Variant report

Variant	nsv976351
Chromosome Location	chr14:70349344-70353065
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr14:70349563-70349626	MCF10A-Er-Src	breast:	n/a	n/a
2	FOXA2	chr14:70349455-70349640	HepG2	liver:	n/a	n/a
3	GATA2	chr14:70352029-70352273	K562	blood:	n/a	n/a
4	HEY1	chr14:70352507-70352872	K562	blood:	n/a	n/a
5	IRF1	chr14:70351548-70351549	K562	blood:	n/a	n/a
6	MYC	chr14:70349693-70349838	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr14:70352482-70352925	GM12892	blood:	n/a	n/a
8	POLR2A	chr14:70352054-70352230	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr14:70349384-70349445	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr14:70352539-70352868	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr14:70352503-70352883	GM12878	blood:	n/a	n/a
12	POLR2A	chr14:70349729-70349765	MCF10A-Er-Src	breast:	n/a	n/a
13	POLR2A	chr14:70352507-70352747	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr14:70352415-70352880	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr14:70352570-70352870	GM12878	blood:	n/a	n/a
16	POLR2A	chr14:70351942-70352156	ProgFib	skin:	n/a	n/a
17	POLR2A	chr14:70352800-70352811	K562	blood:	n/a	n/a
18	POLR2A	chr14:70352453-70352856	GM12878	blood:	n/a	n/a
19	POLR2A	chr14:70349449-70349452	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr14:70350171-70350275	GM12878	blood:	n/a	n/a
21	POLR2A	chr14:70352311-70352943	GM12892	blood:	n/a	n/a
22	POLR2A	chr14:70352028-70352305	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr14:70352784-70352826	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr14:70352476-70352963	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr14:70349902-70350093	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr14:70352556-70352876	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr14:70352446-70352922	GM12878	blood:	n/a	n/a
28	POLR2A	chr14:70349528-70349541	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr14:70352386-70352902	Hela-S3	cervix:	n/a	n/a
30	RCOR1	chr14:70348912-70349578	Hela-S3	cervix:	n/a	n/a
31	SIX5	chr14:70352541-70352772	K562	blood:	n/a	n/a
32	STAT1	chr14:70347715-70349403	Hela-S3	cervix:	n/a	chr14:70349145-70349153 chr14:70349042-70349056
33	STAT3	chr14:70349643-70349733	MCF10A-Er-Src	breast:	n/a	n/a
34	USF2	chr14:70349014-70349638	Hela-S3	cervix:	n/a	n/a
35	ZBTB33	chr14:70352342-70353044	K562	blood:	n/a	n/a
36	ZBTB33	chr14:70352009-70352288	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:70352365-70352415	HMEC	breast:	n/a
2	chr14:70352365-70352415	Hepatocyte	liver:	n/a
3	chr14:70352365-70352415	SK-N-MC	brain:	n/a
4	chr14:70352365-70352415	NH-A	brain:	n/a
5	chr14:70352365-70352415	NT2-D1	testis:	n/a
6	chr14:70352365-70352415	SK-N-SH_RA	brain:	n/a
7	chr14:70352365-70352415	A549	lung:	n/a
8	chr14:70352365-70352415	HEEpiC	esophagus:	n/a
9	chr14:70352365-70352415	Hela-S3	cervix:	n/a
10	chr14:70352365-70352415	GM19239	blood:	n/a
11	chr14:70352365-70352415	NHDF-neo	bronchial:	n/a
12	chr14:70352365-70352415	GM06990	blood:	n/a
13	chr14:70352365-70352415	AG09309	skin:	n/a
14	chr14:70352365-70352415	SK-N-SH	brain:	n/a
15	chr14:70352365-70352415	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:70352365-70352415	CMK	blood:	n/a
17	chr14:70352365-70352415	ECC-1	luminal epithelium:	n/a
18	chr14:70352365-70352415	BJ	skin:	n/a
19	chr14:70352365-70352415	AG04450	lung:	fetal
20	chr14:70352365-70352415	AG09319	gingival:	n/a
21	chr14:70352365-70352415	T-47D	breast:	n/a
22	chr14:70352365-70352415	HEK293	kidney:	embryo
23	chr14:70352365-70352415	MCF10A-Er-Src	breast:	n/a
24	chr14:70352365-70352415	AG04449	skin:	fetal
25	chr14:70352365-70352415	ProgFib	skin:	n/a
26	chr14:70352365-70352415	HCF	heart:	n/a
27	chr14:70352365-70352415	NHBE	bronchial:	n/a
28	chr14:70352365-70352415	HCT-116	colon:	n/a
29	chr14:70352365-70352415	HL-60	blood:	n/a
30	chr14:70352365-70352415	Caco-2	colon:	n/a
31	chr14:70352365-70352415	NB4	blood:	n/a
32	chr14:70352365-70352415	HRCEpiC	kidney:	n/a
33	chr14:70352365-70352415	BE2_C	brain:	n/a
34	chr14:70352365-70352415	HAEpiC	amniotic membrane:	n/a
35	chr14:70352365-70352415	GM12891	blood:	n/a
36	chr14:70352365-70352415	MCF-7	breast:	n/a
37	chr14:70352365-70352415	HUVEC	blood vessel:	n/a
38	chr14:70352365-70352415	HCPEpiC	choroid plexus:	n/a
39	chr14:70352365-70352415	GM12878	blood:	n/a
40	chr14:70352365-70352415	H1-hESC	embryonic stem cell:	embryo
41	chr14:70352365-70352415	HNPCEpiC	eye:	n/a
42	chr14:70352365-70352415	HIPEpiC	eye:	n/a
43	chr14:70352365-70352415	Jurkat	blood:	n/a
44	chr14:70352365-70352415	PFSK-1	brain:	n/a
45	chr14:70352365-70352415	SKMC	muscle:	n/a
46	chr14:70352365-70352415	HCM	heart:	n/a
47	chr14:70352365-70352415	LNCaP	prostate:	n/a
48	chr14:70352365-70352415	HRE	kidney:	n/a
49	chr14:70352365-70352415	IMR90	lung:	fetal
50	chr14:70352365-70352415	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:70345017..70347390-chr14:70347953..70350433,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPL7AP6	TF binding region
RPL7AP6	CpG island
ENSG00000198732	chromatin interactions

