Variant report

Variant	nsv562794
Chromosome Location	chr13:98083262-98086828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:756)
CpG islands
(count:549)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:756 , 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	ARID3A	chr13:98085366-98086241	HepG2	liver:	n/a	n/a
2	ATF2	chr13:98085038-98086272	GM12878	blood:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
3	ATF2	chr13:98085096-98085777	H1-hESC	embryonic stem cell:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
4	ATF2	chr13:98085304-98086176	GM12878	blood:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
5	ATF2	chr13:98085147-98086057	H1-hESC	embryonic stem cell:	n/a	chr13:98085691-98085705 chr13:98085693-98085704
6	ATF3	chr13:98085226-98085687	GM12878	blood:	n/a	chr13:98085404-98085424
7	ATF3	chr13:98085219-98085630	H1-hESC	embryonic stem cell:	n/a	chr13:98085404-98085424
8	ATF3	chr13:98086060-98086274	K562	blood:	n/a	n/a
9	BACH1	chr13:98085062-98085771	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr13:98084855-98085657	A549	lung:	n/a	n/a
11	BCLAF1	chr13:98084876-98085864	GM12878	blood:	n/a	n/a
12	BHLHE40	chr13:98083830-98083878	K562	blood:	n/a	n/a
13	BHLHE40	chr13:98084588-98086514	GM12878	blood:	n/a	chr13:98085193-98085209
14	BHLHE40	chr13:98085211-98086183	K562	blood:	n/a	n/a
15	BHLHE40	chr13:98085153-98086201	HepG2	liver:	n/a	chr13:98085193-98085209
16	BRCA1	chr13:98085288-98085593	HepG2	liver:	n/a	n/a
17	BRCA1	chr13:98085144-98086211	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr13:98085978-98086076	GM12878	blood:	n/a	n/a
19	BRCA1	chr13:98085482-98085634	GM12878	blood:	n/a	n/a
20	BRCA1	chr13:98085034-98085254	GM12878	blood:	n/a	n/a
21	CBX3	chr13:98085076-98085717	K562	blood:	n/a	n/a
22	CBX3	chr13:98085254-98085632	K562	blood:	n/a	n/a
23	CCNT2	chr13:98085530-98087217	K562	blood:	n/a	n/a
24	CEBPB	chr13:98084807-98086028	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:98085277-98086202	GM12878	blood:	n/a	n/a
26	CEBPD	chr13:98086329-98086647	HepG2	liver:	n/a	n/a
27	CHD1	chr13:98084629-98085170	GM12878	blood:	n/a	n/a
28	CHD1	chr13:98085761-98086057	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr13:98084569-98086399	IMR90	lung:	n/a	n/a
30	CHD1	chr13:98085472-98086164	GM12878	blood:	n/a	n/a
31	CHD1	chr13:98086757-98087423	GM12878	blood:	n/a	n/a
32	CHD2	chr13:98086724-98086950	GM12878	blood:	n/a	n/a
33	CHD2	chr13:98085046-98086569	Hela-S3	cervix:	n/a	n/a
34	CHD2	chr13:98085986-98086237	K562	blood:	n/a	n/a
35	CHD2	chr13:98084963-98086180	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr13:98085047-98086204	HepG2	liver:	n/a	n/a
37	CHD2	chr13:98084646-98086472	GM12878	blood:	n/a	n/a
38	CREB1	chr13:98085114-98085802	A549	lung:	n/a	n/a
39	CREB1	chr13:98085042-98086007	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr13:98084846-98086885	HepG2	liver:	n/a	n/a
41	CREB1	chr13:98085063-98085908	A549	lung:	n/a	n/a
42	CREB1	chr13:98086027-98086404	A549	lung:	n/a	n/a
43	CREB1	chr13:98084926-98086607	HepG2	liver:	n/a	n/a
44	CREB1	chr13:98084625-98086337	GM12878	blood:	n/a	n/a
