Variant report

Variant	nsv900445
Chromosome Location	chr13:69240180-69272157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

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	chr13:69266329-69266484	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:69265322-69265590	K562	blood:	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	chr13:69268752-69269047	HepG2	liver:	n/a	n/a
8	CEBPB	chr13:69268765-69268935	A549	lung:	n/a	n/a
9	CEBPB	chr13:69268802-69269108	K562	blood:	n/a	n/a
10	CEBPB	chr13:69268809-69269015	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr13:69268761-69269087	IMR90	lung:	n/a	n/a
12	CTCF	chr13:69259660-69259810	HPAF	blood vessel:	n/a	n/a
13	CTCF	chr13:69271740-69272010	BE2_C	brain:	n/a	n/a
14	CTCF	chr13:69271800-69271950	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr13:69256760-69256910	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:69271740-69271890	SK-N-SH_RA	brain:	n/a	n/a
17	E2F4	chr13:69257947-69257992	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr13:69252919-69253173	GM12878	blood:	n/a	chr13:69253030-69253041
19	EBF1	chr13:69250991-69251502	GM12878	blood:	n/a	n/a
20	EBF1	chr13:69251784-69251838	GM12878	blood:	n/a	n/a
21	ELF1	chr13:69271603-69271966	K562	blood:	n/a	chr13:69271794-69271807
22	EP300	chr13:69271528-69272172	SK-N-SH	brain:	n/a	n/a
23	EP300	chr13:69260123-69261010	MCF-7	breast:	n/a	chr13:69260865-69260875
24	EP300	chr13:69271701-69271955	K562	blood:	n/a	n/a
25	EP300	chr13:69271627-69272125	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr13:69259993-69261092	MCF-7	breast:	n/a	chr13:69260865-69260875
27	EP300	chr13:69271641-69272137	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr13:69268926-69268940	HepG2	liver:	n/a	n/a
29	FOS	chr13:69271907-69271972	MCF10A-Er-Src	breast:	n/a	n/a
30	FOXM1	chr13:69260159-69261228	MCF-7	breast:	n/a	n/a
31	FOXM1	chr13:69260118-69261026	MCF-7	breast:	n/a	n/a
32	GATA3	chr13:69260124-69261119	MCF-7	breast:	n/a	n/a
33	GATA3	chr13:69264612-69264851	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr13:69271582-69272262	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr13:69271578-69272195	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr13:69260086-69261247	MCF-7	breast:	n/a	n/a
37	GATA3	chr13:69260124-69261136	MCF-7	breast:	n/a	n/a
38	GATA3	chr13:69260115-69261157	MCF-7	breast:	n/a	n/a
39	IRF1	chr13:69271771-69272074	K562	blood:	n/a	n/a
40	JUN	chr13:69247954-69248132	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUN	chr13:69262695-69262762	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr13:69271641-69272141	SK-N-SH	brain:	n/a	n/a
43	JUND	chr13:69271670-69272198	SK-N-SH	brain:	n/a	n/a
44	MAFF	chr13:69266009-69266511	K562	blood:	n/a	chr13:69266361-69266379
45	MAFF	chr13:69271995-69272221	HepG2	liver:	n/a	n/a
46	MAFF	chr13:69266298-69266516	HepG2	liver:	n/a	chr13:69266361-69266379
47	MAFF	chr13:69265294-69265529	K562	blood:	n/a	chr13:69265408-69265426
48	MAFF	chr13:69265392-69265521	HepG2	liver:	n/a	chr13:69265408-69265426
49	MAFF	chr13:69271805-69272181	K562	blood:	n/a	n/a
50	MAFK	chr13:69271944-69272271	HepG2	liver:	n/a	chr13:69272119-69272130 chr13:69272120-69272131 chr13:69272120-69272131

