Variant report

Variant	nsv431768
Chromosome Location	chr2:145741527-145981491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1387)
CpG islands
(count:672)
Chromatin interactive
region (count:35)
LncRNA
region (count:126)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:145854319-145854470	K562	blood:	n/a	n/a
2	ATF2	chr2:145876795-145877287	GM12878	blood:	n/a	n/a
3	ATF2	chr2:145876819-145877189	GM12878	blood:	n/a	n/a
4	ATF3	chr2:145775756-145776640	A549	lung:	n/a	n/a
5	ATF3	chr2:145776008-145776571	A549	lung:	n/a	n/a
6	BACH1	chr2:145952298-145952619	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:145895038-145895097	K562	blood:	n/a	n/a
8	BACH1	chr2:145964569-145964731	K562	blood:	n/a	n/a
9	BACH1	chr2:145770748-145770895	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr2:145876770-145877198	GM12878	blood:	n/a	n/a
11	BATF	chr2:145876847-145877219	GM12878	blood:	n/a	n/a
12	BCL3	chr2:145778097-145778750	A549	lung:	n/a	n/a
13	BCL3	chr2:145775876-145776620	A549	lung:	n/a	n/a
14	BCL3	chr2:145780286-145781082	A549	lung:	n/a	n/a
15	BCL3	chr2:145775711-145776533	A549	lung:	n/a	n/a
16	BHLHE40	chr2:145845724-145846046	K562	blood:	n/a	n/a
17	BRCA1	chr2:145915710-145916145	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr2:145764440-145764481	K562	blood:	n/a	n/a
19	CCNT2	chr2:145822065-145822195	K562	blood:	n/a	n/a
20	CCNT2	chr2:145978706-145979038	K562	blood:	n/a	n/a
21	CEBPB	chr2:145775796-145776615	A549	lung:	n/a	n/a
22	CEBPB	chr2:145915576-145916189	A549	lung:	n/a	chr2:145915769-145915782 chr2:145915769-145915782 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915953-145915964 chr2:145915771-145915780 chr2:145915769-145915780 chr2:145915770-145915781
23	CEBPB	chr2:145777889-145778537	A549	lung:	n/a	chr2:145778036-145778047
24	CEBPB	chr2:145764542-145764916	K562	blood:	n/a	chr2:145764717-145764728 chr2:145764716-145764727 chr2:145764716-145764729 chr2:145764716-145764729
25	CEBPB	chr2:145767383-145767529	A549	lung:	n/a	chr2:145767485-145767498 chr2:145767485-145767496
26	CEBPB	chr2:145787470-145787966	A549	lung:	n/a	n/a
27	CEBPB	chr2:145781769-145781853	A549	lung:	n/a	n/a
28	CEBPB	chr2:145793734-145794281	A549	lung:	n/a	chr2:145794001-145794012
29	CEBPB	chr2:145753802-145754388	Hela-S3	cervix:	n/a	chr2:145753987-145753998 chr2:145753987-145754000
30	CEBPB	chr2:145767378-145767550	K562	blood:	n/a	chr2:145767532-145767545 chr2:145767485-145767498 chr2:145767485-145767496
31	CEBPB	chr2:145764411-145765219	IMR90	lung:	n/a	chr2:145764717-145764728 chr2:145764716-145764727 chr2:145764716-145764729 chr2:145764716-145764729
32	CEBPB	chr2:145767396-145767604	IMR90	lung:	n/a	chr2:145767532-145767545 chr2:145767485-145767498 chr2:145767485-145767496
33	CEBPB	chr2:145926904-145927235	Hela-S3	cervix:	n/a	chr2:145927068-145927079
34	CEBPB	chr2:145753072-145753373	HepG2	liver:	n/a	chr2:145753265-145753276 chr2:145753193-145753204 chr2:145753192-145753203
35	CEBPB	chr2:145756087-145756334	A549	lung:	n/a	n/a
36	CEBPB	chr2:145753042-145753395	IMR90	lung:	n/a	chr2:145753265-145753276 chr2:145753193-145753204 chr2:145753192-145753203
37	CEBPB	chr2:145767361-145767640	HepG2	liver:	n/a	chr2:145767532-145767545 chr2:145767485-145767498 chr2:145767485-145767496
38	CEBPB	chr2:145758003-145758337	Hela-S3	cervix:	n/a	chr2:145758150-145758162
39	CEBPB	chr2:145787369-145787889	A549	lung:	n/a	n/a
40	CEBPB	chr2:145915605-145915825	HepG2	liver:	n/a	chr2:145915769-145915782 chr2:145915769-145915782 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915769-145915780 chr2:145915770-145915781
41	CEBPB	chr2:145770264-145770566	A549	lung:	n/a	chr2:145770373-145770386 chr2:145770373-145770386 chr2:145770373-145770384
42	CEBPB	chr2:145778164-145778651	A549	lung:	n/a	n/a
43	CEBPB	chr2:145764334-145765581	A549	lung:	n/a	chr2:145764717-145764728 chr2:145764716-145764727 chr2:145764716-145764729 chr2:145764716-145764729
44	CEBPB	chr2:145775849-145776628	A549	lung:	n/a	n/a
45	CEBPB	chr2:145915521-145916215	IMR90	lung:	n/a	chr2:145915769-145915782 chr2:145915551-145915562 chr2:145915769-145915782 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915953-145915964 chr2:145915771-145915780 chr2:145915769-145915780 chr2:145915770-145915781
46	CEBPB	chr2:145788543-145789198	A549	lung:	n/a	n/a
