Variant report

Variant	nsv882404
Chromosome Location	chr5:97281641-97638743
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	chr5:97386385-97386732	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr5:97405650-97405889	GM12878	blood:	n/a	chr5:97405750-97405760 chr5:97405746-97405756
3	BCL11A	chr5:97378749-97378960	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:97628311-97628485	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:97608531-97608770	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:97397977-97398256	HepG2	liver:	n/a	chr5:97398105-97398116
7	CEBPB	chr5:97378783-97379050	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:97324361-97324490	H1-hESC	embryonic stem cell:	n/a	chr5:97324472-97324483
9	CEBPB	chr5:97398022-97398187	A549	lung:	n/a	chr5:97398105-97398116
10	CEBPB	chr5:97608471-97608702	A549	lung:	n/a	n/a
11	CEBPB	chr5:97445423-97446497	IMR90	lung:	n/a	chr5:97446047-97446060 chr5:97446049-97446060 chr5:97446049-97446060 chr5:97446047-97446060
12	CEBPB	chr5:97431799-97432246	IMR90	lung:	n/a	chr5:97431999-97432010
13	CEBPB	chr5:97523617-97523994	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:97584633-97584906	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:97325294-97325607	IMR90	lung:	n/a	n/a
16	CEBPB	chr5:97540112-97540365	HepG2	liver:	n/a	chr5:97540239-97540250
17	CEBPB	chr5:97403339-97403649	HepG2	liver:	n/a	chr5:97403516-97403527
18	CEBPB	chr5:97315569-97315781	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:97335052-97335326	HepG2	liver:	n/a	chr5:97335304-97335315 chr5:97335304-97335313
20	CEBPB	chr5:97386405-97386694	MCF-7	breast:	n/a	chr5:97386563-97386574
21	CEBPB	chr5:97386366-97386723	IMR90	lung:	n/a	chr5:97386563-97386574
22	CEBPB	chr5:97414103-97414348	A549	lung:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
23	CEBPB	chr5:97597480-97597748	IMR90	lung:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
24	CEBPB	chr5:97385404-97385851	HepG2	liver:	n/a	chr5:97385748-97385759 chr5:97385748-97385761 chr5:97385748-97385759
25	CEBPB	chr5:97414072-97414411	HepG2	liver:	n/a	chr5:97414272-97414285 chr5:97414232-97414243
26	CEBPB	chr5:97584522-97585081	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:97397978-97398244	IMR90	lung:	n/a	chr5:97398105-97398116
28	CEBPB	chr5:97403393-97403603	A549	lung:	n/a	chr5:97403516-97403527
29	CEBPB	chr5:97431855-97432188	Hela-S3	cervix:	n/a	chr5:97431999-97432010
30	CEBPB	chr5:97394381-97394670	A549	lung:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
31	CEBPB	chr5:97288323-97288547	HepG2	liver:	n/a	chr5:97288387-97288400 chr5:97288387-97288400 chr5:97288519-97288532
32	CEBPB	chr5:97431846-97432174	H1-hESC	embryonic stem cell:	n/a	chr5:97431999-97432010
33	CEBPB	chr5:97431847-97432186	HepG2	liver:	n/a	chr5:97431999-97432010
34	CEBPB	chr5:97431850-97432122	A549	lung:	n/a	chr5:97431999-97432010
35	CEBPB	chr5:97431809-97432253	MCF-7	breast:	n/a	chr5:97431999-97432010
36	CEBPB	chr5:97441968-97442351	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:97540115-97540315	A549	lung:	n/a	chr5:97540239-97540250
38	CEBPB	chr5:97386430-97386669	A549	lung:	n/a	chr5:97386563-97386574
39	CEBPB	chr5:97403339-97403632	IMR90	lung:	n/a	chr5:97403516-97403527
40	CEBPB	chr5:97597425-97597751	HepG2	liver:	n/a	chr5:97597602-97597615 chr5:97597603-97597614
41	CEBPB	chr5:97386386-97386756	Hela-S3	cervix:	n/a	chr5:97386563-97386574
42	CEBPB	chr5:97386400-97386600	K562	blood:	n/a	chr5:97386563-97386574
43	CEBPB	chr5:97386421-97386690	HepG2	liver:	n/a	chr5:97386563-97386574
44	CEBPB	chr5:97635212-97636077	IMR90	lung:	n/a	chr5:97635412-97635425
45	CEBPB	chr5:97394376-97394700	HepG2	liver:	n/a	chr5:97394544-97394557 chr5:97394544-97394555
46	CEBPB	chr5:97523691-97523908	A549	lung:	n/a	n/a
47	CEBPB	chr5:97324575-97324602	A549	lung:	n/a	n/a
48	CEBPB	chr5:97324370-97324626	HepG2	liver:	n/a	chr5:97324472-97324483
49	CEBPB	chr5:97462762-97462813	HepG2	liver:	n/a	chr5:97462789-97462800
50	CHD2	chr5:97386435-97386634	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97445281-97445331	NHBE	bronchial:	n/a
2	chr5:97445281-97445331	NHBE	bronchial:	n/a
3	chr5:97315689-97315739	HEEpiC	esophagus:	n/a
4	chr5:97315689-97315739	NHDF-neo	bronchial:	n/a
5	chr5:97445281-97445331	LNCaP	prostate:	n/a
6	chr5:97315689-97315739	T-47D	breast:	n/a
7	chr5:97315689-97315739	CMK	blood:	n/a
8	chr5:97445281-97445331	GM06990	blood:	n/a
9	chr5:97315689-97315739	A549	lung:	n/a
10	chr5:97315689-97315739	AG10803	skin:	n/a
11	chr5:97315689-97315739	Hela-S3	cervix:	n/a
12	chr5:97445281-97445331	GM12891	blood:	n/a
13	chr5:97315689-97315739	AoSMC	blood vessel:	n/a
14	chr5:97315689-97315739	Hepatocyte	liver:	n/a
15	chr5:97315689-97315739	HNPCEpiC	eye:	n/a
16	chr5:97445281-97445331	BJ	skin:	n/a
17	chr5:97445281-97445331	HEEpiC	esophagus:	n/a
18	chr5:97445281-97445331	HRCEpiC	kidney:	n/a
19	chr5:97445281-97445331	T-47D	breast:	n/a
20	chr5:97445281-97445331	HepG2	liver:	n/a
21	chr5:97315689-97315739	HCF	heart:	n/a
22	chr5:97315689-97315739	ovcar-3	ovarian:	n/a
23	chr5:97315689-97315739	PrEC	prostate:	n/a
24	chr5:97315689-97315739	HRCEpiC	kidney:	n/a
25	chr5:97445281-97445331	AG04450	lung:	fetal
26	chr5:97445281-97445331	AG09319	gingival:	n/a
27	chr5:97445281-97445331	NB4	blood:	n/a
28	chr5:97445281-97445331	NT2-D1	testis:	n/a
