Variant report

Variant	nsv832888
Chromosome Location	chr14:105717339-105803170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1881)
CpG islands
(count:4703)
Chromatin interactive
region (count:142)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105748200-105748490	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:105767190-105767604	HepG2	liver:	n/a	n/a
3	ATF3	chr14:105780701-105780901	K562	blood:	n/a	n/a
4	BACH1	chr14:105766424-105767645	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr14:105745670-105745963	GM12878	blood:	n/a	n/a
6	BCL3	chr14:105738400-105738729	GM12878	blood:	n/a	n/a
7	BCL3	chr14:105746228-105746718	GM12878	blood:	n/a	n/a
8	BCL3	chr14:105746226-105746647	GM12878	blood:	n/a	n/a
9	BCL3	chr14:105745638-105745952	GM12878	blood:	n/a	n/a
10	BCLAF1	chr14:105766850-105767395	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:105767853-105768215	K562	blood:	n/a	n/a
12	BHLHE40	chr14:105759635-105759851	GM12878	blood:	n/a	n/a
13	BHLHE40	chr14:105767913-105768111	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:105797122-105797136	K562	blood:	n/a	n/a
15	BHLHE40	chr14:105757536-105757653	K562	blood:	n/a	n/a
16	BHLHE40	chr14:105748289-105748325	HepG2	liver:	n/a	n/a
17	BHLHE40	chr14:105767201-105767636	K562	blood:	n/a	n/a
18	BHLHE40	chr14:105757131-105757351	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:105789597-105789901	K562	blood:	n/a	chr14:105789673-105789689
20	BHLHE40	chr14:105766686-105767711	HepG2	liver:	n/a	chr14:105766760-105766776
21	BHLHE40	chr14:105766831-105767705	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:105780749-105780943	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:105725166-105725434	A549	lung:	n/a	n/a
24	BRCA1	chr14:105766843-105767916	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr14:105766891-105767298	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr14:105766891-105767604	HepG2	liver:	n/a	n/a
27	BRCA1	chr14:105766891-105767649	GM12878	blood:	n/a	n/a
28	CBX3	chr14:105798009-105798308	K562	blood:	n/a	n/a
29	CBX3	chr14:105765911-105766270	K562	blood:	n/a	n/a
30	CBX3	chr14:105767136-105767735	K562	blood:	n/a	n/a
31	CBX3	chr14:105767897-105768155	K562	blood:	n/a	n/a
32	CBX3	chr14:105770918-105771270	K562	blood:	n/a	n/a
33	CBX3	chr14:105765920-105766209	K562	blood:	n/a	n/a
34	CCNT2	chr14:105780628-105781015	K562	blood:	n/a	n/a
35	CCNT2	chr14:105766686-105768120	K562	blood:	n/a	chr14:105767659-105767668
36	CCNT2	chr14:105719576-105719641	K562	blood:	n/a	n/a
37	CEBPB	chr14:105791677-105791877	HepG2	liver:	n/a	chr14:105791720-105791731 chr14:105791718-105791731
38	CEBPB	chr14:105720781-105721070	IMR90	lung:	n/a	n/a
39	CEBPB	chr14:105756826-105757087	Hela-S3	cervix:	n/a	chr14:105756938-105756951 chr14:105756977-105756988
40	CEBPB	chr14:105720824-105721085	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr14:105756881-105757099	IMR90	lung:	n/a	chr14:105756938-105756951 chr14:105756977-105756988
42	CEBPB	chr14:105773598-105773756	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr14:105767925-105768011	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr14:105756851-105757091	A549	lung:	n/a	chr14:105756938-105756951 chr14:105756977-105756988
45	CEBPB	chr14:105725204-105725454	A549	lung:	n/a	n/a
46	CEBPB	chr14:105767004-105767243	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:105756814-105757113	HepG2	liver:	n/a	chr14:105756938-105756951 chr14:105756977-105756988
48	CEBPB	chr14:105758264-105758331	IMR90	lung:	n/a	n/a
49	CEBPB	chr14:105725196-105725494	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:105758265-105758342	A549	lung:	n/a	n/a

