Variant report

Variant	nsv530714
Chromosome Location	chr16:79661581-79925435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2285)
CpG islands
(count:671)
Chromatin interactive
region (count:194)
LncRNA
region (count:103)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:79903455-79904335	K562	blood:	n/a	n/a
2	ARID3A	chr16:79721258-79721396	K562	blood:	n/a	n/a
3	ARID3A	chr16:79692231-79692428	K562	blood:	n/a	n/a
4	ARID3A	chr16:79897219-79898251	K562	blood:	n/a	n/a
5	ARID3A	chr16:79870143-79870400	K562	blood:	n/a	n/a
6	ARID3A	chr16:79861960-79861963	K562	blood:	n/a	n/a
7	ARID3A	chr16:79876767-79877044	K562	blood:	n/a	n/a
8	ARID3A	chr16:79899275-79899534	K562	blood:	n/a	n/a
9	ARID3A	chr16:79774124-79774585	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:79804963-79805399	K562	blood:	n/a	n/a
11	ARID3A	chr16:79915115-79915129	K562	blood:	n/a	n/a
12	ARID3A	chr16:79792844-79793199	HepG2	liver:	n/a	n/a
13	ARID3A	chr16:79872590-79872754	K562	blood:	n/a	n/a
14	ARID3A	chr16:79810451-79810679	K562	blood:	n/a	n/a
15	ARID3A	chr16:79867555-79867917	K562	blood:	n/a	n/a
16	ARID3A	chr16:79791001-79791400	K562	blood:	n/a	n/a
17	ARID3A	chr16:79879300-79880038	K562	blood:	n/a	n/a
18	ARID3A	chr16:79867169-79867175	K562	blood:	n/a	n/a
19	ARID3A	chr16:79804162-79804706	K562	blood:	n/a	n/a
20	ATF1	chr16:79897412-79898173	K562	blood:	n/a	n/a
21	ATF1	chr16:79670313-79670354	K562	blood:	n/a	n/a
22	ATF1	chr16:79857547-79857761	K562	blood:	n/a	n/a
23	ATF1	chr16:79822852-79823054	K562	blood:	n/a	n/a
24	ATF1	chr16:79692140-79692740	K562	blood:	n/a	n/a
25	ATF1	chr16:79791081-79791422	K562	blood:	n/a	n/a
26	ATF1	chr16:79867356-79867830	K562	blood:	n/a	n/a
27	ATF1	chr16:79903468-79903980	K562	blood:	n/a	n/a
28	ATF1	chr16:79801550-79801860	K562	blood:	n/a	n/a
29	ATF1	chr16:79849749-79850192	K562	blood:	n/a	n/a
30	ATF1	chr16:79782336-79782354	K562	blood:	n/a	n/a
31	ATF1	chr16:79721201-79721464	K562	blood:	n/a	n/a
32	ATF1	chr16:79834130-79834404	K562	blood:	n/a	n/a
33	ATF1	chr16:79879627-79880050	K562	blood:	n/a	n/a
34	ATF2	chr16:79791870-79792241	GM12878	blood:	n/a	n/a
35	ATF2	chr16:79878550-79879438	GM12878	blood:	n/a	n/a
36	ATF2	chr16:79878786-79879235	GM12878	blood:	n/a	n/a
37	ATF2	chr16:79662318-79662878	GM12878	blood:	n/a	n/a
38	ATF3	chr16:79692109-79692477	K562	blood:	n/a	n/a
39	ATF3	chr16:79798322-79798662	K562	blood:	n/a	n/a
40	ATF3	chr16:79804703-79804877	K562	blood:	n/a	n/a
41	ATF3	chr16:79903393-79903902	K562	blood:	n/a	chr16:79903443-79903452
42	ATF3	chr16:79692200-79692416	K562	blood:	n/a	n/a
43	ATF3	chr16:79867460-79867734	K562	blood:	n/a	n/a
44	BACH1	chr16:79804668-79804851	K562	blood:	n/a	n/a
45	BACH1	chr16:79757752-79758051	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr16:79879225-79880183	K562	blood:	n/a	n/a
47	BACH1	chr16:79893035-79893056	K562	blood:	n/a	n/a
48	BACH1	chr16:79909812-79909896	K562	blood:	n/a	n/a
49	BACH1	chr16:79879643-79880101	H1-hESC	embryonic stem cell:	n/a	n/a
50	BATF	chr16:79878728-79879258	GM12878	blood:	n/a	chr16:79879034-79879043

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:79692354-79692404	HIPEpiC	eye:	n/a
2	chr16:79804837-79804887	NHDF-neo	bronchial:	n/a
3	chr16:79804683-79804733	NHDF-neo	bronchial:	n/a
4	chr16:79758582-79758632	HEK293	kidney:	embryo
5	chr16:79804561-79804611	AG10803	skin:	n/a
6	chr16:79804438-79804488	HMEC	breast:	n/a
7	chr16:79810788-79810838	SKMC	muscle:	n/a
8	chr16:79800489-79800539	LNCaP	prostate:	n/a
9	chr16:79802467-79802517	NH-A	brain:	n/a
10	chr16:79810788-79810838	MCF10A-Er-Src	breast:	n/a
11	chr16:79804438-79804488	MCF10A-Er-Src	breast:	n/a
12	chr16:79802467-79802517	PrEC	prostate:	n/a
13	chr16:79804837-79804887	NT2-D1	testis:	n/a
14	chr16:79804561-79804611	HPAEpiC	pulmonary alveolar:	n/a
15	chr16:79758582-79758632	GM12892	blood:	n/a
16	chr16:79804561-79804611	HEK293	kidney:	embryo
17	chr16:79692354-79692404	HCPEpiC	choroid plexus:	n/a
18	chr16:79758582-79758632	AG04449	skin:	fetal
19	chr16:79802467-79802517	H1-hESC	embryonic stem cell:	embryo
20	chr16:79802467-79802517	IMR90	lung:	fetal
21	chr16:79810788-79810838	HCPEpiC	choroid plexus:	n/a
22	chr16:79804438-79804488	GM12891	blood:	n/a
