Variant report

Variant	nsv900274
Chromosome Location	chr13:63511841-63864603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1116)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:63818314-63818408	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:63740419-63740523	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:63630119-63630924	K562	blood:	n/a	n/a
4	ATF1	chr13:63618922-63619134	K562	blood:	n/a	n/a
5	ATF2	chr13:63758870-63759176	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:63666693-63666916	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:63805105-63805108	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:63582960-63583004	K562	blood:	n/a	n/a
9	BATF	chr13:63615780-63616039	GM12878	blood:	n/a	n/a
10	BCL3	chr13:63629979-63630226	K562	blood:	n/a	n/a
11	BCL3	chr13:63636565-63636764	K562	blood:	n/a	n/a
12	BDP1	chr13:63621761-63622431	Hela-S3	cervix:	n/a	n/a
13	BHLHE40	chr13:63621363-63621647	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:63646252-63646254	GM12878	blood:	n/a	n/a
15	BRCA1	chr13:63662078-63662155	GM12878	blood:	n/a	n/a
16	BRCA1	chr13:63778099-63778105	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:63621532-63621757	GM12878	blood:	n/a	n/a
18	BRCA1	chr13:63617055-63617144	GM12878	blood:	n/a	n/a
19	BRCA1	chr13:63636779-63637019	GM12878	blood:	n/a	n/a
20	BRCA1	chr13:63631196-63631347	GM12878	blood:	n/a	n/a
21	BRCA1	chr13:63646294-63646772	GM12878	blood:	n/a	n/a
22	BRCA1	chr13:63645994-63646020	Hela-S3	cervix:	n/a	n/a
23	CCNT2	chr13:63636783-63637288	K562	blood:	n/a	n/a
24	CCNT2	chr13:63623533-63624047	K562	blood:	n/a	n/a
25	CCNT2	chr13:63625757-63626259	K562	blood:	n/a	n/a
26	CEBPB	chr13:63845846-63845938	HepG2	liver:	n/a	chr13:63845885-63845896 chr13:63845859-63845870
27	CEBPB	chr13:63776742-63776947	A549	lung:	n/a	n/a
28	CEBPB	chr13:63733024-63733236	HepG2	liver:	n/a	chr13:63733111-63733122
29	CEBPB	chr13:63740269-63740585	HepG2	liver:	n/a	chr13:63740443-63740452 chr13:63740441-63740454 chr13:63740441-63740452
30	CEBPB	chr13:63773680-63773782	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr13:63634182-63634519	K562	blood:	n/a	chr13:63634337-63634348 chr13:63634337-63634350
32	CEBPB	chr13:63558691-63558837	A549	lung:	n/a	n/a
33	CEBPB	chr13:63630292-63630980	K562	blood:	n/a	n/a
34	CEBPB	chr13:63711510-63711861	IMR90	lung:	n/a	chr13:63711684-63711695
35	CEBPB	chr13:63639251-63639536	K562	blood:	n/a	n/a
36	CEBPB	chr13:63695761-63695996	HepG2	liver:	n/a	chr13:63695904-63695915
37	CEBPB	chr13:63711527-63711846	HepG2	liver:	n/a	chr13:63711684-63711695
38	CEBPB	chr13:63862840-63863259	IMR90	lung:	n/a	n/a
39	CEBPB	chr13:63602186-63602386	A549	lung:	n/a	n/a
40	CEBPB	chr13:63773594-63773780	HepG2	liver:	n/a	n/a
41	CEBPB	chr13:63630006-63631026	HepG2	liver:	n/a	chr13:63630260-63630273
42	CEBPB	chr13:63623458-63623824	HepG2	liver:	n/a	chr13:63623529-63623546 chr13:63623716-63623729 chr13:63623627-63623644
43	CEBPB	chr13:63703235-63703442	HepG2	liver:	n/a	chr13:63703327-63703338 chr13:63703326-63703337
44	CEBPB	chr13:63758997-63759239	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr13:63639071-63639547	HepG2	liver:	n/a	n/a
46	CEBPB	chr13:63632992-63633617	HepG2	liver:	n/a	chr13:63633575-63633588 chr13:63633467-63633478 chr13:63633463-63633480
47	CEBPB	chr13:63615917-63616597	IMR90	lung:	n/a	n/a
48	CEBPB	chr13:63836547-63836805	HepG2	liver:	n/a	chr13:63836652-63836663
49	CEBPB	chr13:63783763-63784090	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:63711555-63711746	H1-hESC	embryonic stem cell:	n/a	chr13:63711684-63711695

