Variant report

Variant	nsv869984
Chromosome Location	chr14:20732655-20776216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:751)
CpG islands
(count:488)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20773818-20774422	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:20773991-20774309	K562	blood:	n/a	n/a
3	ARID3A	chr14:20771807-20771811	K562	blood:	n/a	n/a
4	ATF1	chr14:20769953-20770557	K562	blood:	n/a	n/a
5	ATF1	chr14:20774021-20774323	K562	blood:	n/a	n/a
6	ATF2	chr14:20763140-20763708	GM12878	blood:	n/a	n/a
7	ATF2	chr14:20773823-20774338	GM12878	blood:	n/a	n/a
8	ATF2	chr14:20763261-20763704	GM12878	blood:	n/a	n/a
9	ATF3	chr14:20773896-20774392	A549	lung:	n/a	n/a
10	ATF3	chr14:20746654-20746850	K562	blood:	n/a	n/a
11	ATF3	chr14:20773919-20774363	A549	lung:	n/a	n/a
12	BACH1	chr14:20770210-20770858	K562	blood:	n/a	n/a
13	BATF	chr14:20763192-20763680	GM12878	blood:	n/a	n/a
14	BATF	chr14:20763244-20763574	GM12878	blood:	n/a	n/a
15	BATF	chr14:20770190-20770528	GM12878	blood:	n/a	chr14:20770397-20770408
16	BATF	chr14:20770273-20770531	GM12878	blood:	n/a	chr14:20770397-20770408
17	BCL11A	chr14:20763241-20763623	GM12878	blood:	n/a	chr14:20763413-20763422 chr14:20763410-20763419 chr14:20763448-20763457
18	BCL11A	chr14:20763192-20763682	GM12878	blood:	n/a	chr14:20763413-20763422 chr14:20763410-20763419 chr14:20763448-20763457
19	BCL3	chr14:20773699-20774351	A549	lung:	n/a	n/a
20	BCL3	chr14:20763170-20763643	GM12878	blood:	n/a	chr14:20763413-20763422 chr14:20763410-20763419 chr14:20763448-20763457
21	BCL3	chr14:20773540-20774360	A549	lung:	n/a	n/a
22	BCLAF1	chr14:20773893-20774361	K562	blood:	n/a	n/a
23	BCLAF1	chr14:20773758-20774328	GM12878	blood:	n/a	n/a
24	BCLAF1	chr14:20773852-20774368	GM12878	blood:	n/a	n/a
25	BCLAF1	chr14:20763131-20763678	GM12878	blood:	n/a	chr14:20763413-20763422 chr14:20763410-20763419 chr14:20763448-20763457
26	BCLAF1	chr14:20773963-20774395	K562	blood:	n/a	n/a
27	BCLAF1	chr14:20763307-20763668	GM12878	blood:	n/a	chr14:20763413-20763422 chr14:20763410-20763419 chr14:20763448-20763457
28	BHLHE40	chr14:20773831-20774258	K562	blood:	n/a	n/a
29	BHLHE40	chr14:20763278-20763636	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:20773838-20774382	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:20773766-20774327	HepG2	liver:	n/a	n/a
32	BRCA1	chr14:20773913-20774264	HepG2	liver:	n/a	n/a
33	BRCA1	chr14:20773800-20774275	GM12878	blood:	n/a	n/a
34	BRCA1	chr14:20773743-20774316	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr14:20773966-20774239	K562	blood:	n/a	n/a
36	CBX3	chr14:20773803-20774329	HCT-116	colon:	n/a	n/a
37	CEBPB	chr14:20755229-20755482	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:20774055-20774258	K562	blood:	n/a	n/a
39	CEBPB	chr14:20746002-20746165	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:20741552-20741617	A549	lung:	n/a	n/a
41	CHD2	chr14:20773876-20774279	HepG2	liver:	n/a	n/a
42	CHD2	chr14:20773851-20774297	GM12878	blood:	n/a	n/a
43	CHD2	chr14:20773559-20774339	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr14:20763178-20763619	GM12878	blood:	n/a	n/a
45	CHD2	chr14:20774037-20774258	K562	blood:	n/a	n/a
46	CREB1	chr14:20773922-20774233	A549	lung:	n/a	n/a
47	CREB1	chr14:20773987-20774262	A549	lung:	n/a	n/a
48	CTCF	chr14:20774008-20774326	MCF-7	breast:	n/a	chr14:20774164-20774180 chr14:20774158-20774179
49	CTCF	chr14:20755440-20755590	GM06990	blood:	n/a	n/a
50	CTCF	chr14:20774041-20774311	LNCaP	prostate:	n/a	chr14:20774164-20774180 chr14:20774158-20774179

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20773640-20773690	Hela-S3	cervix:	n/a
2	chr14:20774818-20774868	GM12892	blood:	n/a
3	chr14:20773640-20773690	ProgFib	skin:	n/a
4	chr14:20774101-20774151	AG10803	skin:	n/a
5	chr14:20773935-20773985	GM19239	blood:	n/a
6	chr14:20774818-20774868	NH-A	brain:	n/a
7	chr14:20774818-20774868	BE2_C	brain:	n/a
8	chr14:20757727-20757777	HL-60	blood:	n/a
9	chr14:20774818-20774868	U87	brain:	n/a
10	chr14:20773935-20773985	PFSK-1	brain:	n/a
11	chr14:20773640-20773690	PrEC	prostate:	n/a
