Variant report

Variant	nsv1002937
Chromosome Location	chr1:214793813-214994142
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	chr1:214801287-214801860	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:214851580-214852141	HepG2	liver:	n/a	n/a
3	BACH1	chr1:214814708-214816805	K562	blood:	n/a	n/a
4	BACH1	chr1:214819730-214820815	K562	blood:	n/a	n/a
5	BACH1	chr1:214900725-214900844	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:214801311-214801357	K562	blood:	n/a	n/a
7	BHLHE40	chr1:214801338-214801822	K562	blood:	n/a	n/a
8	BHLHE40	chr1:214900647-214900925	HepG2	liver:	n/a	n/a
9	BRCA1	chr1:214982328-214982560	H1-hESC	embryonic stem cell:	n/a	n/a
10	CCNT2	chr1:214967191-214967381	K562	blood:	n/a	n/a
11	CEBPB	chr1:214827391-214827697	A549	lung:	n/a	chr1:214827550-214827561
12	CEBPB	chr1:214965237-214965625	IMR90	lung:	n/a	chr1:214965420-214965431
13	CEBPB	chr1:214918465-214918660	H1-hESC	embryonic stem cell:	n/a	chr1:214918552-214918563
14	CEBPB	chr1:214851794-214851979	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:214927766-214927987	A549	lung:	n/a	n/a
16	CEBPB	chr1:214967058-214967439	IMR90	lung:	n/a	chr1:214967244-214967255
17	CEBPB	chr1:214830671-214831071	A549	lung:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
18	CEBPB	chr1:214810398-214811004	MCF-7	breast:	n/a	chr1:214810843-214810855 chr1:214810773-214810784
19	CEBPB	chr1:214834681-214834734	K562	blood:	n/a	n/a
20	CEBPB	chr1:214834086-214834891	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:214967073-214967433	HepG2	liver:	n/a	chr1:214967244-214967255
22	CEBPB	chr1:214830736-214831011	H1-hESC	embryonic stem cell:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
23	CEBPB	chr1:214965293-214965553	H1-hESC	embryonic stem cell:	n/a	chr1:214965420-214965431
24	CEBPB	chr1:214967046-214967437	MCF-7	breast:	n/a	chr1:214967244-214967255
25	CEBPB	chr1:214880706-214880907	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:214967062-214967392	ECC-1	luminal epithelium:	n/a	chr1:214967244-214967255
27	CEBPB	chr1:214830691-214831040	HepG2	liver:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
28	CEBPB	chr1:214967105-214967408	Hela-S3	cervix:	n/a	chr1:214967244-214967255
29	CEBPB	chr1:214987721-214987756	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:214856975-214857193	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:214967048-214967390	A549	lung:	n/a	chr1:214967244-214967255
32	CEBPB	chr1:214830668-214831233	K562	blood:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
33	CEBPB	chr1:214965254-214965602	A549	lung:	n/a	chr1:214965420-214965431
34	CEBPB	chr1:214927682-214927970	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:214830675-214831037	A549	lung:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
36	CEBPB	chr1:214843415-214843673	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:214919261-214919341	HepG2	liver:	n/a	chr1:214919286-214919297
38	CEBPB	chr1:214967078-214967492	MCF-7	breast:	n/a	chr1:214967244-214967255
39	CEBPB	chr1:214830682-214831003	Hela-S3	cervix:	n/a	chr1:214830847-214830860 chr1:214830847-214830860 chr1:214830848-214830859 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830849-214830858 chr1:214830847-214830858
40	CEBPB	chr1:214820341-214820549	A549	lung:	n/a	n/a
41	CEBPB	chr1:214810530-214810957	MCF-7	breast:	n/a	chr1:214810843-214810855 chr1:214810773-214810784
42	CEBPB	chr1:214801560-214801803	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:214827546-214827625	H1-hESC	embryonic stem cell:	n/a	chr1:214827550-214827561
44	CEBPB	chr1:214843500-214843544	K562	blood:	n/a	n/a
45	CEBPB	chr1:214967066-214967438	A549	lung:	n/a	chr1:214967244-214967255
46	CEBPB	chr1:214827426-214827654	Hela-S3	cervix:	n/a	chr1:214827550-214827561
47	CEBPB	chr1:214967058-214967504	A549	lung:	n/a	chr1:214967244-214967255
48	CEBPB	chr1:214967059-214967443	H1-hESC	embryonic stem cell:	n/a	chr1:214967244-214967255
49	CEBPB	chr1:214965337-214965585	Hela-S3	cervix:	n/a	chr1:214965420-214965431
50	CEBPB	chr1:214965168-214965730	MCF-7	breast:	n/a	chr1:214965420-214965431

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:214926917-214926967	GM12891	blood:	n/a
2	chr1:214842875-214842925	SKMC	muscle:	n/a
3	chr1:214813712-214813762	GM12892	blood:	n/a
4	chr1:214834360-214834410	IMR90	lung:	fetal
5	chr1:214813712-214813762	SAEC	small airway:	n/a
6	chr1:214832208-214832258	SK-N-MC	brain:	n/a
7	chr1:214857122-214857172	Caco-2	colon:	n/a
8	chr1:214837903-214837953	PFSK-1	brain:	n/a
9	chr1:214926946-214926996	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:214842875-214842925	SK-N-MC	brain:	n/a
11	chr1:214832208-214832258	CMK	blood:	n/a
12	chr1:214881338-214881388	NT2-D1	testis:	n/a
