Variant report

Variant	nsv564265
Chromosome Location	chr14:35512335-35624831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1895)
CpG islands
(count:1465)
Chromatin interactive
region (count:159)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35519876-35520224	K562	blood:	n/a	n/a
2	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35521017-35521344	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
6	ARID3A	chr14:35537558-35537700	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:35516133-35516303	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:35547257-35547542	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:35519909-35520120	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
12	ARID3A	chr14:35514746-35515759	HepG2	liver:	n/a	n/a
13	ATF1	chr14:35519862-35520172	K562	blood:	n/a	n/a
14	ATF1	chr14:35515122-35515876	K562	blood:	n/a	n/a
15	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
16	ATF1	chr14:35517147-35517386	K562	blood:	n/a	n/a
17	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
18	ATF2	chr14:35514853-35515586	GM12878	blood:	n/a	n/a
19	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
20	ATF2	chr14:35515000-35515488	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr14:35515054-35515466	GM12878	blood:	n/a	n/a
22	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr14:35515153-35515540	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
26	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
27	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504
28	ATF3	chr14:35591368-35591602	GM12878	blood:	n/a	chr14:35591484-35591504
29	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
30	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
31	ATF3	chr14:35515137-35515513	K562	blood:	n/a	chr14:35515349-35515364 chr14:35515353-35515360 chr14:35515353-35515361 chr14:35515353-35515363 chr14:35515352-35515360 chr14:35515350-35515363 chr14:35515353-35515363
32	ATF3	chr14:35591254-35591787	A549	lung:	n/a	chr14:35591484-35591504
33	BACH1	chr14:35519875-35520207	H1-hESC	embryonic stem cell:	n/a	chr14:35520008-35520022
34	BACH1	chr14:35515145-35516116	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr14:35519638-35520190	K562	blood:	n/a	chr14:35520008-35520022
36	BATF	chr14:35515132-35515392	GM12878	blood:	n/a	chr14:35515350-35515363
37	BATF	chr14:35591663-35591964	GM12878	blood:	n/a	n/a
38	BCL3	chr14:35515089-35515763	GM12878	blood:	n/a	chr14:35515406-35515415
39	BCL3	chr14:35515416-35515871	A549	lung:	n/a	n/a
40	BCL3	chr14:35590950-35592103	A549	lung:	n/a	n/a
41	BCL3	chr14:35590607-35591936	A549	lung:	n/a	n/a
42	BCLAF1	chr14:35590870-35592203	GM12878	blood:	n/a	n/a
43	BCLAF1	chr14:35514960-35515869	GM12878	blood:	n/a	chr14:35515406-35515415
44	BCLAF1	chr14:35590896-35592186	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:35590749-35592231	HepG2	liver:	n/a	n/a
46	BHLHE40	chr14:35590781-35592288	GM12878	blood:	n/a	n/a
47	BHLHE40	chr14:35514837-35515868	HepG2	liver:	n/a	n/a
48	BHLHE40	chr14:35514808-35515688	GM12878	blood:	n/a	n/a
49	BHLHE40	chr14:35590665-35592190	K562	blood:	n/a	n/a
50	BHLHE40	chr14:35514866-35515778	K562	blood:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35515356-35515406	AG04449	skin:	fetal
2	chr14:35515356-35515406	AG04449	skin:	fetal
3	chr14:35540926-35540976	ECC-1	luminal epithelium:	n/a
4	chr14:35591951-35592001	HRE	kidney:	n/a
5	chr14:35592116-35592166	Hela-S3	cervix:	n/a
6	chr14:35591779-35591829	Jurkat	blood:	n/a
7	chr14:35591252-35591302	Hela-S3	cervix:	n/a
8	chr14:35514333-35514383	AG09309	skin:	n/a
9	chr14:35591473-35591523	HUVEC	blood vessel:	n/a
10	chr14:35594356-35594406	HEK293	kidney:	embryo
11	chr14:35512367-35512417	Hela-S3	cervix:	n/a
12	chr14:35512367-35512417	AG04450	lung:	fetal
13	chr14:35587750-35587800	SK-N-SH_RA	brain:	n/a
14	chr14:35587750-35587800	GM12878	blood:	n/a
15	chr14:35591523-35591573	HCM	heart:	n/a
16	chr14:35515858-35515908	K562	blood:	n/a
17	chr14:35589334-35589384	HAEpiC	amniotic membrane:	n/a
18	chr14:35594356-35594406	AG10803	skin:	n/a
19	chr14:35515116-35515166	SKMC	muscle:	n/a
20	chr14:35594356-35594406	HRCEpiC	kidney:	n/a
21	chr14:35591840-35591890	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:35594356-35594406	HIPEpiC	eye:	n/a
23	chr14:35592116-35592166	NH-A	brain:	n/a
24	chr14:35591572-35591622	BE2_C	brain:	n/a
25	chr14:35591625-35591675	NHBE	bronchial:	n/a
26	chr14:35592116-35592166	CMK	blood:	n/a
27	chr14:35515291-35515341	H1-hESC	embryonic stem cell:	embryo
28	chr14:35591473-35591523	HNPCEpiC	eye:	n/a
29	chr14:35587750-35587800	U87	brain:	n/a
30	chr14:35540926-35540976	SAEC	small airway:	n/a
31	chr14:35591695-35591745	H1-hESC	embryonic stem cell:	embryo