23	chr16:79804683-79804733	RPTEC	kidney:	n/a
24	chr16:79692516-79692566	SAEC	small airway:	n/a
25	chr16:79804561-79804611	NT2-D1	testis:	n/a
26	chr16:79692516-79692566	AoSMC	blood vessel:	n/a
27	chr16:79692516-79692566	Hepatocyte	liver:	n/a
28	chr16:79804561-79804611	SK-N-MC	brain:	n/a
29	chr16:79804837-79804887	AG09319	gingival:	n/a
30	chr16:79758582-79758632	HCM	heart:	n/a
31	chr16:79758582-79758632	MCF10A-Er-Src	breast:	n/a
32	chr16:79692354-79692404	PFSK-1	brain:	n/a
33	chr16:79810788-79810838	NHDF-neo	bronchial:	n/a
34	chr16:79804683-79804733	GM12892	blood:	n/a
35	chr16:79802467-79802517	NT2-D1	testis:	n/a
36	chr16:79758582-79758632	SK-N-SH_RA	brain:	n/a
37	chr16:79804837-79804887	HNPCEpiC	eye:	n/a
38	chr16:79804837-79804887	PFSK-1	brain:	n/a
39	chr16:79807631-79807681	Caco-2	colon:	n/a
40	chr16:79804561-79804611	HRCEpiC	kidney:	n/a
41	chr16:79804837-79804887	MCF10A-Er-Src	breast:	n/a
42	chr16:79692354-79692404	HepG2	liver:	n/a
43	chr16:79800489-79800539	HCPEpiC	choroid plexus:	n/a
44	chr16:79810788-79810838	IMR90	lung:	fetal
45	chr16:79692516-79692566	SK-N-SH_RA	brain:	n/a
46	chr16:79802467-79802517	PFSK-1	brain:	n/a
47	chr16:79810788-79810838	HL-60	blood:	n/a
48	chr16:79804837-79804887	NHBE	bronchial:	n/a
49	chr16:79692516-79692566	GM12892	blood:	n/a
50	chr16:79804683-79804733	HCT-116	colon:	n/a

(count:194 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:79699171..79703517-chr16:79703807..79706802,5	MCF-7	breast:
2	chr16:79734831..79736553-chr16:79737131..79738880,2	K562	blood:
3	chr16:79692753..79694381-chr16:79695815..79697614,2	MCF-7	breast:
4	chr16:79877269..79880011-chr16:79882461..79884349,2	K562	blood:
5	chr16:79663456..79665022-chr16:79666568..79669020,2	K562	blood:
6	chr16:79666363..79669932-chr16:79670774..79673864,3	K562	blood:
7	chr16:79918519..79921940-chr16:79923355..79927904,4	MCF-7	breast:
8	chr16:79902555..79905597-chr16:79906895..79909877,3	K562	blood:
9	chr16:79743384..79745275-chr16:79769820..79772303,2	K562	blood:
10	chr16:79757405..79759517-chr16:79760609..79762850,3	MCF-7	breast:
11	chr16:79809357..79812774-chr16:79814579..79816705,4	MCF-7	breast:
12	chr16:79841040..79846419-chr16:79846922..79851463,5	K562	blood:
13	chr16:79875829..79877990-chr16:79901353..79904058,2	K562	blood:
14	chr16:79902555..79905597-chr16:79906895..79909877,3	K562	blood:
15	chr16:79636935..79639673-chr16:79664462..79666392,2	MCF-7	breast:
16	chr16:79872368..79874855-chr16:79875498..79877925,2	MCF-7	breast:
17	chr16:79757085..79759358-chr16:79764740..79767678,2	K562	blood:
18	chr16:79682792..79686602-chr16:79687950..79693094,4	MCF-7	breast:
19	chr16:79685953..79688052-chr16:79693172..79695514,2	MCF-7	breast:
20	chr16:79663911..79665665-chr16:79665779..79668498,2	K562	blood:
21	chr16:79656220..79658984-chr16:79661969..79663711,2	MCF-7	breast:
22	chr16:79870617..79872194-chr16:79875627..79877913,2	K562	blood:
23	chr16:79896418..79898916-chr16:79909922..79912036,2	K562	blood:
24	chr16:79757670..79760367-chr16:79760765..79762545,2	K562	blood:
25	chr16:79913200..79915535-chr16:79917130..79919607,2	MCF-7	breast:
26	chr16:79695985..79698170-chr16:79706715..79709416,2	MCF-7	breast:
27	chr16:79869480..79871405-chr16:79876316..79879081,2	K562	blood:
28	chr16:79777837..79780445-chr16:79803610..79805196,2	K562	blood:
29	chr16:79692753..79694381-chr16:79695815..79697614,2	MCF-7	breast:
30	chr16:79908657..79911589-chr16:79915100..79917663,2	K562	blood:
31	chr16:79673720..79676616-chr16:79676975..79679637,2	MCF-7	breast:
32	chr16:79919007..79921111-chr16:79925288..79927075,2	K562	blood:
33	chr16:79908657..79911589-chr16:79915100..79917663,2	K562	blood:
34	chr16:79691420..79693874-chr16:79695048..79697845,4	MCF-7	breast:
35	chr16:79877945..79879794-chr16:79880017..79882349,2	MCF-7	breast:
36	chr16:79877777..79879938-chr16:79948611..79950631,2	K562	blood:
37	chr16:79902555..79905597-chr16:79906895..79909877,5	K562	blood:
38	chr16:79809357..79812774-chr16:79814579..79816705,4	MCF-7	breast:
39	chr16:79918690..79920713-chr16:79920839..79923822,2	K562	blood:
40	chr16:79791197..79791801-chr16:80117240..80117982,2	MCF-7	breast:
41	chr16:79879070..79882404-chr16:79882481..79885760,4	K562	blood:
42	chr16:79857005..79859687-chr16:79861505..79863503,2	K562	blood:
43	chr16:79890773..79893231-chr16:79899316..79902167,2	K562	blood:
44	chr16:79763806..79766331-chr16:79796283..79799098,2	K562	blood:
45	chr16:79663456..79665022-chr16:79666568..79669020,2	K562	blood:
46	chr16:79712002..79713952-chr16:79716097..79718110,2	K562	blood:
47	chr16:79682792..79686602-chr16:79687950..79693094,4	MCF-7	breast:
48	chr16:79792848..79795161-chr16:79799446..79800979,2	MCF-7	breast:
49	chr16:79897255..79898930-chr16:79902918..79904789,2	MCF-7	breast:
50	chr16:79801497..79802215-chr16:80118580..80119199,3	MCF-7	breast:

(count:103 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WWOX-2	chr16:79747733-79748031	XLOC_011797
2	lnc-WWOX-2	chr16:79748717-79748784	XLOC_011797
3	lnc-WWOX-2	chr16:79747733-79748031	ENSG00000260876.1
4	lnc-WWOX-2	chr16:79831388-79831627	XLOC_011797
5	lnc-MAF-1	chr16:79692081-79692251	XLOC_012016
6	lnc-MAF-2	chr16:79785111-79785173	ENSG00000261390.1
7	lnc-WWOX-2	chr16:79835070-79835240	ENSG00000260876.1
8	lnc-WWOX-2	chr16:79832431-79832587	ENSG00000260876.1
9	lnc-MAF-2	chr16:79804344-79804827	XLOC_012017
10	lnc-MAF-2	chr16:79803910-79803939	XLOC_012017
11	lnc-WWOX-2	chr16:79796223-79796727	NONHSAT143866
12	lnc-WWOX-2	chr16:79709981-79710105	XLOC_011797
13	lnc-WWOX-2	chr16:79832336-79832527	XLOC_011797
14	lnc-MAF-2	chr16:79774044-79774134	ENSG00000261390.1
15	lnc-MAF-2	chr16:79803050-79803119	ENSG00000261390.1
16	lnc-WWOX-2	chr16:79832729-79832987	ENSG00000260876.1
17	lnc-MAF-2	chr16:79804344-79804460	ENSG00000261390.1
18	lnc-MAF-2	chr16:79755372-79755518	XLOC_012017
19	lnc-WWOX-2	chr16:79709981-79710105	XLOC_011797
20	lnc-MAF-2	chr16:79774044-79774093	XLOC_012017
21	lnc-WWOX-2	chr16:79748712-79748784	ENSG00000260876.1
22	lnc-MAF-2	chr16:79803919-79804198	ENSG00000261390.1
23	lnc-MAF-2	chr16:79791548-79791612	ENSG00000261390.1
24	lnc-WWOX-2	chr16:79830650-79830695	ENSG00000260876.1
25	lnc-WWOX-2	chr16:79748717-79748784	XLOC_011797
26	lnc-WWOX-2	chr16:79760254-79760569	XLOC_011797
27	lnc-WWOX-2	chr16:79829000-79829194	ENSG00000260876.1
28	lnc-WWOX-2	chr16:79709981-79710105	XLOC_011797
29	lnc-WWOX-2	chr16:79748712-79748784	XLOC_011797
30	lnc-WWOX-2	chr16:79710005-79710105	ENSG00000260876.1
31	lnc-WWOX-2	chr16:79831388-79831627	ENSG00000260876.1
32	lnc-WWOX-2	chr16:79780936-79781132	NONHSAT143866
33	lnc-WWOX-2	chr16:79747733-79748031	NONHSAT143852
34	lnc-WWOX-2	chr16:79747733-79748031	XLOC_011797
35	lnc-WWOX-2	chr16:79830650-79830695	NR_104661
36	lnc-WWOX-2	chr16:79747733-79748031	XLOC_011797
37	lnc-WWOX-2	chr16:79748717-79748752	XLOC_011797
38	lnc-WWOX-2	chr16:79709981-79710105	XLOC_011797
39	lnc-MAF-2	chr16:79755209-79755518	ENSG00000261390.1
40	lnc-MAF-3	chr16:79860885-79861047	ENSG00000261082.1
41	lnc-MAF-2	chr16:79785111-79785173	ENSG00000261390.1
42	lnc-WWOX-2	chr16:79832490-79832587	ENSG00000260876.1
43	lnc-WWOX-2	chr16:79841318-79841819	ENSG00000260876.1
44	lnc-WWOX-2	chr16:79832080-79832745	NONHSAT143872
45	lnc-WWOX-2	chr16:79804368-79804424	ENSG00000260876.1
46	lnc-MAF-2	chr16:79791548-79791615	XLOC_012017
47	lnc-MAF-2	chr16:79787283-79787373	ENSG00000261390.1
48	lnc-MAF-2	chr16:79749256-79750737	XLOC_012017
49	lnc-WWOX-2	chr16:79830358-79831627	NONHSAT143872
50	lnc-WWOX-2	chr16:79780915-79781075	XLOC_011797

No data

Variant related genes	Relation type
ENSG00000221330	TF binding region
ENSG00000261390	TF binding region
ENSG00000260876	TF binding region
ENSG00000261082	TF binding region
ENSG00000221330	CpG island
ENSG00000261390	CpG island
ENSG00000260876	CpG island
ENSG00000261082	CpG island
ENSG00000260706	chromatin interactions
ENSG00000221330	chromatin interactions
ENSG00000260876	chromatin interactions
ENSG00000261082	chromatin interactions
ENSG00000178573	chromatin interactions
ENSG00000261390	chromatin interactions
DBT	miRNA target sites
CLDND1	miRNA target sites
DAPK1	miRNA target sites
MTX1	miRNA target sites
ABCA1	miRNA target sites
MAPK14	miRNA target sites
DAZAP2	miRNA target sites
CLIC4	miRNA target sites
CLDN12	miRNA target sites
MTUS1	miRNA target sites

Extended variants
information (count: 14517 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:14517 , 50 per page) page: 1 2 3 4 5 6 7 ... 291

