Variant report

Variant	esv3444432
Chromosome Location	chr13:61665252-61781081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:395)
CpG islands
(count:245)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:395 , 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	ATF2	chr13:61776209-61776573	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:61699745-61699887	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:61716704-61716925	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:61697729-61698001	GM12878	blood:	n/a	n/a
5	BATF	chr13:61697697-61698065	GM12878	blood:	n/a	n/a
6	BATF	chr13:61764037-61764369	GM12878	blood:	n/a	n/a
7	BATF	chr13:61748246-61748589	GM12878	blood:	n/a	chr13:61748440-61748451
8	BCL11A	chr13:61669103-61669330	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr13:61776231-61776484	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr13:61697700-61697990	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:61697716-61697959	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:61776262-61776489	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr13:61669022-61669340	H1-hESC	embryonic stem cell:	n/a	n/a
14	CCNT2	chr13:61765414-61765614	K562	blood:	n/a	n/a
15	CEBPB	chr13:61684759-61685050	HepG2	liver:	n/a	chr13:61684892-61684903
16	CEBPB	chr13:61771083-61771089	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:61684789-61685025	A549	lung:	n/a	chr13:61684892-61684903
18	CEBPB	chr13:61761666-61761992	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:61698242-61698305	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr13:61764196-61764402	HepG2	liver:	n/a	chr13:61764313-61764324 chr13:61764310-61764327
21	CEBPB	chr13:61710218-61710570	HepG2	liver:	n/a	chr13:61710376-61710387
22	CEBPB	chr13:61710235-61710525	H1-hESC	embryonic stem cell:	n/a	chr13:61710376-61710387
23	CEBPB	chr13:61668662-61668815	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr13:61710238-61710530	A549	lung:	n/a	chr13:61710376-61710387
25	CEBPB	chr13:61710235-61710545	IMR90	lung:	n/a	chr13:61710376-61710387
26	CEBPB	chr13:61725584-61725856	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:61670167-61670255	HepG2	liver:	n/a	n/a
28	CEBPB	chr13:61723225-61723436	HepG2	liver:	n/a	chr13:61723313-61723324
29	CEBPB	chr13:61723160-61723401	A549	lung:	n/a	chr13:61723313-61723324
30	CHD2	chr13:61669058-61669327	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr13:61699760-61699959	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr13:61699780-61699930	K562	blood:	n/a	n/a
33	CTCF	chr13:61699800-61699950	GM12864	blood:	n/a	n/a
34	CTCF	chr13:61699760-61699910	RPTEC	kidney:	n/a	n/a
35	CTCF	chr13:61699680-61699968	T-47D	breast:	n/a	n/a
36	CTCF	chr13:61699740-61699890	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr13:61699760-61699910	GM12868	blood:	n/a	n/a
38	CTCF	chr13:61699760-61699910	HAc	cerebellar:	n/a	n/a
39	CTCF	chr13:61699740-61699890	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr13:61699800-61699950	HCFaa	heart:	n/a	n/a
41	CTCF	chr13:61699680-61699830	HCT-116	colon:	n/a	n/a
42	CTCF	chr13:61714876-61714892	Fibrobl	skin:	n/a	n/a
43	CTCF	chr13:61699722-61699978	MCF-7	breast:	n/a	n/a
44	CTCF	chr13:61699780-61699930	GM12864	blood:	n/a	n/a
45	CTCF	chr13:61699800-61699950	GM12865	blood:	n/a	n/a
