Variant report

Variant	esv994503
Chromosome Location	chr5:76129230-76144182
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:188)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:188 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr5:76142105-76142119	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr5:76132036-76132284	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:76131985-76132410	A549	lung:	n/a	n/a
4	CEBPB	chr5:76131995-76132322	A549	lung:	n/a	n/a
5	CEBPB	chr5:76134470-76135001	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:76132009-76132318	IMR90	lung:	n/a	n/a
7	CTCF	chr5:76137420-76137570	HEK293	kidney:	n/a	n/a
8	CTCF	chr5:76132120-76132270	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr5:76139880-76140030	HEK293	kidney:	n/a	n/a
10	CTCF	chr5:76132100-76132250	HMF	breast:	n/a	n/a
11	CTCF	chr5:76132096-76132297	HUVEC	blood vessel:	n/a	n/a
12	CTCF	chr5:76132080-76132230	AG09309	skin:	n/a	n/a
13	CTCF	chr5:76132099-76132303	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr5:76132120-76132270	AG10803	skin:	n/a	n/a
15	CTCF	chr5:76132105-76132282	MCF-7	breast:	n/a	n/a
16	CTCF	chr5:76132160-76132310	WI-38	lung:	n/a	n/a
17	CTCF	chr5:76131996-76132350	IMR90	lung:	n/a	n/a
18	CTCF	chr5:76132220-76132370	WI-38	lung:	n/a	n/a
19	CTCF	chr5:76132143-76132250	K562	blood:	n/a	n/a
20	CTCF	chr5:76137480-76137630	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr5:76132100-76132250	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr5:76132100-76132250	AG04449	skin:	n/a	n/a
23	CTCF	chr5:76132120-76132270	AG09319	gingival:	n/a	n/a
24	CTCF	chr5:76132163-76132251	ProgFib	skin:	n/a	n/a
25	CTCF	chr5:76132200-76132350	NHLF	lung:	n/a	n/a
26	CTCF	chr5:76132140-76132290	HFF	foreskin:	n/a	n/a
27	CTCF	chr5:76132160-76132310	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr5:76137534-76137608	K562	blood:	n/a	n/a
29	CTCF	chr5:76132160-76132310	AG09309	skin:	n/a	n/a
30	CTCF	chr5:76132151-76132244	Gliobla	brain:	n/a	n/a
31	CTCF	chr5:76137520-76137670	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:76132019-76132380	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:76132151-76132281	HepG2	liver:	n/a	n/a
34	CTCF	chr5:76132140-76132290	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr5:76132080-76132230	HAc	cerebellar:	n/a	n/a
36	CTCF	chr5:76132180-76132330	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr5:76132120-76132270	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr5:76139920-76140070	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr5:76132260-76132410	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr5:76132140-76132290	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:76132080-76132230	HPF	lung:	n/a	n/a
42	CTCF	chr5:76132240-76132390	A549	lung:	n/a	n/a
43	CTCF	chr5:76132120-76132270	HMEC	breast:	n/a	n/a
44	CTCF	chr5:76139880-76140030	HVMF	connective:	n/a	n/a
45	CTCF	chr5:76131980-76132130	HCM	heart:	n/a	n/a
46	CTCF	chr5:76132080-76132230	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:76132160-76132310	AG09319	gingival:	n/a	n/a
48	CTCF	chr5:76132100-76132250	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr5:76132180-76132330	HCT-116	colon:	n/a	n/a
50	CTCF	chr5:76132100-76132250	HBMEC	blood vessel:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76132547-76132597	A549	lung:	n/a
2	chr5:76132547-76132597	HMEC	breast:	n/a
3	chr5:76132547-76132597	SAEC	small airway:	n/a
4	chr5:76134399-76134449	AoSMC	blood vessel:	n/a
5	chr5:76134399-76134449	HEK293	kidney:	embryo
6	chr5:76132547-76132597	BE2_C	brain:	n/a
7	chr5:76131154-76131204	HMEC	breast:	n/a
8	chr5:76134399-76134449	BE2_C	brain:	n/a
9	chr5:76131154-76131204	HNPCEpiC	eye:	n/a
10	chr5:76131154-76131204	SKMC	muscle:	n/a
11	chr5:76132547-76132597	HIPEpiC	eye:	n/a
12	chr5:76131154-76131204	NH-A	brain:	n/a
13	chr5:76132547-76132597	GM06990	blood:	n/a
14	chr5:76131154-76131204	CMK	blood:	n/a
15	chr5:76134399-76134449	NHDF-neo	bronchial:	n/a
16	chr5:76131154-76131204	AoSMC	blood vessel:	n/a
17	chr5:76134399-76134449	PrEC	prostate:	n/a
18	chr5:76132547-76132597	HCPEpiC	choroid plexus:	n/a
19	chr5:76132547-76132597	NHDF-neo	bronchial:	n/a
20	chr5:76134399-76134449	AG09309	skin:	n/a
21	chr5:76132547-76132597	IMR90	lung:	fetal
22	chr5:76134399-76134449	HepG2	liver:	n/a
23	chr5:76131154-76131204	SK-N-SH_RA	brain:	n/a
24	chr5:76134399-76134449	ovcar-3	ovarian:	n/a
25	chr5:76132547-76132597	MCF10A-Er-Src	breast:	n/a
26	chr5:76131154-76131204	NB4	blood:	n/a
27	chr5:76132547-76132597	PrEC	prostate:	n/a
28	chr5:76131154-76131204	AG09319	gingival:	n/a
29	chr5:76134399-76134449	SK-N-SH_RA	brain:	n/a
30	chr5:76132547-76132597	SK-N-SH	brain:	n/a
31	chr5:76131154-76131204	SK-N-MC	brain:	n/a
32	chr5:76131154-76131204	MCF10A-Er-Src	breast:	n/a
