Variant report

Variant	esv2751147
Chromosome Location	chr13:65872831-66043202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:391)
CpG islands
(count:245)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:391 , 50 per page) page: 1 2 3 4 5 6 7 8

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	BATF	chr13:66041811-66041993	GM12878	blood:	n/a	chr13:66041940-66041951
3	BATF	chr13:65988370-65988595	GM12878	blood:	n/a	n/a
4	BRCA1	chr13:65888304-65888377	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:66035765-66036027	Hela-S3	cervix:	n/a	n/a
6	CBX3	chr13:65953042-65953530	HCT-116	colon:	n/a	n/a
7	CEBPB	chr13:65879841-65879954	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:65935688-65935939	IMR90	lung:	n/a	chr13:65935790-65935801
9	CEBPB	chr13:65985052-65985387	IMR90	lung:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
10	CEBPB	chr13:65911079-65911402	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:65917104-65917425	IMR90	lung:	n/a	chr13:65917266-65917277
12	CEBPB	chr13:66035754-66036255	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr13:65935402-65935876	HepG2	liver:	n/a	chr13:65935790-65935801
14	CEBPB	chr13:65873055-65873231	A549	lung:	n/a	n/a
15	CEBPB	chr13:65942914-65943137	A549	lung:	n/a	chr13:65942991-65943002
16	CEBPB	chr13:66039732-66039775	IMR90	lung:	n/a	n/a
17	CEBPB	chr13:65942890-65943171	HepG2	liver:	n/a	chr13:65942991-65943002
18	CEBPB	chr13:65936220-65936361	HepG2	liver:	n/a	chr13:65936278-65936290
19	CEBPB	chr13:66022805-66023052	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:65917150-65917355	A549	lung:	n/a	chr13:65917266-65917277
21	CEBPB	chr13:66005778-66005860	HepG2	liver:	n/a	chr13:66005831-66005842
22	CEBPB	chr13:65985060-65985370	HepG2	liver:	n/a	chr13:65985203-65985214 chr13:65985204-65985213 chr13:65985202-65985215
23	CEBPB	chr13:65941086-65941290	HepG2	liver:	n/a	chr13:65941156-65941167
24	CEBPB	chr13:65917105-65917448	HepG2	liver:	n/a	chr13:65917266-65917277
25	CEBPB	chr13:65942931-65943178	IMR90	lung:	n/a	chr13:65942991-65943002
26	CTCF	chr13:65989600-65989750	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr13:65888280-65888430	GM12869	blood:	n/a	n/a
28	CTCF	chr13:65897518-65897564	GM10248	blood:	n/a	n/a
29	CTCF	chr13:65914306-65914324	K562	blood:	n/a	n/a
30	CTCF	chr13:65905920-65906070	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr13:66040347-66040446	GM20000	blood:	n/a	n/a
32	CTCF	chr13:65989680-65989830	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr13:65905860-65906010	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr13:65913620-65913770	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr13:65917300-65917450	HPF	lung:	n/a	n/a
36	CTCF	chr13:65938500-65938650	GM12874	blood:	n/a	n/a
37	CTCF	chr13:65888714-65888772	Fibrobl	skin:	n/a	n/a
38	CTCF	chr13:65989741-65989782	LNCaP	prostate:	n/a	n/a
39	CTCF	chr13:65927367-65927392	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr13:66024969-66025059	GM10266	blood:	n/a	n/a
41	CTCF	chr13:65989708-65989800	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr13:65936931-65937013	GM13976	blood:	n/a	n/a
