Variant report

Variant	esv1848030
Chromosome Location	chr14:35602956-35614319
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	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
3	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
4	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
5	CEBPB	chr14:35613295-35613593	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:35612292-35612467	HepG2	liver:	n/a	chr14:35612414-35612425
7	CEBPB	chr14:35612279-35612564	HepG2	liver:	n/a	chr14:35612414-35612425
8	CHD2	chr14:35613402-35613558	GM12878	blood:	n/a	n/a
9	CTCF	chr14:35610029-35610031	LNCaP	prostate:	n/a	n/a
10	CTCF	chr14:35609980-35610130	HCPEpiC	choroid plexus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
11	CTCF	chr14:35610065-35610168	GM13976	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
12	CTCF	chr14:35610000-35610150	GM12865	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
13	CTCF	chr14:35603400-35603550	HepG2	liver:	n/a	n/a
14	CTCF	chr14:35609955-35610239	Spleen_OC	spleen:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
15	CTCF	chr14:35603320-35603470	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr14:35609960-35610110	HMEC	breast:	n/a	n/a
17	CTCF	chr14:35610040-35610190	RPTEC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
18	CTCF	chr14:35610040-35610190	GM12801	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
19	CTCF	chr14:35609857-35610436	IMR90	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
20	CTCF	chr14:35609872-35610234	MCF-7	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
21	CTCF	chr14:35609980-35610130	GM06990	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
22	CTCF	chr14:35610020-35610170	AG10803	skin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
23	CTCF	chr14:35603381-35603557	MCF-7	breast:	n/a	n/a
24	CTCF	chr14:35610000-35610150	GM12868	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
25	CTCF	chr14:35609960-35610110	GM12865	blood:	n/a	n/a
26	CTCF	chr14:35610060-35610210	HMEC	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
27	CTCF	chr14:35602820-35602970	HAc	cerebellar:	n/a	n/a
28	CTCF	chr14:35610000-35610150	NHDF-neo	bronchial:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
29	CTCF	chr14:35609735-35610610	SK-N-SH	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
30	CTCF	chr14:35609921-35610231	H1-hESC	embryonic stem cell:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
31	CTCF	chr14:35610100-35610250	HVMF	connective:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
32	CTCF	chr14:35610020-35610170	AoAF	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
33	CTCF	chr14:35609963-35610210	HepG2	liver:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
34	CTCF	chr14:35609280-35609430	AG10803	skin:	n/a	n/a
35	CTCF	chr14:35610000-35610150	GM12873	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
36	CTCF	chr14:35610040-35610190	HFF-Myc	foreskin:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
37	CTCF	chr14:35602820-35602970	HepG2	liver:	n/a	n/a
38	CTCF	chr14:35610040-35610190	GM12874	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
39	CTCF	chr14:35610018-35610210	Kidney_OC	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
40	CTCF	chr14:35603376-35603560	MCF-7	breast:	n/a	n/a
41	CTCF	chr14:35609977-35610231	Pancreas_OC	pancreas:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
42	CTCF	chr14:35610060-35610210	HMF	breast:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
43	CTCF	chr14:35610000-35610150	SK-N-SH_RA	brain:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
44	CTCF	chr14:35609953-35610237	HUVEC	blood vessel:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
45	CTCF	chr14:35610020-35610170	AG09319	gingival:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
46	CTCF	chr14:35609700-35609850	HMEC	breast:	n/a	n/a
47	CTCF	chr14:35610040-35610190	HPF	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
48	CTCF	chr14:35610039-35610198	GM13977	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
49	CTCF	chr14:35610000-35610150	HRE	kidney:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
50	CTCF	chr14:35610040-35610190	WI-38	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129

No.	Distal block	Cell Line	Cell type
1	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
2	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
3	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
4	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
5	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
6	chr14:35603102..35605461-chr14:35881286..35882903,2	MCF-7	breast:
7	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
8	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
9	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
10	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
11	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
12	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
13	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:
14	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
15	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366

Variant related genes	Relation type
ENSG00000241052	TF binding region
ENSG00000258790	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000100890	chromatin interactions

