Variant report

Variant	esv1816672
Chromosome Location	chr13:51061044-51092946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:193)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:193 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51083366-51083443	HepG2	liver:	n/a	n/a
2	ATF1	chr13:51086067-51086459	K562	blood:	n/a	n/a
3	BACH1	chr13:51068926-51068942	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr13:51086098-51086273	K562	blood:	n/a	n/a
5	CEBPB	chr13:51084214-51084546	HepG2	liver:	n/a	chr13:51084375-51084386
6	CEBPB	chr13:51086122-51086389	K562	blood:	n/a	n/a
7	CEBPB	chr13:51084195-51084538	IMR90	lung:	n/a	chr13:51084375-51084386
8	CTCF	chr13:51087099-51087179	GM19240	blood:	n/a	n/a
9	CTCF	chr13:51087120-51087270	AoAF	blood vessel:	n/a	n/a
10	CTCF	chr13:51087113-51087202	K562	blood:	n/a	n/a
11	CTCF	chr13:51087460-51087610	Caco-2	colon:	n/a	n/a
12	CTCF	chr13:51087260-51087410	HFF	foreskin:	n/a	n/a
13	CTCF	chr13:51087020-51087170	GM12872	blood:	n/a	n/a
14	CTCF	chr13:51087000-51087150	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr13:51087080-51087230	HPF	lung:	n/a	n/a
16	CTCF	chr13:51087040-51087190	AG10803	skin:	n/a	n/a
17	CTCF	chr13:51087100-51087250	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr13:51065369-51065395	MCF-7	breast:	n/a	n/a
19	CTCF	chr13:51087160-51087310	GM12871	blood:	n/a	n/a
20	CTCF	chr13:51087115-51087220	Gliobla	brain:	n/a	n/a
21	CTCF	chr13:51087060-51087210	NHLF	lung:	n/a	n/a
22	CTCF	chr13:51087240-51087390	BJ	skin:	n/a	n/a
23	CTCF	chr13:51087040-51087190	RPTEC	kidney:	n/a	n/a
24	CTCF	chr13:51087100-51087250	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr13:51086976-51087300	K562	blood:	n/a	n/a
26	CTCF	chr13:51087120-51087182	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr13:51087040-51087190	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr13:51087060-51087210	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr13:51087040-51087190	HAc	cerebellar:	n/a	n/a
30	CTCF	chr13:51087000-51087150	RPTEC	kidney:	n/a	n/a
31	CTCF	chr13:51087040-51087190	AG09319	gingival:	n/a	n/a
32	CTCF	chr13:51087000-51087150	GM12873	blood:	n/a	n/a
33	CTCF	chr13:51087000-51087150	HPF	lung:	n/a	n/a
34	CTCF	chr13:51061180-51061330	HPF	lung:	n/a	n/a
35	CTCF	chr13:51066171-51066200	Lung_OC	lung:	n/a	n/a
36	CTCF	chr13:51075620-51075770	MCF-7	breast:	n/a	n/a
37	CTCF	chr13:51087020-51087170	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr13:51087080-51087230	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr13:51092800-51092950	GM12868	blood:	n/a	n/a
40	CTCF	chr13:51087060-51087210	HCFaa	heart:	n/a	n/a
41	CTCF	chr13:51087080-51087230	AG09319	gingival:	n/a	n/a
42	CTCF	chr13:51087080-51087230	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr13:51087060-51087210	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr13:51087106-51087112	K562	blood:	n/a	n/a
45	CTCF	chr13:51087136-51087174	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr13:51086970-51087277	IMR90	lung:	n/a	n/a
47	CTCF	chr13:51086872-51086919	Spleen_OC	spleen:	n/a	n/a
48	CUX1	chr13:51086641-51087069	GM12878	blood:	n/a	n/a
49	CUX1	chr13:51085609-51085671	K562	blood:	n/a	n/a
50	E2F4	chr13:51066794-51066832	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51086835-51086885	AG09309	skin:	n/a
2	chr13:51086835-51086885	LNCaP	prostate:	n/a
3	chr13:51086835-51086885	AG04449	skin:	fetal
4	chr13:51086835-51086885	U87	brain:	n/a
5	chr13:51086835-51086885	MCF10A-Er-Src	breast:	n/a
6	chr13:51086835-51086885	ProgFib	skin:	n/a
7	chr13:51086835-51086885	NH-A	brain:	n/a
8	chr13:51086835-51086885	HCT-116	colon:	n/a
9	chr13:51086835-51086885	A549	lung:	n/a
10	chr13:51086835-51086885	Caco-2	colon:	n/a
11	chr13:51086835-51086885	PFSK-1	brain:	n/a
12	chr13:51086835-51086885	SAEC	small airway:	n/a
13	chr13:51086835-51086885	SKMC	muscle:	n/a
