Variant report

Variant	nsv537888
Chromosome Location	chr5:120375906-120569533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:123)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120480659-120480718	K562	blood:	n/a	n/a
2	CBX3	chr5:120563378-120563655	K562	blood:	n/a	n/a
3	CEBPB	chr5:120497807-120498101	IMR90	lung:	n/a	chr5:120497966-120497977
4	CEBPB	chr5:120497839-120498066	HepG2	liver:	n/a	chr5:120497966-120497977
5	CEBPB	chr5:120535010-120535378	IMR90	lung:	n/a	n/a
6	CEBPB	chr5:120518649-120519214	A549	lung:	n/a	chr5:120518723-120518734
7	CEBPB	chr5:120518774-120519213	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:120386100-120386431	HepG2	liver:	n/a	chr5:120386256-120386267
9	CEBPB	chr5:120489328-120489659	H1-hESC	embryonic stem cell:	n/a	chr5:120489508-120489519
10	CEBPB	chr5:120510128-120510341	K562	blood:	n/a	n/a
11	CEBPB	chr5:120489367-120489679	A549	lung:	n/a	chr5:120489508-120489519
12	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr5:120489382-120489687	HepG2	liver:	n/a	chr5:120489508-120489519
14	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
15	CEBPB	chr5:120500288-120500607	K562	blood:	n/a	n/a
16	CEBPB	chr5:120497794-120498111	K562	blood:	n/a	chr5:120497966-120497977
17	CEBPB	chr5:120465336-120465526	K562	blood:	n/a	chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447 chr5:120465434-120465445 chr5:120465434-120465447 chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447
18	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
19	CEBPB	chr5:120509430-120509502	K562	blood:	n/a	chr5:120509449-120509462 chr5:120509449-120509460
20	CEBPB	chr5:120497904-120498020	A549	lung:	n/a	chr5:120497966-120497977
21	CEBPB	chr5:120511816-120512016	HepG2	liver:	n/a	chr5:120511903-120511914
22	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
23	CEBPB	chr5:120386141-120386392	A549	lung:	n/a	chr5:120386256-120386267
24	CEBPB	chr5:120489377-120489704	K562	blood:	n/a	chr5:120489508-120489519
25	CEBPB	chr5:120518577-120518857	K562	blood:	n/a	chr5:120518723-120518734
26	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
27	CEBPB	chr5:120534992-120535592	Hela-S3	cervix:	n/a	chr5:120534993-120535006
28	CEBPB	chr5:120518614-120519156	HepG2	liver:	n/a	chr5:120518723-120518734
29	CEBPB	chr5:120388712-120389167	MCF-7	breast:	n/a	n/a
30	CEBPB	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
31	CEBPD	chr5:120480469-120480757	K562	blood:	n/a	n/a
32	CEBPD	chr5:120480488-120480808	K562	blood:	n/a	n/a
33	CHD2	chr5:120469053-120469156	K562	blood:	n/a	n/a
34	CTCF	chr5:120480640-120480790	AG09319	gingival:	n/a	n/a
35	CTCF	chr5:120398360-120398510	HVMF	connective:	n/a	n/a
36	CTCF	chr5:120396480-120396630	GM12875	blood:	n/a	n/a
37	CTCF	chr5:120480440-120480590	HCM	heart:	n/a	n/a
38	CTCF	chr5:120525700-120525850	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:120480700-120480850	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr5:120548668-120548698	Fibrobl	skin:	n/a	n/a
41	CTCF	chr5:120525795-120525851	HepG2	liver:	n/a	n/a
42	CTCF	chr5:120480600-120480750	BE2_C	brain:	n/a	n/a
43	CTCF	chr5:120480653-120480819	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr5:120480680-120480830	HMF	breast:	n/a	n/a
45	CTCF	chr5:120480680-120480830	AG09319	gingival:	n/a	n/a
46	CTCF	chr5:120480660-120480810	SAEC	small airway:	n/a	n/a
47	CTCF	chr5:120507640-120507790	AG09319	gingival:	n/a	n/a
48	CTCF	chr5:120480660-120480810	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr5:120504355-120504387	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr5:120480636-120480780	Gliobla	brain:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
2	chr5:120400115-120400165	HNPCEpiC	eye:	n/a
3	chr5:120444080-120444130	CMK	blood:	n/a
4	chr5:120400115-120400165	SK-N-MC	brain:	n/a
5	chr5:120400115-120400165	HEEpiC	esophagus:	n/a
6	chr5:120400115-120400165	AG10803	skin:	n/a
7	chr5:120400115-120400165	NT2-D1	testis:	n/a
8	chr5:120400115-120400165	GM12878	blood:	n/a
9	chr5:120444080-120444130	AG04449	skin:	fetal
10	chr5:120400115-120400165	HUVEC	blood vessel:	n/a
11	chr5:120400115-120400165	AG09319	gingival:	n/a
12	chr5:120444080-120444130	MCF-7	breast:	n/a
13	chr5:120400115-120400165	IMR90	lung:	fetal
14	chr5:120444080-120444130	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:120444080-120444130	HCT-116	colon:	n/a
16	chr5:120444080-120444130	AG10803	skin:	n/a
17	chr5:120400115-120400165	PANC-1	pancreas:	n/a
18	chr5:120444080-120444130	ovcar-3	ovarian:	n/a
19	chr5:120444080-120444130	GM12892	blood:	n/a
20	chr5:120400115-120400165	HEK293	kidney:	embryo
21	chr5:120444080-120444130	PANC-1	pancreas:	n/a
22	chr5:120444080-120444130	ECC-1	luminal epithelium:	n/a
23	chr5:120400115-120400165	GM12892	blood:	n/a
24	chr5:120400115-120400165	Jurkat	blood:	n/a
25	chr5:120444080-120444130	H1-hESC	embryonic stem cell:	embryo
26	chr5:120444080-120444130	Hepatocyte	liver:	n/a
27	chr5:120400115-120400165	Hela-S3	cervix:	n/a
28	chr5:120444080-120444130	SK-N-SH	brain:	n/a
29	chr5:120444080-120444130	HCM	heart:	n/a
30	chr5:120444080-120444130	AoSMC	blood vessel:	n/a
31	chr5:120400115-120400165	Hepatocyte	liver:	n/a
32	chr5:120444080-120444130	HIPEpiC	eye:	n/a
33	chr5:120400115-120400165	H1-hESC	embryonic stem cell:	embryo
34	chr5:120400115-120400165	NH-A	brain:	n/a
