Variant report

Variant	nsv596167
Chromosome Location	chr4:171576294-171672038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 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	ATF2	chr4:171618897-171619876	GM12878	blood:	n/a	n/a
2	ATF2	chr4:171627066-171627444	GM12878	blood:	n/a	n/a
3	BACH1	chr4:171593821-171594062	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:171627041-171627394	GM12878	blood:	n/a	chr4:171627258-171627268 chr4:171627257-171627268
5	BATF	chr4:171596707-171597021	GM12878	blood:	n/a	n/a
6	BATF	chr4:171627059-171627478	GM12878	blood:	n/a	chr4:171627258-171627268 chr4:171627257-171627268
7	BCL11A	chr4:171627044-171627417	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:171619473-171619805	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:171627029-171627473	GM12878	blood:	n/a	n/a
10	BCLAF1	chr4:171619376-171619944	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:171618999-171619874	GM12878	blood:	n/a	n/a
12	CBX3	chr4:171611240-171611559	K562	blood:	n/a	n/a
13	CEBPB	chr4:171644369-171644648	HepG2	liver:	n/a	chr4:171644495-171644506
14	CHD1	chr4:171619823-171619956	GM12878	blood:	n/a	n/a
15	CHD1	chr4:171617847-171617905	GM12878	blood:	n/a	n/a
16	CHD1	chr4:171597560-171597686	GM12878	blood:	n/a	n/a
17	CHD1	chr4:171619102-171619464	GM12878	blood:	n/a	n/a
18	CHD2	chr4:171587836-171588437	GM12878	blood:	n/a	n/a
19	CHD2	chr4:171618952-171620211	GM12878	blood:	n/a	n/a
20	CREB1	chr4:171626954-171627523	GM12878	blood:	n/a	n/a
21	CTCF	chr4:171638095-171638349	MCF-7	breast:	n/a	chr4:171638209-171638227
22	CTCF	chr4:171638140-171638290	HRPEpiC	eye:	n/a	chr4:171638209-171638227
23	CTCF	chr4:171638136-171638300	Medullo	brain:	n/a	chr4:171638209-171638227
24	CTCF	chr4:171638060-171638210	GM12874	blood:	n/a	n/a
25	CTCF	chr4:171671780-171671930	HepG2	liver:	n/a	chr4:171671861-171671879
26	CTCF	chr4:171671760-171671910	GM12869	blood:	n/a	chr4:171671861-171671879
27	CTCF	chr4:171608986-171609151	HepG2	liver:	n/a	n/a
28	CTCF	chr4:171671740-171671890	HVMF	connective:	n/a	chr4:171671861-171671879
29	CTCF	chr4:171671780-171671950	MCF-7	breast:	n/a	chr4:171671861-171671879
30	CTCF	chr4:171638120-171638270	AoAF	blood vessel:	n/a	chr4:171638209-171638227
31	CTCF	chr4:171671732-171671977	MCF-7	breast:	n/a	chr4:171671861-171671879
32	CTCF	chr4:171638160-171638310	HCPEpiC	choroid plexus:	n/a	chr4:171638209-171638227
33	CTCF	chr4:171638160-171638310	GM12865	blood:	n/a	chr4:171638209-171638227
34	CTCF	chr4:171638201-171638242	GM13976	blood:	n/a	chr4:171638209-171638227
35	CTCF	chr4:171638100-171638250	MCF-7	breast:	n/a	chr4:171638209-171638227
36	CTCF	chr4:171638100-171638250	GM06990	blood:	n/a	chr4:171638209-171638227
37	CTCF	chr4:171638203-171638271	MCF-7	breast:	n/a	chr4:171638209-171638227
38	CTCF	chr4:171609118-171609145	K562	blood:	n/a	n/a
39	CTCF	chr4:171671740-171671890	A549	lung:	n/a	chr4:171671861-171671879
40	CTCF	chr4:171638120-171638270	GM12874	blood:	n/a	chr4:171638209-171638227
41	CTCF	chr4:171671900-171672050	HCT-116	colon:	n/a	n/a
42	CTCF	chr4:171671829-171671891	GM13977	blood:	n/a	chr4:171671861-171671879
43	CTCF	chr4:171638160-171638310	GM12873	blood:	n/a	chr4:171638209-171638227
44	CTCF	chr4:171609020-171609170	HepG2	liver:	n/a	n/a
45	CTCF	chr4:171638000-171638150	GM12873	blood:	n/a	n/a
46	CTCF	chr4:171577220-171577370	GM12872	blood:	n/a	n/a
47	CTCF	chr4:171634502-171634539	GM20000	blood:	n/a	n/a
48	CTCF	chr4:171671800-171671918	HepG2	liver:	n/a	chr4:171671861-171671879
49	CTCF	chr4:171671793-171671951	NHEK	skin:	n/a	chr4:171671861-171671879
50	CTCF	chr4:171638027-171638326	SK-N-SH_RA	brain:	n/a	chr4:171638209-171638227

