Variant report

Variant	esv1803100
Chromosome Location	chr13:49576474-49655941
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:122)
Chromatin interactive
region (count:34)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:49638680-49638940	K562	blood:	n/a	n/a
2	ATF1	chr13:49636498-49636856	K562	blood:	n/a	n/a
3	BATF	chr13:49603736-49604000	GM12878	blood:	n/a	n/a
4	BCL11A	chr13:49595347-49595603	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr13:49578416-49578562	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:49636340-49636917	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr13:49634914-49635380	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr13:49595499-49595501	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr13:49637663-49638066	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr13:49636457-49636776	K562	blood:	n/a	n/a
11	CEBPB	chr13:49634839-49635378	Hela-S3	cervix:	n/a	chr13:49635059-49635070
12	CEBPB	chr13:49634872-49635253	K562	blood:	n/a	chr13:49635059-49635070
13	CEBPB	chr13:49634903-49635140	ECC-1	luminal epithelium:	n/a	chr13:49635059-49635070
14	CEBPB	chr13:49601037-49601287	IMR90	lung:	n/a	chr13:49601068-49601076
15	CEBPB	chr13:49634828-49635202	MCF-7	breast:	n/a	chr13:49635059-49635070
16	CEBPB	chr13:49634939-49635198	A549	lung:	n/a	chr13:49635059-49635070
17	CEBPB	chr13:49587234-49587531	HepG2	liver:	n/a	chr13:49587402-49587413
18	CEBPB	chr13:49634879-49635237	HepG2	liver:	n/a	chr13:49635059-49635070
19	CEBPB	chr13:49634879-49635248	MCF-7	breast:	n/a	chr13:49635059-49635070
20	CEBPB	chr13:49616734-49616969	IMR90	lung:	n/a	n/a
21	CEBPB	chr13:49650875-49650904	HepG2	liver:	n/a	chr13:49650890-49650903 chr13:49650890-49650901 chr13:49650892-49650903
22	CEBPB	chr13:49634874-49635253	IMR90	lung:	n/a	chr13:49635059-49635070
23	CEBPB	chr13:49634922-49635214	H1-hESC	embryonic stem cell:	n/a	chr13:49635059-49635070
24	CEBPB	chr13:49634917-49635113	K562	blood:	n/a	chr13:49635059-49635070
25	CEBPB	chr13:49626980-49627181	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:49634858-49635157	K562	blood:	n/a	chr13:49635059-49635070
27	CEBPB	chr13:49634903-49635236	A549	lung:	n/a	chr13:49635059-49635070
28	CEBPB	chr13:49597589-49598035	A549	lung:	n/a	n/a
29	CEBPB	chr13:49587271-49587491	Hela-S3	cervix:	n/a	chr13:49587402-49587413
30	CEBPB	chr13:49597634-49597957	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:49637562-49637969	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr13:49634800-49635299	A549	lung:	n/a	chr13:49635059-49635070
33	CHD2	chr13:49626998-49627315	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr13:49602516-49602531	HepG2	liver:	n/a	n/a
35	CTCF	chr13:49638720-49638870	BE2_C	brain:	n/a	n/a
36	CTCF	chr13:49593565-49593625	GM13977	blood:	n/a	n/a
37	CTCF	chr13:49578049-49578111	K562	blood:	n/a	n/a
38	CTCF	chr13:49628155-49628245	GM10248	blood:	n/a	n/a
39	CTCF	chr13:49638760-49638910	BE2_C	brain:	n/a	n/a
40	CTCF	chr13:49612880-49613030	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr13:49634240-49634390	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr13:49634200-49634350	BJ	skin:	n/a	n/a
43	CTCF	chr13:49653960-49654110	GM12867	blood:	n/a	n/a
44	CTCF	chr13:49638736-49638750	GM10248	blood:	n/a	n/a
45	CTCF	chr13:49638789-49638916	K562	blood:	n/a	n/a
46	CTCF	chr13:49635435-49635468	Fibrobl	skin:	n/a	n/a
47	E2F4	chr13:49627559-49627601	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:49634931-49635198	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:49620754-49620861	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr13:49630291-49630438	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49627807-49627857	Hela-S3	cervix:	n/a
2	chr13:49595616-49595666	SK-N-SH	brain:	n/a
3	chr13:49595616-49595666	NB4	blood:	n/a
4	chr13:49595616-49595666	HCM	heart:	n/a
5	chr13:49627807-49627857	A549	lung:	n/a
6	chr13:49595616-49595666	PrEC	prostate:	n/a
7	chr13:49595616-49595666	HIPEpiC	eye:	n/a
8	chr13:49595616-49595666	HCPEpiC	choroid plexus:	n/a
9	chr13:49627807-49627857	CMK	blood:	n/a
10	chr13:49595616-49595666	NH-A	brain:	n/a
11	chr13:49595616-49595666	HepG2	liver:	n/a
12	chr13:49595616-49595666	AG10803	skin:	n/a
13	chr13:49627807-49627857	BJ	skin:	n/a
14	chr13:49595616-49595666	NHDF-neo	bronchial:	n/a
15	chr13:49627807-49627857	BE2_C	brain:	n/a
