Variant report

Variant	nsv1057791
Chromosome Location	chr16:81515036-81644651
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3876)
CpG islands
(count:3117)
Chromatin interactive
region (count:260)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3876 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81529158-81529984	K562	blood:	n/a	n/a
2	ARID3A	chr16:81634043-81634078	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81592498-81592683	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:81525105-81525223	K562	blood:	n/a	n/a
5	ARID3A	chr16:81517309-81517702	K562	blood:	n/a	n/a
6	ARID3A	chr16:81581673-81581687	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:81517177-81517495	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:81620058-81620332	K562	blood:	n/a	n/a
9	ARID3A	chr16:81538647-81538999	K562	blood:	n/a	n/a
10	ARID3A	chr16:81569226-81569512	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:81582502-81583379	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:81576143-81576703	HepG2	liver:	n/a	n/a
13	ARID3A	chr16:81566312-81566544	HepG2	liver:	n/a	n/a
14	ARID3A	chr16:81547245-81547583	HepG2	liver:	n/a	n/a
15	ARID3A	chr16:81528924-81528927	K562	blood:	n/a	n/a
16	ARID3A	chr16:81567549-81568168	HepG2	liver:	n/a	n/a
17	ARID3A	chr16:81544826-81545290	HepG2	liver:	n/a	n/a
18	ARID3A	chr16:81514897-81515284	K562	blood:	n/a	n/a
19	ARID3A	chr16:81516369-81516519	K562	blood:	n/a	n/a
20	ARID3A	chr16:81601874-81602102	HepG2	liver:	n/a	n/a
21	ARID3A	chr16:81514904-81515338	HepG2	liver:	n/a	n/a
22	ARID3A	chr16:81560007-81560151	K562	blood:	n/a	n/a
23	ATF1	chr16:81529312-81529767	K562	blood:	n/a	n/a
24	ATF1	chr16:81527276-81527612	K562	blood:	n/a	n/a
25	ATF1	chr16:81514976-81515432	K562	blood:	n/a	n/a
26	ATF1	chr16:81555575-81555990	K562	blood:	n/a	n/a
27	ATF1	chr16:81585108-81585429	K562	blood:	n/a	n/a
28	ATF1	chr16:81614592-81614707	K562	blood:	n/a	n/a
29	ATF1	chr16:81532692-81532837	K562	blood:	n/a	n/a
30	ATF1	chr16:81585675-81585986	K562	blood:	n/a	n/a
31	ATF1	chr16:81538547-81538994	K562	blood:	n/a	n/a
32	ATF1	chr16:81633961-81634168	K562	blood:	n/a	n/a
33	ATF1	chr16:81517270-81517572	K562	blood:	n/a	n/a
34	ATF2	chr16:81642090-81642391	GM12878	blood:	n/a	n/a
35	ATF2	chr16:81547449-81548101	GM12878	blood:	n/a	n/a
36	ATF2	chr16:81619432-81619831	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr16:81538531-81539353	GM12878	blood:	n/a	n/a
38	ATF2	chr16:81514642-81515466	GM12878	blood:	n/a	n/a
39	ATF2	chr16:81585021-81585478	GM12878	blood:	n/a	n/a
40	ATF2	chr16:81555591-81556030	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr16:81514843-81515408	GM12878	blood:	n/a	n/a
42	ATF3	chr16:81601623-81602277	A549	lung:	n/a	n/a
43	ATF3	chr16:81616348-81616768	K562	blood:	n/a	n/a
44	ATF3	chr16:81616462-81616716	HepG2	liver:	n/a	n/a
45	ATF3	chr16:81527280-81527553	K562	blood:	n/a	n/a
46	ATF3	chr16:81527245-81527602	K562	blood:	n/a	n/a
47	ATF3	chr16:81529187-81529838	K562	blood:	n/a	n/a
48	ATF3	chr16:81544835-81545326	A549	lung:	n/a	n/a
49	ATF3	chr16:81544695-81545268	A549	lung:	n/a	n/a
50	ATF3	chr16:81516220-81516628	K562	blood:	n/a	n/a

(count:3117 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81564192-81564242	HCM	heart:	n/a
2	chr16:81518122-81518172	LNCaP	prostate:	n/a
3	chr16:81617738-81617788	PANC-1	pancreas:	n/a
4	chr16:81526954-81527004	U87	brain:	n/a
5	chr16:81579629-81579679	AG09309	skin:	n/a
6	chr16:81579244-81579294	NB4	blood:	n/a
7	chr16:81564192-81564242	HCM	heart:	n/a
8	chr16:81518122-81518172	LNCaP	prostate:	n/a
9	chr16:81617738-81617788	PANC-1	pancreas:	n/a
10	chr16:81526954-81527004	U87	brain:	n/a
11	chr16:81579629-81579679	AG09309	skin:	n/a
12	chr16:81579244-81579294	NB4	blood:	n/a
13	chr16:81536171-81536221	T-47D	breast:	n/a
14	chr16:81547907-81547957	HIPEpiC	eye:	n/a
15	chr16:81526954-81527004	AG09319	gingival:	n/a
16	chr16:81547907-81547957	HCM	heart:	n/a
17	chr16:81586800-81586850	RPTEC	kidney:	n/a
18	chr16:81528229-81528279	SKMC	muscle:	n/a
19	chr16:81572405-81572455	HEK293	kidney:	embryo
20	chr16:81634971-81635021	HPAEpiC	pulmonary alveolar:	n/a
21	chr16:81547907-81547957	HCPEpiC	choroid plexus:	n/a
22	chr16:81529947-81529997	HMEC	breast:	n/a
23	chr16:81564161-81564211	SK-N-SH	brain:	n/a
24	chr16:81564527-81564577	SAEC	small airway:	n/a
25	chr16:81564192-81564242	AoSMC	blood vessel:	n/a
26	chr16:81579629-81579679	SKMC	muscle:	n/a