29	chr5:97315689-97315739	HEK293	kidney:	embryo
30	chr5:97445281-97445331	ovcar-3	ovarian:	n/a
31	chr5:97445281-97445331	HUVEC	blood vessel:	n/a
32	chr5:97445281-97445331	HCPEpiC	choroid plexus:	n/a
33	chr5:97445281-97445331	GM19239	blood:	n/a
34	chr5:97445281-97445331	SK-N-MC	brain:	n/a
35	chr5:97445281-97445331	ECC-1	luminal epithelium:	n/a
36	chr5:97445281-97445331	GM12892	blood:	n/a
37	chr5:97445281-97445331	Caco-2	colon:	n/a
38	chr5:97315689-97315739	GM12891	blood:	n/a
39	chr5:97445281-97445331	HAEpiC	amniotic membrane:	n/a
40	chr5:97445281-97445331	HL-60	blood:	n/a
41	chr5:97315689-97315739	HIPEpiC	eye:	n/a
42	chr5:97315689-97315739	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:97445281-97445331	HNPCEpiC	eye:	n/a
44	chr5:97315689-97315739	NT2-D1	testis:	n/a
45	chr5:97445281-97445331	AG10803	skin:	n/a
46	chr5:97445281-97445331	IMR90	lung:	fetal
47	chr5:97445281-97445331	SK-N-SH	brain:	n/a
48	chr5:97315689-97315739	SKMC	muscle:	n/a
49	chr5:97445281-97445331	K562	blood:	n/a
50	chr5:97315689-97315739	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
2	chr5:97615949..97618290-chr5:97620124..97621957,2	MCF-7	breast:
3	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
4	chr5:97535739..97538570-chr5:97541760..97544389,2	K562	blood:
5	chr5:97593547..97596828-chr5:97596937..97599291,3	K562	blood:
6	chr5:97535739..97538570-chr5:97541760..97544389,2	K562	blood:
7	chr5:97490515..97493248-chr5:97494183..97497100,2	K562	blood:
8	chr5:97546193..97548925-chr5:97549441..97552160,2	K562	blood:
9	chr5:97521008..97523916-chr5:97529057..97531855,2	MCF-7	breast:
10	chr5:97331985..97334979-chr5:97337146..97339738,2	K562	blood:
11	chr5:97615949..97618290-chr5:97620124..97621957,2	MCF-7	breast:
12	chr5:97521008..97523916-chr5:97529057..97531855,2	MCF-7	breast:
13	chr5:97546193..97548925-chr5:97549441..97552160,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHD1-2	chr5:97421964-97421988	XLOC_004935
2	lnc-CHD1-2	chr5:97429104-97429275	XLOC_004935
3	lnc-CHD1-2	chr5:97496010-97496123	XLOC_004935
4	lnc-CHD1-2	chr5:97496651-97496897	XLOC_004935
5	lnc-RGMB-7	chr5:97540456-97540897	NONHSAT102941
6	lnc-RGMB-7	chr5:97538763-97538843	NONHSAT102941
7	lnc-CHD1-2	chr5:97496404-97496496	XLOC_004935

Variant related genes	Relation type
ENSG00000249135	TF binding region
ENSG00000248901	TF binding region
ENSG00000249101	TF binding region
ENSG00000238000	TF binding region
ENSG00000249135	CpG island
ENSG00000248901	CpG island
ENSG00000249101	CpG island
ENSG00000238000	CpG island
ENSG00000248901	chromatin interactions
CTLA4	miRNA target sites
AQP1	miRNA target sites
ARFIP1	miRNA target sites
ACTR2	miRNA target sites
IKBKE	miRNA target sites
SEC14L1	miRNA target sites

Extended variants
information (count: 11681 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:11681 , 50 per page) page: 1 2 3 4 5 6 7 ... 234

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555400574	chr5:97291401-97291402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573284541	chr5:97291402-97291403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146523295	chr5:97291452-97291453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189185669	chr5:97291453-97291454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577324106	chr5:97291473-97291474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181544882	chr5:97291507-97291508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376046910	chr5:97291517-97291518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563900216	chr5:97291518-97291519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141077246	chr5:97291569-97291570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186482820	chr5:97291578-97291579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561460262	chr5:97291583-97291584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528462616	chr5:97291584-97291585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147109584	chr5:97297808-97297809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537078860	chr5:97297965-97297966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113111898	chr5:97297978-97297979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17087936	chr5:97298049-97298050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs200003820	chr5:97298072-97298073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113125068	chr5:97298074-97298075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57633984	chr5:97298080-97298081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547164853	chr5:97298132-97298133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190532115	chr5:97298135-97298136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2161544	chr5:97298156-97298157	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs180879136	chr5:97298174-97298175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184930032	chr5:97298184-97298185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536606512	chr5:97298188-97298189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149620313	chr5:97298192-97298193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs542515551	chr5:97307835-97307836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533747494	chr5:97307849-97307850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114809591	