47	CEBPB	chr2:145753777-145754170	A549	lung:	n/a	chr2:145753987-145753998 chr2:145753987-145754000
48	CEBPB	chr2:145793866-145794160	HepG2	liver:	n/a	chr2:145794001-145794012
49	CEBPB	chr2:145915585-145916168	A549	lung:	n/a	chr2:145915769-145915782 chr2:145915769-145915782 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915953-145915964 chr2:145915771-145915780 chr2:145915769-145915780 chr2:145915770-145915781
50	CEBPB	chr2:145915617-145915934	H1-hESC	embryonic stem cell:	n/a	chr2:145915769-145915782 chr2:145915769-145915782 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915771-145915780 chr2:145915769-145915780 chr2:145915770-145915781

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:145780010-145780060	MCF-7	breast:	n/a
2	chr2:145780010-145780060	MCF-7	breast:	n/a
3	chr2:145747877-145747927	ovcar-3	ovarian:	n/a
4	chr2:145764890-145764940	CMK	blood:	n/a
5	chr2:145764890-145764940	A549	lung:	n/a
6	chr2:145942606-145942656	PrEC	prostate:	n/a
7	chr2:145823182-145823232	SAEC	small airway:	n/a
8	chr2:145878989-145879039	PFSK-1	brain:	n/a
9	chr2:145876471-145876521	PFSK-1	brain:	n/a
10	chr2:145795797-145795847	HAEpiC	amniotic membrane:	n/a
11	chr2:145876471-145876521	NB4	blood:	n/a
12	chr2:145779560-145779610	Jurkat	blood:	n/a
13	chr2:145764890-145764940	HCPEpiC	choroid plexus:	n/a
14	chr2:145770038-145770088	AoSMC	blood vessel:	n/a
15	chr2:145753993-145754043	HRCEpiC	kidney:	n/a
16	chr2:145823182-145823232	ovcar-3	ovarian:	n/a
17	chr2:145942606-145942656	Hela-S3	cervix:	n/a
18	chr2:145823182-145823232	Hepatocyte	liver:	n/a
19	chr2:145878989-145879039	RPTEC	kidney:	n/a
20	chr2:145753993-145754043	HRE	kidney:	n/a
21	chr2:145779560-145779610	T-47D	breast:	n/a
22	chr2:145770038-145770088	NH-A	brain:	n/a
23	chr2:145876471-145876521	U87	brain:	n/a
24	chr2:145876471-145876521	A549	lung:	n/a
25	chr2:145770038-145770088	Jurkat	blood:	n/a
26	chr2:145747877-145747927	HEEpiC	esophagus:	n/a
27	chr2:145764890-145764940	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:145878989-145879039	NB4	blood:	n/a
29	chr2:145747877-145747927	HNPCEpiC	eye:	n/a
30	chr2:145780010-145780060	BJ	skin:	n/a
31	chr2:145878989-145879039	HCF	heart:	n/a
32	chr2:145764890-145764940	HRCEpiC	kidney:	n/a
33	chr2:145779560-145779610	HUVEC	blood vessel:	n/a
34	chr2:145878989-145879039	ECC-1	luminal epithelium:	n/a
35	chr2:145795797-145795847	AG10803	skin:	n/a
36	chr2:145878989-145879039	HRE	kidney:	n/a
37	chr2:145795797-145795847	HepG2	liver:	n/a
38	chr2:145753993-145754043	LNCaP	prostate:	n/a
39	chr2:145876471-145876521	HCF	heart:	n/a
40	chr2:145876471-145876521	HCM	heart:	n/a
41	chr2:145764890-145764940	HAEpiC	amniotic membrane:	n/a
42	chr2:145747877-145747927	RPTEC	kidney:	n/a
43	chr2:145747877-145747927	T-47D	breast:	n/a
44	chr2:145747877-145747927	ECC-1	luminal epithelium:	n/a
45	chr2:145753993-145754043	A549	lung:	n/a
46	chr2:145878989-145879039	GM12892	blood:	n/a
47	chr2:145876471-145876521	HMEC	breast:	n/a
48	chr2:145876471-145876521	ECC-1	luminal epithelium:	n/a
49	chr2:145753993-145754043	MCF-7	breast:	n/a
50	chr2:145779560-145779610	GM06990	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:145766027..145767852-chr2:145771285..145773781,2	K562	blood:
2	chr2:145858333..145861336-chr2:145861757..145865772,4	K562	blood:
3	chr2:145737683..145739757-chr2:145742970..145744798,2	K562	blood:
4	chr2:145761619..145763555-chr2:145780660..145782291,2	MCF-7	breast:
5	chr2:145849978..145851703-chr2:145855992..145857835,2	K562	blood:
6	chr2:145282963..145285154-chr2:145751784..145754718,2	K562	blood:
7	chr2:145774729..145777688-chr2:145783583..145786278,2	K562	blood:
8	chr2:145831278..145834150-chr2:145834537..145836320,2	K562	blood:
9	chr2:145831278..145833894-chr2:145834820..145837755,2	K562	blood:
10	chr2:145831278..145834150-chr2:145834537..145836320,2	K562	blood:
11	chr2:145910565..145913077-chr2:145916998..145918613,2	K562	blood:
12	chr2:145841612..145843612-chr2:145843724..145846206,2	K562	blood:
13	chr2:145931426..145934133-chr2:145940517..145942647,2	K562	blood:
14	chr2:145831278..145833894-chr2:145834820..145837755,2	K562	blood:
15	chr2:145831836..145834513-chr2:145842893..145844887,2	K562	blood:
16	chr2:145910565..145913077-chr2:145916998..145918613,2	K562	blood:
17	chr2:145734658..145736993-chr2:145739662..145742200,2	K562	blood:
18	chr2:145785797..145788281-chr2:145794965..145797267,2	K562	blood:
19	chr2:145785797..145788281-chr2:145794965..145797267,2	K562	blood:
20	chr2:145858333..145861336-chr2:145861757..145865772,4	K562	blood:
21	chr2:145935562..145937671-chr2:146251309..146253017,2	K562	blood:
22	chr2:145774729..145777688-chr2:145783583..145786278,2	K562	blood:
23	chr2:145946430..145948396-chr2:145950841..145953089,2	K562	blood:
24	chr2:145846784..145849563-chr2:145851350..145854349,3	K562	blood:
25	chr2:145849978..145851703-chr2:145855992..145857835,2	K562	blood:
26	chr2:145846784..145849563-chr2:145851350..145854349,3	K562	blood:
27	chr2:145884946..145886673-chr2:145889735..145892206,2	K562	blood:
28	chr2:145831836..145834513-chr2:145842893..145844887,2	K562	blood:
29	chr2:145931426..145934133-chr2:145940517..145942647,2	K562	blood:
30	chr2:145841612..145843612-chr2:145843724..145846206,2	K562	blood:
31	chr2:145838780..145841438-chr2:145864698..145867568,2	K562	blood:
32	chr2:145838780..145841438-chr2:145864698..145867568,2	K562	blood:
33	chr2:145884946..145886673-chr2:145889735..145892206,2	K562	blood:
34	chr2:145766027..145767852-chr2:145771285..145773781,2	K562	blood:
35	chr2:145946430..145948396-chr2:145950841..145953089,2	K562	blood:

(count:126 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP15-6	chr2:145780725-145780840	ENSG00000226674
2	lnc-ARHGAP15-6	chr2:145780662-145780840	ENSG00000226674
3	lnc-ZEB2-17	chr2:145805844-145805885	NONHSAT074814
4	lnc-ARHGAP15-6	chr2:145875123-145875220	ENSG00000226674.4
5	lnc-ARHGAP15-6	chr2:145875123-145875220	ENSG00000226674.4
6	lnc-ARHGAP15-6	chr2:145939613-145939660	ENSG00000226674.4
7	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
8	lnc-ARHGAP15-6	chr2:145929565-145929698	ENSG00000226674.4
9	lnc-ARHGAP15-6	chr2:145828387-145828508	ENSG00000226674
10	lnc-ARHGAP15-6	chr2:145828387-145828508	NONHSAT074787
11	lnc-ARHGAP15-6	chr2:145921740-145921879	ENSG00000226674.4
12	lnc-ARHGAP15-6	chr2:145909038-145910069	ENSG00000226674.4
13	lnc-ARHGAP15-6	chr2:145929565-145929698	ENSG00000226674.4
14	lnc-ARHGAP15-6	chr2:145939771-145939941	ENSG00000226674.4
15	lnc-ARHGAP15-6	chr2:145939771-145940030	ENSG00000226674.4
16	lnc-ARHGAP15-6	chr2:145929564-145929698	ENSG00000226674
17	lnc-ARHGAP15-6	chr2:145873980-145874077	ENSG00000226674.4
18	lnc-ARHGAP15-6	chr2:145801933-145802010	ENSG00000226674
19	lnc-ARHGAP15-6	chr2:145939613-145939660	ENSG00000226674
20	lnc-ARHGAP15-6	chr2:145921740-145921879	ENSG00000226674.4
21	lnc-ARHGAP15-6	chr2:145939771-145939991	ENSG00000226674.4
22	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
23	lnc-ARHGAP15-6	chr2:145801454-145801634	ENSG00000226674
24	lnc-ARHGAP15-6	chr2:145815381-145815472	ENSG00000226674.4
25	lnc-ARHGAP15-6	chr2:145938577-145938679	ENSG00000226674.4
26	lnc-ARHGAP15-6	chr2:145870788-145871010	ENSG00000226674.4
27	lnc-ARHGAP15-6	chr2:145939613-145939660	ENSG00000226674.4
28	lnc-ARHGAP15-6	chr2:145938764-145938860	ENSG00000226674.4
29	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
30	lnc-ARHGAP15-6	chr2:145921740-145921879	ENSG00000226674.4
31	lnc-ARHGAP15-6	chr2:145936444-145936534	ENSG00000226674.4
32	lnc-ARHGAP15-6	chr2:145929565-145929698	ENSG00000226674.4
33	lnc-ARHGAP15-6	chr2:145939771-145940082	ENSG00000226674.4
34	lnc-ARHGAP15-6	chr2:145870788-145871010	ENSG00000226674.4
35	lnc-ARHGAP15-6	chr2:145939771-145940208	ENSG00000226674.4
36	lnc-ZEB2-17	chr2:145804735-145804784	NONHSAT074814
37	lnc-ARHGAP15-6	chr2:145939771-145939941	ENSG00000226674.4
38	lnc-ARHGAP15-6	chr2:145929565-145929698	ENSG00000226674.4
39	lnc-ARHGAP15-6	chr2:145780799-145780840	ENSG00000226674.4
40	lnc-ARHGAP15-6	chr2:145939771-145939972	ENSG00000226674
41	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
42	lnc-ARHGAP15-6	chr2:145939771-145939941	ENSG00000226674.4
43	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
44	lnc-ARHGAP15-6	chr2:145870788-145871010	ENSG00000226674.4
45	lnc-ARHGAP15-6	chr2:145939771-145939941	ENSG00000226674.4
46	lnc-ARHGAP15-6	chr2:145780754-145780840	ENSG00000226674
47	lnc-ARHGAP15-6	chr2:145830091-145831662	ENSG00000226674
48	lnc-ARHGAP15-6	chr2:145815218-145815295	ENSG00000226674.4