32	chr14:35516283-35516333	H1-hESC	embryonic stem cell:	embryo
33	chr14:35589334-35589384	SAEC	small airway:	n/a
34	chr14:35515356-35515406	AG10803	skin:	n/a
35	chr14:35587750-35587800	AoSMC	blood vessel:	n/a
36	chr14:35515414-35515464	Hela-S3	cervix:	n/a
37	chr14:35516283-35516333	Jurkat	blood:	n/a
38	chr14:35587750-35587800	HEEpiC	esophagus:	n/a
39	chr14:35516283-35516333	ProgFib	skin:	n/a
40	chr14:35512367-35512417	PrEC	prostate:	n/a
41	chr14:35591625-35591675	HUVEC	blood vessel:	n/a
42	chr14:35591625-35591675	RPTEC	kidney:	n/a
43	chr14:35592116-35592166	NHDF-neo	bronchial:	n/a
44	chr14:35583718-35583768	GM12892	blood:	n/a
45	chr14:35514333-35514383	LNCaP	prostate:	n/a
46	chr14:35591523-35591573	SK-N-MC	brain:	n/a
47	chr14:35589334-35589384	SK-N-SH	brain:	n/a
48	chr14:35591523-35591573	LNCaP	prostate:	n/a
49	chr14:35587750-35587800	HNPCEpiC	eye:	n/a
50	chr14:35591572-35591622	AoSMC	blood vessel:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
2	chr14:35565651..35568101-chr14:35571541..35574493,2	K562	blood:
3	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
4	chr14:35515365..35516134-chr15:65596788..65597492,2	Hela-S3	cervix:
5	chr10:134144877..134145604-chr14:35591124..35591775,2	Hela-S3	cervix:
6	chr11:66056160..66056721-chr14:35590740..35591268,2	Hela-S3	cervix:
7	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
8	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
9	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
10	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
11	chr1:44115905..44116421-chr14:35515198..35515970,2	NB4	blood:
12	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
13	chr14:35520311..35523520-chr14:35872932..35875311,3	MCF-7	breast:
14	chr14:35516520..35518836-chr14:35536161..35537991,2	K562	blood:
15	chr14:35589196..35594400-chr14:35871301..35877730,13	MCF-7	breast:
16	chr14:35576972..35579105-chr14:35589747..35591526,2	MCF-7	breast:
17	chr14:35520110..35522080-chr14:35529783..35531632,2	MCF-7	breast:
18	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
19	chr14:35577807..35579602-chr14:35589893..35592332,3	MCF-7	breast:
20	chr14:35450596..35455465-chr14:35514082..35520003,7	MCF-7	breast:
21	chr14:35513511..35517056-chr14:35517636..35522677,6	K562	blood:
22	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
23	chr14:35519075..35520594-chr14:35524910..35527892,2	MCF-7	breast:
24	chr14:35552593..35554577-chr14:35554998..35557782,3	MCF-7	breast:
25	chr14:35579884..35582908-chr14:35589580..35593400,4	MCF-7	breast:
26	chr14:35579453..35581651-chr14:35585942..35587733,2	K562	blood:
27	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
28	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
29	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
30	chr14:35515355..35516338-chr5:171710986..171711486,2	Hela-S3	cervix:
31	chr14:35514228..35515878-chr14:35780242..35782321,2	MCF-7	breast:
32	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
33	chr14:35591658..35595888-chr14:35872338..35875561,5	K562	blood:
34	chr14:35515655..35516294-chr7:100025920..100026511,2	Hela-S3	cervix:
35	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:
36	chr1:45196086..45196947-chr14:35590878..35591536,2	Hela-S3	cervix:
37	chr14:35590489..35591401-chr15:91445904..91446665,2	Hela-S3	cervix:
38	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:
39	chr14:35524936..35527808-chr14:35546522..35548065,2	MCF-7	breast:
40	chr14:35519987..35522404-chr14:35523498..35526576,3	K562	blood:
41	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
42	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
43	chr14:35500095..35502926-chr14:35557815..35560264,2	MCF-7	breast:
44	chr14:35514169..35519549-chr14:35872431..35877872,11	MCF-7	breast:
45	chr14:35525027..35526542-chr14:35529643..35531640,2	K562	blood:
46	chr14:35514107..35515830-chr14:35872683..35874428,2	MCF-7	breast:
47	chr14:35341498..35344850-chr14:35591184..35593267,3	K562	blood:
48	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
49	chr14:35519075..35520594-chr14:35524910..35527892,2	MCF-7	breast:
50	chr14:35603102..35605461-chr14:35881286..35882903,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
2	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363
3	lnc-RP11-173D9.3.1-1	chr14:35568882-35571935	ENSG00000247658
4	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363
5	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
6	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
7	lnc-RP11-173D9.3.1-1	chr14:35575573-35575690	ENSG00000247658
8	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM177A1	hsa-miR-142-3p	chr14:35551080-35551101
