Variant report

Variant	nsv541809
Chromosome Location	chr13:65495013-66210226
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2087)
CpG islands
(count:1040)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2087 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

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	chr13:65988370-65988595	GM12878	blood:	n/a	n/a
6	BATF	chr13:66041811-66041993	GM12878	blood:	n/a	chr13:66041940-66041951
7	BATF	chr13:65503121-65503331	GM12878	blood:	n/a	n/a
8	BCL11A	chr13:65728776-65729031	GM12878	blood:	n/a	n/a
9	BCL11A	chr13:65512818-65513084	GM12878	blood:	n/a	n/a
10	BCL11A	chr13:65512859-65513178	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:65512810-65513130	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:65728169-65728408	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:65848293-65848391	HepG2	liver:	n/a	n/a
14	BHLHE40	chr13:65735980-65735994	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:65728758-65729389	GM12878	blood:	n/a	n/a
16	BRCA1	chr13:66035765-66036027	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr13:65888304-65888377	GM12878	blood:	n/a	n/a
18	CBX3	chr13:65953042-65953530	HCT-116	colon:	n/a	n/a
19	CEBPB	chr13:65861621-65861890	K562	blood:	n/a	chr13:65861702-65861713 chr13:65861745-65861756
20	CEBPB	chr13:65873055-65873231	A549	lung:	n/a	n/a
21	CEBPB	chr13:65777153-65777273	H1-hESC	embryonic stem cell:	n/a	chr13:65777247-65777258
22	CEBPB	chr13:66071327-66071819	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr13:65659597-65659797	HepG2	liver:	n/a	chr13:65659681-65659692
24	CEBPB	chr13:65942914-65943137	A549	lung:	n/a	chr13:65942991-65943002
25	CEBPB	chr13:66172567-66172901	A549	lung:	n/a	n/a
26	CEBPB	chr13:65549489-65549824	HepG2	liver:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
27	CEBPB	chr13:66095982-66096144	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr13:66048985-66049163	A549	lung:	n/a	n/a
29	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
30	CEBPB	chr13:66035754-66036255	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr13:65499086-65499312	A549	lung:	n/a	chr13:65499202-65499213
32	CEBPB	chr13:65827820-65828305	MCF-7	breast:	n/a	n/a
33	CEBPB	chr13:66172480-66172999	A549	lung:	n/a	chr13:66172550-66172561
34	CEBPB	chr13:65632219-65632478	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr13:66095944-66096227	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:65639346-65639552	A549	lung:	n/a	chr13:65639453-65639464
37	CEBPB	chr13:66005778-66005860	HepG2	liver:	n/a	chr13:66005831-66005842
38	CEBPB	chr13:65632174-65632446	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:66039732-66039775	IMR90	lung:	n/a	n/a
40	CEBPB	chr13:66172575-66172866	A549	lung:	n/a	n/a
41	CEBPB	chr13:65503090-65503733	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr13:65646860-65647060	A549	lung:	n/a	n/a
43	CEBPB	chr13:65942931-65943178	IMR90	lung:	n/a	chr13:65942991-65943002
44	CEBPB	chr13:65911079-65911402	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:65985060-65985370	HepG2	liver:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
46	CEBPB	chr13:65829288-65829450	H1-hESC	embryonic stem cell:	n/a	chr13:65829388-65829399 chr13:65829387-65829400
47	CEBPB	chr13:65985052-65985387	IMR90	lung:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
48	CEBPB	chr13:65637852-65638276	MCF-7	breast:	n/a	n/a
49	CEBPB	chr13:65632148-65632491	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:66172507-66172920	IMR90	lung:	n/a	chr13:66172550-66172561