12	chr14:20774101-20774151	HRE	kidney:	n/a
13	chr14:20773640-20773690	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:20774219-20774269	HUVEC	blood vessel:	n/a
15	chr14:20774219-20774269	HCM	heart:	n/a
16	chr14:20773939-20773989	BJ	skin:	n/a
17	chr14:20774818-20774868	HepG2	liver:	n/a
18	chr14:20773939-20773989	ECC-1	luminal epithelium:	n/a
19	chr14:20773640-20773690	IMR90	lung:	fetal
20	chr14:20773640-20773690	HNPCEpiC	eye:	n/a
21	chr14:20774818-20774868	HL-60	blood:	n/a
22	chr14:20773939-20773989	Jurkat	blood:	n/a
23	chr14:20773939-20773989	HRCEpiC	kidney:	n/a
24	chr14:20773935-20773985	HMEC	breast:	n/a
25	chr14:20757727-20757777	U87	brain:	n/a
26	chr14:20773939-20773989	ProgFib	skin:	n/a
27	chr14:20774003-20774053	RPTEC	kidney:	n/a
28	chr14:20757727-20757777	ECC-1	luminal epithelium:	n/a
29	chr14:20773935-20773985	HCPEpiC	choroid plexus:	n/a
30	chr14:20773939-20773989	HAEpiC	amniotic membrane:	n/a
31	chr14:20774818-20774868	AG09319	gingival:	n/a
32	chr14:20774003-20774053	U87	brain:	n/a
33	chr14:20773939-20773989	SK-N-SH_RA	brain:	n/a
34	chr14:20774818-20774868	AoSMC	blood vessel:	n/a
35	chr14:20774818-20774868	RPTEC	kidney:	n/a
36	chr14:20773935-20773985	SK-N-SH	brain:	n/a
37	chr14:20757727-20757777	HepG2	liver:	n/a
38	chr14:20774003-20774053	HL-60	blood:	n/a
39	chr14:20774101-20774151	NT2-D1	testis:	n/a
40	chr14:20774101-20774151	K562	blood:	n/a
41	chr14:20774101-20774151	U87	brain:	n/a
42	chr14:20774101-20774151	ovcar-3	ovarian:	n/a
43	chr14:20757727-20757777	ProgFib	skin:	n/a
44	chr14:20773939-20773989	AG04450	lung:	fetal
45	chr14:20774101-20774151	NHDF-neo	bronchial:	n/a
46	chr14:20774101-20774151	CMK	blood:	n/a
47	chr14:20773939-20773989	GM19239	blood:	n/a
48	chr14:20757727-20757777	PrEC	prostate:	n/a
49	chr14:20774219-20774269	HCPEpiC	choroid plexus:	n/a
50	chr14:20773935-20773985	AG10803	skin:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20756758..20759737-chr14:20760668..20764234,4	K562	blood:
2	chr14:20738427..20740825-chr14:20746566..20748519,2	K562	blood:
3	chr14:20721089..20723559-chr14:20745289..20746790,2	K562	blood:
4	chr14:20772605..20775038-chr14:20775340..20777178,2	K562	blood:
5	chr14:20768802..20770560-chr14:20773922..20776589,2	MCF-7	breast:
6	chr14:20772552..20774812-chr14:20810086..20811786,2	MCF-7	breast:
7	chr14:20756758..20759737-chr14:20760668..20764234,4	K562	blood:
8	chr1:165035252..165035863-chr14:20763199..20763909,2	MCF-7	breast:
9	chr14:20772687..20775435-chr14:20922031..20924000,2	MCF-7	breast:
10	chr14:20765245..20767756-chr14:20769308..20771305,2	K562	blood:
11	chr14:20764589..20767514-chr14:20772256..20774685,2	K562	blood:
12	chr14:20774180..20774689-chr14:20795248..20796097,2	MCF-7	breast:
13	chr14:20738427..20740825-chr14:20746566..20748519,2	K562	blood:
14	chr14:20765245..20767756-chr14:20769308..20771305,2	K562	blood:
15	chr14:20728878..20731478-chr14:20760523..20763467,2	K562	blood:
16	chr14:20770105..20772048-chr14:20773920..20775883,2	MCF-7	breast:
17	chr14:20770396..20771996-chr14:20811365..20812904,2	MCF-7	breast:
18	chr14:20772439..20773954-chr14:20799516..20802559,3	MCF-7	breast:
19	chr14:20774963..20777741-chr14:20782284..20784767,2	MCF-7	breast:
20	chr14:20755024..20757499-chr14:20761052..20762871,2	MCF-7	breast:
21	chr14:20767452..20770221-chr14:20798521..20800836,2	K562	blood:
22	chr14:20769637..20771954-chr14:20772645..20774173,2	K562	blood:
23	chr14:20769637..20772155-chr14:20772254..20774173,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PARP2-1	chr14:20774596-20774970	ENSG00000258459.1
2	lnc-TTC5-3	chr14:20738080-20742354	ucscGeneNc_uc001vzu_1
3	lnc-TTC5-2	chr14:20755347-20755899	NONHSAT035556
4	lnc-PARP2-1	chr14:20773889-20774261	ENSG00000258459.1

No data

Variant related genes	Relation type
ENSG00000258768	TF binding region
TTC5	TF binding region
ENSG00000258459	TF binding region
ENSG00000258768	CpG island
TTC5	CpG island
ENSG00000258459	CpG island
ENSG00000100814	chromatin interactions
ENSG00000100823	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000258459	chromatin interactions
