Variant report

Variant	nsv882824
Chromosome Location	chr5:124789500-124875058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:124812823-124812953	K562	blood:	n/a	n/a
2	ATF3	chr5:124819888-124820404	A549	lung:	n/a	n/a
3	BACH1	chr5:124800637-124800895	K562	blood:	n/a	n/a
4	BACH1	chr5:124800568-124800831	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:124813513-124813517	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr5:124819832-124820453	A549	lung:	n/a	n/a
7	BCL3	chr5:124819796-124820372	A549	lung:	n/a	n/a
8	BHLHE40	chr5:124863292-124863316	GM12878	blood:	n/a	n/a
9	BRCA1	chr5:124819989-124820582	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr5:124790741-124791102	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:124819878-124820356	MCF-7	breast:	n/a	n/a
12	CEBPB	chr5:124790808-124791044	A549	lung:	n/a	n/a
13	CEBPB	chr5:124835303-124835549	HepG2	liver:	n/a	chr5:124835472-124835489 chr5:124835361-124835372
14	CEBPB	chr5:124822384-124822745	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:124820850-124821280	A549	lung:	n/a	n/a
16	CEBPB	chr5:124819870-124820373	A549	lung:	n/a	n/a
17	CEBPB	chr5:124797388-124797423	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr5:124819791-124820471	HCT-116	colon:	n/a	n/a
19	CEBPB	chr5:124835413-124835544	A549	lung:	n/a	chr5:124835472-124835489
20	CEBPB	chr5:124819991-124820186	HepG2	liver:	n/a	n/a
21	CEBPB	chr5:124820827-124821323	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:124833750-124834200	Hela-S3	cervix:	n/a	chr5:124834054-124834065 chr5:124834053-124834064
23	CEBPB	chr5:124833895-124834227	MCF-7	breast:	n/a	chr5:124834054-124834065 chr5:124834053-124834064
24	CEBPB	chr5:124797774-124797974	A549	lung:	n/a	n/a
25	CEBPB	chr5:124820719-124821348	MCF-7	breast:	n/a	n/a
26	CEBPB	chr5:124820837-124821340	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr5:124819944-124820282	A549	lung:	n/a	n/a
28	CEBPB	chr5:124862366-124862549	HepG2	liver:	n/a	chr5:124862408-124862419
29	CEBPB	chr5:124820610-124821473	HCT-116	colon:	n/a	n/a
30	CEBPB	chr5:124797221-124797918	MCF-7	breast:	n/a	chr5:124797431-124797444
31	CEBPB	chr5:124820615-124821431	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr5:124820680-124821347	HCT-116	colon:	n/a	n/a
33	CEBPB	chr5:124819900-124821287	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:124819869-124820399	MCF-7	breast:	n/a	n/a
35	CEBPB	chr5:124833928-124834135	HepG2	liver:	n/a	chr5:124834054-124834065 chr5:124834053-124834064
36	CEBPB	chr5:124819769-124820528	HCT-116	colon:	n/a	n/a
37	CEBPB	chr5:124819854-124821417	A549	lung:	n/a	n/a
38	CEBPB	chr5:124819933-124820311	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:124819880-124820342	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr5:124835404-124835604	IMR90	lung:	n/a	chr5:124835472-124835489
41	CHD2	chr5:124820928-124821271	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:124819955-124820290	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr5:124820009-124820259	A549	lung:	n/a	n/a
44	CREB1	chr5:124820368-124820782	A549	lung:	n/a	n/a
45	CTCF	chr5:124844825-124844827	GM10248	blood:	n/a	n/a
46	CTCF	chr5:124844860-124844892	GM10248	blood:	n/a	n/a
47	CTCF	chr5:124799000-124799150	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr5:124825029-124825076	Fibrobl	skin:	n/a	n/a
49	CTCF	chr5:124819660-124819810	AoAF	blood vessel:	n/a	chr5:124819686-124819699
50	CTCF	chr5:124843271-124843375	GM13976	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:124852645-124852695	PrEC	prostate:	n/a
2	chr5:124821012-124821062	HEEpiC	esophagus:	n/a
3	chr5:124845866-124845916	BE2_C	brain:	n/a
4	chr5:124835828-124835878	PANC-1	pancreas:	n/a
