Variant report

Variant	nsv1007523
Chromosome Location	chr3:89951855-90144385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:801)
CpG islands
(count:184)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:90140843-90141039	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:90142224-90142549	HepG2	liver:	n/a	n/a
3	BATF	chr3:90057269-90057561	GM12878	blood:	n/a	chr3:90057406-90057415
4	BATF	chr3:90059634-90059882	GM12878	blood:	n/a	n/a
5	BATF	chr3:90084907-90085138	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:89983718-89983928	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr3:90130173-90130430	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr3:90089745-90089993	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:90059633-90059865	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:90089233-90089371	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:90089745-90089969	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:90084913-90085168	GM12878	blood:	n/a	chr3:90085037-90085046
13	BHLHE40	chr3:90089753-90089967	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:90101922-90101932	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:90105845-90105983	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:90065305-90065572	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:90084912-90085190	GM12878	blood:	n/a	n/a
18	CEBPB	chr3:90111939-90112367	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:89986561-89986595	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:90027168-90027321	K562	blood:	n/a	chr3:90027262-90027273 chr3:90027260-90027273 chr3:90027260-90027273 chr3:90027257-90027274
21	CEBPB	chr3:89999416-89999583	H1-hESC	embryonic stem cell:	n/a	chr3:89999498-89999509 chr3:89999497-89999508 chr3:89999497-89999510
22	CEBPB	chr3:90130851-90131195	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:90059170-90059853	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:90111880-90112340	MCF-7	breast:	n/a	n/a
25	CEBPB	chr3:90111852-90112330	MCF-7	breast:	n/a	n/a
26	CEBPB	chr3:90060817-90061003	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:90130910-90131157	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:90057023-90057270	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:90087777-90087892	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:90060754-90061499	HepG2	liver:	n/a	n/a
31	CEBPB	chr3:89999426-89999627	HepG2	liver:	n/a	chr3:89999498-89999509 chr3:89999497-89999508 chr3:89999497-89999510
32	CHD2	chr3:90101737-90101932	GM12878	blood:	n/a	n/a
33	CHD2	chr3:90089757-90089978	GM12878	blood:	n/a	n/a
34	CHD2	chr3:89996735-89996788	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr3:90060425-90060427	GM12878	blood:	n/a	n/a
36	CHD2	chr3:90105739-90105812	GM12878	blood:	n/a	n/a
37	CHD2	chr3:90084886-90085217	GM12878	blood:	n/a	n/a
38	CHD2	chr3:90106035-90106043	GM12878	blood:	n/a	n/a
39	CTCF	chr3:90140960-90141110	GM12870	blood:	n/a	n/a
40	CTCF	chr3:90141980-90142130	SAEC	small airway:	n/a	n/a
41	CTCF	chr3:90140816-90141025	Fibrobl	skin:	n/a	chr3:90140948-90140966
42	CTCF	chr3:90007500-90007650	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr3:90142288-90142480	GM10266	blood:	n/a	chr3:90142361-90142382
44	CTCF	chr3:90140730-90141062	H1-hESC	embryonic stem cell:	n/a	chr3:90140948-90140966
45	CTCF	chr3:89996720-89996870	MCF-7	breast:	n/a	n/a
46	CTCF	chr3:90140855-90141011	GM19240	blood:	n/a	chr3:90140948-90140966
47	CTCF	chr3:90140460-90140610	HMEC	breast:	n/a	chr3:90140527-90140535
48	CTCF	chr3:90109753-90109838	Fibrobl	skin:	n/a	n/a
49	CTCF	chr3:90142280-90142430	GM12871	blood:	n/a	chr3:90142361-90142382
50	CTCF	chr3:90142280-90142430	HCT-116	colon:	n/a	chr3:90142361-90142382

