Variant report

Variant	esv1794348
Chromosome Location	chr1:93090476-93192932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93166432-93166438	K562	blood:	n/a	n/a
2	ARID3A	chr1:93120890-93121035	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:93166804-93167004	K562	blood:	n/a	n/a
4	ARID3A	chr1:93170866-93171250	K562	blood:	n/a	n/a
5	ARID3A	chr1:93175326-93175562	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:93173847-93174509	K562	blood:	n/a	n/a
7	ARID3A	chr1:93177700-93177989	K562	blood:	n/a	n/a
8	ARID3A	chr1:93179508-93179845	HepG2	liver:	n/a	chr1:93179513-93179529
9	ATF1	chr1:93147755-93147985	K562	blood:	n/a	n/a
10	ATF1	chr1:93166705-93166957	K562	blood:	n/a	n/a
11	ATF1	chr1:93173964-93174238	K562	blood:	n/a	n/a
12	BACH1	chr1:93167070-93167279	K562	blood:	n/a	n/a
13	BACH1	chr1:93173457-93174567	K562	blood:	n/a	n/a
14	BACH1	chr1:93173969-93174337	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:93119744-93119935	K562	blood:	n/a	n/a
16	BATF	chr1:93157523-93157814	GM12878	blood:	n/a	n/a
17	BATF	chr1:93157496-93157732	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:93147752-93148026	K562	blood:	n/a	n/a
19	BHLHE40	chr1:93166867-93167031	K562	blood:	n/a	n/a
20	CBX3	chr1:93120766-93121240	HCT-116	colon:	n/a	n/a
21	CBX3	chr1:93120715-93121165	K562	blood:	n/a	n/a
22	CBX3	chr1:93119603-93120100	K562	blood:	n/a	n/a
23	CBX3	chr1:93173893-93174276	K562	blood:	n/a	n/a
24	CCNT2	chr1:93171006-93171308	K562	blood:	n/a	n/a
25	CCNT2	chr1:93175430-93175598	K562	blood:	n/a	chr1:93175457-93175466
26	CCNT2	chr1:93119815-93119887	K562	blood:	n/a	n/a
27	CEBPB	chr1:93171974-93172155	H1-hESC	embryonic stem cell:	n/a	chr1:93172035-93172046
28	CEBPB	chr1:93155761-93156150	ECC-1	luminal epithelium:	n/a	chr1:93155961-93155972
29	CEBPB	chr1:93155805-93156144	A549	lung:	n/a	chr1:93155961-93155972
30	CEBPB	chr1:93129359-93129741	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr1:93118086-93118214	HepG2	liver:	n/a	chr1:93118152-93118163
32	CEBPB	chr1:93160718-93161015	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:93129373-93129697	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:93127655-93127950	IMR90	lung:	n/a	chr1:93127803-93127820
35	CEBPB	chr1:93129299-93129747	A549	lung:	n/a	n/a
36	CEBPB	chr1:93174453-93174675	HepG2	liver:	n/a	chr1:93174591-93174602
37	CEBPB	chr1:93171923-93172178	HepG2	liver:	n/a	chr1:93172035-93172046
38	CEBPB	chr1:93129374-93129702	MCF-7	breast:	n/a	n/a
39	CEBPB	chr1:93155810-93156145	IMR90	lung:	n/a	chr1:93155961-93155972
40	CEBPB	chr1:93129377-93129708	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:93129377-93129731	K562	blood:	n/a	n/a
42	CEBPB	chr1:93155791-93156128	HepG2	liver:	n/a	chr1:93155961-93155972
43	CEBPB	chr1:93129377-93129711	A549	lung:	n/a	n/a
44	CEBPB	chr1:93171957-93171995	A549	lung:	n/a	n/a
45	CEBPB	chr1:93174173-93174766	K562	blood:	n/a	chr1:93174591-93174602
46	CEBPB	chr1:93174460-93174724	IMR90	lung:	n/a	chr1:93174591-93174602
47	CEBPB	chr1:93127671-93127969	A549	lung:	n/a	chr1:93127803-93127820
48	CEBPB	chr1:93155807-93156137	K562	blood:	n/a	chr1:93155961-93155972
49	CEBPB	chr1:93127698-93127937	K562	blood:	n/a	chr1:93127803-93127820
50	CEBPB	chr1:93127659-93127966	Hela-S3	cervix:	n/a	chr1:93127803-93127820

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93176520-93176570	Jurkat	blood:	n/a
2	chr1:93101184-93101234	HAEpiC	amniotic membrane:	n/a
3	chr1:93101184-93101234	LNCaP	prostate:	n/a
4	chr1:93101184-93101234	HEK293	kidney:	embryo
5	chr1:93176520-93176570	SK-N-SH_RA	brain:	n/a
6	chr1:93176520-93176570	HepG2	liver:	n/a
7	chr1:93176520-93176570	HCM	heart:	n/a
8	chr1:93176520-93176570	GM06990	blood:	n/a
9	chr1:93176520-93176570	T-47D	breast:	n/a
10	chr1:93176520-93176570	Caco-2	colon:	n/a
11	chr1:93176520-93176570	HEK293	kidney:	embryo
12	chr1:93101184-93101234	ProgFib	skin:	n/a
13	chr1:93101184-93101234	HRPEpiC	eye:	n/a
14	chr1:93101184-93101234	H1-hESC	embryonic stem cell:	embryo
15	chr1:93101184-93101234	AG09309	skin:	n/a
