Variant report

Variant	nsv1029071
Chromosome Location	chr5:104315342-104447243
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	chr5:104369169-104369636	K562	blood:	n/a	n/a
2	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
3	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
4	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
5	BRCA1	chr5:104325896-104325918	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
7	BRCA1	chr5:104317800-104317805	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
9	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
10	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
11	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
12	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
13	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
14	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
15	CEBPB	chr5:104437342-104437690	HepG2	liver:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
16	CEBPB	chr5:104321962-104322422	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
18	CEBPB	chr5:104437422-104437706	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
19	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
20	CEBPB	chr5:104437386-104437647	IMR90	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
21	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
23	CEBPB	chr5:104369993-104370525	K562	blood:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
24	CEBPB	chr5:104437342-104437688	Hela-S3	cervix:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
25	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
26	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
27	CEBPB	chr5:104437345-104437662	A549	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
28	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
29	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
30	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
31	CEBPB	chr5:104437313-104437709	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
32	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
33	CEBPB	chr5:104334377-104334640	K562	blood:	n/a	chr5:104334524-104334537
34	CEBPB	chr5:104369982-104370331	K562	blood:	n/a	n/a
35	CEBPB	chr5:104437346-104437647	K562	blood:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
36	CEBPB	chr5:104437340-104437708	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
37	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
38	CEBPB	chr5:104437246-104437795	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
39	CEBPB	chr5:104423402-104423724	HepG2	liver:	n/a	chr5:104423566-104423577
40	CEBPB	chr5:104432081-104432193	HepG2	liver:	n/a	n/a
41	CEBPD	chr5:104369352-104369808	K562	blood:	n/a	n/a
42	CEBPD	chr5:104322765-104323144	K562	blood:	n/a	n/a
43	CHD2	chr5:104323100-104323131	K562	blood:	n/a	n/a
44	CTCF	chr5:104394548-104394560	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:104386370-104386472	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr5:104389342-104389378	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:104322420-104322570	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:104322260-104322410	BE2_C	brain:	n/a	n/a
49	CTCF	chr5:104434155-104434241	GM10248	blood:	n/a	n/a
50	CTCF	chr5:104322470-104322512	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104433849-104433899	HEK293	kidney:	embryo
2	chr5:104433849-104433899	HEK293	kidney:	embryo
3	chr5:104345171-104345221	AG09319	gingival:	n/a
4	chr5:104434864-104434914	BJ	skin:	n/a
5	chr5:104434864-104434914	MCF10A-Er-Src	breast:	n/a
6	chr5:104434827-104434877	HL-60	blood:	n/a
7	chr5:104433849-104433899	MCF-7	breast:	n/a
8	chr5:104434827-104434877	HRCEpiC	kidney:	n/a
9	chr5:104435608-104435658	HMEC	breast:	n/a
10	chr5:104434827-104434877	Hela-S3	cervix:	n/a
11	chr5:104435062-104435112	BE2_C	brain:	n/a
12	chr5:104435608-104435658	RPTEC	kidney:	n/a
13	chr5:104345171-104345221	HMEC	breast:	n/a
14	chr5:104434827-104434877	GM12892	blood:	n/a
15	chr5:104345171-104345221	HCPEpiC	choroid plexus:	n/a
16	chr5:104435062-104435112	PrEC	prostate:	n/a
17	chr5:104434827-104434877	SKMC	muscle:	n/a
18	chr5:104345171-104345221	HRCEpiC	kidney:	n/a
19	chr5:104345171-104345221	HEK293	kidney:	embryo
20	chr5:104435062-104435112	PFSK-1	brain:	n/a
21	chr5:104434827-104434877	Hepatocyte	liver:	n/a
22	chr5:104433849-104433899	AG09319	gingival:	n/a
23	chr5:104434827-104434877	U87	brain:	n/a
24	chr5:104434827-104434877	HCPEpiC	choroid plexus:	n/a
25	chr5:104345171-104345221	HRE	kidney:	n/a
26	chr5:104435062-104435112	HEEpiC	esophagus:	n/a
27	chr5:104435608-104435658	HPAEpiC	pulmonary alveolar:	n/a
28	chr5:104435062-104435112	HCT-116	colon:	n/a
29	chr5:104435608-104435658	HL-60	blood:	n/a
30	chr5:104435062-104435112	H1-hESC	embryonic stem cell:	embryo
31	chr5:104434827-104434877	HRE	kidney:	n/a
32	chr5:104345171-104345221	AG09309	skin:	n/a
33	chr5:104433849-104433899	U87	brain:	n/a
34	chr5:104434864-104434914	HepG2	liver:	n/a
35	chr5:104433849-104433899	T-47D	breast:	n/a
36	chr5:104345171-104345221	GM12891	blood:	n/a
37	chr5:104345171-104345221	GM12878	blood:	n/a
38	chr5:104345171-104345221	AG04449	skin:	fetal
39	chr5:104434864-104434914	RPTEC	kidney:	n/a
40	chr5:104434827-104434877	AG09319	gingival:	n/a
41	chr5:104435062-104435112	AG10803	skin:	n/a
42	chr5:104345171-104345221	BE2_C	brain:	n/a
43	chr5:104435062-104435112	AG04449	skin:	fetal
44	chr5:104435608-104435658	NHBE	bronchial:	n/a
45	chr5:104435062-104435112	HepG2	liver:	n/a
46	chr5:104435608-104435658	BJ	skin:	n/a
47	chr5:104435062-104435112	U87	brain:	n/a
48	chr5:104345171-104345221	GM06990	blood:	n/a
49	chr5:104433849-104433899	Hela-S3	cervix:	n/a
50	chr5:104434864-104434914	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
2	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
3	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
4	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
5	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
6	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
7	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
8	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
9	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
