Variant report

Variant	nsv1004381
Chromosome Location	chr1:92968173-93064823
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:886)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:886 , 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	chr1:92981723-92981818	K562	blood:	n/a	n/a
2	ARID3A	chr1:92969957-92970157	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:93010203-93010659	K562	blood:	n/a	n/a
4	ARID3A	chr1:92970529-92971313	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:93002376-93003411	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:93003665-93003865	HepG2	liver:	n/a	n/a
7	ATF1	chr1:93010226-93010719	K562	blood:	n/a	n/a
8	ATF1	chr1:92981505-92981739	K562	blood:	n/a	n/a
9	ATF2	chr1:93003523-93004631	GM12878	blood:	n/a	n/a
10	ATF2	chr1:93049329-93050426	GM12878	blood:	n/a	n/a
11	ATF2	chr1:93049269-93049816	GM12878	blood:	n/a	n/a
12	ATF2	chr1:93052940-93053482	GM12878	blood:	n/a	n/a
13	ATF2	chr1:93003504-93004675	GM12878	blood:	n/a	n/a
14	ATF2	chr1:92968772-92969602	GM12878	blood:	n/a	n/a
15	ATF2	chr1:93028878-93029464	GM12878	blood:	n/a	n/a
16	ATF2	chr1:93002233-93002923	GM12878	blood:	n/a	n/a
17	ATF2	chr1:93052866-93053483	GM12878	blood:	n/a	n/a
18	ATF2	chr1:93002402-93002882	GM12878	blood:	n/a	n/a
19	ATF2	chr1:93049835-93050460	GM12878	blood:	n/a	n/a
20	ATF3	chr1:93010277-93010640	K562	blood:	n/a	n/a
21	BACH1	chr1:92993246-92993248	K562	blood:	n/a	n/a
22	BATF	chr1:93049920-93050305	GM12878	blood:	n/a	chr1:93050185-93050195
23	BATF	chr1:93002526-93002858	GM12878	blood:	n/a	chr1:93002819-93002829
24	BATF	chr1:93049462-93049729	GM12878	blood:	n/a	n/a
25	BATF	chr1:93053049-93053391	GM12878	blood:	n/a	n/a
26	BATF	chr1:93004217-93004611	GM12878	blood:	n/a	n/a
27	BATF	chr1:92975236-92975474	GM12878	blood:	n/a	chr1:92975390-92975401
28	BATF	chr1:93050000-93050266	GM12878	blood:	n/a	chr1:93050185-93050195
29	BATF	chr1:93004020-93004631	GM12878	blood:	n/a	n/a
30	BATF	chr1:93053051-93053397	GM12878	blood:	n/a	n/a
31	BATF	chr1:92975212-92975464	GM12878	blood:	n/a	chr1:92975390-92975401
32	BATF	chr1:93003587-93003947	GM12878	blood:	n/a	n/a
33	BATF	chr1:92969043-92969552	GM12878	blood:	n/a	n/a
34	BATF	chr1:93002480-93002880	GM12878	blood:	n/a	chr1:93002819-93002829
35	BCL11A	chr1:93052959-93053476	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:93004201-93004655	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:93029038-93029400	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:93049857-93050284	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
39	BCL11A	chr1:93002548-93002830	GM12878	blood:	n/a	chr1:93002817-93002826
40	BCL11A	chr1:93053071-93053399	GM12878	blood:	n/a	n/a
41	BCL11A	chr1:93002479-93002869	GM12878	blood:	n/a	chr1:93002817-93002826
42	BCL11A	chr1:93049964-93050273	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
43	BCL11A	chr1:93049426-93049685	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:93004234-93004554	GM12878	blood:	n/a	n/a
45	BCL3	chr1:93002469-93002857	GM12878	blood:	n/a	chr1:93002817-93002826
46	BCL3	chr1:93049974-93050329	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
47	BCL3	chr1:93052972-93053425	GM12878	blood:	n/a	n/a
48	BCLAF1	chr1:93049800-93050322	GM12878	blood:	n/a	chr1:93050184-93050193 chr1:93050234-93050241
49	BCLAF1	chr1:93002416-93002938	GM12878	blood:	n/a	chr1:93002817-93002826
50	BCLAF1	chr1:93028991-93029470	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:92977322-92977372	HNPCEpiC	eye:	n/a
2	chr1:92977322-92977372	NHBE	bronchial:	n/a
3	chr1:92977322-92977372	SK-N-SH	brain:	n/a
4	chr1:92977322-92977372	HUVEC	blood vessel:	n/a
5	chr1:92977322-92977372	HCM	heart:	n/a
6	chr1:92977322-92977372	MCF10A-Er-Src	breast:	n/a
7	chr1:92977322-92977372	HEEpiC	esophagus:	n/a
8	chr1:92977322-92977372	SKMC	muscle:	n/a
9	chr1:92977322-92977372	HRE	kidney:	n/a
10	chr1:92977322-92977372	GM19239	blood:	n/a
11	chr1:92977322-92977372	HCPEpiC	choroid plexus:	n/a