14	chr13:51086835-51086885	IMR90	lung:	fetal
15	chr13:51086835-51086885	Hela-S3	cervix:	n/a
16	chr13:51086835-51086885	HMEC	breast:	n/a
17	chr13:51086835-51086885	HL-60	blood:	n/a
18	chr13:51086835-51086885	NT2-D1	testis:	n/a
19	chr13:51086835-51086885	HCM	heart:	n/a
20	chr13:51086835-51086885	HRPEpiC	eye:	n/a
21	chr13:51086835-51086885	HEK293	kidney:	embryo
22	chr13:51086835-51086885	HAEpiC	amniotic membrane:	n/a
23	chr13:51086835-51086885	SK-N-MC	brain:	n/a
24	chr13:51086835-51086885	AoSMC	blood vessel:	n/a
25	chr13:51086835-51086885	PrEC	prostate:	n/a
26	chr13:51086835-51086885	AG10803	skin:	n/a
27	chr13:51086835-51086885	T-47D	breast:	n/a
28	chr13:51086835-51086885	GM12891	blood:	n/a
29	chr13:51086835-51086885	Hepatocyte	liver:	n/a
30	chr13:51086835-51086885	HEEpiC	esophagus:	n/a
31	chr13:51086835-51086885	HepG2	liver:	n/a
32	chr13:51086835-51086885	HRE	kidney:	n/a
33	chr13:51086835-51086885	HIPEpiC	eye:	n/a
34	chr13:51086835-51086885	HRCEpiC	kidney:	n/a
35	chr13:51086835-51086885	K562	blood:	n/a
36	chr13:51086835-51086885	NHBE	bronchial:	n/a
37	chr13:51086835-51086885	AG04450	lung:	fetal
38	chr13:51086835-51086885	RPTEC	kidney:	n/a
39	chr13:51086835-51086885	SK-N-SH_RA	brain:	n/a
40	chr13:51086835-51086885	Jurkat	blood:	n/a
41	chr13:51086835-51086885	HUVEC	blood vessel:	n/a
42	chr13:51086835-51086885	ECC-1	luminal epithelium:	n/a
43	chr13:51086835-51086885	HNPCEpiC	eye:	n/a
44	chr13:51086835-51086885	HPAEpiC	pulmonary alveolar:	n/a
45	chr13:51086835-51086885	BJ	skin:	n/a
46	chr13:51086835-51086885	H1-hESC	embryonic stem cell:	embryo
47	chr13:51086835-51086885	HCF	heart:	n/a
48	chr13:51086835-51086885	GM06990	blood:	n/a
49	chr13:51086835-51086885	HCPEpiC	choroid plexus:	n/a
50	chr13:51086835-51086885	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:50698955..50699740-chr13:51085777..51086281,2	NB4	blood:
2	chr13:51085819..51089100-chr13:51090794..51093089,4	K562	blood:
3	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
4	chr13:51087212..51089990-chr13:51483181..51484978,2	K562	blood:
5	chr13:51085819..51089100-chr13:51090794..51093089,4	K562	blood:
6	chr13:51065916..51068221-chr13:51075145..51077143,2	K562	blood:
7	chr12:132987438..132988105-chr13:51062911..51063480,2	MCF-7	breast:
8	chr13:50569721..50571547-chr13:51085881..51088680,2	MCF-7	breast:
9	chr13:51059299..51061286-chr13:51063138..51065247,2	MCF-7	breast:
10	chr13:51066276..51068266-chr13:51086109..51088000,2	K562	blood:
11	chr13:50655760..50657850-chr13:51088498..51090922,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-3	chr13:51076948-51077016	XLOC_010390
2	lnc-RNASEH2B-3	chr13:51066780-51066897	NONHSAT033861
3	lnc-RNASEH2B-3	chr13:51067608-51067670	NONHSAT033856
4	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033855
5	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033812
6	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033856
7	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033821
8	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033827
9	lnc-RNASEH2B-3	chr13:51086748-51087029	NONHSAT033861
10	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
11	lnc-RNASEH2B-3	chr13:51069312-51069605	NONHSAT033856
12	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033815
13	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033846
14	lnc-RNASEH2B-3	chr13:51066787-51066897	NR_109974
15	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT140131
16	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
17	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033819
18	lnc-RNASEH2B-3	chr13:51066787-51066897	XLOC_010390
19	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033825
20	lnc-RNASEH2B-3	chr13:51066787-51067189	NONHSAT033842
21	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033817
22	lnc-RNASEH2B-3	chr13:51066787-51066897	NONHSAT033850

