Variant report

Variant	nsv533455
Chromosome Location	chr13:90041897-90255725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:647)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:647 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90166877-90167409	HepG2	liver:	n/a	n/a
2	ATF3	chr13:90166748-90167411	A549	lung:	n/a	n/a
3	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
5	BCL3	chr13:90166728-90167467	A549	lung:	n/a	n/a
6	BCL3	chr13:90166802-90167246	A549	lung:	n/a	n/a
7	BRCA1	chr13:90166960-90167339	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
9	CEBPB	chr13:90110265-90110690	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr13:90216095-90216295	HepG2	liver:	n/a	chr13:90216249-90216262 chr13:90216250-90216261
11	CEBPB	chr13:90177917-90178057	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:90046959-90047120	HepG2	liver:	n/a	n/a
13	CEBPB	chr13:90166942-90167297	MCF-7	breast:	n/a	n/a
14	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
15	CEBPB	chr13:90053451-90053803	HepG2	liver:	n/a	chr13:90053581-90053592
16	CEBPB	chr13:90190413-90190718	IMR90	lung:	n/a	chr13:90190558-90190569
17	CEBPB	chr13:90224834-90224951	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:90076016-90076314	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:90076020-90076326	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:90127840-90128138	A549	lung:	n/a	chr13:90128018-90128029
21	CEBPB	chr13:90177810-90178090	A549	lung:	n/a	n/a
22	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
23	CEBPB	chr13:90190494-90190716	HepG2	liver:	n/a	chr13:90190558-90190569
24	CEBPB	chr13:90127859-90128113	Hela-S3	cervix:	n/a	chr13:90128018-90128029
25	CEBPB	chr13:90120640-90120770	K562	blood:	n/a	chr13:90120722-90120733
26	CEBPB	chr13:90053432-90053763	MCF-7	breast:	n/a	chr13:90053581-90053592
27	CEBPB	chr13:90190415-90190721	H1-hESC	embryonic stem cell:	n/a	chr13:90190558-90190569
28	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
29	CEBPB	chr13:90190545-90190612	K562	blood:	n/a	chr13:90190558-90190569
30	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
31	CEBPB	chr13:90127861-90128178	HepG2	liver:	n/a	chr13:90128018-90128029
32	CEBPB	chr13:90171065-90171290	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr13:90166162-90166377	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:90167086-90167299	HepG2	liver:	n/a	n/a
35	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
36	CEBPB	chr13:90190489-90190619	K562	blood:	n/a	chr13:90190558-90190569
37	CEBPB	chr13:90127850-90128161	IMR90	lung:	n/a	chr13:90128018-90128029
38	CEBPB	chr13:90166750-90167502	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr13:90166987-90167427	A549	lung:	n/a	n/a
40	CEBPB	chr13:90120558-90120849	A549	lung:	n/a	chr13:90120722-90120733
41	CEBPB	chr13:90061199-90061485	A549	lung:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
42	CEBPB	chr13:90166579-90167503	A549	lung:	n/a	n/a
43	CEBPB	chr13:90177821-90178115	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:90166633-90167478	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
46	CEBPB	chr13:90053216-90053959	A549	lung:	n/a	chr13:90053581-90053592
47	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
48	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
49	CEBPB	chr13:90166838-90167348	A549	lung:	n/a	n/a
50	CEBPB	chr13:90053319-90053891	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90045847-90045897	AG10803	skin:	n/a
2	chr13:90053523-90053573	GM12891	blood:	n/a
