Variant report

Variant	esv2752788
Chromosome Location	chr11:5193410-5226318
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	chr11:5218875-5219075	K562	blood:	n/a	n/a
2	ARID3A	chr11:5222439-5222656	K562	blood:	n/a	n/a
3	ARID3A	chr11:5220105-5220182	K562	blood:	n/a	n/a
4	ARID3A	chr11:5226025-5226451	K562	blood:	n/a	n/a
5	ARID3A	chr11:5217315-5217701	K562	blood:	n/a	n/a
6	ARID3A	chr11:5220569-5220574	K562	blood:	n/a	n/a
7	ARID3A	chr11:5194443-5194536	K562	blood:	n/a	n/a
8	ATF1	chr11:5226066-5226378	K562	blood:	n/a	n/a
9	ATF1	chr11:5199045-5199305	K562	blood:	n/a	n/a
10	ATF2	chr11:5226032-5226399	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr11:5226014-5226422	K562	blood:	n/a	n/a
12	BACH1	chr11:5217475-5217660	K562	blood:	n/a	n/a
13	BHLHE40	chr11:5217386-5217656	K562	blood:	n/a	n/a
14	BHLHE40	chr11:5226138-5226199	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:5193299-5193453	K562	blood:	n/a	n/a
16	BRCA1	chr11:5226084-5226312	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr11:5206078-5206231	K562	blood:	n/a	n/a
18	CEBPB	chr11:5218644-5219064	K562	blood:	n/a	n/a
19	CEBPB	chr11:5218668-5219156	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:5199690-5200049	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:5199668-5200048	K562	blood:	n/a	n/a
22	CEBPB	chr11:5218017-5218228	K562	blood:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
23	CEBPB	chr11:5199688-5200003	A549	lung:	n/a	n/a
24	CEBPB	chr11:5199688-5200067	K562	blood:	n/a	n/a
25	CEBPB	chr11:5218052-5218310	H1-hESC	embryonic stem cell:	n/a	chr11:5218173-5218184 chr11:5218171-5218184
26	CEBPB	chr11:5199691-5200054	IMR90	lung:	n/a	n/a
27	CEBPB	chr11:5217466-5217539	K562	blood:	n/a	n/a
28	CHD2	chr11:5195669-5195693	GM12878	blood:	n/a	n/a
29	CHD2	chr11:5226266-5226379	GM12878	blood:	n/a	n/a
30	CTCF	chr11:5217424-5217547	K562	blood:	n/a	n/a
31	CTCF	chr11:5226160-5226310	HUVEC	blood vessel:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
32	CTCF	chr11:5226140-5226290	HPAF	blood vessel:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
33	CTCF	chr11:5226118-5226315	ProgFib	skin:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
34	CTCF	chr11:5226140-5226290	K562	blood:	n/a	chr11:5226196-5226205 chr11:5226193-5226211 chr11:5226195-5226216 chr11:5226194-5226210
35	CTCF	chr11:5226160-5226310	HA-sp	spinal cord:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
36	CTCF	chr11:5226140-5226290	WERI-Rb-1	eye:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
37	CTCF	chr11:5226080-5226230	RPTEC	kidney:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
38	CTCF	chr11:5226160-5226310	HMF	breast:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
39	CTCF	chr11:5226040-5226190	GM12864	blood:	n/a	n/a
40	CTCF	chr11:5225819-5226511	HCT-116	colon:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
41	CTCF	chr11:5226140-5226290	AG09309	skin:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
42	CTCF	chr11:5225800-5226495	A549	lung:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
43	CTCF	chr11:5226120-5226270	GM12801	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
44	CTCF	chr11:5225976-5226439	K562	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
45	CTCF	chr11:5226081-5226325	LNCaP	prostate:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
46	CTCF	chr11:5226120-5226270	HCPEpiC	choroid plexus:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
47	CTCF	chr11:5217340-5217580	K562	blood:	n/a	n/a
48	CTCF	chr11:5226120-5226270	GM12870	blood:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
49	CTCF	chr11:5226117-5226302	Kidney_OC	kidney:	n/a	chr11:5226195-5226216 chr11:5226194-5226210 chr11:5226193-5226211 chr11:5226196-5226205
50	CTCF	chr11:5226060-5226210	NHDF-neo	bronchial:	n/a	chr11:5226194-5226210 chr11:5226196-5226205

