Variant report

Variant	nsv830415
Chromosome Location	chr5:96597763-96764157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:183)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96632846-96633044	HepG2	liver:	n/a	n/a
2	ATF2	chr5:96736132-96736743	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:96736083-96736724	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:96691322-96691778	GM12878	blood:	n/a	n/a
5	BACH1	chr5:96600161-96600267	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr5:96713332-96713631	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:96736252-96736517	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr5:96736211-96736597	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr5:96713335-96713673	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:96691310-96691873	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:96632712-96633177	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:96691380-96691821	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:96761275-96761538	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr5:96675145-96675188	GM12878	blood:	n/a	n/a
15	CBX3	chr5:96632687-96633278	HCT-116	colon:	n/a	n/a
16	CCNT2	chr5:96633727-96633849	K562	blood:	n/a	n/a
17	CCNT2	chr5:96691691-96691850	K562	blood:	n/a	n/a
18	CEBPB	chr5:96658371-96658666	HepG2	liver:	n/a	chr5:96658532-96658543
19	CEBPB	chr5:96728466-96728767	HepG2	liver:	n/a	chr5:96728592-96728603
20	CEBPB	chr5:96608871-96609137	IMR90	lung:	n/a	chr5:96608957-96608968 chr5:96608979-96608990
21	CEBPB	chr5:96719896-96719986	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr5:96658376-96658678	IMR90	lung:	n/a	chr5:96658532-96658543
23	CEBPB	chr5:96608862-96609152	Hela-S3	cervix:	n/a	chr5:96608957-96608968 chr5:96608979-96608990
24	CEBPB	chr5:96608847-96609099	A549	lung:	n/a	chr5:96608957-96608968 chr5:96608979-96608990
25	CEBPB	chr5:96735870-96736169	HepG2	liver:	n/a	chr5:96735998-96736009
26	CEBPB	chr5:96735911-96736086	A549	lung:	n/a	chr5:96735998-96736009
27	CEBPB	chr5:96736408-96736660	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:96658415-96658662	A549	lung:	n/a	chr5:96658532-96658543
29	CEBPB	chr5:96742212-96742225	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:96616438-96616570	IMR90	lung:	n/a	chr5:96616500-96616511
31	CEBPB	chr5:96735886-96736710	H1-hESC	embryonic stem cell:	n/a	chr5:96735998-96736009
32	CEBPB	chr5:96604141-96604264	A549	lung:	n/a	n/a
33	CEBPB	chr5:96608816-96609112	HepG2	liver:	n/a	chr5:96608957-96608968 chr5:96608979-96608990
34	CEBPB	chr5:96616391-96616638	HepG2	liver:	n/a	chr5:96616500-96616511
35	CHD1	chr5:96691326-96691347	GM12878	blood:	n/a	n/a
36	CHD2	chr5:96633012-96633158	HepG2	liver:	n/a	n/a
37	CHD2	chr5:96691511-96691972	GM12878	blood:	n/a	n/a
38	CREB1	chr5:96632777-96633147	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr5:96736193-96736612	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:96632805-96633149	GM12878	blood:	n/a	n/a
41	CTCF	chr5:96763040-96763190	AG10803	skin:	n/a	n/a
42	CTCF	chr5:96761340-96761490	AG09319	gingival:	n/a	n/a
43	CTCF	chr5:96761300-96761450	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr5:96761320-96761470	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr5:96761320-96761470	AG04450	lung:	n/a	n/a
46	CTCF	chr5:96691220-96691370	GM12867	blood:	n/a	n/a
47	CTCF	chr5:96761280-96761430	HEK293	kidney:	n/a	n/a
48	CTCF	chr5:96633187-96633200	GM12891	blood:	n/a	n/a
49	CTCF	chr5:96632920-96633070	GM12878	blood:	n/a	n/a
50	CTCF	chr5:96609420-96609570	BE2_C	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96743054-96743104	RPTEC	kidney:	n/a
2	chr5:96747223-96747273	HRE	kidney:	n/a
3	chr5:96747223-96747273	HNPCEpiC	eye:	n/a
4	chr5:96747223-96747273	GM12891	blood:	n/a
5	chr5:96743054-96743104	K562	blood:	n/a
6	chr5:96747223-96747273	Jurkat	blood:	n/a
7	chr5:96743054-96743104	BJ	skin:	n/a
8	chr5:96747223-96747273	HCT-116	colon:	n/a
9	chr5:96742935-96742985	NHDF-neo	bronchial:	n/a
10	chr5:96747223-96747273	IMR90	lung:	fetal
11	chr5:96742935-96742985	HMEC	breast:	n/a
12	chr5:96743054-96743104	HNPCEpiC	eye:	n/a
13	chr5:96747223-96747273	GM06990	blood:	n/a
14	chr5:96742935-96742985	HepG2	liver:	n/a
15	chr5:96743054-96743104	PrEC	prostate:	n/a
16	chr5:96747223-96747273	HEEpiC	esophagus:	n/a
17	chr5:96742935-96742985	GM06990	blood:	n/a
18	chr5:96743054-96743104	HCT-116	colon:	n/a
19	chr5:96742935-96742985	PANC-1	pancreas:	n/a
20	chr5:96742935-96742985	Caco-2	colon:	n/a
21	chr5:96743054-96743104	A549	lung:	n/a
22	chr5:96747223-96747273	AG10803	skin:	n/a
23	chr5:96747223-96747273	U87	brain:	n/a
24	chr5:96742935-96742985	AG10803	skin:	n/a
25	chr5:96742935-96742985	Hepatocyte	liver:	n/a
26	chr5:96743054-96743104	AG09319	gingival:	n/a
27	chr5:96742935-96742985	HRPEpiC	eye:	n/a
28	chr5:96742935-96742985	U87	brain:	n/a
29	chr5:96742935-96742985	GM12891	blood:	n/a
30	chr5:96747223-96747273	SKMC	muscle:	n/a
31	chr5:96743054-96743104	GM12892	blood:	n/a
32	chr5:96747223-96747273	RPTEC	kidney:	n/a
33	chr5:96743054-96743104	AoSMC	blood vessel:	n/a
34	chr5:96747223-96747273	K562	blood:	n/a
35	chr5:96742935-96742985	BJ	skin:	n/a
36	chr5:96743054-96743104	HCM	heart:	n/a
37	chr5:96747223-96747273	ovcar-3	ovarian:	n/a
