Variant report

Variant	nsv931935
Chromosome Location	chr14:31871658-32117666
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	chr14:31889740-31890190	K562	blood:	n/a	n/a
2	ARID3A	chr14:31919242-31919576	K562	blood:	n/a	n/a
3	ARID3A	chr14:32029929-32030900	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:31926692-31926973	K562	blood:	n/a	n/a
5	ARID3A	chr14:31925760-31927934	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:31998310-31998539	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:31979345-31979767	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:31979285-31979597	K562	blood:	n/a	n/a
9	ARID3A	chr14:31902751-31902786	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:32049609-32049683	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:32013429-32013589	K562	blood:	n/a	n/a
12	ARID3A	chr14:32013394-32013714	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:31919193-31919618	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:32094871-32095254	HepG2	liver:	n/a	chr14:32095223-32095239 chr14:32095224-32095240
15	ARID3A	chr14:31888898-31891391	HepG2	liver:	n/a	n/a
16	ATF1	chr14:31926120-31926865	K562	blood:	n/a	n/a
17	ATF1	chr14:31875168-31875448	K562	blood:	n/a	n/a
18	ATF1	chr14:32030401-32030925	K562	blood:	n/a	chr14:32030577-32030591
19	ATF1	chr14:31919264-31919476	K562	blood:	n/a	n/a
20	ATF2	chr14:31889508-31890142	GM12878	blood:	n/a	n/a
21	ATF2	chr14:31958860-31959365	GM12878	blood:	n/a	n/a
22	ATF2	chr14:32030344-32030839	GM12878	blood:	n/a	chr14:32030577-32030591
23	ATF2	chr14:32030341-32031054	GM12878	blood:	n/a	chr14:32030577-32030591
24	ATF2	chr14:31889628-31890309	GM12878	blood:	n/a	n/a
25	ATF3	chr14:31875173-31875422	K562	blood:	n/a	n/a
26	ATF3	chr14:31889517-31890325	A549	lung:	n/a	n/a
27	ATF3	chr14:32030502-32030817	H1-hESC	embryonic stem cell:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
28	ATF3	chr14:32030510-32030706	GM12878	blood:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
29	ATF3	chr14:32030430-32030998	HepG2	liver:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
30	ATF3	chr14:32030405-32030715	K562	blood:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
31	ATF3	chr14:32030278-32031101	HepG2	liver:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
32	ATF3	chr14:32030435-32030748	K562	blood:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
33	ATF3	chr14:32030480-32030779	K562	blood:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
34	ATF3	chr14:32030376-32030812	GM12878	blood:	n/a	chr14:32030581-32030591 chr14:32030579-32030592 chr14:32030578-32030588 chr14:32030581-32030589 chr14:32030578-32030588 chr14:32030579-32030590 chr14:32030581-32030588 chr14:32030578-32030591 chr14:32030580-32030588 chr14:32030579-32030590 chr14:32030581-32030592 chr14:32030577-32030592 chr14:32030578-32030591 chr14:32030580-32030600
35	BACH1	chr14:31926111-31926143	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr14:31889072-31890103	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr14:32030457-32030747	K562	blood:	n/a	n/a
38	BACH1	chr14:31893454-31893489	K562	blood:	n/a	n/a
39	BATF	chr14:32030472-32030775	GM12878	blood:	n/a	chr14:32030578-32030591
40	BATF	chr14:31890090-31890408	GM12878	blood:	n/a	n/a
41	BATF	chr14:32037936-32038139	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:31887740-31887953	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:31969113-31969289	GM12878	blood:	n/a	n/a
44	BCL3	chr14:31889359-31890148	A549	lung:	n/a	chr14:31889766-31889779
45	BCL3	chr14:31910564-31911423	A549	lung:	n/a	n/a
46	BCL3	chr14:31925991-31926652	A549	lung:	n/a	n/a
47	BCLAF1	chr14:32030305-32030908	GM12878	blood:	n/a	chr14:32030555-32030564
48	BCLAF1	chr14:31926271-31926791	GM12878	blood:	n/a	n/a
49	BCLAF1	chr14:31889496-31890203	GM12878	blood:	n/a	chr14:31889766-31889779
50	BHLHE40	chr14:32030350-32031051	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31929696-31929746	BE2_C	brain:	n/a
2	chr14:32030176-32030226	HRCEpiC	kidney:	n/a
3	chr14:32030457-32030507	BJ	skin:	n/a
4	chr14:32030579-32030629	SAEC	small airway:	n/a
