Variant report

Variant	nsv1001350
Chromosome Location	chr3:51860817-51899966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:489)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:51894914-51895263	K562	blood:	n/a	n/a
2	CBX3	chr3:51867297-51867471	K562	blood:	n/a	n/a
3	CBX3	chr3:51867120-51867478	HCT-116	colon:	n/a	n/a
4	CBX3	chr3:51894802-51895086	K562	blood:	n/a	n/a
5	CBX3	chr3:51867273-51867462	K562	blood:	n/a	n/a
6	CEBPB	chr3:51860724-51861063	A549	lung:	n/a	n/a
7	CEBPB	chr3:51860782-51860955	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr3:51879200-51879350	NHEK	skin:	n/a	n/a
9	CTCF	chr3:51879229-51879289	NHEK	skin:	n/a	n/a
10	CTCF	chr3:51894928-51894950	K562	blood:	n/a	n/a
11	CTCF	chr3:51891482-51891523	GM12891	blood:	n/a	n/a
12	CTCF	chr3:51868720-51868870	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr3:51897835-51897917	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr3:51898915-51898932	LNCaP	prostate:	n/a	n/a
15	CTCF	chr3:51879212-51879305	H1-hESC	embryonic stem cell:	n/a	n/a
16	CUX1	chr3:51878633-51878689	K562	blood:	n/a	n/a
17	EBF1	chr3:51895013-51895795	GM12878	blood:	n/a	n/a
18	EBF1	chr3:51895021-51895561	GM12878	blood:	n/a	n/a
19	EBF1	chr3:51891462-51891616	GM12878	blood:	n/a	n/a
20	EBF1	chr3:51895042-51895631	GM12878	blood:	n/a	n/a
21	EP300	chr3:51894893-51895017	K562	blood:	n/a	chr3:51894895-51894909
22	FAM48A	chr3:51870659-51870693	GM12878	blood:	n/a	n/a
23	FOS	chr3:51889648-51889649	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA2	chr3:51894756-51895165	K562	blood:	n/a	n/a
25	GATA3	chr3:51881323-51881477	SH-SY5Y	brain:	n/a	n/a
26	HEY1	chr3:51891396-51891603	HepG2	liver:	n/a	n/a
27	HEY1	chr3:51891413-51891566	K562	blood:	n/a	n/a
28	JUN	chr3:51882466-51882467	HepG2	liver:	n/a	n/a
29	JUND	chr3:51894838-51895005	K562	blood:	n/a	n/a
30	MAFF	chr3:51894826-51895096	K562	blood:	n/a	n/a
31	MAFK	chr3:51880374-51880529	HepG2	liver:	n/a	chr3:51880493-51880508
32	MAFK	chr3:51894816-51895097	K562	blood:	n/a	n/a
33	MAFK	chr3:51883977-51884051	HepG2	liver:	n/a	n/a
34	MAX	chr3:51894839-51895064	K562	blood:	n/a	n/a
35	MAX	chr3:51895074-51895399	NB4	blood:	n/a	chr3:51895269-51895279
36	MYC	chr3:51894992-51895018	K562	blood:	n/a	n/a
37	MYC	chr3:51897332-51897358	H1-hESC	embryonic stem cell:	n/a	n/a
38	NFYA	chr3:51890326-51890525	K562	blood:	n/a	chr3:51890443-51890461
39	NFYA	chr3:51883698-51884059	K562	blood:	n/a	chr3:51883961-51883979 chr3:51884027-51884045 chr3:51884002-51884020
40	NFYB	chr3:51890191-51890521	GM12878	blood:	n/a	n/a
41	NFYB	chr3:51883742-51884311	K562	blood:	n/a	chr3:51884024-51884039 chr3:51883999-51884014 chr3:51883958-51883973
42	NFYB	chr3:51883845-51884169	Hela-S3	cervix:	n/a	chr3:51884024-51884039 chr3:51883999-51884014 chr3:51883958-51883973
43	NFYB	chr3:51883811-51884198	GM12878	blood:	n/a	chr3:51884024-51884039 chr3:51883999-51884014 chr3:51883958-51883973
44	NFYB	chr3:51890252-51890608	K562	blood:	n/a	n/a
45	NR2F2	chr3:51893236-51893603	K562	blood:	n/a	n/a
46	NR2F2	chr3:51893218-51893664	K562	blood:	n/a	n/a
47	PAX5	chr3:51891650-51892302	GM12878	blood:	n/a	n/a
48	PAX5	chr3:51888000-51888283	GM12878	blood:	n/a	n/a
49	PAX5	chr3:51892101-51892251	GM12878	blood:	n/a	n/a
50	PAX5	chr3:51891698-51892386	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51895692-51895742	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:51895692-51895742	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:51860848-51860898	GM12878	blood:	n/a
4	chr3:51895692-51895742	GM06990	blood:	n/a
5	chr3:51861098-51861148	HPAEpiC	pulmonary alveolar:	n/a
6	chr3:51892252-51892302	SKMC	muscle:	n/a
7	chr3:51861098-51861148	AG10803	skin:	n/a
8	chr3:51860848-51860898	HL-60	blood:	n/a
9	chr3:51892252-51892302	HEK293	kidney:	embryo
10	chr3:51860848-51860898	MCF-7	breast:	n/a
11	chr3:51897222-51897272	SK-N-SH	brain:	n/a
12	chr3:51864587-51864637	HCPEpiC	choroid plexus:	n/a
13	chr3:51897222-51897272	A549	lung:	n/a
14	chr3:51895692-51895742	HRPEpiC	eye:	n/a
15	chr3:51895692-51895742	MCF-7	breast:	n/a
16	chr3:51895692-51895742	HL-60	blood:	n/a
17	chr3:51860848-51860898	Hepatocyte	liver:	n/a
18	chr3:51864587-51864637	HCF	heart:	n/a
19	chr3:51861098-51861148	NHDF-neo	bronchial:	n/a
20	chr3:51860848-51860898	PFSK-1	brain:	n/a
21	chr3:51861098-51861148	U87	brain:	n/a
22	chr3:51861098-51861148	NT2-D1	testis:	n/a
23	chr3:51860848-51860898	HRCEpiC	kidney:	n/a
24	chr3:51897222-51897272	HRCEpiC	kidney:	n/a
25	chr3:51864587-51864637	K562	blood:	n/a
26	chr3:51892692-51892742	PrEC	prostate:	n/a
27	chr3:51861098-51861148	GM19239	blood:	n/a
28	chr3:51895618-51895668	AG04450	lung:	fetal
29	chr3:51861098-51861148	SK-N-MC	brain:	n/a
30	chr3:51861098-51861148	PrEC	prostate:	n/a
31	chr3:51895618-51895668	BJ	skin:	n/a
32	chr3:51895692-51895742	K562	blood:	n/a
33	chr3:51892252-51892302	AG04450	lung:	fetal
