Variant report

Variant	nsv900820
Chromosome Location	chr13:89302824-89686507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:798)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:798 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	ATF2	chr13:89572186-89572643	GM12878	blood:	n/a	n/a
3	ATF2	chr13:89572207-89572528	GM12878	blood:	n/a	n/a
4	BACH1	chr13:89623437-89623444	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:89374937-89374956	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr13:89572277-89572559	GM12878	blood:	n/a	n/a
7	BATF	chr13:89303772-89304165	GM12878	blood:	n/a	n/a
8	BATF	chr13:89561544-89561732	GM12878	blood:	n/a	n/a
9	BATF	chr13:89458729-89458985	GM12878	blood:	n/a	chr13:89458885-89458896
10	BATF	chr13:89572273-89572568	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:89303805-89304131	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:89572223-89572570	GM12878	blood:	n/a	n/a
13	BCL11A	chr13:89303786-89304101	GM12878	blood:	n/a	n/a
14	BCL3	chr13:89303833-89304185	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:89632073-89632317	GM12878	blood:	n/a	n/a
16	BHLHE40	chr13:89643606-89643700	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:89572310-89572510	GM12878	blood:	n/a	n/a
18	BRCA1	chr13:89356772-89357287	Hela-S3	cervix:	n/a	chr13:89357177-89357184
19	CEBPB	chr13:89598063-89598417	A549	lung:	n/a	chr13:89598238-89598249
20	CEBPB	chr13:89598071-89598408	K562	blood:	n/a	chr13:89598238-89598249
21	CEBPB	chr13:89630955-89631172	K562	blood:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
22	CEBPB	chr13:89434392-89434646	HepG2	liver:	n/a	chr13:89434512-89434525 chr13:89434512-89434525 chr13:89434512-89434525 chr13:89434512-89434523 chr13:89434514-89434525
23	CEBPB	chr13:89400880-89401075	A549	lung:	n/a	n/a
24	CEBPB	chr13:89598032-89598441	A549	lung:	n/a	chr13:89598238-89598249
25	CEBPB	chr13:89324303-89324385	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr13:89353798-89354236	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr13:89630930-89631228	H1-hESC	embryonic stem cell:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
28	CEBPB	chr13:89596083-89596253	HepG2	liver:	n/a	chr13:89596117-89596128 chr13:89596118-89596129
29	CEBPB	chr13:89509521-89509939	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:89539359-89539639	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:89630916-89631254	A549	lung:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
32	CEBPB	chr13:89490303-89490550	Hela-S3	cervix:	n/a	chr13:89490429-89490440
33	CEBPB	chr13:89598055-89598434	IMR90	lung:	n/a	chr13:89598238-89598249
34	CEBPB	chr13:89490284-89490572	HepG2	liver:	n/a	chr13:89490429-89490440
35	CEBPB	chr13:89598062-89598430	HepG2	liver:	n/a	chr13:89598238-89598249
36	CEBPB	chr13:89490320-89490562	A549	lung:	n/a	chr13:89490429-89490440
37	CEBPB	chr13:89598060-89598453	ECC-1	luminal epithelium:	n/a	chr13:89598238-89598249
38	CEBPB	chr13:89444187-89444374	HepG2	liver:	n/a	chr13:89444226-89444237 chr13:89444225-89444236
39	CEBPB	chr13:89508592-89508825	HepG2	liver:	n/a	n/a
40	CEBPB	chr13:89598067-89598413	Hela-S3	cervix:	n/a	chr13:89598238-89598249
41	CEBPB	chr13:89598017-89598337	ECC-1	luminal epithelium:	n/a	chr13:89598238-89598249
42	CEBPB	chr13:89370798-89370883	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr13:89490297-89490552	IMR90	lung:	n/a	chr13:89490429-89490440
44	CEBPB	chr13:89630896-89631259	IMR90	lung:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
45	CEBPB	chr13:89630897-89631243	HepG2	liver:	n/a	chr13:89631078-89631089 chr13:89631076-89631093
46	CEBPB	chr13:89311459-89311525	K562	blood:	n/a	n/a
