Variant report

Variant	nsv1001253
Chromosome Location	chr1:77077660-77234093
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:682)
CpG islands
(count:550)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:77139682-77140065	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:77204024-77204337	HepG2	liver:	n/a	n/a
3	ATF1	chr1:77119453-77119559	K562	blood:	n/a	n/a
4	ATF3	chr1:77156408-77156900	HCT-116	colon:	n/a	n/a
5	BATF	chr1:77179188-77179435	GM12878	blood:	n/a	n/a
6	BATF	chr1:77143528-77143773	GM12878	blood:	n/a	chr1:77143665-77143676
7	BCL11A	chr1:77179232-77179520	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:77179313-77179521	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:77133723-77134000	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:77221629-77221756	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:77203965-77204428	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:77204062-77204316	HepG2	liver:	n/a	n/a
13	BHLHE40	chr1:77204025-77204356	HepG2	liver:	n/a	n/a
14	BHLHE40	chr1:77112842-77112874	K562	blood:	n/a	n/a
15	CBX3	chr1:77156384-77156905	HCT-116	colon:	n/a	n/a
16	CCNT2	chr1:77153768-77154264	K562	blood:	n/a	n/a
17	CEBPB	chr1:77225659-77226094	Hela-S3	cervix:	n/a	chr1:77225991-77226002
18	CEBPB	chr1:77105688-77106193	HCT-116	colon:	n/a	n/a
19	CEBPB	chr1:77181194-77181509	Hela-S3	cervix:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
20	CEBPB	chr1:77181185-77181456	IMR90	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
21	CEBPB	chr1:77182007-77182282	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:77181200-77181483	A549	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
23	CEBPB	chr1:77164266-77164461	HepG2	liver:	n/a	chr1:77164405-77164416
24	CEBPB	chr1:77167065-77167392	IMR90	lung:	n/a	chr1:77167220-77167231
25	CEBPB	chr1:77105851-77106102	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:77204028-77204208	HepG2	liver:	n/a	chr1:77204135-77204146
27	CEBPB	chr1:77225635-77226133	IMR90	lung:	n/a	chr1:77225991-77226002
28	CEBPB	chr1:77204029-77204335	HepG2	liver:	n/a	chr1:77204135-77204146
29	CEBPB	chr1:77181235-77181390	K562	blood:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
30	CEBPB	chr1:77167086-77167347	HepG2	liver:	n/a	chr1:77167220-77167231
31	CEBPB	chr1:77105633-77106254	HCT-116	colon:	n/a	n/a
32	CEBPB	chr1:77181111-77181550	HCT-116	colon:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
33	CEBPB	chr1:77181160-77181514	HepG2	liver:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
34	CEBPB	chr1:77167167-77167294	H1-hESC	embryonic stem cell:	n/a	chr1:77167220-77167231
35	CEBPB	chr1:77225708-77226174	HepG2	liver:	n/a	chr1:77225991-77226002
36	CEBPB	chr1:77221430-77221703	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:77203969-77204331	HepG2	liver:	n/a	chr1:77204135-77204146
38	CHD1	chr1:77223338-77223454	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:77232376-77232421	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr1:77148020-77148170	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:77206700-77206850	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:77172801-77172818	GM13976	blood:	n/a	n/a
43	CTCF	chr1:77086180-77086330	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:77165537-77165693	GM12892	blood:	n/a	n/a
45	CTCF	chr1:77165539-77165689	MCF-7	breast:	n/a	n/a
46	CTCF	chr1:77165584-77165663	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr1:77206720-77206870	HCT-116	colon:	n/a	n/a
