Variant report

Variant	nsv4720
Chromosome Location	chr1:225673218-225718009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:547)
CpG islands
(count:305)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:547 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:225696057-225696587	HepG2	liver:	n/a	chr1:225696063-225696079 chr1:225696062-225696078
2	ATF1	chr1:225696204-225696551	K562	blood:	n/a	n/a
3	ATF1	chr1:225712801-225712855	K562	blood:	n/a	n/a
4	ATF2	chr1:225706844-225707334	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:225706932-225707255	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:225678342-225678695	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr1:225696084-225696636	A549	lung:	n/a	n/a
8	ATF3	chr1:225696219-225696573	K562	blood:	n/a	n/a
9	ATF3	chr1:225708346-225708584	K562	blood:	n/a	n/a
10	ATF3	chr1:225696174-225696735	HCT-116	colon:	n/a	n/a
11	ATF3	chr1:225708305-225708592	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr1:225696148-225696607	A549	lung:	n/a	n/a
13	BACH1	chr1:225696262-225696680	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:225686288-225686483	GM12878	blood:	n/a	chr1:225686374-225686385
15	BCL3	chr1:225672714-225673679	A549	lung:	n/a	chr1:225672752-225672765 chr1:225672761-225672769
16	BCL3	chr1:225695926-225696790	A549	lung:	n/a	n/a
17	BHLHE40	chr1:225683837-225684158	K562	blood:	n/a	n/a
18	BHLHE40	chr1:225691105-225691113	K562	blood:	n/a	n/a
19	BHLHE40	chr1:225696319-225696533	K562	blood:	n/a	n/a
20	BRCA1	chr1:225711162-225711398	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr1:225696104-225697230	HCT-116	colon:	n/a	n/a
22	CBX3	chr1:225697388-225698046	HCT-116	colon:	n/a	n/a
23	CBX3	chr1:225697375-225697950	HCT-116	colon:	n/a	n/a
24	CBX3	chr1:225696167-225696753	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:225708327-225708683	HepG2	liver:	n/a	chr1:225708508-225708519
26	CEBPB	chr1:225708331-225708698	A549	lung:	n/a	chr1:225708508-225708519
27	CEBPB	chr1:225696028-225696748	A549	lung:	n/a	n/a
28	CEBPB	chr1:225696043-225696834	HCT-116	colon:	n/a	n/a
29	CEBPB	chr1:225708268-225708618	HCT-116	colon:	n/a	chr1:225708508-225708519
30	CEBPB	chr1:225708327-225708684	K562	blood:	n/a	chr1:225708508-225708519
31	CEBPB	chr1:225696168-225696554	A549	lung:	n/a	n/a
32	CEBPB	chr1:225705442-225705652	A549	lung:	n/a	n/a
33	CEBPB	chr1:225705406-225705625	K562	blood:	n/a	n/a
34	CEBPB	chr1:225696061-225696724	HCT-116	colon:	n/a	n/a
35	CEBPB	chr1:225696177-225696663	IMR90	lung:	n/a	n/a
36	CEBPB	chr1:225708274-225708622	A549	lung:	n/a	chr1:225708508-225708519
37	CEBPB	chr1:225708325-225708582	K562	blood:	n/a	chr1:225708508-225708519
38	CEBPB	chr1:225708333-225708695	H1-hESC	embryonic stem cell:	n/a	chr1:225708508-225708519
39	CEBPB	chr1:225708333-225708624	MCF-7	breast:	n/a	chr1:225708508-225708519
40	CEBPB	chr1:225697347-225697966	HCT-116	colon:	n/a	chr1:225697515-225697528
41	CEBPB	chr1:225696174-225696610	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:225708203-225708730	A549	lung:	n/a	chr1:225708265-225708278 chr1:225708508-225708519
43	CEBPB	chr1:225708343-225708673	Hela-S3	cervix:	n/a	chr1:225708508-225708519
44	CEBPB	chr1:225696153-225696595	A549	lung:	n/a	n/a
45	CEBPB	chr1:225696235-225696494	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:225708324-225708697	IMR90	lung:	n/a	chr1:225708508-225708519
47	CHD2	chr1:225696226-225696602	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr1:225696237-225696541	A549	lung:	n/a	n/a
49	CREB1	chr1:225696240-225696598	ECC-1	luminal epithelium:	n/a	n/a
50	CREB1	chr1:225696181-225696752	H1-hESC	embryonic stem cell:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:225688425-225688475	AoSMC	blood vessel:	n/a
2	chr1:225707049-225707099	HRE	kidney:	n/a
3	chr1:225703895-225703945	U87	brain:	n/a
4	chr1:225676425-225676475	AoSMC	blood vessel:	n/a
5	chr1:225676425-225676475	BJ	skin:	n/a
6	chr1:225703895-225703945	BE2_C	brain:	n/a
7	chr1:225688425-225688475	ECC-1	luminal epithelium:	n/a
8	chr1:225688425-225688475	Jurkat	blood:	n/a
9	chr1:225676425-225676475	HIPEpiC	eye:	n/a
10	chr1:225697019-225697069	HIPEpiC	eye:	n/a
11	chr1:225688425-225688475	ovcar-3	ovarian:	n/a
12	chr1:225676425-225676475	HAEpiC	amniotic membrane:	n/a
13	chr1:225676425-225676475	HNPCEpiC	eye:	n/a
