Variant report

Variant	esv2753866
Chromosome Location	chr13:87260025-87495281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:461)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:87271580-87271813	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr13:87381487-87381725	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr13:87442738-87442952	A549	lung:	n/a	chr13:87442822-87442833
4	CEBPB	chr13:87442694-87442975	HepG2	liver:	n/a	chr13:87442822-87442833
5	CEBPB	chr13:87271522-87271871	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:87271554-87271822	A549	lung:	n/a	n/a
7	CEBPB	chr13:87337420-87337599	HepG2	liver:	n/a	chr13:87337465-87337476
8	CEBPB	chr13:87264131-87264347	HepG2	liver:	n/a	chr13:87264220-87264231
9	CEBPB	chr13:87438052-87438302	HepG2	liver:	n/a	n/a
10	CEBPB	chr13:87438070-87438276	A549	lung:	n/a	n/a
11	CEBPB	chr13:87438092-87438193	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:87475314-87475565	A549	lung:	n/a	chr13:87475414-87475425
13	CEBPB	chr13:87339861-87340160	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:87464869-87465069	IMR90	lung:	n/a	n/a
15	CEBPB	chr13:87325979-87326785	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:87464946-87465050	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:87304795-87305033	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:87409455-87409760	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr13:87271328-87271828	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:87482236-87482598	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:87475265-87475574	HepG2	liver:	n/a	chr13:87475414-87475425
22	CEBPB	chr13:87337405-87337619	Hela-S3	cervix:	n/a	chr13:87337465-87337476
23	CEBPB	chr13:87475251-87475602	IMR90	lung:	n/a	chr13:87475414-87475425
24	CEBPB	chr13:87395927-87396145	H1-hESC	embryonic stem cell:	n/a	chr13:87396008-87396019
25	CEBPB	chr13:87469814-87470097	HepG2	liver:	n/a	chr13:87469948-87469959
26	CEBPB	chr13:87395881-87396169	HepG2	liver:	n/a	chr13:87396008-87396019
27	CEBPB	chr13:87433605-87433805	HepG2	liver:	n/a	chr13:87433727-87433738
28	CHD2	chr13:87409528-87409776	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:87383694-87383698	MCF-7	breast:	n/a	n/a
30	CTCF	chr13:87482460-87482610	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr13:87394136-87394317	Hela-S3	cervix:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
32	CTCF	chr13:87377480-87377630	AG04450	lung:	n/a	n/a
33	CTCF	chr13:87394160-87394310	HRE	kidney:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
34	CTCF	chr13:87377520-87377670	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr13:87394080-87394230	HRPEpiC	eye:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
36	CTCF	chr13:87394100-87394250	AG09319	gingival:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
37	CTCF	chr13:87394180-87394330	SK-N-SH_RA	brain:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
38	CTCF	chr13:87278703-87278765	GM10266	blood:	n/a	n/a
39	CTCF	chr13:87280251-87280292	GM20000	blood:	n/a	n/a
40	CTCF	chr13:87444463-87444586	K562	blood:	n/a	n/a
41	CTCF	chr13:87377483-87377625	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr13:87394160-87394310	HCPEpiC	choroid plexus:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
43	CTCF	chr13:87394040-87394190	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr13:87261164-87261346	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr13:87482480-87482630	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr13:87394100-87394250	BE2_C	brain:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
47	CTCF	chr13:87394160-87394310	HepG2	liver:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
48	CTCF	chr13:87377540-87377690	HPF	lung:	n/a	n/a
49	CTCF	chr13:87261133-87261340	Medullo	brain:	n/a	n/a
50	CTCF	chr13:87377460-87377610	RPTEC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:87444712-87444762	HCF	heart:	n/a
2	chr13:87444696-87444746	HUVEC	blood vessel:	n/a
3	chr13:87444696-87444746	HAEpiC	amniotic membrane:	n/a
4	chr13:87444712-87444762	SK-N-MC	brain:	n/a
5	chr13:87444696-87444746	NHBE	bronchial:	n/a
6	chr13:87444712-87444762	T-47D	breast:	n/a
7	chr13:87444712-87444762	PrEC	prostate:	n/a
8	chr13:87444696-87444746	HRPEpiC	eye:	n/a
9	chr13:87444712-87444762	HRCEpiC	kidney:	n/a
10	chr13:87444712-87444762	ECC-1	luminal epithelium:	n/a
11	chr13:87444712-87444762	BE2_C	brain:	n/a
12	chr13:87444712-87444762	ovcar-3	ovarian:	n/a
13	chr13:87444696-87444746	H1-hESC	embryonic stem cell:	embryo
14	chr13:87444712-87444762	AG04450	lung:	fetal
15	chr13:87444696-87444746	HCF	heart:	n/a
16	chr13:87444712-87444762	HCT-116	colon:	n/a
17	chr13:87444712-87444762	SAEC	small airway:	n/a
18	chr13:87444696-87444746	T-47D	breast:	n/a
19	chr13:87444696-87444746	AoSMC	blood vessel:	n/a
20	chr13:87444696-87444746	NT2-D1	testis:	n/a
21	chr13:87444712-87444762	U87	brain:	n/a
22	chr13:87444712-87444762	BJ	skin:	n/a
23	chr13:87444712-87444762	NHBE	bronchial:	n/a
24	chr13:87444696-87444746	GM06990	blood:	n/a