(count:4703 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105783536-105783586	H1-hESC	embryonic stem cell:	embryo
2	chr14:105784090-105784140	HRCEpiC	kidney:	n/a
3	chr14:105751711-105751761	IMR90	lung:	fetal
4	chr14:105779910-105779960	HCPEpiC	choroid plexus:	n/a
5	chr14:105767409-105767459	SK-N-SH_RA	brain:	n/a
6	chr14:105739057-105739107	SK-N-SH_RA	brain:	n/a
7	chr14:105783536-105783586	H1-hESC	embryonic stem cell:	embryo
8	chr14:105784090-105784140	HRCEpiC	kidney:	n/a
9	chr14:105751711-105751761	IMR90	lung:	fetal
10	chr14:105779910-105779960	HCPEpiC	choroid plexus:	n/a
11	chr14:105767409-105767459	SK-N-SH_RA	brain:	n/a
12	chr14:105739057-105739107	SK-N-SH_RA	brain:	n/a
13	chr14:105780340-105780390	HEEpiC	esophagus:	n/a
14	chr14:105783687-105783737	AG04449	skin:	fetal
15	chr14:105767882-105767932	BE2_C	brain:	n/a
16	chr14:105779826-105779876	MCF10A-Er-Src	breast:	n/a
17	chr14:105783627-105783677	HRCEpiC	kidney:	n/a
18	chr14:105780695-105780745	PrEC	prostate:	n/a
19	chr14:105766346-105766396	SK-N-SH_RA	brain:	n/a
20	chr14:105742034-105742084	K562	blood:	n/a
21	chr14:105768109-105768159	SAEC	small airway:	n/a
22	chr14:105781312-105781362	RPTEC	kidney:	n/a
23	chr14:105738663-105738713	HNPCEpiC	eye:	n/a
24	chr14:105779910-105779960	HEEpiC	esophagus:	n/a
25	chr14:105802918-105802968	CMK	blood:	n/a
26	chr14:105796811-105796861	RPTEC	kidney:	n/a
27	chr14:105802387-105802437	PANC-1	pancreas:	n/a
28	chr14:105768109-105768159	BE2_C	brain:	n/a
29	chr14:105738592-105738642	SAEC	small airway:	n/a
30	chr14:105780695-105780745	Caco-2	colon:	n/a
31	chr14:105789516-105789566	CMK	blood:	n/a
32	chr14:105800169-105800219	PANC-1	pancreas:	n/a
33	chr14:105779826-105779876	HL-60	blood:	n/a
34	chr14:105781312-105781362	HCPEpiC	choroid plexus:	n/a
35	chr14:105767639-105767689	ECC-1	luminal epithelium:	n/a
36	chr14:105779532-105779582	GM12892	blood:	n/a
37	chr14:105793554-105793604	GM12892	blood:	n/a
38	chr14:105793554-105793604	ProgFib	skin:	n/a
39	chr14:105739124-105739174	HCT-116	colon:	n/a
40	chr14:105750676-105750726	HCPEpiC	choroid plexus:	n/a
41	chr14:105782817-105782867	IMR90	lung:	fetal
42	chr14:105738426-105738476	HPAEpiC	pulmonary alveolar:	n/a
43	chr14:105767639-105767689	ProgFib	skin:	n/a
44	chr14:105802918-105802968	HMEC	breast:	n/a
45	chr14:105792853-105792903	MCF-7	breast:	n/a
46	chr14:105794123-105794173	RPTEC	kidney:	n/a
47	chr14:105792505-105792555	HPAEpiC	pulmonary alveolar:	n/a
48	chr14:105739124-105739174	Caco-2	colon:	n/a
49	chr14:105767457-105767507	SK-N-SH	brain:	n/a
50	chr14:105760556-105760606	LNCaP	prostate:	n/a

