Variant report

Variant	nsv526433
Chromosome Location	chr1:77030764-77268215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	BACH1	chr1:77046543-77046571	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:77143528-77143773	GM12878	blood:	n/a	chr1:77143665-77143676
7	BATF	chr1:77179188-77179435	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:77179313-77179521	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:77179232-77179520	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:77048933-77049239	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr1:77204062-77204316	HepG2	liver:	n/a	n/a
12	BHLHE40	chr1:77133723-77134000	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:77112842-77112874	K562	blood:	n/a	n/a
14	BHLHE40	chr1:77203965-77204428	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:77204025-77204356	HepG2	liver:	n/a	n/a
16	BHLHE40	chr1:77221629-77221756	HepG2	liver:	n/a	n/a
17	CBX3	chr1:77156384-77156905	HCT-116	colon:	n/a	n/a
18	CCNT2	chr1:77153768-77154264	K562	blood:	n/a	n/a
19	CEBPB	chr1:77181185-77181456	IMR90	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
20	CEBPB	chr1:77049031-77049343	HepG2	liver:	n/a	chr1:77049192-77049203
21	CEBPB	chr1:77256460-77256657	A549	lung:	n/a	n/a
22	CEBPB	chr1:77105851-77106102	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:77248431-77248783	IMR90	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
24	CEBPB	chr1:77167086-77167347	HepG2	liver:	n/a	chr1:77167220-77167231
25	CEBPB	chr1:77048891-77049375	H1-hESC	embryonic stem cell:	n/a	chr1:77049192-77049203
26	CEBPB	chr1:77105688-77106193	HCT-116	colon:	n/a	n/a
27	CEBPB	chr1:77052571-77052897	HepG2	liver:	n/a	chr1:77052721-77052732
28	CEBPB	chr1:77225708-77226174	HepG2	liver:	n/a	chr1:77225991-77226002
29	CEBPB	chr1:77105633-77106254	HCT-116	colon:	n/a	n/a
30	CEBPB	chr1:77248438-77248766	A549	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
31	CEBPB	chr1:77204028-77204208	HepG2	liver:	n/a	chr1:77204135-77204146
32	CEBPB	chr1:77182007-77182282	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:77225659-77226094	Hela-S3	cervix:	n/a	chr1:77225991-77226002
34	CEBPB	chr1:77203969-77204331	HepG2	liver:	n/a	chr1:77204135-77204146
35	CEBPB	chr1:77181160-77181514	HepG2	liver:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
36	CEBPB	chr1:77052581-77052874	IMR90	lung:	n/a	chr1:77052721-77052732
37	CEBPB	chr1:77248403-77248809	HepG2	liver:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
38	CEBPB	chr1:77055199-77055448	A549	lung:	n/a	chr1:77055290-77055301
39	CEBPB	chr1:77181200-77181483	A549	lung:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
40	CEBPB	chr1:77181235-77181390	K562	blood:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
41	CEBPB	chr1:77248449-77248821	Hela-S3	cervix:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
42	CEBPB	chr1:77249976-77250146	A549	lung:	n/a	chr1:77250003-77250014 chr1:77250003-77250016
43	CEBPB	chr1:77167065-77167392	IMR90	lung:	n/a	chr1:77167220-77167231
44	CEBPB	chr1:77181194-77181509	Hela-S3	cervix:	n/a	chr1:77181291-77181302 chr1:77181330-77181341
45	CEBPB	chr1:77055136-77055460	HepG2	liver:	n/a	chr1:77055290-77055301
46	CEBPB	chr1:77221430-77221703	HepG2	liver:	n/a	n/a
47	CEBPB	chr1:77052547-77052850	A549	lung:	n/a	chr1:77052721-77052732
48	CEBPB	chr1:77204029-77204335	HepG2	liver:	n/a	chr1:77204135-77204146
49	CEBPB	chr1:77225635-77226133	IMR90	lung:	n/a	chr1:77225991-77226002
50	CEBPB	chr1:77167167-77167294	H1-hESC	embryonic stem cell:	n/a	chr1:77167220-77167231

