Variant report

Variant	nsv1018955
Chromosome Location	chr5:119679918-119802014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:1099)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:119741643-119741799	K562	blood:	n/a	n/a
2	ATF1	chr5:119793643-119794138	K562	blood:	n/a	n/a
3	ATF1	chr5:119694688-119694905	K562	blood:	n/a	n/a
4	ATF2	chr5:119793413-119794075	GM12878	blood:	n/a	n/a
5	ATF2	chr5:119793456-119794141	GM12878	blood:	n/a	n/a
6	ATF3	chr5:119793575-119793776	GM12878	blood:	n/a	n/a
7	ATF3	chr5:119793531-119793905	GM12878	blood:	n/a	n/a
8	ATF3	chr5:119793562-119793757	K562	blood:	n/a	n/a
9	ATF3	chr5:119793581-119793842	K562	blood:	n/a	n/a
10	ATF3	chr5:119799801-119800020	K562	blood:	n/a	n/a
11	BACH1	chr5:119697785-119697924	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr5:119793497-119794263	GM12878	blood:	n/a	n/a
13	BATF	chr5:119714603-119715029	GM12878	blood:	n/a	n/a
14	BATF	chr5:119793535-119793841	GM12878	blood:	n/a	n/a
15	BATF	chr5:119714670-119714992	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:119793578-119794002	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:119793538-119794246	GM12878	blood:	n/a	n/a
18	BCL11A	chr5:119714620-119715075	GM12878	blood:	n/a	n/a
19	BCL3	chr5:119722462-119722710	GM12878	blood:	n/a	n/a
20	BCL3	chr5:119721768-119722006	GM12878	blood:	n/a	chr5:119721783-119721792
21	BCLAF1	chr5:119793512-119793944	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:119800557-119800862	K562	blood:	n/a	n/a
23	BHLHE40	chr5:119793468-119794222	K562	blood:	n/a	n/a
24	BHLHE40	chr5:119793451-119794227	HepG2	liver:	n/a	n/a
25	BHLHE40	chr5:119799728-119800086	K562	blood:	n/a	chr5:119799917-119799933
26	BHLHE40	chr5:119793446-119794136	GM12878	blood:	n/a	n/a
27	CBX3	chr5:119686791-119687141	K562	blood:	n/a	n/a
28	CBX3	chr5:119686872-119687070	K562	blood:	n/a	n/a
29	CBX3	chr5:119766328-119766517	K562	blood:	n/a	n/a
30	CBX3	chr5:119793992-119794270	K562	blood:	n/a	n/a
31	CBX3	chr5:119766312-119766599	K562	blood:	n/a	n/a
32	CCNT2	chr5:119801326-119801526	K562	blood:	n/a	chr5:119801482-119801491
33	CCNT2	chr5:119799743-119800201	K562	blood:	n/a	n/a
34	CCNT2	chr5:119800844-119801044	K562	blood:	n/a	n/a
35	CEBPB	chr5:119751624-119752006	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr5:119781713-119782170	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:119702522-119702675	K562	blood:	n/a	chr5:119702615-119702626
38	CEBPB	chr5:119793870-119793873	K562	blood:	n/a	n/a
39	CEBPB	chr5:119696857-119696903	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:119751652-119752056	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr5:119723894-119724463	IMR90	lung:	n/a	n/a
42	CEBPB	chr5:119713168-119713212	K562	blood:	n/a	n/a
43	CEBPB	chr5:119790034-119790418	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr5:119793540-119794182	GM12878	blood:	n/a	n/a
45	CEBPB	chr5:119781622-119782289	IMR90	lung:	n/a	n/a
46	CEBPB	chr5:119751710-119751957	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:119751752-119751990	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:119801582-119802014	K562	blood:	n/a	n/a
49	CEBPB	chr5:119743137-119743337	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr5:119694757-119695008	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119800687-119800737	HAEpiC	amniotic membrane:	n/a
2	chr5:119800687-119800737	HAEpiC	amniotic membrane:	n/a
3	chr5:119799531-119799581	CMK	blood:	n/a
4	chr5:119799862-119799912	AG09319	gingival:	n/a
5	chr5:119801643-119801693	HepG2	liver:	n/a
6	chr5:119799531-119799581	NHBE	bronchial:	n/a
7	chr5:119801431-119801481	NB4	blood:	n/a
8	chr5:119800972-119801022	HL-60	blood:	n/a