(count:142 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:105732454..105734359-chr14:105734769..105737531,2	MCF-7	breast:
2	chr14:105713833..105716142-chr14:105716723..105718932,2	K562	blood:
3	chr14:105766895..105769453-chr14:105788043..105790752,2	K562	blood:
4	chr14:105764841..105767262-chr14:105768886..105771341,2	MCF-7	breast:
5	chr14:105757386..105760349-chr14:105763067..105764806,2	K562	blood:
6	chr14:105717555..105718335-chr3:138200943..138201661,2	MCF-7	breast:
7	chr14:105757651..105762678-chr14:105764586..105768491,12	MCF-7	breast:
8	chr14:105765347..105769263-chr14:105769470..105773685,4	K562	blood:
9	chr14:105443928..105445902-chr14:105765680..105767557,2	MCF-7	breast:
10	chr14:105717901..105719933-chr14:105721820..105724297,3	MCF-7	breast:
11	chr14:105738574..105740940-chr14:105765843..105768156,3	MCF-7	breast:
12	chr14:105753212..105757197-chr14:105757375..105761720,4	MCF-7	breast:
13	chr14:105766490..105767158-chr17:41465540..41466173,2	Hela-S3	cervix:
14	chr14:105765282..105769482-chr14:105778355..105784135,18	K562	blood:
15	chr14:105768384..105770510-chr14:105839259..105840826,2	MCF-7	breast:
16	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
17	chr14:105747048..105750064-chr14:105752369..105754773,3	K562	blood:
18	chr14:105713379..105716522-chr14:105764463..105769159,4	MCF-7	breast:
19	chr14:105791422..105793957-chr14:105861992..105864846,2	K562	blood:
20	chr14:105736589..105738143-chr14:105766736..105768973,2	MCF-7	breast:
21	chr14:105766174..105769085-chr14:105786529..105791325,5	MCF-7	breast:
22	chr14:105788060..105791042-chr14:105819860..105821725,2	MCF-7	breast:
23	chr14:105778878..105784143-chr14:105784229..105795178,22	MCF-7	breast:
24	chr14:105795550..105797452-chr14:105807856..105809392,2	K562	blood:
25	chr14:105744465..105746364-chr14:105757622..105759323,2	K562	blood:
26	chr14:105776327..105778746-chr14:105779695..105781652,2	K562	blood:
27	chr14:105765913..105767563-chr14:105954548..105956473,2	MCF-7	breast:
28	chr14:105748084..105750375-chr14:105752536..105754895,2	MCF-7	breast:
29	chr14:105795771..105798760-chr14:105803162..105807544,4	K562	blood:
30	chr14:105778405..105782273-chr14:105864844..105868439,3	K562	blood:
31	chr14:105798156..105801052-chr14:105809426..105811006,2	MCF-7	breast:
32	chr14:105794770..105795327-chr14:105804546..105805386,2	MCF-7	breast:
33	chr14:105717742..105719473-chr14:105729003..105731764,2	MCF-7	breast:
34	chr14:105668316..105670026-chr14:105722977..105725479,2	MCF-7	breast:
35	chr14:105755787..105757404-chr14:105766249..105769008,2	MCF-7	breast:
36	chr14:105765307..105769571-chr14:105774220..105784135,13	K562	blood:
37	chr14:105761699..105764164-chr14:105811215..105812836,2	MCF-7	breast:
38	chr14:105635176..105636125-chr14:105747875..105748809,5	K562	blood:
39	chr14:105787132..105789177-chr14:105789414..105793167,4	K562	blood:
40	chr14:105721297..105724046-chr14:105725585..105727720,2	MCF-7	breast:
41	chr14:105785639..105787246-chr14:105789793..105792737,2	MCF-7	breast:
42	chr14:105770409..105772942-chr14:105807785..105809717,2	MCF-7	breast:
43	chr14:105667563..105669729-chr14:105747885..105748780,6	MCF-7	breast:
44	chr14:105725348..105727794-chr14:105730448..105732777,2	MCF-7	breast:
45	chr14:105751940..105753785-chr14:105781330..105783374,2	MCF-7	breast:
46	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
47	chr14:105668630..105671458-chr14:105740355..105743089,2	K562	blood:
48	chr14:105795771..105798760-chr14:105803162..105807544,4	K562	blood:
49	chr14:105669972..105673331-chr14:105732479..105735063,3	MCF-7	breast:
50	chr14:105780755..105782993-chr14:105786109..105788994,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-2	chr14:105717014-105717436	NONHSAT040340

No data

Variant related genes	Relation type
BRF1	TF binding region
PACS2	TF binding region
BRF1	CpG island
PACS2	CpG island
ENSG00000201699	chromatin interactions
ENSG00000182809	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000107371	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000122741	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000257341	chromatin interactions
ENSG00000100813	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000051523	chromatin interactions

