Variant report

Variant	nsv902104
Chromosome Location	chr14:77720741-77756321
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	chr14:77736134-77736327	HepG2	liver:	n/a	n/a
2	BACH1	chr14:77736132-77736341	K562	blood:	n/a	n/a
3	BACH1	chr14:77736842-77737281	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr14:77736052-77736216	HepG2	liver:	n/a	n/a
5	BRCA1	chr14:77736133-77736334	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:77734130-77734310	K562	blood:	n/a	n/a
7	CTCF	chr14:77745380-77745530	GM12874	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
8	CTCF	chr14:77745378-77745518	GM19238	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
9	CTCF	chr14:77752000-77752290	GM12868	blood:	n/a	n/a
10	CTCF	chr14:77741940-77742090	BE2_C	brain:	n/a	n/a
11	CTCF	chr14:77745370-77745524	GM12891	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
12	CTCF	chr14:77745392-77745512	GM19239	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
13	CTCF	chr14:77745380-77745530	GM12868	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
14	CTCF	chr14:77745380-77745530	HRE	kidney:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
15	CTCF	chr14:77745320-77745470	Hela-S3	cervix:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
16	CTCF	chr14:77743013-77743141	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr14:77750000-77750150	MCF-7	breast:	n/a	n/a
18	CTCF	chr14:77745352-77745532	MCF-7	breast:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
19	CTCF	chr14:77742020-77742170	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr14:77737756-77737778	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr14:77745381-77745499	ProgFib	skin:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
22	CTCF	chr14:77736005-77736169	Lung_OC	lung:	n/a	n/a
23	CTCF	chr14:77745320-77745470	AG04450	lung:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
24	CTCF	chr14:77741920-77742070	HL-60	blood:	n/a	n/a
25	CTCF	chr14:77741912-77742188	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr14:77735512-77735530	MCF-7	breast:	n/a	n/a
27	CTCF	chr14:77745160-77745310	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr14:77742980-77743130	Caco-2	colon:	n/a	n/a
29	CTCF	chr14:77745378-77745519	GM12892	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
30	CTCF	chr14:77742060-77742210	AG10803	skin:	n/a	n/a
31	CTCF	chr14:77737716-77737751	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr14:77745380-77745530	GM12871	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
33	CTCF	chr14:77745336-77745502	GM12878	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
34	CTCF	chr14:77745380-77745530	A549	lung:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
35	CTCF	chr14:77745390-77745492	MCF-7	breast:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
36	CTCF	chr14:77745280-77745430	GM12873	blood:	n/a	n/a
37	CTCF	chr14:77743051-77743098	K562	blood:	n/a	n/a
38	CTCF	chr14:77744897-77745062	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:77745360-77745510	SK-N-SH_RA	brain:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
40	CTCF	chr14:77745320-77745470	GM12872	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
41	CTCF	chr14:77744916-77745038	MCF-7	breast:	n/a	n/a
42	CTCF	chr14:77745329-77745489	HepG2	liver:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
43	CTCF	chr14:77745240-77745390	GM12869	blood:	n/a	n/a
44	CTCF	chr14:77745348-77745538	A549	lung:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
45	CTCF	chr14:77742003-77742144	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr14:77745340-77745490	GM12875	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
47	CTCF	chr14:77745402-77745526	IMR90	lung:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
48	CTCF	chr14:77745402-77745497	HepG2	liver:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
49	CTCF	chr14:77745320-77745470	GM06990	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
50	CTCF	chr14:77745369-77745511	K562	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:77736734-77736784	MCF10A-Er-Src	breast:	n/a
2	chr14:77732641-77732691	LNCaP	prostate:	n/a
3	chr14:77736734-77736784	MCF10A-Er-Src	breast:	n/a
4	chr14:77732641-77732691	LNCaP	prostate:	n/a
5	chr14:77737621-77737671	HEK293	kidney:	embryo
6	chr14:77732015-77732065	HIPEpiC	eye:	n/a
7	chr14:77737495-77737545	GM12878	blood:	n/a
8	chr14:77738893-77738943	ovcar-3	ovarian:	n/a
9	chr14:77732494-77732544	PFSK-1	brain:	n/a
