Variant report

Variant	esv1832493
Chromosome Location	chr1:144598061-144832598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1307)
CpG islands
(count:612)
Chromatin interactive
region (count:5)
LncRNA
region (count:118)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr1:144618285-144618435	GM12878	blood:	n/a	n/a
2	BATF	chr1:144816815-144817082	GM12878	blood:	n/a	n/a
3	BATF	chr1:144828481-144829126	GM12878	blood:	n/a	n/a
4	BATF	chr1:144618572-144618830	GM12878	blood:	n/a	n/a
5	BATF	chr1:144822457-144822900	GM12878	blood:	n/a	n/a
6	BATF	chr1:144672666-144672904	GM12878	blood:	n/a	n/a
7	BATF	chr1:144604582-144604786	GM12878	blood:	n/a	n/a
8	BATF	chr1:144829153-144829560	GM12878	blood:	n/a	n/a
9	BATF	chr1:144829180-144829396	GM12878	blood:	n/a	n/a
10	BATF	chr1:144617485-144617685	GM12878	blood:	n/a	n/a
11	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
12	BATF	chr1:144614551-144615001	GM12878	blood:	n/a	n/a
13	BATF	chr1:144618840-144619109	GM12878	blood:	n/a	n/a
14	BATF	chr1:144615131-144615468	GM12878	blood:	n/a	n/a
15	BATF	chr1:144679543-144679819	GM12878	blood:	n/a	n/a
16	BATF	chr1:144615010-144615375	GM12878	blood:	n/a	n/a
17	BATF	chr1:144679564-144679880	GM12878	blood:	n/a	n/a
18	BATF	chr1:144614537-144614797	GM12878	blood:	n/a	n/a
19	BATF	chr1:144690283-144690581	GM12878	blood:	n/a	chr1:144690289-144690297 chr1:144690402-144690411
20	BATF	chr1:144816769-144817077	GM12878	blood:	n/a	n/a
21	BATF	chr1:144690796-144691031	GM12878	blood:	n/a	n/a
22	BATF	chr1:144829689-144829978	GM12878	blood:	n/a	n/a
23	BATF	chr1:144811689-144812035	GM12878	blood:	n/a	n/a
24	BATF	chr1:144811804-144812040	GM12878	blood:	n/a	n/a
25	BATF	chr1:144828408-144829114	GM12878	blood:	n/a	n/a
26	BATF	chr1:144822461-144822911	GM12878	blood:	n/a	n/a
27	BCL11A	chr1:144690359-144690638	GM12878	blood:	n/a	n/a
28	BCL11A	chr1:144618530-144618828	GM12878	blood:	n/a	n/a
29	BCL11A	chr1:144828835-144829095	GM12878	blood:	n/a	n/a
30	BCL11A	chr1:144831131-144831365	GM12878	blood:	n/a	n/a
31	BCL11A	chr1:144829792-144829953	GM12878	blood:	n/a	n/a
32	BCL11A	chr1:144618876-144619331	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:144816834-144816993	GM12878	blood:	n/a	n/a
34	BCL11A	chr1:144615162-144615415	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:144811376-144811736	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:144687719-144687979	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:144618887-144619298	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:144828457-144828809	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
40	BCL11A	chr1:144690673-144690958	GM12878	blood:	n/a	n/a
41	BCL11A	chr1:144832400-144832824	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:144829682-144829901	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:144614565-144614849	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:144690657-144691064	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:144828446-144828898	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:144614491-144614868	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:144829265-144829496	GM12878	blood:	n/a	n/a
