Variant report

Variant	nsv522475
Chromosome Location	chr2:112059830-112240636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2517)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:51)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2517 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112142989-112143245	K562	blood:	n/a	n/a
2	ARID3A	chr2:112077982-112078035	K562	blood:	n/a	n/a
3	ARID3A	chr2:112165582-112165606	K562	blood:	n/a	n/a
4	ARID3A	chr2:112078700-112078866	K562	blood:	n/a	n/a
5	ARID3A	chr2:112191601-112191749	K562	blood:	n/a	n/a
6	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:112134733-112134923	HepG2	liver:	n/a	n/a
8	ATF1	chr2:112165410-112165614	K562	blood:	n/a	n/a
9	ATF1	chr2:112139588-112139732	K562	blood:	n/a	n/a
10	ATF1	chr2:112123600-112123901	K562	blood:	n/a	n/a
11	ATF1	chr2:112174751-112174909	K562	blood:	n/a	n/a
12	ATF1	chr2:112191568-112191846	K562	blood:	n/a	n/a
13	ATF1	chr2:112174026-112174226	K562	blood:	n/a	n/a
14	ATF1	chr2:112104247-112104437	K562	blood:	n/a	n/a
15	ATF2	chr2:112183348-112183699	GM12878	blood:	n/a	n/a
16	ATF2	chr2:112183361-112183645	GM12878	blood:	n/a	n/a
17	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
18	BACH1	chr2:112078561-112079019	H1-hESC	embryonic stem cell:	n/a	chr2:112078792-112078806
19	BACH1	chr2:112143146-112143417	K562	blood:	n/a	n/a
20	BACH1	chr2:112078641-112078944	K562	blood:	n/a	chr2:112078792-112078806
21	BATF	chr2:112183252-112183819	GM12878	blood:	n/a	n/a
22	BATF	chr2:112190544-112190853	GM12878	blood:	n/a	n/a
23	BATF	chr2:112072875-112073150	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
24	BATF	chr2:112125609-112126213	GM12878	blood:	n/a	chr2:112125629-112125642
25	BATF	chr2:112195321-112195643	GM12878	blood:	n/a	chr2:112195574-112195583
26	BATF	chr2:112077128-112077551	GM12878	blood:	n/a	n/a
27	BATF	chr2:112074557-112074916	GM12878	blood:	n/a	chr2:112074773-112074784
28	BATF	chr2:112182048-112182971	GM12878	blood:	n/a	n/a
29	BATF	chr2:112186949-112187402	GM12878	blood:	n/a	n/a
30	BATF	chr2:112206432-112206650	GM12878	blood:	n/a	n/a
31	BATF	chr2:112195246-112195683	GM12878	blood:	n/a	chr2:112195574-112195583
32	BATF	chr2:112158868-112159229	GM12878	blood:	n/a	chr2:112159209-112159219
33	BATF	chr2:112074635-112074933	GM12878	blood:	n/a	chr2:112074773-112074784
34	BATF	chr2:112198041-112198360	GM12878	blood:	n/a	n/a
35	BATF	chr2:112190573-112190841	GM12878	blood:	n/a	n/a
36	BATF	chr2:112195786-112196106	GM12878	blood:	n/a	n/a
37	BATF	chr2:112209363-112210356	GM12878	blood:	n/a	n/a
38	BATF	chr2:112073963-112074275	GM12878	blood:	n/a	n/a
39	BATF	chr2:112193854-112194550	GM12878	blood:	n/a	chr2:112194264-112194272
40	BATF	chr2:112211976-112212278	GM12878	blood:	n/a	n/a
41	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
42	BATF	chr2:112158949-112159184	GM12878	blood:	n/a	n/a
43	BATF	chr2:112221408-112221914	GM12878	blood:	n/a	n/a
44	BATF	chr2:112188947-112189209	GM12878	blood:	n/a	n/a
45	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
46	BATF	chr2:112195688-112196162	GM12878	blood:	n/a	n/a
47	BATF	chr2:112131695-112131857	GM12878	blood:	n/a	n/a
48	BATF	chr2:112072847-112073098	GM12878	blood:	n/a	chr2:112073011-112073022 chr2:112072925-112072935
49	BATF	chr2:112182205-112182825	GM12878	blood:	n/a	n/a
50	BATF	chr2:112125762-112126285	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112124380-112124430	Jurkat	blood:	n/a
2	chr2:112124380-112124430	AoSMC	blood vessel:	n/a
3	chr2:112124380-112124430	HCPEpiC	choroid plexus:	n/a
4	chr2:112124118-112124168	HIPEpiC	eye:	n/a
5	chr2:112124380-112124430	HCT-116	colon:	n/a
6	chr2:112124380-112124430	AG04449	skin:	fetal
7	chr2:112124118-112124168	MCF10A-Er-Src	breast:	n/a
8	chr2:112124380-112124430	PFSK-1	brain:	n/a
9	chr2:112124380-112124430	HCF	heart:	n/a
10	chr2:112124118-112124168	PFSK-1	brain:	n/a
11	chr2:112124118-112124168	GM12891	blood:	n/a
12	chr2:112124118-112124168	AG04449	skin:	fetal
13	chr2:112124118-112124168	HEEpiC	esophagus:	n/a
14	chr2:112124118-112124168	LNCaP	prostate:	n/a
15	chr2:112124118-112124168	T-47D	breast:	n/a
16	chr2:112124380-112124430	HIPEpiC	eye:	n/a
17	chr2:112124380-112124430	HCM	heart:	n/a
18	chr2:112124380-112124430	RPTEC	kidney:	n/a
19	chr2:112124118-112124168	AG10803	skin:	n/a
20	chr2:112124380-112124430	HPAEpiC	pulmonary alveolar:	n/a
21	chr2:112124118-112124168	CMK	blood:	n/a
22	chr2:112124380-112124430	NHDF-neo	bronchial:	n/a
23	chr2:112124380-112124430	NT2-D1	testis:	n/a
