Variant report

Variant	esv3335695
Chromosome Location	chr13:111108651-111110599
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	chr13:111108303-111108757	K562	blood:	n/a	n/a
2	ATF2	chr13:111108170-111108771	GM12878	blood:	n/a	n/a
3	ATF2	chr13:111108137-111108738	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:111108215-111108853	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:111108240-111108761	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr13:111108176-111108654	GM12878	blood:	n/a	n/a
7	BCLAF1	chr13:111108146-111108656	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:111108240-111108775	GM12878	blood:	n/a	n/a
9	CBX3	chr13:111108193-111108776	K562	blood:	n/a	n/a
10	CHD1	chr13:111108264-111108720	GM12878	blood:	n/a	n/a
11	CHD2	chr13:111108267-111108694	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr13:111108160-111108771	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr13:111108127-111108768	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr13:111108080-111108953	HCT-116	colon:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
15	CTCF	chr13:111108169-111108661	GM12878	blood:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
16	CTCF	chr13:111108186-111108692	K562	blood:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
17	CTCF	chr13:111108001-111108805	A549	lung:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
18	CTCF	chr13:111108020-111108937	SK-N-SH	brain:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
19	CTCF	chr13:111108150-111108653	H1-hESC	embryonic stem cell:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
20	CTCF	chr13:111108175-111108797	HCT-116	colon:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
21	CTCF	chr13:111108128-111108746	MCF-7	breast:	n/a	chr13:111108403-111108424 chr13:111108354-111108367 chr13:111108404-111108417 chr13:111108401-111108419 chr13:111108402-111108418
22	CTCF	chr13:111108620-111108770	NB4	blood:	n/a	n/a
23	CTCF	chr13:111108647-111108764	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr13:111108643-111108778	Lung_OC	lung:	n/a	n/a
25	E2F6	chr13:111108219-111108744	H1-hESC	embryonic stem cell:	n/a	chr13:111108435-111108449 chr13:111108432-111108446
26	E2F6	chr13:111108289-111108771	A549	lung:	n/a	chr13:111108435-111108449 chr13:111108432-111108446
27	ELF1	chr13:111108185-111108667	GM12878	blood:	n/a	n/a
28	EP300	chr13:111108387-111108755	GM12878	blood:	n/a	n/a
29	EP300	chr13:111108213-111108692	H1-hESC	embryonic stem cell:	n/a	chr13:111108354-111108370
30	EP300	chr13:111108257-111108662	K562	blood:	n/a	chr13:111108354-111108370
31	EP300	chr13:111108360-111108755	GM12878	blood:	n/a	n/a
32	EP300	chr13:111108326-111108707	K562	blood:	n/a	chr13:111108354-111108370
33	FOXM1	chr13:111108087-111108845	GM12878	blood:	n/a	n/a
34	FOXM1	chr13:111108182-111108799	GM12878	blood:	n/a	n/a
35	GTF2F1	chr13:111108238-111108676	Hela-S3	cervix:	n/a	n/a
36	HA-E2F1	chr13:111108003-111108680	MCF-7	breast:	n/a	chr13:111108435-111108449 chr13:111108432-111108446
37	HCFC1	chr13:111108292-111108745	K562	blood:	n/a	n/a
38	IRF4	chr13:111108209-111108662	GM12878	blood:	n/a	n/a
39	JUN	chr13:111108156-111108714	K562	blood:	n/a	n/a
40	JUND	chr13:111109137-111109444	HepG2	liver:	n/a	n/a
41	JUND	chr13:111108238-111108730	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr13:111109449-111109653	HepG2	liver:	n/a	n/a
43	MAFF	chr13:111108284-111108652	HepG2	liver:	n/a	n/a
44	MAFF	chr13:111108270-111108768	K562	blood:	n/a	n/a
45	MAFK	chr13:111108301-111108806	K562	blood:	n/a	n/a
46	MAFK	chr13:111108288-111108660	HepG2	liver:	n/a	n/a
47	MAFK	chr13:111108217-111108936	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAFK	chr13:111108297-111108652	HepG2	liver:	n/a	n/a
49	MAX	chr13:111108221-111108671	A549	lung:	n/a	n/a
50	MAX	chr13:111108161-111108651	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111109651-111109701	AG04449	skin:	fetal
2	chr13:111109651-111109701	NH-A	brain:	n/a
3	chr13:111109651-111109701	HCT-116	colon:	n/a
4	chr13:111109497-111109547	LNCaP	prostate:	n/a
5	chr13:111109140-111109190	HPAEpiC	pulmonary alveolar:	n/a
6	chr13:111109497-111109547	U87	brain:	n/a
7	chr13:111109140-111109190	AG09319	gingival:	n/a
8	chr13:111109140-111109190	GM19239	blood:	n/a
9	chr13:111109651-111109701	IMR90	lung:	fetal
10	chr13:111109140-111109190	U87	brain:	n/a
11	chr13:111109140-111109190	IMR90	lung:	fetal
12	chr13:111109497-111109547	SK-N-SH_RA	brain:	n/a
13	chr13:111109651-111109701	Caco-2	colon:	n/a
14	chr13:111109140-111109190	PFSK-1	brain:	n/a
15	chr13:111109497-111109547	ovcar-3	ovarian:	n/a
16	chr13:111109497-111109547	ProgFib	skin:	n/a
17	chr13:111109497-111109547	GM06990	blood:	n/a
18	chr13:111109651-111109701	SK-N-MC	brain:	n/a
19	chr13:111109651-111109701	K562	blood:	n/a
20	chr13:111109651-111109701	HRPEpiC	eye:	n/a
21	chr13:111109651-111109701	BE2_C	brain:	n/a
22	chr13:111109651-111109701	HEK293	kidney:	embryo
23	chr13:111109140-111109190	Hela-S3	cervix:	n/a
24	chr13:111109140-111109190	HRE	kidney:	n/a
25	chr13:111109140-111109190	AG04449	skin:	fetal
26	chr13:111109140-111109190	HAEpiC	amniotic membrane:	n/a
27	chr13:111109140-111109190	GM12892	blood:	n/a
28	chr13:111109651-111109701	SK-N-SH_RA	brain:	n/a
29	chr13:111109651-111109701	GM19239	blood:	n/a
30	chr13:111109651-111109701	GM12892	blood:	n/a
