Variant report

Variant	nsv826901
Chromosome Location	chr14:24457315-24508468
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	chr14:24483172-24483507	K562	blood:	n/a	n/a
2	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24502290-24502595	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:24505981-24506248	HepG2	liver:	n/a	n/a
5	ATF2	chr14:24505949-24506263	GM12878	blood:	n/a	n/a
6	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
7	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr14:24506432-24506750	GM12878	blood:	n/a	n/a
10	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
11	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
12	BATF	chr14:24506427-24506735	GM12878	blood:	n/a	n/a
13	BCL3	chr14:24505902-24506304	A549	lung:	n/a	n/a
14	BCL3	chr14:24502093-24502738	A549	lung:	n/a	n/a
15	BHLHE40	chr14:24505965-24506313	GM12878	blood:	n/a	n/a
16	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
17	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
18	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
19	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
20	BRCA1	chr14:24505981-24506214	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
22	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
23	CBX3	chr14:24501866-24502194	K562	blood:	n/a	n/a
24	CBX3	chr14:24501883-24502114	K562	blood:	n/a	n/a
25	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
26	CEBPB	chr14:24503786-24503943	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:24502257-24502651	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
28	CEBPB	chr14:24505919-24506258	H1-hESC	embryonic stem cell:	n/a	chr14:24506174-24506185
29	CEBPB	chr14:24506005-24506217	HepG2	liver:	n/a	chr14:24506174-24506185
30	CEBPB	chr14:24502095-24502733	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
31	CEBPB	chr14:24505955-24506340	MCF-7	breast:	n/a	chr14:24506174-24506185
32	CEBPB	chr14:24502240-24502694	Hela-S3	cervix:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
33	CEBPB	chr14:24502235-24502633	MCF-7	breast:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
34	CEBPB	chr14:24502240-24502596	A549	lung:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
35	CEBPB	chr14:24505832-24506370	GM12878	blood:	n/a	chr14:24506174-24506185
36	CEBPB	chr14:24502288-24502568	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
37	CEBPB	chr14:24505953-24506379	MCF-7	breast:	n/a	chr14:24506174-24506185
38	CEBPB	chr14:24502292-24502624	K562	blood:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
39	CEBPB	chr14:24503873-24504233	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:24504095-24504242	HepG2	liver:	n/a	n/a
41	CEBPB	chr14:24503705-24503975	MCF-7	breast:	n/a	n/a
42	CEBPB	chr14:24503875-24503956	A549	lung:	n/a	n/a
43	CEBPB	chr14:24505959-24506192	HepG2	liver:	n/a	chr14:24506174-24506185
44	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
45	CEBPB	chr14:24505923-24506358	A549	lung:	n/a	chr14:24506174-24506185
46	CEBPB	chr14:24505949-24506410	HepG2	liver:	n/a	chr14:24506174-24506185
47	CEBPB	chr14:24502174-24502650	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
48	CEBPB	chr14:24506005-24506241	ECC-1	luminal epithelium:	n/a	chr14:24506174-24506185
49	CEBPB	chr14:24502259-24502654	HepG2	liver:	n/a	chr14:24502436-24502447 chr14:24502436-24502447 chr14:24502434-24502447 chr14:24502434-24502445
50	CEBPB	chr14:24505883-24506354	Hela-S3	cervix:	n/a	chr14:24506174-24506185