ENSG00000136319	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000092094	chromatin interactions

Extended variants
information (count: 1863 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575551325	chr14:20732681-20732682	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs9806017	chr14:20732690-20732691	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs373737328	chr14:20732698-20732699	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs569962130	chr14:20732710-20732711	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs554455883	chr14:20732766-20732767	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs149567801	chr14:20732790-20732791	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs144248136	chr14:20732800-20732801	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs564771853	chr14:20732820-20732821	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs61993943	chr14:20732831-20732832	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs562464794	chr14:20732832-20732833	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs148741797	chr14:20732847-20732848	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs573125356	chr14:20732877-20732878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186131691	chr14:20732910-20732911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60624394	chr14:20732925-20732926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs372264663	chr14:20732936-20732937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375132458	chr14:20732963-20732964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559194070	chr14:20732964-20732965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368405749	chr14:20732979-20732980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574367050	chr14:20733016-20733017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190922132	chr14:20733035-20733036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539075120	chr14:20733048-20733049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182736737	chr14:20733054-20733055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541509487	chr14:20733055-20733056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536269796	chr14:20733066-20733067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186520778	chr14:20733084-20733085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563554606	chr14:20733089-20733090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572785381	chr14:20733094-20733095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530861071	chr14:20733121-20733122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558326209	chr14:20733122-20733123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576975669	chr14:20733132-20733133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544261680	chr14:20733161-20733162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562467672	chr14:20733168-20733169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574503900	chr14:20733175-20733176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4575448	chr14:20733185-20733186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4441175	chr14:20733199-20733200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369488340	chr14:20733282-20733283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541833735	chr14:20733288-20733289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560234207	chr14:20733309-20733310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528794046	chr14:20733327-20733328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547323130	chr14:20733332-20733333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371263698	chr14:20733390-20733391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532609291	chr14:20733458-20733459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551022067	chr14:20733486-20733487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199997709	chr14:20733547-20733548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569230818	