Variant report

Variant	nsv430919
Chromosome Location	chr14:22393148-22969766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9420)
CpG islands
(count:2813)
Chromatin interactive
region (count:248)
LncRNA
region (count:112)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:22694346-22694555	K562	blood:	n/a	n/a
2	ARID3A	chr14:22932684-22932969	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:22579948-22580394	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:22552704-22553020	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:22788290-22788588	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:22446451-22446751	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:22855828-22856172	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:22515400-22515690	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:22929121-22929887	K562	blood:	n/a	n/a
10	ARID3A	chr14:22764524-22765035	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:22843636-22844115	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:22801636-22802916	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:22941997-22942327	K562	blood:	n/a	n/a
14	ARID3A	chr14:22765370-22765613	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:22804392-22804764	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:22580003-22580242	K562	blood:	n/a	n/a
17	ARID3A	chr14:22745215-22745415	K562	blood:	n/a	n/a
18	ARID3A	chr14:22806380-22806660	K562	blood:	n/a	n/a
19	ARID3A	chr14:22802474-22802855	K562	blood:	n/a	n/a
20	ARID3A	chr14:22805545-22805762	K562	blood:	n/a	n/a
21	ARID3A	chr14:22942048-22942302	HepG2	liver:	n/a	n/a
22	ATF1	chr14:22929425-22930088	K562	blood:	n/a	n/a
23	ATF1	chr14:22802422-22802769	K562	blood:	n/a	n/a
24	ATF1	chr14:22598192-22598259	K562	blood:	n/a	n/a
25	ATF1	chr14:22944053-22944079	K562	blood:	n/a	n/a
26	ATF1	chr14:22645817-22646098	K562	blood:	n/a	n/a
27	ATF1	chr14:22966819-22967082	K562	blood:	n/a	n/a
28	ATF1	chr14:22805143-22805343	K562	blood:	n/a	n/a
29	ATF1	chr14:22782653-22782949	K562	blood:	n/a	n/a
30	ATF1	chr14:22898045-22898340	K562	blood:	n/a	n/a
31	ATF1	chr14:22806344-22806684	K562	blood:	n/a	n/a
32	ATF2	chr14:22582661-22583009	GM12878	blood:	n/a	n/a
33	ATF2	chr14:22941903-22942467	GM12878	blood:	n/a	n/a
34	ATF2	chr14:22917031-22918320	GM12878	blood:	n/a	n/a
35	ATF2	chr14:22956719-22958641	GM12878	blood:	n/a	n/a
36	ATF2	chr14:22958727-22960305	GM12878	blood:	n/a	n/a
37	ATF2	chr14:22782586-22782996	GM12878	blood:	n/a	n/a
38	ATF2	chr14:22933087-22934275	GM12878	blood:	n/a	n/a
39	ATF2	chr14:22850800-22851197	GM12878	blood:	n/a	n/a
40	ATF2	chr14:22952938-22953638	GM12878	blood:	n/a	n/a
41	ATF2	chr14:22860192-22860789	GM12878	blood:	n/a	n/a
42	ATF2	chr14:22956958-22958121	GM12878	blood:	n/a	n/a
43	ATF2	chr14:22952266-22954843	GM12878	blood:	n/a	n/a
44	ATF2	chr14:22851477-22853310	GM12878	blood:	n/a	n/a
45	ATF2	chr14:22933150-22934304	GM12878	blood:	n/a	n/a
46	ATF2	chr14:22941742-22942380	GM12878	blood:	n/a	n/a
47	ATF2	chr14:22958725-22960215	GM12878	blood:	n/a	n/a
48	ATF2	chr14:22851242-22852700	GM12878	blood:	n/a	n/a
49	ATF2	chr14:22960628-22961954	GM12878	blood:	n/a	n/a
50	ATF2	chr14:22965462-22966426	GM12878	blood:	n/a	n/a

(count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22457536-22457586	NHDF-neo	bronchial:	n/a
2	chr14:22674549-22674599	LNCaP	prostate:	n/a
3	chr14:22433489-22433539	SKMC	muscle:	n/a
4	chr14:22694601-22694651	AoSMC	blood vessel:	n/a
5	chr14:22963867-22963917	HL-60	blood:	n/a
6	chr14:22969695-22969745	AG09319	gingival:	n/a
7	chr14:22573483-22573533	PANC-1	pancreas:	n/a
8	chr14:22457536-22457586	NHDF-neo	bronchial:	n/a
9	chr14:22674549-22674599	LNCaP	prostate:	n/a
10	chr14:22433489-22433539	SKMC	muscle:	n/a
11	chr14:22694601-22694651	AoSMC	blood vessel:	n/a
12	chr14:22963867-22963917	HL-60	blood:	n/a
