Variant report

Variant	nsv900385
Chromosome Location	chr13:66492872-66611146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr13:66589547-66589747	K562	blood:	n/a	n/a
2	CEBPB	chr13:66539663-66539995	IMR90	lung:	n/a	n/a
3	CEBPB	chr13:66571439-66571773	IMR90	lung:	n/a	n/a
4	CEBPB	chr13:66605742-66605955	H1-hESC	embryonic stem cell:	n/a	chr13:66605818-66605829
5	CEBPB	chr13:66495056-66495370	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:66559601-66560095	MCF-7	breast:	n/a	n/a
7	CEBPB	chr13:66605714-66605963	A549	lung:	n/a	chr13:66605818-66605829
8	CEBPB	chr13:66506381-66506581	HepG2	liver:	n/a	chr13:66506505-66506516
9	CEBPB	chr13:66574571-66574786	HepG2	liver:	n/a	chr13:66574676-66574685 chr13:66574675-66574686 chr13:66574674-66574685
10	CEBPB	chr13:66569441-66569593	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:66605650-66606010	IMR90	lung:	n/a	chr13:66605818-66605829
12	CEBPB	chr13:66605687-66605966	K562	blood:	n/a	chr13:66605818-66605829
13	CEBPB	chr13:66605646-66606003	HepG2	liver:	n/a	chr13:66605818-66605829
14	CEBPB	chr13:66585133-66585269	A549	lung:	n/a	n/a
15	CEBPB	chr13:66506502-66506548	A549	lung:	n/a	chr13:66506505-66506516
16	CEBPB	chr13:66559705-66560073	MCF-7	breast:	n/a	n/a
17	CHD2	chr13:66500909-66501075	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr13:66541238-66541323	GM13977	blood:	n/a	n/a
19	CTCF	chr13:66559900-66560050	HepG2	liver:	n/a	n/a
20	CTCF	chr13:66559840-66559990	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr13:66541180-66541330	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr13:66594220-66594370	SAEC	small airway:	n/a	n/a
23	CTCF	chr13:66501020-66501170	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr13:66500986-66501234	Gliobla	brain:	n/a	n/a
25	CTCF	chr13:66541160-66541310	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr13:66541180-66541330	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr13:66547742-66547802	GM20000	blood:	n/a	n/a
28	CTCF	chr13:66500970-66501252	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:66500959-66501292	K562	blood:	n/a	n/a
30	CTCF	chr13:66541086-66541337	A549	lung:	n/a	n/a
31	CTCF	chr13:66500940-66501090	HMEC	breast:	n/a	n/a
32	CTCF	chr13:66541010-66541452	ECC-1	luminal epithelium:	n/a	n/a
33	CTCF	chr13:66541118-66541409	Gliobla	brain:	n/a	n/a
34	CTCF	chr13:66501040-66501190	HVMF	connective:	n/a	n/a
35	CTCF	chr13:66559909-66560061	HepG2	liver:	n/a	n/a
36	CTCF	chr13:66541128-66541433	K562	blood:	n/a	n/a
37	CTCF	chr13:66541100-66541250	HCM	heart:	n/a	n/a
38	CTCF	chr13:66541140-66541290	MCF-7	breast:	n/a	n/a
39	CTCF	chr13:66559958-66560022	GM12878	blood:	n/a	n/a
40	CTCF	chr13:66541160-66541310	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr13:66541160-66541310	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr13:66560020-66560170	MCF-7	breast:	n/a	n/a
43	CTCF	chr13:66541093-66541381	A549	lung:	n/a	n/a
44	CTCF	chr13:66559941-66559944	NHEK	skin:	n/a	n/a
45	CTCF	chr13:66501080-66501230	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr13:66541220-66541370	HRE	kidney:	n/a	n/a
47	CTCF	chr13:66543800-66543950	AG10803	skin:	n/a	n/a
48	CTCF	chr13:66541141-66541383	MCF-7	breast:	n/a	n/a
