Variant report

Variant	nsv564181
Chromosome Location	chr14:31958761-32363980
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	chr14:32336820-32337151	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:32363573-32363850	K562	blood:	n/a	n/a
3	ARID3A	chr14:32217355-32217854	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:31979285-31979597	K562	blood:	n/a	n/a
5	ARID3A	chr14:32013394-32013714	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:32094871-32095254	HepG2	liver:	n/a	chr14:32095223-32095239 chr14:32095224-32095240
7	ARID3A	chr14:31998310-31998539	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:32029929-32030900	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:32186760-32187276	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:32153639-32153640	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:32328061-32328458	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:32324410-32324953	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:31979345-31979767	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:32013429-32013589	K562	blood:	n/a	n/a
15	ARID3A	chr14:32256644-32256965	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:32256749-32256838	K562	blood:	n/a	n/a
17	ARID3A	chr14:32049609-32049683	HepG2	liver:	n/a	n/a
18	ATF1	chr14:32363503-32363948	K562	blood:	n/a	n/a
19	ATF1	chr14:32030401-32030925	K562	blood:	n/a	chr14:32030577-32030591
20	ATF1	chr14:32346315-32346347	K562	blood:	n/a	n/a
21	ATF2	chr14:32030344-32030839	GM12878	blood:	n/a	chr14:32030577-32030591
22	ATF2	chr14:32030341-32031054	GM12878	blood:	n/a	chr14:32030577-32030591
23	ATF2	chr14:31958860-31959365	GM12878	blood:	n/a	n/a
24	ATF3	chr14:32324566-32324812	HepG2	liver:	n/a	n/a
25	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
26	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
27	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
28	ATF3	chr14:32256603-32256876	K562	blood:	n/a	n/a
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	chr14:32030278-32031101	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
31	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
32	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
33	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
34	BACH1	chr14:32030457-32030747	K562	blood:	n/a	n/a
35	BATF	chr14:32222145-32222496	GM12878	blood:	n/a	chr14:32222322-32222333
36	BATF	chr14:32312682-32312995	GM12878	blood:	n/a	chr14:32312694-32312704
37	BATF	chr14:32030472-32030775	GM12878	blood:	n/a	chr14:32030578-32030591
38	BATF	chr14:32222193-32222405	GM12878	blood:	n/a	chr14:32222322-32222333
39	BATF	chr14:32037936-32038139	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:31969113-31969289	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:32030305-32030908	GM12878	blood:	n/a	chr14:32030555-32030564
42	BHLHE40	chr14:32324441-32324803	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:32363559-32363944	K562	blood:	n/a	n/a
44	BHLHE40	chr14:32346581-32346736	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:32030471-32030975	K562	blood:	n/a	n/a
46	BHLHE40	chr14:32186621-32187204	HepG2	liver:	n/a	n/a
47	BHLHE40	chr14:32186771-32187135	HepG2	liver:	n/a	n/a
48	BHLHE40	chr14:32030350-32031051	GM12878	blood:	n/a	n/a
49	BRCA1	chr14:32144763-32144831	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr14:32030403-32030935	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:32030404-32030454	HepG2	liver:	n/a
2	chr14:32030584-32030634	Hepatocyte	liver:	n/a
3	chr14:32030584-32030634	HCF	heart:	n/a
4	chr14:32030404-32030454	HNPCEpiC	eye:	n/a
5	chr14:32181048-32181098	AG04450	lung:	fetal
6	chr14:32030584-32030634	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:32269554-32269604	ovcar-3	ovarian:	n/a
8	chr14:32029310-32029360	NT2-D1	testis:	n/a
9	chr14:32180736-32180786	K562	blood:	n/a
10	chr14:32030686-32030736	HIPEpiC	eye:	n/a
11	chr14:32073463-32073513	RPTEC	kidney:	n/a
12	chr14:32180736-32180786	HCT-116	colon:	n/a
13	chr14:32030176-32030226	NT2-D1	testis:	n/a
14	chr14:32030546-32030596	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:32029310-32029360	HCF	heart:	n/a
16	chr14:32170077-32170127	Hela-S3	cervix:	n/a
17	chr14:32030457-32030507	U87	brain:	n/a
18	chr14:32030579-32030629	SK-N-SH_RA	brain:	n/a
19	chr14:32029310-32029360	SK-N-SH	brain:	n/a
20	chr14:32029920-32029970	ovcar-3	ovarian:	n/a
21	chr14:32029920-32029970	HMEC	breast:	n/a
22	chr14:32269554-32269604	GM12891	blood:	n/a
23	chr14:32029310-32029360	Hela-S3	cervix:	n/a
24	chr14:32030176-32030226	HRCEpiC	kidney:	n/a
25	chr14:32073463-32073513	SAEC	small airway:	n/a
26	chr14:32109281-32109331	NB4	blood:	n/a