Extended variants
information (count: 3256 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587729593	chr14:105717354-105717355	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs587627352	chr14:105717361-105717362	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs145027396	chr14:105717367-105717368	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs587762569	chr14:105717396-105717397	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs369381211	chr14:105717414-105717415	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs147968356	chr14:105717435-105717436	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs190285898	chr14:105717437-105717438	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs587597013	chr14:105717438-105717439	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs1882846	chr14:105717448-105717449	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs116481945	chr14:105717453-105717454	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149010140	chr14:105717467-105717468	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs58234100	chr14:105717488-105717489	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200482515	chr14:105717493-105717494	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs116165823	chr14:105717512-105717513	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587691801	chr14:105717557-105717558	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs143794595	chr14:105717570-105717571	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs587637217	chr14:105717663-105717664	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs182168154	chr14:105717699-105717700	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs587733516	chr14:105717700-105717701	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs587750681	chr14:105717718-105717719	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs587652386	chr14:105717725-105717726	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141025882	chr14:105717743-105717744	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs2735817	chr14:105717796-105717797	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs186767710	chr14:105717798-105717799	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs587737810	chr14:105717823-105717824	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368150886	chr14:105717830-105717831	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs145073239	chr14:105717886-105717887	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs587704541	chr14:105717927-105717928	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs587600205	chr14:105717933-105717934	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs77413390	chr14:105717941-105717942	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs587736861	chr14:105717950-105717951	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs190797307	chr14:105717951-105717952	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138855713	chr14:105717975-105717976	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112843168	chr14:105717984-105717985	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs587619739	chr14:105718007-105718008	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587691306	chr14:105718080-105718081	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs587753217	chr14:105718103-105718104	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs183959759	chr14:105718130-105718131	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs369292555	chr14:105718131-105718132	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs587647738	chr14:105718134-105718135	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs587705262	chr14:105718135-105718136	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs141992177	chr14:105718199-105718200	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs587658160	chr14:105718218-105718219	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs587735901	chr14:105718230-105718231	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs145632743	chr14:105718257-105718258	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs587646250	chr14:105718288-105718289	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs587720169	chr14:105718291-105718292	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs78778888	chr14:105718300-105718301	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs2816607	chr14:105718385-105718386	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs2816608	chr14:105718407-105718408	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:109)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	20369283	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3946 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105690400-105721400	Weak transcription	K562	blood
2	chr14:105715600-105723600	Weak transcription	Small Intestine	intestine
3	chr14:105715600-105749400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:105715800-105717600	Genic enhancers	Primary B cells from cord blood	blood
5	chr14:105715800-105718000	Weak transcription	NHDF-Ad	bronchial
6	chr14:105715800-105718200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr14:105715800-105718600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr14:105715800-105720400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:105715800-105721400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr14:105715800-105721600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:105715800-105766000	Weak transcription	Fetal Kidney	kidney
12	chr14:105716000-105717400	Strong transcription	HepG2	liver
13	chr14:105716000-105717600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
14	chr14:105716000-105717800	Genic enhancers	Primary T cells fromperipheralblood	blood
15	chr14:105716000-105718400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr14:105716000-105718600	Genic enhancers	Fetal Muscle Leg	muscle
17	chr14:105716000-105719400	Strong transcription	Brain Anterior Caudate	brain
18	chr14:105716000-105719600	Strong transcription	Brain Cingulate Gyrus	brain
19	chr14:105716000-105720400	Strong transcription	Brain Hippocampus Middle	brain
20	chr14:105716000-105720600	Strong transcription	Liver	Liver
21	chr14:105716000-105720600	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr14:105716000-105721200	Weak transcription	Psoas Muscle	Psoas
23	chr14:105716000-105721800	Strong transcription	Fetal Intestine Large	intestine
24	chr14:105716000-105732400	Weak transcription	Primary hematopoietic stem cells	blood
25	chr14:105716200-105717400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:105716200-105717400	Genic enhancers	Fetal Stomach	stomach
27	chr14:105716200-105718000	Genic enhancers	Adipose Nuclei	Adipose
28	chr14:105716200-105718000	Genic enhancers	Fetal Muscle Trunk	muscle
29	chr14:105716200-105718200	Weak transcription	HSMM	muscle
30	chr14:105716200-105718600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:105716200-105718600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr14:105716200-105718600	Strong transcription	NHEK	skin
33	chr14:105716200-105719200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr14:105716200-105719400	Strong transcription	Brain Substantia Nigra	brain
35	chr14:105716200-105719600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr14:105716200-105719600	Strong transcription	Fetal Thymus	thymus
37	chr14:105716200-105719800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr14:105716200-105719800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr14:105716200-105719800	Strong transcription	Ovary	ovary
40	chr14:105716200-105720000	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr14:105716200-105720200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr14:105716200-105720200	Strong transcription	Osteobl	bone
43	chr14:105716200-105720600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr14:105716200-105720600	Strong transcription	NHLF	lung
45	chr14:105716200-105720800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:105716200-105720800	Strong transcription	Colon Smooth Muscle	Colon
47	chr14:105716200-105723400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr14:105716200-105724000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr14:105716200-105724000	Strong transcription	Thymus	Thymus
50	chr14:105716200-105724000	Strong transcription	Monocytes-CD14+_RO01746	blood

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