Variant report

Variant	nsv832638
Chromosome Location	chr13:66342397-66498163
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	CEBPB	chr13:66429428-66429844	A549	lung:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
2	CEBPB	chr13:66429514-66429635	K562	blood:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
3	CEBPB	chr13:66465439-66465644	A549	lung:	n/a	chr13:66465490-66465501 chr13:66465492-66465503 chr13:66465490-66465503 chr13:66465492-66465501 chr13:66465490-66465503
4	CEBPB	chr13:66477786-66478048	HepG2	liver:	n/a	chr13:66477935-66477948 chr13:66477937-66477946 chr13:66477935-66477946
5	CEBPB	chr13:66485915-66486254	HepG2	liver:	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
6	CEBPB	chr13:66442532-66442643	IMR90	lung:	n/a	chr13:66442615-66442624 chr13:66442615-66442624 chr13:66442615-66442624
7	CEBPB	chr13:66460154-66460389	A549	lung:	n/a	chr13:66460271-66460282 chr13:66460252-66460263
8	CEBPB	chr13:66437481-66437831	IMR90	lung:	n/a	chr13:66437636-66437647
9	CEBPB	chr13:66442570-66442664	H1-hESC	embryonic stem cell:	n/a	chr13:66442615-66442624 chr13:66442615-66442624 chr13:66442615-66442624
10	CEBPB	chr13:66460117-66460437	HepG2	liver:	n/a	chr13:66460271-66460282 chr13:66460252-66460263
11	CEBPB	chr13:66405291-66405636	HepG2	liver:	n/a	chr13:66405470-66405481
12	CEBPB	chr13:66491284-66491489	HepG2	liver:	n/a	chr13:66491416-66491427 chr13:66491415-66491426
13	CEBPB	chr13:66487605-66487805	A549	lung:	n/a	n/a
14	CEBPB	chr13:66458063-66458364	IMR90	lung:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
15	CEBPB	chr13:66429405-66429819	IMR90	lung:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
16	CEBPB	chr13:66429419-66429787	H1-hESC	embryonic stem cell:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
17	CEBPB	chr13:66429432-66429777	ECC-1	luminal epithelium:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
18	CEBPB	chr13:66465373-66465649	HepG2	liver:	n/a	chr13:66465490-66465501 chr13:66465492-66465503 chr13:66465490-66465503 chr13:66465492-66465501 chr13:66465490-66465503
19	CEBPB	chr13:66458044-66458358	HepG2	liver:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
20	CEBPB	chr13:66367393-66367619	IMR90	lung:	n/a	n/a
21	CEBPB	chr13:66405318-66405568	A549	lung:	n/a	chr13:66405470-66405481
22	CEBPB	chr13:66458082-66458274	A549	lung:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
23	CEBPB	chr13:66405347-66405602	Hela-S3	cervix:	n/a	chr13:66405470-66405481
24	CEBPB	chr13:66343067-66343334	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr13:66437487-66437849	HepG2	liver:	n/a	chr13:66437636-66437647
26	CEBPB	chr13:66405360-66405560	K562	blood:	n/a	chr13:66405470-66405481
27	CEBPB	chr13:66458026-66458360	Hela-S3	cervix:	n/a	chr13:66458181-66458194 chr13:66458181-66458192 chr13:66458182-66458193
28	CEBPB	chr13:66357410-66357610	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:66429386-66429682	ECC-1	luminal epithelium:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
30	CEBPB	chr13:66343051-66343372	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:66405298-66405623	IMR90	lung:	n/a	chr13:66405470-66405481
32	CEBPB	chr13:66458104-66458297	H1-hESC	embryonic stem cell:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
33	CEBPB	chr13:66429429-66429750	K562	blood:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
34	CEBPB	chr13:66458041-66458308	K562	blood:	n/a	chr13:66458181-66458194 chr13:66458182-66458193 chr13:66458181-66458192
35	CEBPB	chr13:66429414-66429782	Hela-S3	cervix:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
36	CEBPB	chr13:66485905-66486263	Hela-S3	cervix:	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
37	CEBPB	chr13:66348740-66349098	HepG2	liver:	n/a	chr13:66348913-66348924
38	CEBPB	chr13:66485897-66486276	IMR90	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
39	CEBPB	chr13:66495056-66495370	HepG2	liver:	n/a	n/a
40	CEBPB	chr13:66348742-66349098	IMR90	lung:	n/a	chr13:66348913-66348924
41	CEBPB	chr13:66348781-66349093	A549	lung:	n/a	chr13:66348913-66348924
42	CEBPB	chr13:66437606-66437805	K562	blood:	n/a	chr13:66437636-66437647
43	CEBPB	chr13:66429419-66429824	HepG2	liver:	n/a	chr13:66429573-66429584 chr13:66429612-66429623
44	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
45	CTCF	chr13:66457040-66457190	GM12866	blood:	n/a	n/a
46	CTCF	chr13:66457040-66457190	GM12874	blood:	n/a	n/a
47	CTCF	chr13:66457103-66457218	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr13:66432400-66432550	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr13:66350320-66350470	HMF	breast:	n/a	n/a
50	CTCF	chr13:66457060-66457210	Caco-2	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
2	chr13:66355137..66357196-chr13:66362374..66364366,2	K562	blood:
3	chr13:66363582..66364363-chr21:32786060..32786817,2	MCF-7	breast:
4	chr13:66358245..66360880-chr16:71346372..71347872,2	MCF-7	breast:
5	chr13:66423397..66425712-chr13:66435469..66437961,2	K562	blood:
6	chr13:66377468..66378968-chr8:43092929..43094908,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-6	chr13:66410063-66410464	NONHSAT034195
2	lnc-AL445989.1-8	chr13:66451989-66452351	ENSG00000234767
3	lnc-AL445989.1-8	chr13:66449839-66449901	ENSG00000234767
4	lnc-AL445989.1-8	chr13:66440195-66440400	NONHSAT034197
5	lnc-PCDH9-6	chr13:66430425-66430559	NONHSAT034195
6	lnc-AL445989.1-8	chr13:66440306-66440375	ENSG00000234767
7	lnc-AL445989.1-8	chr13:66449839-66449901	NONHSAT034197
8	lnc-AL445989.1-8	chr13:66451989-66452351	NONHSAT034197

