Variant report

Variant	nsv1045844
Chromosome Location	chr13:70038096-70405435
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	chr13:70098686-70098870	K562	blood:	n/a	n/a
2	ARID3A	chr13:70139685-70139885	HepG2	liver:	n/a	n/a
3	ATF1	chr13:70111783-70111864	K562	blood:	n/a	n/a
4	ATF2	chr13:70258281-70258806	GM12878	blood:	n/a	n/a
5	BACH1	chr13:70130741-70131058	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr13:70250741-70250952	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:70139635-70139865	GM12878	blood:	n/a	chr13:70139731-70139742
8	BATF	chr13:70139605-70139900	GM12878	blood:	n/a	chr13:70139731-70139742
9	BATF	chr13:70251604-70251776	GM12878	blood:	n/a	chr13:70251694-70251705
10	BCL11A	chr13:70139578-70139870	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:70140170-70140624	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:70140237-70140557	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:70139623-70139932	GM12878	blood:	n/a	n/a
14	BHLHE40	chr13:70275529-70275573	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:70140226-70140666	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:70251405-70251582	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
18	BRCA1	chr13:70212779-70212821	GM12878	blood:	n/a	n/a
19	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
20	CEBPB	chr13:70231021-70231199	A549	lung:	n/a	chr13:70231088-70231099
21	CEBPB	chr13:70300298-70300460	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr13:70190558-70190930	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:70171142-70171588	HepG2	liver:	n/a	chr13:70171344-70171355
24	CEBPB	chr13:70153505-70153705	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr13:70080175-70080451	HepG2	liver:	n/a	chr13:70080303-70080314
26	CEBPB	chr13:70104870-70105070	HepG2	liver:	n/a	chr13:70104977-70104988
27	CEBPB	chr13:70161792-70161803	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr13:70295769-70296068	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr13:70145475-70145815	HepG2	liver:	n/a	chr13:70145630-70145641
30	CEBPB	chr13:70080171-70080412	A549	lung:	n/a	chr13:70080303-70080314
31	CEBPB	chr13:70115589-70115832	HepG2	liver:	n/a	chr13:70115606-70115617 chr13:70115606-70115617 chr13:70115753-70115764
32	CEBPB	chr13:70161646-70161930	A549	lung:	n/a	chr13:70161769-70161778 chr13:70161769-70161780 chr13:70161769-70161778 chr13:70161769-70161778 chr13:70161767-70161778 chr13:70161769-70161778
33	CEBPB	chr13:70139509-70139939	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:70191691-70191973	HepG2	liver:	n/a	n/a
35	CEBPB	chr13:70111759-70111990	K562	blood:	n/a	n/a
36	CEBPB	chr13:70071354-70071690	HepG2	liver:	n/a	chr13:70071509-70071520 chr13:70071509-70071522 chr13:70071509-70071522 chr13:70071509-70071522 chr13:70071511-70071522
37	CEBPB	chr13:70080155-70080456	IMR90	lung:	n/a	chr13:70080303-70080314
38	CEBPB	chr13:70153488-70153821	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:70296495-70296604	HepG2	liver:	n/a	n/a
40	CEBPB	chr13:70228603-70228905	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr13:70130684-70130981	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr13:70230999-70231245	HepG2	liver:	n/a	chr13:70231088-70231099
43	CEBPB	chr13:70308944-70309274	HepG2	liver:	n/a	chr13:70309100-70309111 chr13:70309099-70309112
44	CEBPB	chr13:70071353-70071606	A549	lung:	n/a	chr13:70071509-70071520 chr13:70071509-70071522 chr13:70071509-70071522 chr13:70071509-70071522 chr13:70071511-70071522
45	CEBPB	chr13:70135776-70135926	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:70329765-70329832	H1-hESC	embryonic stem cell:	n/a	chr13:70329806-70329823
47	CEBPB	chr13:70328822-70329838	HepG2	liver:	n/a	chr13:70328921-70328934 chr13:70329806-70329823 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70328859-70328868 chr13:70329607-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329607-70329618 chr13:70329605-70329616
48	CEBPB	chr13:70139489-70139926	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr13:70161607-70161941	HepG2	liver:	n/a	chr13:70161769-70161778 chr13:70161769-70161780 chr13:70161769-70161778 chr13:70161769-70161778 chr13:70161767-70161778 chr13:70161769-70161778

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70369137-70369187	ovcar-3	ovarian:	n/a
2	chr13:70154624-70154674	BE2_C	brain:	n/a
3	chr13:70154624-70154674	AG04449	skin:	fetal
4	chr13:70369137-70369187	SK-N-SH	brain:	n/a
5	chr13:70154624-70154674	ProgFib	skin:	n/a
6	chr13:70369137-70369187	HCF	heart:	n/a
7	chr13:70154624-70154674	HCF	heart:	n/a
8	chr13:70369137-70369187	HEEpiC	esophagus:	n/a
9	chr13:70154624-70154674	PrEC	prostate:	n/a
10	chr13:70154624-70154674	GM12878	blood:	n/a
11	chr13:70369137-70369187	MCF-7	breast:	n/a
12	chr13:70154624-70154674	HAEpiC	amniotic membrane:	n/a
13	chr13:70369137-70369187	HNPCEpiC	eye:	n/a
14	chr13:70154624-70154674	RPTEC	kidney:	n/a
15	chr13:70154624-70154674	GM12892	blood:	n/a
16	chr13:70154624-70154674	SK-N-MC	brain:	n/a
17	chr13:70154624-70154674	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:70154624-70154674	HEK293	kidney:	embryo
19	chr13:70154624-70154674	HRE	kidney:	n/a
20	chr13:70154624-70154674	AoSMC	blood vessel:	n/a
21	chr13:70369137-70369187	HCPEpiC	choroid plexus:	n/a
22	chr13:70154624-70154674	NH-A	brain:	n/a
23	chr13:70154624-70154674	ECC-1	luminal epithelium:	n/a
24	chr13:70369137-70369187	GM12878	blood:	n/a
25	chr13:70154624-70154674	Hepatocyte	liver:	n/a
26	chr13:70369137-70369187	U87	brain:	n/a
