Variant report

Variant	nsv983206
Chromosome Location	chr11:73565238-73580462
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:124)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 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	ARID3A	chr11:73577409-73577909	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:73579841-73580264	HepG2	liver:	n/a	n/a
3	BCL3	chr11:73577541-73577940	GM12878	blood:	n/a	n/a
4	BCL3	chr11:73577534-73578026	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:73565810-73566116	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:73577613-73577924	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:73570796-73571100	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:73570348-73570400	HepG2	liver:	n/a	chr11:73570382-73570393
9	CEBPB	chr11:73567280-73567544	H1-hESC	embryonic stem cell:	n/a	chr11:73567301-73567312
10	CEBPB	chr11:73567189-73567420	HepG2	liver:	n/a	chr11:73567301-73567312
11	CEBPB	chr11:73571674-73571918	K562	blood:	n/a	n/a
12	CEBPB	chr11:73570829-73571057	K562	blood:	n/a	n/a
13	CEBPB	chr11:73577271-73578045	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:73577571-73578035	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr11:73577674-73577831	GM12878	blood:	n/a	n/a
16	CTCF	chr11:73577580-73577730	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr11:73574280-73574430	HCPEpiC	choroid plexus:	n/a	chr11:73574330-73574339 chr11:73574326-73574339
18	CTCF	chr11:73574300-73574450	HCPEpiC	choroid plexus:	n/a	chr11:73574330-73574339 chr11:73574326-73574339
19	CTCF	chr11:73570040-73570190	GM12873	blood:	n/a	n/a
20	CTCF	chr11:73577740-73577890	MCF-7	breast:	n/a	n/a
21	CUX1	chr11:73577368-73577535	K562	blood:	n/a	n/a
22	E2F4	chr11:73577679-73577844	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:73577232-73577265	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr11:73577119-73578107	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr11:73577585-73577728	HepG2	liver:	n/a	n/a
26	EP300	chr11:73579699-73580187	HepG2	liver:	n/a	n/a
27	EP300	chr11:73568058-73568103	K562	blood:	n/a	n/a
28	EP300	chr11:73577161-73577985	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr11:73577050-73578248	SK-N-SH	brain:	n/a	n/a
30	FOS	chr11:73577199-73577935	MCF10A-Er-Src	breast:	n/a	chr11:73577724-73577736 chr11:73577724-73577735 chr11:73577726-73577734
31	FOS	chr11:73577149-73577956	MCF10A-Er-Src	breast:	n/a	chr11:73577724-73577736 chr11:73577724-73577735 chr11:73577726-73577734
32	FOS	chr11:73577473-73578068	HUVEC	blood vessel:	n/a	chr11:73577724-73577736 chr11:73577724-73577735 chr11:73577726-73577734
33	FOS	chr11:73577150-73577983	MCF10A-Er-Src	breast:	n/a	chr11:73577724-73577736 chr11:73577724-73577735 chr11:73577726-73577734
34	FOS	chr11:73577157-73577979	MCF10A-Er-Src	breast:	n/a	chr11:73577724-73577736 chr11:73577724-73577735 chr11:73577726-73577734
35	FOSL2	chr11:73577254-73578016	A549	lung:	n/a	chr11:73577724-73577736 chr11:73577726-73577734
36	FOSL2	chr11:73577463-73578015	SK-N-SH	brain:	n/a	chr11:73577724-73577736 chr11:73577726-73577734
37	FOSL2	chr11:73577529-73577900	HepG2	liver:	n/a	chr11:73577724-73577736 chr11:73577726-73577734
38	FOSL2	chr11:73577601-73577940	A549	lung:	n/a	chr11:73577724-73577736 chr11:73577726-73577734
39	FOSL2	chr11:73577118-73578197	SK-N-SH	brain:	n/a	chr11:73577724-73577736 chr11:73577726-73577734
40	FOSL2	chr11:73580236-73580640	A549	lung:	n/a	chr11:73580487-73580498
41	FOXA1	chr11:73579762-73580044	HepG2	liver:	n/a	n/a
42	FOXA1	chr11:73568895-73569159	HepG2	liver:	n/a	n/a
43	FOXA2	chr11:73579718-73580090	HepG2	liver:	n/a	n/a
44	GATA2	chr11:73577196-73578117	SH-SY5Y	brain:	n/a	chr11:73577979-73577989
45	GATA2	chr11:73567434-73567729	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr11:73578034-73578100	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr11:73580224-73580818	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr11:73569795-73569936	SH-SY5Y	brain:	n/a	chr11:73569798-73569814 chr11:73569802-73569809 chr11:73569802-73569809 chr11:73569795-73569816 chr11:73569802-73569809 chr11:73569803-73569820
49	GATA3	chr11:73577470-73577658	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr11:73577055-73578187	SK-N-SH	brain:	n/a	chr11:73577979-73577989

(count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73577813-73577863	AG09319	gingival:	n/a
