Variant report

Variant	nsv524753
Chromosome Location	chr13:85864299-86073007
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	ARID3A	chr13:85947684-85947808	HepG2	liver:	n/a	n/a
2	BACH1	chr13:85979800-85979802	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:86009114-86009355	H1-hESC	embryonic stem cell:	n/a	chr13:86009260-86009274
4	BHLHE40	chr13:85933207-85933215	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:86006029-86006048	HepG2	liver:	n/a	n/a
6	BRCA1	chr13:86071289-86072157	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr13:86071751-86072088	A549	lung:	n/a	chr13:86071803-86071820
8	CEBPB	chr13:85987849-85988094	K562	blood:	n/a	chr13:85987993-85988002 chr13:85987981-85987994 chr13:85987992-85988003 chr13:85987927-85987939 chr13:85987991-85988004 chr13:85987981-85987994 chr13:85987981-85987992 chr13:85987991-85988004 chr13:85987991-85988002
9	CEBPB	chr13:85892817-85892995	HepG2	liver:	n/a	chr13:85892866-85892877
10	CEBPB	chr13:86065693-86066048	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:86068032-86068227	A549	lung:	n/a	chr13:86068112-86068123
12	CEBPB	chr13:86071834-86072084	A549	lung:	n/a	n/a
13	CEBPB	chr13:85990647-85990745	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:85987819-85988159	IMR90	lung:	n/a	chr13:85987993-85988002 chr13:85987981-85987994 chr13:85987992-85988003 chr13:85987927-85987939 chr13:85987991-85988004 chr13:85987981-85987994 chr13:85987981-85987992 chr13:85987991-85988004 chr13:85987991-85988002
15	CEBPB	chr13:85927994-85928181	HepG2	liver:	n/a	chr13:85928083-85928092 chr13:85928083-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928094 chr13:85928083-85928092 chr13:85928081-85928092 chr13:85928083-85928094
16	CEBPB	chr13:85903432-85903667	HepG2	liver:	n/a	chr13:85903579-85903590
17	CEBPB	chr13:86001587-86001888	Hela-S3	cervix:	n/a	chr13:86001689-86001700
18	CEBPB	chr13:85869191-85869393	HepG2	liver:	n/a	chr13:85869291-85869302 chr13:85869289-85869300 chr13:85869289-85869302
19	CEBPB	chr13:86016773-86017097	HepG2	liver:	n/a	chr13:86016932-86016943
20	CEBPB	chr13:86016811-86017108	A549	lung:	n/a	chr13:86016932-86016943
21	CEBPB	chr13:85987825-85988157	A549	lung:	n/a	chr13:85987993-85988002 chr13:85987981-85987994 chr13:85987992-85988003 chr13:85987927-85987939 chr13:85987991-85988004 chr13:85987981-85987994 chr13:85987981-85987992 chr13:85987991-85988004 chr13:85987991-85988002
22	CEBPB	chr13:86068041-86068241	HepG2	liver:	n/a	chr13:86068112-86068123
23	CEBPB	chr13:86065660-86066004	IMR90	lung:	n/a	n/a
24	CEBPB	chr13:86016776-86017041	ECC-1	luminal epithelium:	n/a	chr13:86016932-86016943
25	CEBPB	chr13:86070409-86070726	IMR90	lung:	n/a	chr13:86070551-86070562
26	CEBPB	chr13:86070422-86070699	HepG2	liver:	n/a	chr13:86070551-86070562
27	CEBPB	chr13:86070408-86070724	A549	lung:	n/a	chr13:86070551-86070562
28	CEBPB	chr13:86016784-86017068	Hela-S3	cervix:	n/a	chr13:86016932-86016943
29	CEBPB	chr13:85987837-85988166	HepG2	liver:	n/a	chr13:85987993-85988002 chr13:85987981-85987994 chr13:85987992-85988003 chr13:85987927-85987939 chr13:85987991-85988004 chr13:85987981-85987994 chr13:85987981-85987992 chr13:85987991-85988004 chr13:85987991-85988002
30	CEBPB	chr13:85987836-85988170	Hela-S3	cervix:	n/a	chr13:85987993-85988002 chr13:85987981-85987994 chr13:85987992-85988003 chr13:85987927-85987939 chr13:85987991-85988004 chr13:85987981-85987994 chr13:85987981-85987992 chr13:85987991-85988004 chr13:85987991-85988002
31	CEBPB	chr13:85866108-85866245	HepG2	liver:	n/a	chr13:85866196-85866207
32	CEBPB	chr13:86071555-86072281	IMR90	lung:	n/a	chr13:86071803-86071820
33	CEBPB	chr13:86071389-86072263	Hela-S3	cervix:	n/a	chr13:86071803-86071820
34	CHD1	chr13:86071368-86072297	IMR90	lung:	n/a	n/a
35	CHD2	chr13:86071829-86072117	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr13:85972195-85972227	GM20000	blood:	n/a	n/a
37	CTCF	chr13:86004820-86004849	Gliobla	brain:	n/a	n/a
38	CTCF	chr13:86064060-86064210	AG04450	lung:	n/a	n/a
39	CTCF	chr13:85900947-85900982	Lung_OC	lung:	n/a	n/a
40	CTCF	chr13:85994620-85994770	HRE	kidney:	n/a	n/a
41	CTCF	chr13:86064814-86064861	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr13:85952000-85952150	HMEC	breast:	n/a	n/a
43	CTCF	chr13:85939105-85939164	Gliobla	brain:	n/a	n/a
44	CTCF	chr13:86004760-86004910	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr13:85968803-85968858	LNCaP	prostate:	n/a	n/a
46	CTCF	chr13:86004554-86004600	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr13:85922000-85922150	AG10803	skin:	n/a	n/a
48	CTCF	chr13:86064040-86064190	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr13:86032264-86032350	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr13:85925115-85925144	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:85915140-85915190	SKMC	muscle:	n/a
2	chr13:85937926-85937976	HL-60	blood:	n/a
3	chr13:85937788-85937838	Hepatocyte	liver:	n/a
4	chr13:85915140-85915190	A549	lung:	n/a
5	chr13:85937926-85937976	NB4	blood:	n/a
6	chr13:85937788-85937838	GM19239	blood:	n/a
7	chr13:85937926-85937976	AG09309	skin:	n/a
8	chr13:85937957-85938007	GM06990	blood:	n/a
9	chr13:85937788-85937838	NHDF-neo	bronchial:	n/a
10	chr13:85915140-85915190	AG04450	lung:	fetal
11	chr13:85937730-85937780	HL-60	blood:	n/a
12	chr13:85937518-85937568	ECC-1	luminal epithelium:	n/a
13	chr13:85937957-85938007	NHBE	bronchial:	n/a
