Variant report

Variant	nsv430917
Chromosome Location	chr14:22392626-22803906
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:6014)
CpG islands
(count:1343)
Chromatin interactive
region (count:149)
LncRNA
region (count:66)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:6014 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:22801636-22802916	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:22552704-22553020	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:22579948-22580394	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:22802474-22802855	K562	blood:	n/a	n/a
5	ARID3A	chr14:22765370-22765613	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:22515400-22515690	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:22446451-22446751	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:22745215-22745415	K562	blood:	n/a	n/a
9	ARID3A	chr14:22764524-22765035	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:22788290-22788588	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:22580003-22580242	K562	blood:	n/a	n/a
12	ARID3A	chr14:22694346-22694555	K562	blood:	n/a	n/a
13	ATF1	chr14:22802422-22802769	K562	blood:	n/a	n/a
14	ATF1	chr14:22645817-22646098	K562	blood:	n/a	n/a
15	ATF1	chr14:22782653-22782949	K562	blood:	n/a	n/a
16	ATF1	chr14:22598192-22598259	K562	blood:	n/a	n/a
17	ATF2	chr14:22782586-22782996	GM12878	blood:	n/a	n/a
18	ATF2	chr14:22582661-22583009	GM12878	blood:	n/a	n/a
19	ATF3	chr14:22802354-22802903	A549	lung:	n/a	n/a
20	ATF3	chr14:22802478-22802664	K562	blood:	n/a	n/a
21	ATF3	chr14:22802479-22802671	HepG2	liver:	n/a	n/a
22	ATF3	chr14:22802379-22802739	K562	blood:	n/a	n/a
23	BACH1	chr14:22470430-22470522	K562	blood:	n/a	n/a
24	BACH1	chr14:22456148-22456596	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr14:22456212-22456527	K562	blood:	n/a	n/a
26	BACH1	chr14:22568547-22568809	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr14:22465541-22465831	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr14:22802519-22802728	K562	blood:	n/a	n/a
29	BACH1	chr14:22802425-22802636	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:22750875-22751012	K562	blood:	n/a	n/a
31	BATF	chr14:22582631-22583275	GM12878	blood:	n/a	n/a
32	BATF	chr14:22643094-22643302	GM12878	blood:	n/a	n/a
33	BATF	chr14:22736725-22736946	GM12878	blood:	n/a	chr14:22736862-22736873
34	BATF	chr14:22567169-22567469	GM12878	blood:	n/a	n/a
35	BATF	chr14:22582685-22583028	GM12878	blood:	n/a	n/a
36	BATF	chr14:22802471-22802686	GM12878	blood:	n/a	chr14:22802481-22802490 chr14:22802597-22802607 chr14:22802592-22802603
37	BATF	chr14:22670226-22670422	GM12878	blood:	n/a	n/a
38	BATF	chr14:22802392-22802773	GM12878	blood:	n/a	chr14:22802481-22802490 chr14:22802597-22802607 chr14:22802592-22802603
39	BATF	chr14:22773474-22773843	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:22539367-22539609	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:22582704-22583095	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:22539355-22539629	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:22802420-22802769	GM12878	blood:	n/a	n/a
44	BCL3	chr14:22802191-22802955	A549	lung:	n/a	chr14:22802923-22802932
45	BCL3	chr14:22802450-22802759	GM12878	blood:	n/a	n/a
46	BCL3	chr14:22802297-22802913	A549	lung:	n/a	n/a
47	BHLHE40	chr14:22788329-22788517	K562	blood:	n/a	n/a
48	BHLHE40	chr14:22446488-22446678	GM12878	blood:	n/a	n/a
49	BHLHE40	chr14:22516477-22516589	HepG2	liver:	n/a	n/a
50	BHLHE40	chr14:22802374-22802793	HepG2	liver:	n/a	n/a

