Variant report

Variant	nsv875135
Chromosome Location	chr2:133066736-133158922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1533)
CpG islands
(count:977)
Chromatin interactive
region (count:39)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133104731-133105317	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:133106714-133106906	K562	blood:	n/a	n/a
3	ARID3A	chr2:133094781-133094937	K562	blood:	n/a	n/a
4	ARID3A	chr2:133104760-133104980	K562	blood:	n/a	n/a
5	ATF1	chr2:133076152-133076243	K562	blood:	n/a	n/a
6	ATF1	chr2:133104740-133105152	K562	blood:	n/a	n/a
7	ATF1	chr2:133094721-133095082	K562	blood:	n/a	n/a
8	ATF3	chr2:133094797-133095064	K562	blood:	n/a	n/a
9	ATF3	chr2:133110083-133110524	A549	lung:	n/a	n/a
10	BACH1	chr2:133094866-133095024	K562	blood:	n/a	n/a
11	BACH1	chr2:133095528-133095811	K562	blood:	n/a	n/a
12	BACH1	chr2:133095514-133095827	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr2:133111906-133112456	GM12878	blood:	n/a	n/a
14	BATF	chr2:133119317-133119527	GM12878	blood:	n/a	n/a
15	BATF	chr2:133116001-133116199	GM12878	blood:	n/a	n/a
16	BATF	chr2:133112628-133112887	GM12878	blood:	n/a	n/a
17	BATF	chr2:133111916-133112116	GM12878	blood:	n/a	n/a
18	BATF	chr2:133112616-133112878	GM12878	blood:	n/a	n/a
19	BCL11A	chr2:133112627-133112889	GM12878	blood:	n/a	n/a
20	BCL11A	chr2:133151626-133151809	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:133111906-133112137	GM12878	blood:	n/a	n/a
22	BCL11A	chr2:133151603-133151834	GM12878	blood:	n/a	n/a
23	BCL11A	chr2:133119287-133119460	GM12878	blood:	n/a	n/a
24	BCL11A	chr2:133111247-133111451	GM12878	blood:	n/a	chr2:133111306-133111319
25	BCL11A	chr2:133111931-133112298	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:133090083-133090281	K562	blood:	n/a	n/a
27	BHLHE40	chr2:133104680-133105281	K562	blood:	n/a	n/a
28	BHLHE40	chr2:133112167-133112440	HepG2	liver:	n/a	n/a
29	BHLHE40	chr2:133106805-133106889	K562	blood:	n/a	n/a
30	BHLHE40	chr2:133141777-133141786	K562	blood:	n/a	n/a
31	BHLHE40	chr2:133110217-133110224	K562	blood:	n/a	n/a
32	BRCA1	chr2:133102792-133102794	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr2:133110120-133110207	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr2:133110245-133110300	HepG2	liver:	n/a	n/a
35	BRCA1	chr2:133104723-133105160	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr2:133104602-133105322	HepG2	liver:	n/a	n/a
37	CBX3	chr2:133094476-133095161	K562	blood:	n/a	n/a
38	CBX3	chr2:133104565-133105347	K562	blood:	n/a	n/a
39	CBX3	chr2:133095481-133095863	K562	blood:	n/a	n/a
40	CBX3	chr2:133089721-133090145	K562	blood:	n/a	n/a
41	CBX3	chr2:133089877-133090403	K562	blood:	n/a	n/a
42	CEBPB	chr2:133104746-133105113	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:133157682-133158096	IMR90	lung:	n/a	chr2:133157953-133157964 chr2:133157953-133157964 chr2:133157953-133157966
44	CEBPB	chr2:133157636-133158145	K562	blood:	n/a	chr2:133157953-133157964 chr2:133157953-133157964 chr2:133157953-133157966
45	CEBPB	chr2:133122263-133122407	A549	lung:	n/a	n/a
46	CEBPB	chr2:133090548-133090667	K562	blood:	n/a	n/a
47	CEBPB	chr2:133104873-133105065	K562	blood:	n/a	n/a
48	CEBPB	chr2:133090604-133090679	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:133074179-133074481	MCF-7	breast:	n/a	chr2:133074302-133074313
50	CEBPB	chr2:133122254-133122375	HepG2	liver:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133104748-133104798	HPAEpiC	pulmonary alveolar:	n/a
2	chr2:133104748-133104798	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:133090251-133090301	HCT-116	colon:	n/a
4	chr2:133118705-133118755	GM19239	blood:	n/a
5	chr2:133090122-133090172	NB4	blood:	n/a
6	chr2:133111454-133111504	Hepatocyte	liver:	n/a
7	chr2:133110927-133110977	AG10803	skin:	n/a
8	chr2:133090251-133090301	GM12891	blood:	n/a
9	chr2:133111454-133111504	MCF10A-Er-Src	breast:	n/a
10	chr2:133107039-133107089	AoSMC	blood vessel:	n/a
11	chr2:133090122-133090172	SK-N-MC	brain:	n/a
12	chr2:133115033-133115083	NT2-D1	testis:	n/a
13	chr2:133107039-133107089	HIPEpiC	eye:	n/a
14	chr2:133106819-133106869	NHBE	bronchial:	n/a
15	chr2:133110927-133110977	HEK293	kidney:	embryo
16	chr2:133110427-133110477	CMK	blood:	n/a
17	chr2:133110427-133110477	BE2_C	brain:	n/a
18	chr2:133090347-133090397	NB4	blood:	n/a
19	chr2:133107039-133107089	SK-N-SH_RA	brain:	n/a
20	chr2:133118705-133118755	HRE	kidney:	n/a
21	chr2:133104982-133105032	NH-A	brain:	n/a
22	chr2:133105045-133105095	ProgFib	skin:	n/a
23	chr2:133105045-133105095	K562	blood:	n/a
24	chr2:133106819-133106869	MCF10A-Er-Src	breast:	n/a
25	chr2:133090251-133090301	PANC-1	pancreas:	n/a
