Variant report

Variant	nsv1044185
Chromosome Location	chr13:87949735-88096644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:248)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:248 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:88082864-88082918	K562	blood:	n/a	n/a
2	BHLHE40	chr13:88096440-88096715	GM12878	blood:	n/a	n/a
3	CEBPB	chr13:87983468-87983781	MCF-7	breast:	n/a	n/a
4	CEBPB	chr13:87983437-87983890	MCF-7	breast:	n/a	n/a
5	CEBPB	chr13:87983347-87983899	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr13:87983437-87983881	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr13:88078861-88079143	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:88094236-88094497	K562	blood:	n/a	chr13:88094372-88094383
9	CEBPB	chr13:87983456-87983815	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr13:87983487-87983786	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:87999921-87999953	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:88094207-88094561	HepG2	liver:	n/a	chr13:88094372-88094383
13	CTCF	chr13:88050482-88050517	HepG2	liver:	n/a	n/a
14	CTCF	chr13:88050460-88050610	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr13:88057280-88057430	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:88050400-88050550	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr13:88033720-88033870	NB4	blood:	n/a	n/a
18	CTCF	chr13:87972937-87972965	GM10266	blood:	n/a	n/a
19	CTCF	chr13:88050469-88050532	Medullo	brain:	n/a	n/a
20	CTCF	chr13:88057250-88057450	GM12878	blood:	n/a	n/a
21	CTCF	chr13:88050408-88050589	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr13:88020044-88020116	GM20000	blood:	n/a	n/a
23	CTCF	chr13:87985320-87985470	GM12866	blood:	n/a	n/a
24	CTCF	chr13:88050400-88050550	RPTEC	kidney:	n/a	n/a
25	CTCF	chr13:88048420-88048570	GM12867	blood:	n/a	n/a
26	CTCF	chr13:88009128-88009197	GM20000	blood:	n/a	n/a
27	CTCF	chr13:88050360-88050510	RPTEC	kidney:	n/a	n/a
28	CTCF	chr13:88050356-88050608	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:88050400-88050550	HAc	cerebellar:	n/a	n/a
30	CTCF	chr13:88008420-88008570	HEK293	kidney:	n/a	n/a
31	CTCF	chr13:87965840-87965990	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr13:88018772-88018811	GM20000	blood:	n/a	n/a
33	CTCF	chr13:87964080-87964230	SAEC	small airway:	n/a	n/a
34	CTCF	chr13:87964486-87964518	GM20000	blood:	n/a	n/a
35	CTCF	chr13:87964060-87964210	HMEC	breast:	n/a	n/a
36	CTCF	chr13:88050456-88050519	Hela-S3	cervix:	n/a	n/a
37	E2F4	chr13:88007944-88008057	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr13:87962654-87962704	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr13:88092929-88093361	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr13:88022788-88022988	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr13:88060491-88060691	MCF10A-Er-Src	breast:	n/a	n/a
42	EBF1	chr13:88096403-88096631	GM12878	blood:	n/a	n/a
43	ELK1	chr13:87964102-87964163	Hela-S3	cervix:	n/a	n/a
44	ELK4	chr13:87981035-87981108	HEK293	kidney:	n/a	n/a
45	EP300	chr13:88044835-88044852	GM12878	blood:	n/a	n/a
46	EP300	chr13:87983379-87983946	ECC-1	luminal epithelium:	n/a	n/a
47	EP300	chr13:87979114-87979180	GM12878	blood:	n/a	n/a
48	ESR1	chr13:87983444-87983778	ECC-1	luminal epithelium:	n/a	n/a
49	ESR1	chr13:87983394-87983788	ECC-1	luminal epithelium:	n/a	n/a