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65532796-65532846	HMEC	breast:	n/a
2	chr13:65500072-65500122	HL-60	blood:	n/a
3	chr13:65533500-65533550	HepG2	liver:	n/a
4	chr13:65532796-65532846	HMEC	breast:	n/a
5	chr13:65500072-65500122	HL-60	blood:	n/a
6	chr13:65533500-65533550	HepG2	liver:	n/a
7	chr13:65532878-65532928	GM12892	blood:	n/a
8	chr13:65533139-65533189	SAEC	small airway:	n/a
9	chr13:65904937-65904987	AoSMC	blood vessel:	n/a
10	chr13:65724231-65724281	GM12892	blood:	n/a
11	chr13:65532581-65532631	K562	blood:	n/a
12	chr13:65500072-65500122	AoSMC	blood vessel:	n/a
13	chr13:65500124-65500174	MCF10A-Er-Src	breast:	n/a
14	chr13:65533139-65533189	HEK293	kidney:	embryo
15	chr13:65724231-65724281	CMK	blood:	n/a
16	chr13:65532878-65532928	AG09309	skin:	n/a
17	chr13:65532273-65532323	HIPEpiC	eye:	n/a
18	chr13:66156848-66156898	T-47D	breast:	n/a
19	chr13:65532796-65532846	HEEpiC	esophagus:	n/a
20	chr13:65533139-65533189	GM12891	blood:	n/a
21	chr13:65532878-65532928	SAEC	small airway:	n/a
22	chr13:65532581-65532631	HCT-116	colon:	n/a
23	chr13:65724231-65724281	GM06990	blood:	n/a
24	chr13:65500124-65500174	AoSMC	blood vessel:	n/a
25	chr13:65532581-65532631	U87	brain:	n/a
26	chr13:65532878-65532928	HEEpiC	esophagus:	n/a
27	chr13:65532273-65532323	IMR90	lung:	fetal
28	chr13:65532273-65532323	GM12891	blood:	n/a
29	chr13:65724231-65724281	HRPEpiC	eye:	n/a
30	chr13:65532796-65532846	AG09309	skin:	n/a
31	chr13:65532878-65532928	SKMC	muscle:	n/a
32	chr13:65911268-65911318	NHDF-neo	bronchial:	n/a
33	chr13:65532796-65532846	NHBE	bronchial:	n/a
34	chr13:66156848-66156898	AG09309	skin:	n/a
35	chr13:65724231-65724281	HepG2	liver:	n/a
36	chr13:65500072-65500122	SK-N-SH_RA	brain:	n/a
37	chr13:65904937-65904987	ovcar-3	ovarian:	n/a
38	chr13:65532796-65532846	ovcar-3	ovarian:	n/a
39	chr13:65532820-65532870	HepG2	liver:	n/a
40	chr13:66156848-66156898	HRCEpiC	kidney:	n/a
41	chr13:65533139-65533189	Caco-2	colon:	n/a
42	chr13:65884209-65884259	Jurkat	blood:	n/a
43	chr13:65724231-65724281	HCT-116	colon:	n/a
44	chr13:65500072-65500122	HCF	heart:	n/a
45	chr13:65911268-65911318	IMR90	lung:	fetal
46	chr13:65532273-65532323	Caco-2	colon:	n/a
47	chr13:65532581-65532631	MCF10A-Er-Src	breast:	n/a
48	chr13:65500124-65500174	GM06990	blood:	n/a
49	chr13:65884020-65884070	HUVEC	blood vessel:	n/a
50	chr13:65532820-65532870	AG09309	skin:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
2	chr13:65787284..65789901-chr13:65800998..65803685,2	MCF-7	breast:
3	chr13:65713474..65715643-chr13:65725699..65727986,2	K562	blood:
4	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
5	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
6	chr13:65697187..65698862-chr13:65702366..65704985,2	K562	blood:
7	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
8	chr13:65796967..65799458-chr13:65799743..65801550,2	MCF-7	breast:
9	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
10	chr13:65720664..65721646-chr3:80013843..80014668,2	MCF-7	breast:
11	chr13:65697187..65698862-chr13:65702366..65704985,2	K562	blood:
12	chr12:120730575..120731437-chr13:65821446..65821946,4	HCT-116	colon:
13	chr1:106318966..106319467-chr13:66093606..66094106,2	NB4	blood:
14	chr13:65787284..65789901-chr13:65800998..65803685,2	MCF-7	breast:
15	chr12:120729601..120731270-chr13:65821466..65822966,2	K562	blood:
16	chr13:65721248..65723334-chr13:65726895..65729400,2	K562	blood:
17	chr13:65796967..65799458-chr13:65799743..65801550,2	MCF-7	breast:
18	chr12:120729600..120731304-chr13:65821466..65822966,4	K562	blood:
19	chr13:65502724..65504224-chr17:41400395..41402648,2	MCF-7	breast:
20	chr12:120729593..120731262-chr13:65821446..65822946,2	MCF-7	breast:
21	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
22	chr13:65501223..65502743-chr17:41399641..41401888,2	K562	blood:
23	chr13:65501243..65504224-chr17:41399641..41402005,2	K562	blood:
24	chr13:66046639..66047382-chr3:13541452..13542407,2	MCF-7	breast:
25	chr13:65713474..65715643-chr13:65725699..65727986,2	K562	blood:
26	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:
27	chr12:120730653..120731282-chr13:65820966..65821966,3	MCF-7	breast:
28	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
29	chr12:120729617..120731155-chr13:65821446..65822966,3	MCF-7	breast:
30	chr13:65721248..65723334-chr13:65726895..65729400,2	K562	blood:
31	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:

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

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

No data

Variant related genes	Relation type
LGMNP1	TF binding region
STARP1	TF binding region
LGMNP1	CpG island
STARP1	CpG island
ENSG00000200795	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 7217 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7217 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372027667	chr13:65498620-65498621	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs180873693	chr13:65498631-65498632	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185131579	chr13:65498635-65498636	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558034161	chr13:65498652-65498653	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs117614186	chr13:65498702-65498703	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545432564	chr13:65498720-65498721	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs562584593	chr13:65498725-65498726	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs576082024	chr13:65498741-65498742	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs541929448	chr13:65498743-65498744	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs143289532	chr13:65498749-65498750	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs527491235	chr13:65498760-65498761	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs547664697	chr13:65498763-65498764	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs151173953	chr13:65498775-65498776	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs386771810	chr13:65498778-65498779	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs386771811	chr13:65498780-65498781	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs7985378	chr13:65498782-65498783	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549935968	chr13:65498889-65498890	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs570054385	chr13:65498900-65498901	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs191465598	chr13:65498924-65498925	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs182839046	chr13:65498936-65498937	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs187064092	chr13:65498953-65498954	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs376766118	chr13:65498957-65498958	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534935766	chr13:65498960-65498961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs191504630	chr13:65498973-65498974	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs1113141	chr13:65498984-65498985	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534871704	chr13:65499460-65499461	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551584571	chr13:65499531-65499532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs571526339	chr13:65499541-65499542	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537312117	chr13:65499545-65499546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557643899	chr13:65499551-65499552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs1606439	chr13:65499567-65499568	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535480306	chr13:65499590-65499591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564521500	chr13:65499595-65499596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555486329	chr13:65499614-65499615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565640866	chr13:65499664-65499665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7329360	chr13:65499683-65499684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs187719910	chr13:65499684-65499685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs541151328	chr13:65499690-65499691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557951190	chr13:65499703-65499704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577923271	chr13:65499755-65499756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77734545	chr13:65499804-65499805	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs563649525	chr13:65499830-65499831	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs529265179	chr13:65499841-65499842	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs561196116	chr13:65499844-65499845	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs543040485	chr13:65499861-65499862	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs559396257	chr13:65499883-65499884	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs528536218	chr13:65499884-65499885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs551499767	chr13:65499911-65499912	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs574891369	chr13:65499912-65499913	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs191458741	chr13:65499950-65499951	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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	22037309	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:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65498600-65499000	Active TSS	Gastric	stomach
2	chr13:65499400-65499600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:65499400-65499800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:65499600-65502800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:65499800-65500000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:65500000-65500200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr13:65502400-65503400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr13:65502400-65503800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr13:65502400-65504400	Enhancers	Placenta Amnion	Placenta Amnion
10	chr13:65502600-65503800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr13:65502800-65503000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:65502800-65503000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr13:65502800-65503000	Enhancers	Hela-S3	cervix
14	chr13:65502800-65503200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr13:65502800-65503200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:65502800-65503200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr13:65502800-65503200	Enhancers	HMEC	breast
18	chr13:65502800-65503600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr13:65502800-65504400	Enhancers	NH-A	brain
20	chr13:65503000-65503200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:65503000-65503600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr13:65503000-65503600	Enhancers	NHDF-Ad	bronchial
23	chr13:65503000-65503800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr13:65503000-65503800	Enhancers	A549	lung
25	chr13:65503000-65503800	Enhancers	GM12878-XiMat	blood
26	chr13:65503000-65503800	Flanking Active TSS	Hela-S3	cervix
27	chr13:65503000-65504200	Enhancers	HUVEC	blood vessel
28	chr13:65503200-65503600	Flanking Active TSS	HMEC	breast
29	chr13:65503200-65504200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr13:65503200-65504600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr13:65503400-65503800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:65503600-65503800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr13:65503600-65504200	Enhancers	HMEC	breast
34	chr13:65503800-65504200	Enhancers	Hela-S3	cervix
35	chr13:65503800-65504600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr13:65503800-65504600	Weak transcription	GM12878-XiMat	blood
37	chr13:65504200-65504800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr13:65504400-65511600	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr13:65504600-65504800	Enhancers	GM12878-XiMat	blood
40	chr13:65504600-65505400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr13:65511600-65512000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr13:65512000-65512200	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr13:65512200-65512600	Enhancers	Placenta Amnion	Placenta Amnion
44	chr13:65514200-65514800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr13:65514800-65516000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:65516000-65518200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:65518200-65518400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr13:65519000-65519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr13:65519200-65519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr13:65533400-65533600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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