Variant report

Variant	esv2761824
Chromosome Location	chr14:24914008-24993666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:460)
CpG islands
(count:245)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24950760-24951183	HepG2	liver:	n/a	n/a
2	ATF2	chr14:24932426-24932919	GM12878	blood:	n/a	n/a
3	BCLAF1	chr14:24932394-24932853	GM12878	blood:	n/a	chr14:24932495-24932504
4	BHLHE40	chr14:24950873-24951083	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:24988161-24988425	GM12878	blood:	n/a	chr14:24988285-24988298 chr14:24988287-24988296 chr14:24988287-24988296 chr14:24988288-24988297
6	BHLHE40	chr14:24950918-24951048	K562	blood:	n/a	n/a
7	BHLHE40	chr14:24977363-24977725	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:24961460-24961471	A549	lung:	n/a	n/a
9	CEBPB	chr14:24913804-24914037	A549	lung:	n/a	chr14:24913926-24913937
10	CEBPB	chr14:24984093-24984194	HepG2	liver:	n/a	chr14:24984150-24984161
11	CEBPB	chr14:24925409-24925575	A549	lung:	n/a	chr14:24925447-24925460 chr14:24925447-24925458
12	CEBPB	chr14:24936556-24936597	IMR90	lung:	n/a	chr14:24936570-24936581
13	CEBPB	chr14:24933358-24933637	IMR90	lung:	n/a	chr14:24933477-24933488
14	CEBPB	chr14:24936466-24936680	HepG2	liver:	n/a	chr14:24936570-24936581
15	CEBPB	chr14:24933380-24933633	A549	lung:	n/a	chr14:24933477-24933488
16	CEBPB	chr14:24961253-24961544	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:24961363-24961489	HepG2	liver:	n/a	n/a
18	CEBPB	chr14:24961365-24961539	MCF-7	breast:	n/a	n/a
19	CEBPB	chr14:24961288-24961606	HepG2	liver:	n/a	n/a
20	CEBPB	chr14:24991135-24991276	HepG2	liver:	n/a	n/a
21	CEBPB	chr14:24925313-24925621	HepG2	liver:	n/a	chr14:24925447-24925460 chr14:24925447-24925458
22	CEBPB	chr14:24933331-24933629	HepG2	liver:	n/a	chr14:24933477-24933488
23	CEBPB	chr14:24985169-24985265	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:24913817-24914033	HepG2	liver:	n/a	chr14:24913926-24913937
25	CEBPB	chr14:24933322-24933646	K562	blood:	n/a	chr14:24933477-24933488
26	CEBPB	chr14:24991550-24991602	HepG2	liver:	n/a	chr14:24991553-24991564
27	CHD2	chr14:24950790-24951053	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr14:24950846-24951061	HepG2	liver:	n/a	n/a
29	CREB1	chr14:24935061-24935433	GM12878	blood:	n/a	n/a
30	CREB1	chr14:24934957-24935508	GM12878	blood:	n/a	n/a
31	CREB1	chr14:24953109-24953480	GM12878	blood:	n/a	n/a
32	CTCF	chr14:24950825-24951067	Spleen_OC	spleen:	n/a	chr14:24950940-24950958
33	CTCF	chr14:24950880-24951030	NHLF	lung:	n/a	chr14:24950940-24950958
34	CTCF	chr14:24950704-24951229	MCF-7	breast:	n/a	chr14:24950940-24950958
35	CTCF	chr14:24974780-24974930	GM06990	blood:	n/a	n/a
36	CTCF	chr14:24950200-24950350	GM12872	blood:	n/a	n/a
37	CTCF	chr14:24950860-24951010	BE2_C	brain:	n/a	chr14:24950940-24950958
38	CTCF	chr14:24950880-24951030	RPTEC	kidney:	n/a	chr14:24950940-24950958
39	CTCF	chr14:24950880-24951030	HCM	heart:	n/a	chr14:24950940-24950958
40	CTCF	chr14:24950860-24951010	AG09309	skin:	n/a	chr14:24950940-24950958
41	CTCF	chr14:24950826-24951087	GM13976	blood:	n/a	chr14:24950940-24950958
42	CTCF	chr14:24950808-24951100	A549	lung:	n/a	chr14:24950940-24950958
43	CTCF	chr14:24950730-24951129	K562	blood:	n/a	chr14:24950940-24950958
44	CTCF	chr14:24950684-24951263	HepG2	liver:	n/a	chr14:24950940-24950958
45	CTCF	chr14:24950860-24951010	Hela-S3	cervix:	n/a	chr14:24950940-24950958
46	CTCF	chr14:24951460-24951610	AG04449	skin:	n/a	chr14:24951464-24951482
47	CTCF	chr14:24950841-24951058	GM10248	blood:	n/a	chr14:24950940-24950958
48	CTCF	chr14:24950818-24951074	HUVEC	blood vessel:	n/a	chr14:24950940-24950958
49	CTCF	chr14:24950880-24951030	MCF-7	breast:	n/a	chr14:24950940-24950958
50	CTCF	chr14:24950716-24951155	K562	blood:	n/a	chr14:24950940-24950958

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24977773-24977823	K562	blood:	n/a
2	chr14:24977773-24977823	K562	blood:	n/a
3	chr14:24978681-24978731	T-47D	breast:	n/a
4	chr14:24974804-24974854	Caco-2	colon:	n/a
5	chr14:24914181-24914231	HNPCEpiC	eye:	n/a
6	chr14:24978681-24978731	HCT-116	colon:	n/a
7	chr14:24914181-24914231	SK-N-SH	brain:	n/a
8	chr14:24914181-24914231	CMK	blood:	n/a
9	chr14:24978681-24978731	HRPEpiC	eye:	n/a
10	chr14:24978681-24978731	Hepatocyte	liver:	n/a
11	chr14:24978681-24978731	AG04449	skin:	fetal
