Variant report

Variant	esv1792084
Chromosome Location	chr13:49536705-49549571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:355)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:355 , 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	BACH1	chr13:49549313-49551066	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr13:49549214-49551803	GM12878	blood:	n/a	chr13:49549885-49549898 chr13:49550071-49550080 chr13:49550687-49550700 chr13:49550066-49550079 chr13:49550773-49550786 chr13:49550802-49550815
3	BCLAF1	chr13:49549364-49551057	GM12878	blood:	n/a	chr13:49549885-49549898 chr13:49550071-49550080 chr13:49550687-49550700 chr13:49550066-49550079 chr13:49550773-49550786 chr13:49550802-49550815
4	BHLHE40	chr13:49536408-49536811	K562	blood:	n/a	n/a
5	BHLHE40	chr13:49549404-49551675	GM12878	blood:	n/a	chr13:49550800-49550816 chr13:49550542-49550558
6	CBX3	chr13:49549179-49549629	K562	blood:	n/a	n/a
7	CEBPB	chr13:49549295-49549396	K562	blood:	n/a	n/a
8	CEBPB	chr13:49549324-49549866	Hela-S3	cervix:	n/a	n/a
9	CHD1	chr13:49549343-49550544	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr13:49549296-49551023	GM12878	blood:	n/a	n/a
11	CTBP2	chr13:49549211-49550637	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr13:49549200-49549350	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr13:49549020-49549170	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr13:49542940-49543090	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr13:49549260-49549410	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr13:49549220-49549370	BJ	skin:	n/a	n/a
17	CTCF	chr13:49549260-49549410	HCM	heart:	n/a	n/a
18	CTCF	chr13:49549560-49549710	GM12875	blood:	n/a	n/a
19	CTCF	chr13:49537750-49537929	K562	blood:	n/a	n/a
20	CTCF	chr13:49549560-49549710	AG04450	lung:	n/a	n/a
21	CTCF	chr13:49549332-49549371	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr13:49549300-49549450	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr13:49549220-49549370	HMF	breast:	n/a	n/a
24	CTCF	chr13:49549500-49549650	HMEC	breast:	n/a	n/a
25	CTCF	chr13:49537680-49537830	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr13:49549300-49549450	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr13:49549377-49549393	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr13:49549300-49549450	GM12869	blood:	n/a	n/a
29	CTCF	chr13:49537700-49537850	BE2_C	brain:	n/a	n/a
30	CTCF	chr13:49549280-49549430	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr13:49537620-49537770	NB4	blood:	n/a	n/a
32	CTCF	chr13:49549480-49549630	HVMF	connective:	n/a	n/a
33	CTCF	chr13:49549340-49549490	GM12864	blood:	n/a	n/a
34	CTCF	chr13:49549560-49549710	GM12872	blood:	n/a	n/a
35	CTCF	chr13:49549240-49549390	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr13:49549318-49549322	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr13:49549353-49550268	IMR90	lung:	n/a	n/a
38	CTCF	chr13:49537760-49537910	GM12864	blood:	n/a	n/a
39	CTCF	chr13:49549220-49549370	HepG2	liver:	n/a	n/a
40	CTCF	chr13:49549220-49549370	AG10803	skin:	n/a	n/a
41	CTCF	chr13:49549540-49549690	GM12869	blood:	n/a	n/a
42	CTCF	chr13:49549200-49549350	BJ	skin:	n/a	n/a
43	CTCF	chr13:49549240-49549390	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr13:49537740-49537890	HMF	breast:	n/a	n/a
45	CTCF	chr13:49549240-49549390	Caco-2	colon:	n/a	n/a
46	CTCF	chr13:49537680-49537830	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr13:49549540-49549690	GM12871	blood:	n/a	n/a
48	CTCF	chr13:49549300-49549450	NHLF	lung:	n/a	n/a
49	CTCF	chr13:49549280-49549430	HVMF	connective:	n/a	n/a
50	CTCF	chr13:49549540-49549690	GM06990	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:49546137-49546187	PrEC	prostate:	n/a
2	chr13:49549440-49549490	ovcar-3	ovarian:	n/a
3	chr13:49549489-49549539	SK-N-SH	brain:	n/a
4	chr13:49549463-49549513	ProgFib	skin:	n/a
5	chr13:49549489-49549539	AoSMC	blood vessel:	n/a
6	chr13:49549463-49549513	AG04450	lung:	fetal
7	chr13:49549489-49549539	SKMC	muscle:	n/a
8	chr13:49549489-49549539	K562	blood:	n/a
9	chr13:49546137-49546187	HCM	heart:	n/a
10	chr13:49549463-49549513	HRPEpiC	eye:	n/a
11	chr13:49549489-49549539	HCPEpiC	choroid plexus:	n/a
12	chr13:49549489-49549539	SK-N-SH_RA	brain:	n/a
13	chr13:49549489-49549539	Hepatocyte	liver:	n/a
14	chr13:49549440-49549490	Caco-2	colon:	n/a
15	chr13:49546137-49546187	HEEpiC	esophagus:	n/a
16	chr13:49546137-49546187	PANC-1	pancreas:	n/a
17	chr13:49549489-49549539	BJ	skin:	n/a
18	chr13:49549489-49549539	HEK293	kidney:	embryo
19	chr13:49549440-49549490	HMEC	breast:	n/a
20	chr13:49549463-49549513	T-47D	breast:	n/a
21	chr13:49549463-49549513	Jurkat	blood:	n/a
22	chr13:49549489-49549539	HMEC	breast:	n/a
23	chr13:49549463-49549513	NT2-D1	testis:	n/a
24	chr13:49549440-49549490	PrEC	prostate:	n/a
25	chr13:49546137-49546187	GM12878	blood:	n/a
26	chr13:49549440-49549490	IMR90	lung:	fetal
27	chr13:49546137-49546187	HepG2	liver:	n/a
28	chr13:49549489-49549539	AG09309	skin:	n/a
29	chr13:49549489-49549539	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:49549489-49549539	HL-60	blood:	n/a
31	chr13:49546137-49546187	HRPEpiC	eye:	n/a
32	chr13:49549489-49549539	SAEC	small airway:	n/a
33	chr13:49549463-49549513	HCPEpiC	choroid plexus:	n/a
34	chr13:49549440-49549490	SK-N-MC	brain:	n/a
35	chr13:49549463-49549513	HMEC	breast:	n/a
36	chr13:49549463-49549513	U87	brain:	n/a
37	chr13:49549440-49549490	H1-hESC	embryonic stem cell:	embryo
38	chr13:49549440-49549490	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:49549440-49549490	RPTEC	kidney:	n/a
40	chr13:49549489-49549539	AG04449	skin:	fetal
41	chr13:49549440-49549490	BE2_C	brain:	n/a
42	chr13:49549463-49549513	GM12891	blood:	n/a
43	chr13:49546137-49546187	H1-hESC	embryonic stem cell:	embryo
44	chr13:49549440-49549490	NH-A	brain:	n/a
45	chr13:49546137-49546187	NHDF-neo	bronchial:	n/a
46	chr13:49549489-49549539	MCF10A-Er-Src	breast:	n/a
47	chr13:49549463-49549513	HPAEpiC	pulmonary alveolar:	n/a
48	chr13:49546137-49546187	HCT-116	colon:	n/a
49	chr13:49546137-49546187	SK-N-MC	brain:	n/a
50	chr13:49549489-49549539	H1-hESC	embryonic stem cell:	embryo

