Variant report

Variant	nsv537814
Chromosome Location	chr5:96791214-97258383
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1482)
CpG islands
(count:429)
Chromatin interactive
region (count:26)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1482 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96869893-96870174	HepG2	liver:	n/a	n/a
2	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
3	ATF2	chr5:97173832-97174381	GM12878	blood:	n/a	n/a
4	ATF2	chr5:97224125-97224557	GM12878	blood:	n/a	n/a
5	ATF2	chr5:96883703-96884520	GM12878	blood:	n/a	n/a
6	ATF2	chr5:97224163-97224479	GM12878	blood:	n/a	n/a
7	ATF2	chr5:96883636-96884569	GM12878	blood:	n/a	n/a
8	ATF2	chr5:97173902-97174280	GM12878	blood:	n/a	n/a
9	BACH1	chr5:96885956-96886136	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:96861461-96861877	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr5:96883741-96884022	GM12878	blood:	n/a	n/a
12	BATF	chr5:96872418-96872668	GM12878	blood:	n/a	chr5:96872552-96872563
13	BATF	chr5:97224123-97224497	GM12878	blood:	n/a	n/a
14	BATF	chr5:96883695-96884539	GM12878	blood:	n/a	chr5:96884341-96884350
15	BATF	chr5:97224132-97224459	GM12878	blood:	n/a	n/a
16	BATF	chr5:97173882-97174325	GM12878	blood:	n/a	chr5:97174165-97174175 chr5:97174107-97174117
17	BATF	chr5:96872429-96872695	GM12878	blood:	n/a	chr5:96872552-96872563
18	BATF	chr5:96884044-96884526	GM12878	blood:	n/a	chr5:96884341-96884350
19	BATF	chr5:97173837-97174246	GM12878	blood:	n/a	chr5:97174165-97174175 chr5:97174107-97174117
20	BCL11A	chr5:96884033-96884506	GM12878	blood:	n/a	n/a
21	BCL11A	chr5:97173980-97174260	GM12878	blood:	n/a	chr5:97174110-97174119 chr5:97174109-97174118 chr5:97174164-97174173
22	BCL11A	chr5:97173923-97174242	GM12878	blood:	n/a	chr5:97174110-97174119 chr5:97174109-97174118 chr5:97174164-97174173
23	BCL11A	chr5:96883801-96884003	GM12878	blood:	n/a	chr5:96883828-96883837
24	BCL11A	chr5:97224140-97224399	GM12878	blood:	n/a	chr5:97224311-97224320
25	BCL11A	chr5:96884015-96884504	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:97224159-97224505	GM12878	blood:	n/a	chr5:97224311-97224320
27	BCL3	chr5:96928285-96928637	GM12878	blood:	n/a	n/a
28	BCL3	chr5:97224086-97224486	GM12878	blood:	n/a	chr5:97224311-97224320
29	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:96883684-96884500	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:96869825-96870150	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:97173921-97174267	GM12878	blood:	n/a	n/a
34	BHLHE40	chr5:97224143-97224411	GM12878	blood:	n/a	n/a
35	BRCA1	chr5:97175030-97175721	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr5:97173825-97174345	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr5:97205114-97205124	GM12878	blood:	n/a	n/a
38	BRCA1	chr5:97092073-97092104	GM12878	blood:	n/a	n/a
39	CBX3	chr5:97173869-97174377	HCT-116	colon:	n/a	n/a
40	CCNT2	chr5:97137638-97137838	K562	blood:	n/a	n/a
41	CEBPB	chr5:96889595-96889861	Hela-S3	cervix:	n/a	chr5:96889732-96889743 chr5:96889717-96889728
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	chr5:97100446-97100707	K562	blood:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
44	CEBPB	chr5:97205594-97205877	HepG2	liver:	n/a	chr5:97205715-97205726
45	CEBPB	chr5:97182417-97182663	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:96984114-96984366	A549	lung:	n/a	chr5:96984229-96984240
47	CEBPB	chr5:96958462-96958749	HepG2	liver:	n/a	chr5:96958584-96958595 chr5:96958604-96958615
48	CEBPB	chr5:96869837-96870355	MCF-7	breast:	n/a	chr5:96870105-96870116
49	CEBPB	chr5:97100431-97100718	A549	lung:	n/a	chr5:97100575-97100586 chr5:97100573-97100586 chr5:97100573-97100584
50	CEBPB	chr5:97173802-97174567	Hela-S3	cervix:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96890257-96890307	GM06990	blood:	n/a
2	chr5:97191292-97191342	HAEpiC	amniotic membrane:	n/a
3	chr5:96890257-96890307	GM06990	blood:	n/a
4	chr5:97191292-97191342	HAEpiC	amniotic membrane:	n/a
5	chr5:96890257-96890307	ProgFib	skin:	n/a
6	chr5:96890257-96890307	HCM	heart:	n/a
7	chr5:96876834-96876884	NH-A	brain:	n/a
8	chr5:96890257-96890307	HepG2	liver:	n/a
9	chr5:96855476-96855526	RPTEC	kidney:	n/a
10	chr5:96881859-96881909	HIPEpiC	eye:	n/a
11	chr5:96915770-96915820	NB4	blood:	n/a
12	chr5:96915770-96915820	HCF	heart:	n/a
13	chr5:96890257-96890307	BE2_C	brain:	n/a
14	chr5:96845117-96845167	NH-A	brain:	n/a
