Variant report

Variant	nsv562090
Chromosome Location	chr13:65931353-66508344
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	ATF1	chr13:66035822-66036144	K562	blood:	n/a	n/a
2	BATF	chr13:66080137-66080390	GM12878	blood:	n/a	n/a
3	BATF	chr13:65988370-65988595	GM12878	blood:	n/a	n/a
4	BATF	chr13:66041811-66041993	GM12878	blood:	n/a	chr13:66041940-66041951
5	BHLHE40	chr13:66212820-66213067	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:66035765-66036027	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr13:65953042-65953530	HCT-116	colon:	n/a	n/a
8	CBX3	chr13:66212653-66213113	HCT-116	colon:	n/a	n/a
9	CEBPB	chr13:66035754-66036255	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr13:66048985-66049163	A549	lung:	n/a	n/a
11	CEBPB	chr13:66172567-66172901	A549	lung:	n/a	n/a
12	CEBPB	chr13:66491284-66491489	HepG2	liver:	n/a	chr13:66491416-66491427 chr13:66491415-66491426
13	CEBPB	chr13:66485929-66486250	A549	lung:	n/a	chr13:66486079-66486092 chr13:66486081-66486090 chr13:66486081-66486090 chr13:66486079-66486092 chr13:66486081-66486092 chr13:66486079-66486090 chr13:66486081-66486090 chr13:66486081-66486090
14	CEBPB	chr13:66460117-66460437	HepG2	liver:	n/a	chr13:66460271-66460282 chr13:66460252-66460263
15	CEBPB	chr13:66172575-66172866	A549	lung:	n/a	n/a
16	CEBPB	chr13:65942890-65943171	HepG2	liver:	n/a	chr13:65942991-65943002
17	CEBPB	chr13:66405291-66405636	HepG2	liver:	n/a	chr13:66405470-66405481
18	CEBPB	chr13:66429419-66429787	H1-hESC	embryonic stem cell:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
19	CEBPB	chr13:66429386-66429682	ECC-1	luminal epithelium:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
20	CEBPB	chr13:66095982-66096144	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr13:66172469-66172941	Hela-S3	cervix:	n/a	chr13:66172550-66172561
22	CEBPB	chr13:66269598-66269845	A549	lung:	n/a	chr13:66269714-66269727 chr13:66269716-66269727 chr13:66269714-66269725
23	CEBPB	chr13:66437487-66437849	HepG2	liver:	n/a	chr13:66437636-66437647
24	CEBPB	chr13:66367393-66367619	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:66465373-66465649	HepG2	liver:	n/a	chr13:66465490-66465501 chr13:66465492-66465503 chr13:66465490-66465503 chr13:66465492-66465501 chr13:66465490-66465503
26	CEBPB	chr13:66284808-66285037	K562	blood:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
27	CEBPB	chr13:66252098-66252418	HepG2	liver:	n/a	n/a
28	CEBPB	chr13:65936220-65936361	HepG2	liver:	n/a	chr13:65936278-65936290
29	CEBPB	chr13:66405347-66405602	Hela-S3	cervix:	n/a	chr13:66405470-66405481
30	CEBPB	chr13:66252010-66252510	HCT-116	colon:	n/a	n/a
31	CEBPB	chr13:65935688-65935939	IMR90	lung:	n/a	chr13:65935790-65935801
32	CEBPB	chr13:66281605-66281903	HepG2	liver:	n/a	chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281750-66281763 chr13:66281752-66281761 chr13:66281751-66281762 chr13:66281752-66281761 chr13:66281752-66281761 chr13:66281750-66281761
33	CEBPB	chr13:66405360-66405560	K562	blood:	n/a	chr13:66405470-66405481
34	CEBPB	chr13:66302716-66302972	K562	blood:	n/a	chr13:66302825-66302834 chr13:66302825-66302836 chr13:66302823-66302834
35	CEBPB	chr13:66429514-66429635	K562	blood:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
36	CEBPB	chr13:66212723-66213083	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:66458026-66458360	Hela-S3	cervix:	n/a	chr13:66458181-66458194 chr13:66458181-66458192 chr13:66458182-66458193
38	CEBPB	chr13:66284785-66285094	IMR90	lung:	n/a	chr13:66284953-66284964 chr13:66285014-66285031 chr13:66284954-66284963
39	CEBPB	chr13:66252054-66252437	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr13:66437606-66437805	K562	blood:	n/a	chr13:66437636-66437647
41	CEBPB	chr13:66458041-66458308	K562	blood:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
42	CEBPB	chr13:66405318-66405568	A549	lung:	n/a	chr13:66405470-66405481
43	CEBPB	chr13:66495056-66495370	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:66039732-66039775	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:65942931-65943178	IMR90	lung:	n/a	chr13:65942991-65943002
46	CEBPB	chr13:66405298-66405623	IMR90	lung:	n/a	chr13:66405470-66405481