49	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
50	lnc-ARHGAP15-6	chr2:145929565-145929698	ENSG00000226674.4

No data

Variant related genes	Relation type
TEX41	TF binding region
TEX41	CpG island
ENSG00000226674	chromatin interactions

Extended variants
information (count: 7941 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:7941 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544595097	chr2:145744430-145744431	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs2697046	chr2:145744445-145744446	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs144812368	chr2:145744454-145744455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs112032033	chr2:145744461-145744462	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs561102927	chr2:145744495-145744496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs528288384	chr2:145744528-145744529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs551071460	chr2:145744565-145744566	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs546966492	chr2:145744595-145744596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs571523455	chr2:145744607-145744608	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs556035123	chr2:145744631-145744632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs182996457	chr2:145744745-145744746	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs550566587	chr2:145744794-145744795	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs567946166	chr2:145744830-145744831	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs538184436	chr2:145744832-145744833	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs186708819	chr2:145744843-145744844	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs4662412	chr2:145744858-145744859	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191283242	chr2:145744891-145744892	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs184202640	chr2:145744901-145744902	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs534123161	chr2:145744914-145744915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs186983974	chr2:145744975-145744976	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs9973695	chr2:145744988-145744989	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544543315	chr2:145745013-145745014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556541651	chr2:145745022-145745023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116839477	chr2:145745023-145745024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577578801	chr2:145745147-145745148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542385029	chr2:145745177-145745178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs544673821	chr2:145745181-145745182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112228282	chr2:145745184-145745185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527741525	chr2:145745190-145745191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571850999	chr2:145745239-145745240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566041311	chr2:145745244-145745245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540432126	chr2:145745260-145745261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564896328	chr2:145745280-145745281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532460353	chr2:145745319-145745320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77806424	chr2:145745421-145745422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568868986	chr2:145745428-145745429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs529631056	chr2:145745430-145745431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371354041	chr2:145745446-145745447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374039971	chr2:145745455-145745456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547928436	chr2:145745491-145745492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566232756	chr2:145745519-145745520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs786222	chr2:145745530-145745531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs559118894	chr2:145745618-145745619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570927409	chr2:145745662-145745663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193198458	chr2:145745693-145745694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560956288	chr2:145745708-145745709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137888322	chr2:145745750-145745751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185132163	chr2:145745859-145745860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1554826	chr2:145745909-145745910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371368433	chr2:145745944-145745945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
