Variant report

Variant	nsv902427
Chromosome Location	chr14:105508577-105585347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3812)
CpG islands
(count:3239)
Chromatin interactive
region (count:177)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3812 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105512086-105512391	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:105553289-105553458	K562	blood:	n/a	n/a
3	ARID3A	chr14:105512055-105512331	K562	blood:	n/a	n/a
4	ATF1	chr14:105531689-105532059	K562	blood:	n/a	n/a
5	ATF2	chr14:105535270-105535705	GM12878	blood:	n/a	n/a
6	ATF2	chr14:105512921-105514807	GM12878	blood:	n/a	n/a
7	ATF2	chr14:105512072-105512529	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:105531529-105532220	GM12878	blood:	n/a	n/a
9	ATF2	chr14:105533584-105533931	GM12878	blood:	n/a	n/a
10	ATF2	chr14:105527777-105528339	GM12878	blood:	n/a	n/a
11	ATF2	chr14:105533544-105534046	GM12878	blood:	n/a	n/a
12	ATF2	chr14:105553013-105553749	GM12878	blood:	n/a	n/a
13	ATF2	chr14:105527799-105528595	GM12878	blood:	n/a	n/a
14	ATF2	chr14:105536061-105537450	GM12878	blood:	n/a	n/a
15	ATF2	chr14:105532781-105533205	GM12878	blood:	n/a	n/a
16	ATF2	chr14:105512062-105512430	GM12878	blood:	n/a	n/a
17	ATF2	chr14:105535036-105535648	GM12878	blood:	n/a	n/a
18	ATF2	chr14:105529889-105530248	GM12878	blood:	n/a	n/a
19	ATF2	chr14:105514092-105514416	GM12878	blood:	n/a	n/a
20	ATF2	chr14:105512023-105512788	GM12878	blood:	n/a	n/a
21	ATF2	chr14:105531494-105532230	GM12878	blood:	n/a	n/a
22	ATF2	chr14:105536073-105537473	GM12878	blood:	n/a	n/a
23	ATF2	chr14:105531034-105531469	GM12878	blood:	n/a	n/a
24	ATF2	chr14:105532672-105533249	GM12878	blood:	n/a	n/a
25	ATF3	chr14:105557689-105558795	A549	lung:	n/a	n/a
26	ATF3	chr14:105554133-105554962	A549	lung:	n/a	chr14:105554697-105554706
27	ATF3	chr14:105511938-105512481	A549	lung:	n/a	chr14:105512234-105512242
28	ATF3	chr14:105554018-105555597	A549	lung:	n/a	chr14:105554697-105554706
29	ATF3	chr14:105556723-105557180	A549	lung:	n/a	n/a
30	ATF3	chr14:105512057-105512333	HepG2	liver:	n/a	chr14:105512234-105512242
31	ATF3	chr14:105511986-105512491	A549	lung:	n/a	chr14:105512234-105512242
32	ATF3	chr14:105531135-105531272	K562	blood:	n/a	chr14:105531137-105531146 chr14:105531208-105531217
33	ATF3	chr14:105557655-105558363	A549	lung:	n/a	n/a
34	BACH1	chr14:105511954-105512390	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr14:105512083-105512370	K562	blood:	n/a	n/a
36	BACH1	chr14:105554770-105554900	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr14:105554348-105554357	K562	blood:	n/a	n/a
38	BACH1	chr14:105559991-105560466	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr14:105559035-105559660	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr14:105553188-105553726	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr14:105522282-105522707	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr14:105531625-105532007	GM12878	blood:	n/a	n/a
43	BATF	chr14:105537151-105537484	GM12878	blood:	n/a	n/a
44	BATF	chr14:105553188-105553465	GM12878	blood:	n/a	n/a
45	BATF	chr14:105514029-105514517	GM12878	blood:	n/a	n/a
46	BATF	chr14:105536272-105536860	GM12878	blood:	n/a	n/a
47	BATF	chr14:105533597-105533966	GM12878	blood:	n/a	n/a
48	BATF	chr14:105535194-105535500	GM12878	blood:	n/a	n/a
49	BATF	chr14:105527999-105528412	GM12878	blood:	n/a	n/a
50	BATF	chr14:105547887-105548072	GM12878	blood:	n/a	n/a

(count:3239 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105512071-105512121	HCM	heart:	n/a
2	chr14:105562983-105563033	HRCEpiC	kidney:	n/a
3	chr14:105546698-105546748	HUVEC	blood vessel:	n/a
4	chr14:105532252-105532302	MCF10A-Er-Src	breast:	n/a
5	chr14:105562983-105563033	SAEC	small airway:	n/a
6	chr14:105554352-105554402	MCF10A-Er-Src	breast:	n/a
7	chr14:105512071-105512121	HCM	heart:	n/a
8	chr14:105562983-105563033	HRCEpiC	kidney:	n/a
9	chr14:105546698-105546748	HUVEC	blood vessel:	n/a
10	chr14:105532252-105532302	MCF10A-Er-Src	breast:	n/a
11	chr14:105562983-105563033	SAEC	small airway:	n/a
12	chr14:105554352-105554402	MCF10A-Er-Src	breast:	n/a
13	chr14:105557111-105557161	GM12891	blood:	n/a
14	chr14:105521961-105522011	HRCEpiC	kidney:	n/a