12	chr14:24978681-24978731	U87	brain:	n/a
13	chr14:24914181-24914231	Hela-S3	cervix:	n/a
14	chr14:24977773-24977823	MCF-7	breast:	n/a
15	chr14:24914181-24914231	GM19239	blood:	n/a
16	chr14:24914181-24914231	SK-N-MC	brain:	n/a
17	chr14:24977773-24977823	U87	brain:	n/a
18	chr14:24974804-24974854	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:24974804-24974854	Jurkat	blood:	n/a
20	chr14:24978681-24978731	Caco-2	colon:	n/a
21	chr14:24978681-24978731	AG09309	skin:	n/a
22	chr14:24977773-24977823	HepG2	liver:	n/a
23	chr14:24978681-24978731	NHBE	bronchial:	n/a
24	chr14:24977773-24977823	ovcar-3	ovarian:	n/a
25	chr14:24977773-24977823	PFSK-1	brain:	n/a
26	chr14:24977773-24977823	SK-N-MC	brain:	n/a
27	chr14:24977773-24977823	HCPEpiC	choroid plexus:	n/a
28	chr14:24914181-24914231	HL-60	blood:	n/a
29	chr14:24974804-24974854	AG04450	lung:	fetal
30	chr14:24978681-24978731	NT2-D1	testis:	n/a
31	chr14:24974804-24974854	SAEC	small airway:	n/a
32	chr14:24914181-24914231	HCF	heart:	n/a
33	chr14:24974804-24974854	NB4	blood:	n/a
34	chr14:24974804-24974854	SKMC	muscle:	n/a
35	chr14:24974804-24974854	H1-hESC	embryonic stem cell:	embryo
36	chr14:24978681-24978731	AG10803	skin:	n/a
37	chr14:24978681-24978731	A549	lung:	n/a
38	chr14:24974804-24974854	SK-N-SH	brain:	n/a
39	chr14:24977773-24977823	Jurkat	blood:	n/a
40	chr14:24977773-24977823	AG09319	gingival:	n/a
41	chr14:24974804-24974854	HRE	kidney:	n/a
42	chr14:24974804-24974854	HEK293	kidney:	embryo
43	chr14:24978681-24978731	PFSK-1	brain:	n/a
44	chr14:24974804-24974854	ovcar-3	ovarian:	n/a
45	chr14:24977773-24977823	IMR90	lung:	fetal
46	chr14:24914181-24914231	HAEpiC	amniotic membrane:	n/a
47	chr14:24977773-24977823	GM12892	blood:	n/a
48	chr14:24914181-24914231	PrEC	prostate:	n/a
49	chr14:24914181-24914231	IMR90	lung:	fetal
50	chr14:24974804-24974854	AG09309	skin:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
2	chr14:24911704..24914258-chr14:24948506..24950947,2	MCF-7	breast:
3	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
4	chr14:24816528..24849574-chr14:24893305..24914155,145	MCF-7	breast:
5	chr14:24709335..24712189-chr14:24910783..24914037,3	K562	blood:
6	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
7	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
8	chr14:24911289..24913259-chr14:24923385..24925782,2	MCF-7	breast:
9	chr14:24781460..24810019-chr14:24892340..24914262,110	MCF-7	breast:
10	chr14:24929358..24930887-chr8:102503029..102505102,2	MCF-7	breast:
11	chr14:24922420..24924852-chr14:24926664..24928247,2	K562	blood:
12	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
13	chr14:24952643..24955226-chr14:24957985..24960918,2	K562	blood:
14	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:
15	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
16	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
17	chr14:24925537..24927679-chr14:24931012..24933705,2	MCF-7	breast:
18	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
19	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
20	chr14:24910451..24913467-chr14:24926014..24930297,6	MCF-7	breast:
21	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
22	chr14:24977730..24979918-chr14:24980024..24982313,2	MCF-7	breast:
23	chr14:24922420..24924852-chr14:24926664..24928247,2	K562	blood:
24	chr14:24923545..24925251-chr14:24928583..24930504,2	MCF-7	breast:
25	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
26	chr14:24940138..24941029-chr14:24952690..24953556,3	MCF-7	breast:
27	chr14:24987134..24988670-chr14:24989655..24991180,2	K562	blood:
28	chr14:24911857..24913696-chr14:24915123..24916800,2	MCF-7	breast:
29	chr14:24960817..24963613-chr14:24965277..24968190,2	K562	blood:
30	chr14:24941879..24943792-chr14:24944086..24946470,2	MCF-7	breast:
31	chr14:24911430..24913240-chr14:24948207..24950557,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-80A15.1.1-1	chr14:24913490-24914778	ENSG00000251021
2	lnc-RP11-80A15.1.1-1	chr14:24913490-24914778	NR_110032
3	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	ENSG00000251021
4	lnc-RP11-80A15.1.1-1	chr14:24970766-24971403	NR_110032

No data

Variant related genes	Relation type
CMA1	TF binding region
SDR39U1	TF binding region
ENSG00000258744	TF binding region
CMA1	CpG island
SDR39U1	CpG island
ENSG00000258744	CpG island
