Variant report

Variant	nsv518090
Chromosome Location	chr14:35802483-35840241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1738)
CpG islands
(count:549)
Chromatin interactive
region (count:119)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1738 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35828913-35829239	K562	blood:	n/a	n/a
2	ARID3A	chr14:35816401-35817259	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35823045-35823455	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35805605-35806272	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35825248-35826007	K562	blood:	n/a	n/a
6	ARID3A	chr14:35825210-35826108	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:35810902-35811054	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:35836743-35837232	K562	blood:	n/a	n/a
9	ARID3A	chr14:35834810-35835102	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:35803380-35803458	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:35807079-35807330	HepG2	liver:	n/a	n/a
12	ATF1	chr14:35825181-35825633	K562	blood:	n/a	n/a
13	ATF1	chr14:35805813-35806196	K562	blood:	n/a	n/a
14	ATF1	chr14:35834755-35835170	K562	blood:	n/a	n/a
15	ATF2	chr14:35836594-35837330	GM12878	blood:	n/a	n/a
16	ATF3	chr14:35825189-35825603	K562	blood:	n/a	n/a
17	ATF3	chr14:35805645-35806364	A549	lung:	n/a	n/a
18	ATF3	chr14:35805536-35806256	A549	lung:	n/a	n/a
19	ATF3	chr14:35834643-35835073	K562	blood:	n/a	n/a
20	BACH1	chr14:35835358-35835628	K562	blood:	n/a	chr14:35835525-35835539
21	BACH1	chr14:35832628-35832810	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr14:35834809-35835069	K562	blood:	n/a	chr14:35834849-35834863
23	BATF	chr14:35825279-35825686	GM12878	blood:	n/a	chr14:35825397-35825407 chr14:35825393-35825403
24	BATF	chr14:35829886-35830235	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:35836879-35837153	GM12878	blood:	n/a	n/a
26	BCL3	chr14:35805525-35806609	A549	lung:	n/a	chr14:35806078-35806087
27	BCL3	chr14:35804446-35805297	A549	lung:	n/a	n/a
28	BCL3	chr14:35821923-35822498	GM12878	blood:	n/a	chr14:35822120-35822133 chr14:35821936-35821945
29	BCL3	chr14:35805388-35806455	A549	lung:	n/a	chr14:35806078-35806087
30	BCL3	chr14:35831935-35832488	GM12878	blood:	n/a	n/a
31	BCL3	chr14:35832043-35832437	GM12878	blood:	n/a	n/a
32	BCL3	chr14:35822061-35822551	GM12878	blood:	n/a	chr14:35822120-35822133
33	BCL3	chr14:35804460-35805352	A549	lung:	n/a	n/a
34	BCL3	chr14:35834675-35835084	GM12878	blood:	n/a	chr14:35835038-35835047
35	BCLAF1	chr14:35836605-35837297	GM12878	blood:	n/a	n/a
36	BCLAF1	chr14:35836276-35837267	K562	blood:	n/a	n/a
37	BHLHE40	chr14:35825386-35825946	HepG2	liver:	n/a	n/a
38	BHLHE40	chr14:35816962-35817073	K562	blood:	n/a	n/a
39	BHLHE40	chr14:35832181-35832444	HepG2	liver:	n/a	n/a
40	BHLHE40	chr14:35834468-35835502	K562	blood:	n/a	n/a
41	BHLHE40	chr14:35836784-35837117	GM12878	blood:	n/a	n/a
42	BHLHE40	chr14:35834439-35835076	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:35810796-35811188	HepG2	liver:	n/a	n/a
44	BHLHE40	chr14:35805579-35806274	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:35805696-35806242	K562	blood:	n/a	n/a
46	BHLHE40	chr14:35834915-35834936	GM12878	blood:	n/a	n/a
47	BHLHE40	chr14:35816095-35817186	HepG2	liver:	n/a	n/a
48	BHLHE40	chr14:35836819-35837292	K562	blood:	n/a	n/a
49	BHLHE40	chr14:35825458-35826066	GM12878	blood:	n/a	n/a
50	BRCA1	chr14:35816689-35817015	HepG2	liver:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35832310-35832360	Jurkat	blood:	n/a
2	chr14:35822554-35822604	AG10803	skin:	n/a
3	chr14:35822554-35822604	Hepatocyte	liver:	n/a
4	chr14:35838977-35839027	Jurkat	blood:	n/a
5	chr14:35838977-35839027	AG09309	skin:	n/a
6	chr14:35838240-35838290	GM19239	blood:	n/a
7	chr14:35822554-35822604	HPAEpiC	pulmonary alveolar:	n/a
8	chr14:35838885-35838935	SK-N-SH_RA	brain:	n/a
9	chr14:35838240-35838290	HRE	kidney:	n/a
10	chr14:35835511-35835561	BJ	skin:	n/a
11	chr14:35810887-35810937	NT2-D1	testis:	n/a
12	chr14:35810887-35810937	NH-A	brain:	n/a
13	chr14:35835511-35835561	A549	lung:	n/a
14	chr14:35835511-35835561	HUVEC	blood vessel:	n/a
15	chr14:35838413-35838463	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:35835511-35835561	NHBE	bronchial:	n/a
17	chr14:35810887-35810937	SKMC	muscle:	n/a
18	chr14:35805898-35805948	AG10803	skin:	n/a
19	chr14:35822554-35822604	AG04449	skin:	fetal
20	chr14:35838240-35838290	BE2_C	brain:	n/a
21	chr14:35822554-35822604	GM06990	blood:	n/a
22	chr14:35838240-35838290	HCF	heart:	n/a
23	chr14:35822554-35822604	IMR90	lung:	fetal
24	chr14:35838413-35838463	CMK	blood:	n/a
