Variant report

Variant	nsv542035
Chromosome Location	chr14:35563220-35607117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:815)
CpG islands
(count:917)
Chromatin interactive
region (count:71)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:815 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
2	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
3	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
4	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
7	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
8	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
9	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
10	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
11	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504
12	ATF3	chr14:35591254-35591787	A549	lung:	n/a	chr14:35591484-35591504
13	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
14	ATF3	chr14:35591368-35591602	GM12878	blood:	n/a	chr14:35591484-35591504
15	BATF	chr14:35591663-35591964	GM12878	blood:	n/a	n/a
16	BCL3	chr14:35590950-35592103	A549	lung:	n/a	n/a
17	BCL3	chr14:35590607-35591936	A549	lung:	n/a	n/a
18	BCLAF1	chr14:35590896-35592186	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:35590870-35592203	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:35591280-35591665	A549	lung:	n/a	n/a
21	BHLHE40	chr14:35590665-35592190	K562	blood:	n/a	n/a
22	BHLHE40	chr14:35590749-35592231	HepG2	liver:	n/a	n/a
23	BHLHE40	chr14:35590781-35592288	GM12878	blood:	n/a	n/a
24	BRCA1	chr14:35590611-35592191	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr14:35591074-35592013	HepG2	liver:	n/a	n/a
26	BRCA1	chr14:35590603-35591644	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
28	CBX3	chr14:35580902-35581120	K562	blood:	n/a	n/a
29	CBX3	chr14:35590828-35591964	K562	blood:	n/a	n/a
30	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
31	CBX3	chr14:35580846-35581125	K562	blood:	n/a	n/a
32	CCNT2	chr14:35590784-35592019	K562	blood:	n/a	n/a
33	CEBPB	chr14:35590954-35591859	HepG2	liver:	n/a	chr14:35591541-35591552
34	CEBPB	chr14:35590688-35591860	Hela-S3	cervix:	n/a	chr14:35591541-35591552
35	CEBPB	chr14:35583233-35583517	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr14:35590944-35591690	H1-hESC	embryonic stem cell:	n/a	chr14:35591541-35591552
37	CEBPB	chr14:35591348-35591738	IMR90	lung:	n/a	chr14:35591541-35591552
38	CEBPB	chr14:35591219-35591957	A549	lung:	n/a	chr14:35591541-35591552
39	CEBPB	chr14:35590674-35592463	GM12878	blood:	n/a	chr14:35591541-35591552
40	CEBPB	chr14:35590040-35590469	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr14:35591315-35591791	HepG2	liver:	n/a	chr14:35591541-35591552
42	CEBPB	chr14:35583223-35583488	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:35581914-35582023	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:35601915-35601965	HepG2	liver:	n/a	chr14:35601943-35601954
45	CEBPB	chr14:35583186-35583587	IMR90	lung:	n/a	n/a
46	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:35588289-35588318	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:35577839-35577994	HepG2	liver:	n/a	chr14:35577926-35577937
49	CEBPB	chr14:35583266-35583493	K562	blood:	n/a	n/a
50	CEBPB	chr14:35583289-35583522	A549	lung:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35583718-35583768	HEK293	kidney:	embryo
2	chr14:35591695-35591745	PrEC	prostate:	n/a
3	chr14:35583718-35583768	HEK293	kidney:	embryo
4	chr14:35591695-35591745	PrEC	prostate:	n/a
5	chr14:35591572-35591622	GM12891	blood:	n/a
6	chr14:35591252-35591302	AG04449	skin:	fetal
7	chr14:35591779-35591829	HRPEpiC	eye:	n/a
8	chr14:35591695-35591745	LNCaP	prostate:	n/a
9	chr14:35591781-35591831	HRCEpiC	kidney:	n/a
10	chr14:35591473-35591523	HRE	kidney:	n/a
11	chr14:35591951-35592001	AoSMC	blood vessel:	n/a
12	chr14:35591951-35592001	ECC-1	luminal epithelium:	n/a
13	chr14:35591523-35591573	K562	blood:	n/a
14	chr14:35591625-35591675	GM12878	blood:	n/a
15	chr14:35591523-35591573	U87	brain:	n/a
16	chr14:35591695-35591745	IMR90	lung:	fetal
17	chr14:35583718-35583768	K562	blood:	n/a
18	chr14:35587750-35587800	HRCEpiC	kidney:	n/a
19	chr14:35587750-35587800	NHBE	bronchial:	n/a
20	chr14:35589334-35589384	ECC-1	luminal epithelium:	n/a
21	chr14:35591473-35591523	MCF10A-Er-Src	breast:	n/a
22	chr14:35591625-35591675	IMR90	lung:	fetal
23	chr14:35591781-35591831	MCF10A-Er-Src	breast:	n/a
24	chr14:35591572-35591622	GM19239	blood:	n/a
25	chr14:35591779-35591829	NT2-D1	testis:	n/a
26	chr14:35591252-35591302	HAEpiC	amniotic membrane:	n/a
27	chr14:35591473-35591523	AoSMC	blood vessel:	n/a
28	chr14:35589334-35589384	HepG2	liver:	n/a
29	chr14:35583718-35583768	HCF	heart:	n/a
