Variant report

Variant	nsv1016611
Chromosome Location	chr5:97873846-98035559
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	BACH1	chr5:97971338-97971564	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr5:97992216-97992462	H1-hESC	embryonic stem cell:	n/a	chr5:97992446-97992455
3	BCL11A	chr5:97992250-97992404	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:97912432-97912625	K562	blood:	n/a	n/a
5	BHLHE40	chr5:97913597-97913623	GM12878	blood:	n/a	n/a
6	CCNT2	chr5:97987369-97987559	K562	blood:	n/a	n/a
7	CEBPB	chr5:97974512-97974899	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:97934775-97935102	K562	blood:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
9	CEBPB	chr5:97934752-97935098	H1-hESC	embryonic stem cell:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
10	CEBPB	chr5:97934743-97935117	IMR90	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
11	CEBPB	chr5:97934708-97935043	MCF-7	breast:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
12	CEBPB	chr5:97900586-97900903	IMR90	lung:	n/a	chr5:97900726-97900737 chr5:97900724-97900737
13	CEBPB	chr5:97934734-97935106	HepG2	liver:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
14	CEBPB	chr5:97939819-97940054	HepG2	liver:	n/a	chr5:97939901-97939912
15	CEBPB	chr5:97892415-97892773	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:97934745-97935054	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
17	CEBPB	chr5:97900029-97900266	HepG2	liver:	n/a	chr5:97900113-97900124
18	CEBPB	chr5:97958537-97958740	HepG2	liver:	n/a	chr5:97958669-97958680 chr5:97958669-97958678 chr5:97958667-97958678
19	CEBPB	chr5:97934761-97935081	Hela-S3	cervix:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
20	CEBPB	chr5:97993823-97994160	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:98034120-98034490	IMR90	lung:	n/a	chr5:98034300-98034313
22	CEBPB	chr5:97900102-97900172	A549	lung:	n/a	chr5:97900113-97900124
23	CEBPB	chr5:97874291-97874538	HepG2	liver:	n/a	chr5:97874401-97874412
24	CEBPB	chr5:97934750-97935110	A549	lung:	n/a	chr5:97934933-97934946 chr5:97934933-97934944 chr5:97935095-97935103 chr5:97934935-97934944 chr5:97934933-97934946 chr5:97934935-97934944 chr5:97934934-97934945 chr5:97934935-97934944 chr5:97934935-97934944
25	CHD2	chr5:97913543-97913562	GM12878	blood:	n/a	n/a
26	CTCF	chr5:97912320-97912470	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr5:97912440-97912590	K562	blood:	n/a	n/a
28	CTCF	chr5:97912440-97912590	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr5:97912560-97912680	GM13976	blood:	n/a	n/a
30	CTCF	chr5:97912440-97912590	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr5:97912383-97912487	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:97912714-97912777	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr5:97912684-97912689	HepG2	liver:	n/a	n/a
34	CTCF	chr5:97912437-97912718	GM12878	blood:	n/a	n/a
35	CTCF	chr5:97912432-97912772	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr5:97912404-97912499	GM13977	blood:	n/a	n/a
37	CTCF	chr5:97912440-97912590	HCFaa	heart:	n/a	n/a
38	CTCF	chr5:97912420-97912570	NB4	blood:	n/a	n/a
39	CTCF	chr5:97984640-97984790	AG10803	skin:	n/a	n/a
40	CTCF	chr5:97912340-97912490	GM12868	blood:	n/a	n/a
41	CTCF	chr5:97912426-97912707	GM12891	blood:	n/a	n/a
42	CTCF	chr5:97912394-97912465	GM10248	blood:	n/a	n/a
43	CTCF	chr5:97912440-97912590	GM06990	blood:	n/a	n/a
44	CTCF	chr5:97912288-97912510	GM10266	blood:	n/a	n/a
45	CTCF	chr5:97912408-97912717	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:97912080-97912230	GM12873	blood:	n/a	n/a
47	CTCF	chr5:97912299-97912766	K562	blood:	n/a	n/a
48	CTCF	chr5:97912360-97912510	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr5:97912320-97912470	GM12873	blood:	n/a	n/a
50	CTCF	chr5:97912440-97912590	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97912440-97912490	PFSK-1	brain:	n/a
2	chr5:97882639-97882689	HNPCEpiC	eye:	n/a
3	chr5:97912440-97912490	PFSK-1	brain:	n/a
4	chr5:97882639-97882689	HNPCEpiC	eye:	n/a
5	chr5:97992865-97992915	H1-hESC	embryonic stem cell:	embryo
6	chr5:97912440-97912490	HCM	heart:	n/a
7	chr5:97912931-97912981	T-47D	breast:	n/a
8	chr5:97903451-97903501	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:97949352-97949402	BE2_C	brain:	n/a
10	chr5:97971808-97971858	Caco-2	colon:	n/a
11	chr5:97971808-97971858	A549	lung:	n/a
12	chr5:97971808-97971858	HCPEpiC	choroid plexus:	n/a
13	chr5:97912653-97912703	AG04449	skin:	fetal
14	chr5:97903451-97903501	AG04449	skin:	fetal
15	chr5:97882639-97882689	GM12892	blood:	n/a
16	chr5:97912440-97912490	AG09309	skin:	n/a
17	chr5:97949352-97949402	NH-A	brain:	n/a
18	chr5:97912185-97912235	BJ	skin:	n/a
19	chr5:97912653-97912703	PrEC	prostate:	n/a
20	chr5:97912185-97912235	NH-A	brain:	n/a
21	chr5:97970899-97970949	GM06990	blood:	n/a
22	chr5:97992865-97992915	Caco-2	colon:	n/a
23	chr5:97892898-97892948	SK-N-SH	brain:	n/a
24	chr5:97912931-97912981	HEEpiC	esophagus:	n/a
25	chr5:97912931-97912981	K562	blood:	n/a
26	chr5:97949352-97949402	MCF-7	breast:	n/a
27	chr5:97992865-97992915	GM06990	blood:	n/a
28	chr5:97912185-97912235	LNCaP	prostate:	n/a
29	chr5:97882690-97882740	HepG2	liver:	n/a
