Variant report

Variant	nsv823146
Chromosome Location	chr5:95300912-95453557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1815)
CpG islands
(count:427)
Chromatin interactive
region (count:93)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1815 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95305457-95306518	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:95336842-95337451	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:95351898-95352274	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:95323723-95325371	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:95330369-95330382	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:95312516-95312519	K562	blood:	n/a	n/a
7	ARID3A	chr5:95301713-95302152	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:95304820-95305082	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:95359091-95359108	K562	blood:	n/a	n/a
10	ARID3A	chr5:95332827-95333432	HepG2	liver:	n/a	n/a
11	ARID3A	chr5:95446244-95446308	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:95384538-95384656	K562	blood:	n/a	n/a
13	ARID3A	chr5:95309759-95310130	K562	blood:	n/a	n/a
14	ARID3A	chr5:95450977-95451416	HepG2	liver:	n/a	n/a
15	ARID3A	chr5:95322539-95323277	HepG2	liver:	n/a	n/a
16	ARID3A	chr5:95372942-95373299	HepG2	liver:	n/a	n/a
17	ARID3A	chr5:95453250-95454488	HepG2	liver:	n/a	n/a
18	ARID3A	chr5:95353956-95354116	HepG2	liver:	n/a	n/a
19	ARID3A	chr5:95352030-95352315	K562	blood:	n/a	n/a
20	ATF1	chr5:95450456-95450654	K562	blood:	n/a	n/a
21	ATF1	chr5:95309713-95310085	K562	blood:	n/a	n/a
22	ATF1	chr5:95353678-95353980	K562	blood:	n/a	n/a
23	ATF1	chr5:95352046-95352289	K562	blood:	n/a	n/a
24	ATF2	chr5:95309443-95310129	GM12878	blood:	n/a	n/a
25	ATF2	chr5:95309494-95310141	GM12878	blood:	n/a	n/a
26	ATF3	chr5:95309688-95310102	K562	blood:	n/a	n/a
27	BACH1	chr5:95419522-95419564	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr5:95403155-95403208	K562	blood:	n/a	n/a
29	BACH1	chr5:95332618-95332880	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr5:95403879-95404090	K562	blood:	n/a	chr5:95403900-95403914
31	BATF	chr5:95309551-95310064	GM12878	blood:	n/a	n/a
32	BATF	chr5:95309646-95310048	GM12878	blood:	n/a	n/a
33	BCL11A	chr5:95309560-95310076	GM12878	blood:	n/a	n/a
34	BCL11A	chr5:95309598-95309994	GM12878	blood:	n/a	n/a
35	BCL11A	chr5:95419203-95419420	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL3	chr5:95429469-95430215	A549	lung:	n/a	n/a
37	BCLAF1	chr5:95309543-95310083	GM12878	blood:	n/a	n/a
38	BCLAF1	chr5:95403762-95404353	K562	blood:	n/a	chr5:95403903-95403912
39	BCLAF1	chr5:95403803-95404304	K562	blood:	n/a	chr5:95403903-95403912
40	BCLAF1	chr5:95309473-95310082	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:95403758-95403763	K562	blood:	n/a	n/a