26	chr2:133111454-133111504	PANC-1	pancreas:	n/a
27	chr2:133107039-133107089	HRCEpiC	kidney:	n/a
28	chr2:133118667-133118717	Hepatocyte	liver:	n/a
29	chr2:133110427-133110477	HRCEpiC	kidney:	n/a
30	chr2:133110427-133110477	AG09309	skin:	n/a
31	chr2:133105045-133105095	NT2-D1	testis:	n/a
32	chr2:133105420-133105470	A549	lung:	n/a
33	chr2:133111454-133111504	GM12878	blood:	n/a
34	chr2:133090347-133090397	PFSK-1	brain:	n/a
35	chr2:133110427-133110477	AoSMC	blood vessel:	n/a
36	chr2:133118705-133118755	NHBE	bronchial:	n/a
37	chr2:133118705-133118755	Caco-2	colon:	n/a
38	chr2:133110927-133110977	BJ	skin:	n/a
39	chr2:133105045-133105095	GM06990	blood:	n/a
40	chr2:133115033-133115083	GM12892	blood:	n/a
41	chr2:133105045-133105095	GM19239	blood:	n/a
42	chr2:133090122-133090172	GM06990	blood:	n/a
43	chr2:133110927-133110977	ECC-1	luminal epithelium:	n/a
44	chr2:133105420-133105470	GM06990	blood:	n/a
45	chr2:133111454-133111504	SAEC	small airway:	n/a
46	chr2:133111454-133111504	ProgFib	skin:	n/a
47	chr2:133118667-133118717	IMR90	lung:	fetal
48	chr2:133118667-133118717	HEK293	kidney:	embryo
49	chr2:133090347-133090397	HCF	heart:	n/a
50	chr2:133106819-133106869	U87	brain:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:133129937..133132563-chr2:133172940..133174888,2	MCF-7	breast:
2	chr19:44860226..44861181-chr2:133104577..133105347,5	HCT-116	colon:
3	chr2:133109798..133110355-chr20:29611407..29612129,2	MCF-7	breast:
4	chr2:133106605..133107151-chr2:133206153..133207006,2	MCF-7	breast:
5	chr2:133136843..133139726-chr2:133171493..133174059,2	MCF-7	breast:
6	chr19:44859654..44861763-chr2:133102344..133104670,2	K562	blood:
7	chr2:133095694..133097559-chr2:133103404..133105244,2	MCF-7	breast:
8	chr2:133153165..133154899-chr2:133171288..133174191,2	MCF-7	breast:
9	chr2:133026098..133026689-chr2:133106836..133107370,2	MCF-7	breast:
10	chr2:133106447..133107306-chr2:133173079..133174146,3	MCF-7	breast:
11	chr19:44858590..44859395-chr2:133106608..133107319,5	MCF-7	breast:
12	chr2:133133601..133135526-chr2:133136954..133139569,2	MCF-7	breast:
13	chr2:133106413..133107377-chr2:133181739..133182675,3	MCF-7	breast:
14	chr2:133104188..133106579-chr2:133112547..133114980,2	K562	blood:
15	chr2:133106208..133106974-chr2:133928762..133929385,2	MCF-7	breast:
16	chr2:133123487..133125732-chr2:133126959..133129500,2	K562	blood:
17	chr19:44858582..44859085-chr2:133106403..133107293,2	K562	blood:
18	chr2:133152507..133155415-chr2:133160169..133163042,2	MCF-7	breast:
19	chr2:133104869..133106905-chr2:133107987..133110603,2	K562	blood:
20	chr19:44860583..44861870-chr2:133104308..133105302,7	Hela-S3	cervix:
21	chr2:133110121..133110687-chr8:43101237..43102219,2	MCF-7	breast:
22	chr19:44859033..44861169-chr2:133104533..133106354,2	K562	blood:
23	chr2:133124752..133127513-chr2:133337164..133339818,2	MCF-7	breast:
24	chr2:133158017..133160257-chr2:133164655..133167009,2	MCF-7	breast:
25	chr19:44895650..44897507-chr2:133068550..133071124,2	MCF-7	breast:
26	chr2:133106241..133106888-chr2:134318328..134318856,2	K562	blood:
27	chr2:133108915..133111457-chr2:133172343..133174834,3	MCF-7	breast:
28	chr2:133104482..133106618-chr2:133108927..133110502,2	MCF-7	breast:
29	chr2:133123487..133125732-chr2:133126959..133129500,2	K562	blood:
30	chr2:133133601..133135526-chr2:133136954..133139569,2	MCF-7	breast:
31	chr2:133106377..133107304-chr20:29611507..29612208,2	MCF-7	breast:
32	chr2:133104869..133106905-chr2:133107987..133110603,2	K562	blood:
33	chr2:133104482..133106618-chr2:133108927..133110502,2	MCF-7	breast:
34	chr19:44870383..44873063-chr2:133091902..133095007,3	MCF-7	breast:
35	chr2:133129464..133129981-chr2:133206123..133207082,2	MCF-7	breast:
36	chr19:44858569..44859729-chr2:133105937..133107575,6	MCF-7	breast:
37	chr19:44860567..44861162-chr2:133104579..133105358,2	MCF-7	breast:
38	chr2:133108792..133112199-chr2:133172607..133174892,3	MCF-7	breast:
39	chr19:44869272..44873235-chr2:133093559..133096600,6	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR39-2	chr2:133092597-133092734	XLOC_001680
2	lnc-GPR39-2	chr2:133095052-133095288	XLOC_001680
3	lnc-GPR39-2	chr2:133095945-133096192	XLOC_001680
4	lnc-GPR39-2	chr2:133095945-133096184	NONHSAT074528
5	lnc-GPR39-2	chr2:133095158-133095288	NONHSAT074530
6	lnc-GPR39-2	chr2:133095945-133096187	XLOC_001680
7	lnc-GPR39-2	chr2:133094897-133095041	XLOC_001680
8	lnc-GPR39-2	chr2:133094931-133095041	NONHSAT074528
9	lnc-GPR39-2	chr2:133095697-133095736	XLOC_001680
10	lnc-GPR39-2	chr2:133095945-133096184	NONHSAT074530
11	lnc-GPR39-2	chr2:133095000-133095041	NONHSAT074530