9	chr5:119800234-119800284	GM06990	blood:	n/a
10	chr5:119801193-119801243	HRPEpiC	eye:	n/a
11	chr5:119799822-119799872	MCF-7	breast:	n/a
12	chr5:119800143-119800193	Hepatocyte	liver:	n/a
13	chr5:119799862-119799912	RPTEC	kidney:	n/a
14	chr5:119801142-119801192	HMEC	breast:	n/a
15	chr5:119800143-119800193	HIPEpiC	eye:	n/a
16	chr5:119800742-119800792	NH-A	brain:	n/a
17	chr5:119799862-119799912	HCF	heart:	n/a
18	chr5:119800234-119800284	Hepatocyte	liver:	n/a
19	chr5:119801431-119801481	HCF	heart:	n/a
20	chr5:119800687-119800737	T-47D	breast:	n/a
21	chr5:119800403-119800453	HMEC	breast:	n/a
22	chr5:119801643-119801693	HAEpiC	amniotic membrane:	n/a
23	chr5:119800403-119800453	U87	brain:	n/a
24	chr5:119800972-119801022	Hepatocyte	liver:	n/a
25	chr5:119801193-119801243	ECC-1	luminal epithelium:	n/a
26	chr5:119800687-119800737	SK-N-MC	brain:	n/a
27	chr5:119800687-119800737	HCPEpiC	choroid plexus:	n/a
28	chr5:119799862-119799912	HRE	kidney:	n/a
29	chr5:119799822-119799872	Hela-S3	cervix:	n/a
30	chr5:119800403-119800453	NHBE	bronchial:	n/a
31	chr5:119801431-119801481	HIPEpiC	eye:	n/a
32	chr5:119801142-119801192	CMK	blood:	n/a
33	chr5:119800403-119800453	GM12892	blood:	n/a
34	chr5:119800687-119800737	BE2_C	brain:	n/a
35	chr5:119799832-119799882	HPAEpiC	pulmonary alveolar:	n/a
36	chr5:119801193-119801243	NHBE	bronchial:	n/a
37	chr5:119800143-119800193	NT2-D1	testis:	n/a
38	chr5:119800972-119801022	HepG2	liver:	n/a
39	chr5:119800234-119800284	PANC-1	pancreas:	n/a
40	chr5:119800687-119800737	AG09319	gingival:	n/a
41	chr5:119799822-119799872	Hepatocyte	liver:	n/a
42	chr5:119782696-119782746	SK-N-MC	brain:	n/a
43	chr5:119801142-119801192	Jurkat	blood:	n/a
44	chr5:119801431-119801481	GM19239	blood:	n/a
45	chr5:119782696-119782746	SK-N-SH_RA	brain:	n/a
46	chr5:119799822-119799872	PANC-1	pancreas:	n/a
47	chr5:119801643-119801693	K562	blood:	n/a
48	chr5:119799384-119799434	PFSK-1	brain:	n/a
49	chr5:119799220-119799270	MCF-7	breast:	n/a
50	chr5:119782696-119782746	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:119680201..119681861-chr5:119689913..119692510,2	K562	blood:
2	chr5:119775909..119777540-chr5:119783720..119785397,2	K562	blood:
3	chr5:119702205..119704194-chr5:119706645..119708687,2	K562	blood:
4	chr5:119721254..119725042-chr5:119751252..119754462,3	K562	blood:
5	chr5:119775909..119777540-chr5:119783720..119785397,2	K562	blood:
6	chr5:119278619..119279545-chr5:119793318..119794660,3	MCF-7	breast:
7	chr5:119721254..119725042-chr5:119751252..119754462,3	K562	blood:
8	chr5:119785992..119787497-chr5:119792334..119794755,2	K562	blood:
9	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:
10	chr5:119680201..119681861-chr5:119689913..119692510,2	K562	blood:
11	chr5:119792597..119795401-chr5:119799043..119801706,2	K562	blood:
12	chr5:119801561..119803830-chr5:119805628..119808715,3	K562	blood:
13	chr5:119688806..119691602-chr5:119693680..119696391,2	K562	blood:
14	chr5:119702205..119704194-chr5:119706645..119708687,2	K562	blood:
15	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
16	chr5:119795709..119798645-chr5:119801095..119805087,3	K562	blood:
17	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:
18	chr5:119785992..119787497-chr5:119792334..119794755,2	K562	blood:
19	chr5:119719801..119721845-chr5:119723016..119725406,2	K562	blood:
20	chr5:119719801..119721845-chr5:119723016..119725406,2	K562	blood:
21	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
22	chr5:119688806..119691602-chr5:119693680..119696391,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DTWD2-5	chr5:119681602-119682035	ENSG00000261036.1
2	lnc-DTWD2-5	chr5:119740450-119740532	ENSG00000261036.1

