Variant report

Variant	esv3349788
Chromosome Location	chr2:114328582-114360780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2434)
CpG islands
(count:1037)
Chromatin interactive
region (count:4)
LncRNA
region (count:32)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2434 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:114340115-114340374	K562	blood:	n/a	n/a
2	ARID3A	chr2:114341528-114341709	K562	blood:	n/a	n/a
3	ARID3A	chr2:114341464-114341790	HepG2	liver:	n/a	n/a
4	ATF1	chr2:114349732-114349772	K562	blood:	n/a	n/a
5	ATF1	chr2:114340089-114340480	K562	blood:	n/a	n/a
6	ATF2	chr2:114341413-114341806	GM12878	blood:	n/a	n/a
7	ATF2	chr2:114341425-114341694	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr2:114359657-114359767	GM12878	blood:	n/a	n/a
9	ATF3	chr2:114359623-114359862	GM12878	blood:	n/a	n/a
10	ATF3	chr2:114341420-114341810	A549	lung:	n/a	n/a
11	ATF3	chr2:114359653-114359828	K562	blood:	n/a	n/a
12	ATF3	chr2:114341426-114341722	A549	lung:	n/a	n/a
13	ATF3	chr2:114359628-114359819	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr2:114342450-114342472	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr2:114341927-114342368	GM12878	blood:	n/a	n/a
16	BATF	chr2:114358733-114359308	GM12878	blood:	n/a	n/a
17	BATF	chr2:114341254-114341925	GM12878	blood:	n/a	n/a
18	BATF	chr2:114343300-114343492	GM12878	blood:	n/a	chr2:114343416-114343427
19	BATF	chr2:114337655-114337855	GM12878	blood:	n/a	n/a
20	BATF	chr2:114359457-114359883	GM12878	blood:	n/a	n/a
21	BATF	chr2:114356797-114357011	GM12878	blood:	n/a	n/a
22	BATF	chr2:114342145-114342363	GM12878	blood:	n/a	n/a
23	BATF	chr2:114342934-114343135	GM12878	blood:	n/a	n/a
24	BATF	chr2:114340809-114341094	GM12878	blood:	n/a	n/a
25	BATF	chr2:114359584-114359759	GM12878	blood:	n/a	n/a
26	BATF	chr2:114357543-114357728	GM12878	blood:	n/a	n/a
27	BATF	chr2:114356769-114357086	GM12878	blood:	n/a	n/a
28	BATF	chr2:114356527-114356738	GM12878	blood:	n/a	n/a
29	BATF	chr2:114353823-114353988	GM12878	blood:	n/a	n/a
30	BATF	chr2:114340791-114341141	GM12878	blood:	n/a	n/a
31	BATF	chr2:114354654-114354853	GM12878	blood:	n/a	n/a
32	BATF	chr2:114359080-114359259	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:114359452-114359825	GM12878	blood:	n/a	n/a
34	BCL11A	chr2:114345225-114345448	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:114338132-114338304	GM12878	blood:	n/a	n/a
36	BCL11A	chr2:114345523-114345720	GM12878	blood:	n/a	n/a
37	BCL11A	chr2:114357078-114358032	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:114358093-114358502	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:114351923-114352092	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:114357565-114358027	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:114359458-114359824	GM12878	blood:	n/a	n/a
42	BCL11A	chr2:114351273-114351487	GM12878	blood:	n/a	n/a
43	BCL11A	chr2:114340779-114341050	GM12878	blood:	n/a	n/a
44	BCL11A	chr2:114353154-114353342	GM12878	blood:	n/a	n/a
45	BCL11A	chr2:114355506-114355729	GM12878	blood:	n/a	chr2:114355618-114355631
46	BCL11A	chr2:114343200-114343508	GM12878	blood:	n/a	n/a
47	BCL11A	chr2:114346189-114346377	GM12878	blood:	n/a	n/a
48	BCL11A	chr2:114342756-114342990	GM12878	blood:	n/a	n/a
49	BCL11A	chr2:114344807-114345018	GM12878	blood:	n/a	n/a
50	BCL11A	chr2:114344560-114344801	GM12878	blood:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114359736-114359786	K562	blood:	n/a
2	chr2:114360096-114360146	HRPEpiC	eye:	n/a
3	chr2:114346218-114346268	HCT-116	colon:	n/a
4	chr2:114359873-114359923	PFSK-1	brain:	n/a
5	chr2:114341631-114341681	CMK	blood:	n/a
6	chr2:114359736-114359786	HUVEC	blood vessel:	n/a
7	chr2:114334065-114334115	GM12878	blood:	n/a
8	chr2:114360096-114360146	Caco-2	colon:	n/a
9	chr2:114359188-114359238	PrEC	prostate:	n/a
10	chr2:114341631-114341681	HAEpiC	amniotic membrane:	n/a
11	chr2:114359873-114359923	HNPCEpiC	eye:	n/a
12	chr2:114334065-114334115	RPTEC	kidney:	n/a
13	chr2:114359762-114359812	LNCaP	prostate:	n/a
14	chr2:114342108-114342158	HCF	heart:	n/a
15	chr2:114334065-114334115	Caco-2	colon:	n/a
16	chr2:114359188-114359238	HRPEpiC	eye:	n/a