12	chr1:92977322-92977372	RPTEC	kidney:	n/a
13	chr1:92977322-92977372	ovcar-3	ovarian:	n/a
14	chr1:92977322-92977372	NT2-D1	testis:	n/a
15	chr1:92977322-92977372	Jurkat	blood:	n/a
16	chr1:92977322-92977372	AoSMC	blood vessel:	n/a
17	chr1:92977322-92977372	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:92977322-92977372	Hela-S3	cervix:	n/a
19	chr1:92977322-92977372	HepG2	liver:	n/a
20	chr1:92977322-92977372	HMEC	breast:	n/a
21	chr1:92977322-92977372	HIPEpiC	eye:	n/a
22	chr1:92977322-92977372	HEK293	kidney:	embryo
23	chr1:92977322-92977372	H1-hESC	embryonic stem cell:	embryo
24	chr1:92977322-92977372	SK-N-SH_RA	brain:	n/a
25	chr1:92977322-92977372	HL-60	blood:	n/a
26	chr1:92977322-92977372	AG04449	skin:	fetal
27	chr1:92977322-92977372	AG10803	skin:	n/a
28	chr1:92977322-92977372	AG04450	lung:	fetal
29	chr1:92977322-92977372	HCT-116	colon:	n/a
30	chr1:92977322-92977372	GM12892	blood:	n/a
31	chr1:92977322-92977372	A549	lung:	n/a
32	chr1:92977322-92977372	BJ	skin:	n/a
33	chr1:92977322-92977372	HRCEpiC	kidney:	n/a
34	chr1:92977322-92977372	K562	blood:	n/a
35	chr1:92977322-92977372	PrEC	prostate:	n/a
36	chr1:92977322-92977372	NB4	blood:	n/a
37	chr1:92977322-92977372	Caco-2	colon:	n/a
38	chr1:92977322-92977372	HCF	heart:	n/a
39	chr1:92977322-92977372	ProgFib	skin:	n/a
40	chr1:92977322-92977372	PFSK-1	brain:	n/a
41	chr1:92977322-92977372	Hepatocyte	liver:	n/a
42	chr1:92977322-92977372	AG09309	skin:	n/a
43	chr1:92977322-92977372	GM06990	blood:	n/a
44	chr1:92977322-92977372	NHDF-neo	bronchial:	n/a
45	chr1:92977322-92977372	HAEpiC	amniotic membrane:	n/a
46	chr1:92977322-92977372	GM12891	blood:	n/a
47	chr1:92977322-92977372	PANC-1	pancreas:	n/a
48	chr1:92977322-92977372	GM12878	blood:	n/a
49	chr1:92977322-92977372	SK-N-MC	brain:	n/a
50	chr1:92977322-92977372	AG09319	gingival:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:92975440..92978255-chr1:92987459..92989945,2	K562	blood:
2	chr1:92975971..92978255-chr1:92987439..92988959,2	K562	blood:
3	chr1:92971064..92972652-chr1:92984833..92987598,2	MCF-7	breast:
4	chr1:92987883..92989891-chr1:93008621..93010399,2	K562	blood:
5	chr1:93008775..93011605-chr1:93017435..93019676,2	K562	blood:
6	chr1:92966213..92967756-chr1:92973026..92974536,2	K562	blood:
7	chr1:92971064..92972652-chr1:92984833..92987598,2	MCF-7	breast:
8	chr1:93038487..93040567-chr1:93043443..93045326,2	K562	blood:
9	chr1:92975971..92978255-chr1:92987439..92988959,2	K562	blood:
10	chr1:92970721..92973129-chr1:92975876..92977774,2	K562	blood:
11	chr1:93037475..93039657-chr1:93040585..93042175,2	K562	blood:
12	chr1:93037475..93039657-chr1:93040585..93042175,2	K562	blood:
13	chr1:92977725..92979355-chr1:92980937..92983105,2	K562	blood:
14	chr1:92975440..92978255-chr1:92987459..92989945,2	K562	blood:
15	chr1:92987883..92989891-chr1:93008621..93010399,2	K562	blood:
16	chr1:93008775..93011605-chr1:93017435..93019676,2	K562	blood:
17	chr1:93038487..93040567-chr1:93043443..93045326,2	K562	blood:
18	chr1:92977725..92979355-chr1:92980937..92983105,2	K562	blood:
19	chr1:92775257..92776314-chr1:93064696..93065442,3	MCF-7	breast:
20	chr1:93027014..93029326-chr1:93048258..93050872,2	K562	blood:
21	chr1:93027014..93029326-chr1:93048258..93050872,2	K562	blood:
22	chr1:92764183..92766708-chr1:92981582..92984130,2	K562	blood:
23	chr1:92970721..92973129-chr1:92975876..92977774,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GFI1-2	chr1:93046033-93046378	NONHSAT004461

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	EVI5	hsa-miR-124-3p	chr1:92974831-92974850
2	EVI5	hsa-miR-182-5p	chr1:92979039-92979032
3	EVI5	hsa-miR-124-3p	chr1:92974837-92974831
4	EVI5	hsa-miR-182-5p	chr1:92978757-92978786
5	EVI5	hsa-miR-124-3p	chr1:92974288-92974306
6	EVI5	hsa-miR-124-3p	chr1:92974294-92974288
7	EVI5	hsa-miR-96-5p	chr1:92979038-92979032
8	EVI5	hsa-miR-182-5p	chr1:92979033-92979056

Variant related genes	Relation type
ENSG00000223787	TF binding region
ENSG00000223787	CpG island
