Variant report

Variant	esv3350275
Chromosome Location	chr13:76113551-76120649
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76119103-76119402	HepG2	liver:	n/a	n/a
2	ATF1	chr13:76115164-76115846	K562	blood:	n/a	n/a
3	CEBPB	chr13:76119018-76119446	IMR90	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
4	CEBPB	chr13:76119032-76119423	HepG2	liver:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
5	CEBPB	chr13:76117488-76117562	A549	lung:	n/a	n/a
6	CEBPB	chr13:76119008-76119530	Hela-S3	cervix:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
7	CEBPB	chr13:76119116-76119316	A549	lung:	n/a	chr13:76119247-76119258 chr13:76119186-76119203
8	CTCF	chr13:76115320-76115470	AG04449	skin:	n/a	n/a
9	CTCF	chr13:76119240-76119390	AG04449	skin:	n/a	n/a
10	CTCF	chr13:76116200-76116350	AG04449	skin:	n/a	n/a
11	CTCF	chr13:76115400-76115550	HEEpiC	esophagus:	n/a	n/a
12	EGR1	chr13:76114348-76114588	K562	blood:	n/a	chr13:76114443-76114458 chr13:76114444-76114457
13	EP300	chr13:76119097-76119416	Hela-S3	cervix:	n/a	n/a
14	EP300	chr13:76114701-76114707	K562	blood:	n/a	n/a
15	EP300	chr13:76119114-76119287	HepG2	liver:	n/a	n/a
16	FOS	chr13:76119093-76119362	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr13:76113888-76113893	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr13:76119038-76119493	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr13:76119061-76119339	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr13:76119064-76119396	MCF10A-Er-Src	breast:	n/a	n/a
21	JUN	chr13:76115603-76115609	HepG2	liver:	n/a	n/a
22	JUN	chr13:76115481-76115749	K562	blood:	n/a	chr13:76115613-76115621 chr13:76115612-76115621 chr13:76115613-76115620
23	JUN	chr13:76115328-76115922	K562	blood:	n/a	chr13:76115613-76115621 chr13:76115612-76115621 chr13:76115613-76115620
24	JUND	chr13:76119072-76119279	HepG2	liver:	n/a	n/a
25	JUND	chr13:76115408-76115791	K562	blood:	n/a	chr13:76115613-76115621 chr13:76115611-76115622 chr13:76115612-76115621 chr13:76115613-76115620
26	JUND	chr13:76115549-76115695	HepG2	liver:	n/a	chr13:76115613-76115621 chr13:76115611-76115622 chr13:76115612-76115621 chr13:76115613-76115620
27	MAFK	chr13:76115194-76115392	HepG2	liver:	n/a	n/a
28	MAFK	chr13:76115589-76115771	K562	blood:	n/a	n/a
29	MAX	chr13:76119095-76119438	Hela-S3	cervix:	n/a	n/a
30	MAZ	chr13:76117516-76117519	HepG2	liver:	n/a	n/a
31	MAZ	chr13:76119110-76119325	Hela-S3	cervix:	n/a	n/a
32	MEF2A	chr13:76115383-76115882	K562	blood:	n/a	chr13:76115716-76115737 chr13:76115718-76115732 chr13:76115564-76115580
33	MXI1	chr13:76119157-76119455	Hela-S3	cervix:	n/a	n/a
34	MYC	chr13:76119074-76119407	MCF10A-Er-Src	breast:	n/a	n/a
35	MYC	chr13:76114576-76114647	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr13:76119056-76119511	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr13:76120515-76120955	SK-N-MC	brain:	n/a	n/a
38	POLR2A	chr13:76119133-76119236	MCF10A-Er-Src	breast:	n/a	n/a
39	RAD21	chr13:76119124-76119355	Hela-S3	cervix:	n/a	n/a
40	RCOR1	chr13:76119085-76119431	Hela-S3	cervix:	n/a	n/a
41	RCOR1	chr13:76115472-76115776	K562	blood:	n/a	n/a
42	RFX5	chr13:76119159-76119276	HepG2	liver:	n/a	n/a
43	RFX5	chr13:76119097-76119344	Hela-S3	cervix:	n/a	n/a
44	RXRA	chr13:76119018-76119349	HepG2	liver:	n/a	n/a
45	SMC3	chr13:76119236-76119313	HepG2	liver:	n/a	n/a
46	SPI1	chr13:76115438-76115803	GM12891	blood:	n/a	chr13:76115635-76115642 chr13:76115634-76115643 chr13:76115631-76115644
47	SPI1	chr13:76115546-76115728	K562	blood:	n/a	chr13:76115635-76115642 chr13:76115634-76115643 chr13:76115631-76115644
48	SPI1	chr13:76115326-76115895	HL-60	blood:	n/a	chr13:76115635-76115642 chr13:76115634-76115643 chr13:76115631-76115644
49	SPI1	chr13:76115415-76115829	GM12891	blood:	n/a	chr13:76115635-76115642 chr13:76115634-76115643 chr13:76115631-76115644
50	STAT3	chr13:76119142-76119342	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76115526-76115576	HEK293	kidney:	embryo
2	chr13:76119663-76119713	HRPEpiC	eye:	n/a
3	chr13:76115526-76115576	HUVEC	blood vessel:	n/a
4	chr13:76115526-76115576	IMR90	lung:	fetal
5	chr13:76115526-76115576	GM12891	blood:	n/a
6	chr13:76115526-76115576	NT2-D1	testis:	n/a
7	chr13:76115526-76115576	CMK	blood:	n/a
8	chr13:76119663-76119713	K562	blood:	n/a
9	chr13:76115526-76115576	HRCEpiC	kidney:	n/a
10	chr13:76119663-76119713	BE2_C	brain:	n/a
11	chr13:76119663-76119713	HEK293	kidney:	embryo
12	chr13:76115526-76115576	HCT-116	colon:	n/a
13	chr13:76115526-76115576	GM12892	blood:	n/a
14	chr13:76115526-76115576	ovcar-3	ovarian:	n/a
15	chr13:76115526-76115576	BE2_C	brain:	n/a
16	chr13:76115526-76115576	HAEpiC	amniotic membrane:	n/a
17	chr13:76119663-76119713	PFSK-1	brain:	n/a
18	chr13:76119663-76119713	T-47D	breast:	n/a
19	chr13:76119663-76119713	Caco-2	colon:	n/a
20	chr13:76119663-76119713	HepG2	liver:	n/a
21	chr13:76115526-76115576	PFSK-1	brain:	n/a
22	chr13:76115526-76115576	LNCaP	prostate:	n/a
23	chr13:76119663-76119713	RPTEC	kidney:	n/a
24	chr13:76119663-76119713	Jurkat	blood:	n/a
25	chr13:76115526-76115576	HL-60	blood:	n/a
