Variant report

Variant	nsv945328
Chromosome Location	chr1:226015604-226031170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:213)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:213 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr1:226030380-226030585	K562	blood:	n/a	n/a
2	CEBPB	chr1:226022962-226023246	K562	blood:	n/a	n/a
3	CEBPB	chr1:226019895-226019941	HepG2	liver:	n/a	n/a
4	CHD2	chr1:226028611-226028642	K562	blood:	n/a	n/a
5	CHD2	chr1:226029882-226029884	K562	blood:	n/a	n/a
6	CTCF	chr1:226027260-226027410	HRE	kidney:	n/a	n/a
7	CTCF	chr1:226022791-226022861	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr1:226022640-226022790	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr1:226024212-226024245	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr1:226029902-226030056	H1-hESC	embryonic stem cell:	n/a	chr1:226029972-226029985
11	CTCF	chr1:226022760-226022910	HEK293	kidney:	n/a	n/a
12	CTCF	chr1:226029915-226030024	NHEK	skin:	n/a	chr1:226029972-226029985
13	CTCF	chr1:226029898-226029900	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr1:226023791-226023873	Lung_OC	lung:	n/a	n/a
15	CTCF	chr1:226024051-226024111	GM10248	blood:	n/a	n/a
16	EP300	chr1:226022078-226022803	ECC-1	luminal epithelium:	n/a	n/a
17	FOS	chr1:226023540-226023719	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:226022142-226022452	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr1:226023524-226023770	MCF10A-Er-Src	breast:	n/a	n/a
20	FOSL2	chr1:226029875-226030692	HepG2	liver:	n/a	chr1:226030648-226030659 chr1:226030052-226030061
21	JUN	chr1:226025981-226026108	K562	blood:	n/a	n/a
22	MAFF	chr1:226027936-226027971	HepG2	liver:	n/a	n/a
23	MAFF	chr1:226028479-226028757	HepG2	liver:	n/a	chr1:226028605-226028623
24	MAFK	chr1:226028525-226028759	HepG2	liver:	n/a	chr1:226028606-226028621
25	MAFK	chr1:226027826-226028092	HepG2	liver:	n/a	chr1:226027910-226027925
26	MAFK	chr1:226028465-226028777	HepG2	liver:	n/a	chr1:226028606-226028621
27	MAFK	chr1:226027939-226028023	HepG2	liver:	n/a	n/a
28	MYC	chr1:226022082-226022597	MCF10A-Er-Src	breast:	n/a	chr1:226022177-226022186
29	MYC	chr1:226023428-226023817	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr1:226023497-226023824	MCF10A-Er-Src	breast:	n/a	n/a
31	NFIC	chr1:226022099-226022626	SK-N-SH	brain:	n/a	chr1:226022269-226022285
32	NFIC	chr1:226023409-226023936	ECC-1	luminal epithelium:	n/a	n/a
33	NFIC	chr1:226022012-226022709	ECC-1	luminal epithelium:	n/a	chr1:226022269-226022285
34	NFIC	chr1:226022014-226022667	ECC-1	luminal epithelium:	n/a	chr1:226022269-226022285
35	NFIC	chr1:226023365-226023996	ECC-1	luminal epithelium:	n/a	n/a
36	PML	chr1:226030035-226030476	K562	blood:	n/a	n/a
37	POLR2A	chr1:226029273-226035960	HepG2	liver:	n/a	n/a
38	POLR2A	chr1:226026247-226026902	A549	lung:	n/a	n/a
39	POLR2A	chr1:226029446-226038446	K562	blood:	n/a	n/a
40	POLR2A	chr1:226027364-226027895	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr1:226026352-226026441	HepG2	liver:	n/a	n/a
42	POLR2A	chr1:226029725-226029747	ProgFib	skin:	n/a	n/a
43	POLR2A	chr1:226026346-226026574	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr1:226029818-226030046	HepG2	liver:	n/a	n/a
45	POLR2A	chr1:226029800-226032852	K562	blood:	n/a	n/a
46	POLR2A	chr1:226029944-226029958	MCF-7	breast:	n/a	n/a
47	POLR2A	chr1:226029563-226029573	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr1:226026963-226026977	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr1:226030506-226031371	HepG2	liver:	n/a	n/a
50	POLR2A	chr1:226031089-226031414	HCT-116	colon:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226016389-226016439	HL-60	blood:	n/a
2	chr1:226016389-226016439	A549	lung:	n/a
3	chr1:226016389-226016439	Hepatocyte	liver:	n/a
4	chr1:226023590-226023640	MCF-7	breast:	n/a
5	chr1:226023590-226023640	GM19239	blood:	n/a
6	chr1:226016389-226016439	MCF10A-Er-Src	breast:	n/a
7	chr1:226023590-226023640	ProgFib	skin:	n/a
8	chr1:226016389-226016439	K562	blood:	n/a
9	chr1:226023590-226023640	BJ	skin:	n/a
10	chr1:226023590-226023640	HUVEC	blood vessel:	n/a
11	chr1:226023590-226023640	HRPEpiC	eye:	n/a
12	chr1:226023590-226023640	GM12891	blood:	n/a
13	chr1:226016389-226016439	ECC-1	luminal epithelium:	n/a
14	chr1:226023590-226023640	PrEC	prostate:	n/a
15	chr1:226016389-226016439	PANC-1	pancreas:	n/a
16	chr1:226016389-226016439	H1-hESC	embryonic stem cell:	embryo
17	chr1:226016389-226016439	IMR90	lung:	fetal
18	chr1:226023590-226023640	MCF10A-Er-Src	breast:	n/a
19	chr1:226016389-226016439	Hela-S3	cervix:	n/a
20	chr1:226023590-226023640	AG09309	skin:	n/a
21	chr1:226016389-226016439	SK-N-SH_RA	brain:	n/a
22	chr1:226016389-226016439	HRPEpiC	eye:	n/a
23	chr1:226023590-226023640	HEEpiC	esophagus:	n/a
24	chr1:226016389-226016439	MCF-7	breast:	n/a
25	chr1:226023590-226023640	H1-hESC	embryonic stem cell:	embryo
26	chr1:226016389-226016439	GM19239	blood:	n/a
27	chr1:226016389-226016439	Caco-2	colon:	n/a
28	chr1:226016389-226016439	NB4	blood:	n/a
29	chr1:226023590-226023640	HRCEpiC	kidney:	n/a
30	chr1:226016389-226016439	AG10803	skin:	n/a
31	chr1:226023590-226023640	RPTEC	kidney:	n/a
32	chr1:226016389-226016439	HCM	heart:	n/a
33	chr1:226016389-226016439	HRCEpiC	kidney:	n/a
34	chr1:226016389-226016439	AG04449	skin:	fetal
35	chr1:226016389-226016439	T-47D	breast:	n/a
36	chr1:226023590-226023640	A549	lung:	n/a
37	chr1:226023590-226023640	PANC-1	pancreas:	n/a
38	chr1:226023590-226023640	HIPEpiC	eye:	n/a