30	chr14:35591252-35591302	MCF10A-Er-Src	breast:	n/a
31	chr14:35591781-35591831	A549	lung:	n/a
32	chr14:35591572-35591622	SKMC	muscle:	n/a
33	chr14:35591572-35591622	H1-hESC	embryonic stem cell:	embryo
34	chr14:35591473-35591523	ProgFib	skin:	n/a
35	chr14:35589334-35589384	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:35583718-35583768	HCM	heart:	n/a
37	chr14:35594356-35594406	HEK293	kidney:	embryo
38	chr14:35591779-35591829	HL-60	blood:	n/a
39	chr14:35594356-35594406	NHDF-neo	bronchial:	n/a
40	chr14:35591473-35591523	HCF	heart:	n/a
41	chr14:35591523-35591573	AoSMC	blood vessel:	n/a
42	chr14:35591473-35591523	HCT-116	colon:	n/a
43	chr14:35592116-35592166	GM12878	blood:	n/a
44	chr14:35592116-35592166	HRCEpiC	kidney:	n/a
45	chr14:35591840-35591890	NH-A	brain:	n/a
46	chr14:35589334-35589384	NT2-D1	testis:	n/a
47	chr14:35591523-35591573	MCF-7	breast:	n/a
48	chr14:35591951-35592001	SK-N-SH	brain:	n/a
49	chr14:35587750-35587800	NT2-D1	testis:	n/a
50	chr14:35591840-35591890	AoSMC	blood vessel:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:54673261..54673894-chr14:35590757..35591369,2	Hela-S3	cervix:
2	chr14:35593883..35596766-chr14:35627445..35630133,2	MCF-7	breast:
3	chr14:35450245..35452169-chr14:35590215..35593362,3	MCF-7	breast:
4	chr1:1709416..1709919-chr14:35590889..35591481,2	Hela-S3	cervix:
5	chr14:35589240..35593864-chr14:35869008..35876501,20	MCF-7	breast:
6	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
7	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
8	chr14:35590489..35591401-chr15:91445904..91446665,2	Hela-S3	cervix:
9	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:
10	chr10:134144877..134145604-chr14:35591124..35591775,2	Hela-S3	cervix:
11	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
12	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
13	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
14	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
15	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
16	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
17	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
18	chr1:45196086..45196947-chr14:35590878..35591536,2	Hela-S3	cervix:
19	chr14:35016883..35018423-chr14:35574764..35577501,2	MCF-7	breast:
20	chr14:35579453..35581651-chr14:35585942..35587733,2	K562	blood:
21	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
22	chr14:35343360..35345155-chr14:35586268..35588307,2	MCF-7	breast:
23	chr14:35568012..35571090-chr14:35873276..35876327,3	MCF-7	breast:
24	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
25	chr14:35513562..35515919-chr14:35564977..35566594,2	MCF-7	breast:
26	chr14:35568810..35572401-chr14:35587846..35592624,4	MCF-7	breast:
27	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
28	chr14:35603102..35605461-chr14:35881286..35882903,2	MCF-7	breast:
29	chr14:35578569..35580087-chr14:35582011..35583731,2	K562	blood:
30	chr11:66056160..66056721-chr14:35590740..35591268,2	Hela-S3	cervix:
31	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
32	chr14:35565651..35568101-chr14:35571541..35574493,2	K562	blood:
33	chr14:35589196..35594400-chr14:35871301..35877730,13	MCF-7	breast:
34	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
35	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
36	chr14:35341168..35344675-chr14:35590606..35593872,6	MCF-7	breast:
37	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
38	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
39	chr14:35583308..35588876-chr14:35589178..35593731,8	MCF-7	breast:
40	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
41	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
42	chr14:35577807..35579602-chr14:35589893..35592332,3	MCF-7	breast:
43	chr14:35585231..35589339-chr14:35589469..35593386,5	K562	blood:
44	chr14:35589606..35593451-chr14:35594804..35598522,5	K562	blood:
45	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
46	chr14:35560221..35562617-chr14:35563701..35566461,3	MCF-7	breast:
47	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
48	chr14:35591775..35593424-chr14:35873275..35875126,2	K562	blood:
49	chr14:35515621..35517465-chr14:35577132..35579018,2	MCF-7	breast:
50	chr14:35515793..35518719-chr14:35585868..35588915,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
2	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
3	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363
4	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
5	lnc-RP11-173D9.3.1-1	chr14:35575573-35575690	ENSG00000247658
6	lnc-RP11-173D9.3.1-1	chr14:35568882-35571935	ENSG00000247658
7	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363

