Variant report

Variant	nsv832627
Chromosome Location	chr13:61642811-61829217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:489)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	ATF2	chr13:61821690-61822197	GM12878	blood:	n/a	n/a
3	ATF2	chr13:61821778-61822149	GM12878	blood:	n/a	n/a
4	BACH1	chr13:61659801-61659858	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:61716704-61716925	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:61699745-61699887	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:61697729-61698001	GM12878	blood:	n/a	n/a
8	BATF	chr13:61697697-61698065	GM12878	blood:	n/a	n/a
9	BATF	chr13:61821719-61822057	GM12878	blood:	n/a	n/a
10	BATF	chr13:61748246-61748589	GM12878	blood:	n/a	chr13:61748440-61748451
11	BATF	chr13:61764037-61764369	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:61776231-61776484	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr13:61697700-61697990	GM12878	blood:	n/a	n/a
14	BCL11A	chr13:61697716-61697959	GM12878	blood:	n/a	n/a
15	BCL11A	chr13:61821722-61822052	GM12878	blood:	n/a	n/a
16	BCL11A	chr13:61776262-61776489	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr13:61669022-61669340	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr13:61669103-61669330	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr13:61821611-61822203	GM12878	blood:	n/a	n/a
20	BCL3	chr13:61821762-61822135	GM12878	blood:	n/a	n/a
21	BHLHE40	chr13:61827626-61827956	GM12878	blood:	n/a	n/a
22	BHLHE40	chr13:61821740-61822106	GM12878	blood:	n/a	n/a
23	CCNT2	chr13:61765414-61765614	K562	blood:	n/a	n/a
24	CCNT2	chr13:61823509-61823714	K562	blood:	n/a	n/a
25	CEBPB	chr13:61761666-61761992	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:61825237-61825583	IMR90	lung:	n/a	chr13:61825387-61825398
27	CEBPB	chr13:61825313-61825473	K562	blood:	n/a	chr13:61825387-61825398
28	CEBPB	chr13:61664316-61664674	IMR90	lung:	n/a	chr13:61664495-61664506
29	CEBPB	chr13:61664314-61664634	HepG2	liver:	n/a	chr13:61664495-61664506
30	CEBPB	chr13:61698242-61698305	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr13:61684759-61685050	HepG2	liver:	n/a	chr13:61684892-61684903
32	CEBPB	chr13:61764196-61764402	HepG2	liver:	n/a	chr13:61764313-61764324 chr13:61764310-61764327
33	CEBPB	chr13:61664437-61664514	H1-hESC	embryonic stem cell:	n/a	chr13:61664495-61664506
34	CEBPB	chr13:61710238-61710530	A549	lung:	n/a	chr13:61710376-61710387
35	CEBPB	chr13:61684789-61685025	A549	lung:	n/a	chr13:61684892-61684903
36	CEBPB	chr13:61825273-61825447	H1-hESC	embryonic stem cell:	n/a	chr13:61825387-61825398
37	CEBPB	chr13:61710218-61710570	HepG2	liver:	n/a	chr13:61710376-61710387
38	CEBPB	chr13:61723225-61723436	HepG2	liver:	n/a	chr13:61723313-61723324
39	CEBPB	chr13:61668662-61668815	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr13:61664416-61664633	A549	lung:	n/a	chr13:61664495-61664506
41	CEBPB	chr13:61643046-61643246	HepG2	liver:	n/a	chr13:61643149-61643160
42	CEBPB	chr13:61710235-61710525	H1-hESC	embryonic stem cell:	n/a	chr13:61710376-61710387
43	CEBPB	chr13:61723160-61723401	A549	lung:	n/a	chr13:61723313-61723324
44	CEBPB	chr13:61670167-61670255	HepG2	liver:	n/a	n/a
45	CEBPB	chr13:61725584-61725856	HepG2	liver:	n/a	n/a
46	CEBPB	chr13:61825254-61825511	HepG2	liver:	n/a	chr13:61825387-61825398
47	CEBPB	chr13:61710235-61710545	IMR90	lung:	n/a	chr13:61710376-61710387
48	CEBPB	chr13:61646843-61647048	A549	lung:	n/a	n/a
49	CEBPB	chr13:61771083-61771089	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr13:61826536-61826637	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:61780589-61780639	LNCaP	prostate:	n/a
2	chr13:61780589-61780639	LNCaP	prostate:	n/a
3	chr13:61758710-61758760	BE2_C	brain:	n/a
4	chr13:61821307-61821357	MCF10A-Er-Src	breast:	n/a
5	chr13:61791681-61791731	NH-A	brain:	n/a
6	chr13:61758710-61758760	MCF10A-Er-Src	breast:	n/a
7	chr13:61660030-61660080	ovcar-3	ovarian:	n/a
8	chr13:61780589-61780639	U87	brain:	n/a
9	chr13:61780589-61780639	HEK293	kidney:	embryo
10	chr13:61780589-61780639	HNPCEpiC	eye:	n/a
11	chr13:61821307-61821357	GM12891	blood:	n/a
12	chr13:61791652-61791702	SAEC	small airway:	n/a
13	chr13:61821307-61821357	GM19239	blood:	n/a
14	chr13:61660030-61660080	NB4	blood:	n/a
15	chr13:61753592-61753642	HUVEC	blood vessel:	n/a
16	chr13:61660030-61660080	LNCaP	prostate:	n/a
17	chr13:61821307-61821357	HCT-116	colon:	n/a
18	chr13:61780664-61780714	HRE	kidney:	n/a
19	chr13:61791681-61791731	SKMC	muscle:	n/a
20	chr13:61780664-61780714	U87	brain:	n/a
21	chr13:61753592-61753642	ProgFib	skin:	n/a
22	chr13:61758710-61758760	H1-hESC	embryonic stem cell:	embryo
23	chr13:61660030-61660080	RPTEC	kidney:	n/a
24	chr13:61821307-61821357	GM06990	blood:	n/a
25	chr13:61791652-61791702	U87	brain:	n/a
26	chr13:61753592-61753642	MCF10A-Er-Src	breast:	n/a
27	chr13:61791652-61791702	ovcar-3	ovarian:	n/a
28	chr13:61780589-61780639	NH-A	brain:	n/a
29	chr13:61660030-61660080	HL-60	blood:	n/a
30	chr13:61821307-61821357	HIPEpiC	eye:	n/a