24	chr2:112124118-112124168	U87	brain:	n/a
25	chr2:112124380-112124430	NH-A	brain:	n/a
26	chr2:112124118-112124168	ProgFib	skin:	n/a
27	chr2:112124118-112124168	GM12878	blood:	n/a
28	chr2:112124380-112124430	HUVEC	blood vessel:	n/a
29	chr2:112124118-112124168	HMEC	breast:	n/a
30	chr2:112124380-112124430	SK-N-SH_RA	brain:	n/a
31	chr2:112124118-112124168	K562	blood:	n/a
32	chr2:112124380-112124430	HAEpiC	amniotic membrane:	n/a
33	chr2:112124118-112124168	GM19239	blood:	n/a
34	chr2:112124118-112124168	BJ	skin:	n/a
35	chr2:112124118-112124168	H1-hESC	embryonic stem cell:	embryo
36	chr2:112124118-112124168	Hela-S3	cervix:	n/a
37	chr2:112124118-112124168	NH-A	brain:	n/a
38	chr2:112124380-112124430	HRPEpiC	eye:	n/a
39	chr2:112124118-112124168	A549	lung:	n/a
40	chr2:112124380-112124430	HNPCEpiC	eye:	n/a
41	chr2:112124118-112124168	HAEpiC	amniotic membrane:	n/a
42	chr2:112124118-112124168	AG04450	lung:	fetal
43	chr2:112124118-112124168	MCF-7	breast:	n/a
44	chr2:112124380-112124430	SK-N-SH	brain:	n/a
45	chr2:112124380-112124430	GM12892	blood:	n/a
46	chr2:112124118-112124168	PANC-1	pancreas:	n/a
47	chr2:112124380-112124430	MCF10A-Er-Src	breast:	n/a
48	chr2:112124118-112124168	AG09309	skin:	n/a
49	chr2:112124118-112124168	GM12892	blood:	n/a
50	chr2:112124380-112124430	HepG2	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:112158086..112161064-chr8:43095226..43096729,2	MCF-7	breast:
2	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
3	chr2:111879395..111881005-chr2:112073345..112075122,2	MCF-7	breast:
4	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
5	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
6	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
7	chr2:111878316..111879893-chr2:112101721..112103928,2	MCF-7	breast:

(count:51 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
2	lnc-BCL2L11-7	chr2:112141329-112142569	NONHSAT073641
3	lnc-BCL2L11-5	chr2:112085950-112086268	l_1923_chr2:112081839-112086268_testes
4	lnc-AC108463.1-3	chr2:112101638-112101675	ENSG00000172965.10
5	lnc-BCL2L11-8	chr2:112186899-112187197	NONHSAT073647
6	lnc-BCL2L11-6	chr2:112124594-112124991	NONHSAT073618
7	lnc-AC108463.1-3	chr2:112187048-112187197	NONHSAT073639
8	lnc-AC108463.1-3	chr2:112071889-112072139	ENSG00000172965.6
9	lnc-AC108463.1-3	chr2:112125064-112125152	NONHSAT073622
10	lnc-BCL2L11-5	chr2:112081889-112082063	NONHSAT073637
11	lnc-AC108463.1-3	chr2:112101668-112101814	ENSG00000172965.6
12	lnc-AC108463.1-3	chr2:112187020-112187197	ENSG00000172965.6
13	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
14	lnc-AC108463.1-3	chr2:112124591-112125152	NONHSAT073640
15	lnc-BCL2L11-6	chr2:112060981-112061323	NONHSAT073618
16	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
17	lnc-AC108463.1-3	chr2:112186891-112187197	ENSG00000172965.6
18	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
19	lnc-AC108463.1-3	chr2:112101638-112101701	NONHSAT073620
20	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
21	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
22	lnc-AC108463.1-3	chr2:112186886-112187197	NONHSAT073642
23	lnc-AC108463.1-3	chr2:112101789-112101814	NONHSAT073639
24	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
25	lnc-BCL2L11-5	chr2:112081976-112082063	l_1923_chr2:112081839-112086268_testes
26	lnc-AC108463.1-3	chr2:112101638-112101814	NONHSAT073622
27	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
28	lnc-BCL2L11-5	chr2:112085950-112086566	NONHSAT073637
29	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
30	lnc-AC108463.1-3	chr2:112125088-112125152	NONHSAT073639
31	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
32	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
34	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
35	lnc-BCL2L11-5	chr2:112081840-112081972	l_1923_chr2:112081839-112086268_testes
36	lnc-BCL2L11-7	chr2:112141383-112141840	NONHSAT147111
37	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
38	lnc-AC108463.1-3	chr2:112227364-112227564	ENSG00000172965.6
39	lnc-AC108463.1-3	chr2:112199085-112199198	ENSG00000172965.6
40	lnc-AC108463.1-3	chr2:112108185-112108338	ENSG00000172965.6
41	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
42	lnc-BCL2L11-6	chr2:112080919-112081327	NONHSAT073618
43	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
44	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
45	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
