Variant report

Variant	esv275139
Chromosome Location	chr10:54065821-54069336
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	chr10:54067882-54068596	HepG2	liver:	n/a	n/a
2	BACH1	chr10:54068118-54068400	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr10:54067985-54068716	HepG2	liver:	n/a	n/a
4	CEBPB	chr10:54068298-54068716	HepG2	liver:	n/a	n/a
5	CHD2	chr10:54068108-54068304	HepG2	liver:	n/a	chr10:54068152-54068162
6	CHD2	chr10:54068055-54068746	H1-hESC	embryonic stem cell:	n/a	chr10:54068152-54068162
7	CREB1	chr10:54068461-54068745	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr10:54068049-54068244	MCF-7	breast:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
9	CTCF	chr10:54068100-54068250	K562	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
10	CTCF	chr10:54067995-54068218	SK-N-SH_RA	brain:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
11	CTCF	chr10:54068500-54068650	AG04450	lung:	n/a	n/a
12	CTCF	chr10:54068640-54068790	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr10:54068080-54068230	HCM	heart:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
14	CTCF	chr10:54068040-54068190	HMEC	breast:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
15	CTCF	chr10:54068280-54068430	GM12873	blood:	n/a	n/a
16	CTCF	chr10:54068060-54068210	HMF	breast:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
17	CTCF	chr10:54068080-54068230	GM12869	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
18	CTCF	chr10:54068080-54068230	NHDF-neo	bronchial:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
19	CTCF	chr10:54068060-54068210	HBMEC	blood vessel:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
20	CTCF	chr10:54067626-54068765	A549	lung:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
21	CTCF	chr10:54068060-54068210	NHDF-neo	bronchial:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
22	CTCF	chr10:54068014-54068244	Pancreas_OC	pancreas:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
23	CTCF	chr10:54068800-54068950	AG09309	skin:	n/a	n/a
24	CTCF	chr10:54068053-54068243	H1-hESC	embryonic stem cell:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
25	CTCF	chr10:54068022-54068254	GM10248	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
26	CTCF	chr10:54068020-54068170	WERI-Rb-1	eye:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
27	CTCF	chr10:54068060-54068210	BJ	skin:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
28	CTCF	chr10:54068060-54068210	HL-60	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
29	CTCF	chr10:54068080-54068230	AG04449	skin:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
30	CTCF	chr10:54068040-54068190	AoAF	blood vessel:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
31	CTCF	chr10:54067952-54068314	A549	lung:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
32	CTCF	chr10:54068040-54068190	GM12867	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
33	CTCF	chr10:54068060-54068210	GM12873	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
34	CTCF	chr10:54067929-54068282	ECC-1	luminal epithelium:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
35	CTCF	chr10:54067720-54067870	GM06990	blood:	n/a	n/a
36	CTCF	chr10:54068024-54068246	Hela-S3	cervix:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
37	CTCF	chr10:54068056-54068186	GM20000	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
38	CTCF	chr10:54068060-54068210	AG10803	skin:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
39	CTCF	chr10:54068080-54068230	GM12868	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
40	CTCF	chr10:54068060-54068210	GM12878	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
41	CTCF	chr10:54067990-54068246	Spleen_OC	spleen:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
42	CTCF	chr10:54068040-54068190	HEEpiC	esophagus:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
43	CTCF	chr10:54068040-54068190	AG04449	skin:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
44	CTCF	chr10:54068400-54068550	HFF	foreskin:	n/a	n/a
45	CTCF	chr10:54068060-54068210	GM12871	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
46	CTCF	chr10:54068044-54068251	GM12892	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
47	CTCF	chr10:54068120-54068270	BE2_C	brain:	n/a	chr10:54068121-54068131
48	CTCF	chr10:54068060-54068210	Caco-2	colon:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
49	CTCF	chr10:54068080-54068230	GM12874	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131
50	CTCF	chr10:54068100-54068250	GM12867	blood:	n/a	chr10:54068119-54068132 chr10:54068119-54068128 chr10:54068116-54068134 chr10:54068118-54068139 chr10:54068121-54068131

