Variant report

Variant	esv3384312
Chromosome Location	chr13:49063851-49067249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:49066725-49067036	K562	blood:	n/a	n/a
2	ATF2	chr13:49066194-49067099	GM12878	blood:	n/a	n/a
3	ATF2	chr13:49066426-49067129	GM12878	blood:	n/a	n/a
4	BATF	chr13:49066305-49066996	GM12878	blood:	n/a	n/a
5	BCL11A	chr13:49066578-49066990	GM12878	blood:	n/a	n/a
6	BCLAF1	chr13:49066242-49067161	GM12878	blood:	n/a	n/a
7	BCLAF1	chr13:49066270-49067027	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:49066284-49067076	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:49066475-49067023	K562	blood:	n/a	n/a
10	CBX3	chr13:49066598-49066985	K562	blood:	n/a	n/a
11	CEBPB	chr13:49066615-49066999	GM12878	blood:	n/a	n/a
12	CHD1	chr13:49063314-49063851	GM12878	blood:	n/a	n/a
13	CHD1	chr13:49066776-49067001	GM12878	blood:	n/a	n/a
14	CHD2	chr13:49066623-49067019	GM12878	blood:	n/a	n/a
15	CHD2	chr13:49066704-49066898	K562	blood:	n/a	n/a
16	CUX1	chr13:49066424-49066976	GM12878	blood:	n/a	n/a
17	CUX1	chr13:49066789-49066863	K562	blood:	n/a	n/a
18	E2F6	chr13:49066613-49066868	K562	blood:	n/a	n/a
19	E2F6	chr13:49066584-49066947	K562	blood:	n/a	n/a
20	EBF1	chr13:49066281-49067021	GM12878	blood:	n/a	n/a
21	EBF1	chr13:49066591-49066933	GM12878	blood:	n/a	n/a
22	EBF1	chr13:49066620-49066930	GM12878	blood:	n/a	n/a
23	EGR1	chr13:49066629-49066958	GM12878	blood:	n/a	n/a
24	EGR1	chr13:49066637-49066921	GM12878	blood:	n/a	n/a
25	ELF1	chr13:49066379-49067028	GM12878	blood:	n/a	chr13:49066861-49066874 chr13:49066807-49066820
26	ELF1	chr13:49066634-49067015	K562	blood:	n/a	chr13:49066861-49066874 chr13:49066807-49066820
27	ELF1	chr13:49066635-49067027	GM12878	blood:	n/a	chr13:49066861-49066874 chr13:49066807-49066820
28	ELK1	chr13:49066630-49066928	GM12878	blood:	n/a	n/a
29	EP300	chr13:49066575-49067053	GM12878	blood:	n/a	n/a
30	EP300	chr13:49066322-49067022	GM12878	blood:	n/a	n/a
31	EP300	chr13:49066500-49067004	GM12878	blood:	n/a	n/a
32	EP300	chr13:49066688-49066995	K562	blood:	n/a	n/a
33	EP300	chr13:49066405-49066973	GM12878	blood:	n/a	n/a
34	ETS1	chr13:49066534-49067036	GM12878	blood:	n/a	n/a
35	FOS	chr13:49066321-49067022	HUVEC	blood vessel:	n/a	n/a
36	FOXM1	chr13:49066565-49067045	GM12878	blood:	n/a	n/a
37	FOXM1	chr13:49066204-49067233	GM12878	blood:	n/a	n/a
38	FOXP2	chr13:49066614-49066959	SK-N-MC	brain:	n/a	n/a
39	GATA1	chr13:49066497-49067256	PBDE	blood:	n/a	n/a
40	GATA2	chr13:49066294-49067212	HUVEC	blood vessel:	n/a	chr13:49066904-49066918
41	HCFC1	chr13:49066694-49066920	K562	blood:	n/a	n/a
42	IKZF1	chr13:49066198-49067298	GM12878	blood:	n/a	n/a
43	IRF1	chr13:49066673-49066951	K562	blood:	n/a	chr13:49066810-49066831
44	IRF1	chr13:49066555-49067063	K562	blood:	n/a	chr13:49066810-49066831
45	IRF1	chr13:49065577-49065887	K562	blood:	n/a	chr13:49065716-49065730 chr13:49065715-49065727 chr13:49065714-49065728 chr13:49065716-49065726 chr13:49065716-49065727 chr13:49065717-49065728 chr13:49065714-49065727 chr13:49065712-49065726 chr13:49065714-49065727 chr13:49065714-49065727 chr13:49065715-49065732 chr13:49065715-49065727 chr13:49065713-49065727
