Variant report

Variant	nsv1052883
Chromosome Location	chr14:20689721-20743269
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	chr14:20730858-20731162	K562	blood:	n/a	n/a
2	ATF1	chr14:20724352-20724489	K562	blood:	n/a	n/a
3	ATF1	chr14:20730830-20731218	K562	blood:	n/a	n/a
4	ATF3	chr14:20730820-20731074	K562	blood:	n/a	n/a
5	BCL11A	chr14:20730703-20731061	GM12878	blood:	n/a	n/a
6	BHLHE40	chr14:20730817-20731297	K562	blood:	n/a	n/a
7	BHLHE40	chr14:20730754-20731222	GM12878	blood:	n/a	n/a
8	BRCA1	chr14:20716040-20716061	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr14:20730801-20731127	K562	blood:	n/a	n/a
10	CEBPB	chr14:20730821-20731202	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr14:20741552-20741617	A549	lung:	n/a	n/a
12	CEBPB	chr14:20730826-20731185	K562	blood:	n/a	n/a
13	CEBPB	chr14:20730857-20731158	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr14:20730819-20731174	IMR90	lung:	n/a	n/a
15	CHD1	chr14:20730821-20730930	GM12878	blood:	n/a	n/a
16	CHD2	chr14:20730845-20731006	GM12878	blood:	n/a	n/a
17	CHD2	chr14:20730792-20731109	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr14:20715880-20716030	HEEpiC	esophagus:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
19	CTCF	chr14:20715825-20716187	GM12878	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
20	CTCF	chr14:20715879-20716148	LNCaP	prostate:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
21	CTCF	chr14:20715940-20716090	MCF-7	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
22	CTCF	chr14:20724200-20724206	MCF-7	breast:	n/a	n/a
23	CTCF	chr14:20716022-20716053	Fibrobl	skin:	n/a	n/a
24	CTCF	chr14:20715880-20716030	BE2_C	brain:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
25	CTCF	chr14:20715940-20716090	GM12872	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
26	CTCF	chr14:20693369-20693508	HepG2	liver:	n/a	n/a
27	CTCF	chr14:20718697-20718758	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr14:20715840-20715990	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr14:20715940-20716090	GM12870	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
30	CTCF	chr14:20715920-20716070	GM06990	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
31	CTCF	chr14:20715971-20716124	ProgFib	skin:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
32	CTCF	chr14:20715940-20716090	SAEC	small airway:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
33	CTCF	chr14:20693327-20693537	K562	blood:	n/a	n/a
34	CTCF	chr14:20715940-20716090	GM12869	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
35	CTCF	chr14:20716000-20716150	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr14:20715891-20716095	SK-N-SH_RA	brain:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
37	CTCF	chr14:20715920-20716070	GM12871	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
38	CTCF	chr14:20715929-20716087	GM13977	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
39	CTCF	chr14:20693378-20693513	K562	blood:	n/a	n/a
40	CTCF	chr14:20715920-20716070	HepG2	liver:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
41	CTCF	chr14:20715800-20715950	RPTEC	kidney:	n/a	n/a
42	CTCF	chr14:20715940-20716090	GM12873	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
43	CTCF	chr14:20715920-20716070	HMF	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
44	CTCF	chr14:20693420-20693570	A549	lung:	n/a	n/a
45	CTCF	chr14:20715926-20716035	SK-N-SH_RA	brain:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
46	CTCF	chr14:20715960-20716110	WERI-Rb-1	eye:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
47	CTCF	chr14:20715919-20716120	K562	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
48	CTCF	chr14:20731580-20731730	HMF	breast:	n/a	n/a
49	CTCF	chr14:20715940-20716090	GM12864	blood:	n/a	chr14:20715990-20716008 chr14:20715985-20716006
50	CTCF	chr14:20715891-20716084	T-47D	breast:	n/a	chr14:20715990-20716008 chr14:20715985-20716006

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20691777-20691827	H1-hESC	embryonic stem cell:	embryo
2	chr14:20691777-20691827	H1-hESC	embryonic stem cell:	embryo
3	chr14:20710905-20710955	RPTEC	kidney:	n/a
4	chr14:20710905-20710955	HNPCEpiC	eye:	n/a
5	chr14:20704361-20704411	ProgFib	skin:	n/a
6	chr14:20704361-20704411	HCF	heart:	n/a
7	chr14:20710905-20710955	HL-60	blood:	n/a
8	chr14:20710315-20710365	RPTEC	kidney:	n/a
9	chr14:20710881-20710931	U87	brain:	n/a
10	chr14:20692622-20692672	SK-N-SH	brain:	n/a
11	chr14:20692622-20692672	HL-60	blood:	n/a
12	chr14:20711344-20711394	HCF	heart:	n/a
13	chr14:20710315-20710365	SK-N-SH_RA	brain:	n/a
14	chr14:20710315-20710365	Hela-S3	cervix:	n/a
15	chr14:20691777-20691827	HCPEpiC	choroid plexus:	n/a
16	chr14:20692622-20692672	GM19239	blood:	n/a
17	chr14:20704361-20704411	BE2_C	brain:	n/a
18	chr14:20692622-20692672	NHDF-neo	bronchial:	n/a
19	chr14:20710315-20710365	HMEC	breast:	n/a
20	chr14:20704361-20704411	CMK	blood:	n/a
21	chr14:20704361-20704411	Jurkat	blood:	n/a
22	chr14:20692622-20692672	Hela-S3	cervix:	n/a
23	chr14:20691777-20691827	BE2_C	brain:	n/a
24	chr14:20692622-20692672	PFSK-1	brain:	n/a
25	chr14:20704361-20704411	HAEpiC	amniotic membrane:	n/a