ENSG00000122484	chromatin interactions
ENSG00000174842	chromatin interactions

Extended variants
information (count: 3641 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3641 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547635590	chr1:92968234-92968235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552457164	chr1:92968245-92968246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150003016	chr1:92968269-92968270	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547844079	chr1:92968288-92968289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567358567	chr1:92968291-92968292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568042398	chr1:92968301-92968302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535505212	chr1:92968302-92968303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11164654	chr1:92968312-92968313	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs56800608	chr1:92968420-92968421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71091287	chr1:92968421-92968422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549830527	chr1:92968422-92968423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537294480	chr1:92968465-92968466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188663747	chr1:92968466-92968467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577151098	chr1:92968502-92968503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541042208	chr1:92968538-92968539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149178376	chr1:92968556-92968557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558460336	chr1:92968568-92968569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555302629	chr1:92968573-92968574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565594821	chr1:92968661-92968662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76841200	chr1:92968710-92968711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74718581	chr1:92968725-92968726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143947595	chr1:92968731-92968732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146874682	chr1:92968759-92968760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546064535	chr1:92968815-92968816	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs4970696	chr1:92968853-92968854	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542789987	chr1:92968869-92968870	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs556601086	chr1:92968892-92968893	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs140251725	chr1:92968908-92968909	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs376446128	chr1:92968914-92968915	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs145216059	chr1:92969025-92969026	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs150923630	chr1:92969029-92969030	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs140785526	chr1:92969079-92969080	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs568651193	chr1:92969102-92969103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs537232440	chr1:92969211-92969212	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs558752284	chr1:92969213-92969214	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs150103514	chr1:92969256-92969257	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7411724	chr1:92969260-92969261	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570793380	chr1:92969332-92969333	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs201019308	chr1:92969363-92969364	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs575237824	chr1:92969435-92969436	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs539574880	chr1:92969450-92969451	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs553398077	chr1:92969473-92969474	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs35711562	chr1:92969535-92969536	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138589891	