16	chr1:93176520-93176570	HMEC	breast:	n/a
17	chr1:93101184-93101234	IMR90	lung:	fetal
18	chr1:93176520-93176570	NHBE	bronchial:	n/a
19	chr1:93176520-93176570	SK-N-MC	brain:	n/a
20	chr1:93176520-93176570	HL-60	blood:	n/a
21	chr1:93176520-93176570	NHDF-neo	bronchial:	n/a
22	chr1:93101184-93101234	NH-A	brain:	n/a
23	chr1:93176520-93176570	HEEpiC	esophagus:	n/a
24	chr1:93176520-93176570	Hepatocyte	liver:	n/a
25	chr1:93176520-93176570	ovcar-3	ovarian:	n/a
26	chr1:93176520-93176570	PANC-1	pancreas:	n/a
27	chr1:93176520-93176570	HUVEC	blood vessel:	n/a
28	chr1:93176520-93176570	PrEC	prostate:	n/a
29	chr1:93101184-93101234	Hepatocyte	liver:	n/a
30	chr1:93176520-93176570	AG10803	skin:	n/a
31	chr1:93101184-93101234	HNPCEpiC	eye:	n/a
32	chr1:93101184-93101234	T-47D	breast:	n/a
33	chr1:93176520-93176570	AG09319	gingival:	n/a
34	chr1:93176520-93176570	BE2_C	brain:	n/a
35	chr1:93101184-93101234	SAEC	small airway:	n/a
36	chr1:93101184-93101234	GM12891	blood:	n/a
37	chr1:93176520-93176570	GM12892	blood:	n/a
38	chr1:93101184-93101234	GM19239	blood:	n/a
39	chr1:93101184-93101234	AG04449	skin:	fetal
40	chr1:93176520-93176570	U87	brain:	n/a
41	chr1:93101184-93101234	NB4	blood:	n/a
42	chr1:93176520-93176570	GM19239	blood:	n/a
43	chr1:93176520-93176570	NB4	blood:	n/a
44	chr1:93101184-93101234	HCF	heart:	n/a
45	chr1:93176520-93176570	MCF-7	breast:	n/a
46	chr1:93101184-93101234	HCPEpiC	choroid plexus:	n/a
47	chr1:93101184-93101234	A549	lung:	n/a
48	chr1:93101184-93101234	SK-N-MC	brain:	n/a
49	chr1:93101184-93101234	AG09319	gingival:	n/a
50	chr1:93101184-93101234	HUVEC	blood vessel:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93167180..93169532-chr1:93173013..93175472,3	K562	blood:
2	chr1:93110037..93112267-chr1:93116205..93118057,2	K562	blood:
3	chr1:93119617..93122057-chr1:93123545..93126419,2	K562	blood:
4	chr1:93165676..93168735-chr1:93171801..93174880,3	K562	blood:
5	chr1:93114313..93117003-chr1:93124509..93127384,2	K562	blood:
6	chr1:93119617..93122057-chr1:93123545..93126419,2	K562	blood:
7	chr1:93155607..93158060-chr1:93158648..93160493,3	K562	blood:
8	chr1:92762843..92765397-chr1:93103121..93105425,2	K562	blood:
9	chr1:93154026..93155990-chr1:93160380..93162982,2	K562	blood:
10	chr1:93155607..93158060-chr1:93158648..93160493,3	K562	blood:
11	chr1:93168714..93171281-chr1:93175586..93177919,2	K562	blood:
12	chr1:93168714..93171281-chr1:93175586..93177919,2	K562	blood:
13	chr1:93175208..93177703-chr1:93227101..93229847,2	K562	blood:
14	chr1:93175257..93178526-chr1:93178760..93181629,3	K562	blood:
15	chr1:93134641..93136643-chr1:93142209..93143930,2	K562	blood:
16	chr1:93164366..93166063-chr1:93176534..93179501,2	K562	blood:
17	chr1:93154026..93155990-chr1:93160380..93162982,2	K562	blood:
18	chr1:93107293..93109350-chr1:93297737..93299752,2	K562	blood:
19	chr1:93134530..93136643-chr1:93142430..93144187,2	K562	blood:
20	chr1:93167180..93169532-chr1:93173013..93175472,3	K562	blood:
21	chr1:93164366..93166063-chr1:93176534..93179501,2	K562	blood:
22	chr1:93175257..93178526-chr1:93178760..93181629,3	K562	blood:
23	chr1:92762166..92764342-chr1:93135404..93137126,2	K562	blood:
24	chr1:93110037..93112267-chr1:93116205..93118057,2	K562	blood:
25	chr1:93125325..93128274-chr1:93138494..93140203,2	K562	blood:
26	chr1:93114313..93117003-chr1:93124509..93127384,2	K562	blood:
27	chr1:93109943..93111571-chr1:93248352..93250763,2	MCF-7	breast:
28	chr1:93125325..93128274-chr1:93138494..93140203,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM69A-2	chr1:93169415-93169478	NONHSAT004463
2	lnc-FAM69A-2	chr1:93170112-93170301	NONHSAT004463

No data

Variant related genes	Relation type
EVI5	TF binding region
RNU4-59P	TF binding region
HMGB3P9	TF binding region
ENSG00000225505	TF binding region
EVI5	CpG island
RNU4-59P	CpG island
HMGB3P9	CpG island
ENSG00000225505	CpG island
ENSG00000122484	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000174842	chromatin interactions
ENSG00000201317	chromatin interactions
