Variant report

Variant	nsv1042545
Chromosome Location	chr13:65686275-66219510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1800)
CpG islands
(count:367)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1800 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:66035822-66036144	K562	blood:	n/a	n/a
2	ATF2	chr13:65811028-65811336	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:65810994-65811320	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:66080137-66080390	GM12878	blood:	n/a	n/a
5	BATF	chr13:66041811-66041993	GM12878	blood:	n/a	chr13:66041940-66041951
6	BATF	chr13:65988370-65988595	GM12878	blood:	n/a	n/a
7	BCL11A	chr13:65728776-65729031	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:65728758-65729389	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:65735980-65735994	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:65728169-65728408	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:66212820-66213067	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:65848293-65848391	HepG2	liver:	n/a	n/a
13	BRCA1	chr13:65888304-65888377	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:66035765-66036027	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr13:66212653-66213113	HCT-116	colon:	n/a	n/a
16	CBX3	chr13:65953042-65953530	HCT-116	colon:	n/a	n/a
17	CEBPB	chr13:65879841-65879954	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr13:65917105-65917448	HepG2	liver:	n/a	chr13:65917266-65917277
19	CEBPB	chr13:66172575-66172866	A549	lung:	n/a	n/a
20	CEBPB	chr13:65985052-65985387	IMR90	lung:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
21	CEBPB	chr13:66005778-66005860	HepG2	liver:	n/a	chr13:66005831-66005842
22	CEBPB	chr13:65942914-65943137	A549	lung:	n/a	chr13:65942991-65943002
23	CEBPB	chr13:65701753-65702029	K562	blood:	n/a	chr13:65701896-65701907
24	CEBPB	chr13:65871278-65871649	IMR90	lung:	n/a	chr13:65871438-65871449
25	CEBPB	chr13:65853651-65853796	A549	lung:	n/a	n/a
26	CEBPB	chr13:66095982-66096144	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:65936220-65936361	HepG2	liver:	n/a	chr13:65936278-65936290
28	CEBPB	chr13:66071327-66071819	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr13:66172507-66172920	IMR90	lung:	n/a	chr13:66172550-66172561
30	CEBPB	chr13:65686596-65687156	Hela-S3	cervix:	n/a	chr13:65686877-65686890
31	CEBPB	chr13:66048985-66049163	A549	lung:	n/a	n/a
32	CEBPB	chr13:65827820-65828305	MCF-7	breast:	n/a	n/a
33	CEBPB	chr13:66212723-66213083	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:65811009-65811379	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr13:65873055-65873231	A549	lung:	n/a	n/a
36	CEBPB	chr13:66095944-66096227	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:65861564-65861927	HepG2	liver:	n/a	chr13:65861702-65861713 chr13:65861745-65861756
38	CEBPB	chr13:66179445-66179793	IMR90	lung:	n/a	chr13:66179676-66179689 chr13:66179676-66179689 chr13:66179504-66179517 chr13:66179506-66179517 chr13:66179504-66179517 chr13:66179506-66179517 chr13:66179504-66179517 chr13:66179678-66179689
39	CEBPB	chr13:65807064-65807325	HepG2	liver:	n/a	chr13:65807217-65807228
40	CEBPB	chr13:65701718-65702064	IMR90	lung:	n/a	chr13:65701896-65701907
41	CEBPB	chr13:65807097-65807352	A549	lung:	n/a	chr13:65807217-65807228
42	CEBPB	chr13:65853535-65853835	IMR90	lung:	n/a	n/a
43	CEBPB	chr13:65827880-65828240	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr13:65985060-65985370	HepG2	liver:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
45	CEBPB	chr13:65861550-65861926	IMR90	lung:	n/a	chr13:65861702-65861713 chr13:65861745-65861756
46	CEBPB	chr13:65777153-65777273	H1-hESC	embryonic stem cell:	n/a	chr13:65777247-65777258
47	CEBPB	chr13:66172480-66172999	A549	lung:	n/a	chr13:66172550-66172561
48	CEBPB	chr13:66022805-66023052	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:66071382-66071755	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:66071321-66071771	ECC-1	luminal epithelium:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65724231-65724281	HRCEpiC	kidney:	n/a
2	chr13:65724231-65724281	HRCEpiC	kidney:	n/a
3	chr13:65884020-65884070	AG04450	lung:	fetal
4	chr13:65884020-65884070	A549	lung:	n/a
5	chr13:66156848-66156898	BJ	skin:	n/a
6	chr13:66156848-66156898	ECC-1	luminal epithelium:	n/a
7	chr13:65884020-65884070	HAEpiC	amniotic membrane:	n/a
8	chr13:65724231-65724281	HCT-116	colon:	n/a
9	chr13:66156848-66156898	AG04449	skin:	fetal
10	chr13:66156848-66156898	AG04450	lung:	fetal
11	chr13:65884209-65884259	AG09309	skin:	n/a
12	chr13:65724231-65724281	MCF10A-Er-Src	breast:	n/a
13	chr13:65904937-65904987	HAEpiC	amniotic membrane:	n/a
14	chr13:66156848-66156898	Hela-S3	cervix:	n/a
15	chr13:65904937-65904987	NT2-D1	testis:	n/a
16	chr13:65904937-65904987	HepG2	liver:	n/a
17	chr13:65904937-65904987	GM12891	blood:	n/a
18	chr13:65904937-65904987	PrEC	prostate:	n/a
19	chr13:65884020-65884070	ECC-1	luminal epithelium:	n/a
20	chr13:65724231-65724281	HepG2	liver:	n/a
21	chr13:65884020-65884070	ovcar-3	ovarian:	n/a
22	chr13:65724231-65724281	GM12891	blood:	n/a
23	chr13:65911268-65911318	NH-A	brain:	n/a
24	chr13:65884209-65884259	SK-N-SH_RA	brain:	n/a
25	chr13:65884020-65884070	MCF-7	breast:	n/a
26	chr13:66156848-66156898	NHDF-neo	bronchial:	n/a
27	chr13:66156848-66156898	K562	blood:	n/a
28	chr13:66156848-66156898	AG09309	skin:	n/a
29	chr13:65884020-65884070	AG09319	gingival:	n/a
30	chr13:65911268-65911318	HRCEpiC	kidney:	n/a
31	chr13:65911268-65911318	AG04449	skin:	fetal
32	chr13:65904937-65904987	Jurkat	blood:	n/a
33	chr13:65904937-65904987	HCPEpiC	choroid plexus:	n/a