(count:1343 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22694601-22694651	Hela-S3	cervix:	n/a
2	chr14:22694601-22694651	Hela-S3	cervix:	n/a
3	chr14:22573606-22573656	LNCaP	prostate:	n/a
4	chr14:22579242-22579292	AG04450	lung:	fetal
5	chr14:22694601-22694651	AG10803	skin:	n/a
6	chr14:22408982-22409032	NH-A	brain:	n/a
7	chr14:22408982-22409032	SK-N-MC	brain:	n/a
8	chr14:22630004-22630054	SK-N-SH_RA	brain:	n/a
9	chr14:22458634-22458684	IMR90	lung:	fetal
10	chr14:22573483-22573533	AG04449	skin:	fetal
11	chr14:22689870-22689920	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:22465676-22465726	HRE	kidney:	n/a
13	chr14:22689870-22689920	IMR90	lung:	fetal
14	chr14:22433489-22433539	SKMC	muscle:	n/a
15	chr14:22689870-22689920	PANC-1	pancreas:	n/a
16	chr14:22689870-22689920	BJ	skin:	n/a
17	chr14:22573606-22573656	SK-N-SH	brain:	n/a
18	chr14:22465676-22465726	HL-60	blood:	n/a
19	chr14:22694547-22694597	AG04450	lung:	fetal
20	chr14:22465676-22465726	MCF10A-Er-Src	breast:	n/a
21	chr14:22408982-22409032	HAEpiC	amniotic membrane:	n/a
22	chr14:22564251-22564301	HEK293	kidney:	embryo
23	chr14:22689870-22689920	PrEC	prostate:	n/a
24	chr14:22538783-22538833	PANC-1	pancreas:	n/a
25	chr14:22408982-22409032	GM12891	blood:	n/a
26	chr14:22470396-22470446	ECC-1	luminal epithelium:	n/a
27	chr14:22630004-22630054	HCT-116	colon:	n/a
28	chr14:22464490-22464540	HL-60	blood:	n/a
29	chr14:22538783-22538833	SAEC	small airway:	n/a
30	chr14:22408982-22409032	PrEC	prostate:	n/a
31	chr14:22573606-22573656	BJ	skin:	n/a
32	chr14:22465676-22465726	Hela-S3	cervix:	n/a
33	chr14:22457536-22457586	Jurkat	blood:	n/a
34	chr14:22465676-22465726	HMEC	breast:	n/a
35	chr14:22458634-22458684	BE2_C	brain:	n/a
36	chr14:22433489-22433539	T-47D	breast:	n/a
37	chr14:22538783-22538833	GM12878	blood:	n/a
38	chr14:22465676-22465726	LNCaP	prostate:	n/a
39	chr14:22538783-22538833	NHBE	bronchial:	n/a
40	chr14:22674549-22674599	CMK	blood:	n/a
41	chr14:22590704-22590754	HNPCEpiC	eye:	n/a
42	chr14:22564251-22564301	GM12891	blood:	n/a
43	chr14:22538783-22538833	AG04450	lung:	fetal
44	chr14:22694601-22694651	GM12891	blood:	n/a
45	chr14:22470396-22470446	AG04449	skin:	fetal
46	chr14:22465676-22465726	PFSK-1	brain:	n/a
47	chr14:22689870-22689920	NH-A	brain:	n/a
48	chr14:22674549-22674599	NHBE	bronchial:	n/a
49	chr14:22464490-22464540	AG04449	skin:	fetal
50	chr14:22573483-22573533	SK-N-MC	brain:	n/a