Extended variants
information (count: 395 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12590678	chr14:35602956-35602957	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181472181	chr14:35602964-35602965	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551361181	chr14:35602988-35602989	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs571458463	chr14:35603019-35603020	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs534045352	chr14:35603025-35603026	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs527845951	chr14:35603031-35603032	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs553777110	chr14:35603035-35603036	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs373433365	chr14:35603056-35603057	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs12879140	chr14:35603079-35603080	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
10	rs111397396	chr14:35603124-35603125	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs10437989	chr14:35603166-35603167	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs368694114	chr14:35603188-35603189	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs537688823	chr14:35603234-35603235	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs374001111	chr14:35603263-35603264	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs377727477	chr14:35603279-35603280	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs576096165	chr14:35603454-35603455	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs186583265	chr14:35603464-35603465	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs564890486	chr14:35603521-35603522	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs572347998	chr14:35603548-35603549	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs541751280	chr14:35603561-35603562	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs561407772	chr14:35603573-35603574	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs530344982	chr14:35603580-35603581	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs550369010	chr14:35603648-35603649	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188401687	chr14:35603655-35603656	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs371434568	chr14:35603703-35603704	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs180916928	chr14:35603763-35603764	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs531392601	chr14:35603828-35603829	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs551397926	chr14:35603859-35603860	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs111729918	chr14:35603877-35603878	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs571266595	chr14:35603878-35603879	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs140546125	chr14:35603897-35603898	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs149796939	chr14:35603917-35603918	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs567423385	chr14:35603948-35603949	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs144746751	chr14:35603995-35603996	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs555901533	chr14:35604042-35604043	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs569820227	chr14:35604052-35604053	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs538795333	chr14:35604073-35604074	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs558774468	chr14:35604144-35604145	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572437642	chr14:35604152-35604153	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531947225	chr14:35604158-35604159	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148503363	chr14:35604176-35604177	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185183659	chr14:35604222-35604223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574996797	chr14:35604226-35604227	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs76135586	chr14:35604265-35604266	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571641496	chr14:35604286-35604287	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142759670	chr14:35604309-35604310	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559863757	chr14:35604330-35604331	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4494460	chr14:35604350-35604351	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs375170277	chr14:35604359-35604360	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs189651498	chr14:35604366-35604367	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592400-35603000	Weak transcription	Ovary	ovary
2	chr14:35592600-35603000	Weak transcription	Esophagus	oesophagus
3	chr14:35592600-35603000	Weak transcription	Gastric	stomach
4	chr14:35592600-35603200	Weak transcription	Left Ventricle	heart
5	chr14:35592600-35603200	Weak transcription	Pancreas	Pancrea
6	chr14:35592600-35603400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
8	chr14:35592800-35603200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:35593000-35603400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:35593000-35603400	Weak transcription	Right Atrium	heart
12	chr14:35593000-35603800	Weak transcription	Brain Anterior Caudate	brain
13	chr14:35593000-35603800	Weak transcription	Right Ventricle	heart
14	chr14:35593000-35605200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
17	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
18	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr14:35593200-35603000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr14:35593200-35603000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr14:35593200-35603000	Weak transcription	NHLF	lung
22	chr14:35593200-35603400	Weak transcription	Brain Angular Gyrus	brain
23	chr14:35593200-35603400	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:35593200-35603800	Weak transcription	Fetal Heart	heart
25	chr14:35593200-35604000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr14:35593200-35625200	Weak transcription	NH-A	brain
27	chr14:35593200-35625600	Weak transcription	Colon Smooth Muscle	Colon
28	chr14:35593200-35627800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr14:35593200-35635400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr14:35593400-35603600	Weak transcription	HMEC	breast
31	chr14:35593400-35613200	Weak transcription	Osteobl	bone
32	chr14:35593400-35617200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr14:35594000-35615800	Weak transcription	HUVEC	blood vessel
34	chr14:35594400-35629000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr14:35594600-35604000	Weak transcription	Hela-S3	cervix
36	chr14:35594600-35609600	Weak transcription	Colonic Mucosa	Colon
37	chr14:35595200-35613200	Weak transcription	K562	blood
38	chr14:35595600-35603200	Weak transcription	NHEK	skin
39	chr14:35596000-35623600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr14:35596200-35604800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:35597200-35605400	Weak transcription	NHDF-Ad	bronchial
42	chr14:35597400-35625000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr14:35597600-35625000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr14:35597800-35615400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:35598000-35609800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr14:35599200-35603600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr14:35599400-35607200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr14:35599600-35604200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr14:35600000-35604400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr14:35600200-35605400	Strong transcription	Primary B cells from peripheral blood	blood

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