Variant report

Variant	nsv1039814
Chromosome Location	chr14:24414285-24489426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1886)
CpG islands
(count:2565)
Chromatin interactive
region (count:21)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1886 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24423178-24423574	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24422800-24422908	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:24421080-24421116	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
6	ARID3A	chr14:24443416-24443612	HepG2	liver:	n/a	n/a
7	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
8	ATF3	chr14:24423153-24423533	A549	lung:	n/a	n/a
9	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
13	BATF	chr14:24423720-24424085	GM12878	blood:	n/a	n/a
14	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
16	BCL11A	chr14:24423865-24424037	GM12878	blood:	n/a	n/a
17	BCL11A	chr14:24423190-24423452	GM12878	blood:	n/a	n/a
18	BCL3	chr14:24422958-24423594	A549	lung:	n/a	n/a
19	BCLAF1	chr14:24422706-24423635	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:24422878-24423495	HepG2	liver:	n/a	n/a
21	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
22	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:24423117-24423544	K562	blood:	n/a	n/a
24	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
25	BHLHE40	chr14:24422789-24422794	K562	blood:	n/a	n/a
26	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
27	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
28	BHLHE40	chr14:24422805-24422983	GM12878	blood:	n/a	n/a
29	BRCA1	chr14:24423250-24423488	HepG2	liver:	n/a	n/a
30	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
31	BRCA1	chr14:24423242-24423570	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr14:24422911-24423016	HepG2	liver:	n/a	n/a
33	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
34	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
35	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
36	CCNT2	chr14:24422729-24423159	K562	blood:	n/a	chr14:24422739-24422748
37	CEBPB	chr14:24423252-24423596	HepG2	liver:	n/a	chr14:24423462-24423473
38	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
39	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
40	CEBPB	chr14:24422846-24423653	HepG2	liver:	n/a	chr14:24423462-24423473
41	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
42	CEBPB	chr14:24423214-24423650	Hela-S3	cervix:	n/a	chr14:24423462-24423473
43	CEBPB	chr14:24420117-24420317	HepG2	liver:	n/a	chr14:24420174-24420187 chr14:24420176-24420187 chr14:24420176-24420187 chr14:24420231-24420242
44	CEBPB	chr14:24419117-24419298	K562	blood:	n/a	chr14:24419163-24419174 chr14:24419160-24419177
45	CEBPB	chr14:24423180-24423697	A549	lung:	n/a	chr14:24423462-24423473
46	CEBPB	chr14:24423255-24423518	HepG2	liver:	n/a	chr14:24423462-24423473
47	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
48	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
49	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
50	CEBPB	chr14:24419008-24419353	HepG2	liver:	n/a	chr14:24419163-24419174 chr14:24419160-24419177

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24425012-24425062	AG04449	skin:	fetal
2	chr14:24438909-24438959	Caco-2	colon:	n/a
3	chr14:24475906-24475956	SK-N-SH	brain:	n/a
4	chr14:24425012-24425062	AG04449	skin:	fetal
5	chr14:24438909-24438959	Caco-2	colon:	n/a
6	chr14:24475906-24475956	SK-N-SH	brain:	n/a
7	chr14:24439157-24439207	H1-hESC	embryonic stem cell:	embryo
8	chr14:24458345-24458395	AG04449	skin:	fetal
9	chr14:24422419-24422469	PFSK-1	brain:	n/a
10	chr14:24425142-24425192	SK-N-SH_RA	brain:	n/a
11	chr14:24422928-24422978	HCT-116	colon:	n/a
12	chr14:24422837-24422887	ECC-1	luminal epithelium:	n/a
13	chr14:24420715-24420765	NH-A	brain:	n/a
14	chr14:24475053-24475103	HEK293	kidney:	embryo
15	chr14:24423864-24423914	U87	brain:	n/a
16	chr14:24476478-24476528	AG09309	skin:	n/a
17	chr14:24476559-24476609	A549	lung:	n/a
18	chr14:24458099-24458149	GM12878	blood:	n/a
19	chr14:24439157-24439207	SK-N-SH_RA	brain:	n/a
20	chr14:24458099-24458149	HepG2	liver:	n/a
21	chr14:24424191-24424241	HRCEpiC	kidney:	n/a
22	chr14:24439430-24439480	ECC-1	luminal epithelium:	n/a
23	chr14:24425142-24425192	IMR90	lung:	fetal
24	chr14:24457915-24457965	AG09319	gingival:	n/a
25	chr14:24458014-24458064	SK-N-MC	brain:	n/a
26	chr14:24423140-24423190	Hela-S3	cervix:	n/a
27	chr14:24423483-24423533	NB4	blood:	n/a
28	chr14:24458345-24458395	HEK293	kidney:	embryo
29	chr14:24423140-24423190	Jurkat	blood:	n/a
30	chr14:24476478-24476528	HRE	kidney:	n/a
31	chr14:24422837-24422887	HRPEpiC	eye:	n/a
32	chr14:24425012-24425062	NHDF-neo	bronchial:	n/a
33	chr14:24424191-24424241	HIPEpiC	eye:	n/a
34	chr14:24422928-24422978	HRCEpiC	kidney:	n/a
35	chr14:24423483-24423533	HUVEC	blood vessel:	n/a
36	chr14:24422956-24423006	BE2_C	brain:	n/a
37	chr14:24422928-24422978	T-47D	breast:	n/a
38	chr14:24457915-24457965	RPTEC	kidney:	n/a
39	chr14:24425012-24425062	ovcar-3	ovarian:	n/a
40	chr14:24458299-24458349	GM12891	blood:	n/a
41	chr14:24422419-24422469	HRCEpiC	kidney:	n/a
42	chr14:24475906-24475956	PFSK-1	brain:	n/a
43	chr14:24476082-24476132	AG09309	skin:	n/a
44	chr14:24458014-24458064	GM06990	blood:	n/a
45	chr14:24424191-24424241	IMR90	lung:	fetal
46	chr14:24458099-24458149	SK-N-SH	brain:	n/a
47	chr14:24458345-24458395	U87	brain:	n/a
48	chr14:24475053-24475103	GM19239	blood:	n/a
49	chr14:24476478-24476528	GM12891	blood:	n/a
