Variant report

Variant	nsv1037315
Chromosome Location	chr14:44813859-44934602
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:383)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:44918300-44918537	K562	blood:	n/a	n/a
2	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
4	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
5	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
6	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
8	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
9	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
10	CEBPB	chr14:44932945-44933181	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr14:44865546-44865783	Hela-S3	cervix:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
12	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
13	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
14	CEBPB	chr14:44892321-44892509	HepG2	liver:	n/a	chr14:44892371-44892382
15	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
16	CEBPB	chr14:44822857-44823212	IMR90	lung:	n/a	chr14:44823024-44823035
17	CEBPB	chr14:44865449-44865776	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
18	CEBPB	chr14:44825168-44825407	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:44822884-44823206	A549	lung:	n/a	chr14:44823024-44823035
20	CEBPB	chr14:44822861-44823165	K562	blood:	n/a	chr14:44823024-44823035
21	CEBPB	chr14:44822866-44823194	H1-hESC	embryonic stem cell:	n/a	chr14:44823024-44823035
22	CEBPB	chr14:44859620-44859752	H1-hESC	embryonic stem cell:	n/a	chr14:44859701-44859712
23	CEBPB	chr14:44822869-44823209	HepG2	liver:	n/a	chr14:44823024-44823035
24	CEBPB	chr14:44859595-44859755	HepG2	liver:	n/a	chr14:44859701-44859712
25	CEBPB	chr14:44892241-44892441	IMR90	lung:	n/a	chr14:44892371-44892382
26	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
27	CEBPB	chr14:44822632-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
28	CEBPB	chr14:44822915-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
29	CEBPB	chr14:44865478-44865918	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
30	CEBPB	chr14:44865476-44865832	A549	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
31	CEBPB	chr14:44860656-44860866	HepG2	liver:	n/a	chr14:44860752-44860763
32	CEBPD	chr14:44918285-44918591	K562	blood:	n/a	n/a
33	CEBPD	chr14:44918203-44918635	K562	blood:	n/a	n/a
34	CTCF	chr14:44838660-44838810	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr14:44867820-44867970	HepG2	liver:	n/a	n/a
36	CTCF	chr14:44838700-44838850	HMEC	breast:	n/a	n/a
37	CTCF	chr14:44817667-44817768	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:44922602-44923043	T-47D	breast:	n/a	n/a
39	CTCF	chr14:44838760-44838910	MCF-7	breast:	n/a	n/a
40	CTCF	chr14:44930341-44930412	LNCaP	prostate:	n/a	n/a
41	CTCF	chr14:44922829-44922893	K562	blood:	n/a	n/a
42	CTCF	chr14:44838660-44838952	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:44817500-44817650	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:44838750-44838851	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr14:44838712-44838866	HepG2	liver:	n/a	n/a
46	CTCF	chr14:44922804-44922869	NHEK	skin:	n/a	n/a
47	CTCF	chr14:44922746-44922968	GM12878	blood:	n/a	n/a
48	CTCF	chr14:44838680-44838830	HEK293	kidney:	n/a	n/a
49	CTCF	chr14:44838731-44838873	HepG2	liver:	n/a	n/a
50	CTCF	chr14:44884447-44884520	Kidney_OC	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44853952-44854002	GM06990	blood:	n/a
2	chr14:44853952-44854002	GM12892	blood:	n/a
3	chr14:44853952-44854002	SK-N-SH	brain:	n/a
