Variant report

Variant	nsv1361
Chromosome Location	chr14:77707417-77753024
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:1403)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	ATF1	chr14:77712361-77712488	K562	blood:	n/a	n/a
3	BACH1	chr14:77736132-77736341	K562	blood:	n/a	n/a
4	BACH1	chr14:77736842-77737281	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr14:77710087-77710350	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:77736052-77736216	HepG2	liver:	n/a	n/a
7	BRCA1	chr14:77736133-77736334	HepG2	liver:	n/a	n/a
8	CEBPB	chr14:77734130-77734310	K562	blood:	n/a	n/a
9	CTCF	chr14:77712260-77712410	K562	blood:	n/a	n/a
10	CTCF	chr14:77712260-77712410	HA-sp	spinal cord:	n/a	n/a
11	CTCF	chr14:77741912-77742188	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr14:77712220-77712370	SAEC	small airway:	n/a	n/a
13	CTCF	chr14:77736005-77736169	Lung_OC	lung:	n/a	n/a
14	CTCF	chr14:77742000-77742150	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr14:77743051-77743098	K562	blood:	n/a	n/a
16	CTCF	chr14:77712160-77712310	HVMF	connective:	n/a	n/a
17	CTCF	chr14:77745240-77745390	GM12865	blood:	n/a	n/a
18	CTCF	chr14:77712820-77712970	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:77744890-77745057	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:77712220-77712370	GM12870	blood:	n/a	n/a
21	CTCF	chr14:77712340-77712490	GM12871	blood:	n/a	n/a
22	CTCF	chr14:77742060-77742210	A549	lung:	n/a	n/a
23	CTCF	chr14:77712267-77712439	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:77712200-77712350	NHEK	skin:	n/a	n/a
25	CTCF	chr14:77712520-77712670	HAc	cerebellar:	n/a	n/a
26	CTCF	chr14:77745380-77745530	HA-sp	spinal cord:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
27	CTCF	chr14:77712280-77712430	GM12875	blood:	n/a	n/a
28	CTCF	chr14:77712285-77712452	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr14:77712304-77712403	NHEK	skin:	n/a	n/a
30	CTCF	chr14:77712240-77712390	HVMF	connective:	n/a	n/a
31	CTCF	chr14:77712251-77712405	HepG2	liver:	n/a	n/a
32	CTCF	chr14:77745380-77745530	HRPEpiC	eye:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
33	CTCF	chr14:77745360-77745510	HepG2	liver:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
34	CTCF	chr14:77712300-77712450	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr14:77735460-77735610	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:77737716-77737751	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr14:77742020-77742170	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr14:77745360-77745510	HEK293	kidney:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
39	CTCF	chr14:77745320-77745470	GM06990	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
40	CTCF	chr14:77745380-77745530	A549	lung:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
