Variant report

Variant	nsv562624
Chromosome Location	chr13:87304859-87496155
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:393)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:393 , 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	CEBPB	chr13:87395881-87396169	HepG2	liver:	n/a	chr13:87396008-87396019
2	CEBPB	chr13:87438070-87438276	A549	lung:	n/a	n/a
3	CEBPB	chr13:87475251-87475602	IMR90	lung:	n/a	chr13:87475414-87475425
4	CEBPB	chr13:87482236-87482598	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr13:87381487-87381725	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr13:87442694-87442975	HepG2	liver:	n/a	chr13:87442822-87442833
7	CEBPB	chr13:87337405-87337619	Hela-S3	cervix:	n/a	chr13:87337465-87337476
8	CEBPB	chr13:87475265-87475574	HepG2	liver:	n/a	chr13:87475414-87475425
9	CEBPB	chr13:87442738-87442952	A549	lung:	n/a	chr13:87442822-87442833
10	CEBPB	chr13:87337420-87337599	HepG2	liver:	n/a	chr13:87337465-87337476
11	CEBPB	chr13:87409455-87409760	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:87469814-87470097	HepG2	liver:	n/a	chr13:87469948-87469959
13	CEBPB	chr13:87304795-87305033	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:87438052-87438302	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:87464946-87465050	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:87325979-87326785	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr13:87395927-87396145	H1-hESC	embryonic stem cell:	n/a	chr13:87396008-87396019
18	CEBPB	chr13:87438092-87438193	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr13:87464869-87465069	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:87339861-87340160	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:87433605-87433805	HepG2	liver:	n/a	chr13:87433727-87433738
22	CEBPB	chr13:87475314-87475565	A549	lung:	n/a	chr13:87475414-87475425
23	CHD2	chr13:87409528-87409776	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr13:87377531-87377611	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:87377480-87377630	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr13:87394120-87394270	HAc	cerebellar:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
27	CTCF	chr13:87377500-87377650	AG09319	gingival:	n/a	n/a
28	CTCF	chr13:87394136-87394317	Hela-S3	cervix:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
29	CTCF	chr13:87377358-87377761	SK-N-SH	brain:	n/a	n/a
30	CTCF	chr13:87394040-87394190	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr13:87377459-87377625	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr13:87377440-87377590	HAc	cerebellar:	n/a	n/a
33	CTCF	chr13:87394120-87394270	BE2_C	brain:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
34	CTCF	chr13:87377549-87377600	GM12891	blood:	n/a	n/a
35	CTCF	chr13:87444287-87444567	K562	blood:	n/a	n/a
36	CTCF	chr13:87444420-87444570	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr13:87394172-87394292	MCF-7	breast:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
38	CTCF	chr13:87394160-87394310	HCPEpiC	choroid plexus:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
39	CTCF	chr13:87377345-87377645	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr13:87431508-87431537	Lung_OC	lung:	n/a	n/a
41	CTCF	chr13:87377460-87377610	RPTEC	kidney:	n/a	n/a
42	CTCF	chr13:87377459-87377648	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr13:87377480-87377630	BE2_C	brain:	n/a	n/a
44	CTCF	chr13:87383694-87383698	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:87394080-87394230	Caco-2	colon:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
46	CTCF	chr13:87394140-87394290	HRPEpiC	eye:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
47	CTCF	chr13:87377500-87377617	HepG2	liver:	n/a	n/a
48	CTCF	chr13:87394080-87394230	HRPEpiC	eye:	n/a	chr13:87394206-87394222 chr13:87394200-87394221
49	CTCF	chr13:87377483-87377625	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr13:87377480-87377630	HCPEpiC	choroid plexus:	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	AG04449	skin:	fetal
2	chr13:87444712-87444762	ovcar-3	ovarian:	n/a
3	chr13:87444696-87444746	LNCaP	prostate:	n/a
4	chr13:87444696-87444746	SK-N-MC	brain:	n/a
5	chr13:87444712-87444762	HMEC	breast:	n/a
6	chr13:87444712-87444762	T-47D	breast:	n/a
7	chr13:87444696-87444746	AG10803	skin:	n/a
8	chr13:87444712-87444762	ProgFib	skin:	n/a
9	chr13:87444696-87444746	H1-hESC	embryonic stem cell:	embryo
10	chr13:87444696-87444746	AG09319	gingival:	n/a
11	chr13:87444712-87444762	U87	brain:	n/a
12	chr13:87444712-87444762	AG04450	lung:	fetal
13	chr13:87444712-87444762	AG10803	skin:	n/a
14	chr13:87444712-87444762	RPTEC	kidney:	n/a
15	chr13:87444696-87444746	GM12891	blood:	n/a
16	chr13:87444696-87444746	ovcar-3	ovarian:	n/a
17	chr13:87444696-87444746	Hepatocyte	liver:	n/a
18	chr13:87444712-87444762	Jurkat	blood:	n/a
19	chr13:87444712-87444762	GM12892	blood:	n/a
20	chr13:87444712-87444762	NHDF-neo	bronchial:	n/a