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54068408-54068458	AG09309	skin:	n/a
2	chr10:54068408-54068458	AG09309	skin:	n/a
3	chr10:54068630-54068680	GM12891	blood:	n/a
4	chr10:54068572-54068622	SKMC	muscle:	n/a
5	chr10:54068630-54068680	HL-60	blood:	n/a
6	chr10:54068462-54068512	AoSMC	blood vessel:	n/a
7	chr10:54068572-54068622	HepG2	liver:	n/a
8	chr10:54068572-54068622	SK-N-SH_RA	brain:	n/a
9	chr10:54068462-54068512	HUVEC	blood vessel:	n/a
10	chr10:54068462-54068512	NHBE	bronchial:	n/a
11	chr10:54068630-54068680	GM06990	blood:	n/a
12	chr10:54068594-54068644	BJ	skin:	n/a
13	chr10:54068408-54068458	Hela-S3	cervix:	n/a
14	chr10:54068572-54068622	HCF	heart:	n/a
15	chr10:54068630-54068680	SK-N-SH_RA	brain:	n/a
16	chr10:54068372-54068422	GM19239	blood:	n/a
17	chr10:54068572-54068622	GM12891	blood:	n/a
18	chr10:54068162-54068212	HMEC	breast:	n/a
19	chr10:54068372-54068422	SK-N-SH	brain:	n/a
20	chr10:54068162-54068212	AG10803	skin:	n/a
21	chr10:54068162-54068212	NH-A	brain:	n/a
22	chr10:54068462-54068512	PANC-1	pancreas:	n/a
23	chr10:54068572-54068622	HIPEpiC	eye:	n/a
24	chr10:54068408-54068458	Jurkat	blood:	n/a
25	chr10:54068594-54068644	LNCaP	prostate:	n/a
26	chr10:54068594-54068644	AG09309	skin:	n/a
27	chr10:54068462-54068512	HCT-116	colon:	n/a
28	chr10:54068462-54068512	H1-hESC	embryonic stem cell:	embryo
29	chr10:54068408-54068458	HCPEpiC	choroid plexus:	n/a
30	chr10:54068572-54068622	LNCaP	prostate:	n/a
31	chr10:54068594-54068644	Caco-2	colon:	n/a
32	chr10:54068572-54068622	RPTEC	kidney:	n/a
33	chr10:54068462-54068512	HEEpiC	esophagus:	n/a
34	chr10:54068594-54068644	U87	brain:	n/a
35	chr10:54068630-54068680	HAEpiC	amniotic membrane:	n/a
36	chr10:54068630-54068680	AG09309	skin:	n/a
37	chr10:54068572-54068622	NHDF-neo	bronchial:	n/a
38	chr10:54068594-54068644	GM19239	blood:	n/a
39	chr10:54068408-54068458	SAEC	small airway:	n/a
40	chr10:54068408-54068458	H1-hESC	embryonic stem cell:	embryo
41	chr10:54068372-54068422	LNCaP	prostate:	n/a
42	chr10:54068372-54068422	MCF10A-Er-Src	breast:	n/a
43	chr10:54068572-54068622	SAEC	small airway:	n/a
44	chr10:54068372-54068422	H1-hESC	embryonic stem cell:	embryo
45	chr10:54068408-54068458	U87	brain:	n/a
46	chr10:54068162-54068212	AG04449	skin:	fetal
47	chr10:54068372-54068422	Caco-2	colon:	n/a
48	chr10:54068594-54068644	MCF10A-Er-Src	breast:	n/a
49	chr10:54068408-54068458	PANC-1	pancreas:	n/a
50	chr10:54068630-54068680	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:54067709..54068556-chr10:54248148..54249084,3	MCF-7	breast:
2	chr10:54067639..54070008-chr10:54219109..54220773,2	MCF-7	breast:
3	chr10:54067410..54068489-chr10:54326361..54327402,3	MCF-7	breast:
4	chr10:54065637..54068534-chr10:54212590..54214631,2	MCF-7	breast:
5	chr10:54068750..54071230-chr10:54072937..54074524,2	K562	blood:
6	chr10:54067641..54068591-chr10:54326099..54327546,12	MCF-7	breast:
7	chr10:54068768..54071357-chr10:54075695..54080723,4	MCF-7	breast:
8	chr10:54060116..54061619-chr10:54068153..54070919,2	MCF-7	breast:
9	chr10:54064937..54068343-chr10:54326262..54329266,3	MCF-7	breast:
10	chr10:54069192..54071123-chr10:54231891..54233668,2	MCF-7	breast:
11	chr10:54068053..54070294-chr10:54245844..54248114,2	MCF-7	breast:
12	chr10:53145130..53146653-chr10:54068648..54071560,2	K562	blood:
13	chr10:54068229..54070730-chr10:54076005..54078630,2	K562	blood:
14	chr10:54068084..54068588-chr10:54200448..54201287,2	MCF-7	breast:
15	chr10:54064374..54069621-chr10:54325572..54329506,5	MCF-7	breast:
16	chr10:54068619..54069176-chr10:54326482..54327373,2	MCF-7	breast:
17	chr10:54065577..54083492-chr10:54193846..54218961,120	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-5	chr10:54069160-54069297	NONHSAT013418
2	lnc-MBL2-5	chr10:54069160-54069297	ENSG00000236671
3	lnc-MBL2-5	chr10:54069160-54069297	NR_038277

Variant related genes	Relation type
DKK1	TF binding region
PRKG1-AS1	TF binding region
DKK1	CpG island
PRKG1-AS1	CpG island
ENSG00000107984	chromatin interactions
ENSG00000236671	chromatin interactions
ENSG00000231131	chromatin interactions
MAP2K1	miRNA target sites

