Variant report

Variant	esv9932
Chromosome Location	chr1:144618045-144622190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

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	chr1:144618840-144619109	GM12878	blood:	n/a	n/a
3	BATF	chr1:144618572-144618830	GM12878	blood:	n/a	n/a
4	BATF	chr1:144621396-144621792	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:144618530-144618828	GM12878	blood:	n/a	n/a
6	BCL11A	chr1:144618876-144619331	GM12878	blood:	n/a	n/a
7	BCL11A	chr1:144620110-144620305	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:144621190-144621435	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:144618887-144619298	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:144618560-144618873	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:144621538-144621780	HepG2	liver:	n/a	n/a
12	CTCF	chr1:144621046-144621870	A549	lung:	n/a	n/a
13	CTCF	chr1:144621534-144621643	GM10248	blood:	n/a	n/a
14	CTCF	chr1:144621504-144621639	GM20000	blood:	n/a	n/a
15	CTCF	chr1:144621476-144621686	LNCaP	prostate:	n/a	n/a
16	CTCF	chr1:144621560-144621710	RPTEC	kidney:	n/a	n/a
17	CTCF	chr1:144621590-144621606	ProgFib	skin:	n/a	n/a
18	CTCF	chr1:144621540-144621690	BJ	skin:	n/a	n/a
19	CTCF	chr1:144621555-144621610	Lung_OC	lung:	n/a	n/a
20	CTCF	chr1:144621559-144621642	K562	blood:	n/a	n/a
21	CTCF	chr1:144621560-144621710	HMEC	breast:	n/a	n/a
22	CTCF	chr1:144621520-144621670	AG04450	lung:	n/a	n/a
23	CTCF	chr1:144621536-144621653	Medullo	brain:	n/a	n/a
24	CTCF	chr1:144621560-144621710	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:144621509-144621658	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr1:144621522-144621645	GM10266	blood:	n/a	n/a
27	CTCF	chr1:144621487-144621677	GM13977	blood:	n/a	n/a
28	CTCF	chr1:144621582-144621599	GM12878	blood:	n/a	n/a
29	CTCF	chr1:144621407-144621809	A549	lung:	n/a	n/a
30	CTCF	chr1:144621302-144621742	A549	lung:	n/a	n/a
31	CTCF	chr1:144621520-144621670	HPF	lung:	n/a	n/a
32	CTCF	chr1:144621310-144621698	K562	blood:	n/a	n/a
33	CTCF	chr1:144621557-144621640	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr1:144621510-144621644	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr1:144621387-144621708	K562	blood:	n/a	n/a
36	CTCF	chr1:144621500-144621650	HL-60	blood:	n/a	n/a
37	CTCF	chr1:144621520-144621670	AG09309	skin:	n/a	n/a
38	CTCF	chr1:144621520-144621670	GM12871	blood:	n/a	n/a
39	CTCF	chr1:144621571-144621637	A549	lung:	n/a	n/a
40	CTCF	chr1:144621520-144621670	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr1:144621261-144621714	K562	blood:	n/a	n/a
42	CTCF	chr1:144621544-144621623	GM13976	blood:	n/a	n/a
43	CTCF	chr1:144621520-144621670	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:144621403-144621735	A549	lung:	n/a	n/a
45	CTCF	chr1:144621560-144621710	HCM	heart:	n/a	n/a
46	CTCF	chr1:144621520-144621670	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr1:144621520-144621670	HMF	breast:	n/a	n/a
48	CTCF	chr1:144621560-144621710	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr1:144621560-144621710	WI-38	lung:	n/a	n/a
50	CTCF	chr1:144621500-144621650	GM06990	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144619354-144619404	K562	blood:	n/a
2	chr1:144619354-144619404	GM12878	blood:	n/a
3	chr1:144619354-144619404	GM06990	blood:	n/a
4	chr1:144619354-144619404	HCPEpiC	choroid plexus:	n/a
5	chr1:144619354-144619404	AG09319	gingival:	n/a
6	chr1:144619354-144619404	HEEpiC	esophagus:	n/a
7	chr1:144620428-144620478	PrEC	prostate:	n/a
8	chr1:144620428-144620478	U87	brain:	n/a
9	chr1:144620428-144620478	AG09319	gingival:	n/a
10	chr1:144619354-144619404	ProgFib	skin:	n/a
11	chr1:144619354-144619404	T-47D	breast:	n/a
12	chr1:144620428-144620478	IMR90	lung:	fetal
13	chr1:144619354-144619404	HRCEpiC	kidney:	n/a
14	chr1:144620428-144620478	A549	lung:	n/a
15	chr1:144620428-144620478	SAEC	small airway:	n/a
16	chr1:144619354-144619404	HepG2	liver:	n/a
17	chr1:144619354-144619404	HRPEpiC	eye:	n/a
18	chr1:144620428-144620478	HRCEpiC	kidney:	n/a
19	chr1:144620428-144620478	PANC-1	pancreas:	n/a
20	chr1:144619354-144619404	HEK293	kidney:	embryo
21	chr1:144620428-144620478	Hepatocyte	liver:	n/a
22	chr1:144619354-144619404	U87	brain:	n/a
23	chr1:144619354-144619404	HMEC	breast:	n/a
24	chr1:144619354-144619404	LNCaP	prostate:	n/a
25	chr1:144620428-144620478	HAEpiC	amniotic membrane:	n/a
26	chr1:144619354-144619404	NT2-D1	testis:	n/a
27	chr1:144620428-144620478	HMEC	breast:	n/a
28	chr1:144619354-144619404	HCM	heart:	n/a
29	chr1:144619354-144619404	ovcar-3	ovarian:	n/a
30	chr1:144619354-144619404	HNPCEpiC	eye:	n/a
31	chr1:144619354-144619404	SAEC	small airway:	n/a
32	chr1:144619354-144619404	PANC-1	pancreas:	n/a
33	chr1:144619354-144619404	SKMC	muscle:	n/a
34	chr1:144619354-144619404	GM12891	blood:	n/a
35	chr1:144620428-144620478	NHBE	bronchial:	n/a
36	chr1:144619354-144619404	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:144619354-144619404	HRE	kidney:	n/a
38	chr1:144619354-144619404	HIPEpiC	eye:	n/a
39	chr1:144619354-144619404	NB4	blood:	n/a
40	chr1:144620428-144620478	T-47D	breast:	n/a
41	chr1:144620428-144620478	HRE	kidney:	n/a
42	chr1:144620428-144620478	LNCaP	prostate:	n/a
43	chr1:144619354-144619404	AoSMC	blood vessel:	n/a
44	chr1:144620428-144620478	HepG2	liver:	n/a
45	chr1:144620428-144620478	NB4	blood:	n/a
46	chr1:144620428-144620478	AG09309	skin:	n/a
47	chr1:144619354-144619404	HAEpiC	amniotic membrane:	n/a
48	chr1:144620428-144620478	NHDF-neo	bronchial:	n/a
49	chr1:144619354-144619404	SK-N-SH_RA	brain:	n/a
50	chr1:144619354-144619404	BE2_C	brain:	n/a