41	CTCF	chr14:77741960-77742110	HEK293	kidney:	n/a	n/a
42	CTCF	chr14:77710130-77710250	GM19239	blood:	n/a	n/a
43	CTCF	chr14:77712260-77712410	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr14:77745412-77745461	Pancreas_OC	pancreas:	n/a	chr14:77745439-77745457 chr14:77745442-77745455
45	CTCF	chr14:77745362-77745546	K562	blood:	n/a	chr14:77745439-77745457 chr14:77745442-77745455 chr14:77745441-77745462
46	CTCF	chr14:77745300-77745450	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr14:77712200-77712350	GM12871	blood:	n/a	n/a
48	CTCF	chr14:77741940-77742090	BE2_C	brain:	n/a	n/a
49	CTCF	chr14:77742020-77742170	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr14:77749940-77750090	BJ	skin:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:77738080-77738130	ProgFib	skin:	n/a
2	chr14:77737661-77737711	CMK	blood:	n/a
3	chr14:77732283-77732333	AG10803	skin:	n/a
4	chr14:77737800-77737850	GM12892	blood:	n/a
5	chr14:77737621-77737671	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:77737800-77737850	AoSMC	blood vessel:	n/a
7	chr14:77741448-77741498	HMEC	breast:	n/a
8	chr14:77732641-77732691	MCF-7	breast:	n/a
9	chr14:77732468-77732518	AG09319	gingival:	n/a
10	chr14:77738893-77738943	NB4	blood:	n/a
11	chr14:77737146-77737196	HCPEpiC	choroid plexus:	n/a
12	chr14:77736904-77736954	GM12878	blood:	n/a
13	chr14:77736734-77736784	Hepatocyte	liver:	n/a
14	chr14:77732602-77732652	BE2_C	brain:	n/a
15	chr14:77737800-77737850	HEK293	kidney:	embryo
16	chr14:77732015-77732065	ECC-1	luminal epithelium:	n/a
17	chr14:77732641-77732691	BE2_C	brain:	n/a
18	chr14:77737800-77737850	HAEpiC	amniotic membrane:	n/a
19	chr14:77732015-77732065	GM12891	blood:	n/a
20	chr14:77732468-77732518	HEK293	kidney:	embryo
21	chr14:77737771-77737821	ovcar-3	ovarian:	n/a
22	chr14:77737495-77737545	Jurkat	blood:	n/a
23	chr14:77737495-77737545	BJ	skin:	n/a
24	chr14:77737771-77737821	MCF-7	breast:	n/a
25	chr14:77734687-77734737	Jurkat	blood:	n/a
26	chr14:77737749-77737799	HCF	heart:	n/a
27	chr14:77734687-77734737	GM19239	blood:	n/a
28	chr14:77732494-77732544	HRE	kidney:	n/a
29	chr14:77725701-77725751	HCF	heart:	n/a
30	chr14:77738080-77738130	AG04450	lung:	fetal
31	chr14:77738721-77738771	GM19239	blood:	n/a
32	chr14:77737771-77737821	BJ	skin:	n/a
33	chr14:77738893-77738943	PrEC	prostate:	n/a
34	chr14:77737661-77737711	K562	blood:	n/a
35	chr14:77737800-77737850	NHBE	bronchial:	n/a
36	chr14:77738080-77738130	HCPEpiC	choroid plexus:	n/a
37	chr14:77738893-77738943	HRCEpiC	kidney:	n/a
38	chr14:77732602-77732652	NH-A	brain:	n/a
39	chr14:77737771-77737821	AG04450	lung:	fetal
40	chr14:77736734-77736784	HEEpiC	esophagus:	n/a
41	chr14:77732468-77732518	IMR90	lung:	fetal
42	chr14:77738080-77738130	AoSMC	blood vessel:	n/a
43	chr14:77732494-77732544	AG09309	skin:	n/a
44	chr14:77736904-77736954	NT2-D1	testis:	n/a
