Variant report

Variant	nsv878663
Chromosome Location	chr4:9451923-9558344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
4	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
5	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
6	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
7	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
8	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
9	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
11	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
13	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
14	CEBPB	chr4:9530676-9530843	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
16	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a
17	CEBPB	chr4:9530595-9530856	K562	blood:	n/a	n/a
18	CEBPB	chr4:9531399-9531602	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr4:9533998-9534198	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:9533893-9534015	HepG2	liver:	n/a	chr4:9533994-9534004
21	CHD2	chr4:9533949-9534111	H1-hESC	embryonic stem cell:	n/a	chr4:9533994-9534004
22	CTCF	chr4:9497188-9497374	GM13976	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
23	CTCF	chr4:9533795-9533953	Hela-S3	cervix:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
24	CTCF	chr4:9497175-9497440	A549	lung:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
25	CTCF	chr4:9497180-9497330	HFF-Myc	foreskin:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
26	CTCF	chr4:9501258-9501278	MCF-7	breast:	n/a	n/a
27	CTCF	chr4:9533780-9533930	RPTEC	kidney:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
28	CTCF	chr4:9533820-9533970	Hela-S3	cervix:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
29	CTCF	chr4:9533718-9534042	Kidney_OC	kidney:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
30	CTCF	chr4:9533787-9533960	HepG2	liver:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
31	CTCF	chr4:9534280-9534430	GM12865	blood:	n/a	n/a
32	CTCF	chr4:9533800-9533950	HVMF	connective:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
33	CTCF	chr4:9456801-9457127	A549	lung:	n/a	n/a
34	CTCF	chr4:9533780-9533930	MCF-7	breast:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
35	CTCF	chr4:9533780-9533930	GM12871	blood:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
36	CTCF	chr4:9533017-9533143	GM20000	blood:	n/a	n/a
37	CTCF	chr4:9481074-9481548	K562	blood:	n/a	n/a
38	CTCF	chr4:9481140-9481290	GM06990	blood:	n/a	n/a
39	CTCF	chr4:9533800-9533950	GM12873	blood:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
40	CTCF	chr4:9533708-9534008	GM13976	blood:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
41	CTCF	chr4:9497220-9497370	MCF-7	breast:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
42	CTCF	chr4:9481135-9481451	A549	lung:	n/a	n/a
43	CTCF	chr4:9533763-9534043	A549	lung:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
44	CTCF	chr4:9497176-9497416	Fibrobl	skin:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
45	CTCF	chr4:9497200-9497350	GM12872	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
46	CTCF	chr4:9533780-9533930	HCT-116	colon:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
47	CTCF	chr4:9533733-9534000	H1-hESC	embryonic stem cell:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
48	CTCF	chr4:9533753-9533996	K562	blood:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
49	CTCF	chr4:9533820-9533970	BE2_C	brain:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
50	CTCF	chr4:9497200-9497350	HEK293	kidney:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9537404-9537454	NT2-D1	testis:	n/a
2	chr4:9499367-9499417	NHDF-neo	bronchial:	n/a
3	chr4:9508240-9508290	NH-A	brain:	n/a
4	chr4:9476719-9476769	T-47D	breast:	n/a
5	chr4:9557805-9557855	MCF-7	breast:	n/a
6	chr4:9507499-9507549	BJ	skin:	n/a
7	chr4:9479622-9479672	HCPEpiC	choroid plexus:	n/a
8	chr4:9506681-9506731	HCF	heart:	n/a
9	chr4:9537404-9537454	NT2-D1	testis:	n/a
10	chr4:9499367-9499417	NHDF-neo	bronchial:	n/a
11	chr4:9508240-9508290	NH-A	brain:	n/a
12	chr4:9476719-9476769	T-47D	breast:	n/a
13	chr4:9557805-9557855	MCF-7	breast:	n/a
14	chr4:9507499-9507549	BJ	skin:	n/a
15	chr4:9479622-9479672	HCPEpiC	choroid plexus:	n/a
16	chr4:9506681-9506731	HCF	heart:	n/a
17	chr4:9484955-9485005	AoSMC	blood vessel:	n/a
18	chr4:9510572-9510622	RPTEC	kidney:	n/a
19	chr4:9499194-9499244	AG04449	skin:	fetal
20	chr4:9508240-9508290	BJ	skin:	n/a
21	chr4:9537404-9537454	IMR90	lung:	fetal
22	chr4:9493114-9493164	HUVEC	blood vessel:	n/a
23	chr4:9506681-9506731	U87	brain:	n/a
24	chr4:9478126-9478176	MCF10A-Er-Src	breast:	n/a
25	chr4:9457681-9457731	PFSK-1	brain:	n/a
26	chr4:9534062-9534112	MCF10A-Er-Src	breast:	n/a
27	chr4:9523653-9523703	HEK293	kidney:	embryo
28	chr4:9500293-9500343	A549	lung:	n/a
29	chr4:9493114-9493164	AG09309	skin:	n/a
30	chr4:9534041-9534091	BE2_C	brain:	n/a
31	chr4:9475346-9475396	ProgFib	skin:	n/a
32	chr4:9509896-9509946	Hepatocyte	liver:	n/a
33	chr4:9475346-9475396	HCPEpiC	choroid plexus:	n/a
34	chr4:9499194-9499244	ECC-1	luminal epithelium:	n/a
35	chr4:9523653-9523703	BE2_C	brain:	n/a
36	chr4:9479622-9479672	ProgFib	skin:	n/a
37	chr4:9482233-9482283	MCF-7	breast:	n/a
38	chr4:9508976-9509026	A549	lung:	n/a
39	chr4:9508177-9508227	U87	brain:	n/a
40	chr4:9505191-9505241	PrEC	prostate:	n/a
41	chr4:9500293-9500343	HCF	heart:	n/a
42	chr4:9558077-9558127	HCM	heart:	n/a
43	chr4:9510286-9510336	HUVEC	blood vessel:	n/a
44	chr4:9505191-9505241	HNPCEpiC	eye:	n/a
45	chr4:9499194-9499244	PrEC	prostate:	n/a
46	chr4:9509830-9509880	ECC-1	luminal epithelium:	n/a
47	chr4:9503404-9503454	RPTEC	kidney:	n/a
48	chr4:9500174-9500224	Hepatocyte	liver:	n/a
49	chr4:9500293-9500343	PANC-1	pancreas:	n/a
50	chr4:9510572-9510622	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
2	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
3	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
2	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