4	chr14:44853952-44854002	PrEC	prostate:	n/a
5	chr14:44853952-44854002	SK-N-MC	brain:	n/a
6	chr14:44853952-44854002	MCF-7	breast:	n/a
7	chr14:44853952-44854002	Hepatocyte	liver:	n/a
8	chr14:44853952-44854002	ProgFib	skin:	n/a
9	chr14:44853952-44854002	AG09319	gingival:	n/a
10	chr14:44853952-44854002	NH-A	brain:	n/a
11	chr14:44853952-44854002	HCM	heart:	n/a
12	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
13	chr14:44853952-44854002	ovcar-3	ovarian:	n/a
14	chr14:44853952-44854002	AG10803	skin:	n/a
15	chr14:44853952-44854002	HL-60	blood:	n/a
16	chr14:44853952-44854002	HCPEpiC	choroid plexus:	n/a
17	chr14:44853952-44854002	HEK293	kidney:	embryo
18	chr14:44853952-44854002	CMK	blood:	n/a
19	chr14:44853952-44854002	HepG2	liver:	n/a
20	chr14:44853952-44854002	GM12878	blood:	n/a
21	chr14:44853952-44854002	BE2_C	brain:	n/a
22	chr14:44853952-44854002	AG09309	skin:	n/a
23	chr14:44853952-44854002	HRCEpiC	kidney:	n/a
24	chr14:44853952-44854002	H1-hESC	embryonic stem cell:	embryo
25	chr14:44853952-44854002	Jurkat	blood:	n/a
26	chr14:44853952-44854002	HCF	heart:	n/a
27	chr14:44853952-44854002	NHBE	bronchial:	n/a
28	chr14:44853952-44854002	HIPEpiC	eye:	n/a
29	chr14:44853952-44854002	RPTEC	kidney:	n/a
30	chr14:44853952-44854002	NB4	blood:	n/a
31	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
32	chr14:44853952-44854002	BJ	skin:	n/a
33	chr14:44853952-44854002	U87	brain:	n/a
34	chr14:44853952-44854002	SKMC	muscle:	n/a
35	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:44853952-44854002	K562	blood:	n/a
37	chr14:44853952-44854002	HMEC	breast:	n/a
38	chr14:44853952-44854002	T-47D	breast:	n/a
39	chr14:44853952-44854002	ECC-1	luminal epithelium:	n/a
40	chr14:44853952-44854002	Hela-S3	cervix:	n/a
41	chr14:44853952-44854002	SAEC	small airway:	n/a
42	chr14:44853952-44854002	AG04449	skin:	fetal
43	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
44	chr14:44853952-44854002	MCF10A-Er-Src	breast:	n/a
45	chr14:44853952-44854002	IMR90	lung:	fetal
46	chr14:44853952-44854002	PANC-1	pancreas:	n/a
47	chr14:44853952-44854002	HRPEpiC	eye:	n/a
48	chr14:44853952-44854002	PFSK-1	brain:	n/a
49	chr14:44853952-44854002	Caco-2	colon:	n/a
50	chr14:44853952-44854002	AoSMC	blood vessel:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
2	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
3	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
4	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
5	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
6	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
7	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
8	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
9	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
10	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
11	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
12	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
13	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
2	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126
3	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
4	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
5	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
6	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
7	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
8	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
9	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
10	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
11	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
12	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126

