800	Enhancers	Fetal Muscle Trunk	muscle
14	chr2:114121000-114121800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:114121200-114123600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr2:114121800-114122600	Weak transcription	Fetal Muscle Trunk	muscle
17	chr2:114121800-114123800	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr2:114121800-114124400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr2:114122000-114122400	Weak transcription	Fetal Muscle Leg	muscle
20	chr2:114122400-114123600	Enhancers	Fetal Intestine Large	intestine
21	chr2:114122400-114123600	Enhancers	Fetal Muscle Leg	muscle
22	chr2:114122600-114122800	Enhancers	Fetal Muscle Trunk	muscle
23	chr2:114122600-114123200	Enhancers	Psoas Muscle	Psoas
24	chr2:114122600-114124000	Enhancers	Fetal Intestine Small	intestine
25	chr2:114122600-114125400	Enhancers	HSMMtube	muscle
26	chr2:114123000-114123200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr2:114123200-114124000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr2:114123200-114124400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr2:114123200-114124400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr2:114124000-114126000	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr2:114124400-114124600	Enhancers	Lung	lung
32	chr2:114124400-114124800	Enhancers	HMEC	breast
33	chr2:114124400-114125200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:114124400-114125600	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr2:114124400-114125800	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr2:114124600-114125000	Enhancers	A549	lung
37	chr2:114124800-114126600	Weak transcription	HMEC	breast
38	chr2:114125000-114127200	Weak transcription	A549	lung
39	chr2:114125200-114125400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:114125600-114127000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr2:114125800-114126800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr2:114126000-114126800	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr2:114126200-114126800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr2:114126200-114128800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:114126600-114127400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:114126600-114128200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:114126600-114128200	Enhancers	HMEC	breast
48	chr2:114126600-114128400	Enhancers	NHEK	skin
49	chr2:114126800-114131000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr2:114126800-114131200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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