Variant report

Variant	nsv900937
Chromosome Location	chr13:96976345-97275932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:366)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:468 , 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	ARID3A	chr13:97234582-97234671	K562	blood:	n/a	n/a
2	ATF1	chr13:97069847-97069922	K562	blood:	n/a	n/a
3	BACH1	chr13:97128010-97128209	H1-hESC	embryonic stem cell:	n/a	chr13:97128034-97128048
4	BATF	chr13:97061873-97062103	GM12878	blood:	n/a	n/a
5	BATF	chr13:97153302-97153519	GM12878	blood:	n/a	n/a
6	BATF	chr13:97153304-97153567	GM12878	blood:	n/a	n/a
7	BATF	chr13:97184568-97184814	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:97153318-97153519	GM12878	blood:	n/a	n/a
9	BRCA1	chr13:97209846-97209922	HepG2	liver:	n/a	n/a
10	BRCA1	chr13:97131098-97131110	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr13:97090469-97090702	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:96978011-96978121	K562	blood:	n/a	chr13:96978062-96978075 chr13:96978063-96978074
13	CEBPB	chr13:97152045-97152255	Hela-S3	cervix:	n/a	chr13:97152063-97152074
14	CEBPB	chr13:97151965-97152207	H1-hESC	embryonic stem cell:	n/a	chr13:97152063-97152074
15	CEBPB	chr13:97136430-97136616	HepG2	liver:	n/a	chr13:97136479-97136490
16	CEBPB	chr13:97050204-97050372	K562	blood:	n/a	n/a
17	CEBPB	chr13:97225084-97225229	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:97101010-97101080	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:96978029-96978086	Hela-S3	cervix:	n/a	chr13:96978062-96978075 chr13:96978063-96978074
20	CEBPB	chr13:97126889-97127328	MCF-7	breast:	n/a	n/a
21	CEBPB	chr13:96977926-96978221	IMR90	lung:	n/a	chr13:96978062-96978075 chr13:96978063-96978074
22	CEBPB	chr13:97192184-97192315	HepG2	liver:	n/a	chr13:97192213-97192224
23	CEBPB	chr13:97207498-97207517	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr13:97151976-97152339	IMR90	lung:	n/a	chr13:97152063-97152074
25	CEBPB	chr13:97151884-97152329	A549	lung:	n/a	chr13:97152063-97152074
26	CEBPB	chr13:97001769-97001961	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:96977891-96978226	HepG2	liver:	n/a	chr13:96978062-96978075 chr13:96978063-96978074
28	CEBPB	chr13:97151893-97152407	HepG2	liver:	n/a	chr13:97152063-97152074
29	CEBPB	chr13:97203760-97203953	HepG2	liver:	n/a	chr13:97203879-97203890 chr13:97203881-97203892
30	CEBPB	chr13:97151914-97152340	K562	blood:	n/a	chr13:97152063-97152074
31	CTCF	chr13:97185740-97185890	BE2_C	brain:	n/a	n/a
32	CTCF	chr13:97064760-97064910	Caco-2	colon:	n/a	n/a
33	CTCF	chr13:97156520-97156670	BE2_C	brain:	n/a	n/a
34	CTCF	chr13:97179980-97180130	NHEK	skin:	n/a	n/a
35	CTCF	chr13:97204021-97204042	MCF-7	breast:	n/a	n/a
36	CTCF	chr13:97156520-97156670	HRE	kidney:	n/a	n/a
37	CTCF	chr13:97179947-97179989	NHEK	skin:	n/a	n/a
38	CTCF	chr13:97179900-97180050	NHEK	skin:	n/a	n/a
39	CTCF	chr13:97004147-97004210	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr13:97203990-97204063	MCF-7	breast:	n/a	n/a
41	CTCF	chr13:97200477-97200533	ProgFib	skin:	n/a	n/a
42	CTCF	chr13:97179820-97179970	HMEC	breast:	n/a	n/a
43	CTCF	chr13:97179900-97180050	BE2_C	brain:	n/a	n/a
44	CTCF	chr13:97179740-97179890	HCT-116	colon:	n/a	n/a
45	CTCF	chr13:97101467-97101497	Lung_OC	lung:	n/a	n/a
46	CTCF	chr13:97179925-97179963	HepG2	liver:	n/a	n/a
47	CTCF	chr13:97156320-97156470	GM12864	blood:	n/a	n/a
48	CTCF	chr13:97156460-97156610	GM12873	blood:	n/a	n/a
49	CTCF	chr13:97179800-97179950	MCF-7	breast:	n/a	n/a
50	CTCF	chr13:96998957-96999007	GM20000	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96984133-96984183	PrEC	prostate:	n/a
2	chr13:97107445-97107495	HAEpiC	amniotic membrane:	n/a
3	chr13:96984133-96984183	CMK	blood:	n/a
4	chr13:97126731-97126781	Caco-2	colon:	n/a
5	chr13:96984206-96984256	HNPCEpiC	eye:	n/a
6	chr13:97126731-97126781	ProgFib	skin:	n/a
7	chr13:97107445-97107495	NT2-D1	testis:	n/a
8	chr13:97065757-97065807	U87	brain:	n/a
9	chr13:97153748-97153798	AoSMC	blood vessel:	n/a
10	chr13:96984133-96984183	AoSMC	blood vessel:	n/a
11	chr13:97107445-97107495	HL-60	blood:	n/a
12	chr13:96984133-96984183	GM06990	blood:	n/a
13	chr13:97126731-97126781	K562	blood:	n/a
14	chr13:97107445-97107495	RPTEC	kidney:	n/a
