Variant report

Variant	nsv1008130
Chromosome Location	chr3:89837442-90192503
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:306)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:90142224-90142549	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:90140843-90141039	HepG2	liver:	n/a	n/a
3	BATF	chr3:89863737-89864040	GM12878	blood:	n/a	chr3:89863915-89863926
4	BATF	chr3:90084907-90085138	GM12878	blood:	n/a	n/a
5	BATF	chr3:90159937-90160210	GM12878	blood:	n/a	n/a
6	BATF	chr3:90057269-90057561	GM12878	blood:	n/a	chr3:90057406-90057415
7	BATF	chr3:89839448-89839835	GM12878	blood:	n/a	chr3:89839649-89839660
8	BATF	chr3:90059634-90059882	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:90130173-90130430	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr3:89983718-89983928	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr3:90089745-90089969	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:90089745-90089993	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:89839514-89839797	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:90084913-90085168	GM12878	blood:	n/a	chr3:90085037-90085046
15	BCL11A	chr3:90089233-90089371	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:90059633-90059865	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:90101922-90101932	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:90105845-90105983	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:90084912-90085190	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:90089753-90089967	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:90065305-90065572	GM12878	blood:	n/a	n/a
22	CEBPB	chr3:89857981-89858307	A549	lung:	n/a	chr3:89858134-89858145
23	CEBPB	chr3:89889386-89889672	IMR90	lung:	n/a	chr3:89889535-89889546
24	CEBPB	chr3:89999416-89999583	H1-hESC	embryonic stem cell:	n/a	chr3:89999498-89999509 chr3:89999497-89999508 chr3:89999497-89999510
25	CEBPB	chr3:90130851-90131195	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:90060817-90061003	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:90057023-90057270	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:90130910-90131157	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:90060754-90061499	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:89837180-89837605	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr3:90027168-90027321	K562	blood:	n/a	chr3:90027262-90027273 chr3:90027260-90027273 chr3:90027260-90027273 chr3:90027257-90027274
32	CEBPB	chr3:89857971-89858307	IMR90	lung:	n/a	chr3:89858134-89858145
33	CEBPB	chr3:89858584-89858830	HepG2	liver:	n/a	n/a
34	CEBPB	chr3:89889445-89889679	HepG2	liver:	n/a	chr3:89889535-89889546
35	CEBPB	chr3:89999426-89999627	HepG2	liver:	n/a	chr3:89999498-89999509 chr3:89999497-89999508 chr3:89999497-89999510
36	CEBPB	chr3:89857967-89858316	HepG2	liver:	n/a	chr3:89858134-89858145
37	CEBPB	chr3:89855339-89855672	HepG2	liver:	n/a	chr3:89855477-89855488 chr3:89855509-89855522
38	CEBPB	chr3:89855361-89855645	A549	lung:	n/a	chr3:89855477-89855488 chr3:89855509-89855522
39	CEBPB	chr3:89842522-89842749	A549	lung:	n/a	n/a
40	CEBPB	chr3:90087777-90087892	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:90111880-90112340	MCF-7	breast:	n/a	n/a
42	CEBPB	chr3:89837212-89837686	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr3:90111852-90112330	MCF-7	breast:	n/a	n/a
44	CEBPB	chr3:89986561-89986595	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr3:90059170-90059853	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:89838726-89838929	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:90111939-90112367	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:90084886-90085217	GM12878	blood:	n/a	n/a
49	CHD2	chr3:90089757-90089978	GM12878	blood:	n/a	n/a
50	CHD2	chr3:89901199-89901531	H1-hESC	embryonic stem cell:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:90086806-90086856	HRCEpiC	kidney:	n/a
2	chr3:90086806-90086856	HRCEpiC	kidney:	n/a
3	chr3:89909180-89909230	ovcar-3	ovarian:	n/a
4	chr3:90130850-90130900	AG09309	skin:	n/a
5	chr3:89909180-89909230	BJ	skin:	n/a
6	chr3:89901227-89901277	BJ	skin:	n/a
7	chr3:90139296-90139346	LNCaP	prostate:	n/a
8	chr3:89909180-89909230	U87	brain:	n/a
9	chr3:90086806-90086856	HL-60	blood:	n/a
10	chr3:90130850-90130900	SK-N-SH_RA	brain:	n/a
11	chr3:89909180-89909230	AG09319	gingival:	n/a
12	chr3:90139296-90139346	HEK293	kidney:	embryo
13	chr3:89909180-89909230	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:89909180-89909230	ProgFib	skin:	n/a
15	chr3:90086806-90086856	AG10803	skin:	n/a
16	chr3:90086806-90086856	NHBE	bronchial:	n/a
17	chr3:90130850-90130900	GM06990	blood:	n/a
18	chr3:90130850-90130900	GM19239	blood:	n/a
19	chr3:89901227-89901277	IMR90	lung:	fetal
20	chr3:89901227-89901277	BE2_C	brain:	n/a
21	chr3:89901227-89901277	HL-60	blood:	n/a
22	chr3:89901227-89901277	AG04449	skin:	fetal
23	chr3:90130850-90130900	ovcar-3	ovarian:	n/a
24	chr3:90086806-90086856	SK-N-MC	brain:	n/a
25	chr3:89901227-89901277	AG10803	skin:	n/a
26	chr3:89901227-89901277	HRE	kidney:	n/a
27	chr3:90086806-90086856	NHDF-neo	bronchial:	n/a
28	chr3:89909180-89909230	AoSMC	blood vessel:	n/a
29	chr3:90139296-90139346	U87	brain:	n/a
30	chr3:90139296-90139346	NHBE	bronchial:	n/a
31	chr3:90139296-90139346	NHDF-neo	bronchial:	n/a
32	chr3:90139296-90139346	HNPCEpiC	eye:	n/a
33	chr3:90086806-90086856	K562	blood:	n/a
34	chr3:90130850-90130900	AoSMC	blood vessel:	n/a
35	chr3:90086806-90086856	BE2_C	brain:	n/a
