Variant report

Variant	nsv593692
Chromosome Location	chr4:10127301-10153233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:205)
CpG islands
(count:489)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:205 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
2	BATF	chr4:10133064-10133309	GM12878	blood:	n/a	n/a
3	BATF	chr4:10133063-10133313	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:10142964-10143314	K562	blood:	n/a	n/a
5	BHLHE40	chr4:10132206-10132484	K562	blood:	n/a	chr4:10132332-10132353
6	CEBPB	chr4:10130839-10131364	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr4:10142301-10142459	HepG2	liver:	n/a	n/a
8	CHD2	chr4:10130972-10131141	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr4:10143239-10143269	K562	blood:	n/a	n/a
10	CTCF	chr4:10146200-10146350	HEK293	kidney:	n/a	n/a
11	CTCF	chr4:10143160-10143310	GM12873	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
12	CTCF	chr4:10142600-10142750	GM06990	blood:	n/a	n/a
13	CTCF	chr4:10143300-10143450	HCM	heart:	n/a	n/a
14	CTCF	chr4:10142680-10142830	GM12873	blood:	n/a	n/a
15	CTCF	chr4:10143160-10143310	SK-N-SH_RA	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
16	CTCF	chr4:10143121-10143353	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
17	CTCF	chr4:10146240-10146390	GM12875	blood:	n/a	n/a
18	CTCF	chr4:10143220-10143370	BE2_C	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
19	CTCF	chr4:10143216-10143253	NHEK	skin:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
20	CTCF	chr4:10143120-10143270	HCT-116	colon:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
21	CTCF	chr4:10142633-10142773	K562	blood:	n/a	n/a
22	CTCF	chr4:10143120-10143270	HEK293	kidney:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
23	CTCF	chr4:10146180-10146330	GM12864	blood:	n/a	n/a
24	CTCF	chr4:10142737-10143429	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
25	CTCF	chr4:10143180-10143330	HEEpiC	esophagus:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
26	CTCF	chr4:10143200-10143350	GM12870	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
27	CTCF	chr4:10143160-10143310	GM12864	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
28	CTCF	chr4:10142587-10142788	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:10143240-10143390	K562	blood:	n/a	n/a
30	CTCF	chr4:10146080-10146370	GM12866	blood:	n/a	n/a
31	CTCF	chr4:10146240-10146390	HCFaa	heart:	n/a	n/a
32	CTCF	chr4:10146200-10146350	GM12873	blood:	n/a	n/a
33	CTCF	chr4:10143140-10143290	HRPEpiC	eye:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
34	CTCF	chr4:10143135-10143288	HepG2	liver:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
35	CTCF	chr4:10143260-10143410	RPTEC	kidney:	n/a	n/a
36	CTCF	chr4:10142600-10142750	K562	blood:	n/a	n/a
37	CTCF	chr4:10143140-10143290	WERI-Rb-1	eye:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
38	CTCF	chr4:10143120-10143270	Hela-S3	cervix:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
39	CTCF	chr4:10143060-10143210	GM12871	blood:	n/a	n/a
40	CTCF	chr4:10143280-10143430	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:10146200-10146350	GM12872	blood:	n/a	n/a
42	CTCF	chr4:10143180-10143330	SAEC	small airway:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
43	CTCF	chr4:10142560-10143448	H1-hESC	embryonic stem cell:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
44	CTCF	chr4:10142660-10142810	HCT-116	colon:	n/a	n/a
45	CTCF	chr4:10143193-10143253	GM10266	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
46	CTCF	chr4:10143180-10143330	MCF-7	breast:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
47	CTCF	chr4:10143140-10143290	NB4	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
48	CTCF	chr4:10143186-10143191	GM10266	blood:	n/a	n/a
49	CTCF	chr4:10142620-10142770	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr4:10142815-10143400	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10147038-10147088	BE2_C	brain:	n/a
2	chr4:10147038-10147088	BE2_C	brain:	n/a
3	chr4:10147302-10147352	Hela-S3	cervix:	n/a
4	chr4:10147606-10147656	MCF-7	breast:	n/a
5	chr4:10143053-10143103	LNCaP	prostate:	n/a
6	chr4:10149849-10149899	HCPEpiC	choroid plexus:	n/a
7	chr4:10147302-10147352	HMEC	breast:	n/a
8	chr4:10147606-10147656	AoSMC	blood vessel:	n/a
9	chr4:10147606-10147656	HCPEpiC	choroid plexus:	n/a
10	chr4:10149849-10149899	GM06990	blood:	n/a
11	chr4:10147606-10147656	ProgFib	skin:	n/a
12	chr4:10143053-10143103	SAEC	small airway:	n/a
13	chr4:10143053-10143103	ovcar-3	ovarian:	n/a
14	chr4:10147330-10147380	HRPEpiC	eye:	n/a
15	chr4:10147038-10147088	HRE	kidney:	n/a
16	chr4:10143053-10143103	BE2_C	brain:	n/a
17	chr4:10147330-10147380	HRCEpiC	kidney:	n/a
18	chr4:10147100-10147150	HUVEC	blood vessel:	n/a
19	chr4:10147100-10147150	ovcar-3	ovarian:	n/a
20	chr4:10147606-10147656	HRPEpiC	eye:	n/a
21	chr4:10145483-10145533	GM12892	blood:	n/a
22	chr4:10147038-10147088	A549	lung:	n/a
23	chr4:10147302-10147352	U87	brain:	n/a
24	chr4:10147606-10147656	GM12878	blood:	n/a
25	chr4:10147606-10147656	GM06990	blood:	n/a
26	chr4:10147330-10147380	AoSMC	blood vessel:	n/a
27	chr4:10145483-10145533	HEK293	kidney:	embryo
28	chr4:10143053-10143103	Hela-S3	cervix:	n/a
29	chr4:10147038-10147088	HUVEC	blood vessel:	n/a
30	chr4:10147330-10147380	Jurkat	blood:	n/a
31	chr4:10145483-10145533	BE2_C	brain:	n/a
32	chr4:10147038-10147088	Caco-2	colon:	n/a
33	chr4:10143053-10143103	Hepatocyte	liver:	n/a
34	chr4:10149849-10149899	NH-A	brain:	n/a
