Variant report

Variant	nsv878676
Chromosome Location	chr4:9797703-9978094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1363)
CpG islands
(count:489)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9952887-9953127	K562	blood:	n/a	n/a
2	ARID3A	chr4:9965207-9965232	HepG2	liver:	n/a	n/a
3	ATF1	chr4:9850013-9850273	K562	blood:	n/a	n/a
4	ATF1	chr4:9929162-9929613	K562	blood:	n/a	n/a
5	ATF1	chr4:9927280-9927595	K562	blood:	n/a	n/a
6	ATF2	chr4:9814641-9815054	GM12878	blood:	n/a	n/a
7	ATF2	chr4:9972118-9972587	GM12878	blood:	n/a	n/a
8	ATF2	chr4:9809744-9810072	GM12878	blood:	n/a	n/a
9	ATF3	chr4:9849946-9850297	K562	blood:	n/a	n/a
10	BACH1	chr4:9806067-9806321	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:9885168-9885286	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:9813621-9813815	GM12878	blood:	n/a	n/a
13	BATF	chr4:9814742-9814999	GM12878	blood:	n/a	n/a
14	BATF	chr4:9814682-9815071	GM12878	blood:	n/a	n/a
15	BATF	chr4:9972302-9972703	GM12878	blood:	n/a	n/a
16	BATF	chr4:9809777-9810086	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:9851100-9851523	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9851148-9851550	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:9809742-9810117	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:9809752-9810069	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:9972269-9972776	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:9814677-9815008	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:9972312-9972693	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:9814557-9814998	GM12878	blood:	n/a	n/a
25	BCL3	chr4:9826836-9827129	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:9972208-9972590	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:9964308-9964572	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:9872224-9872359	K562	blood:	n/a	n/a
29	BHLHE40	chr4:9802635-9802910	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:9814583-9815072	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:9937928-9938023	K562	blood:	n/a	n/a
32	BHLHE40	chr4:9809308-9809346	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:9809778-9810107	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:9962047-9962396	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:9851061-9851588	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:9882590-9882646	K562	blood:	n/a	n/a
37	BHLHE40	chr4:9972158-9972605	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:9920641-9920828	K562	blood:	n/a	n/a
39	BHLHE40	chr4:9867363-9867483	K562	blood:	n/a	n/a
40	BRCA1	chr4:9871086-9871272	GM12878	blood:	n/a	n/a
41	BRCA1	chr4:9829608-9829617	H1-hESC	embryonic stem cell:	n/a	n/a
42	CCNT2	chr4:9895028-9895704	K562	blood:	n/a	n/a
43	CCNT2	chr4:9937760-9938130	K562	blood:	n/a	n/a
44	CEBPB	chr4:9954023-9954436	MCF-7	breast:	n/a	chr4:9954213-9954224
45	CEBPB	chr4:9849993-9850301	A549	lung:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
46	CEBPB	chr4:9849913-9850318	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
47	CEBPB	chr4:9849824-9850326	HCT-116	colon:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
48	CEBPB	chr4:9954135-9954305	HepG2	liver:	n/a	chr4:9954213-9954224
49	CEBPB	chr4:9849900-9850296	K562	blood:	n/a	chr4:9850045-9850056 chr4:9850120-9850131
50	CEBPB	chr4:9954045-9954390	K562	blood:	n/a	chr4:9954213-9954224