34	chr3:51892692-51892742	GM12891	blood:	n/a
35	chr3:51892692-51892742	HNPCEpiC	eye:	n/a
36	chr3:51892252-51892302	K562	blood:	n/a
37	chr3:51895618-51895668	HEEpiC	esophagus:	n/a
38	chr3:51892692-51892742	AG10803	skin:	n/a
39	chr3:51897222-51897272	HCM	heart:	n/a
40	chr3:51895618-51895668	HEK293	kidney:	embryo
41	chr3:51864587-51864637	HRE	kidney:	n/a
42	chr3:51892252-51892302	Hepatocyte	liver:	n/a
43	chr3:51897222-51897272	AG04450	lung:	fetal
44	chr3:51895692-51895742	GM12891	blood:	n/a
45	chr3:51895692-51895742	GM19239	blood:	n/a
46	chr3:51897222-51897272	IMR90	lung:	fetal
47	chr3:51897222-51897272	CMK	blood:	n/a
48	chr3:51895692-51895742	A549	lung:	n/a
49	chr3:51895692-51895742	BE2_C	brain:	n/a
50	chr3:51895618-51895668	A549	lung:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51873591..51876506-chr3:51881847..51884185,2	MCF-7	breast:
2	chr3:51862209..51864973-chr3:51975409..51978321,2	MCF-7	breast:
3	chr3:51873591..51876506-chr3:51881847..51884185,2	MCF-7	breast:
4	chr3:51878113..51880884-chr3:51974906..51977632,2	MCF-7	breast:
5	chr3:51868432..51870326-chr3:51873852..51875378,2	K562	blood:
6	chr3:51868432..51870326-chr3:51873852..51875378,2	K562	blood:
7	chr3:51859786..51864767-chr3:51865498..51870221,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IQCF2-3	chr3:51863290-51863322	NONHSAT089885
2	lnc-IQCF2-3	chr3:51863290-51863774	NONHSAT089886
3	lnc-IQCF2-3	chr3:51862667-51862823	NONHSAT089886
4	lnc-IQCF2-3	chr3:51863439-51863509	NONHSAT089885
5	lnc-IQCF2-3	chr3:51863681-51863881	NONHSAT089885
6	lnc-IQCF2-3	chr3:51862661-51862823	NONHSAT089885

No data

Variant related genes	Relation type
IQCF2	TF binding region
IQCF3	TF binding region
IQCF2	CpG island
IQCF3	CpG island
ENSG00000229972	chromatin interactions
ENSG00000114767	chromatin interactions
ENSG00000041880	chromatin interactions

Extended variants
information (count: 972 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12639503	chr3:51860817-51860818	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560959405	chr3:51860821-51860822	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534034546	chr3:51860825-51860826	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559005426	chr3:51860929-51860930	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs573764851	chr3:51860953-51860954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs544248149	chr3:51860956-51860957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562422734	chr3:51861051-51861052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546221559	chr3:51861112-51861113	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs35457982	chr3:51861119-51861120	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs367730005	chr3:51861138-51861139	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs564800055	chr3:51861141-51861142	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs561897429	chr3:51862242-51862243	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34004176	chr3:51862272-51862273	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6798175	chr3:51862276-51862277	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs544338225	chr3:51862343-51862344	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs35491658	chr3:51862354-51862355	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs397874843	chr3:51862355-51862356	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190188565	chr3:51862395-51862396	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs141730066	chr3:51862401-51862402	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181336937	chr3:51862414-51862415	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs4975944	chr3:51862421-51862422	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566669131	chr3:51862441-51862442	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs4975943	chr3:51862453-51862454	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs6805941	chr3:51862458-51862459	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549209364	chr3:51862548-51862549	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs77902261	chr3:51862550-51862551	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376742547	chr3:51862711-51862712	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs567509304	chr3:51862717-51862718	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs147097779	chr3:51862724-51862725	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs76998544	chr3:51862761-51862762	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs571307167	chr3:51862775-51862776	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs538274047	chr3:51862809-51862810	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs186857606	chr3:51862810-51862811	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs530333285	chr3:51862839-51862840	