Variant report

Variant	nsv915868
Chromosome Location	chr14:67146757-67351687
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	chr14:67224984-67225061	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:67213116-67213393	K562	blood:	n/a	n/a
3	ATF2	chr14:67218740-67219290	GM12878	blood:	n/a	n/a
4	ATF2	chr14:67218758-67219207	GM12878	blood:	n/a	n/a
5	BACH1	chr14:67305949-67305970	K562	blood:	n/a	n/a
6	BATF	chr14:67218719-67219305	GM12878	blood:	n/a	n/a
7	BATF	chr14:67218778-67219263	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:67218813-67219271	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:67219021-67219287	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:67218905-67219220	GM12878	blood:	n/a	n/a
11	BRCA1	chr14:67288110-67288222	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr14:67202769-67202812	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr14:67198693-67198850	K562	blood:	n/a	n/a
14	CEBPB	chr14:67280308-67280682	HepG2	liver:	n/a	chr14:67280486-67280497
15	CEBPB	chr14:67237139-67237466	IMR90	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
16	CEBPB	chr14:67258805-67259057	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:67280360-67280549	HepG2	liver:	n/a	chr14:67280486-67280497
18	CEBPB	chr14:67280261-67280604	HepG2	liver:	n/a	chr14:67280486-67280497
19	CEBPB	chr14:67280194-67280806	MCF-7	breast:	n/a	chr14:67280486-67280497
20	CEBPB	chr14:67176141-67176415	IMR90	lung:	n/a	n/a
21	CEBPB	chr14:67280214-67280811	MCF-7	breast:	n/a	chr14:67280486-67280497
22	CEBPB	chr14:67280298-67280687	IMR90	lung:	n/a	chr14:67280486-67280497
23	CEBPB	chr14:67310889-67310923	A549	lung:	n/a	n/a
24	CEBPB	chr14:67176094-67176421	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:67164729-67164837	HepG2	liver:	n/a	chr14:67164778-67164789 chr14:67164779-67164790
26	CEBPB	chr14:67237108-67237444	HepG2	liver:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
27	CEBPB	chr14:67176164-67176408	A549	lung:	n/a	n/a
28	CEBPB	chr14:67237135-67237372	H1-hESC	embryonic stem cell:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
29	CEBPB	chr14:67237118-67237434	Hela-S3	cervix:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
30	CEBPB	chr14:67290366-67290605	A549	lung:	n/a	n/a
31	CEBPB	chr14:67326212-67326326	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:67280306-67280665	H1-hESC	embryonic stem cell:	n/a	chr14:67280486-67280497
33	CEBPB	chr14:67325909-67326408	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:67237138-67237439	A549	lung:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
35	CEBPB	chr14:67250483-67250759	A549	lung:	n/a	n/a
36	CEBPB	chr14:67280297-67280677	A549	lung:	n/a	chr14:67280486-67280497
37	CEBPB	chr14:67280274-67280662	A549	lung:	n/a	chr14:67280486-67280497
38	CEBPB	chr14:67250490-67250759	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:67175064-67175343	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:67326120-67326325	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:67290364-67290658	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:67237101-67237436	K562	blood:	n/a	chr14:67237274-67237283 chr14:67237273-67237284 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237274-67237283 chr14:67237272-67237285 chr14:67237272-67237285
43	CEBPB	chr14:67280307-67280679	Hela-S3	cervix:	n/a	chr14:67280486-67280497
44	CEBPB	chr14:67326052-67326430	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:67176089-67176439	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr14:67326090-67326343	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:67280318-67280671	ECC-1	luminal epithelium:	n/a	chr14:67280486-67280497
48	CEBPB	chr14:67326093-67326355	A549	lung:	n/a	n/a
49	CEBPB	chr14:67250550-67250614	K562	blood:	n/a	n/a
50	CEBPB	chr14:67280301-67280681	K562	blood:	n/a	chr14:67280486-67280497

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67292488-67292538	PANC-1	pancreas:	n/a
2	chr14:67292488-67292538	LNCaP	prostate:	n/a
3	chr14:67292488-67292538	HL-60	blood:	n/a
4	chr14:67292488-67292538	HCM	heart:	n/a
5	chr14:67292488-67292538	PFSK-1	brain:	n/a
6	chr14:67292488-67292538	BJ	skin:	n/a
7	chr14:67292488-67292538	GM19239	blood:	n/a
8	chr14:67292488-67292538	HRCEpiC	kidney:	n/a
9	chr14:67292488-67292538	AG10803	skin:	n/a
10	chr14:67292488-67292538	SK-N-SH	brain:	n/a
11	chr14:67292488-67292538	NHBE	bronchial:	n/a
12	chr14:67292488-67292538	T-47D	breast:	n/a
13	chr14:67292488-67292538	HEK293	kidney:	embryo
14	chr14:67292488-67292538	H1-hESC	embryonic stem cell:	embryo
15	chr14:67292488-67292538	MCF10A-Er-Src	breast:	n/a
16	chr14:67292488-67292538	HCT-116	colon:	n/a
17	chr14:67292488-67292538	K562	blood:	n/a
18	chr14:67292488-67292538	NH-A	brain:	n/a
19	chr14:67292488-67292538	HIPEpiC	eye:	n/a
20	chr14:67292488-67292538	IMR90	lung:	fetal
21	chr14:67292488-67292538	GM12891	blood:	n/a
22	chr14:67292488-67292538	NB4	blood:	n/a
23	chr14:67292488-67292538	RPTEC	kidney:	n/a
24	chr14:67292488-67292538	Hela-S3	cervix:	n/a
25	chr14:67292488-67292538	Hepatocyte	liver:	n/a
26	chr14:67292488-67292538	SAEC	small airway:	n/a
27	chr14:67292488-67292538	CMK	blood:	n/a
28	chr14:67292488-67292538	AG09319	gingival:	n/a
29	chr14:67292488-67292538	BE2_C	brain:	n/a
30	chr14:67292488-67292538	HMEC	breast:	n/a
31	chr14:67292488-67292538	HRE	kidney:	n/a
