Variant report

Variant	nsv870345
Chromosome Location	chr13:89164439-89295782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:89238320-89238777	H1-hESC	embryonic stem cell:	n/a	chr13:89238690-89238704
2	BRCA1	chr13:89280576-89280681	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr13:89290092-89290576	IMR90	lung:	n/a	chr13:89290390-89290401
4	CEBPB	chr13:89242865-89243152	IMR90	lung:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
5	CEBPB	chr13:89290188-89290577	HepG2	liver:	n/a	chr13:89290390-89290401
6	CEBPB	chr13:89290214-89290571	Hela-S3	cervix:	n/a	chr13:89290390-89290401
7	CEBPB	chr13:89242868-89243214	HepG2	liver:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
8	CEBPB	chr13:89290206-89290537	H1-hESC	embryonic stem cell:	n/a	chr13:89290390-89290401
9	CEBPB	chr13:89282509-89282768	HepG2	liver:	n/a	chr13:89282641-89282652
10	CEBPB	chr13:89164725-89164947	HepG2	liver:	n/a	chr13:89164855-89164866
11	CEBPB	chr13:89243021-89243158	H1-hESC	embryonic stem cell:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
12	CEBPB	chr13:89270759-89270935	HepG2	liver:	n/a	chr13:89270795-89270806
13	CEBPB	chr13:89242893-89243153	K562	blood:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
14	CEBPB	chr13:89289215-89289541	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:89290248-89290542	A549	lung:	n/a	chr13:89290390-89290401
16	CEBPB	chr13:89290236-89290580	K562	blood:	n/a	chr13:89290390-89290401
17	CEBPB	chr13:89178483-89178781	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr13:89199860-89200010	AG10803	skin:	n/a	n/a
19	CTCF	chr13:89247400-89247550	GM12869	blood:	n/a	n/a
20	CTCF	chr13:89244560-89244710	SAEC	small airway:	n/a	n/a
21	CTCF	chr13:89224967-89225021	GM20000	blood:	n/a	n/a
22	CTCF	chr13:89244136-89244220	GM20000	blood:	n/a	n/a
23	CUX1	chr13:89279287-89279337	GM12878	blood:	n/a	n/a
24	E2F4	chr13:89292346-89292394	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr13:89197220-89197420	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr13:89205826-89206091	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr13:89259115-89259348	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr13:89290254-89290472	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr13:89171437-89171450	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr13:89237749-89238005	GM12878	blood:	n/a	chr13:89237860-89237871
31	EBF1	chr13:89275419-89275829	GM12878	blood:	n/a	n/a
32	EP300	chr13:89217414-89219110	SK-N-SH	brain:	n/a	chr13:89217965-89217975
33	EP300	chr13:89281136-89281539	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr13:89216555-89216558	GM12878	blood:	n/a	n/a
35	EP300	chr13:89188967-89189122	GM12878	blood:	n/a	n/a
36	EP300	chr13:89281131-89281340	SK-N-SH_RA	brain:	n/a	n/a
37	EP300	chr13:89275485-89275742	GM12878	blood:	n/a	n/a
38	EP300	chr13:89254254-89254418	GM12878	blood:	n/a	n/a
39	EP300	chr13:89280807-89281872	SK-N-SH	brain:	n/a	n/a
40	EP300	chr13:89238636-89238715	K562	blood:	n/a	chr13:89238693-89238702
41	EP300	chr13:89189926-89189979	Hela-S3	cervix:	n/a	n/a
42	EP300	chr13:89218001-89218208	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr13:89275460-89275660	GM12878	blood:	n/a	n/a
44	EP300	chr13:89253111-89253336	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr13:89189030-89189045	GM12878	blood:	n/a	n/a
46	FAM48A	chr13:89230446-89230634	GM12878	blood:	n/a	n/a