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5221539-5221589	HEK293	kidney:	embryo
2	chr11:5223080-5223130	ECC-1	luminal epithelium:	n/a
3	chr11:5223080-5223130	ProgFib	skin:	n/a
4	chr11:5221539-5221589	GM12892	blood:	n/a
5	chr11:5223080-5223130	NH-A	brain:	n/a
6	chr11:5221539-5221589	NT2-D1	testis:	n/a
7	chr11:5221539-5221589	GM12878	blood:	n/a
8	chr11:5221539-5221589	HRCEpiC	kidney:	n/a
9	chr11:5221539-5221589	A549	lung:	n/a
10	chr11:5221539-5221589	AG04449	skin:	fetal
11	chr11:5223080-5223130	NHBE	bronchial:	n/a
12	chr11:5223080-5223130	AG10803	skin:	n/a
13	chr11:5221539-5221589	HNPCEpiC	eye:	n/a
14	chr11:5223080-5223130	GM12878	blood:	n/a
15	chr11:5221539-5221589	NHDF-neo	bronchial:	n/a
16	chr11:5223080-5223130	Hepatocyte	liver:	n/a
17	chr11:5223080-5223130	GM12892	blood:	n/a
18	chr11:5223080-5223130	HRCEpiC	kidney:	n/a
19	chr11:5221539-5221589	CMK	blood:	n/a
20	chr11:5223080-5223130	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:5221539-5221589	SK-N-SH_RA	brain:	n/a
22	chr11:5223080-5223130	GM06990	blood:	n/a
23	chr11:5223080-5223130	K562	blood:	n/a
24	chr11:5221539-5221589	IMR90	lung:	fetal
25	chr11:5221539-5221589	HEEpiC	esophagus:	n/a
26	chr11:5221539-5221589	T-47D	breast:	n/a
27	chr11:5223080-5223130	SK-N-MC	brain:	n/a
28	chr11:5223080-5223130	SK-N-SH	brain:	n/a
29	chr11:5221539-5221589	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:5223080-5223130	AoSMC	blood vessel:	n/a
31	chr11:5223080-5223130	GM12891	blood:	n/a
32	chr11:5223080-5223130	HMEC	breast:	n/a
33	chr11:5223080-5223130	HUVEC	blood vessel:	n/a
34	chr11:5221539-5221589	PANC-1	pancreas:	n/a
35	chr11:5223080-5223130	PrEC	prostate:	n/a
36	chr11:5221539-5221589	AG04450	lung:	fetal
37	chr11:5223080-5223130	HCT-116	colon:	n/a
38	chr11:5223080-5223130	MCF-7	breast:	n/a
39	chr11:5223080-5223130	Jurkat	blood:	n/a
40	chr11:5221539-5221589	HMEC	breast:	n/a
41	chr11:5221539-5221589	RPTEC	kidney:	n/a
42	chr11:5221539-5221589	U87	brain:	n/a
43	chr11:5223080-5223130	U87	brain:	n/a
44	chr11:5221539-5221589	ovcar-3	ovarian:	n/a
45	chr11:5223080-5223130	NB4	blood:	n/a
46	chr11:5221539-5221589	Jurkat	blood:	n/a
47	chr11:5221539-5221589	BJ	skin:	n/a
48	chr11:5221539-5221589	SK-N-MC	brain:	n/a
49	chr11:5223080-5223130	SKMC	muscle:	n/a
50	chr11:5221539-5221589	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
2	chr11:5145799..5146631-chr11:5217510..5218294,2	K562	blood:
3	chr11:5191979..5193506-chr11:5217289..5219722,2	K562	blood:
4	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
5	11:5222789-5225325..11:5527719-5533869	K562	blood:
6	11:5146608-5154908..11:5217159-5218976	K562	blood:
7	chr11:5218893..5221432-chr11:5224834..5227380,3	K562	blood:
8	11:5146608-5154908..11:5222789-5225325	K562	blood:
9	chr11:5222818..5224901-chr11:5309713..5311258,2	K562	blood:
10	11:5222789-5225325..11:5533869-5541626	K562	blood:
11	chr11:5149697..5151826-chr11:5212442..5214718,2	K562	blood:
12	chr11:5188106..5190567-chr11:5193129..5195928,3	K562	blood:
13	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
14	chr11:5191942..5195830-chr11:5198178..5202032,4	K562	blood:
15	chr11:5224202..5227710-chr11:5524990..5527435,3	K562	blood:
16	chr11:5192167..5196032-chr11:5198178..5201494,6	K562	blood:
17	chr11:5216417..5219337-chr11:5231565..5234054,2	K562	blood:
18	chr11:5218102..5224405-chr11:5224720..5231093,9	K562	blood:
19	chr11:5152006..5154660-chr11:5213226..5215210,2	K562	blood:
20	11:5222789-5225325..11:5714465-5718134	K562	blood:
21	chr11:5150860..5154299-chr11:5221551..5224711,3	K562	blood:
22	chr11:5192167..5196032-chr11:5198178..5201494,6	K562	blood:
23	11:5222789-5225325..11:5616559-5618985	H1-hESC	embryonic stem cell:	embryo
24	11:5222789-5225325..11:5469844-5475173	K562	blood:
25	11:5217159-5218976..11:5321718-5325668	K562	blood:
26	chr11:5174124..5177497-chr11:5196224..5198159,3	K562	blood:
27	11:5222789-5225325..11:5250847-5268367	K562	blood:
28	11:5222789-5225325..11:5700314-5707362	K562	blood:
29	chr11:5208760..5213541-chr11:5217325..5221735,4	K562	blood:
30	chr11:5216220..5220735-chr11:5221265..5224295,5	K562	blood:
31	chr11:5217946..5220374-chr11:5295563..5297750,2	K562	blood:
32	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
33	chr11:5150178..5155699-chr11:5220911..5225581,8	K562	blood:
34	11:5217159-5218976..11:5700314-5707362	K562	blood:
35	chr11:5191942..5195830-chr11:5198178..5202032,4	K562	blood:
36	chr11:5151076..5153190-chr11:5193820..5196178,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR51B6-1	chr11:5226271-5226317	XLOC_009040