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:63637003-63637053	A549	lung:	n/a
2	chr13:63637003-63637053	RPTEC	kidney:	n/a
3	chr13:63637003-63637053	PFSK-1	brain:	n/a
4	chr13:63617080-63617130	K562	blood:	n/a
5	chr13:63637003-63637053	GM06990	blood:	n/a
6	chr13:63617080-63617130	A549	lung:	n/a
7	chr13:63617080-63617130	NT2-D1	testis:	n/a
8	chr13:63637003-63637053	K562	blood:	n/a
9	chr13:63637003-63637053	Caco-2	colon:	n/a
10	chr13:63637003-63637053	MCF10A-Er-Src	breast:	n/a
11	chr13:63617080-63617130	AG04450	lung:	fetal
12	chr13:63617080-63617130	HCPEpiC	choroid plexus:	n/a
13	chr13:63637003-63637053	CMK	blood:	n/a
14	chr13:63617080-63617130	BE2_C	brain:	n/a
15	chr13:63637003-63637053	NB4	blood:	n/a
16	chr13:63637003-63637053	Hela-S3	cervix:	n/a
17	chr13:63637003-63637053	SK-N-SH_RA	brain:	n/a
18	chr13:63637003-63637053	HRE	kidney:	n/a
19	chr13:63617080-63617130	HRPEpiC	eye:	n/a
20	chr13:63617080-63617130	Caco-2	colon:	n/a
21	chr13:63637003-63637053	ECC-1	luminal epithelium:	n/a
22	chr13:63617080-63617130	IMR90	lung:	fetal
23	chr13:63637003-63637053	SKMC	muscle:	n/a
24	chr13:63637003-63637053	AG10803	skin:	n/a
25	chr13:63617080-63617130	AG09319	gingival:	n/a
26	chr13:63617080-63617130	Hela-S3	cervix:	n/a
27	chr13:63617080-63617130	ProgFib	skin:	n/a
28	chr13:63617080-63617130	HIPEpiC	eye:	n/a
29	chr13:63617080-63617130	ECC-1	luminal epithelium:	n/a
30	chr13:63637003-63637053	HPAEpiC	pulmonary alveolar:	n/a
31	chr13:63617080-63617130	PANC-1	pancreas:	n/a
32	chr13:63617080-63617130	GM19239	blood:	n/a
33	chr13:63637003-63637053	ovcar-3	ovarian:	n/a
34	chr13:63637003-63637053	HNPCEpiC	eye:	n/a
35	chr13:63637003-63637053	Hepatocyte	liver:	n/a
36	chr13:63637003-63637053	HRCEpiC	kidney:	n/a
37	chr13:63617080-63617130	H1-hESC	embryonic stem cell:	embryo
38	chr13:63637003-63637053	HCT-116	colon:	n/a
39	chr13:63637003-63637053	HIPEpiC	eye:	n/a
40	chr13:63617080-63617130	NH-A	brain:	n/a
41	chr13:63617080-63617130	AoSMC	blood vessel:	n/a
42	chr13:63637003-63637053	AG04450	lung:	fetal
43	chr13:63617080-63617130	MCF10A-Er-Src	breast:	n/a
44	chr13:63637003-63637053	NHBE	bronchial:	n/a
45	chr13:63637003-63637053	U87	brain:	n/a
46	chr13:63637003-63637053	HRPEpiC	eye:	n/a
47	chr13:63617080-63617130	CMK	blood:	n/a
48	chr13:63637003-63637053	AG09319	gingival:	n/a
49	chr13:63637003-63637053	GM19239	blood:	n/a
50	chr13:63617080-63617130	NHDF-neo	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:63663754..63665958-chr13:63668093..63670026,2	K562	blood:
2	chr13:63663754..63665958-chr13:63668093..63670026,2	K562	blood:
3	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
4	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:
5	chr13:63647679..63650483-chr20:26148365..26151073,2	K562	blood:
6	chr13:63647686..63648379-chr3:64675736..64676331,2	MCF-7	breast:
7	chr13:63620345..63622864-chr17:21666900..21668712,2	K562	blood:
8	chr13:63647812..63648534-chr20:26148535..26149113,2	MCF-7	breast:
9	chr13:63619880..63624018-chr17:21665172..21668893,6	K562	blood:
10	chr13:63619768..63621405-chr17:21665172..21666856,2	MCF-7	breast:
11	chr12:120076978..120077828-chr13:63812850..63813372,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-20	chr13:63547376-63548145	NONHSAT034156
2	lnc-AL445989.1-3	chr13:63609109-63609165	XLOC_010410
3	lnc-PCDH20-5	chr13:63801112-63801189	XLOC_010639
4	lnc-PCDH20-5	chr13:63757234-63757461	XLOC_010639
5	lnc-AL445989.1-3	chr13:63671473-63671829	XLOC_010410
6	lnc-PCDH20-5	chr13:63768623-63768664	XLOC_010639
7	lnc-AL445989.1-3	chr13:63609108-63609165	NONHSAT034157
8	lnc-AL445989.1-3	chr13:63671472-63671829	NONHSAT034157

