Variant report

Variant	esv17909
Chromosome Location	chr13:111329244-111330419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:111328300-111329671	GM12878	blood:	n/a	n/a
2	BATF	chr13:111329690-111330085	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:111329451-111330173	GM12878	blood:	n/a	n/a
4	BCLAF1	chr13:111328295-111329322	GM12878	blood:	n/a	n/a
5	BCLAF1	chr13:111328372-111329520	GM12878	blood:	n/a	n/a
6	BHLHE40	chr13:111328344-111329778	GM12878	blood:	n/a	chr13:111328790-111328806 chr13:111328782-111328798
7	CHD2	chr13:111328434-111329393	GM12878	blood:	n/a	n/a
8	CREB1	chr13:111328407-111329638	GM12878	blood:	n/a	n/a
9	CTCF	chr13:111330260-111330410	AG09309	skin:	n/a	chr13:111330308-111330326
10	CTCF	chr13:111330240-111330390	AG09309	skin:	n/a	chr13:111330308-111330326
11	CTCF	chr13:111330294-111330378	H1-hESC	embryonic stem cell:	n/a	chr13:111330308-111330326
12	CTCF	chr13:111329160-111329310	GM12870	blood:	n/a	chr13:111329271-111329280
13	CUX1	chr13:111328580-111329471	GM12878	blood:	n/a	n/a
14	EBF1	chr13:111328354-111329649	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
15	EBF1	chr13:111329597-111330195	GM12878	blood:	n/a	n/a
16	EBF1	chr13:111328352-111329629	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
17	EBF1	chr13:111329657-111330177	GM12878	blood:	n/a	n/a
18	EBF1	chr13:111328357-111329570	GM12878	blood:	n/a	chr13:111329363-111329374 chr13:111329386-111329397
19	ELF1	chr13:111328346-111329670	GM12878	blood:	n/a	n/a
20	EP300	chr13:111328368-111329762	GM12878	blood:	n/a	chr13:111329137-111329144
21	EP300	chr13:111328451-111329276	GM12878	blood:	n/a	chr13:111329137-111329144
22	EP300	chr13:111328366-111329571	GM12878	blood:	n/a	chr13:111329137-111329144
23	EP300	chr13:111329686-111330153	GM12878	blood:	n/a	n/a
24	FOXM1	chr13:111328355-111329551	GM12878	blood:	n/a	n/a
25	FOXM1	chr13:111328296-111329361	GM12878	blood:	n/a	n/a
26	IKZF1	chr13:111328464-111329552	GM12878	blood:	n/a	n/a
27	IRF4	chr13:111329601-111330168	GM12878	blood:	n/a	n/a
28	MAX	chr13:111328477-111329339	GM12878	blood:	n/a	n/a
29	MAZ	chr13:111328422-111329787	GM12878	blood:	n/a	n/a
30	MTA3	chr13:111328348-111329353	GM12878	blood:	n/a	n/a
31	MTA3	chr13:111328044-111329851	GM12878	blood:	n/a	n/a
32	MXI1	chr13:111328485-111329477	GM12878	blood:	n/a	n/a
33	NFATC1	chr13:111329129-111329680	GM12878	blood:	n/a	n/a
34	NFIC	chr13:111328301-111329283	GM12878	blood:	n/a	n/a
35	NFIC	chr13:111328328-111329595	GM12878	blood:	n/a	n/a
36	NFIC	chr13:111329367-111329925	GM12878	blood:	n/a	n/a
37	NFIC	chr13:111329631-111330240	GM12878	blood:	n/a	n/a
38	NRF1	chr13:111329072-111329373	GM12878	blood:	n/a	n/a
39	PAX5	chr13:111328351-111329626	GM12878	blood:	n/a	chr13:111329107-111329116
40	PAX5	chr13:111329677-111330195	GM12878	blood:	n/a	n/a
41	PAX5	chr13:111329097-111329427	GM12892	blood:	n/a	chr13:111329107-111329116
42	PAX5	chr13:111328277-111330032	GM12878	blood:	n/a	chr13:111329107-111329116
43	PAX5	chr13:111329685-111330084	GM12878	blood:	n/a	n/a
44	PAX5	chr13:111328292-111330332	GM12878	blood:	n/a	chr13:111329107-111329116
45	PML	chr13:111328339-111329763	GM12878	blood:	n/a	n/a
46	POLR2A	chr13:111328906-111329531	GM12878	blood:	n/a	n/a
47	POLR2A	chr13:111329099-111329299	GM12878	blood:	n/a	n/a
48	POLR2A	chr13:111328457-111329458	GM12878	blood:	n/a	n/a
49	POLR2A	chr13:111329677-111330342	GM12878	blood:	n/a	n/a
50	POLR2A	chr13:111329677-111330279	GM12891	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111329221-111329271	HNPCEpiC	eye:	n/a
2	chr13:111329221-111329271	LNCaP	prostate:	n/a
3	chr13:111329221-111329271	IMR90	lung:	fetal
4	chr13:111329221-111329271	Hela-S3	cervix:	n/a
5	chr13:111329221-111329271	HCF	heart:	n/a
6	chr13:111329221-111329271	HRPEpiC	eye:	n/a
7	chr13:111329221-111329271	GM12878	blood:	n/a
8	chr13:111329221-111329271	NHBE	bronchial:	n/a
9	chr13:111329221-111329271	HCT-116	colon:	n/a
10	chr13:111329221-111329271	Hepatocyte	liver:	n/a
11	chr13:111329221-111329271	AG04449	skin:	fetal
12	chr13:111329221-111329271	AG04450	lung:	fetal
13	chr13:111329221-111329271	PrEC	prostate:	n/a
14	chr13:111329221-111329271	ovcar-3	ovarian:	n/a
15	chr13:111329221-111329271	BJ	skin:	n/a
16	chr13:111329221-111329271	Caco-2	colon:	n/a
17	chr13:111329221-111329271	HEK293	kidney:	embryo
18	chr13:111329221-111329271	AG10803	skin:	n/a
19	chr13:111329221-111329271	SK-N-SH_RA	brain:	n/a
20	chr13:111329221-111329271	GM19239	blood:	n/a
21	chr13:111329221-111329271	SK-N-SH	brain:	n/a
22	chr13:111329221-111329271	HAEpiC	amniotic membrane:	n/a
23	chr13:111329221-111329271	HIPEpiC	eye:	n/a
24	chr13:111329221-111329271	SAEC	small airway:	n/a
25	chr13:111329221-111329271	GM12892	blood:	n/a
26	chr13:111329221-111329271	SKMC	muscle:	n/a
27	chr13:111329221-111329271	HCM	heart:	n/a
28	chr13:111329221-111329271	HRCEpiC	kidney:	n/a
29	chr13:111329221-111329271	AoSMC	blood vessel:	n/a
30	chr13:111329221-111329271	HCPEpiC	choroid plexus:	n/a
