Variant report

Variant	esv3327826
Chromosome Location	chr13:30880377-30882925
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:484)
CpG islands
(count:1039)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:30881565-30881753	K562	blood:	n/a	n/a
2	ARID3A	chr13:30882712-30883117	K562	blood:	n/a	n/a
3	ATF3	chr13:30881135-30881372	HepG2	liver:	n/a	n/a
4	ATF3	chr13:30881143-30881362	K562	blood:	n/a	n/a
5	BACH1	chr13:30882686-30883008	H1-hESC	embryonic stem cell:	n/a	chr13:30882832-30882846
6	BACH1	chr13:30882437-30883242	K562	blood:	n/a	chr13:30882832-30882846
7	BACH1	chr13:30881031-30882053	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:30880487-30880754	GM12878	blood:	n/a	n/a
9	BATF	chr13:30882588-30882917	GM12878	blood:	n/a	chr13:30882760-30882769 chr13:30882835-30882846
10	BATF	chr13:30882670-30883026	GM12878	blood:	n/a	chr13:30882760-30882769 chr13:30882835-30882846
11	BCLAF1	chr13:30880798-30881844	GM12878	blood:	n/a	chr13:30881584-30881593 chr13:30881201-30881214 chr13:30881608-30881621 chr13:30881671-30881680
12	BHLHE40	chr13:30880804-30881895	GM12878	blood:	n/a	chr13:30881610-30881626
13	BHLHE40	chr13:30881231-30881483	A549	lung:	n/a	n/a
14	BHLHE40	chr13:30882728-30882933	K562	blood:	n/a	n/a
15	BHLHE40	chr13:30881000-30881870	HepG2	liver:	n/a	chr13:30881610-30881626
16	BHLHE40	chr13:30880933-30881937	K562	blood:	n/a	chr13:30881610-30881626
17	BRCA1	chr13:30881711-30881766	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr13:30881209-30881669	GM12878	blood:	n/a	n/a
19	BRCA1	chr13:30880786-30881427	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr13:30881793-30881961	HepG2	liver:	n/a	n/a
21	CBX3	chr13:30881633-30881968	K562	blood:	n/a	n/a
22	CBX3	chr13:30882677-30883082	K562	blood:	n/a	n/a
23	CCNT2	chr13:30880910-30882019	K562	blood:	n/a	n/a
24	CEBPB	chr13:30882904-30883189	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:30882735-30883133	K562	blood:	n/a	n/a
26	CEBPB	chr13:30880411-30880833	A549	lung:	n/a	chr13:30880612-30880625
27	CEBPB	chr13:30880533-30881116	Hela-S3	cervix:	n/a	chr13:30880612-30880625
28	CEBPB	chr13:30882833-30883124	K562	blood:	n/a	n/a
29	CEBPB	chr13:30882887-30883166	A549	lung:	n/a	n/a
30	CEBPB	chr13:30882854-30883155	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:30882883-30883068	K562	blood:	n/a	n/a
32	CEBPB	chr13:30882814-30883286	A549	lung:	n/a	n/a
33	CEBPB	chr13:30882827-30883207	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:30880449-30880822	K562	blood:	n/a	chr13:30880612-30880625
35	CEBPB	chr13:30881063-30881427	K562	blood:	n/a	n/a
36	CEBPD	chr13:30881330-30881753	HepG2	liver:	n/a	n/a
37	CHD1	chr13:30880745-30881595	GM12878	blood:	n/a	n/a
38	CHD1	chr13:30881854-30882041	GM12878	blood:	n/a	chr13:30881906-30881913
39	CHD2	chr13:30880991-30881803	HepG2	liver:	n/a	n/a
40	CHD2	chr13:30880887-30881224	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr13:30881476-30882022	H1-hESC	embryonic stem cell:	n/a	chr13:30881906-30881913
42	CHD2	chr13:30880896-30881983	K562	blood:	n/a	chr13:30881906-30881913
43	CHD2	chr13:30880894-30881881	GM12878	blood:	n/a	n/a
44	CHD2	chr13:30880857-30881975	Hela-S3	cervix:	n/a	chr13:30881906-30881913
45	CREB1	chr13:30881103-30881955	A549	lung:	n/a	n/a
46	CTBP2	chr13:30880919-30882100	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr13:30881640-30881790	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr13:30881640-30881790	GM12870	blood:	n/a	n/a
49	CTCF	chr13:30881761-30881823	GM19239	blood:	n/a	n/a
50	CTCF	chr13:30881660-30881810	GM12864	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:30882905-30882955	Hela-S3	cervix:	n/a
2	chr13:30881232-30881282	HUVEC	blood vessel:	n/a
3	chr13:30882905-30882955	Hela-S3	cervix:	n/a
4	chr13:30881232-30881282	HUVEC	blood vessel:	n/a
5	chr13:30881194-30881244	HMEC	breast:	n/a
6	chr13:30881938-30881988	HUVEC	blood vessel:	n/a
7	chr13:30881096-30881146	HIPEpiC	eye:	n/a
8	chr13:30880827-30880877	NHDF-neo	bronchial:	n/a
9	chr13:30881232-30881282	RPTEC	kidney:	n/a
10	chr13:30881323-30881373	K562	blood:	n/a
11	chr13:30881210-30881260	SAEC	small airway:	n/a
12	chr13:30881675-30881725	RPTEC	kidney:	n/a
13	chr13:30881691-30881741	RPTEC	kidney:	n/a
14	chr13:30881210-30881260	A549	lung:	n/a
15	chr13:30880827-30880877	NB4	blood:	n/a
16	chr13:30881703-30881753	PFSK-1	brain:	n/a
17	chr13:30882905-30882955	HL-60	blood:	n/a
18	chr13:30881675-30881725	HAEpiC	amniotic membrane:	n/a
19	chr13:30880900-30880950	SK-N-MC	brain:	n/a
20	chr13:30881675-30881725	AG09309	skin:	n/a
21	chr13:30881437-30881487	AG09319	gingival:	n/a
22	chr13:30881527-30881577	AG09319	gingival:	n/a
23	chr13:30882067-30882117	LNCaP	prostate:	n/a
24	chr13:30881232-30881282	HCF	heart:	n/a
25	chr13:30881267-30881317	HNPCEpiC	eye:	n/a
26	chr13:30881096-30881146	H1-hESC	embryonic stem cell:	embryo
27	chr13:30881194-30881244	HAEpiC	amniotic membrane:	n/a
28	chr13:30881766-30881816	GM12891	blood:	n/a
