Variant report

Variant	nsv518816
Chromosome Location	chr14:46217649-46408343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:607)
CpG islands
(count:367)
Chromatin interactive
region (count:16)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:607 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
2	ATF2	chr14:46337571-46338159	GM12878	blood:	n/a	n/a
3	ATF2	chr14:46336378-46337127	GM12878	blood:	n/a	n/a
4	ATF2	chr14:46337595-46337969	GM12878	blood:	n/a	n/a
5	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:46337483-46337971	GM12878	blood:	n/a	chr14:46337729-46337740
7	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
8	BATF	chr14:46336397-46337076	GM12878	blood:	n/a	n/a
9	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
10	BATF	chr14:46368023-46368235	GM12878	blood:	n/a	n/a
11	BATF	chr14:46337483-46338059	GM12878	blood:	n/a	chr14:46337729-46337740
12	BCL11A	chr14:46338183-46338481	GM12878	blood:	n/a	n/a
13	BCL11A	chr14:46337580-46337867	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:46337474-46337979	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
16	BCL3	chr14:46337522-46337975	GM12878	blood:	n/a	n/a
17	BCL3	chr14:46337578-46337949	GM12878	blood:	n/a	n/a
18	BCL3	chr14:46336621-46336979	GM12878	blood:	n/a	n/a
19	BCLAF1	chr14:46337617-46337960	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:46337665-46337965	GM12878	blood:	n/a	n/a
21	CBX3	chr14:46256472-46256659	K562	blood:	n/a	n/a
22	CEBPB	chr14:46388556-46388893	A549	lung:	n/a	chr14:46388709-46388720
23	CEBPB	chr14:46270317-46270820	A549	lung:	n/a	chr14:46270518-46270529
24	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
25	CEBPB	chr14:46321607-46321769	A549	lung:	n/a	n/a
26	CEBPB	chr14:46309387-46309957	HepG2	liver:	n/a	chr14:46309800-46309811
27	CEBPB	chr14:46248535-46248671	HepG2	liver:	n/a	chr14:46248607-46248618
28	CEBPB	chr14:46232907-46233168	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr14:46242906-46243113	HepG2	liver:	n/a	chr14:46243004-46243015
31	CEBPB	chr14:46242879-46243131	IMR90	lung:	n/a	chr14:46243004-46243015
32	CEBPB	chr14:46270325-46270606	IMR90	lung:	n/a	chr14:46270518-46270529
33	CEBPB	chr14:46388459-46388948	MCF-7	breast:	n/a	chr14:46388709-46388720
34	CEBPB	chr14:46309406-46309962	A549	lung:	n/a	chr14:46309800-46309811
35	CEBPB	chr14:46388507-46388949	MCF-7	breast:	n/a	chr14:46388709-46388720
36	CEBPB	chr14:46270324-46270772	HepG2	liver:	n/a	chr14:46270518-46270529
37	CEBPB	chr14:46388540-46388897	IMR90	lung:	n/a	chr14:46388709-46388720
38	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
39	CREB1	chr14:46337522-46338032	GM12878	blood:	n/a	n/a
40	CREB1	chr14:46276327-46276806	GM12878	blood:	n/a	n/a
41	CTCF	chr14:46340300-46340450	BE2_C	brain:	n/a	n/a
42	CTCF	chr14:46279840-46279990	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr14:46340360-46340510	GM12865	blood:	n/a	n/a
44	CTCF	chr14:46340400-46340550	A549	lung:	n/a	n/a
45	CTCF	chr14:46279827-46279968	ProgFib	skin:	n/a	n/a
46	CTCF	chr14:46340260-46340410	HRE	kidney:	n/a	n/a
47	CTCF	chr14:46279800-46279950	HAc	cerebellar:	n/a	n/a
48	CTCF	chr14:46307920-46308070	HCT-116	colon:	n/a	chr14:46307991-46308009 chr14:46307993-46308014
49	CTCF	chr14:46268840-46268990	NHEK	skin:	n/a	n/a
50	CTCF	chr14:46288322-46288739	MCF-7	breast:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46283172-46283222	GM19239	blood:	n/a
2	chr14:46283172-46283222	GM19239	blood:	n/a
3	chr14:46300358-46300408	Hela-S3	cervix:	n/a
4	chr14:46283172-46283222	GM12892	blood:	n/a
5	chr14:46241576-46241626	SK-N-MC	brain:	n/a
6	chr14:46358279-46358329	LNCaP	prostate:	n/a
7	chr14:46358139-46358189	GM12891	blood:	n/a
8	chr14:46358279-46358329	HCT-116	colon:	n/a
9	chr14:46358279-46358329	AG10803	skin:	n/a
10	chr14:46358279-46358329	AG09319	gingival:	n/a
11	chr14:46300358-46300408	HNPCEpiC	eye:	n/a
12	chr14:46241576-46241626	T-47D	breast:	n/a
13	chr14:46241576-46241626	HCM	heart:	n/a
14	chr14:46358139-46358189	AG09319	gingival:	n/a
15	chr14:46358139-46358189	LNCaP	prostate:	n/a
16	chr14:46283117-46283167	HL-60	blood:	n/a
17	chr14:46283117-46283167	K562	blood:	n/a
18	chr14:46283117-46283167	U87	brain:	n/a
19	chr14:46283172-46283222	SAEC	small airway:	n/a
20	chr14:46300358-46300408	NB4	blood:	n/a
21	chr14:46358279-46358329	HepG2	liver:	n/a
22	chr14:46358279-46358329	HIPEpiC	eye:	n/a
23	chr14:46241576-46241626	ovcar-3	ovarian:	n/a
24	chr14:46283172-46283222	Hepatocyte	liver:	n/a
25	chr14:46300358-46300408	GM12891	blood:	n/a
26	chr14:46241576-46241626	IMR90	lung:	fetal
27	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
28	chr14:46283117-46283167	AG10803	skin:	n/a
29	chr14:46241576-46241626	HCT-116	colon:	n/a
30	chr14:46283172-46283222	BE2_C	brain:	n/a
31	chr14:46300358-46300408	HRE	kidney:	n/a
32	chr14:46300358-46300408	HL-60	blood:	n/a
33	chr14:46283172-46283222	HCM	heart:	n/a
34	chr14:46358279-46358329	GM12878	blood:	n/a
35	chr14:46358139-46358189	Caco-2	colon:	n/a
36	chr14:46358279-46358329	HRPEpiC	eye:	n/a
37	chr14:46241576-46241626	HCF	heart:	n/a
38	chr14:46300358-46300408	MCF-7	breast:	n/a
39	chr14:46283117-46283167	SK-N-SH	brain:	n/a
40	chr14:46358139-46358189	MCF10A-Er-Src	breast:	n/a
41	chr14:46283117-46283167	HEEpiC	esophagus:	n/a
42	chr14:46283117-46283167	AG09319	gingival:	n/a
43	chr14:46300358-46300408	MCF10A-Er-Src	breast:	n/a
44	chr14:46283172-46283222	NH-A	brain:	n/a
45	chr14:46283117-46283167	HRE	kidney:	n/a
46	chr14:46300358-46300408	AG04449	skin:	fetal
47	chr14:46283172-46283222	SK-N-SH_RA	brain:	n/a
48	chr14:46358139-46358189	GM12878	blood:	n/a
49	chr14:46283172-46283222	SK-N-MC	brain:	n/a
50	chr14:46241576-46241626	AG04449	skin:	fetal