48	BCL11A	chr1:144672707-144672942	GM12878	blood:	n/a	n/a
49	BCL11A	chr1:144822517-144822688	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:144620110-144620305	GM12878	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144814628-144814678	AoSMC	blood vessel:	n/a
2	chr1:144620428-144620478	HNPCEpiC	eye:	n/a
3	chr1:144814628-144814678	AoSMC	blood vessel:	n/a
4	chr1:144620428-144620478	HNPCEpiC	eye:	n/a
5	chr1:144814628-144814678	AG04450	lung:	fetal
6	chr1:144612358-144612408	HEK293	kidney:	embryo
7	chr1:144815302-144815352	HEK293	kidney:	embryo
8	chr1:144612358-144612408	PrEC	prostate:	n/a
9	chr1:144811373-144811423	ECC-1	luminal epithelium:	n/a
10	chr1:144620428-144620478	Caco-2	colon:	n/a
11	chr1:144815915-144815965	AG09309	skin:	n/a
12	chr1:144612358-144612408	HEEpiC	esophagus:	n/a
13	chr1:144619354-144619404	K562	blood:	n/a
14	chr1:144619354-144619404	GM12878	blood:	n/a
15	chr1:144814628-144814678	LNCaP	prostate:	n/a
16	chr1:144612646-144612696	BJ	skin:	n/a
17	chr1:144811373-144811423	Hela-S3	cervix:	n/a
18	chr1:144811373-144811423	MCF10A-Er-Src	breast:	n/a
19	chr1:144814628-144814678	HAEpiC	amniotic membrane:	n/a
20	chr1:144615272-144615322	U87	brain:	n/a
21	chr1:144815302-144815352	Hepatocyte	liver:	n/a
22	chr1:144815915-144815965	Caco-2	colon:	n/a
23	chr1:144814628-144814678	ECC-1	luminal epithelium:	n/a
24	chr1:144815302-144815352	Caco-2	colon:	n/a
25	chr1:144620428-144620478	HEEpiC	esophagus:	n/a
26	chr1:144619354-144619404	T-47D	breast:	n/a
27	chr1:144612358-144612408	NH-A	brain:	n/a
28	chr1:144612646-144612696	HMEC	breast:	n/a
29	chr1:144811373-144811423	HIPEpiC	eye:	n/a
30	chr1:144811373-144811423	AG04450	lung:	fetal
31	chr1:144615272-144615322	H1-hESC	embryonic stem cell:	embryo
32	chr1:144619354-144619404	Hela-S3	cervix:	n/a
33	chr1:144612646-144612696	Caco-2	colon:	n/a
34	chr1:144815915-144815965	HRE	kidney:	n/a
35	chr1:144815302-144815352	PFSK-1	brain:	n/a
36	chr1:144692074-144692124	HIPEpiC	eye:	n/a
37	chr1:144619354-144619404	ovcar-3	ovarian:	n/a
38	chr1:144620428-144620478	HCPEpiC	choroid plexus:	n/a
39	chr1:144814628-144814678	SKMC	muscle:	n/a
40	chr1:144814628-144814678	H1-hESC	embryonic stem cell:	embryo
41	chr1:144620428-144620478	SK-N-SH_RA	brain:	n/a
42	chr1:144814628-144814678	HRE	kidney:	n/a
43	chr1:144620428-144620478	GM12878	blood:	n/a
44	chr1:144814628-144814678	BE2_C	brain:	n/a
45	chr1:144815302-144815352	ProgFib	skin:	n/a
46	chr1:144612358-144612408	HCM	heart:	n/a
47	chr1:144815302-144815352	HL-60	blood:	n/a
48	chr1:144619354-144619404	PFSK-1	brain:	n/a
49	chr1:144814628-144814678	RPTEC	kidney:	n/a
50	chr1:144620428-144620478	HAEpiC	amniotic membrane:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144687969..144690729-chr1:144930762..144933228,2	MCF-7	breast:
2	chr1:144535050..144535880-chr1:144697650..144698167,2	MCF-7	breast:
3	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
4	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
5	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:

(count:118 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
2	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
3	lnc-AL592284.1-1	chr1:144824705-144824756	NR_102404
4	lnc-AL592284.1-1	chr1:144598512-144598780	ENSG00000225241
5	lnc-AL592284.1-1	chr1:144816316-144816795	NONHSAT005838
6	lnc-AL592284.1-1	chr1:144606838-144607342	NONHSAT005826
7	lnc-AL592284.1-1	chr1:144598391-144598780	NONHSAT005826
8	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
9	lnc-AL592284.1-1	chr1:144598512-144598780	NONHSAT005823
10	lnc-AL592284.1-1	chr1:144826933-144827105	NR_102405
11	lnc-AL592284.1-1	chr1:144823128-144823179	NR_102404
12	lnc-AL592284.1-1	chr1:144814680-144814894	NR_102404
13	lnc-PDE4DIP-4	chr1:144832200-144833038	NONHSAT005840
14	lnc-AL592284.1-1	chr1:144825353-144825525	NR_102404
15	lnc-AL592284.1-1	chr1:144617150-144617252	NR_102404
16	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102405
17	lnc-AL592284.1-1	chr1:144614388-144614998	ENSG00000225241
18	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
19	lnc-AL592284.1-1	chr1:144618513-144618663	ENSG00000225241
20	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
21	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
22	lnc-AL592284.1-1	chr1:144606129-144606278	ENSG00000225241
23	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
24	lnc-AL592284.1-1	chr1:144614840-144614993	ENSG00000225241
25	lnc-AL592284.1-1	chr1:144617150-144617252	ENSG00000225241
26	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
27	lnc-AL592284.1-1	chr1:144815936-144816049	NONHSAT005837
28	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
29	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102405
30	lnc-AL592284.1-1	chr1:144614840-144614993	ENSG00000225241
31	lnc-AL592284.1-1	chr1:144598512-144598780	NONHSAT005824
32	lnc-AL592284.1-1	chr1:144606369-144606510	ENSG00000225241
33	lnc-AL592284.1-1	chr1:144815936-144816008	NONHSAT005838
34	lnc-AL592284.1-1	chr1:144604478-144604508	ENSG00000225241
35	lnc-AL592284.1-1	chr1:144816473-144816678	NR_102404
36	lnc-AL592284.1-1	chr1:144615096-144615303	ENSG00000225241
37	lnc-AL592284.1-1	chr1:144828973-144830389	NONHSAT005839
38	lnc-AL592284.1-1	chr1:144604410-144604508	ENSG00000225241
39	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
40	lnc-AL592284.1-1	chr1:144817966-144818017	NR_102405
41	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102405
42	lnc-AL592284.1-1	chr1:144815936-144816008	NR_102404
43	lnc-AL592284.1-1	chr1:144614532-144614993	ENSG00000225241
44	lnc-AL592284.1-1	chr1:144598512-144598780	ENSG00000225241
45	lnc-AL592284.1-1	chr1:144598614-144598780	ENSG00000225241
46	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102404
47	lnc-AL592284.1-1	chr1:144617150-144617208	NONHSAT139893
48	lnc-AL592284.1-1	chr1:144614959-144615303	NR_102404
49	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102405
50	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102404

