Variant report

Variant	nsv879080
Chromosome Location	chr4:63255019-63376726
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	ARID3A	chr4:63294757-63294788	K562	blood:	n/a	n/a
2	ATF2	chr4:63320277-63320601	GM12878	blood:	n/a	n/a
3	BATF	chr4:63316519-63316715	GM12878	blood:	n/a	n/a
4	BATF	chr4:63265074-63265292	GM12878	blood:	n/a	n/a
5	BATF	chr4:63320363-63320586	GM12878	blood:	n/a	chr4:63320448-63320461
6	BATF	chr4:63295100-63295326	GM12878	blood:	n/a	chr4:63295282-63295292
7	BATF	chr4:63295109-63295356	GM12878	blood:	n/a	chr4:63295282-63295292
8	BHLHE40	chr4:63268010-63268204	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:63360833-63361155	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:63265023-63265324	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:63280760-63280912	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:63258394-63258425	GM12878	blood:	n/a	n/a
13	CCNT2	chr4:63279209-63279409	K562	blood:	n/a	n/a
14	CEBPB	chr4:63364784-63365082	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:63311320-63311637	HepG2	liver:	n/a	chr4:63311445-63311456
16	CEBPB	chr4:63366019-63366339	IMR90	lung:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
17	CEBPB	chr4:63298894-63299142	HepG2	liver:	n/a	chr4:63299025-63299036 chr4:63299024-63299035
18	CEBPB	chr4:63318348-63318604	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:63297137-63297651	GM12878	blood:	n/a	n/a
20	CEBPB	chr4:63366031-63366359	HepG2	liver:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
21	CEBPB	chr4:63320833-63320835	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:63366022-63366367	K562	blood:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
23	CEBPB	chr4:63364801-63365006	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:63311317-63311630	IMR90	lung:	n/a	chr4:63311445-63311456
25	CEBPB	chr4:63366058-63366371	H1-hESC	embryonic stem cell:	n/a	chr4:63366200-63366213 chr4:63366202-63366211 chr4:63366202-63366211 chr4:63366200-63366211 chr4:63366202-63366211
26	CEBPB	chr4:63300397-63300639	HepG2	liver:	n/a	chr4:63300537-63300548
27	CEBPB	chr4:63311307-63311638	A549	lung:	n/a	chr4:63311445-63311456
28	CEBPB	chr4:63277149-63277437	IMR90	lung:	n/a	chr4:63277267-63277280
29	CHD1	chr4:63297325-63297489	GM12878	blood:	n/a	n/a
30	CHD2	chr4:63297349-63297542	GM12878	blood:	n/a	n/a
31	CREB1	chr4:63320258-63320591	GM12878	blood:	n/a	n/a
32	CREB1	chr4:63296000-63296531	GM12878	blood:	n/a	n/a
33	CREB1	chr4:63316404-63316819	GM12878	blood:	n/a	n/a
34	CTCF	chr4:63298294-63298361	GM13976	blood:	n/a	n/a
35	CTCF	chr4:63341440-63341590	BE2_C	brain:	n/a	n/a
36	CTCF	chr4:63274320-63274470	HPAF	blood vessel:	n/a	chr4:63274360-63274381
37	CTCF	chr4:63358058-63358095	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:63298288-63298293	GM13976	blood:	n/a	n/a
39	CTCF	chr4:63310205-63310270	K562	blood:	n/a	n/a
40	CTCF	chr4:63274280-63274430	HRPEpiC	eye:	n/a	chr4:63274360-63274381
41	CTCF	chr4:63274200-63274350	BE2_C	brain:	n/a	n/a
42	CTCF	chr4:63274022-63274716	SK-N-SH	brain:	n/a	chr4:63274360-63274381
43	CTCF	chr4:63315358-63315541	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:63298364-63298367	GM13976	blood:	n/a	n/a
45	CTCF	chr4:63315460-63315610	HMEC	breast:	n/a	n/a
46	CTCF	chr4:63274304-63274408	LNCaP	prostate:	n/a	chr4:63274360-63274381
47	CTCF	chr4:63309060-63309210	GM12869	blood:	n/a	n/a
48	CTCF	chr4:63376120-63376270	GM12866	blood:	n/a	n/a
49	CTCF	chr4:63274320-63274470	SK-N-SH_RA	brain:	n/a	chr4:63274360-63274381
50	CTCF	chr4:63274260-63274410	HCPEpiC	choroid plexus:	n/a	chr4:63274360-63274381

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:63357670-63357720	LNCaP	prostate:	n/a
2	chr4:63357670-63357720	Jurkat	blood:	n/a
3	chr4:63357670-63357720	BJ	skin:	n/a
4	chr4:63357670-63357720	HEK293	kidney:	embryo
5	chr4:63357670-63357720	T-47D	breast:	n/a
6	chr4:63357670-63357720	HRPEpiC	eye:	n/a
7	chr4:63357670-63357720	HMEC	breast:	n/a
8	chr4:63357670-63357720	SKMC	muscle:	n/a
9	chr4:63357670-63357720	PrEC	prostate:	n/a
10	chr4:63357670-63357720	ECC-1	luminal epithelium:	n/a
11	chr4:63357670-63357720	MCF10A-Er-Src	breast:	n/a
12	chr4:63357670-63357720	SK-N-MC	brain:	n/a
13	chr4:63357670-63357720	GM19239	blood:	n/a
14	chr4:63357670-63357720	AG09319	gingival:	n/a
15	chr4:63357670-63357720	A549	lung:	n/a
16	chr4:63357670-63357720	SAEC	small airway:	n/a
17	chr4:63357670-63357720	PANC-1	pancreas:	n/a
18	chr4:63357670-63357720	NH-A	brain:	n/a
19	chr4:63357670-63357720	Hela-S3	cervix:	n/a
20	chr4:63357670-63357720	HEEpiC	esophagus:	n/a
21	chr4:63357670-63357720	HAEpiC	amniotic membrane:	n/a
22	chr4:63357670-63357720	AoSMC	blood vessel:	n/a
23	chr4:63357670-63357720	H1-hESC	embryonic stem cell:	embryo