12	lnc-ANKRD30BL-7	chr2:133103189-133104870	ENSG00000272769.1
13	lnc-GPR39-2	chr2:133094559-133094792	NONHSAT074528
14	lnc-GPR39-2	chr2:133095945-133096187	XLOC_001680
15	lnc-GPR39-2	chr2:133094769-133095390	NONHSAT074526
16	lnc-GPR39-2	chr2:133095945-133096187	XLOC_001680
17	lnc-GPR39-2	chr2:133095052-133095288	XLOC_001680
18	lnc-GPR39-2	chr2:133095580-133095608	XLOC_001680
19	lnc-GPR39-2	chr2:133092596-133092734	NONHSAT074526
20	lnc-GPR39-2	chr2:133094931-133095041	XLOC_001680
21	lnc-GPR39-2	chr2:133095580-133095736	NONHSAT074528
22	lnc-GPR39-2	chr2:133095435-133096235	NONHSAT074526

No data

Variant related genes	Relation type
ENSG00000272769	TF binding region
ZNF806	TF binding region
FAM201B	TF binding region
ENSG00000272769	CpG island
ZNF806	CpG island
FAM201B	CpG island
ENSG00000062370	chromatin interactions
ENSG00000183840	chromatin interactions
ENSG00000149531	chromatin interactions
ENSG00000230992	chromatin interactions
ENSG00000253884	chromatin interactions
ENSG00000272769	chromatin interactions
FAM49B	miRNA target sites
EXOC5	miRNA target sites
TNPO1	miRNA target sites
TNKS1BP1	miRNA target sites

Extended variants
information (count: 3769 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3769 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11676933	chr2:133066736-133066737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs575349454	chr2:133066762-133066763	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373800184	chr2:133066798-133066799	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564083674	chr2:133066807-133066808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372276018	chr2:133066835-133066836	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs113691386	chr2:133066861-133066862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs2677610	chr2:133066879-133066880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143245912	chr2:133068011-133068012	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs534175534	chr2:133068049-133068050	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs73956622	chr2:133068066-133068067	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs546612192	chr2:133068080-133068081	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs72991506	chr2:133068081-133068082	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs568381750	chr2:133068085-133068086	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs73956624	chr2:133068152-133068153	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs79650315	chr2:133068178-133068179	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs575471739	chr2:133068180-133068181	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs551960982	chr2:133068204-133068205	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs78530417	chr2:133068247-133068248	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs78221600	chr2:133068248-133068249	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs72991507	chr2:133068267-133068268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs539579914	chr2:133068269-133068270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs3867347	chr2:133068337-133068338	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572775825	chr2:133068370-133068371	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs62167622	chr2:133068446-133068447	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs201612659	chr2:133068452-133068453	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs150449488	chr2:133068490-133068491	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs555028792	chr2:133068515-133068516	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs62167623	chr2:133068544-133068545	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs574015999	chr2:133068564-133068565	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs62167624	chr2:133068572-133068573	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs544455293	chr2:133068577-133068578	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs562751803	chr2:133068595-133068596	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs62167625	chr2:133068606-133068607	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs375341863	chr2:133068628-133068629	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs73956626	chr2:133068629-133068630	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs73956627	chr2:133068630-133068631	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs372027389	chr2:133068640-133068641	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs545200688	chr2:133068674-133068675	