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9940566-9940616	HIPEpiC	eye:	n/a
2	chr4:9940566-9940616	HIPEpiC	eye:	n/a
3	chr4:9940566-9940616	GM19239	blood:	n/a
4	chr4:9917839-9917889	SKMC	muscle:	n/a
5	chr4:9917839-9917889	SK-N-SH	brain:	n/a
6	chr4:9892887-9892937	PANC-1	pancreas:	n/a
7	chr4:9950643-9950693	RPTEC	kidney:	n/a
8	chr4:9937674-9937724	K562	blood:	n/a
9	chr4:9884128-9884178	SK-N-SH	brain:	n/a
10	chr4:9917839-9917889	ovcar-3	ovarian:	n/a
11	chr4:9926439-9926489	HCM	heart:	n/a
12	chr4:9926439-9926489	HMEC	breast:	n/a
13	chr4:9926439-9926489	LNCaP	prostate:	n/a
14	chr4:9926439-9926489	BE2_C	brain:	n/a
15	chr4:9884128-9884178	HL-60	blood:	n/a
16	chr4:9940566-9940616	NT2-D1	testis:	n/a
17	chr4:9940566-9940616	HRCEpiC	kidney:	n/a
18	chr4:9922462-9922512	SK-N-MC	brain:	n/a
19	chr4:9892887-9892937	H1-hESC	embryonic stem cell:	embryo
20	chr4:9917839-9917889	GM12892	blood:	n/a
21	chr4:9892887-9892937	HRPEpiC	eye:	n/a
22	chr4:9892887-9892937	BE2_C	brain:	n/a
23	chr4:9884128-9884178	U87	brain:	n/a
24	chr4:9922462-9922512	GM19239	blood:	n/a
25	chr4:9950643-9950693	HCPEpiC	choroid plexus:	n/a
26	chr4:9917839-9917889	HMEC	breast:	n/a
27	chr4:9937674-9937724	MCF10A-Er-Src	breast:	n/a
28	chr4:9926439-9926489	Hela-S3	cervix:	n/a
29	chr4:9926439-9926489	ProgFib	skin:	n/a
30	chr4:9940566-9940616	ovcar-3	ovarian:	n/a
31	chr4:9922462-9922512	GM12878	blood:	n/a
32	chr4:9926439-9926489	A549	lung:	n/a
33	chr4:9940566-9940616	HRE	kidney:	n/a
34	chr4:9937674-9937724	ECC-1	luminal epithelium:	n/a
35	chr4:9926439-9926489	HEK293	kidney:	embryo
36	chr4:9926439-9926489	CMK	blood:	n/a
37	chr4:9926439-9926489	HRCEpiC	kidney:	n/a
38	chr4:9884128-9884178	HEK293	kidney:	embryo
39	chr4:9892887-9892937	NB4	blood:	n/a
40	chr4:9937674-9937724	HepG2	liver:	n/a
41	chr4:9940566-9940616	AG04449	skin:	fetal
42	chr4:9926439-9926489	AoSMC	blood vessel:	n/a
43	chr4:9922462-9922512	PFSK-1	brain:	n/a
44	chr4:9922462-9922512	BE2_C	brain:	n/a
45	chr4:9937674-9937724	HAEpiC	amniotic membrane:	n/a
46	chr4:9940566-9940616	HNPCEpiC	eye:	n/a
47	chr4:9884128-9884178	PrEC	prostate:	n/a
48	chr4:9926439-9926489	AG09319	gingival:	n/a
49	chr4:9950643-9950693	SAEC	small airway:	n/a
50	chr4:9926439-9926489	HAEpiC	amniotic membrane:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9766848..9767385-chr4:9900038..9900893,4	MCF-7	breast:
2	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
3	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
4	chr4:9766226..9767390-chr4:9899951..9901032,8	MCF-7	breast:
5	chr4:9918331..9921142-chr4:10116868..10118418,2	MCF-7	breast:
6	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
7	chr4:9957351..9959521-chr4:10008550..10011275,2	MCF-7	breast:
8	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
9	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
10	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
11	chr4:9898528..9900449-chr4:10019179..10021130,2	MCF-7	breast:
12	chr4:9827283..9829135-chr4:9829200..9831465,2	K562	blood:
13	chr4:9929005..9929948-chr4:10015148..10015863,2	MCF-7	breast:
14	chr4:9841356..9843538-chr4:9847251..9848935,2	K562	blood:
15	chr4:9931197..9931753-chr4:10016553..10017073,2	MCF-7	breast:
16	chr4:9920609..9921128-chr4:10020066..10020974,2	K562	blood:
17	chr4:9869830..9872812-chr4:9880250..9882960,2	K562	blood:
18	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
19	chr4:9959731..9961810-chr4:9971031..9973164,2	K562	blood:
20	chr4:9931454..9932279-chr4:10015120..10015668,2	MCF-7	breast:
21	chr4:9924672..9926796-chr4:10008145..10009788,2	MCF-7	breast:
22	chr4:9920436..9923282-chr4:9925910..9928355,2	MCF-7	breast:
23	chr4:9865151..9867306-chr4:9868074..9870913,3	MCF-7	breast:
24	chr4:9903730..9906582-chr4:9912941..9915065,2	MCF-7	breast:
25	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-13	chr4:9810799-9811038	NONHSAT095145
2	lnc-WDR1-12	chr4:9873428-9874487	NONHSAT095146
3	lnc-WDR1-12	chr4:9870401-9871383	NONHSAT095146
4	lnc-DRD5-13	chr4:9814207-9814604	NONHSAT095145
5	lnc-DRD5-1	chr4:9924438-9924574	ENSG00000249219.1
6	lnc-DRD5-13	chr4:9807330-9807762	NONHSAT095145
7	lnc-DRD5-1	chr4:9925400-9925770	ENSG00000249219.1

