Variant report

Variant	nsv900816
Chromosome Location	chr13:89224649-89392881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 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	ATF2	chr13:89303755-89304204	GM12878	blood:	n/a	n/a
2	BACH1	chr13:89374937-89374956	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:89238320-89238777	H1-hESC	embryonic stem cell:	n/a	chr13:89238690-89238704
4	BATF	chr13:89303772-89304165	GM12878	blood:	n/a	n/a
5	BCL11A	chr13:89303805-89304131	GM12878	blood:	n/a	n/a
6	BCL11A	chr13:89303786-89304101	GM12878	blood:	n/a	n/a
7	BCL3	chr13:89303833-89304185	GM12878	blood:	n/a	n/a
8	BRCA1	chr13:89356772-89357287	Hela-S3	cervix:	n/a	chr13:89357177-89357184
9	BRCA1	chr13:89280576-89280681	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr13:89290214-89290571	Hela-S3	cervix:	n/a	chr13:89290390-89290401
11	CEBPB	chr13:89290188-89290577	HepG2	liver:	n/a	chr13:89290390-89290401
12	CEBPB	chr13:89290206-89290537	H1-hESC	embryonic stem cell:	n/a	chr13:89290390-89290401
13	CEBPB	chr13:89290248-89290542	A549	lung:	n/a	chr13:89290390-89290401
14	CEBPB	chr13:89324303-89324385	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:89290236-89290580	K562	blood:	n/a	chr13:89290390-89290401
16	CEBPB	chr13:89243021-89243158	H1-hESC	embryonic stem cell:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
17	CEBPB	chr13:89370798-89370883	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr13:89282509-89282768	HepG2	liver:	n/a	chr13:89282641-89282652
19	CEBPB	chr13:89270759-89270935	HepG2	liver:	n/a	chr13:89270795-89270806
20	CEBPB	chr13:89290092-89290576	IMR90	lung:	n/a	chr13:89290390-89290401
21	CEBPB	chr13:89242865-89243152	IMR90	lung:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
22	CEBPB	chr13:89242893-89243153	K562	blood:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
23	CEBPB	chr13:89242868-89243214	HepG2	liver:	n/a	chr13:89243024-89243037 chr13:89243024-89243035 chr13:89243067-89243080
24	CEBPB	chr13:89353798-89354236	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:89311459-89311525	K562	blood:	n/a	n/a
26	CEBPB	chr13:89289215-89289541	HepG2	liver:	n/a	n/a
27	CHD2	chr13:89302228-89302309	GM12878	blood:	n/a	n/a
28	CHD2	chr13:89303867-89304192	GM12878	blood:	n/a	n/a
29	CHD2	chr13:89378638-89378699	HepG2	liver:	n/a	n/a
30	CTCF	chr13:89224967-89225021	GM20000	blood:	n/a	n/a
31	CTCF	chr13:89348009-89348071	GM13976	blood:	n/a	n/a
32	CTCF	chr13:89298500-89298650	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr13:89244136-89244220	GM20000	blood:	n/a	n/a
34	CTCF	chr13:89298480-89298630	WERI-Rb-1	eye:	n/a	n/a
35	CTCF	chr13:89338329-89338400	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr13:89298580-89298730	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr13:89298440-89298590	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr13:89298600-89298750	GM12872	blood:	n/a	n/a
39	CTCF	chr13:89298580-89298730	GM12865	blood:	n/a	n/a
40	CTCF	chr13:89298540-89298690	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr13:89298600-89298750	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr13:89298580-89298730	NB4	blood:	n/a	n/a
43	CTCF	chr13:89298560-89298710	BE2_C	brain:	n/a	n/a
44	CTCF	chr13:89347107-89347146	GM10248	blood:	n/a	n/a