31	chr13:111109497-111109547	GM12878	blood:	n/a
32	chr13:111109497-111109547	HRPEpiC	eye:	n/a
33	chr13:111109497-111109547	ECC-1	luminal epithelium:	n/a
34	chr13:111109497-111109547	Hela-S3	cervix:	n/a
35	chr13:111109497-111109547	MCF10A-Er-Src	breast:	n/a
36	chr13:111109140-111109190	H1-hESC	embryonic stem cell:	embryo
37	chr13:111109140-111109190	HL-60	blood:	n/a
38	chr13:111109140-111109190	BE2_C	brain:	n/a
39	chr13:111109497-111109547	HNPCEpiC	eye:	n/a
40	chr13:111109497-111109547	HRCEpiC	kidney:	n/a
41	chr13:111109651-111109701	BJ	skin:	n/a
42	chr13:111109651-111109701	T-47D	breast:	n/a
43	chr13:111109140-111109190	NT2-D1	testis:	n/a
44	chr13:111109497-111109547	HUVEC	blood vessel:	n/a
45	chr13:111109140-111109190	AoSMC	blood vessel:	n/a
46	chr13:111109651-111109701	NHDF-neo	bronchial:	n/a
47	chr13:111109651-111109701	CMK	blood:	n/a
48	chr13:111109140-111109190	NHDF-neo	bronchial:	n/a
49	chr13:111109651-111109701	SAEC	small airway:	n/a
50	chr13:111109497-111109547	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:111107847..111110592-chr13:111111239..111113236,3	MCF-7	breast:
2	chr13:111108605..111110640-chr13:111363694..111365787,2	MCF-7	breast:
3	chr13:111107610..111109499-chr13:111162077..111163995,2	K562	blood:
4	chr13:111107007..111108826-chr13:111174960..111176925,2	MCF-7	breast:
5	chr13:111107216..111109712-chr13:111113064..111115037,2	K562	blood:
6	chr13:111106557..111109185-chr13:111212224..111215375,3	MCF-7	breast:
7	chr13:111104435..111110355-chr13:111364229..111367898,5	MCF-7	breast:
8	chr13:111107958..111109838-chr2:11209436..11210956,2	MCF-7	breast:
9	chr13:111106451..111110358-chr13:111364193..111366968,4	K562	blood:
10	chr13:111107824..111108748-chr13:111297271..111297854,2	MCF-7	breast:
11	chr13:111106850..111109675-chr13:111241801..111244096,2	MCF-7	breast:
12	chr13:111108088..111108850-chr13:111179257..111180150,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A2-AS2-1	chr13:111110438-111110633	ENSG00000224821.5
2	lnc-COL4A2-AS2-1	chr13:111110030-111110066	ENSG00000224821.5
3	lnc-COL4A2-AS2-1	chr13:111108743-111109703	ENSG00000224821.5
4	lnc-COL4A2-AS2-1	chr13:111109872-111109934	ENSG00000224821.5

Variant related genes	Relation type
COL4A2	TF binding region
COL4A2	CpG island
ENSG00000139832	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000134871	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112023853	chr13:111108682-111108683	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs552551449	chr13:111108693-111108694	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs541451105	chr13:111108750-111108751	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs537442497	chr13:111108772-111108773	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs148750475	chr13:111108789-111108790	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs184361034	chr13:111108792-111108793	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs113592700	chr13:111108808-111108809	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs113383711	chr13:111108818-111108819	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs7996349	chr13:111108819-111108820	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs375950522	chr13:111108823-111108824	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs533246355	chr13:111108826-111108827	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs551897920	chr13:111108859-111108860	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs7996702	chr13:111108874-111108875	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs553567325	chr13:111108897-111108898	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs549220123	chr13:111108901-111108902	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs567641489	chr13:111108927-111108928	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs190095024	chr13:111108939-111108940	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs553475777	chr13:111108940-111108941	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs192745272	chr13:111108956-111108957	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs539147096	chr13:111108979-111108980	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs557841726	chr13:111109020-111109021	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs184799226	chr13:111109051-111109052	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs189304849	chr13:111109059-111109060	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs568697567	chr13:111109060-111109061	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs555665336	chr13:111109093-111109094	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs573966887	chr13:111109095-111109096	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs113122708	chr13:111109129-111109130	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs139012252	chr13:111109133-111109134	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs545470705	chr13:111109140-111109141	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs71201249	chr13:111109153-111109154	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs9583497	chr13:111109156-111109157	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs28502737	chr13:111109157-111109158	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs186587913	chr13:111109163-111109164	