30	chr5:97912440-97912490	ECC-1	luminal epithelium:	n/a
31	chr5:97971808-97971858	HPAEpiC	pulmonary alveolar:	n/a
32	chr5:97992865-97992915	NB4	blood:	n/a
33	chr5:97970899-97970949	HRE	kidney:	n/a
34	chr5:97892898-97892948	RPTEC	kidney:	n/a
35	chr5:97949352-97949402	U87	brain:	n/a
36	chr5:97970899-97970949	MCF-7	breast:	n/a
37	chr5:97882690-97882740	PANC-1	pancreas:	n/a
38	chr5:97912653-97912703	PFSK-1	brain:	n/a
39	chr5:97912931-97912981	HCT-116	colon:	n/a
40	chr5:97912185-97912235	T-47D	breast:	n/a
41	chr5:97912440-97912490	ProgFib	skin:	n/a
42	chr5:97882639-97882689	MCF10A-Er-Src	breast:	n/a
43	chr5:97912653-97912703	ovcar-3	ovarian:	n/a
44	chr5:97992865-97992915	HRCEpiC	kidney:	n/a
45	chr5:97912931-97912981	SK-N-MC	brain:	n/a
46	chr5:97912440-97912490	U87	brain:	n/a
47	chr5:97912440-97912490	AG04449	skin:	fetal
48	chr5:97912653-97912703	HCPEpiC	choroid plexus:	n/a
49	chr5:97882690-97882740	HMEC	breast:	n/a
50	chr5:97912185-97912235	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:114624344..114625029-chr5:97973309..97973944,2	MCF-7	breast:
2	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:
3	chr5:97880735..97882855-chr5:98107997..98110735,2	MCF-7	breast:
4	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:
5	chr5:97980901..97982903-chr5:97985969..97988620,2	K562	blood:
6	chr5:97899000..97899520-chr6:119558658..119559166,2	MCF-7	breast:
7	chr5:97966444..97968012-chr5:98368423..98370387,2	K562	blood:
8	chr5:97927404..97929282-chr5:97932064..97934664,2	K562	blood:
9	chr5:97960709..97962831-chr5:97972137..97973848,2	K562	blood:
10	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
11	chr5:97947803..97949307-chr5:97953669..97956460,2	K562	blood:
12	chr5:98006117..98008420-chr5:98011449..98013351,2	MCF-7	breast:
13	chr5:98034269..98036713-chr5:98038711..98041425,2	K562	blood:
14	chr5:97980901..97982903-chr5:97985969..97988620,2	K562	blood:
15	chr5:98006117..98008420-chr5:98011449..98013351,2	MCF-7	breast:
16	chr5:97960709..97962831-chr5:97972137..97973848,2	K562	blood:
17	chr5:97927782..97929943-chr5:97931809..97933564,2	K562	blood:

Variant related genes	Relation type
CTBP2P4	TF binding region
ENSG00000223053	TF binding region
ENSG00000251553	TF binding region
CTBP2P4	CpG island
ENSG00000223053	CpG island
ENSG00000251553	CpG island
ENSG00000174136	chromatin interactions
ENSG00000246763	chromatin interactions

Extended variants
information (count: 6039 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:6039 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77778300	chr5:97873886-97873887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115617995	chr5:97873890-97873891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs182674811	chr5:97873908-97873909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146031560	chr5:97873970-97873971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573226816	chr5:97873972-97873973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540505793	chr5:97873985-97873986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565402685	chr5:97874005-97874006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187528442	chr5:97874042-97874043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532559338	chr5:97874110-97874111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190481807	chr5:97874132-97874133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375739800	chr5:97874142-97874143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568385100	chr5:97874147-97874148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563011375	chr5:97874170-97874171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs374624252	chr5:97874190-97874191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6867574	chr5:97874200-97874201	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184111345	chr5:97874206-97874207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13179799	chr5:97874210-97874211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147478161	chr5:97874227-97874228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547635841	chr5:97874333-97874334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552421816	chr5:97874375-97874376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528430672	chr5:97874407-97874408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188675799	chr5:97874579-97874580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377595959	chr5:97874590-97874591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571423833	chr5:97874600-97874601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6868315	chr5:97874652-97874653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372013538	chr5:97874663-97874664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570968829	chr5:97874689-97874690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539550910	chr5:97874699-97874700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs559702611	chr5:97874710-97874711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193234577	chr5:97874721-97874722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs929739	