10	chr14:77737749-77737799	PFSK-1	brain:	n/a
11	chr14:77738721-77738771	HCM	heart:	n/a
12	chr14:77732494-77732544	HAEpiC	amniotic membrane:	n/a
13	chr14:77731074-77731124	NH-A	brain:	n/a
14	chr14:77725701-77725751	NB4	blood:	n/a
15	chr14:77737495-77737545	NHBE	bronchial:	n/a
16	chr14:77735102-77735152	HIPEpiC	eye:	n/a
17	chr14:77737495-77737545	HCT-116	colon:	n/a
18	chr14:77736904-77736954	SK-N-MC	brain:	n/a
19	chr14:77732283-77732333	SAEC	small airway:	n/a
20	chr14:77737146-77737196	U87	brain:	n/a
21	chr14:77737800-77737850	HEK293	kidney:	embryo
22	chr14:77736904-77736954	HIPEpiC	eye:	n/a
23	chr14:77732283-77732333	AoSMC	blood vessel:	n/a
24	chr14:77732602-77732652	HRCEpiC	kidney:	n/a
25	chr14:77738080-77738130	CMK	blood:	n/a
26	chr14:77731074-77731124	HAEpiC	amniotic membrane:	n/a
27	chr14:77737146-77737196	MCF-7	breast:	n/a
28	chr14:77737771-77737821	PFSK-1	brain:	n/a
29	chr14:77738721-77738771	GM19239	blood:	n/a
30	chr14:77737621-77737671	HRPEpiC	eye:	n/a
31	chr14:77732015-77732065	PANC-1	pancreas:	n/a
32	chr14:77741448-77741498	HCM	heart:	n/a
33	chr14:77737661-77737711	T-47D	breast:	n/a
34	chr14:77738893-77738943	HMEC	breast:	n/a
35	chr14:77737661-77737711	AG09319	gingival:	n/a
36	chr14:77734687-77734737	HAEpiC	amniotic membrane:	n/a
37	chr14:77738080-77738130	GM06990	blood:	n/a
38	chr14:77732641-77732691	AoSMC	blood vessel:	n/a
39	chr14:77737749-77737799	AG04450	lung:	fetal
40	chr14:77732015-77732065	CMK	blood:	n/a
41	chr14:77737495-77737545	HCF	heart:	n/a
42	chr14:77732468-77732518	CMK	blood:	n/a
43	chr14:77741448-77741498	NHBE	bronchial:	n/a
44	chr14:77737146-77737196	PANC-1	pancreas:	n/a
45	chr14:77741448-77741498	HRPEpiC	eye:	n/a
46	chr14:77737661-77737711	HCPEpiC	choroid plexus:	n/a
47	chr14:77732494-77732544	NHBE	bronchial:	n/a
48	chr14:77737495-77737545	HCM	heart:	n/a
49	chr14:77737621-77737671	GM12891	blood:	n/a
50	chr14:77737749-77737799	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:77748044..77750512-chr14:77785605..77787632,2	MCF-7	breast:
2	chr14:77741494..77746628-chr14:77751488..77756217,6	MCF-7	breast:
3	chr14:77735572..77739063-chr14:77740094..77742423,3	K562	blood:
4	chr14:77742580..77744356-chr14:77768244..77771004,2	MCF-7	breast:
5	chr14:77719388..77722055-chr14:77734428..77736002,2	K562	blood:
6	chr14:77752243..77754429-chr14:77756635..77759049,2	MCF-7	breast:
7	chr14:77626056..77627919-chr14:77723714..77725727,2	MCF-7	breast:
8	chr14:77738568..77742274-chr14:77786037..77788783,3	MCF-7	breast:
9	chr14:77738903..77740778-chr14:77763967..77766805,2	MCF-7	breast:
10	chr14:77751328..77755884-chr14:77785355..77788655,4	MCF-7	breast:
11	chr14:77750609..77752387-chr14:77785082..77786796,2	MCF-7	breast:
12	chr14:77734159..77735864-chr14:77768086..77770638,2	MCF-7	breast:
13	chr14:77704827..77706771-chr14:77719324..77721062,2	MCF-7	breast:
14	chr14:77745441..77747775-chr14:77749161..77750911,2	MCF-7	breast:
15	chr13:102030233..102030781-chr14:77734735..77735360,2	MCF-7	breast:
16	chr14:77734678..77737344-chr14:77778616..77780685,2	MCF-7	breast:
17	chr14:77726824..77729314-chr14:78083022..78085300,2	K562	blood:
18	chr14:77744963..77747141-chr14:77762245..77764781,2	MCF-7	breast:
19	chr14:77646430..77648233-chr14:77722733..77725408,2	MCF-7	breast:
20	chr14:77746501..77748869-chr14:77754519..77757381,3	MCF-7	breast:
21	chr14:77746501..77748869-chr14:77754519..77757381,3	MCF-7	breast:
22	chr14:77730051..77733003-chr14:77740176..77742640,2	MCF-7	breast:
23	chr14:77745441..77747775-chr14:77749161..77750911,2	MCF-7	breast:
24	chr14:77644659..77647131-chr14:77754541..77756569,2	MCF-7	breast:
25	chr14:77736936..77738767-chr14:77739466..77741351,2	MCF-7	breast:
26	chr14:77597295..77599304-chr14:77739506..77741172,2	MCF-7	breast:
27	chr14:77754082..77755889-chr14:77757491..77759643,2	MCF-7	breast:
28	chr14:77723065..77723902-chr3:79134805..79135701,2	MCF-7	breast:
29	chr14:77656618..77658691-chr14:77734209..77736747,2	MCF-7	breast:
30	chr14:77741661..77744211-chr14:77747237..77749936,2	MCF-7	breast:
31	chr14:77719388..77722055-chr14:77734428..77736002,2	K562	blood:
32	chr14:77741661..77744211-chr14:77747237..77749936,2	MCF-7	breast:
33	chr14:77720307..77722761-chr14:77737382..77738891,2	MCF-7	breast:
34	chr14:77749701..77751347-chr14:77755395..77757544,2	K562	blood:
35	chr14:77741494..77746628-chr14:77751488..77756217,6	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NGB-1	chr14:77744737-77744851	NONHSAT037969
2	lnc-NGB-1	chr14:77745072-77745212	NONHSAT037969