42	BHLHE40	chr5:95322641-95323582	HepG2	liver:	n/a	n/a
43	BHLHE40	chr5:95414995-95415053	K562	blood:	n/a	n/a
44	BHLHE40	chr5:95416311-95416524	K562	blood:	n/a	n/a
45	BHLHE40	chr5:95305399-95305961	HepG2	liver:	n/a	n/a
46	BHLHE40	chr5:95384654-95384708	K562	blood:	n/a	n/a
47	BHLHE40	chr5:95309494-95310097	GM12878	blood:	n/a	n/a
48	BHLHE40	chr5:95351971-95352249	K562	blood:	n/a	n/a
49	BHLHE40	chr5:95309600-95310023	K562	blood:	n/a	n/a
50	BRCA1	chr5:95403730-95404260	Hela-S3	cervix:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95310237-95310287	NH-A	brain:	n/a
2	chr5:95361197-95361247	HMEC	breast:	n/a
3	chr5:95413871-95413921	PANC-1	pancreas:	n/a
4	chr5:95413861-95413911	HRE	kidney:	n/a
5	chr5:95419503-95419553	SK-N-SH	brain:	n/a
6	chr5:95409135-95409185	PANC-1	pancreas:	n/a
7	chr5:95413861-95413911	SAEC	small airway:	n/a
8	chr5:95409135-95409185	AG10803	skin:	n/a
9	chr5:95413861-95413911	HCT-116	colon:	n/a
10	chr5:95409135-95409185	HRCEpiC	kidney:	n/a
11	chr5:95310237-95310287	AG09319	gingival:	n/a
12	chr5:95413861-95413911	IMR90	lung:	fetal
13	chr5:95310237-95310287	NB4	blood:	n/a
14	chr5:95321963-95322013	HRE	kidney:	n/a
15	chr5:95413871-95413921	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:95413861-95413911	A549	lung:	n/a
17	chr5:95413871-95413921	HUVEC	blood vessel:	n/a
18	chr5:95419503-95419553	HepG2	liver:	n/a
19	chr5:95361197-95361247	U87	brain:	n/a
20	chr5:95409135-95409185	NT2-D1	testis:	n/a
21	chr5:95310237-95310287	GM06990	blood:	n/a
22	chr5:95413861-95413911	PANC-1	pancreas:	n/a
23	chr5:95361197-95361247	SK-N-MC	brain:	n/a
24	chr5:95409135-95409185	HRPEpiC	eye:	n/a
25	chr5:95419503-95419553	CMK	blood:	n/a
26	chr5:95310237-95310287	SK-N-SH_RA	brain:	n/a
27	chr5:95419503-95419553	T-47D	breast:	n/a
28	chr5:95310237-95310287	PFSK-1	brain:	n/a
29	chr5:95419503-95419553	AG09319	gingival:	n/a
30	chr5:95409135-95409185	HEEpiC	esophagus:	n/a
31	chr5:95310237-95310287	PrEC	prostate:	n/a
32	chr5:95409135-95409185	HCM	heart:	n/a
33	chr5:95419503-95419553	SK-N-SH_RA	brain:	n/a
34	chr5:95413871-95413921	SK-N-SH_RA	brain:	n/a
35	chr5:95409135-95409185	Caco-2	colon:	n/a
36	chr5:95409135-95409185	NHBE	bronchial:	n/a
37	chr5:95419503-95419553	RPTEC	kidney:	n/a
38	chr5:95361197-95361247	Hela-S3	cervix:	n/a
39	chr5:95419503-95419553	GM19239	blood:	n/a
40	chr5:95361197-95361247	ovcar-3	ovarian:	n/a
41	chr5:95361197-95361247	HRPEpiC	eye:	n/a
42	chr5:95409135-95409185	MCF-7	breast:	n/a
43	chr5:95413861-95413911	AG10803	skin:	n/a
44	chr5:95310237-95310287	SAEC	small airway:	n/a
45	chr5:95409135-95409185	Jurkat	blood:	n/a
46	chr5:95413871-95413921	PrEC	prostate:	n/a
47	chr5:95409135-95409185	CMK	blood:	n/a
48	chr5:95361197-95361247	AG04450	lung:	fetal
49	chr5:95409135-95409185	HAEpiC	amniotic membrane:	n/a
50	chr5:95321963-95322013	AG04450	lung:	fetal

