Variant report

Variant	nsv977365
Chromosome Location	chr13:37576107-37580409
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:37576364-37576597	K562	blood:	n/a	n/a
2	BACH1	chr13:37576507-37576522	K562	blood:	n/a	n/a
3	CHD1	chr13:37576926-37576974	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr13:37579176-37579256	GM13976	blood:	n/a	n/a
5	FOS	chr13:37577209-37577484	MCF10A-Er-Src	breast:	n/a	n/a
6	FOS	chr13:37577273-37577477	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr13:37577194-37577482	MCF10A-Er-Src	breast:	n/a	n/a
8	IRF1	chr13:37576913-37576921	K562	blood:	n/a	n/a
9	MAFF	chr13:37576042-37576489	K562	blood:	n/a	n/a
10	MXI1	chr13:37576040-37576517	K562	blood:	n/a	n/a
11	MXI1	chr13:37572479-37576541	SK-N-SH	brain:	n/a	n/a
12	MXI1	chr13:37579333-37579475	K562	blood:	n/a	n/a
13	MYC	chr13:37576156-37576569	K562	blood:	n/a	chr13:37576396-37576403
14	MYC	chr13:37579761-37579800	MCF-7	breast:	n/a	n/a
15	POLR2A	chr13:37577412-37577424	MCF-7	breast:	n/a	n/a
16	POLR2A	chr13:37578473-37578475	HepG2	liver:	n/a	n/a
17	POLR2A	chr13:37577010-37577191	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr13:37575540-37576775	GM12878	blood:	n/a	n/a
19	POLR2A	chr13:37572561-37576455	MCF-7	breast:	n/a	n/a
20	POLR2A	chr13:37579309-37579324	MCF-7	breast:	n/a	n/a
21	POLR2A	chr13:37578492-37578499	MCF-7	breast:	n/a	n/a
22	POLR2A	chr13:37580059-37580122	MCF-7	breast:	n/a	n/a
23	POLR2A	chr13:37578447-37578464	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr13:37576963-37577169	MCF-7	breast:	n/a	n/a
25	POLR2A	chr13:37576172-37576173	K562	blood:	n/a	n/a
26	POLR2A	chr13:37575981-37576257	ProgFib	skin:	n/a	n/a
27	POLR2A	chr13:37579622-37579811	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr13:37573181-37576379	K562	blood:	n/a	n/a
29	POLR2A	chr13:37572468-37576172	GM18505	blood:	n/a	n/a
30	POLR2A	chr13:37579039-37579079	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr13:37578461-37578547	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr13:37578505-37578510	MCF-7	breast:	n/a	n/a
33	POLR2A	chr13:37578532-37578567	HUVEC	blood vessel:	n/a	n/a
34	POLR2A	chr13:37579905-37579949	GM12878	blood:	n/a	n/a
35	POLR2A	chr13:37578349-37578775	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr13:37578970-37579027	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr13:37579778-37579813	MCF-7	breast:	n/a	n/a
38	POLR2A	chr13:37578398-37578672	HepG2	liver:	n/a	n/a
39	POLR2A	chr13:37579596-37580145	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr13:37572632-37576457	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr13:37577275-37577438	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr13:37579642-37580025	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr13:37579635-37579983	MCF-7	breast:	n/a	n/a
44	POLR2A	chr13:37577574-37577862	HepG2	liver:	n/a	n/a
45	POLR2A	chr13:37572373-37576273	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr13:37575465-37576317	U87	brain:	n/a	n/a
47	POLR2A	chr13:37572272-37576402	HepG2	liver:	n/a	n/a
48	POLR2A	chr13:37574342-37576370	SK-N-SH	brain:	n/a	n/a