32	chr14:67292488-67292538	HNPCEpiC	eye:	n/a
33	chr14:67292488-67292538	SKMC	muscle:	n/a
34	chr14:67292488-67292538	HepG2	liver:	n/a
35	chr14:67292488-67292538	NT2-D1	testis:	n/a
36	chr14:67292488-67292538	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:67292488-67292538	ECC-1	luminal epithelium:	n/a
38	chr14:67292488-67292538	HCF	heart:	n/a
39	chr14:67292488-67292538	U87	brain:	n/a
40	chr14:67292488-67292538	ovcar-3	ovarian:	n/a
41	chr14:67292488-67292538	AG04450	lung:	fetal
42	chr14:67292488-67292538	HCPEpiC	choroid plexus:	n/a
43	chr14:67292488-67292538	AoSMC	blood vessel:	n/a
44	chr14:67292488-67292538	HRPEpiC	eye:	n/a
45	chr14:67292488-67292538	PrEC	prostate:	n/a
46	chr14:67292488-67292538	AG09309	skin:	n/a
47	chr14:67292488-67292538	Caco-2	colon:	n/a
48	chr14:67292488-67292538	GM12892	blood:	n/a
49	chr14:67292488-67292538	SK-N-SH_RA	brain:	n/a
50	chr14:67292488-67292538	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
2	chr14:67154703..67157341-chr14:67158405..67161202,2	MCF-7	breast:
3	chr14:67145360..67148245-chr14:67155765..67157650,2	MCF-7	breast:
4	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
5	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
6	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
7	chr14:67292902..67294544-chr14:67295956..67298374,2	MCF-7	breast:
8	chr14:67091099..67091710-chr14:67212729..67213799,3	MCF-7	breast:
9	chr14:67273370..67275073-chr14:67291638..67294473,2	K562	blood:
10	chr14:66868171..66869202-chr14:67212732..67213746,3	MCF-7	breast:
11	chr14:67347067..67349521-chr14:67447070..67449089,2	MCF-7	breast:
12	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
13	chr14:67145360..67148245-chr14:67155765..67157650,2	MCF-7	breast:
14	chr14:67221145..67223857-chr14:67240535..67242119,2	K562	blood:
15	chr14:67297492..67297992-chr6:10786994..10787529,2	MCF-7	breast:
16	chr14:67310130..67311981-chr14:67312589..67315388,2	MCF-7	breast:
17	chr14:67154703..67157341-chr14:67158405..67161202,2	MCF-7	breast:
18	chr14:66974629..66976267-chr14:67206447..67208432,2	MCF-7	breast:
19	chr14:67247462..67249948-chr14:67251250..67254048,2	MCF-7	breast:
20	chr14:67290864..67292814-chr14:67296432..67298009,2	MCF-7	breast:
21	chr14:67249480..67250181-chr17:59494053..59494794,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71D-3	chr14:67227250-67227736	NONHSAT037427
2	lnc-ATP6V1D-6	chr14:67184597-67184862	expRegAs_chr14_4324_-
3	lnc-ATP6V1D-5	chr14:67187470-67188083	predAs_ge08_ARG2_2

Variant related genes	Relation type
GPHN	TF binding region
ENSG00000258796	TF binding region
GPHN	CpG island
ENSG00000258796	CpG island
ENSG00000171723	chromatin interactions
ENSG00000258561	chromatin interactions

Extended variants
information (count: 7348 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7348 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17182817	chr14:67146763-67146764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574753501	chr14:67146788-67146789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138913016	chr14:67146829-67146830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17103682	chr14:67146839-67146840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556192775	chr14:67146850-67146851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12587681	chr14:67146871-67146872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs544825068	chr14:67146880-67146881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186029261	chr14:67146897-67146898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571835746	chr14:67146930-67146931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78969404	chr14:67146943-67146944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10136366	chr14:67146945-67146946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs529668755	chr14:67146959-67146960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543361553	chr14:67147007-67147008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117845601	chr14:67147027-67147028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs111420697	chr14:67147052-67147053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552035644	chr14:67147068-67147069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs4294753	chr14:67147073-67147074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs527831124	chr14:67147119-67147120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117610336	chr14:67147148-67147149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200003253	chr14:67147218-67147219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567710658	chr14:67147219-67147220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558054568	chr14:67147230-67147231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs941808	chr14:67147286-67147287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs78453952	chr14:67147369-67147370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144560221	chr14:67147412-67147413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73287803	chr14:67147442-67147443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558377946	chr14:67147457-67147458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs77525109	chr14:67147480-67147481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576780135	chr14:67147498-67147499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs541180748	