31	chr13:111329221-111329271	HRE	kidney:	n/a
32	chr13:111329221-111329271	AG09319	gingival:	n/a
33	chr13:111329221-111329271	MCF10A-Er-Src	breast:	n/a
34	chr13:111329221-111329271	HEEpiC	esophagus:	n/a
35	chr13:111329221-111329271	T-47D	breast:	n/a
36	chr13:111329221-111329271	HL-60	blood:	n/a
37	chr13:111329221-111329271	K562	blood:	n/a
38	chr13:111329221-111329271	AG09309	skin:	n/a
39	chr13:111329221-111329271	HepG2	liver:	n/a
40	chr13:111329221-111329271	Jurkat	blood:	n/a
41	chr13:111329221-111329271	ECC-1	luminal epithelium:	n/a
42	chr13:111329221-111329271	BE2_C	brain:	n/a
43	chr13:111329221-111329271	NH-A	brain:	n/a
44	chr13:111329221-111329271	RPTEC	kidney:	n/a
45	chr13:111329221-111329271	PANC-1	pancreas:	n/a
46	chr13:111329221-111329271	HPAEpiC	pulmonary alveolar:	n/a
47	chr13:111329221-111329271	MCF-7	breast:	n/a
48	chr13:111329221-111329271	PFSK-1	brain:	n/a
49	chr13:111329221-111329271	NHDF-neo	bronchial:	n/a
50	chr13:111329221-111329271	GM06990	blood:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:111328800..111330834-chr13:111364440..111366788,2	K562	blood:
2	chr13:111328800..111332502-chr13:111363272..111367932,6	K562	blood:

No data

Variant related genes	Relation type
CARS2	TF binding region
CARS2	CpG island
ENSG00000134905	chromatin interactions
ENSG00000153487	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371196794	chr13:111329306-111329307	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374751888	chr13:111329325-111329326	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145315422	chr13:111329326-111329327	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs369056410	chr13:111329344-111329345	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs149601283	chr13:111329353-111329354	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs557671802	chr13:111329354-111329355	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575915087	chr13:111329355-111329356	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs144283051	chr13:111329361-111329362	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372177940	chr13:111329367-111329368	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs140056876	chr13:111329389-111329390	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs143818816	chr13:111329404-111329405	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs537075451	chr13:111329422-111329423	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199589765	chr13:111329435-111329436	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201064390	chr13:111329444-111329445	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375938059	chr13:111329449-111329450	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs541127961	chr13:111329450-111329451	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs559902282	chr13:111329465-111329466	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs578236157	chr13:111329470-111329471	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs369686025	chr13:111329471-111329472	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs545607309	chr13:111329475-111329476	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs200627513	chr13:111329486-111329487	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs562781182	chr13:111329504-111329505	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs185147145	chr13:111329514-111329515	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs189085438	chr13:111329529-111329530	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs113622654	chr13:111329579-111329580	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs74125032	chr13:111329589-111329590	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs56131494	chr13:111329596-111329597	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs76103038	chr13:111329610-111329611	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs78214217	chr13:111329612-111329613	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs56405935	chr13:111329613-111329614	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs56260830	chr13:111329619-111329620	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs11069862	chr13:111329632-111329633	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs80279244	chr13:111329655-111329656	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs11069863	chr13:111329665-111329666	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
35	rs372446455	chr13:111329673-111329674	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs369148346	chr13:111329679-111329680	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs386774764	chr13:111329680-111329681	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs151026419	chr13:111329686-111329687	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs12431291	chr13:111329688-111329689	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs12431292	chr13:111329689-111329690	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs112411948	chr13:111329731-111329732	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