No data

Variant related genes	Relation type
FAM177A1	TF binding region
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
FAM177A1	CpG island
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
ENSG00000259090	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000258790	chromatin interactions
FNDC3A	miRNA target sites
NEFM	miRNA target sites
SAMD4B	miRNA target sites
C2CD4A	miRNA target sites

Extended variants
information (count: 1696 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1696 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541640520	chr14:35563229-35563230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113882299	chr14:35563327-35563328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560028530	chr14:35563341-35563342	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570776281	chr14:35563378-35563379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533653786	chr14:35563401-35563402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547351861	chr14:35563501-35563502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567058872	chr14:35563572-35563573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536101042	chr14:35563631-35563632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556006429	chr14:35563632-35563633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71435854	chr14:35563679-35563680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34162171	chr14:35563680-35563681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149818775	chr14:35563686-35563687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs397701886	chr14:35563687-35563688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568114928	chr14:35563689-35563690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536768769	chr14:35563696-35563697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556895363	chr14:35563700-35563701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76520532	chr14:35563701-35563702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs57490113	chr14:35563748-35563749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs397977733	chr14:35563750-35563751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190765057	chr14:35563800-35563801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183536584	chr14:35563808-35563809	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368142369	chr14:35563814-35563815	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs68042411	chr14:35563864-35563865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs34870339	chr14:35563865-35563866	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs552898295	chr14:35563867-35563868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs572806090	chr14:35563891-35563892	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs188782061	chr14:35563912-35563913	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs561748137	chr14:35564020-35564021	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530899582	chr14:35564026-35564027	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575662873	chr14:35564030-35564031	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs544405854	chr14:35564085-35564086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112396573	chr14:35564087-35564088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192873712	chr14:35564138-35564139	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79347211	chr14:35564159-35564160	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566863539	chr14:35564160-35564161	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs369008918	chr14:35564213-35564214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199881823	chr14:35564217-35564218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs372312834	chr14:35564231-35564232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs199936272	chr14:35564275-35564276	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148710642	chr14:35564291-35564292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142279359	chr14:35564295-35564296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150007051	chr14:35564302-35564303	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377037544	chr14:35564324-35564325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs369410792	chr14:35564330-35564331	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs373692237	chr14:35564331-35564332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs61741202	chr14:35564389-35564390	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs200055292	chr14:35564420-35564421	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369969591	chr14:35564464-35564465	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs529629615	chr14:35564479-35564480	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs551578801	chr14:35564553-35564554	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD

Chromatin state (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
2	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
3	chr14:35530600-35563600	Weak transcription	Small Intestine	intestine
4	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
5	chr14:35531400-35563400	Weak transcription	Gastric	stomach
6	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
8	chr14:35543200-35580800	Weak transcription	K562	blood
9	chr14:35545600-35564600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:35545600-35568600	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr14:35545600-35569800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:35545600-35580800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:35545600-35582800	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:35545800-35566400	Strong transcription	Primary T helper cells PMA-I stimulated	--
16	chr14:35546000-35568000	Strong transcription	Osteobl	bone
17	chr14:35546000-35581200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr14:35546000-35585800	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr14:35546000-35587200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr14:35546200-35564800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:35546200-35566000	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr14:35546200-35585000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr14:35546800-35571800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:35547000-35580800	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr14:35547200-35574400	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr14:35547200-35577600	Strong transcription	Placenta	Placenta
27	chr14:35547400-35565800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr14:35547400-35574000	Strong transcription	Adipose Nuclei	Adipose
29	chr14:35547400-35577800	Strong transcription	Primary B cells from peripheral blood	blood
30	chr14:35547400-35580600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr14:35548000-35581000	Strong transcription	HepG2	liver
32	chr14:35548200-35580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:35548400-35578800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:35548600-35563400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr14:35549600-35569000	Strong transcription	Liver	Liver
36	chr14:35550200-35586000	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr14:35550800-35581000	Strong transcription	Dnd41	blood
38	chr14:35551000-35572800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr14:35551400-35563400	Weak transcription	NHLF	lung
40	chr14:35551600-35579400	Weak transcription	NHEK	skin
41	chr14:35552000-35586600	Strong transcription	Fetal Thymus	thymus
42	chr14:35552600-35566000	Strong transcription	Fetal Muscle Trunk	muscle
43	chr14:35552600-35568400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr14:35552600-35577600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr14:35552800-35568000	Strong transcription	Brain Germinal Matrix	brain
46	chr14:35553000-35570600	Strong transcription	Fetal Intestine Large	intestine
47	chr14:35553400-35589800	Weak transcription	Pancreas	Pancrea
48	chr14:35554200-35566200	Weak transcription	Spleen	Spleen
49	chr14:35554800-35563400	Weak transcription	Brain Substantia Nigra	brain
50	chr14:35554800-35563400	Weak transcription	Psoas Muscle	Psoas

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