45	CREB1	chr13:98084933-98086350	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr13:98085953-98086408	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr13:98085104-98085958	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr13:98084992-98085906	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr13:98084883-98086360	GM12878	blood:	n/a	n/a
50	CTCF	chr13:98085980-98086130	SAEC	small airway:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:98084247-98084297	GM12891	blood:	n/a
2	chr13:98084247-98084297	PrEC	prostate:	n/a
3	chr13:98085463-98085513	SK-N-MC	brain:	n/a
4	chr13:98085463-98085513	AG09319	gingival:	n/a
5	chr13:98085375-98085425	ovcar-3	ovarian:	n/a
6	chr13:98085375-98085425	Caco-2	colon:	n/a
7	chr13:98085375-98085425	Jurkat	blood:	n/a
8	chr13:98085375-98085425	LNCaP	prostate:	n/a
9	chr13:98085463-98085513	HUVEC	blood vessel:	n/a
10	chr13:98085375-98085425	BJ	skin:	n/a
11	chr13:98085375-98085425	HPAEpiC	pulmonary alveolar:	n/a
12	chr13:98084247-98084297	HRPEpiC	eye:	n/a
13	chr13:98085463-98085513	HepG2	liver:	n/a
14	chr13:98085375-98085425	HUVEC	blood vessel:	n/a
15	chr13:98086635-98086685	U87	brain:	n/a
16	chr13:98086635-98086685	HRCEpiC	kidney:	n/a
17	chr13:98085463-98085513	PrEC	prostate:	n/a
18	chr13:98084247-98084297	T-47D	breast:	n/a
19	chr13:98086635-98086685	ECC-1	luminal epithelium:	n/a
20	chr13:98086427-98086477	HMEC	breast:	n/a
21	chr13:98085463-98085513	T-47D	breast:	n/a
22	chr13:98085949-98085999	HRPEpiC	eye:	n/a
23	chr13:98085463-98085513	NH-A	brain:	n/a
24	chr13:98085375-98085425	Hela-S3	cervix:	n/a
25	chr13:98085949-98085999	ProgFib	skin:	n/a
26	chr13:98085949-98085999	HCM	heart:	n/a
27	chr13:98085949-98085999	NT2-D1	testis:	n/a
28	chr13:98084247-98084297	HRE	kidney:	n/a
29	chr13:98086635-98086685	HNPCEpiC	eye:	n/a
30	chr13:98085375-98085425	ECC-1	luminal epithelium:	n/a
31	chr13:98085463-98085513	HCM	heart:	n/a
32	chr13:98086433-98086483	AG09319	gingival:	n/a
33	chr13:98084247-98084297	H1-hESC	embryonic stem cell:	embryo
34	chr13:98085463-98085513	HPAEpiC	pulmonary alveolar:	n/a
35	chr13:98085949-98085999	HL-60	blood:	n/a
36	chr13:98085375-98085425	H1-hESC	embryonic stem cell:	embryo
37	chr13:98086784-98086834	ECC-1	luminal epithelium:	n/a
38	chr13:98085947-98085997	MCF10A-Er-Src	breast:	n/a
39	chr13:98086784-98086834	H1-hESC	embryonic stem cell:	embryo
40	chr13:98086635-98086685	HUVEC	blood vessel:	n/a
41	chr13:98086784-98086834	HMEC	breast:	n/a
42	chr13:98085949-98085999	PrEC	prostate:	n/a
43	chr13:98084247-98084297	Hela-S3	cervix:	n/a
44	chr13:98086635-98086685	AoSMC	blood vessel:	n/a
45	chr13:98086427-98086477	LNCaP	prostate:	n/a
46	chr13:98086635-98086685	Hela-S3	cervix:	n/a
47	chr13:98084247-98084297	MCF-7	breast:	n/a
48	chr13:98085947-98085997	HCT-116	colon:	n/a
49	chr13:98086635-98086685	NT2-D1	testis:	n/a
50	chr13:98086427-98086477	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:98078675..98081221-chr13:98083499..98086151,3	MCF-7	breast:
2	chr13:98084839..98085346-chr3:186764394..186765071,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OXGR1-6	chr13:98081597-98086236	NONHSAT034832

