Variant report

Variant	esv2329300
Chromosome Location	chr1:78353435-78353852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:89)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:89 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr1:78353836-78354370	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr1:78353820-78354234	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr1:78353820-78353970	HBMEC	blood vessel:	n/a	n/a
4	CTCF	chr1:78353840-78353990	HRPEpiC	eye:	n/a	n/a
5	CTCF	chr1:78353840-78353990	HCPEpiC	choroid plexus:	n/a	n/a
6	CTCF	chr1:78353840-78353990	K562	blood:	n/a	n/a
7	CTCF	chr1:78353820-78353970	BJ	skin:	n/a	n/a
8	CTCF	chr1:78353840-78353990	HepG2	liver:	n/a	n/a
9	CTCF	chr1:78353740-78353890	AG04450	lung:	n/a	n/a
10	CTCF	chr1:78353780-78353930	HepG2	liver:	n/a	n/a
11	CTCF	chr1:78353820-78353970	HPF	lung:	n/a	n/a
12	CTCF	chr1:78353807-78354018	HepG2	liver:	n/a	n/a
13	CTCF	chr1:78353780-78353930	AG09319	gingival:	n/a	n/a
14	CTCF	chr1:78353826-78354019	ProgFib	skin:	n/a	n/a
15	CTCF	chr1:78353840-78353990	HRE	kidney:	n/a	n/a
16	CTCF	chr1:78353760-78353910	HFF	foreskin:	n/a	n/a
17	CTCF	chr1:78353786-78354119	IMR90	lung:	n/a	n/a
18	CTCF	chr1:78353840-78353990	AG09319	gingival:	n/a	n/a
19	CTCF	chr1:78353840-78353990	HPF	lung:	n/a	n/a
20	CTCF	chr1:78353760-78353910	AG09309	skin:	n/a	n/a
21	CTCF	chr1:78353839-78353874	Lung_OC	lung:	n/a	n/a
22	CTCF	chr1:78353846-78354002	HepG2	liver:	n/a	n/a
23	CTCF	chr1:78353624-78353663	Lung_OC	lung:	n/a	n/a
24	CTCF	chr1:78353680-78353830	RPTEC	kidney:	n/a	n/a
25	CTCF	chr1:78353840-78353990	BJ	skin:	n/a	n/a
26	CTCF	chr1:78353800-78353950	NHLF	lung:	n/a	n/a
27	CTCF	chr1:78353820-78353970	GM12873	blood:	n/a	n/a
28	CTCF	chr1:78353800-78353950	AG10803	skin:	n/a	n/a
29	CTCF	chr1:78353840-78353990	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr1:78353800-78353950	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr1:78353780-78353930	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr1:78353820-78353970	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:78353840-78353990	A549	lung:	n/a	n/a
34	CTCF	chr1:78353760-78353910	HVMF	connective:	n/a	n/a
35	CTCF	chr1:78353840-78353990	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr1:78353840-78353990	NHDF-neo	bronchial:	n/a	n/a
37	EP300	chr1:78353826-78354076	K562	blood:	n/a	n/a
38	EP300	chr1:78353711-78354797	SK-N-SH	brain:	n/a	n/a
39	GTF2F1	chr1:78353840-78354783	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr1:78353832-78354040	K562	blood:	n/a	n/a
41	KAP1	chr1:78353754-78354281	HEK293	kidney:	n/a	n/a
42	MAX	chr1:78353736-78354705	A549	lung:	n/a	n/a
43	MAX	chr1:78353738-78354725	SK-N-SH	brain:	n/a	n/a