13	chr14:22969695-22969745	AG09319	gingival:	n/a
14	chr14:22573483-22573533	PANC-1	pancreas:	n/a
15	chr14:22958399-22958449	MCF-7	breast:	n/a
16	chr14:22968031-22968081	HRPEpiC	eye:	n/a
17	chr14:22694547-22694597	HRPEpiC	eye:	n/a
18	chr14:22966633-22966683	T-47D	breast:	n/a
19	chr14:22945181-22945231	U87	brain:	n/a
20	chr14:22630004-22630054	HEEpiC	esophagus:	n/a
21	chr14:22968031-22968081	HRCEpiC	kidney:	n/a
22	chr14:22573483-22573533	GM12891	blood:	n/a
23	chr14:22963867-22963917	HRE	kidney:	n/a
24	chr14:22590704-22590754	NHDF-neo	bronchial:	n/a
25	chr14:22457536-22457586	HCT-116	colon:	n/a
26	chr14:22564251-22564301	MCF10A-Er-Src	breast:	n/a
27	chr14:22902298-22902348	HEEpiC	esophagus:	n/a
28	chr14:22958399-22958449	LNCaP	prostate:	n/a
29	chr14:22464490-22464540	SK-N-SH	brain:	n/a
30	chr14:22433693-22433743	GM12892	blood:	n/a
31	chr14:22470396-22470446	HAEpiC	amniotic membrane:	n/a
32	chr14:22564251-22564301	SKMC	muscle:	n/a
33	chr14:22902226-22902276	HCF	heart:	n/a
34	chr14:22457536-22457586	HepG2	liver:	n/a
35	chr14:22938675-22938725	NH-A	brain:	n/a
36	chr14:22965472-22965522	AG04450	lung:	fetal
37	chr14:22902226-22902276	IMR90	lung:	fetal
38	chr14:22471111-22471161	HL-60	blood:	n/a
39	chr14:22579242-22579292	HRCEpiC	kidney:	n/a
40	chr14:22433693-22433743	AG09309	skin:	n/a
41	chr14:22538783-22538833	PFSK-1	brain:	n/a
42	chr14:22471111-22471161	AG04450	lung:	fetal
43	chr14:22902298-22902348	SKMC	muscle:	n/a
44	chr14:22938675-22938725	HIPEpiC	eye:	n/a
45	chr14:22465676-22465726	HMEC	breast:	n/a
46	chr14:22941183-22941233	PrEC	prostate:	n/a
47	chr14:22408982-22409032	GM12892	blood:	n/a
48	chr14:22694601-22694651	NT2-D1	testis:	n/a
49	chr14:22941183-22941233	HNPCEpiC	eye:	n/a
50	chr14:22925659-22925709	GM12878	blood:	n/a

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr14:22770476..22771415-chr14:22843857..22844546,2	MCF-7	breast:
2	chr14:22532215..22535183-chr14:22535899..22538751,3	K562	blood:
3	chr14:22859602..22861601-chr14:22940820..22943707,2	K562	blood:
4	chr14:22855941..22856510-chr14:22940240..22941260,3	K562	blood:
5	chr14:22381747..22382682-chr14:22568612..22569505,2	MCF-7	breast:
6	chr14:22554611..22556111-chr3:73158574..73161594,3	K562	blood:
7	chr14:22772559..22774851-chr14:22778654..22780201,2	MCF-7	breast:
8	chr14:22859979..22860926-chr14:22941284..22942679,19	MCF-7	breast:
9	chr14:22552370..22552947-chr14:22565151..22565758,2	MCF-7	breast:
10	chr14:22887752..22889710-chr14:22893066..22895246,2	K562	blood:
11	chr14:22870770..22873189-chr14:22873992..22876321,2	MCF-7	breast:
12	chr14:22787883..22788821-chr14:22855804..22856459,3	K562	blood:
13	chr14:22688367..22691201-chr14:22731721..22733853,2	MCF-7	breast:
14	chr14:22465637..22466187-chr14:22508234..22509353,3	MCF-7	breast:
15	chr14:22643813..22646697-chr14:22651857..22653999,3	MCF-7	breast:
16	chr14:22508432..22509169-chr14:22568256..22569068,4	MCF-7	breast:
17	chr14:22714064..22716296-chr14:22718223..22720052,2	MCF-7	breast:
18	chr14:22788394..22789082-chr14:22855740..22856285,2	MCF-7	breast:
19	chr14:22555233..22555822-chr14:22568280..22569073,2	MCF-7	breast:
20	chr14:22235335..22237919-chr14:22567739..22569727,2	MCF-7	breast:
21	chr14:22862824..22864416-chr14:22864446..22866192,2	K562	blood:
22	chr14:22860207..22860973-chr14:22940190..22940778,2	MCF-7	breast:
23	chr14:22855481..22856874-chr14:22941338..22942713,6	K562	blood:
24	chr14:22758101..22760043-chr14:22761332..22763107,2	MCF-7	breast:
25	chr14:22755065..22755565-chr9:131709348..131709852,2	MCF-7	breast:
26	chr14:22862824..22864416-chr14:22864446..22866192,2	K562	blood:
27	chr14:22753988..22755736-chr14:22757103..22759788,3	MCF-7	breast:
28	chr14:22689474..22690035-chr14:22940633..22941202,2	MCF-7	breast:
29	chr14:22782982..22783495-chr14:22848904..22849615,2	MCF-7	breast:
30	chr14:22859967..22861216-chr14:22940144..22941196,30	MCF-7	breast:
31	chr14:22731859..22733753-chr14:22735251..22737043,2	MCF-7	breast:
32	chr14:22788466..22789134-chr14:22842373..22842880,2	MCF-7	breast:
33	chr14:22862055..22864692-chr14:22920966..22922475,2	MCF-7	breast:
34	chr14:22465297..22466231-chr14:22568070..22569095,4	MCF-7	breast:
35	chr14:22448554..22450231-chr14:22452075..22453975,2	MCF-7	breast:
36	chr14:22746753..22748555-chr14:23355124..23357041,2	MCF-7	breast:
37	chr14:22772559..22774851-chr14:22778654..22780201,2	MCF-7	breast:
38	chr14:22615286..22617241-chr14:22632058..22634012,2	MCF-7	breast:
39	chr14:22532215..22534018-chr14:22536841..22538751,2	K562	blood:
40	chr14:22643970..22646253-chr14:22648103..22650894,3	MCF-7	breast:
41	chr14:22859945..22861319-chr14:22940207..22941157,15	MCF-7	breast:
42	chr14:22693865..22694927-chr14:22782327..22783376,6	MCF-7	breast:
43	chr14:22631349..22633623-chr14:22639459..22642568,4	MCF-7	breast:
44	chr14:22782662..22783265-chr14:22941744..22942480,2	MCF-7	breast:
45	chr14:22694397..22696930-chr14:22740010..22742025,2	MCF-7	breast:
46	chr14:22860207..22860973-chr14:22940190..22940778,2	MCF-7	breast:
47	chr14:22692942..22694471-chr14:22843442..22844484,5	MCF-7	breast:
48	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
49	chr14:22632562..22633124-chr4:143395110..143395748,2	MCF-7	breast:
50	chr14:22632384..22633121-chr14:22741174..22741692,2	MCF-7	breast:

(count:112 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-7	chr14:22653668-22653953	NONHSAT035760
2	lnc-DAD1-2	chr14:22929014-22930299	NONHSAT035772
3	lnc-AE000662.92.1-10	chr14:22958475-22958531	NONHSAT035716
4	lnc-AE000662.92.1-10	chr14:22466181-22466398	NONHSAT035728
5	lnc-OR10G2-8	chr14:22508841-22508960	NONHSAT035748
6	lnc-AE000662.92.1-9	chr14:22623012-22623063	NONHSAT035757
7	lnc-DAD1-2	chr14:22869445-22869575	ENSG00000251002
8	lnc-DAD1-2	chr14:22950274-22950347	NONHSAT035774
9	lnc-DAD1-2	chr14:22872095-22872164	ENSG00000251002
10	lnc-AE000662.92.1-10	chr14:22466181-22466411	NONHSAT035729
11	lnc-OR10G2-7	chr14:22432255-22433844	l_935_chr14:22432254-22434316_brain
12	lnc-OR4E2-9	chr14:22564599-22564896	NONHSAT035752
13	lnc-DAD1-2	chr14:22953008-22953424	NONHSAT035774
14	lnc-AE000662.92.1-6	chr14:22658319-22658607	NONHSAT035761
15	lnc-AE000662.92.1-10	chr14:22539277-22539475	NONHSAT035751
16	lnc-AE000662.92.1-10	chr14:22466246-22466398	NONHSAT035742
17	lnc-DAD1-2	chr14:22869445-22869575	ENSG00000251002
18	lnc-DAD1-4	chr14:22801352-22801906	NONHSAT035764
19	lnc-OR10G2-8	chr14:22509116-22509392	NONHSAT035748
20	lnc-AE000662.92.1-10	chr14:22968667-22968762	NONHSAT035727
21	lnc-AE000662.92.1-10	chr14:22958462-22958531	NONHSAT035718
22	lnc-AE000662.92.1-10	chr14:22459042-22459181	NONHSAT035725
23	lnc-AE000662.92.1-2	chr14:22886826-22886962	ENSG00000259042.1
24	lnc-AE000662.92.1-10	chr14:22538907-22539002	NONHSAT035750
25	lnc-DAD1-2	chr14:22953490-22953600	NONHSAT035772
26	lnc-AE000662.92.1-10	chr14:22466181-22466398	NONHSAT035727
27	lnc-AE000662.92.1-10	chr14:22466182-22466411	NONHSAT035730
28	lnc-AE000662.92.1-10	chr14:22958473-22958555	NONHSAT035742
29	lnc-AE000662.92.1-10	chr14:22947870-22947923	NONHSAT035725
30	lnc-DAD1-2	chr14:22901658-22901731	ENSG00000251002
31	lnc-DAD1-2	chr14:22930055-22930303	NONHSAT035774
32	lnc-DAD1-2	chr14:22849083-22850808	ENSG00000251002
33	lnc-DAD1-2	chr14:22950230-22950347	ENSG00000251002
34	lnc-DAD1-2	chr14:22901658-22901719	ENSG00000251002
35	lnc-AE000662.92.1-10	chr14:22508939-22508960	NONHSAT035749
36	lnc-AE000662.92.1-10	chr14:22466225-22466411	NONHSAT035734
37	lnc-DAD1-2	chr14:22850754-22850808	ENSG00000251002
38	lnc-DAD1-2	chr14:22850247-22850383	ENSG00000251002
39	lnc-AE000662.92.1-10	chr14:22962395-22962451	NONHSAT035730
