Variant report

Variant	nsv1029048
Chromosome Location	chr5:114345201-114408136
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	ARID3A	chr5:114389914-114390321	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:114404334-114404677	HepG2	liver:	n/a	n/a
3	ATF2	chr5:114404436-114404906	GM12878	blood:	n/a	n/a
4	BATF	chr5:114404549-114404883	GM12878	blood:	n/a	chr5:114404702-114404713
5	BATF	chr5:114404446-114404925	GM12878	blood:	n/a	chr5:114404702-114404713
6	BCL11A	chr5:114404592-114404917	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:114404558-114404767	GM12878	blood:	n/a	n/a
8	CEBPB	chr5:114367287-114367466	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:114367353-114367583	A549	lung:	n/a	n/a
10	CEBPB	chr5:114367286-114367573	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:114367276-114367583	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:114388697-114388980	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:114388673-114388975	HepG2	liver:	n/a	n/a
14	CHD2	chr5:114404073-114404247	HepG2	liver:	n/a	n/a
15	CHD2	chr5:114369722-114369774	GM12878	blood:	n/a	n/a
16	CTCF	chr5:114405171-114405362	Kidney_OC	kidney:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
17	CTCF	chr5:114369660-114369810	HCT-116	colon:	n/a	n/a
18	CTCF	chr5:114405115-114405401	MCF-7	breast:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
19	CTCF	chr5:114405057-114405453	GM12878	blood:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
20	CTCF	chr5:114405114-114405392	Medullo	brain:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
21	CTCF	chr5:114405119-114405387	HepG2	liver:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
22	CTCF	chr5:114405160-114405310	GM12864	blood:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
23	CTCF	chr5:114369649-114369849	IMR90	lung:	n/a	n/a
24	CTCF	chr5:114405240-114405390	NHEK	skin:	n/a	chr5:114405245-114405261 chr5:114405244-114405262
25	CTCF	chr5:114405136-114405376	Pancreas_OC	pancreas:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
26	CTCF	chr5:114369658-114369856	HepG2	liver:	n/a	n/a
27	CTCF	chr5:114405180-114405330	BJ	skin:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
28	CTCF	chr5:114405200-114405350	K562	blood:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
29	CTCF	chr5:114369700-114369850	AG04449	skin:	n/a	n/a
30	CTCF	chr5:114405200-114405350	HEEpiC	esophagus:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
31	CTCF	chr5:114369566-114369944	GM12878	blood:	n/a	n/a
32	CTCF	chr5:114351760-114351829	GM13976	blood:	n/a	n/a
33	CTCF	chr5:114405180-114405330	Caco-2	colon:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
34	CTCF	chr5:114405180-114405330	HFF-Myc	foreskin:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
35	CTCF	chr5:114369640-114369790	BJ	skin:	n/a	n/a
36	CTCF	chr5:114389100-114389250	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr5:114369550-114369991	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:114369560-114369830	HVMF	connective:	n/a	n/a
39	CTCF	chr5:114405220-114405370	HRE	kidney:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
40	CTCF	chr5:114405240-114405390	BJ	skin:	n/a	chr5:114405245-114405261 chr5:114405244-114405262
41	CTCF	chr5:114405140-114405290	GM12867	blood:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
42	CTCF	chr5:114405200-114405350	HPF	lung:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
43	CTCF	chr5:114369673-114369839	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr5:114405180-114405330	AG04449	skin:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
45	CTCF	chr5:114405051-114405462	A549	lung:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
46	CTCF	chr5:114405160-114405310	HepG2	liver:	n/a	chr5:114405245-114405261 chr5:114405244-114405262 chr5:114405239-114405260
47	CTCF	chr5:114400667-114400693	GM13976	blood:	n/a	n/a
48	CTCF	chr5:114369680-114369830	BJ	skin:	n/a	n/a
49	CTCF	chr5:114369660-114369810	NB4	blood:	n/a	n/a
50	CTCF	chr5:114369680-114369830	AG09309	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114365928-114365978	HEK293	kidney:	embryo
2	chr5:114365928-114365978	AG09309	skin:	n/a
3	chr5:114365928-114365978	BE2_C	brain:	n/a
4	chr5:114365928-114365978	Caco-2	colon:	n/a
5	chr5:114365928-114365978	SK-N-SH	brain:	n/a
6	chr5:114365928-114365978	SAEC	small airway:	n/a
7	chr5:114365928-114365978	SK-N-SH_RA	brain:	n/a
8	chr5:114365928-114365978	CMK	blood:	n/a
9	chr5:114365928-114365978	Hepatocyte	liver:	n/a
10	chr5:114365928-114365978	NH-A	brain:	n/a
11	chr5:114365928-114365978	AG10803	skin:	n/a
12	chr5:114365928-114365978	HRCEpiC	kidney:	n/a
13	chr5:114365928-114365978	AoSMC	blood vessel:	n/a
14	chr5:114365928-114365978	ECC-1	luminal epithelium:	n/a
15	chr5:114365928-114365978	ovcar-3	ovarian:	n/a
16	chr5:114365928-114365978	AG04449	skin:	fetal
17	chr5:114365928-114365978	HNPCEpiC	eye:	n/a
18	chr5:114365928-114365978	NHBE	bronchial:	n/a
19	chr5:114365928-114365978	HL-60	blood:	n/a
20	chr5:114365928-114365978	PrEC	prostate:	n/a
21	chr5:114365928-114365978	HCF	heart:	n/a
22	chr5:114365928-114365978	HCT-116	colon:	n/a
