Variant report

Variant	esv34743
Chromosome Location	chr13:54313729-54424593
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	BHLHE40	chr13:54356605-54356862	GM12878	blood:	n/a	n/a
2	CEBPB	chr13:54356588-54356906	A549	lung:	n/a	n/a
3	CEBPB	chr13:54356591-54356893	K562	blood:	n/a	n/a
4	CEBPB	chr13:54356551-54356967	ECC-1	luminal epithelium:	n/a	chr13:54356928-54356936
5	CEBPB	chr13:54356549-54356924	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr13:54361120-54361404	HepG2	liver:	n/a	chr13:54361258-54361269
7	CEBPB	chr13:54356561-54356901	HepG2	liver:	n/a	n/a
8	CEBPB	chr13:54356658-54356771	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:54404485-54404673	HepG2	liver:	n/a	chr13:54404618-54404629
10	CEBPB	chr13:54356576-54356912	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:54356561-54356898	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:54356619-54356839	MCF-7	breast:	n/a	n/a
13	CEBPB	chr13:54356622-54356826	A549	lung:	n/a	n/a
14	CEBPB	chr13:54376269-54376545	HepG2	liver:	n/a	chr13:54376521-54376534 chr13:54376318-54376331
15	CTCF	chr13:54336091-54336200	Fibrobl	skin:	n/a	n/a
16	CTCF	chr13:54356660-54356810	GM12871	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
17	CTCF	chr13:54356158-54356335	HepG2	liver:	n/a	chr13:54356250-54356266
18	CTCF	chr13:54356580-54356730	HL-60	blood:	n/a	n/a
19	CTCF	chr13:54356220-54356370	HEK293	kidney:	n/a	chr13:54356250-54356266
20	CTCF	chr13:54356602-54356838	Pancreas_OC	pancreas:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
21	CTCF	chr13:54356620-54356770	GM12865	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
22	CTCF	chr13:54356180-54356330	HRE	kidney:	n/a	chr13:54356250-54356266
23	CTCF	chr13:54356035-54356398	MCF-7	breast:	n/a	chr13:54356250-54356266
24	CTCF	chr13:54356588-54356865	Lung_OC	lung:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
25	CTCF	chr13:54339556-54339585	GM10266	blood:	n/a	n/a
26	CTCF	chr13:54356740-54356890	NHLF	lung:	n/a	n/a
27	CTCF	chr13:54356578-54356869	Medullo	brain:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
28	CTCF	chr13:54356620-54356770	GM12873	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
29	CTCF	chr13:54356620-54356770	GM12878	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
30	CTCF	chr13:54356642-54356834	Fibrobl	skin:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
31	CTCF	chr13:54356260-54356410	HMEC	breast:	n/a	n/a
32	CTCF	chr13:54356680-54356830	A549	lung:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
33	CTCF	chr13:54356670-54356839	GM19238	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
34	CTCF	chr13:54356470-54356905	T-47D	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
35	CTCF	chr13:54356160-54356310	WERI-Rb-1	eye:	n/a	chr13:54356250-54356266
36	CTCF	chr13:54356660-54356810	GM12864	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
37	CTCF	chr13:54356580-54356730	GM12878	blood:	n/a	n/a
38	CTCF	chr13:54356711-54356755	MCF-7	breast:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
39	CTCF	chr13:54350041-54350192	GM12878	blood:	n/a	n/a
40	CTCF	chr13:54356640-54356790	GM12870	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
41	CTCF	chr13:54356660-54356810	AG04450	lung:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
42	CTCF	chr13:54356700-54356850	RPTEC	kidney:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
43	CTCF	chr13:54356680-54356830	NHDF-neo	bronchial:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
44	CTCF	chr13:54356660-54356810	BJ	skin:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
45	CTCF	chr13:54353180-54353330	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr13:54356580-54356844	Spleen_OC	spleen:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
47	CTCF	chr13:54356143-54356362	H1-hESC	embryonic stem cell:	n/a	chr13:54356250-54356266
48	CTCF	chr13:54357000-54357150	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr13:54356620-54356770	GM12872	blood:	n/a	chr13:54356716-54356737 chr13:54356714-54356732 chr13:54356715-54356731
50	CTCF	chr13:54357824-54357854	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54422912-54422962	ovcar-3	ovarian:	n/a
2	chr13:54422912-54422962	NT2-D1	testis:	n/a
3	chr13:54422912-54422962	AG09319	gingival:	n/a
4	chr13:54422912-54422962	SK-N-SH_RA	brain:	n/a
5	chr13:54362844-54362894	HRPEpiC	eye:	n/a
6	chr13:54362844-54362894	AoSMC	blood vessel:	n/a
7	chr13:54362844-54362894	GM12892	blood:	n/a
8	chr13:54422912-54422962	Jurkat	blood:	n/a
9	chr13:54362844-54362894	Hepatocyte	liver:	n/a
10	chr13:54422912-54422962	Hela-S3	cervix:	n/a
11	chr13:54422912-54422962	PFSK-1	brain:	n/a
12	chr13:54422912-54422962	AG04450	lung:	fetal
13	chr13:54362844-54362894	HRE	kidney:	n/a
14	chr13:54422912-54422962	MCF-7	breast:	n/a
15	chr13:54362844-54362894	HEK293	kidney:	embryo
16	chr13:54362844-54362894	GM12891	blood:	n/a
17	chr13:54422912-54422962	IMR90	lung:	fetal
18	chr13:54422912-54422962	HUVEC	blood vessel:	n/a
19	chr13:54422912-54422962	HCPEpiC	choroid plexus:	n/a
20	chr13:54422912-54422962	H1-hESC	embryonic stem cell:	embryo
21	chr13:54422912-54422962	AG09309	skin:	n/a
22	chr13:54362844-54362894	RPTEC	kidney:	n/a
23	chr13:54362844-54362894	HCF	heart:	n/a
24	chr13:54422912-54422962	HCF	heart:	n/a