29	chr13:30881527-30881577	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:30881096-30881146	HRCEpiC	kidney:	n/a
31	chr13:30881267-30881317	HepG2	liver:	n/a
32	chr13:30881938-30881988	HRPEpiC	eye:	n/a
33	chr13:30881766-30881816	SAEC	small airway:	n/a
34	chr13:30881675-30881725	AG04449	skin:	fetal
35	chr13:30881267-30881317	NB4	blood:	n/a
36	chr13:30881691-30881741	AoSMC	blood vessel:	n/a
37	chr13:30881766-30881816	Jurkat	blood:	n/a
38	chr13:30881691-30881741	HAEpiC	amniotic membrane:	n/a
39	chr13:30881675-30881725	HMEC	breast:	n/a
40	chr13:30881437-30881487	GM12891	blood:	n/a
41	chr13:30881703-30881753	RPTEC	kidney:	n/a
42	chr13:30882067-30882117	HL-60	blood:	n/a
43	chr13:30881210-30881260	HEK293	kidney:	embryo
44	chr13:30881527-30881577	HEEpiC	esophagus:	n/a
45	chr13:30881527-30881577	HNPCEpiC	eye:	n/a
46	chr13:30881703-30881753	HEK293	kidney:	embryo
47	chr13:30881527-30881577	A549	lung:	n/a
48	chr13:30881703-30881753	ProgFib	skin:	n/a
49	chr13:30881323-30881373	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:30881691-30881741	ProgFib	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:30882921..30884448-chr13:30901661..30903319,2	K562	blood:
2	chr13:30880213..30882773-chr13:31038194..31039987,2	K562	blood:
3	chr13:30881311..30882964-chr13:31038012..31040659,2	K562	blood:
4	chr13:30882203..30884087-chr13:30995822..30997883,2	MCF-7	breast:

No data

Variant related genes	Relation type
KATNAL1	TF binding region
KATNAL1	CpG island
ENSG00000225039	chromatin interactions
ENSG00000189403	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368032845	chr13:30880430-30880431	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs557452770	chr13:30880494-30880495	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577211209	chr13:30880534-30880535	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs202081	chr13:30880547-30880548	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200494989	chr13:30880588-30880589	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201576199	chr13:30880589-30880590	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs199568716	chr13:30880591-30880592	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111726921	chr13:30880593-30880594	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs573067536	chr13:30880594-30880595	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs56034729	chr13:30880598-30880599	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2073952	chr13:30880599-30880600	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs191275841	chr13:30880639-30880640	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146304919	chr13:30880706-30880707	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545835333	chr13:30880720-30880721	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183081992	chr13:30880738-30880739	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543942176	chr13:30880802-30880803	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537626618	chr13:30880836-30880837	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116650258	chr13:30880965-30880966	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs532971775	chr13:30880970-30880971	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546262718	chr13:30881014-30881015	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs560060245	chr13:30881020-30881021	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs202082	chr13:30881026-30881027	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs187288450	chr13:30881065-30881066	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs571092938	chr13:30881125-30881126	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192230306	chr13:30881134-30881135	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531933299	chr13:30881149-30881150	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138390939	chr13:30881150-30881151	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs386378683	chr13:30881152-30881153	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201466969	chr13:30881157-30881158	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs10624978	chr13:30881158-30881159	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551144222	chr13:30881177-30881178	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs570837798	chr13:30881185-30881186	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539884403	chr13:30881192-30881193	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs202083	chr13:30881316-30881317	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs566808480	chr13:30881355-30881356	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs535368773	chr13:30881368-30881369	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139045051	chr13:30881369-30881370	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs575141384	chr13:30881388-30881389	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs543980916	chr13:30881412-30881413	