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:90139296-90139346	ProgFib	skin:	n/a
2	chr3:90139296-90139346	ProgFib	skin:	n/a
3	chr3:90130850-90130900	Jurkat	blood:	n/a
4	chr3:90139296-90139346	HEK293	kidney:	embryo
5	chr3:90139296-90139346	SK-N-MC	brain:	n/a
6	chr3:90139296-90139346	HCT-116	colon:	n/a
7	chr3:90139296-90139346	PrEC	prostate:	n/a
8	chr3:90139296-90139346	HIPEpiC	eye:	n/a
9	chr3:90130850-90130900	HUVEC	blood vessel:	n/a
10	chr3:90139296-90139346	GM19239	blood:	n/a
11	chr3:90086806-90086856	NHBE	bronchial:	n/a
12	chr3:90130850-90130900	HL-60	blood:	n/a
13	chr3:90130850-90130900	H1-hESC	embryonic stem cell:	embryo
14	chr3:90130850-90130900	MCF-7	breast:	n/a
15	chr3:90086806-90086856	RPTEC	kidney:	n/a
16	chr3:90086806-90086856	GM12878	blood:	n/a
17	chr3:90086806-90086856	NH-A	brain:	n/a
18	chr3:90086806-90086856	PFSK-1	brain:	n/a
19	chr3:90086806-90086856	LNCaP	prostate:	n/a
20	chr3:90086806-90086856	A549	lung:	n/a
21	chr3:90130850-90130900	SK-N-SH	brain:	n/a
22	chr3:90139296-90139346	HEEpiC	esophagus:	n/a
23	chr3:90139296-90139346	IMR90	lung:	fetal
24	chr3:90086806-90086856	HNPCEpiC	eye:	n/a
25	chr3:90086806-90086856	HUVEC	blood vessel:	n/a
26	chr3:90139296-90139346	GM06990	blood:	n/a
27	chr3:90086806-90086856	SK-N-MC	brain:	n/a
28	chr3:90139296-90139346	U87	brain:	n/a
29	chr3:90130850-90130900	HCM	heart:	n/a
30	chr3:90130850-90130900	BE2_C	brain:	n/a
31	chr3:90130850-90130900	GM12891	blood:	n/a
32	chr3:90130850-90130900	GM12878	blood:	n/a
33	chr3:90130850-90130900	K562	blood:	n/a
34	chr3:90139296-90139346	HUVEC	blood vessel:	n/a
35	chr3:90130850-90130900	AG04449	skin:	fetal
36	chr3:90130850-90130900	NT2-D1	testis:	n/a
37	chr3:90130850-90130900	HRPEpiC	eye:	n/a
38	chr3:90139296-90139346	HRPEpiC	eye:	n/a
39	chr3:90139296-90139346	RPTEC	kidney:	n/a
40	chr3:90130850-90130900	GM12892	blood:	n/a
41	chr3:90139296-90139346	MCF-7	breast:	n/a
42	chr3:90086806-90086856	BE2_C	brain:	n/a
43	chr3:90086806-90086856	HMEC	breast:	n/a
44	chr3:90139296-90139346	HNPCEpiC	eye:	n/a
45	chr3:90086806-90086856	SKMC	muscle:	n/a
46	chr3:90086806-90086856	HRPEpiC	eye:	n/a
47	chr3:90139296-90139346	AG04449	skin:	fetal
48	chr3:90086806-90086856	GM12892	blood:	n/a
49	chr3:90139296-90139346	HL-60	blood:	n/a
50	chr3:90130850-90130900	T-47D	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:89611242..89611987-chr3:90140381..90141293,2	MCF-7	breast:
2	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:
3	chr3:89900833..89901811-chr3:90140473..90141334,4	MCF-7	breast:
4	chr3:90096383..90097903-chr8:137113417..137115130,2	MCF-7	breast:
5	chr3:89996596..89997810-chr3:90140377..90141392,6	MCF-7	breast:
6	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
7	chr3:90075388..90077133-chr3:90078504..90080483,2	MCF-7	breast:
8	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:
9	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
10	chr3:89996596..89997810-chr3:90140377..90141392,6	MCF-7	breast:
11	chr3:89996606..89997218-chr3:90142348..90142978,2	MCF-7	breast:
12	chr3:89996606..89997218-chr3:90142348..90142978,2	MCF-7	breast:
13	chr3:90001450..90003026-chr3:90006244..90008333,2	MCF-7	breast:
14	chr3:89954956..89957239-chr3:89973715..89976586,2	MCF-7	breast:
15	chr3:89996325..89997175-chr3:90140367..90141418,4	MCF-7	breast:
16	chr3:89954956..89957239-chr3:89973715..89976586,2	MCF-7	breast:
17	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:
18	chr3:89996325..89997175-chr3:90140367..90141418,4	MCF-7	breast:
19	chr3:90001450..90003026-chr3:90006244..90008333,2	MCF-7	breast:
20	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPHA3-1	chr3:90079434-90079644	NONHSAT090712

No data

Variant related genes	Relation type
ENSG00000212598	TF binding region
ENSG00000212598	CpG island
ENSG00000212598	chromatin interactions