34	chr13:65904937-65904987	H1-hESC	embryonic stem cell:	embryo
35	chr13:65724231-65724281	AG09309	skin:	n/a
36	chr13:65884209-65884259	HL-60	blood:	n/a
37	chr13:66156848-66156898	HAEpiC	amniotic membrane:	n/a
38	chr13:65884209-65884259	AoSMC	blood vessel:	n/a
39	chr13:65884209-65884259	ovcar-3	ovarian:	n/a
40	chr13:66156848-66156898	PFSK-1	brain:	n/a
41	chr13:65724231-65724281	HPAEpiC	pulmonary alveolar:	n/a
42	chr13:65724231-65724281	Jurkat	blood:	n/a
43	chr13:66156848-66156898	SK-N-SH	brain:	n/a
44	chr13:65911268-65911318	HMEC	breast:	n/a
45	chr13:65884020-65884070	LNCaP	prostate:	n/a
46	chr13:65884020-65884070	K562	blood:	n/a
47	chr13:65911268-65911318	AG10803	skin:	n/a
48	chr13:65884209-65884259	IMR90	lung:	fetal
49	chr13:65904937-65904987	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:65884209-65884259	HRCEpiC	kidney:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
2	chr13:65721248..65723334-chr13:65726895..65729400,2	K562	blood:
3	chr13:65721248..65723334-chr13:65726895..65729400,2	K562	blood:
4	chr13:65045929..65046727-chr13:66212514..66213321,2	MCF-7	breast:
5	chr13:65697187..65698862-chr13:65702366..65704985,2	K562	blood:
6	chr12:120729600..120731304-chr13:65821466..65822966,4	K562	blood:
7	chr13:65796967..65799458-chr13:65799743..65801550,2	MCF-7	breast:
8	chr13:65697187..65698862-chr13:65702366..65704985,2	K562	blood:
9	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
10	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
11	chr13:65713474..65715643-chr13:65725699..65727986,2	K562	blood:
12	chr12:120729601..120731270-chr13:65821466..65822966,2	K562	blood:
13	chr13:65796967..65799458-chr13:65799743..65801550,2	MCF-7	breast:
14	chr13:65787284..65789901-chr13:65800998..65803685,2	MCF-7	breast:
15	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
16	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
17	chr12:120730575..120731437-chr13:65821446..65821946,4	HCT-116	colon:
18	chr13:65713474..65715643-chr13:65725699..65727986,2	K562	blood:
19	chr12:120729617..120731155-chr13:65821446..65822966,3	MCF-7	breast:
20	chr13:65020257..65021157-chr13:66212532..66213123,2	MCF-7	breast:
21	chr13:65720664..65721646-chr3:80013843..80014668,2	MCF-7	breast:
22	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
23	chr12:120730653..120731282-chr13:65820966..65821966,3	MCF-7	breast:
24	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:
25	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:
26	chr1:106318966..106319467-chr13:66093606..66094106,2	NB4	blood:
27	chr13:66046639..66047382-chr3:13541452..13542407,2	MCF-7	breast:
28	chr12:120729593..120731262-chr13:65821446..65822946,2	MCF-7	breast:
29	chr13:65787284..65789901-chr13:65800998..65803685,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-7	chr13:66035510-66035584	NONHSAT034194
2	lnc-PCDH9-10	chr13:65880203-65881304	ucscGeneNc_uc001vim_2
3	lnc-PCDH9-7	chr13:66015947-66016044	NONHSAT034194
4	lnc-PCDH9-7	chr13:66017513-66017582	NONHSAT034194

No data

Variant related genes	Relation type
STARP1	TF binding region
STARP1	CpG island
ENSG00000200795	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 6189 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:6189 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145505710	chr13:65686309-65686310	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs549779143	chr13:65686336-65686337	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs367728178	chr13:65686337-65686338	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs147696211	chr13:65686378-65686379	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs537859525	chr13:65686426-65686427	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs377533444	chr13:65686427-65686428	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs9540357	chr13:65686458-65686459	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs548765324	chr13:65686462-65686463	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs565885497	chr13:65686486-65686487	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs57840683	chr13:65686492-65686493	Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs143251731	chr13:65686510-65686511	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs148294651	chr13:65686517-65686518	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs571603800	chr13:65686522-65686523	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs140427793	chr13:65686581-65686582	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs71820722	chr13:65686616-65686617	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs557345855	chr13:65686735-65686736	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs189565881	chr13:65686761-65686762	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs112952043	chr13:65686768-65686769	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs536759787	chr13:65686779-65686780	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs553142356	chr13:65686785-65686786	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs572996787	chr13:65686798-65686799	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs545234450	chr13:65686854-65686855	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs374843977	chr13:65686872-65686873	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs79959664	chr13:65686969-65686970	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs377324756	chr13:65686996-65686997	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182218950	chr13:65687047-65687048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575557949	