Variant report

Variant	esv14404
Chromosome Location	chr13:76107773-76119573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:708)
CpG islands
(count:918)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76111847-76112381	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76119103-76119402	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:76111988-76112275	K562	blood:	n/a	n/a
4	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
5	ATF2	chr13:76111559-76112389	GM12878	blood:	n/a	n/a
6	ATF2	chr13:76112008-76112514	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:76111716-76112543	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr13:76112015-76112538	A549	lung:	n/a	n/a
9	BCLAF1	chr13:76111591-76112186	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:76111845-76112497	K562	blood:	n/a	n/a
11	BHLHE40	chr13:76111942-76112433	A549	lung:	n/a	n/a
12	BHLHE40	chr13:76111626-76112484	HepG2	liver:	n/a	n/a
13	BHLHE40	chr13:76111540-76112825	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:76111988-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr13:76111808-76112292	GM12878	blood:	n/a	n/a
16	BRCA1	chr13:76111576-76112481	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr13:76111647-76112440	HepG2	liver:	n/a	n/a
18	CCNT2	chr13:76111554-76112436	K562	blood:	n/a	n/a
19	CEBPB	chr13:76119018-76119446	IMR90	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
20	CEBPB	chr13:76119116-76119316	A549	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
21	CEBPB	chr13:76119032-76119423	HepG2	liver:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
22	CEBPB	chr13:76119008-76119530	Hela-S3	cervix:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
23	CEBPB	chr13:76117488-76117562	A549	lung:	n/a	n/a
24	CEBPD	chr13:76111665-76112069	HepG2	liver:	n/a	n/a
25	CHD1	chr13:76111515-76112632	GM12878	blood:	n/a	n/a
26	CHD1	chr13:76111504-76112506	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr13:76111165-76112724	IMR90	lung:	n/a	n/a
28	CHD2	chr13:76111594-76112513	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr13:76111725-76112523	GM12878	blood:	n/a	n/a
30	CHD2	chr13:76111873-76112550	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr13:76111795-76112421	K562	blood:	n/a	n/a
32	CHD2	chr13:76111716-76112448	HepG2	liver:	n/a	n/a
33	CREB1	chr13:76111785-76112474	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr13:76111842-76112398	A549	lung:	n/a	n/a
35	CTBP2	chr13:76111695-76112410	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr13:76111980-76112130	BJ	skin:	n/a	n/a
37	CTCF	chr13:76111920-76112070	GM06990	blood:	n/a	n/a
38	CTCF	chr13:76111960-76112110	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr13:76111980-76112130	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr13:76111720-76111870	GM12871	blood:	n/a	n/a
41	CTCF	chr13:76110840-76110990	AG04450	lung:	n/a	n/a
42	CTCF	chr13:76111920-76112070	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr13:76111980-76112130	GM12871	blood:	n/a	n/a
44	CTCF	chr13:76111900-76112050	GM12864	blood:	n/a	n/a
45	CTCF	chr13:76111860-76112010	HRE	kidney:	n/a	n/a
46	CTCF	chr13:76111920-76112070	GM12868	blood:	n/a	n/a
47	CTCF	chr13:76111680-76111830	GM12873	blood:	n/a	n/a
48	CTCF	chr13:76116200-76116350	AG04449	skin:	n/a	n/a
49	CTCF	chr13:76111920-76112070	RPTEC	kidney:	n/a	n/a
50	CTCF	chr13:76110600-76110750	AG04450	lung:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76112980-76113030	ovcar-3	ovarian:	n/a
2	chr13:76111785-76111835	NH-A	brain:	n/a
3	chr13:76111751-76111801	HRPEpiC	eye:	n/a
4	chr13:76112980-76113030	ovcar-3	ovarian:	n/a
5	chr13:76111785-76111835	NH-A	brain:	n/a
6	chr13:76111751-76111801	HRPEpiC	eye:	n/a
7	chr13:76112980-76113030	Hela-S3	cervix:	n/a
8	chr13:76112973-76113023	HRPEpiC	eye:	n/a
9	chr13:76112980-76113030	SK-N-SH_RA	brain:	n/a
10	chr13:76111980-76112030	HUVEC	blood vessel:	n/a
11	chr13:76111751-76111801	HIPEpiC	eye:	n/a
12	chr13:76111980-76112030	GM19239	blood:	n/a
13	chr13:76113014-76113064	GM06990	blood:	n/a
14	chr13:76112973-76113023	NT2-D1	testis:	n/a
15	chr13:76115526-76115576	AG04449	skin:	fetal
16	chr13:76111980-76112030	Caco-2	colon:	n/a
17	chr13:76111980-76112030	HCM	heart:	n/a
18	chr13:76112980-76113030	NHDF-neo	bronchial:	n/a
19	chr13:76112980-76113030	NH-A	brain:	n/a
20	chr13:76111751-76111801	GM12891	blood:	n/a
21	chr13:76115526-76115576	Hepatocyte	liver:	n/a
22	chr13:76109220-76109270	HEEpiC	esophagus:	n/a
23	chr13:76112187-76112237	BE2_C	brain:	n/a
24	chr13:76112039-76112089	NHDF-neo	bronchial:	n/a
25	chr13:76111751-76111801	Jurkat	blood:	n/a
26	chr13:76115526-76115576	H1-hESC	embryonic stem cell:	embryo
27	chr13:76111785-76111835	Hepatocyte	liver:	n/a
28	chr13:76111107-76111157	HRE	kidney:	n/a
29	chr13:76113014-76113064	SK-N-MC	brain:	n/a
30	chr13:76112973-76113023	IMR90	lung:	fetal
31	chr13:76112980-76113030	HRCEpiC	kidney:	n/a
32	chr13:76111785-76111835	AG09319	gingival:	n/a
33	chr13:76115526-76115576	SKMC	muscle:	n/a
34	chr13:76115526-76115576	IMR90	lung:	fetal
35	chr13:76115526-76115576	PrEC	prostate:	n/a
36	chr13:76112232-76112282	HAEpiC	amniotic membrane:	n/a
37	chr13:76112030-76112080	SAEC	small airway:	n/a
38	chr13:76112274-76112324	AG10803	skin:	n/a
39	chr13:76115526-76115576	CMK	blood:	n/a
40	chr13:76111918-76111968	Hepatocyte	liver:	n/a
41	chr13:76112039-76112089	Jurkat	blood:	n/a
42	chr13:76113014-76113064	NT2-D1	testis:	n/a
43	chr13:76111107-76111157	HL-60	blood:	n/a
44	chr13:76115526-76115576	ECC-1	luminal epithelium:	n/a
45	chr13:76112232-76112282	AG04449	skin:	fetal
46	chr13:76112187-76112237	ECC-1	luminal epithelium:	n/a
47	chr13:76112187-76112237	MCF-7	breast:	n/a
48	chr13:76113014-76113064	AG04449	skin:	fetal
49	chr13:76111980-76112030	SK-N-SH_RA	brain:	n/a
50	chr13:76111918-76111968	H1-hESC	embryonic stem cell:	embryo