50	chr14:24473832-24473882	HCF	heart:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24099084..24100809-chr14:24421080..24423663,2	MCF-7	breast:
2	chr14:24421589..24424746-chr14:24425153..24428957,4	MCF-7	breast:
3	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
4	chr14:24421741..24423927-chr14:24582561..24584260,2	K562	blood:
5	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
6	chr1:186344468..186345047-chr14:24423051..24423847,2	MCF-7	breast:
7	chr14:24422915..24424427-chr14:24563237..24565374,2	MCF-7	breast:
8	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
9	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:
10	chr14:24197895..24200996-chr14:24421897..24424681,3	MCF-7	breast:
11	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
12	chr14:24422551..24423442-chr5:180229136..180229785,2	HCT-116	colon:
13	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
14	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
15	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
16	chr14:24398247..24400471-chr14:24419661..24421717,2	MCF-7	breast:
17	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
18	chr14:24407257..24409021-chr14:24418766..24420278,2	MCF-7	breast:
19	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
20	chr14:24036767..24038500-chr14:24420729..24424068,4	MCF-7	breast:
21	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24422783-24423392	NONHSAT035954
2	lnc-NRL-1	chr14:24422983-24423061	ENSG00000215256.3
3	lnc-NRL-1	chr14:24422783-24423331	ENSG00000215256.3
4	lnc-NRL-1	chr14:24422983-24423242	NR_023923
5	lnc-NRL-1	chr14:24422518-24422578	ENSG00000215256.3
6	lnc-NRL-1	chr14:24423334-24423392	NONHSAT035952
7	lnc-NRL-1	chr14:24422983-24423242	ENSG00000215256.3
8	lnc-NRL-1	chr14:24422783-24423406	NR_023921
9	lnc-NRL-1	chr14:24422983-24423406	ENSG00000215256.3
10	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3
11	lnc-NRL-1	chr14:24422983-24423242	NONHSAT035952
12	lnc-NRL-1	chr14:24423957-24424298	NONHSAT035953
13	lnc-NRL-1	chr14:24423334-24423406	NR_023923
14	lnc-NRL-1	chr14:24422199-24422628	ENSG00000215256.3
15	lnc-NRL-1	chr14:24423334-24423375	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4-AS1	TF binding region
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	CpG island
DHRS4	CpG island
DHRS4L2	CpG island
ENSG00000100897	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000100867	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000258464	chromatin interactions
ENSG00000157181	chromatin interactions
ENSG00000197775	chromatin interactions
ENSG00000047410	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000131446	chromatin interactions

Extended variants
information (count: 3839 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:3839 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78197088	chr14:24414311-24414312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75956384	chr14:24414319-24414320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532723413	chr14:24414340-24414341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552523488	chr14:24414349-24414350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545057483	chr14:24414364-24414365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185670995	chr14:24414374-24414375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75658348	chr14:24414379-24414380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547736501	chr14:24414385-24414386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567716007	chr14:24414542-24414543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386775658	chr14:24414624-24414625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs58786866	chr14:24414625-24414626	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs570483856	chr14:24414629-24414630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533492019	chr14:24414633-24414634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539594354	chr14:24414643-24414644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs55897938	chr14:24414654-24414655	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs139983293	chr14:24414686-24414687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
17	rs111571149	chr14:24414712-24414713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs111652247	chr14:24414719-24414720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs112608884	chr14:24414795-24414796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs112256515	chr14:24414798-24414799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs554215385	chr14:24414807-24414808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112782991	chr14:24414811-24414812	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs143514281	chr14:24414822-24414823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562752024	chr14:24414841-24414842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs531832391	chr14:24414844-24414845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542108615	chr14:24414848-24414849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562079919	chr14:24414849-24414850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191210032	chr14:24414851-24414852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543015850	chr14:24414858-24414859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140820089	chr14:24414876-24414877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146235009	