Variant report

Variant	nsv471044
Chromosome Location	chr5:120917249-121056045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120992127-120992130	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:121027167-121027618	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:121027284-121027484	K562	blood:	n/a	n/a
4	ARID3A	chr5:121034548-121034610	K562	blood:	n/a	n/a
5	ATF1	chr5:121027234-121027535	K562	blood:	n/a	n/a
6	ATF1	chr5:121034439-121034794	K562	blood:	n/a	n/a
7	ATF1	chr5:121017032-121017258	K562	blood:	n/a	n/a
8	ATF3	chr5:121027203-121027431	K562	blood:	n/a	n/a
9	BHLHE40	chr5:121017021-121017277	K562	blood:	n/a	n/a
10	BRCA1	chr5:121027229-121027541	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr5:121016894-121017597	K562	blood:	n/a	n/a
12	CCNT2	chr5:121034456-121034611	K562	blood:	n/a	n/a
13	CCNT2	chr5:121002914-121003211	K562	blood:	n/a	n/a
14	CEBPB	chr5:120964549-120964732	K562	blood:	n/a	chr5:120964658-120964669
15	CEBPB	chr5:121027168-121027662	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:120964486-120965003	HepG2	liver:	n/a	chr5:120964658-120964669
17	CEBPB	chr5:120935701-120935939	IMR90	lung:	n/a	n/a
18	CEBPB	chr5:120943154-120943354	HepG2	liver:	n/a	chr5:120943250-120943261
19	CEBPB	chr5:120924909-120925158	HepG2	liver:	n/a	chr5:120925022-120925033
20	CEBPB	chr5:121029652-121030001	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr5:121029752-121029861	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:120964568-120964931	H1-hESC	embryonic stem cell:	n/a	chr5:120964658-120964669
23	CEBPB	chr5:121038311-121038477	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:121038365-121038468	A549	lung:	n/a	n/a
25	CEBPB	chr5:121037547-121037873	K562	blood:	n/a	chr5:121037702-121037715
26	CEBPB	chr5:121029595-121029978	A549	lung:	n/a	n/a
27	CEBPB	chr5:120964500-120964914	K562	blood:	n/a	chr5:120964658-120964669
28	CEBPB	chr5:120943177-120943331	IMR90	lung:	n/a	chr5:120943250-120943261
29	CEBPB	chr5:120943249-120943280	K562	blood:	n/a	chr5:120943250-120943261
30	CEBPB	chr5:121052340-121052423	HepG2	liver:	n/a	chr5:121052363-121052374
31	CEBPB	chr5:120964509-120964898	A549	lung:	n/a	chr5:120964658-120964669
32	CEBPB	chr5:121027286-121027622	K562	blood:	n/a	n/a
33	CEBPB	chr5:121017502-121017514	K562	blood:	n/a	n/a
34	CEBPB	chr5:121029686-121029950	K562	blood:	n/a	n/a
35	CEBPB	chr5:121027210-121027530	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:120964527-120964910	MCF-7	breast:	n/a	chr5:120964658-120964669
37	CEBPB	chr5:120964485-120964948	Hela-S3	cervix:	n/a	chr5:120964658-120964669
38	CEBPB	chr5:121037621-121037804	H1-hESC	embryonic stem cell:	n/a	chr5:121037702-121037715
39	CEBPB	chr5:121029672-121029976	K562	blood:	n/a	n/a
40	CEBPB	chr5:121027127-121027625	K562	blood:	n/a	n/a
41	CEBPB	chr5:120924908-120925203	IMR90	lung:	n/a	chr5:120925022-120925033
42	CEBPB	chr5:121027205-121027644	A549	lung:	n/a	n/a
43	CEBPB	chr5:121034315-121034697	K562	blood:	n/a	chr5:121034489-121034501
44	CEBPB	chr5:120964504-120965017	A549	lung:	n/a	chr5:120964658-120964669
45	CEBPB	chr5:121027278-121027539	A549	lung:	n/a	n/a
46	CEBPB	chr5:120964481-120964818	K562	blood:	n/a	chr5:120964658-120964669
47	CEBPB	chr5:121034411-121034679	K562	blood:	n/a	chr5:121034489-121034501
48	CEBPD	chr5:121002967-121003385	K562	blood:	n/a	n/a
49	CEBPD	chr5:121034412-121034849	K562	blood:	n/a	n/a
50	CEBPD	chr5:121027289-121027604	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:121022314-121022364	BJ	skin:	n/a
2	chr5:121022314-121022364	HL-60	blood:	n/a
3	chr5:120953129-120953179	K562	blood:	n/a
4	chr5:121022314-121022364	SKMC	muscle:	n/a
5	chr5:120953129-120953179	GM12878	blood:	n/a
6	chr5:120953129-120953179	HMEC	breast:	n/a
7	chr5:120953129-120953179	IMR90	lung:	fetal
8	chr5:121022314-121022364	HCT-116	colon:	n/a
9	chr5:120953129-120953179	LNCaP	prostate:	n/a
10	chr5:121022314-121022364	ProgFib	skin:	n/a
11	chr5:121022314-121022364	AG04450	lung:	fetal
12	chr5:121022314-121022364	A549	lung:	n/a
13	chr5:120953129-120953179	PANC-1	pancreas:	n/a
14	chr5:121022314-121022364	AG09319	gingival:	n/a
15	chr5:121022314-121022364	LNCaP	prostate:	n/a
16	chr5:120953129-120953179	HRE	kidney:	n/a
17	chr5:120953129-120953179	AG09319	gingival:	n/a
18	chr5:120953129-120953179	NHBE	bronchial:	n/a
19	chr5:120953129-120953179	AG04450	lung:	fetal
20	chr5:121022314-121022364	HMEC	breast:	n/a
21	chr5:120953129-120953179	HepG2	liver:	n/a
22	chr5:120953129-120953179	GM06990	blood:	n/a
23	chr5:120953129-120953179	NB4	blood:	n/a
24	chr5:121022314-121022364	MCF-7	breast:	n/a
25	chr5:121022314-121022364	MCF10A-Er-Src	breast:	n/a
26	chr5:121022314-121022364	HIPEpiC	eye:	n/a
27	chr5:121022314-121022364	NB4	blood:	n/a
28	chr5:121022314-121022364	GM06990	blood:	n/a
29	chr5:121022314-121022364	Jurkat	blood:	n/a
30	chr5:121022314-121022364	CMK	blood:	n/a
31	chr5:121022314-121022364	NHBE	bronchial:	n/a
32	chr5:120953129-120953179	NH-A	brain:	n/a
33	chr5:121022314-121022364	HCF	heart:	n/a
34	chr5:121022314-121022364	HRE	kidney:	n/a
35	chr5:121022314-121022364	T-47D	breast:	n/a