47	CEBPB	chr13:89431756-89431994	IMR90	lung:	n/a	n/a
48	CEBPB	chr13:89598062-89598418	H1-hESC	embryonic stem cell:	n/a	chr13:89598238-89598249
49	CHD2	chr13:89557803-89557932	GM12878	blood:	n/a	n/a
50	CHD2	chr13:89572254-89572531	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89370107-89370157	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:89370422-89370472	RPTEC	kidney:	n/a
3	chr13:89370107-89370157	NT2-D1	testis:	n/a
4	chr13:89370107-89370157	PANC-1	pancreas:	n/a
5	chr13:89370422-89370472	PANC-1	pancreas:	n/a
6	chr13:89370229-89370279	HL-60	blood:	n/a
7	chr13:89370229-89370279	HCPEpiC	choroid plexus:	n/a
8	chr13:89370107-89370157	SKMC	muscle:	n/a
9	chr13:89370422-89370472	HAEpiC	amniotic membrane:	n/a
10	chr13:89370229-89370279	GM12878	blood:	n/a
11	chr13:89370107-89370157	K562	blood:	n/a
12	chr13:89370422-89370472	HL-60	blood:	n/a
13	chr13:89370422-89370472	AG10803	skin:	n/a
14	chr13:89370422-89370472	NB4	blood:	n/a
15	chr13:89370229-89370279	ProgFib	skin:	n/a
16	chr13:89370422-89370472	PrEC	prostate:	n/a
17	chr13:89370422-89370472	AG09309	skin:	n/a
18	chr13:89370229-89370279	GM12892	blood:	n/a
19	chr13:89370422-89370472	SK-N-MC	brain:	n/a
20	chr13:89370107-89370157	SK-N-SH_RA	brain:	n/a
21	chr13:89370107-89370157	H1-hESC	embryonic stem cell:	embryo
22	chr13:89370107-89370157	HAEpiC	amniotic membrane:	n/a
23	chr13:89370107-89370157	SK-N-SH	brain:	n/a
24	chr13:89370229-89370279	NH-A	brain:	n/a
25	chr13:89370229-89370279	PFSK-1	brain:	n/a
26	chr13:89370229-89370279	NB4	blood:	n/a
27	chr13:89370229-89370279	GM06990	blood:	n/a
28	chr13:89370422-89370472	BE2_C	brain:	n/a
29	chr13:89370229-89370279	AoSMC	blood vessel:	n/a
30	chr13:89370422-89370472	Caco-2	colon:	n/a
31	chr13:89370107-89370157	U87	brain:	n/a
32	chr13:89370422-89370472	HEK293	kidney:	embryo
33	chr13:89370107-89370157	HUVEC	blood vessel:	n/a
34	chr13:89370107-89370157	ProgFib	skin:	n/a
35	chr13:89370229-89370279	Jurkat	blood:	n/a
36	chr13:89370422-89370472	ECC-1	luminal epithelium:	n/a
37	chr13:89370107-89370157	HepG2	liver:	n/a
38	chr13:89370229-89370279	LNCaP	prostate:	n/a
39	chr13:89370107-89370157	PrEC	prostate:	n/a
40	chr13:89370107-89370157	BE2_C	brain:	n/a
41	chr13:89370107-89370157	HCPEpiC	choroid plexus:	n/a
42	chr13:89370107-89370157	AG10803	skin:	n/a
43	chr13:89370107-89370157	AoSMC	blood vessel:	n/a
44	chr13:89370229-89370279	HMEC	breast:	n/a
45	chr13:89370422-89370472	NT2-D1	testis:	n/a
46	chr13:89370229-89370279	AG09309	skin:	n/a
47	chr13:89370422-89370472	HRE	kidney:	n/a
48	chr13:89370422-89370472	GM12878	blood:	n/a
49	chr13:89370107-89370157	AG09309	skin:	n/a
50	chr13:89370107-89370157	MCF10A-Er-Src	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:89446778..89447282-chr20:52691355..52691999,2	MCF-7	breast:
2	chr13:89528545..89531167-chr13:91999570..92001170,2	K562	blood:
3	chr13:89369839..89371609-chr13:89377639..89379655,2	K562	blood:
4	chr13:89369839..89371609-chr13:89377639..89379655,2	K562	blood:
5	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:
6	chr13:89606576..89609218-chr13:89612592..89614304,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-22	chr13:89630701-89631039	NONHSAT034619
2	lnc-SLITRK6-23	chr13:89633752-89633831	l_898_chr13:89627586-89633831_testes
3	lnc-SLITRK6-21	chr13:89556163-89556457	l_897_chr13:89556162-89558584_testes
4	lnc-SLITRK5-7	chr13:89324069-89324311	NONHSAT034614
5	lnc-SLITRK6-21	chr13:89558109-89558584	l_897_chr13:89556162-89558584_testes
6	lnc-SLITRK6-23	chr13:89627871-89627986	l_898_chr13:89627586-89633831_testes
7	lnc-SLITRK6-23	chr13:89627587-89627859	l_898_chr13:89627586-89633831_testes

