Variant report

Variant	nsv974316
Chromosome Location	chr14:24423787-24424426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr14:24423720-24424085	GM12878	blood:	n/a	n/a
2	BCL11A	chr14:24423865-24424037	GM12878	blood:	n/a	n/a
3	CTCF	chr14:24424349-24424394	GM13976	blood:	n/a	n/a
4	CTCF	chr14:24424310-24424354	LNCaP	prostate:	n/a	n/a
5	CTCF	chr14:24424328-24424348	GM13976	blood:	n/a	n/a
6	CTCF	chr14:24424355-24424361	LNCaP	prostate:	n/a	n/a
7	CTCF	chr14:24423960-24424031	GM13976	blood:	n/a	n/a
8	CTCF	chr14:24424020-24424170	GM12872	blood:	n/a	n/a
9	CTCF	chr14:24424320-24424470	AG04449	skin:	n/a	n/a
10	CTCF	chr14:24423969-24423991	GM13977	blood:	n/a	n/a
11	CTCF	chr14:24424267-24424297	GM13976	blood:	n/a	n/a
12	CTCF	chr14:24423923-24423983	LNCaP	prostate:	n/a	n/a
13	CTCF	chr14:24423953-24424065	GM20000	blood:	n/a	n/a
14	CTCF	chr14:24424240-24424261	GM13976	blood:	n/a	n/a
15	CTCF	chr14:24423740-24423890	HepG2	liver:	n/a	n/a
16	CTCF	chr14:24423700-24423850	HMF	breast:	n/a	n/a
17	CTCF	chr14:24422723-24423866	A549	lung:	n/a	chr14:24423405-24423426 chr14:24423411-24423427 chr14:24423410-24423428
18	EBF1	chr14:24423795-24424109	GM12878	blood:	n/a	chr14:24423962-24423973
19	EBF1	chr14:24423759-24424086	GM12878	blood:	n/a	chr14:24423962-24423973
20	EBF1	chr14:24423857-24424077	GM12878	blood:	n/a	chr14:24423962-24423973
21	MAFK	chr14:24423658-24423847	HepG2	liver:	n/a	n/a
22	MBD4	chr14:24422642-24423826	HepG2	liver:	n/a	n/a
23	MXI1	chr14:24422274-24423831	SK-N-SH	brain:	n/a	chr14:24423256-24423265 chr14:24423258-24423267
24	MYBL2	chr14:24422110-24423826	HepG2	liver:	n/a	n/a
25	MYBL2	chr14:24422368-24423806	HepG2	liver:	n/a	n/a
26	MYC	chr14:24424348-24424365	MCF-7	breast:	n/a	n/a
27	MYC	chr14:24424366-24424374	MCF-7	breast:	n/a	n/a
28	MYC	chr14:24424117-24424478	MCF10A-Er-Src	breast:	n/a	n/a
29	MYC	chr14:24424181-24424479	MCF10A-Er-Src	breast:	n/a	n/a
30	MYC	chr14:24424350-24424386	MCF-7	breast:	n/a	n/a
31	POLR2A	chr14:24423844-24423969	K562	blood:	n/a	n/a
32	POLR2A	chr14:24424097-24424319	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr14:24424309-24424421	MCF-7	breast:	n/a	n/a
34	POLR2A	chr14:24424005-24424050	K562	blood:	n/a	n/a
35	POLR2A	chr14:24424256-24424286	MCF10A-Er-Src	breast:	n/a	n/a
36	SPI1	chr14:24423773-24424079	GM12878	blood:	n/a	n/a
37	TEAD4	chr14:24422372-24423865	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24424191-24424241	NHBE	bronchial:	n/a
2	chr14:24423864-24423914	HUVEC	blood vessel:	n/a
3	chr14:24424191-24424241	ProgFib	skin:	n/a
4	chr14:24423864-24423914	NB4	blood:	n/a
5	chr14:24423864-24423914	SAEC	small airway:	n/a
