Variant report

Variant	nsv969928
Chromosome Location	chr5:107132237-107143800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:126)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:126 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:107140530-107140842	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:107140568-107140830	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:107140492-107140923	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr5:107140487-107140903	IMR90	lung:	n/a	n/a
5	CEBPB	chr5:107139974-107140064	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:107140557-107140891	A549	lung:	n/a	n/a
7	CEBPB	chr5:107142464-107142785	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr5:107132620-107132770	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr5:107132640-107132790	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr5:107132560-107132710	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr5:107132580-107132730	HRE	kidney:	n/a	n/a
12	CTCF	chr5:107132620-107132770	AG10803	skin:	n/a	n/a
13	CTCF	chr5:107132560-107132710	HepG2	liver:	n/a	n/a
14	CTCF	chr5:107132620-107132770	HMF	breast:	n/a	n/a
15	CTCF	chr5:107132620-107132770	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr5:107132580-107132730	GM06990	blood:	n/a	n/a
17	CTCF	chr5:107132600-107132750	GM12864	blood:	n/a	n/a
18	CTCF	chr5:107132620-107132770	HCFaa	heart:	n/a	n/a
19	CTCF	chr5:107132560-107132710	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr5:107141560-107141710	BE2_C	brain:	n/a	chr5:107141651-107141664
21	CTCF	chr5:107140180-107140330	HAc	cerebellar:	n/a	n/a
22	CTCF	chr5:107132620-107132770	AG09309	skin:	n/a	n/a
23	CTCF	chr5:107132640-107132790	GM12864	blood:	n/a	n/a
24	CTCF	chr5:107132780-107132930	GM12871	blood:	n/a	n/a
25	CTCF	chr5:107132580-107132730	GM12878	blood:	n/a	n/a
26	CTCF	chr5:107132620-107132770	AG09319	gingival:	n/a	n/a
27	CTCF	chr5:107132620-107132770	HRE	kidney:	n/a	n/a
28	CTCF	chr5:107132580-107132730	A549	lung:	n/a	n/a
29	CTCF	chr5:107132629-107132761	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr5:107132640-107132790	AG09309	skin:	n/a	n/a
31	CTCF	chr5:107132620-107132770	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr5:107132660-107132810	GM06990	blood:	n/a	n/a
33	CTCF	chr5:107132600-107132750	MCF-7	breast:	n/a	n/a
34	CTCF	chr5:107132560-107132710	HCT-116	colon:	n/a	n/a
35	CTCF	chr5:107132580-107132730	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr5:107132720-107132870	AG10803	skin:	n/a	n/a
37	CTCF	chr5:107132540-107132690	WI-38	lung:	n/a	n/a
38	CTCF	chr5:107132580-107132730	HCT-116	colon:	n/a	n/a
39	CTCF	chr5:107132640-107132790	HEK293	kidney:	n/a	n/a
40	CTCF	chr5:107132580-107132730	HAc	cerebellar:	n/a	n/a
41	CTCF	chr5:107132684-107132723	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:107132600-107132750	RPTEC	kidney:	n/a	n/a
43	CTCF	chr5:107132640-107132790	HMEC	breast:	n/a	n/a
44	CTCF	chr5:107132620-107132770	HPF	lung:	n/a	n/a
45	CTCF	chr5:107132640-107132790	AG09319	gingival:	n/a	n/a
46	CTCF	chr5:107132640-107132790	NHEK	skin:	n/a	n/a
47	CTCF	chr5:107132600-107132750	AG04449	skin:	n/a	n/a
48	CTCF	chr5:107132580-107132730	HMEC	breast:	n/a	n/a
49	CTCF	chr5:107132560-107132710	AG04449	skin:	n/a	n/a
50	CTCF	chr5:107132660-107132810	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:107135281-107135331	SK-N-SH_RA	brain:	n/a
2	chr5:107135281-107135331	AG09319	gingival:	n/a
3	chr5:107135281-107135331	MCF-7	breast:	n/a
4	chr5:107135281-107135331	HUVEC	blood vessel:	n/a
5	chr5:107135281-107135331	CMK	blood:	n/a
6	chr5:107135281-107135331	AG10803	skin:	n/a
7	chr5:107135281-107135331	ECC-1	luminal epithelium:	n/a
8	chr5:107135281-107135331	K562	blood:	n/a
9	chr5:107135281-107135331	PANC-1	pancreas:	n/a
10	chr5:107135281-107135331	HEEpiC	esophagus:	n/a
11	chr5:107135281-107135331	SKMC	muscle:	n/a
12	chr5:107135281-107135331	NHBE	bronchial:	n/a
13	chr5:107135281-107135331	HRPEpiC	eye:	n/a
14	chr5:107135281-107135331	GM12892	blood:	n/a
15	chr5:107135281-107135331	HNPCEpiC	eye:	n/a
16	chr5:107135281-107135331	AG09309	skin:	n/a
17	chr5:107135281-107135331	BJ	skin:	n/a
18	chr5:107135281-107135331	ProgFib	skin:	n/a
19	chr5:107135281-107135331	NHDF-neo	bronchial:	n/a
20	chr5:107135281-107135331	T-47D	breast:	n/a
21	chr5:107135281-107135331	HCM	heart:	n/a
22	chr5:107135281-107135331	Caco-2	colon:	n/a
23	chr5:107135281-107135331	NB4	blood:	n/a
24	chr5:107135281-107135331	HMEC	breast:	n/a
25	chr5:107135281-107135331	SK-N-SH	brain:	n/a
26	chr5:107135281-107135331	PrEC	prostate:	n/a
27	chr5:107135281-107135331	SK-N-MC	brain:	n/a
28	chr5:107135281-107135331	NH-A	brain:	n/a
29	chr5:107135281-107135331	HEK293	kidney:	embryo
30	chr5:107135281-107135331	Jurkat	blood:	n/a
31	chr5:107135281-107135331	IMR90	lung:	fetal
32	chr5:107135281-107135331	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:107135281-107135331	HCPEpiC	choroid plexus:	n/a