46	CTCF	chr13:61699774-61699921	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr13:61699780-61699930	GM12869	blood:	n/a	n/a
48	CTCF	chr13:61699808-61699940	K562	blood:	n/a	n/a
49	CTCF	chr13:61699780-61699930	Caco-2	colon:	n/a	n/a
50	CTCF	chr13:61699760-61699910	GM12870	blood:	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	chr13:61780589-61780639	SK-N-SH	brain:	n/a
2	chr13:61780589-61780639	SK-N-SH	brain:	n/a
3	chr13:61753592-61753642	HNPCEpiC	eye:	n/a
4	chr13:61780589-61780639	AG10803	skin:	n/a
5	chr13:61753592-61753642	NT2-D1	testis:	n/a
6	chr13:61758710-61758760	HepG2	liver:	n/a
7	chr13:61780664-61780714	SKMC	muscle:	n/a
8	chr13:61753592-61753642	NH-A	brain:	n/a
9	chr13:61758710-61758760	Caco-2	colon:	n/a
10	chr13:61780589-61780639	A549	lung:	n/a
11	chr13:61753592-61753642	SKMC	muscle:	n/a
12	chr13:61780589-61780639	K562	blood:	n/a
13	chr13:61780664-61780714	AG09319	gingival:	n/a
14	chr13:61780589-61780639	HEK293	kidney:	embryo
15	chr13:61753592-61753642	AoSMC	blood vessel:	n/a
16	chr13:61758710-61758760	NT2-D1	testis:	n/a
17	chr13:61758710-61758760	AG04450	lung:	fetal
18	chr13:61758710-61758760	Jurkat	blood:	n/a
19	chr13:61753592-61753642	HCPEpiC	choroid plexus:	n/a
20	chr13:61758710-61758760	Hepatocyte	liver:	n/a
21	chr13:61780589-61780639	AG04449	skin:	fetal
22	chr13:61758710-61758760	BJ	skin:	n/a
23	chr13:61780664-61780714	U87	brain:	n/a
24	chr13:61753592-61753642	ECC-1	luminal epithelium:	n/a
25	chr13:61780589-61780639	HIPEpiC	eye:	n/a
26	chr13:61780664-61780714	Hepatocyte	liver:	n/a
27	chr13:61753592-61753642	HRPEpiC	eye:	n/a
28	chr13:61780664-61780714	SK-N-SH	brain:	n/a
29	chr13:61758710-61758760	GM12878	blood:	n/a
30	chr13:61780589-61780639	PANC-1	pancreas:	n/a
31	chr13:61758710-61758760	AG09319	gingival:	n/a
32	chr13:61758710-61758760	PFSK-1	brain:	n/a
33	chr13:61753592-61753642	NHDF-neo	bronchial:	n/a
34	chr13:61780589-61780639	GM06990	blood:	n/a
35	chr13:61780589-61780639	AG09319	gingival:	n/a
36	chr13:61780589-61780639	ECC-1	luminal epithelium:	n/a
37	chr13:61780664-61780714	A549	lung:	n/a
38	chr13:61780589-61780639	ProgFib	skin:	n/a
39	chr13:61780664-61780714	NH-A	brain:	n/a
40	chr13:61780664-61780714	HRPEpiC	eye:	n/a
41	chr13:61758710-61758760	Hela-S3	cervix:	n/a
42	chr13:61753592-61753642	U87	brain:	n/a
43	chr13:61780664-61780714	T-47D	breast:	n/a
44	chr13:61758710-61758760	ovcar-3	ovarian:	n/a
45	chr13:61753592-61753642	GM06990	blood:	n/a
46	chr13:61758710-61758760	NB4	blood:	n/a
47	chr13:61753592-61753642	MCF-7	breast:	n/a
48	chr13:61753592-61753642	SK-N-MC	brain:	n/a
49	chr13:61780664-61780714	NT2-D1	testis:	n/a
50	chr13:61780589-61780639	SAEC	small airway:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:61732713..61735428-chr13:61747940..61750203,2	K562	blood:
2	chr13:61229131..61230781-chr13:61693406..61695295,2	MCF-7	breast:
3	chr11:27527514..27528297-chr13:61775281..61775781,2	Hela-S3	cervix:
4	chr13:61718056..61720899-chr13:61723464..61726288,2	K562	blood:
5	chr13:61718056..61720899-chr13:61723464..61726288,2	K562	blood:
6	chr13:61732713..61735428-chr13:61747940..61750203,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TDRD3-8	chr13:61721961-61722081	NONHSAT034123
2	lnc-TDRD3-8	chr13:61699768-61699866	NONHSAT034123
3	lnc-TDRD3-8	chr13:61696231-61696328	NONHSAT034123

