Variant report

Variant	esv3321721
Chromosome Location	chr11:63705201-63707749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:63706182-63706239	K562	blood:	n/a	n/a
2	ATF1	chr11:63705937-63706485	K562	blood:	n/a	n/a
3	ATF2	chr11:63706043-63706706	GM12878	blood:	n/a	n/a
4	ATF3	chr11:63706122-63706462	HepG2	liver:	n/a	chr11:63706413-63706422 chr11:63706259-63706268
5	ATF3	chr11:63706052-63706878	H1-hESC	embryonic stem cell:	n/a	chr11:63706413-63706422 chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706259-63706268 chr11:63706655-63706675 chr11:63706655-63706664
6	ATF3	chr11:63706536-63706803	HepG2	liver:	n/a	chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706655-63706675 chr11:63706655-63706664
7	ATF3	chr11:63706037-63706912	H1-hESC	embryonic stem cell:	n/a	chr11:63706413-63706422 chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706259-63706268 chr11:63706655-63706675 chr11:63706655-63706664
8	ATF3	chr11:63706440-63706852	K562	blood:	n/a	chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706655-63706675 chr11:63706655-63706664
9	ATF3	chr11:63706147-63706420	GM12878	blood:	n/a	chr11:63706259-63706268
10	ATF3	chr11:63706538-63706774	GM12878	blood:	n/a	chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706655-63706675 chr11:63706655-63706664
11	ATF3	chr11:63705559-63705815	K562	blood:	n/a	n/a
12	ATF3	chr11:63705695-63706421	A549	lung:	n/a	chr11:63706259-63706268
13	ATF3	chr11:63706106-63706749	K562	blood:	n/a	chr11:63706413-63706422 chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706259-63706268 chr11:63706655-63706675 chr11:63706655-63706664
14	ATF3	chr11:63706070-63706435	K562	blood:	n/a	chr11:63706413-63706422 chr11:63706259-63706268
15	ATF3	chr11:63706024-63706435	GM12878	blood:	n/a	chr11:63706413-63706422 chr11:63706259-63706268
16	ATF3	chr11:63706479-63706896	GM12878	blood:	n/a	chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706655-63706675 chr11:63706655-63706664
17	ATF3	chr11:63705992-63706851	HepG2	liver:	n/a	chr11:63706413-63706422 chr11:63706681-63706701 chr11:63706681-63706690 chr11:63706259-63706268 chr11:63706655-63706675 chr11:63706655-63706664
18	BCL3	chr11:63706082-63706764	A549	lung:	n/a	n/a
19	BCL3	chr11:63705482-63706126	A549	lung:	n/a	n/a
20	BCLAF1	chr11:63705986-63706731	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:63705474-63707341	K562	blood:	n/a	chr11:63706681-63706690 chr11:63706653-63706666 chr11:63705687-63705700 chr11:63707303-63707319 chr11:63706655-63706664 chr11:63705683-63705704 chr11:63705689-63705698 chr11:63707297-63707313 chr11:63705688-63705697 chr11:63706679-63706692 chr11:63706656-63706665 chr11:63706681-63706690 chr11:63706682-63706691 chr11:63705689-63705698 chr11:63706675-63706696 chr11:63706655-63706664
22	BHLHE40	chr11:63705508-63706900	HepG2	liver:	n/a	chr11:63706681-63706690 chr11:63706653-63706666 chr11:63705687-63705700 chr11:63706655-63706664 chr11:63705683-63705704 chr11:63705689-63705698 chr11:63705688-63705697 chr11:63706679-63706692 chr11:63706656-63706665 chr11:63706681-63706690 chr11:63706682-63706691 chr11:63705689-63705698 chr11:63706675-63706696 chr11:63706655-63706664
23	BHLHE40	chr11:63706456-63706854	A549	lung:	n/a	chr11:63706681-63706690 chr11:63706653-63706666 chr11:63706655-63706664 chr11:63706679-63706692 chr11:63706656-63706665 chr11:63706681-63706690 chr11:63706682-63706691 chr11:63706675-63706696 chr11:63706655-63706664
24	BHLHE40	chr11:63705503-63706878	GM12878	blood:	n/a	chr11:63706681-63706690 chr11:63706653-63706666 chr11:63705687-63705700 chr11:63706655-63706664 chr11:63705683-63705704 chr11:63705689-63705698 chr11:63705688-63705697 chr11:63706679-63706692 chr11:63706656-63706665 chr11:63706681-63706690 chr11:63706682-63706691 chr11:63705689-63705698 chr11:63706675-63706696 chr11:63706655-63706664
25	BHLHE40	chr11:63705506-63705970	A549	lung:	n/a	chr11:63705687-63705700 chr11:63705683-63705704 chr11:63705689-63705698 chr11:63705688-63705697 chr11:63705689-63705698
26	BRCA1	chr11:63706052-63706637	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr11:63706451-63706628	GM12878	blood:	n/a	n/a
28	BRCA1	chr11:63705539-63706662	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr11:63707002-63707078	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr11:63706230-63706429	HepG2	liver:	n/a	n/a
31	CBX3	chr11:63705760-63706690	K562	blood:	n/a	n/a