46	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
47	lnc-AC108463.1-3	chr2:112125064-112125102	ENSG00000172965.10
48	lnc-AC108463.1-3	chr2:112125064-112125152	ENSG00000172965.6
49	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.6
50	lnc-AC108463.1-3	chr2:112101638-112101814	ENSG00000172965.10

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4435	chr2:112078638-112078659	MIMAT0018951_1

No data

Variant related genes	Relation type
MIR4435-1HG	TF binding region
ENSG00000223973	TF binding region
MIR4435-1	TF binding region
MIR4435-1HG	CpG island
ENSG00000223973	CpG island
MIR4435-1	CpG island
ENSG00000153094	chromatin interactions

Extended variants
information (count: 4565 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4565 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56215408	chr2:112059830-112059831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528883631	chr2:112059864-112059865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575914618	chr2:112059867-112059868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568954963	chr2:112059933-112059934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537963701	chr2:112059972-112059973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551651811	chr2:112060004-112060005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571821771	chr2:112060098-112060099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199702825	chr2:112060118-112060119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535304714	chr2:112060152-112060153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554444204	chr2:112060194-112060195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146194416	chr2:112060196-112060197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147839446	chr2:112060204-112060205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs56180248	chr2:112060205-112060206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576092346	chr2:112060219-112060220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545107554	chr2:112060241-112060242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557619064	chr2:112060318-112060319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577761750	chr2:112060387-112060388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540091823	chr2:112060401-112060402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560383288	chr2:112060531-112060532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529235466	chr2:112060550-112060551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62161614	chr2:112060570-112060571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542618522	chr2:112060593-112060594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148031215	chr2:112060641-112060642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562485682	chr2:112060704-112060705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531394578	chr2:112060731-112060732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200095050	chr2:112060868-112060869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551460498	chr2:112060869-112060870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571301961	chr2:112060870-112060871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370417919	chr2:112060979-112060980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79662174	chr2:112060996-112060997	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs150107864	chr2:112060999-112061000	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs547701546	chr2:112061014-112061015	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs192114101	chr2:112061045-112061046	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs200576501	chr2:112061048-112061049	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs556097169	chr2:112061074-112061075	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs184505639	chr2:112061090-112061091	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs138536001	chr2:112061128-112061129	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs374523574	chr2:112061279-112061280	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs141490854	chr2:112061358-112061359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558997194	chr2:112061434-112061435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62161615	chr2:112061485-112061486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540403241	