ENSG00000067208	chromatin interactions

Extended variants
information (count: 3945 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3945 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1415296	chr1:93090476-93090477	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557832225	chr1:93090541-93090542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75412038	chr1:93090575-93090576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564704224	chr1:93090649-93090650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539728091	chr1:93090696-93090697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181356374	chr1:93090697-93090698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565742133	chr1:93090751-93090752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78378977	chr1:93090788-93090789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572989581	chr1:93090827-93090828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541167038	chr1:93090830-93090831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10874725	chr1:93090850-93090851	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114441192	chr1:93090853-93090854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554173284	chr1:93090861-93090862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538131621	chr1:93090927-93090928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs3790451	chr1:93090934-93090935	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs185628242	chr1:93090963-93090964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139441463	chr1:93091015-93091016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376829751	chr1:93091018-93091019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538981501	chr1:93091062-93091063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553751402	chr1:93091064-93091065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs3790450	chr1:93091065-93091066	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs552450242	chr1:93091119-93091120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72966728	chr1:93091130-93091131	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191728486	chr1:93091146-93091147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559703174	chr1:93091243-93091244	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576215090	chr1:93091254-93091255	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528645861	chr1:93091286-93091287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201552619	chr1:93091306-93091307	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568236554	chr1:93091315-93091316	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200027454	chr1:93091349-93091350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565226429	chr1:93091385-93091386	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200025759	chr1:93091387-93091388	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374514734	chr1:93091388-93091389	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374417183	chr1:93091401-93091402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137964507	chr1:93091411-93091412	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202244393	chr1:93091416-93091417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200126355	chr1:93091420-93091421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201223473	chr1:93091456-93091457	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202242710	chr1:93091458-93091459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368450494	chr1:93091495-93091496	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs202038233	chr1:93091508-93091509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200167597	chr1:93091525-93091526	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201538456	chr1:93091527-93091528	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529796924	chr1:93091726-93091727	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548330199	chr1:93091737-93091738	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs139266738	chr1:93091791-93091792	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs538472363	chr1:93091859-93091860	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs149558435	chr1:93091944-93091945	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs571862121	chr1:93091959-93091960	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs183628544	chr1:93091970-93091971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93014800-93100200	Weak transcription	Right Ventricle	heart