40	lnc-DAD1-2	chr14:22901658-22901731	ENSG00000251002
41	lnc-AE000662.92.1-10	chr14:22466246-22466413	NONHSAT035743
42	lnc-DAD1-2	chr14:22850773-22850808	ENSG00000251002
43	lnc-OR10G2-9	chr14:22518799-22519031	expReg_chr14_765_-
44	lnc-AE000662.92.1-10	chr14:22951262-22951335	NONHSAT035712
45	lnc-OR4E2-9	chr14:22564302-22564393	NONHSAT035752
46	lnc-OR10G2-7	chr14:22434299-22434316	l_935_chr14:22432254-22434316_brain
47	lnc-AE000662.92.1-5	chr14:22733632-22733683	NONHSAT035763
48	lnc-AE000662.92.1-10	chr14:22466224-22466411	NONHSAT035733
49	lnc-AE000662.92.1-10	chr14:22466242-22466411	NONHSAT035738
50	lnc-AE000662.92.1-10	chr14:22946710-22946778	NONHSAT035743

No data

Variant related genes	Relation type
TRAV33	TF binding region
TRAV8-7	TF binding region
TRAJ44	TF binding region
TRAV41	TF binding region
TRAV26-1	TF binding region
TRDD2	TF binding region
ENSG00000238634	TF binding region
TRAV23DV6	TF binding region
TRDV1	TF binding region
TRAJ52	TF binding region
TRAJ37	TF binding region
ENSG00000258557	TF binding region
TRAJ51	TF binding region
TRDD3	TF binding region
ENSG00000258705	TF binding region
TRDV3	TF binding region
TRAV9-2	TF binding region
TRAV38-1	TF binding region
TRAJ39	TF binding region
TRAJ43	TF binding region
TRAJ49	TF binding region
TRAV12-3	TF binding region
TRAJ55	TF binding region
TRAJ36	TF binding region
TRAJ45	TF binding region
TRAV8-6	TF binding region
TRAJ56	TF binding region
TRAJ48	TF binding region
TRAV34	TF binding region
TRAJ54	TF binding region
TRAV32	TF binding region
TRAJ61	TF binding region
TRAV15	TF binding region
TRAV40	TF binding region
TRAV37	TF binding region
TRDV2	TF binding region
TRAJ50	TF binding region
TRDJ2	TF binding region
TRAV25	TF binding region
TRAJ42	TF binding region
TRDD1	TF binding region
TRAV19	TF binding region
TRDJ1	TF binding region
TRAV39	TF binding region
TRAJ38	TF binding region
TRAV38-2DV8	TF binding region
TRDJ3	TF binding region
TRAJ57	TF binding region
TRAV24	TF binding region
TRAV30	TF binding region
ENSG00000256221	TF binding region
TRAV36DV7	TF binding region
TRAV17	TF binding region
TRAJ58	TF binding region
TRAV21	TF binding region
TRAV18	TF binding region
TRAJ41	TF binding region
TRAV20	TF binding region
TRAV31	TF binding region
TRAV16	TF binding region
ENSG00000251002	TF binding region
TRDJ4	TF binding region
TRAV26-2	TF binding region
TRAJ47	TF binding region
TRAV22	TF binding region
TRAJ59	TF binding region
ENSG00000259042	TF binding region
TRAJ46	TF binding region
TRAJ60	TF binding region
TRAJ40	TF binding region
TRAV28	TF binding region
TRAV35	TF binding region
TRDC	TF binding region
TRAV27	TF binding region
TRAV29DV5	TF binding region
TRAJ53	TF binding region
TRAV33	CpG island
TRAV8-7	CpG island
TRAJ44	CpG island
TRAV41	CpG island
TRAV26-1	CpG island
TRDD2	CpG island
ENSG00000238634	CpG island
TRAV23DV6	CpG island
TRDV1	CpG island
TRAJ52	CpG island
TRAJ37	CpG island
ENSG00000258557	CpG island
TRAJ51	CpG island
TRDD3	CpG island
ENSG00000258705	CpG island
TRDV3	CpG island
TRAV9-2	CpG island
TRAV38-1	CpG island
TRAJ39	CpG island
TRAJ43	CpG island
TRAJ49	CpG island
TRAV12-3	CpG island
TRAJ55	CpG island
TRAJ36	CpG island
TRAJ45	CpG island
TRAV8-6	CpG island
TRAJ56	CpG island
TRAJ48	CpG island
TRAV34	CpG island
TRAJ54	CpG island
TRAV32	CpG island
TRAJ61	CpG island
TRAV15	CpG island
TRAV40	CpG island
TRAV37	CpG island
TRDV2	CpG island
TRAJ50	CpG island
TRDJ2	CpG island
TRAV25	CpG island
TRAJ42	CpG island
TRDD1	CpG island
TRAV19	CpG island
TRDJ1	CpG island
TRAV39	CpG island
TRAJ38	CpG island
TRAV38-2DV8	CpG island
TRDJ3	CpG island
TRAJ57	CpG island
TRAV24	CpG island
TRAV30	CpG island
ENSG00000256221	CpG island
TRAV36DV7	CpG island
TRAV17	CpG island
TRAJ58	CpG island
TRAV21	CpG island
TRAV18	CpG island
TRAJ41	CpG island
TRAV20	CpG island
TRAV31	CpG island
