Variant report

Variant	nsv522324
Chromosome Location	chr2:134085665-134174032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:402)
CpG islands
(count:489)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:134097037-134097041	K562	blood:	n/a	n/a
2	BCL3	chr2:134104177-134104553	GM12878	blood:	n/a	n/a
3	BHLHE40	chr2:134119719-134119882	GM12878	blood:	n/a	n/a
4	BHLHE40	chr2:134173057-134173395	GM12878	blood:	n/a	n/a
5	BRCA1	chr2:134103274-134103787	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr2:134119678-134120195	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr2:134102290-134102899	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:134172108-134172326	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:134170046-134171171	Hela-S3	cervix:	n/a	chr2:134170438-134170451
10	CEBPB	chr2:134170352-134170525	IMR90	lung:	n/a	chr2:134170438-134170451
11	CEBPB	chr2:134134628-134134894	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:134119668-134119880	A549	lung:	n/a	n/a
13	CEBPB	chr2:134170221-134170687	A549	lung:	n/a	chr2:134170438-134170451
14	CEBPB	chr2:134147286-134147396	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:134092482-134092903	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:134120886-134121183	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr2:134095890-134096128	Hela-S3	cervix:	n/a	chr2:134096054-134096065
18	CEBPB	chr2:134102267-134102854	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:134103185-134103584	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:134119529-134120325	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:134170306-134170630	A549	lung:	n/a	chr2:134170438-134170451
22	CEBPB	chr2:134161665-134161926	HepG2	liver:	n/a	chr2:134161818-134161829 chr2:134161819-134161830 chr2:134161818-134161831 chr2:134161861-134161874
23	CEBPB	chr2:134095788-134096225	IMR90	lung:	n/a	chr2:134096054-134096065
24	CEBPB	chr2:134119542-134119916	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:134104155-134104720	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:134119608-134119881	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:134104232-134104595	A549	lung:	n/a	n/a
28	CEBPB	chr2:134104177-134104699	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr2:134102392-134102835	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr2:134119196-134119209	GM12878	blood:	n/a	n/a
31	CHD2	chr2:134117528-134117539	GM12878	blood:	n/a	n/a
32	CTCF	chr2:134111918-134111979	GM10266	blood:	n/a	n/a
33	CTCF	chr2:134169500-134169650	HAc	cerebellar:	n/a	chr2:134169607-134169625
34	CTCF	chr2:134138620-134138770	GM12872	blood:	n/a	n/a
35	CTCF	chr2:134111892-134112010	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr2:134169500-134169650	BE2_C	brain:	n/a	chr2:134169607-134169625
37	CTCF	chr2:134122214-134122555	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr2:134169540-134169690	WERI-Rb-1	eye:	n/a	chr2:134169607-134169625
39	CTCF	chr2:134169540-134169690	HBMEC	blood vessel:	n/a	chr2:134169607-134169625
40	CTCF	chr2:134169542-134169658	IMR90	lung:	n/a	chr2:134169607-134169625
41	CTCF	chr2:134122315-134122513	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:134111840-134111990	GM12867	blood:	n/a	n/a
43	CTCF	chr2:134169580-134169730	GM12872	blood:	n/a	chr2:134169607-134169625
44	CTCF	chr2:134122240-134122390	AG09319	gingival:	n/a	n/a
45	CTCF	chr2:134111880-134112030	GM12874	blood:	n/a	n/a
46	CTCF	chr2:134122343-134122481	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:134122346-134122473	A549	lung:	n/a	n/a
48	CTCF	chr2:134111784-134112141	GM12878	blood:	n/a	n/a
49	CTCF	chr2:134122260-134122410	GM12864	blood:	n/a	n/a
50	CTCF	chr2:134111840-134111990	GM12872	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:134104516-134104566	NH-A	brain:	n/a
2	chr2:134104516-134104566	NH-A	brain:	n/a
3	chr2:134147854-134147904	HRE	kidney:	n/a
4	chr2:134104516-134104566	HEK293	kidney:	embryo
5	chr2:134169851-134169901	U87	brain:	n/a
6	chr2:134169851-134169901	NHDF-neo	bronchial:	n/a
7	chr2:134169851-134169901	HAEpiC	amniotic membrane:	n/a
8	chr2:134099762-134099812	NHDF-neo	bronchial:	n/a
9	chr2:134135267-134135317	AG09319	gingival:	n/a
10	chr2:134119805-134119855	K562	blood:	n/a
11	chr2:134135267-134135317	SK-N-SH	brain:	n/a
12	chr2:134169851-134169901	GM12892	blood:	n/a
13	chr2:134169851-134169901	HCT-116	colon:	n/a
14	chr2:134147854-134147904	HMEC	breast:	n/a
15	chr2:134169851-134169901	ECC-1	luminal epithelium:	n/a
16	chr2:134104516-134104566	NB4	blood:	n/a
17	chr2:134163531-134163581	HCT-116	colon:	n/a
18	chr2:134119805-134119855	PFSK-1	brain:	n/a
19	chr2:134099762-134099812	AG04449	skin:	fetal
20	chr2:134119805-134119855	SK-N-MC	brain:	n/a
21	chr2:134169851-134169901	SKMC	muscle:	n/a
22	chr2:134104516-134104566	HCM	heart:	n/a
23	chr2:134127568-134127618	GM19239	blood:	n/a
24	chr2:134119805-134119855	HepG2	liver:	n/a
25	chr2:134127568-134127618	HCPEpiC	choroid plexus:	n/a
26	chr2:134127568-134127618	HepG2	liver:	n/a
27	chr2:134147854-134147904	K562	blood:	n/a
28	chr2:134147854-134147904	NH-A	brain:	n/a
29	chr2:134147854-134147904	BJ	skin:	n/a
30	chr2:134127568-134127618	GM12891	blood:	n/a
31	chr2:134169851-134169901	HCF	heart:	n/a
32	chr2:134099762-134099812	GM12892	blood:	n/a
33	chr2:134147854-134147904	HEK293	kidney:	embryo
34	chr2:134147854-134147904	HepG2	liver:	n/a