chr1:92969541-92969542	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs114376285	chr1:92969547-92969548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs114800608	chr1:92969587-92969588	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs557483792	chr1:92969594-92969595	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs116784038	chr1:92969635-92969636	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs545999380	chr1:92969747-92969748	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs564245632	chr1:92969778-92969779	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioma	20126413	CNVD

Chromatin state (count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92952800-92991400	Weak transcription	Pancreas	Pancrea
2	chr1:92961600-92969800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr1:92965200-92968600	Weak transcription	Fetal Thymus	thymus
4	chr1:92967400-92969800	Enhancers	Dnd41	blood
5	chr1:92967600-92968200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:92967600-92968200	Enhancers	HSMM	muscle
7	chr1:92967600-92968200	Enhancers	NHDF-Ad	bronchial
8	chr1:92967600-92968200	Enhancers	Osteobl	bone
9	chr1:92967600-92969600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:92967800-92968200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:92967800-92969000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:92967800-92970000	Enhancers	HMEC	breast
13	chr1:92967800-92978400	Weak transcription	Fetal Intestine Small	intestine
14	chr1:92967800-92986000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:92968000-92968200	Flanking Active TSS	GM12878-XiMat	blood
16	chr1:92968000-92968200	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr1:92968000-92968400	Enhancers	Muscle Satellite Cultured Cells	--
18	chr1:92968000-92970000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:92968200-92968400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr1:92968200-92968800	Enhancers	GM12878-XiMat	blood
21	chr1:92968200-92968800	Weak transcription	Osteobl	bone
22	chr1:92968200-92969200	Enhancers	HepG2	liver
23	chr1:92968200-92969400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:92968200-92975200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:92968200-92977400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:92968200-93042800	Weak transcription	HSMM	muscle
27	chr1:92968400-92997600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:92968600-92971800	Enhancers	Fetal Thymus	thymus
29	chr1:92968800-92969200	Flanking Active TSS	GM12878-XiMat	blood
30	chr1:92968800-92969400	Enhancers	Osteobl	bone
31	chr1:92969000-92969800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:92969000-92969800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr1:92969000-92970200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:92969000-92971400	Enhancers	Thymus	Thymus
35	chr1:92969200-92969400	Enhancers	HSMMtube	muscle
36	chr1:92969200-92970800	Enhancers	GM12878-XiMat	blood
37	chr1:92969200-92970800	Flanking Active TSS	HepG2	liver
38	chr1:92969400-92969600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr1:92969400-92969800	Enhancers	NH-A	brain
40	chr1:92969400-92969800	Flanking Active TSS	Osteobl	bone
41	chr1:92969400-92970000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:92969400-92979800	Weak transcription	HSMMtube	muscle
43	chr1:92969600-92970000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:92969600-92970200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr1:92969600-92970600	Enhancers	Primary B cells from cord blood	blood
46	chr1:92969600-92970800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr1:92969600-92984200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr1:92969800-92970000	Enhancers	Spleen	Spleen
49	chr1:92969800-92970000	Enhancers	Osteobl	bone
50	chr1:92969800-92970600	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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