Variant report

Variant	nsv882596
Chromosome Location	chr5:104470386-105095250
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1552)
CpG islands
(count:184)
Chromatin interactive
region (count:112)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1552 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104729126-104729280	K562	blood:	n/a	n/a
2	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
3	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
4	ARID3A	chr5:104728602-104728921	K562	blood:	n/a	n/a
5	ARID3A	chr5:104726542-104727019	K562	blood:	n/a	n/a
6	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
7	ATF1	chr5:104728486-104728895	K562	blood:	n/a	n/a
8	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
9	ATF1	chr5:105089710-105089962	K562	blood:	n/a	n/a
10	ATF1	chr5:104733331-104733371	K562	blood:	n/a	n/a
11	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
12	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
13	ATF3	chr5:104890433-104890632	K562	blood:	n/a	n/a
14	BACH1	chr5:104923763-104924073	K562	blood:	n/a	n/a
15	BACH1	chr5:104738330-104738373	K562	blood:	n/a	n/a
16	BACH1	chr5:104923724-104924138	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:104541248-104541265	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:104779909-104779930	K562	blood:	n/a	n/a
19	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr5:104928859-104929002	K562	blood:	n/a	n/a
21	BHLHE40	chr5:104728493-104728748	K562	blood:	n/a	n/a
22	BRCA1	chr5:105023264-105023360	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr5:104868861-104868905	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr5:104755081-104755354	K562	blood:	n/a	n/a
26	CBX3	chr5:104728363-104729015	K562	blood:	n/a	n/a
27	CBX3	chr5:104866542-104866887	K562	blood:	n/a	n/a
28	CBX3	chr5:104928778-104929345	K562	blood:	n/a	n/a
29	CBX3	chr5:104686453-104686733	K562	blood:	n/a	n/a
30	CBX3	chr5:104796414-104796740	K562	blood:	n/a	n/a
31	CBX3	chr5:105037977-105038410	HCT-116	colon:	n/a	n/a
32	CBX3	chr5:104699005-104699210	K562	blood:	n/a	n/a
33	CBX3	chr5:104796463-104796676	K562	blood:	n/a	n/a
34	CBX3	chr5:104866626-104866912	K562	blood:	n/a	n/a
35	CBX3	chr5:104923689-104924055	K562	blood:	n/a	n/a
36	CBX3	chr5:104728451-104728993	K562	blood:	n/a	n/a
37	CBX3	chr5:104755037-104755389	K562	blood:	n/a	n/a
38	CBX3	chr5:104939067-104939376	K562	blood:	n/a	n/a
39	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
40	CCNT2	chr5:104890165-104890637	K562	blood:	n/a	n/a
41	CCNT2	chr5:104928811-104929257	K562	blood:	n/a	n/a
42	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
43	CCNT2	chr5:104727769-104728552	K562	blood:	n/a	n/a
44	CEBPB	chr5:104876322-104876498	K562	blood:	n/a	n/a
45	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:104965103-104965346	HepG2	liver:	n/a	chr5:104965201-104965212
47	CEBPB	chr5:104890358-104890650	K562	blood:	n/a	n/a
48	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
49	CEBPB	chr5:104665990-104666190	H1-hESC	embryonic stem cell:	n/a	chr5:104666084-104666093 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666082-104666095 chr5:104666082-104666093 chr5:104666082-104666095 chr5:104666084-104666093 chr5:104666083-104666094
50	CEBPB	chr5:104709840-104710114	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104728220-104728270	T-47D	breast:	n/a
2	chr5:104728220-104728270	T-47D	breast:	n/a
3	chr5:104728220-104728270	HEK293	kidney:	embryo
4	chr5:104728220-104728270	PrEC	prostate:	n/a
5	chr5:104728427-104728477	HEK293	kidney:	embryo
6	chr5:104728220-104728270	PFSK-1	brain:	n/a
7	chr5:104728220-104728270	NT2-D1	testis:	n/a
8	chr5:104728220-104728270	NH-A	brain:	n/a
9	chr5:104728220-104728270	ProgFib	skin:	n/a
10	chr5:104728427-104728477	HAEpiC	amniotic membrane:	n/a
11	chr5:104728220-104728270	HUVEC	blood vessel:	n/a
12	chr5:104728427-104728477	AoSMC	blood vessel:	n/a
13	chr5:104728427-104728477	PANC-1	pancreas:	n/a
14	chr5:104854808-104854858	NH-A	brain:	n/a
15	chr5:104728220-104728270	U87	brain:	n/a
16	chr5:104728220-104728270	HCF	heart:	n/a
17	chr5:104728427-104728477	SK-N-SH_RA	brain:	n/a
18	chr5:104728220-104728270	HCT-116	colon:	n/a
19	chr5:104728427-104728477	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:104728427-104728477	PFSK-1	brain:	n/a
21	chr5:104854808-104854858	HRCEpiC	kidney:	n/a
22	chr5:104728427-104728477	NHDF-neo	bronchial:	n/a
23	chr5:104854808-104854858	NHBE	bronchial:	n/a
24	chr5:104728220-104728270	HIPEpiC	eye:	n/a
25	chr5:104728220-104728270	HL-60	blood:	n/a
26	chr5:104728220-104728270	NHBE	bronchial:	n/a
27	chr5:104728427-104728477	GM12891	blood:	n/a
28	chr5:104728220-104728270	RPTEC	kidney:	n/a
29	chr5:104728220-104728270	GM12878	blood:	n/a
30	chr5:104728427-104728477	HNPCEpiC	eye:	n/a
31	chr5:104728220-104728270	ECC-1	luminal epithelium:	n/a
32	chr5:104854808-104854858	HAEpiC	amniotic membrane:	n/a
33	chr5:104728427-104728477	GM12878	blood:	n/a
34	chr5:104854808-104854858	NB4	blood:	n/a
35	chr5:104728220-104728270	Jurkat	blood:	n/a
36	chr5:104854808-104854858	HCPEpiC	choroid plexus:	n/a
37	chr5:104728427-104728477	HCF	heart:	n/a
38	chr5:104728220-104728270	HCM	heart:	n/a
39	chr5:104728220-104728270	MCF10A-Er-Src	breast:	n/a
40	chr5:104728427-104728477	GM12892	blood:	n/a
41	chr5:104854808-104854858	HCT-116	colon:	n/a
42	chr5:104854808-104854858	HCF	heart:	n/a
43	chr5:104728427-104728477	HCM	heart:	n/a
44	chr5:104728220-104728270	IMR90	lung:	fetal
45	chr5:104728427-104728477	AG04450	lung:	fetal
46	chr5:104854808-104854858	HL-60	blood:	n/a
47	chr5:104854808-104854858	AG04449	skin:	fetal