21	chr13:87444712-87444762	Caco-2	colon:	n/a
22	chr13:87444712-87444762	HCM	heart:	n/a
23	chr13:87444696-87444746	Jurkat	blood:	n/a
24	chr13:87444696-87444746	RPTEC	kidney:	n/a
25	chr13:87444696-87444746	GM19239	blood:	n/a
26	chr13:87444696-87444746	ECC-1	luminal epithelium:	n/a
27	chr13:87444696-87444746	HCM	heart:	n/a
28	chr13:87444712-87444762	MCF-7	breast:	n/a
29	chr13:87444712-87444762	A549	lung:	n/a
30	chr13:87444712-87444762	IMR90	lung:	fetal
31	chr13:87444696-87444746	GM06990	blood:	n/a
32	chr13:87444696-87444746	MCF-7	breast:	n/a
33	chr13:87444696-87444746	NHDF-neo	bronchial:	n/a
34	chr13:87444696-87444746	BJ	skin:	n/a
35	chr13:87444712-87444762	GM06990	blood:	n/a
36	chr13:87444696-87444746	AG09309	skin:	n/a
37	chr13:87444712-87444762	NB4	blood:	n/a
38	chr13:87444712-87444762	HEK293	kidney:	embryo
39	chr13:87444696-87444746	SK-N-SH_RA	brain:	n/a
40	chr13:87444696-87444746	T-47D	breast:	n/a
41	chr13:87444696-87444746	BE2_C	brain:	n/a
42	chr13:87444712-87444762	Hepatocyte	liver:	n/a
43	chr13:87444712-87444762	HepG2	liver:	n/a
44	chr13:87444712-87444762	BJ	skin:	n/a
45	chr13:87444712-87444762	CMK	blood:	n/a
46	chr13:87444696-87444746	PrEC	prostate:	n/a
47	chr13:87444696-87444746	HUVEC	blood vessel:	n/a
48	chr13:87444696-87444746	CMK	blood:	n/a
49	chr13:87444696-87444746	HepG2	liver:	n/a
50	chr13:87444712-87444762	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:
2	chr13:87315449..87317669-chr13:87358524..87360044,2	K562	blood:
3	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:
4	chr13:87219118..87219726-chr13:87393723..87394529,2	MCF-7	breast:
5	chr13:87219074..87220049-chr13:87393792..87394360,2	MCF-7	breast:
6	chr11:3376919..3379551-chr13:87416799..87418315,2	K562	blood:
7	chr13:87315449..87317669-chr13:87358524..87360044,2	K562	blood:
8	chr13:87422380..87424249-chr13:87425366..87427570,2	K562	blood:
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: 2312 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138052460	chr13:87316229-87316230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532201277	chr13:87316234-87316235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532853359	chr13:87316242-87316243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370608363	chr13:87316245-87316246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188463873	chr13:87316253-87316254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550329771	chr13:87316292-87316293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568871833	chr13:87316293-87316294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562926431	chr13:87316316-87316317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76815382	chr13:87316317-87316318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548739360	chr13:87316381-87316382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566978722	chr13:87316393-87316394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536300887	chr13:87326496-87326497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570629392	chr13:87326531-87326532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs13378384	chr13:87326538-87326539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2996395	chr13:87326574-87326575	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375899380	chr13:87326727-87326728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543461240	chr13:87326743-87326744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188917601	chr13:87326764-87326765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573717149	chr13:87326799-87326800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542245873	chr13:87333607-87333608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551399416	chr13:87333611-87333612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533391485	chr13:87333638-87333639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144096911	chr13:87333644-87333645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531080776	chr13:87333650-87333651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76233711	chr13:87333705-87333706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200832890	chr13:87333712-87333713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150572737	chr13:87333781-87333782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140746773	chr13:87333787-87333788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535294671	chr13:87333794-87333795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375414649	chr13:87333795-87333796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377518320	chr13:87333796-87333797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs35612245	chr13:87333797-87333798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568186826	chr13:87336606-87336607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs118094872	chr13:87336628-87336629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs550375676	