13	chr1:214857122-214857172	H1-hESC	embryonic stem cell:	embryo
14	chr1:214835694-214835744	IMR90	lung:	fetal
15	chr1:214835694-214835744	PFSK-1	brain:	n/a
16	chr1:214857122-214857172	SK-N-SH_RA	brain:	n/a
17	chr1:214813712-214813762	GM19239	blood:	n/a
18	chr1:214837903-214837953	GM12891	blood:	n/a
19	chr1:214857122-214857172	MCF10A-Er-Src	breast:	n/a
20	chr1:214846567-214846617	ECC-1	luminal epithelium:	n/a
21	chr1:214926917-214926967	ProgFib	skin:	n/a
22	chr1:214832208-214832258	AG04450	lung:	fetal
23	chr1:214846567-214846617	HEEpiC	esophagus:	n/a
24	chr1:214832208-214832258	NHBE	bronchial:	n/a
25	chr1:214857122-214857172	Jurkat	blood:	n/a
26	chr1:214857122-214857172	Hepatocyte	liver:	n/a
27	chr1:214926740-214926790	CMK	blood:	n/a
28	chr1:214846567-214846617	SK-N-MC	brain:	n/a
29	chr1:214842875-214842925	HIPEpiC	eye:	n/a
30	chr1:214837903-214837953	ovcar-3	ovarian:	n/a
31	chr1:214834360-214834410	SK-N-MC	brain:	n/a
32	chr1:214857122-214857172	HMEC	breast:	n/a
33	chr1:214837903-214837953	HAEpiC	amniotic membrane:	n/a
34	chr1:214926740-214926790	U87	brain:	n/a
35	chr1:214926946-214926996	BJ	skin:	n/a
36	chr1:214857122-214857172	GM06990	blood:	n/a
37	chr1:214846567-214846617	HRPEpiC	eye:	n/a
38	chr1:214837903-214837953	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:214837903-214837953	HCF	heart:	n/a
40	chr1:214835694-214835744	GM12878	blood:	n/a
41	chr1:214881338-214881388	MCF10A-Er-Src	breast:	n/a
42	chr1:214834360-214834410	HAEpiC	amniotic membrane:	n/a
43	chr1:214813712-214813762	HUVEC	blood vessel:	n/a
44	chr1:214846567-214846617	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:214846567-214846617	NHDF-neo	bronchial:	n/a
46	chr1:214832208-214832258	AG04449	skin:	fetal
47	chr1:214832208-214832258	GM06990	blood:	n/a
48	chr1:214926946-214926996	GM19239	blood:	n/a
49	chr1:214926946-214926996	MCF-7	breast:	n/a
50	chr1:214842875-214842925	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:214834027..214834925-chr1:214981557..214982784,3	MCF-7	breast:
2	chr1:214848173..214850892-chr1:214855334..214857551,2	K562	blood:
3	chr1:214453018..214454782-chr1:214930192..214932149,2	K562	blood:
4	chr1:214801262..214803726-chr1:214809634..214812012,2	MCF-7	breast:
5	chr1:214796160..214799538-chr1:214799766..214802874,3	K562	blood:
6	chr1:214867721..214869870-chr1:214873799..214876588,2	K562	blood:
7	chr1:214961510..214963625-chr1:214964294..214966473,3	K562	blood:
8	chr1:214826908..214828411-chr1:214831248..214833515,2	K562	blood:
9	chr1:214811484..214813559-chr20:55681705..55683750,3	MCF-7	breast:
10	chr1:214904477..214906839-chr1:214908051..214910386,2	K562	blood:
11	chr1:214834027..214834925-chr1:214981557..214982784,3	MCF-7	breast:
12	chr1:214801262..214803726-chr1:214809634..214812012,2	MCF-7	breast:
13	chr1:214808186..214810904-chr1:214813905..214816278,2	K562	blood:
14	chr1:214916105..214918875-chr1:214919117..214921438,3	K562	blood:
15	chr1:214831928..214832819-chr1:215249703..215250277,2	MCF-7	breast:
16	chr1:214833894..214834885-chr1:215699492..215700543,5	MCF-7	breast:
17	chr1:214981501..214983168-chr1:215319349..215320262,5	MCF-7	breast:
18	chr1:214867721..214869870-chr1:214873799..214876588,2	K562	blood:
19	chr1:214850136..214853701-chr1:214856174..214859270,3	MCF-7	breast:
20	chr1:214515058..214515630-chr1:214810706..214811356,2	MCF-7	breast:
21	chr1:214808186..214810904-chr1:214813905..214816278,2	K562	blood:
22	chr1:214800940..214802210-chr1:214810478..214811783,6	MCF-7	breast:
23	chr1:214916105..214918875-chr1:214919117..214921438,2	K562	blood:
24	chr1:214916105..214918875-chr1:214919117..214921438,3	K562	blood:
25	chr1:214839860..214842177-chr1:214843539..214846062,2	K562	blood:
26	chr1:214964650..214967515-chr1:214968725..214970577,2	MCF-7	breast:
27	chr1:214764019..214764657-chr1:214801288..214801935,2	MCF-7	breast:
28	chr1:214961510..214963625-chr1:214964294..214966473,3	K562	blood:
29	chr1:214822003..214824820-chr1:214825524..214828117,3	K562	blood:
30	chr1:214848812..214851960-chr1:214852511..214855713,3	MCF-7	breast:
31	chr1:214775848..214778755-chr1:214793553..214795303,2	K562	blood:
32	chr1:214836037..214839768-chr1:214843506..214845441,3	K562	blood:
33	chr1:214834101..214834893-chr1:215690806..215691569,6	MCF-7	breast:
34	chr1:214840354..214842406-chr1:215740144..215741858,2	MCF-7	breast:
35	chr1:214836037..214839768-chr1:214843506..214845441,3	K562	blood:
36	chr1:214832044..214832744-chr1:215319419..215320008,2	MCF-7	breast:
37	chr1:214505527..214506582-chr1:214801187..214801906,3	MCF-7	breast:
38	chr1:214989020..214991888-chr1:214992425..214995415,2	K562	blood:
39	chr1:214833941..214834902-chr1:215696603..215697420,3	MCF-7	breast:
40	chr1:214848173..214850892-chr1:214853976..214857551,3	K562	blood:
41	chr1:214836037..214838803-chr1:214843803..214845441,2	K562	blood:
42	chr1:214775592..214777676-chr1:214805586..214808335,2	MCF-7	breast:
43	chr1:214831934..214833558-chr1:215696482..215697599,5	MCF-7	breast:
44	chr1:214833968..214834951-chr1:215319332..215320214,6	MCF-7	breast:
45	chr1:214981924..214982642-chr1:215319314..215319817,2	MCF-7	breast:
46	chr1:214776329..214778755-chr1:214793412..214795053,3	K562	blood:
47	chr1:214818661..214820186-chr17:59886646..59888355,2	MCF-7	breast:
48	chr1:214833954..214834916-chr1:215249431..215250403,7	MCF-7	breast:
49	chr1:214800806..214805673-chr1:214807375..214811280,6	MCF-7	breast:
50	chr1:214804097..214806246-chr1:214807582..214811806,3	K562	blood:

Variant related genes	Relation type
CENPF	TF binding region
CENPF	CpG island
ENSG00000143499	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000136636	chromatin interactions
ENSG00000117724	chromatin interactions
ENSG00000224584	chromatin interactions

Extended variants
information (count: 4258 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:4258 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17023277	chr1:214793813-214793814	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150232732	chr1:214793856-214793857	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs59561763	chr1:214793868-214793869	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs564246899	chr1:214793876-214793877	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs117213302	chr1:214793895-214793896	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549953162	chr1:214793955-214793956	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376767238	chr1:214793996-214793997	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs569811667	chr1:214794037-214794038	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376653860	chr1:214794040-214794041	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373857309	chr1:214794041-214794042	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141779900	chr1:214794043-214794044	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148125567	chr1:214794049-214794050	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs141892982	chr1:214794059-214794060	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369501655	chr1:214794067-214794068	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201702404	chr1:214794075-214794076	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372789993	chr1:214794119-214794120	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs139700147	chr1:214794155-214794156	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548936057	chr1:214794171-214794172	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs1050065	chr1:214794173-214794174	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs377444877	chr1:214794190-214794191	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs147545168	chr1:214794191-214794192	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs370239629	chr1:214794228-214794229	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs565713136	chr1:214794234-214794235	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1050066	chr1:214794239-214794240	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145606920	chr1:214794241-214794242	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375031145	chr1:214794278-214794279	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs114104425	chr1:214794279-214794280	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs368399001	chr1:214794301-214794302	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372009319	chr1:214794305-214794306	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558829228	chr1:214794370-214794371	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181891605	chr1:214794397-214794398	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs578082958	chr1:214794400-214794401	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374658044	chr1:214794419-214794420	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565184463	chr1:214794430-214794431	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185608878	chr1:214794492-214794493	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138973567	chr1:214794496-214794497	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140577329	chr1:214794511-214794512	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543322742	chr1:214794523-214794524	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs80220869	chr1:214794526-214794527	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79383566	chr1:214794556-214794557	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541070494	chr1:214794562-214794563	