3	chr13:90045847-90045897	HEEpiC	esophagus:	n/a
4	chr13:90053523-90053573	HCM	heart:	n/a
5	chr13:90053523-90053573	SK-N-SH	brain:	n/a
6	chr13:90045847-90045897	GM12892	blood:	n/a
7	chr13:90045847-90045897	HNPCEpiC	eye:	n/a
8	chr13:90053523-90053573	AG04450	lung:	fetal
9	chr13:90053523-90053573	T-47D	breast:	n/a
10	chr13:90053523-90053573	BE2_C	brain:	n/a
11	chr13:90045847-90045897	SAEC	small airway:	n/a
12	chr13:90045847-90045897	CMK	blood:	n/a
13	chr13:90045847-90045897	GM12878	blood:	n/a
14	chr13:90053523-90053573	HRCEpiC	kidney:	n/a
15	chr13:90053523-90053573	SK-N-SH_RA	brain:	n/a
16	chr13:90045847-90045897	U87	brain:	n/a
17	chr13:90045847-90045897	IMR90	lung:	fetal
18	chr13:90045847-90045897	HCF	heart:	n/a
19	chr13:90045847-90045897	Caco-2	colon:	n/a
20	chr13:90053523-90053573	H1-hESC	embryonic stem cell:	embryo
21	chr13:90045847-90045897	ECC-1	luminal epithelium:	n/a
22	chr13:90053523-90053573	A549	lung:	n/a
23	chr13:90045847-90045897	PANC-1	pancreas:	n/a
24	chr13:90045847-90045897	SK-N-MC	brain:	n/a
25	chr13:90053523-90053573	HCT-116	colon:	n/a
26	chr13:90053523-90053573	NT2-D1	testis:	n/a
27	chr13:90053523-90053573	LNCaP	prostate:	n/a
28	chr13:90045847-90045897	HepG2	liver:	n/a
29	chr13:90045847-90045897	LNCaP	prostate:	n/a
30	chr13:90045847-90045897	SK-N-SH_RA	brain:	n/a
31	chr13:90053523-90053573	RPTEC	kidney:	n/a
32	chr13:90053523-90053573	U87	brain:	n/a
33	chr13:90045847-90045897	PrEC	prostate:	n/a
34	chr13:90053523-90053573	HIPEpiC	eye:	n/a
35	chr13:90045847-90045897	AG04449	skin:	fetal
36	chr13:90053523-90053573	PFSK-1	brain:	n/a
37	chr13:90045847-90045897	SKMC	muscle:	n/a
38	chr13:90053523-90053573	MCF10A-Er-Src	breast:	n/a
39	chr13:90053523-90053573	HEK293	kidney:	embryo
40	chr13:90053523-90053573	AG09309	skin:	n/a
41	chr13:90045847-90045897	HRCEpiC	kidney:	n/a
42	chr13:90053523-90053573	Jurkat	blood:	n/a
43	chr13:90053523-90053573	HPAEpiC	pulmonary alveolar:	n/a
44	chr13:90053523-90053573	Hepatocyte	liver:	n/a
45	chr13:90045847-90045897	AG04450	lung:	fetal
46	chr13:90053523-90053573	HNPCEpiC	eye:	n/a
47	chr13:90045847-90045897	SK-N-SH	brain:	n/a
48	chr13:90045847-90045897	NH-A	brain:	n/a
49	chr13:90045847-90045897	HCM	heart:	n/a
50	chr13:90053523-90053573	HAEpiC	amniotic membrane:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
2	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
3	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
4	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
5	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
6	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-12	chr13:90205985-90206049	NONHSAT034632
2	lnc-SLITRK5-28	chr13:90186444-90186646	NONHSAT034630
3	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685
4	lnc-SLITRK6-12	chr13:90216586-90216667	NONHSAT034632
5	lnc-SLITRK6-12	chr13:90203455-90203544	NONHSAT034632
6	lnc-SLITRK6-12	chr13:90205985-90206058	XLOC_010686
7	lnc-SLITRK6-12	chr13:90204359-90204643	XLOC_010686
8	lnc-GPC5-4	chr13:90203487-90203531	ENSG00000271395.1
9	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
10	lnc-SLITRK6-12	chr13:90203455-90203544	XLOC_010686
11	lnc-GPC5-4	chr13:90204359-90204606	XLOC_010468
12	lnc-GPC5-4	chr13:90203039-90203531	XLOC_010468
13	lnc-GPC5-4	chr13:90204359-90204643	ENSG00000271395.1
14	lnc-SLITRK6-12	chr13:90201048-90201465	NONHSAT034632
15	lnc-SLITRK5-28	chr13:90186815-90187120	NONHSAT034630
16	lnc-SLITRK6-12	chr13:90203487-90203531	XLOC_010686
17	lnc-SLITRK6-12	chr13:90200945-90201465	XLOC_010686