26	chr13:76119663-76119713	Hela-S3	cervix:	n/a
27	chr13:76115526-76115576	AoSMC	blood vessel:	n/a
28	chr13:76119663-76119713	HRCEpiC	kidney:	n/a
29	chr13:76119663-76119713	SKMC	muscle:	n/a
30	chr13:76115526-76115576	MCF10A-Er-Src	breast:	n/a
31	chr13:76115526-76115576	Hela-S3	cervix:	n/a
32	chr13:76119663-76119713	AG04450	lung:	fetal
33	chr13:76119663-76119713	GM12891	blood:	n/a
34	chr13:76115526-76115576	NB4	blood:	n/a
35	chr13:76115526-76115576	SAEC	small airway:	n/a
36	chr13:76119663-76119713	SK-N-MC	brain:	n/a
37	chr13:76119663-76119713	NB4	blood:	n/a
38	chr13:76115526-76115576	Hepatocyte	liver:	n/a
39	chr13:76119663-76119713	HUVEC	blood vessel:	n/a
40	chr13:76119663-76119713	SAEC	small airway:	n/a
41	chr13:76115526-76115576	NHDF-neo	bronchial:	n/a
42	chr13:76115526-76115576	HCM	heart:	n/a
43	chr13:76119663-76119713	NHBE	bronchial:	n/a
44	chr13:76119663-76119713	HPAEpiC	pulmonary alveolar:	n/a
45	chr13:76115526-76115576	ECC-1	luminal epithelium:	n/a
46	chr13:76115526-76115576	AG10803	skin:	n/a
47	chr13:76119663-76119713	HAEpiC	amniotic membrane:	n/a
48	chr13:76119663-76119713	HCM	heart:	n/a
49	chr13:76115526-76115576	K562	blood:	n/a
50	chr13:76119663-76119713	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr13:76109717..76113590-chr13:76122029..76126081,5	MCF-7	breast:
2	chr13:76111452..76114150-chr13:76122087..76125338,6	MCF-7	breast:
3	chr13:76109687..76114004-chr13:76118514..76122227,3	K562	blood:
4	chr13:76115839..76118347-chr13:76129572..76131579,2	K562	blood:
5	chr13:76118168..76119687-chr13:76122527..76125250,2	MCF-7	breast:
6	chr13:76109113..76111805-chr13:76112674..76114626,2	K562	blood:

Variant related genes	Relation type
COMMD6	TF binding region
ENSG00000261553	TF binding region
UCHL3	TF binding region
COMMD6	CpG island
ENSG00000261553	CpG island
UCHL3	CpG island
ENSG00000261553	chromatin interactions
ENSG00000118939	chromatin interactions
ENSG00000188243	chromatin interactions

Extended variants
information (count: 282 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79480156	chr13:76113552-76113553	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs1138188	chr13:76113572-76113573	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs371534290	chr13:76113584-76113585	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs76562318	chr13:76113607-76113608	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs9573581	chr13:76113612-76113613	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs141195563	chr13:76113640-76113641	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs9543965	chr13:76113721-76113722	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs543718054	chr13:76113748-76113749	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs565223415	chr13:76113836-76113837	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs58213492	chr13:76113859-76113860	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs61015249	chr13:76113895-76113896	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181466810	chr13:76113909-76113910	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs367925680	chr13:76113930-76113931	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs9530445	chr13:76113938-76113939	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs541634046	chr13:76113940-76113941	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs367916061	chr13:76113964-76113965	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs58441165	chr13:76113965-76113966	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529034984	chr13:76114016-76114017	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs116429985	chr13:76114017-76114018	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs77721973	chr13:76114037-76114038	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs185998847	chr13:76114084-76114085	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs142007959	chr13:76114105-76114106	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs34796430	chr13:76114106-76114107	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs191281948	chr13:76114144-76114145	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140709763	chr13:76114156-76114157	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368160513	chr13:76114159-76114160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9543966	chr13:76114195-76114196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs572074888	chr13:76114203-76114204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145829192	chr13:76114209-76114210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183094540	chr13:76114251-76114252	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs187690401	chr13:76114260-76114261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs529356051	chr13:76114272-76114273	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs376812309	chr13:76114279-76114280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570371094	chr13:76114316-76114317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs543482511	