Variant report

Variant	esv3429935
Chromosome Location	chr13:52694751-52735744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1151)
CpG islands
(count:2197)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52701870-52702197	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:52701599-52702201	K562	blood:	n/a	n/a
3	ARID3A	chr13:52703090-52703386	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:52735380-52735683	HepG2	liver:	n/a	chr13:52735628-52735644 chr13:52735627-52735643
5	BACH1	chr13:52703283-52703494	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:52733037-52733825	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr13:52732932-52733442	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:52701899-52702501	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:52703185-52703444	K562	blood:	n/a	n/a
10	BHLHE40	chr13:52733530-52734030	HepG2	liver:	n/a	n/a
11	BHLHE40	chr13:52733132-52734017	K562	blood:	n/a	n/a
12	BHLHE40	chr13:52733135-52733991	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:52701862-52702479	K562	blood:	n/a	n/a
14	BRCA1	chr13:52701897-52702538	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr13:52703224-52703419	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr13:52733684-52733754	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:52703151-52703255	HepG2	liver:	n/a	n/a
18	CBX3	chr13:52733555-52734397	HCT-116	colon:	n/a	n/a
19	CBX3	chr13:52701679-52702219	K562	blood:	n/a	n/a
20	CBX3	chr13:52733509-52734229	HCT-116	colon:	n/a	n/a
21	CBX3	chr13:52733579-52734234	K562	blood:	n/a	n/a
22	CBX3	chr13:52733696-52734095	K562	blood:	n/a	n/a
23	CCNT2	chr13:52722436-52722540	K562	blood:	n/a	n/a
24	CCNT2	chr13:52733331-52733804	K562	blood:	n/a	n/a
25	CCNT2	chr13:52703038-52703694	K562	blood:	n/a	n/a
26	CEBPB	chr13:52733770-52734105	A549	lung:	n/a	n/a
27	CEBPB	chr13:52722107-52722382	K562	blood:	n/a	n/a
28	CEBPB	chr13:52703108-52703497	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:52733674-52734120	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:52701916-52702347	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr13:52733907-52734117	HepG2	liver:	n/a	n/a
32	CEBPB	chr13:52733857-52734200	HepG2	liver:	n/a	n/a
33	CEBPD	chr13:52699755-52700107	K562	blood:	n/a	n/a
34	CHD1	chr13:52733657-52733804	GM12878	blood:	n/a	n/a
35	CHD1	chr13:52734225-52734288	GM12878	blood:	n/a	n/a
36	CHD1	chr13:52733095-52733390	GM12878	blood:	n/a	n/a
37	CHD1	chr13:52733502-52733547	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr13:52701888-52702191	HepG2	liver:	n/a	n/a
39	CHD2	chr13:52733211-52733295	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr13:52701890-52702274	GM12878	blood:	n/a	n/a
41	CHD2	chr13:52733566-52733905	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr13:52733668-52734186	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr13:52702491-52702663	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr13:52733773-52733981	K562	blood:	n/a	n/a
45	CHD2	chr13:52701918-52702233	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr13:52703168-52703208	HepG2	liver:	n/a	n/a
47	CHD2	chr13:52733563-52733922	HepG2	liver:	n/a	n/a
48	CHD2	chr13:52733023-52733992	GM12878	blood:	n/a	n/a
49	CHD2	chr13:52732995-52733312	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr13:52701883-52702231	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52702460-52702510	HCPEpiC	choroid plexus:	n/a
2	chr13:52702460-52702510	HCPEpiC	choroid plexus:	n/a
3	chr13:52733382-52733432	GM06990	blood:	n/a
4	chr13:52703373-52703423	H1-hESC	embryonic stem cell:	embryo
5	chr13:52702845-52702895	GM12878	blood:	n/a
6	chr13:52703935-52703985	HCM	heart:	n/a
7	chr13:52701033-52701083	GM06990	blood:	n/a
8	chr13:52734134-52734184	HPAEpiC	pulmonary alveolar:	n/a
9	chr13:52703328-52703378	Hela-S3	cervix:	n/a
10	chr13:52733628-52733678	HepG2	liver:	n/a
11	chr13:52733373-52733423	PFSK-1	brain:	n/a
12	chr13:52703615-52703665	HUVEC	blood vessel:	n/a
13	chr13:52733565-52733615	HAEpiC	amniotic membrane:	n/a
14	chr13:52699305-52699355	HCT-116	colon:	n/a
15	chr13:52701033-52701083	K562	blood:	n/a
16	chr13:52733860-52733910	AoSMC	blood vessel:	n/a