chr5:97307904-97307905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73772518	chr5:97307950-97307951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148878919	chr5:97307974-97307975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113836880	chr5:97308001-97308002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374270580	chr5:97308002-97308003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56041625	chr5:97308009-97308010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114355017	chr5:97308029-97308030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550499405	chr5:97308088-97308089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76727938	chr5:97308090-97308091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367667316	chr5:97308094-97308095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576548967	chr5:97308125-97308126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11959302	chr5:97308232-97308233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550739684	chr5:97308242-97308243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569437160	chr5:97308281-97308282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs555967994	chr5:97308328-97308329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs6557022	chr5:97308351-97308352	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150572464	chr5:97308358-97308359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372893328	chr5:97308372-97308373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139560060	chr5:97308376-97308377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534260186	chr5:97308383-97308384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7735809	chr5:97310604-97310605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541869765	chr5:97310651-97310652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:750 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97291400-97291600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:97297800-97298200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:97297800-97298200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:97297800-97298200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:97307800-97308400	Enhancers	Duodenum Mucosa	Duodenum
6	chr5:97310600-97321800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:97313200-97313800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:97313800-97315000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:97314800-97321400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:97315000-97315600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:97315000-97316000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr5:97315000-97316400	Enhancers	Fetal Lung	lung
13	chr5:97315400-97316600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:97315600-97316000	Enhancers	Fetal Stomach	stomach
15	chr5:97315600-97316800	Enhancers	HUVEC	blood vessel
16	chr5:97315800-97316200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:97316200-97321600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:97316400-97316600	Weak transcription	Fetal Lung	lung
19	chr5:97318200-97318400	Enhancers	Fetal Lung	lung
20	chr5:97321400-97321800	Enhancers	Osteobl	bone
21	chr5:97321400-97322400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:97321400-97322400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr5:97321400-97322600	Enhancers	NHDF-Ad	bronchial
24	chr5:97321600-97321800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:97321600-97321800	Enhancers	NH-A	brain
26	chr5:97321800-97322000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr5:97321800-97322200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:97321800-97322200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr5:97321800-97322200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:97321800-97322200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr5:97321800-97322200	Enhancers	HSMM	muscle
32	chr5:97321800-97322200	Flanking Active TSS	NH-A	brain
33	chr5:97321800-97322200	Flanking Active TSS	Osteobl	bone
34	chr5:97322000-97322200	Enhancers	NHLF	lung
35	chr5:97322200-97322400	Enhancers	NH-A	brain
36	chr5:97333200-97334600	Enhancers	Fetal Lung	lung
37	chr5:97333400-97335200	Enhancers	Brain Cingulate Gyrus	brain
38	chr5:97333600-97335400	Enhancers	Brain Anterior Caudate	brain
39	chr5:97333600-97336400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:97333800-97334600	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr5:97333800-97335600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr5:97333800-97336000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:97334000-97334200	Enhancers	Brain Hippocampus Middle	brain
44	chr5:97334000-97334800	Enhancers	Brain Angular Gyrus	brain
45	chr5:97334000-97335200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr5:97334000-97336000	Enhancers	Brain Substantia Nigra	brain
47	chr5:97334200-97335000	Enhancers	Brain Germinal Matrix	brain
48	chr5:97334400-97335000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:97334400-97335200	Weak transcription	Brain Hippocampus Middle	brain
50	chr5:97334600-97335200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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