Variant report

Variant	nsv1001588
Chromosome Location	chr1:209908876-209938243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:1037)
Chromatin interactive
region (count:31)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:209919806-209920006	K562	blood:	n/a	n/a
2	ARID3A	chr1:209921013-209921570	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:209921054-209921380	K562	blood:	n/a	n/a
4	ATF1	chr1:209919889-209920413	K562	blood:	n/a	n/a
5	ATF1	chr1:209925463-209925855	K562	blood:	n/a	n/a
6	ATF1	chr1:209920995-209921484	K562	blood:	n/a	n/a
7	ATF2	chr1:209930143-209930708	GM12878	blood:	n/a	n/a
8	ATF2	chr1:209924743-209925745	GM12878	blood:	n/a	n/a
9	ATF2	chr1:209920963-209921452	GM12878	blood:	n/a	n/a
10	ATF2	chr1:209929110-209929765	GM12878	blood:	n/a	n/a
11	ATF2	chr1:209924760-209925773	GM12878	blood:	n/a	n/a
12	ATF2	chr1:209920921-209921459	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:209920873-209921547	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr1:209921004-209921479	GM12878	blood:	n/a	n/a
15	ATF3	chr1:209920985-209921395	H1-hESC	embryonic stem cell:	n/a	chr1:209921002-209921016
16	ATF3	chr1:209920949-209921477	K562	blood:	n/a	chr1:209921002-209921016
17	ATF3	chr1:209920988-209921485	K562	blood:	n/a	chr1:209921002-209921016
18	BACH1	chr1:209921024-209921536	H1-hESC	embryonic stem cell:	n/a	chr1:209921240-209921254
19	BACH1	chr1:209921114-209921379	K562	blood:	n/a	chr1:209921240-209921254
20	BATF	chr1:209925147-209925724	GM12878	blood:	n/a	n/a
21	BATF	chr1:209924829-209925131	GM12878	blood:	n/a	n/a
22	BATF	chr1:209924750-209925876	GM12878	blood:	n/a	n/a
23	BATF	chr1:209929263-209929670	GM12878	blood:	n/a	n/a
24	BATF	chr1:209921030-209921441	GM12878	blood:	n/a	chr1:209921244-209921254 chr1:209921243-209921254
25	BATF	chr1:209922600-209922847	GM12878	blood:	n/a	n/a
26	BCL11A	chr1:209925293-209925660	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:209924883-209925713	GM12878	blood:	n/a	chr1:209925691-209925698
28	BCL3	chr1:209920881-209921526	A549	lung:	n/a	n/a
29	BCL3	chr1:209924918-209925636	GM12878	blood:	n/a	n/a
30	BCLAF1	chr1:209924809-209925780	GM12878	blood:	n/a	chr1:209925691-209925698
31	BCLAF1	chr1:209929104-209929760	GM12878	blood:	n/a	n/a
32	BCLAF1	chr1:209920878-209921575	GM12878	blood:	n/a	n/a
33	BCLAF1	chr1:209920918-209921564	GM12878	blood:	n/a	n/a
34	BCLAF1	chr1:209925143-209925814	GM12878	blood:	n/a	chr1:209925691-209925698
35	BHLHE40	chr1:209915413-209915613	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:209919882-209919980	K562	blood:	n/a	n/a
37	BHLHE40	chr1:209915353-209915409	K562	blood:	n/a	n/a
38	BHLHE40	chr1:209920814-209921542	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:209920979-209921554	HepG2	liver:	n/a	n/a
40	BHLHE40	chr1:209929950-209930349	GM12878	blood:	n/a	n/a
41	BHLHE40	chr1:209920956-209921651	K562	blood:	n/a	n/a
42	BHLHE40	chr1:209924890-209925736	GM12878	blood:	n/a	n/a
43	BRCA1	chr1:209921135-209921510	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr1:209921049-209921376	HepG2	liver:	n/a	n/a
45	BRCA1	chr1:209921051-209921486	H1-hESC	embryonic stem cell:	n/a	n/a
46	CBX3	chr1:209920861-209921773	HCT-116	colon:	n/a	n/a
47	CBX3	chr1:209920861-209921572	K562	blood:	n/a	n/a
48	CBX3	chr1:209920945-209921499	K562	blood:	n/a	n/a
49	CCNT2	chr1:209920937-209921544	K562	blood:	n/a	n/a
50	CEBPB	chr1:209921003-209921366	IMR90	lung:	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	chr1:209922102-209922152	GM12892	blood:	n/a
2	chr1:209922102-209922152	GM12878	blood:	n/a
3	chr1:209929512-209929562	HUVEC	blood vessel:	n/a
4	chr1:209929496-209929546	SK-N-SH	brain:	n/a
5	chr1:209929622-209929672	SKMC	muscle:	n/a
6	chr1:209922102-209922152	AoSMC	blood vessel:	n/a
7	chr1:209917237-209917287	HIPEpiC	eye:	n/a
8	chr1:209921232-209921282	GM12878	blood:	n/a
9	chr1:209921096-209921146	HAEpiC	amniotic membrane:	n/a
10	chr1:209930127-209930177	PANC-1	pancreas:	n/a
11	chr1:209921096-209921146	BJ	skin:	n/a
12	chr1:209929546-209929596	HUVEC	blood vessel:	n/a
13	chr1:209930127-209930177	AG09319	gingival:	n/a
14	chr1:209929496-209929546	Hepatocyte	liver:	n/a
15	chr1:209921370-209921420	HNPCEpiC	eye:	n/a
16	chr1:209921129-209921179	Hepatocyte	liver:	n/a