16	chr13:49627807-49627857	Caco-2	colon:	n/a
17	chr13:49627807-49627857	Jurkat	blood:	n/a
18	chr13:49595616-49595666	AG04449	skin:	fetal
19	chr13:49627807-49627857	U87	brain:	n/a
20	chr13:49627807-49627857	ProgFib	skin:	n/a
21	chr13:49595616-49595666	PANC-1	pancreas:	n/a
22	chr13:49627807-49627857	HCF	heart:	n/a
23	chr13:49595616-49595666	CMK	blood:	n/a
24	chr13:49595616-49595666	NT2-D1	testis:	n/a
25	chr13:49595616-49595666	AG09309	skin:	n/a
26	chr13:49627807-49627857	K562	blood:	n/a
27	chr13:49595616-49595666	K562	blood:	n/a
28	chr13:49627807-49627857	GM12891	blood:	n/a
29	chr13:49627807-49627857	PrEC	prostate:	n/a
30	chr13:49595616-49595666	GM12891	blood:	n/a
31	chr13:49595616-49595666	HCF	heart:	n/a
32	chr13:49627807-49627857	AoSMC	blood vessel:	n/a
33	chr13:49627807-49627857	Hepatocyte	liver:	n/a
34	chr13:49627807-49627857	PFSK-1	brain:	n/a
35	chr13:49595616-49595666	GM06990	blood:	n/a
36	chr13:49595616-49595666	H1-hESC	embryonic stem cell:	embryo
37	chr13:49595616-49595666	MCF10A-Er-Src	breast:	n/a
38	chr13:49595616-49595666	AG09319	gingival:	n/a
39	chr13:49595616-49595666	AG04450	lung:	fetal
40	chr13:49627807-49627857	GM12892	blood:	n/a
41	chr13:49627807-49627857	T-47D	breast:	n/a
42	chr13:49595616-49595666	NHBE	bronchial:	n/a
43	chr13:49627807-49627857	NT2-D1	testis:	n/a
44	chr13:49595616-49595666	HRE	kidney:	n/a
45	chr13:49627807-49627857	HUVEC	blood vessel:	n/a
46	chr13:49627807-49627857	ECC-1	luminal epithelium:	n/a
47	chr13:49595616-49595666	PFSK-1	brain:	n/a
48	chr13:49627807-49627857	GM06990	blood:	n/a
49	chr13:49627807-49627857	SK-N-SH	brain:	n/a
50	chr13:49595616-49595666	LNCaP	prostate:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:49604135..49605802-chr13:49605947..49607714,2	K562	blood:
2	chr13:49604135..49605802-chr13:49605947..49607714,2	K562	blood:
3	chr13:49593632..49596233-chr13:49598271..49600480,2	K562	blood:
4	chr13:49549971..49551740-chr13:49593482..49595514,2	MCF-7	breast:
5	chr13:49595139..49597075-chr13:49604093..49605906,2	MCF-7	breast:
6	chr13:49612653..49615001-chr13:49616623..49619316,2	K562	blood:
7	chr13:49466661..49468822-chr13:49580224..49582626,2	K562	blood:
8	chr13:49554450..49556211-chr13:49593897..49596163,2	MCF-7	breast:
9	chr13:49548649..49550609-chr13:49593444..49595263,2	MCF-7	breast:
10	chr13:49612653..49615001-chr13:49616623..49619316,2	K562	blood:
11	chr13:49578756..49580621-chr13:49592368..49595270,2	K562	blood:
12	chr13:49597126..49599869-chr13:49609048..49611243,2	MCF-7	breast:
13	chr13:49639889..49641763-chr13:49644416..49646733,2	MCF-7	breast:
14	chr13:49595139..49597075-chr13:49604093..49605906,2	MCF-7	breast:
15	chr13:49561507..49563277-chr13:49591979..49593773,2	MCF-7	breast:
16	chr13:49649325..49651270-chr13:49659429..49661263,2	K562	blood:
17	chr13:49552747..49554579-chr13:49576987..49579021,2	K562	blood:
18	chr13:49548847..49551677-chr13:49633338..49635251,2	K562	blood:
19	chr13:49578756..49580621-chr13:49592368..49595270,2	K562	blood:
20	chr13:49596195..49598292-chr13:49601731..49604447,2	MCF-7	breast:
21	chr13:49593632..49596233-chr13:49598271..49600480,2	K562	blood:
22	chr13:49596195..49598292-chr13:49601731..49604447,2	MCF-7	breast:
23	chr13:49570124..49572139-chr13:49576079..49578417,2	K562	blood:
24	chr13:49548397..49551326-chr13:49595569..49598537,2	MCF-7	breast:
25	chr13:49548799..49551073-chr13:49618380..49620404,2	K562	blood:
26	chr13:49597126..49599869-chr13:49609048..49611243,2	MCF-7	breast:
27	chr13:49638488..49641005-chr13:49654158..49656722,2	K562	blood:
28	chr13:49549824..49551719-chr13:49578466..49580949,2	MCF-7	breast:
29	chr13:49549529..49551263-chr13:49654719..49657031,2	MCF-7	breast:
30	chr13:49575322..49578422-chr13:49581779..49585645,3	K562	blood:
31	chr13:49639889..49641763-chr13:49644416..49646733,2	MCF-7	breast:
32	chr13:49548698..49552354-chr13:49633913..49636847,3	MCF-7	breast:
33	chr13:49638488..49641005-chr13:49654158..49656722,2	K562	blood:
34	chr13:49575322..49578422-chr13:49581779..49585645,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAB39L-3	chr13:49618215-49618518	NONHSAT033729
2	lnc-CAB39L-3	chr13:49618821-49619154	NONHSAT033729
3	lnc-CAB39L-3	chr13:49619592-49620930	NONHSAT033729

No data

Variant related genes	Relation type
RAD17P2	TF binding region
RAD17P2	CpG island
ENSG00000102531	chromatin interactions
