Variant report

Variant	nsv882560
Chromosome Location	chr5:104288558-104404642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:229)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:229 , 50 per page) page: 1 2 3 4 5

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	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:104317800-104317805	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr5:104325896-104325918	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
9	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
10	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
11	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
12	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
13	CCNT2	chr5:104306891-104307038	K562	blood:	n/a	n/a
14	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
16	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
17	CEBPB	chr5:104297579-104297662	HepG2	liver:	n/a	chr5:104297618-104297629 chr5:104297617-104297630
18	CEBPB	chr5:104369982-104370331	K562	blood:	n/a	n/a
19	CEBPB	chr5:104334377-104334640	K562	blood:	n/a	chr5:104334524-104334537
20	CEBPB	chr5:104321962-104322422	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
22	CEBPB	chr5:104369993-104370525	K562	blood:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
23	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
24	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
25	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
26	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
27	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
28	CEBPD	chr5:104322765-104323144	K562	blood:	n/a	n/a
29	CEBPD	chr5:104369352-104369808	K562	blood:	n/a	n/a
30	CHD2	chr5:104323100-104323131	K562	blood:	n/a	n/a
31	CTCF	chr5:104322470-104322512	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:104322420-104322570	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:104311439-104311504	GM12892	blood:	n/a	n/a
34	CTCF	chr5:104386380-104386454	GM10248	blood:	n/a	n/a
35	CTCF	chr5:104288608-104288628	Medullo	brain:	n/a	n/a
36	CTCF	chr5:104389342-104389378	MCF-7	breast:	n/a	n/a
37	CTCF	chr5:104300088-104300155	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:104322260-104322410	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:104394548-104394560	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:104297909-104297968	Lung_OC	lung:	n/a	n/a
41	CTCF	chr5:104300157-104300162	LNCaP	prostate:	n/a	n/a
42	CTCF	chr5:104305321-104305354	GM10248	blood:	n/a	n/a
43	CTCF	chr5:104311457-104311553	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:104386370-104386472	Kidney_OC	kidney:	n/a	n/a
45	CUX1	chr5:104314298-104314324	GM12878	blood:	n/a	n/a
46	CUX1	chr5:104369453-104370241	K562	blood:	n/a	n/a
47	E2F4	chr5:104358206-104358406	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr5:104378291-104378393	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:104368954-104369463	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr5:104399543-104399743	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104345171-104345221	Hepatocyte	liver:	n/a
2	chr5:104345171-104345221	HEEpiC	esophagus:	n/a
3	chr5:104345171-104345221	HIPEpiC	eye:	n/a
4	chr5:104345171-104345221	Hela-S3	cervix:	n/a
5	chr5:104345171-104345221	RPTEC	kidney:	n/a
6	chr5:104345171-104345221	CMK	blood:	n/a
7	chr5:104345171-104345221	K562	blood:	n/a
8	chr5:104345171-104345221	AoSMC	blood vessel:	n/a
9	chr5:104345171-104345221	IMR90	lung:	fetal
10	chr5:104345171-104345221	GM12892	blood:	n/a
11	chr5:104345171-104345221	MCF-7	breast:	n/a
12	chr5:104345171-104345221	H1-hESC	embryonic stem cell:	embryo
13	chr5:104345171-104345221	GM06990	blood:	n/a
14	chr5:104345171-104345221	HepG2	liver:	n/a
15	chr5:104345171-104345221	PANC-1	pancreas:	n/a
16	chr5:104345171-104345221	NT2-D1	testis:	n/a
17	chr5:104345171-104345221	SK-N-SH_RA	brain:	n/a
18	chr5:104345171-104345221	HL-60	blood:	n/a
19	chr5:104345171-104345221	GM12878	blood:	n/a
20	chr5:104345171-104345221	HMEC	breast:	n/a
21	chr5:104345171-104345221	MCF10A-Er-Src	breast:	n/a
22	chr5:104345171-104345221	Jurkat	blood:	n/a
23	chr5:104345171-104345221	T-47D	breast:	n/a
24	chr5:104345171-104345221	ProgFib	skin:	n/a
25	chr5:104345171-104345221	BE2_C	brain:	n/a
26	chr5:104345171-104345221	A549	lung:	n/a
27	chr5:104345171-104345221	GM12891	blood:	n/a
28	chr5:104345171-104345221	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:104345171-104345221	HCPEpiC	choroid plexus:	n/a
30	chr5:104345171-104345221	HRPEpiC	eye:	n/a
31	chr5:104345171-104345221	HUVEC	blood vessel:	n/a
32	chr5:104345171-104345221	SAEC	small airway:	n/a
33	chr5:104345171-104345221	HAEpiC	amniotic membrane:	n/a
34	chr5:104345171-104345221	PrEC	prostate:	n/a
35	chr5:104345171-104345221	BJ	skin:	n/a
36	chr5:104345171-104345221	HRCEpiC	kidney:	n/a
37	chr5:104345171-104345221	AG04449	skin:	fetal
38	chr5:104345171-104345221	NH-A	brain:	n/a
39	chr5:104345171-104345221	NHDF-neo	bronchial:	n/a
40	chr5:104345171-104345221	ovcar-3	ovarian:	n/a
41	chr5:104345171-104345221	ECC-1	luminal epithelium:	n/a
42	chr5:104345171-104345221	NHBE	bronchial:	n/a
43	chr5:104345171-104345221	U87	brain:	n/a
44	chr5:104345171-104345221	HNPCEpiC	eye:	n/a
45	chr5:104345171-104345221	HCT-116	colon:	n/a
46	chr5:104345171-104345221	AG04450	lung:	fetal
47	chr5:104345171-104345221	PFSK-1	brain:	n/a
48	chr5:104345171-104345221	HCF	heart:	n/a
49	chr5:104345171-104345221	Caco-2	colon:	n/a
50	chr5:104345171-104345221	SK-N-SH	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
2	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
3	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
4	chr17:57921408..57924296-chr5:104291652..104294224,2	MCF-7	breast:
5	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
6	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
7	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
8	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
9	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
10	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
11	chr5:104294786..104295742-chr9:99125283..99126098,2	MCF-7	breast:
12	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
13	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
14	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
15	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584
2	lnc-NUDT12-7	chr5:104308988-104309359	ENSG00000253584
3	lnc-NUDT12-7	chr5:104311375-104311586	ENSG00000253584
4	lnc-NUDT12-7	chr5:104315392-104315477	ENSG00000253584
5	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584