ENSG00000254024	chromatin interactions
ENSG00000083307	chromatin interactions
ENSG00000129465	chromatin interactions
ENSG00000258973	chromatin interactions
ENSG00000129467	chromatin interactions
ENSG00000100445	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000100968	chromatin interactions
ENSG00000207141	chromatin interactions
ENSG00000213903	chromatin interactions
CYP2C8	miRNA target sites

Extended variants
information (count: 2509 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2509 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11158709	chr14:24914008-24914009	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184358293	chr14:24914028-24914029	Weak transcription	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
3	rs541349199	chr14:24914049-24914050	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
4	rs187757178	chr14:24914051-24914052	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
5	rs193115648	chr14:24914114-24914115	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
6	rs147341780	chr14:24914121-24914122	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
7	rs116265618	chr14:24914128-24914129	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
8	rs4981518	chr14:24914129-24914130	Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs529021142	chr14:24914156-24914157	Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs74797678	chr14:24914191-24914192	Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs4981519	chr14:24914227-24914228	Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs528260028	chr14:24914253-24914254	Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
13	rs80192295	chr14:24914326-24914327	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs559597814	chr14:24914411-24914412	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs4981520	chr14:24914431-24914432	Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs116818120	chr14:24914550-24914551	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs185829799	chr14:24914574-24914575	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs569990039	chr14:24914586-24914587	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs189382706	chr14:24914643-24914644	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs536378985	chr14:24914663-24914664	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs555806318	chr14:24914664-24914665	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs4981521	chr14:24914681-24914682	Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs541263530	chr14:24914682-24914683	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs557910696	chr14:24914704-24914705	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs4981522	chr14:24914727-24914728	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs4981523	chr14:24914730-24914731	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs557725631	chr14:24914733-24914734	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs528852743	chr14:24914736-24914737	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs4982919	chr14:24914739-24914740	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs4982920	chr14:24914802-24914803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs528172493	chr14:24914879-24914880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551646918	chr14:24914903-24914904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192339841	chr14:24914923-24914924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4981524	chr14:24914929-24914930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs559543555	chr14:24914932-24914933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528939899	chr14:24914948-24914949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs78261011	chr14:24914978-24914979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184508077	chr14:24914987-24914988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188725293	chr14:24915038-24915039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555462287	chr14:24915060-24915061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565865057	chr14:24915123-24915124	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112193461	chr14:24915151-24915152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs181107879	chr14:24915166-24915167	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs533330554	chr14:24915174-24915175	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs78663777	chr14:24915196-24915197	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112265330	chr14:24915236-24915237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs77673327	chr14:24915271-24915272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