ENSG00000201662	chromatin interactions

Extended variants
information (count: 2796 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:2796 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9526512	chr13:49576474-49576475	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142175726	chr13:49576590-49576591	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs117913180	chr13:49576634-49576635	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs9526513	chr13:49576635-49576636	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs549631955	chr13:49576747-49576748	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs73492392	chr13:49576755-49576756	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs189682883	chr13:49576782-49576783	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs151191948	chr13:49576934-49576935	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs571015102	chr13:49576956-49576957	Enhancers Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs369022583	chr13:49577021-49577022	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs553370668	chr13:49577029-49577030	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs192376982	chr13:49577100-49577101	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs139216571	chr13:49577118-49577119	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs542587636	chr13:49577121-49577122	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs114148477	chr13:49577165-49577166	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs576203913	chr13:49577172-49577173	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs77265452	chr13:49577213-49577214	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs543645488	chr13:49577220-49577221	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs4942795	chr13:49577327-49577328	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs538106105	chr13:49577345-49577346	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs533480947	chr13:49577356-49577357	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs533276228	chr13:49577410-49577411	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs560313723	chr13:49577476-49577477	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs184334532	chr13:49577487-49577488	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs9596052	chr13:49577496-49577497	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567948243	chr13:49577498-49577499	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs142345479	chr13:49577501-49577502	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs549849991	chr13:49577509-49577510	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs571438331	chr13:49577510-49577511	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs538420800	chr13:49577529-49577530	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs189431995	chr13:49577553-49577554	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs565797850	chr13:49577559-49577560	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs149560890	chr13:49577597-49577598	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs546926341	chr13:49577628-49577629	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs536552783	chr13:49577740-49577741	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs566798733	chr13:49577747-49577748	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs576099095	chr13:49577773-49577774	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs543478363	chr13:49577781-49577782	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs568288086	chr13:49577794-49577795	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs181829017	chr13:49577839-49577840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186050422	chr13:49577871-49577872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534909424	chr13:49577876-49577877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554476353	chr13:49577898-49577899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61950691	chr13:49577910-49577911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545582954	chr13:49577911-49577912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560745344	chr13:49577995-49577996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567890862	chr13:49577997-49577998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536819919	chr13:49578002-49578003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74075845	chr13:49578035-49578036	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs561462458	chr13:49578069-49578070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Breast cancer	17899364	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