5	chr14:31929696-31929746	BE2_C	brain:	n/a
6	chr14:32030176-32030226	HRCEpiC	kidney:	n/a
7	chr14:32030457-32030507	BJ	skin:	n/a
8	chr14:32030579-32030629	SAEC	small airway:	n/a
9	chr14:32030546-32030596	HCM	heart:	n/a
10	chr14:32073463-32073513	GM06990	blood:	n/a
11	chr14:32030916-32030966	HCF	heart:	n/a
12	chr14:31927974-31928024	PFSK-1	brain:	n/a
13	chr14:31996486-31996536	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:32029920-32029970	HUVEC	blood vessel:	n/a
15	chr14:32030916-32030966	HIPEpiC	eye:	n/a
16	chr14:31926792-31926842	HepG2	liver:	n/a
17	chr14:32029310-32029360	MCF-7	breast:	n/a
18	chr14:31926792-31926842	Hepatocyte	liver:	n/a
19	chr14:31915923-31915973	HCM	heart:	n/a
20	chr14:31890052-31890102	PrEC	prostate:	n/a
21	chr14:31996486-31996536	AoSMC	blood vessel:	n/a
22	chr14:31889640-31889690	Caco-2	colon:	n/a
23	chr14:31926483-31926533	NHDF-neo	bronchial:	n/a
24	chr14:31926776-31926826	AG04450	lung:	fetal
25	chr14:31892296-31892346	LNCaP	prostate:	n/a
26	chr14:31889912-31889962	NB4	blood:	n/a
27	chr14:31889640-31889690	BJ	skin:	n/a
28	chr14:31889912-31889962	ovcar-3	ovarian:	n/a
29	chr14:32030546-32030596	T-47D	breast:	n/a
30	chr14:32073463-32073513	HEK293	kidney:	embryo
31	chr14:32109281-32109331	AG09309	skin:	n/a
32	chr14:31889912-31889962	GM12878	blood:	n/a
33	chr14:31926216-31926266	HCPEpiC	choroid plexus:	n/a
34	chr14:31926483-31926533	HAEpiC	amniotic membrane:	n/a
35	chr14:32109281-32109331	HUVEC	blood vessel:	n/a
36	chr14:31996486-31996536	HCT-116	colon:	n/a
37	chr14:31926792-31926842	MCF-7	breast:	n/a
38	chr14:31923667-31923717	Hepatocyte	liver:	n/a
39	chr14:32031012-32031062	RPTEC	kidney:	n/a
40	chr14:32030404-32030454	GM19239	blood:	n/a
41	chr14:32030205-32030255	HRPEpiC	eye:	n/a
42	chr14:32030546-32030596	HRPEpiC	eye:	n/a
43	chr14:31889912-31889962	LNCaP	prostate:	n/a
44	chr14:32030916-32030966	BJ	skin:	n/a
45	chr14:31926564-31926614	PANC-1	pancreas:	n/a
46	chr14:32029310-32029360	PrEC	prostate:	n/a
47	chr14:31926299-31926349	RPTEC	kidney:	n/a
48	chr14:32109281-32109331	HCM	heart:	n/a
49	chr14:31915923-31915973	GM12891	blood:	n/a
50	chr14:31926299-31926349	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:31887818..31891601-chr14:31923594..31927929,15	K562	blood:
2	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
3	chr14:31675912..31678861-chr14:31887650..31889789,3	K562	blood:
4	chr14:31889321..31891710-chr14:31909671..31912287,4	K562	blood:
5	chr14:32045847..32047973-chr14:32058333..32059909,2	MCF-7	breast:
6	chr14:31913970..31917383-chr14:31917651..31919831,3	MCF-7	breast:
7	chr14:32044780..32047478-chr14:32049514..32051528,2	MCF-7	breast:
8	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
9	chr14:31887046..31892106-chr14:31923824..31928892,9	K562	blood:
10	chr13:37574206..37574708-chr14:31889229..31890178,2	Hela-S3	cervix:
11	chr14:31905050..31906707-chr14:31906776..31909428,2	K562	blood:
12	chr14:32031985..32034611-chr14:32035178..32036787,2	MCF-7	breast:
13	chr14:32025880..32027814-chr14:32029222..32031344,2	MCF-7	breast:
14	chr14:31909214..31911851-chr14:31915493..31917225,2	K562	blood:
15	chr14:32030832..32032361-chr14:32036434..32038297,2	MCF-7	breast:
16	chr14:32034560..32036452-chr14:32038131..32040324,3	MCF-7	breast:
17	chr14:31923625..31927013-chr14:32030157..32032112,3	K562	blood:
18	chr14:31909214..31911851-chr14:31915493..31917225,2	K562	blood:
19	chr14:31950717..31953457-chr14:31954097..31956557,2	MCF-7	breast:
20	chr14:31874749..31876483-chr14:31879400..31881889,2	MCF-7	breast:
21	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
22	chr14:31889308..31890174-chr6:31795417..31795943,2	Hela-S3	cervix:
23	chr14:32031985..32034611-chr14:32035178..32036787,2	MCF-7	breast:
24	chr14:31675912..31678861-chr14:31887661..31889789,2	K562	blood:
25	chr14:31888444..31892446-chr14:31892724..31897271,5	K562	blood:
26	chr14:31888249..31890715-chr14:31905768..31907591,2	MCF-7	breast:
27	chr14:31888336..31890825-chr14:31917653..31919383,2	MCF-7	breast:
28	chr14:31926057..31926979-chr20:2632755..2633485,2	NB4	blood:
29	chr14:31925687..31926473-chr17:8076447..8076967,2	Hela-S3	cervix:
30	chr14:31907031..31909539-chr14:31909575..31912143,2	K562	blood:
31	chr14:31905050..31906638-chr14:31906776..31909651,2	K562	blood:
32	chr14:31905050..31906707-chr14:31906776..31909428,2	K562	blood:
33	chr14:32034560..32036452-chr14:32038131..32040324,3	MCF-7	breast:
34	chr14:31906586..31908599-chr14:31913797..31916070,2	MCF-7	breast:
35	chr14:32045847..32047973-chr14:32058333..32059909,2	MCF-7	breast:
36	chr14:31888742..31889382-chr3:41241031..41241649,2	Hela-S3	cervix:
37	chr14:31888318..31891005-chr14:31919529..31921805,3	MCF-7	breast:
38	chr14:31857830..31860114-chr14:31922683..31925572,2	K562	blood:
39	chr11:65189842..65190451-chr14:31926170..31926697,2	Hela-S3	cervix:
40	chr14:31925036..31927590-chr14:31947189..31950405,3	MCF-7	breast:
41	chr14:32025880..32027814-chr14:32029222..32031344,2	MCF-7	breast:
42	chr14:31914833..31916596-chr14:31919367..31920967,2	MCF-7	breast:
43	chr14:31900629..31902248-chr14:31924546..31926804,2	MCF-7	breast:
44	chr14:31676619..31677277-chr14:31889333..31889964,2	K562	blood:
45	chr11:122932393..122933144-chr14:31926505..31927244,2	NB4	blood:
46	chr14:32030832..32032361-chr14:32036434..32038297,2	MCF-7	breast:
47	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
48	chr14:31871925..31874502-chr14:31880911..31883683,2	K562	blood:
49	chr14:31888596..31889246-chr8:110346351..110347121,2	Hela-S3	cervix:
50	chr14:31874749..31876483-chr14:31879400..31881889,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUBPL-1	chr14:31914850-31914940	ENSG00000250365
2	lnc-C14orf126-1	chr14:32027624-32027704	ENSG00000258196.1
3	lnc-C14orf126-1	chr14:32022564-32022836	ENSG00000258196.1
4	lnc-RP11-187E13.1.1-1	chr14:31995361-31995382	NONHSAT036285
5	lnc-NUBPL-1	chr14:31908878-31909151	ENSG00000250365
6	lnc-NUBPL-1	chr14:31890150-31890183	ENSG00000250365
7	lnc-RP11-187E13.1.1-1	chr14:32023231-32023433	XLOC_010790
8	lnc-RP11-187E13.1.1-1	chr14:32027031-32027301	NONHSAT036285
9	lnc-NUBPL-1	chr14:31891050-31891174	ENSG00000250365
10	lnc-C14orf126-2	chr14:32030317-32030540	ENSG00000257155.1
11	lnc-RP11-187E13.1.1-1	chr14:32019977-32020133	NONHSAT036285
12	lnc-NUBPL-1	chr14:31921313-31922089	ENSG00000250365
13	lnc-AP4S1-2	chr14:31959233-31959309	XLOC_010789
14	lnc-AP4S1-2	chr14:31995258-31995393	XLOC_010789
15	lnc-NUBPL-1	chr14:31889492-31889791	ENSG00000250365
16	lnc-RP11-187E13.1.1-1	chr14:32020114-32020133	XLOC_010790
17	lnc-C14orf126-1	chr14:32023194-32023269	ENSG00000258196.1
18	lnc-C14orf126-2	chr14:32027713-32027776	ENSG00000257155.1
19	lnc-NUBPL-1	chr14:31908878-31909155	ENSG00000250365
20	lnc-NUBPL-1	chr14:31889964-31890183	ENSG00000250365
21	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
22	lnc-C14orf126-7	chr14:31932001-31932577	NONHSAT036283
23	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C14orf126	hsa-miR-181b-5p	chr14:31915941-31915963

Variant related genes	Relation type
NUBPL	TF binding region
ENSG00000257155	TF binding region
ENSG00000250365	TF binding region
ENSG00000239323	TF binding region
ENSG00000258196	TF binding region
ENSG00000203546	TF binding region
DTD2	TF binding region
HEATR5A	TF binding region
GPR33	TF binding region
NUBPL	CpG island
ENSG00000257155	CpG island
ENSG00000250365	CpG island
ENSG00000239323	CpG island
ENSG00000258196	CpG island
ENSG00000203546	CpG island
DTD2	CpG island
HEATR5A	CpG island
GPR33	CpG island
ENSG00000214943	chromatin interactions
ENSG00000257155	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000270820	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000168036	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000119969	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000258196	chromatin interactions
ENSG00000142188	chromatin interactions
ENSG00000221062	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000101361	chromatin interactions
ENSG00000200463	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000129480	chromatin interactions
SERPINB5	miRNA target sites
CD274	miRNA target sites
CCNG1	miRNA target sites
ALG2	miRNA target sites
SLC26A2	miRNA target sites
YTHDC1	miRNA target sites

Extended variants