27	chr14:31996632-31996682	GM12891	blood:	n/a
28	chr14:32030579-32030629	MCF-7	breast:	n/a
29	chr14:32169802-32169852	GM12878	blood:	n/a
30	chr14:32109281-32109331	NHBE	bronchial:	n/a
31	chr14:32029310-32029360	HL-60	blood:	n/a
32	chr14:32350428-32350478	T-47D	breast:	n/a
33	chr14:32328771-32328821	PFSK-1	brain:	n/a
34	chr14:32109281-32109331	HCPEpiC	choroid plexus:	n/a
35	chr14:32073463-32073513	ovcar-3	ovarian:	n/a
36	chr14:32030584-32030634	NH-A	brain:	n/a
37	chr14:32180736-32180786	ovcar-3	ovarian:	n/a
38	chr14:32073463-32073513	Caco-2	colon:	n/a
39	chr14:32350324-32350374	GM12878	blood:	n/a
40	chr14:32030354-32030404	IMR90	lung:	fetal
41	chr14:31996632-31996682	HCPEpiC	choroid plexus:	n/a
42	chr14:32030584-32030634	GM19239	blood:	n/a
43	chr14:32031012-32031062	HMEC	breast:	n/a
44	chr14:32030354-32030404	U87	brain:	n/a
45	chr14:32029310-32029360	AG09319	gingival:	n/a
46	chr14:32030916-32030966	GM12891	blood:	n/a
47	chr14:32030354-32030404	HRE	kidney:	n/a
48	chr14:32030584-32030634	BE2_C	brain:	n/a
49	chr14:32350428-32350478	HCT-116	colon:	n/a
50	chr14:32029310-32029360	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:32044780..32047478-chr14:32049514..32051528,2	MCF-7	breast:
2	chr14:32031985..32034611-chr14:32035178..32036787,2	MCF-7	breast:
3	chr14:32044780..32047478-chr14:32049514..32051528,2	MCF-7	breast:
4	chr14:32025880..32027814-chr14:32029222..32031344,2	MCF-7	breast:
5	chr14:32058170..32059829-chr14:32063421..32066274,2	MCF-7	breast:
6	chr14:32068418..32071070-chr14:32073502..32076049,2	K562	blood:
7	chr14:32146895..32147481-chr14:32713372..32714254,2	MCF-7	breast:
8	chr14:32295269..32297310-chr14:32302685..32304466,2	K562	blood:
9	chr14:32195719..32197688-chr14:32198704..32200404,2	MCF-7	breast:
10	chr14:32067637..32070373-chr14:32072834..32075613,2	MCF-7	breast:
11	chr14:32026102..32028468-chr14:32029065..32030751,2	K562	blood:
12	chr14:32303855..32305860-chr14:32313557..32315760,2	MCF-7	breast:
13	chr14:32290973..32293409-chr14:32296887..32298672,2	K562	blood:
14	chr14:32030832..32032361-chr14:32036434..32038297,2	MCF-7	breast:
15	chr14:32290973..32293409-chr14:32296388..32299179,4	K562	blood:
16	chr14:32316314..32318915-chr14:32319714..32322323,3	K562	blood:
17	chr14:32303855..32305860-chr14:32313557..32315760,2	MCF-7	breast:
18	chr14:31923625..31927013-chr14:32030157..32032112,3	K562	blood:
19	chr14:32023534..32025380-chr14:32030147..32032486,2	K562	blood:
20	chr14:32247374..32249738-chr14:32259732..32262061,2	MCF-7	breast:
21	chr14:32195719..32197688-chr14:32198704..32200404,2	MCF-7	breast:
22	chr14:32045847..32047973-chr14:32058333..32059909,2	MCF-7	breast:
23	chr14:32039155..32042058-chr14:32047091..32049607,2	K562	blood:
24	chr14:32030832..32032361-chr14:32036434..32038297,2	MCF-7	breast:
25	chr14:32045847..32047973-chr14:32058333..32059909,2	MCF-7	breast:
26	chr14:32247374..32249738-chr14:32259732..32262061,2	MCF-7	breast:
27	chr14:32058170..32059829-chr14:32063421..32066274,2	MCF-7	breast:
28	chr14:32039155..32042058-chr14:32047091..32049607,2	K562	blood:
29	chr14:32250042..32252755-chr14:32254053..32255704,2	MCF-7	breast:
30	chr14:32034560..32036452-chr14:32038131..32040324,3	MCF-7	breast:
31	chr14:32340007..32341798-chr14:32343859..32345846,2	K562	blood:
32	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
33	chr14:32341518..32343411-chr14:32344329..32346208,2	MCF-7	breast:
34	chr14:32029880..32032465-chr14:32040379..32041979,2	K562	blood:
35	chr14:32123058..32124663-chr14:32126123..32128762,2	K562	blood:
36	chr14:31979147..31979905-chr14:32256388..32256891,2	MCF-7	breast:
37	chr14:31979520..31980020-chr14:32542725..32543442,2	MCF-7	breast:
38	chr14:32290973..32293409-chr14:32296388..32299179,4	K562	blood:
39	chr14:32031985..32034611-chr14:32035178..32036787,2	MCF-7	breast:
40	chr14:32341518..32343411-chr14:32344329..32346208,2	MCF-7	breast:
41	chr14:32026102..32028468-chr14:32029065..32030751,2	K562	blood:
42	chr14:32340007..32341798-chr14:32343859..32345846,2	K562	blood:
43	chr14:32029434..32031919-chr14:32034723..32037100,2	MCF-7	breast:
44	chr14:32290973..32293409-chr14:32296887..32298672,2	K562	blood:
45	chr14:32360805..32362723-chr14:32544749..32546621,2	K562	blood:
46	chr14:32034560..32036452-chr14:32038131..32040324,3	MCF-7	breast:
47	chr14:32250042..32252755-chr14:32254053..32255704,2	MCF-7	breast:
48	chr14:32025880..32027814-chr14:32029222..32031344,2	MCF-7	breast:
49	chr14:32295269..32297310-chr14:32302685..32304466,2	K562	blood:
50	chr10:96305060..96305666-chr14:32030841..32031784,2	Hela-S3	cervix:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf126-1	chr14:32023194-32023269	ENSG00000258196.1