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

Extended variants
information (count: 3440 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3440 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549176183	chr13:66342632-66342633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541451479	chr13:66342648-66342649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559558964	chr13:66342652-66342653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528589369	chr13:66342660-66342661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs112595611	chr13:66342661-66342662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551319999	chr13:66342718-66342719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561563812	chr13:66342721-66342722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73500523	chr13:66342752-66342753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537327749	chr13:66342787-66342788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550898085	chr13:66342810-66342811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567964728	chr13:66342813-66342814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190927391	chr13:66342853-66342854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536420201	chr13:66342858-66342859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs9540547	chr13:66342918-66342919	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183448525	chr13:66342926-66342927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76500518	chr13:66342928-66342929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs527399624	chr13:66342930-66342931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117692987	chr13:66342961-66342962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543722345	chr13:66343211-66343212	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs188914607	chr13:66343227-66343228	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs9592426	chr13:66343234-66343235	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs573901347	chr13:66343245-66343246	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs542410872	chr13:66343332-66343333	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs193146240	chr13:66343343-66343344	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs559507972	chr13:66343348-66343349	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs146076417	chr13:66343350-66343351	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs138599233	chr13:66343358-66343359	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs183600215	chr13:66343378-66343379	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs571243454	chr13:66343386-66343387	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs188098060	chr13:66343389-66343390	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs576518834	chr13:66347035-66347036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs188901917	chr13:66347042-66347043	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs562481204	chr13:66347081-66347082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs193102330	chr13:66347088-66347089	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs185176777	chr13:66347156-66347157	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs561787407	chr13:66347157-66347158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs189138020	chr13:66347225-66347226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547605070	chr13:66347226-66347227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564321510	chr13:66347244-66347245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533445956	chr13:66347409-66347410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115364837	chr13:66347421-66347422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570151858	chr13:66347569-66347570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535450836	chr13:66347590-66347591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549358363	chr13:66347598-66347599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151217110	chr13:66347602-66347603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573854965	chr13:66347637-66347638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534988449	chr13:66347665-66347666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529600229	chr13:66347705-66347706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375901650	chr13:66347716-66347717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112402727	chr13:66347717-66347718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:210 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66342600-66343200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:66343000-66343400	Enhancers	H1 Cell Line	embryonic stem cell
3	chr13:66343000-66343400	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr13:66347000-66347200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr13:66347200-66349800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr13:66357600-66358000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr13:66358000-66358400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr13:66363800-66364200	Enhancers	Osteobl	bone
9	chr13:66363800-66364600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:66363800-66364600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr13:66363800-66364600	Enhancers	HSMMtube	muscle
12	chr13:66364200-66364600	Flanking Active TSS	Osteobl	bone
13	chr13:66372000-66373600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr13:66373600-66376400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr13:66376400-66377200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr13:66376600-66377000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr13:66377000-66379000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:66377200-66379000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:66379000-66379200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:66379000-66379400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr13:66379200-66379600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr13:66379400-66382200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr13:66379600-66379800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:66379800-66382400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:66380800-66382000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr13:66381000-66382800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr13:66381000-66382800	Enhancers	Osteobl	bone
28	chr13:66381400-66383200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr13:66381800-66383400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:66382000-66382200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr13:66382200-66382600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr13:66382200-66383000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr13:66382400-66382800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:66387200-66387400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr13:66399200-66399600	Enhancers	HUVEC	blood vessel
36	chr13:66401000-66401400	Enhancers	Brain Germinal Matrix	brain
37	chr13:66404600-66404800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr13:66410000-66410200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:66410200-66410400	Enhancers	Pancreas	Pancrea
40	chr13:66410200-66413600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr13:66412800-66417400	Weak transcription	Gastric	stomach
42	chr13:66413600-66413800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr13:66413600-66415600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:66415600-66420600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:66417400-66417600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr13:66417400-66417800	Enhancers	Gastric	stomach
47	chr13:66417600-66418600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:66417800-66419000	Weak transcription	Gastric	stomach
49	chr13:66418600-66418800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr13:66418800-66419000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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