17	chr1:209928895-209928945	ECC-1	luminal epithelium:	n/a
18	chr1:209922102-209922152	GM19239	blood:	n/a
19	chr1:209929496-209929546	PrEC	prostate:	n/a
20	chr1:209921370-209921420	NB4	blood:	n/a
21	chr1:209917237-209917287	HL-60	blood:	n/a
22	chr1:209917237-209917287	HRE	kidney:	n/a
23	chr1:209929546-209929596	NHBE	bronchial:	n/a
24	chr1:209921577-209921627	T-47D	breast:	n/a
25	chr1:209929546-209929596	GM12892	blood:	n/a
26	chr1:209917237-209917287	NT2-D1	testis:	n/a
27	chr1:209928895-209928945	HIPEpiC	eye:	n/a
28	chr1:209929622-209929672	AG09319	gingival:	n/a
29	chr1:209921232-209921282	NH-A	brain:	n/a
30	chr1:209915875-209915925	LNCaP	prostate:	n/a
31	chr1:209921370-209921420	HEEpiC	esophagus:	n/a
32	chr1:209921096-209921146	A549	lung:	n/a
33	chr1:209929496-209929546	HUVEC	blood vessel:	n/a
34	chr1:209919394-209919444	MCF10A-Er-Src	breast:	n/a
35	chr1:209921096-209921146	Hela-S3	cervix:	n/a
36	chr1:209929546-209929596	RPTEC	kidney:	n/a
37	chr1:209928526-209928576	RPTEC	kidney:	n/a
38	chr1:209921232-209921282	HIPEpiC	eye:	n/a
39	chr1:209928895-209928945	CMK	blood:	n/a
40	chr1:209929512-209929562	NB4	blood:	n/a
41	chr1:209930127-209930177	HCPEpiC	choroid plexus:	n/a
42	chr1:209921096-209921146	AG09319	gingival:	n/a
43	chr1:209919394-209919444	GM12878	blood:	n/a
44	chr1:209921232-209921282	GM12891	blood:	n/a
45	chr1:209921031-209921081	SK-N-SH_RA	brain:	n/a
46	chr1:209921129-209921179	Jurkat	blood:	n/a
47	chr1:209921129-209921179	NHBE	bronchial:	n/a
48	chr1:209921031-209921081	GM06990	blood:	n/a
49	chr1:209930127-209930177	GM12892	blood:	n/a
50	chr1:209922102-209922152	GM12891	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:209742263..209743556-chr1:209920676..209921449,8	K562	blood:
2	chr1:209920917..209921835-chr1:210162910..210163551,2	K562	blood:
3	chr1:209865847..209866908-chr1:209920647..209921937,5	K562	blood:
4	chr1:209921622..209924785-chr1:209954989..209957828,3	MCF-7	breast:
5	chr1:209913450..209916086-chr1:209919671..209921571,2	K562	blood:
6	chr1:209865971..209866599-chr1:209921080..209921833,2	MCF-7	breast:
7	chr1:209750094..209750827-chr1:209920765..209921786,7	K562	blood:
8	chr1:209897489..209898995-chr1:209918699..209920810,2	K562	blood:
9	chr1:209917192..209919277-chr1:209920875..209922464,2	K562	blood:
10	chr1:209916474..209918920-chr1:209920104..209922211,2	MCF-7	breast:
11	chr1:209937467..209939616-chr1:209957476..209959399,2	K562	blood:
12	chr1:209819912..209820560-chr1:209920680..209921530,2	MCF-7	breast:
13	chr1:209739097..209740094-chr1:209921398..209921982,2	K562	blood:
14	chr1:209921608..209924525-chr1:209928498..209931459,3	K562	blood:
15	chr1:209775181..209776051-chr1:209920704..209921451,3	MCF-7	breast:
16	chr1:209775290..209776004-chr1:209920694..209921561,3	K562	blood:
17	chr1:209931478..209933302-chr1:209941660..209944063,2	K562	blood:
18	chr1:209754061..209755961-chr1:209923961..209926598,2	K562	blood:
19	chr1:209739402..209740077-chr1:209920611..209921381,2	K562	blood:
20	chr1:209898728..209900231-chr1:209914075..209916050,2	K562	blood:
21	chr1:209913450..209916086-chr1:209919671..209921571,2	K562	blood:
22	chr1:209887863..209889453-chr1:209910765..209912630,2	K562	blood:
23	chr1:209742327..209743226-chr1:209920951..209921587,3	MCF-7	breast:
24	chr1:209898273..209898882-chr1:209921133..209921700,3	MCF-7	breast:
25	chr1:209921083..209924525-chr1:209927225..209931869,7	K562	blood:
26	chr1:209935010..209937588-chr1:209955355..209957792,2	K562	blood:
27	chr1:209763958..209764607-chr1:209920721..209921610,2	MCF-7	breast:
28	chr1:209900061..209902674-chr1:209907942..209909580,2	K562	blood:
29	chr1:209920122..209922907-chr1:209973621..209976183,2	MCF-7	breast:
30	chr1:209749839..209750375-chr1:209920675..209921983,3	MCF-7	breast:
31	chr1:209800921..209801627-chr1:209920949..209921660,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD11B1-3	chr1:209935860-209935941	NONHSAT009232
2	lnc-HSD11B1-1	chr1:209917718-209918559	NONHSAT009230
3	lnc-TRAF3IP3-1	chr1:209926487-209926547	NONHSAT009231
4	lnc-TRAF3IP3-1	chr1:209929911-209930068	NONHSAT009231
5	lnc-TRAF3IP3-1	chr1:209927491-209927732	NONHSAT009231
6	lnc-HSD11B1-3	chr1:209933517-209933729	NONHSAT009232
7	lnc-HSD11B1-3	chr1:209932379-209932479	NONHSAT009232