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
2	chr13:76106394..76109955-chr13:76110419..76113939,6	MCF-7	breast:
3	chr13:76101020..76103303-chr13:76108939..76111291,2	K562	blood:
4	chr11:65339613..65340413-chr13:76111532..76112034,2	NB4	blood:
5	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
6	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
7	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
8	chr13:76055919..76057695-chr13:76110507..76112437,2	MCF-7	breast:
9	chr13:76118168..76119687-chr13:76122527..76125250,2	MCF-7	breast:
10	chr13:76111404..76112078-chr17:26989037..26989702,2	Hela-S3	cervix:
11	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:
12	chr1:151253613..151254502-chr13:76111700..76112352,2	Hela-S3	cervix:
13	chr13:76101122..76104303-chr13:76108576..76110569,3	K562	blood:
14	chr13:76055248..76057886-chr13:76110224..76112780,4	MCF-7	breast:
15	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
16	chr13:76111578..76112381-chrX:73511953..73512510,2	Hela-S3	cervix:
17	chr13:76109687..76114004-chr13:76118514..76122227,3	K562	blood:
18	chr13:76102775..76109881-chr13:76110381..76113047,9	MCF-7	breast:
19	chr13:76107791..76110428-chr13:76144234..76145882,2	K562	blood:
20	chr13:76111859..76112746-chr13:76123326..76123936,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D4-2	chr13:76111635-76111811	NONHSAT034360

No data

Variant related genes	Relation type
COMMD6	TF binding region
ENSG00000261553	TF binding region
UCHL3	TF binding region
COMMD6	CpG island
ENSG00000261553	CpG island
UCHL3	CpG island
ENSG00000230590	chromatin interactions
ENSG00000109111	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000136111	chromatin interactions
ENSG00000261553	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000188243	chromatin interactions
ENSG00000176973	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000132581	chromatin interactions