45	chr14:77732641-77732691	AG09319	gingival:	n/a
46	chr14:77732468-77732518	K562	blood:	n/a
47	chr14:77735102-77735152	GM12892	blood:	n/a
48	chr14:77737495-77737545	HRCEpiC	kidney:	n/a
49	chr14:77741448-77741498	GM06990	blood:	n/a
50	chr14:77738893-77738943	Hela-S3	cervix:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:77742580..77744356-chr14:77768244..77771004,2	MCF-7	breast:
2	chr14:77707273..77709179-chr14:77710972..77713210,2	MCF-7	breast:
3	chr14:77734678..77737344-chr14:77778616..77780685,2	MCF-7	breast:
4	chr14:77626056..77627919-chr14:77723714..77725727,2	MCF-7	breast:
5	chr14:77720307..77722761-chr14:77737382..77738891,2	MCF-7	breast:
6	chr14:77741494..77746628-chr14:77751488..77756217,6	MCF-7	breast:
7	chr14:77741661..77744211-chr14:77747237..77749936,2	MCF-7	breast:
8	chr14:77744963..77747141-chr14:77762245..77764781,2	MCF-7	breast:
9	chr14:77707273..77709179-chr14:77710972..77713210,2	MCF-7	breast:
10	chr14:77723065..77723902-chr3:79134805..79135701,2	MCF-7	breast:
11	chr14:77745441..77747775-chr14:77749161..77750911,2	MCF-7	breast:
12	chr14:77750609..77752387-chr14:77785082..77786796,2	MCF-7	breast:
13	chr14:77726824..77729314-chr14:78083022..78085300,2	K562	blood:
14	chr14:77734159..77735864-chr14:77768086..77770638,2	MCF-7	breast:
15	chr14:77597295..77599304-chr14:77739506..77741172,2	MCF-7	breast:
16	chr14:77646430..77648233-chr14:77722733..77725408,2	MCF-7	breast:
17	chr14:77748044..77750512-chr14:77785605..77787632,2	MCF-7	breast:
18	chr14:77719388..77722055-chr14:77734428..77736002,2	K562	blood:
19	chr14:77736936..77738767-chr14:77739466..77741351,2	MCF-7	breast:
20	chr14:77719388..77722055-chr14:77734428..77736002,2	K562	blood:
21	chr14:77746501..77748869-chr14:77754519..77757381,3	MCF-7	breast:
22	chr14:77712852..77714702-chr14:77715843..77718574,2	K562	blood:
23	chr14:77656618..77658691-chr14:77734209..77736747,2	MCF-7	breast:
24	chr14:77730051..77733003-chr14:77740176..77742640,2	MCF-7	breast:
25	chr14:77698665..77701683-chr14:77707359..77710603,3	MCF-7	breast:
26	chr14:77741494..77746628-chr14:77751488..77756217,6	MCF-7	breast:
27	chr14:77741661..77744211-chr14:77747237..77749936,2	MCF-7	breast:
28	chr14:77745441..77747775-chr14:77749161..77750911,2	MCF-7	breast:
29	chr14:77738568..77742274-chr14:77786037..77788783,3	MCF-7	breast:
30	chr14:77752243..77754429-chr14:77756635..77759049,2	MCF-7	breast:
31	chr14:77606518..77608062-chr14:77708276..77710654,2	MCF-7	breast:
32	chr13:102030233..102030781-chr14:77734735..77735360,2	MCF-7	breast:
33	chr14:77751328..77755884-chr14:77785355..77788655,4	MCF-7	breast:
34	chr14:77738903..77740778-chr14:77763967..77766805,2	MCF-7	breast:
35	chr14:77704827..77706771-chr14:77719324..77721062,2	MCF-7	breast:
36	chr14:77735572..77739063-chr14:77740094..77742423,3	K562	blood:

(count:4 , 50 per page) page: 1

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

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

No data

Variant related genes	Relation type
NGB	TF binding region
POMT2	TF binding region
TMEM63C	TF binding region
MIR1260A	TF binding region
NGB	CpG island
POMT2	CpG island
TMEM63C	CpG island
MIR1260A	CpG island
ENSG00000165553	chromatin interactions
ENSG00000100577	chromatin interactions
ENSG00000009830	chromatin interactions
ENSG00000269883	chromatin interactions
ENSG00000100596	chromatin interactions
ENSG00000165548	chromatin interactions
ENSG00000177108	chromatin interactions
ENSG00000221754	chromatin interactions
TMEM41A	Mature miRNA region
ZNF432	Mature miRNA region
DDX1	Mature miRNA region
HNRNPAB	Mature miRNA region

Extended variants
information (count: 1985 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1985 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374404395	chr14:77707442-77707443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs144509713	chr14:77707443-77707444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570073420	chr14:77707516-77707517	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112228490	chr14:77707543-77707544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555837976	chr14:77707572-77707573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575759567	chr14:77707580-77707581	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548679285	chr14:77707585-77707586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375131097	chr14:77707586-77707587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572225598	chr14:77707614-77707615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77101169	chr14:77707626-77707627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17812490	chr14:77707632-77707633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2540887	chr14:77707635-77707636	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs577304139	chr14:77707666-77707667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184499714	chr14:77707668-77707669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562949293	chr14:77707698-77707699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531746702	chr14:77707735-77707736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542326612	chr14:77707736-77707737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189381216	chr14:77707743-77707744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527895427	chr14:77707869-77707870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374988507	chr14:77707877-77707878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547673048	chr14:77707920-77707921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193149817	chr14:77707930-77707931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147142676	chr14:77707961-77707962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549397526	chr14:77707981-77707982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534194603	chr14:77708015-77708016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140268599	chr14:77708058-77708059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555442468	chr14:77708095-77708096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185653039	chr14:77708098-77708099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546794837	chr14:77708113-77708114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534861498	chr14:77708156-77708157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558084272	chr14:77708163-77708164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571398791	chr14:77708165-77708166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534384255	chr14:77708204-77708205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs578022614	chr14:77708216-77708217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546204585	chr14:77708224-77708225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556563276	chr14:77708240-77708241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189114640	chr14:77708284-77708285	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78143881	chr14:77708357-77708358	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs79664403	chr14:77708388-77708389	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527876720	chr14:77708389-77708390	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs541255104	chr14:77708417-77708418	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs8007762	chr14:77708465-77708466	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs557065018	chr14:77708506-77708507	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368415163	chr14:77708516-77708517	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs550080370	chr14:77708581-77708582	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs116832486	chr14:77708600-77708601	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs142228943	chr14:77708618-77708619	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs151218235	chr14:77708688-77708689	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs201848457	chr14:77708695-77708696	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201023823	chr14:77708755-77708756	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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

Chromatin state (count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77654200-77709400	Weak transcription	Esophagus	oesophagus
2	chr14:77686400-77712400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:77692800-77712400	Weak transcription	Fetal Intestine Small	intestine
4	chr14:77697600-77726800	Weak transcription	Brain Substantia Nigra	brain
5	chr14:77698400-77720000	Weak transcription	Pancreas	Pancrea
6	chr14:77701400-77708400	Weak transcription	Brain Angular Gyrus	brain
7	chr14:77701600-77710000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr14:77704800-77719200	Weak transcription	Brain Hippocampus Middle	brain
9	chr14:77705000-77707800	Strong transcription	Brain Germinal Matrix	brain
10	chr14:77705600-77714400	Weak transcription	Brain Anterior Caudate	brain
11	chr14:77705800-77709600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr14:77706200-77710000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:77706800-77709000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr14:77706800-77709000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr14:77706800-77709600	Weak transcription	Spleen	Spleen
16	chr14:77707000-77708000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr14:77707000-77708400	Weak transcription	Fetal Brain Female	brain
18	chr14:77707000-77710000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:77707200-77712800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:77707800-77709800	Weak transcription	Brain Germinal Matrix	brain
21	chr14:77707800-77710800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr14:77708000-77710600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:77708000-77711400	Enhancers	Primary B cells from cord blood	blood
24	chr14:77708000-77711400	Enhancers	Primary hematopoietic stem cells	blood
25	chr14:77708000-77711800	Enhancers	Primary B cells from peripheral blood	blood
26	chr14:77708400-77713400	Strong transcription	Brain Angular Gyrus	brain
27	chr14:77708400-77720600	Strong transcription	Fetal Brain Female	brain
28	chr14:77708600-77710800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr14:77708600-77711000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr14:77708600-77714800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr14:77709000-77711400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr14:77709000-77718400	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr14:77709400-77712800	Strong transcription	Esophagus	oesophagus
34	chr14:77709600-77710200	Strong transcription	Pancreatic Islets	Pancreatic Islet
35	chr14:77709600-77711200	Enhancers	Spleen	Spleen
36	chr14:77709800-77711800	Strong transcription	Brain Germinal Matrix	brain
37	chr14:77709800-77729600	Weak transcription	Fetal Brain Male	brain
38	chr14:77710000-77710200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr14:77710000-77710600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:77710000-77713200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:77710200-77712400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr14:77710600-77714600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:77711000-77717600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr14:77711200-77731000	Weak transcription	Spleen	Spleen
45	chr14:77711400-77712400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr14:77711800-77714800	Weak transcription	Brain Germinal Matrix	brain
47	chr14:77712400-77712800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr14:77712400-77713000	Strong transcription	Fetal Intestine Small	intestine
49	chr14:77712400-77713200	Strong transcription	Brain Cingulate Gyrus	brain
50	chr14:77712400-77720800	Strong transcription	Pancreatic Islets	Pancreatic Islet

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