Variant report

Variant	nsv968977
Chromosome Location	chr5:114599737-114602288
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	IRF1	chr5:114599853-114600042	K562	blood:	n/a	n/a
2	MYC	chr5:114600570-114600595	MCF-7	breast:	n/a	n/a
3	MYC	chr5:114600597-114600754	MCF-7	breast:	n/a	n/a
4	POLR2A	chr5:114600798-114600809	MCF-7	breast:	n/a	n/a
5	POLR2A	chr5:114601384-114601558	MCF10A-Er-Src	breast:	n/a	n/a
6	POLR2A	chr5:114600655-114600660	MCF-7	breast:	n/a	n/a
7	POLR2A	chr5:114600618-114600624	MCF-7	breast:	n/a	n/a
8	POLR2A	chr5:114598362-114600207	K562	blood:	n/a	n/a
9	POLR2A	chr5:114599975-114600164	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr5:114600979-114600994	Gliobla	brain:	n/a	n/a
11	POLR2A	chr5:114600665-114600767	MCF-7	breast:	n/a	n/a
12	POLR2A	chr5:114600438-114600491	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr5:114600560-114600705	MCF-7	breast:	n/a	n/a
14	POLR2A	chr5:114600377-114600618	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr5:114600961-114601158	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr5:114600630-114600639	MCF-7	breast:	n/a	n/a
17	POLR2A	chr5:114600531-114600780	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr5:114600584-114600599	A549	lung:	n/a	n/a
19	SPI1	chr5:114601498-114601674	GM12891	blood:	n/a	n/a
20	TBP	chr5:114599752-114599910	K562	blood:	n/a	n/a
21	UBTF	chr5:114599731-114599826	K562	blood:	n/a	n/a
22	ZNF143	chr5:114599739-114599741	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114601105-114601155	HepG2	liver:	n/a
2	chr5:114601105-114601155	CMK	blood:	n/a
3	chr5:114601105-114601155	NB4	blood:	n/a
4	chr5:114601105-114601155	U87	brain:	n/a
5	chr5:114601105-114601155	BE2_C	brain:	n/a
6	chr5:114601105-114601155	Jurkat	blood:	n/a
7	chr5:114601105-114601155	HUVEC	blood vessel:	n/a
8	chr5:114601105-114601155	Hela-S3	cervix:	n/a
9	chr5:114601105-114601155	SK-N-MC	brain:	n/a
10	chr5:114601105-114601155	PrEC	prostate:	n/a
11	chr5:114601105-114601155	AG10803	skin:	n/a
12	chr5:114601105-114601155	T-47D	breast:	n/a
13	chr5:114601105-114601155	HEEpiC	esophagus:	n/a
14	chr5:114601105-114601155	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:114601105-114601155	GM12878	blood:	n/a
16	chr5:114601105-114601155	HEK293	kidney:	embryo
17	chr5:114601105-114601155	MCF10A-Er-Src	breast:	n/a
18	chr5:114601105-114601155	SK-N-SH_RA	brain:	n/a
19	chr5:114601105-114601155	LNCaP	prostate:	n/a
20	chr5:114601105-114601155	GM12891	blood:	n/a
21	chr5:114601105-114601155	PFSK-1	brain:	n/a
22	chr5:114601105-114601155	NT2-D1	testis:	n/a
23	chr5:114601105-114601155	GM12892	blood:	n/a
24	chr5:114601105-114601155	HRCEpiC	kidney:	n/a
25	chr5:114601105-114601155	Caco-2	colon:	n/a
26	chr5:114601105-114601155	HCM	heart:	n/a
27	chr5:114601105-114601155	ovcar-3	ovarian:	n/a
28	chr5:114601105-114601155	NHBE	bronchial:	n/a
29	chr5:114601105-114601155	GM06990	blood:	n/a
30	chr5:114601105-114601155	ECC-1	luminal epithelium:	n/a
31	chr5:114601105-114601155	HL-60	blood:	n/a
32	chr5:114601105-114601155	HCT-116	colon:	n/a
33	chr5:114601105-114601155	AG04449	skin:	fetal
34	chr5:114601105-114601155	GM19239	blood:	n/a
35	chr5:114601105-114601155	HCF	heart:	n/a
36	chr5:114601105-114601155	A549	lung:	n/a
37	chr5:114601105-114601155	BJ	skin:	n/a
38	chr5:114601105-114601155	SKMC	muscle:	n/a
39	chr5:114601105-114601155	RPTEC	kidney:	n/a
40	chr5:114601105-114601155	AG09319	gingival:	n/a
41	chr5:114601105-114601155	HRE	kidney:	n/a
42	chr5:114601105-114601155	NHDF-neo	bronchial:	n/a
43	chr5:114601105-114601155	PANC-1	pancreas:	n/a
44	chr5:114601105-114601155	HCPEpiC	choroid plexus:	n/a
45	chr5:114601105-114601155	SAEC	small airway:	n/a
46	chr5:114601105-114601155	AG09309	skin:	n/a
47	chr5:114601105-114601155	H1-hESC	embryonic stem cell:	embryo
48	chr5:114601105-114601155	HIPEpiC	eye:	n/a
49	chr5:114601105-114601155	HMEC	breast:	n/a
50	chr5:114601105-114601155	HAEpiC	amniotic membrane:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:114599046..114601822-chr5:114630160..114632443,2	K562	blood:
2	chr5:114552265..114553912-chr5:114598605..114600282,2	K562	blood:
3	chr5:114598208..114599898-chr5:114601355..114602888,2	MCF-7	breast:
4	chr5:114598595..114600612-chr5:114607394..114609348,2	MCF-7	breast:
5	chr5:114598335..114600352-chr5:114624872..114627572,2	K562	blood:
6	chr5:114599500..114601272-chr5:114611165..114613598,2	K562	blood:
7	chr5:114598026..114600265-chr5:114601043..114603821,2	K562	blood:
8	chr5:114598026..114600265-chr5:114601043..114603821,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000243304	TF binding region
PGGT1B	TF binding region
ENSG00000243304	CpG island
PGGT1B	CpG island
ENSG00000250197	chromatin interactions
ENSG00000164221	chromatin interactions
ENSG00000271797	chromatin interactions
ENSG00000164219	chromatin interactions
ENSG00000243304	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73257443	chr5:114599790-114599791	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547422497	chr5:114599795-114599796	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs560987324	chr5:114599811-114599812	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs529900174	chr5:114599822-114599823	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs143077934	chr5:114599964-114599965	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs148221291	chr5:114599996-114599997	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs532479288	chr5:114600029-114600030	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs552199715	chr5:114600067-114600068	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs77733418	chr5:114600068-114600069	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs187894226	chr5:114600078-114600079	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs554611475	chr5:114600160-114600161	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs568245987	chr5:114600163-114600164	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537223180	chr5:114600180-114600181	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs9688262	chr5:114600197-114600198	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192360313	chr5:114600199-114600200	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs185725148	chr5:114600213-114600214	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs369812708	chr5:114600279-114600280	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs546434755	chr5:114600410-114600411	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553392198	