45	CTCF	chr13:89247400-89247550	GM12869	blood:	n/a	n/a
46	CTCF	chr13:89323950-89324028	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr13:89298520-89298670	HPF	lung:	n/a	n/a
48	CTCF	chr13:89313590-89313651	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr13:89298520-89298670	HEK293	kidney:	n/a	n/a
50	CTCF	chr13:89298600-89298750	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89370229-89370279	HepG2	liver:	n/a
2	chr13:89370422-89370472	NHDF-neo	bronchial:	n/a
3	chr13:89370107-89370157	SK-N-MC	brain:	n/a
4	chr13:89370422-89370472	RPTEC	kidney:	n/a
5	chr13:89370107-89370157	PrEC	prostate:	n/a
6	chr13:89370229-89370279	GM19239	blood:	n/a
7	chr13:89370107-89370157	HUVEC	blood vessel:	n/a
8	chr13:89370422-89370472	HPAEpiC	pulmonary alveolar:	n/a
9	chr13:89370422-89370472	IMR90	lung:	fetal
10	chr13:89370107-89370157	ECC-1	luminal epithelium:	n/a
11	chr13:89370229-89370279	HEK293	kidney:	embryo
12	chr13:89370229-89370279	A549	lung:	n/a
13	chr13:89370229-89370279	HCPEpiC	choroid plexus:	n/a
14	chr13:89370107-89370157	SAEC	small airway:	n/a
15	chr13:89370422-89370472	HEK293	kidney:	embryo
16	chr13:89370107-89370157	HAEpiC	amniotic membrane:	n/a
17	chr13:89370229-89370279	HCF	heart:	n/a
18	chr13:89370229-89370279	GM12891	blood:	n/a
19	chr13:89370107-89370157	HRCEpiC	kidney:	n/a
20	chr13:89370422-89370472	HCM	heart:	n/a
21	chr13:89370229-89370279	AG09319	gingival:	n/a
22	chr13:89370422-89370472	SK-N-SH	brain:	n/a
23	chr13:89370107-89370157	CMK	blood:	n/a
24	chr13:89370107-89370157	HIPEpiC	eye:	n/a
25	chr13:89370229-89370279	HRCEpiC	kidney:	n/a
26	chr13:89370422-89370472	GM12878	blood:	n/a
27	chr13:89370229-89370279	PrEC	prostate:	n/a
28	chr13:89370422-89370472	AG09319	gingival:	n/a
29	chr13:89370107-89370157	A549	lung:	n/a
30	chr13:89370229-89370279	SK-N-SH_RA	brain:	n/a
31	chr13:89370107-89370157	T-47D	breast:	n/a
32	chr13:89370229-89370279	NHDF-neo	bronchial:	n/a
33	chr13:89370422-89370472	NT2-D1	testis:	n/a
34	chr13:89370422-89370472	HUVEC	blood vessel:	n/a
35	chr13:89370422-89370472	HRPEpiC	eye:	n/a
36	chr13:89370229-89370279	ProgFib	skin:	n/a
37	chr13:89370229-89370279	HUVEC	blood vessel:	n/a
38	chr13:89370422-89370472	GM06990	blood:	n/a
39	chr13:89370107-89370157	HCF	heart:	n/a
40	chr13:89370422-89370472	HCF	heart:	n/a
41	chr13:89370107-89370157	GM12891	blood:	n/a
42	chr13:89370422-89370472	HEEpiC	esophagus:	n/a
43	chr13:89370422-89370472	HepG2	liver:	n/a
44	chr13:89370422-89370472	K562	blood:	n/a
45	chr13:89370422-89370472	MCF-7	breast:	n/a
46	chr13:89370229-89370279	Caco-2	colon:	n/a
47	chr13:89370107-89370157	HEK293	kidney:	embryo
48	chr13:89370229-89370279	Hepatocyte	liver:	n/a
49	chr13:89370229-89370279	NHBE	bronchial:	n/a
50	chr13:89370107-89370157	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:89369839..89371609-chr13:89377639..89379655,2	K562	blood:
2	chr13:89369839..89371609-chr13:89377639..89379655,2	K562	blood:
3	chr13:89273831..89276576-chr13:89278587..89280292,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-8	chr13:89282351-89282651	ENSG00000261666.1
2	lnc-SLITRK5-8	chr13:89279107-89280404	ENSG00000261666.1
3	lnc-SLITRK5-7	chr13:89279107-89279587	NONHSAT034614
4	lnc-SLITRK5-7	chr13:89324069-89324311	NONHSAT034614

