Variant report

Variant	nsv900440
Chromosome Location	chr13:69171580-69282276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:249)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:249 , 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	chr13:69271864-69271997	K562	blood:	n/a	n/a
2	BACH1	chr13:69265322-69265590	K562	blood:	n/a	n/a
3	BACH1	chr13:69266329-69266484	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:69240994-69241236	GM12878	blood:	n/a	n/a
5	CBX3	chr13:69271695-69271977	K562	blood:	n/a	n/a
6	CCNT2	chr13:69271798-69271998	K562	blood:	n/a	n/a
7	CEBPB	chr13:69228540-69228837	K562	blood:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
8	CEBPB	chr13:69189035-69189348	IMR90	lung:	n/a	chr13:69189217-69189228
9	CEBPB	chr13:69268802-69269108	K562	blood:	n/a	n/a
10	CEBPB	chr13:69189070-69189346	A549	lung:	n/a	chr13:69189217-69189228
11	CEBPB	chr13:69223398-69223677	Hela-S3	cervix:	n/a	chr13:69223512-69223524
12	CEBPB	chr13:69268765-69268935	A549	lung:	n/a	n/a
13	CEBPB	chr13:69189188-69189331	H1-hESC	embryonic stem cell:	n/a	chr13:69189217-69189228
14	CEBPB	chr13:69189054-69189377	HepG2	liver:	n/a	chr13:69189217-69189228
15	CEBPB	chr13:69228505-69228846	HepG2	liver:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
16	CEBPB	chr13:69268752-69269047	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:69268761-69269087	IMR90	lung:	n/a	n/a
18	CEBPB	chr13:69228553-69228762	A549	lung:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
19	CEBPB	chr13:69189114-69189314	Hela-S3	cervix:	n/a	chr13:69189217-69189228
20	CEBPB	chr13:69228532-69228846	IMR90	lung:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
21	CEBPB	chr13:69268809-69269015	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr13:69228574-69228763	H1-hESC	embryonic stem cell:	n/a	chr13:69228659-69228670 chr13:69228661-69228672
23	CTCF	chr13:69259660-69259810	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr13:69190769-69190832	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:69256760-69256910	RPTEC	kidney:	n/a	n/a
26	CTCF	chr13:69271800-69271950	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr13:69271740-69272010	BE2_C	brain:	n/a	n/a
28	CTCF	chr13:69190792-69190857	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:69280578-69280650	GM10248	blood:	n/a	n/a
30	CTCF	chr13:69271740-69271890	SK-N-SH_RA	brain:	n/a	n/a
31	E2F4	chr13:69209275-69209634	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr13:69231410-69231610	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr13:69257947-69257992	MCF10A-Er-Src	breast:	n/a	n/a
34	EBF1	chr13:69250991-69251502	GM12878	blood:	n/a	n/a
35	EBF1	chr13:69252919-69253173	GM12878	blood:	n/a	chr13:69253030-69253041
36	EBF1	chr13:69251784-69251838	GM12878	blood:	n/a	n/a
37	EBF1	chr13:69181299-69181562	GM12878	blood:	n/a	chr13:69181435-69181446 chr13:69181436-69181446
38	EBF1	chr13:69182410-69182568	GM12878	blood:	n/a	chr13:69182432-69182443
39	ELF1	chr13:69271603-69271966	K562	blood:	n/a	chr13:69271794-69271807
40	EP300	chr13:69271641-69272137	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr13:69268926-69268940	HepG2	liver:	n/a	n/a
42	EP300	chr13:69260123-69261010	MCF-7	breast:	n/a	chr13:69260865-69260875
43	EP300	chr13:69281713-69282108	K562	blood:	n/a	chr13:69282086-69282093
44	EP300	chr13:69271528-69272172	SK-N-SH	brain:	n/a	n/a
45	EP300	chr13:69271627-69272125	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr13:69271701-69271955	K562	blood:	n/a	n/a
47	EP300	chr13:69259993-69261092	MCF-7	breast:	n/a	chr13:69260865-69260875
48	EP300	chr13:69226110-69226485	MCF-7	breast:	n/a	n/a
49	FAM48A	chr13:69203397-69203508	GM12878	blood:	n/a	n/a
50	FOS	chr13:69226295-69226498	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	chr13:69261665-69261715	T-47D	breast:	n/a
2	chr13:69261665-69261715	PFSK-1	brain:	n/a
3	chr13:69261665-69261715	NHBE	bronchial:	n/a
4	chr13:69261665-69261715	BE2_C	brain:	n/a
5	chr13:69261665-69261715	SAEC	small airway:	n/a
6	chr13:69261665-69261715	HRPEpiC	eye:	n/a
7	chr13:69261665-69261715	AG09319	gingival:	n/a
8	chr13:69261665-69261715	NB4	blood:	n/a
9	chr13:69261665-69261715	HepG2	liver:	n/a
10	chr13:69261665-69261715	NT2-D1	testis:	n/a
11	chr13:69261665-69261715	AG09309	skin:	n/a
12	chr13:69261665-69261715	K562	blood:	n/a
13	chr13:69261665-69261715	IMR90	lung:	fetal
14	chr13:69261665-69261715	HNPCEpiC	eye:	n/a
15	chr13:69261665-69261715	HUVEC	blood vessel:	n/a
16	chr13:69261665-69261715	ECC-1	luminal epithelium:	n/a
17	chr13:69261665-69261715	AG04450	lung:	fetal
18	chr13:69261665-69261715	Hela-S3	cervix:	n/a
19	chr13:69261665-69261715	SK-N-SH_RA	brain:	n/a
20	chr13:69261665-69261715	MCF-7	breast:	n/a
21	chr13:69261665-69261715	HEEpiC	esophagus:	n/a
22	chr13:69261665-69261715	AG04449	skin:	fetal
23	chr13:69261665-69261715	BJ	skin:	n/a
24	chr13:69261665-69261715	AoSMC	blood vessel:	n/a
25	chr13:69261665-69261715	Jurkat	blood:	n/a
26	chr13:69261665-69261715	GM12892	blood:	n/a
27	chr13:69261665-69261715	U87	brain:	n/a
28	chr13:69261665-69261715	AG10803	skin:	n/a
29	chr13:69261665-69261715	Hepatocyte	liver:	n/a
30	chr13:69261665-69261715	GM06990	blood:	n/a
31	chr13:69261665-69261715	HAEpiC	amniotic membrane:	n/a
32	chr13:69261665-69261715	A549	lung:	n/a
33	chr13:69261665-69261715	ovcar-3	ovarian:	n/a
34	chr13:69261665-69261715	HEK293	kidney:	embryo
35	chr13:69261665-69261715	HL-60	blood:	n/a
36	chr13:69261665-69261715	HMEC	breast:	n/a
37	chr13:69261665-69261715	HRCEpiC	kidney:	n/a