15	chr14:105538414-105538464	SK-N-SH_RA	brain:	n/a
16	chr14:105527251-105527301	AG04450	lung:	fetal
17	chr14:105560110-105560160	K562	blood:	n/a
18	chr14:105509376-105509426	GM12878	blood:	n/a
19	chr14:105557746-105557796	H1-hESC	embryonic stem cell:	embryo
20	chr14:105557746-105557796	Hela-S3	cervix:	n/a
21	chr14:105532252-105532302	HAEpiC	amniotic membrane:	n/a
22	chr14:105516255-105516305	NHBE	bronchial:	n/a
23	chr14:105512213-105512263	HCPEpiC	choroid plexus:	n/a
24	chr14:105517573-105517623	ProgFib	skin:	n/a
25	chr14:105509229-105509279	GM12878	blood:	n/a
26	chr14:105522348-105522398	GM19239	blood:	n/a
27	chr14:105521894-105521944	HCT-116	colon:	n/a
28	chr14:105582624-105582674	SKMC	muscle:	n/a
29	chr14:105532208-105532258	K562	blood:	n/a
30	chr14:105516255-105516305	AG04450	lung:	fetal
31	chr14:105560008-105560058	HCM	heart:	n/a
32	chr14:105584224-105584274	HNPCEpiC	eye:	n/a
33	chr14:105512213-105512263	BJ	skin:	n/a
34	chr14:105518248-105518298	GM12892	blood:	n/a
35	chr14:105522902-105522952	HUVEC	blood vessel:	n/a
36	chr14:105555223-105555273	H1-hESC	embryonic stem cell:	embryo
37	chr14:105517946-105517996	AG09309	skin:	n/a
38	chr14:105532252-105532302	NH-A	brain:	n/a
39	chr14:105560199-105560249	AG04450	lung:	fetal
40	chr14:105553520-105553570	MCF-7	breast:	n/a
41	chr14:105546698-105546748	Caco-2	colon:	n/a
42	chr14:105509229-105509279	SAEC	small airway:	n/a
43	chr14:105512071-105512121	AG09319	gingival:	n/a
44	chr14:105522902-105522952	HRPEpiC	eye:	n/a
45	chr14:105521961-105522011	NHBE	bronchial:	n/a
46	chr14:105557746-105557796	HL-60	blood:	n/a
47	chr14:105581043-105581093	HRCEpiC	kidney:	n/a
48	chr14:105522348-105522398	PrEC	prostate:	n/a
49	chr14:105522348-105522398	H1-hESC	embryonic stem cell:	embryo
50	chr14:105562983-105563033	GM19239	blood:	n/a

(count:177 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:105440744..105442653-chr14:105551168..105553091,2	MCF-7	breast:
2	chr14:105483268..105491279-chr14:105504611..105511531,14	MCF-7	breast:
3	chr14:105511484..105514787-chr14:105515650..105518482,3	MCF-7	breast:
4	chr14:105537608..105540428-chr14:105542339..105544754,4	MCF-7	breast:
5	chr14:105447414..105449078-chr14:105542830..105544424,2	MCF-7	breast:
6	chr14:105555507..105557532-chr14:105644874..105649259,4	MCF-7	breast:
7	chr14:105455819..105458793-chr14:105513628..105516107,2	MCF-7	breast:
8	chr14:105519148..105521520-chr14:105539109..105541488,2	K562	blood:
9	chr14:105444336..105445214-chr14:105553267..105554067,2	K562	blood:
10	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
11	chr14:105512283..105515187-chr14:105515395..105518440,3	MCF-7	breast:
12	chr14:105461096..105464805-chr14:105509582..105512379,4	MCF-7	breast:
13	chr14:105499189..105502656-chr14:105506829..105510545,6	MCF-7	breast:
14	chr14:105451525..105454488-chr14:105528251..105530075,2	MCF-7	breast:
15	chr14:105441925..105443131-chr14:105511722..105512739,17	K562	blood:
16	chr14:105557521..105561291-chr14:105561691..105564473,4	MCF-7	breast:
17	chr14:105519950..105521697-chr14:105523622..105526334,2	MCF-7	breast:
18	chr14:105441607..105442989-chr14:105532142..105533415,5	MCF-7	breast:
19	chr14:105541940..105543448-chr14:105558104..105559608,2	K562	blood:
20	chr14:105521494..105526312-chr14:105528458..105531564,4	MCF-7	breast:
21	chr14:105437250..105440570-chr14:105553722..105556644,3	MCF-7	breast:
22	chr14:105488161..105488707-chr14:105511957..105512657,2	MCF-7	breast:
23	chr14:105458011..105458613-chr14:105511934..105512703,4	MCF-7	breast:
24	chr14:105522574..105524801-chr14:105525749..105528494,2	K562	blood:
25	chr14:105538481..105541276-chr14:105553556..105555941,2	K562	blood:
26	chr14:105399823..105400369-chr14:105511778..105512655,3	MCF-7	breast:
27	chr14:105440892..105442421-chr14:105508272..105511059,2	MCF-7	breast:
28	chr14:105500093..105502246-chr14:105511409..105512946,2	MCF-7	breast:
29	chr14:105478222..105479179-chr14:105511711..105512689,8	MCF-7	breast:
30	chr14:105457715..105458591-chr14:105511755..105512731,6	MCF-7	breast:
31	chr14:105450535..105452638-chr14:105507886..105509886,2	MCF-7	breast:
32	chr14:105438202..105442375-chr14:105515554..105517419,4	MCF-7	breast:
33	chr14:105571300..105574874-chr14:105580786..105584672,4	MCF-7	breast:
34	chr14:105556545..105557474-chr14:105818256..105819211,4	K562	blood:
35	chr14:105550667..105552367-chr14:105554467..105556280,2	K562	blood:
36	chr14:105433754..105435630-chr14:105557991..105559597,2	MCF-7	breast:
37	chr14:105515500..105519468-chr14:105521561..105526194,6	K562	blood:
38	chr14:105362754..105363622-chr14:105511827..105512699,2	MCF-7	breast:
39	chr14:105443860..105446448-chr14:105515601..105519489,3	MCF-7	breast:
40	chr14:105485865..105488702-chr14:105521834..105523359,2	K562	blood:
41	chr14:105293283..105294221-chr14:105511851..105512622,2	MCF-7	breast:
42	chr14:105432444..105435171-chr14:105511281..105513551,2	MCF-7	breast:
43	chr14:105567398..105568987-chr14:105582432..105584780,2	MCF-7	breast:
44	chr14:105441809..105443191-chr14:105552782..105553787,10	MCF-7	breast:
45	chr14:105362768..105363662-chr14:105553187..105553782,2	MCF-7	breast:
46	chr14:105443757..105444660-chr14:105510431..105511022,2	MCF-7	breast:
47	chr14:105551472..105556224-chr14:105557135..105561197,4	K562	blood:
48	chr14:105552947..105555057-chr14:105555509..105557119,2	K562	blood:
49	chr14:105526612..105528156-chr14:105531987..105533882,2	MCF-7	breast:
50	chr14:105441376..105443921-chr14:105550710..105553221,2	MCF-7	breast:

(count:33 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf79-2	chr14:105561597-105562105	NONHSAT040321
2	lnc-C14orf79-2	chr14:105561877-105562105	XLOC_010952
3	lnc-C14orf79-2	chr14:105564810-105565172	XLOC_010952
4	lnc-C14orf79-2	chr14:105564810-105564823	XLOC_010952
5	lnc-C14orf79-2	chr14:105564810-105564853	NONHSAT040321
6	lnc-C14orf79-2	chr14:105560484-105560553	NR_110546
7	lnc-C14orf79-2	chr14:105561473-105561779	XLOC_010952
8	lnc-C14orf79-2	chr14:105565381-105565891	XLOC_010952
9	lnc-C14orf79-2	chr14:105560857-105562105	XLOC_010952
10	lnc-GPR132-1	chr14:105536959-105537000	XLOC_011152
11	lnc-C14orf79-2	chr14:105559831-105560057	XLOC_010952
12	lnc-C14orf79-2	chr14:105561662-105561779	ENSG00000257556
13	lnc-C14orf79-2	chr14:105564810-105564910	ENSG00000257556
14	lnc-C14orf79-2	chr14:105565056-105565341	ENSG00000257556
15	lnc-GPR132-1	chr14:105533801-105534066	XLOC_011152
16	lnc-C14orf79-2	chr14:105565090-105565227	XLOC_010952
17	lnc-C14orf79-2	chr14:105561877-105562266	XLOC_010952
18	lnc-C14orf79-2	chr14:105561877-105562105	NR_110546
19	lnc-C14orf79-2	chr14:105561877-105562104	ENSG00000257556
20	lnc-GPR132-1	chr14:105538497-105539070	XLOC_011152
21	lnc-C14orf79-2	chr14:105559108-105559211	NONHSAT040321
22	lnc-C14orf79-2	chr14:105565381-105565468	XLOC_010952
23	lnc-GPR132-1	chr14:105532071-105532089	XLOC_011152
24	lnc-C14orf79-2	chr14:105561664-105561779	NR_110546
25	lnc-GPR132-2	chr14:105509257-105509821	XLOC_011151
26	lnc-C14orf79-2	chr14:105565619-105565833	NR_110546
27	lnc-C14orf79-2	chr14:105559946-105560157	ENSG00000257556
28	lnc-C14orf79-2	chr14:105561528-105562105	ENSG00000257556
29	lnc-C14orf79-2	chr14:105565056-105565227	NR_110546
30	lnc-C14orf79-1	chr14:105543887-105543911	XLOC_010951
31	lnc-C14orf79-2	chr14:105564810-105564910	NR_110546
32	lnc-C14orf79-2	chr14:105561877-105562036	ENSG00000257556
33	lnc-C14orf79-1	chr14:105543608-105543786	XLOC_010951

No data

Variant related genes	Relation type
ENSG00000257556	TF binding region
GPR132	TF binding region
ENSG00000258154	TF binding region
ENSG00000257556	CpG island
GPR132	CpG island
ENSG00000258154	CpG island
ENSG00000226174	chromatin interactions
ENSG00000226950	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000213228	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000264585	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000183484	chromatin interactions
KIF1B	miRNA target sites
PLDN	miRNA target sites
MBD1	miRNA target sites
MBD6	miRNA target sites
COPS3	miRNA target sites
NUP160	miRNA target sites
ECHDC1	miRNA target sites
NASP	miRNA target sites
PDCD4	miRNA target sites
DFFA	miRNA target sites

Extended variants