No data

Variant related genes	Relation type
RAP2A	TF binding region
RAP2A	CpG island

Extended variants
information (count: 144 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:144 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3818590	chr13:98083262-98083263	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555689529	chr13:98083264-98083265	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs572494867	chr13:98083327-98083328	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs576717044	chr13:98083406-98083407	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs143674424	chr13:98083429-98083430	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs144891435	chr13:98083462-98083463	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs558267610	chr13:98083520-98083521	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs78109546	chr13:98083541-98083542	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs543773730	chr13:98083542-98083543	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs149040425	chr13:98083583-98083584	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs376595030	chr13:98083599-98083600	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs190057899	chr13:98083685-98083686	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs578116265	chr13:98083689-98083690	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs543137113	chr13:98083734-98083735	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs542020412	chr13:98083785-98083786	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs59888293	chr13:98083802-98083803	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs181258868	chr13:98083817-98083818	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs143069762	chr13:98083822-98083823	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs186485839	chr13:98083851-98083852	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs565151707	chr13:98083907-98083908	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs74741050	chr13:98084008-98084009	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs572338940	chr13:98084019-98084020	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs550630934	chr13:98084036-98084037	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs368819009	chr13:98084059-98084060	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs567108029	chr13:98084089-98084090	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs372780551	chr13:98084129-98084130	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs377661853	chr13:98084191-98084192	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs191018484	chr13:98084236-98084237	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs546286062	chr13:98084241-98084242	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs566181570	chr13:98084311-98084312	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs540845987	chr13:98084324-98084325	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs34442666	chr13:98084377-98084378	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs538353395	chr13:98084394-98084395	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs558490989	chr13:98084412-98084413	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs74105076	chr13:98084479-98084480	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs74105078	chr13:98084485-98084486	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs74105079	chr13:98084499-98084500	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574284623	chr13:98084511-98084512	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs543199909	chr13:98084538-98084539	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs553614138	chr13:98084553-98084554	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs527960058	chr13:98084559-98084560	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs147088562	chr13:98084592-98084593	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs565262846	chr13:98084613-98084614	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs368841852	chr13:98084631-98084632	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs370194145	chr13:98084632-98084633	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs9584575	chr13:98084675-98084676	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs138516343	chr13:98084692-98084693	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs116411868	chr13:98084699-98084700	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs571563911	chr13:98084746-98084747	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs182336505	chr13:98084791-98084792	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
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
Breast cancer	21785460	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:98076400-98084800	Weak transcription	Esophagus	oesophagus
2	chr13:98079400-98084200	Weak transcription	Liver	Liver
3	chr13:98080400-98084400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:98081000-98083800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr13:98081000-98084000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr13:98081200-98083600	Enhancers	Dnd41	blood
7	chr13:98081800-98084200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:98081800-98084400	Enhancers	Fetal Heart	heart
9	chr13:98081800-98084400	Enhancers	Fetal Intestine Small	intestine
10	chr13:98082000-98084600	Enhancers	Fetal Intestine Large	intestine
11	chr13:98082200-98083800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr13:98082200-98083800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr13:98082200-98084000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr13:98082200-98084400	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr13:98082200-98084400	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr13:98082200-98084400	Weak transcription	Adipose Nuclei	Adipose
17	chr13:98082200-98084600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:98082200-98084600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr13:98082200-98084600	Weak transcription	Aorta	Aorta
20	chr13:98082200-98084600	Weak transcription	Colon Smooth Muscle	Colon
21	chr13:98082200-98084600	Weak transcription	Left Ventricle	heart
22	chr13:98082200-98084600	Weak transcription	Hela-S3	cervix
23	chr13:98082200-98085000	Weak transcription	K562	blood
24	chr13:98082400-98083600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:98082400-98083600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr13:98082400-98083600	Enhancers	Fetal Stomach	stomach
27	chr13:98082400-98083600	Weak transcription	HepG2	liver
28	chr13:98082400-98084000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr13:98082400-98084000	Weak transcription	Fetal Kidney	kidney
30	chr13:98082400-98084400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr13:98082400-98084400	Weak transcription	Rectal Smooth Muscle	rectum
32	chr13:98082400-98084400	Weak transcription	Right Atrium	heart
33	chr13:98082400-98084400	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr13:98082400-98084400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr13:98082400-98084600	Weak transcription	Fetal Muscle Trunk	muscle
36	chr13:98082400-98084600	Weak transcription	Placenta	Placenta
37	chr13:98082400-98084800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:98082600-98083600	Flanking Active TSS	Brain Cingulate Gyrus	brain
39	chr13:98082600-98083800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr13:98082600-98084400	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr13:98082800-98083600	Enhancers	Brain Angular Gyrus	brain
42	chr13:98082800-98083800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr13:98082800-98083800	Enhancers	Psoas Muscle	Psoas
44	chr13:98082800-98084000	Enhancers	NHDF-Ad	bronchial
45	chr13:98082800-98084000	Enhancers	NHLF	lung
46	chr13:98082800-98084000	Weak transcription	Osteobl	bone
47	chr13:98082800-98084200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:98082800-98084200	Enhancers	Brain Substantia Nigra	brain
49	chr13:98082800-98084400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr13:98082800-98084400	Enhancers	Fetal Lung	lung

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