Variant report

Variant	nsv1014275
Chromosome Location	chr3:22796228-22880732
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:22838379-22838488	K562	blood:	n/a	n/a
2	BACH1	chr3:22876658-22876746	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr3:22866807-22866832	GM12878	blood:	n/a	n/a
4	CEBPB	chr3:22813116-22813156	H1-hESC	embryonic stem cell:	n/a	chr3:22813118-22813131
5	CEBPB	chr3:22808988-22809235	HepG2	liver:	n/a	chr3:22809074-22809085
6	CEBPB	chr3:22876602-22876809	A549	lung:	n/a	n/a
7	CEBPB	chr3:22807857-22808071	H1-hESC	embryonic stem cell:	n/a	chr3:22807955-22807966
8	CEBPB	chr3:22830014-22830272	HepG2	liver:	n/a	chr3:22830144-22830155
9	CEBPB	chr3:22877091-22877663	HepG2	liver:	n/a	chr3:22877489-22877498 chr3:22877489-22877500 chr3:22877487-22877498 chr3:22877487-22877500
10	CEBPB	chr3:22808900-22809217	A549	lung:	n/a	chr3:22809074-22809085
11	CEBPB	chr3:22830026-22830226	H1-hESC	embryonic stem cell:	n/a	chr3:22830144-22830155
12	CEBPB	chr3:22877342-22877660	A549	lung:	n/a	chr3:22877489-22877498 chr3:22877489-22877500 chr3:22877487-22877498 chr3:22877487-22877500
13	CEBPB	chr3:22824674-22824851	A549	lung:	n/a	chr3:22824780-22824791
14	CEBPB	chr3:22807797-22808121	HepG2	liver:	n/a	chr3:22807955-22807966
15	CEBPB	chr3:22807874-22808037	Hela-S3	cervix:	n/a	chr3:22807955-22807966
16	CEBPB	chr3:22817438-22817635	HepG2	liver:	n/a	chr3:22817570-22817581
17	CEBPB	chr3:22807813-22808145	A549	lung:	n/a	chr3:22807955-22807966
18	CEBPB	chr3:22808930-22809139	K562	blood:	n/a	chr3:22809074-22809085
19	CEBPB	chr3:22854791-22855109	A549	lung:	n/a	chr3:22854853-22854864
20	CEBPB	chr3:22829967-22830308	IMR90	lung:	n/a	chr3:22830144-22830155
21	CEBPB	chr3:22824731-22824944	HepG2	liver:	n/a	chr3:22824780-22824791
22	CEBPB	chr3:22830066-22830284	K562	blood:	n/a	chr3:22830144-22830155
23	CEBPB	chr3:22807788-22808115	IMR90	lung:	n/a	chr3:22807955-22807966
24	CTCF	chr3:22837546-22837685	GM12878	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
25	CTCF	chr3:22837480-22837630	GM12872	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
26	CTCF	chr3:22837552-22837642	Hela-S3	cervix:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
27	CTCF	chr3:22837500-22837650	HepG2	liver:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
28	CTCF	chr3:22837540-22837690	HL-60	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
29	CTCF	chr3:22837520-22837670	GM12873	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
30	CTCF	chr3:22837061-22837145	GM13977	blood:	n/a	n/a
31	CTCF	chr3:22837446-22837756	GM12878	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
32	CTCF	chr3:22806988-22806992	GM10248	blood:	n/a	n/a
33	CTCF	chr3:22837524-22837684	MCF-7	breast:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
34	CTCF	chr3:22811217-22811309	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:22837549-22837682	MCF-7	breast:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
36	CTCF	chr3:22866767-22866792	ProgFib	skin:	n/a	n/a
37	CTCF	chr3:22815180-22815220	GM10248	blood:	n/a	n/a
38	CTCF	chr3:22837124-22837158	GM20000	blood:	n/a	n/a
39	CTCF	chr3:22837568-22837639	Medullo	brain:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
40	CTCF	chr3:22837580-22837657	GM12892	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
41	CTCF	chr3:22837545-22837658	GM19239	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
42	CTCF	chr3:22837500-22837650	GM12873	blood:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
43	CTCF	chr3:22837660-22837810	A549	lung:	n/a	n/a
44	CTCF	chr3:22797104-22797158	Medullo	brain:	n/a	n/a
45	CTCF	chr3:22837509-22837671	H1-hESC	embryonic stem cell:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
46	CTCF	chr3:22837566-22837646	HepG2	liver:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
47	CTCF	chr3:22837500-22837650	WERI-Rb-1	eye:	n/a	chr3:22837608-22837624 chr3:22837609-22837630 chr3:22837607-22837625
48	CTCF	chr3:22837460-22837610	NB4	blood:	n/a	n/a
49	CTCF	chr3:22822548-22822603	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr3:22837640-22837790	RPTEC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22834726-22834776	HAEpiC	amniotic membrane:	n/a
2	chr3:22843137-22843187	Jurkat	blood:	n/a
3	chr3:22834726-22834776	BJ	skin:	n/a
4	chr3:22834726-22834776	PrEC	prostate:	n/a
5	chr3:22843137-22843187	AG09319	gingival:	n/a
6	chr3:22843137-22843187	AoSMC	blood vessel:	n/a
7	chr3:22834726-22834776	AG09319	gingival:	n/a
8	chr3:22843137-22843187	MCF10A-Er-Src	breast:	n/a
9	chr3:22843137-22843187	ovcar-3	ovarian:	n/a
10	chr3:22843137-22843187	SAEC	small airway:	n/a
11	chr3:22843137-22843187	LNCaP	prostate:	n/a
12	chr3:22843137-22843187	H1-hESC	embryonic stem cell:	embryo
13	chr3:22843137-22843187	IMR90	lung:	fetal
14	chr3:22834726-22834776	NHBE	bronchial:	n/a
15	chr3:22843137-22843187	HIPEpiC	eye:	n/a
16	chr3:22834726-22834776	LNCaP	prostate:	n/a
17	chr3:22834726-22834776	GM19239	blood:	n/a
18	chr3:22834726-22834776	HEK293	kidney:	embryo
19	chr3:22834726-22834776	GM06990	blood:	n/a
20	chr3:22834726-22834776	AG04449	skin:	fetal
21	chr3:22834726-22834776	Hepatocyte	liver:	n/a
22	chr3:22834726-22834776	HIPEpiC	eye:	n/a
23	chr3:22843137-22843187	T-47D	breast:	n/a