27	chr13:70369137-70369187	AoSMC	blood vessel:	n/a
28	chr13:70154624-70154674	PFSK-1	brain:	n/a
29	chr13:70154624-70154674	AG09309	skin:	n/a
30	chr13:70369137-70369187	NHBE	bronchial:	n/a
31	chr13:70154624-70154674	HEEpiC	esophagus:	n/a
32	chr13:70154624-70154674	T-47D	breast:	n/a
33	chr13:70369137-70369187	ProgFib	skin:	n/a
34	chr13:70369137-70369187	H1-hESC	embryonic stem cell:	embryo
35	chr13:70154624-70154674	BJ	skin:	n/a
36	chr13:70154624-70154674	NB4	blood:	n/a
37	chr13:70369137-70369187	AG04450	lung:	fetal
38	chr13:70154624-70154674	HUVEC	blood vessel:	n/a
39	chr13:70369137-70369187	AG09319	gingival:	n/a
40	chr13:70369137-70369187	CMK	blood:	n/a
41	chr13:70154624-70154674	SK-N-SH_RA	brain:	n/a
42	chr13:70154624-70154674	PANC-1	pancreas:	n/a
43	chr13:70154624-70154674	GM06990	blood:	n/a
44	chr13:70369137-70369187	HRCEpiC	kidney:	n/a
45	chr13:70154624-70154674	HCM	heart:	n/a
46	chr13:70369137-70369187	A549	lung:	n/a
47	chr13:70154624-70154674	HIPEpiC	eye:	n/a
48	chr13:70154624-70154674	NHDF-neo	bronchial:	n/a
49	chr13:70369137-70369187	SAEC	small airway:	n/a
50	chr13:70154624-70154674	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr13:70281102..70281979-chr16:2731851..2732580,2	MCF-7	breast:
2	chr13:70111760..70112275-chr13:70431222..70431945,2	K562	blood:
3	chr13:70139358..70139986-chr13:70431208..70431784,2	MCF-7	breast:
4	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
5	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
6	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
7	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
8	chr13:70159737..70160485-chr3:63899719..63900444,2	MCF-7	breast:
9	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
10	chr11:65198093..65198776-chr13:70273636..70274136,2	Hela-S3	cervix:
11	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
12	chr13:70138280..70140328-chr13:70148714..70150548,2	MCF-7	breast:
13	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
14	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
15	chr13:70138280..70140328-chr13:70148714..70150548,2	MCF-7	breast:
16	chr13:70207003..70207565-chr6:110796356..110796874,2	MCF-7	breast:
17	chr13:70111047..70112123-chr13:70431019..70432110,4	MCF-7	breast:
18	chr13:70145786..70147691-chr13:70150305..70153180,2	K562	blood:
19	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
20	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
21	chr13:70139732..70140265-chr13:71142279..71142907,2	MCF-7	breast:
22	chr13:70145786..70147691-chr13:70150305..70153180,2	K562	blood:
23	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
24	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
25	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-2	chr13:70050502-70050530	NONHSAT034247
2	lnc-KLHL1-2	chr13:70046963-70047356	NONHSAT034247

Variant related genes	Relation type
RNY3P10	TF binding region
RNY3P10	CpG island
ENSG00000139842	chromatin interactions
ENSG00000167977	chromatin interactions

Extended variants
information (count: 5465 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5465 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372750133	chr13:70041812-70041813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183121402	chr13:70041838-70041839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568975931	chr13:70041868-70041869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112558309	chr13:70041876-70041877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs78067447	chr13:70041883-70041884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35382504	chr13:70041888-70041889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76657393	chr13:70041895-70041896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs62506644	chr13:70041933-70041934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs34330148	chr13:70041939-70041940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191442035	chr13:70041940-70041941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112524565	chr13:70041969-70041970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574757475	chr13:70041983-70041984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs74764144	chr13:70042052-70042053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs77062519	chr13:70042055-70042056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370721780	chr13:70042068-70042069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554442038	chr13:70042081-70042082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3997644	chr13:70042115-70042116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34609216	chr13:70042116-70042117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376773927	chr13:70042118-70042119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397774065	chr13:70042119-70042120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573346504	chr13:70042230-70042231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577518459	chr13:70042269-70042270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546380521	chr13:70042270-70042271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562589978	chr13:70042308-70042309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531408855	chr13:70042381-70042382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375579973	chr13:70042448-70042449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9541948	chr13:70042589-70042590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs527271572	