14	chr13:85937788-85937838	GM12878	blood:	n/a
15	chr13:85937957-85938007	GM12891	blood:	n/a
16	chr13:85937518-85937568	BE2_C	brain:	n/a
17	chr13:85937730-85937780	SK-N-MC	brain:	n/a
18	chr13:85937730-85937780	CMK	blood:	n/a
19	chr13:85937518-85937568	NT2-D1	testis:	n/a
20	chr13:85937730-85937780	HCF	heart:	n/a
21	chr13:85937861-85937911	PFSK-1	brain:	n/a
22	chr13:85937788-85937838	K562	blood:	n/a
23	chr13:85937788-85937838	AoSMC	blood vessel:	n/a
24	chr13:85937926-85937976	ovcar-3	ovarian:	n/a
25	chr13:85915140-85915190	HPAEpiC	pulmonary alveolar:	n/a
26	chr13:85937518-85937568	GM12892	blood:	n/a
27	chr13:85937861-85937911	AG04449	skin:	fetal
28	chr13:85937861-85937911	RPTEC	kidney:	n/a
29	chr13:85937730-85937780	HNPCEpiC	eye:	n/a
30	chr13:85937518-85937568	GM19239	blood:	n/a
31	chr13:85937730-85937780	HMEC	breast:	n/a
32	chr13:85937788-85937838	HEK293	kidney:	embryo
33	chr13:85937957-85938007	K562	blood:	n/a
34	chr13:85915140-85915190	HAEpiC	amniotic membrane:	n/a
35	chr13:85937926-85937976	MCF-7	breast:	n/a
36	chr13:85937861-85937911	SK-N-SH	brain:	n/a
37	chr13:85937957-85938007	HMEC	breast:	n/a
38	chr13:85937957-85938007	PrEC	prostate:	n/a
39	chr13:85937957-85938007	ovcar-3	ovarian:	n/a
40	chr13:85937861-85937911	HUVEC	blood vessel:	n/a
41	chr13:85937926-85937976	SKMC	muscle:	n/a
42	chr13:85937957-85938007	HL-60	blood:	n/a
43	chr13:85937518-85937568	HEEpiC	esophagus:	n/a
44	chr13:85937926-85937976	Hela-S3	cervix:	n/a
45	chr13:85937518-85937568	PFSK-1	brain:	n/a
46	chr13:85937926-85937976	PFSK-1	brain:	n/a
47	chr13:85915140-85915190	PrEC	prostate:	n/a
48	chr13:85937788-85937838	NT2-D1	testis:	n/a
49	chr13:85937957-85938007	HRCEpiC	kidney:	n/a
50	chr13:85937730-85937780	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:
2	chr13:85919914..85922732-chr13:85924658..85927029,2	K562	blood:
3	chr13:86033358..86036212-chr13:86039864..86042849,2	MCF-7	breast:
4	chr13:86012041..86014222-chr13:86015485..86017247,2	K562	blood:
5	chr13:86012041..86014222-chr13:86015485..86017247,2	K562	blood:
6	chr13:86033358..86036212-chr13:86039864..86042849,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-11	chr13:85937736-85938230	XLOC_010460
2	lnc-SLITRK5-11	chr13:85985736-85986331	XLOC_010460
3	lnc-SLITRK5-11	chr13:85937981-85938230	XLOC_010460
4	lnc-SLITRK5-11	chr13:85937736-85938230	ENSG00000226317.2
5	lnc-SLITRK5-11	chr13:85937738-85938230	NONHSAT034564
6	lnc-SLITRK5-11	chr13:85982740-85982882	XLOC_010460

Variant related genes	Relation type
LINC00351	TF binding region
LINC00351	CpG island
PDE3B	miRNA target sites
PDE4D	miRNA target sites

Extended variants
information (count: 2482 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2482 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186728394	chr13:85867614-85867615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140605657	chr13:85867618-85867619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556724786	chr13:85867634-85867635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs34301588	chr13:85867649-85867650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575175519	chr13:85867652-85867653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542384434	chr13:85867672-85867673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560632338	chr13:85867734-85867735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572566415	chr13:85867740-85867741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150480399	chr13:85867810-85867811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs113728023	chr13:85867819-85867820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375249918	chr13:85867821-85867822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368112160	chr13:85867826-85867827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571665794	chr13:85867886-85867887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142932627	chr13:85867890-85867891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553864116	chr13:85867891-85867892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548568774	chr13:85867911-85867912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566993233	chr13:85867922-85867923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148810811	chr13:85867957-85867958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527792991	chr13:85867975-85867976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552744274	chr13:85867979-85867980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534240875	chr13:85867981-85867982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1490097	chr13:85868600-85868601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs568754716	chr13:85868636-85868637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535702141	chr13:85868647-85868648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77832761	chr13:85868678-85868679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566120705	chr13:85868695-85868696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533686168	chr13:85868723-85868724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558598400	chr13:85868729-85868730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372883329	chr13:85868744-85868745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370882138	chr13:85868750-85868751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576831507	