15	chr5:97191292-97191342	NH-A	brain:	n/a
16	chr5:96890257-96890307	HAEpiC	amniotic membrane:	n/a
17	chr5:96915770-96915820	SAEC	small airway:	n/a
18	chr5:96915770-96915820	HIPEpiC	eye:	n/a
19	chr5:97191292-97191342	ECC-1	luminal epithelium:	n/a
20	chr5:96855476-96855526	Hela-S3	cervix:	n/a
21	chr5:96881859-96881909	HUVEC	blood vessel:	n/a
22	chr5:96876834-96876884	ECC-1	luminal epithelium:	n/a
23	chr5:96881859-96881909	AG04450	lung:	fetal
24	chr5:96845117-96845167	GM06990	blood:	n/a
25	chr5:97191292-97191342	AG04450	lung:	fetal
26	chr5:97191292-97191342	HL-60	blood:	n/a
27	chr5:96876834-96876884	GM12878	blood:	n/a
28	chr5:96915770-96915820	GM19239	blood:	n/a
29	chr5:96845117-96845167	AG10803	skin:	n/a
30	chr5:97191292-97191342	LNCaP	prostate:	n/a
31	chr5:96876834-96876884	Hela-S3	cervix:	n/a
32	chr5:96845117-96845167	AG09319	gingival:	n/a
33	chr5:97191292-97191342	HCPEpiC	choroid plexus:	n/a
34	chr5:96881859-96881909	HNPCEpiC	eye:	n/a
35	chr5:96876834-96876884	HCF	heart:	n/a
36	chr5:96845117-96845167	SK-N-SH	brain:	n/a
37	chr5:96915770-96915820	GM12891	blood:	n/a
38	chr5:96915770-96915820	NT2-D1	testis:	n/a
39	chr5:96855476-96855526	PANC-1	pancreas:	n/a
40	chr5:96876834-96876884	AG04449	skin:	fetal
41	chr5:96855476-96855526	NT2-D1	testis:	n/a
42	chr5:96876834-96876884	PANC-1	pancreas:	n/a
43	chr5:96881859-96881909	HCM	heart:	n/a
44	chr5:96876834-96876884	GM06990	blood:	n/a
45	chr5:97191292-97191342	NT2-D1	testis:	n/a
46	chr5:96876834-96876884	HL-60	blood:	n/a
47	chr5:96881859-96881909	HRPEpiC	eye:	n/a
48	chr5:96876834-96876884	ProgFib	skin:	n/a
49	chr5:96890257-96890307	HEK293	kidney:	embryo
50	chr5:96845117-96845167	HRPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:97160876..97163358-chr5:97164775..97167035,2	K562	blood:
2	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
3	chr5:97162501..97165001-chr5:97167662..97169407,2	MCF-7	breast:
4	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:
5	chr5:97160876..97163358-chr5:97164775..97167035,2	K562	blood:
6	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
7	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
8	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
9	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
10	chr5:97207148..97208975-chr5:97213192..97214894,2	K562	blood:
11	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
12	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
13	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:
14	chr5:97162501..97165001-chr5:97167662..97169407,2	MCF-7	breast:
15	chr5:96869180..96869850-chr5:98103055..98104021,2	MCF-7	breast:
16	chr5:97063042..97065906-chr5:97067363..97069421,2	MCF-7	breast:
17	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
18	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:
19	chr5:97063042..97065906-chr5:97067363..97069421,2	MCF-7	breast:
20	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
21	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
22	chr5:97203818..97206757-chr5:97208812..97211809,2	K562	blood:
23	chr5:97113626..97116438-chr5:97121561..97123647,2	K562	blood:
24	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
25	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
26	chr5:97113626..97116438-chr5:97121561..97123647,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-2	chr5:97004254-97004366	NONHSAT102931
2	lnc-CTD-2215E18.1.1-3	chr5:97235342-97235457	XLOC_004484
3	lnc-CTD-2215E18.1.1-3	chr5:97217132-97217271	XLOC_004484
4	lnc-CTD-2215E18.1.1-6	chr5:97073598-97074617	NONHSAT102935
5	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
6	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	XLOC_004483
7	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006755	NR_105028
8	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	NR_105028
9	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931
10	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
11	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006750	XLOC_004483
12	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	XLOC_004483
13	lnc-CTD-2215E18.1.1-3	chr5:97217124-97217271	XLOC_004484
14	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	NR_105028
15	lnc-CTD-2215E18.1.1-2	chr5:97006297-97006750	NONHSAT102931
16	lnc-CTD-2215E18.1.1-2	chr5:96856932-96856994	NONHSAT102931
17	lnc-CTD-2215E18.1.1-3	chr5:97257835-97258399	XLOC_004484

