Variant report

Variant	nsv1025654
Chromosome Location	chr5:96613448-96817528
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:921)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr5:96691322-96691778	GM12878	blood:	n/a	n/a
3	ATF2	chr5:96736132-96736743	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:96736083-96736724	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr5:96713332-96713631	GM12878	blood:	n/a	n/a
6	BCL11A	chr5:96736252-96736517	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr5:96736211-96736597	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr5:96713335-96713673	GM12878	blood:	n/a	n/a
9	BCLAF1	chr5:96691310-96691873	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:96632712-96633177	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:96691380-96691821	GM12878	blood:	n/a	n/a
12	BRCA1	chr5:96761275-96761538	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr5:96675145-96675188	GM12878	blood:	n/a	n/a
14	CBX3	chr5:96632687-96633278	HCT-116	colon:	n/a	n/a
15	CCNT2	chr5:96691691-96691850	K562	blood:	n/a	n/a
16	CCNT2	chr5:96633727-96633849	K562	blood:	n/a	n/a
17	CEBPB	chr5:96742212-96742225	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:96767484-96767678	Hela-S3	cervix:	n/a	chr5:96767561-96767572
19	CEBPB	chr5:96767482-96767701	A549	lung:	n/a	chr5:96767561-96767572
20	CEBPB	chr5:96735911-96736086	A549	lung:	n/a	chr5:96735998-96736009
21	CEBPB	chr5:96728466-96728767	HepG2	liver:	n/a	chr5:96728592-96728603
22	CEBPB	chr5:96735870-96736169	HepG2	liver:	n/a	chr5:96735998-96736009
23	CEBPB	chr5:96658371-96658666	HepG2	liver:	n/a	chr5:96658532-96658543
24	CEBPB	chr5:96616438-96616570	IMR90	lung:	n/a	chr5:96616500-96616511
25	CEBPB	chr5:96616391-96616638	HepG2	liver:	n/a	chr5:96616500-96616511
26	CEBPB	chr5:96658415-96658662	A549	lung:	n/a	chr5:96658532-96658543
27	CEBPB	chr5:96658376-96658678	IMR90	lung:	n/a	chr5:96658532-96658543
28	CEBPB	chr5:96769639-96770035	MCF-7	breast:	n/a	n/a
29	CEBPB	chr5:96719896-96719986	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr5:96767418-96767754	MCF-7	breast:	n/a	chr5:96767561-96767572
31	CEBPB	chr5:96736408-96736660	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:96767396-96767709	HepG2	liver:	n/a	chr5:96767561-96767572
33	CEBPB	chr5:96735886-96736710	H1-hESC	embryonic stem cell:	n/a	chr5:96735998-96736009
34	CEBPB	chr5:96782630-96782690	HepG2	liver:	n/a	chr5:96782638-96782649
35	CHD1	chr5:96691326-96691347	GM12878	blood:	n/a	n/a
36	CHD2	chr5:96691511-96691972	GM12878	blood:	n/a	n/a
37	CHD2	chr5:96633012-96633158	HepG2	liver:	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	chr5:96761293-96761506	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:96633320-96633470	GM12869	blood:	n/a	n/a
42	CTCF	chr5:96632920-96633070	K562	blood:	n/a	n/a
43	CTCF	chr5:96761280-96761430	GM12870	blood:	n/a	n/a
44	CTCF	chr5:96633312-96633324	GM12892	blood:	n/a	n/a
45	CTCF	chr5:96632960-96633110	NB4	blood:	n/a	n/a
46	CTCF	chr5:96691274-96691447	GM12891	blood:	n/a	n/a
47	CTCF	chr5:96761290-96761514	GM12878	blood:	n/a	n/a
48	CTCF	chr5:96632960-96633110	HAc	cerebellar:	n/a	n/a
49	CTCF	chr5:96761320-96761470	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr5:96693788-96693874	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96789385-96789435	NHDF-neo	bronchial:	n/a
2	chr5:96789385-96789435	LNCaP	prostate:	n/a
3	chr5:96789385-96789435	Hela-S3	cervix:	n/a
4	chr5:96747223-96747273	NHDF-neo	bronchial:	n/a
5	chr5:96789385-96789435	SK-N-SH_RA	brain:	n/a
6	chr5:96747223-96747273	HAEpiC	amniotic membrane:	n/a
7	chr5:96743054-96743104	SK-N-SH_RA	brain:	n/a
8	chr5:96747223-96747273	HL-60	blood:	n/a
9	chr5:96747223-96747273	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:96742935-96742985	HAEpiC	amniotic membrane:	n/a
11	chr5:96742935-96742985	GM19239	blood:	n/a
12	chr5:96743054-96743104	K562	blood:	n/a
13	chr5:96742935-96742985	HepG2	liver:	n/a
14	chr5:96747223-96747273	GM12878	blood:	n/a
15	chr5:96742935-96742985	AG04449	skin:	fetal
16	chr5:96789385-96789435	HCT-116	colon:	n/a
17	chr5:96747223-96747273	GM12891	blood:	n/a
18	chr5:96743054-96743104	HCPEpiC	choroid plexus:	n/a
19	chr5:96789385-96789435	HRE	kidney:	n/a
20	chr5:96789385-96789435	BJ	skin:	n/a
21	chr5:96747223-96747273	AG10803	skin:	n/a
22	chr5:96743054-96743104	Hepatocyte	liver:	n/a
23	chr5:96747223-96747273	CMK	blood:	n/a
24	chr5:96747223-96747273	MCF-7	breast:	n/a
25	chr5:96789385-96789435	ProgFib	skin:	n/a
26	chr5:96789385-96789435	A549	lung:	n/a
27	chr5:96742935-96742985	HRPEpiC	eye:	n/a
28	chr5:96743054-96743104	PrEC	prostate:	n/a
29	chr5:96742935-96742985	Hela-S3	cervix:	n/a
30	chr5:96742935-96742985	HRCEpiC	kidney:	n/a
31	chr5:96747223-96747273	HEEpiC	esophagus:	n/a