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:171663610-171663660	ECC-1	luminal epithelium:	n/a
2	chr4:171663610-171663660	HEK293	kidney:	embryo
3	chr4:171663610-171663660	NH-A	brain:	n/a
4	chr4:171604188-171604238	MCF-7	breast:	n/a
5	chr4:171663610-171663660	GM12878	blood:	n/a
6	chr4:171663610-171663660	HCPEpiC	choroid plexus:	n/a
7	chr4:171604188-171604238	H1-hESC	embryonic stem cell:	embryo
8	chr4:171663610-171663660	H1-hESC	embryonic stem cell:	embryo
9	chr4:171663610-171663660	A549	lung:	n/a
10	chr4:171663610-171663660	RPTEC	kidney:	n/a
11	chr4:171663610-171663660	NHBE	bronchial:	n/a
12	chr4:171663610-171663660	U87	brain:	n/a
13	chr4:171604188-171604238	HMEC	breast:	n/a
14	chr4:171604188-171604238	NHBE	bronchial:	n/a
15	chr4:171663610-171663660	SK-N-MC	brain:	n/a
16	chr4:171604188-171604238	AG09319	gingival:	n/a
17	chr4:171604188-171604238	RPTEC	kidney:	n/a
18	chr4:171604188-171604238	GM19239	blood:	n/a
19	chr4:171663610-171663660	BJ	skin:	n/a
20	chr4:171663610-171663660	HCF	heart:	n/a
21	chr4:171663610-171663660	Jurkat	blood:	n/a
22	chr4:171663610-171663660	SK-N-SH_RA	brain:	n/a
23	chr4:171604188-171604238	NB4	blood:	n/a
24	chr4:171663610-171663660	AG04449	skin:	fetal
25	chr4:171604188-171604238	SKMC	muscle:	n/a
26	chr4:171604188-171604238	ECC-1	luminal epithelium:	n/a
27	chr4:171604188-171604238	GM12891	blood:	n/a
28	chr4:171604188-171604238	U87	brain:	n/a
29	chr4:171663610-171663660	GM12892	blood:	n/a
30	chr4:171604188-171604238	LNCaP	prostate:	n/a
31	chr4:171663610-171663660	AG04450	lung:	fetal
32	chr4:171604188-171604238	BE2_C	brain:	n/a
33	chr4:171604188-171604238	HNPCEpiC	eye:	n/a
34	chr4:171604188-171604238	HCF	heart:	n/a
35	chr4:171663610-171663660	HAEpiC	amniotic membrane:	n/a
36	chr4:171604188-171604238	AG04449	skin:	fetal
37	chr4:171604188-171604238	AG10803	skin:	n/a
38	chr4:171604188-171604238	AG09309	skin:	n/a
39	chr4:171663610-171663660	HepG2	liver:	n/a
40	chr4:171663610-171663660	GM19239	blood:	n/a
41	chr4:171663610-171663660	NB4	blood:	n/a
42	chr4:171604188-171604238	AG04450	lung:	fetal
43	chr4:171663610-171663660	HRCEpiC	kidney:	n/a
44	chr4:171663610-171663660	K562	blood:	n/a
45	chr4:171663610-171663660	AG10803	skin:	n/a
46	chr4:171663610-171663660	HEEpiC	esophagus:	n/a
47	chr4:171604188-171604238	SK-N-MC	brain:	n/a
48	chr4:171663610-171663660	HCM	heart:	n/a
49	chr4:171663610-171663660	T-47D	breast:	n/a
50	chr4:171604188-171604238	PANC-1	pancreas:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:171510484..171511294-chr4:171637729..171638500,2	MCF-7	breast:
2	chr4:171515518..171516388-chr4:171637945..171638514,2	MCF-7	breast:
3	chr4:171510470..171511103-chr4:171637783..171638586,3	MCF-7	breast:
4	chr4:171577282..171579007-chr4:171581596..171583717,2	K562	blood:
5	chr4:171577282..171579007-chr4:171581596..171583717,2	K562	blood:
6	chr4:171616881..171619381-chr4:171620954..171623355,2	K562	blood:
7	chr4:171671477..171672293-chr4:171774330..171775293,5	MCF-7	breast:
8	chr4:171616881..171619381-chr4:171620954..171623355,2	K562	blood:
9	chr11:104200333..104200963-chr4:171635355..171636168,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AADAT-3	chr4:171663746-171664179	NONHSAT099189
2	lnc-AADAT-3	chr4:171664816-171664886	NONHSAT099189
3	lnc-AADAT-3	chr4:171663620-171664179	XLOC_004157
4	lnc-AADAT-3	chr4:171663302-171663311	NONHSAT099189
5	lnc-AADAT-3	chr4:171664816-171664869	XLOC_004157

