Variant report

Variant	nsv1044086
Chromosome Location	chr13:49331713-49350131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:364)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:49343281-49343609	HepG2	liver:	n/a	n/a
2	BATF	chr13:49343230-49343558	GM12878	blood:	n/a	n/a
3	BRCA1	chr13:49343223-49343600	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr13:49348022-49348374	Hela-S3	cervix:	n/a	chr13:49348182-49348193
5	CEBPB	chr13:49343300-49343499	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:49343209-49343567	K562	blood:	n/a	n/a
7	CEBPB	chr13:49343292-49343600	MCF-7	breast:	n/a	n/a
8	CEBPB	chr13:49348023-49348345	HepG2	liver:	n/a	chr13:49348182-49348193
9	CEBPB	chr13:49343210-49343563	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:49348073-49348323	A549	lung:	n/a	chr13:49348182-49348193
11	CEBPB	chr13:49343230-49343559	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:49343202-49343615	A549	lung:	n/a	n/a
13	CEBPB	chr13:49343101-49343662	A549	lung:	n/a	n/a
14	CEBPB	chr13:49343196-49343539	K562	blood:	n/a	n/a
15	CEBPB	chr13:49341989-49342026	HepG2	liver:	n/a	n/a
16	CEBPB	chr13:49343178-49343559	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:49347995-49348376	IMR90	lung:	n/a	chr13:49348182-49348193
18	CEBPB	chr13:49343213-49343614	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:49343203-49343582	IMR90	lung:	n/a	n/a
20	CHD2	chr13:49343294-49343660	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr13:49343400-49343550	AG04450	lung:	n/a	chr13:49343448-49343469
22	CTCF	chr13:49343300-49343450	WI-38	lung:	n/a	n/a
23	CTCF	chr13:49343259-49343533	A549	lung:	n/a	chr13:49343448-49343469
24	CTCF	chr13:49343380-49343530	NHDF-neo	bronchial:	n/a	chr13:49343448-49343469
25	CTCF	chr13:49342866-49344007	HCT-116	colon:	n/a	chr13:49343448-49343469
26	CTCF	chr13:49343740-49343890	GM12872	blood:	n/a	n/a
27	CTCF	chr13:49343420-49343570	NHLF	lung:	n/a	chr13:49343448-49343469
28	CTCF	chr13:49343281-49343595	LNCaP	prostate:	n/a	chr13:49343448-49343469
29	CTCF	chr13:49343179-49343685	K562	blood:	n/a	chr13:49343448-49343469
30	CTCF	chr13:49343360-49343510	HA-sp	spinal cord:	n/a	chr13:49343448-49343469
31	CTCF	chr13:49343255-49343595	Kidney_OC	kidney:	n/a	chr13:49343448-49343469
32	CTCF	chr13:49343323-49343564	MCF-7	breast:	n/a	chr13:49343448-49343469
33	CTCF	chr13:49343360-49343510	GM12866	blood:	n/a	chr13:49343448-49343469
34	CTCF	chr13:49343380-49343530	HUVEC	blood vessel:	n/a	chr13:49343448-49343469
35	CTCF	chr13:49343278-49343581	GM10248	blood:	n/a	chr13:49343448-49343469
36	CTCF	chr13:49343360-49343510	HCT-116	colon:	n/a	chr13:49343448-49343469
37	CTCF	chr13:49343294-49343628	GM19238	blood:	n/a	chr13:49343448-49343469
38	CTCF	chr13:49343380-49343530	GM12874	blood:	n/a	chr13:49343448-49343469
39	CTCF	chr13:49343340-49343533	MCF-7	breast:	n/a	chr13:49343448-49343469
40	CTCF	chr13:49343129-49343754	MCF-7	breast:	n/a	chr13:49343448-49343469
41	CTCF	chr13:49343360-49343510	SK-N-SH_RA	brain:	n/a	chr13:49343448-49343469
42	CTCF	chr13:49343360-49343510	HEK293	kidney:	n/a	chr13:49343448-49343469
43	CTCF	chr13:49343087-49343692	A549	lung:	n/a	chr13:49343448-49343469
44	CTCF	chr13:49343282-49343608	Fibrobl	skin:	n/a	chr13:49343448-49343469
45	CTCF	chr13:49343340-49343490	HRE	kidney:	n/a	chr13:49343448-49343469
46	CTCF	chr13:49343360-49343510	NHEK	skin:	n/a	chr13:49343448-49343469
47	CTCF	chr13:49343360-49343510	BE2_C	brain:	n/a	chr13:49343448-49343469
48	CTCF	chr13:49343340-49343490	HRPEpiC	eye:	n/a	chr13:49343448-49343469
49	CTCF	chr13:49343266-49343634	GM13977	blood:	n/a	chr13:49343448-49343469
50	CTCF	chr13:49343234-49343653	SK-N-SH_RA	brain:	n/a	chr13:49343448-49343469