35	chr4:10143053-10143103	GM12892	blood:	n/a
36	chr4:10149849-10149899	AG04449	skin:	fetal
37	chr4:10147330-10147380	GM12891	blood:	n/a
38	chr4:10147038-10147088	IMR90	lung:	fetal
39	chr4:10145483-10145533	RPTEC	kidney:	n/a
40	chr4:10145483-10145533	GM19239	blood:	n/a
41	chr4:10145483-10145533	AoSMC	blood vessel:	n/a
42	chr4:10147330-10147380	LNCaP	prostate:	n/a
43	chr4:10149849-10149899	AG09319	gingival:	n/a
44	chr4:10143053-10143103	HAEpiC	amniotic membrane:	n/a
45	chr4:10147038-10147088	MCF-7	breast:	n/a
46	chr4:10147302-10147352	GM12891	blood:	n/a
47	chr4:10147100-10147150	GM12878	blood:	n/a
48	chr4:10147606-10147656	NT2-D1	testis:	n/a
49	chr4:10143053-10143103	HIPEpiC	eye:	n/a
50	chr4:10143053-10143103	U87	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:10121162..10125014-chr4:10131852..10134322,3	MCF-7	breast:
2	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
3	chr4:10126622..10128433-chr4:10132503..10134257,2	MCF-7	breast:
4	chr4:10124627..10126326-chr4:10129593..10131682,2	MCF-7	breast:
5	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
6	chr4:10126622..10128433-chr4:10132503..10134257,2	MCF-7	breast:
7	chr4:10142468..10145387-chr4:10146611..10148310,2	MCF-7	breast:
8	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
9	chr4:10110208..10112839-chr4:10141638..10144449,2	MCF-7	breast:
10	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
11	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
12	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
13	chr4:10124578..10127302-chr4:10186119..10188725,2	K562	blood:
14	chr4:10147623..10149514-chr4:10156130..10157999,2	K562	blood:
15	chr4:10117985..10121218-chr4:10149186..10152668,4	MCF-7	breast:
16	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
17	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
18	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
19	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
20	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
21	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
22	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
23	chr4:10133192..10134746-chr4:10556529..10559334,2	K562	blood:
24	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
25	chr4:10118110..10120453-chr4:10131867..10134092,3	MCF-7	breast:
26	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
27	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
28	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
29	chr4:10143164..10147494-chr4:10150670..10153852,4	K562	blood:
30	chr4:10117528..10120943-chr4:10131939..10133897,4	MCF-7	breast:
31	chr4:10117694..10121179-chr4:10148695..10151564,3	MCF-7	breast:
32	chr4:10137029..10138548-chr4:10444331..10446997,2	K562	blood:
33	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
34	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
35	chr4:10132922..10135214-chr4:10181103..10182859,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
2	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429

No data

Variant related genes	Relation type
ENSG00000250393	TF binding region
ENSG00000250393	CpG island
ENSG00000250393	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions

Extended variants
information (count: 2234 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2234 , 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	rs11724184	chr4:10127301-10127302	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367781577	chr4:10127307-10127308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551162687	chr4:10127313-10127314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371565481	chr4:10127315-10127316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190307921	chr4:10127316-10127317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139053580	chr4:10127323-10127324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551456326	chr4:10127324-10127325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193191804	chr4:10127330-10127331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200993173	chr4:10127351-10127352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185120093	chr4:10127352-10127353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533742115	chr4:10127366-10127367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143059242	chr4:10127367-10127368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188851016	chr4:10127380-10127381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147064356	chr4:10127381-10127382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376302052	chr4:10127385-10127386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577393917	chr4:10127402-10127403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539592738	chr4:10127408-10127409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534986941	chr4:10127414-10127415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181080685	chr4:10127427-10127428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573163942	chr4:10127435-10127436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10001106	chr4:10127441-10127442	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs562385430	chr4:10127445-10127446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188147809	chr4:10127447-10127448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150165633	chr4:10127448-10127449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182207569	