47	FOS	chr13:89255408-89256076	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr13:89275078-89275260	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr13:89275016-89275333	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr13:89255704-89255927	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89179261-89179311	IMR90	lung:	fetal
2	chr13:89179261-89179311	HRPEpiC	eye:	n/a
3	chr13:89179261-89179311	NHBE	bronchial:	n/a
4	chr13:89179261-89179311	HEEpiC	esophagus:	n/a
5	chr13:89179261-89179311	ovcar-3	ovarian:	n/a
6	chr13:89179261-89179311	AG09309	skin:	n/a
7	chr13:89179261-89179311	HAEpiC	amniotic membrane:	n/a
8	chr13:89179261-89179311	BJ	skin:	n/a
9	chr13:89179261-89179311	LNCaP	prostate:	n/a
10	chr13:89179261-89179311	GM12892	blood:	n/a
11	chr13:89179261-89179311	HCM	heart:	n/a
12	chr13:89179261-89179311	HPAEpiC	pulmonary alveolar:	n/a
13	chr13:89179261-89179311	NHDF-neo	bronchial:	n/a
14	chr13:89179261-89179311	GM12878	blood:	n/a
15	chr13:89179261-89179311	HepG2	liver:	n/a
16	chr13:89179261-89179311	CMK	blood:	n/a
17	chr13:89179261-89179311	NB4	blood:	n/a
18	chr13:89179261-89179311	GM19239	blood:	n/a
19	chr13:89179261-89179311	RPTEC	kidney:	n/a
20	chr13:89179261-89179311	HNPCEpiC	eye:	n/a
21	chr13:89179261-89179311	GM12891	blood:	n/a
22	chr13:89179261-89179311	HRE	kidney:	n/a
23	chr13:89179261-89179311	MCF-7	breast:	n/a
24	chr13:89179261-89179311	SK-N-SH_RA	brain:	n/a
25	chr13:89179261-89179311	HMEC	breast:	n/a
26	chr13:89179261-89179311	BE2_C	brain:	n/a
27	chr13:89179261-89179311	NH-A	brain:	n/a
28	chr13:89179261-89179311	Jurkat	blood:	n/a
29	chr13:89179261-89179311	AoSMC	blood vessel:	n/a
30	chr13:89179261-89179311	PrEC	prostate:	n/a
31	chr13:89179261-89179311	ECC-1	luminal epithelium:	n/a
32	chr13:89179261-89179311	Caco-2	colon:	n/a
33	chr13:89179261-89179311	PANC-1	pancreas:	n/a
34	chr13:89179261-89179311	HCT-116	colon:	n/a
35	chr13:89179261-89179311	NT2-D1	testis:	n/a
36	chr13:89179261-89179311	HIPEpiC	eye:	n/a
37	chr13:89179261-89179311	SAEC	small airway:	n/a
38	chr13:89179261-89179311	SK-N-SH	brain:	n/a
39	chr13:89179261-89179311	ProgFib	skin:	n/a
40	chr13:89179261-89179311	PFSK-1	brain:	n/a
41	chr13:89179261-89179311	H1-hESC	embryonic stem cell:	embryo
42	chr13:89179261-89179311	AG04450	lung:	fetal
43	chr13:89179261-89179311	SK-N-MC	brain:	n/a
44	chr13:89179261-89179311	T-47D	breast:	n/a
45	chr13:89179261-89179311	K562	blood:	n/a
46	chr13:89179261-89179311	HCPEpiC	choroid plexus:	n/a
47	chr13:89179261-89179311	HUVEC	blood vessel:	n/a
48	chr13:89179261-89179311	AG04449	skin:	fetal
49	chr13:89179261-89179311	GM06990	blood:	n/a
50	chr13:89179261-89179311	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:89273831..89276576-chr13:89278587..89280292,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-7	chr13:89194157-89194227	XLOC_010466
2	lnc-SLITRK5-7	chr13:89197598-89197764	NONHSAT034615
3	lnc-SLITRK5-7	chr13:89193084-89193698	NONHSAT034615
4	lnc-SLITRK5-8	chr13:89282351-89282651	ENSG00000261666.1
5	lnc-SLITRK5-8	chr13:89279107-89280404	ENSG00000261666.1
6	lnc-SLITRK5-7	chr13:89194157-89194227	NONHSAT034615
7	lnc-SLITRK5-7	chr13:89193084-89193698	NONHSAT034614
8	lnc-SLITRK5-7	chr13:89279107-89279587	NONHSAT034614
9	lnc-SLITRK5-7	chr13:89194157-89194227	NONHSAT034614
10	lnc-SLITRK5-7	chr13:89193119-89193698	XLOC_010466
11	lnc-SLITRK5-7	chr13:89194540-89194679	XLOC_010466
12	lnc-SLITRK5-7	chr13:89197598-89197764	XLOC_010466
13	lnc-SLITRK5-7	chr13:89194525-89194761	XLOC_010466