36	chr3:89909180-89909230	CMK	blood:	n/a
37	chr3:90139296-90139346	HRE	kidney:	n/a
38	chr3:89901227-89901277	A549	lung:	n/a
39	chr3:90130850-90130900	HIPEpiC	eye:	n/a
40	chr3:89901227-89901277	CMK	blood:	n/a
41	chr3:89901227-89901277	SK-N-SH	brain:	n/a
42	chr3:89901227-89901277	GM12878	blood:	n/a
43	chr3:90139296-90139346	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:90130850-90130900	HRE	kidney:	n/a
45	chr3:90086806-90086856	MCF-7	breast:	n/a
46	chr3:90139296-90139346	GM12878	blood:	n/a
47	chr3:90086806-90086856	CMK	blood:	n/a
48	chr3:90086806-90086856	GM12891	blood:	n/a
49	chr3:90139296-90139346	Hepatocyte	liver:	n/a
50	chr3:89909180-89909230	AG09309	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:90096383..90097903-chr8:137113417..137115130,2	MCF-7	breast:
2	chr3:89858428..89860418-chr3:89862912..89865718,2	MCF-7	breast:
3	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:
4	chr3:90068533..90070645-chr3:90092564..90094236,2	MCF-7	breast:
5	chr3:90001450..90003026-chr3:90006244..90008333,2	MCF-7	breast:
6	chr3:89954956..89957239-chr3:89973715..89976586,2	MCF-7	breast:
7	chr3:89996596..89997810-chr3:90140377..90141392,6	MCF-7	breast:
8	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:
9	chr3:89996325..89997175-chr3:90140367..90141418,4	MCF-7	breast:
10	chr3:89611023..89612234-chr3:89900845..89901820,5	MCF-7	breast:
11	chr3:89858428..89860418-chr3:89862912..89865718,2	MCF-7	breast:
12	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
13	chr3:89900833..89901811-chr3:90140473..90141334,4	MCF-7	breast:
14	chr3:90068937..90071174-chr3:90072001..90074074,2	MCF-7	breast:
15	chr3:89996596..89997810-chr3:90140377..90141392,6	MCF-7	breast:
16	chr3:89996606..89997218-chr3:90142348..90142978,2	MCF-7	breast:
17	chr3:90184075..90187070-chr3:90192628..90194644,2	MCF-7	breast:
18	chr3:89829884..89832447-chr3:89837199..89839743,2	K562	blood:
19	chr3:89900833..89901811-chr3:90140473..90141334,4	MCF-7	breast:
20	chr3:89163095..89164119-chr3:89900902..89901799,5	MCF-7	breast:
21	chr3:89147543..89148341-chr3:89900953..89901507,2	MCF-7	breast:
22	chr3:88690038..88690583-chr3:89901209..89901840,2	MCF-7	breast:
23	chr3:88252675..88253298-chr3:89900974..89901665,3	MCF-7	breast:
24	chr3:90067745..90070170-chr3:90100154..90102360,2	MCF-7	breast:
25	chr3:89892604..89895274-chr3:89895825..89897588,2	MCF-7	breast:
26	chr3:90001450..90003026-chr3:90006244..90008333,2	MCF-7	breast:
27	chr3:89892604..89895274-chr3:89895825..89897588,2	MCF-7	breast:
28	chr3:89611242..89611987-chr3:90140381..90141293,2	MCF-7	breast:
29	chr3:89954956..89957239-chr3:89973715..89976586,2	MCF-7	breast:
30	chr3:90075388..90077133-chr3:90078504..90080483,2	MCF-7	breast:
31	chr3:89996606..89997218-chr3:90142348..90142978,2	MCF-7	breast:
32	chr3:89996325..89997175-chr3:90140367..90141418,4	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: 10567 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:10567 , 50 per page) page: 1 2 3 4 5 6 7 ... 212

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76929374	chr3:89839413-89839414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545557271	chr3:89839415-89839416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557952568	chr3:89839421-89839422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543895024	chr3:89839449-89839450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571304592	chr3:89839460-89839461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1520594	chr3:89839468-89839469	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184582891	chr3:89839476-89839477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569062541	chr3:89839481-89839482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4572791	chr3:89839503-89839504	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs187621413	chr3:89839547-89839548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566403322	chr3:89839570-89839571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533772415	chr3:89839571-89839572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558630107	chr3:89839584-89839585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561601442	chr3:89839592-89839593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545748440	chr3:89839627-89839628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs61487225	chr3:89839636-89839637	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs529147576	chr3:89839643-89839644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139692618	chr3:89839662-89839663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115795783	chr3:89839721-89839722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561440561	chr3:89839722-89839723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7628828	chr3:89839807-89839808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs74878589	chr3:89839808-89839809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79922279	chr3:89839809-89839810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371576387	chr3:89839810-89839811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77600871	chr3:89839811-89839812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76979402	chr3:89839812-89839813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192059079	chr3:89839859-89839860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs528609929	chr3:89839860-89839861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184331218	