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
2	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
3	chr14:46079191..46080200-chr14:46279301..46280311,3	MCF-7	breast:
4	chr14:46119850..46120526-chr14:46279646..46280307,2	MCF-7	breast:
5	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
6	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
7	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
8	chr14:46253596..46255101-chr14:46269085..46271326,2	K562	blood:
9	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
10	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
11	chr14:46185495..46186349-chr14:46307923..46308469,2	MCF-7	breast:
12	chr14:46185447..46186022-chr14:46279860..46280372,3	MCF-7	breast:
13	chr14:46147376..46147982-chr14:46279500..46280082,2	MCF-7	breast:
14	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
15	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
16	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-5	chr14:46241339-46241424	XLOC_010816
2	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
3	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675
4	lnc-FANCM-5	chr14:46217809-46217840	NONHSAT036670
5	lnc-FANCM-5	chr14:46217539-46217865	NONHSAT036671
6	lnc-FANCM-5	chr14:46217809-46217893	NONHSAT036668
7	lnc-FANCM-5	chr14:46217809-46217860	XLOC_010816
8	lnc-FANCM-5	chr14:46241613-46241659	XLOC_010816
9	lnc-FANCM-5	chr14:46241338-46241424	NONHSAT036671
10	lnc-FANCM-5	chr14:46241612-46241659	NONHSAT036671

No data

Variant related genes	Relation type
ENSG00000264420	TF binding region
LINC00871	TF binding region
ENSG00000264420	CpG island
LINC00871	CpG island