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24505671-24505721	SK-N-SH_RA	brain:	n/a
2	chr14:24457993-24458043	A549	lung:	n/a
3	chr14:24457509-24457559	ovcar-3	ovarian:	n/a
4	chr14:24505671-24505721	SK-N-SH_RA	brain:	n/a
5	chr14:24457993-24458043	A549	lung:	n/a
6	chr14:24457509-24457559	ovcar-3	ovarian:	n/a
7	chr14:24458004-24458054	AG04450	lung:	fetal
8	chr14:24505898-24505948	NH-A	brain:	n/a
9	chr14:24505537-24505587	BJ	skin:	n/a
10	chr14:24475906-24475956	SAEC	small airway:	n/a
11	chr14:24505547-24505597	HIPEpiC	eye:	n/a
12	chr14:24458000-24458050	HCPEpiC	choroid plexus:	n/a
13	chr14:24457993-24458043	GM19239	blood:	n/a
14	chr14:24505554-24505604	AG04449	skin:	fetal
15	chr14:24458299-24458349	ProgFib	skin:	n/a
16	chr14:24458299-24458349	SK-N-MC	brain:	n/a
17	chr14:24503311-24503361	HCF	heart:	n/a
18	chr14:24457893-24457943	ovcar-3	ovarian:	n/a
19	chr14:24476478-24476528	IMR90	lung:	fetal
20	chr14:24505653-24505703	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:24476478-24476528	HRPEpiC	eye:	n/a
22	chr14:24458345-24458395	HMEC	breast:	n/a
23	chr14:24457509-24457559	A549	lung:	n/a
24	chr14:24458099-24458149	SK-N-SH	brain:	n/a
25	chr14:24457915-24457965	ProgFib	skin:	n/a
26	chr14:24505653-24505703	HMEC	breast:	n/a
27	chr14:24457893-24457943	HEEpiC	esophagus:	n/a
28	chr14:24475053-24475103	AG04450	lung:	fetal
29	chr14:24457915-24457965	NHBE	bronchial:	n/a
30	chr14:24475906-24475956	GM12891	blood:	n/a
31	chr14:24505743-24505793	HRPEpiC	eye:	n/a
32	chr14:24505537-24505587	HCT-116	colon:	n/a
33	chr14:24476082-24476132	HNPCEpiC	eye:	n/a
34	chr14:24457915-24457965	GM12878	blood:	n/a
35	chr14:24503311-24503361	AG04449	skin:	fetal
36	chr14:24505898-24505948	AG09309	skin:	n/a
37	chr14:24458299-24458349	GM19239	blood:	n/a
38	chr14:24457893-24457943	SK-N-MC	brain:	n/a
39	chr14:24475906-24475956	H1-hESC	embryonic stem cell:	embryo
40	chr14:24505898-24505948	HCPEpiC	choroid plexus:	n/a
41	chr14:24505898-24505948	GM12878	blood:	n/a
42	chr14:24458014-24458064	HRE	kidney:	n/a
43	chr14:24476478-24476528	CMK	blood:	n/a
44	chr14:24478620-24478670	HRE	kidney:	n/a
45	chr14:24458099-24458149	HIPEpiC	eye:	n/a
46	chr14:24458099-24458149	RPTEC	kidney:	n/a
47	chr14:24476082-24476132	HL-60	blood:	n/a
48	chr14:24476478-24476528	NHBE	bronchial:	n/a
49	chr14:24475053-24475103	HEEpiC	esophagus:	n/a
50	chr14:24458299-24458349	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
2	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
3	chr14:24503791..24508058-chr14:24562194..24566408,5	MCF-7	breast:
4	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
5	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
6	chr14:24505359..24507247-chr14:24702110..24704400,2	MCF-7	breast:
7	chr14:24504090..24505966-chr14:24768791..24770568,2	MCF-7	breast:
8	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
9	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
10	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
11	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
12	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
13	chr14:24504490..24506127-chr14:24583788..24585514,2	MCF-7	breast:
14	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
15	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
16	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
17	chr14:24505124..24506975-chr14:24520204..24522367,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

Variant related genes	Relation type
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
ENSG00000225766	TF binding region
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000225766	CpG island
ENSG00000100938	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000186648	chromatin interactions
ENSG00000196943	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000157379	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000225766	chromatin interactions

