Variant report

Variant	esv3360645
Chromosome Location	chr1:113375959-113414652
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:613)
Chromatin interactive
region (count:15)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:113412037-113412274	K562	blood:	n/a	n/a
2	ATF1	chr1:113412031-113412267	K562	blood:	n/a	n/a
3	ATF3	chr1:113406594-113406740	K562	blood:	n/a	n/a
4	BACH1	chr1:113391962-113392548	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:113387894-113388170	GM12878	blood:	n/a	chr1:113388042-113388053
6	BHLHE40	chr1:113383269-113383658	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:113397800-113398144	IMR90	lung:	n/a	chr1:113397958-113397969
8	CEBPB	chr1:113394293-113394634	K562	blood:	n/a	n/a
9	CEBPB	chr1:113394323-113394637	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:113397795-113398109	HepG2	liver:	n/a	chr1:113397958-113397969
11	CEBPB	chr1:113394303-113394797	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:113383779-113384209	MCF-7	breast:	n/a	n/a
13	CEBPB	chr1:113386872-113387013	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:113383814-113384195	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:113394315-113394515	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:113386785-113387076	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:113386784-113387058	K562	blood:	n/a	n/a
18	CEBPB	chr1:113397822-113398064	K562	blood:	n/a	chr1:113397958-113397969
19	CEBPB	chr1:113383834-113384109	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:113394351-113394537	A549	lung:	n/a	n/a
21	CEBPB	chr1:113397788-113398124	A549	lung:	n/a	chr1:113397958-113397969
22	CEBPB	chr1:113386774-113387098	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:113394312-113394617	K562	blood:	n/a	n/a
24	CEBPB	chr1:113394309-113394671	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:113399996-113400299	K562	blood:	n/a	n/a
26	CEBPB	chr1:113380987-113381014	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:113386881-113387074	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:113399987-113400263	K562	blood:	n/a	n/a
29	CEBPB	chr1:113386765-113387060	A549	lung:	n/a	n/a
30	CHD2	chr1:113392081-113392251	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr1:113393341-113393404	GM10248	blood:	n/a	n/a
32	CTCF	chr1:113392180-113392330	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr1:113411460-113411610	K562	blood:	n/a	n/a
34	CTCF	chr1:113411400-113411550	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:113414409-113414440	GM12891	blood:	n/a	chr1:113414410-113414423
36	CTCF	chr1:113411460-113411610	HMEC	breast:	n/a	n/a
37	CTCF	chr1:113392300-113392450	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:113385600-113385750	GM12867	blood:	n/a	n/a
39	CTCF	chr1:113411480-113411630	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr1:113411440-113411590	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr1:113411420-113411570	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:113411338-113411679	K562	blood:	n/a	n/a
43	CTCF	chr1:113414380-113414530	HEK293	kidney:	n/a	chr1:113414410-113414423
44	CTCF	chr1:113381080-113381230	GM06990	blood:	n/a	n/a
45	CTCF	chr1:113382449-113382529	GM10248	blood:	n/a	n/a
46	CTCF	chr1:113414461-113414480	K562	blood:	n/a	n/a
47	CTCF	chr1:113414392-113414452	MCF-7	breast:	n/a	chr1:113414410-113414423
48	CTCF	chr1:113411440-113411590	HFF	foreskin:	n/a	n/a
49	CTCF	chr1:113414380-113414530	GM12868	blood:	n/a	chr1:113414410-113414423
50	CTCF	chr1:113411460-113411610	HMF	breast:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:113392617-113392667	GM12892	blood:	n/a
2	chr1:113392781-113392831	HEK293	kidney:	embryo
3	chr1:113394877-113394927	PANC-1	pancreas:	n/a
4	chr1:113392617-113392667	GM12892	blood:	n/a
5	chr1:113392781-113392831	HEK293	kidney:	embryo
6	chr1:113394877-113394927	PANC-1	pancreas:	n/a
7	chr1:113392781-113392831	Hela-S3	cervix:	n/a
8	chr1:113393179-113393229	GM06990	blood:	n/a
9	chr1:113390019-113390069	PFSK-1	brain:	n/a
10	chr1:113393176-113393226	SK-N-MC	brain:	n/a
11	chr1:113393322-113393372	HepG2	liver:	n/a
12	chr1:113392781-113392831	A549	lung:	n/a
13	chr1:113392781-113392831	AG09309	skin:	n/a
14	chr1:113390019-113390069	MCF-7	breast:	n/a
15	chr1:113392781-113392831	PFSK-1	brain:	n/a
16	chr1:113393322-113393372	HCPEpiC	choroid plexus:	n/a
17	chr1:113393179-113393229	MCF-7	breast:	n/a
18	chr1:113392116-113392166	NT2-D1	testis:	n/a
19	chr1:113393176-113393226	T-47D	breast:	n/a
20	chr1:113390019-113390069	ovcar-3	ovarian:	n/a
21	chr1:113392617-113392667	PANC-1	pancreas:	n/a
22	chr1:113392388-113392438	MCF-7	breast:	n/a
23	chr1:113393179-113393229	PrEC	prostate:	n/a
24	chr1:113390019-113390069	PANC-1	pancreas:	n/a
25	chr1:113392617-113392667	AG09309	skin:	n/a
26	chr1:113393176-113393226	H1-hESC	embryonic stem cell:	embryo
27	chr1:113390019-113390069	HRE	kidney:	n/a
28	chr1:113392617-113392667	NHDF-neo	bronchial:	n/a
29	chr1:113392388-113392438	MCF10A-Er-Src	breast:	n/a
30	chr1:113393322-113393372	Hela-S3	cervix:	n/a
31	chr1:113393176-113393226	LNCaP	prostate:	n/a
32	chr1:113392116-113392166	ovcar-3	ovarian:	n/a
33	chr1:113393322-113393372	HRCEpiC	kidney:	n/a
34	chr1:113393322-113393372	HIPEpiC	eye:	n/a
35	chr1:113394877-113394927	HCPEpiC	choroid plexus:	n/a
36	chr1:113392116-113392166	BE2_C	brain:	n/a
37	chr1:113393176-113393226	HCF	heart:	n/a
38	chr1:113392617-113392667	HAEpiC	amniotic membrane:	n/a
39	chr1:113393322-113393372	SK-N-MC	brain:	n/a
40	chr1:113392162-113392212	GM19239	blood:	n/a
41	chr1:113392781-113392831	ProgFib	skin:	n/a
42	chr1:113390019-113390069	HCF	heart:	n/a