33	chr5:76132547-76132597	CMK	blood:	n/a
34	chr5:76134399-76134449	AG04450	lung:	fetal
35	chr5:76132547-76132597	GM19239	blood:	n/a
36	chr5:76131154-76131204	HRE	kidney:	n/a
37	chr5:76131154-76131204	HEK293	kidney:	embryo
38	chr5:76134399-76134449	HCT-116	colon:	n/a
39	chr5:76132547-76132597	NB4	blood:	n/a
40	chr5:76132547-76132597	HEEpiC	esophagus:	n/a
41	chr5:76131154-76131204	GM12878	blood:	n/a
42	chr5:76132547-76132597	NH-A	brain:	n/a
43	chr5:76134399-76134449	PANC-1	pancreas:	n/a
44	chr5:76131154-76131204	Hepatocyte	liver:	n/a
45	chr5:76134399-76134449	NT2-D1	testis:	n/a
46	chr5:76132547-76132597	RPTEC	kidney:	n/a
47	chr5:76132547-76132597	ProgFib	skin:	n/a
48	chr5:76132547-76132597	HEK293	kidney:	embryo
49	chr5:76134399-76134449	HCF	heart:	n/a
50	chr5:76132547-76132597	GM12892	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
2	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
3	chr5:76132665..76134749-chr5:76137165..76139299,2	K562	blood:
4	chr5:75973826..75975865-chr5:76141935..76143640,2	MCF-7	breast:
5	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
6	chr5:76136037..76139434-chr5:76141594..76145921,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F2RL2-4	chr5:76132727-76133020	NONHSAT102252

No data

Variant related genes	Relation type
RN7SL208P	TF binding region
S100Z	TF binding region
RN7SL208P	CpG island
S100Z	CpG island
ENSG00000171643	chromatin interactions
ENSG00000264391	chromatin interactions

Extended variants
information (count: 593 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:593 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114050394	chr5:76129239-76129240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369747168	chr5:76129240-76129241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2243062	chr5:76129241-76129242	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs373708895	chr5:76129249-76129250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187106934	chr5:76129277-76129278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370713776	chr5:76129291-76129292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2243083	chr5:76129303-76129304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376163464	chr5:76129309-76129310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs267600695	chr5:76129377-76129378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144257769	chr5:76129449-76129450	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146609770	chr5:76129458-76129459	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141069352	chr5:76129476-76129477	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563654389	chr5:76129504-76129505	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138965893	chr5:76129521-76129522	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149001132	chr5:76129526-76129527	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114618359	chr5:76129550-76129551	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115274241	chr5:76129560-76129561	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376878559	chr5:76129567-76129568	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2243084	chr5:76129647-76129648	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs187721390	chr5:76129648-76129649	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376212863	chr5:76129653-76129654	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189860773	chr5:76129654-76129655	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2243063	chr5:76129655-76129656	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569299379	chr5:76129661-76129662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529274010	chr5:76129681-76129682	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146054906	chr5:76129692-76129693	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2243064	chr5:76129704-76129705	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535427440	chr5:76129734-76129735	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143647822	chr5:76129738-76129739	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565779111	chr5:76129762-76129763	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534668337	chr5:76129771-76129772	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557576114	chr5:76129779-76129780	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2243065	chr5:76129806-76129807	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376383495	chr5:76129870-76129871	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62365147	chr5:76129961-76129962	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62365148	chr5:76129965-76129966	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35323826	