31	chr13:61780664-61780714	CMK	blood:	n/a
32	chr13:61821307-61821357	GM12878	blood:	n/a
33	chr13:61780664-61780714	NHBE	bronchial:	n/a
34	chr13:61660030-61660080	GM12878	blood:	n/a
35	chr13:61791652-61791702	HRE	kidney:	n/a
36	chr13:61780589-61780639	PFSK-1	brain:	n/a
37	chr13:61780664-61780714	NH-A	brain:	n/a
38	chr13:61660030-61660080	T-47D	breast:	n/a
39	chr13:61660030-61660080	K562	blood:	n/a
40	chr13:61791652-61791702	MCF10A-Er-Src	breast:	n/a
41	chr13:61780589-61780639	IMR90	lung:	fetal
42	chr13:61660030-61660080	GM19239	blood:	n/a
43	chr13:61753592-61753642	ovcar-3	ovarian:	n/a
44	chr13:61791652-61791702	MCF-7	breast:	n/a
45	chr13:61780664-61780714	A549	lung:	n/a
46	chr13:61758710-61758760	NH-A	brain:	n/a
47	chr13:61758710-61758760	HCF	heart:	n/a
48	chr13:61821307-61821357	HRCEpiC	kidney:	n/a
49	chr13:61753592-61753642	NHDF-neo	bronchial:	n/a
50	chr13:61660030-61660080	H1-hESC	embryonic stem cell:	embryo

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:61718056..61720899-chr13:61723464..61726288,2	K562	blood:
2	chr13:61718056..61720899-chr13:61723464..61726288,2	K562	blood:
3	chr13:61201360..61202127-chr13:61829066..61830170,3	MCF-7	breast:
4	chr13:61732713..61735428-chr13:61747940..61750203,2	K562	blood:
5	chr13:61229131..61230781-chr13:61693406..61695295,2	MCF-7	breast:
6	chr11:27527514..27528297-chr13:61775281..61775781,2	Hela-S3	cervix:
7	chr13:61732713..61735428-chr13:61747940..61750203,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TDRD3-8	chr13:61696231-61696328	NONHSAT034123
2	lnc-TDRD3-10	chr13:61794060-61794532	NONHSAT034125
3	lnc-TDRD3-8	chr13:61699768-61699866	NONHSAT034123
4	lnc-TDRD3-10	chr13:61793439-61793520	NONHSAT034125
5	lnc-TDRD3-8	chr13:61721961-61722081	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: 5543 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:5543 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182308813	chr13:61642839-61642840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575180265	chr13:61642861-61642862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184471825	chr13:61642915-61642916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554859121	chr13:61642935-61642936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572921117	chr13:61642943-61642944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548095322	chr13:61642985-61642986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189196198	chr13:61643001-61643002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139897298	chr13:61643002-61643003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577052875	chr13:61643075-61643076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17234420	chr13:61643097-61643098	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs142847066	chr13:61643099-61643100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529700408	chr13:61643105-61643106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147431220	chr13:61643136-61643137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs181133990	chr13:61643156-61643157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34690960	chr13:61643177-61643178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542920516	chr13:61643178-61643179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540629232	chr13:61643181-61643182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527861550	chr13:61643245-61643246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552390505	chr13:61643276-61643277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs57252817	chr13:61643379-61643380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561467253	chr13:61643413-61643414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570605175	chr13:61643426-61643427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531738873	chr13:61643457-61643458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61954581	chr13:61643462-61643463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549866327	chr13:61643486-61643487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568324057	chr13:61643541-61643542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185763108	chr13:61643588-61643589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs374734469	chr13:61643614-61643615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80157096	chr13:61643820-61643821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533738858	chr13:61643969-61643970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs112229088	chr13:61643986-61643987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577113443	chr13:61644029-61644030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544282316	chr13:61644038-61644039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556308106	chr13:61644097-61644098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574324839	chr13:61644131-61644132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10507661	chr13:61644179-61644180	