34	chr5:107135281-107135331	AG04449	skin:	fetal
35	chr5:107135281-107135331	PFSK-1	brain:	n/a
36	chr5:107135281-107135331	GM12878	blood:	n/a
37	chr5:107135281-107135331	ovcar-3	ovarian:	n/a
38	chr5:107135281-107135331	Hela-S3	cervix:	n/a
39	chr5:107135281-107135331	LNCaP	prostate:	n/a
40	chr5:107135281-107135331	HL-60	blood:	n/a
41	chr5:107135281-107135331	HCT-116	colon:	n/a
42	chr5:107135281-107135331	HAEpiC	amniotic membrane:	n/a
43	chr5:107135281-107135331	GM06990	blood:	n/a
44	chr5:107135281-107135331	RPTEC	kidney:	n/a
45	chr5:107135281-107135331	HepG2	liver:	n/a
46	chr5:107135281-107135331	MCF10A-Er-Src	breast:	n/a
47	chr5:107135281-107135331	NT2-D1	testis:	n/a
48	chr5:107135281-107135331	GM12891	blood:	n/a
49	chr5:107135281-107135331	BE2_C	brain:	n/a
50	chr5:107135281-107135331	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:107125029..107126613-chr5:107139861..107141985,2	MCF-7	breast:
2	chr5:107139921..107141469-chr5:107142790..107144472,2	K562	blood:
3	chr5:107141836..107143424-chr5:107150743..107153310,2	MCF-7	breast:
4	chr5:107135763..107138365-chr5:107141825..107143430,2	K562	blood:
5	chr1:69106008..69107508-chr5:107141802..107143595,2	MCF-7	breast:
6	chr5:107135763..107138365-chr5:107141825..107143430,2	K562	blood:
7	chr5:107139921..107141469-chr5:107142790..107144472,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FER-10	chr5:107142478-107142625	l_2992_chr5:107142477-107144693_heart

No data

Variant related genes	Relation type
RN7SKP122	TF binding region
RN7SKP122	CpG island

Extended variants
information (count: 497 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:497 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186323473	chr5:107132240-107132241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192081689	chr5:107132247-107132248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6868417	chr5:107132270-107132271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs139875686	chr5:107132293-107132294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143236110	chr5:107132342-107132343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552333473	chr5:107132350-107132351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571712833	chr5:107132359-107132360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537675777	chr5:107132368-107132369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146691329	chr5:107132370-107132371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13159249	chr5:107132384-107132385	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182732159	chr5:107132538-107132539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143444975	chr5:107132583-107132584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186308702	chr5:107132590-107132591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190760951	chr5:107132610-107132611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565395285	chr5:107132640-107132641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575298136	chr5:107132646-107132647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544405362	chr5:107132680-107132681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs6869199	chr5:107132694-107132695	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs151127750	chr5:107132727-107132728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73780421	chr5:107132745-107132746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs182273380	chr5:107132755-107132756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141076608	chr5:107132787-107132788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56714753	chr5:107132793-107132794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11742515	chr5:107132802-107132803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs397955703	chr5:107132805-107132806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552276920	chr5:107132839-107132840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150246164	chr5:107132868-107132869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs537209280	chr5:107132921-107132922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576923928	chr5:107132923-107132924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1862309	chr5:107132934-107132935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372965980	chr5:107132947-107132948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536527621	chr5:107132962-107132963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78666967	chr5:107132963-107132964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566495514	chr5:107132981-107132982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538650213	chr5:107132984-107132985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1862308	chr5:107132991-107132992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187986106	