39	chr1:226023590-226023640	HAEpiC	amniotic membrane:	n/a
40	chr1:226016389-226016439	HUVEC	blood vessel:	n/a
41	chr1:226023590-226023640	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:226016389-226016439	HNPCEpiC	eye:	n/a
43	chr1:226023590-226023640	HNPCEpiC	eye:	n/a
44	chr1:226016389-226016439	HCPEpiC	choroid plexus:	n/a
45	chr1:226016389-226016439	CMK	blood:	n/a
46	chr1:226016389-226016439	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:226016389-226016439	AG09309	skin:	n/a
48	chr1:226023590-226023640	HRE	kidney:	n/a
49	chr1:226023590-226023640	SK-N-SH	brain:	n/a
50	chr1:226023590-226023640	AG10803	skin:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226025881..226027741-chr1:226105867..226108259,2	K562	blood:
2	chr1:226030085..226032295-chr1:226067898..226070113,2	MCF-7	breast:
3	chr1:225662368..225663228-chr1:226027050..226027785,2	K562	blood:
4	chr1:226027447..226029935-chr1:226154706..226156516,2	K562	blood:
5	chr1:225966034..225968187-chr1:226022147..226024459,2	MCF-7	breast:
6	chr1:226022223..226024431-chr1:226025111..226027659,2	MCF-7	breast:
7	chr1:225655109..225657230-chr1:226022691..226024869,2	K562	blood:
8	chr1:225992085..225994324-chr1:226013953..226015752,2	K562	blood:
9	chr1:226025653..226027789-chr1:226114675..226116510,2	K562	blood:
10	chr1:226011523..226014376-chr1:226017221..226018923,2	MCF-7	breast:
11	chr1:225998663..226000298-chr1:226028489..226031143,2	MCF-7	breast:
12	chr1:225964257..225969087-chr1:226030786..226035881,7	K562	blood:
13	chr1:226022223..226024431-chr1:226025111..226027659,2	MCF-7	breast:
14	chr1:226028800..226031173-chr1:226165446..226167469,2	MCF-7	breast:
15	chr1:226025810..226027984-chr1:226031798..226033532,2	MCF-7	breast:
16	chr1:225964435..225966967-chr1:226028850..226030577,3	MCF-7	breast:
17	chr1:225965253..225967050-chr1:226028471..226030639,2	K562	blood:
18	chr1:225839806..225841875-chr1:226019865..226022618,2	MCF-7	breast:
19	chr1:226021203..226023917-chr1:226026955..226030143,3	K562	blood:
20	chr1:226015474..226017647-chr1:226024996..226027298,2	MCF-7	breast:
21	chr1:226021203..226023917-chr1:226026955..226030143,3	K562	blood:
22	chr1:225821970..225824548-chr1:226027169..226028727,2	K562	blood:
23	chr1:226016918..226019631-chr1:226062636..226064658,2	K562	blood:
24	chr1:225840519..225842068-chr1:226029667..226032109,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM63A-1	chr1:226028584-226028888	ENSG00000242861.1

No data

Variant related genes	Relation type
EPHX1	TF binding region
EPHX1	CpG island
ENSG00000154380	chromatin interactions
ENSG00000196187	chromatin interactions
ENSG00000143742	chromatin interactions
ENSG00000143819	chromatin interactions

Extended variants
information (count: 792 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566671174	chr1:226015605-226015606	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs199974928	chr1:226015615-226015616	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs144793415	chr1:226015618-226015619	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372684614	chr1:226015619-226015620	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112201930	chr1:226015620-226015621	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112984494	chr1:226015621-226015622	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111695074	chr1:226015622-226015623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533963161	chr1:226015704-226015705	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555278479	chr1:226015768-226015769	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139752880	chr1:226015780-226015781	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373140482	chr1:226015813-226015814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556933760	chr1:226015822-226015823	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12747413	chr1:226015828-226015829	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546074002	chr1:226015859-226015860	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557999395	chr1:226015970-226015971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573461291	chr1:226016004-226016005	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540780094	chr1:226016041-226016042	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540486252	chr1:226016043-226016044	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146784345	chr1:226016073-226016074	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528977777	chr1:226016074-226016075	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140462041	chr1:226016119-226016120	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144207603	chr1:226016134-226016135	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs45437093	chr1:226016218-226016219	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374855618	chr1:226016266-226016267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs41266227	chr1:226016267-226016268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551420461	chr1:226016313-226016314	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs45540836	chr1:226016332-226016333	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527602539	chr1:226016336-226016337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549155583	chr1:226016380-226016381	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs41266229	chr1:226016381-226016382	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs370888055	chr1:226016394-226016395	