No data

Variant related genes	Relation type
RNA5SP154	TF binding region
ENSG00000249219	TF binding region
SLC2A9	TF binding region
RNA5SP154	CpG island
ENSG00000249219	CpG island
SLC2A9	CpG island
ENSG00000109667	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 8044 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:8044 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13106539	chr4:9797703-9797704	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527476094	chr4:9797706-9797707	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548916550	chr4:9797750-9797751	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs190391101	chr4:9797768-9797769	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs182272137	chr4:9797771-9797772	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs550917924	chr4:9797772-9797773	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569258776	chr4:9797810-9797811	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539869009	chr4:9797813-9797814	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558486106	chr4:9797823-9797824	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs567210567	chr4:9797824-9797825	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs534361600	chr4:9797888-9797889	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs555682551	chr4:9797889-9797890	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs141183770	chr4:9797916-9797917	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184387875	chr4:9797919-9797920	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs552068620	chr4:9798015-9798016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556255403	chr4:9798027-9798028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189070632	chr4:9798030-9798031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146955774	chr4:9798079-9798080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559976332	chr4:9798085-9798086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2139240	chr4:9798092-9798093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181452584	chr4:9798098-9798099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138052838	chr4:9798126-9798127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113406918	chr4:9798139-9798140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550775065	chr4:9798164-9798165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569420851	chr4:9798179-9798180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377529549	chr4:9798196-9798197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2867389	chr4:9798201-9798202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554272228	chr4:9798220-9798221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533354134	chr4:9798222-9798223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2867390	chr4:9798237-9798238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2867391	chr4:9798246-9798247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2867392	chr4:9798248-9798249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185646091	chr4:9798257-9798258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs3060762	chr4:9798260-9798261	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs567121521	chr4:9798290-9798291	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs10015812	chr4:9798316-9798317	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs377537223	chr4:9798354-9798355	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555892702	chr4:9798372-9798373	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs150463413	chr4:9798395-9798396	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs138311708	chr4:9798519-9798520	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs58691214	chr4:9798557-9798558	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs149644486	chr4:9798566-9798567	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577330300	chr4:9798569-9798570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs544559200	chr4:9798597-9798598	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs61020282	chr4:9798604-9798605	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs6449000	chr4:9798612-9798613	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs35800794	chr4:9798645-9798646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs555175537	chr4:9798646-9798647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs367672511	chr4:9798651-9798652	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547597979	chr4:9798665-9798666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
early-passage human iPS cells	21368824	CNVD
Sinonasal adenocarcinoma	21360264	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ependymoma	20639864	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Obesity	21131291	CNVD
Schizophrenia	23813976	CNVD
Hepatocellular carcinoma	22267523	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9794400-9798000	Weak transcription	HMEC	breast
2	chr4:9794600-9805800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:9794600-9812600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:9797200-9806400	Weak transcription	HepG2	liver
5	chr4:9798200-9799200	Enhancers	HMEC	breast
6	chr4:9798800-9815000	Weak transcription	Lung	lung
7	chr4:9799200-9802000	Weak transcription	Liver	Liver
8	chr4:9799200-9819600	Weak transcription	HMEC	breast
9	chr4:9802400-9803400	Enhancers	Thymus	Thymus
10	chr4:9802600-9803800	Enhancers	Fetal Thymus	thymus
11	chr4:9803200-9803800	Enhancers	Fetal Muscle Trunk	muscle
12	chr4:9803200-9803800	Enhancers	Fetal Muscle Leg	muscle
13	chr4:9804600-9808800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr4:9805800-9807000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:9806000-9806800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:9806000-9807000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:9806200-9806600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:9806200-9806800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr4:9806200-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:9806200-9821200	Weak transcription	Fetal Intestine Small	intestine
21	chr4:9806400-9807200	Enhancers	Placenta	Placenta
22	chr4:9806400-9807400	Strong transcription	HepG2	liver
23	chr4:9806600-9807000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:9806800-9807000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:9807000-9808800	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr4:9807000-9809400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr4:9807000-9810400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:9807000-9819800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:9807200-9807600	Weak transcription	Placenta	Placenta
30	chr4:9807400-9808600	Weak transcription	HepG2	liver
31	chr4:9807600-9808200	Enhancers	Placenta	Placenta
32	chr4:9808200-9809600	ZNF genes & repeats	Placenta	Placenta
33	chr4:9808200-9832000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr4:9808400-9809400	Enhancers	Fetal Stomach	stomach
35	chr4:9808600-9813400	Strong transcription	HepG2	liver
36	chr4:9808800-9810800	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr4:9808800-9813200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr4:9808800-9834400	Weak transcription	NHEK	skin
39	chr4:9809400-9810000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:9809600-9810000	Enhancers	Fetal Muscle Trunk	muscle
41	chr4:9809600-9810000	Enhancers	Placenta	Placenta
42	chr4:9809600-9810400	Enhancers	Fetal Muscle Leg	muscle
43	chr4:9810000-9830600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr4:9810400-9811000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr4:9810800-9811600	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr4:9811000-9827000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:9811600-9813000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr4:9812600-9813600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:9813000-9813800	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr4:9813000-9814600	Enhancers	Primary neutrophils fromperipheralblood	blood

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