32	CCNT2	chr11:63705940-63706585	K562	blood:	n/a	n/a
33	CEBPB	chr11:63705581-63706587	Hela-S3	cervix:	n/a	chr11:63706013-63706025
34	CEBPB	chr11:63706950-63707285	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:63706969-63707275	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:63706971-63707285	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:63707067-63707267	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr11:63706986-63707393	K562	blood:	n/a	n/a
39	CEBPB	chr11:63706971-63707242	K562	blood:	n/a	n/a
40	CEBPD	chr11:63706089-63706858	HepG2	liver:	n/a	n/a
41	CHD1	chr11:63706497-63706722	GM12878	blood:	n/a	n/a
42	CHD2	chr11:63707178-63707341	K562	blood:	n/a	n/a
43	CHD2	chr11:63706087-63706576	K562	blood:	n/a	n/a
44	CHD2	chr11:63706900-63707379	GM12878	blood:	n/a	n/a
45	CHD2	chr11:63705548-63706589	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr11:63705898-63706690	GM12878	blood:	n/a	n/a
47	CHD2	chr11:63707267-63707406	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr11:63706170-63706589	HepG2	liver:	n/a	n/a
49	CHD2	chr11:63705830-63706820	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr11:63707196-63707458	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63705760-63705810	PANC-1	pancreas:	n/a
2	chr11:63706477-63706527	AG04450	lung:	fetal
3	chr11:63706312-63706362	SK-N-SH	brain:	n/a
4	chr11:63705760-63705810	PANC-1	pancreas:	n/a
5	chr11:63706477-63706527	AG04450	lung:	fetal
6	chr11:63706312-63706362	SK-N-SH	brain:	n/a
7	chr11:63705697-63705747	NB4	blood:	n/a
8	chr11:63706246-63706296	BJ	skin:	n/a
9	chr11:63706491-63706541	HL-60	blood:	n/a
10	chr11:63706275-63706325	IMR90	lung:	fetal
11	chr11:63705760-63705810	HRPEpiC	eye:	n/a
12	chr11:63706275-63706325	HRCEpiC	kidney:	n/a
13	chr11:63705693-63705743	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:63706312-63706362	AoSMC	blood vessel:	n/a
15	chr11:63706477-63706527	Caco-2	colon:	n/a
16	chr11:63705760-63705810	LNCaP	prostate:	n/a
17	chr11:63705946-63705996	T-47D	breast:	n/a
18	chr11:63707354-63707404	IMR90	lung:	fetal
19	chr11:63706491-63706541	HCM	heart:	n/a
20	chr11:63706246-63706296	HRCEpiC	kidney:	n/a
21	chr11:63706279-63706329	AG09319	gingival:	n/a
22	chr11:63706279-63706329	HepG2	liver:	n/a
23	chr11:63706477-63706527	HMEC	breast:	n/a
24	chr11:63706312-63706362	HEK293	kidney:	embryo
25	chr11:63706312-63706362	Hela-S3	cervix:	n/a
26	chr11:63706275-63706325	NHDF-neo	bronchial:	n/a
27	chr11:63705946-63705996	HNPCEpiC	eye:	n/a
28	chr11:63706491-63706541	Hela-S3	cervix:	n/a
29	chr11:63707354-63707404	H1-hESC	embryonic stem cell:	embryo
30	chr11:63705760-63705810	HCF	heart:	n/a
31	chr11:63706491-63706541	SK-N-MC	brain:	n/a
32	chr11:63705946-63705996	BJ	skin:	n/a
33	chr11:63706491-63706541	PANC-1	pancreas:	n/a
34	chr11:63706312-63706362	U87	brain:	n/a
35	chr11:63706279-63706329	LNCaP	prostate:	n/a
36	chr11:63706312-63706362	HRPEpiC	eye:	n/a
37	chr11:63705693-63705743	HIPEpiC	eye:	n/a
38	chr11:63707354-63707404	BJ	skin:	n/a
39	chr11:63705693-63705743	AG04449	skin:	fetal
40	chr11:63706312-63706362	K562	blood:	n/a
41	chr11:63705697-63705747	Hela-S3	cervix:	n/a
42	chr11:63705693-63705743	CMK	blood:	n/a
43	chr11:63707354-63707404	SAEC	small airway:	n/a
44	chr11:63705693-63705743	HRE	kidney:	n/a
45	chr11:63706279-63706329	T-47D	breast:	n/a
46	chr11:63706279-63706329	HL-60	blood:	n/a
47	chr11:63706491-63706541	ProgFib	skin:	n/a
48	chr11:63707354-63707404	U87	brain:	n/a
49	chr11:63706477-63706527	HCM	heart:	n/a
50	chr11:63706246-63706296	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:63704733..63706426-chr11:63742021..63745098,3	K562	blood:
2	chr11:63697160..63699564-chr11:63703957..63705699,2	MCF-7	breast:
3	chr11:63703471..63707661-chr11:63741980..63743610,3	K562	blood:
4	chr11:63683456..63690158-chr11:63704393..63714412,17	K562	blood:
5	chr11:63655390..63658583-chr11:63705235..63708313,3	K562	blood:
6	chr11:63704888..63707484-chr11:63951709..63953319,2	MCF-7	breast:
7	chr11:63705424..63708366-chr11:63719461..63721078,2	MCF-7	breast:
8	chr11:63683018..63687693-chr11:63704987..63708969,9	MCF-7	breast:
9	chr11:63682242..63690244-chr11:63703955..63713214,18	K562	blood:
10	chr11:63531277..63535286-chr11:63705300..63707994,3	MCF-7	breast:
11	chr1:43312160..43312711-chr11:63705230..63706062,2	Hela-S3	cervix:
12	chr11:63683295..63687930-chr11:63703819..63708534,6	MCF-7	breast:
13	chr11:63706023..63706544-chr2:197036114..197036681,2	Hela-S3	cervix:
14	chr11:62606149..62609197-chr11:63704613..63706388,3	MCF-7	breast:
15	chr11:63601389..63603149-chr11:63706339..63708895,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCOR2-2	chr11:63706941-63707041	l_489_chr11:63700870-63707041_76bGuttman_hES

Variant related genes	Relation type
NAA40	TF binding region
NAA40	CpG island
ENSG00000168439	chromatin interactions
ENSG00000110583	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000081320	chromatin interactions
ENSG00000164011	chromatin interactions
ENSG00000188070	chromatin interactions
ENSG00000072518	chromatin interactions
ENSG00000167771	chromatin interactions
ENSG00000256280	chromatin interactions
ENSG00000256100	chromatin interactions
ENSG00000176340	chromatin interactions

Extended variants
information (count: 121 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:121 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572654299	chr11:63705276-63705277	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs146707097	chr11:63705288-63705289	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs34920769	chr11:63705291-63705292	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs35195208	chr11:63705296-63705297	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs537174440	chr11:63705297-63705298	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs35313359	chr11:63705306-63705307	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs192094198	chr11:63705342-63705343	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs35316184	chr11:63705359-63705360	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs557525969	chr11:63705368-63705369	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs570996743	chr11:63705398-63705399	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs540046648	chr11:63705437-63705438	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
12	rs183604733	chr11:63705454-63705455	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
13	rs573600998	chr11:63705457-63705458	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
14	rs113371384	chr11:63705458-63705459	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs541811374	chr11:63705478-63705479	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
16	rs138050800	chr11:63705520-63705521	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs575276784	chr11:63705548-63705549	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs188493568	chr11:63705550-63705551	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs564297859	chr11:63705551-63705552	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs143517545	chr11:63705554-63705555	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs552787242	chr11:63705561-63705562	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs540043158	chr11:63705562-63705563	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs559989921	chr11:63705599-63705600	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs143909481	chr11:63705632-63705633	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs548538870	chr11:63705686-63705687	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs561985462	chr11:63705697-63705698	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs531023348	chr11:63705723-63705724	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs550754906	chr11:63705730-63705731	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs148194905	chr11:63705842-63705843	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs546912734	chr11:63705879-63705880	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs540009886	chr11:63705891-63705892	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs12272430	chr11:63705927-63705928	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs117072054	chr11:63705931-63705932	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs536184017	chr11:63705955-63705956	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs555340329	chr11:63706019-63706020	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs141129984	chr11:63706084-63706085	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs116758591	chr11:63706085-63706086	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs552255510	chr11:63706103-63706104	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs374800106	chr11:63706121-63706122	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs73494181	