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69261665-69261715	H1-hESC	embryonic stem cell:	embryo
2	chr13:69261665-69261715	HNPCEpiC	eye:	n/a
3	chr13:69261665-69261715	HepG2	liver:	n/a
4	chr13:69261665-69261715	NT2-D1	testis:	n/a
5	chr13:69261665-69261715	K562	blood:	n/a
6	chr13:69261665-69261715	SKMC	muscle:	n/a
7	chr13:69261665-69261715	SK-N-SH	brain:	n/a
8	chr13:69261665-69261715	NHBE	bronchial:	n/a
9	chr13:69261665-69261715	GM12878	blood:	n/a
10	chr13:69261665-69261715	HEEpiC	esophagus:	n/a
11	chr13:69261665-69261715	SK-N-MC	brain:	n/a
12	chr13:69261665-69261715	GM19239	blood:	n/a
13	chr13:69261665-69261715	GM12892	blood:	n/a
14	chr13:69261665-69261715	AG04449	skin:	fetal
15	chr13:69261665-69261715	BE2_C	brain:	n/a
16	chr13:69261665-69261715	NB4	blood:	n/a
17	chr13:69261665-69261715	HL-60	blood:	n/a
18	chr13:69261665-69261715	HCPEpiC	choroid plexus:	n/a
19	chr13:69261665-69261715	AG04450	lung:	fetal
20	chr13:69261665-69261715	A549	lung:	n/a
21	chr13:69261665-69261715	HRPEpiC	eye:	n/a
22	chr13:69261665-69261715	Caco-2	colon:	n/a
23	chr13:69261665-69261715	Hela-S3	cervix:	n/a
24	chr13:69261665-69261715	ECC-1	luminal epithelium:	n/a
25	chr13:69261665-69261715	Jurkat	blood:	n/a
26	chr13:69261665-69261715	NH-A	brain:	n/a
27	chr13:69261665-69261715	HMEC	breast:	n/a
28	chr13:69261665-69261715	MCF-7	breast:	n/a
29	chr13:69261665-69261715	GM06990	blood:	n/a
30	chr13:69261665-69261715	AG09319	gingival:	n/a
31	chr13:69261665-69261715	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:69261665-69261715	RPTEC	kidney:	n/a
33	chr13:69261665-69261715	Hepatocyte	liver:	n/a
34	chr13:69261665-69261715	CMK	blood:	n/a
35	chr13:69261665-69261715	ProgFib	skin:	n/a
36	chr13:69261665-69261715	HCM	heart:	n/a
37	chr13:69261665-69261715	HCT-116	colon:	n/a
38	chr13:69261665-69261715	PFSK-1	brain:	n/a
39	chr13:69261665-69261715	AG10803	skin:	n/a
40	chr13:69261665-69261715	HRCEpiC	kidney:	n/a
41	chr13:69261665-69261715	NHDF-neo	bronchial:	n/a
42	chr13:69261665-69261715	HEK293	kidney:	embryo
43	chr13:69261665-69261715	HCF	heart:	n/a
44	chr13:69261665-69261715	GM12891	blood:	n/a
45	chr13:69261665-69261715	IMR90	lung:	fetal
46	chr13:69261665-69261715	PrEC	prostate:	n/a
47	chr13:69261665-69261715	HUVEC	blood vessel:	n/a
48	chr13:69261665-69261715	T-47D	breast:	n/a
49	chr13:69261665-69261715	SK-N-SH_RA	brain:	n/a
50	chr13:69261665-69261715	HAEpiC	amniotic membrane:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
2	chr13:69269070..69271450-chr13:69274161..69276898,2	K562	blood:
3	chr13:69259973..69261382-chr13:69319364..69320393,8	MCF-7	breast:
4	chr13:69254844..69257160-chr13:69257337..69259897,2	K562	blood:
5	chr13:69258057..69262640-chr13:69318281..69322115,7	MCF-7	breast:
6	chr13:69259897..69261382-chr13:69319281..69320393,15	MCF-7	breast:
7	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
8	chr13:69266497..69268743-chr13:69269469..69272027,2	MCF-7	breast:
9	chr13:69259880..69261273-chr13:69319408..69320273,7	MCF-7	breast:
10	chr13:69260117..69261169-chr13:69319440..69320437,6	MCF-7	breast:
11	chr13:69259986..69260836-chr13:69285583..69286413,2	MCF-7	breast:
12	chr13:69255286..69258231-chr13:69263633..69265493,2	K562	blood:
13	chr13:69261144..69263388-chr13:69284618..69286596,2	MCF-7	breast:
14	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
15	chr13:69258923..69261156-chr13:69263100..69265480,2	K562	blood:
16	chr13:69259900..69260965-chr13:69319275..69320290,3	MCF-7	breast:
17	chr13:69260112..69260846-chr13:69285482..69286306,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-8	chr13:69267938-69268213	NONHSAT034237