47	CEBPB	chr13:66465439-66465644	A549	lung:	n/a	chr13:66465490-66465501 chr13:66465492-66465503 chr13:66465490-66465503 chr13:66465492-66465501 chr13:66465490-66465503
48	CEBPB	chr13:66252168-66252428	MCF-7	breast:	n/a	n/a
49	CEBPB	chr13:65941086-65941290	HepG2	liver:	n/a	chr13:65941156-65941167
50	CEBPB	chr13:66252073-66252455	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66252177-66252227	T-47D	breast:	n/a
2	chr13:66156848-66156898	HUVEC	blood vessel:	n/a
3	chr13:66252177-66252227	BJ	skin:	n/a
4	chr13:66501111-66501161	HEK293	kidney:	embryo
5	chr13:66252177-66252227	MCF-7	breast:	n/a
6	chr13:66501111-66501161	K562	blood:	n/a
7	chr13:66252177-66252227	Caco-2	colon:	n/a
8	chr13:66252177-66252227	ECC-1	luminal epithelium:	n/a
9	chr13:66322551-66322601	HCF	heart:	n/a
10	chr13:66252177-66252227	U87	brain:	n/a
11	chr13:66501111-66501161	SAEC	small airway:	n/a
12	chr13:66322551-66322601	MCF-7	breast:	n/a
13	chr13:66252177-66252227	GM12878	blood:	n/a
14	chr13:66156848-66156898	HCPEpiC	choroid plexus:	n/a
15	chr13:66156848-66156898	GM12878	blood:	n/a
16	chr13:66156848-66156898	BE2_C	brain:	n/a
17	chr13:66252177-66252227	MCF10A-Er-Src	breast:	n/a
18	chr13:66156848-66156898	PANC-1	pancreas:	n/a
19	chr13:66252177-66252227	CMK	blood:	n/a
20	chr13:66322551-66322601	GM12892	blood:	n/a
21	chr13:66156848-66156898	HIPEpiC	eye:	n/a
22	chr13:66252177-66252227	AG09319	gingival:	n/a
23	chr13:66322551-66322601	PrEC	prostate:	n/a
24	chr13:66322551-66322601	ovcar-3	ovarian:	n/a
25	chr13:66501111-66501161	HRPEpiC	eye:	n/a
26	chr13:66322551-66322601	SAEC	small airway:	n/a
27	chr13:66501111-66501161	MCF10A-Er-Src	breast:	n/a
28	chr13:66501111-66501161	SKMC	muscle:	n/a
29	chr13:66252177-66252227	H1-hESC	embryonic stem cell:	embryo
30	chr13:66252177-66252227	NH-A	brain:	n/a
31	chr13:66322551-66322601	HRE	kidney:	n/a
32	chr13:66501111-66501161	HCF	heart:	n/a
33	chr13:66322551-66322601	NHBE	bronchial:	n/a
34	chr13:66501111-66501161	PrEC	prostate:	n/a
35	chr13:66156848-66156898	AoSMC	blood vessel:	n/a
36	chr13:66252177-66252227	HIPEpiC	eye:	n/a
37	chr13:66252177-66252227	AG04450	lung:	fetal
38	chr13:66252177-66252227	SK-N-SH_RA	brain:	n/a
39	chr13:66252177-66252227	HEEpiC	esophagus:	n/a
40	chr13:66322551-66322601	BJ	skin:	n/a
41	chr13:66322551-66322601	SK-N-SH	brain:	n/a
42	chr13:66156848-66156898	U87	brain:	n/a
43	chr13:66322551-66322601	GM19239	blood:	n/a
44	chr13:66322551-66322601	NHDF-neo	bronchial:	n/a
45	chr13:66156848-66156898	NHBE	bronchial:	n/a
46	chr13:66501111-66501161	T-47D	breast:	n/a
47	chr13:66156848-66156898	AG10803	skin:	n/a
48	chr13:66252177-66252227	ovcar-3	ovarian:	n/a
49	chr13:66322551-66322601	AG10803	skin:	n/a
50	chr13:66252177-66252227	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:65045929..65046727-chr13:66212514..66213321,2	MCF-7	breast:
2	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:
3	chr1:106318966..106319467-chr13:66093606..66094106,2	NB4	blood:
4	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
5	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
6	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
7	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
8	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:
9	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
10	chr13:66046639..66047382-chr3:13541452..13542407,2	MCF-7	breast:
11	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
12	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
13	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
14	chr13:65802985..65805270-chr13:66070535..66073117,2	K562	blood:
15	chr13:66014665..66017459-chr13:66017619..66020223,2	MCF-7	breast:
16	chr13:66206471..66208391-chr13:66217892..66220664,2	K562	blood:
17	chr13:66296680..66298971-chr13:66300615..66302352,2	MCF-7	breast:
18	chr13:65020257..65021157-chr13:66212532..66213123,2	MCF-7	breast:
19	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-8	chr13:66451989-66452351	ENSG00000234767
2	lnc-AL445989.1-8	chr13:66440195-66440400	NONHSAT034197
3	lnc-PCDH9-6	chr13:66410063-66410464	NONHSAT034195
4	lnc-AL445989.1-8	chr13:66451989-66452351	NONHSAT034197
5	lnc-PCDH9-6	chr13:66430425-66430559	NONHSAT034195
6	lnc-PCDH9-7	chr13:66015947-66016044	NONHSAT034194
7	lnc-PCDH9-7	chr13:66035510-66035584	NONHSAT034194
8	lnc-PCDH9-7	chr13:66017513-66017582	NONHSAT034194