chr13:65687048-65687049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565134578	chr13:65687079-65687080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79884270	chr13:65687102-65687103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150172738	chr13:65687125-65687126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138724014	chr13:65687129-65687130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572006751	chr13:65687170-65687171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559532213	chr13:65687180-65687181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147609058	chr13:65707010-65707011	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190106744	chr13:65707020-65707021	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs540658948	chr13:65707049-65707050	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532288726	chr13:65707058-65707059	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs367803749	chr13:65707069-65707070	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs544460215	chr13:65707077-65707078	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577790202	chr13:65707095-65707096	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370232546	chr13:65707096-65707097	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs373342727	chr13:65707113-65707114	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs181578456	chr13:65707134-65707135	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs563432316	chr13:65707147-65707148	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs529178613	chr13:65707156-65707157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs542956655	chr13:65707207-65707208	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs559379805	chr13:65707216-65707217	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs528522746	chr13:65707284-65707285	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs551342370	chr13:65707331-65707332	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs78648028	chr13:65707357-65707358	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Osteosarcoma	21215367	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65686000-65687200	Enhancers	Muscle Satellite Cultured Cells	--
2	chr13:65686200-65686400	Enhancers	NH-A	brain
3	chr13:65686200-65686600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:65686200-65686600	Enhancers	Hela-S3	cervix
5	chr13:65686200-65686800	Active TSS	NHDF-Ad	bronchial
6	chr13:65686400-65686600	Flanking Active TSS	NH-A	brain
7	chr13:65686400-65687000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr13:65686400-65687000	Enhancers	A549	lung
9	chr13:65686600-65686800	Enhancers	NH-A	brain
10	chr13:65686800-65687000	Active TSS	NH-A	brain
11	chr13:65707000-65707800	Active TSS	A549	lung
12	chr13:65707200-65707600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr13:65723800-65724200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:65724200-65724600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr13:65726800-65727000	Enhancers	GM12878-XiMat	blood
16	chr13:65727000-65727200	Flanking Active TSS	GM12878-XiMat	blood
17	chr13:65727000-65727400	Active TSS	A549	lung
18	chr13:65727000-65728400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr13:65727200-65727400	Active TSS	GM12878-XiMat	blood
20	chr13:65727200-65728200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr13:65727400-65727800	Enhancers	GM12878-XiMat	blood
22	chr13:65727800-65728600	Weak transcription	GM12878-XiMat	blood
23	chr13:65728200-65728600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr13:65728600-65729000	Enhancers	GM12878-XiMat	blood
25	chr13:65731400-65732400	Enhancers	HUVEC	blood vessel
26	chr13:65763000-65763400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr13:65763400-65763800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr13:65777400-65778200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr13:65779000-65780800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr13:65791200-65791800	Enhancers	Fetal Brain Male	brain
31	chr13:65791200-65792400	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr13:65791800-65792200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr13:65799600-65800400	Enhancers	Fetal Heart	heart
34	chr13:65810800-65811200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr13:65811200-65812000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr13:65814000-65814800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr13:65823400-65823600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:65823600-65824400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:65824400-65825400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:65824800-65825000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr13:65830200-65830400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr13:65833200-65834400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr13:65834200-65834800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr13:65834200-65834800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr13:65834200-65836600	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr13:65834400-65834800	Enhancers	Primary hematopoietic stem cells	blood
47	chr13:65834400-65834800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr13:65834400-65834800	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr13:65834400-65836000	Enhancers	Fetal Lung	lung
50	chr13:65834600-65834800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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