Variant report

Variant	nsv882558
Chromosome Location	chr5:104239861-104283002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
2	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:104278321-104278989	MCF-7	breast:	n/a	n/a
4	CEBPB	chr5:104273290-104273692	Hela-S3	cervix:	n/a	chr5:104273426-104273439 chr5:104273423-104273440
5	CEBPB	chr5:104278381-104278967	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:104278464-104278803	MCF-7	breast:	n/a	n/a
7	CEBPB	chr5:104246629-104247018	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr5:104246611-104246974	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr5:104278471-104278830	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr5:104268257-104268260	Gliobla	brain:	n/a	n/a
11	CTCF	chr5:104268240-104268390	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:104268258-104268288	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:104249600-104249750	BE2_C	brain:	n/a	n/a
14	CTCF	chr5:104268240-104268390	Caco-2	colon:	n/a	n/a
15	CTCF	chr5:104268246-104268249	MCF-7	breast:	n/a	n/a
16	CTCF	chr5:104268256-104268367	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:104268319-104268324	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr5:104268261-104268324	Gliobla	brain:	n/a	n/a
19	CTCF	chr5:104268250-104268254	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:104274403-104274483	GM20000	blood:	n/a	n/a
21	CTCF	chr5:104268274-104268340	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:104268295-104268333	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:104249560-104249710	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:104268210-104268328	LNCaP	prostate:	n/a	n/a
25	CTCF	chr5:104281767-104281872	Spleen_OC	spleen:	n/a	n/a
26	E2F4	chr5:104253014-104253201	MCF10A-Er-Src	breast:	n/a	n/a
27	ELK4	chr5:104278175-104278785	Hela-S3	cervix:	n/a	n/a
28	EP300	chr5:104249508-104249993	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr5:104276898-104277665	SK-N-SH	brain:	n/a	n/a
30	EP300	chr5:104278502-104278764	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr5:104273307-104273655	Hela-S3	cervix:	n/a	chr5:104273427-104273441
32	EP300	chr5:104278448-104278833	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr5:104246519-104247127	MCF-7	breast:	n/a	n/a
34	EP300	chr5:104245506-104245885	SK-N-SH_RA	brain:	n/a	chr5:104245546-104245555
35	EP300	chr5:104242180-104242326	K562	blood:	n/a	n/a
36	EP300	chr5:104249074-104250805	SK-N-SH	brain:	n/a	chr5:104250292-104250306 chr5:104250761-104250769 chr5:104249376-104249390 chr5:104250723-104250731
37	EP300	chr5:104249508-104249809	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr5:104278279-104279085	SK-N-SH	brain:	n/a	n/a
39	EP300	chr5:104278387-104278898	Hela-S3	cervix:	n/a	n/a
40	EP300	chr5:104278284-104278952	MCF-7	breast:	n/a	n/a
41	EP300	chr5:104245533-104245803	SK-N-SH_RA	brain:	n/a	chr5:104245546-104245555
42	EP300	chr5:104246543-104247084	MCF-7	breast:	n/a	n/a
43	FOS	chr5:104246554-104246964	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr5:104278426-104279011	Hela-S3	cervix:	n/a	n/a
45	FOS	chr5:104246661-104246934	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:104246641-104246949	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr5:104246550-104246973	MCF10A-Er-Src	breast:	n/a	n/a
48	FOSL2	chr5:104246547-104246999	MCF-7	breast:	n/a	n/a
49	FOXA1	chr5:104278466-104278692	T-47D	breast:	n/a	n/a