49	POLR2A	chr13:37578431-37578629	HepG2	liver:	n/a	n/a
50	POLR2A	chr13:37580004-37580345	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:37578846-37578896	HUVEC	blood vessel:	n/a
2	chr13:37578846-37578896	SKMC	muscle:	n/a
3	chr13:37578846-37578896	A549	lung:	n/a
4	chr13:37578846-37578896	Hela-S3	cervix:	n/a
5	chr13:37578846-37578896	K562	blood:	n/a
6	chr13:37578846-37578896	NB4	blood:	n/a
7	chr13:37578846-37578896	IMR90	lung:	fetal
8	chr13:37578846-37578896	AG04449	skin:	fetal
9	chr13:37578846-37578896	HMEC	breast:	n/a
10	chr13:37578846-37578896	PFSK-1	brain:	n/a
11	chr13:37578846-37578896	HepG2	liver:	n/a
12	chr13:37578846-37578896	HCT-116	colon:	n/a
13	chr13:37578846-37578896	Hepatocyte	liver:	n/a
14	chr13:37578846-37578896	HL-60	blood:	n/a
15	chr13:37578846-37578896	BJ	skin:	n/a
16	chr13:37578846-37578896	HIPEpiC	eye:	n/a
17	chr13:37578846-37578896	BE2_C	brain:	n/a
18	chr13:37578846-37578896	PrEC	prostate:	n/a
19	chr13:37578846-37578896	AG10803	skin:	n/a
20	chr13:37578846-37578896	SAEC	small airway:	n/a
21	chr13:37578846-37578896	HEEpiC	esophagus:	n/a
22	chr13:37578846-37578896	ovcar-3	ovarian:	n/a
23	chr13:37578846-37578896	HCPEpiC	choroid plexus:	n/a
24	chr13:37578846-37578896	GM06990	blood:	n/a
25	chr13:37578846-37578896	SK-N-MC	brain:	n/a
26	chr13:37578846-37578896	AG09319	gingival:	n/a
27	chr13:37578846-37578896	Caco-2	colon:	n/a
28	chr13:37578846-37578896	HRPEpiC	eye:	n/a
29	chr13:37578846-37578896	ECC-1	luminal epithelium:	n/a
30	chr13:37578846-37578896	NHBE	bronchial:	n/a
31	chr13:37578846-37578896	PANC-1	pancreas:	n/a
32	chr13:37578846-37578896	ProgFib	skin:	n/a
33	chr13:37578846-37578896	HAEpiC	amniotic membrane:	n/a
34	chr13:37578846-37578896	RPTEC	kidney:	n/a
35	chr13:37578846-37578896	GM12891	blood:	n/a
36	chr13:37578846-37578896	H1-hESC	embryonic stem cell:	embryo
37	chr13:37578846-37578896	SK-N-SH	brain:	n/a
38	chr13:37578846-37578896	HNPCEpiC	eye:	n/a
39	chr13:37578846-37578896	LNCaP	prostate:	n/a
40	chr13:37578846-37578896	U87	brain:	n/a
41	chr13:37578846-37578896	HCF	heart:	n/a
42	chr13:37578846-37578896	MCF10A-Er-Src	breast:	n/a
43	chr13:37578846-37578896	HRE	kidney:	n/a
44	chr13:37578846-37578896	GM19239	blood:	n/a
45	chr13:37578846-37578896	MCF-7	breast:	n/a
46	chr13:37578846-37578896	AG04450	lung:	fetal
47	chr13:37578846-37578896	SK-N-SH_RA	brain:	n/a
48	chr13:37578846-37578896	HPAEpiC	pulmonary alveolar:	n/a
49	chr13:37578846-37578896	HCM	heart:	n/a
50	chr13:37578846-37578896	T-47D	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:37573339..37577948-chr13:37631578..37635345,7	K562	blood:
2	chr13:37573411..37578166-chr13:37631570..37635674,7	MCF-7	breast:
3	chr13:37570200..37576399-chr13:37580273..37587423,15	MCF-7	breast:
4	chr13:37572134..37576910-chr13:37632372..37635841,8	MCF-7	breast:
5	chr13:37572711..37577948-chr13:37631792..37635345,6	K562	blood:
6	chr13:37571989..37576230-chr13:37592486..37599969,7	MCF-7	breast:
7	chr13:37571801..37576368-chr13:37598708..37601979,7	MCF-7	breast:
8	chr13:37570200..37576399-chr13:37580273..37587423,15	MCF-7	breast:

No data

Variant related genes	Relation type
EXOSC8	TF binding region
ALG5	TF binding region
EXOSC8	CpG island
ALG5	CpG island
ENSG00000102710	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000120697	chromatin interactions

Extended variants
information (count: 172 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545164221	chr13:37576122-37576123	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs184031999	chr13:37576134-37576135	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs370582511	chr13:37576137-37576138	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs530532439	chr13:37576146-37576147	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs140192725	chr13:37576212-37576213	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs143855245	chr13:37576229-37576230	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs535572723	chr13:37576281-37576282	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs188372980	chr13:37576283-37576284	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs551091674	chr13:37576324-37576325	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs201843398	chr13:37576375-37576376	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs377264694	chr13:37576389-37576390	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs566342827	chr13:37576413-37576414	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs533406536	chr13:37576414-37576415	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs77177263	chr13:37576466-37576467	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368766707	chr13:37576472-37576473	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs570221508	chr13:37576547-37576548	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs537545724	chr13:37576567-37576568	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs555869080	chr13:37576577-37576578	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs3819029	chr13:37576598-37576599	Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs144158336	chr13:37576613-37576614	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs111604467	chr13:37576615-37576616	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs138423344	chr13:37576683-37576684	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs371499255	chr13:37576686-37576687	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs140557324	chr13:37576695-37576696	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs369415503	chr13:37576699-37576700	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368725606	chr13:37576707-37576708	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs372690048	chr13:37576724-37576725	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs534999679	chr13:37576741-37576742	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553019262	chr13:37576749-37576750	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs544440175	chr13:37576789-37576790	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs577863189	chr13:37576811-37576812	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544913389	chr13:37576820-37576821	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs116120295	chr13:37576844-37576845	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs142795092	chr13:37576852-37576853	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs35560394	chr13:37576867-37576868	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs181023796	chr13:37576918-37576919	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs374256517	chr13:37576951-37576952	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528103305	chr13:37576976-37576977	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs540222395	chr13:37576977-37576978	Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs559836541	chr13:37577011-37577012	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs377141803	chr13:37577042-37577043	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533688679	chr13:37577043-37577044	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs114554307	chr13:37577046-37577047	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11550133	chr13:37577094-37577095	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs570284201	chr13:37577111-37577112	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs531091502	chr13:37577118-37577119	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs112146399	chr13:37577130-37577131	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs370644485	chr13:37577136-37577137	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201694694	chr13:37577149-37577150	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs185050901	chr13:37577189-37577190	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	18641027	CNVD
Prostate cancer	16573809	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
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21965145	CNVD
Hirschsprung''s Disease	21712996	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Monoclonal gammopathy of undetermined significance	19135901	CNVD
Prostate cancer	19242612	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
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37571600-37576200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:37571800-37576200	Active TSS	GM12878-XiMat	blood
3	chr13:37571800-37576400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr13:37571800-37576400	Active TSS	K562	blood
5	chr13:37572200-37576200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr13:37572200-37576200	Active TSS	Hela-S3	cervix
7	chr13:37572200-37576400	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr13:37572200-37576400	Active TSS	H1 Cell Line	embryonic stem cell
9	chr13:37572400-37576200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr13:37572400-37576200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:37572400-37576400	Active TSS	A549	lung
12	chr13:37572400-37576600	Active TSS	NHLF	lung
13	chr13:37572600-37576200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr13:37572600-37576200	Active TSS	NHEK	skin
15	chr13:37572600-37576400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr13:37572600-37576400	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr13:37572600-37576400	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr13:37572600-37576600	Active TSS	HMEC	breast
19	chr13:37572800-37576200	Active TSS	Thymus	Thymus
20	chr13:37573000-37576400	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr13:37573200-37576200	Active TSS	Primary T cells fromperipheralblood	blood
22	chr13:37573400-37576400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr13:37574000-37576600	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr13:37575400-37576200	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr13:37575400-37576200	Flanking Active TSS	Liver	Liver
26	chr13:37575400-37576400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr13:37575400-37576400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:37575400-37576400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr13:37575400-37576400	Flanking Active TSS	Fetal Brain Female	brain
30	chr13:37575400-37580600	Weak transcription	Small Intestine	intestine
31	chr13:37575400-37583800	Weak transcription	Spleen	Spleen
32	chr13:37575400-37631200	Weak transcription	Stomach Mucosa	stomach
33	chr13:37575600-37576200	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr13:37575600-37576200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
35	chr13:37575600-37576200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr13:37575600-37576200	Flanking Active TSS	Brain Germinal Matrix	brain
37	chr13:37575600-37576400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr13:37575600-37576400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:37575600-37576400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
40	chr13:37575600-37576400	Flanking Active TSS	HUVEC	blood vessel
41	chr13:37575600-37576400	Flanking Active TSS	NH-A	brain
42	chr13:37575600-37576400	Flanking Active TSS	Osteobl	bone
43	chr13:37575600-37577600	Weak transcription	Left Ventricle	heart
44	chr13:37575600-37577600	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr13:37575600-37578000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:37575600-37578000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr13:37575600-37578200	Weak transcription	Lung	lung
48	chr13:37575600-37578200	Weak transcription	Ovary	ovary
49	chr13:37575600-37578800	Weak transcription	Aorta	Aorta
50	chr13:37575600-37583800	Weak transcription	Esophagus	oesophagus

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