35	chr5:120400115-120400165	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:120400115-120400165	NB4	blood:	n/a
37	chr5:120444080-120444130	HRCEpiC	kidney:	n/a
38	chr5:120444080-120444130	HUVEC	blood vessel:	n/a
39	chr5:120400115-120400165	AG09309	skin:	n/a
40	chr5:120400115-120400165	SKMC	muscle:	n/a
41	chr5:120400115-120400165	MCF-7	breast:	n/a
42	chr5:120444080-120444130	HAEpiC	amniotic membrane:	n/a
43	chr5:120444080-120444130	NHBE	bronchial:	n/a
44	chr5:120444080-120444130	U87	brain:	n/a
45	chr5:120400115-120400165	SAEC	small airway:	n/a
46	chr5:120400115-120400165	SK-N-SH	brain:	n/a
47	chr5:120444080-120444130	Caco-2	colon:	n/a
48	chr5:120444080-120444130	HMEC	breast:	n/a
49	chr5:120444080-120444130	K562	blood:	n/a
50	chr5:120400115-120400165	BE2_C	brain:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
2	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
3	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
4	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
5	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
6	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
7	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
8	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
9	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
10	chr5:120539543..120541398-chr5:120544523..120546831,2	K562	blood:
11	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
12	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
13	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
14	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
15	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
16	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
17	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
18	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
19	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
20	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
21	chr5:120544152..120546595-chr5:120554469..120557280,2	K562	blood:
22	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
2	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
3	lnc-FTMT-2	chr5:120535399-120535503	ENSG00000229855.4
4	lnc-FTMT-2	chr5:120540703-120540825	ENSG00000229855.4
5	lnc-LOX-8	chr5:120531675-120531905	NONHSAT103452
6	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450
7	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
8	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451

No data

Variant related genes	Relation type
ENSG00000229855	TF binding region
ENSG00000248853	TF binding region
ENSG00000250847	TF binding region
ENSG00000229855	CpG island
ENSG00000248853	CpG island
ENSG00000250847	CpG island

Extended variants
information (count: 3646 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3646 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147843959	chr5:120375928-120375929	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs576048263	chr5:120375950-120375951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs543330753	chr5:120375960-120375961	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs375362364	chr5:120375975-120375976	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs191133331	chr5:120375994-120375995	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs573531358	chr5:120376005-120376006	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs541137909	chr5:120376043-120376044	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs73787319	chr5:120376062-120376063	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533041555	chr5:120376065-120376066	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs544841418	chr5:120376124-120376125	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs183223951	chr5:120376185-120376186	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs17446646	chr5:120376188-120376189	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548835544	chr5:120376193-120376194	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs76684525	chr5:120376204-120376205	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs77837436	chr5:120376208-120376209	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs141146190	chr5:120376209-120376210	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs571697015	chr5:120376210-120376211	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs376627565	chr5:120376211-120376212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs539127317	chr5:120376216-120376217	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs187549944	chr5:120376220-120376221	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs17147273	chr5:120376238-120376239	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs369319336	chr5:120376242-120376243	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs144988835	chr5:120376248-120376249	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs112655844	chr5:120376265-120376266	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs555269628	chr5:120376270-120376271	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs111587673	chr5:120376277-120376278	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs17506227	chr5:120376386-120376387	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs542522444	chr5:120376410-120376411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs201908451	chr5:120376432-120376433	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs561582517	