14	chr1:225697019-225697069	HEK293	kidney:	embryo
15	chr1:225688425-225688475	HepG2	liver:	n/a
16	chr1:225707049-225707099	SK-N-SH	brain:	n/a
17	chr1:225703895-225703945	AG10803	skin:	n/a
18	chr1:225688425-225688475	HCT-116	colon:	n/a
19	chr1:225703895-225703945	HNPCEpiC	eye:	n/a
20	chr1:225703895-225703945	SAEC	small airway:	n/a
21	chr1:225703895-225703945	HRCEpiC	kidney:	n/a
22	chr1:225688425-225688475	K562	blood:	n/a
23	chr1:225688425-225688475	RPTEC	kidney:	n/a
24	chr1:225697019-225697069	HRPEpiC	eye:	n/a
25	chr1:225707049-225707099	IMR90	lung:	fetal
26	chr1:225676425-225676475	HCT-116	colon:	n/a
27	chr1:225688425-225688475	SK-N-SH_RA	brain:	n/a
28	chr1:225688425-225688475	ProgFib	skin:	n/a
29	chr1:225676425-225676475	IMR90	lung:	fetal
30	chr1:225703895-225703945	ovcar-3	ovarian:	n/a
31	chr1:225707049-225707099	AG04450	lung:	fetal
32	chr1:225707049-225707099	HUVEC	blood vessel:	n/a
33	chr1:225688425-225688475	HRCEpiC	kidney:	n/a
34	chr1:225707049-225707099	SK-N-SH_RA	brain:	n/a
35	chr1:225697019-225697069	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:225676425-225676475	SKMC	muscle:	n/a
37	chr1:225676425-225676475	HMEC	breast:	n/a
38	chr1:225697019-225697069	ovcar-3	ovarian:	n/a
39	chr1:225688425-225688475	HCM	heart:	n/a
40	chr1:225707049-225707099	HL-60	blood:	n/a
41	chr1:225676425-225676475	Jurkat	blood:	n/a
42	chr1:225703895-225703945	PANC-1	pancreas:	n/a
43	chr1:225688425-225688475	GM06990	blood:	n/a
44	chr1:225697019-225697069	HL-60	blood:	n/a
45	chr1:225676425-225676475	NHDF-neo	bronchial:	n/a
46	chr1:225688425-225688475	AG04450	lung:	fetal
47	chr1:225676425-225676475	CMK	blood:	n/a
48	chr1:225697019-225697069	AG09309	skin:	n/a
49	chr1:225697019-225697069	AoSMC	blood vessel:	n/a
50	chr1:225676425-225676475	HEK293	kidney:	embryo

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:225682780..225684982-chr1:225687181..225690046,2	MCF-7	breast:
2	chr1:225716258..225718106-chr1:225719282..225721032,2	MCF-7	breast:
3	chr1:225704786..225708350-chr1:225708492..225710197,3	K562	blood:
4	chr1:225713990..225716472-chr1:225723399..225725793,2	K562	blood:
5	chr1:225710717..225715059-chr1:225715137..225718400,6	K562	blood:
6	chr1:225667455..225673405-chr1:225674170..225678275,6	MCF-7	breast:
7	chr1:225662746..225665144-chr1:225672666..225674544,2	MCF-7	breast:
8	chr1:225692749..225695160-chr1:225840876..225842568,2	MCF-7	breast:
9	chr1:225674187..225676643-chr1:225684973..225688505,3	K562	blood:
10	chr1:225689503..225693745-chr1:225697165..225700935,4	K562	blood:
11	chr1:225704786..225708350-chr1:225708492..225710197,3	K562	blood:
12	chr1:225662561..225663268-chr1:225685078..225685619,2	K562	blood:
13	chr1:225674187..225676643-chr1:225684973..225688505,3	K562	blood:
14	chr1:225668756..225671445-chr1:225674981..225676551,3	K562	blood:
15	chr1:225692705..225694841-chr1:225697963..225699635,2	K562	blood:
16	chr1:225703740..225706678-chr1:225717251..225719258,2	K562	blood:
17	chr1:225703740..225706678-chr1:225717251..225719258,2	K562	blood:
18	chr1:225710717..225715059-chr1:225715137..225718400,6	K562	blood:
19	chr1:225674280..225677221-chr1:225997663..226000316,2	MCF-7	breast:
20	chr1:225710178..225712804-chr1:225725363..225728293,2	MCF-7	breast:
21	chr1:225712577..225715165-chr1:225716923..225719442,2	MCF-7	breast:
22	chr1:225712577..225715165-chr1:225716923..225719442,2	MCF-7	breast:
23	chr1:225668772..225671386-chr1:225671515..225673412,2	K562	blood:
24	chr1:225712005..225714955-chr1:225715137..225718400,3	K562	blood:
25	chr1:225686982..225689320-chr1:225964805..225966549,2	MCF-7	breast:
26	chr1:225691003..225692885-chr1:225694759..225696360,2	K562	blood:
27	chr1:225712005..225714955-chr1:225715137..225718400,3	K562	blood:
28	chr1:225694216..225695016-chr2:43701955..43702730,2	MCF-7	breast:
29	chr1:225701844..225704859-chr1:225708519..225712628,3	MCF-7	breast:
30	chr1:225667455..225673405-chr1:225674170..225678275,6	MCF-7	breast:
31	chr1:225684757..225686780-chr1:225840497..225842307,2	MCF-7	breast:
32	chr1:225662457..225663199-chr1:225705258..225705789,2	MCF-7	breast:
33	chr1:225698646..225701113-chr1:225965307..225966901,2	MCF-7	breast:
34	chr1:225692705..225694841-chr1:225697963..225699635,2	K562	blood:
35	chr1:225717290..225720018-chr1:225721925..225724393,2	K562	blood:

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ENAH	hsa-miR-375	chr1:225684946-225684940
2	ENAH	hsa-miR-124-3p	chr1:225683220-225683214
3	ENAH	hsa-miR-181a-5p	chr1:225682671-225682665
4	ENAH	hsa-miR-124-3p	chr1:225674888-225674882
5	ENAH	hsa-miR-181a-5p	chr1:225682791-225682784

Variant related genes	Relation type
ENAH	TF binding region
ENAH	CpG island
ENSG00000154380	chromatin interactions
ENSG00000143819	chromatin interactions
ENSG00000143742	chromatin interactions

Extended variants
information (count: 1524 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545933631	chr1:225673248-225673249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17500562	chr1:225673293-225673294	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs61850569	chr1:225673330-225673331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528647573	chr1:225673331-225673332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556619221	chr1:225673390-225673391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540951633	chr1:225673401-225673402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562355823	chr1:225673410-225673411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528939291	chr1:225673442-225673443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550594858	chr1:225673467-225673468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372260666	chr1:225673473-225673474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs17500604	chr1:225673474-225673475	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs12042698	chr1:225673483-225673484	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs35144270	chr1:225673492-225673493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs17500639	chr1:225673516-225673517	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566686140	chr1:225673518-225673519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184305697	chr1:225673545-225673546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548905659	chr1:225673587-225673588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567220170	chr1:225673611-225673612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537697725	chr1:225673656-225673657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535957051	chr1:225673671-225673672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556943775	chr1:225673722-225673723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199699991	chr1:225673767-225673768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188209815	chr1:225673783-225673784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17500644	chr1:225673784-225673785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs148654648	chr1:225673800-225673801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9804142	chr1:225673847-225673848	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs575508458	chr1:225673909-225673910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386369807	chr1:225673932-225673933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71170085	chr1:225673955-225673956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562418583	chr1:225673972-225673973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574389926	chr1:225674012-225674013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545899365	chr1:225674017-225674018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544879349	chr1:225674018-225674019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562483957	chr1:225674061-225674062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6656170	chr1:225674069-225674070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12137602	chr1:225674074-225674075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532765390	chr1:225674076-225674077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551487069	chr1:225674122-225674123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559982131	chr1:225674178-225674179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370178773	chr1:225674182-225674183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374437122	chr1:225674236-225674237	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114316392	chr1:225674240-225674241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17500679	