Variant report

Variant	nsv878683
Chromosome Location	chr4:9844621-9911843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:538)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
2	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
3	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
7	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
8	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
9	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
10	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
11	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
12	CEBPB	chr4:9900230-9900797	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:9849998-9850279	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
14	CEBPB	chr4:9849980-9850299	H1-hESC	embryonic stem cell:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
15	CEBPB	chr4:9876089-9876404	IMR90	lung:	n/a	chr4:9876241-9876252
16	CEBPB	chr4:9895305-9895547	K562	blood:	n/a	n/a
17	CEBPB	chr4:9849942-9850300	IMR90	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
18	CEBPB	chr4:9849994-9850220	MCF-7	breast:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
19	CEBPB	chr4:9895337-9895676	K562	blood:	n/a	n/a
20	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
21	CEBPB	chr4:9849949-9850302	HepG2	liver:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
22	CEBPB	chr4:9900393-9900739	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:9876209-9876280	K562	blood:	n/a	chr4:9876241-9876252
24	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
25	CEBPB	chr4:9888675-9888963	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
27	CEBPB	chr4:9900383-9900669	K562	blood:	n/a	n/a
28	CEBPB	chr4:9900375-9900657	K562	blood:	n/a	n/a
29	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
30	CEBPB	chr4:9876127-9876348	HepG2	liver:	n/a	chr4:9876241-9876252
31	CEBPB	chr4:9849869-9850308	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
32	CEBPB	chr4:9849953-9850289	Hela-S3	cervix:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
33	CEBPB	chr4:9867161-9867312	HepG2	liver:	n/a	chr4:9867238-9867249
34	CEBPD	chr4:9895204-9895804	K562	blood:	n/a	chr4:9895425-9895436
35	CEBPD	chr4:9895295-9895750	K562	blood:	n/a	chr4:9895425-9895436
36	CEBPZ	chr4:9901305-9901320	HepG2	liver:	n/a	n/a
37	CHD2	chr4:9850691-9850877	GM12878	blood:	n/a	n/a
38	CHD2	chr4:9851191-9851526	GM12878	blood:	n/a	n/a
39	CHD2	chr4:9900292-9900700	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:9900344-9900605	Medullo	brain:	n/a	n/a
41	CTCF	chr4:9900340-9900490	GM12875	blood:	n/a	n/a
42	CTCF	chr4:9900343-9900599	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:9900340-9900490	GM12874	blood:	n/a	n/a
44	CTCF	chr4:9878840-9878990	GM06990	blood:	n/a	n/a
45	CTCF	chr4:9900380-9900530	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr4:9900328-9900583	Fibrobl	skin:	n/a	n/a
47	CTCF	chr4:9900400-9900550	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:9878840-9878990	HepG2	liver:	n/a	n/a
49	CTCF	chr4:9900300-9900450	GM12869	blood:	n/a	n/a
50	CTCF	chr4:9900365-9900566	Kidney_OC	kidney:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9884128-9884178	NHBE	bronchial:	n/a
2	chr4:9884128-9884178	PANC-1	pancreas:	n/a
3	chr4:9884128-9884178	HepG2	liver:	n/a
4	chr4:9892887-9892937	HepG2	liver:	n/a
5	chr4:9892887-9892937	HMEC	breast:	n/a
6	chr4:9884128-9884178	BJ	skin:	n/a
7	chr4:9892887-9892937	HIPEpiC	eye:	n/a
8	chr4:9884128-9884178	AG09319	gingival:	n/a
9	chr4:9884128-9884178	HMEC	breast:	n/a
10	chr4:9884128-9884178	Hepatocyte	liver:	n/a
11	chr4:9884128-9884178	NH-A	brain:	n/a
12	chr4:9892887-9892937	AG10803	skin:	n/a
13	chr4:9892887-9892937	MCF10A-Er-Src	breast:	n/a
14	chr4:9892887-9892937	CMK	blood:	n/a
15	chr4:9884128-9884178	SAEC	small airway:	n/a
16	chr4:9884128-9884178	SKMC	muscle:	n/a
17	chr4:9892887-9892937	NB4	blood:	n/a
18	chr4:9884128-9884178	GM12892	blood:	n/a
19	chr4:9892887-9892937	PFSK-1	brain:	n/a
20	chr4:9884128-9884178	CMK	blood:	n/a
21	chr4:9884128-9884178	HRE	kidney:	n/a
22	chr4:9884128-9884178	LNCaP	prostate:	n/a
23	chr4:9892887-9892937	SAEC	small airway:	n/a
24	chr4:9884128-9884178	HCPEpiC	choroid plexus:	n/a
25	chr4:9884128-9884178	AG04450	lung:	fetal
26	chr4:9892887-9892937	GM19239	blood:	n/a
27	chr4:9884128-9884178	K562	blood:	n/a
28	chr4:9892887-9892937	HRE	kidney:	n/a
29	chr4:9884128-9884178	HEK293	kidney:	embryo
30	chr4:9892887-9892937	SK-N-MC	brain:	n/a
31	chr4:9892887-9892937	ECC-1	luminal epithelium:	n/a
32	chr4:9884128-9884178	NB4	blood:	n/a
33	chr4:9884128-9884178	HEEpiC	esophagus:	n/a
34	chr4:9892887-9892937	HCM	heart:	n/a
35	chr4:9884128-9884178	IMR90	lung:	fetal
36	chr4:9892887-9892937	MCF-7	breast:	n/a
37	chr4:9884128-9884178	Hela-S3	cervix:	n/a
38	chr4:9892887-9892937	Hepatocyte	liver:	n/a
39	chr4:9892887-9892937	NHBE	bronchial:	n/a
40	chr4:9884128-9884178	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:9884128-9884178	NT2-D1	testis:	n/a
42	chr4:9884128-9884178	RPTEC	kidney:	n/a
43	chr4:9892887-9892937	AG09319	gingival:	n/a
44	chr4:9892887-9892937	A549	lung:	n/a
45	chr4:9892887-9892937	Jurkat	blood:	n/a
46	chr4:9892887-9892937	GM12892	blood:	n/a
47	chr4:9884128-9884178	HCM	heart:	n/a
48	chr4:9884128-9884178	H1-hESC	embryonic stem cell:	embryo
49	chr4:9892887-9892937	HUVEC	blood vessel:	n/a
50	chr4:9892887-9892937	SK-N-SH	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
2	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
3	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
4	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
5	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
6	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
7	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
8	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
9	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
10	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
2	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146