chr5:97874728-97874729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs568658902	chr5:97874757-97874758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369642270	chr5:97874780-97874781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76525418	chr5:97874811-97874812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138743543	chr5:97874819-97874820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76749961	chr5:97874820-97874821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199808509	chr5:97874821-97874822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs929738	chr5:97874839-97874840	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs34068242	chr5:97874902-97874903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573115088	chr5:97875043-97875044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs6888021	chr5:97875055-97875056	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs141763317	chr5:97875069-97875070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs577426603	chr5:97875098-97875099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373020497	chr5:97875099-97875100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572327235	chr5:97875146-97875147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150768232	chr5:97875153-97875154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577896531	chr5:97875166-97875167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs3919570	chr5:97875199-97875200	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs115374843	chr5:97875214-97875215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528317377	chr5:97875242-97875243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97873400-97874000	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr5:97873400-97874200	Enhancers	H1 Cell Line	embryonic stem cell
3	chr5:97873400-97874200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:97873400-97874200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:97873400-97874200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:97873600-97874000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:97873600-97874200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:97873600-97874200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr5:97873800-97874200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:97874200-97877000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:97875000-97876200	Enhancers	NHDF-Ad	bronchial
12	chr5:97876600-97876800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr5:97877000-97882000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:97888800-97889800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:97889800-97895600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:97892400-97893000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:97892400-97893200	Enhancers	NHDF-Ad	bronchial
18	chr5:97892400-97894000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr5:97892400-97894400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr5:97892400-97894400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr5:97892600-97893000	Enhancers	NHLF	lung
22	chr5:97892600-97893200	Enhancers	NH-A	brain
23	chr5:97892600-97894400	Enhancers	Osteobl	bone
24	chr5:97893000-97894000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr5:97893000-97905200	Weak transcription	NHLF	lung
26	chr5:97893200-97893600	Weak transcription	NH-A	brain
27	chr5:97893200-97893600	Weak transcription	NHDF-Ad	bronchial
28	chr5:97893600-97894000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:97893600-97894400	Enhancers	NH-A	brain
30	chr5:97893600-97894400	Enhancers	NHDF-Ad	bronchial
31	chr5:97894000-97894600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr5:97895600-97896400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:97896400-97899200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:97897400-97897600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr5:97897400-97902800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:97897600-97898200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr5:97897800-97898200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:97898000-97899400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr5:97898000-97899600	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr5:97898200-97898400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:97898200-97898800	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:97898200-97899000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr5:97898200-97899400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:97898400-97898800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:97898400-97898800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:97898400-97898800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:97898600-97898800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:97898600-97899400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr5:97898600-97899800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr5:97898800-97899400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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