9	lnc-AL445989.1-9	chr13:66503637-66503853	XLOC_010414
10	lnc-AL445989.1-8	chr13:66449839-66449901	ENSG00000234767
11	lnc-AL445989.1-8	chr13:66449839-66449901	NONHSAT034197
12	lnc-AL445989.1-8	chr13:66440306-66440375	ENSG00000234767

Variant related genes	Relation type
HNRNPA3P5	TF binding region
ENSG00000221685	TF binding region
LINC01052	TF binding region
HNRNPA3P5	CpG island
ENSG00000221685	CpG island
LINC01052	CpG island
ENSG00000236565	chromatin interactions

Extended variants
information (count: 8731 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:8731 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576970651	chr13:65943328-65943329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs371619609	chr13:65943336-65943337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556389607	chr13:65943339-65943340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs80233894	chr13:65943347-65943348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542126180	chr13:65943359-65943360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369994484	chr13:65943386-65943387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572424265	chr13:65943421-65943422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541028025	chr13:65943422-65943423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373717308	chr13:65943425-65943426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139923400	chr13:65943457-65943458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571020304	chr13:65943473-65943474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540987951	chr13:65943486-65943487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145346690	chr13:65943519-65943520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549992875	chr13:65943520-65943521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563525654	chr13:65943534-65943535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529412907	chr13:65943535-65943536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549673107	chr13:65943583-65943584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566194560	chr13:65943596-65943597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559395232	chr13:65943602-65943603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114095017	chr13:65943655-65943656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528534956	chr13:65943656-65943657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369951078	chr13:65943679-65943680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374006799	chr13:65943681-65943682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577636521	chr13:65943692-65943693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547067949	chr13:65943718-65943719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555130569	chr13:65943747-65943748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570607633	chr13:65943756-65943757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539516572	chr13:65943778-65943779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545104979	chr13:65943787-65943788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371649906	chr13:65943820-65943821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145157229	chr13:65943849-65943850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576317567	chr13:65943854-65943855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113674670	chr13:65943871-65943872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181750447	chr13:65943881-65943882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555646349	chr13:65943914-65943915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185615708	chr13:65943917-65943918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559782885	chr13:65943967-65943968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190377682	chr13:65943978-65943979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564304475	chr13:65944011-65944012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563316153	chr13:65944015-65944016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543525793	chr13:65944025-65944026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148483090	