No data

Variant related genes	Relation type
PRR16	TF binding region
ENSG00000261036	TF binding region
PRR16	CpG island
ENSG00000261036	CpG island
ENSG00000184838	chromatin interactions

Extended variants
information (count: 4943 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4943 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183784436	chr5:119680237-119680238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542406988	chr5:119680271-119680272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189293743	chr5:119680328-119680329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531241686	chr5:119680369-119680370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs544571728	chr5:119680384-119680385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551154588	chr5:119680391-119680392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564462244	chr5:119680469-119680470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533401214	chr5:119680515-119680516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547262250	chr5:119680544-119680545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72784167	chr5:119680547-119680548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs182173700	chr5:119680569-119680570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79267567	chr5:119680575-119680576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150079752	chr5:119680623-119680624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538262870	chr5:119680644-119680645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187254092	chr5:119680652-119680653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368414363	chr5:119680692-119680693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191885802	chr5:119680693-119680694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533885204	chr5:119680731-119680732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182112302	chr5:119680741-119680742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138533833	chr5:119680776-119680777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542793471	chr5:119680784-119680785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555856693	chr5:119680819-119680820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575703869	chr5:119680820-119680821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544608424	chr5:119680849-119680850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185861747	chr5:119680878-119680879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572003874	chr5:119680899-119680900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540596262	chr5:119680940-119680941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11948803	chr5:119680955-119680956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs17146484	chr5:119680964-119680965	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs141616079	chr5:119680965-119680966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552777153	chr5:119680991-119680992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146228046	chr5:119681000-119681001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531795289	chr5:119681007-119681008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375871971	chr5:119681017-119681018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368715149	chr5:119681018-119681019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190128862	chr5:119681025-119681026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563290291	chr5:119681057-119681058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534177374	chr5:119681067-119681068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182399758	chr5:119681103-119681104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530377205	chr5:119681121-119681122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545791666	chr5:119681127-119681128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17146485	chr5:119681139-119681140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs368878429	chr5:119681145-119681146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532874911	chr5:119681148-119681149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555893477	chr5:119681162-119681163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186711482	chr5:119681170-119681171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190923708	chr5:119681215-119681216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140125934	chr5:119681234-119681235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372938484	chr5:119681278-119681279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149393657	chr5:119681279-119681280	Weak transcription	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119680200-119680400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:119680400-119686400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:119681600-119682000	Enhancers	HMEC	breast
4	chr5:119686400-119687400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:119687400-119689800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:119689400-119691800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:119689800-119690200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:119689800-119690400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:119689800-119691600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:119690000-119690800	Enhancers	HMEC	breast
11	chr5:119690200-119691600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:119690200-119701400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:119697400-119701600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:119697800-119699000	Active TSS	K562	blood
15	chr5:119698200-119698400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:119698200-119699200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:119698400-119703600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:119699200-119701600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:119700800-119702200	Enhancers	HMEC	breast
20	chr5:119701400-119702000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr5:119701400-119702000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr5:119701600-119702000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:119701600-119702200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:119701600-119702400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:119701600-119703000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:119702000-119703800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:119702000-119703800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr5:119702200-119703800	Weak transcription	HMEC	breast
29	chr5:119702200-119704000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr5:119702400-119707800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:119703600-119703800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:119703800-119704000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr5:119703800-119704200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr5:119703800-119704200	Enhancers	Esophagus	oesophagus
35	chr5:119703800-119704600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:119703800-119705400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr5:119703800-119705400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:119703800-119705600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:119703800-119705600	Enhancers	HMEC	breast
40	chr5:119704000-119704200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:119704000-119704400	Active TSS	Gastric	stomach
42	chr5:119704000-119705000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr5:119704000-119705200	ZNF genes & repeats	Dnd41	blood
44	chr5:119704200-119704400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:119704400-119705000	Enhancers	Colonic Mucosa	Colon
46	chr5:119704400-119705400	Enhancers	Gastric	stomach
47	chr5:119704400-119708600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr5:119704600-119705000	Enhancers	Duodenum Mucosa	Duodenum
49	chr5:119704600-119705000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
50	chr5:119704600-119705200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin

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