38	chr5:96743054-96743104	HRCEpiC	kidney:	n/a
39	chr5:96747223-96747273	HEK293	kidney:	embryo
40	chr5:96743054-96743104	HRPEpiC	eye:	n/a
41	chr5:96747223-96747273	AoSMC	blood vessel:	n/a
42	chr5:96747223-96747273	CMK	blood:	n/a
43	chr5:96743054-96743104	NT2-D1	testis:	n/a
44	chr5:96743054-96743104	ECC-1	luminal epithelium:	n/a
45	chr5:96743054-96743104	HCF	heart:	n/a
46	chr5:96743054-96743104	SKMC	muscle:	n/a
47	chr5:96742935-96742985	HCM	heart:	n/a
48	chr5:96742935-96742985	PrEC	prostate:	n/a
49	chr5:96743054-96743104	GM12891	blood:	n/a
50	chr5:96743054-96743104	AG09309	skin:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
2	chr5:96518180..96520707-chr5:96752048..96753718,2	K562	blood:
3	chr5:96697302..96697824-chr5:146587593..146588113,2	Hela-S3	cervix:
4	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
5	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
6	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
7	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
8	chr17:41464548..41466257-chr5:96697324..96698824,2	MCF-7	breast:
9	chr3:73159507..73161444-chr5:96697302..96698824,2	K562	blood:
10	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
11	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
12	chr17:41380182..41383629-chr5:96695802..96698822,5	K562	blood:
13	chr17:41398650..41400853-chr5:96695801..96698804,5	K562	blood:
14	chr17:41463734..41465366-chr5:96695802..96697324,2	MCF-7	breast:
15	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
16	chr17:41398860..41401971-chr5:96695801..96698802,6	K562	blood:
17	chr5:96735260..96736761-chr7:31786509..31788468,2	MCF-7	breast:
18	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
19	chr17:41380186..41382311-chr5:96695804..96697321,3	MCF-7	breast:
20	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
21	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
22	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
23	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
24	chr17:41462273..41467084-chr5:96695804..96698803,5	K562	blood:
25	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
26	chr17:41380182..41383606-chr5:96695801..96698822,3	K562	blood:
27	chr17:41398605..41400432-chr5:96695803..96698802,4	MCF-7	breast:
28	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-5	chr5:96704480-96706125	NONHSAT102928

No data

Variant related genes	Relation type
ENSG00000249761	TF binding region
YTHDF1P1	TF binding region
ENSG00000249761	CpG island
YTHDF1P1	CpG island
ENSG00000058729	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2982 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2982 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34385977	chr5:96601022-96601023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76859864	chr5:96601044-96601045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551820709	chr5:96601058-96601059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35949841	chr5:96601076-96601077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563701018	chr5:96601154-96601155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531214076	chr5:96601171-96601172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185178918	chr5:96601215-96601216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190057792	chr5:96601216-96601217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181888837	chr5:96601259-96601260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71654364	chr5:96601284-96601285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565662129	chr5:96601285-96601286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571639033	chr5:96601290-96601291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539177014	chr5:96601299-96601300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186532131	chr5:96601325-96601326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557318152	chr5:96601336-96601337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569355481	chr5:96601367-96601368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs536942782	chr5:96601431-96601432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2548419	chr5:96601508-96601509	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs573738057	chr5:96601509-96601510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144857678	chr5:96601513-96601514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138453253	chr5:96601533-96601534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111580395	chr5:96601571-96601572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189836758	chr5:96601598-96601599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373455392	chr5:96601754-96601755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35724466	chr5:96601755-96601756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs5869749	chr5:96601758-96601759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563663880	chr5:96601844-96601845	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530931977	chr5:96601859-96601860	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115553850	chr5:96601885-96601886	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1528598	chr5:96601924-96601925	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs528658108	