Variant report

Variant	nsv541767
Chromosome Location	chr13:48703732-48765860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:48718534-48718925	K562	blood:	n/a	n/a
2	ATF1	chr13:48716630-48716977	K562	blood:	n/a	n/a
3	ATF1	chr13:48735984-48736360	K562	blood:	n/a	n/a
4	ATF2	chr13:48716507-48716868	GM12878	blood:	n/a	n/a
5	ATF2	chr13:48758357-48758664	GM12878	blood:	n/a	n/a
6	ATF2	chr13:48760474-48760725	GM12878	blood:	n/a	n/a
7	BACH1	chr13:48730234-48730388	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:48758389-48758607	GM12878	blood:	n/a	n/a
9	BATF	chr13:48730015-48730326	GM12878	blood:	n/a	n/a
10	BATF	chr13:48758348-48758653	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:48716605-48716864	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:48760463-48760712	GM12878	blood:	n/a	n/a
13	BCL11A	chr13:48758376-48758786	GM12878	blood:	n/a	n/a
14	BCLAF1	chr13:48716496-48716945	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:48758425-48758694	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:48736057-48736323	K562	blood:	n/a	n/a
17	BHLHE40	chr13:48716608-48716991	GM12878	blood:	n/a	chr13:48716865-48716886 chr13:48716872-48716881
18	BHLHE40	chr13:48716681-48716958	K562	blood:	n/a	chr13:48716865-48716886 chr13:48716872-48716881
19	CBX3	chr13:48729907-48730442	HCT-116	colon:	n/a	n/a
20	CCNT2	chr13:48716692-48716892	K562	blood:	n/a	n/a
21	CCNT2	chr13:48730795-48730916	K562	blood:	n/a	n/a
22	CCNT2	chr13:48736020-48736338	K562	blood:	n/a	n/a
23	CEBPB	chr13:48711142-48711270	HepG2	liver:	n/a	chr13:48711196-48711207
24	CEBPB	chr13:48729991-48730431	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:48736513-48736646	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:48750598-48750784	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:48729861-48730590	HCT-116	colon:	n/a	n/a
28	CEBPB	chr13:48760541-48760878	HepG2	liver:	n/a	chr13:48760708-48760719
29	CEBPB	chr13:48760581-48760857	K562	blood:	n/a	chr13:48760708-48760719
30	CEBPB	chr13:48729940-48730549	HCT-116	colon:	n/a	n/a
31	CEBPB	chr13:48729998-48730339	A549	lung:	n/a	n/a
32	CEBPB	chr13:48707187-48707320	K562	blood:	n/a	n/a
33	CEBPB	chr13:48730243-48730443	K562	blood:	n/a	n/a
34	CEBPB	chr13:48729391-48729501	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr13:48758493-48758717	GM12878	blood:	n/a	n/a
36	CHD2	chr13:48760554-48760767	GM12878	blood:	n/a	n/a
37	CTCF	chr13:48720827-48720922	Lung_OC	lung:	n/a	n/a
38	CTCF	chr13:48756660-48756810	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr13:48756595-48756692	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:48756620-48756770	MCF-7	breast:	n/a	n/a
41	CTCF	chr13:48756680-48756830	HFF	foreskin:	n/a	n/a
42	CTCF	chr13:48746199-48746262	GM13977	blood:	n/a	n/a
43	CTCF	chr13:48756720-48756870	A549	lung:	n/a	n/a
44	CTCF	chr13:48743046-48743145	ProgFib	skin:	n/a	n/a
45	CTCF	chr13:48756660-48756810	HepG2	liver:	n/a	n/a
46	CTCF	chr13:48762900-48763050	HEK293	kidney:	n/a	n/a
47	CTCF	chr13:48756660-48756810	HRE	kidney:	n/a	n/a
48	CTCF	chr13:48756701-48756706	K562	blood:	n/a	n/a
49	CTCF	chr13:48756680-48756830	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr13:48756620-48756770	HEK293	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:48761357-48761407	HUVEC	blood vessel:	n/a
2	chr13:48712008-48712058	PANC-1	pancreas:	n/a
3	chr13:48761357-48761407	H1-hESC	embryonic stem cell:	embryo
4	chr13:48761357-48761407	HepG2	liver:	n/a
5	chr13:48712008-48712058	PrEC	prostate:	n/a
6	chr13:48761357-48761407	Jurkat	blood:	n/a
7	chr13:48761357-48761407	GM12892	blood:	n/a
8	chr13:48761357-48761407	U87	brain:	n/a
9	chr13:48761357-48761407	AG09309	skin:	n/a
10	chr13:48712008-48712058	ProgFib	skin:	n/a
11	chr13:48712008-48712058	CMK	blood:	n/a
12	chr13:48712008-48712058	MCF-7	breast:	n/a
13	chr13:48761357-48761407	BE2_C	brain:	n/a
14	chr13:48712008-48712058	HPAEpiC	pulmonary alveolar:	n/a
15	chr13:48712008-48712058	NB4	blood:	n/a
16	chr13:48712008-48712058	GM12878	blood:	n/a
17	chr13:48761357-48761407	SKMC	muscle:	n/a
18	chr13:48761357-48761407	AG04450	lung:	fetal
19	chr13:48761357-48761407	GM12878	blood:	n/a
20	chr13:48761357-48761407	HCF	heart:	n/a
21	chr13:48761357-48761407	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:48761357-48761407	HCPEpiC	choroid plexus:	n/a
23	chr13:48761357-48761407	HIPEpiC	eye:	n/a
24	chr13:48712008-48712058	U87	brain:	n/a
25	chr13:48761357-48761407	HAEpiC	amniotic membrane:	n/a
26	chr13:48761357-48761407	BJ	skin:	n/a
27	chr13:48712008-48712058	MCF10A-Er-Src	breast:	n/a
28	chr13:48761357-48761407	NH-A	brain:	n/a
29	chr13:48712008-48712058	PFSK-1	brain:	n/a
30	chr13:48712008-48712058	HRCEpiC	kidney:	n/a
31	chr13:48712008-48712058	SK-N-MC	brain:	n/a
32	chr13:48712008-48712058	Caco-2	colon:	n/a
33	chr13:48712008-48712058	HepG2	liver:	n/a
34	chr13:48761357-48761407	MCF-7	breast:	n/a
35	chr13:48761357-48761407	SAEC	small airway:	n/a
36	chr13:48761357-48761407	AG10803	skin:	n/a
37	chr13:48712008-48712058	Hela-S3	cervix:	n/a
38	chr13:48712008-48712058	A549	lung:	n/a
39	chr13:48761357-48761407	HRCEpiC	kidney:	n/a
40	chr13:48712008-48712058	ECC-1	luminal epithelium:	n/a
41	chr13:48761357-48761407	RPTEC	kidney:	n/a