2	FAM177A1	hsa-miR-186-5p	chr14:35551034-35551055
3	FAM177A1	hsa-miR-124-3p	chr14:35552531-35552538
4	FAM177A1	hsa-miR-186-5p	chr14:35550483-35550504
5	FAM177A1	hsa-miR-124-3p	chr14:35552521-35552538
6	FAM177A1	hsa-miR-155-5p	chr14:35551927-35551947

Variant related genes	Relation type
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
ENSG00000241052	TF binding region
FAM177A1	TF binding region
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
ENSG00000241052	CpG island
FAM177A1	CpG island
ENSG00000202077	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000185634	chromatin interactions
ENSG00000115275	chromatin interactions
ENSG00000100902	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000058262	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000255302	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000066135	chromatin interactions
ENSG00000168246	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000235883	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000200156	chromatin interactions
FNDC3A	miRNA target sites
SAMD4B	miRNA target sites
C2CD4A	miRNA target sites
NEFM	miRNA target sites

Extended variants
information (count: 4377 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4377 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs799477	chr14:35512335-35512336	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113597207	chr14:35512364-35512365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563007739	chr14:35512368-35512369	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs576329980	chr14:35512456-35512457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570202324	chr14:35512492-35512493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs799476	chr14:35512612-35512613	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs565424617	chr14:35512652-35512653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528020466	chr14:35512655-35512656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548009995	chr14:35512672-35512673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531081841	chr14:35512684-35512685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80282026	chr14:35512685-35512686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530331342	chr14:35512697-35512698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs8009093	chr14:35512703-35512704	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs568952210	chr14:35512717-35512718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190700128	chr14:35512752-35512753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs200449451	chr14:35512789-35512790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61989480	chr14:35512807-35512808	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs559720617	chr14:35512836-35512837	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs5807807	chr14:35512911-35512912	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs397852891	chr14:35512917-35512918	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs181987933	chr14:35512937-35512938	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs372158410	chr14:35512939-35512940	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs1028449	chr14:35512995-35512996	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs533878688	chr14:35513001-35513002	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs553541993	chr14:35513030-35513031	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368716161	chr14:35513031-35513032	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs76667742	chr14:35513057-35513058	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs5807808	chr14:35513062-35513063	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs567082031	chr14:35513162-35513163	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536064906	chr14:35513214-35513215	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs556348282	chr14:35513236-35513237	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs74243590	chr14:35513246-35513247	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs545053468	chr14:35513306-35513307	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs537429289	chr14:35513317-35513318	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs558959662	chr14:35513328-35513329	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs10146343	chr14:35513466-35513467	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs541708768	chr14:35513475-35513476	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs561573208	chr14:35513477-35513478	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs530286565	chr14:35513482-35513483	