chr5:114600411-114600412	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571978621	chr5:114600517-114600518	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187490435	chr5:114600544-114600545	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560944337	chr5:114600557-114600558	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs73780090	chr5:114600598-114600599	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543633507	chr5:114600633-114600634	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs563459516	chr5:114600638-114600639	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs376988531	chr5:114600662-114600663	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs114922779	chr5:114600720-114600721	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565854726	chr5:114600721-114600722	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs528468506	chr5:114600778-114600779	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570326311	chr5:114600791-114600792	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548202900	chr5:114600800-114600801	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374851371	chr5:114600808-114600809	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs147357747	chr5:114600833-114600834	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs539676612	chr5:114600856-114600857	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537188014	chr5:114600870-114600871	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs557044041	chr5:114600992-114600993	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534934463	chr5:114601040-114601041	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs139485580	chr5:114601065-114601066	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs553263388	chr5:114601083-114601084	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs539667407	chr5:114601090-114601091	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs35118853	chr5:114601111-114601112	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573487359	chr5:114601147-114601148	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs541024925	chr5:114601168-114601169	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550024717	chr5:114601171-114601172	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs188675199	chr5:114601193-114601194	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs574495510	chr5:114601194-114601195	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs571580208	chr5:114601195-114601196	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs563262221	chr5:114601198-114601199	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs557185843	chr5:114601201-114601202	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs143713988	chr5:114601235-114601236	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114598800-114600400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:114598800-114600600	Weak transcription	Lung	lung
3	chr5:114598800-114602600	Weak transcription	Spleen	Spleen
4	chr5:114598800-114608200	Weak transcription	Small Intestine	intestine
5	chr5:114598800-114612200	Weak transcription	Gastric	stomach
6	chr5:114598800-114613000	Weak transcription	Esophagus	oesophagus
7	chr5:114599000-114599800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:114599000-114600200	Weak transcription	Fetal Muscle Leg	muscle
9	chr5:114599000-114600400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr5:114599000-114600400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:114599000-114600400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr5:114599000-114600400	Weak transcription	Aorta	Aorta
13	chr5:114599000-114600400	Weak transcription	Brain Germinal Matrix	brain
14	chr5:114599000-114600400	Weak transcription	Fetal Intestine Small	intestine
15	chr5:114599000-114600400	Weak transcription	Fetal Stomach	stomach
16	chr5:114599000-114600400	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr5:114599000-114600600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:114599000-114601000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr5:114599000-114601600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr5:114599000-114603200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:114599000-114606200	Weak transcription	HSMMtube	muscle
22	chr5:114599000-114606400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:114599000-114606400	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr5:114599000-114608800	Weak transcription	Brain Substantia Nigra	brain
25	chr5:114599000-114610200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr5:114599000-114610200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:114599000-114610400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr5:114599000-114610600	Weak transcription	Pancreas	Pancrea
29	chr5:114599000-114610600	Weak transcription	NHLF	lung
30	chr5:114599000-114612200	Weak transcription	Right Ventricle	heart
31	chr5:114599000-114612800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:114599000-114612800	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr5:114599000-114612800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:114599000-114612800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr5:114599000-114612800	Weak transcription	Fetal Intestine Large	intestine
36	chr5:114599000-114612800	Weak transcription	Fetal Thymus	thymus
37	chr5:114599000-114614200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:114599000-114617000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr5:114599000-114617200	Weak transcription	Thymus	Thymus
40	chr5:114599000-114624000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr5:114599000-114626600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr5:114599000-114630800	Weak transcription	Psoas Muscle	Psoas
43	chr5:114599000-114631200	Weak transcription	Primary hematopoietic stem cells	blood
44	chr5:114599000-114631200	Weak transcription	HSMM	muscle
45	chr5:114599000-114631400	Weak transcription	Left Ventricle	heart
46	chr5:114599200-114600000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:114599200-114600000	Weak transcription	Fetal Brain Female	brain
48	chr5:114599200-114600400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:114599200-114600400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:114599200-114600400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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