3	lnc-NGB-1	chr14:77746166-77746275	NONHSAT037969
4	lnc-NGB-1	chr14:77743326-77743621	NONHSAT037969

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1260a	chr14:77732574-77732591	MIMAT0005911

Variant related genes	Relation type
MIR1260A	TF binding region
NGB	TF binding region
POMT2	TF binding region
MIR1260A	CpG island
NGB	CpG island
POMT2	CpG island
ENSG00000221754	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000165553	chromatin interactions
ENSG00000100596	chromatin interactions
ENSG00000165548	chromatin interactions
ENSG00000100577	chromatin interactions
TMEM41A	Mature miRNA region
ZNF432	Mature miRNA region
HNRNPAB	Mature miRNA region
DDX1	Mature miRNA region

Extended variants
information (count: 1528 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs877896	chr14:77720741-77720742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564067376	chr14:77720766-77720767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532827924	chr14:77720797-77720798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187780759	chr14:77720900-77720901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192931752	chr14:77720901-77720902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs147101527	chr14:77720924-77720925	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183806402	chr14:77720945-77720946	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576513641	chr14:77720950-77720951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs8016994	chr14:77720957-77720958	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs188294128	chr14:77721026-77721027	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562430194	chr14:77721040-77721041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570817978	chr14:77721085-77721086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs193006926	chr14:77721086-77721087	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556219936	chr14:77721128-77721129	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183953611	chr14:77721141-77721142	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs151095088	chr14:77721160-77721161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560274232	chr14:77721184-77721185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188204898	chr14:77721200-77721201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541700203	chr14:77721207-77721208	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558212460	chr14:77721218-77721219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs577543509	chr14:77721254-77721255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543084314	chr14:77721262-77721263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563288550	chr14:77721335-77721336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs422642	chr14:77721374-77721375	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542747615	chr14:77721380-77721381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559550067	chr14:77721400-77721401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548074311	chr14:77721412-77721413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141023940	chr14:77721458-77721459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546175507	chr14:77721460-77721461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551652536	chr14:77721487-77721488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs375526996	chr14:77721501-77721502	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191109242	chr14:77721578-77721579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10151490	chr14:77721581-77721582	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs12437257	chr14:77721586-77721587	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184786727	chr14:77721626-77721627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs735477	chr14:77721723-77721724	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs571478749	chr14:77721736-77721737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537500352	chr14:77721794-77721795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs116228646	chr14:77721909-77721910	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549103944	chr14:77721960-77721961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs55841851	chr14:77721983-77721984	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs534933331	chr14:77722002-77722003	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs140851947	