TRAV16	CpG island
ENSG00000251002	CpG island
TRDJ4	CpG island
TRAV26-2	CpG island
TRAJ47	CpG island
TRAV22	CpG island
TRAJ59	CpG island
ENSG00000259042	CpG island
TRAJ46	CpG island
TRAJ60	CpG island
TRAJ40	CpG island
TRAV28	CpG island
TRAV35	CpG island
TRDC	CpG island
TRAV27	CpG island
TRAV29DV5	CpG island
TRAJ53	CpG island
ENSG00000258905	chromatin interactions
ENSG00000211812	chromatin interactions
ENSG00000211834	chromatin interactions
ENSG00000259092	chromatin interactions
ENSG00000211810	chromatin interactions
ENSG00000211820	chromatin interactions
ENSG00000259054	chromatin interactions
ENSG00000211851	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000211850	chromatin interactions
ENSG00000237235	chromatin interactions
ENSG00000256590	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000211802	chromatin interactions
ENSG00000211798	chromatin interactions
ENSG00000211831	chromatin interactions
ENSG00000211832	chromatin interactions
ENSG00000259068	chromatin interactions
ENSG00000211839	chromatin interactions
ENSG00000211837	chromatin interactions
ENSG00000211827	chromatin interactions
ENSG00000211836	chromatin interactions
ENSG00000256221	chromatin interactions
ENSG00000211840	chromatin interactions
ENSG00000211809	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000249446	chromatin interactions
ENSG00000251002	chromatin interactions
ENSG00000211804	chromatin interactions
ENSG00000211796	chromatin interactions
ENSG00000211835	chromatin interactions
ENSG00000211829	chromatin interactions
ENSG00000211797	chromatin interactions
ENSG00000211791	chromatin interactions
ENSG00000109452	chromatin interactions
ENSG00000249048	chromatin interactions
ENSG00000212335	chromatin interactions
ENSG00000211807	chromatin interactions
ENSG00000223997	chromatin interactions
ENSG00000211795	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000250688	chromatin interactions
ENSG00000211818	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000211803	chromatin interactions
ENSG00000211817	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000211816	chromatin interactions
ENSG00000211849	chromatin interactions
ENSG00000211780	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000211814	chromatin interactions
ENSG00000211800	chromatin interactions
ENSG00000211819	chromatin interactions
ENSG00000211815	chromatin interactions
ENSG00000248366	chromatin interactions
ENSG00000258705	chromatin interactions
GRB10	miRNA target sites
CNOT4	miRNA target sites
MREG	miRNA target sites
CCNE1	miRNA target sites
GPAM	miRNA target sites
DPY19L3	miRNA target sites
BCL2	miRNA target sites
ZFAND5	miRNA target sites
LSM1	miRNA target sites
KPNA2	miRNA target sites
RECK	miRNA target sites
ARID4B	miRNA target sites
CACNB2	miRNA target sites
ELOVL4	miRNA target sites
CCL20	miRNA target sites
MYT1	miRNA target sites
HSPA1L	miRNA target sites
RPS6KA6	miRNA target sites
RB1	miRNA target sites
RASGRP3	miRNA target sites

Extended variants
information (count: 22649 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:22649 , 50 per page) page: 1 2 3 4 5 6 7 ... 453

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8007645	chr14:22393148-22393149	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531993122	chr14:22393154-22393155	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115228655	chr14:22393174-22393175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568644440	chr14:22393182-22393183	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs8007794	chr14:22393199-22393200	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs8007804	chr14:22393214-22393215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs566588330	chr14:22393240-22393241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs8007829	