No data

Variant related genes	Relation type
ENSG00000258969	TF binding region
ENSG00000259126	TF binding region
ENSG00000258969	CpG island
ENSG00000259126	CpG island
ENSG00000259126	chromatin interactions
B4GALT1	miRNA target sites
FAM134B	miRNA target sites

Extended variants
information (count: 2220 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2220 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10484182	chr14:44813859-44813860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576528082	chr14:44813871-44813872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537103436	chr14:44813911-44813912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11845596	chr14:44813967-44813968	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs574118286	chr14:44813989-44813990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139894885	chr14:44814024-44814025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138407889	chr14:44814054-44814055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374366923	chr14:44814058-44814059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560119618	chr14:44814076-44814077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17543100	chr14:44814080-44814081	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs10484181	chr14:44814084-44814085	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563617655	chr14:44814121-44814122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563268447	chr14:44814144-44814145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530630529	chr14:44814154-44814155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548761334	chr14:44814177-44814178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538599675	chr14:44814181-44814182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191962063	chr14:44814200-44814201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561150126	chr14:44814205-44814206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528244308	chr14:44814239-44814240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546365956	chr14:44814267-44814268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs5808271	chr14:44814283-44814284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs397783485	chr14:44814286-44814287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199893289	chr14:44814287-44814288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376564049	chr14:44814289-44814290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571242625	chr14:44814329-44814330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117772486	chr14:44814346-44814347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546050491	chr14:44814349-44814350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386776985	chr14:44814353-44814354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74632276	chr14:44814355-44814356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145372346	chr14:44814388-44814389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548415000	chr14:44814390-44814391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555552247	chr14:44814393-44814394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541175284	chr14:44814394-44814395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35716666	chr14:44814423-44814424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116626120	chr14:44814459-44814460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1959207	chr14:44814517-44814518	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs530850194	chr14:44814573-44814574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76800551	chr14:44814598-44814599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545668527	chr14:44814618-44814619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62013202	chr14:44814626-44814627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556923972	chr14:44814639-44814640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575095216	chr14:44814668-44814669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147845339	chr14:44814698-44814699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369708330	chr14:44814725-44814726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184501355	chr14:44814739-44814740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs140413763	chr14:44814811-44814812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574968163	chr14:44814818-44814819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187307120	chr14:44814856-44814857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544011590	chr14:44814862-44814863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56400721	chr14:44814882-44814883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

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
Acute lymphoblastic leukemia	21098271	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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44807600-44818400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:44815800-44816200	Active TSS	Fetal Brain Male	brain
3	chr14:44817400-44817600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:44837000-44837400	Enhancers	Fetal Heart	heart
5	chr14:44837400-44839200	Weak transcription	Fetal Heart	heart
6	chr14:44838200-44839400	Enhancers	Fetal Intestine Large	intestine
7	chr14:44838200-44839600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr14:44838400-44842600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr14:44838600-44839400	Enhancers	NHEK	skin
10	chr14:44838800-44839200	Enhancers	HMEC	breast
11	chr14:44839200-44839600	Weak transcription	HMEC	breast
12	chr14:44839200-44840200	Enhancers	Fetal Heart	heart
13	chr14:44839400-44841200	Weak transcription	Fetal Intestine Large	intestine
14	chr14:44839600-44839800	Enhancers	HMEC	breast
15	chr14:44839600-44840000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:44839600-44840200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:44839600-44841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr14:44839800-44841200	Weak transcription	HMEC	breast
19	chr14:44840200-44841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:44840800-44842400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:44841200-44841800	Enhancers	HMEC	breast
22	chr14:44841200-44842400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:44841200-44842600	Enhancers	Fetal Intestine Large	intestine
24	chr14:44841400-44841800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:44841800-44842400	Weak transcription	HMEC	breast
26	chr14:44842400-44842600	Enhancers	HMEC	breast
27	chr14:44843400-44850200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:44845200-44846600	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr14:44848000-44849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr14:44848400-44849200	Enhancers	Adipose Nuclei	Adipose
31	chr14:44849200-44851000	Weak transcription	Adipose Nuclei	Adipose
32	chr14:44849200-44851600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:44850200-44851000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr14:44851000-44852800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr14:44851000-44853600	Enhancers	Adipose Nuclei	Adipose
36	chr14:44851600-44853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr14:44852600-44852800	Enhancers	Ovary	ovary
38	chr14:44852800-44853600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:44853000-44853600	Enhancers	Fetal Stomach	stomach
40	chr14:44853400-44853600	Enhancers	Ovary	ovary
41	chr14:44853400-44853800	Enhancers	Fetal Brain Female	brain
42	chr14:44853800-44857400	Weak transcription	Fetal Brain Female	brain
43	chr14:44854200-44854400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr14:44857400-44857600	Enhancers	Fetal Brain Female	brain
45	chr14:44861800-44862400	Enhancers	Fetal Intestine Large	intestine
46	chr14:44862400-44862800	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr14:44872000-44872600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr14:44872000-44874400	Enhancers	Fetal Brain Male	brain
49	chr14:44872400-44874600	Enhancers	Fetal Brain Female	brain
50	chr14:44872600-44874000	Enhancers	Fetal Heart	heart

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