No data

Variant related genes	Relation type
LINC00376	TF binding region
LINC00376	CpG island
DNMT1	miRNA target sites
PHF14	miRNA target sites

Extended variants
information (count: 6564 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6564 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116798686	chr13:63518618-63518619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538272814	chr13:63518670-63518671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183998118	chr13:63518705-63518706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112015722	chr13:63518748-63518749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113302347	chr13:63518770-63518771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111996639	chr13:63518776-63518777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1194443	chr13:63518823-63518824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536719102	chr13:63518838-63518839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542334260	chr13:63518867-63518868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35394654	chr13:63518887-63518888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386771613	chr13:63518889-63518890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375918688	chr13:63518890-63518891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374116974	chr13:63518900-63518901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76538055	chr13:63518959-63518960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534964527	chr13:63518972-63518973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552970529	chr13:63518983-63518984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77363825	chr13:63518984-63518985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs573025911	chr13:63518988-63518989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577804019	chr13:63519029-63519030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184196960	chr13:63519043-63519044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78586583	chr13:63519066-63519067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557167289	chr13:63519154-63519155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578010651	chr13:63519172-63519173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576615847	chr13:63519183-63519184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113794440	chr13:63519187-63519188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562107723	chr13:63519207-63519208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12429399	chr13:63519236-63519237	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs541735219	chr13:63519254-63519255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559778199	chr13:63519283-63519284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533638877	chr13:63519300-63519301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551703297	chr13:63519352-63519353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368571135	chr13:63519369-63519370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553691321	chr13:63519393-63519394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150005360	chr13:63519405-63519406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573741980	chr13:63519417-63519418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12429419	chr13:63519423-63519424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562269463	chr13:63519456-63519457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs375794508	chr13:63519459-63519460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11841177	chr13:63519522-63519523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs544618597	chr13:63519551-63519552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187027491	chr13:63519583-63519584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149137564	chr13:63519589-63519590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552900152	chr13:63519590-63519591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112098628	chr13:63519591-63519592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557204149	chr13:63519659-63519660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549514966	chr13:63519720-63519721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537591077	chr13:63519728-63519729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77228009	chr13:63519739-63519740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555873478	chr13:63519751-63519752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574009552	chr13:63519777-63519778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63518600-63520200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:63533800-63534600	Enhancers	Dnd41	blood
3	chr13:63534600-63538400	Weak transcription	Dnd41	blood
4	chr13:63534800-63535200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr13:63534800-63535200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr13:63534800-63536200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:63535000-63535400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr13:63536200-63537000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:63537000-63537400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:63537400-63537800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:63537800-63539000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:63538400-63539600	Enhancers	Dnd41	blood
13	chr13:63551400-63554600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr13:63554400-63555000	Enhancers	Dnd41	blood
15	chr13:63554600-63555000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:63555000-63563000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr13:63558600-63559000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr13:63559400-63560000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:63569800-63570000	Enhancers	Dnd41	blood
20	chr13:63570000-63571200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr13:63570000-63572200	Flanking Active TSS	Dnd41	blood
22	chr13:63570200-63571000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:63570200-63572200	Enhancers	Fetal Thymus	thymus
24	chr13:63570400-63571400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr13:63570600-63572200	Enhancers	Primary hematopoietic stem cells	blood
26	chr13:63571000-63572200	Enhancers	Primary T cells from cord blood	blood
27	chr13:63571000-63572200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:63571200-63572000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr13:63571200-63572000	Enhancers	Thymus	Thymus
30	chr13:63571400-63571600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr13:63571600-63571800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr13:63571800-63572000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr13:63572000-63573000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr13:63572000-63573200	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr13:63572200-63572800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr13:63572200-63573800	Enhancers	Dnd41	blood
37	chr13:63573800-63575600	Weak transcription	Dnd41	blood
38	chr13:63575600-63576000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr13:63575600-63577000	Enhancers	Dnd41	blood
40	chr13:63582600-63584800	ZNF genes & repeats	Dnd41	blood
41	chr13:63583400-63585000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:63583800-63584200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr13:63584000-63584600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:63596200-63596800	Enhancers	Dnd41	blood
45	chr13:63597600-63597800	Enhancers	Brain Anterior Caudate	brain
46	chr13:63597800-63600400	Weak transcription	Brain Anterior Caudate	brain
47	chr13:63598600-63598800	Enhancers	Brain Hippocampus Middle	brain
48	chr13:63598800-63601000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr13:63599000-63600000	Weak transcription	Brain Hippocampus Middle	brain
50	chr13:63599600-63600800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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