Variant report

Variant	nsv542144
Chromosome Location	chr14:81468860-81599074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:549)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81475877-81476082	K562	blood:	n/a	n/a
2	ARID3A	chr14:81472752-81472934	K562	blood:	n/a	n/a
3	ARID3A	chr14:81489472-81490101	K562	blood:	n/a	n/a
4	ARID3A	chr14:81471969-81472276	K562	blood:	n/a	n/a
5	ATF1	chr14:81471911-81472280	K562	blood:	n/a	n/a
6	ATF1	chr14:81500365-81500413	K562	blood:	n/a	n/a
7	ATF1	chr14:81475715-81476025	K562	blood:	n/a	n/a
8	ATF1	chr14:81489462-81489779	K562	blood:	n/a	n/a
9	ATF1	chr14:81472660-81472919	K562	blood:	n/a	n/a
10	ATF2	chr14:81588590-81589068	GM12878	blood:	n/a	n/a
11	ATF2	chr14:81588558-81589111	GM12878	blood:	n/a	n/a
12	ATF3	chr14:81471966-81472205	K562	blood:	n/a	chr14:81472094-81472109 chr14:81472098-81472105 chr14:81472097-81472105 chr14:81472095-81472106
13	BATF	chr14:81529132-81529373	GM12878	blood:	n/a	n/a
14	BATF	chr14:81588763-81589047	GM12878	blood:	n/a	n/a
15	BATF	chr14:81529161-81529458	GM12878	blood:	n/a	n/a
16	BCL11A	chr14:81588605-81588983	GM12878	blood:	n/a	n/a
17	BCLAF1	chr14:81588557-81589102	GM12878	blood:	n/a	n/a
18	BHLHE40	chr14:81588744-81588970	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:81548788-81548800	K562	blood:	n/a	n/a
20	BRCA1	chr14:81529183-81529431	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr14:81530687-81530815	HepG2	liver:	n/a	n/a
22	CBX3	chr14:81536945-81537161	K562	blood:	n/a	n/a
23	CBX3	chr14:81593970-81594216	K562	blood:	n/a	n/a
24	CBX3	chr14:81522301-81522679	K562	blood:	n/a	n/a
25	CBX3	chr14:81489349-81489976	K562	blood:	n/a	n/a
26	CCNT2	chr14:81489520-81490219	K562	blood:	n/a	n/a
27	CEBPB	chr14:81472742-81473090	K562	blood:	n/a	n/a
28	CEBPB	chr14:81489401-81489877	K562	blood:	n/a	n/a
29	CEBPB	chr14:81573790-81573835	A549	lung:	n/a	n/a
30	CEBPB	chr14:81575032-81575337	IMR90	lung:	n/a	chr14:81575171-81575182
31	CEBPB	chr14:81494983-81495157	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:81594280-81594446	H1-hESC	embryonic stem cell:	n/a	chr14:81594363-81594374
33	CEBPB	chr14:81494979-81495215	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:81594246-81594554	K562	blood:	n/a	chr14:81594363-81594374
35	CEBPB	chr14:81591620-81591820	HepG2	liver:	n/a	chr14:81591775-81591786 chr14:81591664-81591675
36	CEBPB	chr14:81470968-81471182	K562	blood:	n/a	n/a
37	CEBPB	chr14:81567401-81567639	A549	lung:	n/a	chr14:81567507-81567518
38	CEBPB	chr14:81471918-81472255	K562	blood:	n/a	n/a
39	CEBPB	chr14:81568589-81568916	IMR90	lung:	n/a	chr14:81568758-81568771 chr14:81568758-81568769
40	CEBPB	chr14:81568592-81568907	HepG2	liver:	n/a	chr14:81568758-81568771 chr14:81568758-81568769
41	CEBPB	chr14:81575024-81575317	A549	lung:	n/a	chr14:81575171-81575182
42	CEBPB	chr14:81594186-81594520	A549	lung:	n/a	chr14:81594363-81594374
43	CEBPB	chr14:81568692-81568892	H1-hESC	embryonic stem cell:	n/a	chr14:81568758-81568771 chr14:81568758-81568769
44	CEBPB	chr14:81494951-81495141	A549	lung:	n/a	n/a
45	CEBPB	chr14:81567350-81567667	HepG2	liver:	n/a	chr14:81567507-81567518
46	CEBPB	chr14:81489664-81489738	K562	blood:	n/a	n/a
47	CEBPB	chr14:81575018-81575325	HepG2	liver:	n/a	chr14:81575171-81575182
48	CEBPB	chr14:81594190-81594520	HepG2	liver:	n/a	chr14:81594363-81594374
49	CEBPB	chr14:81594188-81594536	IMR90	lung:	n/a	chr14:81594363-81594374
50	CEBPB	chr14:81484701-81484823	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81580765-81580815	HRE	kidney:	n/a
2	chr14:81580765-81580815	HMEC	breast:	n/a
3	chr14:81580765-81580815	AoSMC	blood vessel:	n/a
4	chr14:81580765-81580815	GM19239	blood:	n/a
5	chr14:81580765-81580815	H1-hESC	embryonic stem cell:	embryo
6	chr14:81580765-81580815	AG04449	skin:	fetal
7	chr14:81580765-81580815	HCT-116	colon:	n/a
8	chr14:81580765-81580815	GM12891	blood:	n/a
9	chr14:81580765-81580815	IMR90	lung:	fetal
10	chr14:81580765-81580815	ProgFib	skin:	n/a
11	chr14:81580765-81580815	HUVEC	blood vessel:	n/a
12	chr14:81580765-81580815	SAEC	small airway:	n/a
13	chr14:81580765-81580815	Hepatocyte	liver:	n/a
14	chr14:81580765-81580815	NT2-D1	testis:	n/a
15	chr14:81580765-81580815	RPTEC	kidney:	n/a