10	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
11	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
12	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
2	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584
3	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584
4	lnc-NUDT12-7	chr5:104315392-104315477	ENSG00000253584
5	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096

Variant related genes	Relation type
ENSG00000253584	TF binding region
RAB9BP1	TF binding region
ENSG00000253584	CpG island
RAB9BP1	CpG island
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1112 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528738165	chr5:104315403-104315404	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs551494546	chr5:104315404-104315405	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs564978992	chr5:104315405-104315406	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs530791163	chr5:104315414-104315415	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs73210379	chr5:104315422-104315423	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs529541600	chr5:104315435-104315436	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs80108303	chr5:104321210-104321211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373961415	chr5:104321233-104321234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571374077	chr5:104321243-104321244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75890009	chr5:104321245-104321246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186352314	chr5:104321259-104321260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544601978	chr5:104321278-104321279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549520087	chr5:104321309-104321310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569739609	chr5:104321334-104321335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556942936	chr5:104321336-104321337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535787563	chr5:104321400-104321401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3993310	chr5:104322016-104322017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138139649	chr5:104322032-104322033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560522900	chr5:104322068-104322069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538989569	chr5:104322076-104322077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558999490	chr5:104322096-104322097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368884191	chr5:104322100-104322101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs557163977	chr5:104322117-104322118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371559648	chr5:104322175-104322176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373298039	chr5:104322241-104322242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77272076	chr5:104322249-104322250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556761595	chr5:104322263-104322264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143521616	chr5:104322269-104322270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376753686	chr5:104322302-104322303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542820239	chr5:104322303-104322304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113874602	chr5:104322329-104322330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553651576	chr5:104322332-104322333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573155815	chr5:104322336-104322337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545012585	chr5:104322342-104322343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572654183	chr5:104322346-104322347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2964705	chr5:104322379-104322380	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183359764	chr5:104322418-104322419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs544726020	chr5:104322431-104322432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10477841	chr5:104322481-104322482	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186544719	chr5:104322529-104322530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145903254	chr5:104322548-104322549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565987996	chr5:104322558-104322559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528438613	chr5:104322563-104322564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112040542	chr5:104322588-104322589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138358621	chr5:104322596-104322597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533087157	chr5:104322600-104322601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149245374	chr5:104322607-104322608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567592434	chr5:104322627-104322628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536626770	chr5:104322647-104322648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551606476	chr5:104322650-104322651	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104321200-104321400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:104322000-104322200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:104322000-104323400	Enhancers	Fetal Intestine Small	intestine
4	chr5:104322000-104323600	Enhancers	Fetal Intestine Large	intestine
5	chr5:104322600-104324600	Enhancers	K562	blood
6	chr5:104324800-104326000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:104325200-104326400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:104369400-104369800	Enhancers	K562	blood
9	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr5:104369800-104370200	Flanking Active TSS	K562	blood
12	chr5:104370200-104370400	Enhancers	K562	blood
13	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
14	chr5:104370400-104371600	Weak transcription	K562	blood
15	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
17	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
19	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
20	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
21	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
31	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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