Variant related genes	Relation type
OR7E85P	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
MIR548I2	TF binding region
ENSG00000249443	TF binding region
OR7E83P	TF binding region
ENSG00000266246	TF binding region
UNC93B7	TF binding region
ENSG00000242034	TF binding region
OR7E85P	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
MIR548I2	CpG island
ENSG00000249443	CpG island
OR7E83P	CpG island
ENSG00000266246	CpG island
UNC93B7	CpG island
ENSG00000242034	CpG island

Extended variants
information (count: 5488 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5488 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537410607	chr4:9452609-9452610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6844838	chr4:9452616-9452617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs374375700	chr4:9452633-9452634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569142784	chr4:9452636-9452637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368860322	chr4:9452654-9452655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539847520	chr4:9452659-9452660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557751217	chr4:9452677-9452678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114632096	chr4:9452703-9452704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534036878	chr4:9452714-9452715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555491475	chr4:9452715-9452716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574219430	chr4:9452717-9452718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544566260	chr4:9452724-9452725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556848457	chr4:9452725-9452726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6849780	chr4:9452734-9452735	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs544765009	chr4:9452743-9452744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79170033	chr4:9452749-9452750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185095772	chr4:9452758-9452759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574808314	chr4:9452779-9452780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527336851	chr4:9452797-9452798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541396307	chr4:9452808-9452809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111302495	chr4:9452810-9452811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189219906	chr4:9452822-9452823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545922485	chr4:9452829-9452830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181620289	chr4:9452832-9452833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549786881	chr4:9452849-9452850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140452798	chr4:9452876-9452877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377498261	chr4:9452887-9452888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553539978	chr4:9452890-9452891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10011737	chr4:9452894-9452895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs6856153	chr4:9452898-9452899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs183977421	chr4:9452900-9452901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540306373	chr4:9452909-9452910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566531219	chr4:9452917-9452918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534023370	chr4:9452928-9452929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188756038	chr4:9452930-9452931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567741021	chr4:9452934-9452935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6850194	chr4:9452936-9452937	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs111879603	chr4:9452953-9452954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529303827	chr4:9452959-9452960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186217911	chr4:9452973-9452974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11935532	chr4:9452974-9452975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544233867	chr4:9452978-9452979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561932784	chr4:9452979-9452980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553799455	chr4:9452982-9452983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572114999	chr4:9452993-9452994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542731062	chr4:9453000-9453001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561067952	chr4:9453010-9453011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191891649	chr4:9453025-9453026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543567502	chr4:9453030-9453031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10011866	chr4:9453032-9453033	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9452600-9453800	Enhancers	Small Intestine	intestine
2	chr4:9453000-9453800	Enhancers	Duodenum Mucosa	Duodenum
3	chr4:9453600-9454800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr4:9453600-9456200	Enhancers	Fetal Intestine Large	intestine
5	chr4:9453600-9456800	Enhancers	Fetal Intestine Small	intestine
6	chr4:9453600-9457200	Enhancers	Stomach Mucosa	stomach
7	chr4:9453800-9454600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:9454600-9454800	Enhancers	Duodenum Mucosa	Duodenum
9	chr4:9454800-9455200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr4:9454800-9455800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:9455200-9457200	Enhancers	Duodenum Mucosa	Duodenum
12	chr4:9455800-9456800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:9455800-9457200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr4:9456400-9456800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:9456400-9457200	Enhancers	Gastric	stomach
16	chr4:9476200-9477000	Bivalent Enhancer	Fetal Brain Male	brain
17	chr4:9476600-9477000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
18	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr4:9477000-9477400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
24	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
25	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
26	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:9496200-9496800	Enhancers	Thymus	Thymus
28	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr4:9499000-9499600	Enhancers	Liver	Liver
36	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
39	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
42	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
43	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
44	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell
47	chr4:9499200-9500600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr4:9499200-9500600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr4:9499200-9500600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr4:9499200-9500600	Active TSS	Breast Myoepithelial Primary Cells	Breast

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