Variant report

Variant	nsv1034347
Chromosome Location	chr5:97062961-97241450
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	ATF2	chr5:97224163-97224479	GM12878	blood:	n/a	n/a
2	ATF2	chr5:97173832-97174381	GM12878	blood:	n/a	n/a
3	ATF2	chr5:97224125-97224557	GM12878	blood:	n/a	n/a
4	ATF2	chr5:97173902-97174280	GM12878	blood:	n/a	n/a
5	BATF	chr5:97173837-97174246	GM12878	blood:	n/a	chr5:97174165-97174175 chr5:97174107-97174117
6	BATF	chr5:97224132-97224459	GM12878	blood:	n/a	n/a
7	BATF	chr5:97224123-97224497	GM12878	blood:	n/a	n/a
8	BATF	chr5:97173882-97174325	GM12878	blood:	n/a	chr5:97174165-97174175 chr5:97174107-97174117
9	BCL11A	chr5:97224159-97224505	GM12878	blood:	n/a	chr5:97224311-97224320
10	BCL11A	chr5:97173923-97174242	GM12878	blood:	n/a	chr5:97174110-97174119 chr5:97174109-97174118 chr5:97174164-97174173
11	BCL11A	chr5:97173980-97174260	GM12878	blood:	n/a	chr5:97174110-97174119 chr5:97174109-97174118 chr5:97174164-97174173
12	BCL11A	chr5:97224140-97224399	GM12878	blood:	n/a	chr5:97224311-97224320
13	BCL3	chr5:97224086-97224486	GM12878	blood:	n/a	chr5:97224311-97224320
14	BHLHE40	chr5:97224143-97224411	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:97173921-97174267	GM12878	blood:	n/a	n/a
16	BRCA1	chr5:97205114-97205124	GM12878	blood:	n/a	n/a
17	BRCA1	chr5:97092073-97092104	GM12878	blood:	n/a	n/a
18	BRCA1	chr5:97175030-97175721	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:97173825-97174345	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr5:97173869-97174377	HCT-116	colon:	n/a	n/a
21	CCNT2	chr5:97137638-97137838	K562	blood:	n/a	n/a
22	CEBPB	chr5:97100431-97100718	A549	lung:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
23	CEBPB	chr5:97173802-97174567	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:97179837-97180102	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:97173787-97174423	HCT-116	colon:	n/a	n/a
26	CEBPB	chr5:97100307-97100770	MCF-7	breast:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
27	CEBPB	chr5:97179849-97180425	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:97182393-97182686	IMR90	lung:	n/a	n/a
29	CEBPB	chr5:97182417-97182663	MCF-7	breast:	n/a	n/a
30	CEBPB	chr5:97100446-97100707	K562	blood:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
31	CEBPB	chr5:97175289-97175447	HepG2	liver:	n/a	chr5:97175378-97175389 chr5:97175380-97175391
32	CEBPB	chr5:97173852-97174388	HCT-116	colon:	n/a	n/a
33	CEBPB	chr5:97100304-97100855	MCF-7	breast:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
34	CEBPB	chr5:97175006-97175801	Hela-S3	cervix:	n/a	chr5:97175378-97175389 chr5:97175380-97175391 chr5:97175031-97175044 chr5:97175030-97175047
35	CEBPB	chr5:97227989-97228292	HepG2	liver:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
36	CEBPB	chr5:97173876-97174272	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:97205594-97205877	HepG2	liver:	n/a	chr5:97205715-97205726
38	CEBPB	chr5:97100388-97100797	Hela-S3	cervix:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
39	CEBPB	chr5:97085589-97085836	HepG2	liver:	n/a	chr5:97085700-97085711
40	CEBPB	chr5:97205605-97205797	IMR90	lung:	n/a	chr5:97205715-97205726
41	CEBPB	chr5:97100346-97100779	IMR90	lung:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
42	CEBPB	chr5:97227985-97228252	IMR90	lung:	n/a	chr5:97228176-97228188 chr5:97228138-97228151 chr5:97228138-97228151 chr5:97228138-97228149 chr5:97228139-97228150
43	CEBPB	chr5:97202094-97202237	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:97121118-97121214	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:97070883-97071301	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:97100392-97100766	HepG2	liver:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
47	CEBPB	chr5:97135889-97136000	A549	lung:	n/a	n/a
48	CEBPB	chr5:97182424-97182719	Hela-S3	cervix:	n/a	n/a
49	CHD1	chr5:97155897-97155903	GM12878	blood:	n/a	n/a
50	CHD2	chr5:97173946-97174401	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97191292-97191342	HRE	kidney:	n/a
2	chr5:97191292-97191342	MCF10A-Er-Src	breast:	n/a
3	chr5:97191292-97191342	HEK293	kidney:	embryo
4	chr5:97191292-97191342	GM06990	blood:	n/a
5	chr5:97191292-97191342	GM12892	blood:	n/a
6	chr5:97191292-97191342	T-47D	breast:	n/a
7	chr5:97191292-97191342	NT2-D1	testis:	n/a
8	chr5:97191292-97191342	LNCaP	prostate:	n/a
9	chr5:97191292-97191342	ProgFib	skin:	n/a
10	chr5:97191292-97191342	HUVEC	blood vessel:	n/a
11	chr5:97191292-97191342	Hela-S3	cervix:	n/a
12	chr5:97191292-97191342	HRCEpiC	kidney:	n/a
13	chr5:97191292-97191342	ovcar-3	ovarian:	n/a
14	chr5:97191292-97191342	HAEpiC	amniotic membrane:	n/a
15	chr5:97191292-97191342	NB4	blood:	n/a
16	chr5:97191292-97191342	PFSK-1	brain:	n/a
17	chr5:97191292-97191342	BJ	skin:	n/a
18	chr5:97191292-97191342	CMK	blood:	n/a
19	chr5:97191292-97191342	Caco-2	colon:	n/a
20	chr5:97191292-97191342	MCF-7	breast:	n/a
21	chr5:97191292-97191342	SK-N-MC	brain:	n/a
22	chr5:97191292-97191342	A549	lung:	n/a
23	chr5:97191292-97191342	SAEC	small airway:	n/a
24	chr5:97191292-97191342	AG10803	skin:	n/a
25	chr5:97191292-97191342	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:97191292-97191342	HepG2	liver:	n/a