2	chr11:73567838-73567888	NT2-D1	testis:	n/a
3	chr11:73577813-73577863	AG09319	gingival:	n/a
4	chr11:73567838-73567888	NT2-D1	testis:	n/a
5	chr11:73567838-73567888	HCM	heart:	n/a
6	chr11:73567838-73567888	NB4	blood:	n/a
7	chr11:73567838-73567888	HEK293	kidney:	embryo
8	chr11:73577813-73577863	HIPEpiC	eye:	n/a
9	chr11:73577813-73577863	HCF	heart:	n/a
10	chr11:73577813-73577863	HEK293	kidney:	embryo
11	chr11:73577813-73577863	SK-N-SH_RA	brain:	n/a
12	chr11:73567838-73567888	K562	blood:	n/a
13	chr11:73577813-73577863	SK-N-MC	brain:	n/a
14	chr11:73577813-73577863	GM06990	blood:	n/a
15	chr11:73577813-73577863	MCF-7	breast:	n/a
16	chr11:73567838-73567888	NHBE	bronchial:	n/a
17	chr11:73577813-73577863	Hela-S3	cervix:	n/a
18	chr11:73567838-73567888	PFSK-1	brain:	n/a
19	chr11:73577813-73577863	H1-hESC	embryonic stem cell:	embryo
20	chr11:73577813-73577863	T-47D	breast:	n/a
21	chr11:73577813-73577863	HNPCEpiC	eye:	n/a
22	chr11:73577813-73577863	HCPEpiC	choroid plexus:	n/a
23	chr11:73577813-73577863	Caco-2	colon:	n/a
24	chr11:73567838-73567888	GM06990	blood:	n/a
25	chr11:73577813-73577863	ECC-1	luminal epithelium:	n/a
26	chr11:73567838-73567888	HNPCEpiC	eye:	n/a
27	chr11:73567838-73567888	RPTEC	kidney:	n/a
28	chr11:73567838-73567888	AG09319	gingival:	n/a
29	chr11:73577813-73577863	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:73577813-73577863	NHBE	bronchial:	n/a
31	chr11:73567838-73567888	SK-N-MC	brain:	n/a
32	chr11:73577813-73577863	HCM	heart:	n/a
33	chr11:73567838-73567888	HEEpiC	esophagus:	n/a
34	chr11:73577813-73577863	GM12878	blood:	n/a
35	chr11:73567838-73567888	BE2_C	brain:	n/a
36	chr11:73577813-73577863	NH-A	brain:	n/a
37	chr11:73567838-73567888	H1-hESC	embryonic stem cell:	embryo
38	chr11:73577813-73577863	BJ	skin:	n/a
39	chr11:73567838-73567888	BJ	skin:	n/a
40	chr11:73577813-73577863	HepG2	liver:	n/a
41	chr11:73577813-73577863	Hepatocyte	liver:	n/a
42	chr11:73577813-73577863	NB4	blood:	n/a
43	chr11:73577813-73577863	Jurkat	blood:	n/a
44	chr11:73567838-73567888	GM12892	blood:	n/a
45	chr11:73577813-73577863	AoSMC	blood vessel:	n/a
46	chr11:73567838-73567888	Caco-2	colon:	n/a
47	chr11:73567838-73567888	HCPEpiC	choroid plexus:	n/a
48	chr11:73567838-73567888	NH-A	brain:	n/a
49	chr11:73577813-73577863	PANC-1	pancreas:	n/a
50	chr11:73577813-73577863	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:73575595..73577982-chr11:73579126..73581143,2	K562	blood:
2	chr11:73572050..73574537-chr11:73596940..73598526,2	MCF-7	breast:
3	chr11:73559337..73560863-chr11:73574694..73577336,2	K562	blood:
4	chr11:73570812..73572958-chr11:73578378..73580627,2	K562	blood:
5	chr11:73569201..73571625-chr11:73578467..73580588,2	MCF-7	breast:
6	chr11:73579249..73581313-chr11:73590994..73593823,2	K562	blood:
7	chr11:73547802..73550044-chr11:73567818..73570244,2	MCF-7	breast:
8	chr11:73572749..73574418-chr11:73579241..73582235,3	MCF-7	breast:
9	chr11:73570812..73572971-chr11:73578378..73580940,3	K562	blood:
10	chr11:73484187..73487136-chr11:73577769..73579675,2	K562	blood:
11	chr11:73568778..73570652-chr11:73588089..73591014,2	MCF-7	breast:
12	chr11:73568596..73571925-chr11:73573759..73576003,3	K562	blood:
13	chr11:73570812..73572971-chr11:73578378..73580940,3	K562	blood:
14	chr11:73578838..73580724-chr11:73585708..73589795,5	MCF-7	breast:
15	chr11:73572749..73574418-chr11:73579241..73582235,3	MCF-7	breast:
16	chr11:73568596..73571925-chr11:73573759..73576003,3	K562	blood:
17	chr11:73572742..73574859-chr11:73586899..73588515,2	MCF-7	breast:
18	chr11:73528552..73530776-chr11:73572316..73575159,2	K562	blood:
19	chr11:73563616..73566513-chr11:73584114..73587031,2	K562	blood:
20	chr11:73567413..73569720-chr11:73578293..73583542,5	MCF-7	breast:
21	chr11:73470677..73473057-chr11:73568563..73570885,3	K562	blood:
22	chr11:73576374..73578756-chr11:73637961..73639798,2	MCF-7	breast:
23	chr11:73569201..73571625-chr11:73578467..73580588,2	MCF-7	breast:
24	chr11:73569512..73571560-chr11:73581546..73584245,2	K562	blood:
25	chr11:73576169..73580357-chr11:73581447..73584221,5	MCF-7	breast:
26	chr11:73573157..73576108-chr11:73585479..73588302,2	MCF-7	breast:
27	chr11:73574387..73575953-chr11:73575970..73577570,2	MCF-7	breast:
28	chr11:73565085..73567966-chr11:73582133..73584937,2	K562	blood:
29	chr11:73567413..73569720-chr11:73578293..73583542,5	MCF-7	breast:
30	chr11:73570812..73572958-chr11:73578378..73580627,2	K562	blood:
31	chr11:73574387..73575953-chr11:73575970..73577570,2	MCF-7	breast:
32	chr11:73575595..73577982-chr11:73579126..73581143,2	K562	blood:
33	chr11:73571127..73573037-chr11:73586377..73589618,4	MCF-7	breast:
34	chr11:73561541..73564055-chr11:73569091..73571372,2	K562	blood:

No data

Variant related genes	Relation type
CCDC58P5	TF binding region
CCDC58P5	CpG island
ENSG00000181924	chromatin interactions
ENSG00000256681	chromatin interactions
ENSG00000256360	chromatin interactions
ENSG00000256034	chromatin interactions
ENSG00000175575	chromatin interactions
ENSG00000175582	chromatin interactions

Extended variants
information (count: 537 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181037475	chr11:73565254-73565255	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs561141783	chr11:73565275-73565276	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529811977	chr11:73565294-73565295	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs540576609	chr11:73565295-73565296	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370603720	chr11:73565334-73565335	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529282956	chr11:73565367-73565368	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184323002	chr11:73565368-73565369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs58695771	chr11:73565392-73565393	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs552587568	chr11:73565483-73565484	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569239929	chr11:73565511-73565512	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12421077	chr11:73565554-73565555	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548344960	chr11:73565567-73565568	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376733110	chr11:73565579-73565580	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529847666	chr11:73565592-73565593	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568647370	chr11:73565621-73565622	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12791617	chr11:73565640-73565641	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs554090255	chr11:73565712-73565713	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190039333	chr11:73565759-73565760	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs539710163	chr11:73565818-73565819	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181220641	chr11:73565826-73565827	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs575084159	chr11:73565850-73565851	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs544306438	chr11:73565899-73565900	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs17132397	chr11:73565917-73565918	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs185310440	chr11:73565931-73565932	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540409946	chr11:73565953-73565954	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376470747	chr11:73565956-73565957	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551733199	chr11:73565971-73565972	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs532461425	chr11:73566089-73566090	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35683504	chr11:73566090-73566091	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150123755	chr11:73566204-73566205	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs568090191	chr11:73566214-73566215	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570994063	chr11:73566217-73566218	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs548702636	chr11:73566220-73566221	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562038595	chr11:73566224-73566225	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs140272395	chr11:73566228-73566229	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs61177720	chr11:73566238-73566239	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190568194	chr11:73566286-73566287	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs2511262	chr11:73566340-73566341	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs550022889	chr11:73566341-73566342	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181442038	chr11:73566352-73566353	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145243174	chr11:73566402-73566403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs137859893	chr11:73566414-73566415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34046676	