8	lnc-HSD11B1-3	chr1:209929481-209929654	NONHSAT009232

No data

Variant related genes	Relation type
TRAF3IP3	TF binding region
ENSG00000236136	TF binding region
TRAF3IP3	CpG island
ENSG00000236136	CpG island
ENSG00000009790	chromatin interactions
ENSG00000117595	chromatin interactions
ENSG00000162757	chromatin interactions
ENSG00000236136	chromatin interactions

Extended variants
information (count: 1058 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1058 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10863785	chr1:209908876-209908877	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543364033	chr1:209908877-209908878	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12123431	chr1:209908899-209908900	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569255314	chr1:209908946-209908947	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537815967	chr1:209909003-209909004	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528880470	chr1:209909004-209909005	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs566803144	chr1:209909060-209909061	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150870355	chr1:209909093-209909094	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs139373402	chr1:209909137-209909138	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145645426	chr1:209909166-209909167	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147756323	chr1:209909186-209909187	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559456683	chr1:209909201-209909202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142341274	chr1:209909208-209909209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549425274	chr1:209909253-209909254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190602301	chr1:209909254-209909255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374063402	chr1:209909258-209909259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367872132	chr1:209909314-209909315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115516780	chr1:209909318-209909319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558434294	chr1:209909355-209909356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2064148	chr1:209909385-209909386	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs80337405	chr1:209909409-209909410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78059492	chr1:209909422-209909423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115145015	chr1:209909433-209909434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111488558	chr1:209909509-209909510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543675340	chr1:209909522-209909523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116687539	chr1:209909569-209909570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573286740	chr1:209909572-209909573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540666110	chr1:209909627-209909628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117538664	chr1:209909674-209909675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553933227	chr1:209909679-209909680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144574791	chr1:209909708-209909709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574457594	chr1:209909710-209909711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563869770	chr1:209909728-209909729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541549838	chr1:209909811-209909812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531032592	chr1:209909842-209909843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549628109	chr1:209909858-209909859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183174637	chr1:209909860-209909861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189210202	chr1:209909873-209909874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370728806	chr1:209909874-209909875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192301296	chr1:209909914-209909915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375345042	chr1:209909927-209909928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182862884	chr1:209910112-209910113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575206213	