6	chr14:24423864-24423914	GM12892	blood:	n/a
7	chr14:24423864-24423914	HRCEpiC	kidney:	n/a
8	chr14:24424191-24424241	NB4	blood:	n/a
9	chr14:24423864-24423914	PFSK-1	brain:	n/a
10	chr14:24424191-24424241	SK-N-SH	brain:	n/a
11	chr14:24423864-24423914	AG04450	lung:	fetal
12	chr14:24423864-24423914	HCT-116	colon:	n/a
13	chr14:24424191-24424241	HRE	kidney:	n/a
14	chr14:24424191-24424241	Hepatocyte	liver:	n/a
15	chr14:24423864-24423914	MCF-7	breast:	n/a
16	chr14:24423864-24423914	AG09309	skin:	n/a
17	chr14:24423864-24423914	AoSMC	blood vessel:	n/a
18	chr14:24424191-24424241	NHDF-neo	bronchial:	n/a
19	chr14:24424191-24424241	RPTEC	kidney:	n/a
20	chr14:24424191-24424241	PrEC	prostate:	n/a
21	chr14:24423864-24423914	U87	brain:	n/a
22	chr14:24424191-24424241	A549	lung:	n/a
23	chr14:24424191-24424241	NH-A	brain:	n/a
24	chr14:24424191-24424241	ECC-1	luminal epithelium:	n/a
25	chr14:24423864-24423914	MCF10A-Er-Src	breast:	n/a
26	chr14:24423864-24423914	NHBE	bronchial:	n/a
27	chr14:24424191-24424241	AG04449	skin:	fetal
28	chr14:24424191-24424241	Caco-2	colon:	n/a
29	chr14:24423864-24423914	GM12878	blood:	n/a
30	chr14:24424191-24424241	GM06990	blood:	n/a
31	chr14:24423864-24423914	HNPCEpiC	eye:	n/a
32	chr14:24423864-24423914	PrEC	prostate:	n/a
33	chr14:24423864-24423914	BE2_C	brain:	n/a
34	chr14:24423864-24423914	AG09319	gingival:	n/a
35	chr14:24423864-24423914	SKMC	muscle:	n/a
36	chr14:24424191-24424241	U87	brain:	n/a
37	chr14:24424191-24424241	HCM	heart:	n/a
38	chr14:24423864-24423914	SK-N-SH_RA	brain:	n/a
39	chr14:24424191-24424241	CMK	blood:	n/a
40	chr14:24424191-24424241	NT2-D1	testis:	n/a
41	chr14:24424191-24424241	HNPCEpiC	eye:	n/a
42	chr14:24423864-24423914	RPTEC	kidney:	n/a
43	chr14:24424191-24424241	AG04450	lung:	fetal
44	chr14:24423864-24423914	AG10803	skin:	n/a
45	chr14:24423864-24423914	K562	blood:	n/a
46	chr14:24424191-24424241	HAEpiC	amniotic membrane:	n/a
47	chr14:24424191-24424241	HEK293	kidney:	embryo
48	chr14:24424191-24424241	SK-N-SH_RA	brain:	n/a
49	chr14:24423864-24423914	IMR90	lung:	fetal
50	chr14:24423864-24423914	BJ	skin:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24422915..24424427-chr14:24563237..24565374,2	MCF-7	breast:
2	chr14:24422701..24424551-chr14:24504249..24506129,2	MCF-7	breast:
3	chr14:24197895..24200996-chr14:24421897..24424681,3	MCF-7	breast:
4	chr14:24421741..24423927-chr14:24582561..24584260,2	K562	blood:
5	chr14:24036767..24038500-chr14:24420729..24424068,4	MCF-7	breast:
6	chr1:186344468..186345047-chr14:24423051..24423847,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24423957-24424298	NONHSAT035953