43	chr1:113392116-113392166	HRCEpiC	kidney:	n/a
44	chr1:113393322-113393372	AG10803	skin:	n/a
45	chr1:113392388-113392438	RPTEC	kidney:	n/a
46	chr1:113393176-113393226	BJ	skin:	n/a
47	chr1:113392617-113392667	HNPCEpiC	eye:	n/a
48	chr1:113392388-113392438	HAEpiC	amniotic membrane:	n/a
49	chr1:113390019-113390069	AG04450	lung:	fetal
50	chr1:113393176-113393226	HRPEpiC	eye:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:113379016..113381976-chr1:113384140..113386902,2	MCF-7	breast:
2	chr1:113393846..113396397-chr1:113410611..113412289,2	K562	blood:
3	chr1:113382661..113385204-chr1:113393197..113394858,2	MCF-7	breast:
4	chr1:113379016..113381976-chr1:113384140..113386902,2	MCF-7	breast:
5	chr1:113411911..113414258-chr1:113419696..113422107,2	MCF-7	breast:
6	chr1:113405858..113408757-chr1:113410736..113413457,2	K562	blood:
7	chr1:113405858..113408757-chr1:113410736..113413457,2	K562	blood:
8	chr1:113383663..113385223-chr1:113386866..113389078,2	MCF-7	breast:
9	chr1:113360437..113362050-chr1:113412669..113415625,2	K562	blood:
10	chr1:113413685..113416683-chr1:113491542..113494143,2	K562	blood:
11	chr1:113346242..113347922-chr1:113394008..113395856,2	MCF-7	breast:
12	chr1:113413526..113415499-chr1:113588812..113591393,2	MCF-7	breast:
13	chr1:113257969..113259766-chr1:113414429..113416544,2	K562	blood:
14	chr1:113383663..113385223-chr1:113386866..113389078,2	MCF-7	breast:
15	chr1:113393846..113396397-chr1:113410611..113412289,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A1-1	chr1:113392302-113392437	XLOC_000966
2	lnc-FAM19A3-7	chr1:113400759-113400763	NONHSAT005292
3	lnc-FAM19A3-2	chr1:113392650-113393049	XLOC_000348
4	lnc-SLC16A1-1	chr1:113383110-113383202	NONHSAT005284
5	lnc-SLC16A1-1	chr1:113383110-113383202	XLOC_000966
6	lnc-SLC16A1-1	chr1:113383110-113383202	ENSG00000215866.3
7	lnc-SLC16A1-1	chr1:113392302-113392401	XLOC_000966
8	lnc-FAM19A3-2	chr1:113392392-113393049	NONHSAT005289
9	lnc-SLC16A1-1	chr1:113391576-113391672	NONHSAT005284
10	lnc-SLC16A1-1	chr1:113392568-113392706	ucscGeneNc_uc001ede_1
11	lnc-FAM19A3-7	chr1:113400131-113400686	NONHSAT005292
12	lnc-FAM19A3-6	chr1:113377818-113377983	NONHSAT005288
13	lnc-SLC16A1-1	chr1:113392302-113392399	ENSG00000215866.3
14	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005288
15	lnc-FAM19A3-6	chr1:113390931-113391200	NONHSAT005281
16	lnc-SLC16A1-1	chr1:113391576-113391672	XLOC_000966
17	lnc-SLC16A1-1	chr1:113392302-113393265	NONHSAT005284
18	lnc-FAM19A3-2	chr1:113392698-113393049	XLOC_000348
19	lnc-SLC16A1-1	chr1:113392302-113393265	XLOC_000966
20	lnc-FAM19A3-7	chr1:113399850-113401156	NONHSAT005291
21	lnc-SLC16A1-1	chr1:113383110-113383202	XLOC_000966

No data

Variant related genes	Relation type
ENSG00000224167	TF binding region
ENSG00000215866	TF binding region
ENSG00000224167	CpG island
ENSG00000215866	CpG island
ENSG00000215866	chromatin interactions
ENSG00000155367	chromatin interactions
ENSG00000261595	chromatin interactions
CDH12	miRNA target sites
CREB5	miRNA target sites
CTDSPL	miRNA target sites
NCOR2	miRNA target sites
PPIF	miRNA target sites
HAUS6	miRNA target sites

Extended variants
information (count: 1608 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1608 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6679888	chr1:113375970-113375971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563991686	chr1:113375971-113375972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529588275	chr1:113375972-113375973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548962844	chr1:113375992-113375993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572673641	chr1:113376004-113376005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565776721	chr1:113376027-113376028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528526059	chr1:113376034-113376035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147449869	chr1:113376055-113376056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35813568	chr1:113376056-113376057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139989366	chr1:113376072-113376073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4501838	chr1:113376077-113376078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs4348718	chr1:113376110-113376111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184705872	chr1:113376129-113376130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536589603	chr1:113376182-113376183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190076130	chr1:113376203-113376204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572876915	chr1:113376256-113376257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs545096015	chr1:113376281-113376282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558635256	chr1:113376292-113376293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575277887	chr1:113376360-113376361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543975676	chr1:113376378-113376379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563778027	chr1:113376403-113376404	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs149202176	chr1:113376413-113376414	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs542923739	chr1:113376465-113376466	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs6688777	chr1:113376497-113376498	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs142394584	chr1:113376505-113376506	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs375285202	chr1:113376520-113376521	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs6688787	chr1:113376527-113376528	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs6688789	