42	rs116445785	chr13:111329741-111329742	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375733871	chr13:111329749-111329750	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs111861692	chr13:111329762-111329763	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs555745014	chr13:111329790-111329791	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs573906307	chr13:111329792-111329793	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs111337923	chr13:111329806-111329807	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535011932	chr13:111329807-111329808	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs553542826	chr13:111329812-111329813	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs56390422	chr13:111329813-111329814	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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
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

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111297800-111336400	Weak transcription	Small Intestine	intestine
2	chr13:111302200-111351400	Weak transcription	Stomach Mucosa	stomach
3	chr13:111310800-111352200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr13:111311600-111352000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr13:111312800-111357400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr13:111316200-111330600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr13:111316600-111332800	Weak transcription	K562	blood
8	chr13:111319400-111337600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr13:111319800-111348400	Weak transcription	Fetal Brain Male	brain
10	chr13:111319800-111354600	Weak transcription	Fetal Heart	heart
11	chr13:111320200-111339200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr13:111321800-111332800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:111322000-111330000	Weak transcription	NHDF-Ad	bronchial
14	chr13:111322800-111333800	Weak transcription	Fetal Kidney	kidney
15	chr13:111322800-111349600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr13:111327600-111329600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr13:111327800-111329400	Strong transcription	Placenta Amnion	Placenta Amnion
18	chr13:111327800-111331400	Strong transcription	Colonic Mucosa	Colon
19	chr13:111327800-111336000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:111327800-111344200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr13:111327800-111347400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr13:111327800-111355000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr13:111328000-111329400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
24	chr13:111328000-111329400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr13:111328000-111329400	Flanking Active TSS	GM12878-XiMat	blood
26	chr13:111328000-111329400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr13:111328000-111329600	Strong transcription	Brain Anterior Caudate	brain
28	chr13:111328000-111330400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr13:111328000-111331000	Strong transcription	Fetal Lung	lung
30	chr13:111328000-111331200	Strong transcription	Fetal Muscle Trunk	muscle
31	chr13:111328000-111331600	Strong transcription	Duodenum Smooth Muscle	Duodenum
32	chr13:111328000-111331800	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr13:111328000-111331800	Strong transcription	Gastric	stomach
34	chr13:111328000-111331800	Strong transcription	Ovary	ovary
35	chr13:111328000-111331800	Strong transcription	Thymus	Thymus
36	chr13:111328000-111332400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr13:111328000-111333200	Strong transcription	NHLF	lung
38	chr13:111328000-111335200	Strong transcription	Brain Cingulate Gyrus	brain
39	chr13:111328000-111335200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr13:111328000-111335400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr13:111328000-111335400	Strong transcription	HepG2	liver
42	chr13:111328000-111335600	Strong transcription	Liver	Liver
43	chr13:111328000-111335600	Strong transcription	Duodenum Mucosa	Duodenum
44	chr13:111328000-111336000	Strong transcription	Fetal Intestine Large	intestine
45	chr13:111328000-111336600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr13:111328000-111336800	Strong transcription	Left Ventricle	heart
47	chr13:111328000-111337800	Strong transcription	Brain Germinal Matrix	brain
48	chr13:111328000-111338200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr13:111328000-111339800	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr13:111328000-111340200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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