chr5:120379434-120379435	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs528982485	chr5:120379455-120379456	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs78186234	chr5:120379471-120379472	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs141055703	chr5:120379492-120379493	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs533087649	chr5:120379520-120379521	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs180798161	chr5:120379570-120379571	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs185934308	chr5:120379592-120379593	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs534668841	chr5:120379600-120379601	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs145091270	chr5:120379607-120379608	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs201399663	chr5:120379615-120379616	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs371767890	chr5:120379623-120379624	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs375561759	chr5:120379625-120379626	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs549354053	chr5:120379653-120379654	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs567693413	chr5:120379670-120379671	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs17147274	chr5:120379679-120379680	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs146879001	chr5:120379681-120379682	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs571841222	chr5:120379691-120379692	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs539356822	chr5:120379729-120379730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557648441	chr5:120379744-120379745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576111557	chr5:120379799-120379800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs140746231	chr5:120379815-120379816	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
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
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120379400-120380200	Enhancers	Dnd41	blood
2	chr5:120380200-120383800	Weak transcription	Dnd41	blood
3	chr5:120383800-120384200	Enhancers	Dnd41	blood
4	chr5:120384200-120385000	Weak transcription	Dnd41	blood
5	chr5:120385000-120386400	Enhancers	Dnd41	blood
6	chr5:120385200-120385600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:120385200-120385600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr5:120385600-120386000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:120386400-120386800	Weak transcription	Dnd41	blood
10	chr5:120386800-120388800	Enhancers	Dnd41	blood
11	chr5:120388200-120389400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:120388400-120389400	Enhancers	Hela-S3	cervix
13	chr5:120388400-120389600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:120388800-120389600	Flanking Active TSS	Dnd41	blood
15	chr5:120389000-120389600	Enhancers	Fetal Kidney	kidney
16	chr5:120389600-120392200	Enhancers	Dnd41	blood
17	chr5:120399800-120400200	Enhancers	H1 Cell Line	embryonic stem cell
18	chr5:120399800-120400400	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr5:120399800-120400400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr5:120399800-120400400	Active TSS	HUES6 Cell Line	embryonic stem cell
21	chr5:120400000-120400200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr5:120400000-120400400	Active TSS	H9 Cell Line	embryonic stem cell
23	chr5:120400000-120400400	Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr5:120400000-120400400	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr5:120400000-120400400	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr5:120400000-120400400	Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr5:120413000-120414200	Enhancers	Dnd41	blood
28	chr5:120423200-120424400	ZNF genes & repeats	Dnd41	blood
29	chr5:120424400-120425400	Weak transcription	Dnd41	blood
30	chr5:120425400-120427000	Enhancers	Dnd41	blood
31	chr5:120440400-120440800	Enhancers	Spleen	Spleen
32	chr5:120442200-120442800	ZNF genes & repeats	Dnd41	blood
33	chr5:120442800-120444000	Weak transcription	Dnd41	blood
34	chr5:120443000-120447600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:120443400-120445000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:120443800-120444000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:120444000-120444400	ZNF genes & repeats	Dnd41	blood
38	chr5:120444000-120444600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr5:120444000-120444600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:120444000-120444800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr5:120444200-120444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr5:120444200-120444600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr5:120444400-120444600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr5:120444400-120444800	Enhancers	Placenta	Placenta
45	chr5:120444400-120444800	Active TSS	Hela-S3	cervix
46	chr5:120444400-120445600	Enhancers	Dnd41	blood
47	chr5:120444600-120444800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:120445000-120449000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:120447600-120447800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:120449000-120449600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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