No data

Variant related genes	Relation type
GRPEL2P1	TF binding region
GRPEL2P1	CpG island
ENSG00000215417	chromatin interactions

Extended variants
information (count: 3342 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3342 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187113832	chr13:89307811-89307812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192697743	chr13:89307845-89307846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150043519	chr13:89307931-89307932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183021846	chr13:89307958-89307959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563671058	chr13:89307961-89307962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530910344	chr13:89307996-89307997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs17628712	chr13:89308835-89308836	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs374863492	chr13:89308872-89308873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537588892	chr13:89308917-89308918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536244664	chr13:89308918-89308919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548010809	chr13:89308972-89308973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1326444	chr13:89308999-89309000	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141309897	chr13:89309007-89309008	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs557479686	chr13:89309009-89309010	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs570269868	chr13:89309024-89309025	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs537787972	chr13:89309032-89309033	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs556419106	chr13:89309033-89309034	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs575577857	chr13:89309054-89309055	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs114835465	chr13:89309138-89309139	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs372112020	chr13:89309154-89309155	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs7993257	chr13:89309155-89309156	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs573397140	chr13:89309197-89309198	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs9583475	chr13:89309210-89309211	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs565489558	chr13:89309227-89309228	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs532745954	chr13:89309231-89309232	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs544627373	chr13:89309247-89309248	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563177567	chr13:89309254-89309255	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs529693439	chr13:89309285-89309286	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs548187964	chr13:89309290-89309291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566082384	chr13:89309343-89309344	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs527393159	chr13:89309350-89309351	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs74840510	chr13:89309356-89309357	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs112219724	chr13:89309363-89309364	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs570359254	chr13:89309475-89309476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538021869	chr13:89309477-89309478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556219206	chr13:89309483-89309484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186096861	chr13:89309505-89309506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189054786	chr13:89309548-89309549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181916016	chr13:89309592-89309593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs80245370	chr13:89309599-89309600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs17628718	chr13:89309600-89309601	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs35772222	chr13:89324082-89324083	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs181071758	chr13:89324120-89324121	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs186051721	chr13:89324160-89324161	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs191994840	chr13:89324200-89324201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs541141182	chr13:89324247-89324248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs564200830	chr13:89324249-89324250	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370873499	chr13:89324250-89324251	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs113244257	chr13:89324254-89324255	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs185960746	chr13:89324258-89324259	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Osteosarcoma	21215367	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Burkitt''s lymphoma	19759907	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89307800-89308000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr13:89308800-89309000	Enhancers	Hela-S3	cervix
3	chr13:89309000-89309400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr13:89309000-89309400	Flanking Active TSS	Hela-S3	cervix
5	chr13:89309400-89309600	Enhancers	Hela-S3	cervix
6	chr13:89344400-89344600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:89344600-89345800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr13:89345800-89346400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:89346200-89346600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:89346400-89351200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr13:89351200-89351400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:89351400-89357000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:89353400-89353800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:89353800-89354200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr13:89353800-89354200	Enhancers	Hela-S3	cervix
16	chr13:89354200-89354400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr13:89354200-89355600	Weak transcription	Hela-S3	cervix
18	chr13:89354400-89356200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr13:89355600-89355800	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr13:89355600-89356200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr13:89355600-89356200	Enhancers	Hela-S3	cervix
22	chr13:89355600-89357000	Enhancers	Primary hematopoietic stem cells	blood
23	chr13:89355800-89356400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr13:89356200-89356400	Enhancers	Stomach Mucosa	stomach
25	chr13:89356200-89357000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr13:89356200-89357200	Active TSS	Hela-S3	cervix
27	chr13:89356200-89357400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr13:89356200-89357400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr13:89356400-89356600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr13:89356400-89356600	Enhancers	Fetal Intestine Small	intestine
31	chr13:89356400-89356600	Enhancers	NHEK	skin
32	chr13:89356400-89356800	Flanking Active TSS	Stomach Mucosa	stomach
33	chr13:89356400-89357000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr13:89356400-89357200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:89356400-89357200	Active TSS	Duodenum Mucosa	Duodenum
36	chr13:89356400-89357200	Active TSS	Right Atrium	heart
37	chr13:89356400-89357200	Active TSS	Monocytes-CD14+_RO01746	blood
38	chr13:89356400-89357400	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr13:89356400-89357400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr13:89356400-89357400	Active TSS	Adipose Nuclei	Adipose
41	chr13:89356400-89357400	Active TSS	Fetal Lung	lung
42	chr13:89356400-89357400	Active TSS	Fetal Stomach	stomach
43	chr13:89356600-89356800	Enhancers	Fetal Heart	heart
44	chr13:89356600-89357000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr13:89356600-89357000	Active TSS	Fetal Intestine Small	intestine
46	chr13:89356600-89357000	Active TSS	Placenta	Placenta
47	chr13:89356600-89357000	Active TSS	Rectal Mucosa Donor 29	rectum
48	chr13:89356600-89357000	Active TSS	Rectal Mucosa Donor 31	rectum
49	chr13:89356600-89357000	Flanking Active TSS	NHEK	skin
50	chr13:89356600-89357200	Active TSS	Duodenum Smooth Muscle	Duodenum

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