24	chr4:63357670-63357720	K562	blood:	n/a
25	chr4:63357670-63357720	ovcar-3	ovarian:	n/a
26	chr4:63357670-63357720	HUVEC	blood vessel:	n/a
27	chr4:63357670-63357720	HPAEpiC	pulmonary alveolar:	n/a
28	chr4:63357670-63357720	HIPEpiC	eye:	n/a
29	chr4:63357670-63357720	AG09309	skin:	n/a
30	chr4:63357670-63357720	BE2_C	brain:	n/a
31	chr4:63357670-63357720	NHDF-neo	bronchial:	n/a
32	chr4:63357670-63357720	U87	brain:	n/a
33	chr4:63357670-63357720	HCM	heart:	n/a
34	chr4:63357670-63357720	GM12892	blood:	n/a
35	chr4:63357670-63357720	HCPEpiC	choroid plexus:	n/a
36	chr4:63357670-63357720	HCF	heart:	n/a
37	chr4:63357670-63357720	ProgFib	skin:	n/a
38	chr4:63357670-63357720	HRCEpiC	kidney:	n/a
39	chr4:63357670-63357720	HepG2	liver:	n/a
40	chr4:63357670-63357720	NB4	blood:	n/a
41	chr4:63357670-63357720	IMR90	lung:	fetal
42	chr4:63357670-63357720	NT2-D1	testis:	n/a
43	chr4:63357670-63357720	NHBE	bronchial:	n/a
44	chr4:63357670-63357720	SK-N-SH	brain:	n/a
45	chr4:63357670-63357720	GM12878	blood:	n/a
46	chr4:63357670-63357720	MCF-7	breast:	n/a
47	chr4:63357670-63357720	AG04449	skin:	fetal
48	chr4:63357670-63357720	Hepatocyte	liver:	n/a
49	chr4:63357670-63357720	RPTEC	kidney:	n/a
50	chr4:63357670-63357720	GM12891	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TECRL-3	chr4:63320310-63320355	XLOC_003967
2	lnc-TECRL-15	chr4:63355213-63355936	NONHSAT096630
3	lnc-TECRL-3	chr4:63316228-63316413	XLOC_003967
4	lnc-LPHN3-12	chr4:63376187-63376489	NONHSAT096631

Variant related genes	Relation type
HMGN1P11	TF binding region
ENSG00000248847	TF binding region
HMGN1P11	CpG island
ENSG00000248847	CpG island

Extended variants
information (count: 1982 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1982 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543412151	chr4:63260430-63260431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542538300	chr4:63260501-63260502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116830916	chr4:63260542-63260543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139472651	chr4:63260544-63260545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560725604	chr4:63260629-63260630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556819228	chr4:63260669-63260670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541123422	chr4:63260683-63260684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114565988	chr4:63260692-63260693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374702357	chr4:63260737-63260738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561658669	chr4:63260738-63260739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527868191	chr4:63260739-63260740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs5858761	chr4:63260744-63260745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186287034	chr4:63260753-63260754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76224277	chr4:63260769-63260770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531904533	chr4:63260811-63260812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549730649	chr4:63260822-63260823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs571627967	chr4:63260843-63260844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35167504	chr4:63260848-63260849	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547868249	chr4:63260849-63260850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545245925	chr4:63260871-63260872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566083681	chr4:63260900-63260901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190748871	chr4:63260979-63260980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1564224	chr4:63260992-63260993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142769772	chr4:63260999-63261000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537352659	chr4:63261029-63261030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558220255	chr4:63261063-63261064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576768762	chr4:63261115-63261116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540709911	chr4:63261130-63261131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553018488	chr4:63261139-63261140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146091061	chr4:63261157-63261158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115771312	chr4:63261175-63261176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs778945	chr4:63261213-63261214	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116345546	chr4:63261253-63261254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148755240	chr4:63261269-63261270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565488864	chr4:63261285-63261286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532530020	