16	chr14:81580765-81580815	SK-N-SH	brain:	n/a
17	chr14:81580765-81580815	MCF-7	breast:	n/a
18	chr14:81580765-81580815	A549	lung:	n/a
19	chr14:81580765-81580815	HIPEpiC	eye:	n/a
20	chr14:81580765-81580815	HAEpiC	amniotic membrane:	n/a
21	chr14:81580765-81580815	HNPCEpiC	eye:	n/a
22	chr14:81580765-81580815	PANC-1	pancreas:	n/a
23	chr14:81580765-81580815	CMK	blood:	n/a
24	chr14:81580765-81580815	AG09309	skin:	n/a
25	chr14:81580765-81580815	PFSK-1	brain:	n/a
26	chr14:81580765-81580815	AG10803	skin:	n/a
27	chr14:81580765-81580815	Hela-S3	cervix:	n/a
28	chr14:81580765-81580815	GM12892	blood:	n/a
29	chr14:81580765-81580815	HCF	heart:	n/a
30	chr14:81580765-81580815	HRCEpiC	kidney:	n/a
31	chr14:81580765-81580815	GM06990	blood:	n/a
32	chr14:81580765-81580815	Jurkat	blood:	n/a
33	chr14:81580765-81580815	SK-N-MC	brain:	n/a
34	chr14:81580765-81580815	AG09319	gingival:	n/a
35	chr14:81580765-81580815	T-47D	breast:	n/a
36	chr14:81580765-81580815	K562	blood:	n/a
37	chr14:81580765-81580815	Caco-2	colon:	n/a
38	chr14:81580765-81580815	HCM	heart:	n/a
39	chr14:81580765-81580815	ovcar-3	ovarian:	n/a
40	chr14:81580765-81580815	NH-A	brain:	n/a
41	chr14:81580765-81580815	NHBE	bronchial:	n/a
42	chr14:81580765-81580815	SKMC	muscle:	n/a
43	chr14:81580765-81580815	NHDF-neo	bronchial:	n/a
44	chr14:81580765-81580815	HCPEpiC	choroid plexus:	n/a
45	chr14:81580765-81580815	AG04450	lung:	fetal
46	chr14:81580765-81580815	HepG2	liver:	n/a
47	chr14:81580765-81580815	HEEpiC	esophagus:	n/a
48	chr14:81580765-81580815	GM12878	blood:	n/a
49	chr14:81580765-81580815	LNCaP	prostate:	n/a
50	chr14:81580765-81580815	NB4	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81476596..81478510-chr14:81478665..81481342,2	K562	blood:
2	chr14:81487256..81489215-chr14:81492840..81494538,2	K562	blood:
3	chr14:81467255..81470490-chr14:81470537..81472087,4	K562	blood:
4	chr14:81586845..81589081-chr14:81590020..81592537,2	MCF-7	breast:
5	chr14:81462345..81463310-chr14:81528942..81529784,4	MCF-7	breast:
6	chr14:81495440..81498431-chr14:81685185..81687345,2	K562	blood:
7	chr14:81462591..81463541-chr14:81528802..81529444,3	MCF-7	breast:
8	chr14:81536154..81536750-chr14:81547094..81547647,2	MCF-7	breast:
9	chr14:81596731..81598312-chr14:81628484..81630801,2	K562	blood:
10	chr14:81586845..81589081-chr14:81590020..81592537,2	MCF-7	breast:
11	chr14:81496857..81499197-chr14:81502024..81503758,2	K562	blood:
12	chr14:81468835..81472649-chr14:81474348..81477215,3	K562	blood:
13	chr14:81522510..81524954-chr14:81528365..81530619,2	MCF-7	breast:
14	chr14:81479552..81481692-chr14:81684705..81687037,3	K562	blood:
15	chr14:81489891..81491738-chr14:81496835..81498987,2	K562	blood:
16	chr14:81486385..81489423-chr14:81489812..81494340,5	K562	blood:
17	chr14:81525678..81528643-chr14:81528934..81531190,2	MCF-7	breast:
18	chr14:81420680..81421622-chr14:81528974..81529745,4	MCF-7	breast:
19	chr14:81512399..81512969-chr3:86511334..86512054,2	MCF-7	breast:
20	chr14:81486385..81489423-chr14:81489812..81494340,5	K562	blood:
21	chr14:81522510..81524954-chr14:81528365..81530619,2	MCF-7	breast:
22	chr14:81462340..81462871-chr14:81529168..81529817,2	K562	blood:
23	chr14:81476596..81478510-chr14:81478665..81481342,2	K562	blood:
24	chr14:81574238..81576394-chr14:81685477..81688391,2	K562	blood:
25	chr14:81472830..81475161-chr14:81475745..81477749,2	MCF-7	breast:
26	chr14:81464422..81467304-chr14:81478351..81480140,2	MCF-7	breast:
27	chr14:81487256..81489215-chr14:81492840..81494538,2	K562	blood:
28	chr14:81472830..81475161-chr14:81475745..81477749,2	MCF-7	breast:
29	chr14:81512955..81515863-chr14:81686957..81688607,2	K562	blood:
30	chr14:81564551..81566339-chr14:81684688..81687460,2	MCF-7	breast:
31	chr14:81525678..81528643-chr14:81528934..81531190,2	MCF-7	breast:
32	chr14:81494625..81496593-chr14:81498314..81499995,2	K562	blood:
33	chr14:81536154..81536750-chr14:81547094..81547647,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN3-5	chr14:81574693-81574796	NONHSAT038049
2	lnc-GTF2A1-1	chr14:81573377-81573482	ENSG00000258999.1
3	lnc-NRXN3-5	chr14:81574956-81575184	NONHSAT038049
4	lnc-CEP128-2	chr14:81469669-81469989	NONHSAT038047