27	chr16:81529947-81529997	T-47D	breast:	n/a
28	chr16:81579629-81579679	HUVEC	blood vessel:	n/a
29	chr16:81564553-81564603	GM19239	blood:	n/a
30	chr16:81564161-81564211	NHDF-neo	bronchial:	n/a
31	chr16:81639791-81639841	GM12892	blood:	n/a
32	chr16:81536171-81536221	GM12892	blood:	n/a
33	chr16:81586800-81586850	IMR90	lung:	fetal
34	chr16:81564553-81564603	AG04450	lung:	fetal
35	chr16:81547907-81547957	AG09309	skin:	n/a
36	chr16:81579629-81579679	HEEpiC	esophagus:	n/a
37	chr16:81547907-81547957	HepG2	liver:	n/a
38	chr16:81527427-81527477	NH-A	brain:	n/a
39	chr16:81579400-81579450	SAEC	small airway:	n/a
40	chr16:81527360-81527410	SK-N-SH_RA	brain:	n/a
41	chr16:81533152-81533202	SKMC	muscle:	n/a
42	chr16:81520589-81520639	IMR90	lung:	fetal
43	chr16:81580500-81580550	HCT-116	colon:	n/a
44	chr16:81567375-81567425	HAEpiC	amniotic membrane:	n/a
45	chr16:81528989-81529039	NHBE	bronchial:	n/a
46	chr16:81564314-81564364	AG09309	skin:	n/a
47	chr16:81564314-81564364	SKMC	muscle:	n/a
48	chr16:81580500-81580550	CMK	blood:	n/a
49	chr16:81520244-81520294	MCF-7	breast:	n/a
50	chr16:81639791-81639841	HEEpiC	esophagus:	n/a

(count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr16:81565757..81568380-chr16:81569280..81572909,4	K562	blood:
2	chr16:81522073..81525174-chr16:81527539..81530591,4	MCF-7	breast:
3	chr16:81595733..81597797-chr16:81598756..81601475,2	MCF-7	breast:
4	chr16:81621915..81623701-chr16:81627145..81629070,2	MCF-7	breast:
5	chr16:81568196..81570082-chr16:81573508..81576113,2	K562	blood:
6	chr16:81548752..81553118-chr16:81553470..81556973,6	K562	blood:
7	chr16:81596628..81600367-chr16:81601999..81604973,3	MCF-7	breast:
8	chr16:81536056..81540431-chr16:81540581..81543691,4	K562	blood:
9	chr16:81476822..81479616-chr16:81528551..81531319,2	MCF-7	breast:
10	chr16:81587351..81589044-chr16:81811838..81813407,2	K562	blood:
11	chr16:81538598..81540305-chr16:81552129..81554762,2	K562	blood:
12	chr16:81586015..81589398-chr16:81589613..81592514,4	MCF-7	breast:
13	chr16:81578943..81580979-chr16:81604433..81607387,2	K562	blood:
14	chr16:81607192..81611602-chr16:81637708..81641189,4	MCF-7	breast:
15	chr16:81478376..81479918-chr16:81612129..81613848,2	MCF-7	breast:
16	chr16:81479204..81482002-chr16:81562835..81564936,2	MCF-7	breast:
17	chr16:81545018..81547272-chr16:81553455..81555320,2	MCF-7	breast:
18	chr16:81589280..81593699-chr16:81599147..81604604,6	MCF-7	breast:
19	chr16:81575502..81578399-chr16:81587269..81589357,4	MCF-7	breast:
20	chr16:81513398..81515319-chr16:81515579..81518063,2	MCF-7	breast:
21	chr16:81515266..81518031-chr16:81784330..81786216,2	K562	blood:
22	chr16:81477018..81482401-chr16:81598968..81605345,9	MCF-7	breast:
23	chr16:81629952..81632348-chr16:81634208..81635852,3	K562	blood:
24	chr16:81477859..81481266-chr16:81523834..81526339,3	MCF-7	breast:
25	chr16:81602073..81603967-chr16:81621534..81623080,2	K562	blood:
26	chr16:81506233..81509171-chr16:81529935..81531469,2	MCF-7	breast:
27	chr16:81613896..81616758-chr16:81641074..81643658,2	MCF-7	breast:
28	chr16:81578640..81580177-chr16:81596522..81598545,2	MCF-7	breast:
29	chr16:81600677..81603897-chr16:81613066..81616910,4	MCF-7	breast:
30	chr16:81602073..81603967-chr16:81621534..81623080,2	K562	blood:
31	chr16:81477202..81480429-chr16:81614800..81620694,9	MCF-7	breast:
32	chr16:81515452..81518298-chr16:81547120..81549781,2	MCF-7	breast:
33	chr16:81576839..81579779-chr16:81583456..81585257,2	K562	blood:
34	chr16:81477897..81480070-chr16:81586724..81588364,2	MCF-7	breast:
35	chr16:81596623..81599518-chr16:81602688..81606938,4	MCF-7	breast:
36	chr16:81550713..81552453-chr16:81584328..81586999,2	K562	blood:
37	chr16:81632422..81634895-chr16:81653001..81657177,3	MCF-7	breast:
38	chr16:81476449..81480009-chr16:81614671..81617341,4	MCF-7	breast:
39	chr16:81628673..81631001-chr16:81631996..81634111,2	K562	blood:
40	chr16:81556103..81558627-chr16:81562997..81564545,2	K562	blood:
41	chr16:81640517..81643022-chr16:81644201..81646459,2	K562	blood:
42	chr16:81557086..81559213-chr16:81591248..81592791,2	MCF-7	breast:
43	chr16:81538598..81540305-chr16:81552129..81554762,2	K562	blood:
44	chr16:81487188..81490116-chr16:81629347..81631108,2	MCF-7	breast:
45	chr16:81515811..81518675-chr16:81530848..81533048,2	MCF-7	breast:
46	chr16:81523253..81525338-chr16:81546964..81549202,2	MCF-7	breast:
