Variant report

Variant	nsv1018714
Chromosome Location	chr5:115586834-115625245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:115614176-115614178	K562	blood:	n/a	n/a
2	BATF	chr5:115609206-115609493	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
3	BATF	chr5:115609200-115609492	GM12878	blood:	n/a	chr5:115609356-115609366 chr5:115609352-115609362 chr5:115609355-115609366
4	CBX3	chr5:115612735-115612979	K562	blood:	n/a	n/a
5	CBX3	chr5:115612653-115612965	K562	blood:	n/a	n/a
6	CBX3	chr5:115612612-115613059	HCT-116	colon:	n/a	n/a
7	CEBPB	chr5:115601292-115601498	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:115608269-115608767	MCF-7	breast:	n/a	chr5:115608483-115608494
9	CEBPB	chr5:115608311-115608872	IMR90	lung:	n/a	chr5:115608483-115608494
10	CEBPB	chr5:115608227-115608718	MCF-7	breast:	n/a	chr5:115608483-115608494
11	CEBPB	chr5:115608357-115608659	A549	lung:	n/a	chr5:115608483-115608494
12	CEBPB	chr5:115608381-115608622	HepG2	liver:	n/a	chr5:115608483-115608494
13	CEBPB	chr5:115612611-115612811	A549	lung:	n/a	n/a
14	CEBPB	chr5:115615956-115616164	HepG2	liver:	n/a	n/a
15	CHD2	chr5:115609186-115609453	GM12878	blood:	n/a	n/a
16	CHD2	chr5:115608466-115608624	GM12878	blood:	n/a	n/a
17	CTCF	chr5:115625060-115625210	HFF-Myc	foreskin:	n/a	chr5:115625169-115625182
18	CTCF	chr5:115608400-115608550	GM12871	blood:	n/a	n/a
19	CTCF	chr5:115625129-115625224	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
20	CTCF	chr5:115625060-115625210	GM12865	blood:	n/a	chr5:115625169-115625182
21	CTCF	chr5:115625040-115625190	HMF	breast:	n/a	chr5:115625169-115625182
22	CTCF	chr5:115625040-115625190	AG09319	gingival:	n/a	chr5:115625169-115625182
23	CTCF	chr5:115625080-115625230	HAc	cerebellar:	n/a	chr5:115625169-115625182
24	CTCF	chr5:115625133-115625254	MCF-7	breast:	n/a	chr5:115625169-115625182
25	CTCF	chr5:115625120-115625270	SAEC	small airway:	n/a	chr5:115625169-115625182
26	CTCF	chr5:115625060-115625210	AoAF	blood vessel:	n/a	chr5:115625169-115625182
27	CTCF	chr5:115608320-115608470	HVMF	connective:	n/a	n/a
28	CTCF	chr5:115605340-115605490	AG10803	skin:	n/a	n/a
29	CTCF	chr5:115625120-115625270	AG04450	lung:	n/a	chr5:115625169-115625182
30	CTCF	chr5:115625000-115625150	HFF	foreskin:	n/a	n/a
31	CTCF	chr5:115625080-115625230	K562	blood:	n/a	chr5:115625169-115625182
32	CTCF	chr5:115625000-115625150	GM12872	blood:	n/a	n/a
33	CTCF	chr5:115608440-115608590	A549	lung:	n/a	n/a
34	CTCF	chr5:115625100-115625250	GM12868	blood:	n/a	chr5:115625169-115625182
35	CTCF	chr5:115608440-115608590	HVMF	connective:	n/a	n/a
36	CTCF	chr5:115625133-115625238	NHEK	skin:	n/a	chr5:115625169-115625182
37	CTCF	chr5:115608440-115608590	AG04450	lung:	n/a	n/a
38	CTCF	chr5:115608080-115608230	BE2_C	brain:	n/a	n/a
39	CTCF	chr5:115608420-115608570	AG09319	gingival:	n/a	n/a
40	CTCF	chr5:115608420-115608570	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr5:115608300-115608651	GM12878	blood:	n/a	n/a
42	CTCF	chr5:115608300-115608450	GM12874	blood:	n/a	n/a
43	CTCF	chr5:115608440-115608590	HRE	kidney:	n/a	n/a
44	CTCF	chr5:115625080-115625230	NB4	blood:	n/a	chr5:115625169-115625182
45	CTCF	chr5:115624940-115625090	GM12866	blood:	n/a	n/a
46	CTCF	chr5:115608400-115608550	GM06990	blood:	n/a	n/a