49	CTCF	chr13:66541160-66541310	NB4	blood:	n/a	n/a
50	CTCF	chr13:66541180-66541330	SK-N-SH_RA	brain:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66501111-66501161	AG04449	skin:	fetal
2	chr13:66583686-66583736	HUVEC	blood vessel:	n/a
3	chr13:66583583-66583633	IMR90	lung:	fetal
4	chr13:66501111-66501161	NH-A	brain:	n/a
5	chr13:66583583-66583633	HPAEpiC	pulmonary alveolar:	n/a
6	chr13:66583583-66583633	MCF-7	breast:	n/a
7	chr13:66583686-66583736	HRPEpiC	eye:	n/a
8	chr13:66583583-66583633	HepG2	liver:	n/a
9	chr13:66583686-66583736	GM12892	blood:	n/a
10	chr13:66607275-66607325	ECC-1	luminal epithelium:	n/a
11	chr13:66583583-66583633	BE2_C	brain:	n/a
12	chr13:66501111-66501161	Caco-2	colon:	n/a
13	chr13:66583583-66583633	GM19239	blood:	n/a
14	chr13:66583686-66583736	K562	blood:	n/a
15	chr13:66583583-66583633	GM06990	blood:	n/a
16	chr13:66583583-66583633	NHBE	bronchial:	n/a
17	chr13:66583583-66583633	ovcar-3	ovarian:	n/a
18	chr13:66583686-66583736	NHBE	bronchial:	n/a
19	chr13:66583686-66583736	Hepatocyte	liver:	n/a
20	chr13:66607275-66607325	U87	brain:	n/a
21	chr13:66607275-66607325	CMK	blood:	n/a
22	chr13:66607275-66607325	AG10803	skin:	n/a
23	chr13:66607275-66607325	NHDF-neo	bronchial:	n/a
24	chr13:66583583-66583633	AG09319	gingival:	n/a
25	chr13:66501111-66501161	HIPEpiC	eye:	n/a
26	chr13:66583583-66583633	SK-N-SH_RA	brain:	n/a
27	chr13:66583583-66583633	GM12878	blood:	n/a
28	chr13:66607275-66607325	HMEC	breast:	n/a
29	chr13:66607275-66607325	AoSMC	blood vessel:	n/a
30	chr13:66583686-66583736	GM12891	blood:	n/a
31	chr13:66583583-66583633	U87	brain:	n/a
32	chr13:66607275-66607325	K562	blood:	n/a
33	chr13:66501111-66501161	HCT-116	colon:	n/a
34	chr13:66501111-66501161	SAEC	small airway:	n/a
35	chr13:66583686-66583736	AG04450	lung:	fetal
36	chr13:66501111-66501161	PrEC	prostate:	n/a
37	chr13:66501111-66501161	HL-60	blood:	n/a
38	chr13:66501111-66501161	SK-N-SH_RA	brain:	n/a
39	chr13:66583583-66583633	HIPEpiC	eye:	n/a
40	chr13:66583686-66583736	HNPCEpiC	eye:	n/a
41	chr13:66607275-66607325	IMR90	lung:	fetal
42	chr13:66501111-66501161	LNCaP	prostate:	n/a
43	chr13:66501111-66501161	Hela-S3	cervix:	n/a
44	chr13:66583686-66583736	GM12878	blood:	n/a
45	chr13:66583686-66583736	RPTEC	kidney:	n/a
46	chr13:66607275-66607325	HIPEpiC	eye:	n/a
47	chr13:66583686-66583736	PrEC	prostate:	n/a
48	chr13:66501111-66501161	NT2-D1	testis:	n/a
49	chr13:66583583-66583633	SK-N-MC	brain:	n/a
50	chr13:66607275-66607325	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
2	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
3	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
4	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
5	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
6	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
7	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-10	chr13:66515195-66515334	XLOC_010415
2	lnc-AL445989.1-9	chr13:66510419-66510480	XLOC_010414
3	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
4	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
5	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416
6	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548x-3p	chr13:66540484-66540503	MIMAT0015081