42	chr13:48761357-48761407	HL-60	blood:	n/a
43	chr13:48712008-48712058	LNCaP	prostate:	n/a
44	chr13:48761357-48761407	A549	lung:	n/a
45	chr13:48712008-48712058	HCT-116	colon:	n/a
46	chr13:48712008-48712058	BJ	skin:	n/a
47	chr13:48761357-48761407	HCT-116	colon:	n/a
48	chr13:48712008-48712058	AG09319	gingival:	n/a
49	chr13:48712008-48712058	AG09309	skin:	n/a
50	chr13:48712008-48712058	ovcar-3	ovarian:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:48719328..48721688-chr13:48725913..48727426,2	MCF-7	breast:
2	chr13:48759722..48761535-chr13:48765446..48768314,2	K562	blood:
3	chr13:48610445..48612287-chr13:48722206..48724817,2	K562	blood:
4	chr13:48730879..48733755-chr13:48736482..48738295,2	MCF-7	breast:
5	chr13:48759722..48761535-chr13:48765446..48768314,2	K562	blood:
6	chr13:48738757..48741557-chr13:48751933..48753971,2	K562	blood:
7	chr13:48707167..48708993-chr13:48709200..48711032,2	MCF-7	breast:
8	chr13:48730571..48732164-chr13:48738258..48740910,2	K562	blood:
9	chr13:48730879..48733755-chr13:48736482..48738295,2	MCF-7	breast:
10	chr13:48738757..48741557-chr13:48751933..48753971,2	K562	blood:
11	chr13:48705406..48707742-chr13:48718152..48719712,2	K562	blood:
12	chr13:48719328..48721688-chr13:48725913..48727426,2	MCF-7	breast:
13	chr13:48705406..48707742-chr13:48718152..48719712,2	K562	blood:
14	chr11:134888413..134889240-chr13:48703699..48704350,2	MCF-7	breast:
15	chr13:48730571..48732164-chr13:48738258..48740910,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MED4-1	chr13:48707668-48708098	l_836_chr13:48707667-48719987_testes
2	lnc-MED4-1	chr13:48719596-48719987	l_836_chr13:48707667-48719987_testes

No data

Variant related genes	Relation type
POLR2KP2	TF binding region
POLR2KP2	CpG island
ENSG00000136143	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000224510	chromatin interactions

Extended variants
information (count: 2224 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:2224 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373257435	chr13:48703740-48703741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570269914	chr13:48703754-48703755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537470233	chr13:48703787-48703788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114830198	chr13:48703820-48703821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577481584	chr13:48703844-48703845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187896034	chr13:48703955-48703956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553291413	chr13:48703964-48703965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115723930	chr13:48703976-48703977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553206546	chr13:48703977-48703978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541510937	chr13:48703999-48704000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563073548	chr13:48704007-48704008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574868159	chr13:48704012-48704013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545411898	chr13:48704033-48704034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564367156	chr13:48704048-48704049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79224756	chr13:48704066-48704067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548373523	chr13:48704200-48704201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535418944	chr13:48704233-48704234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150605438	chr13:48704337-48704338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139796251	chr13:48704369-48704370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548679061	chr13:48704414-48704415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376224948	chr13:48704434-48704435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192140015	chr13:48704456-48704457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552296121	chr13:48704470-48704471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571075876	chr13:48704513-48704514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553666073	chr13:48704515-48704516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149805469	chr13:48704532-48704533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74982162	chr13:48704545-48704546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558394711	chr13:48704608-48704609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs578101360	chr13:48704632-48704633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556608058	chr13:48704655-48704656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs115604882	chr13:48704690-48704691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377169863	chr13:48704692-48704693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367873079	chr13:48704743-48704744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146810716	chr13:48704822-48704823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572837121	chr13:48704831-48704832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540141265	chr13:48704862-48704863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs5803425	