chr5:76129966-76129967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566827130	chr5:76129970-76129971	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs70982645	chr5:76129975-76129976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2243085	chr5:76130039-76130040	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537268108	chr5:76130044-76130045	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3135469	chr5:76130059-76130060	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs2243066	chr5:76130113-76130114	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs542600555	chr5:76130114-76130115	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559366027	chr5:76130129-76130130	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2243067	chr5:76130196-76130197	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571965986	chr5:76130210-76130211	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2243068	chr5:76130229-76130230	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182575884	chr5:76130249-76130250	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565259436	chr5:76130284-76130285	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76116000-76131600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr5:76116400-76131600	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr5:76116800-76134200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:76117400-76130800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr5:76117400-76134200	Weak transcription	Stomach Mucosa	stomach
6	chr5:76117400-76135200	Weak transcription	Colonic Mucosa	Colon
7	chr5:76118800-76134600	Weak transcription	HepG2	liver
8	chr5:76123000-76132400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:76123600-76132400	Strong transcription	Fetal Intestine Small	intestine
10	chr5:76126000-76130800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr5:76126000-76132800	Weak transcription	Aorta	Aorta
12	chr5:76127000-76131800	Strong transcription	Fetal Intestine Large	intestine
13	chr5:76127000-76134600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr5:76127200-76130200	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr5:76127200-76131800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:76127200-76134600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr5:76127400-76129400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:76127400-76134200	Weak transcription	Osteobl	bone
19	chr5:76127600-76132800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr5:76127800-76134400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr5:76128000-76132800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:76128000-76134600	Weak transcription	Small Intestine	intestine
23	chr5:76128200-76130400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:76128200-76130600	Strong transcription	H1 Cell Line	embryonic stem cell
25	chr5:76128200-76130600	Strong transcription	NHEK	skin
26	chr5:76128200-76133400	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:76128400-76130200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr5:76128400-76130400	Strong transcription	HUES48 Cell Line	embryonic stem cell
29	chr5:76128400-76130400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr5:76128400-76130800	Strong transcription	Duodenum Mucosa	Duodenum
31	chr5:76128400-76132000	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:76128400-76132400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:76128400-76133000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:76128600-76129400	Strong transcription	Liver	Liver
35	chr5:76128600-76129600	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr5:76128600-76129600	Strong transcription	Primary T cells from cord blood	blood
37	chr5:76128600-76129600	Strong transcription	NH-A	brain
38	chr5:76128600-76129800	Strong transcription	Pancreas	Pancrea
39	chr5:76128600-76129800	Strong transcription	A549	lung
40	chr5:76128600-76129800	Strong transcription	NHLF	lung
41	chr5:76128600-76130000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr5:76128600-76130000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:76128600-76130000	Strong transcription	HUVEC	blood vessel
44	chr5:76128600-76130200	Strong transcription	H9 Cell Line	embryonic stem cell
45	chr5:76128600-76130200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:76128600-76130200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr5:76128600-76130200	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr5:76128600-76130200	Strong transcription	HMEC	breast
49	chr5:76128600-76130400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
50	chr5:76128600-76130400	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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