50	FOS	chr13:87983505-87983762	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88078884-88078934	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:88078884-88078934	MCF-7	breast:	n/a
3	chr13:88078884-88078934	ECC-1	luminal epithelium:	n/a
4	chr13:88078884-88078934	HUVEC	blood vessel:	n/a
5	chr13:88078884-88078934	CMK	blood:	n/a
6	chr13:88078884-88078934	HRCEpiC	kidney:	n/a
7	chr13:88078884-88078934	SK-N-MC	brain:	n/a
8	chr13:88078884-88078934	GM12891	blood:	n/a
9	chr13:88078884-88078934	HCT-116	colon:	n/a
10	chr13:88078884-88078934	HEK293	kidney:	embryo
11	chr13:88078884-88078934	U87	brain:	n/a
12	chr13:88078884-88078934	HepG2	liver:	n/a
13	chr13:88078884-88078934	AoSMC	blood vessel:	n/a
14	chr13:88078884-88078934	LNCaP	prostate:	n/a
15	chr13:88078884-88078934	HCM	heart:	n/a
16	chr13:88078884-88078934	AG09319	gingival:	n/a
17	chr13:88078884-88078934	HRE	kidney:	n/a
18	chr13:88078884-88078934	T-47D	breast:	n/a
19	chr13:88078884-88078934	Caco-2	colon:	n/a
20	chr13:88078884-88078934	Hela-S3	cervix:	n/a
21	chr13:88078884-88078934	GM06990	blood:	n/a
22	chr13:88078884-88078934	ovcar-3	ovarian:	n/a
23	chr13:88078884-88078934	AG10803	skin:	n/a
24	chr13:88078884-88078934	HL-60	blood:	n/a
25	chr13:88078884-88078934	AG04450	lung:	fetal
26	chr13:88078884-88078934	HIPEpiC	eye:	n/a
27	chr13:88078884-88078934	SK-N-SH_RA	brain:	n/a
28	chr13:88078884-88078934	GM12878	blood:	n/a
29	chr13:88078884-88078934	HEEpiC	esophagus:	n/a
30	chr13:88078884-88078934	ProgFib	skin:	n/a
31	chr13:88078884-88078934	Jurkat	blood:	n/a
32	chr13:88078884-88078934	HRPEpiC	eye:	n/a
33	chr13:88078884-88078934	BE2_C	brain:	n/a
34	chr13:88078884-88078934	MCF10A-Er-Src	breast:	n/a
35	chr13:88078884-88078934	AG09309	skin:	n/a
36	chr13:88078884-88078934	SKMC	muscle:	n/a
37	chr13:88078884-88078934	SK-N-SH	brain:	n/a
38	chr13:88078884-88078934	NH-A	brain:	n/a
39	chr13:88078884-88078934	Hepatocyte	liver:	n/a
40	chr13:88078884-88078934	AG04449	skin:	fetal
41	chr13:88078884-88078934	PrEC	prostate:	n/a
42	chr13:88078884-88078934	RPTEC	kidney:	n/a
43	chr13:88078884-88078934	PFSK-1	brain:	n/a
44	chr13:88078884-88078934	NHBE	bronchial:	n/a
45	chr13:88078884-88078934	PANC-1	pancreas:	n/a
46	chr13:88078884-88078934	HAEpiC	amniotic membrane:	n/a
47	chr13:88078884-88078934	H1-hESC	embryonic stem cell:	embryo
48	chr13:88078884-88078934	HNPCEpiC	eye:	n/a
49	chr13:88078884-88078934	SAEC	small airway:	n/a
50	chr13:88078884-88078934	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:87944988..87946530-chr13:87947239..87950149,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-8	chr13:88079469-88079802	XLOC_010682
2	lnc-SLITRK6-9	chr13:88079469-88079802	ENSG00000228824.2
3	lnc-SLITRK5-14	chr13:87995599-87995765	NONHSAT034585
4	lnc-SLITRK6-9	chr13:88096247-88097385	ENSG00000228824
5	lnc-SLITRK6-9	chr13:88096242-88097385	XLOC_010683
6	lnc-SLITRK5-14	chr13:87992541-87992680	NONHSAT034585
7	lnc-SLITRK5-14	chr13:87992158-87992228	NONHSAT034584
8	lnc-SLITRK5-14	chr13:87991120-87991699	NONHSAT034584
9	lnc-SLITRK6-9	chr13:88079455-88079802	ENSG00000232636.2
10	lnc-SLITRK5-14	chr13:87992526-87992762	NONHSAT034584
11	lnc-SLITRK6-8	chr13:88080353-88080528	XLOC_010682
12	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000232636.2
13	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000228824.2