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs9583498	chr13:111109177-111109178	Weak transcription Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs563808677	chr13:111109187-111109188	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs530982663	chr13:111109190-111109191	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs9583499	chr13:111109205-111109206	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs189476385	chr13:111109208-111109209	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs561182370	chr13:111109209-111109210	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs528741657	chr13:111109213-111109214	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs547318994	chr13:111109219-111109220	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs181801540	chr13:111109228-111109229	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs370055942	chr13:111109251-111109252	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs373423717	chr13:111109273-111109274	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs539420098	chr13:111109274-111109275	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs9588168	chr13:111109283-111109284	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs28660620	chr13:111109289-111109290	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs551159570	chr13:111109292-111109293	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs112463686	chr13:111109303-111109304	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs111791213	chr13:111109313-111109314	Weak transcription Strong transcription	Chromatin interactive region lncRNA	3 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
Cancer	20164919	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
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111078200-111136800	Weak transcription	Colonic Mucosa	Colon
2	chr13:111083600-111110000	Weak transcription	Esophagus	oesophagus
3	chr13:111097000-111109000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:111099000-111123400	Strong transcription	Fetal Muscle Trunk	muscle
5	chr13:111099800-111116400	Strong transcription	Fetal Muscle Leg	muscle
6	chr13:111100000-111120000	Weak transcription	Pancreas	Pancrea
7	chr13:111100400-111118200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr13:111101600-111130200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr13:111101800-111127800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr13:111102200-111122000	Strong transcription	Placenta	Placenta
11	chr13:111103600-111112000	Weak transcription	HSMMtube	muscle
12	chr13:111103800-111125600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:111104200-111111600	Weak transcription	Fetal Lung	lung
14	chr13:111104400-111111400	Weak transcription	HSMM	muscle
15	chr13:111105800-111108800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:111105800-111108800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr13:111105800-111138000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr13:111106200-111110400	Strong transcription	Adipose Nuclei	Adipose
19	chr13:111106400-111108800	Strong transcription	NH-A	brain
20	chr13:111106400-111115200	Weak transcription	Fetal Kidney	kidney
21	chr13:111106600-111111800	Strong transcription	Aorta	Aorta
22	chr13:111106600-111112400	Strong transcription	NHLF	lung
23	chr13:111106800-111110600	Strong transcription	Lung	lung
24	chr13:111107000-111109800	Weak transcription	Left Ventricle	heart
25	chr13:111107000-111111600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr13:111107400-111108800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr13:111107400-111110200	Weak transcription	HUVEC	blood vessel
28	chr13:111107400-111114600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr13:111107600-111109800	Weak transcription	Spleen	Spleen
30	chr13:111107600-111118000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:111107600-111130400	Weak transcription	Right Atrium	heart
32	chr13:111107800-111108800	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr13:111108000-111108800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr13:111108000-111108800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr13:111108000-111108800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr13:111108000-111108800	Enhancers	Primary hematopoietic stem cells	blood
37	chr13:111108000-111108800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr13:111108000-111108800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:111108000-111108800	Enhancers	Liver	Liver
40	chr13:111108000-111109800	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr13:111108200-111108800	Enhancers	Primary B cells from peripheral blood	blood
42	chr13:111108200-111108800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr13:111108200-111108800	Enhancers	Duodenum Mucosa	Duodenum
44	chr13:111108200-111108800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr13:111108200-111108800	Enhancers	Fetal Brain Male	brain
46	chr13:111108200-111108800	Genic enhancers	Fetal Intestine Small	intestine
47	chr13:111108200-111108800	Enhancers	Stomach Mucosa	stomach
48	chr13:111108200-111108800	Enhancers	K562	blood
49	chr13:111108200-111108800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr13:111108200-111108800	Enhancers	NHEK	skin

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