Variant report

Variant	nsv975393
Chromosome Location	chr11:72954333-72969696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:72959863-72960158	H1-hESC	embryonic stem cell:	n/a	chr11:72960028-72960042
2	BACH1	chr11:72959903-72960189	K562	blood:	n/a	chr11:72960028-72960042
3	CEBPB	chr11:72961086-72961398	A549	lung:	n/a	chr11:72961240-72961251
4	CEBPB	chr11:72957396-72957645	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:72968408-72968737	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:72961118-72961319	IMR90	lung:	n/a	chr11:72961240-72961251
7	CEBPB	chr11:72961084-72961401	HepG2	liver:	n/a	chr11:72961240-72961251
8	CEBPB	chr11:72961070-72961441	ECC-1	luminal epithelium:	n/a	chr11:72961240-72961251
9	CEBPB	chr11:72961097-72961361	Hela-S3	cervix:	n/a	chr11:72961240-72961251
10	CEBPB	chr11:72961120-72961296	H1-hESC	embryonic stem cell:	n/a	chr11:72961240-72961251
11	CHD2	chr11:72961802-72961818	HepG2	liver:	n/a	n/a
12	CREB1	chr11:72968449-72968832	A549	lung:	n/a	n/a
13	CTCF	chr11:72953006-72954348	A549	lung:	n/a	chr11:72953825-72953846 chr11:72953836-72953845 chr11:72953531-72953549 chr11:72953830-72953848
14	CTCF	chr11:72964020-72964170	HepG2	liver:	n/a	n/a
15	CTCF	chr11:72969072-72969105	Fibrobl	skin:	n/a	n/a
16	CTCF	chr11:72964000-72964150	GM12864	blood:	n/a	n/a
17	CTCF	chr11:72964020-72964170	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr11:72963960-72964110	AG04449	skin:	n/a	n/a
19	CTCF	chr11:72964046-72964139	HepG2	liver:	n/a	n/a
20	CTCF	chr11:72964040-72964190	GM12865	blood:	n/a	n/a
21	CTCF	chr11:72956240-72956390	BE2_C	brain:	n/a	n/a
22	CTCF	chr11:72964020-72964170	BE2_C	brain:	n/a	n/a
23	CTCF	chr11:72969060-72969210	HRPEpiC	eye:	n/a	chr11:72969105-72969123
24	CTCF	chr11:72964000-72964150	GM12866	blood:	n/a	n/a
25	CTCF	chr11:72964010-72964202	MCF-7	breast:	n/a	n/a
26	CTCF	chr11:72964020-72964170	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr11:72963931-72964191	K562	blood:	n/a	n/a
28	CTCF	chr11:72964000-72964150	GM12878	blood:	n/a	n/a
29	CTCF	chr11:72954300-72954450	GM12878	blood:	n/a	n/a
30	CTCF	chr11:72964000-72964150	K562	blood:	n/a	n/a
31	CTCF	chr11:72969142-72969200	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr11:72969085-72969177	ProgFib	skin:	n/a	chr11:72969105-72969123
33	CTCF	chr11:72963936-72964192	K562	blood:	n/a	n/a
34	CTCF	chr11:72964020-72964170	GM12870	blood:	n/a	n/a
35	CTCF	chr11:72964033-72964177	MCF-7	breast:	n/a	n/a
36	CTCF	chr11:72964047-72964174	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:72964060-72964210	GM06990	blood:	n/a	n/a
38	CTCF	chr11:72964020-72964170	GM12872	blood:	n/a	n/a
39	CTCF	chr11:72964040-72964190	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr11:72964020-72964170	GM12867	blood:	n/a	n/a
41	CTCF	chr11:72963940-72964090	BE2_C	brain:	n/a	n/a
42	CTCF	chr11:72954320-72954470	AG04450	lung:	n/a	n/a
43	CTCF	chr11:72963840-72963990	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr11:72963980-72964130	HRE	kidney:	n/a	n/a
45	CTCF	chr11:72963960-72964110	HCFaa	heart:	n/a	n/a
46	CTCF	chr11:72964020-72964170	HCT-116	colon:	n/a	n/a
47	CTCF	chr11:72964000-72964150	GM12865	blood:	n/a	n/a
48	CTCF	chr11:72964020-72964170	GM12865	blood:	n/a	n/a
49	CTCF	chr11:72954480-72954630	GM12873	blood:	n/a	n/a
50	CTCF	chr11:72968940-72969090	RPTEC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72968848-72968898	HNPCEpiC	eye:	n/a
2	chr11:72968848-72968898	ProgFib	skin:	n/a
3	chr11:72968848-72968898	HRE	kidney:	n/a
4	chr11:72968848-72968898	LNCaP	prostate:	n/a
5	chr11:72968848-72968898	HRPEpiC	eye:	n/a
6	chr11:72968848-72968898	HIPEpiC	eye:	n/a
7	chr11:72968848-72968898	AG04449	skin:	fetal