chr1:209910195-209910196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113353370	chr1:209910263-209910264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539091457	chr1:209910286-209910287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541765649	chr1:209910312-209910313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145715013	chr1:209910347-209910348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543816194	chr1:209910383-209910384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148946907	chr1:209910384-209910385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143723245	chr1:209910404-209910405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	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
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:879 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209902400-209915000	Weak transcription	Brain Substantia Nigra	brain
2	chr1:209902400-209915400	Weak transcription	Brain Angular Gyrus	brain
3	chr1:209903000-209915200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr1:209906200-209909200	Genic enhancers	Liver	Liver
5	chr1:209906400-209914200	Weak transcription	Left Ventricle	heart
6	chr1:209906600-209909400	Weak transcription	Fetal Heart	heart
7	chr1:209906600-209914800	Weak transcription	Right Atrium	heart
8	chr1:209907600-209914800	Weak transcription	Spleen	Spleen
9	chr1:209907600-209920800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:209907800-209914600	Weak transcription	Right Ventricle	heart
11	chr1:209908000-209909000	Weak transcription	Ovary	ovary
12	chr1:209908000-209909400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:209908000-209909600	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr1:209908000-209909600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr1:209908600-209909200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:209909000-209909800	Enhancers	Ovary	ovary
17	chr1:209909200-209910600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:209909200-209910800	Enhancers	Liver	Liver
19	chr1:209909400-209910400	Enhancers	Fetal Heart	heart
20	chr1:209909400-209910800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:209909600-209909800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr1:209909800-209910000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr1:209909800-209914600	Weak transcription	Ovary	ovary
24	chr1:209910600-209914600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:209910800-209914000	Weak transcription	Liver	Liver
26	chr1:209910800-209915200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:209913600-209915200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr1:209914000-209917200	Enhancers	Liver	Liver
29	chr1:209914200-209914400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr1:209914200-209914800	Enhancers	Duodenum Mucosa	Duodenum
31	chr1:209914200-209916800	Enhancers	Fetal Intestine Large	intestine
32	chr1:209914200-209916800	Enhancers	Left Ventricle	heart
33	chr1:209914400-209915000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr1:209914400-209915600	Enhancers	Fetal Heart	heart
35	chr1:209914400-209915600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr1:209914600-209914800	Enhancers	Right Ventricle	heart
37	chr1:209914600-209915000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:209914600-209915800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:209914600-209916600	Enhancers	Fetal Intestine Small	intestine
40	chr1:209914600-209917000	Enhancers	Ovary	ovary
41	chr1:209914800-209915000	Flanking Active TSS	Duodenum Mucosa	Duodenum
42	chr1:209914800-209915200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr1:209914800-209915200	Enhancers	Spleen	Spleen
44	chr1:209914800-209915400	Enhancers	Esophagus	oesophagus
45	chr1:209914800-209915800	Weak transcription	Right Ventricle	heart
46	chr1:209914800-209916200	Enhancers	Adipose Nuclei	Adipose
47	chr1:209914800-209917800	Enhancers	Pancreas	Pancrea
48	chr1:209914800-209917800	Enhancers	Right Atrium	heart
49	chr1:209915000-209915200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr1:209915000-209915400	Enhancers	Duodenum Mucosa	Duodenum

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