(count:149 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:22689184..22689709-chr14:22782522..22783262,2	MCF-7	breast:
2	chr14:22782982..22783495-chr14:22848904..22849615,2	MCF-7	breast:
3	chr14:22693535..22694449-chr14:22788132..22788768,2	MCF-7	breast:
4	chr14:22634286..22636790-chr14:22741155..22742671,2	MCF-7	breast:
5	chr14:22603782..22606179-chr14:22607430..22609520,2	MCF-7	breast:
6	chr14:22643970..22646253-chr14:22648103..22650894,3	MCF-7	breast:
7	chr14:22755065..22755565-chr9:131709348..131709852,2	MCF-7	breast:
8	chr14:22668551..22669387-chr14:22782298..22783291,2	MCF-7	breast:
9	chr14:22456047..22456782-chr14:22465298..22465973,2	MCF-7	breast:
10	chr14:22758101..22760043-chr14:22761332..22763107,2	MCF-7	breast:
11	chr14:22729687..22734778-chr14:22736945..22742365,6	MCF-7	breast:
12	chr14:22758101..22760043-chr14:22761332..22763107,2	MCF-7	breast:
13	chr11:62609148..62609720-chr14:22554611..22555111,2	Hela-S3	cervix:
14	chr14:22771659..22772159-chr14:22782640..22783274,2	MCF-7	breast:
15	chr14:22555233..22555822-chr14:22568280..22569073,2	MCF-7	breast:
16	chr11:68295992..68298851-chr14:22471442..22473971,2	MCF-7	breast:
17	chr14:22745355..22746897-chr14:22749281..22751192,2	MCF-7	breast:
18	chr14:22747893..22750330-chr14:22755217..22757122,2	MCF-7	breast:
19	chr14:22626421..22628658-chr14:22786907..22788886,2	MCF-7	breast:
20	chr14:22668647..22670800-chr14:22675533..22677492,2	MCF-7	breast:
21	chr14:22446154..22446833-chr14:22568339..22569132,2	MCF-7	breast:
22	chr14:22551979..22553343-chr14:22567813..22568845,8	MCF-7	breast:
23	chr14:22652889..22653705-chr14:22668945..22669592,2	MCF-7	breast:
24	chr14:22776089..22777923-chr14:22781026..22782759,2	MCF-7	breast:
25	chr11:62609117..62609718-chr14:22554611..22555131,5	HCT-116	colon:
26	chr14:22759513..22761832-chr14:22763808..22765631,2	MCF-7	breast:
27	chr14:22381747..22382682-chr14:22568612..22569505,2	MCF-7	breast:
28	chr14:22735413..22737011-chr14:22760439..22762105,2	MCF-7	breast:
29	chr14:22551979..22553343-chr14:22567813..22568845,8	MCF-7	breast:
30	chr14:22455914..22456898-chr14:22568288..22568800,3	MCF-7	breast:
31	chr14:22795690..22798301-chr14:22837296..22840159,2	MCF-7	breast:
32	chr14:22632384..22633121-chr14:22741174..22741692,2	MCF-7	breast:
33	chr14:22514895..22516734-chr14:22567994..22569123,6	MCF-7	breast:
34	chr14:22458147..22458872-chr14:22568199..22569106,2	MCF-7	breast:
35	chr14:22731859..22733753-chr14:22735251..22737043,2	MCF-7	breast:
36	chr14:22538808..22541789-chr14:22546919..22548697,2	K562	blood:
37	chr14:22532215..22534018-chr14:22536841..22538751,2	K562	blood:
38	chr14:22553176..22555268-chr14:22563550..22566303,2	MCF-7	breast:
39	chr14:22714064..22716296-chr14:22718223..22720052,2	MCF-7	breast:
40	chr14:22771659..22772159-chr14:22782640..22783274,2	MCF-7	breast:
41	chr14:22455914..22456450-chr14:22507743..22508393,2	MCF-7	breast:
42	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
43	chr14:22694156..22694958-chr14:22744677..22745780,4	MCF-7	breast:
44	chr14:22772559..22774851-chr14:22778654..22780201,2	MCF-7	breast:
45	chr14:22731205..22733963-chr14:22736080..22737631,2	K562	blood:
46	chr14:22471344..22472858-chr14:22480146..22483054,2	MCF-7	breast:
47	chr14:22470490..22471667-chr14:22568300..22569059,4	MCF-7	breast:
48	chr14:22552187..22553607-chr14:22567385..22569180,17	MCF-7	breast:
49	chr14:22634997..22636619-chr14:22639097..22641198,2	MCF-7	breast:
50	chr14:22235335..22237919-chr14:22567739..22569727,2	MCF-7	breast:

(count:66 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4E2-8	chr14:22522131-22522790	l_936_chr14:22521733-22524438_thyroid
2	lnc-AE000662.92.1-10	chr14:22466182-22466411	NONHSAT035731
3	lnc-AE000662.92.1-10	chr14:22466242-22466395	NONHSAT035740
4	lnc-AE000662.92.1-10	chr14:22466246-22466413	NONHSAT035743
5	lnc-AE000662.92.1-10	chr14:22539191-22539462	NONHSAT035750
6	lnc-AE000662.92.1-10	chr14:22466240-22466404	NONHSAT035736
7	lnc-AE000662.92.1-10	chr14:22458896-22459009	NONHSAT035725
8	lnc-OR4E2-8	chr14:22523887-22524438	l_936_chr14:22521733-22524438_thyroid
9	lnc-DAD1-4	chr14:22801352-22801906	NONHSAT035764
10	lnc-OR4E2-8	chr14:22521734-22521793	l_936_chr14:22521733-22524438_thyroid
11	lnc-AE000662.92.1-10	chr14:22508939-22508960	NONHSAT035749
12	lnc-AE000662.92.1-10	chr14:22392628-22392831	NONHSAT035716
13	lnc-AE000662.92.1-10	chr14:22466235-22466408	NONHSAT035735
14	lnc-AE000662.92.1-10	chr14:22392662-22392811	NONHSAT035718
15	lnc-AE000662.92.1-10	chr14:22466181-22466398	NONHSAT035728
16	lnc-AE000662.92.1-10	chr14:22466207-22466395	NONHSAT035732
17	lnc-OR4E2-7	chr14:22480149-22483203	NONHSAT035747
18	lnc-OR10G2-8	chr14:22508841-22508960	NONHSAT035748
19	lnc-AE000662.92.1-10	chr14:22466182-22466411	NONHSAT035730
20	lnc-OR10G2-9	chr14:22518799-22519031	expReg_chr14_765_-
21	lnc-AE000662.92.1-10	chr14:22459042-22459181	NONHSAT035725
22	lnc-AE000662.92.1-10	chr14:22509116-22509387	NONHSAT035749
23	lnc-AE000662.92.1-10	chr14:22466247-22466411	NONHSAT035744
24	lnc-AE000662.92.1-10	chr14:22392658-22392811	NONHSAT035717
25	lnc-OR10G2-7	chr14:22432255-22433844	l_935_chr14:22432254-22434316_brain
26	lnc-OR10G2-10	chr14:22563724-22563978	expReg_chr14_828_-
27	lnc-OR4E2-9	chr14:22564302-22564393	NONHSAT035752
28	lnc-AE000662.92.1-10	chr14:22466242-22466411	NONHSAT035737
29	lnc-OR4E2-9	chr14:22564610-22564680	NONHSAT035753
30	lnc-AE000662.92.1-8	chr14:22645469-22645761	NONHSAT035759
31	lnc-AE000662.92.1-10	chr14:22466224-22466411	NONHSAT035733
32	lnc-AE000662.92.1-5	chr14:22733858-22734147	NONHSAT035763
33	lnc-AE000662.92.1-10	chr14:22538907-22539002	NONHSAT035750
34	lnc-AE000662.92.1-9	chr14:22623301-22623571	NONHSAT035757
35	lnc-DAD1-4	chr14:22802820-22803115	NONHSAT035764
36	lnc-AE000662.92.1-10	chr14:22458751-22458780	NONHSAT035725
37	lnc-OR10G2-8	chr14:22509116-22509392	NONHSAT035748
38	lnc-OR4E2-8	chr14:22521802-22522130	l_936_chr14:22521733-22524438_thyroid
39	lnc-OR4E2-9	chr14:22564763-22564894	NONHSAT035753
40	lnc-AE000662.92.1-10	chr14:22466242-22466395	NONHSAT035739
41	lnc-AE000662.92.1-10	chr14:22466181-22466411	NONHSAT035729
42	lnc-AE000662.92.1-5	chr14:22733632-22733683	NONHSAT035763
43	lnc-AE000662.92.1-6	chr14:22658319-22658607	NONHSAT035761
44	lnc-AE000662.92.1-10	chr14:22466242-22466411	NONHSAT035738
45	lnc-AE000662.92.1-7	chr14:22653668-22653953	NONHSAT035760
46	lnc-DAD1-5	chr14:22631526-22631754	NONHSAT035758
47	lnc-AE000662.92.1-10	chr14:22466225-22466411	NONHSAT035734
48	lnc-AE000662.92.1-10	chr14:22466247-22466411	NONHSAT035745
49	lnc-AE000662.92.1-10	chr14:22466272-22466395	NONHSAT035746
50	lnc-OR4E2-8	chr14:22523701-22523885	l_936_chr14:22521733-22524438_thyroid