information (count: 8612 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:8612 , 50 per page) page: 1 2 3 4 5 6 7 ... 173

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573564679	chr14:31871742-31871743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540883742	chr14:31871743-31871744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115879161	chr14:31871765-31871766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193213853	chr14:31871784-31871785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199805804	chr14:31871801-31871802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10483352	chr14:31871875-31871876	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543982429	chr14:31871953-31871954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528561855	chr14:31872023-31872024	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562557917	chr14:31872027-31872028	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533002611	chr14:31872061-31872062	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200514372	chr14:31872064-31872065	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201968171	chr14:31872119-31872120	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560043962	chr14:31872129-31872130	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs35562864	chr14:31872184-31872185	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs138226506	chr14:31872213-31872214	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs370173506	chr14:31872226-31872227	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs185568163	chr14:31872264-31872265	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs546629266	chr14:31872280-31872281	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs147557302	chr14:31872314-31872315	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs568122655	chr14:31872320-31872321	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529238935	chr14:31872376-31872377	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs550816059	chr14:31872418-31872419	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs569296573	chr14:31872477-31872478	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs374952351	chr14:31872486-31872487	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs539677558	chr14:31872495-31872496	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs189519481	chr14:31872510-31872511	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs567220794	chr14:31872529-31872530	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs534490415	chr14:31872550-31872551	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374617649	chr14:31872598-31872599	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs76570241	chr14:31872660-31872661	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573559644	chr14:31872684-31872685	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs117277415	chr14:31872749-31872750	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556002520	chr14:31872755-31872756	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577651929	chr14:31872759-31872760	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs142086012	chr14:31872813-31872814	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs192068087	chr14:31872863-31872864	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569378365	chr14:31872929-31872930	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542516207	chr14:31873023-31873024	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs7359020	chr14:31873038-31873039	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs74776258	chr14:31873046-31873047	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs550935888	chr14:31873056-31873057	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551070079	chr14:31873065-31873066	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs569283462	chr14:31873097-31873098	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs150104460	chr14:31873109-31873110	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs539611626	chr14:31873122-31873123	