Alveolar rhabdomyosarcoma	16790082	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
Chronic lymphocytic leukemia	21670202	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
Congenital anomalies of the kidney and urinary tract	20467480	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
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD

Chromatin state (count:1087 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49551400-49638800	Weak transcription	Pancreas	Pancrea
2	chr13:49553600-49596200	Weak transcription	Ovary	ovary
3	chr13:49555000-49581600	Weak transcription	Left Ventricle	heart
4	chr13:49557000-49579800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:49557000-49626800	Weak transcription	Right Ventricle	heart
6	chr13:49560000-49587600	Weak transcription	Fetal Kidney	kidney
7	chr13:49560200-49578000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr13:49560200-49581000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr13:49560800-49587200	Weak transcription	Small Intestine	intestine
10	chr13:49563800-49583400	Weak transcription	Fetal Heart	heart
11	chr13:49566000-49585400	Weak transcription	Fetal Stomach	stomach
12	chr13:49567000-49580200	Weak transcription	HSMM	muscle
13	chr13:49568000-49598200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr13:49568600-49580400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr13:49568800-49626800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:49568800-49627000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:49569000-49580200	Weak transcription	Placenta	Placenta
18	chr13:49570400-49584400	Weak transcription	Gastric	stomach
19	chr13:49571200-49584200	Weak transcription	Thymus	Thymus
20	chr13:49572000-49604800	Weak transcription	Aorta	Aorta
21	chr13:49572400-49581400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr13:49573400-49634800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr13:49573600-49584000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr13:49573600-49595600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr13:49574000-49580200	Weak transcription	Hela-S3	cervix
26	chr13:49574200-49585800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr13:49574400-49581400	Weak transcription	HMEC	breast
28	chr13:49574600-49580400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr13:49574600-49580800	Weak transcription	NH-A	brain
30	chr13:49574800-49580200	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr13:49574800-49580200	Weak transcription	Dnd41	blood
32	chr13:49574800-49580400	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr13:49574800-49580800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr13:49574800-49580800	Weak transcription	Duodenum Mucosa	Duodenum
35	chr13:49574800-49583600	Weak transcription	HUVEC	blood vessel
36	chr13:49574800-49585800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr13:49575000-49580800	Weak transcription	Primary B cells from cord blood	blood
38	chr13:49575000-49581400	Weak transcription	Primary T cells from cord blood	blood
39	chr13:49575000-49587200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr13:49575200-49580400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr13:49575600-49580800	Weak transcription	Primary T helper cells PMA-I stimulated	--
42	chr13:49575800-49580200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr13:49576000-49584200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr13:49576000-49587000	Weak transcription	Brain Germinal Matrix	brain
45	chr13:49576200-49577800	ZNF genes & repeats	GM12878-XiMat	blood
46	chr13:49576200-49595400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr13:49576400-49577000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr13:49576800-49577000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr13:49576800-49579800	Weak transcription	NHDF-Ad	bronchial
50	chr13:49576800-49580600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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