Variant report

Variant	nsv900375
Chromosome Location	chr13:65501587-65577032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:255)
CpG islands
(count:491)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:65503121-65503331	GM12878	blood:	n/a	n/a
2	BCL11A	chr13:65512859-65513178	GM12878	blood:	n/a	n/a
3	BCL11A	chr13:65512818-65513084	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:65512810-65513130	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:65503090-65503733	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr13:65549486-65549834	IMR90	lung:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
7	CEBPB	chr13:65503142-65503716	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:65549489-65549824	HepG2	liver:	n/a	chr13:65549674-65549685 chr13:65549616-65549627
9	CEBPB	chr13:65530999-65531037	HepG2	liver:	n/a	chr13:65531013-65531026 chr13:65531015-65531026 chr13:65531010-65531027 chr13:65531013-65531024 chr13:65531013-65531026
10	CHD1	chr13:65568223-65568415	GM12878	blood:	n/a	n/a
11	CHD2	chr13:65567966-65568470	GM12878	blood:	n/a	n/a
12	CTCF	chr13:65571700-65571850	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr13:65571640-65571790	HCT-116	colon:	n/a	n/a
14	CTCF	chr13:65519380-65519530	HMEC	breast:	n/a	chr13:65519402-65519423
15	CTCF	chr13:65559841-65559911	Lung_OC	lung:	n/a	n/a
16	CTCF	chr13:65532360-65532510	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr13:65571760-65571910	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr13:65571680-65571830	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr13:65571720-65571870	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr13:65502073-65502093	Fibrobl	skin:	n/a	n/a
21	CTCF	chr13:65515436-65515516	GM10248	blood:	n/a	n/a
22	CTCF	chr13:65571800-65571950	HMEC	breast:	n/a	n/a
23	CTCF	chr13:65566920-65567070	AG04449	skin:	n/a	n/a
24	CTCF	chr13:65571720-65571870	BE2_C	brain:	n/a	n/a
25	CTCF	chr13:65571700-65571850	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr13:65571800-65571950	HepG2	liver:	n/a	n/a
27	CTCF	chr13:65571680-65571830	AG04450	lung:	n/a	n/a
28	CTCF	chr13:65519280-65519430	HPAF	blood vessel:	n/a	chr13:65519402-65519423
29	CTCF	chr13:65571760-65571910	Caco-2	colon:	n/a	n/a
30	CTCF	chr13:65571780-65571930	AG04450	lung:	n/a	n/a
31	CTCF	chr13:65502048-65502064	Fibrobl	skin:	n/a	n/a
32	CTCF	chr13:65571794-65571840	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr13:65519300-65519450	AG10803	skin:	n/a	chr13:65519402-65519423
34	CTCF	chr13:65503954-65504015	GM10248	blood:	n/a	n/a
35	CTCF	chr13:65519300-65519450	HMEC	breast:	n/a	chr13:65519402-65519423
36	CTCF	chr13:65571760-65571910	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr13:65571760-65571910	HMEC	breast:	n/a	n/a
38	CTCF	chr13:65519389-65519419	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr13:65571780-65571930	AG10803	skin:	n/a	n/a
40	CTCF	chr13:65551897-65551982	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr13:65519389-65519432	ProgFib	skin:	n/a	chr13:65519402-65519423
42	CTCF	chr13:65519390-65519427	Gliobla	brain:	n/a	chr13:65519402-65519423