No data

Variant related genes	Relation type
LINC00560	TF binding region
LINC00560	CpG island
ENSG00000261666	chromatin interactions

Extended variants
information (count: 2151 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2151 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9587857	chr13:89224649-89224650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565230894	chr13:89224651-89224652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs386773138	chr13:89224674-89224675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544461579	chr13:89224675-89224676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1334183	chr13:89224678-89224679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs548435662	chr13:89224689-89224690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143634644	chr13:89224714-89224715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147215960	chr13:89224738-89224739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185240419	chr13:89224768-89224769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1360712	chr13:89224785-89224786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544383598	chr13:89224813-89224814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80046503	chr13:89224870-89224871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568604401	chr13:89224871-89224872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145849471	chr13:89224883-89224884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58599542	chr13:89224887-89224888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556572427	chr13:89224975-89224976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576057085	chr13:89224997-89224998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535806515	chr13:89225023-89225024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189563545	chr13:89225048-89225049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556107150	chr13:89225093-89225094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181894277	chr13:89225132-89225133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561171958	chr13:89225187-89225188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1334182	chr13:89225203-89225204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377509134	chr13:89225236-89225237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs9521351	chr13:89225265-89225266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs554062198	chr13:89225276-89225277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187085324	chr13:89225352-89225353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9521352	chr13:89225353-89225354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs369051595	chr13:89225388-89225389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559041448	chr13:89225408-89225409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577243339	chr13:89225411-89225412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559904546	chr13:89225413-89225414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528113373	chr13:89225450-89225451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544662752	chr13:89225461-89225462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562952276	chr13:89225532-89225533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79382744	chr13:89225541-89225542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542167138	chr13:89225575-89225576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149343943	chr13:89225607-89225608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59457121	chr13:89225623-89225624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551866558	chr13:89225661-89225662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372034828	chr13:89225696-89225697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144695531	chr13:89225721-89225722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9587858	chr13:89225793-89225794	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12583174	chr13:89225816-89225817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs568263641	chr13:89225830-89225831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535641943	chr13:89225848-89225849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554148405	chr13:89226008-89226009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531325392	chr13:89226017-89226018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537173150	chr13:89226029-89226030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs17545883	chr13:89226063-89226064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89221600-89233000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:89233000-89233200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:89237600-89238000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr13:89237600-89238800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr13:89237600-89238800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr13:89238000-89238200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:89238200-89238400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr13:89238200-89238600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr13:89238400-89238600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr13:89238600-89238800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:89244200-89244800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:89244400-89244600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr13:89247000-89247400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr13:89252400-89253000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr13:89255000-89255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:89255000-89255400	Enhancers	Esophagus	oesophagus
17	chr13:89255000-89256400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr13:89255200-89256000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:89255400-89256400	Enhancers	NHEK	skin
20	chr13:89267800-89268800	Enhancers	Pancreatic Islets	Pancreatic Islet
21	chr13:89268800-89270000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr13:89270200-89270400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr13:89271400-89274400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr13:89273800-89276000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr13:89274000-89276400	Enhancers	Primary T cells from cord blood	blood
26	chr13:89274400-89274600	Active TSS	Primary T helper naive cells from peripheral blood	blood
27	chr13:89274400-89274800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr13:89274400-89275000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr13:89274400-89275600	Enhancers	NHEK	skin
30	chr13:89274400-89275800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:89274600-89274800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
32	chr13:89274600-89274800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr13:89274600-89275000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr13:89274600-89275200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr13:89274800-89275000	Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr13:89274800-89275200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr13:89274800-89275200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr13:89274800-89276000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr13:89275000-89276600	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr13:89275200-89275600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr13:89275200-89277200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr13:89275600-89276200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr13:89275600-89278600	Weak transcription	NHEK	skin
44	chr13:89276400-89276600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr13:89276600-89277200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr13:89277200-89277400	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr13:89277400-89278600	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr13:89278600-89280000	Enhancers	NHEK	skin
49	chr13:89280200-89281200	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr13:89281200-89281400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--

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