Extended variants
information (count: 151 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:151 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7100461	chr10:54065821-54065822	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563824941	chr10:54065827-54065828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12248083	chr10:54065830-54065831	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577410993	chr10:54065840-54065841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571508181	chr10:54065845-54065846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12249544	chr10:54065862-54065863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532463102	chr10:54065883-54065884	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544917687	chr10:54065935-54065936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565077095	chr10:54066010-54066011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530744607	chr10:54066034-54066035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544519545	chr10:54066076-54066077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560815490	chr10:54066078-54066079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529650930	chr10:54066081-54066082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546143807	chr10:54066083-54066084	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566270186	chr10:54066084-54066085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532060828	chr10:54066092-54066093	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552525134	chr10:54066094-54066095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569455311	chr10:54066095-54066096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184591740	chr10:54066100-54066101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113736045	chr10:54066141-54066142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370055841	chr10:54066150-54066151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548869293	chr10:54066225-54066226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548538745	chr10:54066236-54066237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189873441	chr10:54066310-54066311	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534230411	chr10:54066313-54066314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs181505253	chr10:54066317-54066318	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139447090	chr10:54066344-54066345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200743152	chr10:54066385-54066386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10540789	chr10:54066386-54066387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs398054343	chr10:54066390-54066391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143849590	chr10:54066433-54066434	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577450372	chr10:54066463-54066464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34395134	chr10:54066583-54066584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34532016	chr10:54066592-54066593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs199515304	chr10:54066594-54066595	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539903911	chr10:54066626-54066627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs138528147	chr10:54066696-54066697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141609793	chr10:54066707-54066708	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371904536	chr10:54066772-54066773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184678941	chr10:54066780-54066781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544036638	chr10:54066814-54066815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546302424	chr10:54066827-54066828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576406281	chr10:54066831-54066832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs189608217	chr10:54066836-54066837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560853619	chr10:54066877-54066878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs574389553	chr10:54066882-54066883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539874719	chr10:54066885-54066886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559697082	chr10:54066947-54066948	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115467716	chr10:54066987-54066988	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs552264386	chr10:54067015-54067016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	20164919	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54041400-54068200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:54042800-54068200	Weak transcription	Aorta	Aorta
3	chr10:54043200-54067800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:54045000-54068000	Weak transcription	HSMMtube	muscle
5	chr10:54057200-54068200	Weak transcription	HSMM	muscle
6	chr10:54064600-54067800	Weak transcription	A549	lung
7	chr10:54066800-54067000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr10:54067800-54068000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr10:54067800-54068000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:54067800-54068000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr10:54067800-54068000	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr10:54067800-54068200	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr10:54067800-54068200	Bivalent Enhancer	Primary B cells from cord blood	blood
14	chr10:54067800-54068200	Enhancers	Primary B cells from peripheral blood	blood
15	chr10:54067800-54068200	Enhancers	A549	lung
16	chr10:54067800-54068200	Active TSS	HepG2	liver
17	chr10:54068000-54068200	Active TSS	H1 Cell Line	embryonic stem cell
18	chr10:54068000-54068200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:54068000-54068200	Active TSS	H9 Cell Line	embryonic stem cell
20	chr10:54068000-54068200	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr10:54068000-54068200	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr10:54068000-54068200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr10:54068000-54068200	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr10:54068000-54068200	Active TSS	Primary hematopoietic stem cells	blood
25	chr10:54068000-54068200	Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr10:54068000-54068200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr10:54068000-54068200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:54068000-54068200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr10:54068000-54068200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr10:54068000-54068200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:54068000-54068200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr10:54068000-54068200	Enhancers	Adipose Nuclei	Adipose
33	chr10:54068000-54068200	Active TSS	Brain Germinal Matrix	brain
34	chr10:54068000-54068200	Active TSS	Fetal Intestine Large	intestine
35	chr10:54068000-54068200	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
36	chr10:54068000-54068200	Active TSS	Fetal Muscle Leg	muscle
37	chr10:54068000-54068200	Enhancers	Pancreas	Pancrea
38	chr10:54068000-54068200	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr10:54068000-54068200	Active TSS	Rectal Mucosa Donor 31	rectum
40	chr10:54068000-54068200	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr10:54068000-54068200	Enhancers	HMEC	breast
42	chr10:54068000-54068200	Active TSS	HUVEC	blood vessel
43	chr10:54068000-54068200	Active TSS	NHEK	skin
44	chr10:54068000-54068200	Enhancers	NHLF	lung
45	chr10:54068000-54068400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr10:54068000-54068400	Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr10:54068000-54068400	Active TSS	Fetal Brain Female	brain
48	chr10:54068000-54068400	Active TSS	Fetal Intestine Small	intestine
49	chr10:54068000-54068400	Active TSS	Thymus	Thymus
50	chr10:54068000-54068400	Active TSS	Osteobl	bone

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