48	chr5:104728427-104728477	Hela-S3	cervix:	n/a
49	chr5:104854808-104854858	Jurkat	blood:	n/a
50	chr5:104854808-104854858	NT2-D1	testis:	n/a

(count:112 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
2	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
3	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
4	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
5	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
6	chr5:104952188..104952864-chr5:105577091..105577886,5	MCF-7	breast:
7	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
8	chr5:104686842..104688917-chr5:104691899..104693400,2	K562	blood:
9	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:
10	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
11	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
12	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
13	chr5:104727296..104728816-chr5:104790778..104793743,2	K562	blood:
14	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
15	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
16	chr5:104928031..104930264-chr5:104952247..104955234,2	MCF-7	breast:
17	chr5:103843512..103846064-chr5:104654970..104657716,2	K562	blood:
18	chr5:104722652..104724763-chr5:104741861..104743629,2	K562	blood:
19	chr5:104740786..104743331-chr5:104745586..104748363,2	K562	blood:
20	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
21	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
22	chr5:104778136..104780320-chr5:104785388..104787017,2	K562	blood:
23	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
24	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
25	chr4:114611671..114612572-chr5:104870661..104871343,2	MCF-7	breast:
26	chr5:104682989..104685447-chr5:104726579..104728705,2	K562	blood:
27	chr5:104682524..104684533-chr5:104692732..104695457,2	MCF-7	breast:
28	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
29	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
30	chr5:104723018..104724952-chr5:104737690..104739211,2	K562	blood:
31	chr1:184434764..184435543-chr5:104792004..104792524,3	MCF-7	breast:
32	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
33	chr5:104805339..104808156-chr5:104810446..104813222,2	MCF-7	breast:
34	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
35	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
36	chr5:104733236..104736068-chr5:104886596..104888346,2	MCF-7	breast:
37	chr5:104955261..104956180-chr5:105577014..105577827,4	MCF-7	breast:
38	chr5:104926004..104928970-chr5:104930124..104932222,3	K562	blood:
39	chr5:104926004..104928970-chr5:104930124..104932222,3	K562	blood:
40	chr5:104712112..104715391-chr5:104727182..104729595,3	K562	blood:
41	chr5:104952005..104953083-chr5:105576858..105577888,9	MCF-7	breast:
42	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
43	chr5:104726359..104728666-chr5:105131284..105132821,2	K562	blood:
44	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
45	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
46	chr5:104729079..104730844-chr5:104733038..104734650,2	K562	blood:
47	chr5:104679097..104680828-chr5:104708980..104711591,2	K562	blood:
48	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
49	chr5:103982040..103982621-chr5:104952113..104952873,2	MCF-7	breast:
50	chr5:104833860..104836077-chr5:104839152..104841039,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
2	lnc-NUDT12-6	chr5:104728462-104728671	ENSG00000251574
3	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097
4	lnc-NUDT12-7	chr5:104728462-104728989	NONHSAT103097

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	TF binding region
ENSG00000253584	CpG island
ENSG00000251574	CpG island
ENSG00000168298	chromatin interactions
ENSG00000145743	chromatin interactions
ENSG00000251574	chromatin interactions
ENSG00000132874	chromatin interactions

Extended variants
information (count: 7178 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:7178 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs211090	chr5:104470386-104470387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370898151	chr5:104470392-104470393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562678617	chr5:104470426-104470427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200801461	chr5:104470438-104470439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531710477	chr5:104470487-104470488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557415177	chr5:104470503-104470504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548240998	chr5:104470523-104470524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560754619	chr5:104470560-104470561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373406168	chr5:104470593-104470594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549939609	chr5:104472684-104472685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371818295	chr5:104472703-104472704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569887399	chr5:104472708-104472709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114404330	chr5:104472728-104472729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549371884	chr5:104472736-104472737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566068392	chr5:104472799-104472800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143254685	chr5:104472809-104472810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188324647	chr5:104472867-104472868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181064342	chr5:104472912-104472913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578134097	