24	chr3:22843137-22843187	HNPCEpiC	eye:	n/a
25	chr3:22834726-22834776	HRCEpiC	kidney:	n/a
26	chr3:22843137-22843187	PrEC	prostate:	n/a
27	chr3:22834726-22834776	GM12878	blood:	n/a
28	chr3:22834726-22834776	HMEC	breast:	n/a
29	chr3:22843137-22843187	GM06990	blood:	n/a
30	chr3:22843137-22843187	GM12878	blood:	n/a
31	chr3:22834726-22834776	SK-N-MC	brain:	n/a
32	chr3:22843137-22843187	HCT-116	colon:	n/a
33	chr3:22834726-22834776	NH-A	brain:	n/a
34	chr3:22834726-22834776	HUVEC	blood vessel:	n/a
35	chr3:22843137-22843187	ProgFib	skin:	n/a
36	chr3:22843137-22843187	HepG2	liver:	n/a
37	chr3:22843137-22843187	HL-60	blood:	n/a
38	chr3:22843137-22843187	HEK293	kidney:	embryo
39	chr3:22843137-22843187	Hepatocyte	liver:	n/a
40	chr3:22834726-22834776	RPTEC	kidney:	n/a
41	chr3:22834726-22834776	BE2_C	brain:	n/a
42	chr3:22843137-22843187	MCF-7	breast:	n/a
43	chr3:22834726-22834776	MCF10A-Er-Src	breast:	n/a
44	chr3:22834726-22834776	HCT-116	colon:	n/a
45	chr3:22843137-22843187	GM12891	blood:	n/a
46	chr3:22843137-22843187	AG04449	skin:	fetal
47	chr3:22843137-22843187	PFSK-1	brain:	n/a
48	chr3:22843137-22843187	SKMC	muscle:	n/a
49	chr3:22834726-22834776	MCF-7	breast:	n/a
50	chr3:22843137-22843187	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:22837140..22837804-chr3:22903829..22904564,2	MCF-7	breast:
2	chr3:22794268..22797124-chr3:22799597..22801489,2	MCF-7	breast:
3	chr3:22803714..22805482-chr3:22807294..22809398,2	K562	blood:
4	chr3:22808136..22810861-chr3:22815889..22818179,2	K562	blood:
5	chr3:22804037..22805757-chr3:23957373..23959128,2	K562	blood:
6	chr3:22837465..22837989-chr3:22929309..22930132,2	MCF-7	breast:
7	chr3:22784017..22786866-chr3:22809414..22812166,2	MCF-7	breast:
8	chr3:22808136..22810861-chr3:22815889..22818179,2	K562	blood:
9	chr3:22874201..22876969-chr3:22880901..22883798,2	MCF-7	breast:
10	chr10:118596641..118597304-chr3:22865951..22866785,2	MCF-7	breast:
11	chr3:22794268..22797124-chr3:22799597..22801489,2	MCF-7	breast:
12	chr3:22803714..22805482-chr3:22807294..22809398,2	K562	blood:
13	chr3:22786053..22788405-chr3:22793906..22796307,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF385D-4	chr3:22852881-22853115	NONHSAT088659
2	lnc-ZNF385D-4	chr3:22853169-22853538	NONHSAT088659

Variant related genes	Relation type
ENSG00000271235	TF binding region
ENSG00000271235	CpG island
ENSG00000174748	chromatin interactions
ENSG00000197885	chromatin interactions

Extended variants
information (count: 2614 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2614 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537232819	chr3:22796293-22796294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114342175	chr3:22796453-22796454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576527148	chr3:22796457-22796458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553301365	chr3:22796478-22796479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140870239	chr3:22796513-22796514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146416809	chr3:22796591-22796592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573381373	chr3:22796637-22796638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544551335	chr3:22796640-22796641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370601293	chr3:22796642-22796643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386659311	chr3:22796646-22796647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563411335	chr3:22796682-22796683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535813875	chr3:22796733-22796734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530858841	chr3:22796738-22796739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60437162	chr3:22796761-22796762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs59051301	chr3:22796762-22796763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139000852	chr3:22796839-22796840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143123351	chr3:22796847-22796848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532614089	chr3:22796848-22796849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547929891	chr3:22796849-22796850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566039597	chr3:22796876-22796877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574943740	chr3:22796902-22796903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370018038	chr3:22796909-22796910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147471882	chr3:22796928-22796929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548598842	chr3:22796933-22796934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530289873	chr3:22796943-22796944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370203672	chr3:22796954-22796955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558679611	chr3:22796959-22796960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192044637	chr3:22796965-22796966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117453796	chr3:22796985-22796986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534379536	chr3:22797015-22797016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552813186	