chr1:113376535-113376536	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs376618777	chr1:113376629-113376630	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs567803567	chr1:113376632-113376633	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs535210387	chr1:113376633-113376634	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs181662687	chr1:113376679-113376680	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs115126303	chr1:113376704-113376705	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs553324631	chr1:113376738-113376739	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs187357881	chr1:113376793-113376794	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs564754392	chr1:113376798-113376799	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs538620742	chr1:113376825-113376826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532045597	chr1:113376831-113376832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189244878	chr1:113376852-113376853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181013546	chr1:113376858-113376859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551957883	chr1:113376956-113376957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537585364	chr1:113377002-113377003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557489280	chr1:113377027-113377028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561724610	chr1:113377049-113377050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79587905	chr1:113377055-113377056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542888740	chr1:113377078-113377079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150238672	chr1:113377085-113377086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200350744	chr1:113377093-113377094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559638595	chr1:113377099-113377100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201362635	chr1:113377107-113377108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113364200-113392000	Weak transcription	Right Atrium	heart
2	chr1:113365200-113382600	Weak transcription	HUVEC	blood vessel
3	chr1:113369200-113392000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr1:113369600-113383600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr1:113370000-113376400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr1:113370000-113379400	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr1:113370000-113383400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:113370600-113383400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:113370600-113383400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:113370800-113376400	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:113371600-113376400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr1:113374600-113383200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:113375600-113379400	Weak transcription	Placenta	Placenta
14	chr1:113375800-113376200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:113376200-113376800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:113376400-113376800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr1:113376400-113376800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr1:113376400-113376800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr1:113376400-113376800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr1:113376400-113377000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:113376600-113376800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr1:113376800-113378000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr1:113376800-113379400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:113376800-113379400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr1:113376800-113383400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr1:113378200-113378400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:113378200-113378400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:113378200-113378400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:113378200-113378600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:113378200-113379400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:113378200-113379800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:113378200-113379800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr1:113378400-113379400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:113378400-113379600	Enhancers	NHDF-Ad	bronchial
35	chr1:113378400-113379800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:113378400-113379800	Enhancers	Osteobl	bone
37	chr1:113378400-113380000	Enhancers	NHEK	skin
38	chr1:113378600-113378800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:113378600-113379600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:113378600-113379600	Enhancers	HMEC	breast
41	chr1:113378600-113380600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:113378800-113383000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:113379400-113379600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:113379400-113379600	Enhancers	Right Ventricle	heart
45	chr1:113379400-113379600	Enhancers	Hela-S3	cervix
46	chr1:113379400-113379800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr1:113379400-113380000	Enhancers	Placenta	Placenta
48	chr1:113379400-113380200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr1:113379400-113380200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr1:113379400-113381000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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