26	chr14:20691777-20691827	A549	lung:	n/a
27	chr14:20692622-20692672	Hepatocyte	liver:	n/a
28	chr14:20710315-20710365	GM12892	blood:	n/a
29	chr14:20710905-20710955	SK-N-SH	brain:	n/a
30	chr14:20711344-20711394	HRE	kidney:	n/a
31	chr14:20691777-20691827	SKMC	muscle:	n/a
32	chr14:20711344-20711394	NT2-D1	testis:	n/a
33	chr14:20710905-20710955	GM06990	blood:	n/a
34	chr14:20704361-20704411	U87	brain:	n/a
35	chr14:20710315-20710365	NHDF-neo	bronchial:	n/a
36	chr14:20704361-20704411	HRE	kidney:	n/a
37	chr14:20710315-20710365	H1-hESC	embryonic stem cell:	embryo
38	chr14:20704361-20704411	HEK293	kidney:	embryo
39	chr14:20691777-20691827	HIPEpiC	eye:	n/a
40	chr14:20710881-20710931	HIPEpiC	eye:	n/a
41	chr14:20710881-20710931	MCF10A-Er-Src	breast:	n/a
42	chr14:20711344-20711394	T-47D	breast:	n/a
43	chr14:20710881-20710931	BJ	skin:	n/a
44	chr14:20711344-20711394	MCF-7	breast:	n/a
45	chr14:20710315-20710365	ECC-1	luminal epithelium:	n/a
46	chr14:20691777-20691827	HAEpiC	amniotic membrane:	n/a
47	chr14:20691777-20691827	MCF10A-Er-Src	breast:	n/a
48	chr14:20711344-20711394	HIPEpiC	eye:	n/a
49	chr14:20692622-20692672	LNCaP	prostate:	n/a
50	chr14:20710881-20710931	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:20721089..20723559-chr14:20745289..20746790,2	K562	blood:
2	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:
3	chr14:20716993..20719012-chr14:20810406..20812740,2	MCF-7	breast:
4	chr14:20674085..20677001-chr14:20687478..20690164,2	MCF-7	breast:
5	chr14:20738427..20740825-chr14:20746566..20748519,2	K562	blood:
6	chr14:20691139..20693631-chr14:20695657..20698105,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC5-3	chr14:20738080-20742354	ucscGeneNc_uc001vzu_1
2	lnc-TTC5-2	chr14:20726344-20726358	NONHSAT035556
3	lnc-TTC5-2	chr14:20728639-20732467	ENSG00000258768.2
4	lnc-TTC5-2	chr14:20724717-20724844	NONHSAT035556
5	lnc-TTC5-2	chr14:20729548-20729773	NONHSAT035558
6	lnc-TTC5-2	chr14:20725877-20725934	NONHSAT035556
7	lnc-TTC5-2	chr14:20728743-20729137	NONHSAT035558
8	lnc-TTC5-2	chr14:20729772-20729892	NONHSAT035556

Variant related genes	Relation type
ENSG00000266336	TF binding region
ENSG00000258768	TF binding region
OR11H6	TF binding region
TTC5	TF binding region
OR11H4	TF binding region
OR11H7	TF binding region
ENSG00000266336	CpG island
ENSG00000258768	CpG island
OR11H6	CpG island
TTC5	CpG island
OR11H4	CpG island
OR11H7	CpG island
ENSG00000258806	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000176219	chromatin interactions

Extended variants
information (count: 1508 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1508 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556189018	chr14:20689732-20689733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373726951	chr14:20689748-20689749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28700222	chr14:20689751-20689752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs558998889	chr14:20689765-20689766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577159720	chr14:20689780-20689781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539355365	chr14:20689792-20689793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554052272	chr14:20689797-20689798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11406460	chr14:20689798-20689799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs397958088	chr14:20689803-20689804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556290152	chr14:20689813-20689814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574530936	chr14:20689818-20689819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs193249226	chr14:20689831-20689832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182323950	chr14:20689865-20689866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559810843	chr14:20689877-20689878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199877569	chr14:20689898-20689899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374519737	chr14:20689912-20689913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545347522	chr14:20689925-20689926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563760949	chr14:20689956-20689957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532805576	chr14:20690010-20690011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368493055	chr14:20690033-20690034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550979517	chr14:20690038-20690039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10148193	chr14:20690052-20690053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200410856	chr14:20690067-20690068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186679560	chr14:20690099-20690100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191086594	chr14:20690105-20690106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184057386	chr14:20690106-20690107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13379219	chr14:20690108-20690109	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552573496	chr14:20690152-20690153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7154460	chr14:20690168-20690169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs538272318	