Non-syndromic sensorineural hearing loss	20456320	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145744400-145744800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:145744800-145745000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr2:145745000-145747600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr2:145746200-145746400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr2:145746200-145746600	Enhancers	HUVEC	blood vessel
6	chr2:145746400-145746600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:145746400-145746600	Enhancers	Brain Cingulate Gyrus	brain
8	chr2:145746400-145747600	Enhancers	Brain Anterior Caudate	brain
9	chr2:145746400-145748800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:145746600-145747200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr2:145746600-145747600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:145747200-145747600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:145747200-145748800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr2:145747200-145749400	Enhancers	Brain Cingulate Gyrus	brain
15	chr2:145747200-145749400	Enhancers	Brain Hippocampus Middle	brain
16	chr2:145747400-145748000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:145747400-145748800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:145747400-145749200	Enhancers	Brain Substantia Nigra	brain
19	chr2:145747600-145748000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:145747600-145748000	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr2:145747600-145748400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr2:145747600-145748800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr2:145747600-145748800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:145747600-145749000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr2:145747600-145749200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr2:145747800-145748600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr2:145747800-145748600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:145747800-145748600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr2:145747800-145748600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:145747800-145748600	Enhancers	Dnd41	blood
31	chr2:145747800-145748800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr2:145747800-145749200	Enhancers	Brain Angular Gyrus	brain
33	chr2:145748000-145748200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr2:145748000-145748600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:145748000-145749000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:145748000-145749400	Enhancers	Brain Anterior Caudate	brain
37	chr2:145748200-145748400	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:145748200-145748800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:145748400-145748600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr2:145748600-145749000	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr2:145748600-145756800	Weak transcription	Dnd41	blood
42	chr2:145748800-145753400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:145749000-145749200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr2:145749200-145750000	Weak transcription	Brain Substantia Nigra	brain
45	chr2:145749200-145753400	Weak transcription	Brain Angular Gyrus	brain
46	chr2:145749400-145753600	Weak transcription	Brain Hippocampus Middle	brain
47	chr2:145750000-145750200	Enhancers	Brain Substantia Nigra	brain
48	chr2:145751400-145751600	Enhancers	Ovary	ovary
49	chr2:145751600-145752400	Enhancers	Fetal Lung	lung
50	chr2:145751600-145754200	Weak transcription	Ovary	ovary

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