Variant report

Variant	nsv900088
Chromosome Location	chr13:53250839-53274936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:119)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:119 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:53269894-53270461	GM12878	blood:	n/a	n/a
2	ATF2	chr13:53269953-53270338	GM12878	blood:	n/a	n/a
3	BATF	chr13:53269992-53270317	GM12878	blood:	n/a	n/a
4	BATF	chr13:53269961-53270417	GM12878	blood:	n/a	n/a
5	BCL3	chr13:53258541-53258847	GM12878	blood:	n/a	n/a
6	BCL3	chr13:53269920-53270452	GM12878	blood:	n/a	n/a
7	BHLHE40	chr13:53270080-53270290	GM12878	blood:	n/a	n/a
8	CEBPB	chr13:53255146-53255178	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:53269919-53270278	HepG2	liver:	n/a	n/a
10	CEBPB	chr13:53269917-53270303	IMR90	lung:	n/a	n/a
11	CREB1	chr13:53269983-53270419	GM12878	blood:	n/a	n/a
12	CTCF	chr13:53270818-53270899	GM10248	blood:	n/a	n/a
13	CTCF	chr13:53252842-53252930	Fibrobl	skin:	n/a	n/a
14	CTCF	chr13:53263990-53264096	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:53263935-53264093	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr13:53256200-53256350	Caco-2	colon:	n/a	n/a
17	E2F4	chr13:53267495-53267683	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr13:53270107-53270332	GM12878	blood:	n/a	n/a
19	EP300	chr13:53269503-53269506	GM12878	blood:	n/a	n/a
20	EP300	chr13:53251518-53252891	SK-N-SH	brain:	n/a	n/a
21	EP300	chr13:53252053-53252287	K562	blood:	n/a	n/a
22	EP300	chr13:53257471-53257811	K562	blood:	n/a	n/a
23	EP300	chr13:53269998-53270253	GM12878	blood:	n/a	n/a
24	EP300	chr13:53269838-53270309	GM12878	blood:	n/a	n/a
25	FAM48A	chr13:53273632-53273780	GM12878	blood:	n/a	n/a
26	FOS	chr13:53265019-53265219	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr13:53265117-53265192	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:53269994-53270316	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr13:53270023-53270297	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr13:53265095-53265201	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:53269983-53270309	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:53270024-53270315	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA1	chr13:53270460-53270688	HepG2	liver:	n/a	n/a
34	FOXA2	chr13:53269989-53270238	HepG2	liver:	n/a	n/a
35	FOXM1	chr13:53269921-53270286	GM12878	blood:	n/a	n/a
36	GATA1	chr13:53251803-53252694	PBDE	blood:	n/a	n/a
37	GATA3	chr13:53251841-53252507	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr13:53252084-53252333	SH-SY5Y	brain:	n/a	n/a
39	HMGN3	chr13:53252026-53252223	K562	blood:	n/a	n/a
40	IRF4	chr13:53269965-53270291	GM12878	blood:	n/a	n/a
41	MAFK	chr13:53268572-53268660	HepG2	liver:	n/a	chr13:53268588-53268599 chr13:53268587-53268598 chr13:53268587-53268598 chr13:53268583-53268599 chr13:53268586-53268600 chr13:53268588-53268599
42	MAZ	chr13:53268647-53268659	HepG2	liver:	n/a	n/a
43	MYC	chr13:53266052-53266064	MCF10A-Er-Src	breast:	n/a	n/a
44	MYC	chr13:53252891-53252947	MCF-7	breast:	n/a	n/a
45	MYC	chr13:53270086-53270282	MCF10A-Er-Src	breast:	n/a	n/a
46	NFATC1	chr13:53269825-53270385	GM12878	blood:	n/a	n/a
47	NFATC1	chr13:53269880-53270506	GM12878	blood:	n/a	n/a
48	NFE2	chr13:53262334-53262423	GM12878	blood:	n/a	n/a
49	NFIC	chr13:53269840-53270370	GM12878	blood:	n/a	n/a
50	NFYB	chr13:53270094-53270235	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53262275-53262325	HCT-116	colon:	n/a
2	chr13:53262275-53262325	AG09319	gingival:	n/a
3	chr13:53262275-53262325	Jurkat	blood:	n/a
4	chr13:53262275-53262325	PANC-1	pancreas:	n/a
5	chr13:53262275-53262325	A549	lung:	n/a
6	chr13:53262275-53262325	PrEC	prostate:	n/a
7	chr13:53262275-53262325	HRCEpiC	kidney:	n/a
8	chr13:53262275-53262325	LNCaP	prostate:	n/a
9	chr13:53262275-53262325	SAEC	small airway:	n/a
10	chr13:53262275-53262325	GM06990	blood:	n/a
11	chr13:53262275-53262325	HCPEpiC	choroid plexus:	n/a
12	chr13:53262275-53262325	GM12891	blood:	n/a
13	chr13:53262275-53262325	SKMC	muscle:	n/a
14	chr13:53262275-53262325	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:53262275-53262325	CMK	blood:	n/a
16	chr13:53262275-53262325	NB4	blood:	n/a
17	chr13:53262275-53262325	GM19239	blood:	n/a
18	chr13:53262275-53262325	NT2-D1	testis:	n/a
19	chr13:53262275-53262325	Hepatocyte	liver:	n/a
20	chr13:53262275-53262325	HNPCEpiC	eye:	n/a
21	chr13:53262275-53262325	GM12892	blood:	n/a
22	chr13:53262275-53262325	HRE	kidney:	n/a
23	chr13:53262275-53262325	HEK293	kidney:	embryo
24	chr13:53262275-53262325	BJ	skin:	n/a
25	chr13:53262275-53262325	HRPEpiC	eye:	n/a
26	chr13:53262275-53262325	ProgFib	skin:	n/a
27	chr13:53262275-53262325	HAEpiC	amniotic membrane:	n/a
28	chr13:53262275-53262325	ECC-1	luminal epithelium:	n/a
29	chr13:53262275-53262325	NHDF-neo	bronchial:	n/a
30	chr13:53262275-53262325	T-47D	breast:	n/a
31	chr13:53262275-53262325	HEEpiC	esophagus:	n/a
32	chr13:53262275-53262325	AG10803	skin:	n/a
33	chr13:53262275-53262325	HCF	heart:	n/a
34	chr13:53262275-53262325	MCF10A-Er-Src	breast:	n/a
35	chr13:53262275-53262325	HL-60	blood:	n/a
36	chr13:53262275-53262325	HepG2	liver:	n/a
37	chr13:53262275-53262325	ovcar-3	ovarian:	n/a
38	chr13:53262275-53262325	PFSK-1	brain:	n/a
39	chr13:53262275-53262325	AG04450	lung:	fetal
40	chr13:53262275-53262325	SK-N-SH_RA	brain:	n/a
41	chr13:53262275-53262325	Caco-2	colon:	n/a
42	chr13:53262275-53262325	BE2_C	brain:	n/a
43	chr13:53262275-53262325	AG09309	skin:	n/a
44	chr13:53262275-53262325	MCF-7	breast:	n/a
45	chr13:53262275-53262325	SK-N-SH	brain:	n/a
46	chr13:53262275-53262325	HMEC	breast:	n/a
47	chr13:53262275-53262325	HIPEpiC	eye:	n/a
48	chr13:53262275-53262325	AoSMC	blood vessel:	n/a
49	chr13:53262275-53262325	U87	brain:	n/a
50	chr13:53262275-53262325	AG04449	skin:	fetal