chr5:96601940-96601941	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116350477	chr5:96601967-96601968	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553193414	chr5:96601969-96601970	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571845956	chr5:96601990-96601991	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142981626	chr5:96602010-96602011	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551110844	chr5:96602022-96602023	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569260227	chr5:96602031-96602032	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536655177	chr5:96602032-96602033	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1528599	chr5:96602047-96602048	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs374057179	chr5:96602075-96602076	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534945754	chr5:96602123-96602124	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78190599	chr5:96602162-96602163	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577953034	chr5:96602209-96602210	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545515317	chr5:96602231-96602232	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181030714	chr5:96602283-96602284	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185996719	chr5:96602294-96602295	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367899521	chr5:96602299-96602300	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542679280	chr5:96602337-96602338	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561364990	chr5:96602354-96602355	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191243761	chr5:96602358-96602359	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96601000-96601800	Enhancers	Fetal Muscle Leg	muscle
2	chr5:96601400-96601800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:96601400-96603800	Enhancers	Adipose Nuclei	Adipose
4	chr5:96601800-96602200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr5:96601800-96602200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:96601800-96602400	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:96602200-96602400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr5:96602200-96602600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:96602200-96602800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:96602400-96602600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:96602400-96602600	Enhancers	Fetal Muscle Leg	muscle
12	chr5:96602600-96602800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:96602800-96603000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:96603000-96604200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr5:96603400-96603800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:96603400-96603800	Enhancers	Brain Anterior Caudate	brain
17	chr5:96607800-96609200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:96609200-96609600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:96612400-96612800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:96612400-96612800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:96632800-96633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:96632800-96633800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr5:96633000-96633200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:96633000-96633800	Enhancers	NHDF-Ad	bronchial
25	chr5:96633200-96633800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr5:96633200-96636600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:96633400-96633800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:96633400-96633800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:96636600-96637200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:96641200-96645400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:96658400-96661400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:96659600-96660400	Enhancers	NHDF-Ad	bronchial
33	chr5:96659600-96660800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr5:96660200-96660600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:96666800-96667000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
36	chr5:96666800-96667000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:96671800-96672200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:96672000-96672200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:96672200-96672400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:96675000-96675800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr5:96691000-96691200	Enhancers	GM12878-XiMat	blood
42	chr5:96691200-96691800	Enhancers	Primary B cells from peripheral blood	blood
43	chr5:96691200-96692200	Flanking Active TSS	GM12878-XiMat	blood
44	chr5:96692200-96695800	Active TSS	GM12878-XiMat	blood
45	chr5:96693400-96694000	Enhancers	NHEK	skin
46	chr5:96693800-96694000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:96698200-96699000	Enhancers	Fetal Lung	lung
48	chr5:96698400-96699400	Enhancers	Primary hematopoietic stem cells	blood
49	chr5:96699000-96699400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr5:96699000-96700600	Weak transcription	Fetal Lung	lung

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