36	chr5:120953129-120953179	H1-hESC	embryonic stem cell:	embryo
37	chr5:120953129-120953179	BJ	skin:	n/a
38	chr5:120953129-120953179	ECC-1	luminal epithelium:	n/a
39	chr5:120953129-120953179	PFSK-1	brain:	n/a
40	chr5:120953129-120953179	AoSMC	blood vessel:	n/a
41	chr5:121022314-121022364	HCPEpiC	choroid plexus:	n/a
42	chr5:120953129-120953179	GM19239	blood:	n/a
43	chr5:120953129-120953179	AG10803	skin:	n/a
44	chr5:120953129-120953179	HRCEpiC	kidney:	n/a
45	chr5:121022314-121022364	PrEC	prostate:	n/a
46	chr5:120953129-120953179	Hela-S3	cervix:	n/a
47	chr5:120953129-120953179	MCF10A-Er-Src	breast:	n/a
48	chr5:120953129-120953179	NHDF-neo	bronchial:	n/a
49	chr5:120953129-120953179	A549	lung:	n/a
50	chr5:120953129-120953179	SK-N-SH_RA	brain:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:121037717..121040177-chr5:121042706..121044340,2	K562	blood:
2	chr5:120928236..120930477-chr5:120934461..120936328,2	K562	blood:
3	chr5:120972976..120975022-chr5:120976329..120977904,2	K562	blood:
4	chr5:120953693..120956473-chr5:120986186..120988872,2	K562	blood:
5	chr5:121037717..121040177-chr5:121042706..121044340,2	K562	blood:
6	chr5:120928236..120930477-chr5:120934461..120936328,2	K562	blood:
7	chr5:120966174..120966865-chr5:121226297..121226810,2	MCF-7	breast:
8	chr5:120972976..120975022-chr5:120976329..120977904,2	K562	blood:
9	chr5:120953693..120956473-chr5:120986186..120988872,2	K562	blood:
10	chr5:121048396..121050681-chr5:121053038..121054727,2	K562	blood:
11	chr5:121045011..121047566-chr5:121108750..121111081,2	K562	blood:
12	chr5:120966119..120966759-chr5:121285387..121286002,2	MCF-7	breast:
13	chr5:120965691..120966274-chr5:121206074..121206765,2	MCF-7	breast:
14	chr5:121048396..121050681-chr5:121053038..121054727,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213661	TF binding region
ENSG00000249600	TF binding region
ENSG00000213661	CpG island
ENSG00000249600	CpG island

Extended variants
information (count: 2531 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:2531 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183664435	chr5:120917434-120917435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12521671	chr5:120917454-120917455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554516510	chr5:120917461-120917462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6886054	chr5:120917498-120917499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552567385	chr5:120917539-120917540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6886220	chr5:120917583-120917584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78035857	chr5:120917599-120917600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200581976	chr5:120917632-120917633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560727236	chr5:120917657-120917658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143777057	chr5:120917671-120917672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114694125	chr5:120917700-120917701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189550203	chr5:120917713-120917714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371097079	chr5:120917724-120917725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147216165	chr5:120917748-120917749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550680206	chr5:120917752-120917753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568152034	chr5:120917754-120917755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529610956	chr5:120917757-120917758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535582255	chr5:120917768-120917769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116323185	chr5:120917785-120917786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs77496646	chr5:120917787-120917788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556647690	chr5:120917799-120917800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6886456	chr5:120917823-120917824	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs539068598	chr5:120917842-120917843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181847423	chr5:120917889-120917890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73790936	chr5:120917920-120917921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537665163	chr5:120917948-120917949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577502702	chr5:120917964-120917965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556586592	chr5:120917977-120917978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76691294	chr5:120918031-120918032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542197760	chr5:120918040-120918041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545460832	chr5:120918044-120918045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186909742	chr5:120918047-120918048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11949226	chr5:120918058-120918059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546554546	chr5:120918075-120918076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191804362	