50	FOXA1	chr5:104246614-104246888	T-47D	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104265747-104265797	GM19239	blood:	n/a
2	chr5:104265747-104265797	NB4	blood:	n/a
3	chr5:104265747-104265797	SKMC	muscle:	n/a
4	chr5:104265747-104265797	HRPEpiC	eye:	n/a
5	chr5:104265747-104265797	A549	lung:	n/a
6	chr5:104265747-104265797	U87	brain:	n/a
7	chr5:104265747-104265797	HAEpiC	amniotic membrane:	n/a
8	chr5:104265747-104265797	HepG2	liver:	n/a
9	chr5:104265747-104265797	MCF-7	breast:	n/a
10	chr5:104265747-104265797	Jurkat	blood:	n/a
11	chr5:104265747-104265797	HRCEpiC	kidney:	n/a
12	chr5:104265747-104265797	PrEC	prostate:	n/a
13	chr5:104265747-104265797	HMEC	breast:	n/a
14	chr5:104265747-104265797	CMK	blood:	n/a
15	chr5:104265747-104265797	HRE	kidney:	n/a
16	chr5:104265747-104265797	SAEC	small airway:	n/a
17	chr5:104265747-104265797	HL-60	blood:	n/a
18	chr5:104265747-104265797	PANC-1	pancreas:	n/a
19	chr5:104265747-104265797	AoSMC	blood vessel:	n/a
20	chr5:104265747-104265797	HCM	heart:	n/a
21	chr5:104265747-104265797	AG04450	lung:	fetal
22	chr5:104265747-104265797	ProgFib	skin:	n/a
23	chr5:104265747-104265797	NH-A	brain:	n/a
24	chr5:104265747-104265797	GM12878	blood:	n/a
25	chr5:104265747-104265797	PFSK-1	brain:	n/a
26	chr5:104265747-104265797	HEK293	kidney:	embryo
27	chr5:104265747-104265797	Hepatocyte	liver:	n/a
28	chr5:104265747-104265797	K562	blood:	n/a
29	chr5:104265747-104265797	NT2-D1	testis:	n/a
30	chr5:104265747-104265797	HCF	heart:	n/a
31	chr5:104265747-104265797	HEEpiC	esophagus:	n/a
32	chr5:104265747-104265797	Caco-2	colon:	n/a
33	chr5:104265747-104265797	HIPEpiC	eye:	n/a
34	chr5:104265747-104265797	ovcar-3	ovarian:	n/a
35	chr5:104265747-104265797	IMR90	lung:	fetal
36	chr5:104265747-104265797	MCF10A-Er-Src	breast:	n/a
37	chr5:104265747-104265797	RPTEC	kidney:	n/a
38	chr5:104265747-104265797	SK-N-SH_RA	brain:	n/a
39	chr5:104265747-104265797	HCT-116	colon:	n/a
40	chr5:104265747-104265797	Hela-S3	cervix:	n/a
41	chr5:104265747-104265797	BJ	skin:	n/a
42	chr5:104265747-104265797	GM12892	blood:	n/a
43	chr5:104265747-104265797	BE2_C	brain:	n/a
44	chr5:104265747-104265797	HUVEC	blood vessel:	n/a
45	chr5:104265747-104265797	ECC-1	luminal epithelium:	n/a
46	chr5:104265747-104265797	SK-N-SH	brain:	n/a
47	chr5:104265747-104265797	GM06990	blood:	n/a
48	chr5:104265747-104265797	GM12891	blood:	n/a
49	chr5:104265747-104265797	AG10803	skin:	n/a
50	chr5:104265747-104265797	SK-N-MC	brain:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
2	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
3	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
4	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
5	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
6	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
7	chr5:104245189..104247786-chr5:104277262..104279951,2	MCF-7	breast:
8	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
9	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
10	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
11	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
12	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
13	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
14	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
15	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
16	chr17:57939158..57941470-chr5:104246724..104248724,2	MCF-7	breast:
17	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104253193-104253599	ENSG00000253584
2	lnc-NUDT12-6	chr5:104246363-104246434	ENSG00000251574