No data

Variant related genes	Relation type
LINC01040	TF binding region
LINC00353	TF binding region
ENSG00000271395	TF binding region
LINC01040	CpG island
LINC00353	CpG island
ENSG00000271395	CpG island
MBNL1	miRNA target sites
HSP90B1	miRNA target sites

Extended variants
information (count: 4433 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4433 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576017283	chr13:90045411-90045412	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs146831134	chr13:90045450-90045451	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs9522542	chr13:90045486-90045487	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs573551481	chr13:90045504-90045505	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs183268413	chr13:90045510-90045511	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs373726639	chr13:90045512-90045513	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs140493722	chr13:90045530-90045531	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs374560206	chr13:90045546-90045547	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs569668034	chr13:90045547-90045548	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs564407127	chr13:90045552-90045553	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531771051	chr13:90045586-90045587	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550197585	chr13:90045607-90045608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs59426569	chr13:90045619-90045620	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs529572523	chr13:90045621-90045622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150465641	chr13:90045631-90045632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567495685	chr13:90045685-90045686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566237692	chr13:90045688-90045689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376618831	chr13:90045690-90045691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539626287	chr13:90045735-90045736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557870381	chr13:90045766-90045767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569644137	chr13:90045879-90045880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192221438	chr13:90045914-90045915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112961154	chr13:90045944-90045945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188248973	chr13:90045958-90045959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553046083	chr13:90046016-90046017	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs540895710	chr13:90046026-90046027	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs552970336	chr13:90046059-90046060	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs367724141	chr13:90046078-90046079	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs192961941	chr13:90046090-90046091	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs35208914	chr13:90046125-90046126	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs544865434	chr13:90046203-90046204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs564649201	chr13:90046294-90046295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531662386	chr13:90046317-90046318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs543848954	chr13:90046406-90046407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562027648	chr13:90046424-90046425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529635831	chr13:90046428-90046429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548140718	chr13:90046448-90046449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199785334	chr13:90046463-90046464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566229131	chr13:90046495-90046496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533617775	chr13:90046500-90046501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145327112	chr13:90046553-90046554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536711046	chr13:90046573-90046574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9588599	chr13:90046583-90046584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs67949454	chr13:90046615-90046616	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs534303428	chr13:90046634-90046635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553271855	chr13:90046637-90046638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184560752	chr13:90046678-90046679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538831049	chr13:90046753-90046754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188324428	chr13:90046930-90046931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576625749	chr13:90047015-90047016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90045400-90045600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:90045400-90045800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:90045600-90046000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:90045800-90046600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:90046000-90046200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:90046000-90046600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:90046000-90046600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr13:90046000-90046600	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr13:90046200-90046600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:90046200-90046600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr13:90046200-90047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:90046600-90052800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr13:90049200-90052800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr13:90052800-90053000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr13:90052800-90053000	Enhancers	Fetal Brain Male	brain
16	chr13:90052800-90053000	Enhancers	Gastric	stomach
17	chr13:90052800-90053200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr13:90052800-90053200	Enhancers	Muscle Satellite Cultured Cells	--
19	chr13:90052800-90053400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr13:90052800-90053400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:90052800-90054000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr13:90052800-90054000	Enhancers	Primary hematopoietic stem cells	blood
23	chr13:90052800-90054200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr13:90052800-90054200	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr13:90052800-90054200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr13:90052800-90054200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr13:90052800-90054600	Enhancers	Hela-S3	cervix
28	chr13:90053000-90053600	Weak transcription	Fetal Brain Male	brain
29	chr13:90053000-90053800	Weak transcription	Gastric	stomach
30	chr13:90053000-90054200	Enhancers	NHEK	skin
31	chr13:90053000-90059200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr13:90053200-90053400	Enhancers	A549	lung
33	chr13:90053200-90053400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr13:90053200-90053600	Enhancers	Adipose Nuclei	Adipose
35	chr13:90053200-90054000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr13:90053200-90054000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr13:90053400-90053600	Enhancers	Liver	Liver
38	chr13:90053400-90053800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:90053400-90053800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr13:90053400-90053800	Flanking Active TSS	A549	lung
41	chr13:90053400-90054000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr13:90053400-90054000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr13:90053400-90054000	Enhancers	HUVEC	blood vessel
44	chr13:90053400-90054000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr13:90053600-90054000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr13:90053600-90054000	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr13:90053600-90054000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr13:90053600-90054000	Flanking Active TSS	Adipose Nuclei	Adipose
49	chr13:90053600-90054000	Flanking Active TSS	Liver	Liver
50	chr13:90053600-90054000	Enhancers	Fetal Brain Male	brain

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