Variant report

Variant	nsv562643
Chromosome Location	chr13:90383458-90487155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:321)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90462884-90462897	HepG2	liver:	n/a	n/a
2	ATF1	chr13:90466783-90467103	K562	blood:	n/a	n/a
3	ATF1	chr13:90448578-90448855	K562	blood:	n/a	n/a
4	ATF1	chr13:90446074-90446297	K562	blood:	n/a	n/a
5	ATF1	chr13:90445517-90445688	K562	blood:	n/a	n/a
6	ATF1	chr13:90458876-90459006	K562	blood:	n/a	n/a
7	ATF1	chr13:90483482-90484025	K562	blood:	n/a	n/a
8	ATF1	chr13:90452879-90452924	K562	blood:	n/a	n/a
9	ATF1	chr13:90459939-90460250	K562	blood:	n/a	n/a
10	ATF1	chr13:90468064-90468577	K562	blood:	n/a	n/a
11	ATF1	chr13:90477390-90477952	K562	blood:	n/a	n/a
12	ATF1	chr13:90463731-90464784	K562	blood:	n/a	n/a
13	BACH1	chr13:90394961-90395002	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr13:90472685-90473042	K562	blood:	n/a	n/a
15	BRCA1	chr13:90385982-90386497	Hela-S3	cervix:	n/a	n/a
16	CCNT2	chr13:90449354-90449592	K562	blood:	n/a	n/a
17	CCNT2	chr13:90479195-90479749	K562	blood:	n/a	n/a
18	CCNT2	chr13:90445561-90446205	K562	blood:	n/a	n/a
19	CEBPB	chr13:90385946-90386684	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:90450048-90450640	K562	blood:	n/a	chr13:90450190-90450201
21	CEBPB	chr13:90454196-90454358	A549	lung:	n/a	n/a
22	CEBPB	chr13:90441356-90441425	K562	blood:	n/a	n/a
23	CEBPB	chr13:90480867-90481108	HepG2	liver:	n/a	chr13:90480973-90480984 chr13:90480974-90480985 chr13:90480973-90480984
24	CEBPB	chr13:90450117-90450276	HepG2	liver:	n/a	chr13:90450190-90450201
25	CEBPB	chr13:90415253-90415658	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:90445760-90446127	K562	blood:	n/a	n/a
27	CEBPB	chr13:90461947-90462055	H1-hESC	embryonic stem cell:	n/a	chr13:90462026-90462039
28	CHD1	chr13:90414472-90414534	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:90485180-90485241	GM10248	blood:	n/a	n/a
30	CTCF	chr13:90451340-90451704	K562	blood:	n/a	n/a
31	CTCF	chr13:90429160-90429310	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr13:90456986-90457112	K562	blood:	n/a	n/a
33	CTCF	chr13:90402355-90402423	Lung_OC	lung:	n/a	n/a
34	CTCF	chr13:90458020-90458170	HRE	kidney:	n/a	n/a
35	CTCF	chr13:90451600-90451750	BE2_C	brain:	n/a	n/a
36	CTCF	chr13:90429220-90429370	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr13:90429200-90429350	BE2_C	brain:	n/a	n/a
38	CTCF	chr13:90450320-90450470	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr13:90435800-90435950	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr13:90451640-90451790	HPF	lung:	n/a	n/a
41	CTCF	chr13:90436720-90436870	GM12867	blood:	n/a	n/a
42	CTCF	chr13:90469786-90469842	GM20000	blood:	n/a	n/a
43	E2F4	chr13:90392326-90392608	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr13:90479330-90479593	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr13:90439246-90439247	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr13:90404915-90405238	MCF10A-Er-Src	breast:	n/a	chr13:90404970-90404979 chr13:90405008-90405017
47	E2F4	chr13:90427052-90427248	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:90397173-90397373	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:90486471-90486643	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr13:90424402-90424602	GM12878	blood:	n/a	chr13:90424486-90424497 chr13:90424426-90424436