chr14:22393246-22393247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs8012874	chr14:22393266-22393267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568767387	chr14:22393267-22393268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201209200	chr14:22393295-22393296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35954874	chr14:22393352-22393353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs139109583	chr14:22393354-22393355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377191138	chr14:22393382-22393383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116056119	chr14:22393434-22393435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs36012830	chr14:22393439-22393440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs35167138	chr14:22393446-22393447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145117669	chr14:22393458-22393459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35583044	chr14:22393465-22393466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562856793	chr14:22393511-22393512	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs34567185	chr14:22393513-22393514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs34808520	chr14:22393541-22393542	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs368476068	chr14:22393567-22393568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562404158	chr14:22393574-22393575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74692207	chr14:22393596-22393597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs548054863	chr14:22393602-22393603	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141724318	chr14:22393607-22393608	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532189691	chr14:22393639-22393640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371193180	chr14:22393651-22393652	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs568807609	chr14:22393698-22393699	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs35389538	chr14:22393702-22393703	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145663078	chr14:22393708-22393709	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113783617	chr14:22393714-22393715	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34688734	chr14:22393737-22393738	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs533729961	chr14:22393744-22393745	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553892075	chr14:22393766-22393767	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545485928	chr14:22393772-22393773	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61979701	chr14:22393784-22393785	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs373834173	chr14:22393785-22393786	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs28790913	chr14:22393789-22393790	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556401204	chr14:22393803-22393804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540329670	chr14:22393808-22393809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11844921	chr14:22393845-22393846	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs116150555	chr14:22393855-22393856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544503535	chr14:22393880-22393881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562364036	chr14:22393918-22393919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191999400	chr14:22393961-22393962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78531734	chr14:22393970-22393971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28888478	chr14:22394012-22394013	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs11157302	chr14:22394019-22394020	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Barrett''s syndrome	19417022	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5244 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22389200-22395200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr14:22391400-22393200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