23	chr5:114365928-114365978	GM19239	blood:	n/a
24	chr5:114365928-114365978	RPTEC	kidney:	n/a
25	chr5:114365928-114365978	IMR90	lung:	fetal
26	chr5:114365928-114365978	HepG2	liver:	n/a
27	chr5:114365928-114365978	NB4	blood:	n/a
28	chr5:114365928-114365978	ProgFib	skin:	n/a
29	chr5:114365928-114365978	SK-N-MC	brain:	n/a
30	chr5:114365928-114365978	BJ	skin:	n/a
31	chr5:114365928-114365978	PANC-1	pancreas:	n/a
32	chr5:114365928-114365978	GM06990	blood:	n/a
33	chr5:114365928-114365978	SKMC	muscle:	n/a
34	chr5:114365928-114365978	PFSK-1	brain:	n/a
35	chr5:114365928-114365978	NT2-D1	testis:	n/a
36	chr5:114365928-114365978	HRPEpiC	eye:	n/a
37	chr5:114365928-114365978	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:114365928-114365978	GM12891	blood:	n/a
39	chr5:114365928-114365978	HEEpiC	esophagus:	n/a
40	chr5:114365928-114365978	HAEpiC	amniotic membrane:	n/a
41	chr5:114365928-114365978	NHDF-neo	bronchial:	n/a
42	chr5:114365928-114365978	HCM	heart:	n/a
43	chr5:114365928-114365978	LNCaP	prostate:	n/a
44	chr5:114365928-114365978	HMEC	breast:	n/a
45	chr5:114365928-114365978	MCF-7	breast:	n/a
46	chr5:114365928-114365978	AG09319	gingival:	n/a
47	chr5:114365928-114365978	AG04450	lung:	fetal
48	chr5:114365928-114365978	U87	brain:	n/a
49	chr5:114365928-114365978	MCF10A-Er-Src	breast:	n/a
50	chr5:114365928-114365978	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:114138711..114139387-chr5:114369334..114369873,2	MCF-7	breast:
2	chr22:21978725..21981306-chr5:114359469..114360989,2	K562	blood:
3	chr5:113014328..113015260-chr5:114404740..114405272,3	K562	blood:
4	chr5:113785328..113785951-chr5:114369489..114370463,2	MCF-7	breast:
5	chr5:114133331..114134215-chr5:114369304..114370183,3	MCF-7	breast:
6	chr5:113785791..113786752-chr5:114405185..114405973,2	MCF-7	breast:
7	chr5:114139185..114139978-chr5:114404825..114405439,2	MCF-7	breast:
8	chr5:114234220..114234829-chr5:114405733..114406270,2	MCF-7	breast:
9	chr5:114139161..114139984-chr5:114369361..114370136,2	MCF-7	breast:
10	chr5:114404877..114405516-chr5:114433463..114434454,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000251132	TF binding region
ENSG00000251132	CpG island

Extended variants
information (count: 903 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538377551	chr5:114352000-114352001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113209966	chr5:114352130-114352131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551939088	chr5:114352132-114352133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114219398	chr5:114352139-114352140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568662802	chr5:114352191-114352192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11949019	chr5:114352216-114352217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534431372	chr5:114352231-114352232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs191453145	chr5:114352257-114352258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541946068	chr5:114352278-114352279	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554571675	chr5:114352279-114352280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574734845	chr5:114352301-114352302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72474067	chr5:114352313-114352314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537041798	chr5:114352323-114352324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56997174	chr5:114352325-114352326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369415373	chr5:114352380-114352381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568652695	chr5:114352421-114352422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76174910	chr5:114352487-114352488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557436571	chr5:114352562-114352563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577388773	chr5:114352565-114352566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73782659	chr5:114352599-114352600	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553567297	chr5:114352619-114352620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573377484	chr5:114352663-114352664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542471795	chr5:114352676-114352677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562237881	chr5:114352679-114352680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546697469	chr5:114352684-114352685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542995122	chr5:114352719-114352720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs61002768	chr5:114352744-114352745	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs74382717	chr5:114352745-114352746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs551875737	chr5:114352772-114352773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183237316	chr5:114352773-114352774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528283117	chr5:114352788-114352789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113498135	chr5:114352792-114352793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73245620	chr5:114352798-114352799	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs568260853	