chr13:85868773-85868774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544417891	chr13:85868781-85868782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537593694	chr13:85868795-85868796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183919759	chr13:85868796-85868797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542138470	chr13:85868814-85868815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12430097	chr13:85868829-85868830	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs527666406	chr13:85868944-85868945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76049600	chr13:85868958-85868959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546351934	chr13:85868976-85868977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188469269	chr13:85868977-85868978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531681517	chr13:85868997-85868998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551296464	chr13:85872420-85872421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563488499	chr13:85872430-85872431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530762382	chr13:85872447-85872448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144372327	chr13:85872469-85872470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs74349557	chr13:85872506-85872507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567359452	chr13:85872542-85872543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560794860	chr13:85872546-85872547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534715554	chr13:85872585-85872586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9319133	chr13:85872609-85872610	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	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
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Congenital anomalies of the kidney and urinary tract	18316590	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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85867600-85868000	Enhancers	Fetal Lung	lung
2	chr13:85868600-85869000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:85872400-85873000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:85883600-85883800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr13:85883800-85887600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:85884200-85887600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr13:85885800-85887400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr13:85886200-85886400	Enhancers	Brain Substantia Nigra	brain
9	chr13:85887400-85887800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:85887400-85888200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr13:85887600-85888400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr13:85887600-85888400	Enhancers	HUVEC	blood vessel
13	chr13:85887600-85888600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr13:85887600-85888800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr13:85887600-85889000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:85887800-85888400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:85887800-85888400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr13:85887800-85888400	Enhancers	NHEK	skin
19	chr13:85888000-85888400	Enhancers	Brain Cingulate Gyrus	brain
20	chr13:85888000-85888400	Enhancers	Brain Substantia Nigra	brain
21	chr13:85888000-85888600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr13:85888000-85889200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:85888200-85888600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:85888200-85889200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr13:85888200-85889200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr13:85888400-85888800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr13:85888400-85890800	Weak transcription	HUVEC	blood vessel
28	chr13:85888600-85889000	Enhancers	Brain Substantia Nigra	brain
29	chr13:85888800-85889200	Enhancers	Brain Cingulate Gyrus	brain
30	chr13:85888800-85890600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr13:85889200-85890200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:85890400-85890600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:85890600-85891000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:85890600-85891000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr13:85890600-85891000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr13:85890800-85891200	Active TSS	Fetal Muscle Leg	muscle
37	chr13:85890800-85891200	Enhancers	HUVEC	blood vessel
38	chr13:85891000-85895400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr13:85895400-85895800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr13:85911800-85912000	Bivalent Enhancer	Liver	Liver
41	chr13:85915600-85915800	Enhancers	HSMM	muscle
42	chr13:85915600-85916000	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr13:85931200-85933600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr13:85940400-85940600	Enhancers	NH-A	brain
45	chr13:85940600-85941600	Weak transcription	NH-A	brain
46	chr13:85940800-85942600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr13:85941000-85941800	Enhancers	A549	lung
48	chr13:85941400-85943000	Enhancers	Dnd41	blood
49	chr13:85941600-85942000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr13:85941600-85942400	Enhancers	NH-A	brain

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