No data

Variant related genes	Relation type
MIR548X2	TF binding region
MIR548X2	CpG island
INO80D	miRNA target sites

Extended variants
information (count: 2398 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2398 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17079434	chr13:66492872-66492873	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147967790	chr13:66492929-66492930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544714656	chr13:66492979-66492980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141109821	chr13:66492992-66492993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530516676	chr13:66493004-66493005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543909567	chr13:66493008-66493009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145057417	chr13:66493010-66493011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144932444	chr13:66493040-66493041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180736862	chr13:66493044-66493045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546842554	chr13:66493075-66493076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566686718	chr13:66493076-66493077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532302711	chr13:66493177-66493178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17079454	chr13:66493180-66493181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs185892689	chr13:66493207-66493208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554009031	chr13:66493224-66493225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538323878	chr13:66493260-66493261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61453947	chr13:66493264-66493265	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs191140963	chr13:66493295-66493296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17079456	chr13:66493352-66493353	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs534241542	chr13:66493353-66493354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183867714	chr13:66493378-66493379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557835154	chr13:66493391-66493392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554006004	chr13:66493418-66493419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112671264	chr13:66493429-66493430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186567952	chr13:66493451-66493452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543503839	chr13:66493464-66493465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556328131	chr13:66493470-66493471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17079457	chr13:66493474-66493475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs544273481	chr13:66493481-66493482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143109981	chr13:66493541-66493542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565844448	chr13:66493559-66493560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529655355	chr13:66493591-66493592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540163853	chr13:66493592-66493593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs151196229	chr13:66493660-66493661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560439753	chr13:66493661-66493662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532440604	chr13:66493671-66493672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552438366	chr13:66493673-66493674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140365142	chr13:66493681-66493682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369892256	chr13:66493701-66493702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531736569	chr13:66493758-66493759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548629640	chr13:66493766-66493767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541395474	chr13:66493769-66493770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35409306	chr13:66493788-66493789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568372437	chr13:66493793-66493794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35231292	chr13:66493813-66493814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1929206	chr13:66493872-66493873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551691627	chr13:66493893-66493894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149827395	chr13:66493922-66493923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547385199	chr13:66493925-66493926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145547627	chr13:66493966-66493967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66489600-66496400	Weak transcription	HSMM	muscle
2	chr13:66490000-66496200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:66490400-66495600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr13:66491200-66493000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr13:66492600-66495800	Weak transcription	NHDF-Ad	bronchial
6	chr13:66492800-66495800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr13:66495600-66497000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr13:66495800-66496200	Enhancers	NHDF-Ad	bronchial
9	chr13:66495800-66496600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:66495800-66497000	Enhancers	Osteobl	bone
11	chr13:66496000-66496600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr13:66496200-66496400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr13:66496200-66496600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr13:66496400-66496600	Enhancers	HSMM	muscle
15	chr13:66497000-66501200	Weak transcription	Osteobl	bone
16	chr13:66500400-66500800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:66500600-66500800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr13:66500600-66501000	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr13:66500800-66501000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr13:66500800-66501000	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr13:66500800-66501000	Enhancers	Fetal Muscle Trunk	muscle
22	chr13:66500800-66501200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr13:66500800-66501200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr13:66500800-66501200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr13:66500800-66501200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:66500800-66501200	Enhancers	Liver	Liver
27	chr13:66500800-66501200	Enhancers	HMEC	breast
28	chr13:66500800-66501400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr13:66500800-66501400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr13:66500800-66501400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:66500800-66501400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr13:66500800-66501400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr13:66500800-66501400	Enhancers	Right Atrium	heart
34	chr13:66500800-66501600	Enhancers	H1 Cell Line	embryonic stem cell
35	chr13:66500800-66501600	Enhancers	Fetal Lung	lung
36	chr13:66500800-66501600	Enhancers	Left Ventricle	heart
37	chr13:66500800-66501600	Enhancers	Pancreas	Pancrea
38	chr13:66501000-66501200	Active TSS	iPS-15b Cell Line	embryonic stem cell
39	chr13:66501000-66501200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
40	chr13:66501000-66501200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr13:66501000-66501400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr13:66501000-66501400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr13:66501200-66501400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:66501200-66501400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr13:66501200-66501400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr13:66501200-66501600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr13:66501200-66501600	Enhancers	Brain Cingulate Gyrus	brain
48	chr13:66501200-66501800	Enhancers	Psoas Muscle	Psoas
49	chr13:66501400-66501600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr13:66501800-66513400	Weak transcription	Psoas Muscle	Psoas

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