No data

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

Extended variants
information (count: 738 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534926649	chr13:69247415-69247416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557733878	chr13:69247482-69247483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76910076	chr13:69247513-69247514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183202341	chr13:69247519-69247520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559411259	chr13:69247522-69247523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532941429	chr13:69247536-69247537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187370027	chr13:69247537-69247538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191818006	chr13:69247541-69247542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563436524	chr13:69247572-69247573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541920325	chr13:69247586-69247587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182553634	chr13:69247591-69247592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374740530	chr13:69247630-69247631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs287372	chr13:69247634-69247635	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541728868	chr13:69247646-69247647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564650446	chr13:69247760-69247761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533659706	chr13:69247764-69247765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558228947	chr13:69250618-69250619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543854423	chr13:69250670-69250671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373541137	chr13:69250734-69250735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560756516	chr13:69250751-69250752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150092900	chr13:69250756-69250757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529804155	chr13:69250776-69250777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567929868	chr13:69250790-69250791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565574758	chr13:69250795-69250796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540177795	chr13:69250854-69250855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78757405	chr13:69250875-69250876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112889042	chr13:69250910-69250911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553143695	chr13:69250916-69250917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551306143	chr13:69250935-69250936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76354629	chr13:69250937-69250938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186159673	chr13:69251019-69251020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190529329	chr13:69251023-69251024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376681274	chr13:69251225-69251226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551793220	chr13:69251269-69251270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556552340	chr13:69251363-69251364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571665916	chr13:69251381-69251382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531031946	chr13:69251392-69251393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551056093	chr13:69251401-69251402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373358925	chr13:69251407-69251408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536829489	chr13:69251425-69251426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117743025	chr13:69251429-69251430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112432615	chr13:69251479-69251480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567190683	chr13:69251518-69251519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538957437	chr13:69251583-69251584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182958184	chr13:69251587-69251588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188140602	chr13:69251588-69251589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537562739	chr13:69251632-69251633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554214730	chr13:69251814-69251815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574172848	chr13:69251828-69251829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145854410	chr13:69251844-69251845	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69247400-69247800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:69250600-69252000	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr13:69250800-69251000	Enhancers	HSMM	muscle
4	chr13:69251000-69251400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:69251000-69252000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:69251200-69252200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:69252000-69253000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr13:69252000-69253000	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr13:69252800-69253200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr13:69253000-69253200	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:69253000-69253200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr13:69253000-69253400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr13:69253200-69256400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr13:69253200-69260200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr13:69258400-69260200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr13:69260200-69260600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:69260200-69260800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:69260200-69260800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr13:69260200-69264600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:69260400-69260800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr13:69260600-69261400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr13:69260600-69262800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr13:69260800-69262200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:69260800-69262200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr13:69260800-69262200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr13:69262000-69262800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr13:69262200-69262400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:69262200-69262600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr13:69262200-69262600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr13:69262200-69262600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr13:69262200-69262800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr13:69262200-69262800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr13:69262400-69262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr13:69262600-69282600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:69264600-69265000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:69264600-69265000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr13:69264600-69265000	Enhancers	Brain Germinal Matrix	brain
38	chr13:69266000-69266800	Enhancers	K562	blood
39	chr13:69266800-69272400	Weak transcription	K562	blood
40	chr13:69271200-69272600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr13:69271600-69271800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr13:69271800-69272000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr13:69271800-69272200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr13:69271800-69272400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr13:69272000-69275000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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