32	chr5:96742935-96742985	A549	lung:	n/a
33	chr5:96789385-96789435	BE2_C	brain:	n/a
34	chr5:96743054-96743104	IMR90	lung:	fetal
35	chr5:96789385-96789435	RPTEC	kidney:	n/a
36	chr5:96789385-96789435	HCPEpiC	choroid plexus:	n/a
37	chr5:96747223-96747273	HUVEC	blood vessel:	n/a
38	chr5:96789385-96789435	AG09319	gingival:	n/a
39	chr5:96747223-96747273	NHBE	bronchial:	n/a
40	chr5:96743054-96743104	HMEC	breast:	n/a
41	chr5:96743054-96743104	AG04449	skin:	fetal
42	chr5:96743054-96743104	SK-N-MC	brain:	n/a
43	chr5:96742935-96742985	NH-A	brain:	n/a
44	chr5:96742935-96742985	HUVEC	blood vessel:	n/a
45	chr5:96747223-96747273	K562	blood:	n/a
46	chr5:96747223-96747273	GM19239	blood:	n/a
47	chr5:96747223-96747273	RPTEC	kidney:	n/a
48	chr5:96742935-96742985	HEK293	kidney:	embryo
49	chr5:96742935-96742985	SAEC	small airway:	n/a
50	chr5:96742935-96742985	AG10803	skin:	n/a

(count:29 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-1	chr5:96767448-96767604	ENSG00000251513.1
2	lnc-CTD-2215E18.1.1-5	chr5:96704480-96706125	NONHSAT102928
3	lnc-RIOK2-3	chr5:96785062-96785445	NONHSAT102929
4	lnc-CTD-2215E18.1.1-1	chr5:96772257-96772921	ENSG00000251513.1
5	lnc-RIOK2-4	chr5:96786031-96786319	NONHSAT102930

No data

Variant related genes	Relation type
ENSG00000249761	TF binding region
YTHDF1P1	TF binding region
ENSG00000249977	TF binding region
ENSG00000249761	CpG island
YTHDF1P1	CpG island
ENSG00000249977	CpG island
ENSG00000058729	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 3468 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3468 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543140728	chr5:96632806-96632807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561102082	chr5:96632816-96632817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs721801	chr5:96632830-96632831	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs546602716	chr5:96632847-96632848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186587099	chr5:96632881-96632882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs1609326	chr5:96632891-96632892	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571166640	chr5:96632904-96632905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1852739	chr5:96632947-96632948	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536728191	chr5:96632948-96632949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34356111	chr5:96632951-96632952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570410855	chr5:96632993-96632994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529502372	chr5:96632994-96632995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534559100	chr5:96633001-96633002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553007719	chr5:96633021-96633022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183642831	chr5:96633051-96633052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570197479	chr5:96633068-96633069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538964741	chr5:96633073-96633074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1609327	chr5:96633109-96633110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575422421	chr5:96633125-96633126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs75462250	chr5:96633138-96633139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561011352	chr5:96633142-96633143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1581662	chr5:96633171-96633172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs142162084	chr5:96633190-96633191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540232665	chr5:96633191-96633192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188352365	chr5:96633201-96633202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146576852	chr5:96633205-96633206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112760744	chr5:96633256-96633257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551286687	chr5:96633266-96633267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563062628	chr5:96633267-96633268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376201216	chr5:96633287-96633288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139095913	chr5:96633307-96633308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548507032	chr5:96633382-96633383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2643500	chr5:96633389-96633390	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs73780715	chr5:96633406-96633407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541136467	chr5:96633488-96633489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs148387845	chr5:96633511-96633512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75993295	