chr5:120918076-120918077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374763428	chr5:120918125-120918126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs72791278	chr5:120918130-120918131	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs11949251	chr5:120918141-120918142	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562565959	chr5:120918146-120918147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529783604	chr5:120918157-120918158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181461442	chr5:120918177-120918178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs28517831	chr5:120918192-120918193	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs386691817	chr5:120918243-120918244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547910560	chr5:120918301-120918302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566163318	chr5:120918302-120918303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567566783	chr5:120918308-120918309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186568118	chr5:120918309-120918310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189948297	chr5:120918332-120918333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370489155	chr5:120918334-120918335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570670726	chr5:120918422-120918423	Enhancers	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
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
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:152 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120917400-120920000	Enhancers	Dnd41	blood
2	chr5:120918800-120919200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:120921400-120921800	Enhancers	Fetal Heart	heart
4	chr5:120925000-120926400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr5:120951400-120953800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:120964400-120964800	Enhancers	Dnd41	blood
7	chr5:120964600-120964800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:120964600-120964800	Enhancers	Psoas Muscle	Psoas
9	chr5:120964600-120964800	Active TSS	Skeletal Muscle Female	skeletal muscle
10	chr5:120964600-120965000	Enhancers	Adipose Nuclei	Adipose
11	chr5:120964800-120965000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:120964800-120965000	Enhancers	Right Atrium	heart
13	chr5:120964800-120965000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr5:120964800-120965200	Enhancers	Fetal Heart	heart
15	chr5:120964800-120965400	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr5:120964800-120976000	Weak transcription	Psoas Muscle	Psoas
17	chr5:120965000-120966200	Weak transcription	Adipose Nuclei	Adipose
18	chr5:120965000-120966400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:120965000-120966600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr5:120965400-120966600	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr5:120966000-120966800	Enhancers	Fetal Brain Female	brain
22	chr5:120966400-120966600	Enhancers	Adipose Nuclei	Adipose
23	chr5:120966400-120966800	Enhancers	Fetal Stomach	stomach
24	chr5:120966400-120967400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:120966600-120966800	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr5:120967200-120968000	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr5:120969400-120969600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:120975800-120976000	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr5:120975800-120976200	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr5:120976000-120976800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
31	chr5:120976200-120976400	Enhancers	Psoas Muscle	Psoas
32	chr5:120976200-120976600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr5:120976200-120976600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr5:120985800-120987000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:120986200-120987600	Enhancers	Dnd41	blood
36	chr5:120991800-120992600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:120996000-120996200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:121002000-121003800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr5:121002000-121004400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:121002800-121003000	Enhancers	Primary hematopoietic stem cells	blood
41	chr5:121003200-121004400	Weak transcription	Primary hematopoietic stem cells	blood
42	chr5:121003800-121004200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:121004200-121005000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr5:121004400-121004800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr5:121004400-121005000	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:121004400-121005000	Enhancers	NH-A	brain
47	chr5:121004800-121005200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:121007200-121007600	Enhancers	HepG2	liver
49	chr5:121011200-121011800	Enhancers	Primary hematopoietic stem cells	blood
50	chr5:121011200-121012200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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