44	MAX	chr1:78353771-78354881	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr1:78353770-78354889	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr1:78353781-78354487	SK-N-SH	brain:	n/a	n/a
47	MAZ	chr1:78353812-78354570	K562	blood:	n/a	n/a
48	MAZ	chr1:78353684-78356140	IMR90	lung:	n/a	n/a
49	MYC	chr1:78353848-78354243	K562	blood:	n/a	n/a
50	POLR2A	chr1:78353729-78354692	HUVEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:78353422-78353472	HCPEpiC	choroid plexus:	n/a
2	chr1:78353422-78353472	NT2-D1	testis:	n/a
3	chr1:78353422-78353472	HCF	heart:	n/a
4	chr1:78353422-78353472	SKMC	muscle:	n/a
5	chr1:78353422-78353472	H1-hESC	embryonic stem cell:	embryo
6	chr1:78353422-78353472	GM06990	blood:	n/a
7	chr1:78353422-78353472	AG04450	lung:	fetal
8	chr1:78353422-78353472	HUVEC	blood vessel:	n/a
9	chr1:78353422-78353472	SK-N-MC	brain:	n/a
10	chr1:78353422-78353472	GM19239	blood:	n/a
11	chr1:78353422-78353472	BE2_C	brain:	n/a
12	chr1:78353422-78353472	Hepatocyte	liver:	n/a
13	chr1:78353422-78353472	MCF-7	breast:	n/a
14	chr1:78353422-78353472	MCF10A-Er-Src	breast:	n/a
15	chr1:78353422-78353472	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:78353422-78353472	LNCaP	prostate:	n/a
17	chr1:78353422-78353472	ovcar-3	ovarian:	n/a
18	chr1:78353422-78353472	NH-A	brain:	n/a
19	chr1:78353422-78353472	U87	brain:	n/a
20	chr1:78353422-78353472	AG10803	skin:	n/a
21	chr1:78353422-78353472	ECC-1	luminal epithelium:	n/a
22	chr1:78353422-78353472	NHBE	bronchial:	n/a
23	chr1:78353422-78353472	SAEC	small airway:	n/a
24	chr1:78353422-78353472	IMR90	lung:	fetal
25	chr1:78353422-78353472	HRE	kidney:	n/a
26	chr1:78353422-78353472	NB4	blood:	n/a
27	chr1:78353422-78353472	HRPEpiC	eye:	n/a
28	chr1:78353422-78353472	HEEpiC	esophagus:	n/a
29	chr1:78353422-78353472	HMEC	breast:	n/a
30	chr1:78353422-78353472	ProgFib	skin:	n/a
31	chr1:78353422-78353472	HIPEpiC	eye:	n/a
32	chr1:78353422-78353472	AoSMC	blood vessel:	n/a
33	chr1:78353422-78353472	HepG2	liver:	n/a
34	chr1:78353422-78353472	AG09309	skin:	n/a
35	chr1:78353422-78353472	HL-60	blood:	n/a
36	chr1:78353422-78353472	Hela-S3	cervix:	n/a
37	chr1:78353422-78353472	PANC-1	pancreas:	n/a
38	chr1:78353422-78353472	HCT-116	colon:	n/a
39	chr1:78353422-78353472	BJ	skin:	n/a
40	chr1:78353422-78353472	A549	lung:	n/a
41	chr1:78353422-78353472	T-47D	breast:	n/a
42	chr1:78353422-78353472	GM12878	blood:	n/a
43	chr1:78353422-78353472	Caco-2	colon:	n/a
44	chr1:78353422-78353472	HNPCEpiC	eye:	n/a
45	chr1:78353422-78353472	SK-N-SH_RA	brain:	n/a
46	chr1:78353422-78353472	NHDF-neo	bronchial:	n/a
47	chr1:78353422-78353472	GM12892	blood:	n/a
48	chr1:78353422-78353472	K562	blood:	n/a
49	chr1:78353422-78353472	PFSK-1	brain:	n/a
50	chr1:78353422-78353472	PrEC	prostate:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FUBP1-1	chr1:78353285-78354953	ENSG00000235927