48	CTCF	chr1:77165603-77165650	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:77206660-77206810	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr1:77148034-77148058	MCF-7	breast:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77230704-77230754	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:77230704-77230754	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:77230704-77230754	HCT-116	colon:	n/a
4	chr1:77165565-77165615	HCM	heart:	n/a
5	chr1:77230704-77230754	LNCaP	prostate:	n/a
6	chr1:77165604-77165654	HMEC	breast:	n/a
7	chr1:77230837-77230887	GM12878	blood:	n/a
8	chr1:77224035-77224085	AG04450	lung:	fetal
9	chr1:77096137-77096187	A549	lung:	n/a
10	chr1:77165604-77165654	IMR90	lung:	fetal
11	chr1:77221292-77221342	AG04449	skin:	fetal
12	chr1:77165604-77165654	AG04449	skin:	fetal
13	chr1:77096137-77096187	SAEC	small airway:	n/a
14	chr1:77224035-77224085	IMR90	lung:	fetal
15	chr1:77165565-77165615	AG10803	skin:	n/a
16	chr1:77096137-77096187	SK-N-SH_RA	brain:	n/a
17	chr1:77165461-77165511	Caco-2	colon:	n/a
18	chr1:77230704-77230754	Hela-S3	cervix:	n/a
19	chr1:77096137-77096187	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:77221292-77221342	AG04450	lung:	fetal
21	chr1:77165604-77165654	GM06990	blood:	n/a
22	chr1:77230704-77230754	HAEpiC	amniotic membrane:	n/a
23	chr1:77230619-77230669	RPTEC	kidney:	n/a
24	chr1:77096137-77096187	HRE	kidney:	n/a
25	chr1:77165461-77165511	MCF-7	breast:	n/a
26	chr1:77165565-77165615	U87	brain:	n/a
27	chr1:77221292-77221342	SKMC	muscle:	n/a
28	chr1:77230619-77230669	Hela-S3	cervix:	n/a
29	chr1:77096137-77096187	IMR90	lung:	fetal
30	chr1:77230704-77230754	Hepatocyte	liver:	n/a
31	chr1:77165604-77165654	HCPEpiC	choroid plexus:	n/a
32	chr1:77165565-77165615	Hepatocyte	liver:	n/a
33	chr1:77221292-77221342	PFSK-1	brain:	n/a
34	chr1:77096137-77096187	HNPCEpiC	eye:	n/a
35	chr1:77224035-77224085	PFSK-1	brain:	n/a
36	chr1:77165604-77165654	ovcar-3	ovarian:	n/a
37	chr1:77165604-77165654	GM19239	blood:	n/a
38	chr1:77221292-77221342	MCF10A-Er-Src	breast:	n/a
39	chr1:77230704-77230754	HMEC	breast:	n/a
40	chr1:77221292-77221342	HIPEpiC	eye:	n/a
41	chr1:77221292-77221342	HCF	heart:	n/a
42	chr1:77165604-77165654	HCT-116	colon:	n/a
43	chr1:77165604-77165654	PANC-1	pancreas:	n/a
44	chr1:77224035-77224085	ProgFib	skin:	n/a
45	chr1:77224035-77224085	Caco-2	colon:	n/a
46	chr1:77230837-77230887	T-47D	breast:	n/a
47	chr1:77165565-77165615	HL-60	blood:	n/a
48	chr1:77224035-77224085	HRE	kidney:	n/a
49	chr1:77230619-77230669	K562	blood:	n/a
50	chr1:77165565-77165615	K562	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:77152003..77153806-chr1:77226748..77229399,2	MCF-7	breast:
2	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
3	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
4	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
5	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:
6	chr1:77152003..77153806-chr1:77226748..77229399,2	MCF-7	breast:
7	chr1:77160313..77162146-chr1:77164141..77166438,2	K562	blood:
8	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
9	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
10	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
11	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGK-2	chr1:77223809-77223853	XLOC_000873
2	lnc-ST6GALNAC3-3	chr1:77102562-77103024	ENSG00000272855.1
3	lnc-PIGK-2	chr1:77223965-77224089	XLOC_000873