46	IRF1	chr13:49066615-49067021	K562	blood:	n/a	chr13:49066810-49066831
47	IRF4	chr13:49066635-49067031	GM12878	blood:	n/a	chr13:49066810-49066831
48	IRF4	chr13:49066517-49067110	GM12878	blood:	n/a	chr13:49066810-49066831
49	JUND	chr13:49066713-49067073	K562	blood:	n/a	n/a
50	MAFK	chr13:49066710-49067092	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49066969-49067019	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:49066868-49066918	Hela-S3	cervix:	n/a
3	chr13:49066969-49067019	ProgFib	skin:	n/a
4	chr13:49066868-49066918	HEEpiC	esophagus:	n/a
5	chr13:49066969-49067019	NT2-D1	testis:	n/a
6	chr13:49066868-49066918	NB4	blood:	n/a
7	chr13:49066969-49067019	SKMC	muscle:	n/a
8	chr13:49066868-49066918	HRPEpiC	eye:	n/a
9	chr13:49066868-49066918	HCT-116	colon:	n/a
10	chr13:49066868-49066918	MCF10A-Er-Src	breast:	n/a
11	chr13:49066969-49067019	SK-N-SH_RA	brain:	n/a
12	chr13:49066868-49066918	HEK293	kidney:	embryo
13	chr13:49066969-49067019	AG10803	skin:	n/a
14	chr13:49066969-49067019	CMK	blood:	n/a
15	chr13:49066868-49066918	HCF	heart:	n/a
16	chr13:49066868-49066918	NHBE	bronchial:	n/a
17	chr13:49066868-49066918	IMR90	lung:	fetal
18	chr13:49066969-49067019	SK-N-SH	brain:	n/a
19	chr13:49066868-49066918	NT2-D1	testis:	n/a
20	chr13:49066868-49066918	GM12891	blood:	n/a
21	chr13:49066868-49066918	SK-N-SH	brain:	n/a
22	chr13:49066969-49067019	NB4	blood:	n/a
23	chr13:49066868-49066918	NH-A	brain:	n/a
24	chr13:49066868-49066918	GM19239	blood:	n/a
25	chr13:49066969-49067019	LNCaP	prostate:	n/a
26	chr13:49066969-49067019	GM12891	blood:	n/a
27	chr13:49066868-49066918	HCPEpiC	choroid plexus:	n/a
28	chr13:49066969-49067019	PANC-1	pancreas:	n/a
29	chr13:49066868-49066918	T-47D	breast:	n/a
30	chr13:49066969-49067019	Caco-2	colon:	n/a
31	chr13:49066969-49067019	Jurkat	blood:	n/a
32	chr13:49066969-49067019	PrEC	prostate:	n/a
33	chr13:49066969-49067019	HRE	kidney:	n/a
34	chr13:49066969-49067019	PFSK-1	brain:	n/a
35	chr13:49066868-49066918	AG10803	skin:	n/a
36	chr13:49066969-49067019	Hepatocyte	liver:	n/a
37	chr13:49066969-49067019	ECC-1	luminal epithelium:	n/a
38	chr13:49066868-49066918	SKMC	muscle:	n/a
39	chr13:49066868-49066918	LNCaP	prostate:	n/a
40	chr13:49066868-49066918	K562	blood:	n/a
41	chr13:49066969-49067019	NHDF-neo	bronchial:	n/a
42	chr13:49066868-49066918	BJ	skin:	n/a
43	chr13:49066969-49067019	K562	blood:	n/a
44	chr13:49066868-49066918	AG04449	skin:	fetal
45	chr13:49066868-49066918	Hepatocyte	liver:	n/a
46	chr13:49066969-49067019	HRCEpiC	kidney:	n/a
47	chr13:49066969-49067019	AG04449	skin:	fetal
48	chr13:49066969-49067019	HRPEpiC	eye:	n/a
49	chr13:49066868-49066918	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:49066868-49066918	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:49063272..49066257-chr13:49067561..49069081,2	K562	blood:

Variant related genes	Relation type
RCBTB2	TF binding region
RCBTB2	CpG island

Extended variants
information (count: 133 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9332079	chr13:49063874-49063875	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9332078	chr13:49063880-49063881	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs147666176	chr13:49063886-49063887	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527884886	chr13:49063914-49063915	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs7981750	chr13:49063921-49063922	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs149175309	chr13:49063927-49063928	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs531316923	chr13:49063945-49063946	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs549830602	chr13:49063971-49063972	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs192693021	chr13:49063997-49063998	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs143282542	chr13:49064076-49064077	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs9332077	chr13:49064090-49064091	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565818978	chr13:49064103-49064104	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs549721757	chr13:49064198-49064199	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs536075595	chr13:49064206-49064207	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs555818636	chr13:49064214-49064215	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs369594536	chr13:49064216-49064217	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs9332076	chr13:49064221-49064222	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537846460	chr13:49064242-49064243	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs145466956	chr13:49064250-49064251	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs147261845	chr13:49064274-49064275	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs201477264	chr13:49064286-49064287	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs569552454	chr13:49064323-49064324	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs34823603	chr13:49064329-49064330	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs140924847	chr13:49064344-49064345	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs371775666	chr13:49064345-49064346	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs9332075	chr13:49064359-49064360	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs556132273	chr13:49064373-49064374	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs556179166	chr13:49064387-49064388	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs200254911	chr13:49064408-49064409	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs373952680	chr13:49064413-49064414	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545636810	chr13:49064422-49064423	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541137455	chr13:49064446-49064447	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560643436	chr13:49064512-49064513	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs9332074	chr13:49064514-49064515	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs56318255	chr13:49064515-49064516	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538670033	chr13:49064523-49064524	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs188087751	chr13:49064534-49064535	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9332073	chr13:49064569-49064570	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs41284770	chr13:49064653-49064654	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs9332072	chr13:49064702-49064703	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs369357506	chr13:49064776-49064777	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532012417	chr13:49064797-49064798	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs9332071	chr13:49064808-49064809	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs534873862	chr13:49064819-49064820	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs551386879	chr13:49064826-49064827	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs75650024	chr13:49064833-49064834	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs9332070	chr13:49064846-49064847	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs553366374	chr13:49064876-49064877	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs371501573	chr13:49064877-49064878	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs9332069	chr13:49064878-49064879	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Autism	22495309	CNVD

Chromatin state (count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49023800-49073800	Weak transcription	NH-A	brain
2	chr13:49025600-49066200	Weak transcription	Psoas Muscle	Psoas
3	chr13:49028000-49071000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr13:49030600-49070600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr13:49031600-49066200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr13:49031800-49065400	Weak transcription	Brain Substantia Nigra	brain
7	chr13:49032000-49065600	Weak transcription	Brain Anterior Caudate	brain
8	chr13:49032000-49066200	Weak transcription	Colonic Mucosa	Colon
9	chr13:49032400-49066200	Weak transcription	Spleen	Spleen
10	chr13:49032400-49066600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr13:49032400-49066600	Weak transcription	Ovary	ovary
12	chr13:49032400-49067400	Weak transcription	Pancreas	Pancrea
13	chr13:49032400-49067600	Weak transcription	Gastric	stomach
14	chr13:49032800-49066200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr13:49034400-49073800	Weak transcription	Esophagus	oesophagus
16	chr13:49035200-49073400	Weak transcription	Fetal Intestine Small	intestine
17	chr13:49035600-49065400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr13:49035600-49066000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr13:49035800-49066400	Weak transcription	NHEK	skin
20	chr13:49049800-49066200	Weak transcription	Lung	lung
21	chr13:49050000-49065600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr13:49051200-49064800	Weak transcription	Brain Hippocampus Middle	brain
23	chr13:49051800-49065400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr13:49052800-49064800	Weak transcription	Liver	Liver
25	chr13:49053600-49071200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr13:49053800-49066600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr13:49054000-49094000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:49054200-49064800	Weak transcription	Thymus	Thymus
29	chr13:49054200-49066600	Weak transcription	Aorta	Aorta
30	chr13:49054400-49064800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr13:49054400-49065600	Weak transcription	HUVEC	blood vessel
32	chr13:49054400-49065800	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr13:49054400-49065800	Weak transcription	NHLF	lung
34	chr13:49054400-49066200	Weak transcription	Brain Angular Gyrus	brain
35	chr13:49054400-49066200	Weak transcription	Placenta	Placenta
36	chr13:49054400-49066200	Weak transcription	HSMMtube	muscle
37	chr13:49054400-49066400	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr13:49054400-49066600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:49054600-49065600	Weak transcription	Duodenum Mucosa	Duodenum
40	chr13:49054600-49065600	Weak transcription	Osteobl	bone
41	chr13:49054600-49066000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr13:49054600-49066200	Weak transcription	HMEC	breast
43	chr13:49055000-49065600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr13:49056600-49065600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr13:49057400-49064600	Weak transcription	Primary hematopoietic stem cells	blood
46	chr13:49057400-49068400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr13:49058800-49065400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr13:49060400-49064600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr13:49060600-49067400	Weak transcription	Stomach Mucosa	stomach
50	chr13:49061200-49065400	Weak transcription	Small Intestine	intestine

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