Variant report

Variant	nsv456146
Chromosome Location	chr14:21361384-21432455
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	chr14:21423410-21423550	HepG2	liver:	n/a	n/a
2	CEBPB	chr14:21387301-21387487	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
3	CEBPB	chr14:21387140-21387598	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
4	CEBPB	chr14:21362247-21362271	H1-hESC	embryonic stem cell:	n/a	chr14:21362250-21362261
5	CEBPB	chr14:21387199-21387544	A549	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
6	CEBPB	chr14:21362153-21362361	IMR90	lung:	n/a	chr14:21362250-21362261
7	CEBPB	chr14:21387278-21387542	IMR90	lung:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
8	CEBPB	chr14:21387189-21387569	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
9	CEBPB	chr14:21432359-21432575	K562	blood:	n/a	n/a
10	CEBPB	chr14:21432387-21432631	A549	lung:	n/a	n/a
11	CEBPB	chr14:21373948-21374221	HepG2	liver:	n/a	chr14:21374057-21374070
12	CEBPB	chr14:21387196-21387557	Hela-S3	cervix:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
13	CEBPB	chr14:21404892-21405089	MCF-7	breast:	n/a	n/a
14	CEBPB	chr14:21387183-21387567	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
15	CEBPB	chr14:21362091-21362409	HepG2	liver:	n/a	chr14:21362250-21362261
16	CEBPB	chr14:21423393-21423620	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
17	CEBPB	chr14:21372661-21372946	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr14:21404959-21405123	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:21423391-21423541	Hela-S3	cervix:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
20	CEBPB	chr14:21404946-21405126	K562	blood:	n/a	n/a
21	CEBPB	chr14:21423250-21423720	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
22	CEBPB	chr14:21390806-21390847	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr14:21423326-21423702	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
24	CEBPB	chr14:21362201-21362274	K562	blood:	n/a	chr14:21362250-21362261
25	CEBPB	chr14:21432362-21432664	MCF-7	breast:	n/a	n/a
26	CEBPB	chr14:21362168-21362307	Hela-S3	cervix:	n/a	chr14:21362250-21362261
27	CEBPB	chr14:21362130-21362293	A549	lung:	n/a	chr14:21362250-21362261
28	CEBPB	chr14:21387296-21387479	HepG2	liver:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
29	CEBPB	chr14:21387197-21387553	H1-hESC	embryonic stem cell:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
30	CEBPB	chr14:21390675-21390974	A549	lung:	n/a	n/a
31	CEBPB	chr14:21387328-21387608	MCF-7	breast:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
32	CEBPB	chr14:21432386-21432650	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:21387184-21387565	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
34	CEBPB	chr14:21390663-21390987	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:21423483-21423531	A549	lung:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
36	CEBPB	chr14:21390705-21391054	MCF-7	breast:	n/a	n/a
37	CEBPB	chr14:21432342-21432666	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:21390712-21390883	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr14:21390780-21390974	K562	blood:	n/a	n/a
40	CEBPB	chr14:21387233-21387541	K562	blood:	n/a	chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387368-21387377 chr14:21387366-21387379 chr14:21387368-21387377
41	CEBPB	chr14:21423324-21423698	HepG2	liver:	n/a	chr14:21423498-21423509 chr14:21423498-21423511
42	CEBPD	chr14:21387228-21387447	HepG2	liver:	n/a	chr14:21387366-21387377 chr14:21387368-21387377
43	CEBPD	chr14:21423329-21423575	HepG2	liver:	n/a	chr14:21423499-21423510
44	CTCF	chr14:21402387-21402658	H1-hESC	embryonic stem cell:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
45	CTCF	chr14:21401920-21402070	AG09319	gingival:	n/a	n/a
46	CTCF	chr14:21402420-21402570	BJ	skin:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
47	CTCF	chr14:21372620-21372770	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr14:21429520-21429670	GM12873	blood:	n/a	n/a
49	CTCF	chr14:21402420-21402570	HPF	lung:	n/a	chr14:21402496-21402514 chr14:21402498-21402511 chr14:21402497-21402513 chr14:21402498-21402511
50	CTCF	chr14:21429520-21429670	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21422205-21422255	T-47D	breast:	n/a
2	chr14:21422965-21423015	NB4	blood:	n/a
3	chr14:21423837-21423887	ProgFib	skin:	n/a
4	chr14:21422205-21422255	SK-N-MC	brain:	n/a
5	chr14:21422965-21423015	U87	brain:	n/a
6	chr14:21423769-21423819	Caco-2	colon:	n/a
7	chr14:21422965-21423015	ECC-1	luminal epithelium:	n/a
8	chr14:21424117-21424167	T-47D	breast:	n/a
9	chr14:21423684-21423734	H1-hESC	embryonic stem cell:	embryo
10	chr14:21386453-21386503	AoSMC	blood vessel:	n/a
11	chr14:21422605-21422655	SK-N-MC	brain:	n/a
12	chr14:21424117-21424167	NT2-D1	testis:	n/a
13	chr14:21422605-21422655	NB4	blood:	n/a
14	chr14:21386453-21386503	NHBE	bronchial:	n/a
15	chr14:21424117-21424167	CMK	blood:	n/a
16	chr14:21422965-21423015	AoSMC	blood vessel:	n/a
17	chr14:21422205-21422255	NHBE	bronchial:	n/a
18	chr14:21424117-21424167	NHBE	bronchial:	n/a
19	chr14:21423837-21423887	HEK293	kidney:	embryo
20	chr14:21423837-21423887	Hela-S3	cervix:	n/a
21	chr14:21422965-21423015	HepG2	liver:	n/a
22	chr14:21422205-21422255	HEEpiC	esophagus:	n/a
23	chr14:21422205-21422255	NT2-D1	testis:	n/a
24	chr14:21423769-21423819	HEEpiC	esophagus:	n/a
25	chr14:21386453-21386503	GM06990	blood:	n/a