35	chr2:134099762-134099812	AoSMC	blood vessel:	n/a
36	chr2:134135267-134135317	SK-N-MC	brain:	n/a
37	chr2:134163531-134163581	Hepatocyte	liver:	n/a
38	chr2:134119805-134119855	GM12891	blood:	n/a
39	chr2:134127568-134127618	HL-60	blood:	n/a
40	chr2:134135267-134135317	MCF-7	breast:	n/a
41	chr2:134147854-134147904	HCT-116	colon:	n/a
42	chr2:134119805-134119855	A549	lung:	n/a
43	chr2:134147854-134147904	Caco-2	colon:	n/a
44	chr2:134135267-134135317	HCT-116	colon:	n/a
45	chr2:134135267-134135317	ECC-1	luminal epithelium:	n/a
46	chr2:134099762-134099812	A549	lung:	n/a
47	chr2:134163531-134163581	HepG2	liver:	n/a
48	chr2:134169851-134169901	HUVEC	blood vessel:	n/a
49	chr2:134163531-134163581	Jurkat	blood:	n/a
50	chr2:134127568-134127618	ECC-1	luminal epithelium:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:134168124..134170815-chr2:134171824..134174647,2	K562	blood:
2	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
3	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
4	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
5	chr2:134084453..134086561-chr2:134089070..134091697,3	MCF-7	breast:
6	chr2:134101590..134103181-chr2:134107237..134110074,2	K562	blood:
7	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
8	chr2:134086116..134088912-chr2:134093493..134094997,2	MCF-7	breast:
9	chr2:134089345..134089856-chr2:134262223..134263005,2	MCF-7	breast:
10	chr2:134159517..134161483-chr2:134169565..134171940,2	MCF-7	breast:
11	chr2:134147354..134149666-chr2:134150601..134153236,2	K562	blood:
12	chr2:134154022..134156001-chr2:134158455..134161393,2	MCF-7	breast:
13	chr2:134083491..134086031-chr2:134262913..134265457,2	MCF-7	breast:
14	chr2:134088192..134090911-chr2:134099454..134100959,2	MCF-7	breast:
15	chr2:134089010..134089877-chr2:134262426..134263057,3	MCF-7	breast:
16	chr2:134088967..134089889-chr2:134250249..134251166,2	MCF-7	breast:
17	chr2:134159517..134161483-chr2:134169565..134171940,2	MCF-7	breast:
18	chr2:134168124..134170815-chr2:134171824..134174647,2	K562	blood:
19	chr2:134148626..134150845-chr2:134154535..134156780,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LYPD1-4	chr2:134148681-134148970	NONHSAT074547

No data

Variant related genes	Relation type
RNU6-579P	TF binding region
RN7SKP154	TF binding region
RNU6-579P	CpG island
RN7SKP154	CpG island
ENSG00000222068	chromatin interactions
ENSG00000252688	chromatin interactions

Extended variants
information (count: 3246 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3246 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1430165	chr2:134085665-134085666	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561490322	chr2:134085668-134085669	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112612327	chr2:134085773-134085774	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534469569	chr2:134085819-134085820	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528946293	chr2:134085834-134085835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs35651234	chr2:134085933-134085934	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147641334	chr2:134086006-134086007	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111303972	chr2:134086011-134086012	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142227177	chr2:134086012-134086013	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536729514	chr2:134086026-134086027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs112095921	chr2:134086061-134086062	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113824154	chr2:134086088-134086089	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537464232	chr2:134086139-134086140	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs111962653	chr2:134086179-134086180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs112687773	chr2:134086188-134086189	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35697369	chr2:134086204-134086205	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10928450	chr2:134086271-134086272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs541401367	chr2:134086311-134086312	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559893767	chr2:134086312-134086313	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548407378	chr2:134086347-134086348	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35725271	chr2:134086367-134086368	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143137182	chr2:134086424-134086425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541890667	chr2:134086439-134086440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563058852	chr2:134086451-134086452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs530393645	chr2:134086492-134086493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148237569	chr2:134086573-134086574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371615399	chr2:134086582-134086583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563782496	chr2:134086605-134086606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79582014	chr2:134086646-134086647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10928451	chr2:134086647-134086648	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112853336	chr2:134086655-134086656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535307570	