17	chr13:52734432-52734482	PFSK-1	brain:	n/a
18	chr13:52733382-52733432	H1-hESC	embryonic stem cell:	embryo
19	chr13:52707286-52707336	HepG2	liver:	n/a
20	chr13:52703160-52703210	PFSK-1	brain:	n/a
21	chr13:52703362-52703412	AG09309	skin:	n/a
22	chr13:52733860-52733910	ovcar-3	ovarian:	n/a
23	chr13:52733628-52733678	HRE	kidney:	n/a
24	chr13:52703373-52703423	MCF10A-Er-Src	breast:	n/a
25	chr13:52733628-52733678	SK-N-MC	brain:	n/a
26	chr13:52703373-52703423	MCF-7	breast:	n/a
27	chr13:52735075-52735125	HUVEC	blood vessel:	n/a
28	chr13:52707286-52707336	SKMC	muscle:	n/a
29	chr13:52703615-52703665	AG09319	gingival:	n/a
30	chr13:52703373-52703423	T-47D	breast:	n/a
31	chr13:52733292-52733342	ProgFib	skin:	n/a
32	chr13:52701588-52701638	HRE	kidney:	n/a
33	chr13:52733664-52733714	HIPEpiC	eye:	n/a
34	chr13:52703328-52703378	NHBE	bronchial:	n/a
35	chr13:52703362-52703412	SKMC	muscle:	n/a
36	chr13:52733292-52733342	BE2_C	brain:	n/a
37	chr13:52733586-52733636	HCF	heart:	n/a
38	chr13:52733373-52733423	MCF10A-Er-Src	breast:	n/a
39	chr13:52733373-52733423	AG04449	skin:	fetal
40	chr13:52703373-52703423	GM12878	blood:	n/a
41	chr13:52703362-52703412	HIPEpiC	eye:	n/a
42	chr13:52702431-52702481	BJ	skin:	n/a
43	chr13:52733373-52733423	AG09319	gingival:	n/a
44	chr13:52703615-52703665	NHBE	bronchial:	n/a
45	chr13:52701033-52701083	HRE	kidney:	n/a
46	chr13:52733586-52733636	H1-hESC	embryonic stem cell:	embryo
47	chr13:52734018-52734068	HAEpiC	amniotic membrane:	n/a
48	chr13:52733664-52733714	K562	blood:	n/a
49	chr13:52733382-52733432	HCT-116	colon:	n/a
50	chr13:52702856-52702906	HEK293	kidney:	embryo

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52509591..52510539-chr13:52701676..52702543,4	MCF-7	breast:
2	chr13:52469831..52471115-chr13:52701846..52702769,5	MCF-7	breast:
3	chr13:52699126..52701652-chr13:52702989..52705135,2	K562	blood:
4	chr13:52376747..52380251-chr13:52704508..52706445,3	MCF-7	breast:
5	chr13:52578352..52579378-chr13:52701728..52702446,3	MCF-7	breast:
6	chr13:52377335..52378174-chr13:52702786..52703324,2	K562	blood:
7	chr13:52718895..52720527-chr13:52725427..52728131,2	MCF-7	breast:
8	chr13:52701771..52705558-chr13:52767896..52769871,3	MCF-7	breast:
9	chr13:52729535..52732308-chr13:52732328..52734703,4	K562	blood:
10	chr13:52584477..52586943-chr13:52701489..52703372,3	K562	blood:
11	chr13:52486050..52486951-chr13:52701619..52702125,2	MCF-7	breast:
12	chr13:52725842..52728742-chr13:52731896..52733455,2	MCF-7	breast:
13	chr13:52714165..52716732-chr13:52726469..52728185,2	MCF-7	breast:
14	chr13:52699126..52701652-chr13:52702989..52705135,2	K562	blood:
15	chr13:52730788..52732496-chr13:52768343..52769860,2	MCF-7	breast:
16	chr13:52693297..52694930-chr13:52700506..52703282,2	MCF-7	breast:
17	chr13:52735080..52737033-chr13:52768484..52770040,2	MCF-7	breast:
18	chr13:52726747..52729442-chr13:52731857..52734601,2	K562	blood:
19	chr13:52714165..52716732-chr13:52726469..52728185,2	MCF-7	breast:
20	chr13:52728953..52731151-chr13:52731981..52733789,2	MCF-7	breast:
21	chr13:52600318..52601043-chr13:52701669..52702499,2	MCF-7	breast:
22	chr13:52729535..52732308-chr13:52732328..52734703,4	K562	blood:
23	chr13:52522795..52524482-chr13:52694291..52697001,2	K562	blood:
24	chr13:52725842..52728742-chr13:52731896..52733455,2	MCF-7	breast:
25	chr13:52388965..52389862-chr13:52701684..52702477,3	K562	blood:
26	chr13:52718895..52720527-chr13:52725427..52728131,2	MCF-7	breast:
27	chr13:52584477..52586900-chr13:52700506..52703372,3	K562	blood:
28	chr13:52691024..52693567-chr13:52694230..52696395,3	K562	blood:
29	chr13:52376169..52378547-chr13:52701514..52703656,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UTP14C-1	chr13:52703031-52706193	NR_110306
2	lnc-UTP14C-1	chr13:52703027-52706193	NONHSAT033962
3	lnc-UTP14C-1	chr13:52706594-52706859	NR_110306
4	lnc-UTP14C-1	chr13:52706594-52706859	NONHSAT033962

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NEK3	hsa-miR-98-5p	chr13:52706911-52706932
2	NEK3	hsa-miR-98-5p	chr13:52706917-52706910

Variant related genes	Relation type
NEK5	TF binding region
NEK3	TF binding region
NEK5	CpG island
NEK3	CpG island