25	chr13:87444696-87444746	ProgFib	skin:	n/a
26	chr13:87444696-87444746	AG10803	skin:	n/a
27	chr13:87444712-87444762	HRPEpiC	eye:	n/a
28	chr13:87444696-87444746	HEK293	kidney:	embryo
29	chr13:87444712-87444762	IMR90	lung:	fetal
30	chr13:87444696-87444746	SKMC	muscle:	n/a
31	chr13:87444712-87444762	HRE	kidney:	n/a
32	chr13:87444712-87444762	HEK293	kidney:	embryo
33	chr13:87444696-87444746	AG04450	lung:	fetal
34	chr13:87444696-87444746	SAEC	small airway:	n/a
35	chr13:87444696-87444746	Hela-S3	cervix:	n/a
36	chr13:87444712-87444762	RPTEC	kidney:	n/a
37	chr13:87444696-87444746	HMEC	breast:	n/a
38	chr13:87444696-87444746	SK-N-SH	brain:	n/a
39	chr13:87444696-87444746	ovcar-3	ovarian:	n/a
40	chr13:87444696-87444746	NHDF-neo	bronchial:	n/a
41	chr13:87444696-87444746	NB4	blood:	n/a
42	chr13:87444696-87444746	HL-60	blood:	n/a
43	chr13:87444712-87444762	LNCaP	prostate:	n/a
44	chr13:87444712-87444762	ProgFib	skin:	n/a
45	chr13:87444696-87444746	HCM	heart:	n/a
46	chr13:87444712-87444762	MCF-7	breast:	n/a
47	chr13:87444696-87444746	U87	brain:	n/a
48	chr13:87444712-87444762	SK-N-SH	brain:	n/a
49	chr13:87444696-87444746	SK-N-MC	brain:	n/a
50	chr13:87444712-87444762	AG09319	gingival:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:87219118..87219726-chr13:87393723..87394529,2	MCF-7	breast:
2	chr11:3376919..3379551-chr13:87416799..87418315,2	K562	blood:
3	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:
4	chr13:87315449..87317669-chr13:87358524..87360044,2	K562	blood:
5	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:
6	chr13:87422380..87424249-chr13:87425366..87427570,2	K562	blood:
7	chr13:87315449..87317669-chr13:87358524..87360044,2	K562	blood:
8	chr13:87219074..87220049-chr13:87393792..87394360,2	MCF-7	breast:
9	chr13:87422380..87424249-chr13:87425366..87427570,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-19	chr13:87377755-87378308	NONHSAT034580

No data

Variant related genes	Relation type
TXNL1P1	TF binding region
TXNL1P1	CpG island

Extended variants
information (count: 2397 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2397 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9588793	chr13:87275200-87275201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs557832251	chr13:87275206-87275207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576387975	chr13:87275281-87275282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs73551444	chr13:87275309-87275310	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181368011	chr13:87275310-87275311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534576975	chr13:87275314-87275315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574681043	chr13:87275315-87275316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542072729	chr13:87275319-87275320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560377414	chr13:87275330-87275331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577644585	chr13:87275336-87275337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185251287	chr13:87275363-87275364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190008869	chr13:87275378-87275379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113664940	chr13:87275413-87275414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116400314	chr13:87275433-87275434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531217850	chr13:87275444-87275445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142776265	chr13:87275450-87275451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2996414	chr13:87275471-87275472	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs183359361	chr13:87275478-87275479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529426915	chr13:87275514-87275515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187910303	chr13:87275550-87275551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191286275	chr13:87276417-87276418	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs537425285	chr13:87276440-87276441	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs184545834	chr13:87276489-87276490	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576065595	chr13:87276498-87276499	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374877151	chr13:87276501-87276502	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs534764623	chr13:87276532-87276533	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs190692896	chr13:87276536-87276537	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs181538230	chr13:87276586-87276587	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs572140071	chr13:87276593-87276594	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539668507	chr13:87276614-87276615	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs557748068	chr13:87276622-87276623	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs575966120	chr13:87276640-87276641	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs576174739	chr13:87276658-87276659	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369235003	chr13:87276674-87276675	