chr11:63706160-63706161	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs139381927	chr11:63706175-63706176	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs573593168	chr11:63706177-63706178	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs144112381	chr11:63706197-63706198	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs542593686	chr11:63706249-63706250	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs60668438	chr11:63706276-63706277	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530763934	chr11:63706277-63706278	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs550973132	chr11:63706365-63706366	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs564537289	chr11:63706369-63706370	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs374574752	chr11:63706384-63706385	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs376507315	chr11:63706441-63706442	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63697000-63705600	Weak transcription	Right Atrium	heart
2	chr11:63698800-63705600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:63698800-63705600	Weak transcription	Esophagus	oesophagus
4	chr11:63699000-63705600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:63699600-63705400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:63699600-63705600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr11:63699800-63705600	Weak transcription	Fetal Lung	lung
8	chr11:63699800-63705600	Weak transcription	Fetal Muscle Trunk	muscle
9	chr11:63700000-63705400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:63701400-63705600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:63701400-63705600	Weak transcription	Left Ventricle	heart
12	chr11:63702200-63705600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:63702200-63705600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr11:63702200-63705600	Weak transcription	Adipose Nuclei	Adipose
15	chr11:63702400-63705600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:63702400-63705600	Weak transcription	Osteobl	bone
17	chr11:63703000-63705400	Weak transcription	Placenta	Placenta
18	chr11:63703400-63705400	Weak transcription	Right Ventricle	heart
19	chr11:63703600-63705400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:63705000-63705400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:63705000-63705400	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:63705000-63705400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:63705000-63705400	Enhancers	A549	lung
24	chr11:63705000-63705400	Enhancers	HepG2	liver
25	chr11:63705000-63705400	Enhancers	HMEC	breast
26	chr11:63705000-63705400	Enhancers	K562	blood
27	chr11:63705000-63705400	Enhancers	NHEK	skin
28	chr11:63705000-63705600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:63705000-63705600	Weak transcription	Fetal Brain Male	brain
30	chr11:63705000-63705600	Enhancers	Pancreas	Pancrea
31	chr11:63705000-63706000	Flanking Active TSS	Hela-S3	cervix
32	chr11:63705000-63707400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:63705200-63705400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr11:63705200-63705400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:63705200-63705400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:63705200-63705400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:63705200-63705400	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr11:63705200-63705400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr11:63705200-63705400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr11:63705200-63705400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr11:63705200-63705400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:63705200-63705400	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:63705200-63705400	Enhancers	Fetal Intestine Small	intestine
44	chr11:63705200-63705400	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr11:63705200-63705400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr11:63705200-63705400	Enhancers	GM12878-XiMat	blood
47	chr11:63705200-63705600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:63705200-63705600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:63705200-63705600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr11:63705200-63705600	Enhancers	Fetal Kidney	kidney

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