No data

Variant related genes	Relation type
TRAV39	TF binding region
TRAV38-2DV8	TF binding region
TRAV33	TF binding region
TRAV8-7	TF binding region
TRAV24	TF binding region
TRAV41	TF binding region
TRAV30	TF binding region
TRAV26-1	TF binding region
ENSG00000256221	TF binding region
TRAV36DV7	TF binding region
ENSG00000238634	TF binding region
TRAV23DV6	TF binding region
TRDV1	TF binding region
TRAV17	TF binding region
ENSG00000258557	TF binding region
TRAV21	TF binding region
TRAV18	TF binding region
ENSG00000258705	TF binding region
TRAV9-2	TF binding region
TRAV38-1	TF binding region
TRAV12-3	TF binding region
TRAV20	TF binding region
TRAV31	TF binding region
TRAV16	TF binding region
TRAV8-6	TF binding region
TRAV34	TF binding region
TRAV26-2	TF binding region
TRAV32	TF binding region
TRAV15	TF binding region
TRAV22	TF binding region
TRAV40	TF binding region
TRAV37	TF binding region
TRAV28	TF binding region
TRAV35	TF binding region
TRAV25	TF binding region
TRAV27	TF binding region
TRAV29DV5	TF binding region
TRAV19	TF binding region
TRAV39	CpG island
TRAV38-2DV8	CpG island
TRAV33	CpG island
TRAV8-7	CpG island
TRAV24	CpG island
TRAV41	CpG island
TRAV30	CpG island
TRAV26-1	CpG island
ENSG00000256221	CpG island
TRAV36DV7	CpG island
ENSG00000238634	CpG island
TRAV23DV6	CpG island
TRDV1	CpG island
TRAV17	CpG island
ENSG00000258557	CpG island
TRAV21	CpG island
TRAV18	CpG island
ENSG00000258705	CpG island
TRAV9-2	CpG island
TRAV38-1	CpG island
TRAV12-3	CpG island
TRAV20	CpG island
TRAV31	CpG island
TRAV16	CpG island
TRAV8-6	CpG island
TRAV34	CpG island
TRAV26-2	CpG island
TRAV32	CpG island
TRAV15	CpG island
TRAV22	CpG island
TRAV40	CpG island
TRAV37	CpG island
TRAV28	CpG island
TRAV35	CpG island
TRAV25	CpG island
TRAV27	CpG island
TRAV29DV5	CpG island
TRAV19	CpG island
ENSG00000211800	chromatin interactions
ENSG00000211804	chromatin interactions
ENSG00000211810	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000211802	chromatin interactions
ENSG00000211780	chromatin interactions
ENSG00000211791	chromatin interactions
ENSG00000249048	chromatin interactions
ENSG00000211814	chromatin interactions
ENSG00000259092	chromatin interactions
ENSG00000211812	chromatin interactions
ENSG00000211815	chromatin interactions
ENSG00000211819	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000258705	chromatin interactions
ENSG00000211820	chromatin interactions
ENSG00000109452	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000256221	chromatin interactions
ENSG00000211798	chromatin interactions
ENSG00000211818	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000211796	chromatin interactions
ENSG00000211816	chromatin interactions
ENSG00000211807	chromatin interactions
ENSG00000211809	chromatin interactions
ENSG00000211797	chromatin interactions
ENSG00000259068	chromatin interactions
ENSG00000211817	chromatin interactions
ENSG00000258905	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000211803	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000211795	chromatin interactions

Extended variants
information (count: 16857 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:16857 , 50 per page) page: 1 2 3 4 5 6 7 ... 338