27	chr5:97191292-97191342	NHBE	bronchial:	n/a
28	chr5:97191292-97191342	H1-hESC	embryonic stem cell:	embryo
29	chr5:97191292-97191342	NH-A	brain:	n/a
30	chr5:97191292-97191342	HMEC	breast:	n/a
31	chr5:97191292-97191342	SK-N-SH_RA	brain:	n/a
32	chr5:97191292-97191342	RPTEC	kidney:	n/a
33	chr5:97191292-97191342	HRPEpiC	eye:	n/a
34	chr5:97191292-97191342	Jurkat	blood:	n/a
35	chr5:97191292-97191342	HCF	heart:	n/a
36	chr5:97191292-97191342	U87	brain:	n/a
37	chr5:97191292-97191342	PrEC	prostate:	n/a
38	chr5:97191292-97191342	PANC-1	pancreas:	n/a
39	chr5:97191292-97191342	BE2_C	brain:	n/a
40	chr5:97191292-97191342	AG04450	lung:	fetal
41	chr5:97191292-97191342	HEEpiC	esophagus:	n/a
42	chr5:97191292-97191342	HCT-116	colon:	n/a
43	chr5:97191292-97191342	HL-60	blood:	n/a
44	chr5:97191292-97191342	GM12891	blood:	n/a
45	chr5:97191292-97191342	IMR90	lung:	fetal
46	chr5:97191292-97191342	ECC-1	luminal epithelium:	n/a
47	chr5:97191292-97191342	AoSMC	blood vessel:	n/a
48	chr5:97191292-97191342	HNPCEpiC	eye:	n/a
49	chr5:97191292-97191342	AG09309	skin:	n/a
50	chr5:97191292-97191342	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:97162501..97165001-chr5:97167662..97169407,2	MCF-7	breast:
2	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
3	chr5:97160876..97163358-chr5:97164775..97167035,2	K562	blood:
4	chr5:97063042..97065906-chr5:97067363..97069421,2	MCF-7	breast:
5	chr5:97162501..97165001-chr5:97167662..97169407,2	MCF-7	breast:
6	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
7	chr5:97160876..97163358-chr5:97164775..97167035,2	K562	blood:
8	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
9	chr5:97113626..97116438-chr5:97121561..97123647,2	K562	blood:
10	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
11	chr5:97113626..97116438-chr5:97121561..97123647,2	K562	blood:
12	chr5:97063042..97065906-chr5:97067363..97069421,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-3	chr5:97235342-97235457	XLOC_004484
2	lnc-CTD-2215E18.1.1-3	chr5:97217132-97217271	XLOC_004484
3	lnc-CTD-2215E18.1.1-3	chr5:97217124-97217271	XLOC_004484
4	lnc-CTD-2215E18.1.1-6	chr5:97073598-97074617	NONHSAT102935

Variant related genes	Relation type
ENSG00000248202	TF binding region
ENSG00000251193	TF binding region
ENSG00000248202	CpG island
ENSG00000251193	CpG island
DNAJB12	miRNA target sites

Extended variants
information (count: 2610 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2610 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7709586	chr5:97062961-97062962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116283488	chr5:97063013-97063014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113849702	chr5:97063067-97063068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563580716	chr5:97063094-97063095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530996129	chr5:97063152-97063153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17087760	chr5:97063231-97063232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139041510	chr5:97063279-97063280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377630739	chr5:97063382-97063383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528950650	chr5:97063421-97063422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536672088	chr5:97063461-97063462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185837158	chr5:97063494-97063495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142996380	chr5:97063495-97063496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7731431	chr5:97063545-97063546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs147546799	chr5:97063547-97063548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140175487	chr5:97063602-97063603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191016273	chr5:97063609-97063610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536870687	chr5:97063723-97063724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183778558	chr5:97063728-97063729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112341022	chr5:97063767-97063768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186162027	chr5:97063776-97063777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552996291	chr5:97063792-97063793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577605577	chr5:97063879-97063880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545328797	chr5:97063883-97063884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190635126	chr5:97063922-97063923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183305867	chr5:97063923-97063924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370770911	chr5:97063956-97063957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561494697	chr5:97063967-97063968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74690079	chr5:97063971-97063972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547514478	chr5:97064100-97064101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150672473	chr5:97064107-97064108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186991251	