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs111529648	chr1:214794563-214794564	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs563981107	chr1:214794569-214794570	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533059664	chr1:214794584-214794585	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs115870166	chr1:214794595-214794596	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554641688	chr1:214794622-214794623	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145725578	chr1:214794627-214794628	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529079961	chr1:214794633-214794634	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548847627	chr1:214794659-214794660	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543784520	chr1:214794669-214794670	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22522925	CNVD
Primary hepatocellular	22912832	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1144 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214777600-214800400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:214777600-214810800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:214777600-214838600	Weak transcription	Esophagus	oesophagus
4	chr1:214777800-214838400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr1:214778000-214839200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr1:214778200-214803600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr1:214778400-214794200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:214778800-214794000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr1:214781200-214818000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:214781800-214794000	Weak transcription	Fetal Stomach	stomach
11	chr1:214781800-214795800	Weak transcription	Fetal Intestine Small	intestine
12	chr1:214782000-214803800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:214782800-214794000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:214783200-214794000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:214783200-214817800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr1:214783400-214838800	Weak transcription	Fetal Kidney	kidney
17	chr1:214784600-214834000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:214784800-214803600	Weak transcription	Brain Germinal Matrix	brain
19	chr1:214784800-214807400	Weak transcription	Fetal Brain Female	brain
20	chr1:214785600-214819400	Strong transcription	K562	blood
21	chr1:214785600-214843800	Strong transcription	Fetal Thymus	thymus
22	chr1:214785800-214800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr1:214786000-214794600	Weak transcription	Primary T cells from cord blood	blood
24	chr1:214786200-214843000	Strong transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:214786600-214797200	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr1:214786600-214800200	Strong transcription	HUES48 Cell Line	embryonic stem cell
27	chr1:214786600-214833800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:214786600-214843200	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr1:214786800-214800400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr1:214786800-214805200	Strong transcription	Dnd41	blood
31	chr1:214786800-214843800	Strong transcription	Monocytes-CD14+_RO01746	blood
32	chr1:214787200-214798200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:214787600-214796600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:214787600-214842200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr1:214787800-214798600	Strong transcription	HepG2	liver
36	chr1:214787800-214800400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr1:214788000-214803800	Weak transcription	Placenta	Placenta
38	chr1:214788000-214810400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:214788200-214820600	Weak transcription	Fetal Heart	heart
40	chr1:214788600-214803800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:214789000-214794200	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr1:214789000-214837400	Weak transcription	Small Intestine	intestine
43	chr1:214789200-214794400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:214789200-214796800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr1:214789600-214796200	Strong transcription	A549	lung
46	chr1:214789800-214796800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr1:214790400-214797600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:214790600-214795000	Strong transcription	Fetal Muscle Trunk	muscle
49	chr1:214790600-214795000	Strong transcription	Fetal Muscle Leg	muscle
50	chr1:214790600-214795800	Strong transcription	HMEC	breast

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