Variant report

Variant	nsv882562
Chromosome Location	chr5:104311833-104452655
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	chr5:104370024-104370214	K562	blood:	n/a	n/a
3	ATF1	chr5:104373680-104373755	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	chr5:104428357-104428592	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	CBX3	chr5:104370642-104370939	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	chr5:104369982-104370331	K562	blood:	n/a	n/a
15	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
16	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
17	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
18	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
19	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
20	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
21	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
22	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
23	CEBPB	chr5:104423402-104423724	HepG2	liver:	n/a	chr5:104423566-104423577
24	CEBPB	chr5:104369993-104370525	K562	blood:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
25	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
26	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
27	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
28	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
29	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
30	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
31	CEBPB	chr5:104334377-104334640	K562	blood:	n/a	chr5:104334524-104334537
32	CEBPB	chr5:104432081-104432193	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
34	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
35	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
36	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
37	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
38	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
39	CEBPB	chr5:104321962-104322422	MCF-7	breast:	n/a	n/a
40	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
41	CEBPD	chr5:104322765-104323144	K562	blood:	n/a	n/a
42	CEBPD	chr5:104369352-104369808	K562	blood:	n/a	n/a
43	CHD2	chr5:104323100-104323131	K562	blood:	n/a	n/a
44	CTCF	chr5:104448719-104448771	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:104434155-104434241	GM10248	blood:	n/a	n/a
46	CTCF	chr5:104386380-104386454	GM10248	blood:	n/a	n/a
47	CTCF	chr5:104322470-104322512	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr5:104389342-104389378	MCF-7	breast:	n/a	n/a
49	CTCF	chr5:104394548-104394560	LNCaP	prostate:	n/a	n/a
50	CTCF	chr5:104322420-104322570	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104434864-104434914	HNPCEpiC	eye:	n/a
2	chr5:104434864-104434914	HNPCEpiC	eye:	n/a
3	chr5:104435062-104435112	SK-N-SH	brain:	n/a
4	chr5:104435062-104435112	LNCaP	prostate:	n/a
5	chr5:104345171-104345221	SK-N-SH_RA	brain:	n/a
6	chr5:104345171-104345221	Hela-S3	cervix:	n/a
7	chr5:104434864-104434914	HMEC	breast:	n/a
8	chr5:104435062-104435112	ovcar-3	ovarian:	n/a
9	chr5:104433849-104433899	AG04449	skin:	fetal
10	chr5:104435062-104435112	HL-60	blood:	n/a
11	chr5:104435608-104435658	HEK293	kidney:	embryo
12	chr5:104435608-104435658	GM06990	blood:	n/a
13	chr5:104433849-104433899	HCM	heart:	n/a
14	chr5:104345171-104345221	GM12878	blood:	n/a
15	chr5:104435608-104435658	AG04450	lung:	fetal
16	chr5:104433849-104433899	NHBE	bronchial:	n/a
17	chr5:104434827-104434877	HCT-116	colon:	n/a
18	chr5:104345171-104345221	HEK293	kidney:	embryo
19	chr5:104434864-104434914	HepG2	liver:	n/a
20	chr5:104434864-104434914	HEK293	kidney:	embryo
21	chr5:104435062-104435112	AG04450	lung:	fetal
22	chr5:104435608-104435658	NHBE	bronchial:	n/a
23	chr5:104435608-104435658	HEEpiC	esophagus:	n/a
24	chr5:104434827-104434877	AoSMC	blood vessel:	n/a
25	chr5:104345171-104345221	AG09319	gingival:	n/a
26	chr5:104435062-104435112	HEEpiC	esophagus:	n/a
27	chr5:104434827-104434877	SKMC	muscle:	n/a
28	chr5:104433849-104433899	PrEC	prostate:	n/a
29	chr5:104434827-104434877	H1-hESC	embryonic stem cell:	embryo
30	chr5:104435062-104435112	NHBE	bronchial:	n/a
31	chr5:104435608-104435658	ovcar-3	ovarian:	n/a
32	chr5:104433849-104433899	AG10803	skin:	n/a
33	chr5:104435062-104435112	AG09309	skin:	n/a
34	chr5:104434827-104434877	PANC-1	pancreas:	n/a
35	chr5:104433849-104433899	GM06990	blood:	n/a
36	chr5:104435062-104435112	GM12891	blood:	n/a
37	chr5:104434827-104434877	AG04449	skin:	fetal
38	chr5:104345171-104345221	ovcar-3	ovarian:	n/a
39	chr5:104434864-104434914	GM12878	blood:	n/a
40	chr5:104433849-104433899	HCT-116	colon:	n/a
41	chr5:104433849-104433899	Caco-2	colon:	n/a
42	chr5:104434827-104434877	SK-N-SH_RA	brain:	n/a
43	chr5:104434864-104434914	NB4	blood:	n/a
44	chr5:104435062-104435112	AG09319	gingival:	n/a
45	chr5:104434827-104434877	AG09319	gingival:	n/a
46	chr5:104435608-104435658	ProgFib	skin:	n/a
47	chr5:104435608-104435658	AG09319	gingival:	n/a
48	chr5:104345171-104345221	HMEC	breast:	n/a
49	chr5:104434864-104434914	AoSMC	blood vessel:	n/a
50	chr5:104345171-104345221	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
2	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
3	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
4	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
5	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
6	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
7	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
8	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
9	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
10	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
11	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
12	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
13	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:

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

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: 1181 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10066783	chr5:104311833-104311834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375434763	chr5:104311838-104311839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56412076	chr5:104311863-104311864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557894927	chr5:104311906-104311907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184260148	chr5:104311980-104311981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540016747	chr5:104311999-104312000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188940359	chr5:104312028-104312029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532257041	chr5:104312047-104312048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192200846	chr5:104312090-104312091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530739070	chr5:104312153-104312154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574064838	chr5:104312172-104312173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12652392	chr5:104312183-104312184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs184739332	chr5:104312197-104312198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567801261	chr5:104312199-104312200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534421597	chr5:104312238-104312239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12656727	chr5:104312242-104312243	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs571133387	chr5:104312249-104312250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563425904	chr5:104312329-104312330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545229345	chr5:104312378-104312379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371729837	chr5:104312395-104312396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150748143	chr5:104312396-104312397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535832018	chr5:104312399-104312400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73777381	chr5:104312404-104312405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552538224	chr5:104312410-104312411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139407392	chr5:104312476-104312477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4703323	chr5:104312484-104312485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560051576	chr5:104312487-104312488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528789350	chr5:104312596-104312597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546928816	chr5:104312601-104312602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75545364	chr5:104312626-104312627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545741655	chr5:104312707-104312708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562423164	chr5:104312711-104312712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531241842	chr5:104312733-104312734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146481542	chr5:104312738-104312739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6866409	chr5:104312745-104312746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs539772656	chr5:104312765-104312766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147316842	chr5:104312779-104312780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527349948	chr5:104312846-104312847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34140932	chr5:104312899-104312900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35846657	chr5:104312931-104312932	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528833794	chr5:104312978-104312979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569748223	chr5:104313036-104313037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149859228	chr5:104313072-104313073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550529140	chr5:104313074-104313075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182313568	chr5:104313076-104313077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535871631	chr5:104313175-104313176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555748816	chr5:104313197-104313198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs377765510	chr5:104313220-104313221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185984677	chr5:104313302-104313303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537092210	chr5:104313304-104313305	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104310600-104312800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:104310600-104312800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:104312800-104313200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:104312800-104313400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:104312800-104313600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:104313000-104313600	Enhancers	Aorta	Aorta
7	chr5:104321200-104321400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:104322000-104322200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:104322000-104323400	Enhancers	Fetal Intestine Small	intestine
10	chr5:104322000-104323600	Enhancers	Fetal Intestine Large	intestine
11	chr5:104322600-104324600	Enhancers	K562	blood
12	chr5:104324800-104326000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:104325200-104326400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:104369400-104369800	Enhancers	K562	blood
15	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr5:104369800-104370200	Flanking Active TSS	K562	blood
18	chr5:104370200-104370400	Enhancers	K562	blood
19	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
20	chr5:104370400-104371600	Weak transcription	K562	blood
21	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
23	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
25	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
26	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
27	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
37	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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