Extended variants
information (count: 469 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567706712	chr13:76107785-76107786	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs537979608	chr13:76107804-76107805	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549732713	chr13:76107824-76107825	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571292307	chr13:76107862-76107863	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs114275685	chr13:76107910-76107911	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs78939515	chr13:76107934-76107935	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548115600	chr13:76107956-76107957	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549844126	chr13:76107976-76107977	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111573912	chr13:76108072-76108073	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536813129	chr13:76108084-76108085	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs554865919	chr13:76108093-76108094	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576059920	chr13:76108118-76108119	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs75770932	chr13:76108122-76108123	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs543558145	chr13:76108156-76108157	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558718051	chr13:76108158-76108159	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2328952	chr13:76108173-76108174	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs370581392	chr13:76108250-76108251	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs145186634	chr13:76108422-76108423	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559586906	chr13:76108423-76108424	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147909137	chr13:76108438-76108439	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541982237	chr13:76108443-76108444	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs563356885	chr13:76108512-76108513	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs7338768	chr13:76108558-76108559	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs549841689	chr13:76108568-76108569	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs67051742	chr13:76108649-76108650	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs145380133	chr13:76108697-76108698	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs186788323	chr13:76108738-76108739	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs115701355	chr13:76108751-76108752	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536566111	chr13:76108864-76108865	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs555109642	chr13:76108917-76108918	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564700437	chr13:76108928-76108929	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs190542091	chr13:76108964-76108965	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183033551	chr13:76108995-76108996	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs140113456	chr13:76108997-76108998	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs371067683	chr13:76109021-76109022	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs117264184	chr13:76109024-76109025	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs531742388	chr13:76109057-76109058	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577050838	chr13:76109087-76109088	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs118037415	chr13:76109154-76109155	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs151030353	chr13:76109158-76109159	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs141122316	chr13:76109198-76109199	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs9600489	chr13:76109221-76109222	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563628730	chr13:76109258-76109259	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375747095	chr13:76109261-76109262	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs4885309	chr13:76109285-76109286	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201363947	chr13:76109289-76109290	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs576241355	chr13:76109290-76109291	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs55887720	chr13:76109292-76109293	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201959512	chr13:76109293-76109294	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs398056568	chr13:76109294-76109295	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76093600-76109400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr13:76095600-76109200	Weak transcription	Gastric	stomach
3	chr13:76095800-76111400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:76096600-76110400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:76096600-76111400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:76097000-76111000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr13:76097000-76111600	Weak transcription	Spleen	Spleen
8	chr13:76097800-76110400	Weak transcription	Brain Angular Gyrus	brain
9	chr13:76097800-76110600	Weak transcription	Fetal Brain Male	brain
10	chr13:76097800-76110600	Weak transcription	Fetal Kidney	kidney
11	chr13:76097800-76110600	Weak transcription	Psoas Muscle	Psoas
12	chr13:76097800-76111200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr13:76098000-76110400	Weak transcription	A549	lung
14	chr13:76098000-76110400	Weak transcription	HUVEC	blood vessel
15	chr13:76098000-76110600	Weak transcription	Brain Anterior Caudate	brain
16	chr13:76098000-76110600	Weak transcription	Rectal Smooth Muscle	rectum
17	chr13:76098000-76111200	Weak transcription	Aorta	Aorta
18	chr13:76098200-76108200	Weak transcription	NHEK	skin
19	chr13:76098200-76109600	Weak transcription	Brain Germinal Matrix	brain
20	chr13:76098200-76110400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr13:76098400-76110200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr13:76098600-76111000	Weak transcription	Colonic Mucosa	Colon
23	chr13:76098800-76110400	Weak transcription	Brain Cingulate Gyrus	brain
24	chr13:76098800-76111400	Weak transcription	Esophagus	oesophagus
25	chr13:76099400-76109400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr13:76099400-76110400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:76099600-76109400	Weak transcription	HSMMtube	muscle
28	chr13:76099600-76110200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:76099600-76111000	Weak transcription	K562	blood
30	chr13:76100000-76109000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr13:76100000-76109200	Weak transcription	Lung	lung
32	chr13:76100000-76109400	Weak transcription	Left Ventricle	heart
33	chr13:76100000-76109400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr13:76100000-76110600	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr13:76100000-76111200	Weak transcription	Ovary	ovary
36	chr13:76100200-76109200	Weak transcription	Colon Smooth Muscle	Colon
37	chr13:76100200-76109200	Weak transcription	Thymus	Thymus
38	chr13:76100200-76110400	Weak transcription	Brain Substantia Nigra	brain
39	chr13:76100200-76110600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr13:76100400-76107800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr13:76100400-76110600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr13:76100600-76109400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr13:76100800-76110000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr13:76100800-76110600	Weak transcription	Right Ventricle	heart
45	chr13:76101200-76109200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:76101400-76107800	Weak transcription	NH-A	brain
47	chr13:76102200-76110400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr13:76102400-76109000	Weak transcription	Stomach Smooth Muscle	stomach
49	chr13:76103200-76108000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr13:76103600-76111000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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