chr13:48704868-48704869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34340621	chr13:48704869-48704870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs386379103	chr13:48704870-48704871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3082886	chr13:48704871-48704872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1998989	chr13:48704938-48704939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs529071010	chr13:48705096-48705097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184864176	chr13:48705170-48705171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563729657	chr13:48705243-48705244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77419736	chr13:48705268-48705269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552683338	chr13:48705273-48705274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35536952	chr13:48705278-48705279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189283071	chr13:48705296-48705297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76029036	chr13:48705305-48705306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201046391	chr13:48705346-48705347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Malignant fibrous histiocytomas	21085701	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
Ovarian cancer	22355333	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
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	21750150	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Phyllodes tumor	17334353	CNVD
Retinoblastoma	22278416	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
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:48700400-48705600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr13:48701600-48704000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr13:48701800-48705000	Weak transcription	HMEC	breast
4	chr13:48701800-48705800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr13:48701800-48725800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr13:48702000-48704800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr13:48702000-48705200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr13:48702000-48705200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr13:48702000-48705200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr13:48702000-48705200	Weak transcription	NHEK	skin
11	chr13:48702000-48705600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr13:48702200-48704800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr13:48702200-48705600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr13:48702200-48705600	Weak transcription	HepG2	liver
15	chr13:48702200-48713800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr13:48702600-48704400	Weak transcription	Brain Hippocampus Middle	brain
17	chr13:48703200-48703800	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr13:48703200-48704000	Enhancers	Fetal Thymus	thymus
19	chr13:48703200-48704000	Enhancers	Dnd41	blood
20	chr13:48703200-48704200	Enhancers	Primary T cells from cord blood	blood
21	chr13:48703600-48703800	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr13:48703600-48705800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr13:48703800-48705600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr13:48704000-48705400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr13:48704000-48705400	Weak transcription	Fetal Thymus	thymus
26	chr13:48704800-48705400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr13:48705000-48706200	Enhancers	HMEC	breast
28	chr13:48705200-48705600	Enhancers	NHEK	skin
29	chr13:48705200-48705800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr13:48705200-48706000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr13:48705200-48706200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr13:48705400-48706600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr13:48705600-48705800	Enhancers	Brain Hippocampus Middle	brain
34	chr13:48705600-48706000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr13:48705600-48706000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:48705600-48706000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr13:48705600-48706000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:48705600-48706000	Flanking Active TSS	NHEK	skin
39	chr13:48705600-48706200	Enhancers	HepG2	liver
40	chr13:48705800-48706000	Enhancers	Primary B cells from peripheral blood	blood
41	chr13:48705800-48706000	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr13:48705800-48706000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr13:48705800-48706000	Enhancers	Fetal Thymus	thymus
44	chr13:48705800-48706200	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr13:48705800-48707000	Enhancers	Primary hematopoietic stem cells	blood
46	chr13:48706000-48706200	Enhancers	NHEK	skin
47	chr13:48706000-48710600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr13:48706800-48707000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr13:48710600-48711000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr13:48711800-48712200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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