chr14:20733629-20733630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200939945	chr14:20733658-20733659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187523951	chr14:20733660-20733661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200093161	chr14:20733673-20733674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200248811	chr14:20733674-20733675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369808679	chr14:20733743-20733744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1316 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20719400-20741000	Weak transcription	Aorta	Aorta
2	chr14:20722600-20755000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:20723000-20739400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:20724400-20755200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr14:20725400-20748200	Weak transcription	Ovary	ovary
6	chr14:20729600-20732800	Enhancers	NHEK	skin
7	chr14:20730000-20732800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr14:20731200-20743200	Weak transcription	Psoas Muscle	Psoas
9	chr14:20731400-20732800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr14:20731400-20755600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr14:20731400-20757000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:20731600-20732800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr14:20731600-20754400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr14:20732400-20732800	Enhancers	A549	lung
15	chr14:20736400-20737200	Enhancers	HepG2	liver
16	chr14:20739200-20739600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr14:20739400-20743600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
18	chr14:20739600-20741000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:20739800-20742600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
20	chr14:20740200-20745400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr14:20740200-20755200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr14:20740600-20754600	Weak transcription	Brain Hippocampus Middle	brain
23	chr14:20740800-20741000	Weak transcription	Gastric	stomach
24	chr14:20741000-20741200	ZNF genes & repeats	Gastric	stomach
25	chr14:20741000-20741200	ZNF genes & repeats	Right Ventricle	heart
26	chr14:20741000-20741400	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
27	chr14:20741000-20741600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr14:20741000-20741600	ZNF genes & repeats	Aorta	Aorta
29	chr14:20741200-20756400	Weak transcription	Gastric	stomach
30	chr14:20741200-20757400	Weak transcription	Right Ventricle	heart
31	chr14:20741400-20755800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr14:20741600-20742800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:20741600-20743000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr14:20741600-20744200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr14:20741600-20755200	Weak transcription	Aorta	Aorta
36	chr14:20741600-20755200	Weak transcription	Pancreas	Pancrea
37	chr14:20741800-20743400	ZNF genes & repeats	Fetal Lung	lung
38	chr14:20742000-20742800	ZNF genes & repeats	Dnd41	blood
39	chr14:20742200-20742400	ZNF genes & repeats	Spleen	Spleen
40	chr14:20742200-20742800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
41	chr14:20742200-20742800	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr14:20742200-20742800	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
43	chr14:20742400-20756600	Weak transcription	Spleen	Spleen
44	chr14:20742400-20759000	Weak transcription	Colon Smooth Muscle	Colon
45	chr14:20742600-20742800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr14:20742600-20742800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr14:20742600-20742800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr14:20742600-20742800	ZNF genes & repeats	Adipose Nuclei	Adipose
49	chr14:20742600-20742800	ZNF genes & repeats	Colonic Mucosa	Colon
50	chr14:20742600-20742800	Enhancers	Lung	lung

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