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:95385578..95387448-chr5:95403301..95405273,2	K562	blood:
2	chr5:95411135..95413386-chr5:95414339..95416415,2	K562	blood:
3	chr5:95296726..95298627-chr5:95417154..95418671,2	MCF-7	breast:
4	chr5:95262626..95265334-chr5:95402014..95404790,2	K562	blood:
5	chr5:95416575..95419199-chr5:95425271..95427989,2	K562	blood:
6	chr5:95385578..95388383-chr5:95402339..95405273,2	K562	blood:
7	chr5:95401885..95403759-chr5:95409386..95411340,2	K562	blood:
8	chr5:95390171..95391884-chr5:95392902..95395243,2	K562	blood:
9	chr5:95398261..95399913-chr5:95401508..95403607,2	K562	blood:
10	chr5:95363657..95366374-chr5:95368522..95371027,2	MCF-7	breast:
11	chr5:95445238..95446778-chr5:95449413..95451842,2	K562	blood:
12	chr11:64013141..64015957-chr5:95386899..95388399,2	MCF-7	breast:
13	chr5:95309496..95312774-chr5:95317440..95321403,4	K562	blood:
14	chr5:95417552..95419052-chr5:95421414..95423793,2	MCF-7	breast:
15	chr5:95398261..95399913-chr5:95401508..95403607,2	K562	blood:
16	chr5:95394397..95397979-chr5:95402204..95405493,4	K562	blood:
17	chr5:95362269..95364371-chr5:95402115..95403817,2	K562	blood:
18	chr5:95296910..95298799-chr5:95356285..95359042,2	K562	blood:
19	chr5:95296314..95298555-chr5:95397660..95400268,2	K562	blood:
20	chr5:95331250..95333197-chr5:95339157..95340673,2	K562	blood:
21	chr5:95359766..95362858-chr5:95371780..95373834,3	MCF-7	breast:
22	chr5:95403553..95405838-chr5:95406923..95410499,3	K562	blood:
23	chr5:95406044..95407989-chr5:95410489..95412810,2	K562	blood:
24	chr5:95259027..95261912-chr5:95403568..95405178,2	K562	blood:
25	chr5:95363683..95365395-chr5:95366901..95369484,2	K562	blood:
26	chr5:95330891..95333849-chr5:95334417..95336264,2	K562	blood:
27	chr5:95351011..95353911-chr5:95402617..95404215,2	K562	blood:
28	chr5:95294561..95296390-chr5:95300649..95302787,2	MCF-7	breast:
29	chr5:95321789..95324191-chr5:95329308..95331429,2	MCF-7	breast:
30	chr5:95295795..95298001-chr5:95305862..95309802,3	MCF-7	breast:
31	chr5:95295944..95298185-chr5:95343206..95345084,2	K562	blood:
32	chr5:95401831..95405579-chr5:95411274..95417557,7	K562	blood:
33	chr5:95296782..95299195-chr5:95402497..95405358,3	K562	blood:
34	chr5:95322628..95324639-chr5:95325581..95328091,2	K562	blood:
35	chr5:95330891..95333849-chr5:95334417..95336264,2	K562	blood:
36	chr5:95295987..95299495-chr5:95427071..95430521,5	MCF-7	breast:
37	chr5:95294835..95302887-chr5:95306601..95313873,11	K562	blood:
38	chr5:95297972..95300750-chr5:95328029..95330073,2	K562	blood:
39	chr5:95328505..95331232-chr5:95332077..95333739,2	K562	blood:
40	chr5:95304291..95306265-chr5:95309546..95312179,2	K562	blood:
41	chr5:95399534..95401780-chr5:95407826..95410205,2	K562	blood:
42	chr5:95417552..95419052-chr5:95421414..95423793,2	MCF-7	breast:
43	chr5:95408446..95411161-chr5:95411273..95412980,2	K562	blood:
44	chr5:95328505..95331232-chr5:95332077..95333739,2	K562	blood:
45	chr5:95194068..95196070-chr5:95401310..95403656,2	K562	blood:
46	chr5:95408446..95411161-chr5:95411273..95412980,2	K562	blood:
47	chr5:95359766..95362858-chr5:95371780..95373834,3	MCF-7	breast:
48	chr5:95372818..95374675-chr5:95378795..95380652,2	MCF-7	breast:
49	chr5:95334613..95336349-chr5:95402257..95404926,2	K562	blood:
50	chr5:95315592..95318103-chr5:95322606..95324931,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELL2-2	chr5:95338604-95339260	NONHSAT102881
2	lnc-C5orf27-3	chr5:95446638-95446709	ENSG00000250551
3	lnc-ELL2-1	chr5:95300703-95300955	ENSG00000250955.1
4	lnc-ELL2-1	chr5:95305926-95306000	ENSG00000250955.1
5	lnc-ELL2-1	chr5:95321964-95322015	ENSG00000250955.1
6	lnc-ELL2-1	chr5:95316041-95316231	ENSG00000250955.1
7	lnc-C5orf27-3	chr5:95385819-95385905	ENSG00000250551