chr4:63261295-63261296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182270062	chr4:63261305-63261306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187685442	chr4:63261369-63261370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530230903	chr4:63261443-63261444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114004326	chr4:63261487-63261488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28661043	chr4:63261521-63261522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537288908	chr4:63261568-63261569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73820007	chr4:63261578-63261579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs370569000	chr4:63261602-63261603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77411967	chr4:63261613-63261614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151306751	chr4:63261634-63261635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192665212	chr4:63261743-63261744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs80082664	chr4:63261840-63261841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576229404	chr4:63261901-63261902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547350792	chr4:63261902-63261903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Medulloblastoma	21163964	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63260400-63261000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr4:63260400-63261200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr4:63260800-63261200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr4:63260800-63261200	Enhancers	Primary hematopoietic stem cells	blood
5	chr4:63260800-63261200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr4:63261200-63263600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr4:63264200-63264400	Enhancers	Left Ventricle	heart
8	chr4:63265000-63265200	Enhancers	Brain Hippocampus Middle	brain
9	chr4:63265000-63265200	Enhancers	Left Ventricle	heart
10	chr4:63265000-63265400	Enhancers	Adipose Nuclei	Adipose
11	chr4:63268000-63268400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr4:63268400-63273000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr4:63272800-63273400	Enhancers	Right Ventricle	heart
14	chr4:63273000-63273800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr4:63273200-63273800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr4:63276000-63277200	Enhancers	Fetal Heart	heart
17	chr4:63276200-63276600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:63276200-63276600	Enhancers	Left Ventricle	heart
19	chr4:63294000-63294200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr4:63295400-63295800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:63295800-63296400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:63295800-63297000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:63296200-63296800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:63297000-63297200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:63297000-63297400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:63314800-63315400	Enhancers	Fetal Brain Male	brain
27	chr4:63318200-63318600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:63318600-63320400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:63320200-63320600	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr4:63320400-63320800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:63320400-63320800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:63320400-63320800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:63320400-63321800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:63320600-63321000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr4:63321800-63322200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:63322000-63323200	Enhancers	HMEC	breast
37	chr4:63322200-63322600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr4:63322600-63323400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:63323200-63326000	Weak transcription	HMEC	breast
40	chr4:63326000-63326800	Enhancers	HMEC	breast
41	chr4:63333200-63333800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:63333400-63333800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:63335800-63336000	Active TSS	HSMM	muscle
44	chr4:63336000-63336200	Flanking Active TSS	HSMM	muscle
45	chr4:63336000-63336200	Enhancers	HSMMtube	muscle
46	chr4:63337200-63337800	Enhancers	Fetal Brain Male	brain
47	chr4:63340400-63341400	Enhancers	HMEC	breast
48	chr4:63341200-63341600	Enhancers	Fetal Muscle Leg	muscle
49	chr4:63341200-63342200	Enhancers	Spleen	Spleen
50	chr4:63341600-63341800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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