chr2:112061617-112061618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553709699	chr2:112061679-112061680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573949151	chr2:112061696-112061697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542955645	chr2:112061714-112061715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529610275	chr2:112061757-112061758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562422808	chr2:112061832-112061833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531329323	chr2:112061897-112061898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544721151	chr2:112061925-112061926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564977599	chr2:112061957-112061958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	17483303	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
Ovarian cancer	21781307	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
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1737 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112025600-112116600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:112048800-112069600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:112055000-112070600	Weak transcription	NHLF	lung
4	chr2:112058200-112069600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:112058200-112071000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:112058600-112068400	Weak transcription	HepG2	liver
7	chr2:112059800-112060400	Enhancers	HSMMtube	muscle
8	chr2:112059800-112060600	Enhancers	Left Ventricle	heart
9	chr2:112059800-112060800	Enhancers	Fetal Thymus	thymus
10	chr2:112059800-112061000	Enhancers	Dnd41	blood
11	chr2:112059800-112061000	Enhancers	HSMM	muscle
12	chr2:112060000-112060800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr2:112060400-112079200	Weak transcription	HSMMtube	muscle
14	chr2:112060600-112060800	Enhancers	NH-A	brain
15	chr2:112060800-112062600	Weak transcription	NH-A	brain
16	chr2:112062200-112062400	Enhancers	Osteobl	bone
17	chr2:112062200-112062800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr2:112062400-112070200	Weak transcription	Osteobl	bone
19	chr2:112062600-112062800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr2:112062600-112062800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:112062600-112062800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:112062600-112062800	Enhancers	NH-A	brain
23	chr2:112062800-112063400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:112062800-112070600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr2:112062800-112070600	Weak transcription	NH-A	brain
26	chr2:112063000-112067200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:112063400-112063600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:112063600-112070000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:112063600-112086200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:112066800-112067000	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr2:112067200-112067400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:112067200-112067400	Enhancers	Fetal Muscle Leg	muscle
33	chr2:112067200-112068600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr2:112067400-112069600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:112067400-112070400	Weak transcription	Fetal Muscle Leg	muscle
36	chr2:112068000-112068200	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr2:112068000-112068800	Enhancers	Fetal Muscle Trunk	muscle
38	chr2:112068000-112072800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr2:112068600-112071600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr2:112068800-112069000	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr2:112068800-112070000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr2:112068800-112072200	Enhancers	Liver	Liver
43	chr2:112069600-112069800	Enhancers	Brain Anterior Caudate	brain
44	chr2:112069600-112070200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr2:112069600-112070800	Enhancers	Brain Hippocampus Middle	brain
46	chr2:112069600-112070800	Enhancers	Brain Substantia Nigra	brain
47	chr2:112069600-112071400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:112069600-112071400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr2:112069600-112071600	Enhancers	NHDF-Ad	bronchial
50	chr2:112069600-112072000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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