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10140810	chr14:22392626-22392627	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368500210	chr14:22392628-22392629	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs186083191	chr14:22392629-22392630	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs17197613	chr14:22392639-22392640	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs35290879	chr14:22392654-22392655	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs538052424	chr14:22392657-22392658	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs376944986	chr14:22392660-22392661	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs548840265	chr14:22392673-22392674	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs148614554	chr14:22392699-22392700	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs367651915	chr14:22392702-22392703	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs8021861	chr14:22392703-22392704	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73595132	chr14:22392718-22392719	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs17197620	chr14:22392760-22392761	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs117541445	chr14:22392774-22392775	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs8008040	chr14:22392807-22392808	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs369927923	chr14:22392818-22392819	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs267603932	chr14:22392819-22392820	Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs35379740	chr14:22392838-22392839	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs17112255	chr14:22392845-22392846	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370071188	chr14:22392849-22392850	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372434720	chr14:22392902-22392903	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528062825	chr14:22392909-22392910	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556566797	chr14:22392910-22392911	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554302537	chr14:22392970-22392971	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs76791097	chr14:22392979-22392980	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs8007442	chr14:22392983-22392984	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs367899535	chr14:22392986-22392987	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12882476	chr14:22393086-22393087	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532382043	chr14:22393114-22393115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141955459	chr14:22393118-22393119	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs8006384	chr14:22393124-22393125	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs8007645	chr14:22393148-22393149	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs531993122	chr14:22393154-22393155	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115228655	chr14:22393174-22393175	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs568644440	chr14:22393182-22393183	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs8007794	chr14:22393199-22393200	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs8007804	chr14:22393214-22393215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs566588330	chr14:22393240-22393241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs8007829	chr14:22393246-22393247	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs8012874	chr14:22393266-22393267	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs568767387	chr14:22393267-22393268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201209200	chr14:22393295-22393296	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs35954874	chr14:22393352-22393353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139109583	chr14:22393354-22393355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377191138	chr14:22393382-22393383	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs116056119	chr14:22393434-22393435	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs36012830	chr14:22393439-22393440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs35167138	chr14:22393446-22393447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs145117669	chr14:22393458-22393459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs35583044	chr14:22393465-22393466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

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

Chromatin state (count:2715 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

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	chr14:22391600-22392800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
5	chr14:22391800-22393200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:22392000-22392800	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr14:22392000-22392800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
8	chr14:22392000-22393000	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr14:22392200-22392800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
10	chr14:22392200-22392800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr14:22392200-22392800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr14:22392200-22392800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
13	chr14:22392200-22393000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr14:22392200-22393000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr14:22392200-22393000	Flanking Active TSS	Thymus	Thymus
16	chr14:22392200-22393200	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr14:22392400-22392800	Flanking Active TSS	Primary B cells from peripheral blood	blood
18	chr14:22392400-22392800	Flanking Active TSS	Primary hematopoietic stem cells	blood
19	chr14:22392400-22392800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
20	chr14:22392400-22392800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
21	chr14:22392400-22392800	Flanking Active TSS	Fetal Thymus	thymus
22	chr14:22392400-22392800	Flanking Active TSS	Dnd41	blood
23	chr14:22392400-22393000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:22392400-22393000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr14:22392600-22392800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr14:22392600-22393000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:22392600-22394200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr14:22392800-22393600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr14:22392800-22393600	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr14:22392800-22393800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr14:22392800-22394000	Enhancers	Primary B cells from peripheral blood	blood
32	chr14:22392800-22394000	Enhancers	Primary T cells fromperipheralblood	blood
33	chr14:22392800-22394200	Enhancers	Primary hematopoietic stem cells	blood
34	chr14:22392800-22394200	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr14:22392800-22394200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr14:22392800-22394400	Enhancers	Primary B cells from cord blood	blood
37	chr14:22392800-22394400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr14:22392800-22394400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr14:22392800-22394400	Enhancers	Fetal Thymus	thymus
40	chr14:22392800-22394400	Enhancers	Dnd41	blood
41	chr14:22392800-22395000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr14:22393000-22393600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr14:22393000-22394200	Enhancers	Thymus	Thymus
44	chr14:22393000-22394400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr14:22393000-22395000	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr14:22393000-22399800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr14:22393200-22394200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr14:22393200-22394400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:22393200-22395200	Enhancers	Primary T cells from cord blood	blood
50	chr14:22393600-22393800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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