chr13:76114331-76114332	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113478281	chr13:76114343-76114344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs376505939	chr13:76114354-76114355	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs9543967	chr13:76114377-76114378	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs35556048	chr13:76114397-76114398	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs117834171	chr13:76114398-76114399	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553455715	chr13:76114402-76114403	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529932572	chr13:76114407-76114408	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549208333	chr13:76114442-76114443	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs9543968	chr13:76114474-76114475	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371744441	chr13:76114477-76114478	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs66889294	chr13:76114478-76114479	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372640334	chr13:76114480-76114481	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs59520333	chr13:76114481-76114482	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs55703295	chr13:76114508-76114509	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200357117	chr13:76114509-76114510	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	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
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76112200-76123000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:76112600-76113600	Weak transcription	Osteobl	bone
3	chr13:76112600-76114600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr13:76112600-76115000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr13:76112600-76115000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr13:76112600-76119200	Weak transcription	NHLF	lung
7	chr13:76112600-76122800	Weak transcription	Fetal Brain Male	brain
8	chr13:76112600-76123000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr13:76112600-76123000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr13:76112600-76123600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:76112800-76113600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr13:76112800-76114600	Weak transcription	HepG2	liver
13	chr13:76112800-76115000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr13:76112800-76115200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr13:76112800-76115200	Weak transcription	GM12878-XiMat	blood
16	chr13:76112800-76115200	Weak transcription	K562	blood
17	chr13:76112800-76116000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr13:76112800-76118600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr13:76112800-76119200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr13:76112800-76122800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:76112800-76122800	Weak transcription	Brain Anterior Caudate	brain
22	chr13:76112800-76123000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr13:76112800-76123000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:76112800-76123000	Weak transcription	Adipose Nuclei	Adipose
25	chr13:76113000-76114400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:76113600-76114200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:76113600-76114200	Enhancers	Osteobl	bone
28	chr13:76114200-76114600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:76114200-76118600	Weak transcription	Osteobl	bone
30	chr13:76114400-76118800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:76114600-76114800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:76114600-76115600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr13:76114600-76116200	Enhancers	HepG2	liver
34	chr13:76114800-76117800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:76115000-76116000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr13:76115000-76116400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr13:76115000-76117400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr13:76115200-76115800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:76115200-76115800	Enhancers	K562	blood
40	chr13:76115200-76116000	Enhancers	GM12878-XiMat	blood
41	chr13:76115600-76120200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr13:76115800-76119200	Weak transcription	K562	blood
43	chr13:76115800-76120400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr13:76116000-76117000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:76116000-76123000	Weak transcription	GM12878-XiMat	blood
46	chr13:76116200-76116600	Weak transcription	HepG2	liver
47	chr13:76116400-76123200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr13:76116600-76119600	Enhancers	HepG2	liver
49	chr13:76117400-76118800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr13:76117800-76119600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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