15	chr13:97153748-97153798	GM12892	blood:	n/a
16	chr13:97126731-97126781	U87	brain:	n/a
17	chr13:97126731-97126781	ovcar-3	ovarian:	n/a
18	chr13:97126731-97126781	SKMC	muscle:	n/a
19	chr13:97107445-97107495	MCF-7	breast:	n/a
20	chr13:97126731-97126781	AG04449	skin:	fetal
21	chr13:97153748-97153798	GM19239	blood:	n/a
22	chr13:96984206-96984256	NHBE	bronchial:	n/a
23	chr13:96984206-96984256	HRCEpiC	kidney:	n/a
24	chr13:96984206-96984256	NT2-D1	testis:	n/a
25	chr13:97126731-97126781	HRPEpiC	eye:	n/a
26	chr13:97107445-97107495	GM06990	blood:	n/a
27	chr13:96984206-96984256	HCPEpiC	choroid plexus:	n/a
28	chr13:97065757-97065807	K562	blood:	n/a
29	chr13:97153748-97153798	SK-N-SH	brain:	n/a
30	chr13:97153748-97153798	HRPEpiC	eye:	n/a
31	chr13:97065757-97065807	Hepatocyte	liver:	n/a
32	chr13:97153748-97153798	AG04449	skin:	fetal
33	chr13:96984133-96984183	GM12892	blood:	n/a
34	chr13:97126731-97126781	AG04450	lung:	fetal
35	chr13:97126731-97126781	LNCaP	prostate:	n/a
36	chr13:97065757-97065807	T-47D	breast:	n/a
37	chr13:97153748-97153798	PANC-1	pancreas:	n/a
38	chr13:97153748-97153798	HCM	heart:	n/a
39	chr13:96984133-96984183	HAEpiC	amniotic membrane:	n/a
40	chr13:96984133-96984183	H1-hESC	embryonic stem cell:	embryo
41	chr13:96984206-96984256	AG04449	skin:	fetal
42	chr13:96984133-96984183	AG09319	gingival:	n/a
43	chr13:96984206-96984256	HAEpiC	amniotic membrane:	n/a
44	chr13:96984133-96984183	IMR90	lung:	fetal
45	chr13:97153748-97153798	LNCaP	prostate:	n/a
46	chr13:96984206-96984256	BE2_C	brain:	n/a
47	chr13:97107445-97107495	ovcar-3	ovarian:	n/a
48	chr13:97107445-97107495	HRE	kidney:	n/a
49	chr13:97153748-97153798	SAEC	small airway:	n/a
50	chr13:97126731-97126781	RPTEC	kidney:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:97123948..97125852-chr13:97129896..97131619,2	K562	blood:
2	chr13:97169094..97173338-chr13:97202267..97205317,4	MCF-7	breast:
3	chr13:97045257..97047343-chr13:97050874..97053623,2	MCF-7	breast:
4	chr13:97241737..97243330-chr13:97271160..97273681,2	MCF-7	breast:
5	chr13:97265116..97268425-chr13:97269725..97272716,3	K562	blood:
6	chr13:97047617..97050128-chr13:97056674..97059617,2	K562	blood:
7	chr13:97150259..97153204-chr13:97154134..97156231,2	K562	blood:
8	chr13:97171093..97173298-chr13:97369679..97371227,2	MCF-7	breast:
9	chr13:97124837..97125524-chr14:96449119..96449841,2	MCF-7	breast:
10	chr13:97130348..97132078-chr13:97148789..97150424,2	MCF-7	breast:
11	chr13:97263515..97266118-chr13:97267550..97269207,2	K562	blood:
12	chr13:97169094..97173338-chr13:97202267..97205317,4	MCF-7	breast:
13	chr13:97130348..97132078-chr13:97148789..97150424,2	MCF-7	breast:
14	chr1:121485222..121485724-chr13:97251489..97252005,2	MCF-7	breast:
15	chr13:97123948..97125852-chr13:97129896..97131619,2	K562	blood:
16	chr13:97045257..97047343-chr13:97050874..97053623,2	MCF-7	breast:
17	chr13:97127272..97129084-chr13:97157433..97159683,2	MCF-7	breast:
18	chr13:97047617..97050128-chr13:97056674..97059617,2	K562	blood:
19	chr13:97263515..97266118-chr13:97267550..97269207,2	K562	blood:
20	chr13:97127272..97129084-chr13:97157433..97159683,2	MCF-7	breast:
21	chr13:97241737..97243330-chr13:97271160..97273681,2	MCF-7	breast:
22	chr13:97150259..97153204-chr13:97154134..97156231,2	K562	blood:
23	chr13:96705085..96707362-chr13:97040004..97041510,2	MCF-7	breast:
24	chr13:97265116..97268425-chr13:97269725..97272716,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGGT2-4	chr13:97128046-97128218	NONHSAT034785
2	lnc-UGGT2-4	chr13:97125266-97125784	NONHSAT034785
3	lnc-DNAJC3-4	chr13:96991437-96991547	l_903_chr13:96989763-96999042_testes
4	lnc-DNAJC3-4	chr13:96998816-96999042	l_903_chr13:96989763-96999042_testes
5	lnc-MBNL2-4	chr13:97225913-97226753	NONHSAT034786
6	lnc-DNAJC3-4	chr13:96989764-96989936	l_903_chr13:96989763-96999042_testes

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4501	chr13:97079483-97079503	MIMAT0019037

No data

Variant related genes	Relation type
AMMECR1LP1	TF binding region
AMMECR1LP1	CpG island
ENSG00000102595	chromatin interactions
ZNF280C	miRNA target sites
FSTL1	miRNA target sites

Extended variants