25	chr13:54362844-54362894	Hela-S3	cervix:	n/a
26	chr13:54362844-54362894	NH-A	brain:	n/a
27	chr13:54362844-54362894	HCT-116	colon:	n/a
28	chr13:54362844-54362894	HCPEpiC	choroid plexus:	n/a
29	chr13:54362844-54362894	HEEpiC	esophagus:	n/a
30	chr13:54362844-54362894	AG09309	skin:	n/a
31	chr13:54362844-54362894	MCF-7	breast:	n/a
32	chr13:54422912-54422962	GM12891	blood:	n/a
33	chr13:54362844-54362894	CMK	blood:	n/a
34	chr13:54362844-54362894	HUVEC	blood vessel:	n/a
35	chr13:54422912-54422962	BE2_C	brain:	n/a
36	chr13:54362844-54362894	SKMC	muscle:	n/a
37	chr13:54362844-54362894	PANC-1	pancreas:	n/a
38	chr13:54362844-54362894	HIPEpiC	eye:	n/a
39	chr13:54362844-54362894	SK-N-SH_RA	brain:	n/a
40	chr13:54422912-54422962	K562	blood:	n/a
41	chr13:54422912-54422962	RPTEC	kidney:	n/a
42	chr13:54362844-54362894	GM12878	blood:	n/a
43	chr13:54422912-54422962	NH-A	brain:	n/a
44	chr13:54362844-54362894	SK-N-SH	brain:	n/a
45	chr13:54362844-54362894	HMEC	breast:	n/a
46	chr13:54362844-54362894	HPAEpiC	pulmonary alveolar:	n/a
47	chr13:54422912-54422962	AG04449	skin:	fetal
48	chr13:54422912-54422962	GM12892	blood:	n/a
49	chr13:54362844-54362894	HepG2	liver:	n/a
50	chr13:54422912-54422962	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:53824138..53824998-chr13:54353117..54353653,2	MCF-7	breast:
2	chr13:53824070..53825129-chr13:54355995..54357044,7	MCF-7	breast:
3	chr13:53824183..53825128-chr13:54355772..54356571,3	MCF-7	breast:
4	chr13:53824154..53825004-chr13:54349752..54350528,4	MCF-7	breast:
5	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:
6	chr13:53824156..53824674-chr13:54349734..54350480,3	MCF-7	breast:
7	chr13:54411879..54413790-chr13:54440349..54442010,2	K562	blood:
8	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-2	chr13:54334856-54334931	XLOC_010398
2	lnc-OLFM4-3	chr13:54418480-54418657	ENSG00000261517.1
3	lnc-OLFM4-3	chr13:54414818-54414945	ENSG00000261517.1
4	lnc-OLFM4-10	chr13:54424439-54424529	l_854_chr13:54424438-54458818_testes
5	lnc-OLFM4-2	chr13:54348953-54349119	XLOC_010398
6	lnc-OLFM4-3	chr13:54389554-54389628	ENSG00000261517.1
7	lnc-OLFM4-3	chr13:54412874-54412924	ENSG00000261517.1

Variant related genes	Relation type
LINC00558	TF binding region
LINC00558	CpG island

Extended variants
information (count: 1078 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:1078 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558533621	chr13:54320013-54320014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs189033941	chr13:54320029-54320030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567263610	chr13:54320071-54320072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs9596846	chr13:54320170-54320171	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs560358415	chr13:54320176-54320177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148311278	chr13:54320253-54320254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77274453	chr13:54320268-54320269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78845190	chr13:54320312-54320313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531656294	chr13:54320326-54320327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570387289	chr13:54332817-54332818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373188237	chr13:54332900-54332901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74507610	chr13:54332924-54332925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374638845	chr13:54332929-54332930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4483741	chr13:54332972-54332973	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
15	rs567150655	chr13:54332994-54332995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113657181	chr13:54333063-54333064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536191138	chr13:54333075-54333076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566053909	chr13:54333127-54333128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184934900	chr13:54333171-54333172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544644272	chr13:54333205-54333206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4293248	chr13:54333209-54333210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs143877037	chr13:54333215-54333216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540290431	chr13:54333228-54333229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs148599240	chr13:54333230-54333231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528361284	chr13:54333251-54333252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189395962	chr13:54333295-54333296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561500307	chr13:54333352-54333353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376068529	chr13:54333362-54333363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530628085	chr13:54333370-54333371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141385538	chr13:54333380-54333381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147428232	chr13:54333419-54333420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533078137	chr13:54333443-54333444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139697642	chr13:54333452-54333453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555052969	