Variant report

Variant	nsv827069
Chromosome Location	chr14:104027502-104028019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr14:104027988-104028292	H1-hESC	embryonic stem cell:	n/a	n/a
2	CREB1	chr14:104027540-104028133	H1-hESC	embryonic stem cell:	n/a	n/a
3	CREB1	chr14:104027594-104028041	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr14:104027860-104028010	GM12864	blood:	n/a	n/a
5	CTCF	chr14:104027760-104027910	Caco-2	colon:	n/a	n/a
6	CTCF	chr14:104027860-104028010	GM12873	blood:	n/a	n/a
7	CTCF	chr14:104027840-104028110	MCF-7	breast:	n/a	n/a
8	CTCF	chr14:104027800-104027950	GM12875	blood:	n/a	n/a
9	CTCF	chr14:104027820-104027970	AoAF	blood vessel:	n/a	n/a
10	CTCF	chr14:104027820-104027970	NHEK	skin:	n/a	n/a
11	CTCF	chr14:104027780-104027930	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr14:104027820-104027970	SAEC	small airway:	n/a	n/a
13	CTCF	chr14:104027800-104027950	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr14:104027700-104027850	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr14:104027800-104027950	HepG2	liver:	n/a	n/a
16	CTCF	chr14:104027740-104027890	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:104027820-104027970	HMEC	breast:	n/a	n/a
18	CTCF	chr14:104027840-104027990	HEK293	kidney:	n/a	n/a
19	CTCF	chr14:104027760-104027910	GM12873	blood:	n/a	n/a
20	CTCF	chr14:104027880-104028030	GM12868	blood:	n/a	n/a
21	E2F4	chr14:104027650-104028455	MCF10A-Er-Src	breast:	n/a	chr14:104028207-104028221 chr14:104028209-104028217 chr14:104028209-104028217
22	EGR1	chr14:104027582-104027841	K562	blood:	n/a	n/a
23	EGR1	chr14:104027602-104027903	K562	blood:	n/a	n/a
24	EGR1	chr14:104027429-104028040	MCF-7	breast:	n/a	n/a
25	EP300	chr14:104027440-104028566	ECC-1	luminal epithelium:	n/a	n/a
26	FOS	chr14:104027624-104028020	MCF10A-Er-Src	breast:	n/a	chr14:104027897-104027906
27	FOS	chr14:104027624-104027991	MCF10A-Er-Src	breast:	n/a	chr14:104027897-104027906
28	FOS	chr14:104027634-104027979	MCF10A-Er-Src	breast:	n/a	chr14:104027897-104027906
29	FOS	chr14:104027545-104027933	MCF10A-Er-Src	breast:	n/a	chr14:104027897-104027906
30	FOSL2	chr14:104027539-104028006	MCF-7	breast:	n/a	chr14:104027897-104027906
31	FOSL2	chr14:104027595-104027975	HepG2	liver:	n/a	chr14:104027897-104027906
32	GABPA	chr14:104027612-104029881	MCF-7	breast:	n/a	n/a
33	GTF2F1	chr14:104028013-104028132	H1-hESC	embryonic stem cell:	n/a	n/a
34	GTF2F1	chr14:104027666-104028011	Hela-S3	cervix:	n/a	n/a
35	HA-E2F1	chr14:104027559-104029847	MCF-7	breast:	n/a	chr14:104028207-104028221 chr14:104028209-104028217 chr14:104028209-104028217 chr14:104028673-104028688 chr14:104029236-104029245
36	HCFC1	chr14:104027237-104030166	Hela-S3	cervix:	n/a	n/a
37	HCFC1	chr14:104027871-104028005	K562	blood:	n/a	n/a
38	JUND	chr14:104027696-104027910	K562	blood:	n/a	chr14:104027796-104027807 chr14:104027897-104027906
39	JUND	chr14:104027675-104027913	HepG2	liver:	n/a	chr14:104027796-104027807 chr14:104027897-104027906
40	JUND	chr14:104027577-104028272	H1-hESC	embryonic stem cell:	n/a	chr14:104027796-104027807 chr14:104027897-104027906
41	MAX	chr14:104027574-104029883	MCF-7	breast:	n/a	n/a
42	MAX	chr14:104027750-104030033	Hela-S3	cervix:	n/a	n/a
43	MAX	chr14:104027988-104029903	ECC-1	luminal epithelium:	n/a	n/a
44	MXI1	chr14:104027798-104030910	SK-N-SH	brain:	n/a	chr14:104030620-104030635 chr14:104030622-104030637
45	MXI1	chr14:104027853-104029809	Hela-S3	cervix:	n/a	n/a
46	MXI1	chr14:104027879-104029711	GM12878	blood:	n/a	n/a
47	MYC	chr14:104027773-104028332	MCF10A-Er-Src	breast:	n/a	n/a
48	NRF1	chr14:104027932-104027984	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr14:104027702-104027939	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr14:104027795-104027981	H1-hESC	embryonic stem cell:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104027995-104028045	Hela-S3	cervix:	n/a