17	chr2:114342108-114342158	ovcar-3	ovarian:	n/a
18	chr2:114341631-114341681	SK-N-SH_RA	brain:	n/a
19	chr2:114345644-114345694	K562	blood:	n/a
20	chr2:114340391-114340441	T-47D	breast:	n/a
21	chr2:114342621-114342671	H1-hESC	embryonic stem cell:	embryo
22	chr2:114360096-114360146	Jurkat	blood:	n/a
23	chr2:114342621-114342671	PrEC	prostate:	n/a
24	chr2:114359251-114359301	HEK293	kidney:	embryo
25	chr2:114342108-114342158	AG04449	skin:	fetal
26	chr2:114334065-114334115	NHDF-neo	bronchial:	n/a
27	chr2:114359736-114359786	Caco-2	colon:	n/a
28	chr2:114359736-114359786	U87	brain:	n/a
29	chr2:114359736-114359786	HL-60	blood:	n/a
30	chr2:114359188-114359238	A549	lung:	n/a
31	chr2:114341680-114341730	HMEC	breast:	n/a
32	chr2:114340391-114340441	U87	brain:	n/a
33	chr2:114360096-114360146	HCT-116	colon:	n/a
34	chr2:114359762-114359812	HCF	heart:	n/a
35	chr2:114333496-114333546	HMEC	breast:	n/a
36	chr2:114334065-114334115	HCM	heart:	n/a
37	chr2:114359736-114359786	HMEC	breast:	n/a
38	chr2:114357261-114357311	Hepatocyte	liver:	n/a
39	chr2:114333496-114333546	HL-60	blood:	n/a
40	chr2:114333496-114333546	SAEC	small airway:	n/a
41	chr2:114342621-114342671	HL-60	blood:	n/a
42	chr2:114359251-114359301	A549	lung:	n/a
43	chr2:114342621-114342671	Hepatocyte	liver:	n/a
44	chr2:114346218-114346268	GM12891	blood:	n/a
45	chr2:114340391-114340441	HRE	kidney:	n/a
46	chr2:114359736-114359786	AG04450	lung:	fetal
47	chr2:114342108-114342158	BE2_C	brain:	n/a
48	chr2:114345644-114345694	AG09319	gingival:	n/a
49	chr2:114359762-114359812	GM19239	blood:	n/a
50	chr2:114357261-114357311	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:114344560..114345063-chr2:114361338..114362244,2	MCF-7	breast:
2	chr12:77529..78029-chr2:114344487..114344997,2	MCF-7	breast:
3	chr2:114359257..114359811-chr2:114457510..114458087,2	MCF-7	breast:
4	chr12:77501..78029-chr2:114344484..114344991,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RABL2A-2	chr2:114335866-114336429	ENSG00000226516.3
2	lnc-SLC35F5-16	chr2:114358789-114358838	NONHSAT073813
3	lnc-RABL2A-2	chr2:114335559-114335763	ENSG00000226516.3
4	lnc-RABL2A-2	chr2:114335559-114335763	ENSG00000226516
5	lnc-SLC35F5-16	chr2:114356613-114357795	NONHSAT073813
6	lnc-SLC35F5-17	chr2:114347802-114348156	l_1931_chr2:114347801-114356084_testes
7	lnc-RABL2A-2	chr2:114334959-114335319	XLOC_001632
8	lnc-RABL2A-2	chr2:114334959-114335319	ENSG00000226516.3
9	lnc-RABL2A-2	chr2:114335559-114336429	ENSG00000226516.3
10	lnc-RABL2A-2	chr2:114335559-114335961	XLOC_001632
11	lnc-SLC35F5-16	chr2:114358295-114358403	NONHSAT073810
12	lnc-SLC35F5-16	chr2:114358789-114359153	NONHSAT073810
13	lnc-SLC35F5-16	chr2:114356605-114357791	NONHSAT073810
14	lnc-RABL2A-2	chr2:114336158-114336486	XLOC_001632
15	lnc-RABL2A-2	chr2:114335192-114335319	ENSG00000226516
16	lnc-SLC35F5-16	chr2:114358789-114359006	NONHSAT073809
17	lnc-RABL2A-2	chr2:114334959-114335319	ENSG00000226516.3
18	lnc-SLC35F5-16	chr2:114358789-114358838	NONHSAT073812
19	lnc-RABL2A-2	chr2:114335559-114335763	XLOC_001632
20	lnc-SLC35F5-16	chr2:114357939-114358040	NONHSAT073812
21	lnc-SLC35F5-17	chr2:114355758-114356084	l_1931_chr2:114347801-114356084_testes
22	lnc-SLC35F5-16	chr2:114356605-114358403	NONHSAT073811
23	lnc-SLC35F5-16	chr2:114358789-114359153	NONHSAT073811
24	lnc-AC016745.1-6	chr2:114335509-114335609	l_1930_chr2:114303057-114317403_testes
25	lnc-SLC35F5-16	chr2:114356605-114358421	NONHSAT073809
26	lnc-RABL2A-2	chr2:114334959-114335319	XLOC_001632
27	lnc-SLC35F5-16	chr2:114356613-114357773	NONHSAT073812
28	lnc-RABL2A-2	chr2:114335866-114336428	XLOC_001632
29	lnc-SLC35F5-17	chr2:114349194-114349311	l_1931_chr2:114347801-114356084_testes
30	lnc-SLC35F5-16	chr2:114358319-114358403	NONHSAT073812
31	lnc-SLC35F5-16	chr2:114358319-114358403	NONHSAT073813
32	lnc-RABL2A-2	chr2:114335866-114336353	ENSG00000226516

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1302	chr2:114340581-114340601	MIMAT0005890_4

No data

Variant related genes	Relation type
DDX11L2	TF binding region
WASH2P	TF binding region
MIR1302-3	TF binding region
FAM138B	TF binding region
DDX11L2	CpG island
WASH2P	CpG island
MIR1302-3	CpG island