2	chr1:93026000-93091800	Weak transcription	Hela-S3	cervix
3	chr1:93052000-93119400	Weak transcription	NHEK	skin
4	chr1:93053600-93166200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:93055000-93100200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:93062000-93118800	Weak transcription	HMEC	breast
7	chr1:93063000-93100600	Weak transcription	Gastric	stomach
8	chr1:93064400-93100800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr1:93065200-93101000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr1:93065200-93118600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:93065800-93119600	Weak transcription	NH-A	brain
12	chr1:93066800-93103000	Weak transcription	NHDF-Ad	bronchial
13	chr1:93066800-93114600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:93067200-93101000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr1:93067400-93100800	Weak transcription	Brain Angular Gyrus	brain
16	chr1:93068200-93100600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr1:93068600-93100400	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr1:93068600-93112600	Weak transcription	Brain Substantia Nigra	brain
19	chr1:93068800-93103200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr1:93069400-93104600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr1:93069600-93119600	Weak transcription	Colon Smooth Muscle	Colon
22	chr1:93070000-93100800	Weak transcription	Brain Cingulate Gyrus	brain
23	chr1:93070600-93100200	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr1:93070600-93100600	Weak transcription	Colonic Mucosa	Colon
25	chr1:93070600-93101000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr1:93070800-93100800	Weak transcription	Brain Hippocampus Middle	brain
27	chr1:93077200-93100600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:93078400-93096200	Weak transcription	Fetal Heart	heart
29	chr1:93080200-93100800	Weak transcription	Esophagus	oesophagus
30	chr1:93080800-93092600	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr1:93081200-93100800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:93081200-93100800	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr1:93082200-93101000	Weak transcription	HSMMtube	muscle
34	chr1:93082400-93101200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:93082600-93108600	Weak transcription	Psoas Muscle	Psoas
36	chr1:93082800-93100600	Weak transcription	Lung	lung
37	chr1:93082800-93100800	Weak transcription	Aorta	Aorta
38	chr1:93083400-93100400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:93083600-93101000	Weak transcription	Primary B cells from cord blood	blood
40	chr1:93083600-93101000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr1:93083600-93101000	Weak transcription	Stomach Smooth Muscle	stomach
42	chr1:93083600-93106400	Weak transcription	Pancreas	Pancrea
43	chr1:93083800-93101000	Weak transcription	Fetal Kidney	kidney
44	chr1:93084000-93100800	Weak transcription	Left Ventricle	heart
45	chr1:93084000-93101000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr1:93084000-93101000	Weak transcription	Duodenum Mucosa	Duodenum
47	chr1:93084200-93091200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr1:93084200-93100200	Weak transcription	Fetal Lung	lung
49	chr1:93084200-93100600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr1:93084200-93100600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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