25	chr14:35832310-35832360	SAEC	small airway:	n/a
26	chr14:35838977-35839027	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:35838977-35839027	PANC-1	pancreas:	n/a
28	chr14:35822554-35822604	ProgFib	skin:	n/a
29	chr14:35832310-35832360	HCPEpiC	choroid plexus:	n/a
30	chr14:35838977-35839027	Hepatocyte	liver:	n/a
31	chr14:35838240-35838290	GM12891	blood:	n/a
32	chr14:35805898-35805948	H1-hESC	embryonic stem cell:	embryo
33	chr14:35805898-35805948	SK-N-MC	brain:	n/a
34	chr14:35838977-35839027	AoSMC	blood vessel:	n/a
35	chr14:35838240-35838290	A549	lung:	n/a
36	chr14:35835511-35835561	HEK293	kidney:	embryo
37	chr14:35838240-35838290	HRCEpiC	kidney:	n/a
38	chr14:35810887-35810937	GM19239	blood:	n/a
39	chr14:35838413-35838463	K562	blood:	n/a
40	chr14:35838240-35838290	HIPEpiC	eye:	n/a
41	chr14:35838413-35838463	AG04450	lung:	fetal
42	chr14:35832310-35832360	HCF	heart:	n/a
43	chr14:35832310-35832360	HRPEpiC	eye:	n/a
44	chr14:35835511-35835561	PFSK-1	brain:	n/a
45	chr14:35838240-35838290	H1-hESC	embryonic stem cell:	embryo
46	chr14:35805898-35805948	NHDF-neo	bronchial:	n/a
47	chr14:35835511-35835561	Hela-S3	cervix:	n/a
48	chr14:35838977-35839027	U87	brain:	n/a
49	chr14:35838240-35838290	ovcar-3	ovarian:	n/a
50	chr14:35832310-35832360	NHBE	bronchial:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:35816577..35819351-chr14:35832841..35834841,2	K562	blood:
2	chr14:35821416..35823849-chr14:35826359..35828501,2	K562	blood:
3	chr14:35803428..35804017-chr14:35872984..35873546,2	MCF-7	breast:
4	chr14:35804902..35807934-chr14:35810651..35813744,3	K562	blood:
5	chr14:35790365..35792681-chr14:35809651..35811760,2	MCF-7	breast:
6	chr14:35757408..35763930-chr14:35809319..35813404,11	MCF-7	breast:
7	chr14:35781062..35784992-chr14:35805086..35807917,3	MCF-7	breast:
8	chr14:35759553..35761751-chr14:35821894..35823859,2	MCF-7	breast:
9	chr14:35801529..35804372-chr14:35808012..35809578,2	K562	blood:
10	chr14:35804352..35806289-chr16:30623113..30625899,2	MCF-7	breast:
11	chr14:35816577..35819351-chr14:35832841..35834841,2	K562	blood:
12	chr14:35799325..35802587-chr14:35803466..35807668,8	K562	blood:
13	chr14:35839386..35842775-chr14:35870921..35874153,4	K562	blood:
14	chr14:35808792..35810743-chr14:35815553..35817945,2	K562	blood:
15	chr14:35821416..35824471-chr14:35826109..35828501,4	K562	blood:
16	chr14:35792762..35795033-chr14:35804615..35806413,2	MCF-7	breast:
17	chr14:35801529..35804372-chr14:35808012..35809578,2	K562	blood:
18	chr14:35805577..35806437-chr14:35872990..35873527,2	MCF-7	breast:
19	chr14:35803831..35805653-chr8:102502064..102503841,2	MCF-7	breast:
20	chr14:35801385..35810310-chr14:35830739..35838852,15	K562	blood:
21	chr14:35590118..35592539-chr14:35839205..35841309,2	MCF-7	breast:
22	chr14:35810790..35811847-chr14:35873610..35874301,3	MCF-7	breast:
23	chr14:35829669..35831731-chr14:35831828..35834789,2	MCF-7	breast:
24	chr14:35342362..35344896-chr14:35804305..35806891,2	MCF-7	breast:
25	chr14:35806177..35808702-chr14:35872439..35875223,3	K562	blood:
26	chr14:35701570..35704183-chr14:35804617..35807506,4	MCF-7	breast:
27	chr14:35500902..35503626-chr14:35810015..35811675,2	MCF-7	breast:
28	chr14:35797442..35799693-chr14:35801625..35803378,2	K562	blood:
29	chr14:35800587..35801136-chr14:35810062..35810609,2	MCF-7	breast:
30	chr14:35827417..35829276-chr14:35829488..35832046,2	K562	blood:
31	chr14:35826145..35827656-chr14:35829547..35831516,2	MCF-7	breast:
32	chr14:21736090..21738167-chr14:35834973..35837752,2	MCF-7	breast:
33	chr14:35759417..35767612-chr14:35799689..35808998,23	MCF-7	breast:
34	chr14:35833474..35838463-chr14:35839143..35843538,8	K562	blood:
35	chr14:35802904..35803808-chr14:35875773..35876572,4	K562	blood:
36	chr14:35783009..35785578-chr14:35809337..35811839,2	MCF-7	breast:
37	chr14:35698922..35700571-chr14:35810245..35812248,2	MCF-7	breast:
38	chr14:35702282..35704520-chr14:35800753..35803790,5	MCF-7	breast:
39	chr14:35825567..35827487-chr14:35834461..35837123,2	MCF-7	breast:
40	chr14:35817047..35819303-chr14:35821094..35823025,2	K562	blood:
41	chr14:35773332..35776624-chr14:35804894..35807958,4	MCF-7	breast:
42	chr14:35728670..35731490-chr14:35834675..35836936,2	K562	blood:
43	chr14:35311937..35314117-chr14:35804578..35807465,2	MCF-7	breast:
44	chr14:35804902..35807934-chr14:35810651..35813744,3	K562	blood:
45	chr14:35801529..35803038-chr14:35808078..35809983,2	K562	blood:
46	chr14:35825704..35827505-chr14:35837776..35839385,2	MCF-7	breast:
47	chr14:35835946..35837731-chr14:35866883..35868831,2	K562	blood:
48	chr14:35515127..35516753-chr14:35810234..35812265,2	MCF-7	breast:
49	chr14:35778351..35785006-chr14:35799640..35807255,11	MCF-7	breast:
50	chr14:35785092..35787628-chr14:35800075..35803024,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NFKBIA-4	chr14:35811376-35812101	l_964_chr14:35808028-35812101_thyroid
2	lnc-NFKBIA-1	chr14:35831438-35832000	ENSG00000258860.1
3	lnc-NFKBIA-1	chr14:35832774-35832834	ENSG00000258860.1
4	lnc-PSMA6-4	chr14:35804609-35805475	NONHSAT036376
5	lnc-NFKBIA-4	chr14:35808029-35808268	l_964_chr14:35808028-35812101_thyroid

No data

Variant related genes	Relation type
ENSG00000258860	TF binding region
ENSG00000258860	CpG island
ENSG00000199004	chromatin interactions
ENSG00000265530	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000256243	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000258860	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000240392	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000100902	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000092020	chromatin interactions

Extended variants
information (count: 1600 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10147645	chr14:35802483-35802484	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558294129	chr14:35802509-35802510	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs567663049	chr14:35802544-35802545	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs10147734	chr14:35802564-35802565	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs140666755	chr14:35802586-35802587	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs576360126	chr14:35802601-35802602	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs12436274	chr14:35802623-35802624	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs142285439	chr14:35802624-35802625	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs150895807	chr14:35802685-35802686	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs139429118	chr14:35802697-35802698	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs150030175	chr14:35802702-35802703	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs528906025	chr14:35802703-35802704	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs542286664	chr14:35802710-35802711	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs201937177	chr14:35802720-35802721	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs562453475	chr14:35802753-35802754	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs186281122	chr14:35802758-35802759	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs551701548	chr14:35802766-35802767	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs571473176	chr14:35802780-35802781	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs12436351	chr14:35802786-35802787	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs146620177	chr14:35802853-35802854	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs567680979	chr14:35802868-35802869	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs536733172	chr14:35802887-35802888	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs112190003	chr14:35802912-35802913	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs189139101	chr14:35802986-35802987	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs182546034	chr14:35802987-35802988	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs187117469	chr14:35802991-35802992	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs538733883	chr14:35802992-35802993	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs192185358	chr14:35802997-35802998	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs572321257	chr14:35803006-35803007	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs534876903	chr14:35803039-35803040	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs182946345	chr14:35803043-35803044	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs573689589	chr14:35803087-35803088	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs185696346	chr14:35803095-35803096	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs562515558	chr14:35803100-35803101	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs190105526	chr14:35803121-35803122	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs576064356	chr14:35803125-35803126	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs140283824	chr14:35803178-35803179	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs372112224	chr14:35803206-35803207	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs17512725	chr14:35803243-35803244	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557713823	chr14:35803285-35803286	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs547309534	