information (count: 3055 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4633639	chr14:105508577-105508578	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150715961	chr14:105508639-105508640	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs536145824	chr14:105508664-105508665	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs4424849	chr14:105508666-105508667	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs535116496	chr14:105508674-105508675	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs192048998	chr14:105508687-105508688	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577945849	chr14:105508770-105508771	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs572519787	chr14:105508771-105508772	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs140032287	chr14:105508811-105508812	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs556998543	chr14:105508860-105508861	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs573567171	chr14:105508948-105508949	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs12890617	chr14:105508998-105508999	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs149845156	chr14:105509090-105509091	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs183178954	chr14:105509108-105509109	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs147939942	chr14:105509115-105509116	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs564923186	chr14:105509177-105509178	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs141770564	chr14:105509178-105509179	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532312468	chr14:105509183-105509184	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs12433546	chr14:105509234-105509235	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs529562223	chr14:105509239-105509240	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs12436313	chr14:105509242-105509243	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566264655	chr14:105509246-105509247	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs12436388	chr14:105509267-105509268	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs145526378	chr14:105509286-105509287	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs147694937	chr14:105509289-105509290	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs537068520	chr14:105509327-105509328	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs557284791	chr14:105509337-105509338	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs573601774	chr14:105509344-105509345	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs547322519	chr14:105509376-105509377	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs552791374	chr14:105509427-105509428	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs186796618	chr14:105509435-105509436	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs34513219	chr14:105509442-105509443	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs545158483	chr14:105509446-105509447	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs564842236	chr14:105509574-105509575	Weak transcription Enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs530587379	chr14:105509619-105509620	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs149154306	chr14:105509639-105509640	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs143259194	chr14:105509680-105509681	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs529653802	chr14:105509714-105509715	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs189699493	chr14:105509740-105509741	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs528870553	chr14:105509760-105509761	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs566307491	chr14:105509809-105509810	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs528720354	chr14:105509868-105509869	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551920318	chr14:105509892-105509893	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548957502	chr14:105509945-105509946	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114733319	chr14:105509976-105509977	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs148298189	chr14:105509997-105509998	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs7159920	chr14:105510027-105510028	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs374699219	chr14:105510035-105510036	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs567314169	chr14:105510052-105510053	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75610061	chr14:105510077-105510078	ZNF genes & repeats Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	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