2	lnc-C14orf126-2	chr14:32030317-32030540	ENSG00000257155.1
3	lnc-RP11-187E13.1.1-1	chr14:32020114-32020133	XLOC_010790
4	lnc-AP4S1-2	chr14:31995258-31995393	XLOC_010789
5	lnc-C14orf126-1	chr14:32022564-32022836	ENSG00000258196.1
6	lnc-C14orf126-2	chr14:32027713-32027776	ENSG00000257155.1
7	lnc-RP11-187E13.1.1-1	chr14:32027031-32027301	NONHSAT036285
8	lnc-RP11-187E13.1.1-1	chr14:31995361-31995382	NONHSAT036285
9	lnc-RP11-187E13.1.1-1	chr14:32019977-32020133	NONHSAT036285
10	lnc-C14orf126-1	chr14:32027624-32027704	ENSG00000258196.1
11	lnc-AP4S1-2	chr14:31959233-31959309	XLOC_010789
12	lnc-RP11-187E13.1.1-1	chr14:32023231-32023433	XLOC_010790

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NUBPL	hsa-miR-24-3p	chr14:32329735-32329757

Variant related genes	Relation type
NUBPL	TF binding region
RNU6-602P	TF binding region
ENSG00000257155	TF binding region
ENSG00000258196	TF binding region
RNU6-455P	TF binding region
NUBPL	CpG island
RNU6-602P	CpG island
ENSG00000257155	CpG island
ENSG00000258196	CpG island
RNU6-455P	CpG island
ENSG00000129480	chromatin interactions
ENSG00000258196	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000258655	chromatin interactions
ENSG00000100852	chromatin interactions
ENSG00000257155	chromatin interactions
ENSG00000151413	chromatin interactions
ENSG00000119969	chromatin interactions

Extended variants
information (count: 15325 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:15325 , 50 per page) page: 1 2 3 4 5 6 7 ... 307

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2183631	chr14:31958761-31958762	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs575257832	chr14:31958781-31958782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546055566	chr14:31958866-31958867	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs139303031	chr14:31958907-31958908	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs150045440	chr14:31958913-31958914	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs540465821	chr14:31958935-31958936	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs10139022	chr14:31958956-31958957	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528964979	chr14:31959017-31959018	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181533486	chr14:31959030-31959031	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144326643	chr14:31959038-31959039	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs532970637	chr14:31959043-31959044	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs1013394	chr14:31959086-31959087	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs75305514	chr14:31959117-31959118	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs202160146	chr14:31959203-31959204	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs144893980	chr14:31959224-31959225	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs548892237	chr14:31959266-31959267	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs567484648	chr14:31959298-31959299	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs544306672	chr14:31959437-31959438	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535550504	chr14:31959473-31959474	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77971576	chr14:31959479-31959480	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs113550740	chr14:31959498-31959499	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs557444175	chr14:31959543-31959544	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs568872792	chr14:31959568-31959569	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs116622913	chr14:31959607-31959608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557775956	chr14:31959621-31959622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573190107	chr14:31959639-31959640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79194714	chr14:31959641-31959642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114806415	chr14:31959663-31959664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372569341	chr14:31959673-31959674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115662893	chr14:31959681-31959682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574196252	chr14:31959793-31959794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57110356	chr14:31959827-31959828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565065253	chr14:31959833-31959834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200454329	chr14:31959844-31959845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs186145219	chr14:31959848-31959849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535987624	