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77224035-77224085	GM12878	blood:	n/a
2	chr1:77224035-77224085	GM12878	blood:	n/a
3	chr1:77165604-77165654	AG04450	lung:	fetal
4	chr1:77165461-77165511	BE2_C	brain:	n/a
5	chr1:77230704-77230754	MCF10A-Er-Src	breast:	n/a
6	chr1:77221292-77221342	AG09319	gingival:	n/a
7	chr1:77230704-77230754	NT2-D1	testis:	n/a
8	chr1:77165565-77165615	GM19239	blood:	n/a
9	chr1:77230619-77230669	HNPCEpiC	eye:	n/a
10	chr1:77230837-77230887	HRCEpiC	kidney:	n/a
11	chr1:77165565-77165615	SK-N-SH	brain:	n/a
12	chr1:77042560-77042610	AG04450	lung:	fetal
13	chr1:77096137-77096187	NHDF-neo	bronchial:	n/a
14	chr1:77165604-77165654	T-47D	breast:	n/a
15	chr1:77230619-77230669	HepG2	liver:	n/a
16	chr1:77043128-77043178	HIPEpiC	eye:	n/a
17	chr1:77165461-77165511	NT2-D1	testis:	n/a
18	chr1:77096137-77096187	IMR90	lung:	fetal
19	chr1:77043128-77043178	CMK	blood:	n/a
20	chr1:77043128-77043178	SKMC	muscle:	n/a
21	chr1:77230837-77230887	GM12878	blood:	n/a
22	chr1:77096137-77096187	HCM	heart:	n/a
23	chr1:77221292-77221342	NB4	blood:	n/a
24	chr1:77165461-77165511	IMR90	lung:	fetal
25	chr1:77165604-77165654	HIPEpiC	eye:	n/a
26	chr1:77049380-77049430	HL-60	blood:	n/a
27	chr1:77165604-77165654	GM06990	blood:	n/a
28	chr1:77165461-77165511	AG04450	lung:	fetal
29	chr1:77043128-77043178	HCT-116	colon:	n/a
30	chr1:77096137-77096187	HRPEpiC	eye:	n/a
31	chr1:77230837-77230887	Jurkat	blood:	n/a
32	chr1:77230837-77230887	PrEC	prostate:	n/a
33	chr1:77230704-77230754	ECC-1	luminal epithelium:	n/a
34	chr1:77165565-77165615	GM06990	blood:	n/a
35	chr1:77230619-77230669	AG10803	skin:	n/a
36	chr1:77221292-77221342	BE2_C	brain:	n/a
37	chr1:77230837-77230887	ProgFib	skin:	n/a
38	chr1:77230619-77230669	MCF10A-Er-Src	breast:	n/a
39	chr1:77230619-77230669	HMEC	breast:	n/a
40	chr1:77049380-77049430	AG10803	skin:	n/a
41	chr1:77165565-77165615	HRE	kidney:	n/a
42	chr1:77224035-77224085	RPTEC	kidney:	n/a
43	chr1:77230619-77230669	HRE	kidney:	n/a
44	chr1:77165565-77165615	SKMC	muscle:	n/a
45	chr1:77221292-77221342	AG04450	lung:	fetal
46	chr1:77224035-77224085	SK-N-SH	brain:	n/a
47	chr1:77042560-77042610	GM06990	blood:	n/a
48	chr1:77224035-77224085	CMK	blood:	n/a
49	chr1:77165604-77165654	AG10803	skin:	n/a
50	chr1:77224035-77224085	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
2	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
3	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
4	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
5	chr1:77152003..77153806-chr1:77226748..77229399,2	MCF-7	breast:
6	chr1:77263566..77264086-chr12:6643239..6643753,2	HCT-116	colon:
7	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:
8	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
9	chr1:77147990..77150135-chr1:77152468..77154920,2	MCF-7	breast:
10	chr1:77056837..77059200-chr1:77061368..77063126,2	K562	blood:
11	chr1:77152003..77153806-chr1:77226748..77229399,2	MCF-7	breast:
12	chr1:77268124..77270530-chr1:77274080..77275666,2	MCF-7	breast:
13	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
14	chr1:77160313..77162146-chr1:77164141..77166438,2	K562	blood:
15	chr1:77180012..77182664-chr1:77186329..77188985,2	MCF-7	breast:
16	chr1:77056837..77059200-chr1:77061368..77063126,2	K562	blood:

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
4	lnc-PIGK-2	chr1:77244675-77244952	XLOC_000873