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs118093333	chr13:30881457-30881458	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs375800636	chr13:30881460-30881461	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs537259935	chr13:30881466-30881467	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs540758502	chr13:30881532-30881533	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542904058	chr13:30881538-30881539	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531775135	chr13:30881540-30881541	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs540295703	chr13:30881564-30881565	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs6490453	chr13:30881573-30881574	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528844771	chr13:30881579-30881580	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183198202	chr13:30881596-30881597	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs563013376	chr13:30881599-30881600	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Squamous cell cancer	20885788	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Malignant glioma	17146433	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
Acute lymphoblastic leukemia	21339820	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Retinoblastoma	22278416	CNVD
Peters Plus syndrome	16909395	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Ovarian cancer	19047089	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21147910	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30861000-30880800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:30866800-30880800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr13:30868400-30880800	Weak transcription	Left Ventricle	heart
4	chr13:30870800-30880400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr13:30871000-30880400	Weak transcription	Fetal Intestine Small	intestine
6	chr13:30871000-30880400	Weak transcription	Right Ventricle	heart
7	chr13:30876000-30880600	Enhancers	Fetal Brain Male	brain
8	chr13:30876200-30880400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:30876200-30880600	Weak transcription	Ovary	ovary
10	chr13:30876400-30880800	Weak transcription	Lung	lung
11	chr13:30876600-30880600	Enhancers	Fetal Heart	heart
12	chr13:30877000-30880600	Enhancers	Primary B cells from cord blood	blood
13	chr13:30877200-30880400	Enhancers	HepG2	liver
14	chr13:30877200-30880600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr13:30877400-30880600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:30877400-30880600	Enhancers	Primary B cells from peripheral blood	blood
17	chr13:30877800-30880400	Flanking Active TSS	Dnd41	blood
18	chr13:30877800-30880800	Weak transcription	Spleen	Spleen
19	chr13:30878000-30880600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr13:30878000-30880600	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr13:30878200-30880400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr13:30878200-30880600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr13:30878400-30880600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr13:30878800-30880400	Enhancers	Brain Anterior Caudate	brain
25	chr13:30878800-30880600	Weak transcription	Brain Hippocampus Middle	brain
26	chr13:30878800-30880800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:30879000-30880400	Enhancers	Rectal Smooth Muscle	rectum
28	chr13:30879000-30880600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr13:30879400-30880400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr13:30879400-30880400	Enhancers	Fetal Lung	lung
31	chr13:30879400-30880400	Enhancers	HSMM	muscle
32	chr13:30879400-30880600	Enhancers	Brain Substantia Nigra	brain
33	chr13:30879400-30880800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
34	chr13:30879400-30881000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:30879600-30880400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:30879600-30880400	Enhancers	Fetal Muscle Leg	muscle
37	chr13:30879600-30880400	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr13:30879600-30880600	Enhancers	Primary hematopoietic stem cells	blood
39	chr13:30879600-30880600	Enhancers	Hela-S3	cervix
40	chr13:30879600-30880600	Enhancers	HSMMtube	muscle
41	chr13:30879600-30881000	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr13:30879600-30881000	Flanking Active TSS	HUVEC	blood vessel
43	chr13:30879600-30881600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr13:30879600-30882000	Active TSS	A549	lung
45	chr13:30879800-30880400	Enhancers	Fetal Intestine Large	intestine
46	chr13:30879800-30880400	Weak transcription	Right Atrium	heart
47	chr13:30879800-30880600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr13:30879800-30880600	Weak transcription	Fetal Kidney	kidney
49	chr13:30879800-30880600	Flanking Active TSS	NHEK	skin
50	chr13:30879800-30880800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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