No data

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

Extended variants
information (count: 983 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:983 , 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	rs10479304	chr5:104288558-104288559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529169837	chr5:104288609-104288610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs369033213	chr5:104288612-104288613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368814552	chr5:104288619-104288620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535696447	chr5:104288636-104288637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183131728	chr5:104288647-104288648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528127947	chr5:104288680-104288681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188021561	chr5:104288697-104288698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111459504	chr5:104288703-104288704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571404509	chr5:104288722-104288723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530589031	chr5:104288738-104288739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377729713	chr5:104288743-104288744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551220300	chr5:104288751-104288752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571458489	chr5:104288765-104288766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191642157	chr5:104288865-104288866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557525830	chr5:104288960-104288961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369565598	chr5:104288965-104288966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567814853	chr5:104288979-104288980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536554282	chr5:104288996-104288997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576243524	chr5:104289034-104289035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148478827	chr5:104289055-104289056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114166142	chr5:104289064-104289065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567049206	chr5:104289068-104289069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34730510	chr5:104289165-104289166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112192789	chr5:104289191-104289192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539050879	chr5:104289232-104289233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558636613	chr5:104289250-104289251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142739758	chr5:104289291-104289292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575348730	chr5:104289295-104289296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73208397	chr5:104289305-104289306	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576934953	chr5:104289354-104289355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183426526	chr5:104289383-104289384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573457990	chr5:104289397-104289398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114425697	chr5:104289402-104289403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371237709	chr5:104289408-104289409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553021349	chr5:104289432-104289433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559630611	chr5:104289471-104289472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3844308	chr5:104289484-104289485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs368362799	chr5:104289556-104289557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3852174	chr5:104289566-104289567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541699530	chr5:104289575-104289576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564849037	chr5:104289611-104289612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs386690743	chr5:104289640-104289641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17498869	chr5:104289641-104289642	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs560956652	chr5:104289667-104289668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192441099	chr5:104289675-104289676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150977844	chr5:104289694-104289695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367548178	chr5:104289717-104289718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567188365	chr5:104289724-104289725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3852175	chr5:104289725-104289726	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104288000-104290600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:104307400-104307600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:104310000-104310200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:104310000-104310600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:104310200-104310600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:104310600-104312800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:104310600-104312800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:104312800-104313200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:104312800-104313400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:104312800-104313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:104313000-104313600	Enhancers	Aorta	Aorta
12	chr5:104321200-104321400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:104322000-104322200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:104322000-104323400	Enhancers	Fetal Intestine Small	intestine
15	chr5:104322000-104323600	Enhancers	Fetal Intestine Large	intestine
16	chr5:104322600-104324600	Enhancers	K562	blood
17	chr5:104324800-104326000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:104325200-104326400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:104369400-104369800	Enhancers	K562	blood
20	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr5:104369800-104370200	Flanking Active TSS	K562	blood
23	chr5:104370200-104370400	Enhancers	K562	blood
24	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
25	chr5:104370400-104371600	Weak transcription	K562	blood
26	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
28	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
30	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
31	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
32	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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