chr4:10127456-10127457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577803871	chr4:10127457-10127458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187587025	chr4:10127468-10127469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533560431	chr4:10127469-10127470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs11722643	chr4:10127484-10127485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs191914172	chr4:10127485-10127486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553260988	chr4:10127492-10127493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548928175	chr4:10127502-10127503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182183882	chr4:10127520-10127521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566904990	chr4:10127521-10127522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117240423	chr4:10127527-10127528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557072968	chr4:10127532-10127533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113768021	chr4:10127540-10127541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571149676	chr4:10127544-10127545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs74664438	chr4:10127549-10127550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557972210	chr4:10127558-10127559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573206674	chr4:10127559-10127560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566927041	chr4:10127571-10127572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141489061	chr4:10127576-10127577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534020621	chr4:10127587-10127588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555826567	chr4:10127621-10127622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185683974	chr4:10127635-10127636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs544962010	chr4:10127638-10127639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74859631	chr4:10127647-10127648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575056168	chr4:10127672-10127673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190144993	chr4:10127676-10127677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10120600-10127400	Enhancers	Primary T helper cells PMA-I stimulated	--
2	chr4:10120800-10127400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr4:10121800-10127400	Enhancers	Dnd41	blood
4	chr4:10123400-10127800	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr4:10124600-10128200	Enhancers	Right Ventricle	heart
6	chr4:10125200-10128400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:10125800-10128600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:10125800-10129200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:10125800-10130000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:10125800-10130400	Weak transcription	HSMMtube	muscle
11	chr4:10126000-10127600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:10126000-10130200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:10126000-10130200	Weak transcription	Hela-S3	cervix
14	chr4:10126000-10131400	Weak transcription	Fetal Lung	lung
15	chr4:10126200-10130600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr4:10126200-10130800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr4:10126400-10128800	Weak transcription	Placenta	Placenta
18	chr4:10126400-10130200	Weak transcription	HSMM	muscle
19	chr4:10126600-10131000	Weak transcription	Adipose Nuclei	Adipose
20	chr4:10126600-10131000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr4:10126600-10131000	Weak transcription	Right Atrium	heart
22	chr4:10126600-10131600	Weak transcription	Spleen	Spleen
23	chr4:10126800-10128600	Enhancers	Fetal Heart	heart
24	chr4:10127000-10130400	Weak transcription	HUVEC	blood vessel
25	chr4:10127000-10130600	Weak transcription	Fetal Muscle Leg	muscle
26	chr4:10127200-10128000	Enhancers	Left Ventricle	heart
27	chr4:10128000-10131000	Weak transcription	Left Ventricle	heart
28	chr4:10128200-10131400	Weak transcription	Right Ventricle	heart
29	chr4:10128400-10129200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:10128600-10129000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr4:10129000-10129200	Enhancers	Placenta	Placenta
32	chr4:10129200-10129600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:10129400-10130200	Enhancers	K562	blood
34	chr4:10129600-10129800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr4:10129600-10132000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:10129800-10130200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:10129800-10131400	Enhancers	NHEK	skin
38	chr4:10130000-10131600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:10130200-10131400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:10130200-10131400	Enhancers	NHDF-Ad	bronchial
41	chr4:10130200-10131600	Enhancers	Hela-S3	cervix
42	chr4:10130200-10132400	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:10130200-10132600	Enhancers	HSMM	muscle
44	chr4:10130400-10131000	Enhancers	HMEC	breast
45	chr4:10130400-10131000	Enhancers	HUVEC	blood vessel
46	chr4:10130400-10132200	Enhancers	HSMMtube	muscle
47	chr4:10130600-10133000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr4:10130600-10133200	Enhancers	Fetal Muscle Leg	muscle
49	chr4:10130800-10131200	Enhancers	Psoas Muscle	Psoas
50	chr4:10130800-10132200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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