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201339170	chr13:61644191-61644192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9570442	chr13:61644194-61644195	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528031306	chr13:61644198-61644199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139224433	chr13:61644202-61644203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149928060	chr13:61644215-61644216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530286486	chr13:61644223-61644224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201012363	chr13:61644227-61644228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200317471	chr13:61644228-61644229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34224006	chr13:61644229-61644230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs36029431	chr13:61644230-61644231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9539032	chr13:61644231-61644232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140380381	chr13:61644235-61644236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28701101	chr13:61644239-61644240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202214334	chr13:61644243-61644244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Breast cancer	22522925	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61642800-61649800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:61649800-61652600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:61652600-61652800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:61652800-61653000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:61652800-61653400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr13:61652800-61653600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:61652800-61653600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr13:61652800-61654000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr13:61652800-61654200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:61652800-61654200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr13:61652800-61654200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:61652800-61654600	Enhancers	H9 Cell Line	embryonic stem cell
13	chr13:61653000-61653200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:61653000-61654400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr13:61653200-61653600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:61653200-61653600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr13:61653600-61654000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:61653600-61654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:61653600-61654000	Enhancers	Placenta Amnion	Placenta Amnion
20	chr13:61654000-61654200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr13:61654000-61657000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr13:61654200-61654600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr13:61654200-61659200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr13:61654600-61655200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:61654600-61663800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr13:61655200-61662000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:61655800-61656600	Enhancers	Brain Germinal Matrix	brain
28	chr13:61656600-61659600	Weak transcription	Brain Germinal Matrix	brain
29	chr13:61657000-61661000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:61658200-61660800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr13:61658200-61661000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr13:61658600-61660800	Enhancers	NHEK	skin
33	chr13:61659200-61659600	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr13:61659200-61659800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr13:61659200-61660200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:61659600-61659800	Enhancers	Brain Germinal Matrix	brain
37	chr13:61659600-61660400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr13:61659600-61660600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr13:61659800-61660200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr13:61659800-61660600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr13:61659800-61660600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr13:61659800-61668600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr13:61660200-61668600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr13:61660400-61660600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr13:61660600-61662000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr13:61660600-61662000	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr13:61660600-61662200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr13:61660600-61663600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr13:61660600-61664000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr13:61660800-61662000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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