Extended variants
information (count: 2314 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2314 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531084256	chr14:24457336-24457337	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs55714428	chr14:24457352-24457353	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs55869357	chr14:24457373-24457374	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368777546	chr14:24457457-24457458	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536236624	chr14:24457464-24457465	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs61999794	chr14:24457482-24457483	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs139460417	chr14:24457509-24457510	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs535566758	chr14:24457510-24457511	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs142554673	chr14:24457513-24457514	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs377112432	chr14:24457521-24457522	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs369419477	chr14:24457522-24457523	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs66845024	chr14:24457531-24457532	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146010672	chr14:24457536-24457537	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs184297225	chr14:24457537-24457538	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs371723757	chr14:24457546-24457547	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs374680042	chr14:24457592-24457593	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs61999795	chr14:24457614-24457615	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142125693	chr14:24457624-24457625	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs553123813	chr14:24457633-24457634	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374959750	chr14:24457659-24457660	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs572965242	chr14:24457674-24457675	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs71405824	chr14:24457818-24457819	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188543568	chr14:24457825-24457826	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs531020923	chr14:24457846-24457847	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs544521231	chr14:24457861-24457862	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs561623428	chr14:24457863-24457864	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs369774973	chr14:24457900-24457901	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs530356551	chr14:24457904-24457905	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs72692114	chr14:24457918-24457919	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs180953787	chr14:24457921-24457922	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs72692115	chr14:24457923-24457924	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552311031	chr14:24457934-24457935	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs569012255	chr14:24457943-24457944	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs541511957	chr14:24457951-24457952	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs538034877	chr14:24457957-24457958	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs554494097	chr14:24457961-24457962	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs149890493	chr14:24457967-24457968	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs111695788	chr14:24457990-24457991	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs55774579	chr14:24458001-24458002	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs117487342	chr14:24458013-24458014	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	mRNA abundance
41	rs374553574	chr14:24458031-24458032	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs78442944	chr14:24458037-24458038	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs377346223	chr14:24458045-24458046	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs373029131	chr14:24458046-24458047	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs55643821	chr14:24458048-24458049	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs575382198	chr14:24458053-24458054	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
47	rs55911718	chr14:24458055-24458056	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561357892	chr14:24458061-24458062	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
49	rs112919965	chr14:24458075-24458076	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs540573403	chr14:24458077-24458078	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1247 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
2	chr14:24439400-24457600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr14:24446200-24458000	Weak transcription	Gastric	stomach
4	chr14:24446600-24457400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr14:24448000-24457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:24448400-24457400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr14:24450400-24457400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr14:24450400-24457600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr14:24451800-24457400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr14:24452600-24457600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr14:24453600-24457600	Enhancers	Dnd41	blood
12	chr14:24453800-24457600	Enhancers	Fetal Thymus	thymus
13	chr14:24454800-24457600	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr14:24455000-24457800	Weak transcription	HMEC	breast
15	chr14:24455000-24458000	Weak transcription	HSMM	muscle
16	chr14:24455200-24457400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr14:24455200-24457600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr14:24455200-24457600	Weak transcription	Osteobl	bone
19	chr14:24455400-24457600	Enhancers	Fetal Intestine Large	intestine
20	chr14:24455400-24457800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr14:24455600-24457600	Enhancers	A549	lung
22	chr14:24455800-24457600	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr14:24455800-24458000	Enhancers	Fetal Lung	lung
24	chr14:24455800-24459400	Enhancers	Fetal Brain Female	brain
25	chr14:24456200-24457400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr14:24456200-24457600	Weak transcription	Psoas Muscle	Psoas
27	chr14:24456200-24457600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr14:24456200-24457600	Weak transcription	NHDF-Ad	bronchial
29	chr14:24456200-24457800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:24456200-24457800	Weak transcription	Brain Hippocampus Middle	brain
31	chr14:24456200-24457800	Weak transcription	Colonic Mucosa	Colon
32	chr14:24456200-24458000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr14:24456200-24458200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr14:24456200-24458200	Weak transcription	Placenta	Placenta
35	chr14:24456400-24457600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:24456400-24457600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr14:24456400-24457600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr14:24456400-24457600	Weak transcription	Fetal Intestine Small	intestine
39	chr14:24456400-24457800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:24456400-24458200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:24456400-24458200	Weak transcription	Brain Substantia Nigra	brain
42	chr14:24456400-24459200	Weak transcription	Brain Cingulate Gyrus	brain
43	chr14:24456600-24457600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:24456600-24457600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr14:24456600-24457600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr14:24456600-24457800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr14:24456600-24457800	Weak transcription	Brain Anterior Caudate	brain
48	chr14:24456600-24457800	Weak transcription	Fetal Brain Male	brain
49	chr14:24456600-24458000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr14:24456600-24458000	Weak transcription	Esophagus	oesophagus

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