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TSHR	hsa-miR-181a-5p	chr14:81575149-81575171

Variant related genes	Relation type
TSHR	TF binding region
ENSG00000271656	TF binding region
RPL17P3	TF binding region
NMNAT1P1	TF binding region
TSHR	CpG island
ENSG00000271656	CpG island
RPL17P3	CpG island
NMNAT1P1	CpG island
ENSG00000271656	chromatin interactions
ENSG00000165409	chromatin interactions
ENSG00000259167	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000271705	chromatin interactions

Extended variants
information (count: 4781 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4781 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555815167	chr14:81468896-81468897	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs187083918	chr14:81468953-81468954	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs4903964	chr14:81468954-81468955	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs543697012	chr14:81469043-81469044	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200281092	chr14:81469126-81469127	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199677500	chr14:81469128-81469129	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12889568	chr14:81469129-81469130	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201833602	chr14:81469130-81469131	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373832725	chr14:81469152-81469153	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs374950501	chr14:81469154-81469155	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs56340312	chr14:81469168-81469169	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs374612939	chr14:81469169-81469170	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562190978	chr14:81469174-81469175	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534922737	chr14:81469242-81469243	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs577195908	chr14:81469322-81469323	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs7151548	chr14:81469340-81469341	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs55699123	chr14:81469349-81469350	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs190652543	chr14:81469420-81469421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560013050	chr14:81469426-81469427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527334046	chr14:81469427-81469428	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548916517	chr14:81469438-81469439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs56278849	chr14:81469456-81469457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75887592	chr14:81469458-81469459	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531686340	chr14:81469472-81469473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550079915	chr14:81469496-81469497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199943510	chr14:81469505-81469506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539047686	chr14:81469559-81469560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371030518	chr14:81469560-81469561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547738897	chr14:81469569-81469570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566041030	chr14:81469571-81469572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7152373	chr14:81469592-81469593	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs545163523	chr14:81469597-81469598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180718539	chr14:81469644-81469645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569911952	chr14:81469699-81469700	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs556979212	chr14:81469728-81469729	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs537376525	chr14:81469732-81469733	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs375756390	chr14:81469766-81469767	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs142508825	chr14:81469788-81469789	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs544682576	chr14:81469793-81469794	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs368487366	chr14:81469821-81469822	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs575158418	