Extended variants
information (count: 6741 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6741 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563057261	chr3:89953410-89953411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74482834	chr3:89953415-89953416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372561115	chr3:89953420-89953421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555897141	chr3:89953434-89953435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373549206	chr3:89953456-89953457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530491761	chr3:89953476-89953477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541171280	chr3:89953522-89953523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs58593183	chr3:89953532-89953533	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs577619942	chr3:89953538-89953539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545347057	chr3:89953566-89953567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs116230294	chr3:89953577-89953578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375653216	chr3:89953667-89953668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188413606	chr3:89953668-89953669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151054472	chr3:89953684-89953685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141003216	chr3:89953690-89953691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561100998	chr3:89953715-89953716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181243822	chr3:89953731-89953732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144362764	chr3:89953764-89953765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371171477	chr3:89953778-89953779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147826723	chr3:89953806-89953807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528289919	chr3:89953812-89953813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538647065	chr3:89953822-89953823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550513519	chr3:89953849-89953850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552097529	chr3:89953866-89953867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570271508	chr3:89953897-89953898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs55743058	chr3:89953905-89953906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs141430016	chr3:89953943-89953944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375514263	chr3:89953948-89953949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34792399	chr3:89953953-89953954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534844271	chr3:89953961-89953962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553062136	chr3:89953967-89953968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36035829	chr3:89954004-89954005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577683873	chr3:89954017-89954018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112668081	chr3:89954036-89954037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571503084	chr3:89954084-89954085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147017297	chr3:89954112-89954113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546608170	chr3:89954129-89954130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575535124	chr3:89954147-89954148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528575158	chr3:89954154-89954155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542948530	chr3:89954173-89954174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186072172	chr3:89954201-89954202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528298704	chr3:89954206-89954207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76963855	chr3:89954229-89954230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs137889010	chr3:89954230-89954231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532201939	chr3:89954235-89954236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550381494	chr3:89954248-89954249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568452190	chr3:89954263-89954264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568867107	chr3:89954297-89954298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529656612	chr3:89954308-89954309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72917604	chr3:89954314-89954315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Soft tissue tumor	16732325	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Lung cancer	19547694	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:739 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89953400-89963600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:89963600-89964200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:89972400-89973200	Enhancers	Fetal Lung	lung
4	chr3:89973200-89973600	Flanking Active TSS	Fetal Lung	lung
5	chr3:89973200-89973600	Enhancers	HSMMtube	muscle
6	chr3:89973200-89974000	Enhancers	Fetal Brain Male	brain
7	chr3:89973600-89974200	Enhancers	Fetal Lung	lung
8	chr3:89974200-89975000	Weak transcription	Fetal Lung	lung
9	chr3:89975000-89975400	Enhancers	Fetal Lung	lung
10	chr3:89975200-89976000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr3:89975400-89977400	Weak transcription	Fetal Lung	lung
12	chr3:89975600-89976600	Enhancers	Stomach Mucosa	stomach
13	chr3:89976400-89976800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:89977000-89977200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:89977200-89984200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:89977400-89977600	Enhancers	Fetal Lung	lung
17	chr3:89982000-89982200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:89982000-89983000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:89982200-89982600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr3:89982200-89982600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:89982200-89982600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr3:89982200-89982800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
23	chr3:89982200-89983400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr3:89982600-89984400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr3:89982600-89998000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:89982800-89984000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr3:89982800-89984000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr3:89983000-89983800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:89983200-89984600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr3:89983200-89984600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr3:89983400-89984400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:89983400-89984400	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:89983800-89984000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr3:89983800-89984000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:89984000-89984600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr3:89984200-89984400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr3:89993800-89994200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr3:89994200-89994600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr3:89995200-89996200	Enhancers	Hela-S3	cervix
40	chr3:89995600-89997200	Enhancers	Stomach Mucosa	stomach
41	chr3:89996000-89996800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:89996000-89997200	Enhancers	Duodenum Mucosa	Duodenum
43	chr3:89996200-89996600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr3:89996200-89996600	Enhancers	Right Ventricle	heart
45	chr3:89996200-89997000	Enhancers	Fetal Muscle Leg	muscle
46	chr3:89996200-89997000	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr3:89996200-89997000	Flanking Active TSS	Hela-S3	cervix
48	chr3:89996200-89997200	Enhancers	Adipose Nuclei	Adipose
49	chr3:89996200-89998200	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr3:89996200-89998400	Enhancers	Fetal Heart	heart

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