chr13:87336637-87336638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535853969	chr13:87336658-87336659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530215546	chr13:87336690-87336691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370708285	chr13:87336715-87336716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187594495	chr13:87336716-87336717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556050987	chr13:87336718-87336719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558802057	chr13:87337235-87337236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564857760	chr13:87337290-87337291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576728892	chr13:87337310-87337311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544228234	chr13:87337317-87337318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562420337	chr13:87337368-87337369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529845519	chr13:87337378-87337379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530742152	chr13:87337379-87337380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs202162246	chr13:87337380-87337381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374540766	chr13:87337381-87337382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61546883	chr13:87337397-87337398	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
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
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87316200-87316400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:87326400-87326800	Enhancers	Hela-S3	cervix
3	chr13:87333600-87333800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:87336600-87336800	Enhancers	NH-A	brain
5	chr13:87337200-87337800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr13:87339600-87340000	Enhancers	Fetal Lung	lung
7	chr13:87340000-87341800	Weak transcription	Fetal Lung	lung
8	chr13:87341800-87342200	Enhancers	Fetal Lung	lung
9	chr13:87347600-87349800	Enhancers	Adipose Nuclei	Adipose
10	chr13:87363200-87363600	Enhancers	Fetal Brain Female	brain
11	chr13:87363400-87363800	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr13:87366000-87368200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:87374200-87375000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr13:87403200-87403600	Enhancers	Gastric	stomach
15	chr13:87409200-87409800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr13:87409200-87410000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:87409200-87411200	Enhancers	HMEC	breast
18	chr13:87409400-87409800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr13:87409400-87410000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr13:87409400-87410000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr13:87409600-87410000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr13:87409600-87410400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr13:87409800-87411400	Active TSS	Primary T cells fromperipheralblood	blood
24	chr13:87409800-87411400	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
25	chr13:87409800-87416800	Active TSS	Fetal Thymus	thymus
26	chr13:87416800-87417000	Flanking Active TSS	Fetal Thymus	thymus
27	chr13:87417000-87417200	Active TSS	Fetal Thymus	thymus
28	chr13:87417200-87417800	Flanking Active TSS	Fetal Thymus	thymus
29	chr13:87417800-87418400	Active TSS	Fetal Thymus	thymus
30	chr13:87418000-87418200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr13:87439800-87442600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr13:87440200-87441200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr13:87440400-87441200	Enhancers	Brain Angular Gyrus	brain
34	chr13:87440600-87441200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr13:87440800-87441200	Enhancers	Brain Anterior Caudate	brain
36	chr13:87440800-87441200	Enhancers	Brain Substantia Nigra	brain
37	chr13:87441200-87441800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr13:87441200-87444400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr13:87441800-87442000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr13:87443800-87444400	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr13:87444000-87444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr13:87444400-87444600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr13:87444400-87444600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr13:87450200-87450600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:87450200-87450600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:87452600-87453200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:87455200-87455600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:87456600-87478400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr13:87462200-87463400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:87462200-87463400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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