information (count: 6801 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:6801 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535351490	chr13:96984092-96984093	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12583401	chr13:96984099-96984100	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs36163593	chr13:96984105-96984106	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs577599761	chr13:96984141-96984142	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs181528672	chr13:96984144-96984145	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs76281900	chr13:96984145-96984146	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs557031917	chr13:96984154-96984155	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573797868	chr13:96984155-96984156	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs546600817	chr13:96984171-96984172	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs11616787	chr13:96984177-96984178	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11616767	chr13:96984198-96984199	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs138241501	chr13:96984207-96984208	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551200856	chr13:96984208-96984209	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545264315	chr13:96984215-96984216	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs142758593	chr13:96984230-96984231	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs185859871	chr13:96984231-96984232	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs550600684	chr13:96984254-96984255	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs191201404	chr13:96984271-96984272	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs529812940	chr13:96984280-96984281	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs367701829	chr13:96984284-96984285	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs549284148	chr13:96984290-96984291	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs566241774	chr13:96984308-96984309	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534940869	chr13:96984309-96984310	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs558019543	chr13:96984313-96984314	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs183825485	chr13:96984320-96984321	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs537000609	chr13:96984324-96984325	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs556944140	chr13:96984360-96984361	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs7139408	chr13:96984390-96984391	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536503006	chr13:96984399-96984400	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs187928201	chr13:96984402-96984403	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs553215913	chr13:96984406-96984407	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs148378620	chr13:96984417-96984418	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs544923909	chr13:96984423-96984424	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs375213620	chr13:96984425-96984426	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs369823288	chr13:96984426-96984427	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs141550210	chr13:96984441-96984442	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs575620665	chr13:96984459-96984460	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs544194770	chr13:96984506-96984507	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs560889644	chr13:96984527-96984528	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373039795	chr13:96984531-96984532	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs370439811	chr13:96984601-96984602	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs529686992	chr13:96984617-96984618	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546659660	chr13:96984630-96984631	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs560031009	chr13:96984635-96984636	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs567759405	chr13:96984645-96984646	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs190450885	chr13:96984683-96984684	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs551561763	chr13:96984706-96984707	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs571566375	chr13:96984739-96984740	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs544662144	chr13:96984748-96984749	Active TSS Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs537362624	chr13:96984757-96984758	Active TSS Enhancers ZNF genes & repeats	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