chr13:54333453-54333454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566512386	chr13:54333477-54333478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145209913	chr13:54333509-54333510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568691261	chr13:54333516-54333517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537607110	chr13:54333547-54333548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181715899	chr13:54333590-54333591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547458452	chr13:54334885-54334886	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs372331516	chr13:54334902-54334903	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs145116985	chr13:54334911-54334912	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs148340322	chr13:54334912-54334913	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs140778352	chr13:54335073-54335074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556132074	chr13:54335074-54335075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150112946	chr13:54335076-54335077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554930227	chr13:54335090-54335091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116136843	chr13:54335103-54335104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188449952	chr13:54335120-54335121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573445585	chr13:54335139-54335140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
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
Acute lymphoblastic leukemia	22237106	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
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
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54320000-54320400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:54332800-54333600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr13:54332800-54333600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr13:54332800-54333600	Enhancers	H9 Cell Line	embryonic stem cell
5	chr13:54332800-54333600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr13:54333000-54333600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:54333000-54333600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr13:54333000-54333600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr13:54335000-54335800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:54335200-54335600	Enhancers	Spleen	Spleen
11	chr13:54335600-54336000	Active TSS	Spleen	Spleen
12	chr13:54335800-54336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr13:54336000-54336200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:54348400-54348600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:54350200-54350400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:54350200-54350400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr13:54350400-54353000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr13:54350600-54351600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:54351600-54352600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:54351600-54352800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:54352600-54356000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr13:54353000-54353200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr13:54353200-54356800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr13:54355400-54356200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr13:54355600-54355800	Enhancers	Fetal Brain Male	brain
26	chr13:54355600-54356200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr13:54355600-54356200	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr13:54355600-54356400	Enhancers	Fetal Heart	heart
29	chr13:54355600-54356800	Enhancers	Fetal Brain Female	brain
30	chr13:54355800-54356000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:54355800-54356200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr13:54355800-54356200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr13:54355800-54356200	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr13:54355800-54356800	Weak transcription	Fetal Brain Male	brain
35	chr13:54356000-54356200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr13:54356000-54356400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:54356000-54356800	Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr13:54356000-54358800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:54356200-54356400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:54356200-54356400	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr13:54356200-54356600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr13:54356200-54356600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr13:54356200-54356600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr13:54356200-54356600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr13:54356200-54356600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr13:54356200-54356600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr13:54356200-54356600	Active TSS	Fetal Muscle Leg	muscle
48	chr13:54356200-54356800	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr13:54356200-54356800	Enhancers	Fetal Lung	lung
50	chr13:54356200-54357000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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