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568552839	chr16:79661602-79661603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531136038	chr16:79661621-79661622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs550833008	chr16:79661655-79661656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567011503	chr16:79661659-79661660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78417178	chr16:79661692-79661693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549409328	chr16:79661715-79661716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184472362	chr16:79661719-79661720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs538204823	chr16:79661725-79661726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143021523	chr16:79661777-79661778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189187565	chr16:79661778-79661779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146150607	chr16:79661785-79661786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553939261	chr16:79661835-79661836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112560979	chr16:79661845-79661846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570527036	chr16:79661853-79661854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs4889002	chr16:79661912-79661913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs561783851	chr16:79661944-79661945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116239468	chr16:79661979-79661980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544204083	chr16:79661993-79661994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192701658	chr16:79662014-79662015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139721042	chr16:79662102-79662103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373158749	chr16:79662107-79662108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376608539	chr16:79662114-79662115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs67361426	chr16:79662144-79662145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs149766388	chr16:79662156-79662157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527439334	chr16:79662163-79662164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185054685	chr16:79662171-79662172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117521817	chr16:79662183-79662184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537881778	chr16:79662193-79662194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549749211	chr16:79662196-79662197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562468800	chr16:79662227-79662228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144751811	chr16:79662274-79662275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538946145	chr16:79662285-79662286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553999891	chr16:79662288-79662289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572562925	chr16:79662368-79662369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536825279	chr16:79662373-79662374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555568935	chr16:79662413-79662414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555196936	chr16:79662415-79662416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189614612	chr16:79662439-79662440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544262211	chr16:79662468-79662469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556192084	chr16:79662522-79662523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575326158	chr16:79662535-79662536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544542266	chr16:79662540-79662541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148524750	chr16:79662545-79662546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144433490	chr16:79662565-79662566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545329606	chr16:79662592-79662593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs560360794	chr16:79662595-79662596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180700977	chr16:79662613-79662614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185172500	chr16:79662615-79662616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147811665	chr16:79662632-79662633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141448034	chr16:79662640-79662641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Adrenocortical carcinoma	18281524	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Hypoplastic left heart syndrome	22349727	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	22495309	CNVD