No data

Variant related genes	Relation type
ENSG00000248202	TF binding region
ENSG00000248931	TF binding region
ENSG00000250331	TF binding region
ENSG00000251193	TF binding region
ENSG00000248202	CpG island
ENSG00000248931	CpG island
ENSG00000250331	CpG island
ENSG00000251193	CpG island
DNAJB12	miRNA target sites

Extended variants
information (count: 9213 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:9213 , 50 per page) page: 1 2 3 4 5 6 7 ... 185

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75405956	chr5:96791813-96791814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563964802	chr5:96791841-96791842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376255878	chr5:96791853-96791854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574078112	chr5:96791877-96791878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146730811	chr5:96791881-96791882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199612073	chr5:96791973-96791974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543266903	chr5:96792013-96792014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561664021	chr5:96792022-96792023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185537438	chr5:96792079-96792080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190456510	chr5:96792084-96792085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559783684	chr5:96792106-96792107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533307991	chr5:96792177-96792178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78025249	chr5:96792197-96792198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543093772	chr5:96792315-96792316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191324995	chr5:96792338-96792339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537465671	chr5:96792348-96792349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548702957	chr5:96792365-96792366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549660395	chr5:96792415-96792416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567979493	chr5:96792417-96792418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535207010	chr5:96792426-96792427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12657210	chr5:96792455-96792456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs77930511	chr5:96792494-96792495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs386690297	chr5:96792508-96792509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145277503	chr5:96792509-96792510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575907626	chr5:96792520-96792521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543036243	chr5:96792597-96792598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561627778	chr5:96792607-96792608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183887902	chr5:96792645-96792646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573634130	chr5:96792716-96792717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149163122	chr5:96792718-96792719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188608648	chr5:96792784-96792785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201404872	chr5:96792798-96792799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533157738	chr5:96792851-96792852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545133443	chr5:96792895-96792896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563823138	chr5:96792926-96792927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530896239	chr5:96792927-96792928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549424525	chr5:96792932-96792933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181392053	chr5:96792978-96792979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569429723	chr5:96792988-96792989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13180130	chr5:96792990-96792991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12517149	chr5:96793016-96793017	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs147104918	chr5:96793017-96793018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57377966	chr5:96793025-96793026	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs376430721	chr5:96793026-96793027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554986279	chr5:96793029-96793030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573597308	chr5:96793114-96793115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555488457	chr5:96793118-96793119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540883071	chr5:96793131-96793132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141960061	chr5:96793146-96793147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34055946	chr5:96793148-96793149	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96791800-96794600	Weak transcription	Pancreas	Pancrea
2	chr5:96794200-96794400	Enhancers	GM12878-XiMat	blood
3	chr5:96794400-96794800	Flanking Active TSS	GM12878-XiMat	blood
4	chr5:96794600-96794800	ZNF genes & repeats	Pancreas	Pancrea
5	chr5:96794800-96795400	Enhancers	GM12878-XiMat	blood
6	chr5:96797400-96798400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr5:96801600-96802600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:96802600-96803200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr5:96806000-96808000	ZNF genes & repeats	Pancreas	Pancrea
10	chr5:96807000-96808000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:96808000-96808200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr5:96811800-96812400	Enhancers	GM12878-XiMat	blood
13	chr5:96812200-96813000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:96812400-96812800	Enhancers	NHEK	skin
15	chr5:96812400-96813000	Flanking Active TSS	GM12878-XiMat	blood
16	chr5:96813000-96815600	Enhancers	GM12878-XiMat	blood
17	chr5:96814000-96814600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:96814200-96814600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:96814200-96814600	Enhancers	Fetal Lung	lung
20	chr5:96814200-96814600	Enhancers	Ovary	ovary
21	chr5:96814400-96815000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr5:96814600-96816200	Weak transcription	Ovary	ovary
23	chr5:96815600-96816600	Flanking Active TSS	GM12878-XiMat	blood
24	chr5:96816200-96816600	Enhancers	Ovary	ovary
25	chr5:96816600-96816800	Enhancers	GM12878-XiMat	blood
26	chr5:96816600-96818600	Weak transcription	Ovary	ovary
27	chr5:96817400-96817600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:96818400-96818600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:96818600-96819000	Enhancers	Ovary	ovary
30	chr5:96818800-96819000	Enhancers	Gastric	stomach
31	chr5:96821400-96821600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr5:96821600-96823800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:96822000-96824000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:96823800-96824000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr5:96823800-96824000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:96823800-96824200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:96823800-96824200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr5:96824000-96824200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:96824000-96824200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr5:96824200-96824800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:96824800-96825200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:96825000-96825200	Enhancers	Pancreas	Pancrea
43	chr5:96825200-96830200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:96829200-96831600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:96830200-96830400	Enhancers	Ovary	ovary
46	chr5:96830200-96831000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr5:96830200-96831200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:96830200-96831400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:96830200-96831400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr5:96830400-96831000	Weak transcription	Ovary	ovary

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