47	chr16:81613179..81615947-chr16:81637579..81640462,2	MCF-7	breast:
48	chr16:81520528..81523163-chr16:81525818..81527534,2	MCF-7	breast:
49	chr16:81522805..81524809-chr17:56735512..56737887,2	MCF-7	breast:
50	chr16:81515811..81518675-chr16:81530848..81533048,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLCG2-7	chr16:81643912-81644145	NONHSAT143949

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7854-3p	chr16:81567547-81567567	MIMAT0030429

No data

Variant related genes	Relation type
ENSG00000260229	TF binding region
CMIP	TF binding region
ENSG00000260229	CpG island
CMIP	CpG island
ENSG00000197943	chromatin interactions
ENSG00000153815	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 6986 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6986 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185319919	chr16:81515060-81515061	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs566510130	chr16:81515085-81515086	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534010950	chr16:81515109-81515110	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs553168543	chr16:81515120-81515121	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs568576549	chr16:81515134-81515135	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs535473372	chr16:81515148-81515149	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs557440707	chr16:81515150-81515151	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575714620	chr16:81515154-81515155	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190286662	chr16:81515155-81515156	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181490158	chr16:81515199-81515200	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573330991	chr16:81515210-81515211	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540851393	chr16:81515247-81515248	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184978151	chr16:81515264-81515265	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79501848	chr16:81515319-81515320	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140844911	chr16:81515320-81515321	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115508388	chr16:81515345-81515346	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs56140527	chr16:81515361-81515362	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551232041	chr16:81515368-81515369	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs13330589	chr16:81515377-81515378	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527481680	chr16:81515421-81515422	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs2966082	chr16:81515428-81515429	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2926000	chr16:81515440-81515441	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs189442442	chr16:81515477-81515478	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551105197	chr16:81515510-81515511	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs180970850	chr16:81515525-81515526	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142996157	chr16:81515544-81515545	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185000300	chr16:81515545-81515546	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573520342	chr16:81515548-81515549	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191073785	chr16:81515555-81515556	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569543997	chr16:81515571-81515572	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555882481	chr16:81515609-81515610	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs113595319	chr16:81515632-81515633	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543866136	chr16:81515637-81515638	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs35081994	chr16:81515640-81515641	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181848314	chr16:81515709-81515710	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs555154751	chr16:81515715-81515716	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2966083	chr16:81515722-81515723	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145551412	chr16:81515724-81515725	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549012894	chr16:81515769-81515770	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557931802	chr16:81515864-81515865	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561099501	chr16:81515954-81515955	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11859878	