chr14:31959856-31959857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373418668	chr14:31959909-31959910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142007408	chr14:31959961-31959962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs72672700	chr14:31960000-31960001	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs77522360	chr14:31960008-31960009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369206811	chr14:31960022-31960023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373514443	chr14:31960101-31960102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549282349	chr14:31960109-31960110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560459865	chr14:31960276-31960277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533256019	chr14:31960289-31960290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560884982	chr14:31960331-31960332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72672702	chr14:31960359-31960360	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs117662819	chr14:31960434-31960435	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569006495	chr14:31960489-31960490	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151178374	chr14:31960499-31960500	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	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:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31953400-31960400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:31955800-31961200	Enhancers	Primary B cells from cord blood	blood
3	chr14:31956400-31963800	Enhancers	Primary B cells from peripheral blood	blood
4	chr14:31957600-31959400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:31957800-31960000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr14:31957800-31960200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr14:31958600-31959000	Enhancers	GM12878-XiMat	blood
8	chr14:31959000-31959600	Flanking Active TSS	GM12878-XiMat	blood
9	chr14:31959200-31959600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:31959400-31959600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:31959400-31959600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:31959400-31960200	Enhancers	Fetal Brain Male	brain
13	chr14:31959600-31959800	Enhancers	GM12878-XiMat	blood
14	chr14:31959600-31961800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:31959800-31961800	Weak transcription	GM12878-XiMat	blood
16	chr14:31960000-31960200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:31960400-31960600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
18	chr14:31960400-31961600	Enhancers	HepG2	liver
19	chr14:31961200-31961600	Weak transcription	Primary B cells from cord blood	blood
20	chr14:31961600-31962200	Bivalent Enhancer	HepG2	liver
21	chr14:31961600-31962600	Enhancers	HMEC	breast
22	chr14:31961600-31962800	Enhancers	Primary B cells from cord blood	blood
23	chr14:31961800-31962200	Enhancers	Hela-S3	cervix
24	chr14:31961800-31962400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:31961800-31962600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:31961800-31962800	Enhancers	GM12878-XiMat	blood
27	chr14:31962000-31962200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr14:31962000-31962400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:31962000-31962600	Enhancers	Esophagus	oesophagus
30	chr14:31962000-31962600	Enhancers	NHEK	skin
31	chr14:31962000-31968000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:31962200-31963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr14:31962400-31962600	Enhancers	A549	lung
34	chr14:31963400-31963600	Enhancers	GM12878-XiMat	blood
35	chr14:31963400-31964400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:31972000-31974200	Enhancers	Fetal Heart	heart
37	chr14:31972400-31972600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:31972400-31972600	Enhancers	Aorta	Aorta
39	chr14:31972400-31974200	Weak transcription	Right Atrium	heart
40	chr14:31972600-31973400	Weak transcription	Aorta	Aorta
41	chr14:31972800-31974000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:31973000-31974400	Enhancers	Fetal Brain Male	brain
43	chr14:31973400-31973800	Enhancers	Aorta	Aorta
44	chr14:31973400-31976200	Enhancers	Ovary	ovary
45	chr14:31973600-31974400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:31973600-31974800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:31973800-31974000	Weak transcription	Aorta	Aorta
48	chr14:31973800-31974400	Enhancers	Left Ventricle	heart
49	chr14:31973800-31974400	Enhancers	Lung	lung
50	chr14:31974000-31974200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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