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3169	chr13:61773982-61774003	MIMAT0015044

No data

Variant related genes	Relation type
MIR3169	TF binding region
MIR3169	CpG island

Extended variants
information (count: 3435 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3435 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535330409	chr13:61665252-61665253	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs555548230	chr13:61665260-61665261	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs575300121	chr13:61665301-61665302	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs140097377	chr13:61665313-61665314	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143568942	chr13:61665314-61665315	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs577749437	chr13:61665323-61665324	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs386771482	chr13:61665324-61665325	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373548040	chr13:61665325-61665326	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs567402975	chr13:61665327-61665328	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs186919805	chr13:61665357-61665358	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs190609921	chr13:61665358-61665359	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs182040669	chr13:61665370-61665371	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs9539035	chr13:61665377-61665378	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs184901243	chr13:61665381-61665382	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs550896118	chr13:61665400-61665401	Weak transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs145543943	chr13:61665421-61665422	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs533201174	chr13:61665448-61665449	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs9570459	chr13:61665455-61665456	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs568886848	chr13:61665461-61665462	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs189760313	chr13:61665471-61665472	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs182406604	chr13:61665472-61665473	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs77218514	chr13:61665497-61665498	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs540910716	chr13:61665523-61665524	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs555552042	chr13:61665524-61665525	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs569050261	chr13:61665534-61665535	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs544317753	chr13:61665564-61665565	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs371488188	chr13:61665590-61665591	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs369115798	chr13:61665602-61665603	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs562605422	chr13:61665625-61665626	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs530109349	chr13:61665631-61665632	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs541905783	chr13:61665637-61665638	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs186647267	chr13:61665646-61665647	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs528410865	chr13:61665670-61665671	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs112618923	chr13:61665721-61665722	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs35646555	chr13:61665722-61665723	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs57638281	chr13:61665724-61665725	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs558115018	chr13:61665775-61665776	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs546893221	chr13:61665788-61665789	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs146996016	chr13:61665791-61665792	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs532311248	chr13:61665837-61665838	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs550704926	chr13:61665844-61665845	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs568810290	chr13:61665848-61665849	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs536340813	chr13:61665849-61665850	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs80232334	chr13:61665851-61665852	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs547914836	chr13:61665855-61665856	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs557533853	chr13:61665873-61665874	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs191284435	chr13:61665931-61665932	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs138002333	chr13:61665947-61665948	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs558793365	chr13:61665961-61665962	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs573527300	chr13:61666032-61666033	Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
small cell lung cancer	20016488	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
Lung cancer	18438408	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
Esophageal squamous carcinoma	20200074	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61659800-61668600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr13:61660200-61668600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr13:61662600-61665400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:61662800-61668400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:61664200-61668400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:61664200-61668600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr13:61664400-61668600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr13:61665400-61666600	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:61666600-61669400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:61668400-61668600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr13:61668400-61669600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr13:61668400-61669600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr13:61668600-61668800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr13:61668600-61669600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr13:61668600-61669600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:61668600-61669800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:61668600-61669800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr13:61668600-61669800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr13:61668600-61669800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr13:61668600-61670200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr13:61668800-61669000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr13:61668800-61669200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr13:61669200-61669600	Enhancers	H9 Cell Line	embryonic stem cell
24	chr13:61669400-61670400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr13:61669600-61670600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:61669800-61670000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:61669800-61670800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr13:61670400-61670600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:61670600-61671200	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:61670800-61671800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr13:61671200-61671600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:61671600-61671800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:61671800-61672600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:61672600-61677000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:61672800-61673000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr13:61677000-61677800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:61677800-61687000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:61684200-61685200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:61684400-61684600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr13:61684600-61686000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr13:61685000-61685400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr13:61685400-61685600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr13:61686000-61686400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:61687000-61694400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:61687400-61688000	ZNF genes & repeats	Gastric	stomach
46	chr13:61687400-61688200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:61694400-61699800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr13:61698000-61698400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr13:61698000-61698400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr13:61698000-61698600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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