No data

Variant related genes	Relation type
SLC2A9	TF binding region
SLC2A9	CpG island
ENSG00000109667	chromatin interactions

Extended variants
information (count: 3019 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3019 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6449050	chr4:9844621-9844622	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs115090236	chr4:9844647-9844648	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs186429004	chr4:9844648-9844649	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs6449051	chr4:9844711-9844712	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs114316846	chr4:9844714-9844715	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs6449052	chr4:9844732-9844733	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs189365277	chr4:9844760-9844761	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs78785836	chr4:9844767-9844768	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs372129839	chr4:9844772-9844773	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs532071395	chr4:9844822-9844823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs180864691	chr4:9844824-9844825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs143731237	chr4:9844843-9844844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375492818	chr4:9845039-9845040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60065895	chr4:9845065-9845066	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs386671548	chr4:9845079-9845080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11938161	chr4:9845080-9845081	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79150862	chr4:9845094-9845095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536996657	chr4:9845117-9845118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551906289	chr4:9845164-9845165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549125772	chr4:9845173-9845174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186472223	chr4:9845178-9845179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538724140	chr4:9845206-9845207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554262348	chr4:9845218-9845219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190857425	chr4:9845231-9845232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569723749	chr4:9845252-9845253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577508014	chr4:9845264-9845265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs560805385	chr4:9845265-9845266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536631664	chr4:9845299-9845300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537268348	chr4:9845334-9845335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183098281	chr4:9845343-9845344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116551294	chr4:9845390-9845391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565445633	chr4:9845417-9845418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577393168	chr4:9845434-9845435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541293740	chr4:9845488-9845489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369138285	chr4:9845558-9845559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529791602	chr4:9845596-9845597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs16889496	chr4:9845597-9845598	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs141664687	chr4:9845669-9845670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560070393	chr4:9845696-9845697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530674713	chr4:9845750-9845751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552067952	chr4:9845770-9845771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146298159	chr4:9845774-9845775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78847128	chr4:9845776-9845777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376976572	chr4:9845780-9845781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146263615	chr4:9845783-9845784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566549469	chr4:9845784-9845785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150659411	chr4:9845787-9845788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13141248	chr4:9845790-9845791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566152319	chr4:9845874-9845875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549679953	chr4:9845896-9845897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Neuroblastoma	20406844	CNVD
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Breast cancer	17142309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9838400-9844800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:9842400-9844800	ZNF genes & repeats	HepG2	liver
3	chr4:9843200-9847800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:9843400-9844800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:9843600-9847800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:9844400-9847600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr4:9844600-9847600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr4:9844800-9845000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:9844800-9850600	Weak transcription	HepG2	liver
10	chr4:9844800-9851000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:9845000-9851600	Weak transcription	Fetal Intestine Small	intestine
12	chr4:9845000-9874800	Weak transcription	NHEK	skin
13	chr4:9847600-9848200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
14	chr4:9847600-9848200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
15	chr4:9847800-9848200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:9847800-9848200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:9848200-9848600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:9848200-9849200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:9848200-9849200	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr4:9848200-9850600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr4:9848400-9849400	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr4:9848600-9848800	Enhancers	Fetal Kidney	kidney
23	chr4:9848600-9853200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:9848600-9861800	Weak transcription	HMEC	breast
25	chr4:9848800-9850200	Weak transcription	Fetal Kidney	kidney
26	chr4:9849200-9849800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:9849200-9852400	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr4:9849400-9850200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr4:9849800-9850600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:9850200-9851600	Enhancers	Fetal Kidney	kidney
31	chr4:9850200-9858800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr4:9850600-9851200	Enhancers	GM12878-XiMat	blood
33	chr4:9850600-9851400	Strong transcription	HepG2	liver
34	chr4:9850600-9852200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:9850600-9853000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr4:9850800-9851000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr4:9851000-9851600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:9851200-9869800	Weak transcription	Gastric	stomach
39	chr4:9851400-9859000	Weak transcription	HepG2	liver
40	chr4:9851600-9852400	Strong transcription	Fetal Intestine Small	intestine
41	chr4:9851600-9852800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:9851600-9857200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:9852200-9858200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:9852400-9852800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr4:9852400-9852800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:9852400-9858400	Weak transcription	Monocytes-CD14+_RO01746	blood
47	chr4:9852400-9858800	Weak transcription	Fetal Intestine Small	intestine
48	chr4:9852600-9852800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:9852600-9853000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:9852800-9853200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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