47	CTCF	chr5:115625080-115625230	HMF	breast:	n/a	chr5:115625169-115625182
48	CTCF	chr5:115625040-115625190	HUVEC	blood vessel:	n/a	chr5:115625169-115625182
49	CTCF	chr5:115608440-115608590	RPTEC	kidney:	n/a	n/a
50	CTCF	chr5:115608400-115608550	AG09319	gingival:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:115599680-115599730	HMEC	breast:	n/a
2	chr5:115599680-115599730	HL-60	blood:	n/a
3	chr5:115599680-115599730	Caco-2	colon:	n/a
4	chr5:115599680-115599730	GM06990	blood:	n/a
5	chr5:115599680-115599730	HUVEC	blood vessel:	n/a
6	chr5:115599680-115599730	HCM	heart:	n/a
7	chr5:115599680-115599730	Hela-S3	cervix:	n/a
8	chr5:115599680-115599730	HRE	kidney:	n/a
9	chr5:115599680-115599730	Jurkat	blood:	n/a
10	chr5:115599680-115599730	HIPEpiC	eye:	n/a
11	chr5:115599680-115599730	HRPEpiC	eye:	n/a
12	chr5:115599680-115599730	HNPCEpiC	eye:	n/a
13	chr5:115599680-115599730	GM12878	blood:	n/a
14	chr5:115599680-115599730	HAEpiC	amniotic membrane:	n/a
15	chr5:115599680-115599730	ovcar-3	ovarian:	n/a
16	chr5:115599680-115599730	PrEC	prostate:	n/a
17	chr5:115599680-115599730	BJ	skin:	n/a
18	chr5:115599680-115599730	NHBE	bronchial:	n/a
19	chr5:115599680-115599730	MCF10A-Er-Src	breast:	n/a
20	chr5:115599680-115599730	GM19239	blood:	n/a
21	chr5:115599680-115599730	HEEpiC	esophagus:	n/a
22	chr5:115599680-115599730	NHDF-neo	bronchial:	n/a
23	chr5:115599680-115599730	AG10803	skin:	n/a
24	chr5:115599680-115599730	SKMC	muscle:	n/a
25	chr5:115599680-115599730	AG04450	lung:	fetal
26	chr5:115599680-115599730	AG09319	gingival:	n/a
27	chr5:115599680-115599730	IMR90	lung:	fetal
28	chr5:115599680-115599730	ECC-1	luminal epithelium:	n/a
29	chr5:115599680-115599730	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:115599680-115599730	NH-A	brain:	n/a
31	chr5:115599680-115599730	AoSMC	blood vessel:	n/a
32	chr5:115599680-115599730	U87	brain:	n/a
33	chr5:115599680-115599730	NT2-D1	testis:	n/a
34	chr5:115599680-115599730	ProgFib	skin:	n/a
35	chr5:115599680-115599730	T-47D	breast:	n/a
36	chr5:115599680-115599730	A549	lung:	n/a
37	chr5:115599680-115599730	NB4	blood:	n/a
38	chr5:115599680-115599730	SAEC	small airway:	n/a
39	chr5:115599680-115599730	HEK293	kidney:	embryo
40	chr5:115599680-115599730	H1-hESC	embryonic stem cell:	embryo
41	chr5:115599680-115599730	AG09309	skin:	n/a
42	chr5:115599680-115599730	HepG2	liver:	n/a
43	chr5:115599680-115599730	SK-N-SH_RA	brain:	n/a
44	chr5:115599680-115599730	BE2_C	brain:	n/a
45	chr5:115599680-115599730	LNCaP	prostate:	n/a
46	chr5:115599680-115599730	Hepatocyte	liver:	n/a
47	chr5:115599680-115599730	MCF-7	breast:	n/a
48	chr5:115599680-115599730	RPTEC	kidney:	n/a
49	chr5:115599680-115599730	CMK	blood:	n/a
50	chr5:115599680-115599730	K562	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:115473639..115474170-chr5:115607611..115608509,2	MCF-7	breast:
2	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
3	chr5:115473058..115473763-chr5:115624723..115625238,2	MCF-7	breast:
4	chr5:115607181..115609929-chr5:115613382..115615949,2	K562	blood:
5	chr5:115573428..115574084-chr5:115607901..115608709,2	MCF-7	breast:
6	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:
7	chr5:115611187..115613784-chr5:115614610..115617269,2	MCF-7	breast:

No data

Variant related genes	Relation type
COMMD10	TF binding region
COMMD10	CpG island

Extended variants
information (count: 2034 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2034 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187380681	chr5:115586841-115586842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527564317	chr5:115586905-115586906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192564165	chr5:115586912-115586913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549845001	chr5:115586923-115586924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs568497633	chr5:115586955-115586956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139799729	chr5:115586964-115586965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560766936	chr5:115586970-115586971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529860050	chr5:115586973-115586974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184790030	chr5:115586982-115586983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150014726	chr5:115586983-115586984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551489448	chr5:115586987-115586988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs28658343	chr5:115586991-115586992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6874582	chr5:115586995-115586996	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190291266	chr5:115587005-115587006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535313572	chr5:115587091-115587092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555273696	chr5:115587098-115587099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147969183	chr5:115587123-115587124	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs6896405	chr5:115587139-115587140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184348291	chr5:115587157-115587158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201292846	chr5:115587189-115587190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537614377	chr5:115587210-115587211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555990448	chr5:115587214-115587215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373017342	chr5:115587259-115587260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544637068	chr5:115587264-115587265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377045808	chr5:115587297-115587298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371163687	chr5:115587338-115587339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374214094	chr5:115587355-115587356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377612861	chr5:115587398-115587399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370940801	chr5:115587422-115587423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377150615	chr5:115587469-115587470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540940470	chr5:115587531-115587532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374117574	chr5:115587558-115587559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10062898	chr5:115587561-115587562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs529852101	chr5:115587565-115587566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370306371	chr5:115587580-115587581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62385977	chr5:115587610-115587611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532624131	chr5:115587616-115587617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370639081	chr5:115587656-115587657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552633643	chr5:115587671-115587672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs55885663	chr5:115587702-115587703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368706153	chr5:115587734-115587735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528460933	chr5:115587752-115587753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376934035	chr5:115587792-115587793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548911112	chr5:115587860-115587861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568693838	chr5:115587868-115587869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372082995	chr5:115587872-115587873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537295848	chr5:115587912-115587913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374313575	chr5:115587914-115587915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368447066	chr5:115587920-115587921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372436093	chr5:115587945-115587946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
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	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
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
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:115560400-115610600	Weak transcription	Left Ventricle	heart
2	chr5:115562400-115589000	Weak transcription	Ovary	ovary
3	chr5:115579600-115610600	Weak transcription	Primary B cells from cord blood	blood
4	chr5:115581400-115591600	Weak transcription	Primary T cells from cord blood	blood
5	chr5:115582600-115594600	Weak transcription	Fetal Intestine Large	intestine
6	chr5:115583600-115589000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:115584800-115603600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:115585200-115587800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:115585800-115601200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr5:115586000-115587000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:115586600-115595600	Weak transcription	Aorta	Aorta
12	chr5:115586600-115603000	Weak transcription	Dnd41	blood
13	chr5:115586800-115587200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr5:115586800-115588400	Weak transcription	Brain Hippocampus Middle	brain
15	chr5:115586800-115597000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr5:115586800-115608000	Weak transcription	Adipose Nuclei	Adipose
17	chr5:115586800-115609800	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr5:115586800-115610800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr5:115587000-115599800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:115590800-115610200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr5:115591000-115607200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr5:115591600-115592000	ZNF genes & repeats	Primary T cells from cord blood	blood
23	chr5:115592000-115599600	Weak transcription	Primary T cells from cord blood	blood
24	chr5:115592000-115607800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr5:115592200-115593400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr5:115592800-115593200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr5:115593000-115601400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr5:115594400-115595400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:115595000-115601200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr5:115595200-115595400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:115595200-115597800	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr5:115595400-115597000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:115595600-115596600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr5:115595800-115603800	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr5:115596200-115596400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr5:115596200-115596800	Enhancers	Colon Smooth Muscle	Colon
37	chr5:115596400-115598400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:115596600-115597600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:115596800-115597800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr5:115597000-115597400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:115597000-115597600	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr5:115597000-115599000	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr5:115597000-115608200	Weak transcription	NHDF-Ad	bronchial
44	chr5:115597400-115599600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:115597600-115599800	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr5:115597800-115599800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr5:115597800-115603400	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr5:115598400-115598600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr5:115598600-115598800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:115599000-115601400	Weak transcription	Monocytes-CD14+_RO01746	blood

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