43	CTCF	chr13:65896800-65896950	NB4	blood:	n/a	n/a
44	CTCF	chr13:65976940-65977090	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr13:65927451-65927495	LNCaP	prostate:	n/a	n/a
46	CTCF	chr13:65989716-65989802	LNCaP	prostate:	n/a	n/a
47	CTCF	chr13:66035120-66035270	AG04449	skin:	n/a	n/a
48	CTCF	chr13:65877435-65877523	Fibrobl	skin:	n/a	n/a
49	CTCF	chr13:65938235-65938259	ProgFib	skin:	n/a	n/a
50	E2F4	chr13:65954652-65954895	MCF10A-Er-Src	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65911268-65911318	HRCEpiC	kidney:	n/a
2	chr13:65911268-65911318	HRCEpiC	kidney:	n/a
3	chr13:65884020-65884070	ECC-1	luminal epithelium:	n/a
4	chr13:65884209-65884259	HMEC	breast:	n/a
5	chr13:65884209-65884259	MCF-7	breast:	n/a
6	chr13:65911268-65911318	AG09309	skin:	n/a
7	chr13:65911268-65911318	HEK293	kidney:	embryo
8	chr13:65884020-65884070	A549	lung:	n/a
9	chr13:65911268-65911318	PrEC	prostate:	n/a
10	chr13:65904937-65904987	NHBE	bronchial:	n/a
11	chr13:65884209-65884259	Caco-2	colon:	n/a
12	chr13:65884209-65884259	HNPCEpiC	eye:	n/a
13	chr13:65911268-65911318	Hepatocyte	liver:	n/a
14	chr13:65884020-65884070	HNPCEpiC	eye:	n/a
15	chr13:65884209-65884259	BJ	skin:	n/a
16	chr13:65911268-65911318	ProgFib	skin:	n/a
17	chr13:65904937-65904987	HepG2	liver:	n/a
18	chr13:65911268-65911318	AG09319	gingival:	n/a
19	chr13:65884020-65884070	ProgFib	skin:	n/a
20	chr13:65904937-65904987	HUVEC	blood vessel:	n/a
21	chr13:65884020-65884070	AoSMC	blood vessel:	n/a
22	chr13:65884020-65884070	AG09319	gingival:	n/a
23	chr13:65884209-65884259	SKMC	muscle:	n/a
24	chr13:65904937-65904987	ProgFib	skin:	n/a
25	chr13:65884209-65884259	AG09319	gingival:	n/a
26	chr13:65904937-65904987	NT2-D1	testis:	n/a
27	chr13:65904937-65904987	HNPCEpiC	eye:	n/a
28	chr13:65884020-65884070	SK-N-SH_RA	brain:	n/a
29	chr13:65904937-65904987	HEEpiC	esophagus:	n/a
30	chr13:65884020-65884070	HCPEpiC	choroid plexus:	n/a
31	chr13:65884020-65884070	HRE	kidney:	n/a
32	chr13:65884020-65884070	AG04450	lung:	fetal
33	chr13:65911268-65911318	NB4	blood:	n/a
34	chr13:65904937-65904987	AG09319	gingival:	n/a
35	chr13:65911268-65911318	U87	brain:	n/a
36	chr13:65911268-65911318	GM06990	blood:	n/a
37	chr13:65884020-65884070	NHBE	bronchial:	n/a
38	chr13:65884209-65884259	PFSK-1	brain:	n/a
39	chr13:65884209-65884259	SK-N-MC	brain:	n/a
40	chr13:65904937-65904987	SAEC	small airway:	n/a
41	chr13:65884209-65884259	H1-hESC	embryonic stem cell:	embryo
42	chr13:65884209-65884259	GM19239	blood:	n/a
43	chr13:65911268-65911318	Caco-2	colon:	n/a
44	chr13:65911268-65911318	HEEpiC	esophagus:	n/a
45	chr13:65884020-65884070	PrEC	prostate:	n/a
46	chr13:65904937-65904987	GM06990	blood:	n/a
47	chr13:65884020-65884070	K562	blood:	n/a
48	chr13:65904937-65904987	SK-N-SH_RA	brain:	n/a
49	chr13:65884209-65884259	HRPEpiC	eye:	n/a
50	chr13:65911268-65911318	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
2	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:
3	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
4	chr13:65913509..65915186-chr13:65916545..65919418,2	K562	blood:

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

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

No data

Variant related genes	Relation type
STARP1	TF binding region
STARP1	CpG island

Extended variants
information (count: 2904 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:2904 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553439117	chr13:65880250-65880251	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs9564233	chr13:65880279-65880280	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs200121494	chr13:65880280-65880281	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs117830637	chr13:65880309-65880310	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs557299457	chr13:65880342-65880343	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs559674975	chr13:65880360-65880361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs182705968	chr13:65880394-65880395	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs185118647	chr13:65880418-65880419	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs146912279	chr13:65880438-65880439	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs139347066	chr13:65880461-65880462	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs75539378	chr13:65880473-65880474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs559396861	chr13:65880483-65880484	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs528351699	chr13:65880542-65880543	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs115375059	chr13:65880554-65880555	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs376056170	chr13:65880585-65880586	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs559824072	chr13:65880619-65880620	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs565308217	chr13:65880622-65880623	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs573297393	chr13:65880634-65880635	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs189824632	chr13:65880661-65880662	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs143255493	chr13:65880662-65880663	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs567746141	chr13:65880677-65880678	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs111793923	chr13:65880716-65880717	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs9634923	chr13:65880748-65880749	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs567069393	chr13:65880816-65880817	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs545225307	chr13:65880828-65880829	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
26	rs114574062	chr13:65880844-65880845	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
27	rs577256464	chr13:65880902-65880903	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
28	rs117590977	chr13:65880903-65880904	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
29	rs536644339	chr13:65881097-65881098	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs551912079	chr13:65881116-65881117	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs556781759	chr13:65881124-65881125	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs200533519	chr13:65881129-65881130	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs542472468	chr13:65881144-65881145	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs116560406	chr13:65881147-65881148	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs573051774	chr13:65881155-65881156	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs182720384	chr13:65881237-65881238	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs565168100	chr13:65881304-65881305	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs144765192	chr13:65881368-65881369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531082216	chr13:65881424-65881425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550949910	chr13:65881449-65881450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150459266	chr13:65881477-65881478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188991819	chr13:65881493-65881494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546902326	chr13:65881507-65881508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567086266	chr13:65881509-65881510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532556827	chr13:65881533-65881534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374322720	chr13:65881535-65881536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549285421	chr13:65881543-65881544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12430856	chr13:65881606-65881607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535464013	chr13:65881622-65881623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115420458	chr13:65881624-65881625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65880600-65880800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:65880800-65881000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:65881000-65883400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:65884000-65884600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:65884000-65884600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr13:65885200-65885400	ZNF genes & repeats	Pancreas	Pancrea
7	chr13:65885400-65887400	Weak transcription	Pancreas	Pancrea
8	chr13:65887400-65888800	ZNF genes & repeats	Pancreas	Pancrea
9	chr13:65888400-65888800	Enhancers	Gastric	stomach
10	chr13:65905000-65905200	Enhancers	Gastric	stomach
11	chr13:65905200-65910400	Weak transcription	Gastric	stomach
12	chr13:65907400-65907600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr13:65909600-65911400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr13:65910000-65911000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr13:65910000-65911400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:65910200-65910400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr13:65910200-65911000	Enhancers	Fetal Muscle Trunk	muscle
18	chr13:65910400-65911200	Enhancers	Fetal Muscle Leg	muscle
19	chr13:65910400-65911200	Enhancers	Gastric	stomach
20	chr13:65910400-65911400	Enhancers	Brain Germinal Matrix	brain
21	chr13:65910400-65913200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr13:65910600-65911600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr13:65911000-65913400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr13:65911200-65911600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr13:65913200-65914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr13:65913400-65913600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr13:65913600-65913800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:65913600-65914400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:65913800-65914000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr13:65914000-65914800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:65914400-65917400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr13:65914800-65915600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr13:65914800-65915800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr13:65915600-65917600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr13:65915800-65917600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr13:65916400-65917600	Enhancers	Primary hematopoietic stem cells	blood
37	chr13:65916800-65917600	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr13:65917200-65918800	Enhancers	Fetal Heart	heart
39	chr13:65917400-65917600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr13:65917600-65920600	Weak transcription	Primary hematopoietic stem cells	blood
41	chr13:65943200-65943600	Enhancers	Fetal Heart	heart
42	chr13:65943600-65944000	Weak transcription	Fetal Heart	heart
43	chr13:65944000-65944600	Enhancers	Fetal Heart	heart
44	chr13:65952200-65953000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr13:65959600-65960000	Enhancers	Fetal Lung	lung
46	chr13:65960000-65960400	Weak transcription	Fetal Lung	lung
47	chr13:65960400-65960600	Enhancers	Fetal Lung	lung
48	chr13:65960600-65961400	Weak transcription	Fetal Lung	lung
49	chr13:65961000-65962000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr13:65961400-65961600	ZNF genes & repeats	Fetal Lung	lung

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