26	chr14:21422205-21422255	HMEC	breast:	n/a
27	chr14:21423837-21423887	NH-A	brain:	n/a
28	chr14:21423837-21423887	HNPCEpiC	eye:	n/a
29	chr14:21386453-21386503	HRCEpiC	kidney:	n/a
30	chr14:21422605-21422655	CMK	blood:	n/a
31	chr14:21423684-21423734	CMK	blood:	n/a
32	chr14:21424117-21424167	HCPEpiC	choroid plexus:	n/a
33	chr14:21423837-21423887	LNCaP	prostate:	n/a
34	chr14:21423684-21423734	U87	brain:	n/a
35	chr14:21386453-21386503	HRE	kidney:	n/a
36	chr14:21422605-21422655	SK-N-SH	brain:	n/a
37	chr14:21422965-21423015	IMR90	lung:	fetal
38	chr14:21423837-21423887	ovcar-3	ovarian:	n/a
39	chr14:21422965-21423015	SK-N-SH	brain:	n/a
40	chr14:21422605-21422655	Jurkat	blood:	n/a
41	chr14:21422205-21422255	HUVEC	blood vessel:	n/a
42	chr14:21424117-21424167	MCF10A-Er-Src	breast:	n/a
43	chr14:21422205-21422255	U87	brain:	n/a
44	chr14:21423684-21423734	HCT-116	colon:	n/a
45	chr14:21422605-21422655	GM12891	blood:	n/a
46	chr14:21423837-21423887	MCF10A-Er-Src	breast:	n/a
47	chr14:21423769-21423819	HMEC	breast:	n/a
48	chr14:21422605-21422655	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:21423684-21423734	NHDF-neo	bronchial:	n/a
50	chr14:21423684-21423734	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:21429229..21430249-chr14:21438962..21439710,3	MCF-7	breast:
2	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
3	chr14:21417758..21420748-chr14:21423705..21426897,3	MCF-7	breast:
4	chr14:21429613..21431283-chr14:21433107..21435716,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDRG2-3	chr14:21366144-21366340	ENSG00000258918
2	lnc-RNASE2-1	chr14:21418698-21418708	NONHSAT035618
3	lnc-NDRG2-2	chr14:21396396-21396739	ENSG00000258772
4	lnc-NDRG2-2	chr14:21384925-21385029	ENSG00000258772
5	lnc-RNASE2-2	chr14:21431738-21432024	NONHSAT035619
6	lnc-RNASE3-1	chr14:21387795-21388335	ENSG00000136315
7	lnc-RNASE3-1	chr14:21387500-21387563	ENSG00000136315
8	lnc-NDRG2-3	chr14:21404261-21404414	ENSG00000258918
9	lnc-RNASE2-1	chr14:21419045-21419476	NONHSAT035618

Variant related genes	Relation type
ENSG00000258772	TF binding region
ENSG00000136315	TF binding region
RNASE2	TF binding region
RN7SL189P	TF binding region
ENSG00000258918	TF binding region
ENSG00000258772	CpG island
ENSG00000136315	CpG island
RNASE2	CpG island
RN7SL189P	CpG island
ENSG00000258918	CpG island

Extended variants
information (count: 2140 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2140 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11849372	chr14:21361384-21361385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533975011	chr14:21361414-21361415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537197774	chr14:21361425-21361426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114358359	chr14:21361429-21361430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573821113	chr14:21361440-21361441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542556943	chr14:21361468-21361469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35263286	chr14:21361475-21361476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116865868	chr14:21361504-21361505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370994032	chr14:21361568-21361569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs573141269	chr14:21361614-21361615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2007798	chr14:21361621-21361622	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs10129333	chr14:21361631-21361632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs145856855	chr14:21361637-21361638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550718649	chr14:21361642-21361643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556721820	chr14:21361653-21361654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561311906	chr14:21361674-21361675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530365768	chr14:21361718-21361719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546955550	chr14:21361760-21361761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180718643	chr14:21361767-21361768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138349092	chr14:21361788-21361789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551401943	chr14:21361801-21361802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571325500	chr14:21361811-21361812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34578507	chr14:21361855-21361856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370586107	chr14:21361927-21361928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185112785	chr14:21361971-21361972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567329720	chr14:21361982-21361983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543587789	chr14:21362043-21362044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564074973	chr14:21362058-21362059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536483563	chr14:21362069-21362070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565045586	chr14:21362078-21362079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374665944	chr14:21362082-21362083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552960218	chr14:21362093-21362094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190707557	chr14:21362119-21362120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544953392	