Autism	21865298	CNVD
Schizophrenia	21346763	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2479 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79657600-79662000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr16:79658000-79661800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr16:79660400-79662600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr16:79660800-79662000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr16:79661400-79663400	Enhancers	HMEC	breast
6	chr16:79661600-79663200	Enhancers	NH-A	brain
7	chr16:79661600-79663200	Enhancers	Osteobl	bone
8	chr16:79661800-79663000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr16:79661800-79663000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr16:79661800-79663000	Enhancers	NHEK	skin
11	chr16:79661800-79663200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr16:79661800-79663200	Enhancers	Primary hematopoietic stem cells	blood
13	chr16:79661800-79663200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr16:79661800-79663200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr16:79662000-79662600	Enhancers	HSMM	muscle
16	chr16:79662000-79663000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr16:79662000-79663000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr16:79662000-79663200	Enhancers	Primary T cells fromperipheralblood	blood
19	chr16:79662000-79663200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
20	chr16:79662000-79663200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr16:79662000-79663200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr16:79662200-79662400	Enhancers	HSMMtube	muscle
23	chr16:79662200-79662600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr16:79662200-79662800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr16:79662200-79662800	Enhancers	Placenta	Placenta
26	chr16:79662200-79663000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr16:79662200-79663200	Enhancers	GM12878-XiMat	blood
28	chr16:79662200-79663600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr16:79662400-79662800	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr16:79662400-79663000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr16:79662400-79663400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr16:79662600-79663000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr16:79662600-79666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr16:79663000-79665800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr16:79663000-79665800	Weak transcription	NHEK	skin
36	chr16:79663000-79666000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr16:79663000-79666200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr16:79663200-79665800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr16:79663200-79665800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr16:79663200-79666000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr16:79663200-79666000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr16:79663200-79666200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr16:79663400-79665800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr16:79663400-79666000	Weak transcription	HMEC	breast
45	chr16:79664600-79667000	Weak transcription	Fetal Intestine Small	intestine
46	chr16:79665000-79666000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr16:79665800-79666400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:79665800-79666800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr16:79665800-79666800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr16:79665800-79666800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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