FAM138B	CpG island
C11orf41	miRNA target sites
C10orf88	miRNA target sites
C11orf54	miRNA target sites

Extended variants
information (count: 1421 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1421 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567907942	chr2:114328582-114328583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536546128	chr2:114328683-114328684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556093674	chr2:114328719-114328720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575962296	chr2:114328749-114328750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538328763	chr2:114328762-114328763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558260902	chr2:114328793-114328794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573451171	chr2:114328830-114328831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571908564	chr2:114328875-114328876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1665350	chr2:114328936-114328937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs28720009	chr2:114328997-114328998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375041396	chr2:114329069-114329070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368054030	chr2:114329080-114329081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562868373	chr2:114329084-114329085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531644346	chr2:114329118-114329119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549062841	chr2:114329193-114329194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565418295	chr2:114329234-114329235	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs199925993	chr2:114329240-114329241	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs190213521	chr2:114329247-114329248	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs547964037	chr2:114329264-114329265	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs567781891	chr2:114329270-114329271	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs550239378	chr2:114329312-114329313	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs3893136	chr2:114329326-114329327	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs538296125	chr2:114329331-114329332	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs370689040	chr2:114329338-114329339	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs62159298	chr2:114329385-114329386	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs10174451	chr2:114329388-114329389	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553521825	chr2:114329389-114329390	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs534418369	chr2:114329391-114329392	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554722101	chr2:114329402-114329403	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369769590	chr2:114329408-114329409	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs62159299	chr2:114329429-114329430	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs116123247	chr2:114329463-114329464	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs376632576	chr2:114329467-114329468	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs10197529	chr2:114329491-114329492	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs200007050	chr2:114329508-114329509	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs543687665	chr2:114329522-114329523	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs377371570	chr2:114329545-114329546	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs557002938	chr2:114329560-114329561	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs111850597	chr2:114329576-114329577	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs375562746	chr2:114329584-114329585	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs111690791	chr2:114329599-114329600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs184176180	chr2:114329626-114329627	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs373731623	chr2:114329628-114329629	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs140408439	chr2:114329663-114329664	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs565283333	chr2:114329664-114329665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs2019963	chr2:114329677-114329678	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs527755657	chr2:114329691-114329692	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs541550961	chr2:114329699-114329700	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs561515304	chr2:114329703-114329704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs530256663	chr2:114329730-114329731	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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