chr5:104472919-104472920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115449339	chr5:104472931-104472932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556418134	chr5:104472946-104472947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148054214	chr5:104472979-104472980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542146280	chr5:104472980-104472981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140906816	chr5:104473035-104473036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564427304	chr5:104473081-104473082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572046107	chr5:104473084-104473085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111718977	chr5:104473099-104473100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558594908	chr5:104473161-104473162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185617876	chr5:104473223-104473224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145346382	chr5:104473250-104473251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs376109856	chr5:104473251-104473252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5870149	chr5:104473252-104473253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201545202	chr5:104473253-104473254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199819651	chr5:104473255-104473256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200744607	chr5:104473256-104473257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201753840	chr5:104473258-104473259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs397998915	chr5:104473266-104473267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545279293	chr5:104473308-104473309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112373460	chr5:104473325-104473326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138680403	chr5:104473340-104473341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542592768	chr5:104473394-104473395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368922470	chr5:104473396-104473397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113914947	chr5:104473415-104473416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549699282	chr5:104473488-104473489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188806111	chr5:104473516-104473517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs294158	chr5:104473561-104473562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181652270	chr5:104473602-104473603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186845630	chr5:104473649-104473650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537560371	chr5:104473751-104473752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557442480	chr5:104473764-104473765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104469400-104470600	Enhancers	Liver	Liver
2	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
8	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
9	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
10	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
11	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
12	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
17	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast
20	chr5:104541800-104542600	Enhancers	Brain Germinal Matrix	brain
21	chr5:104550000-104550400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:104550200-104550600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:104550200-104550600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr5:104550200-104550600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:104550200-104550800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr5:104550400-104550600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:104550600-104552600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr5:104550800-104554800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:104552600-104553600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:104553000-104553800	Enhancers	Brain Germinal Matrix	brain
31	chr5:104553200-104554200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:104553600-104555200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:104554200-104554600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:104554600-104555400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr5:104554800-104555200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr5:104555000-104556600	Enhancers	Primary hematopoietic stem cells	blood
37	chr5:104555200-104555400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:104555400-104555800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:104555800-104557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:104556200-104556600	Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr5:104565200-104565400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:104565400-104565800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:104565600-104566600	Enhancers	K562	blood
44	chr5:104565800-104566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:104565800-104566800	Enhancers	Colon Smooth Muscle	Colon
46	chr5:104566000-104566400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr5:104566200-104566800	Enhancers	Fetal Lung	lung
48	chr5:104566800-104567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:104567600-104567800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:104575600-104576000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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