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:53253633..53256352-chr13:53264459..53267100,2	K562	blood:
2	chr13:53225429..53228125-chr13:53249748..53252503,2	K562	blood:
3	chr13:53258335..53260690-chr13:53267146..53270145,2	K562	blood:
4	chr13:53272168..53275270-chr13:53277522..53280783,3	K562	blood:
5	chr13:53031068..53033072-chr13:53251817..53253830,2	K562	blood:
6	chr13:53258383..53260639-chr13:53264833..53266950,2	MCF-7	breast:
7	chr13:53225756..53229849-chr13:53255678..53259863,4	K562	blood:
8	chr13:53270072..53270943-chr2:854831..855664,2	MCF-7	breast:
9	chr13:53264710..53266234-chr13:53267984..53269930,2	K562	blood:
10	chr13:53258383..53260639-chr13:53264833..53266950,2	MCF-7	breast:
11	chr13:53264710..53266234-chr13:53267984..53269930,2	K562	blood:
12	chr13:53258335..53260690-chr13:53267146..53270145,2	K562	blood:
13	chr13:53253633..53256352-chr13:53264459..53267100,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LECT1-1	chr13:53268955-53274883	ENSG00000248190
2	lnc-LECT1-1	chr13:53263722-53263958	ENSG00000248190

No data

Variant related genes	Relation type
SUGT1	TF binding region
SUGT1	CpG island
ENSG00000165416	chromatin interactions
STXBP1	miRNA target sites
EZH2	miRNA target sites