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs190131325	chr14:35513489-35513490	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs559036418	chr14:35513546-35513547	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs562426404	chr14:35513633-35513634	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs115149959	chr14:35513662-35513663	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs551085846	chr14:35513702-35513703	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs8013540	chr14:35513760-35513761	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs527300643	chr14:35513875-35513876	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs547241316	chr14:35513923-35513924	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs143205316	chr14:35513949-35513950	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs536044048	chr14:35513969-35513970	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs556353594	chr14:35514016-35514017	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:4066 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35485800-35514800	Weak transcription	Right Ventricle	heart
2	chr14:35488600-35514200	Weak transcription	Small Intestine	intestine
3	chr14:35490200-35514600	Weak transcription	NHLF	lung
4	chr14:35496800-35514600	Weak transcription	HSMMtube	muscle
5	chr14:35498000-35514200	Weak transcription	Fetal Kidney	kidney
6	chr14:35498600-35514600	Weak transcription	Colon Smooth Muscle	Colon
7	chr14:35500400-35514200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr14:35501800-35514400	Weak transcription	NH-A	brain
9	chr14:35502800-35514600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr14:35503000-35514400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr14:35503400-35514200	Weak transcription	Primary T cells from cord blood	blood
12	chr14:35503600-35514400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr14:35503600-35514400	Weak transcription	Fetal Lung	lung
14	chr14:35503800-35514200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:35503800-35514200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr14:35503800-35514400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr14:35503800-35514600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr14:35503800-35514600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr14:35503800-35514800	Weak transcription	Aorta	Aorta
20	chr14:35504000-35514200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr14:35504000-35514400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr14:35504000-35514400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:35504000-35514600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr14:35504000-35514600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr14:35504000-35514800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr14:35504000-35515000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr14:35504600-35514200	Weak transcription	Fetal Intestine Small	intestine
28	chr14:35510600-35514800	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr14:35510800-35514200	Weak transcription	HepG2	liver
30	chr14:35512600-35512800	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr14:35512600-35514000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr14:35513000-35514200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr14:35513600-35514600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:35513800-35514000	Enhancers	Esophagus	oesophagus
35	chr14:35513800-35514000	Enhancers	Pancreas	Pancrea
36	chr14:35514000-35514200	Enhancers	Primary hematopoietic stem cells	blood
37	chr14:35514000-35514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr14:35514200-35514400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:35514200-35514400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:35514200-35514400	Enhancers	Primary B cells from cord blood	blood
41	chr14:35514200-35514400	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr14:35514200-35514400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr14:35514200-35514400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr14:35514200-35514400	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr14:35514200-35514400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr14:35514200-35514400	Enhancers	Primary T killer memory cells from peripheral blood	blood
47	chr14:35514200-35514400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr14:35514200-35514400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:35514200-35514400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr14:35514200-35514400	Enhancers	Brain Substantia Nigra	brain

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