5	chr5:124835828-124835878	RPTEC	kidney:	n/a
6	chr5:124835828-124835878	GM12878	blood:	n/a
7	chr5:124821012-124821062	K562	blood:	n/a
8	chr5:124835828-124835878	NHBE	bronchial:	n/a
9	chr5:124852645-124852695	HRPEpiC	eye:	n/a
10	chr5:124821012-124821062	PFSK-1	brain:	n/a
11	chr5:124835828-124835878	CMK	blood:	n/a
12	chr5:124852645-124852695	AoSMC	blood vessel:	n/a
13	chr5:124835828-124835878	HCPEpiC	choroid plexus:	n/a
14	chr5:124821012-124821062	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:124835828-124835878	GM19239	blood:	n/a
16	chr5:124835828-124835878	HepG2	liver:	n/a
17	chr5:124835828-124835878	GM06990	blood:	n/a
18	chr5:124852645-124852695	A549	lung:	n/a
19	chr5:124845866-124845916	K562	blood:	n/a
20	chr5:124852645-124852695	Caco-2	colon:	n/a
21	chr5:124845866-124845916	GM12891	blood:	n/a
22	chr5:124835828-124835878	LNCaP	prostate:	n/a
23	chr5:124835828-124835878	IMR90	lung:	fetal
24	chr5:124821012-124821062	SK-N-MC	brain:	n/a
25	chr5:124835828-124835878	Hepatocyte	liver:	n/a
26	chr5:124835828-124835878	PFSK-1	brain:	n/a
27	chr5:124835828-124835878	SKMC	muscle:	n/a
28	chr5:124852645-124852695	HCT-116	colon:	n/a
29	chr5:124852645-124852695	AG04450	lung:	fetal
30	chr5:124845866-124845916	GM19239	blood:	n/a
31	chr5:124821012-124821062	RPTEC	kidney:	n/a
32	chr5:124821012-124821062	A549	lung:	n/a
33	chr5:124821012-124821062	NT2-D1	testis:	n/a
34	chr5:124852645-124852695	AG04449	skin:	fetal
35	chr5:124852645-124852695	HUVEC	blood vessel:	n/a
36	chr5:124845866-124845916	AG04449	skin:	fetal
37	chr5:124852645-124852695	AG10803	skin:	n/a
38	chr5:124852645-124852695	NB4	blood:	n/a
39	chr5:124845866-124845916	HCM	heart:	n/a
40	chr5:124821012-124821062	ECC-1	luminal epithelium:	n/a
41	chr5:124845866-124845916	Hela-S3	cervix:	n/a
42	chr5:124852645-124852695	H1-hESC	embryonic stem cell:	embryo
43	chr5:124845866-124845916	AG09319	gingival:	n/a
44	chr5:124835828-124835878	AG04449	skin:	fetal
45	chr5:124835828-124835878	AoSMC	blood vessel:	n/a
46	chr5:124845866-124845916	AoSMC	blood vessel:	n/a
47	chr5:124821012-124821062	H1-hESC	embryonic stem cell:	embryo
48	chr5:124852645-124852695	HL-60	blood:	n/a
49	chr5:124821012-124821062	GM19239	blood:	n/a
50	chr5:124845866-124845916	HCF	heart:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:124787637..124789614-chr5:124795687..124797598,2	MCF-7	breast:
2	chr5:124787637..124789614-chr5:124795687..124797598,2	MCF-7	breast:
3	chr5:124855835..124858574-chr5:124862134..124863991,2	K562	blood:
4	chr5:124797532..124799322-chr5:124800167..124802283,2	MCF-7	breast:
5	chr5:124812779..124814356-chr5:124815356..124817386,2	K562	blood:
6	chr5:124812779..124814356-chr5:124815356..124817386,2	K562	blood:
7	chr5:124783033..124786221-chr5:124790428..124792959,3	MCF-7	breast:
8	chr5:124816573..124819551-chr5:124822797..124825714,2	MCF-7	breast:
9	chr5:124804057..124805782-chr5:124806040..124809032,2	MCF-7	breast:
10	chr5:124804057..124805782-chr5:124806040..124809032,2	MCF-7	breast:
11	chr5:23483811..23484735-chr5:124818892..124819399,2	MCF-7	breast:
12	chr5:124745519..124746394-chr5:124819221..124820024,3	MCF-7	breast:
13	chr5:124855835..124858574-chr5:124862134..124863991,2	K562	blood:
14	chr5:124797532..124799322-chr5:124800167..124802283,2	MCF-7	breast:
15	chr5:124816573..124819551-chr5:124822797..124825714,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRAMD3-2	chr5:124828954-124829028	ENSG00000260192.1
2	lnc-GRAMD3-2	chr5:124834469-124834649	NONHSAT103560
3	lnc-GRAMD3-2	chr5:124828954-124829028	NONHSAT103560
4	lnc-GRAMD3-2	chr5:124855221-124855288	NONHSAT103560
5	lnc-GRAMD3-2	chr5:124834469-124834649	ENSG00000260192.1
6	lnc-GRAMD3-2	chr5:124855221-124855288	ENSG00000260192.1