ENSG00000102796	chromatin interactions
ENSG00000243406	chromatin interactions
ENSG00000197168	chromatin interactions
ENSG00000253710	chromatin interactions
ENSG00000231856	chromatin interactions
ENSG00000123191	chromatin interactions
ENSG00000136098	chromatin interactions

Extended variants
information (count: 1517 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1517 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539081567	chr13:52694776-52694777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145466210	chr13:52694807-52694808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs9535871	chr13:52694813-52694814	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs9535872	chr13:52694817-52694818	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs376067602	chr13:52694908-52694909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188471348	chr13:52694922-52694923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs201888113	chr13:52695048-52695049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76615049	chr13:52695060-52695061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs9535873	chr13:52695139-52695140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs537764686	chr13:52695170-52695171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557544618	chr13:52695195-52695196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143234487	chr13:52695273-52695274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373296419	chr13:52695281-52695282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559201415	chr13:52695295-52695296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547228500	chr13:52695296-52695297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34187285	chr13:52695312-52695313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148311702	chr13:52695358-52695359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192895461	chr13:52695388-52695389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199821768	chr13:52695435-52695436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540634251	chr13:52695454-52695455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560571936	chr13:52695456-52695457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529890969	chr13:52695516-52695517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549673369	chr13:52695534-52695535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563133621	chr13:52695541-52695542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532253177	chr13:52695605-52695606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs9535874	chr13:52695613-52695614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376546831	chr13:52695618-52695619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543677091	chr13:52695620-52695621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183424869	chr13:52695670-52695671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530565761	chr13:52695693-52695694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370711559	chr13:52695717-52695718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78586711	chr13:52695803-52695804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187691089	chr13:52695848-52695849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544134610	chr13:52695939-52695940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1004576	chr13:52695981-52695982	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs577343963	chr13:52695990-52695991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539677550	chr13:52695991-52695992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553545605	chr13:52696031-52696032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147103991	chr13:52696037-52696038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541123282	chr13:52696039-52696040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560507054	chr13:52696040-52696041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572365980	chr13:52696059-52696060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543309481	chr13:52696102-52696103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138558422	