Non-syndromic sensorineural hearing loss	19587683	CNVD
Recurrent pregnancy loss	19789632	CNVD
Multiple sclerosis	20428171	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:2665 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105500600-105512000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:105504800-105512000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:105507000-105509600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:105507600-105508800	Enhancers	A549	lung
5	chr14:105507800-105508600	Bivalent Enhancer	HepG2	liver
6	chr14:105507800-105508600	Enhancers	NHEK	skin
7	chr14:105508000-105508600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:105508000-105508600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:105508000-105509600	Enhancers	Fetal Heart	heart
10	chr14:105508000-105509800	Enhancers	Esophagus	oesophagus
11	chr14:105508200-105508600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr14:105508200-105508800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr14:105508200-105508800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:105508400-105509000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr14:105508600-105508800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:105508600-105508800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr14:105508800-105509000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr14:105508800-105509200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr14:105508800-105509600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:105509400-105509800	Enhancers	Primary B cells from cord blood	blood
21	chr14:105509400-105509800	Bivalent Enhancer	Placenta	Placenta
22	chr14:105509400-105511200	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr14:105509600-105510000	Weak transcription	Fetal Heart	heart
24	chr14:105509600-105510200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr14:105509600-105512000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:105509600-105512800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr14:105509800-105510600	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr14:105509800-105511200	Weak transcription	Primary B cells from cord blood	blood
29	chr14:105509800-105514600	Enhancers	GM12878-XiMat	blood
30	chr14:105509800-105516600	Weak transcription	Esophagus	oesophagus
31	chr14:105510000-105510200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr14:105510200-105510400	Enhancers	Fetal Lung	lung
33	chr14:105510200-105512400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr14:105510200-105512600	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr14:105510600-105511200	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr14:105510600-105512200	Weak transcription	Fetal Lung	lung
37	chr14:105511000-105511200	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr14:105511000-105511800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:105511000-105512000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr14:105511200-105511400	Enhancers	Primary B cells from cord blood	blood
41	chr14:105511200-105511600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
42	chr14:105511200-105511800	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr14:105511200-105512600	Enhancers	Primary hematopoietic stem cells	blood
44	chr14:105511200-105512800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr14:105511200-105513000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
46	chr14:105511400-105511600	Bivalent Enhancer	HepG2	liver
47	chr14:105511400-105511800	Weak transcription	Primary B cells from cord blood	blood
48	chr14:105511400-105512800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr14:105511600-105512000	Enhancers	HepG2	liver
50	chr14:105511600-105513200	Enhancers	Primary monocytes fromperipheralblood	blood

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