No data

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
2	lnc-AL592284.1-1	chr1:144618513-144618663	ENSG00000225241
3	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
4	lnc-AL592284.1-1	chr1:144618082-144618296	NR_102405
5	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102405
6	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
7	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
8	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102405
9	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
10	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
11	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
12	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102405
13	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
14	lnc-AL592284.1-1	chr1:144618082-144618296	NR_102404
15	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
16	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
17	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
18	lnc-AL592284.1-1	chr1:144619883-144620039	ENSG00000225241
19	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
20	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
21	lnc-AL592284.1-1	chr1:144619347-144619419	NR_102404
22	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
23	lnc-AL592284.1-1	chr1:144619883-144620094	ENSG00000225241
24	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
25	lnc-AL592284.1-1	chr1:144621447-144621656	NR_102404
26	lnc-AL592284.1-1	chr1:144621447-144621655	ENSG00000225241
27	lnc-AL592284.1-1	chr1:144619883-144620094	NR_102404
28	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241
29	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
30	lnc-AL592284.1-1	chr1:144619347-144619419	ENSG00000225241
31	lnc-AL592284.1-1	chr1:144621447-144621656	ENSG00000225241
32	lnc-AL592284.1-1	chr1:144618082-144618296	ENSG00000225241

No data

Variant related genes	Relation type
ENSG00000225241	TF binding region
ENSG00000225241	CpG island

Extended variants
information (count: 282 )
Associated
traits (count: 164 )