No data

Variant related genes	Relation type
PFN1P2	TF binding region
NBPF9	TF binding region
ENSG00000225241	TF binding region
ENSG00000215861	TF binding region
PFN1P2	CpG island
NBPF9	CpG island
ENSG00000225241	CpG island
ENSG00000215861	CpG island
ENSG00000178104	chromatin interactions

Extended variants
information (count: 3678 )
Associated
traits (count: 168 )

Variant overlapped rSNPs/rCNVs (count:3678 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10399799	chr1:144598069-144598070	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs587672058	chr1:144598074-144598075	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs1698690	chr1:144598179-144598180	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1698689	chr1:144598213-144598214	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs61807921	chr1:144598245-144598246	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs587631779	chr1:144598261-144598262	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs587688841	chr1:144598263-144598264	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs200072377	chr1:144598288-144598289	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs587748186	chr1:144598295-144598296	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs587616908	chr1:144598301-144598302	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs587660705	chr1:144598332-144598333	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs587734275	chr1:144598339-144598340	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs587617539	chr1:144598369-144598370	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs587696044	chr1:144598422-144598423	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs368525779	chr1:144598580-144598581	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs587755855	chr1:144598606-144598607	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs1698687	chr1:144598641-144598642	Weak transcription Strong transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs587628673	chr1:144598656-144598657	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs1699854	chr1:144598659-144598660	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs149760427	chr1:144598691-144598692	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs587687965	chr1:144598721-144598722	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs372140203	chr1:144598744-144598745	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs2660554	chr1:144598755-144598756	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs2655813	chr1:144598889-144598890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587722816	chr1:144598922-144598923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs2660553	chr1:144598927-144598928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2660552	chr1:144598950-144598951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74116456	chr1:144598974-144598975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2655812	chr1:144598975-144598976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587754474	chr1:144599009-144599010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78268502	chr1:144599051-144599052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112181187	chr1:144599069-144599070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587677011	chr1:144599076-144599077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6666535	chr1:144599105-144599106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201187209	chr1:144599117-144599118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111636993	chr1:144599126-144599127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587631737	chr1:144599131-144599132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2938646	chr1:144599147-144599148	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74116914	chr1:144599161-144599162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587725546	chr1:144599168-144599169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587605888	chr1:144599169-144599170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587653581	chr1:144599172-144599173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61807923	chr1:144599186-144599187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587739602	chr1:144599192-144599193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111764388	chr1:144599259-144599260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587611684	chr1:144599311-144599312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200231374	chr1:144599360-144599361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587675616	chr1:144599364-144599365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587734548	chr1:144599387-144599388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201088020	chr1:144599407-144599408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:168)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Cancer	17440070	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144594400-144604600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:144594600-144598200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:144594600-144598600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:144594600-144598600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr1:144594600-144600800	Weak transcription	Colonic Mucosa	Colon
6	chr1:144594600-144601800	Weak transcription	Esophagus	oesophagus
7	chr1:144594600-144603800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr1:144594600-144621200	Weak transcription	Gastric	stomach
9	chr1:144594600-144622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:144594600-144622000	Weak transcription	Placenta	Placenta
11	chr1:144594800-144598400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:144594800-144598600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:144594800-144598600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:144594800-144598600	Weak transcription	Brain Anterior Caudate	brain
15	chr1:144594800-144598600	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr1:144594800-144598600	Weak transcription	Spleen	Spleen
17	chr1:144594800-144598800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr1:144594800-144599000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:144594800-144602200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:144594800-144602800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr1:144594800-144604000	Weak transcription	K562	blood
22	chr1:144594800-144607200	Weak transcription	Left Ventricle	heart
23	chr1:144594800-144607200	Weak transcription	Lung	lung
24	chr1:144594800-144607200	Weak transcription	Stomach Smooth Muscle	stomach
25	chr1:144594800-144607600	Weak transcription	Brain Substantia Nigra	brain
26	chr1:144594800-144608000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr1:144594800-144608000	Weak transcription	Fetal Brain Male	brain
28	chr1:144594800-144608600	Weak transcription	Psoas Muscle	Psoas
29	chr1:144594800-144609000	Weak transcription	A549	lung
30	chr1:144594800-144609000	Weak transcription	GM12878-XiMat	blood
31	chr1:144594800-144609200	Weak transcription	Brain Hippocampus Middle	brain
32	chr1:144594800-144618000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:144594800-144618000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr1:144594800-144618000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr1:144594800-144618000	Weak transcription	Adipose Nuclei	Adipose
36	chr1:144594800-144619400	Weak transcription	Aorta	Aorta
37	chr1:144594800-144620000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr1:144594800-144620200	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr1:144594800-144620600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:144594800-144621200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr1:144594800-144621200	Weak transcription	Fetal Lung	lung
42	chr1:144594800-144621200	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr1:144594800-144621400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:144594800-144621400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr1:144594800-144621600	Weak transcription	HSMM	muscle
46	chr1:144594800-144621800	Weak transcription	Brain Germinal Matrix	brain
47	chr1:144594800-144621800	Weak transcription	HSMMtube	muscle
48	chr1:144594800-144622000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:144594800-144622000	Weak transcription	Duodenum Mucosa	Duodenum
50	chr1:144594800-144623400	Weak transcription	Primary T cells from cord blood	blood

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