chr3:89839890-89839891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564973000	chr3:89839960-89839961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530776228	chr3:89839986-89839987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs532351661	chr3:89840003-89840004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80103495	chr3:89840004-89840005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188523497	chr3:89840036-89840037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569021959	chr3:89840089-89840090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192341184	chr3:89840095-89840096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184355054	chr3:89840111-89840112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11915412	chr3:89840140-89840141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs551797345	chr3:89843604-89843605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116735809	chr3:89843608-89843609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537383851	chr3:89843628-89843629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555349508	chr3:89843668-89843669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs573522630	chr3:89843701-89843702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539414656	chr3:89843717-89843718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534476083	chr3:89843722-89843723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550171483	chr3:89843746-89843747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370135738	chr3:89843755-89843756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577270977	chr3:89843773-89843774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544696281	chr3:89843863-89843864	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs568842458	chr3:89843887-89843888	Flanking Active TSS	n/a	n/a	Overlapped CNVs	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:942 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:89839400-89840200	Enhancers	Stomach Mucosa	stomach
2	chr3:89843600-89843800	Enhancers	Duodenum Mucosa	Duodenum
3	chr3:89843800-89844000	Flanking Active TSS	Duodenum Mucosa	Duodenum
4	chr3:89844000-89844400	Active TSS	Duodenum Mucosa	Duodenum
5	chr3:89844000-89845200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:89844400-89844600	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr3:89844600-89845400	Enhancers	Duodenum Mucosa	Duodenum
8	chr3:89844800-89845200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:89844800-89845200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:89844800-89845200	Enhancers	Fetal Heart	heart
11	chr3:89852800-89853200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:89852800-89853800	Enhancers	Adipose Nuclei	Adipose
13	chr3:89853200-89858200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:89854000-89854200	Enhancers	Brain Germinal Matrix	brain
15	chr3:89855200-89856400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:89855400-89855600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr3:89855400-89855800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr3:89855400-89855800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:89855600-89855800	Enhancers	Brain Germinal Matrix	brain
20	chr3:89855600-89856200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:89855600-89856200	Enhancers	Fetal Lung	lung
22	chr3:89855600-89857200	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr3:89855800-89856200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:89855800-89856400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:89855800-89856800	Weak transcription	Brain Germinal Matrix	brain
26	chr3:89856000-89856400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr3:89856200-89857400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr3:89856800-89857000	Enhancers	Brain Germinal Matrix	brain
29	chr3:89857200-89858000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr3:89857600-89858000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr3:89858000-89858400	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr3:89858200-89859000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr3:89858400-89859000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr3:89859000-89861600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:89860400-89867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:89860800-89861200	ZNF genes & repeats	Pancreas	Pancrea
37	chr3:89861600-89861800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:89867000-89867400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:89867400-89868200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:89868200-89868400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:89887600-89888400	Enhancers	Duodenum Mucosa	Duodenum
42	chr3:89890000-89890200	Enhancers	Duodenum Mucosa	Duodenum
43	chr3:89890000-89890400	Enhancers	Stomach Mucosa	stomach
44	chr3:89890400-89890800	Weak transcription	Stomach Mucosa	stomach
45	chr3:89890800-89891800	Enhancers	Stomach Mucosa	stomach
46	chr3:89899800-89901000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:89900200-89900800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:89900200-89900800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr3:89900200-89901600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:89900200-89901600	Enhancers	HUES64 Cell Line	embryonic stem cell

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