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90419012-90419062	HCT-116	colon:	n/a
2	chr13:90419012-90419062	AG09309	skin:	n/a
3	chr13:90419012-90419062	MCF-7	breast:	n/a
4	chr13:90419012-90419062	GM12892	blood:	n/a
5	chr13:90419012-90419062	NHDF-neo	bronchial:	n/a
6	chr13:90419012-90419062	MCF10A-Er-Src	breast:	n/a
7	chr13:90419012-90419062	SKMC	muscle:	n/a
8	chr13:90419012-90419062	HEEpiC	esophagus:	n/a
9	chr13:90419012-90419062	NHBE	bronchial:	n/a
10	chr13:90419012-90419062	SK-N-MC	brain:	n/a
11	chr13:90419012-90419062	NB4	blood:	n/a
12	chr13:90419012-90419062	A549	lung:	n/a
13	chr13:90419012-90419062	LNCaP	prostate:	n/a
14	chr13:90419012-90419062	AG10803	skin:	n/a
15	chr13:90419012-90419062	GM06990	blood:	n/a
16	chr13:90419012-90419062	ECC-1	luminal epithelium:	n/a
17	chr13:90419012-90419062	IMR90	lung:	fetal
18	chr13:90419012-90419062	ProgFib	skin:	n/a
19	chr13:90419012-90419062	HCF	heart:	n/a
20	chr13:90419012-90419062	AG04450	lung:	fetal
21	chr13:90419012-90419062	HCM	heart:	n/a
22	chr13:90419012-90419062	HRE	kidney:	n/a
23	chr13:90419012-90419062	AG09319	gingival:	n/a
24	chr13:90419012-90419062	T-47D	breast:	n/a
25	chr13:90419012-90419062	AoSMC	blood vessel:	n/a
26	chr13:90419012-90419062	HCPEpiC	choroid plexus:	n/a
27	chr13:90419012-90419062	HL-60	blood:	n/a
28	chr13:90419012-90419062	AG04449	skin:	fetal
29	chr13:90419012-90419062	HRCEpiC	kidney:	n/a
30	chr13:90419012-90419062	SK-N-SH	brain:	n/a
31	chr13:90419012-90419062	PFSK-1	brain:	n/a
32	chr13:90419012-90419062	BJ	skin:	n/a
33	chr13:90419012-90419062	Jurkat	blood:	n/a
34	chr13:90419012-90419062	NH-A	brain:	n/a
35	chr13:90419012-90419062	HAEpiC	amniotic membrane:	n/a
36	chr13:90419012-90419062	PANC-1	pancreas:	n/a
37	chr13:90419012-90419062	Hela-S3	cervix:	n/a
38	chr13:90419012-90419062	SAEC	small airway:	n/a
39	chr13:90419012-90419062	HepG2	liver:	n/a
40	chr13:90419012-90419062	SK-N-SH_RA	brain:	n/a
41	chr13:90419012-90419062	HUVEC	blood vessel:	n/a
42	chr13:90419012-90419062	HIPEpiC	eye:	n/a
43	chr13:90419012-90419062	K562	blood:	n/a
44	chr13:90419012-90419062	HEK293	kidney:	embryo
45	chr13:90419012-90419062	ovcar-3	ovarian:	n/a
46	chr13:90419012-90419062	HMEC	breast:	n/a
47	chr13:90419012-90419062	PrEC	prostate:	n/a
48	chr13:90419012-90419062	NT2-D1	testis:	n/a
49	chr13:90419012-90419062	CMK	blood:	n/a
50	chr13:90419012-90419062	H1-hESC	embryonic stem cell:	embryo

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90471832..90475214-chr13:90475498..90478937,3	K562	blood:
2	chr13:90482310..90483904-chr13:90487174..90489682,2	K562	blood:
3	chr13:90418481..90420847-chr13:90437525..90440214,2	MCF-7	breast:
4	chr13:90449351..90452223-chr13:90453733..90455503,2	K562	blood:
5	chr13:90438180..90442021-chr13:90442191..90444686,4	K562	blood:
6	chr13:90451472..90453159-chr13:90467765..90470147,2	K562	blood:
7	chr13:81107224..81110748-chr13:90439942..90442170,3	K562	blood:
8	chr13:90451578..90453716-chr13:90460021..90462776,2	K562	blood:
9	chr13:90471832..90475214-chr13:90475498..90478937,3	K562	blood:
10	chr13:90462886..90465501-chr13:90466757..90468821,2	K562	blood:
11	chr13:81104877..81107145-chr13:90439895..90442181,2	K562	blood:
12	chr13:90458920..90462227-chr13:90462309..90464800,3	K562	blood:
13	chr13:90476201..90479176-chr13:90479802..90482619,4	K562	blood:
14	chr13:90449351..90452223-chr13:90453733..90455503,2	K562	blood:
15	chr13:90476201..90479176-chr13:90479802..90482619,4	K562	blood:
16	chr13:90451578..90453716-chr13:90460021..90462776,2	K562	blood:
17	chr13:90418481..90420847-chr13:90437525..90440214,2	MCF-7	breast:
18	chr13:90436471..90441172-chr13:90442955..90446450,4	K562	blood:
19	chr13:90442816..90446344-chr13:90446714..90450498,3	K562	blood:
20	chr13:90438180..90442021-chr13:90442191..90444686,4	K562	blood:
21	chr13:90461092..90463944-chr13:90499339..90502245,2	K562	blood:
22	chr13:90458920..90462227-chr13:90462309..90464800,3	K562	blood:
23	chr13:90462886..90465501-chr13:90466757..90468821,2	K562	blood:
24	chr13:90442816..90446344-chr13:90446714..90450498,3	K562	blood:
25	chr13:90436471..90441172-chr13:90442955..90446450,4	K562	blood:
26	chr13:81107870..81110072-chr13:90437576..90439628,3	K562	blood:
27	chr13:81108572..81110898-chr13:90437772..90440257,3	K562	blood:
28	chr13:90451472..90453159-chr13:90467765..90470147,2	K562	blood:

No data

Variant related genes	Relation type
RPL7L1P1	TF binding region
ENSG00000200733	TF binding region
RPL7L1P1	CpG island
ENSG00000200733	CpG island
ENSG00000200733	chromatin interactions

Extended variants
information (count: 2322 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9522667	chr13:90383458-90383459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs180943344	chr13:90383470-90383471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528973472	chr13:90383536-90383537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9522668	chr13:90383557-90383558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9555935	chr13:90383682-90383683	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557297499	chr13:90383706-90383707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575617526	chr13:90383718-90383719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73595751	chr13:90383721-90383722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561616778	chr13:90383731-90383732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376278629	chr13:90383732-90383733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528993107	chr13:90383737-90383738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544612520	chr13:90383760-90383761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534941446	chr13:90383796-90383797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9588740	chr13:90383824-90383825	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374331160	chr13:90383827-90383828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560688758	chr13:90383835-90383836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9522669	chr13:90383848-90383849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs552885298	chr13:90383849-90383850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9583726	chr13:90383931-90383932	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs531604248	chr13:90383932-90383933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537393580	chr13:90383953-90383954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550191145	chr13:90383957-90383958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568424418	chr13:90383966-90383967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535951031	chr13:90383967-90383968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9522670	chr13:90383974-90383975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144723157	chr13:90383996-90383997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34373916	chr13:90384008-90384009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574906660	chr13:90384010-90384011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71798358	chr13:90384019-90384020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs398056689	chr13:90384030-90384031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542738877	chr13:90384032-90384033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557610306	chr13:90384073-90384074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377361713	chr13:90384160-90384161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142336858	chr13:90384177-90384178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575978503	chr13:90384242-90384243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190874476	chr13:90384327-90384328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9522671	chr13:90384331-90384332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs573626495	chr13:90384461-90384462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183905290	chr13:90384496-90384497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559521904	chr13:90384585-90384586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572653042	chr13:90384586-90384587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371925302	chr13:90384587-90384588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188947800	chr13:90384627-90384628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568232055	chr13:90384644-90384645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564758764	chr13:90384672-90384673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532043375	chr13:90384697-90384698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191658185	chr13:90384717-90384718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182983875	chr13:90384833-90384834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142907663	chr13:90384856-90384857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547470607	chr13:90384858-90384859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Burkitt''s lymphoma	20823134	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90375600-90389600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:90380400-90385200	Weak transcription	Hela-S3	cervix
3	chr13:90385200-90387200	Enhancers	Hela-S3	cervix
4	chr13:90387200-90402400	Weak transcription	Hela-S3	cervix
5	chr13:90389800-90390600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:90390000-90390600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr13:90390200-90390800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:90392200-90394600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr13:90393200-90394800	Enhancers	Fetal Heart	heart
10	chr13:90393400-90393800	Enhancers	Fetal Muscle Leg	muscle
11	chr13:90393400-90393800	Enhancers	Left Ventricle	heart
12	chr13:90394800-90398600	Weak transcription	Fetal Heart	heart
13	chr13:90398200-90401200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:90398400-90399200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr13:90398400-90399400	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr13:90398600-90399200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr13:90398600-90399400	Enhancers	Fetal Heart	heart
18	chr13:90398800-90399200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr13:90398800-90399200	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr13:90399200-90399600	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr13:90399200-90400400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr13:90399400-90400600	Weak transcription	Fetal Heart	heart
23	chr13:90399600-90399800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr13:90399800-90400800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr13:90400600-90400800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr13:90400600-90401400	Enhancers	Fetal Heart	heart
27	chr13:90400800-90401400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr13:90401200-90401400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:90401200-90406200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:90401400-90408000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr13:90401600-90402600	Enhancers	HUVEC	blood vessel
32	chr13:90402000-90402800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:90402200-90402600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr13:90402400-90402600	Enhancers	Hela-S3	cervix
35	chr13:90402400-90402800	Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr13:90403600-90404200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:90406200-90406400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:90406400-90406600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:90406600-90406800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:90406800-90408800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:90408000-90408600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:90408600-90415600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr13:90414200-90415800	Enhancers	HUVEC	blood vessel
44	chr13:90414800-90415800	Enhancers	NH-A	brain
45	chr13:90415200-90416000	Enhancers	Hela-S3	cervix
46	chr13:90415600-90415800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr13:90418400-90419400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:90419000-90419400	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr13:90425200-90425600	Enhancers	HUVEC	blood vessel
50	chr13:90431600-90438600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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