3	chr14:22391400-22393400	Enhancers	HUVEC	blood vessel
4	chr14:22391800-22393200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:22392200-22393200	Flanking Active TSS	Primary T cells from cord blood	blood
6	chr14:22392600-22394200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr14:22392800-22393600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr14:22392800-22393600	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr14:22392800-22393800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr14:22392800-22394000	Enhancers	Primary B cells from peripheral blood	blood
11	chr14:22392800-22394000	Enhancers	Primary T cells fromperipheralblood	blood
12	chr14:22392800-22394200	Enhancers	Primary hematopoietic stem cells	blood
13	chr14:22392800-22394200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr14:22392800-22394200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr14:22392800-22394400	Enhancers	Primary B cells from cord blood	blood
16	chr14:22392800-22394400	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr14:22392800-22394400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr14:22392800-22394400	Enhancers	Fetal Thymus	thymus
19	chr14:22392800-22394400	Enhancers	Dnd41	blood
20	chr14:22392800-22395000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr14:22393000-22393600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr14:22393000-22394200	Enhancers	Thymus	Thymus
23	chr14:22393000-22394400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:22393000-22395000	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr14:22393000-22399800	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr14:22393200-22394200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr14:22393200-22394400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr14:22393200-22395200	Enhancers	Primary T cells from cord blood	blood
29	chr14:22393600-22393800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr14:22393800-22394000	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr14:22394000-22394200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
32	chr14:22394200-22394800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr14:22394200-22395200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr14:22394200-22397200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr14:22394200-22399600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr14:22394200-22399600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr14:22394400-22396200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr14:22394400-22397000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr14:22394400-22399400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:22394400-22399600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr14:22394800-22395000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr14:22395000-22396200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr14:22395000-22397200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr14:22395200-22396200	Weak transcription	Primary T cells from cord blood	blood
45	chr14:22395200-22397000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr14:22396200-22396400	Enhancers	Primary T cells from cord blood	blood
47	chr14:22396200-22396400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr14:22396200-22396400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr14:22396400-22396800	Weak transcription	Primary T cells from cord blood	blood
50	chr14:22396400-22396800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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