No data

Variant related genes	Relation type
DLEU1	TF binding region
DLEU1	CpG island
ENSG00000231607	chromatin interactions
ENSG00000264864	chromatin interactions
ENSG00000136104	chromatin interactions
ENSG00000233672	chromatin interactions
ENSG00000204977	chromatin interactions
ENSG00000176124	chromatin interactions
NAGK	miRNA target sites

Extended variants
information (count: 963 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149340	chr13:51061044-51061045	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370755322	chr13:51061052-51061053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186296351	chr13:51061142-51061143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113236292	chr13:51061206-51061207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191081893	chr13:51061218-51061219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201444895	chr13:51061248-51061249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527612258	chr13:51061253-51061254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61964387	chr13:51061300-51061301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549213053	chr13:51061350-51061351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544358689	chr13:51061360-51061361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115624754	chr13:51061364-51061365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531442267	chr13:51061394-51061395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74076636	chr13:51061432-51061433	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs374163093	chr13:51061486-51061487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182147283	chr13:51061516-51061517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538328924	chr13:51061529-51061530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547090341	chr13:51061564-51061565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117935294	chr13:51061581-51061582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115192861	chr13:51061647-51061648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141373168	chr13:51061810-51061811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574385717	chr13:51061847-51061848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556478204	chr13:51061872-51061873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185400920	chr13:51061878-51061879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538471298	chr13:51061901-51061902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556781251	chr13:51061908-51061909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578156055	chr13:51061918-51061919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201764	chr13:51061932-51061933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560289114	chr13:51061955-51061956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs169321	chr13:51061976-51061977	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs61964388	chr13:51061980-51061981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191144520	chr13:51062016-51062017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531480290	chr13:51062031-51062032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549597659	chr13:51062051-51062052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564702753	chr13:51062082-51062083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561985965	chr13:51062095-51062096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182924902	chr13:51062106-51062107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188449626	chr13:51062115-51062116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371782641	chr13:51062209-51062210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192807784	chr13:51062337-51062338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536294200	chr13:51062424-51062425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367643377	chr13:51062449-51062450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182915120	chr13:51062516-51062517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150762956	chr13:51062531-51062532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139140155	chr13:51062555-51062556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77743573	chr13:51062602-51062603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs157175	chr13:51062697-51062698	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553081108	chr13:51062701-51062702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369037696	chr13:51062947-51062948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28896278	chr13:51062960-51062961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192581208	chr13:51062993-51062994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

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
Trisomy	24170809	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Sezary syndrome	18413736	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51058400-51061400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr13:51058400-51061400	Enhancers	Fetal Heart	heart
3	chr13:51059000-51061200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr13:51059200-51061200	Enhancers	Brain Anterior Caudate	brain
5	chr13:51059200-51061400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:51060000-51061200	Enhancers	NHLF	lung
7	chr13:51060200-51061200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr13:51060200-51061200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:51060200-51061200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr13:51060400-51061200	Enhancers	K562	blood
11	chr13:51060600-51061600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr13:51060800-51061200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr13:51060800-51063000	Weak transcription	Fetal Kidney	kidney
14	chr13:51060800-51064000	Weak transcription	Aorta	Aorta
15	chr13:51061000-51061200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr13:51061000-51061200	Enhancers	Fetal Stomach	stomach
17	chr13:51061000-51061200	Enhancers	Osteobl	bone
18	chr13:51064000-51064200	Enhancers	Aorta	Aorta
19	chr13:51065600-51068600	Weak transcription	HepG2	liver
20	chr13:51067200-51068000	Enhancers	Dnd41	blood
21	chr13:51067600-51069400	Enhancers	Fetal Thymus	thymus
22	chr13:51067800-51068000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr13:51067800-51068200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr13:51067800-51068400	Enhancers	K562	blood
25	chr13:51067800-51069000	Enhancers	Primary hematopoietic stem cells	blood
26	chr13:51067800-51069200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr13:51067800-51069200	Enhancers	Thymus	Thymus
28	chr13:51068000-51068200	Flanking Active TSS	Dnd41	blood
29	chr13:51068000-51068600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr13:51068000-51068600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr13:51068000-51069200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr13:51068000-51069400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr13:51068200-51068400	Enhancers	Dnd41	blood
34	chr13:51068200-51068800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:51068200-51069200	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr13:51068200-51069200	Enhancers	Primary T cells from cord blood	blood
37	chr13:51068400-51068600	Flanking Active TSS	Dnd41	blood
38	chr13:51068400-51068800	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr13:51068600-51070000	Enhancers	Dnd41	blood
40	chr13:51069000-51069400	Enhancers	Adipose Nuclei	Adipose
41	chr13:51075000-51075400	Enhancers	Thymus	Thymus
42	chr13:51075000-51075800	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr13:51075000-51075800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr13:51075000-51075800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr13:51075200-51075800	Enhancers	K562	blood
46	chr13:51075400-51083400	Weak transcription	Thymus	Thymus
47	chr13:51075800-51084800	Weak transcription	K562	blood
48	chr13:51082800-51086000	Weak transcription	Gastric	stomach
49	chr13:51083000-51083800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
50	chr13:51083200-51086200	Enhancers	HepG2	liver

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