chr14:24414911-24414912	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs570495259	chr14:24414917-24414918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139321762	chr14:24414921-24414922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs539751734	chr14:24414972-24414973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549953241	chr14:24414981-24414982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9671870	chr14:24415009-24415010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs535686149	chr14:24415012-24415013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555683122	chr14:24415027-24415028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565861910	chr14:24415033-24415034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150174008	chr14:24415059-24415060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183436629	chr14:24415091-24415092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144021639	chr14:24415099-24415100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77266968	chr14:24415163-24415164	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs561510832	chr14:24415185-24415186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186344597	chr14:24415205-24415206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191146444	chr14:24415207-24415208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140802224	chr14:24415219-24415220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9671445	chr14:24415230-24415231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs562018610	chr14:24415274-24415275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182243165	chr14:24415306-24415307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1903 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24400000-24420000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr14:24400600-24421000	Weak transcription	Colon Smooth Muscle	Colon
3	chr14:24402200-24421200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr14:24405600-24422400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr14:24405800-24421400	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr14:24405800-24422400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr14:24406600-24416200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:24406800-24414600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr14:24407000-24420000	Weak transcription	HSMM	muscle
10	chr14:24407000-24421000	Weak transcription	Fetal Intestine Large	intestine
11	chr14:24407000-24421200	Weak transcription	Fetal Kidney	kidney
12	chr14:24407400-24422400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr14:24407600-24422200	Weak transcription	Primary B cells from cord blood	blood
14	chr14:24407800-24422400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr14:24408400-24421200	Weak transcription	Brain Substantia Nigra	brain
16	chr14:24408600-24419600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr14:24409800-24421000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:24410200-24420800	Weak transcription	Spleen	Spleen
19	chr14:24410200-24421000	Weak transcription	Left Ventricle	heart
20	chr14:24410400-24419600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:24410400-24421000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr14:24410400-24421000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:24410400-24421000	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:24410400-24421000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr14:24410400-24421200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr14:24410600-24419400	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr14:24410600-24420600	Weak transcription	Ovary	ovary
28	chr14:24410600-24420800	Weak transcription	Brain Cingulate Gyrus	brain
29	chr14:24410600-24421000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr14:24410600-24421200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:24410600-24421800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr14:24410800-24420000	Weak transcription	Adipose Nuclei	Adipose
33	chr14:24410800-24420200	Weak transcription	Duodenum Mucosa	Duodenum
34	chr14:24410800-24420600	Weak transcription	Fetal Muscle Leg	muscle
35	chr14:24410800-24420800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:24410800-24421000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr14:24410800-24421000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr14:24410800-24421800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:24410800-24422000	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr14:24410800-24422400	Weak transcription	Aorta	Aorta
41	chr14:24411000-24420800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr14:24411000-24421000	Weak transcription	Fetal Muscle Trunk	muscle
43	chr14:24411200-24417400	Weak transcription	Stomach Smooth Muscle	stomach
44	chr14:24411400-24420800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr14:24412000-24414600	Weak transcription	Primary T cells from cord blood	blood
46	chr14:24412000-24420800	Weak transcription	Lung	lung
47	chr14:24412200-24415400	Weak transcription	Fetal Stomach	stomach
48	chr14:24412200-24422400	Weak transcription	Esophagus	oesophagus
49	chr14:24412400-24415000	Weak transcription	Fetal Intestine Small	intestine
50	chr14:24412400-24420800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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