8	chr11:72968848-72968898	AG04450	lung:	fetal
9	chr11:72968848-72968898	ovcar-3	ovarian:	n/a
10	chr11:72968848-72968898	A549	lung:	n/a
11	chr11:72968848-72968898	NHDF-neo	bronchial:	n/a
12	chr11:72968848-72968898	HRCEpiC	kidney:	n/a
13	chr11:72968848-72968898	Caco-2	colon:	n/a
14	chr11:72968848-72968898	PANC-1	pancreas:	n/a
15	chr11:72968848-72968898	RPTEC	kidney:	n/a
16	chr11:72968848-72968898	HCT-116	colon:	n/a
17	chr11:72968848-72968898	NT2-D1	testis:	n/a
18	chr11:72968848-72968898	HMEC	breast:	n/a
19	chr11:72968848-72968898	HepG2	liver:	n/a
20	chr11:72968848-72968898	NH-A	brain:	n/a
21	chr11:72968848-72968898	NB4	blood:	n/a
22	chr11:72968848-72968898	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:72968848-72968898	HUVEC	blood vessel:	n/a
24	chr11:72968848-72968898	Hepatocyte	liver:	n/a
25	chr11:72968848-72968898	AoSMC	blood vessel:	n/a
26	chr11:72968848-72968898	AG09309	skin:	n/a
27	chr11:72968848-72968898	HEK293	kidney:	embryo
28	chr11:72968848-72968898	MCF-7	breast:	n/a
29	chr11:72968848-72968898	HCM	heart:	n/a
30	chr11:72968848-72968898	SK-N-MC	brain:	n/a
31	chr11:72968848-72968898	HCPEpiC	choroid plexus:	n/a
32	chr11:72968848-72968898	SKMC	muscle:	n/a
33	chr11:72968848-72968898	GM12878	blood:	n/a
34	chr11:72968848-72968898	U87	brain:	n/a
35	chr11:72968848-72968898	PFSK-1	brain:	n/a
36	chr11:72968848-72968898	GM12891	blood:	n/a
37	chr11:72968848-72968898	MCF10A-Er-Src	breast:	n/a
38	chr11:72968848-72968898	AG10803	skin:	n/a
39	chr11:72968848-72968898	SAEC	small airway:	n/a
40	chr11:72968848-72968898	K562	blood:	n/a
41	chr11:72968848-72968898	BE2_C	brain:	n/a
42	chr11:72968848-72968898	IMR90	lung:	fetal
43	chr11:72968848-72968898	AG09319	gingival:	n/a
44	chr11:72968848-72968898	HAEpiC	amniotic membrane:	n/a
45	chr11:72968848-72968898	GM06990	blood:	n/a
46	chr11:72968848-72968898	BJ	skin:	n/a
47	chr11:72968848-72968898	T-47D	breast:	n/a
48	chr11:72968848-72968898	PrEC	prostate:	n/a
49	chr11:72968848-72968898	H1-hESC	embryonic stem cell:	embryo
50	chr11:72968848-72968898	HL-60	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:72542208..72542723-chr11:72953527..72954347,2	MCF-7	breast:
2	chr11:72952611..72954570-chr11:72995302..72997462,2	MCF-7	breast:
3	chr11:72953671..72955860-chr11:72968822..72970580,2	K562	blood:
4	chr11:72944490..72946453-chr11:72952891..72955306,2	MCF-7	breast:
5	chr11:72943180..72944892-chr11:72951598..72954377,2	K562	blood:
6	chr11:72895927..72897022-chr11:72953325..72954606,11	MCF-7	breast:
7	chr11:72952515..72955647-chr11:72999946..73001920,3	MCF-7	breast:
8	chr11:72968010..72971100-chr11:72972272..72977350,4	MCF-7	breast:
9	chr11:72953671..72955860-chr11:72968822..72970580,2	K562	blood:
10	chr11:72948068..72951441-chr11:72952296..72954651,3	K562	blood:
11	chr11:72956033..72957650-chr11:72958875..72961424,2	K562	blood:
12	chr11:72635726..72636238-chr11:72953409..72954338,2	K562	blood:
13	chr11:72951072..72954969-chr11:72955033..72959684,5	MCF-7	breast:
14	chr11:72938389..72940654-chr11:72953845..72956300,2	MCF-7	breast:
15	chr11:72968142..72972004-chr11:72979481..72982441,3	MCF-7	breast:
16	chr11:72536642..72539499-chr11:72952238..72954950,2	K562	blood:
17	chr11:72951072..72954969-chr11:72955033..72959684,5	MCF-7	breast:
18	chr11:72955205..72958712-chr11:72959687..72962653,3	MCF-7	breast:
19	chr11:72953739..72954341-chr11:73000494..73001410,2	MCF-7	breast:
20	chr11:72969464..72972035-chr11:72974532..72976271,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-P2RY6-1	chr11:72969046-72970234	XLOC_009208
2	lnc-P2RY6-1	chr11:72964638-72964852	XLOC_009208
3	lnc-P2RY2-4	chr11:72960369-72960912	NONHSAT022818
4	lnc-P2RY2-4	chr11:72959824-72960043	NONHSAT022818