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:49549492..49550320-chr15:73075454..73076164,2	NB4	blood:
2	chr13:49549219..49550138-chr16:75669158..75670004,2	NB4	blood:
3	chr13:49538660..49540724-chr13:49542814..49545257,2	MCF-7	breast:
4	chr13:49344498..49346343-chr13:49548446..49550486,2	MCF-7	breast:
5	chr13:49548036..49549716-chr13:49570249..49572622,2	K562	blood:
6	chr13:49538660..49540724-chr13:49542814..49545257,2	MCF-7	breast:
7	chr13:49535111..49537978-chr13:49544443..49546396,2	K562	blood:
8	chr13:49546080..49548216-chr13:49556766..49558384,2	MCF-7	breast:
9	chr13:49535149..49536967-chr13:49548289..49550226,2	K562	blood:
10	chr13:49511991..49514025-chr13:49547058..49549833,2	K562	blood:
11	chr13:49535111..49537978-chr13:49544443..49546396,2	K562	blood:
12	chr13:49549495..49551590-chr13:49668953..49673259,5	MCF-7	breast:
13	chr10:81106936..81108869-chr13:49549506..49551759,2	MCF-7	breast:
14	chr13:49547950..49551813-chr13:49821954..49825536,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAB39L-4	chr13:49546319-49550047	NONHSAT033727
2	lnc-FNDC3A-2	chr13:49538238-49538736	NONHSAT033726
3	lnc-CAB39L-4	chr13:49547696-49547790	ucscGeneNc_uc001vdx_2
4	lnc-CAB39L-4	chr13:49540234-49540300	ucscGeneNc_uc001vdx_2
5	lnc-FNDC3A-2	chr13:49536817-49537104	NONHSAT033726

No data

Variant related genes	Relation type
FNDC3A	TF binding region
FNDC3A	CpG island
ENSG00000108179	chromatin interactions
ENSG00000225131	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000102531	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000199788	chromatin interactions
ENSG00000065427	chromatin interactions