No data

Variant related genes	Relation type
ENSG00000250968	TF binding region
ENSG00000250968	CpG island
KHSRP	miRNA target sites
KEAP1	miRNA target sites

Extended variants
information (count: 2239 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2239 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1596248	chr4:171576294-171576295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146368345	chr4:171576299-171576300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200055332	chr4:171576347-171576348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs74736833	chr4:171576389-171576390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80187844	chr4:171576412-171576413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139654763	chr4:171576448-171576449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs111728236	chr4:171576494-171576495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569772656	chr4:171576499-171576500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537096045	chr4:171576505-171576506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555649963	chr4:171576507-171576508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1442904	chr4:171576508-171576509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs10016268	chr4:171576521-171576522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs1442903	chr4:171576578-171576579	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs181392631	chr4:171576634-171576635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146088427	chr4:171576638-171576639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186765512	chr4:171576647-171576648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs67304008	chr4:171576648-171576649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192073036	chr4:171576650-171576651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2030542	chr4:171576695-171576696	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs564091459	chr4:171576701-171576702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs6553535	chr4:171589600-171589601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141308865	chr4:171589625-171589626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533708011	chr4:171589630-171589631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28780788	chr4:171589643-171589644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs28831112	chr4:171589647-171589648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112358011	chr4:171589653-171589654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528016005	chr4:171589684-171589685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527337461	chr4:171589748-171589749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150773515	chr4:171589757-171589758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568684914	chr4:171589758-171589759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370848015	chr4:171589807-171589808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139254975	chr4:171589808-171589809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115025132	chr4:171589836-171589837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548076600	chr4:171589882-171589883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539993810	chr4:171589922-171589923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35922126	chr4:171589929-171589930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573368052	chr4:171589959-171589960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540304950	chr4:171589987-171589988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144069195	chr4:171589997-171589998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145965924	chr4:171590025-171590026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372837823	chr4:171590125-171590126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373315259	chr4:171590133-171590134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182366767	chr4:171590169-171590170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113165114	chr4:171590192-171590193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533004930	chr4:171590250-171590251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544792635	chr4:171590251-171590252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9997272	chr4:171590316-171590317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs139830583	chr4:171590338-171590339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149672592	chr4:171590365-171590366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34704211	chr4:171590389-171590390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Developmental delay	22127048	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:171575400-171576600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:171576600-171576800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr4:171589600-171590000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr4:171590000-171593000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr4:171591000-171591200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr4:171591600-171595200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:171592200-171593200	Enhancers	GM12878-XiMat	blood
8	chr4:171592800-171596800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:171593000-171593600	Enhancers	Fetal Intestine Large	intestine
10	chr4:171593000-171593800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr4:171593000-171594000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:171593000-171594000	Enhancers	Osteobl	bone
13	chr4:171593000-171595000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:171593000-171596400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr4:171593400-171594000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:171593400-171594400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:171593400-171594400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr4:171593400-171597200	Enhancers	HMEC	breast
19	chr4:171593400-171597200	Enhancers	NH-A	brain
20	chr4:171593600-171594000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:171593600-171594000	Enhancers	NHEK	skin
22	chr4:171593600-171594400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr4:171593600-171594600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:171593600-171594600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr4:171593800-171594000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:171593800-171594600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:171593800-171594600	Enhancers	Hela-S3	cervix
28	chr4:171593800-171602200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:171594000-171594400	Weak transcription	Osteobl	bone
30	chr4:171594000-171601400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:171594400-171594600	Enhancers	Osteobl	bone
32	chr4:171594400-171596000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr4:171594600-171595800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr4:171594600-171595800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:171594600-171596400	Weak transcription	Osteobl	bone
36	chr4:171594600-171596600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr4:171595000-171595400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:171595200-171595800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:171595400-171595600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr4:171595400-171596800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:171595600-171596400	Enhancers	Primary hematopoietic stem cells	blood
42	chr4:171595800-171596000	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr4:171595800-171596400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr4:171595800-171596600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:171596000-171596400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr4:171596000-171596600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:171596400-171596800	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr4:171596400-171597000	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:171596400-171597200	Enhancers	Osteobl	bone
50	chr4:171596400-171597400	Enhancers	GM12878-XiMat	blood

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