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs2987537	chr13:87276688-87276689	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185196039	chr13:87276697-87276698	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs540759984	chr13:87276716-87276717	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs559444760	chr13:87276767-87276768	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs182373038	chr13:87285603-87285604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568894142	chr13:87285616-87285617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs74505327	chr13:87285652-87285653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568663432	chr13:87285684-87285685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7318164	chr13:87285713-87285714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567058371	chr13:87285731-87285732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569202002	chr13:87285750-87285751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534210708	chr13:87285784-87285785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187183717	chr13:87285785-87285786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576804013	chr13:87285791-87285792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191659692	chr13:87285823-87285824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556533722	chr13:87285855-87285856	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
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
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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87275200-87275600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:87276400-87276600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:87276600-87276800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr13:87285600-87286000	Enhancers	Fetal Heart	heart
5	chr13:87285600-87286800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr13:87286800-87287600	Enhancers	Adipose Nuclei	Adipose
7	chr13:87316200-87316400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr13:87326400-87326800	Enhancers	Hela-S3	cervix
9	chr13:87333600-87333800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:87336600-87336800	Enhancers	NH-A	brain
11	chr13:87337200-87337800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr13:87339600-87340000	Enhancers	Fetal Lung	lung
13	chr13:87340000-87341800	Weak transcription	Fetal Lung	lung
14	chr13:87341800-87342200	Enhancers	Fetal Lung	lung
15	chr13:87347600-87349800	Enhancers	Adipose Nuclei	Adipose
16	chr13:87363200-87363600	Enhancers	Fetal Brain Female	brain
17	chr13:87363400-87363800	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr13:87366000-87368200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:87374200-87375000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr13:87403200-87403600	Enhancers	Gastric	stomach
21	chr13:87409200-87409800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr13:87409200-87410000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr13:87409200-87411200	Enhancers	HMEC	breast
24	chr13:87409400-87409800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr13:87409400-87410000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr13:87409400-87410000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr13:87409600-87410000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr13:87409600-87410400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:87409800-87411400	Active TSS	Primary T cells fromperipheralblood	blood
30	chr13:87409800-87411400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
31	chr13:87409800-87416800	Active TSS	Fetal Thymus	thymus
32	chr13:87416800-87417000	Flanking Active TSS	Fetal Thymus	thymus
33	chr13:87417000-87417200	Active TSS	Fetal Thymus	thymus
34	chr13:87417200-87417800	Flanking Active TSS	Fetal Thymus	thymus
35	chr13:87417800-87418400	Active TSS	Fetal Thymus	thymus
36	chr13:87418000-87418200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr13:87439800-87442600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr13:87440200-87441200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr13:87440400-87441200	Enhancers	Brain Angular Gyrus	brain
40	chr13:87440600-87441200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr13:87440800-87441200	Enhancers	Brain Anterior Caudate	brain
42	chr13:87440800-87441200	Enhancers	Brain Substantia Nigra	brain
43	chr13:87441200-87441800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:87441200-87444400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr13:87441800-87442000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr13:87443800-87444400	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr13:87444000-87444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr13:87444400-87444600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr13:87444400-87444600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr13:87450200-87450600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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