chr11:73566445-73566446	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs149650841	chr11:73566563-73566564	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533835481	chr11:73566568-73566569	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554028378	chr11:73566595-73566596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577063286	chr11:73566596-73566597	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370394355	chr11:73566689-73566690	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562629945	chr11:73566708-73566709	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372624637	chr11:73566729-73566730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	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
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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73499600-73583800	Weak transcription	Aorta	Aorta
2	chr11:73500200-73574200	Weak transcription	Right Ventricle	heart
3	chr11:73500400-73571400	Weak transcription	Fetal Brain Male	brain
4	chr11:73500400-73583800	Weak transcription	Colonic Mucosa	Colon
5	chr11:73508400-73570600	Weak transcription	Psoas Muscle	Psoas
6	chr11:73508800-73573800	Weak transcription	Spleen	Spleen
7	chr11:73508800-73575400	Weak transcription	Gastric	stomach
8	chr11:73518400-73584000	Weak transcription	Pancreas	Pancrea
9	chr11:73533000-73580400	Weak transcription	Stomach Mucosa	stomach
10	chr11:73537400-73582600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr11:73539000-73577200	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:73539200-73574200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:73539200-73583800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr11:73540000-73571200	Weak transcription	NHDF-Ad	bronchial
15	chr11:73540800-73577400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:73541600-73567000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:73541800-73574000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr11:73541800-73583600	Weak transcription	Esophagus	oesophagus
19	chr11:73542400-73577400	Weak transcription	HUVEC	blood vessel
20	chr11:73542600-73577200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr11:73548800-73582000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:73549400-73567000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr11:73549800-73567200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr11:73549800-73583600	Weak transcription	GM12878-XiMat	blood
25	chr11:73550000-73567000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr11:73550000-73567000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:73550000-73567000	Weak transcription	Primary B cells from cord blood	blood
28	chr11:73550000-73574000	Weak transcription	A549	lung
29	chr11:73550000-73577200	Weak transcription	HSMMtube	muscle
30	chr11:73550400-73565400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:73550400-73565600	Weak transcription	Osteobl	bone
32	chr11:73550400-73574200	Weak transcription	HSMM	muscle
33	chr11:73550400-73577200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:73550400-73577200	Weak transcription	NH-A	brain
35	chr11:73550400-73582400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:73554200-73571200	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr11:73554200-73574800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr11:73554400-73566800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:73554800-73575200	Weak transcription	Ovary	ovary
40	chr11:73555000-73567200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr11:73555000-73570800	Weak transcription	HepG2	liver
42	chr11:73555000-73571400	Weak transcription	Hela-S3	cervix
43	chr11:73555000-73577200	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr11:73555600-73571600	Weak transcription	Colon Smooth Muscle	Colon
45	chr11:73555600-73573800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr11:73556000-73570800	Weak transcription	Brain Germinal Matrix	brain
47	chr11:73556000-73570800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr11:73556200-73567000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:73556200-73570600	Weak transcription	Placenta	Placenta
50	chr11:73556200-73580400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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