chr14:20690303-20690304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76903989	chr14:20690304-20690305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200064273	chr14:20690343-20690344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574720804	chr14:20690371-20690372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75859755	chr14:20690374-20690375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140533167	chr14:20690431-20690432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61993861	chr14:20690450-20690451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192962586	chr14:20690498-20690499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546889718	chr14:20690535-20690536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150451922	chr14:20690554-20690555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138288172	chr14:20690556-20690557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185282044	chr14:20690563-20690564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7150608	chr14:20690569-20690570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs563032576	chr14:20690575-20690576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149217863	chr14:20690580-20690581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7143108	chr14:20690599-20690600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7143113	chr14:20690605-20690606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs8020960	chr14:20690606-20690607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs190552120	chr14:20690643-20690644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76486806	chr14:20690666-20690667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537846951	chr14:20690712-20690713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20687800-20691200	Weak transcription	K562	blood
2	chr14:20691200-20692600	Enhancers	K562	blood
3	chr14:20695400-20695600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:20698000-20698400	Active TSS	Fetal Heart	heart
5	chr14:20704000-20704400	Active TSS	HepG2	liver
6	chr14:20707000-20707200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:20718600-20719200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
8	chr14:20718800-20724200	Weak transcription	Ovary	ovary
9	chr14:20719200-20719400	ZNF genes & repeats	Aorta	Aorta
10	chr14:20719400-20741000	Weak transcription	Aorta	Aorta
11	chr14:20720800-20721400	ZNF genes & repeats	Liver	Liver
12	chr14:20721400-20730400	Weak transcription	Liver	Liver
13	chr14:20722600-20755000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr14:20722800-20723000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
15	chr14:20723000-20739400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr14:20724000-20724400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr14:20724200-20724600	ZNF genes & repeats	Ovary	ovary
18	chr14:20724400-20755200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr14:20724600-20725200	Weak transcription	Ovary	ovary
20	chr14:20725200-20725400	ZNF genes & repeats	Ovary	ovary
21	chr14:20725400-20748200	Weak transcription	Ovary	ovary
22	chr14:20728800-20730400	Weak transcription	Fetal Brain Male	brain
23	chr14:20729600-20732200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:20729600-20732800	Enhancers	NHEK	skin
25	chr14:20730000-20732000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:20730000-20732600	Enhancers	HMEC	breast
27	chr14:20730000-20732800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr14:20730200-20731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:20730200-20731400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr14:20730200-20731800	Enhancers	Hela-S3	cervix
31	chr14:20730400-20730600	Enhancers	Osteobl	bone
32	chr14:20730400-20731200	Enhancers	NHDF-Ad	bronchial
33	chr14:20730400-20731400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr14:20730400-20731400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:20730400-20731600	Enhancers	HSMM	muscle
36	chr14:20730400-20732000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr14:20730400-20732000	Enhancers	K562	blood
38	chr14:20730600-20730800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr14:20730600-20730800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr14:20730600-20731200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr14:20730600-20731200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr14:20730600-20731200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr14:20730600-20731200	Flanking Active TSS	Osteobl	bone
44	chr14:20730600-20731400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr14:20730600-20731400	Enhancers	A549	lung
46	chr14:20730600-20731600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr14:20730800-20731000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:20730800-20731200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr14:20730800-20731200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr14:20730800-20731200	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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