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	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
Metanephric adenoma	20802469	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
prenatal diagnosis	22389664	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:96984000-96984200	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr13:96984000-96984400	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr13:96984000-96984800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr13:96984000-96984800	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr13:96984200-96984400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr13:96984400-96984800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr13:96984400-96985200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr13:96985200-96985400	Enhancers	Fetal Intestine Large	intestine
9	chr13:96986000-96986200	Enhancers	Fetal Intestine Large	intestine
10	chr13:96994600-96995600	Enhancers	Fetal Brain Female	brain
11	chr13:96994800-96995400	Enhancers	Fetal Brain Male	brain
12	chr13:96994800-96995400	Enhancers	Fetal Intestine Small	intestine
13	chr13:96994800-96995600	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr13:96994800-96995600	Enhancers	Brain Germinal Matrix	brain
15	chr13:96995200-96995600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr13:96995400-96998800	Weak transcription	Fetal Brain Male	brain
17	chr13:96995400-96999400	Weak transcription	Fetal Intestine Small	intestine
18	chr13:96995600-96995800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr13:96995600-96999200	Weak transcription	Fetal Brain Female	brain
20	chr13:96995800-96996800	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr13:96996600-96997000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr13:96996800-96997800	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr13:96997800-97001800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr13:96998800-96999800	Enhancers	Fetal Brain Male	brain
25	chr13:96999200-96999600	Enhancers	Fetal Brain Female	brain
26	chr13:97001800-97002400	Enhancers	Brain Germinal Matrix	brain
27	chr13:97001800-97003000	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr13:97003000-97006200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr13:97006200-97006400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr13:97006400-97007000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr13:97007000-97007200	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr13:97008800-97009600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:97009600-97013200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:97013200-97013800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:97013800-97014200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:97013800-97014400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr13:97013800-97014400	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr13:97014200-97014400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:97019800-97020400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr13:97020200-97020400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr13:97020400-97021400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:97021400-97021800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr13:97027200-97027400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:97027400-97033800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr13:97031600-97032400	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr13:97032400-97033800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr13:97032600-97032800	Enhancers	Pancreas	Pancrea
48	chr13:97032800-97033800	Weak transcription	Pancreas	Pancrea
49	chr13:97033600-97034600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr13:97033800-97034200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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