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs41266231	chr1:226016397-226016398	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs368412064	chr1:226016416-226016417	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs368254083	chr1:226016429-226016430	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs200493338	chr1:226016460-226016461	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs148398736	chr1:226016466-226016467	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372505975	chr1:226016492-226016493	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs200146699	chr1:226016507-226016508	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs11540967	chr1:226016551-226016552	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs3738046	chr1:226016558-226016559	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs375797693	chr1:226016565-226016566	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2234697	chr1:226016575-226016576	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557100177	chr1:226016593-226016594	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182154631	chr1:226016595-226016596	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11540969	chr1:226016605-226016606	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374642223	chr1:226016613-226016614	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555904871	chr1:226016622-226016623	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368099525	chr1:226016630-226016631	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs3738047	chr1:226016633-226016634	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376462097	chr1:226016635-226016636	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
abnormal development	18461090	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:706 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226000000-226019400	Weak transcription	Fetal Brain Female	brain
2	chr1:226000400-226015800	Enhancers	Ovary	ovary
3	chr1:226001800-226019200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:226005600-226019400	Weak transcription	Brain Germinal Matrix	brain
5	chr1:226005800-226019200	Weak transcription	NHLF	lung
6	chr1:226005800-226019400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:226005800-226019400	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr1:226006200-226016600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:226006200-226019400	Weak transcription	HSMM	muscle
10	chr1:226006200-226022000	Weak transcription	NHDF-Ad	bronchial
11	chr1:226006400-226016800	Weak transcription	Colonic Mucosa	Colon
12	chr1:226006400-226018600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:226006400-226019400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr1:226006400-226019600	Weak transcription	Hela-S3	cervix
15	chr1:226006600-226016600	Weak transcription	Aorta	Aorta
16	chr1:226008800-226019400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:226010800-226016600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:226010800-226019200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr1:226011000-226015800	Enhancers	Fetal Muscle Trunk	muscle
20	chr1:226011000-226015800	Genic enhancers	Fetal Muscle Leg	muscle
21	chr1:226011000-226016800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:226011200-226016600	Enhancers	Pancreas	Pancrea
23	chr1:226011800-226016600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr1:226012600-226016400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:226012600-226016600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:226012600-226016800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr1:226012600-226018000	Weak transcription	Fetal Brain Male	brain
28	chr1:226013400-226019200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:226013400-226019200	Weak transcription	Brain Angular Gyrus	brain
30	chr1:226013400-226031800	Weak transcription	Fetal Kidney	kidney
31	chr1:226013600-226016200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:226013600-226016400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr1:226013600-226016400	Weak transcription	Brain Substantia Nigra	brain
34	chr1:226013600-226016600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:226013600-226016800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr1:226013600-226019200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr1:226013600-226052600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:226013800-226016600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:226013800-226016800	Weak transcription	Brain Anterior Caudate	brain
40	chr1:226013800-226018000	Weak transcription	A549	lung
41	chr1:226013800-226019200	Weak transcription	Osteobl	bone
42	chr1:226013800-226019400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:226013800-226019400	Weak transcription	HSMMtube	muscle
44	chr1:226013800-226032000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr1:226013800-226037200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:226014000-226016800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr1:226014000-226032800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:226014200-226016800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:226014400-226015800	Flanking Active TSS	Liver	Liver
50	chr1:226014400-226019400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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