No data

Variant related genes	Relation type
NEXN	TF binding region
NEXN-AS1	TF binding region
NEXN	CpG island
NEXN-AS1	CpG island
UNC45A	miRNA target sites

Extended variants
information (count: 52 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:52 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113300435	chr1:78353553-78353554	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
2	rs77761183	chr1:78353561-78353562	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
3	rs542967845	chr1:78353571-78353572	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557747578	chr1:78353572-78353573	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
5	rs572705689	chr1:78353596-78353597	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs561104451	chr1:78353597-78353598	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs371594560	chr1:78353602-78353603	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs114020893	chr1:78353605-78353606	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs146391268	chr1:78353606-78353607	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs139722383	chr1:78353611-78353612	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs564678587	chr1:78353616-78353617	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs77520905	chr1:78353617-78353618	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs368323568	chr1:78353620-78353621	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs74825111	chr1:78353623-78353624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs371919352	chr1:78353626-78353627	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs74726685	chr1:78353629-78353630	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs376385686	chr1:78353632-78353633	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs76614617	chr1:78353635-78353636	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs369992247	chr1:78353638-78353639	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs74632794	chr1:78353641-78353642	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs373879306	chr1:78353644-78353645	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs80143518	chr1:78353647-78353648	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs374832568	chr1:78353650-78353651	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs535351568	chr1:78353652-78353653	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs75411573	chr1:78353653-78353654	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs553219078	chr1:78353655-78353656	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs368808527	chr1:78353656-78353657	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs74631226	chr1:78353659-78353660	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs574727255	chr1:78353661-78353662	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs372865332	chr1:78353662-78353663	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs541998205	chr1:78353664-78353665	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs79987664	chr1:78353665-78353666	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs563488639	chr1:78353670-78353671	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs79782190	chr1:78353671-78353672	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs575703066	chr1:78353673-78353674	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs375869668	chr1:78353674-78353675	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs77842697	chr1:78353677-78353678	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs201884406	chr1:78353680-78353681	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs199894090	chr1:78353686-78353687	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs200366722	chr1:78353687-78353688	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs139426808	chr1:78353689-78353690	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs546825035	chr1:78353690-78353691	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs545577141	chr1:78353691-78353692	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs386367397	chr1:78353692-78353693	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs538778659	chr1:78353693-78353694	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs74092324	chr1:78353704-78353705	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184458454	chr1:78353726-78353727	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs374026384	chr1:78353727-78353728	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs570539625	chr1:78353756-78353757	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs187603385	chr1:78353761-78353762	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:78299600-78353800	Weak transcription	Brain Substantia Nigra	brain
2	chr1:78324600-78353800	Weak transcription	Esophagus	oesophagus
3	chr1:78327200-78353600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr1:78327400-78353800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:78333400-78353800	Weak transcription	Lung	lung
6	chr1:78333600-78354000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr1:78333800-78353800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:78334400-78353600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr1:78334400-78353600	Weak transcription	Adipose Nuclei	Adipose
10	chr1:78334400-78353800	Weak transcription	Brain Hippocampus Middle	brain
11	chr1:78334400-78353800	Weak transcription	Fetal Kidney	kidney
12	chr1:78334600-78353600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:78334600-78353600	Weak transcription	Fetal Brain Female	brain
14	chr1:78334600-78353800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr1:78334600-78353800	Weak transcription	Placenta	Placenta
16	chr1:78334600-78353800	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr1:78337000-78353600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr1:78340800-78353800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:78341000-78353600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:78341000-78353800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr1:78341200-78353600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:78341200-78353800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:78341200-78353800	Weak transcription	Fetal Intestine Large	intestine
24	chr1:78341200-78353800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr1:78341400-78353600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:78341400-78353600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:78341400-78353800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr1:78346200-78354000	Weak transcription	Spleen	Spleen
29	chr1:78346800-78353800	Weak transcription	Primary T cells from cord blood	blood
30	chr1:78349200-78353600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr1:78350600-78353800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:78352400-78353800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:78352400-78359800	Active TSS	Right Ventricle	heart
34	chr1:78352600-78353600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr1:78352600-78353600	Enhancers	Fetal Muscle Leg	muscle
36	chr1:78352600-78353600	Enhancers	Stomach Smooth Muscle	stomach
37	chr1:78352800-78353800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr1:78353000-78353600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr1:78353000-78353600	Enhancers	Colon Smooth Muscle	Colon
40	chr1:78353000-78353600	Enhancers	Fetal Muscle Trunk	muscle
41	chr1:78353000-78353600	Enhancers	Ovary	ovary
42	chr1:78353000-78353600	Enhancers	Rectal Smooth Muscle	rectum
43	chr1:78353000-78353800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
44	chr1:78353000-78354000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr1:78353000-78354200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chr1:78353200-78353600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:78353200-78353600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr1:78353200-78353600	Enhancers	Fetal Lung	lung
49	chr1:78353200-78353600	Enhancers	Fetal Stomach	stomach
50	chr1:78353200-78353600	Enhancers	HMEC	breast

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