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372721535	chr3:51862858-51862859	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138536476	chr3:51862920-51862921	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs540482879	chr3:51862936-51862937	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs555629144	chr3:51862999-51863000	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573941359	chr3:51863000-51863001	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377646018	chr3:51863027-51863028	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs544769275	chr3:51863085-51863086	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs562875530	chr3:51863091-51863092	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533431195	chr3:51863138-51863139	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs545094877	chr3:51863151-51863152	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560456698	chr3:51863169-51863170	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149218474	chr3:51863185-51863186	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs548814088	chr3:51863263-51863264	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549346292	chr3:51863267-51863268	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs561146472	chr3:51863298-51863299	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs35776716	chr3:51863303-51863304	Inactive region	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51870400-51871200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:51875800-51876600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:51876600-51878600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:51878600-51879600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:51878600-51879600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:51878600-51880200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr3:51878600-51880400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:51878800-51880000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:51878800-51880000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:51878800-51880200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:51879000-51879600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr3:51879200-51879600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:51879200-51880000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:51879600-51880000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr3:51879600-51880200	Enhancers	H9 Cell Line	embryonic stem cell
16	chr3:51879600-51881400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:51879800-51880000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr3:51879800-51880400	ZNF genes & repeats	Right Atrium	heart
19	chr3:51887000-51888200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:51888200-51888400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:51888400-51889200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:51889200-51889400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:51889400-51890400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:51890400-51892000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:51890600-51891600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:51892000-51893800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:51893800-51895000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:51894600-51894800	Enhancers	GM12878-XiMat	blood
29	chr3:51894800-51895200	Flanking Active TSS	GM12878-XiMat	blood
30	chr3:51894800-51895400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:51894800-51895800	Enhancers	Primary B cells from peripheral blood	blood
32	chr3:51895000-51895200	Enhancers	Primary hematopoietic stem cells	blood
33	chr3:51895000-51895800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr3:51895200-51895400	Enhancers	GM12878-XiMat	blood
35	chr3:51895400-51895800	Flanking Active TSS	GM12878-XiMat	blood
36	chr3:51895800-51896000	Enhancers	GM12878-XiMat	blood
37	chr3:51896400-51896600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr3:51896600-51896800	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr3:51896600-51897000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:51896600-51897000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr3:51896600-51897400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:51896600-51897400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:51896800-51897200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr3:51897000-51897400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr3:51897000-51897400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr3:51897400-51902800	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr3:51897400-51902800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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