48	rs542635782	chr14:24915330-24915331	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141560418	chr14:24915331-24915332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571480363	chr14:24915352-24915353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24912000-24925800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:24912400-24922400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:24912600-24925800	Weak transcription	Ovary	ovary
4	chr14:24912800-24915800	Weak transcription	Aorta	Aorta
5	chr14:24912800-24922800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:24912800-24950800	Weak transcription	Gastric	stomach
7	chr14:24913000-24914800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr14:24913000-24914800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr14:24913000-24914800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr14:24913000-24914800	Weak transcription	Fetal Muscle Leg	muscle
11	chr14:24913000-24915000	Weak transcription	Brain Substantia Nigra	brain
12	chr14:24913000-24915000	Weak transcription	K562	blood
13	chr14:24913000-24915600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:24913000-24917000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:24913000-24917400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:24913000-24917600	Weak transcription	Placenta	Placenta
17	chr14:24913000-24917800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr14:24913000-24918000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr14:24913000-24922200	Weak transcription	Fetal Intestine Small	intestine
20	chr14:24913000-24922400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr14:24913000-24922800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:24913000-24923600	Weak transcription	NHEK	skin
23	chr14:24913000-24925400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:24913000-24925800	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr14:24913000-24926400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:24913000-24930000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:24913000-24931600	Weak transcription	Fetal Kidney	kidney
28	chr14:24913000-24932400	Weak transcription	Primary B cells from cord blood	blood
29	chr14:24913000-24932800	Weak transcription	Primary T cells from cord blood	blood
30	chr14:24913200-24915000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr14:24913200-24916000	Weak transcription	HSMM	muscle
32	chr14:24913200-24921800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr14:24913200-24925400	Weak transcription	HMEC	breast
34	chr14:24913600-24923600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr14:24914000-24914400	Weak transcription	Fetal Stomach	stomach
36	chr14:24914000-24923200	Weak transcription	HepG2	liver
37	chr14:24920800-24927400	Weak transcription	Spleen	Spleen
38	chr14:24921800-24923600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:24922000-24925800	Weak transcription	Liver	Liver
40	chr14:24922200-24924200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:24922200-24924200	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr14:24922200-24946000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr14:24922400-24922800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
44	chr14:24922400-24923000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
45	chr14:24922400-24924600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr14:24922800-24924200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr14:24922800-24924200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr14:24922800-24951000	Weak transcription	Pancreas	Pancrea
49	chr14:24923000-24925800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr14:24923200-24924000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived

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