Extended variants
information (count: 212 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:212 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9568139	chr13:49536705-49536706	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188312057	chr13:49536708-49536709	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546576466	chr13:49536723-49536724	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192992834	chr13:49536725-49536726	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184743564	chr13:49536749-49536750	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79361640	chr13:49536756-49536757	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189663478	chr13:49536776-49536777	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563738523	chr13:49536831-49536832	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs569441129	chr13:49536833-49536834	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs192386265	chr13:49536839-49536840	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs557853825	chr13:49536893-49536894	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs531631391	chr13:49536897-49536898	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs117593087	chr13:49536915-49536916	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs555392001	chr13:49536919-49536920	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs183525439	chr13:49536933-49536934	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs544505286	chr13:49536943-49536944	Inactive region	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs532045696	chr13:49537058-49537059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs562608002	chr13:49537059-49537060	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs189439486	chr13:49537091-49537092	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs544855190	chr13:49537102-49537103	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs555879953	chr13:49538349-49538350	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs116092803	chr13:49538371-49538372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs538562533	chr13:49538391-49538392	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs566280314	chr13:49538409-49538410	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs553611742	chr13:49538422-49538423	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs565903084	chr13:49538477-49538478	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs181620837	chr13:49538511-49538512	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs7325026	chr13:49538512-49538513	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs186374195	chr13:49538548-49538549	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs574032025	chr13:49538552-49538553	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs139100373	chr13:49538649-49538650	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs376189319	chr13:49538675-49538676	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs191275843	chr13:49538719-49538720	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs532066699	chr13:49540234-49540235	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs188068737	chr13:49540273-49540274	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs147852539	chr13:49540285-49540286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs9596044	chr13:49540297-49540298	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs189694425	chr13:49541604-49541605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs117023478	chr13:49541649-49541650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566216020	chr13:49541657-49541658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530205575	chr13:49541663-49541664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548344696	chr13:49541667-49541668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7322842	chr13:49541672-49541673	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543079151	chr13:49541703-49541704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563067169	chr13:49541704-49541705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181197772	chr13:49541712-49541713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558844520	chr13:49541796-49541797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574890276	chr13:49542007-49542008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141005569	chr13:49542008-49542009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556749276	chr13:49542025-49542026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49536400-49536800	Enhancers	K562	blood
2	chr13:49541600-49541800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:49542000-49542800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:49545600-49546200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:49546200-49546400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:49546400-49547000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:49546600-49549000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr13:49546800-49549000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
9	chr13:49546800-49549400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr13:49547400-49548800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:49547600-49548000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
12	chr13:49547600-49549200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr13:49547800-49549000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:49548000-49548800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr13:49548400-49548600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr13:49548400-49548600	Enhancers	Dnd41	blood
17	chr13:49548400-49548800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
18	chr13:49548400-49548800	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr13:49548400-49548800	ZNF genes & repeats	Fetal Intestine Small	intestine
20	chr13:49548400-49549000	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr13:49548400-49551200	Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr13:49548400-49552200	Active TSS	Aorta	Aorta
23	chr13:49548600-49548800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:49548600-49548800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr13:49548600-49548800	Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr13:49548600-49548800	Enhancers	Primary hematopoietic stem cells	blood
27	chr13:49548600-49548800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:49548600-49548800	Enhancers	Muscle Satellite Cultured Cells	--
29	chr13:49548600-49548800	Enhancers	Colon Smooth Muscle	Colon
30	chr13:49548600-49548800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr13:49548600-49548800	Enhancers	Rectal Smooth Muscle	rectum
32	chr13:49548600-49549000	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr13:49548600-49549000	Active TSS	Liver	Liver
34	chr13:49548600-49549000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr13:49548600-49549000	Enhancers	Fetal Stomach	stomach
36	chr13:49548600-49549200	Enhancers	Fetal Brain Female	brain
37	chr13:49548600-49549200	Enhancers	Fetal Heart	heart
38	chr13:49548600-49549200	Enhancers	Thymus	Thymus
39	chr13:49548600-49549200	ZNF genes & repeats	GM12878-XiMat	blood
40	chr13:49548600-49549600	Flanking Active TSS	Dnd41	blood
41	chr13:49548600-49550000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr13:49548600-49551600	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr13:49548800-49549000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr13:49548800-49549000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:49548800-49549000	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr13:49548800-49549000	Active TSS	Primary T cells from cord blood	blood
47	chr13:49548800-49549000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr13:49548800-49549000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr13:49548800-49549000	Enhancers	Adipose Nuclei	Adipose
50	chr13:49548800-49549000	Enhancers	Brain Germinal Matrix	brain

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