Variant overlapped rSNPs/rCNVs (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs55646423	chr1:144618070-144618071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112111762	chr1:144618113-144618114	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs61809735	chr1:144618123-144618124	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs587685970	chr1:144618139-144618140	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs28691033	chr1:144618144-144618145	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs587707459	chr1:144618157-144618158	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs587610566	chr1:144618159-144618160	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs200951275	chr1:144618176-144618177	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs587742048	chr1:144618188-144618189	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs61809737	chr1:144618201-144618202	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs587621381	chr1:144618210-144618211	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs587700849	chr1:144618221-144618222	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs587756378	chr1:144618222-144618223	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs587606867	chr1:144618224-144618225	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs587660821	chr1:144618229-144618230	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs587734368	chr1:144618235-144618236	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs201136836	chr1:144618254-144618255	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs201757242	chr1:144618281-144618282	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs587671273	chr1:144618339-144618340	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs374193618	chr1:144618351-144618352	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs61809738	chr1:144618354-144618355	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
22	rs370405965	chr1:144618381-144618382	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs113916638	chr1:144618403-144618404	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs61810891	chr1:144618407-144618408	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs201799917	chr1:144618414-144618415	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs372378580	chr1:144618432-144618433	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs587685744	chr1:144618453-144618454	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs370297578	chr1:144618464-144618465	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs35428490	chr1:144618465-144618466	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs61810892	chr1:144618477-144618478	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs587763330	chr1:144618491-144618492	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs587625097	chr1:144618523-144618524	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
33	rs587688171	chr1:144618535-144618536	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
34	rs587762725	chr1:144618556-144618557	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
35	rs200350896	chr1:144618557-144618558	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
36	rs9441144	chr1:144618559-144618560	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
37	rs587662167	chr1:144618562-144618563	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs367795225	chr1:144618581-144618582	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
39	rs372344087	chr1:144618587-144618588	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
40	rs9441145	chr1:144618603-144618604	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs587747859	chr1:144618604-144618605	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs587773023	chr1:144618609-144618610	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs587676942	chr1:144618621-144618622	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs367956732	chr1:144618631-144618632	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs3979879	chr1:144618663-144618664	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs587727473	chr1:144618675-144618676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs587605933	chr1:144618677-144618678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112374863	chr1:144618752-144618753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs113290782	chr1:144618765-144618766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587653295	chr1:144618767-144618768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:164)

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
Breast cancer	22522925	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144594600-144621200	Weak transcription	Gastric	stomach
2	chr1:144594600-144622000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:144594600-144622000	Weak transcription	Placenta	Placenta
4	chr1:144594800-144619400	Weak transcription	Aorta	Aorta
5	chr1:144594800-144620000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr1:144594800-144620200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr1:144594800-144620600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:144594800-144621200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:144594800-144621200	Weak transcription	Fetal Lung	lung
10	chr1:144594800-144621200	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:144594800-144621400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:144594800-144621400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:144594800-144621600	Weak transcription	HSMM	muscle
14	chr1:144594800-144621800	Weak transcription	Brain Germinal Matrix	brain
15	chr1:144594800-144621800	Weak transcription	HSMMtube	muscle
16	chr1:144594800-144622000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:144594800-144622000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr1:144594800-144623400	Weak transcription	Primary T cells from cord blood	blood
19	chr1:144594800-144623400	Weak transcription	HUVEC	blood vessel
20	chr1:144594800-144624000	Weak transcription	Right Ventricle	heart
21	chr1:144595800-144623200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr1:144596200-144618200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:144596200-144621400	Weak transcription	Pancreas	Pancrea
24	chr1:144596400-144622000	Weak transcription	NH-A	brain
25	chr1:144598800-144621400	Weak transcription	Colon Smooth Muscle	Colon
26	chr1:144598800-144623600	Weak transcription	Hela-S3	cervix
27	chr1:144599000-144621200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr1:144599200-144621600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr1:144599400-144618200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr1:144599400-144619400	Weak transcription	Fetal Muscle Leg	muscle
31	chr1:144599400-144619400	Weak transcription	Osteobl	bone
32	chr1:144599400-144619600	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr1:144599400-144620400	Weak transcription	Fetal Muscle Trunk	muscle
34	chr1:144599400-144621600	Weak transcription	HMEC	breast
35	chr1:144599400-144621800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr1:144599400-144622000	Weak transcription	Fetal Stomach	stomach
37	chr1:144599400-144623400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr1:144599600-144618400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:144599800-144623800	Weak transcription	Fetal Intestine Small	intestine
40	chr1:144600000-144620200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr1:144601400-144618600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:144601600-144618200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr1:144601600-144621000	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr1:144604400-144620200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr1:144604400-144621600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:144607800-144618200	Weak transcription	Lung	lung
47	chr1:144607800-144619400	Weak transcription	Primary B cells from peripheral blood	blood
48	chr1:144607800-144619400	Weak transcription	Dnd41	blood
49	chr1:144607800-144621400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr1:144607800-144622000	Weak transcription	Fetal Intestine Large	intestine

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