2	chr14:104027995-104028045	AG04450	lung:	fetal
3	chr14:104027995-104028045	GM12891	blood:	n/a
4	chr14:104027995-104028045	U87	brain:	n/a
5	chr14:104027995-104028045	HRCEpiC	kidney:	n/a
6	chr14:104027995-104028045	NB4	blood:	n/a
7	chr14:104027995-104028045	IMR90	lung:	fetal
8	chr14:104027995-104028045	HMEC	breast:	n/a
9	chr14:104027995-104028045	SK-N-MC	brain:	n/a
10	chr14:104027995-104028045	PANC-1	pancreas:	n/a
11	chr14:104027995-104028045	AG10803	skin:	n/a
12	chr14:104027995-104028045	HAEpiC	amniotic membrane:	n/a
13	chr14:104027995-104028045	HEEpiC	esophagus:	n/a
14	chr14:104027995-104028045	LNCaP	prostate:	n/a
15	chr14:104027995-104028045	NH-A	brain:	n/a
16	chr14:104027995-104028045	NHBE	bronchial:	n/a
17	chr14:104027995-104028045	BJ	skin:	n/a
18	chr14:104027995-104028045	SK-N-SH_RA	brain:	n/a
19	chr14:104027995-104028045	T-47D	breast:	n/a
20	chr14:104027995-104028045	GM12878	blood:	n/a
21	chr14:104027995-104028045	AG09319	gingival:	n/a
22	chr14:104027995-104028045	SAEC	small airway:	n/a
23	chr14:104027995-104028045	H1-hESC	embryonic stem cell:	embryo
24	chr14:104027995-104028045	GM06990	blood:	n/a
25	chr14:104027995-104028045	SK-N-SH	brain:	n/a
26	chr14:104027995-104028045	AG09309	skin:	n/a
27	chr14:104027995-104028045	ECC-1	luminal epithelium:	n/a
28	chr14:104027995-104028045	NT2-D1	testis:	n/a
29	chr14:104027995-104028045	Jurkat	blood:	n/a
30	chr14:104027995-104028045	ProgFib	skin:	n/a
31	chr14:104027995-104028045	HepG2	liver:	n/a
32	chr14:104027995-104028045	AoSMC	blood vessel:	n/a
33	chr14:104027995-104028045	HL-60	blood:	n/a
34	chr14:104027995-104028045	RPTEC	kidney:	n/a
35	chr14:104027995-104028045	HNPCEpiC	eye:	n/a
36	chr14:104027995-104028045	CMK	blood:	n/a
37	chr14:104027995-104028045	MCF-7	breast:	n/a
38	chr14:104027995-104028045	HRPEpiC	eye:	n/a
39	chr14:104027995-104028045	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:104027995-104028045	MCF10A-Er-Src	breast:	n/a
41	chr14:104027995-104028045	Hepatocyte	liver:	n/a
42	chr14:104027995-104028045	HIPEpiC	eye:	n/a
43	chr14:104027995-104028045	HCM	heart:	n/a
44	chr14:104027995-104028045	HUVEC	blood vessel:	n/a
45	chr14:104027995-104028045	A549	lung:	n/a
46	chr14:104027995-104028045	PFSK-1	brain:	n/a
47	chr14:104027995-104028045	K562	blood:	n/a
48	chr14:104027995-104028045	HCT-116	colon:	n/a
49	chr14:104027995-104028045	HRE	kidney:	n/a
50	chr14:104027995-104028045	BE2_C	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:103992298..103994293-chr14:104026567..104028145,2	K562	blood:
2	chr14:103799415..103801924-chr14:104027086..104029565,3	MCF-7	breast:
3	chr14:104009722..104012574-chr14:104026131..104028003,2	K562	blood:
4	chr14:104027061..104029959-chr14:104033088..104037337,3	K562	blood:
5	chr14:104016689..104020988-chr14:104027518..104030448,6	MCF-7	breast:
6	chr14:103992721..103998040-chr14:104027797..104030842,4	MCF-7	breast:
7	chr14:104014533..104016298-chr14:104025800..104028102,2	K562	blood:
8	chr14:104026574..104032100-chr14:104033737..104038565,9	MCF-7	breast:
9	chr14:103983696..103988397-chr14:104026059..104029809,6	K562	blood:
10	chr14:104018005..104022715-chr14:104023184..104028959,7	K562	blood:
11	chr14:104026026..104030833-chr14:104180410..104184978,6	MCF-7	breast:
12	chr14:104027610..104029440-chr14:104145265..104147418,2	MCF-7	breast:
13	chr14:104027886..104033252-chr14:104178637..104183670,7	MCF-7	breast:
14	chr14:104026767..104030601-chr14:104092111..104097061,5	MCF-7	breast:
15	chr14:104003474..104006501-chr14:104024765..104028078,3	MCF-7	breast:
16	chr14:103985364..103989946-chr14:104026445..104030227,8	MCF-7	breast:
17	chr14:104026845..104031617-chr14:104090112..104098528,12	MCF-7	breast:
18	chr14:104027275..104029645-chr9:131939860..131941591,2	MCF-7	breast:

No data

Variant related genes	Relation type
KLC1	TF binding region
APOPT1	TF binding region
ENSG00000256500	TF binding region
KLC1	CpG island
APOPT1	CpG island
ENSG00000256500	CpG island
ENSG00000188483	chromatin interactions
ENSG00000126214	chromatin interactions
ENSG00000126215	chromatin interactions
ENSG00000166166	chromatin interactions
ENSG00000260285	chromatin interactions
ENSG00000258851	chromatin interactions
ENSG00000269963	chromatin interactions
ENSG00000201184	chromatin interactions
ENSG00000100711	chromatin interactions
ENSG00000166165	chromatin interactions
ENSG00000256053	chromatin interactions
ENSG00000100664	chromatin interactions

Extended variants
information (count: 30 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372359623	chr14:104027506-104027507	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs555123878	chr14:104027509-104027510	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs375948162	chr14:104027529-104027530	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs201848541	chr14:104027544-104027545	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs147379559	chr14:104027551-104027552	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs11625397	chr14:104027557-104027558	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs371829112	chr14:104027558-104027559	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs189484565	chr14:104027569-104027570	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs544166690	chr14:104027578-104027579	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs113117376	chr14:104027579-104027580	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs34186780	chr14:104027595-104027596	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181803004	chr14:104027636-104027637	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
13	rs531015389	chr14:104027664-104027665	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
14	rs139608073	chr14:104027673-104027674	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
15	rs112554013	chr14:104027682-104027683	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs561324521	chr14:104027757-104027758	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs530334804	chr14:104027771-104027772	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs183855527	chr14:104027789-104027790	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
19	rs540319612	chr14:104027790-104027791	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
20	rs566743619	chr14:104027802-104027803	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
21	rs539825341	chr14:104027804-104027805	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
22	rs538812372	chr14:104027838-104027839	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
23	rs74088040	chr14:104027851-104027852	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs568953749	chr14:104027893-104027894	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs189346403	chr14:104027918-104027919	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs111328512	chr14:104027934-104027935	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
27	rs150939989	chr14:104027946-104027947	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
28	rs140682113	chr14:104027990-104027991	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs34896432	chr14:104027995-104027996	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532325768	chr14:104027997-104027998	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
Lung cancer	18438408	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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21364760	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104011400-104027800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:104013600-104027600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:104019200-104027600	Weak transcription	Colonic Mucosa	Colon
4	chr14:104019800-104027600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:104023200-104027600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr14:104023600-104027600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr14:104025200-104027600	Weak transcription	Ovary	ovary
8	chr14:104025400-104027800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr14:104026000-104027600	Genic enhancers	Fetal Muscle Leg	muscle
10	chr14:104026000-104027600	Genic enhancers	Left Ventricle	heart
11	chr14:104026200-104027600	Genic enhancers	Primary T cells fromperipheralblood	blood
12	chr14:104026200-104027600	Enhancers	Colon Smooth Muscle	Colon
13	chr14:104026200-104027600	Enhancers	Right Atrium	heart
14	chr14:104026400-104027600	Genic enhancers	Fetal Stomach	stomach
15	chr14:104026400-104027800	Enhancers	Fetal Brain Male	brain
16	chr14:104026800-104027600	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr14:104026800-104027600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr14:104026800-104027600	Enhancers	Placenta Amnion	Placenta Amnion
19	chr14:104026800-104028000	Enhancers	Spleen	Spleen
20	chr14:104027000-104027600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr14:104027000-104027600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr14:104027000-104027600	Enhancers	Primary T cells from cord blood	blood
23	chr14:104027000-104027600	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr14:104027000-104027600	Enhancers	Brain Hippocampus Middle	brain
25	chr14:104027000-104027600	Enhancers	Brain Substantia Nigra	brain
26	chr14:104027000-104027600	Weak transcription	Esophagus	oesophagus
27	chr14:104027000-104027600	Enhancers	Placenta	Placenta
28	chr14:104027000-104027600	Weak transcription	Gastric	stomach
29	chr14:104027000-104027600	Weak transcription	Lung	lung
30	chr14:104027000-104027600	Weak transcription	Pancreas	Pancrea
31	chr14:104027000-104027600	Enhancers	Right Ventricle	heart
32	chr14:104027000-104027600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr14:104027000-104027800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr14:104027000-104027800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr14:104027000-104027800	Genic enhancers	Primary B cells from cord blood	blood
36	chr14:104027000-104027800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr14:104027000-104028000	Enhancers	Primary B cells from peripheral blood	blood
38	chr14:104027000-104028400	Flanking Active TSS	Brain Germinal Matrix	brain
39	chr14:104027000-104028400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr14:104027000-104028400	Flanking Active TSS	Stomach Smooth Muscle	stomach
41	chr14:104027000-104028600	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr14:104027200-104027600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr14:104027200-104027600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr14:104027200-104027600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr14:104027200-104027600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr14:104027200-104027600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr14:104027200-104027600	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr14:104027200-104027600	Enhancers	Fetal Kidney	kidney
49	chr14:104027200-104027600	Genic enhancers	Fetal Thymus	thymus
50	chr14:104027200-104027600	Enhancers	Small Intestine	intestine

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