No data

Variant related genes	Relation type
OR8R1P	TF binding region
OR8R1P	CpG island
ENSG00000256347	chromatin interactions
ENSG00000171631	chromatin interactions
ENSG00000260401	chromatin interactions

Extended variants
information (count: 611 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554412557	chr11:72954373-72954374	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs375725424	chr11:72954374-72954375	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540062461	chr11:72954386-72954387	Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs536400823	chr11:72954416-72954417	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs3814728	chr11:72954449-72954450	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs369660296	chr11:72954479-72954480	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs190064850	chr11:72954484-72954485	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs531786938	chr11:72954485-72954486	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs139092607	chr11:72954541-72954542	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562052086	chr11:72954666-72954667	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs576371238	chr11:72954667-72954668	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527841952	chr11:72954697-72954698	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373260800	chr11:72954702-72954703	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144516158	chr11:72954717-72954718	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1557452	chr11:72954731-72954732	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533428527	chr11:72954741-72954742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76823251	chr11:72954763-72954764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146625321	chr11:72954767-72954768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183058278	chr11:72954800-72954801	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1791923	chr11:72954809-72954810	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568064995	chr11:72954831-72954832	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533961029	chr11:72954844-72954845	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553670782	chr11:72954849-72954850	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs577138321	chr11:72954948-72954949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546117398	chr11:72954949-72954950	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565764796	chr11:72954953-72954954	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187298773	chr11:72954969-72954970	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556538946	chr11:72955017-72955018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112628758	chr11:72955033-72955034	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372730150	chr11:72955034-72955035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs34284315	chr11:72955045-72955046	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535313748	chr11:72955049-72955050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs539659707	chr11:72955068-72955069	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562186260	chr11:72955097-72955098	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75965639	chr11:72955101-72955102	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527801936	chr11:72955104-72955105	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs558939816	chr11:72955113-72955114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs559598	chr11:72955157-72955158	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576762568	chr11:72955185-72955186	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142418800	chr11:72955202-72955203	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564498436	chr11:72955207-72955208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs59648065	chr11:72955215-72955216	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs78428226	chr11:72955217-72955218	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs193288202	chr11:72955231-72955232	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547898381	chr11:72955244-72955245	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs574722	chr11:72955248-72955249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375743064	chr11:72955264-72955265	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568113064	chr11:72955286-72955287	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7109731	chr11:72955314-72955315	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553880400	chr11:72955357-72955358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72946600-72954400	Enhancers	Right Ventricle	heart
2	chr11:72949600-72954400	Enhancers	HMEC	breast
3	chr11:72951600-72954400	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr11:72951800-72956200	Weak transcription	Lung	lung
5	chr11:72952000-72956800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:72952600-72954400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:72953000-72962000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr11:72953200-72954400	Enhancers	NHEK	skin
9	chr11:72953200-72954800	Enhancers	Placenta Amnion	Placenta Amnion
10	chr11:72953200-72955400	Enhancers	Spleen	Spleen
11	chr11:72953400-72954400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:72953400-72954400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:72953400-72954400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr11:72953400-72954600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr11:72953400-72954800	Enhancers	Placenta	Placenta
16	chr11:72953600-72954400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr11:72953800-72954400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr11:72953800-72956000	Weak transcription	Osteobl	bone
19	chr11:72953800-72956600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr11:72954000-72954400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr11:72954000-72955400	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr11:72954000-72963600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr11:72954200-72954400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr11:72954200-72954400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:72954200-72954600	Enhancers	A549	lung
26	chr11:72954200-72954600	Enhancers	GM12878-XiMat	blood
27	chr11:72954200-72954600	Enhancers	HepG2	liver
28	chr11:72954200-72954800	Strong transcription	Esophagus	oesophagus
29	chr11:72954200-72954800	Enhancers	Fetal Lung	lung
30	chr11:72954200-72955600	Weak transcription	Brain Germinal Matrix	brain
31	chr11:72954200-72955600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:72954200-72955800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:72954200-72955800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:72954200-72955800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr11:72954200-72955800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr11:72954200-72955800	Weak transcription	Fetal Heart	heart
37	chr11:72954200-72956000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:72954200-72956000	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr11:72954200-72956000	Weak transcription	Right Atrium	heart
40	chr11:72954200-72956200	Weak transcription	NHDF-Ad	bronchial
41	chr11:72954200-72956400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr11:72954200-72956800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr11:72954200-72956800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:72954200-72957000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr11:72954200-72958200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:72954200-72959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr11:72954200-72959800	Weak transcription	Hela-S3	cervix
48	chr11:72954200-72961000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr11:72954200-72964000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr11:72954200-72968600	Weak transcription	Left Ventricle	heart

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