Extended variants
information (count: 907 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs973198	chr13:53250839-53250840	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189402228	chr13:53250857-53250858	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373830068	chr13:53250893-53250894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs180921569	chr13:53250923-53250924	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148293870	chr13:53250958-53250959	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs376523326	chr13:53250984-53250985	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565441655	chr13:53250999-53251000	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532906508	chr13:53251011-53251012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141595289	chr13:53251017-53251018	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs9526974	chr13:53251040-53251041	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs535073469	chr13:53251048-53251049	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs7325840	chr13:53251087-53251088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs568821085	chr13:53251096-53251097	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537714134	chr13:53251105-53251106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557554869	chr13:53251127-53251128	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577748581	chr13:53251134-53251135	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs10603223	chr13:53251214-53251215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534069920	chr13:53251240-53251241	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561048437	chr13:53251355-53251356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554233599	chr13:53251369-53251370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs367972257	chr13:53251383-53251384	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574000514	chr13:53251434-53251435	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185965046	chr13:53251445-53251446	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs34626108	chr13:53251447-53251448	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562827653	chr13:53251462-53251463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576822410	chr13:53251497-53251498	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545687059	chr13:53251503-53251504	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565365695	chr13:53251514-53251515	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201309450	chr13:53251622-53251623	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs191188467	chr13:53251640-53251641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527870531	chr13:53251688-53251689	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539994023	chr13:53251692-53251693	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7996692	chr13:53251733-53251734	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs77113789	chr13:53251762-53251763	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7995188	chr13:53251766-53251767	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs568486436	chr13:53251767-53251768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs67319452	chr13:53251839-53251840	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200236906	chr13:53251842-53251843	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201513655	chr13:53251843-53251844	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199656709	chr13:53251846-53251847	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200674146	chr13:53251847-53251848	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs61644578	chr13:53251861-53251862	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs181114128	chr13:53251890-53251891	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs79389888	chr13:53251923-53251924	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs67330553	chr13:53251924-53251925	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547637121	chr13:53251947-53251948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185426708	chr13:53251983-53251984	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559276466	chr13:53252043-53252044	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528079307	chr13:53252049-53252050	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553636384	chr13:53252064-53252065	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

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
Urothelial carcinoma	21177765	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53227800-53260000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:53228000-53251000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr13:53228200-53256400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:53228400-53254600	Weak transcription	Colonic Mucosa	Colon
5	chr13:53228600-53254600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr13:53229000-53276600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr13:53229200-53268000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr13:53229400-53254600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr13:53229800-53255000	Weak transcription	Spleen	Spleen
10	chr13:53230200-53263600	Weak transcription	Stomach Mucosa	stomach
11	chr13:53230400-53266400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:53230600-53266400	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr13:53230800-53253800	Weak transcription	Fetal Heart	heart
14	chr13:53230800-53277400	Weak transcription	Gastric	stomach
15	chr13:53231200-53262400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr13:53231800-53266400	Strong transcription	Primary monocytes fromperipheralblood	blood
17	chr13:53235200-53276000	Weak transcription	Right Ventricle	heart
18	chr13:53236600-53254600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr13:53236600-53255000	Weak transcription	Lung	lung
20	chr13:53236800-53254400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr13:53236800-53255000	Weak transcription	Aorta	Aorta
22	chr13:53237200-53261800	Weak transcription	Fetal Brain Male	brain
23	chr13:53239000-53255600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:53239200-53254000	Weak transcription	Brain Hippocampus Middle	brain
25	chr13:53239200-53265600	Weak transcription	Brain Angular Gyrus	brain
26	chr13:53239400-53254200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr13:53239400-53255000	Weak transcription	Ovary	ovary
28	chr13:53240400-53255800	Strong transcription	GM12878-XiMat	blood
29	chr13:53240600-53255000	Weak transcription	Esophagus	oesophagus
30	chr13:53240600-53255000	Weak transcription	Pancreas	Pancrea
31	chr13:53240600-53264200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr13:53240600-53275800	Weak transcription	K562	blood
33	chr13:53242000-53254200	Weak transcription	Colon Smooth Muscle	Colon
34	chr13:53242000-53255600	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr13:53242600-53252200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr13:53242600-53252800	Weak transcription	Fetal Intestine Small	intestine
37	chr13:53242600-53253000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr13:53242600-53254600	Weak transcription	Fetal Brain Female	brain
39	chr13:53242600-53254600	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr13:53242600-53255000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr13:53242600-53255000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr13:53242600-53258000	Weak transcription	Small Intestine	intestine
43	chr13:53242800-53253800	Weak transcription	Brain Anterior Caudate	brain
44	chr13:53242800-53254200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr13:53242800-53278600	Weak transcription	Psoas Muscle	Psoas
46	chr13:53243000-53254000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr13:53243200-53259000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr13:53243400-53254400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr13:53243800-53258200	Weak transcription	NHEK	skin
50	chr13:53244200-53253800	Weak transcription	Brain Cingulate Gyrus	brain

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