chr2:134086674-134086675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs78194793	chr2:134086679-134086680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570166271	chr2:134086699-134086700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140219615	chr2:134086714-134086715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557146584	chr2:134086730-134086731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558982335	chr2:134086742-134086743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570209330	chr2:134086763-134086764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374451709	chr2:134086768-134086769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537361787	chr2:134086790-134086791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111698765	chr2:134086833-134086834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs72987683	chr2:134086865-134086866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574939852	chr2:134086904-134086905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542038995	chr2:134086917-134086918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150318095	chr2:134086946-134086947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575002658	chr2:134086974-134086975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545543523	chr2:134087020-134087021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181498569	chr2:134087032-134087033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528110709	chr2:134087049-134087050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540489524	chr2:134087099-134087100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	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
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	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
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134070400-134094600	Weak transcription	NHEK	skin
2	chr2:134081000-134087000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:134083400-134090400	Weak transcription	NHDF-Ad	bronchial
4	chr2:134084600-134089000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:134084800-134092200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:134085000-134086600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:134085000-134087000	Enhancers	A549	lung
8	chr2:134085000-134087400	Enhancers	Hela-S3	cervix
9	chr2:134085000-134092000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:134085000-134093000	Weak transcription	Brain Substantia Nigra	brain
11	chr2:134085200-134086200	Enhancers	Brain Anterior Caudate	brain
12	chr2:134085200-134088400	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:134085600-134086200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr2:134086200-134087600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:134086200-134092200	Weak transcription	Brain Anterior Caudate	brain
16	chr2:134086600-134087200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:134087000-134088400	Weak transcription	A549	lung
18	chr2:134087000-134090400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr2:134087200-134090800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr2:134087400-134088800	Weak transcription	Hela-S3	cervix
21	chr2:134087400-134103800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:134087600-134095600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:134088400-134089400	Enhancers	A549	lung
24	chr2:134088400-134090000	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr2:134088800-134093800	Enhancers	Hela-S3	cervix
26	chr2:134089000-134089400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:134089000-134089400	Enhancers	Right Atrium	heart
28	chr2:134089000-134089600	Enhancers	Left Ventricle	heart
29	chr2:134089400-134090600	Weak transcription	A549	lung
30	chr2:134090400-134091000	Enhancers	Osteobl	bone
31	chr2:134090400-134091200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr2:134090400-134091200	Enhancers	NHDF-Ad	bronchial
33	chr2:134090600-134091200	Enhancers	A549	lung
34	chr2:134090800-134091400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr2:134091200-134094800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:134091400-134091800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:134091800-134092800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr2:134092000-134092800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:134092000-134092800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr2:134092000-134093000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:134092000-134093000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr2:134092000-134093200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:134092200-134092800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr2:134092200-134092800	Enhancers	Brain Anterior Caudate	brain
45	chr2:134092200-134093200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr2:134092200-134093200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr2:134092200-134093400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr2:134092400-134092800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:134092400-134092800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr2:134092600-134093000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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