No data

Variant related genes	Relation type
DHRS4-AS1	TF binding region
DHRS4-AS1	CpG island
ENSG00000157181	chromatin interactions
ENSG00000100897	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000047410	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000258464	chromatin interactions

Extended variants
information (count: 57 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181529896	chr14:24423788-24423789	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs370779641	chr14:24423829-24423830	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs184293697	chr14:24423851-24423852	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs575266309	chr14:24423857-24423858	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs188537860	chr14:24423864-24423865	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs148181627	chr14:24423875-24423876	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs11158470	chr14:24423918-24423919	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs199842000	chr14:24423921-24423922	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs563397587	chr14:24423947-24423948	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs113151112	chr14:24423992-24423993	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
11	rs564170732	chr14:24423994-24423995	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
12	rs113367887	chr14:24424013-24424014	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
13	rs527714467	chr14:24424033-24424034	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
14	rs547466225	chr14:24424035-24424036	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
15	rs149860092	chr14:24424062-24424063	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
16	rs539603870	chr14:24424080-24424081	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs556719649	chr14:24424098-24424099	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs561117787	chr14:24424111-24424112	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs570201640	chr14:24424128-24424129	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs536134518	chr14:24424147-24424148	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs180985433	chr14:24424155-24424156	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs572047087	chr14:24424161-24424162	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs146356650	chr14:24424181-24424182	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs61999765	chr14:24424182-24424183	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs61999766	chr14:24424186-24424187	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs557854878	chr14:24424209-24424210	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs139708761	chr14:24424224-24424225	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs373010678	chr14:24424225-24424226	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs146373042	chr14:24424247-24424248	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs543208779	chr14:24424248-24424249	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs563498507	chr14:24424252-24424253	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs138564114	chr14:24424253-24424254	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs374151392	chr14:24424260-24424261	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs377038259	chr14:24424264-24424265	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
35	rs199663128	chr14:24424266-24424267	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
36	rs559251300	chr14:24424267-24424268	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
37	rs527652442	chr14:24424280-24424281	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
38	rs1127278	chr14:24424281-24424282	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
39	rs1127279	chr14:24424289-24424290	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
40	rs533460137	chr14:24424292-24424293	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs550046703	chr14:24424305-24424306	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs79086208	chr14:24424306-24424307	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs148405684	chr14:24424326-24424327	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs142533242	chr14:24424331-24424332	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs150588702	chr14:24424333-24424334	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs139648244	chr14:24424339-24424340	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs549668516	chr14:24424340-24424341	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs4981491	chr14:24424346-24424347	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs566393352	chr14:24424362-24424363	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs12147221	chr14:24424367-24424368	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

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

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24421000-24423800	Active TSS	K562	blood
2	chr14:24421200-24423800	Active TSS	Fetal Kidney	kidney
3	chr14:24421600-24424200	Active TSS	Duodenum Mucosa	Duodenum
4	chr14:24421800-24423800	Active TSS	GM12878-XiMat	blood
5	chr14:24421800-24424200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr14:24422000-24423800	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr14:24422200-24423800	Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr14:24422200-24423800	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr14:24422200-24423800	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr14:24422200-24423800	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr14:24422200-24423800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr14:24422200-24423800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:24422200-24423800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr14:24422200-24423800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:24422200-24423800	Active TSS	Brain Germinal Matrix	brain
16	chr14:24422200-24423800	Active TSS	A549	lung
17	chr14:24422200-24423800	Active TSS	HMEC	breast
18	chr14:24422200-24423800	Active TSS	HSMM	muscle
19	chr14:24422200-24424000	Active TSS	NHLF	lung
20	chr14:24422200-24424200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr14:24422400-24423800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr14:24422400-24423800	Active TSS	Aorta	Aorta
23	chr14:24422400-24423800	Active TSS	NH-A	brain
24	chr14:24422400-24424000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:24422600-24423800	Active TSS	Fetal Intestine Large	intestine
26	chr14:24422600-24423800	Active TSS	Fetal Intestine Small	intestine
27	chr14:24422600-24423800	Active TSS	Left Ventricle	heart
28	chr14:24422600-24423800	Active TSS	Right Atrium	heart
29	chr14:24422600-24423800	Active TSS	Right Ventricle	heart
30	chr14:24422600-24423800	Active TSS	NHDF-Ad	bronchial
31	chr14:24422600-24424000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr14:24422600-24424200	Active TSS	Primary hematopoietic stem cells short term culture	blood
33	chr14:24422800-24423800	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr14:24422800-24423800	Active TSS	Fetal Muscle Trunk	muscle
35	chr14:24423000-24424400	Active TSS	Fetal Brain Female	brain
36	chr14:24423200-24423800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:24423200-24424000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr14:24423200-24424000	Flanking Active TSS	Dnd41	blood
39	chr14:24423200-24424200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
40	chr14:24423400-24423800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:24423400-24423800	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr14:24423400-24423800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:24423400-24423800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr14:24423400-24423800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr14:24423400-24423800	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr14:24423400-24423800	Flanking Active TSS	Brain Angular Gyrus	brain
47	chr14:24423400-24423800	Flanking Active TSS	Brain Anterior Caudate	brain
48	chr14:24423400-24423800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr14:24423400-24423800	Weak transcription	Esophagus	oesophagus
50	chr14:24423400-24423800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland

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