chr5:114352824-114352825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537371010	chr5:114352833-114352834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs148006345	chr5:114352843-114352844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570873208	chr5:114352926-114352927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115148098	chr5:114352929-114352930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564122171	chr5:114352930-114352931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573330159	chr5:114352949-114352950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542057126	chr5:114352990-114352991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142496302	chr5:114353008-114353009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528352802	chr5:114353014-114353015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs56203091	chr5:114353023-114353024	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs187052537	chr5:114353053-114353054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190883940	chr5:114353054-114353055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs531983869	chr5:114353069-114353070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545452674	chr5:114353077-114353078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374465767	chr5:114353078-114353079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559174042	chr5:114353091-114353092	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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	16774939	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
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114352000-114352400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr5:114352000-114354800	Enhancers	Fetal Lung	lung
3	chr5:114358400-114358600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:114364000-114364800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:114364200-114364800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:114364200-114365000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:114364400-114364800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr5:114364400-114364800	Enhancers	H1 Cell Line	embryonic stem cell
9	chr5:114364400-114364800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:114364400-114365000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr5:114364400-114365000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:114364400-114365000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr5:114364400-114365000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:114364600-114365000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:114364600-114365000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:114383000-114383400	Enhancers	Brain Cingulate Gyrus	brain
17	chr5:114383000-114384000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:114384000-114389200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr5:114385600-114386200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:114385800-114386200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:114386400-114387000	Enhancers	Liver	Liver
22	chr5:114387000-114390000	Weak transcription	Liver	Liver
23	chr5:114388200-114390800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr5:114388400-114388800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:114388400-114389000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr5:114388600-114389000	Enhancers	H9 Cell Line	embryonic stem cell
27	chr5:114388800-114390600	Enhancers	HepG2	liver
28	chr5:114389200-114389400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr5:114389200-114390400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:114389800-114390400	Enhancers	Pancreas	Pancrea
31	chr5:114390000-114390400	Enhancers	Liver	Liver
32	chr5:114391800-114392800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:114403800-114404000	Enhancers	Primary T cells fromperipheralblood	blood
34	chr5:114403800-114404000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr5:114403800-114404000	Enhancers	HepG2	liver
36	chr5:114403800-114404200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr5:114403800-114404400	Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr5:114404000-114404200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr5:114404000-114404200	Enhancers	Placenta	Placenta
40	chr5:114404000-114404200	Flanking Active TSS	HepG2	liver
41	chr5:114404000-114404400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
42	chr5:114404000-114404400	Enhancers	Hela-S3	cervix
43	chr5:114404000-114404600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:114404000-114404600	Active TSS	Liver	Liver
45	chr5:114404000-114404600	Active TSS	Duodenum Mucosa	Duodenum
46	chr5:114404000-114404600	Enhancers	Lung	lung
47	chr5:114404000-114404600	Active TSS	Pancreas	Pancrea
48	chr5:114404000-114404600	Active TSS	K562	blood
49	chr5:114404000-114405600	ZNF genes & repeats	GM12878-XiMat	blood
50	chr5:114404200-114404600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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