No data

Variant related genes	Relation type
LIN28AP2	TF binding region
LIN28AP2	CpG island
DENR	miRNA target sites

Extended variants
information (count: 2800 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2800 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111969591	chr13:87982227-87982228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547918705	chr13:87982248-87982249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567151861	chr13:87982262-87982263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527996697	chr13:87982321-87982322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370689574	chr13:87982360-87982361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117715288	chr13:87982375-87982376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575046847	chr13:87982376-87982377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371918349	chr13:87982383-87982384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540475855	chr13:87982396-87982397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28406865	chr13:87982413-87982414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs66470505	chr13:87982423-87982424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9516799	chr13:87982440-87982441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376026221	chr13:87982442-87982443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111953930	chr13:87982463-87982464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58973296	chr13:87982469-87982470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373627788	chr13:87982470-87982471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571074640	chr13:87982501-87982502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538311714	chr13:87982503-87982504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370482253	chr13:87982506-87982507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112685311	chr13:87982525-87982526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572386234	chr13:87982547-87982548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568493464	chr13:87982619-87982620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574781559	chr13:87982622-87982623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78365407	chr13:87982690-87982691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs66882955	chr13:87982707-87982708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs540145794	chr13:87982799-87982800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558295706	chr13:87982841-87982842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148236922	chr13:87982844-87982845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544113632	chr13:87982855-87982856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376934265	chr13:87982873-87982874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140279731	chr13:87982890-87982891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564224440	chr13:87982947-87982948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529799627	chr13:87982964-87982965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563916885	chr13:87983025-87983026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559905178	chr13:87983031-87983032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374172965	chr13:87983086-87983087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527958847	chr13:87983140-87983141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552923740	chr13:87983158-87983159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571187621	chr13:87983164-87983165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531923447	chr13:87983169-87983170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529395210	chr13:87983172-87983173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs376076628	chr13:87983218-87983219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575891099	chr13:87983273-87983274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543226385	chr13:87983277-87983278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568535722	chr13:87983298-87983299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386773065	chr13:87983309-87983310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535579276	chr13:87983414-87983415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74824989	chr13:87983442-87983443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565751533	chr13:87983449-87983450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368944270	chr13:87983454-87983455	Enhancers Weak transcription	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
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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87982200-87998600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:87983200-87984000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:87983200-87984200	Enhancers	Liver	Liver
4	chr13:87983400-87983800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:87983400-87983800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:87983400-87983800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr13:87983400-87983800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr13:87983400-87983800	Enhancers	NHEK	skin
9	chr13:87983400-87984600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr13:87984200-87985000	Weak transcription	Liver	Liver
11	chr13:87985000-87985200	Enhancers	Liver	Liver
12	chr13:87985200-87986200	Weak transcription	Liver	Liver
13	chr13:87986200-87987000	Active TSS	Liver	Liver
14	chr13:87987800-87989200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr13:87993400-87993800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:87993800-88005800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr13:87996200-87996800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr13:87996400-87996800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr13:87996400-87997000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr13:87996600-87997000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:87996600-87997000	Enhancers	HMEC	breast
22	chr13:87996600-87997200	Enhancers	NHEK	skin
23	chr13:87996800-88005600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr13:87997200-87997800	Weak transcription	NHEK	skin
25	chr13:87997800-87998000	Enhancers	NHEK	skin
26	chr13:87998600-87999000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr13:87999000-88012600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr13:88005600-88006200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr13:88008600-88009000	Enhancers	NHEK	skin
30	chr13:88010800-88011400	Enhancers	Fetal Brain Female	brain
31	chr13:88012600-88013800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:88013800-88014400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:88014400-88015200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:88015200-88025000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:88020600-88021200	Active TSS	Hela-S3	cervix
36	chr13:88025000-88026200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:88026200-88038800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:88038400-88039200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr13:88056200-88056800	Enhancers	Liver	Liver
40	chr13:88059400-88060000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
41	chr13:88060000-88062000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr13:88078400-88079600	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr13:88078800-88080000	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr13:88079000-88079400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:88079000-88079400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr13:88079000-88079800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr13:88079000-88081000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr13:88079200-88080000	Enhancers	HUES6 Cell Line	embryonic stem cell

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