No data

Variant related genes	Relation type
ENSG00000264686	TF binding region
RNU6-161P	TF binding region
ENSG00000272855	TF binding region
TPI1P1	TF binding region
ENSG00000264686	CpG island
RNU6-161P	CpG island
ENSG00000272855	CpG island
TPI1P1	CpG island
ENSG00000226415	chromatin interactions

Extended variants
information (count: 3453 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3453 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181451017	chr1:77077680-77077681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554365252	chr1:77077709-77077710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150526018	chr1:77077744-77077745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533537606	chr1:77077763-77077764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372780579	chr1:77077802-77077803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558559826	chr1:77077808-77077809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs139486043	chr1:77077836-77077837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544879423	chr1:77077874-77077875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185542952	chr1:77077875-77077876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575086857	chr1:77077906-77077907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568620350	chr1:77077907-77077908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542339162	chr1:77078015-77078016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558907173	chr1:77078072-77078073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560370557	chr1:77078153-77078154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527748710	chr1:77078165-77078166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552309987	chr1:77078218-77078219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564090182	chr1:77078225-77078226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532280281	chr1:77078230-77078231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550450330	chr1:77078279-77078280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369292952	chr1:77078303-77078304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537760599	chr1:77078347-77078348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149666568	chr1:77078389-77078390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536036014	chr1:77078416-77078417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146764751	chr1:77078465-77078466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188492142	chr1:77078558-77078559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533838288	chr1:77078600-77078601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557650871	chr1:77078602-77078603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs377197443	chr1:77078640-77078641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139394434	chr1:77078646-77078647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180953464	chr1:77078738-77078739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs341026	chr1:77078750-77078751	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs186078541	chr1:77078822-77078823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17684029	chr1:77078848-77078849	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
34	rs542075417	chr1:77078889-77078890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554313124	chr1:77078901-77078902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572448892	chr1:77078903-77078904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558521038	chr1:77078912-77078913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs236019	chr1:77078925-77078926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs192101630	chr1:77078932-77078933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112566350	chr1:77078947-77078948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571244065	chr1:77079012-77079013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs180467	chr1:77079025-77079026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs548086536	chr1:77079034-77079035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560771051	chr1:77079035-77079036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146492908	chr1:77079040-77079041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543199581	chr1:77079075-77079076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527436598	chr1:77079112-77079113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552300996	chr1:77079145-77079146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184093268	chr1:77079206-77079207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537826882	chr1:77079265-77079266	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77074400-77078600	Weak transcription	Small Intestine	intestine
2	chr1:77076400-77080800	Weak transcription	Fetal Stomach	stomach
3	chr1:77077800-77078200	Enhancers	Pancreas	Pancrea
4	chr1:77078200-77078600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:77078400-77078800	Enhancers	Pancreas	Pancrea
6	chr1:77079200-77079400	Enhancers	Left Ventricle	heart
7	chr1:77079200-77079800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr1:77079200-77079800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr1:77079400-77079600	Enhancers	Fetal Lung	lung
10	chr1:77079600-77080600	Weak transcription	Left Ventricle	heart
11	chr1:77079600-77080800	Weak transcription	Fetal Lung	lung
12	chr1:77080600-77081200	Enhancers	Left Ventricle	heart
13	chr1:77080600-77081800	Enhancers	Ovary	ovary
14	chr1:77080800-77081400	Enhancers	Colon Smooth Muscle	Colon
15	chr1:77080800-77081800	Enhancers	Fetal Stomach	stomach
16	chr1:77080800-77082400	Enhancers	Fetal Lung	lung
17	chr1:77081000-77081800	Enhancers	Adipose Nuclei	Adipose
18	chr1:77081000-77082400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:77081000-77088600	Weak transcription	Right Atrium	heart
20	chr1:77081800-77082000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:77081800-77082800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr1:77082400-77092000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:77082400-77094400	Weak transcription	Fetal Lung	lung
24	chr1:77082600-77082800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr1:77082800-77086200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr1:77084600-77086000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr1:77086000-77086200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr1:77086000-77086200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr1:77086200-77088200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr1:77086200-77088400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:77088200-77098000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr1:77088400-77089600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:77088400-77089800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr1:77088600-77088800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:77088600-77088800	Enhancers	Right Atrium	heart
36	chr1:77088800-77092000	Weak transcription	Right Atrium	heart
37	chr1:77088800-77094600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:77089200-77089800	Enhancers	Fetal Kidney	kidney
39	chr1:77089600-77089800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr1:77089800-77090000	Enhancers	Brain Angular Gyrus	brain
41	chr1:77089800-77091000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr1:77089800-77094400	Weak transcription	Fetal Kidney	kidney
43	chr1:77090000-77091200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr1:77090000-77099000	Weak transcription	Brain Angular Gyrus	brain
45	chr1:77091000-77092400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:77091200-77092400	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr1:77091400-77092400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr1:77092000-77095000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:77092200-77092400	Enhancers	Right Atrium	heart
50	chr1:77092200-77093800	Weak transcription	Primary B cells from cord blood	blood

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