chr5:97064130-97064131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139843667	chr5:97064166-97064167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191768207	chr5:97064174-97064175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149907248	chr5:97064201-97064202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548906605	chr5:97064204-97064205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567450633	chr5:97064216-97064217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534830861	chr5:97064242-97064243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553033469	chr5:97064249-97064250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183173786	chr5:97064259-97064260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538670589	chr5:97064284-97064285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557290726	chr5:97064346-97064347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs565905703	chr5:97064446-97064447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575859055	chr5:97064484-97064485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373877333	chr5:97064514-97064515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12651959	chr5:97064517-97064518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs554912977	chr5:97064527-97064528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573468630	chr5:97064539-97064540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369169033	chr5:97064612-97064613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541165601	chr5:97064694-97064695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144937540	chr5:97064720-97064721	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	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97059600-97064800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:97062000-97063800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr5:97063800-97064400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr5:97064200-97064600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:97064800-97065000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:97065000-97065200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr5:97066600-97067800	Enhancers	Fetal Heart	heart
8	chr5:97067000-97067600	Enhancers	Psoas Muscle	Psoas
9	chr5:97067000-97067600	Enhancers	HSMMtube	muscle
10	chr5:97069000-97075000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr5:97070400-97071800	Enhancers	HMEC	breast
12	chr5:97070600-97071800	Enhancers	NHEK	skin
13	chr5:97070800-97071200	Enhancers	HUVEC	blood vessel
14	chr5:97070800-97071200	Enhancers	NHLF	lung
15	chr5:97070800-97071400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr5:97070800-97071600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:97070800-97071600	Enhancers	Muscle Satellite Cultured Cells	--
18	chr5:97070800-97071600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:97070800-97071600	Enhancers	NHDF-Ad	bronchial
20	chr5:97070800-97071600	Enhancers	Osteobl	bone
21	chr5:97070800-97071800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:97070800-97071800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:97071200-97072000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:97071400-97072000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:97072600-97075200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr5:97085800-97086600	Enhancers	Dnd41	blood
27	chr5:97086000-97087200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr5:97086400-97087400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:97086400-97087600	Enhancers	Adipose Nuclei	Adipose
30	chr5:97091800-97092200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:97097000-97097800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:97097800-97100000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:97100000-97101200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:97100200-97100600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:97100200-97100800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr5:97100200-97100800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:97100200-97101400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:97100400-97101000	Enhancers	Muscle Satellite Cultured Cells	--
39	chr5:97107400-97107800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr5:97107600-97107800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr5:97107800-97108200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr5:97108000-97108400	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr5:97126800-97127200	Weak transcription	Gastric	stomach
44	chr5:97127200-97127400	ZNF genes & repeats	Gastric	stomach
45	chr5:97131800-97132000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:97131800-97132200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:97132000-97132800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:97132200-97133400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:97132800-97134400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:97133400-97136400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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