chr5:96633556-96633557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571297395	chr5:96633578-96633579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1406326	chr5:96633611-96633612	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs140457537	chr5:96633653-96633654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77702220	chr5:96633670-96633671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1830367	chr5:96633720-96633721	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs554343464	chr5:96633778-96633779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181343535	chr5:96633821-96633822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540364261	chr5:96633832-96633833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558509485	chr5:96633833-96633834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113825337	chr5:96633865-96633866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150393858	chr5:96633897-96633898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563157395	chr5:96633903-96633904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2697598	chr5:96633928-96633929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:266 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96632800-96633800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr5:96632800-96633800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:96633000-96633200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:96633000-96633800	Enhancers	NHDF-Ad	bronchial
5	chr5:96633200-96633800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr5:96633200-96636600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:96633400-96633800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:96633400-96633800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr5:96636600-96637200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:96641200-96645400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:96658400-96661400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:96659600-96660400	Enhancers	NHDF-Ad	bronchial
13	chr5:96659600-96660800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:96660200-96660600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr5:96666800-96667000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
16	chr5:96666800-96667000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:96671800-96672200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:96672000-96672200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:96672200-96672400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:96675000-96675800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr5:96691000-96691200	Enhancers	GM12878-XiMat	blood
22	chr5:96691200-96691800	Enhancers	Primary B cells from peripheral blood	blood
23	chr5:96691200-96692200	Flanking Active TSS	GM12878-XiMat	blood
24	chr5:96692200-96695800	Active TSS	GM12878-XiMat	blood
25	chr5:96693400-96694000	Enhancers	NHEK	skin
26	chr5:96693800-96694000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:96698200-96699000	Enhancers	Fetal Lung	lung
28	chr5:96698400-96699400	Enhancers	Primary hematopoietic stem cells	blood
29	chr5:96699000-96699400	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr5:96699000-96700600	Weak transcription	Fetal Lung	lung
31	chr5:96699200-96699800	Enhancers	GM12878-XiMat	blood
32	chr5:96699400-96699600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr5:96699400-96699600	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:96699400-96699600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr5:96699400-96699800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr5:96699400-96699800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr5:96699400-96700000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr5:96699400-96702000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:96699600-96699800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:96699600-96699800	Enhancers	Ovary	ovary
41	chr5:96699600-96700200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:96699600-96700600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr5:96699600-96701000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr5:96699600-96703200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:96699800-96701000	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr5:96699800-96701000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:96699800-96701000	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr5:96700000-96701000	Weak transcription	Ovary	ovary
49	chr5:96700000-96701400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:96700200-96700600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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