chr14:67147501-67147502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113170655	chr14:67147502-67147503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574448335	chr14:67147509-67147510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367927315	chr14:67147512-67147513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192062977	chr14:67147539-67147540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs141688628	chr14:67147562-67147563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8021087	chr14:67147586-67147587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184151992	chr14:67147614-67147615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186297599	chr14:67147628-67147629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190637963	chr14:67147639-67147640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs570679721	chr14:67147718-67147719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575220854	chr14:67147719-67147720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77211110	chr14:67147729-67147730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs370364971	chr14:67147781-67147782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201109534	chr14:67147794-67147795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560521073	chr14:67147795-67147796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373821253	chr14:67147813-67147814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3759753	chr14:67147816-67147817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs144247888	chr14:67147846-67147847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371802458	chr14:67147851-67147852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530173903	chr14:67147861-67147862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Autism	22495309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67144400-67168200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:67146000-67156600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr14:67146000-67172000	Weak transcription	Liver	Liver
4	chr14:67146400-67148400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:67146600-67149000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:67146800-67148400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr14:67147400-67151000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:67148000-67162000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr14:67148200-67151000	Weak transcription	Dnd41	blood
10	chr14:67148400-67148800	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr14:67148400-67149000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:67148800-67169400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:67149000-67156200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr14:67151000-67151400	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
15	chr14:67151000-67151400	ZNF genes & repeats	Dnd41	blood
16	chr14:67151400-67151600	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr14:67154200-67164200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:67154600-67154800	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr14:67157400-67157800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr14:67157600-67158200	Enhancers	Gastric	stomach
21	chr14:67157600-67174800	Weak transcription	HepG2	liver
22	chr14:67158000-67158200	Enhancers	Lung	lung
23	chr14:67162000-67163200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:67166600-67168200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr14:67166600-67170600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr14:67167800-67168200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr14:67168000-67168400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:67168200-67168400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr14:67168200-67168400	ZNF genes & repeats	Esophagus	oesophagus
30	chr14:67168200-67168600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr14:67168200-67168600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr14:67168200-67168600	Enhancers	NHEK	skin
33	chr14:67168200-67168800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr14:67168200-67168800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:67168200-67168800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:67168200-67168800	ZNF genes & repeats	Fetal Intestine Small	intestine
37	chr14:67168200-67168800	ZNF genes & repeats	Lung	lung
38	chr14:67168200-67169000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:67168200-67169000	Enhancers	HMEC	breast
40	chr14:67168400-67168600	Enhancers	Esophagus	oesophagus
41	chr14:67168400-67168600	Enhancers	Pancreas	Pancrea
42	chr14:67168400-67168800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:67168800-67170200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr14:67168800-67171400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr14:67169000-67176000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:67172600-67172800	Weak transcription	Liver	Liver
47	chr14:67173000-67173200	ZNF genes & repeats	Psoas Muscle	Psoas
48	chr14:67174200-67174400	Enhancers	Gastric	stomach
49	chr14:67174200-67174400	Enhancers	Ovary	ovary
50	chr14:67174400-67176800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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