chr3:22797020-22797021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556078060	chr3:22797032-22797033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574501886	chr3:22797065-22797066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541442505	chr3:22797089-22797090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542236384	chr3:22797106-22797107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575736399	chr3:22797116-22797117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544636705	chr3:22797125-22797126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575604243	chr3:22797126-22797127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373150121	chr3:22797132-22797133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564436994	chr3:22797170-22797171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546131303	chr3:22797174-22797175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564241656	chr3:22797206-22797207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528319268	chr3:22797243-22797244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13085890	chr3:22797261-22797262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559579524	chr3:22797311-22797312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530255454	chr3:22797316-22797317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534883070	chr3:22797350-22797351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184866077	chr3:22797359-22797360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569718039	chr3:22797429-22797430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs35819075	chr3:22797444-22797445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22786000-22802000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:22797400-22797600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:22798600-22799200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:22799200-22801000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:22801000-22801400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:22801200-22801400	Enhancers	Fetal Lung	lung
7	chr3:22801400-22802000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:22801600-22802800	Weak transcription	Fetal Lung	lung
9	chr3:22802000-22803000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr3:22802000-22807400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:22802600-22803200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:22802800-22803200	Enhancers	Fetal Lung	lung
13	chr3:22808400-22812000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:22811000-22811200	Enhancers	Esophagus	oesophagus
15	chr3:22811600-22811800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:22812400-22812600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:22820800-22821400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:22821000-22821600	Enhancers	HMEC	breast
19	chr3:22823800-22834000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr3:22834000-22834400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:22834000-22834400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:22834000-22834800	Enhancers	H9 Cell Line	embryonic stem cell
23	chr3:22834000-22835000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:22834200-22834600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:22834200-22834600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:22834200-22834600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:22834200-22835000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:22834400-22839800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:22834600-22842400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr3:22839800-22840600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr3:22840200-22840600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr3:22840200-22840600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:22842400-22843000	Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr3:22842600-22843200	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr3:22842800-22843200	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr3:22853000-22853400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr3:22853400-22860400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:22857000-22857200	Enhancers	Gastric	stomach
39	chr3:22859600-22859800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:22859800-22861000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:22860400-22861000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:22861000-22866600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:22865800-22866000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:22866000-22866600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:22866600-22866800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:22866600-22867000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:22866600-22867000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:22866600-22867400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:22866800-22877600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:22867400-22867800	Enhancers	H1 Cell Line	embryonic stem cell

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