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49349649-49349699	HRCEpiC	kidney:	n/a
2	chr13:49349649-49349699	HL-60	blood:	n/a
3	chr13:49349649-49349699	SK-N-MC	brain:	n/a
4	chr13:49349649-49349699	GM12892	blood:	n/a
5	chr13:49349649-49349699	MCF10A-Er-Src	breast:	n/a
6	chr13:49349649-49349699	RPTEC	kidney:	n/a
7	chr13:49349649-49349699	HRE	kidney:	n/a
8	chr13:49349649-49349699	AG09319	gingival:	n/a
9	chr13:49349649-49349699	HCT-116	colon:	n/a
10	chr13:49349649-49349699	U87	brain:	n/a
11	chr13:49349649-49349699	PANC-1	pancreas:	n/a
12	chr13:49349649-49349699	NHDF-neo	bronchial:	n/a
13	chr13:49349649-49349699	K562	blood:	n/a
14	chr13:49349649-49349699	ProgFib	skin:	n/a
15	chr13:49349649-49349699	Caco-2	colon:	n/a
16	chr13:49349649-49349699	HEK293	kidney:	embryo
17	chr13:49349649-49349699	HCM	heart:	n/a
18	chr13:49349649-49349699	BJ	skin:	n/a
19	chr13:49349649-49349699	SK-N-SH_RA	brain:	n/a
20	chr13:49349649-49349699	ECC-1	luminal epithelium:	n/a
21	chr13:49349649-49349699	NB4	blood:	n/a
22	chr13:49349649-49349699	HCF	heart:	n/a
23	chr13:49349649-49349699	CMK	blood:	n/a
24	chr13:49349649-49349699	AG09309	skin:	n/a
25	chr13:49349649-49349699	MCF-7	breast:	n/a
26	chr13:49349649-49349699	Hela-S3	cervix:	n/a
27	chr13:49349649-49349699	HEEpiC	esophagus:	n/a
28	chr13:49349649-49349699	SK-N-SH	brain:	n/a
29	chr13:49349649-49349699	AG04450	lung:	fetal
30	chr13:49349649-49349699	HNPCEpiC	eye:	n/a
31	chr13:49349649-49349699	H1-hESC	embryonic stem cell:	embryo
32	chr13:49349649-49349699	HepG2	liver:	n/a
33	chr13:49349649-49349699	LNCaP	prostate:	n/a
34	chr13:49349649-49349699	GM12891	blood:	n/a
35	chr13:49349649-49349699	HAEpiC	amniotic membrane:	n/a
36	chr13:49349649-49349699	GM19239	blood:	n/a
37	chr13:49349649-49349699	BE2_C	brain:	n/a
38	chr13:49349649-49349699	AoSMC	blood vessel:	n/a
39	chr13:49349649-49349699	SKMC	muscle:	n/a
40	chr13:49349649-49349699	HRPEpiC	eye:	n/a
41	chr13:49349649-49349699	GM06990	blood:	n/a
42	chr13:49349649-49349699	HPAEpiC	pulmonary alveolar:	n/a
43	chr13:49349649-49349699	HUVEC	blood vessel:	n/a
44	chr13:49349649-49349699	NH-A	brain:	n/a
45	chr13:49349649-49349699	Hepatocyte	liver:	n/a
46	chr13:49349649-49349699	HMEC	breast:	n/a
47	chr13:49349649-49349699	PrEC	prostate:	n/a
48	chr13:49349649-49349699	A549	lung:	n/a
49	chr13:49349649-49349699	SAEC	small airway:	n/a
50	chr13:49349649-49349699	NHBE	bronchial:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:49342359..49344964-chr13:49345478..49349332,4	K562	blood:
2	chr13:49169501..49170445-chr13:49342944..49343864,14	MCF-7	breast:
3	chr13:49323521..49324509-chr13:49342836..49343780,6	MCF-7	breast:
4	chr13:49342669..49345130-chr13:49347475..49349741,3	K562	blood:
5	chr13:49305851..49306691-chr13:49342839..49343554,2	MCF-7	breast:
6	chr13:49169339..49170769-chr13:49342414..49344167,53	MCF-7	breast:
7	chr13:49344498..49346343-chr13:49548446..49550486,2	MCF-7	breast:
8	chr13:47337286..47337846-chr13:49343111..49343875,2	MCF-7	breast:
9	chr13:48908385..48909298-chr13:49342938..49343582,2	MCF-7	breast:
10	chr13:49066707..49067590-chr13:49343362..49343898,2	K562	blood:
11	chr13:48700764..48701721-chr13:49342977..49343886,4	K562	blood:
12	chr13:49323717..49324650-chr13:49343067..49343837,2	K562	blood:
13	chr13:49169482..49170418-chr13:49342940..49343870,6	K562	blood:
14	chr13:49323328..49325913-chr13:49330163..49332626,2	MCF-7	breast:
15	chr13:49342669..49345130-chr13:49347475..49349741,3	K562	blood:
16	chr13:49343209..49343771-chr13:49550554..49551136,2	MCF-7	breast:
17	chr13:49217399..49217979-chr13:49342910..49343628,2	MCF-7	breast:
18	chr13:49348522..49350092-chr13:49351651..49354289,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYSLTR2-1	chr13:49345759-49345965	NONHSAT033724