No data

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

Extended variants
information (count: 929 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1153987	chr5:104239861-104239862	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73777346	chr5:104239863-104239864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560202765	chr5:104239889-104239890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572025256	chr5:104239907-104239908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552247835	chr5:104239946-104239947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563117220	chr5:104239962-104239963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546690789	chr5:104239987-104239988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370180711	chr5:104240062-104240063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548925524	chr5:104240092-104240093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181224498	chr5:104240093-104240094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534213171	chr5:104240139-104240140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547431581	chr5:104240151-104240152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570925965	chr5:104240155-104240156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185001015	chr5:104240162-104240163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556226025	chr5:104240178-104240179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568186929	chr5:104240197-104240198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189884053	chr5:104240215-104240216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554461919	chr5:104240223-104240224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574604776	chr5:104240240-104240241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540226736	chr5:104240242-104240243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559940127	chr5:104240282-104240283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181623469	chr5:104240300-104240301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545614362	chr5:104240305-104240306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs17157310	chr5:104240310-104240311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531964596	chr5:104240313-104240314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73777349	chr5:104240319-104240320	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs556921371	chr5:104240332-104240333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562375717	chr5:104240338-104240339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149094590	chr5:104240364-104240365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548065134	chr5:104240371-104240372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570794806	chr5:104240449-104240450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560191504	chr5:104240488-104240489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143060873	chr5:104240497-104240498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529292621	chr5:104240504-104240505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115647975	chr5:104240568-104240569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539739368	chr5:104240592-104240593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148225668	chr5:104240602-104240603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141125707	chr5:104240608-104240609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17157313	chr5:104240609-104240610	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs111942717	chr5:104240625-104240626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564654391	chr5:104240626-104240627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370238123	chr5:104240682-104240683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186289806	chr5:104240728-104240729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191021381	chr5:104240729-104240730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558368637	chr5:104240750-104240751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576790786	chr5:104240753-104240754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115450085	chr5:104240767-104240768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556308489	chr5:104240768-104240769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540899567	chr5:104240777-104240778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs137905835	chr5:104240781-104240782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104237800-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:104239600-104240600	Enhancers	A549	lung
3	chr5:104240200-104240800	Enhancers	HepG2	liver
4	chr5:104243000-104243200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:104243200-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:104245400-104246800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:104245400-104247200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:104245600-104246400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:104245600-104246600	Enhancers	Hela-S3	cervix
10	chr5:104245600-104247800	Active TSS	A549	lung
11	chr5:104245800-104246200	Enhancers	NHEK	skin
12	chr5:104245800-104247600	Enhancers	HMEC	breast
13	chr5:104246000-104246600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:104246000-104247000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:104246200-104246600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr5:104246200-104247000	Flanking Active TSS	NHEK	skin
17	chr5:104246400-104246600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr5:104246400-104246600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:104246400-104247600	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr5:104246600-104246800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr5:104246600-104246800	Flanking Active TSS	Hela-S3	cervix
22	chr5:104246600-104247000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr5:104246600-104247000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:104246800-104247000	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:104246800-104247000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104246800-104247200	Active TSS	Hela-S3	cervix
27	chr5:104247000-104247200	Active TSS	HUES6 Cell Line	embryonic stem cell
28	chr5:104247000-104247200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:104247000-104247200	Enhancers	NHEK	skin
30	chr5:104247000-104247400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:104247200-104247800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:104247400-104247600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr5:104247800-104250400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:104249400-104251600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:104249600-104250000	Enhancers	Fetal Brain Male	brain
36	chr5:104249600-104251000	Enhancers	Brain Germinal Matrix	brain
37	chr5:104250400-104251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr5:104250800-104251400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:104255800-104256200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:104260000-104260800	Enhancers	Fetal Intestine Large	intestine
41	chr5:104264600-104265200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:104265200-104268200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:104268200-104268400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:104268200-104268400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:104268400-104268600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:104277200-104277400	Enhancers	Fetal Intestine Large	intestine
47	chr5:104277200-104277400	Enhancers	Fetal Intestine Small	intestine
48	chr5:104277400-104278400	Weak transcription	Fetal Intestine Large	intestine
49	chr5:104277600-104283000	Weak transcription	Fetal Intestine Small	intestine
50	chr5:104277800-104278600	Enhancers	Hela-S3	cervix

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