chr1:225674255-225674256	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs537761657	chr1:225674294-225674295	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72753025	chr1:225674295-225674296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569261371	chr1:225674306-225674307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539437363	chr1:225674343-225674344	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543559206	chr1:225674348-225674349	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191611963	chr1:225674364-225674365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573256187	chr1:225674395-225674396	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:225655600-225677000	Weak transcription	Right Atrium	heart
2	chr1:225663200-225683800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr1:225663200-225686400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:225663200-225696400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr1:225663400-225686000	Weak transcription	A549	lung
6	chr1:225666000-225696800	Weak transcription	Esophagus	oesophagus
7	chr1:225667400-225684400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:225669000-225687800	Weak transcription	Placenta	Placenta
9	chr1:225669200-225673600	Enhancers	Fetal Muscle Leg	muscle
10	chr1:225669800-225673400	Enhancers	Fetal Brain Male	brain
11	chr1:225669800-225696800	Weak transcription	Pancreas	Pancrea
12	chr1:225670600-225680200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:225670600-225680200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:225670600-225684200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr1:225670800-225674000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:225670800-225674000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:225670800-225674000	Weak transcription	Aorta	Aorta
18	chr1:225670800-225676400	Weak transcription	Fetal Lung	lung
19	chr1:225670800-225676600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:225670800-225676600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:225670800-225676600	Weak transcription	Brain Anterior Caudate	brain
22	chr1:225670800-225676600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:225670800-225677000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:225670800-225680000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:225670800-225680800	Weak transcription	NH-A	brain
26	chr1:225670800-225681000	Weak transcription	HSMM	muscle
27	chr1:225670800-225682200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:225670800-225683800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:225670800-225683800	Weak transcription	HSMMtube	muscle
30	chr1:225670800-225686400	Weak transcription	Ovary	ovary
31	chr1:225670800-225688400	Weak transcription	Duodenum Mucosa	Duodenum
32	chr1:225671000-225676400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr1:225671600-225683800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:225671600-225685000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:225671800-225680200	Weak transcription	Osteobl	bone
36	chr1:225672000-225676000	Weak transcription	Brain Hippocampus Middle	brain
37	chr1:225672000-225681600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr1:225672000-225683600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr1:225672200-225673400	Enhancers	Fetal Thymus	thymus
40	chr1:225672200-225676000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr1:225672200-225676000	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr1:225672200-225682000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:225672200-225685200	Weak transcription	NHDF-Ad	bronchial
44	chr1:225672200-225696800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:225672200-225696800	Weak transcription	Brain Germinal Matrix	brain
46	chr1:225672400-225676000	Weak transcription	Colon Smooth Muscle	Colon
47	chr1:225672400-225676000	Weak transcription	Rectal Smooth Muscle	rectum
48	chr1:225672400-225676400	Weak transcription	Brain Angular Gyrus	brain
49	chr1:225672400-225676600	Weak transcription	Brain Substantia Nigra	brain
50	chr1:225672400-225676600	Weak transcription	Stomach Smooth Muscle	stomach

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