No data

Variant related genes	Relation type
ENSG00000260192	TF binding region
ENSG00000260192	CpG island

Extended variants
information (count: 3154 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3154 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4472260	chr5:124789500-124789501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143595524	chr5:124789504-124789505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189171877	chr5:124789569-124789570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541873280	chr5:124789580-124789581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13353869	chr5:124789612-124789613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs556733255	chr5:124789621-124789622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527761873	chr5:124789652-124789653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199740134	chr5:124789680-124789681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373203448	chr5:124789683-124789684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs147199399	chr5:124789684-124789685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181008007	chr5:124789693-124789694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576165169	chr5:124789700-124789701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200872233	chr5:124789701-124789702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148636718	chr5:124789707-124789708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185078341	chr5:124789711-124789712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561846573	chr5:124789718-124789719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370638723	chr5:124789755-124789756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188663010	chr5:124789793-124789794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545874966	chr5:124789832-124789833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142133662	chr5:124789876-124789877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10477664	chr5:124789905-124789906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs528603157	chr5:124789934-124789935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181231243	chr5:124790000-124790001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551102811	chr5:124790006-124790007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186359564	chr5:124790009-124790010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538057914	chr5:124790052-124790053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58917396	chr5:124790060-124790061	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs191669432	chr5:124790110-124790111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs80118693	chr5:124790117-124790118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561948891	chr5:124790139-124790140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553862925	chr5:124790157-124790158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572510719	chr5:124790165-124790166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs151171124	chr5:124790179-124790180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531189640	chr5:124790200-124790201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574256811	chr5:124790270-124790271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533455888	chr5:124790296-124790297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551343112	chr5:124790297-124790298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113479732	chr5:124790300-124790301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs78730845	chr5:124790319-124790320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138987342	chr5:124790359-124790360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144000744	chr5:124790423-124790424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556582672	chr5:124790462-124790463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529155073	chr5:124790508-124790509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367869470	chr5:124790514-124790515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6888542	chr5:124790536-124790537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558915827	chr5:124790538-124790539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183465878	chr5:124790548-124790549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146867576	chr5:124790573-124790574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569427980	chr5:124790625-124790626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538406763	chr5:124790670-124790671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	16397240	CNVD
Parathyroid adenoma	22454399	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124787200-124790400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr5:124787600-124797400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:124790200-124790800	Enhancers	Brain Hippocampus Middle	brain
4	chr5:124790400-124790800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:124790400-124790800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:124790400-124790800	Enhancers	Brain Substantia Nigra	brain
7	chr5:124790400-124790800	Enhancers	NH-A	brain
8	chr5:124792200-124792400	Enhancers	Brain Substantia Nigra	brain
9	chr5:124793400-124794000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
10	chr5:124796800-124797800	Enhancers	Dnd41	blood
11	chr5:124797200-124797800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:124797200-124798000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:124797200-124798200	Enhancers	Brain Germinal Matrix	brain
14	chr5:124797400-124797800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:124797400-124797800	Enhancers	HSMMtube	muscle
16	chr5:124797800-124799200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:124797800-124800600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr5:124798000-124799200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:124798200-124798600	Weak transcription	Brain Germinal Matrix	brain
20	chr5:124798600-124800000	Enhancers	Brain Germinal Matrix	brain
21	chr5:124798800-124799400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr5:124798800-124799800	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr5:124799000-124800000	Enhancers	Fetal Brain Female	brain
24	chr5:124799200-124799600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:124799200-124799600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:124799200-124799800	Enhancers	Fetal Brain Male	brain
27	chr5:124799400-124799800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr5:124799600-124804800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr5:124799600-124805000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:124799800-124801600	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr5:124800600-124801200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:124801200-124805400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:124801400-124801800	Enhancers	Fetal Lung	lung
34	chr5:124801600-124802000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr5:124802600-124803200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:124802600-124803400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr5:124802600-124803400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:124802600-124803400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr5:124802800-124803200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr5:124803000-124803200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr5:124803000-124803400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:124804200-124805000	Enhancers	HSMMtube	muscle
43	chr5:124804800-124807200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:124805000-124806000	Weak transcription	HSMMtube	muscle
45	chr5:124805000-124806800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:124805400-124805600	Enhancers	Brain Substantia Nigra	brain
47	chr5:124805400-124806400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr5:124805400-124806400	Enhancers	Brain Hippocampus Middle	brain
49	chr5:124805800-124806400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr5:124806000-124806400	Enhancers	HSMMtube	muscle

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