chr13:70042592-70042593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs664401	chr13:70042679-70042680	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs563789	chr13:70042709-70042710	Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532975603	chr13:70042711-70042712	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs549536485	chr13:70042719-70042720	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs569489121	chr13:70042728-70042729	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs550939190	chr13:70042782-70042783	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs17683235	chr13:70042839-70042840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs548652117	chr13:70042865-70042866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568406858	chr13:70042871-70042872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76172646	chr13:70042890-70042891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554179696	chr13:70042912-70042913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368113876	chr13:70042931-70042932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138863146	chr13:70042936-70042937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536923954	chr13:70042938-70042939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534252035	chr13:70042972-70042973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577581828	chr13:70042976-70042977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555036458	chr13:70043048-70043049	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs116196511	chr13:70043087-70043088	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549217012	chr13:70043088-70043089	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs200006147	chr13:70043146-70043147	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541027284	chr13:70043148-70043149	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs183644490	chr13:70043175-70043176	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70041800-70044800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:70042600-70042800	Flanking Active TSS	Liver	Liver
3	chr13:70042800-70043000	Enhancers	Liver	Liver
4	chr13:70043000-70043200	Flanking Active TSS	Liver	Liver
5	chr13:70043200-70043400	Enhancers	Liver	Liver
6	chr13:70044800-70045000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:70048400-70048600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr13:70048600-70049200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:70049200-70049400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:70049400-70051000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr13:70051000-70051400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr13:70057600-70058400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr13:70058200-70059400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
14	chr13:70060400-70062200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr13:70069000-70069600	Enhancers	Fetal Brain Male	brain
16	chr13:70069200-70069600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:70069200-70069600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr13:70069200-70069600	Enhancers	Fetal Brain Female	brain
19	chr13:70069600-70070600	Weak transcription	Fetal Brain Female	brain
20	chr13:70069600-70072200	Weak transcription	Fetal Brain Male	brain
21	chr13:70070600-70072000	Enhancers	Fetal Brain Female	brain
22	chr13:70072200-70072600	Enhancers	Fetal Brain Male	brain
23	chr13:70072600-70082200	Weak transcription	Fetal Brain Male	brain
24	chr13:70082200-70082400	Enhancers	Fetal Brain Male	brain
25	chr13:70092600-70093000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:70098600-70099400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr13:70098800-70099200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:70099000-70099400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr13:70099000-70099400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr13:70099000-70099400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr13:70099400-70101600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr13:70101600-70102200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr13:70104600-70104800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:70105000-70110800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:70110800-70111000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:70115400-70115800	Enhancers	Liver	Liver
37	chr13:70117600-70118000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr13:70118000-70119200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr13:70119000-70119800	Enhancers	Fetal Intestine Small	intestine
40	chr13:70119000-70119800	Enhancers	Stomach Mucosa	stomach
41	chr13:70119200-70119400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr13:70119400-70119600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr13:70119400-70120000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:70119400-70121000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr13:70119800-70122000	Weak transcription	Stomach Mucosa	stomach
46	chr13:70121000-70122600	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr13:70122000-70122400	Enhancers	Stomach Mucosa	stomach
48	chr13:70129000-70129200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr13:70129200-70137600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:70130200-70131000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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