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs112974398	chr2:133068694-133068695	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs141370537	chr2:133068699-133068700	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs140472651	chr2:133068700-133068701	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs150427864	chr2:133068701-133068702	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs370095984	chr2:133068704-133068705	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs2677611	chr2:133068720-133068721	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs2598816	chr2:133068755-133068756	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs527750027	chr2:133068758-133068759	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs549382910	chr2:133068760-133068761	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs2598815	chr2:133068796-133068797	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs529216363	chr2:133068848-133068849	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs4096121	chr2:133068860-133068861	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133068000-133068200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:133068000-133068400	ZNF genes & repeats	Brain Cingulate Gyrus	brain
3	chr2:133068200-133068400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:133068200-133068400	ZNF genes & repeats	Brain Hippocampus Middle	brain
5	chr2:133068200-133069200	ZNF genes & repeats	Aorta	Aorta
6	chr2:133068400-133074200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr2:133068400-133076000	Weak transcription	Brain Hippocampus Middle	brain
8	chr2:133068400-133076400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:133069000-133076200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr2:133071400-133076800	Weak transcription	Brain Angular Gyrus	brain
11	chr2:133071800-133075800	Weak transcription	Brain Substantia Nigra	brain
12	chr2:133072400-133073000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:133072600-133072800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:133072600-133072800	ZNF genes & repeats	Spleen	Spleen
15	chr2:133072800-133073200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:133073000-133074000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:133073200-133074200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:133073600-133074600	Enhancers	Osteobl	bone
19	chr2:133074000-133074400	Weak transcription	Spleen	Spleen
20	chr2:133074000-133074600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr2:133074000-133075400	Enhancers	NHEK	skin
22	chr2:133074000-133075800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr2:133074200-133074400	Enhancers	Esophagus	oesophagus
24	chr2:133074200-133075200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:133074200-133075200	Enhancers	HMEC	breast
26	chr2:133074400-133074600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:133074400-133075200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr2:133074400-133075600	Weak transcription	Esophagus	oesophagus
29	chr2:133074600-133075800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr2:133075600-133075800	Enhancers	Esophagus	oesophagus
31	chr2:133075600-133076600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr2:133075800-133076400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr2:133075800-133076400	Enhancers	Brain Substantia Nigra	brain
34	chr2:133075800-133080400	Weak transcription	Esophagus	oesophagus
35	chr2:133076000-133076400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr2:133076000-133076600	Enhancers	Brain Hippocampus Middle	brain
37	chr2:133076200-133076400	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:133076400-133076600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:133076400-133076600	Enhancers	Brain Cingulate Gyrus	brain
40	chr2:133076600-133077000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr2:133078600-133079000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:133078600-133080200	Enhancers	Fetal Brain Male	brain
43	chr2:133079000-133080800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:133080800-133081600	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr2:133080800-133082000	Enhancers	Psoas Muscle	Psoas
46	chr2:133081600-133082000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:133081600-133082000	Enhancers	Brain Anterior Caudate	brain
48	chr2:133089200-133102400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:133089600-133090200	Active TSS	Duodenum Mucosa	Duodenum
50	chr2:133089600-133090400	Active TSS	K562	blood

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