chr14:21362147-21362148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149137546	chr14:21362183-21362184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575273423	chr14:21362222-21362223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544297056	chr14:21362223-21362224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561460697	chr14:21362246-21362247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530215538	chr14:21362267-21362268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34727082	chr14:21362279-21362280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77981733	chr14:21362290-21362291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35346389	chr14:21362295-21362296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540264511	chr14:21362374-21362375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs184026185	chr14:21362403-21362404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs36105440	chr14:21362424-21362425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532866584	chr14:21362429-21362430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540671367	chr14:21362439-21362440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs57320287	chr14:21362457-21362458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188928091	chr14:21362520-21362521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530552361	chr14:21362555-21362556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	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
Developmental delay	21147756	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
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:220 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21356000-21362200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:21360400-21362400	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr14:21361200-21362200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr14:21362200-21363200	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr14:21362200-21364600	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr14:21362400-21363400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr14:21363200-21363800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr14:21363400-21364200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr14:21363800-21364600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr14:21364200-21364400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr14:21364400-21364800	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr14:21364600-21365600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr14:21364600-21365600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr14:21364800-21365400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr14:21365400-21365600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr14:21365600-21372400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr14:21370400-21370600	Enhancers	Gastric	stomach
18	chr14:21371800-21373000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr14:21371800-21375600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr14:21372400-21372600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr14:21372400-21372800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:21372400-21373000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr14:21372400-21373000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr14:21372400-21373200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:21372400-21373200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr14:21372400-21373200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr14:21372400-21373200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr14:21372600-21373000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:21372600-21373000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr14:21372600-21373000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr14:21372600-21374600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr14:21372600-21374800	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr14:21372800-21373200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr14:21373000-21373400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:21373400-21374000	Enhancers	Primary B cells from cord blood	blood
36	chr14:21373400-21374800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr14:21374800-21375400	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr14:21378800-21379000	Flanking Active TSS	HepG2	liver
39	chr14:21379000-21379200	Active TSS	HepG2	liver
40	chr14:21385000-21386000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr14:21385000-21387400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr14:21385000-21389400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr14:21385200-21387000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr14:21385400-21385800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:21386000-21386200	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr14:21386000-21386400	Enhancers	Fetal Intestine Large	intestine
47	chr14:21386400-21387400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr14:21387000-21387800	Enhancers	Primary hematopoietic stem cells	blood
49	chr14:21387000-21388400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:21387000-21388400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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