chr14:35803290-35803291	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs561125461	chr14:35803292-35803293	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs530178544	chr14:35803293-35803294	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs371436895	chr14:35803313-35803314	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs182510856	chr14:35803332-35803333	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs569256710	chr14:35803375-35803376	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs569723967	chr14:35803376-35803377	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs538612080	chr14:35803391-35803392	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs144019598	chr14:35803411-35803412	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs374706732	chr14:35803441-35803442	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 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
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD
Cancer	20164920	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	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

Chromatin state (count:1732 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35784800-35804600	Weak transcription	Ovary	ovary
2	chr14:35784800-35804600	Weak transcription	Psoas Muscle	Psoas
3	chr14:35787600-35803200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr14:35788000-35804600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:35788600-35805800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:35789000-35804600	Weak transcription	Brain Anterior Caudate	brain
7	chr14:35796000-35803000	Weak transcription	Liver	Liver
8	chr14:35800000-35815000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr14:35800600-35803600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:35800600-35803800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr14:35800600-35803800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr14:35800600-35804000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:35800600-35805000	Enhancers	Fetal Intestine Large	intestine
14	chr14:35800600-35807000	Enhancers	Primary hematopoietic stem cells	blood
15	chr14:35800600-35807200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr14:35800600-35807400	Enhancers	Placenta Amnion	Placenta Amnion
17	chr14:35800600-35814400	Enhancers	Placenta	Placenta
18	chr14:35800800-35802600	Enhancers	Fetal Heart	heart
19	chr14:35800800-35803000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr14:35800800-35803000	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr14:35800800-35803200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:35800800-35803200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr14:35800800-35803200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr14:35800800-35803400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:35800800-35803400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:35800800-35803400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr14:35800800-35803400	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr14:35800800-35803400	Enhancers	Fetal Lung	lung
29	chr14:35800800-35803600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr14:35800800-35803600	Enhancers	GM12878-XiMat	blood
31	chr14:35800800-35803800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:35800800-35803800	Enhancers	Colonic Mucosa	Colon
33	chr14:35800800-35804000	Enhancers	Gastric	stomach
34	chr14:35800800-35804000	Enhancers	HMEC	breast
35	chr14:35800800-35804000	Enhancers	K562	blood
36	chr14:35800800-35804200	Enhancers	Esophagus	oesophagus
37	chr14:35800800-35804400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:35800800-35804400	Enhancers	Rectal Mucosa Donor 29	rectum
39	chr14:35800800-35804600	Enhancers	Duodenum Mucosa	Duodenum
40	chr14:35800800-35804600	Enhancers	A549	lung
41	chr14:35800800-35805000	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr14:35800800-35806000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:35800800-35806600	Enhancers	Stomach Mucosa	stomach
44	chr14:35800800-35807000	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr14:35800800-35812200	Enhancers	Fetal Thymus	thymus
46	chr14:35800800-35813800	Enhancers	Lung	lung
47	chr14:35801000-35802600	Enhancers	Primary T cells fromperipheralblood	blood
48	chr14:35801000-35802800	Enhancers	Small Intestine	intestine
49	chr14:35801000-35803000	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr14:35801000-35803400	Genic enhancers	Fetal Intestine Small	intestine

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