miRNA name	Chromosome Location	mirBase accession
hsa-miR-583	chr5:95414857-95414877	MIMAT0003248

No data

Variant related genes	Relation type
ELL2	TF binding region
FABP5P5	TF binding region
MIR583	TF binding region
ENSG00000250551	TF binding region
ENSG00000250955	TF binding region
ELL2	CpG island
FABP5P5	CpG island
MIR583	CpG island
ENSG00000250551	CpG island
ENSG00000250955	CpG island
ENSG00000251314	chromatin interactions
ENSG00000207578	chromatin interactions
ENSG00000173457	chromatin interactions
ENSG00000250955	chromatin interactions
ENSG00000213716	chromatin interactions
ENSG00000250551	chromatin interactions
ENSG00000118985	chromatin interactions
ENSG00000256940	chromatin interactions
ENSG00000153113	chromatin interactions

Extended variants
information (count: 4930 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4930 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3832379	chr5:95300942-95300943	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs397882302	chr5:95300951-95300952	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs552138167	chr5:95301011-95301012	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571900738	chr5:95301038-95301039	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs534175697	chr5:95301039-95301040	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs184706680	chr5:95301095-95301096	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs368513213	chr5:95301111-95301112	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs144770549	chr5:95301121-95301122	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs556215974	chr5:95301172-95301173	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs563638727	chr5:95301174-95301175	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs576060873	chr5:95301215-95301216	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs116769769	chr5:95301245-95301246	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs371790540	chr5:95301262-95301263	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs529501111	chr5:95301325-95301326	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs189423224	chr5:95301347-95301348	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs918629	chr5:95301463-95301464	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
17	rs540880573	chr5:95301490-95301491	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs561105118	chr5:95301491-95301492	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs569316786	chr5:95301535-95301536	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs115037351	chr5:95301549-95301550	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs563357990	chr5:95301560-95301561	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs114080728	chr5:95301568-95301569	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs372155812	chr5:95301641-95301642	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs200993292	chr5:95301705-95301706	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs571856400	chr5:95301715-95301716	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs181953731	chr5:95301748-95301749	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs117933362	chr5:95301828-95301829	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs184265894	chr5:95301834-95301835	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs536430059	chr5:95301861-95301862	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs147874524	chr5:95301869-95301870	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs569809699	chr5:95301884-95301885	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs375715317	chr5:95301922-95301923	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs149539667	chr5:95301942-95301943	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs528612632	chr5:95301954-95301955	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs374060787	chr5:95301978-95301979	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs148918439	chr5:95302002-95302003	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs572268997	chr5:95302008-95302009	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs143657732	chr5:95302009-95302010	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs111693284	chr5:95302010-95302011	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs551567208	chr5:95302049-95302050	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs554547528	chr5:95302057-95302058	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs189261308	chr5:95302136-95302137	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs543633665	chr5:95302142-95302143	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs563420511	chr5:95302159-95302160	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs148160002	chr5:95302236-95302237	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545829576	chr5:95302259-95302260	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs559272733	chr5:95302260-95302261	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs571459756	chr5:95302278-95302279	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs181149159	chr5:95302300-95302301	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs548103411	chr5:95302302-95302303	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1607 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95298400-95301600	Weak transcription	Fetal Intestine Small	intestine
2	chr5:95298400-95309200	Weak transcription	NHLF	lung
3	chr5:95298600-95301400	Weak transcription	A549	lung
4	chr5:95298600-95302000	Weak transcription	Fetal Intestine Large	intestine
5	chr5:95298600-95305000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:95298600-95305200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr5:95298800-95301400	Weak transcription	Stomach Mucosa	stomach
8	chr5:95298800-95302000	Weak transcription	Gastric	stomach
9	chr5:95298800-95322600	Weak transcription	Pancreas	Pancrea
10	chr5:95299600-95309000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:95300000-95308600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr5:95300200-95303000	Enhancers	HepG2	liver
13	chr5:95300600-95301000	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr5:95300600-95302600	Enhancers	Liver	Liver
15	chr5:95301000-95302200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr5:95301400-95302400	Enhancers	A549	lung
17	chr5:95301400-95302800	Enhancers	Stomach Mucosa	stomach
18	chr5:95301600-95303400	Enhancers	Fetal Intestine Small	intestine
19	chr5:95302000-95302600	Enhancers	Gastric	stomach
20	chr5:95302000-95303400	Enhancers	Fetal Intestine Large	intestine
21	chr5:95302200-95302400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:95302600-95305200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:95302600-95305200	Weak transcription	Liver	Liver
24	chr5:95302800-95309000	Weak transcription	Stomach Mucosa	stomach
25	chr5:95303000-95304200	Weak transcription	HepG2	liver
26	chr5:95303400-95304600	Weak transcription	Fetal Intestine Large	intestine
27	chr5:95303400-95304600	Weak transcription	Fetal Intestine Small	intestine
28	chr5:95304200-95305200	Enhancers	HepG2	liver
29	chr5:95304600-95305200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr5:95304600-95305200	Enhancers	Fetal Intestine Small	intestine
31	chr5:95304800-95306800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr5:95305000-95306000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:95305000-95306000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr5:95305000-95306200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:95305000-95306200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:95305200-95305400	Enhancers	Fetal Intestine Large	intestine
37	chr5:95305200-95305600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:95305200-95305800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:95305200-95305800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr5:95305200-95306000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr5:95305200-95306000	Enhancers	Osteobl	bone
42	chr5:95305200-95306400	Enhancers	Liver	Liver
43	chr5:95305200-95306400	Flanking Active TSS	HepG2	liver
44	chr5:95305200-95310600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:95305600-95305800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:95305800-95306000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:95305800-95309200	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr5:95306000-95309000	Weak transcription	Osteobl	bone
49	chr5:95306000-95309400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr5:95306400-95306600	Weak transcription	Pancreatic Islets	Pancreatic Islet

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