chr13:65944042-65944043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115104484	chr13:65944043-65944044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180731008	chr13:65944157-65944158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560033672	chr13:65944190-65944191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528777966	chr13:65944249-65944250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547397812	chr13:65944254-65944255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs530779451	chr13:65944269-65944270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570444398	chr13:65944309-65944310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142664462	chr13:65944371-65944372	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:65943200-65943600	Enhancers	Fetal Heart	heart
2	chr13:65943600-65944000	Weak transcription	Fetal Heart	heart
3	chr13:65944000-65944600	Enhancers	Fetal Heart	heart
4	chr13:65952200-65953000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr13:65959600-65960000	Enhancers	Fetal Lung	lung
6	chr13:65960000-65960400	Weak transcription	Fetal Lung	lung
7	chr13:65960400-65960600	Enhancers	Fetal Lung	lung
8	chr13:65960600-65961400	Weak transcription	Fetal Lung	lung
9	chr13:65961000-65962000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:65961400-65961600	ZNF genes & repeats	Fetal Lung	lung
11	chr13:65961400-65962400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr13:65962000-65962600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr13:65962600-65964400	Weak transcription	Fetal Brain Male	brain
14	chr13:65967600-65970000	Weak transcription	Fetal Brain Male	brain
15	chr13:65971400-65972600	Enhancers	Placenta Amnion	Placenta Amnion
16	chr13:65971800-65973400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr13:65972600-65973800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr13:65973400-65974800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr13:65974200-65975000	Enhancers	Fetal Lung	lung
20	chr13:65974400-65974600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr13:65974800-65975000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr13:65978600-65978800	Enhancers	Fetal Brain Female	brain
23	chr13:65981800-65982000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:65990800-65991200	Enhancers	Fetal Lung	lung
25	chr13:65991200-65992200	Weak transcription	Fetal Lung	lung
26	chr13:65992000-65992400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr13:65992000-65993400	Enhancers	Fetal Kidney	kidney
28	chr13:65992200-65992400	Enhancers	Fetal Lung	lung
29	chr13:65992200-65992600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:65992600-65993800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr13:65992800-65993800	Enhancers	Brain Germinal Matrix	brain
32	chr13:65993800-65994200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr13:65993800-65994400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr13:66009000-66010400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:66009400-66010200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
36	chr13:66009600-66010200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr13:66009800-66010200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr13:66010200-66015800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr13:66010200-66031600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr13:66015800-66016000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr13:66016000-66018600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr13:66018800-66019000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr13:66028200-66028800	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr13:66031600-66031800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr13:66031800-66035800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr13:66033400-66034000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr13:66033400-66036000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:66033600-66034000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr13:66033600-66036200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr13:66033800-66034800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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