38	chr13:69261665-69261715	NHDF-neo	bronchial:	n/a
39	chr13:69261665-69261715	GM12878	blood:	n/a
40	chr13:69261665-69261715	LNCaP	prostate:	n/a
41	chr13:69261665-69261715	SK-N-MC	brain:	n/a
42	chr13:69261665-69261715	HIPEpiC	eye:	n/a
43	chr13:69261665-69261715	NH-A	brain:	n/a
44	chr13:69261665-69261715	MCF10A-Er-Src	breast:	n/a
45	chr13:69261665-69261715	CMK	blood:	n/a
46	chr13:69261665-69261715	SKMC	muscle:	n/a
47	chr13:69261665-69261715	ProgFib	skin:	n/a
48	chr13:69261665-69261715	GM12891	blood:	n/a
49	chr13:69261665-69261715	RPTEC	kidney:	n/a
50	chr13:69261665-69261715	PANC-1	pancreas:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69259986..69260836-chr13:69285583..69286413,2	MCF-7	breast:
2	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
3	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
4	chr13:69218941..69220747-chr13:69221001..69223260,2	K562	blood:
5	chr13:69259900..69260965-chr13:69319275..69320290,3	MCF-7	breast:
6	chr13:69213639..69216422-chr13:69230531..69232946,2	K562	blood:
7	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
8	chr13:69261144..69263388-chr13:69284618..69286596,2	MCF-7	breast:
9	chr13:69260117..69261169-chr13:69319440..69320437,6	MCF-7	breast:
10	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
11	chr13:69213639..69216422-chr13:69230531..69232946,2	K562	blood:
12	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
13	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
14	chr13:69259880..69261273-chr13:69319408..69320273,7	MCF-7	breast:
15	chr13:69197810..69200163-chr13:69200816..69203067,2	K562	blood:
16	chr13:69197810..69200163-chr13:69200816..69203067,2	K562	blood:
17	chr13:69232704..69235680-chr13:69237810..69239831,2	K562	blood:
18	chr13:69260112..69260846-chr13:69285482..69286306,2	MCF-7	breast:
19	chr13:69259897..69261382-chr13:69319281..69320393,15	MCF-7	breast:
20	chr13:69232704..69235680-chr13:69237810..69239831,2	K562	blood:
21	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
22	chr13:69258057..69262640-chr13:69318281..69322115,7	MCF-7	breast:
23	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
24	chr13:69218941..69220747-chr13:69221001..69223260,2	K562	blood:
25	chr13:69266497..69268743-chr13:69269469..69272027,2	MCF-7	breast:
26	chr13:69281888..69284510-chr13:69284969..69287100,2	K562	blood:
27	chr13:69259973..69261382-chr13:69319364..69320393,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-8	chr13:69267938-69268213	NONHSAT034237
2	lnc-BORA-27	chr13:69208322-69208618	NONHSAT034235
3	lnc-BORA-26	chr13:69228704-69229182	NONHSAT034236

No data

Variant related genes	Relation type
RPL12P34	TF binding region
RN7SL761P	TF binding region
RPS3AP52	TF binding region
RPL12P34	CpG island
RN7SL761P	CpG island
RPS3AP52	CpG island
ENSG00000243671	chromatin interactions

Extended variants
information (count: 1658 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1658 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs287312	chr13:69171580-69171581	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563075525	chr13:69171583-69171584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144775435	chr13:69171641-69171642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542457238	chr13:69171642-69171643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559493657	chr13:69171651-69171652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186640061	chr13:69171668-69171669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9541458	chr13:69171697-69171698	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs564347413	chr13:69171754-69171755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs533325709	chr13:69171755-69171756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528380291	chr13:69171776-69171777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550185280	chr13:69171796-69171797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs287313	chr13:69171801-69171802	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs535949631	chr13:69171874-69171875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9571962	chr13:69171916-69171917	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs192499798	chr13:69171933-69171934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535027930	chr13:69171975-69171976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571216755	chr13:69172028-69172029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148234506	chr13:69172069-69172070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571830558	chr13:69172116-69172117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs287314	chr13:69172144-69172145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs575629070	chr13:69172162-69172163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs556533984	chr13:69172244-69172245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184548033	chr13:69172255-69172256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367688883	chr13:69172259-69172260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573439634	chr13:69172323-69172324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141264567	chr13:69172354-69172355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376161073	chr13:69172360-69172361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552897034	chr13:69172438-69172439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572967816	chr13:69172443-69172444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs67450654	