chr13:52696108-52696109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35975511	chr13:52696120-52696121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532320313	chr13:52696137-52696138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552052836	chr13:52696207-52696208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559522508	chr13:52696213-52696214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573929365	chr13:52696277-52696278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374670892	chr13:52696409-52696410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1786 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52693800-52699000	Weak transcription	K562	blood
2	chr13:52694400-52701600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr13:52699000-52701800	Enhancers	K562	blood
4	chr13:52701000-52701800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr13:52701200-52701800	Enhancers	Fetal Intestine Small	intestine
6	chr13:52701400-52701600	Enhancers	Stomach Smooth Muscle	stomach
7	chr13:52701400-52701800	Enhancers	NHEK	skin
8	chr13:52701600-52701800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr13:52701600-52701800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:52701600-52701800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr13:52701600-52701800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:52701600-52701800	Enhancers	Brain Cingulate Gyrus	brain
13	chr13:52701600-52701800	Active TSS	Colon Smooth Muscle	Colon
14	chr13:52701600-52701800	Enhancers	Duodenum Mucosa	Duodenum
15	chr13:52701600-52701800	Enhancers	Fetal Heart	heart
16	chr13:52701600-52701800	Enhancers	Fetal Kidney	kidney
17	chr13:52701600-52701800	Enhancers	Rectal Smooth Muscle	rectum
18	chr13:52701600-52701800	Enhancers	Stomach Mucosa	stomach
19	chr13:52701600-52701800	Enhancers	HepG2	liver
20	chr13:52701600-52702000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
21	chr13:52701600-52702000	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr13:52701600-52702000	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr13:52701600-52702000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:52701600-52702000	Enhancers	Adipose Nuclei	Adipose
25	chr13:52701600-52702000	Enhancers	Colonic Mucosa	Colon
26	chr13:52701600-52702000	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr13:52701600-52702000	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr13:52701600-52702200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:52701600-52702200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr13:52701600-52702200	Enhancers	Fetal Stomach	stomach
31	chr13:52701600-52702200	Flanking Active TSS	Stomach Smooth Muscle	stomach
32	chr13:52701600-52702200	Enhancers	HMEC	breast
33	chr13:52701600-52702200	Enhancers	HSMMtube	muscle
34	chr13:52701800-52702000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:52701800-52702000	Enhancers	H1 Cell Line	embryonic stem cell
36	chr13:52701800-52702000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr13:52701800-52702000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr13:52701800-52702000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr13:52701800-52702000	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr13:52701800-52702000	Enhancers	Primary T cells from cord blood	blood
41	chr13:52701800-52702000	Enhancers	Primary hematopoietic stem cells	blood
42	chr13:52701800-52702000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
43	chr13:52701800-52702000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr13:52701800-52702000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
45	chr13:52701800-52702000	Enhancers	Primary T helper cells PMA-I stimulated	--
46	chr13:52701800-52702000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr13:52701800-52702000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr13:52701800-52702000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr13:52701800-52702000	Enhancers	Muscle Satellite Cultured Cells	--
50	chr13:52701800-52702000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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