Variant related genes	Relation type
OR51V1	TF binding region
OR51A1P	TF binding region
OR52A1	TF binding region
OR52Z1	TF binding region
ENSG00000224091	TF binding region
OR51V1	CpG island
OR51A1P	CpG island
OR52A1	CpG island
OR52Z1	CpG island
ENSG00000224091	CpG island
ENSG00000258588	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000187918	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000176748	chromatin interactions
ENSG00000175520	chromatin interactions
ENSG00000171944	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000167355	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000224091	chromatin interactions
ENSG00000176752	chromatin interactions
HSPA13	miRNA target sites

Extended variants
information (count: 1258 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1258 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10768634	chr11:5193410-5193411	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181139604	chr11:5193422-5193423	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546950651	chr11:5193428-5193429	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs568148877	chr11:5193446-5193447	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74051397	chr11:5193475-5193476	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73398616	chr11:5193502-5193503	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs568665167	chr11:5193553-5193554	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs145187517	chr11:5193554-5193555	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs73398618	chr11:5193569-5193570	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs145459184	chr11:5193593-5193594	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs79010688	chr11:5193598-5193599	Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs149177608	chr11:5193677-5193678	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs540188266	chr11:5193730-5193731	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs533957207	chr11:5193765-5193766	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs143291856	chr11:5193776-5193777	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573699188	chr11:5193779-5193780	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138845638	chr11:5193782-5193783	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544276246	chr11:5193858-5193859	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562577267	chr11:5193863-5193864	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186375838	chr11:5193877-5193878	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73398619	chr11:5193899-5193900	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370940396	chr11:5193926-5193927	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs140352255	chr11:5193947-5193948	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs61880399	chr11:5193959-5193960	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545601088	chr11:5193965-5193966	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs59759843	chr11:5193970-5193971	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs58961546	chr11:5193975-5193976	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs61315948	chr11:5193985-5193986	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs151095854	chr11:5193994-5193995	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs59972901	chr11:5193995-5193996	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145427802	chr11:5194052-5194053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568086043	chr11:5194095-5194096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs529254513	chr11:5194116-5194117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs74407219	chr11:5194153-5194154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs10742559	chr11:5194180-5194181	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs56940740	chr11:5194222-5194223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79596209	chr11:5194257-5194258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79769480	chr11:5194261-5194262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189527572	chr11:5194286-5194287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182350202	chr11:5194287-5194288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555701514	chr11:5194289-5194290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377521917	chr11:5194330-5194331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs78884386	chr11:5194408-5194409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187726207	chr11:5194422-5194423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577645499	chr11:5194438-5194439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544809598	chr11:5194450-5194451	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs564667132	chr11:5194481-5194482	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs10742560	chr11:5194503-5194504	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs4910540	chr11:5194530-5194531	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79906388	chr11:5194546-5194547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5193200-5193600	Flanking Active TSS	K562	blood
2	chr11:5193600-5194000	Enhancers	K562	blood
3	chr11:5194000-5199000	Weak transcription	K562	blood
4	chr11:5199000-5200000	Enhancers	K562	blood
5	chr11:5217000-5217200	Enhancers	K562	blood
6	chr11:5217200-5217800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:5217200-5217800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:5217200-5217800	Flanking Active TSS	K562	blood
9	chr11:5217400-5217600	Enhancers	NHLF	lung
10	chr11:5217400-5217800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr11:5217600-5220200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:5217600-5226000	Weak transcription	NHLF	lung
13	chr11:5217800-5219200	Enhancers	K562	blood
14	chr11:5218200-5219400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:5218600-5219800	Enhancers	Osteobl	bone
16	chr11:5219200-5220400	Weak transcription	K562	blood
17	chr11:5219400-5222800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:5220200-5224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:5220400-5223200	Enhancers	K562	blood
20	chr11:5221000-5221800	Enhancers	Brain Germinal Matrix	brain
21	chr11:5221600-5221800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:5221800-5222600	Weak transcription	Brain Germinal Matrix	brain
23	chr11:5222600-5222800	Enhancers	Brain Germinal Matrix	brain
24	chr11:5222600-5223000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:5222800-5223200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:5223000-5229600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:5223200-5224800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:5223200-5224800	Weak transcription	K562	blood
29	chr11:5224200-5226200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:5224800-5225000	Enhancers	K562	blood
31	chr11:5224800-5225200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr11:5225000-5225400	Weak transcription	K562	blood
33	chr11:5225200-5231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr11:5225400-5226400	Enhancers	K562	blood
35	chr11:5226000-5226200	Enhancers	NHLF	lung
36	chr11:5226000-5226400	Enhancers	Osteobl	bone

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