Extended variants
information (count: 3305 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3305 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1268595	chr14:46217649-46217650	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146984734	chr14:46217681-46217682	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs191843404	chr14:46217699-46217700	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557044645	chr14:46217714-46217715	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs376024741	chr14:46217720-46217721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs542664719	chr14:46217729-46217730	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs554367651	chr14:46217806-46217807	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs182687963	chr14:46217808-46217809	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs137970896	chr14:46217818-46217819	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs149488034	chr14:46217847-46217848	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs186960453	chr14:46217892-46217893	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs111712183	chr14:46225000-46225001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543799771	chr14:46225021-46225022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147718383	chr14:46225058-46225059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563989822	chr14:46225074-46225075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs374148638	chr14:46225103-46225104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1906816	chr14:46225134-46225135	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566842424	chr14:46225139-46225140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549468002	chr14:46225161-46225162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534199185	chr14:46225163-46225164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142488828	chr14:46225164-46225165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577295026	chr14:46225175-46225176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546396021	chr14:46225223-46225224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146782181	chr14:46225240-46225241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114387664	chr14:46225243-46225244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1266308	chr14:46225284-46225285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs541691840	chr14:46225287-46225288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187667999	chr14:46225308-46225309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77637356	chr14:46225368-46225369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139105988	chr14:46225369-46225370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141479058	chr14:46225379-46225380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527391093	chr14:46225387-46225388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143538636	chr14:46231844-46231845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575110447	chr14:46231857-46231858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542475931	chr14:46231866-46231867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112734925	chr14:46231876-46231877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561433617	chr14:46231948-46231949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148042476	chr14:46231995-46231996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527665607	chr14:46232030-46232031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185211703	chr14:46232071-46232072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564514311	chr14:46232081-46232082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143511556	chr14:46232083-46232084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145905602	chr14:46232188-46232189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75833425	chr14:46232387-46232388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535297747	chr14:46232400-46232401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547645603	chr14:46232470-46232471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191106652	chr14:46232484-46232485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1266296	chr14:46232501-46232502	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs138724896	chr14:46232504-46232505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376877268	chr14:46232650-46232651	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46225000-46225400	Enhancers	Esophagus	oesophagus
2	chr14:46231800-46232800	Enhancers	Colon Smooth Muscle	Colon
3	chr14:46232800-46241200	Weak transcription	Colon Smooth Muscle	Colon
4	chr14:46237600-46238000	Enhancers	Rectal Smooth Muscle	rectum
5	chr14:46241200-46242000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr14:46241200-46242200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr14:46241200-46242200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr14:46241200-46242200	Enhancers	Colon Smooth Muscle	Colon
9	chr14:46241200-46242400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr14:46241200-46242400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr14:46241200-46242400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr14:46252200-46252600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:46252600-46252800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:46252800-46253600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:46253200-46256800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr14:46253400-46253800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:46253400-46254000	ZNF genes & repeats	NHEK	skin
18	chr14:46253400-46254200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:46253600-46253800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:46253600-46254000	Enhancers	Stomach Mucosa	stomach
21	chr14:46253600-46255600	Enhancers	HMEC	breast
22	chr14:46253800-46254000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:46253800-46254200	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr14:46253800-46255400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr14:46254000-46254200	Enhancers	NHEK	skin
26	chr14:46254000-46254800	Weak transcription	Stomach Mucosa	stomach
27	chr14:46254000-46255400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr14:46254200-46254400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chr14:46254200-46254600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr14:46254200-46254600	Flanking Active TSS	NHEK	skin
31	chr14:46254400-46254600	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr14:46254600-46255000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr14:46254600-46255000	Enhancers	NHEK	skin
34	chr14:46254600-46255600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:46254800-46255600	Enhancers	Stomach Mucosa	stomach
36	chr14:46254800-46256400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:46255000-46255600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr14:46255000-46256000	ZNF genes & repeats	NHEK	skin
39	chr14:46255200-46255800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr14:46255400-46255600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:46255400-46256400	ZNF genes & repeats	Liver	Liver
42	chr14:46255600-46255800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:46255800-46256200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:46255800-46258400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr14:46258400-46262000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr14:46258600-46258800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
47	chr14:46259600-46260400	Enhancers	Colon Smooth Muscle	Colon
48	chr14:46260400-46261000	Weak transcription	Colon Smooth Muscle	Colon
49	chr14:46261000-46261200	Enhancers	Colon Smooth Muscle	Colon
50	chr14:46261800-46262600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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