43	CTCF	chr13:65530122-65530177	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr13:65532436-65532505	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr13:65552346-65552377	GM13976	blood:	n/a	n/a
46	E2F4	chr13:65574843-65575043	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr13:65547649-65547844	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:65503219-65503293	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:65517477-65517669	MCF10A-Er-Src	breast:	n/a	n/a
50	EBF1	chr13:65557179-65557449	GM12878	blood:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:65532820-65532870	SK-N-SH	brain:	n/a
2	chr13:65533500-65533550	ECC-1	luminal epithelium:	n/a
3	chr13:65533500-65533550	CMK	blood:	n/a
4	chr13:65532820-65532870	SK-N-SH	brain:	n/a
5	chr13:65533500-65533550	ECC-1	luminal epithelium:	n/a
6	chr13:65533500-65533550	CMK	blood:	n/a
7	chr13:65532581-65532631	K562	blood:	n/a
8	chr13:65532796-65532846	SKMC	muscle:	n/a
9	chr13:65532581-65532631	PrEC	prostate:	n/a
10	chr13:65532796-65532846	LNCaP	prostate:	n/a
11	chr13:65532408-65532458	Caco-2	colon:	n/a
12	chr13:65532408-65532458	HEK293	kidney:	embryo
13	chr13:65533500-65533550	SKMC	muscle:	n/a
14	chr13:65533139-65533189	SK-N-MC	brain:	n/a
15	chr13:65532796-65532846	HepG2	liver:	n/a
16	chr13:65532408-65532458	PFSK-1	brain:	n/a
17	chr13:65532581-65532631	HIPEpiC	eye:	n/a
18	chr13:65532581-65532631	HCF	heart:	n/a
19	chr13:65533139-65533189	HAEpiC	amniotic membrane:	n/a
20	chr13:65532408-65532458	HRCEpiC	kidney:	n/a
21	chr13:65533139-65533189	MCF10A-Er-Src	breast:	n/a
22	chr13:65532273-65532323	SK-N-SH_RA	brain:	n/a
23	chr13:65532273-65532323	NHBE	bronchial:	n/a
24	chr13:65532878-65532928	SKMC	muscle:	n/a
25	chr13:65533139-65533189	Hepatocyte	liver:	n/a
26	chr13:65532820-65532870	BE2_C	brain:	n/a
27	chr13:65533139-65533189	HRE	kidney:	n/a
28	chr13:65533139-65533189	H1-hESC	embryonic stem cell:	embryo
29	chr13:65532408-65532458	HCM	heart:	n/a
30	chr13:65532820-65532870	Caco-2	colon:	n/a
31	chr13:65532408-65532458	AG10803	skin:	n/a
32	chr13:65533139-65533189	PFSK-1	brain:	n/a
33	chr13:65533500-65533550	NHBE	bronchial:	n/a
34	chr13:65532878-65532928	Hela-S3	cervix:	n/a
35	chr13:65532820-65532870	AG09319	gingival:	n/a
36	chr13:65532878-65532928	HCM	heart:	n/a
37	chr13:65532581-65532631	U87	brain:	n/a
38	chr13:65533500-65533550	SK-N-SH	brain:	n/a
39	chr13:65533139-65533189	NHDF-neo	bronchial:	n/a
40	chr13:65532878-65532928	NHDF-neo	bronchial:	n/a
41	chr13:65533500-65533550	ovcar-3	ovarian:	n/a
42	chr13:65532796-65532846	CMK	blood:	n/a
43	chr13:65532273-65532323	AG04450	lung:	fetal
44	chr13:65532581-65532631	HRCEpiC	kidney:	n/a
45	chr13:65532581-65532631	AoSMC	blood vessel:	n/a
46	chr13:65532408-65532458	SAEC	small airway:	n/a
47	chr13:65532878-65532928	GM06990	blood:	n/a
48	chr13:65532820-65532870	ovcar-3	ovarian:	n/a
49	chr13:65533139-65533189	GM12891	blood:	n/a
50	chr13:65532581-65532631	HAEpiC	amniotic membrane:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
2	chr13:65501223..65502743-chr17:41399641..41401888,2	K562	blood:
3	chr13:65502724..65504224-chr17:41400395..41402648,2	MCF-7	breast:
4	chr13:65512386..65514959-chr13:65519104..65520898,2	K562	blood:
5	chr13:65501243..65504224-chr17:41399641..41402005,2	K562	blood:

No data

Variant related genes	Relation type
LGMNP1	TF binding region
LGMNP1	CpG island

Extended variants
information (count: 758 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2137512	chr13:65501587-65501588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537113148	chr13:65501591-65501592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189069122	chr13:65501637-65501638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562061425	chr13:65501722-65501723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9317459	chr13:65501730-65501731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569746182	chr13:65501761-65501762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536087566	chr13:65501767-65501768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536713334	chr13:65501771-65501772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572834669	chr13:65501834-65501835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76501629	chr13:65501842-65501843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181522570	chr13:65501903-65501904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575559909	chr13:65501904-65501905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544648206	chr13:65501929-65501930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139142197	chr13:65501949-65501950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575078779	chr13:65502021-65502022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186306407	chr13:65502024-65502025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531388460	chr13:65502074-65502075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9540268	chr13:65502102-65502103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192034164	chr13:65502128-65502129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35164015	chr13:65502280-65502281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143939405	chr13:65502283-65502284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552607364	chr13:65502298-65502299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140330510	chr13:65502331-65502332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113930399	chr13:65502345-65502346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181541989	chr13:65502392-65502393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185673131	chr13:65502404-65502405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190921150	chr13:65502438-65502439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532798785	chr13:65502450-65502451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144215979	chr13:65502451-65502452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552893210	chr13:65502478-65502479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566345545	chr13:65502494-65502495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538505918	chr13:65502508-65502509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563207439	chr13:65502605-65502606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569233394	chr13:65502626-65502627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537895843	chr13:65502650-65502651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183109221	chr13:65502656-65502657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575017819	chr13:65502666-65502667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540749047	chr13:65502675-65502676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554369206	chr13:65502815-65502816	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534863649	chr13:65502831-65502832	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546428428	chr13:65502843-65502844	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563084552	chr13:65502862-65502863	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530516990	chr13:65502875-65502876	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs552836710	chr13:65502941-65502942	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141869665	chr13:65502942-65502943	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187951265	chr13:65502952-65502953	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529706368	chr13:65502980-65502981	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73202411	chr13:65503006-65503007	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566284626	chr13:65503009-65503010	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs142971783	chr13:65503030-65503031	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65499600-65502800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:65502400-65503400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr13:65502400-65503800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr13:65502400-65504400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr13:65502600-65503800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr13:65502800-65503000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:65502800-65503000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr13:65502800-65503000	Enhancers	Hela-S3	cervix
9	chr13:65502800-65503200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr13:65502800-65503200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:65502800-65503200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:65502800-65503200	Enhancers	HMEC	breast
13	chr13:65502800-65503600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr13:65502800-65504400	Enhancers	NH-A	brain
15	chr13:65503000-65503200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr13:65503000-65503600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr13:65503000-65503600	Enhancers	NHDF-Ad	bronchial
18	chr13:65503000-65503800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr13:65503000-65503800	Enhancers	A549	lung
20	chr13:65503000-65503800	Enhancers	GM12878-XiMat	blood
21	chr13:65503000-65503800	Flanking Active TSS	Hela-S3	cervix
22	chr13:65503000-65504200	Enhancers	HUVEC	blood vessel
23	chr13:65503200-65503600	Flanking Active TSS	HMEC	breast
24	chr13:65503200-65504200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr13:65503200-65504600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:65503400-65503800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr13:65503600-65503800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr13:65503600-65504200	Enhancers	HMEC	breast
29	chr13:65503800-65504200	Enhancers	Hela-S3	cervix
30	chr13:65503800-65504600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr13:65503800-65504600	Weak transcription	GM12878-XiMat	blood
32	chr13:65504200-65504800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr13:65504400-65511600	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr13:65504600-65504800	Enhancers	GM12878-XiMat	blood
35	chr13:65504600-65505400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr13:65511600-65512000	Enhancers	Placenta Amnion	Placenta Amnion
37	chr13:65512000-65512200	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr13:65512200-65512600	Enhancers	Placenta Amnion	Placenta Amnion
39	chr13:65514200-65514800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:65514800-65516000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr13:65516000-65518200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr13:65518200-65518400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr13:65519000-65519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr13:65519200-65519600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:65533400-65533600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr13:65536000-65537400	Enhancers	Fetal Intestine Small	intestine
47	chr13:65566800-65567600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr13:65567000-65567600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:65576000-65576400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr13:65576000-65576600	Enhancers	HUES48 Cell Line	embryonic stem cell

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