No data

Variant related genes	Relation type
LINC00433	TF binding region
LINC00560	TF binding region
LINC00433	CpG island
LINC00560	CpG island
ENSG00000261666	chromatin interactions
VEGFA	miRNA target sites
MUC17	miRNA target sites

Extended variants
information (count: 1873 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531546570	chr13:89164459-89164460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543303525	chr13:89164462-89164463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562552201	chr13:89164593-89164594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529991704	chr13:89164631-89164632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533950291	chr13:89164648-89164649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200816383	chr13:89164650-89164651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs67109994	chr13:89164672-89164673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535887612	chr13:89164746-89164747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143929876	chr13:89164760-89164761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113469605	chr13:89164815-89164816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527770489	chr13:89164816-89164817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs552767811	chr13:89164851-89164852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182430479	chr13:89164871-89164872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546200297	chr13:89164882-89164883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs640020	chr13:89164883-89164884	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs568082892	chr13:89164884-89164885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535404744	chr13:89164898-89164899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76290708	chr13:89164918-89164919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113043366	chr13:89164938-89164939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543555190	chr13:89164957-89164958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368640312	chr13:89164992-89164993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117921230	chr13:89165025-89165026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139210376	chr13:89165079-89165080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563479709	chr13:89165080-89165081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561621893	chr13:89165081-89165082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111380940	chr13:89165086-89165087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113477784	chr13:89165103-89165104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149410300	chr13:89165119-89165120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560267057	chr13:89165152-89165153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527835460	chr13:89165164-89165165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552383736	chr13:89165169-89165170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571056883	chr13:89165177-89165178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531910935	chr13:89165179-89165180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550509082	chr13:89165182-89165183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568803108	chr13:89165184-89165185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111315625	chr13:89165209-89165210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536133424	chr13:89165216-89165217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553776416	chr13:89165221-89165222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9514921	chr13:89165239-89165240	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539530024	chr13:89165278-89165279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557521440	chr13:89165296-89165297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368150986	chr13:89165299-89165300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543179402	chr13:89165312-89165313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555128957	chr13:89165339-89165340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573628122	chr13:89165366-89165367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540966765	chr13:89165367-89165368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371992258	chr13:89165410-89165411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560577549	chr13:89165411-89165412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575557359	chr13:89165420-89165421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572301411	chr13:89165425-89165426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
High-grade prostatic intraepithelial neoplasia	16573809	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
Congenital anomalies of the kidney and urinary tract	18316590	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
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89163600-89165000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr13:89163600-89165000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr13:89163600-89165000	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:89163800-89165200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:89163800-89165200	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr13:89163800-89165200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:89165000-89168000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr13:89168000-89168400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr13:89169800-89171000	Active TSS	H9 Cell Line	embryonic stem cell
10	chr13:89170600-89171400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr13:89171400-89172400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:89172400-89172800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr13:89172800-89176600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:89176000-89178400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr13:89177600-89179400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:89178400-89179000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:89178400-89179000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr13:89178400-89179200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr13:89178600-89179000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:89178600-89179000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:89178600-89179400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr13:89178600-89179400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:89178800-89179400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr13:89210400-89210800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr13:89221600-89233000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:89233000-89233200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:89237600-89238000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:89237600-89238800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:89237600-89238800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr13:89238000-89238200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:89238200-89238400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr13:89238200-89238600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:89238400-89238600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr13:89238600-89238800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:89244200-89244800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr13:89244400-89244600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:89247000-89247400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:89252400-89253000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:89255000-89255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr13:89255000-89255400	Enhancers	Esophagus	oesophagus
41	chr13:89255000-89256400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr13:89255200-89256000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr13:89255400-89256400	Enhancers	NHEK	skin
44	chr13:89267800-89268800	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr13:89268800-89270000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr13:89270200-89270400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr13:89271400-89274400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr13:89273800-89276000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr13:89274000-89276400	Enhancers	Primary T cells from cord blood	blood
50	chr13:89274400-89274600	Active TSS	Primary T helper naive cells from peripheral blood	blood

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