chr16:81515956-81515957	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs111765530	chr16:81515985-81515986	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551066610	chr16:81515989-81515990	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs113182456	chr16:81516005-81516006	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs186990456	chr16:81516028-81516029	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539828474	chr16:81516029-81516030	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551799072	chr16:81516038-81516039	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs117312299	chr16:81516039-81516040	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534465408	chr16:81516042-81516043	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:5895 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81485600-81516800	Weak transcription	Hela-S3	cervix
2	chr16:81486600-81525200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr16:81501800-81515200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr16:81503000-81516600	Weak transcription	Brain Germinal Matrix	brain
5	chr16:81504000-81517800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr16:81504200-81518200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr16:81505200-81525600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr16:81505400-81521800	Weak transcription	Fetal Kidney	kidney
9	chr16:81505800-81523600	Weak transcription	Fetal Brain Male	brain
10	chr16:81506000-81546600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr16:81506600-81547000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr16:81506800-81517600	Weak transcription	HMEC	breast
13	chr16:81507600-81516400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr16:81507600-81518400	Enhancers	Spleen	Spleen
15	chr16:81507800-81516400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr16:81507800-81519400	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr16:81508000-81516400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr16:81508000-81518000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr16:81508600-81519400	Weak transcription	Ovary	ovary
20	chr16:81509400-81518000	Enhancers	Primary T cells fromperipheralblood	blood
21	chr16:81509800-81517600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr16:81509800-81518600	Enhancers	Lung	lung
23	chr16:81510000-81516000	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr16:81510000-81517200	Enhancers	Small Intestine	intestine
25	chr16:81510000-81518400	Enhancers	Placenta	Placenta
26	chr16:81510000-81518800	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr16:81510200-81516000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:81510200-81517000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr16:81510400-81522400	Weak transcription	Fetal Brain Female	brain
30	chr16:81510400-81533200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr16:81510600-81518000	Enhancers	Liver	Liver
32	chr16:81510600-81521200	Enhancers	Stomach Mucosa	stomach
33	chr16:81511000-81517000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr16:81511200-81515200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr16:81511400-81527000	Enhancers	Fetal Muscle Leg	muscle
36	chr16:81511600-81517200	Enhancers	Pancreas	Pancrea
37	chr16:81511600-81518200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr16:81511800-81515800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr16:81512000-81516200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr16:81512400-81515800	Weak transcription	Colon Smooth Muscle	Colon
41	chr16:81512400-81515800	Weak transcription	Right Ventricle	heart
42	chr16:81512400-81525000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr16:81512600-81515800	Weak transcription	Left Ventricle	heart
44	chr16:81512800-81515400	Enhancers	Primary T cells from cord blood	blood
45	chr16:81512800-81516400	Weak transcription	Dnd41	blood
46	chr16:81512800-81518600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr16:81513000-81515200	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr16:81513000-81517200	Genic enhancers	A549	lung
49	chr16:81513200-81515200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr16:81513200-81517800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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