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs115909580	chr14:31873139-31873140	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs184464279	chr14:31873180-31873181	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs188466762	chr14:31873223-31873224	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534343600	chr14:31873274-31873275	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs138592847	chr14:31873332-31873333	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3319 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31771000-31888800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr14:31782200-31875200	Weak transcription	Gastric	stomach
3	chr14:31801200-31883800	Weak transcription	Small Intestine	intestine
4	chr14:31801400-31875600	Weak transcription	Brain Germinal Matrix	brain
5	chr14:31801600-31872400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:31802800-31872000	Weak transcription	Fetal Brain Male	brain
7	chr14:31803600-31872600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr14:31808000-31872600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr14:31809600-31872000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr14:31813200-31872800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr14:31816000-31888800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr14:31825600-31872800	Weak transcription	Fetal Kidney	kidney
13	chr14:31825600-31878600	Weak transcription	Pancreas	Pancrea
14	chr14:31827400-31874400	Weak transcription	Spleen	Spleen
15	chr14:31837200-31871800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr14:31838000-31875000	Weak transcription	K562	blood
17	chr14:31841400-31872800	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr14:31841600-31872200	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr14:31847000-31878600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr14:31847600-31875000	Weak transcription	Stomach Mucosa	stomach
21	chr14:31847800-31887400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr14:31851000-31872600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr14:31851200-31872400	Strong transcription	HepG2	liver
24	chr14:31851600-31872800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:31853200-31875200	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr14:31853200-31880600	Weak transcription	HSMMtube	muscle
27	chr14:31854600-31880600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr14:31855000-31888400	Weak transcription	Primary T cells from cord blood	blood
29	chr14:31859200-31871800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:31859200-31872000	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr14:31859200-31875200	Weak transcription	Colon Smooth Muscle	Colon
32	chr14:31859200-31880600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr14:31859800-31871800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr14:31860200-31871800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:31861600-31872000	Strong transcription	Placenta	Placenta
36	chr14:31861600-31888400	Weak transcription	Psoas Muscle	Psoas
37	chr14:31863000-31879000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:31863000-31889000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr14:31863200-31874400	Weak transcription	Lung	lung
40	chr14:31863400-31872000	Weak transcription	Aorta	Aorta
41	chr14:31863400-31883200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr14:31863400-31884400	Weak transcription	Brain Anterior Caudate	brain
43	chr14:31863600-31872000	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr14:31863800-31877600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr14:31864600-31888400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr14:31865400-31872200	Strong transcription	Duodenum Mucosa	Duodenum
47	chr14:31865600-31878200	Weak transcription	HMEC	breast
48	chr14:31865600-31883200	Weak transcription	NHEK	skin
49	chr14:31865600-31884200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:31865800-31874000	Weak transcription	Brain Inferior Temporal Lobe	brain

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