chr14:81469823-81469824	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs372842219	chr14:81469854-81469855	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs374839663	chr14:81469859-81469860	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs553690197	chr14:81469860-81469861	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs72478821	chr14:81469887-81469888	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs542705639	chr14:81469917-81469918	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs146908702	chr14:81470002-81470003	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs55960644	chr14:81470024-81470025	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs543605256	chr14:81470050-81470051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs55957493	chr14:81470054-81470055	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
2	chr14:81463200-81469000	Weak transcription	K562	blood
3	chr14:81467000-81470400	Strong transcription	Dnd41	blood
4	chr14:81468000-81486600	Weak transcription	Thymus	Thymus
5	chr14:81468400-81469600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr14:81468400-81472600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr14:81469000-81469200	Bivalent Enhancer	Primary T cells from cord blood	blood
8	chr14:81469000-81469200	Enhancers	Primary hematopoietic stem cells	blood
9	chr14:81469000-81469200	Enhancers	HSMM	muscle
10	chr14:81469000-81469200	Flanking Active TSS	K562	blood
11	chr14:81469200-81469400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
12	chr14:81469200-81469400	Enhancers	K562	blood
13	chr14:81469400-81470800	Weak transcription	K562	blood
14	chr14:81469600-81469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr14:81470400-81477200	Weak transcription	Dnd41	blood
16	chr14:81470800-81474800	Enhancers	K562	blood
17	chr14:81471400-81471600	Enhancers	Left Ventricle	heart
18	chr14:81471400-81472800	Enhancers	Fetal Heart	heart
19	chr14:81472600-81472800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:81474800-81475200	Weak transcription	K562	blood
21	chr14:81475200-81476400	Enhancers	K562	blood
22	chr14:81476400-81477200	Weak transcription	K562	blood
23	chr14:81477200-81477400	Enhancers	K562	blood
24	chr14:81477200-81478000	ZNF genes & repeats	Dnd41	blood
25	chr14:81478000-81482600	Weak transcription	Dnd41	blood
26	chr14:81482600-81487000	Strong transcription	Dnd41	blood
27	chr14:81483400-81484000	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr14:81484000-81484400	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr14:81484000-81485000	Enhancers	NHDF-Ad	bronchial
30	chr14:81484000-81485600	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr14:81484200-81484400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:81484200-81484400	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr14:81484200-81485000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr14:81484400-81484600	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr14:81484400-81484600	Enhancers	Adipose Nuclei	Adipose
36	chr14:81484400-81484800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr14:81484400-81485000	Active TSS	Duodenum Mucosa	Duodenum
38	chr14:81484400-81485200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:81484400-81485200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr14:81484600-81484800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:81484600-81485000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr14:81484600-81485200	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr14:81484600-81502400	Weak transcription	Liver	Liver
44	chr14:81484800-81485000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr14:81484800-81485000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:81484800-81485800	Enhancers	K562	blood
47	chr14:81485000-81485200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr14:81485000-81485400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:81485000-81485600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr14:81485200-81485400	Enhancers	Adipose Nuclei	Adipose

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