No data

Variant related genes	Relation type
PSME2P2	TF binding region
PSME2P2	CpG island
ENSG00000225131	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000136161	chromatin interactions

Extended variants
information (count: 665 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567256021	chr13:49331713-49331714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs7320191	chr13:49331767-49331768	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs57408197	chr13:49331794-49331795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571177814	chr13:49331807-49331808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185924104	chr13:49331845-49331846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7319904	chr13:49331856-49331857	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs148987758	chr13:49331857-49331858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377072655	chr13:49331890-49331891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534306041	chr13:49331902-49331903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115621006	chr13:49331971-49331972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552460333	chr13:49331972-49331973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190249560	chr13:49331979-49331980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544591766	chr13:49331985-49331986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547072427	chr13:49331987-49331988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533076674	chr13:49332045-49332046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1323554	chr13:49332057-49332058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs182578760	chr13:49332058-49332059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560713029	chr13:49332077-49332078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527832826	chr13:49332095-49332096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542713730	chr13:49332108-49332109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560784263	chr13:49332130-49332131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531359488	chr13:49332140-49332141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544987594	chr13:49332143-49332144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60826934	chr13:49332157-49332158	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570894198	chr13:49332216-49332217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532311787	chr13:49332237-49332238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187935923	chr13:49332285-49332286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565877746	chr13:49332294-49332295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35570463	chr13:49332369-49332370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11617699	chr13:49332386-49332387	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs555852027	chr13:49332431-49332432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569249614	chr13:49332445-49332446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58220941	chr13:49332495-49332496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556638181	chr13:49332515-49332516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578069266	chr13:49332527-49332528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545717679	chr13:49332551-49332552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554128163	chr13:49332746-49332747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59162799	chr13:49332759-49332760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142654062	chr13:49332778-49332779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542822485	chr13:49332831-49332832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs74648258	chr13:49332920-49332921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs531338336	chr13:49332938-49332939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543103443	chr13:49332942-49332943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370054851	chr13:49332953-49332954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10220120	chr13:49332973-49332974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530298777	chr13:49332974-49332975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531942560	chr13:49332998-49332999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146884879	chr13:49332999-49333000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565808376	chr13:49333011-49333012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548471906	chr13:49333030-49333031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49331200-49341800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:49334000-49336600	Enhancers	Fetal Intestine Small	intestine
3	chr13:49335000-49335400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:49335000-49335800	Enhancers	Fetal Intestine Large	intestine
5	chr13:49337000-49337200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:49337600-49338400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr13:49338000-49338400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr13:49338200-49338400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:49341200-49341400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:49341600-49341800	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr13:49341800-49342000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:49342800-49343600	Enhancers	Dnd41	blood
13	chr13:49343000-49343200	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr13:49343000-49343400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr13:49343000-49343400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr13:49343000-49343600	Enhancers	Brain Hippocampus Middle	brain
17	chr13:49343000-49343600	Enhancers	Stomach Mucosa	stomach
18	chr13:49343000-49343800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr13:49343000-49344400	Enhancers	Hela-S3	cervix
20	chr13:49343200-49343400	Enhancers	Primary T cells from cord blood	blood
21	chr13:49343400-49343800	Enhancers	Brain Anterior Caudate	brain
22	chr13:49343600-49344000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr13:49343600-49345800	Weak transcription	Dnd41	blood
24	chr13:49343800-49346000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr13:49344000-49349000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr13:49344400-49347400	Weak transcription	Hela-S3	cervix
27	chr13:49345800-49348000	Enhancers	Dnd41	blood
28	chr13:49346000-49346400	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr13:49346000-49346400	Enhancers	Right Ventricle	heart
30	chr13:49346000-49346800	Enhancers	Left Ventricle	heart
31	chr13:49346000-49346800	Enhancers	Right Atrium	heart
32	chr13:49346000-49348400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr13:49346200-49346600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr13:49346200-49346800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr13:49346200-49346800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr13:49346200-49346800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr13:49346200-49346800	Enhancers	Fetal Heart	heart
38	chr13:49346200-49347600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr13:49346400-49346600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr13:49346400-49346800	Enhancers	Fetal Lung	lung
41	chr13:49346400-49350600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr13:49346600-49347600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr13:49346600-49357200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:49346800-49348800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr13:49346800-49352200	Weak transcription	Left Ventricle	heart
46	chr13:49347400-49352000	Enhancers	Hela-S3	cervix
47	chr13:49347600-49349200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr13:49347800-49348400	Enhancers	Placenta	Placenta
49	chr13:49347800-49352000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr13:49348400-49350000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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