chr13:69172464-69172465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544993026	chr13:69172469-69172470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574347127	chr13:69172472-69172473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs398023244	chr13:69172483-69172484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527480866	chr13:69172495-69172496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71196204	chr13:69172510-69172511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs66488668	chr13:69172511-69172512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79765150	chr13:69172516-69172517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376874418	chr13:69172517-69172518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565220543	chr13:69172520-69172521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs207806	chr13:69172521-69172522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112017340	chr13:69172526-69172527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568988127	chr13:69172571-69172572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79217022	chr13:69177412-69177413	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs74895450	chr13:69177416-69177417	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs556795701	chr13:69177426-69177427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs369548104	chr13:69177441-69177442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs374060919	chr13:69177512-69177513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs1855701	chr13:69177548-69177549	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs191822155	chr13:69177648-69177649	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs184039995	chr13:69177660-69177661	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69170600-69172600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:69171400-69171800	Weak transcription	Fetal Heart	heart
3	chr13:69171800-69172600	Enhancers	Fetal Heart	heart
4	chr13:69177400-69177800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr13:69177800-69185200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr13:69182000-69182400	Active TSS	Hela-S3	cervix
7	chr13:69190800-69191800	Enhancers	HepG2	liver
8	chr13:69191400-69192000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:69191600-69191800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:69191800-69192000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:69194400-69194600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:69194600-69194800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr13:69194800-69195200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:69217800-69219200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr13:69218800-69219200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr13:69224000-69224400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:69238800-69239000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:69247400-69247800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:69250600-69252000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr13:69250800-69251000	Enhancers	HSMM	muscle
21	chr13:69251000-69251400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr13:69251000-69252000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr13:69251200-69252200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:69252000-69253000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr13:69252000-69253000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr13:69252800-69253200	Enhancers	Placenta Amnion	Placenta Amnion
27	chr13:69253000-69253200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:69253000-69253200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:69253000-69253400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr13:69253200-69256400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr13:69253200-69260200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr13:69258400-69260200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr13:69260200-69260600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr13:69260200-69260800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:69260200-69260800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr13:69260200-69264600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:69260400-69260800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr13:69260600-69261400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr13:69260600-69262800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr13:69260800-69262200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr13:69260800-69262200	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr13:69260800-69262200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr13:69262000-69262800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr13:69262200-69262400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr13:69262200-69262600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr13:69262200-69262600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr13:69262200-69262600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr13:69262200-69262800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr13:69262200-69262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr13:69262400-69262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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