chr14:77722011-77722012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568378334	chr14:77722055-77722056	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs144600811	chr14:77722056-77722057	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7144033	chr14:77722088-77722089	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs888059	chr14:77722148-77722149	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs553601618	chr14:77722158-77722159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190505116	chr14:77722184-77722185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs182001091	chr14:77722209-77722210	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Biliary cancer	19435499	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Intracranial aneurysm	16715129	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77697600-77726800	Weak transcription	Brain Substantia Nigra	brain
2	chr14:77709800-77729600	Weak transcription	Fetal Brain Male	brain
3	chr14:77711200-77731000	Weak transcription	Spleen	Spleen
4	chr14:77712400-77720800	Strong transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:77712800-77720800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr14:77713200-77726800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr14:77714000-77723400	Weak transcription	Fetal Intestine Large	intestine
8	chr14:77714800-77720800	Strong transcription	Brain Germinal Matrix	brain
9	chr14:77715800-77721400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:77716200-77724200	Weak transcription	Brain Angular Gyrus	brain
11	chr14:77718200-77720800	Strong transcription	Esophagus	oesophagus
12	chr14:77718400-77726800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr14:77719800-77720800	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr14:77719800-77720800	Strong transcription	Brain Anterior Caudate	brain
15	chr14:77720000-77724600	Weak transcription	Fetal Intestine Small	intestine
16	chr14:77720400-77724000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:77720600-77721800	Weak transcription	Fetal Brain Female	brain
18	chr14:77720600-77725000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:77720800-77723400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr14:77720800-77724600	Weak transcription	Brain Germinal Matrix	brain
21	chr14:77720800-77725600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr14:77720800-77725800	Weak transcription	Esophagus	oesophagus
23	chr14:77720800-77726800	Weak transcription	Brain Anterior Caudate	brain
24	chr14:77720800-77727000	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr14:77721800-77725000	Strong transcription	Fetal Brain Female	brain
26	chr14:77722800-77723000	Enhancers	Gastric	stomach
27	chr14:77723000-77734000	Weak transcription	Gastric	stomach
28	chr14:77723400-77724000	Strong transcription	Pancreatic Islets	Pancreatic Islet
29	chr14:77723800-77724000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
30	chr14:77724000-77724400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:77724000-77725800	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr14:77724400-77725800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr14:77724600-77725000	Strong transcription	Brain Germinal Matrix	brain
34	chr14:77725000-77727000	Weak transcription	Brain Germinal Matrix	brain
35	chr14:77725000-77730400	Weak transcription	Fetal Brain Female	brain
36	chr14:77725400-77725600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr14:77725600-77725800	Bivalent Enhancer	Fetal Stomach	stomach
38	chr14:77725600-77726000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
39	chr14:77725600-77726000	Enhancers	H1 Cell Line	embryonic stem cell
40	chr14:77725600-77726000	Bivalent Enhancer	HepG2	liver
41	chr14:77725600-77727600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr14:77725800-77726000	Enhancers	Esophagus	oesophagus
43	chr14:77725800-77726800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr14:77725800-77727200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr14:77726000-77727000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr14:77726000-77727600	Weak transcription	Esophagus	oesophagus
47	chr14:77726200-77728000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:77726600-77727800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr14:77726600-77728000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:77726800-77727000	Enhancers	Brain Cingulate Gyrus	brain

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