chr5:107133096-107133097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544425189	chr5:107133117-107133118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554726059	chr5:107133134-107133135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138877227	chr5:107133147-107133148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113468385	chr5:107133170-107133171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553537948	chr5:107133176-107133177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1422436	chr5:107133199-107133200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs542581581	chr5:107133204-107133205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532099820	chr5:107133247-107133248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545795961	chr5:107133248-107133249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192259790	chr5:107133252-107133253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113717067	chr5:107133261-107133262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550398505	chr5:107133326-107133327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531434410	chr5:107133351-107133352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107127800-107135400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:107130200-107135200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:107130800-107140400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:107132600-107135000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:107134800-107136000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:107135000-107135200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:107135000-107135400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:107135000-107135400	Enhancers	H9 Cell Line	embryonic stem cell
9	chr5:107135000-107135600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr5:107135000-107135600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:107135000-107135800	Enhancers	H1 Cell Line	embryonic stem cell
12	chr5:107135000-107135800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:107135000-107135800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr5:107135000-107135800	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr5:107135000-107136000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:107135000-107136200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr5:107135000-107136400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr5:107135200-107135400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:107135200-107135400	Enhancers	Right Atrium	heart
20	chr5:107135200-107135600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:107135200-107135600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr5:107135200-107136000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:107135200-107136000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:107135400-107135800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr5:107135400-107135800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr5:107135400-107136600	Enhancers	Fetal Lung	lung
27	chr5:107135400-107137000	Enhancers	Primary T cells from cord blood	blood
28	chr5:107135400-107137800	Enhancers	Pancreatic Islets	Pancreatic Islet
29	chr5:107135400-107138400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:107135400-107140600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr5:107135400-107143000	Weak transcription	Right Atrium	heart
32	chr5:107135600-107135800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:107135600-107140800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:107135600-107140800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:107135800-107140400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr5:107135800-107140600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr5:107135800-107140800	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:107135800-107140800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:107135800-107141400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:107136000-107140400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:107136000-107141000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:107136200-107140400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr5:107136400-107140200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr5:107137000-107140400	Weak transcription	Primary T cells from cord blood	blood
45	chr5:107137800-107141400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr5:107138400-107144800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:107139200-107141200	Enhancers	Dnd41	blood
48	chr5:107139400-107139600	Enhancers	NHDF-Ad	bronchial
49	chr5:107139800-107142000	Weak transcription	NHDF-Ad	bronchial
50	chr5:107140200-107144200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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