Extended variants
information (count: 152 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:152 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554893473	chr14:70349358-70349359	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs35732834	chr14:70349361-70349362	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190602649	chr14:70349378-70349379	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149592359	chr14:70349383-70349384	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117541286	chr14:70349413-70349414	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183200298	chr14:70349414-70349415	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578144147	chr14:70349420-70349421	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149722780	chr14:70349453-70349454	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557501837	chr14:70349467-70349468	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs540077671	chr14:70349478-70349479	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544622827	chr14:70349546-70349547	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs575762337	chr14:70349566-70349567	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543141297	chr14:70349676-70349677	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs8003374	chr14:70349682-70349683	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs528463341	chr14:70349683-70349684	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570392293	chr14:70349750-70349751	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559360440	chr14:70349757-70349758	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs187807687	chr14:70349765-70349766	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs530758171	chr14:70349785-70349786	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145608694	chr14:70349789-70349790	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148915630	chr14:70349791-70349792	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193287856	chr14:70349833-70349834	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74455586	chr14:70349836-70349837	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567288596	chr14:70349862-70349863	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112004890	chr14:70349874-70349875	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs145634582	chr14:70349915-70349916	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560878426	chr14:70349984-70349985	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375695370	chr14:70349988-70349989	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547288252	chr14:70349992-70349993	Weak transcription ZNF genes & repeats Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs71423378	chr14:70350024-70350025	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138179879	chr14:70350054-70350055	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs539238056	chr14:70350107-70350108	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141224600	chr14:70350135-70350136	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369205272	chr14:70350250-70350251	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528296917	chr14:70350268-70350269	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536780820	chr14:70350344-70350345	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554745344	chr14:70350395-70350396	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs547087228	chr14:70350396-70350397	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573213641	chr14:70350402-70350403	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540225795	chr14:70350403-70350404	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10138095	chr14:70350467-70350468	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs577465666	chr14:70350499-70350500	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549731368	chr14:70350562-70350563	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185637993	chr14:70350588-70350589	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs34300667	chr14:70350606-70350607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527389025	chr14:70350607-70350608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs138668964	chr14:70350637-70350638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563182848	chr14:70350639-70350640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372215265	chr14:70350647-70350648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532535017	chr14:70350655-70350656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70345800-70349400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:70346000-70349600	Active TSS	Fetal Brain Female	brain
3	chr14:70347200-70349600	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr14:70347400-70349400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr14:70347400-70349800	Enhancers	Fetal Stomach	stomach
6	chr14:70348000-70354200	Weak transcription	Psoas Muscle	Psoas
7	chr14:70348200-70349400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr14:70348200-70349400	Flanking Active TSS	Hela-S3	cervix
9	chr14:70348400-70353400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr14:70348600-70349400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr14:70348600-70349400	Flanking Active TSS	Brain Germinal Matrix	brain
12	chr14:70348600-70349600	Enhancers	Fetal Brain Male	brain
13	chr14:70348600-70350600	Enhancers	Liver	Liver
14	chr14:70348800-70349600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr14:70349000-70349400	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:70349000-70349400	Enhancers	Fetal Muscle Trunk	muscle
17	chr14:70349000-70349600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr14:70349000-70349600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr14:70349000-70349600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr14:70349000-70353000	Weak transcription	Brain Substantia Nigra	brain
21	chr14:70349200-70349400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr14:70349200-70349400	Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr14:70349200-70349400	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr14:70349200-70349600	Flanking Active TSS	HepG2	liver
25	chr14:70349200-70353000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr14:70349400-70349600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:70349400-70349600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr14:70349400-70349600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr14:70349400-70349600	Bivalent Enhancer	HSMMtube	muscle
30	chr14:70349400-70349800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr14:70349400-70349800	Active TSS	Brain Germinal Matrix	brain
32	chr14:70349400-70350000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr14:70349400-70350000	Transcr. at gene 5' and 3'	Hela-S3	cervix
34	chr14:70349400-70350600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr14:70349400-70353000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr14:70349400-70353400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:70349400-70354000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr14:70349600-70349800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:70349600-70350200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr14:70349600-70351200	Enhancers	HepG2	liver
41	chr14:70349600-70352800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:70349600-70353200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr14:70349600-70353400	Weak transcription	Fetal Brain Male	brain
44	chr14:70349600-70354800	Weak transcription	Fetal Brain Female	brain
45	chr14:70349600-70356000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr14:70349800-70350200	Enhancers	Brain Germinal Matrix	brain
47	chr14:70349800-70350400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr14:70349800-70351000	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:70349800-70352800	Weak transcription	Fetal Stomach	stomach
50	chr14:70350000-70350200	Flanking Active TSS	Hela-S3	cervix

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