Variant related genes	Relation type
ENSG00000264686	TF binding region
RNU6-161P	TF binding region
TPI1P1	TF binding region
ENSG00000272855	TF binding region
ENSG00000237552	TF binding region
ENSG00000264686	CpG island
RNU6-161P	CpG island
TPI1P1	CpG island
ENSG00000272855	CpG island
ENSG00000237552	CpG island
ENSG00000226415	chromatin interactions
ENSG00000111640	chromatin interactions

Extended variants
information (count: 5944 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:5944 , 50 per page) page: 1 2 3 4 5 6 7 ... 119

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185651588	chr1:77034256-77034257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190456026	chr1:77034260-77034261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549019038	chr1:77034277-77034278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567508245	chr1:77034311-77034312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534862856	chr1:77034388-77034389	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139504855	chr1:77034400-77034401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577847594	chr1:77034406-77034407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs72991832	chr1:77034407-77034408	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12077082	chr1:77034444-77034445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575140227	chr1:77034473-77034474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542561942	chr1:77034672-77034673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561471105	chr1:77034681-77034682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114147175	chr1:77034691-77034692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113816083	chr1:77034692-77034693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565113652	chr1:77034698-77034699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575491832	chr1:77034708-77034709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181870684	chr1:77034718-77034719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs550808112	chr1:77034735-77034736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs315015	chr1:77034771-77034772	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530047288	chr1:77034793-77034794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149676052	chr1:77034822-77034823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567608174	chr1:77034882-77034883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116717368	chr1:77034959-77034960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546845923	chr1:77034967-77034968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571489420	chr1:77034982-77034983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564478566	chr1:77034995-77034996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538785582	chr1:77035021-77035022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61103299	chr1:77035029-77035030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34427182	chr1:77035094-77035095	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs186943286	chr1:77035109-77035110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs417415	chr1:77035168-77035169	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs367208	chr1:77035173-77035174	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs573226934	chr1:77035174-77035175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111586982	chr1:77035191-77035192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148816788	chr1:77035192-77035193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs61773281	chr1:77037426-77037427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs315020	chr1:77037430-77037431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs150733143	chr1:77037433-77037434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531340883	chr1:77037489-77037490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192255999	chr1:77037494-77037495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117172824	chr1:77037522-77037523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571640902	chr1:77037590-77037591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536133291	chr1:77037679-77037680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548080665	chr1:77037714-77037715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11806882	chr1:77037734-77037735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs183627934	chr1:77037792-77037793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35323311	chr1:77037799-77037800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397732681	chr1:77037807-77037808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112953264	chr1:77037808-77037809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112256943	chr1:77037809-77037810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	18451855	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:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77034200-77034600	Enhancers	Fetal Kidney	kidney
2	chr1:77034400-77035200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr1:77037400-77048400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:77038200-77039000	Enhancers	Fetal Brain Female	brain
5	chr1:77038400-77038800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr1:77038800-77039200	ZNF genes & repeats	Primary B cells from cord blood	blood
7	chr1:77038800-77042200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr1:77039000-77039200	Enhancers	Gastric	stomach
9	chr1:77042200-77042400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:77042200-77043600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:77042400-77042800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr1:77042400-77043000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr1:77042400-77043000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:77042400-77043400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:77042600-77043800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr1:77042800-77045800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr1:77043000-77043600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr1:77043000-77045800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:77043400-77044000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr1:77043400-77045800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr1:77043600-77045800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr1:77043600-77048000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr1:77043800-77045600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr1:77044000-77051800	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr1:77045600-77046800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:77045800-77046400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:77045800-77046400	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr1:77045800-77046600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr1:77045800-77046600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr1:77045800-77046800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:77045800-77049800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr1:77045800-77050600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr1:77046200-77046600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr1:77046400-77048000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:77046600-77048000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr1:77046600-77048400	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr1:77046600-77048600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr1:77046800-77048000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr1:77046800-77048200	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr1:77047800-77050600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:77048000-77048200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr1:77048000-77049200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr1:77048000-77049600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:77048000-77050200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:77048000-77050200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr1:77048200-77048600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:77048200-77049200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:77048200-77050200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr1:77048400-77049600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr1:77048400-77049800	Enhancers	H1 Cell Line	embryonic stem cell

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