Chromatin state (count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114311400-114340400	Weak transcription	Fetal Stomach	stomach
2	chr2:114314600-114339000	Weak transcription	NHLF	lung
3	chr2:114326200-114332600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:114327600-114328600	Enhancers	K562	blood
5	chr2:114327600-114329200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr2:114327600-114329800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr2:114328600-114330600	Weak transcription	K562	blood
8	chr2:114329200-114329800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr2:114329200-114329800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr2:114329400-114329600	Enhancers	NHDF-Ad	bronchial
11	chr2:114329600-114341000	Weak transcription	NHDF-Ad	bronchial
12	chr2:114329800-114330000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr2:114329800-114333000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr2:114330000-114332600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr2:114330600-114334400	Enhancers	K562	blood
16	chr2:114332600-114333200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:114332600-114333200	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr2:114333000-114333200	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:114333200-114334000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:114333200-114340000	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr2:114333200-114340200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr2:114334000-114335000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr2:114334200-114334800	Enhancers	Fetal Muscle Leg	muscle
24	chr2:114334400-114336600	Weak transcription	K562	blood
25	chr2:114334800-114340200	Weak transcription	Fetal Muscle Leg	muscle
26	chr2:114335000-114336600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:114336600-114336800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:114336600-114337000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr2:114336600-114337000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr2:114336600-114340200	Enhancers	K562	blood
31	chr2:114336800-114340200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:114337000-114338600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:114337000-114340200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr2:114338600-114339000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:114339000-114339200	Enhancers	NHLF	lung
36	chr2:114339000-114340200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:114339200-114340200	Weak transcription	NHLF	lung
38	chr2:114340000-114340200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:114340000-114340200	Active TSS	Breast Myoepithelial Primary Cells	Breast
40	chr2:114340000-114340200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr2:114340000-114340200	Enhancers	Fetal Kidney	kidney
42	chr2:114340000-114340200	Enhancers	Dnd41	blood
43	chr2:114340000-114340600	Bivalent Enhancer	HepG2	liver
44	chr2:114340000-114340800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr2:114340000-114341000	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr2:114340000-114341000	Enhancers	Fetal Muscle Trunk	muscle
47	chr2:114340000-114341000	Enhancers	Placenta	Placenta
48	chr2:114340000-114341000	Enhancers	HSMMtube	muscle
49	chr2:114340000-114341200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:114340200-114340400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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