Variant report

Variant	nsv593558
Chromosome Location	chr4:7109083-7136998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:306)
CpG islands
(count:671)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:7122098-7122348	K562	blood:	n/a	n/a
2	BCL3	chr4:7133556-7133887	GM12878	blood:	n/a	n/a
3	BCL3	chr4:7135011-7135294	GM12878	blood:	n/a	n/a
4	BCL3	chr4:7133549-7133962	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:7126714-7127101	K562	blood:	n/a	n/a
6	BHLHE40	chr4:7129826-7130186	K562	blood:	n/a	chr4:7130017-7130026
7	BHLHE40	chr4:7129458-7129606	K562	blood:	n/a	n/a
8	CBX3	chr4:7134741-7135064	K562	blood:	n/a	n/a
9	CBX3	chr4:7134685-7135077	K562	blood:	n/a	n/a
10	CEBPB	chr4:7127760-7128075	K562	blood:	n/a	chr4:7127957-7127968
11	CEBPB	chr4:7126761-7127241	IMR90	lung:	n/a	chr4:7127078-7127089
12	CEBPB	chr4:7124201-7124223	K562	blood:	n/a	chr4:7124210-7124223
13	CEBPB	chr4:7127770-7128098	K562	blood:	n/a	chr4:7127957-7127968
14	CEBPB	chr4:7127867-7128099	HepG2	liver:	n/a	chr4:7127957-7127968
15	CEBPB	chr4:7126425-7126668	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr4:7122096-7122393	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr4:7122140-7122405	K562	blood:	n/a	n/a
18	CTCF	chr4:7126840-7126990	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr4:7126873-7127019	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr4:7126884-7126979	HepG2	liver:	n/a	n/a
21	CTCF	chr4:7131540-7131690	HepG2	liver:	n/a	n/a
22	CTCF	chr4:7126720-7126870	WI-38	lung:	n/a	n/a
23	CTCF	chr4:7135600-7135750	HepG2	liver:	n/a	n/a
24	CTCF	chr4:7135600-7135750	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr4:7128173-7128265	GM12892	blood:	n/a	n/a
26	CTCF	chr4:7131636-7131776	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:7135640-7135790	GM12873	blood:	n/a	n/a
28	CTCF	chr4:7126820-7126970	SAEC	small airway:	n/a	n/a
29	CTCF	chr4:7126851-7127020	K562	blood:	n/a	n/a
30	CTCF	chr4:7126860-7127010	HRE	kidney:	n/a	n/a
31	CTCF	chr4:7126880-7127030	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr4:7126920-7127070	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr4:7126840-7126990	RPTEC	kidney:	n/a	n/a
34	CTCF	chr4:7135620-7135770	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr4:7126940-7127090	HMF	breast:	n/a	n/a
36	CTCF	chr4:7126880-7126970	GM12891	blood:	n/a	n/a
37	CTCF	chr4:7126880-7127030	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr4:7126680-7126830	NHLF	lung:	n/a	n/a
39	CTCF	chr4:7135560-7135710	GM12870	blood:	n/a	n/a
40	CTCF	chr4:7124060-7124210	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:7135680-7135830	GM12864	blood:	n/a	n/a
42	CTCF	chr4:7135600-7135750	K562	blood:	n/a	n/a
43	CTCF	chr4:7126800-7126950	HRE	kidney:	n/a	n/a
44	CTCF	chr4:7133360-7133758	GM19239	blood:	n/a	n/a
45	CTCF	chr4:7126860-7127010	K562	blood:	n/a	n/a
46	CTCF	chr4:7135600-7135750	AG04449	skin:	n/a	n/a
47	CTCF	chr4:7126913-7127034	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr4:7135640-7135790	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:7126820-7126970	NHEK	skin:	n/a	n/a
50	CTCF	chr4:7126800-7126950	HEEpiC	esophagus:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7131247-7131297	Hela-S3	cervix:	n/a
2	chr4:7131061-7131111	SK-N-SH	brain:	n/a
3	chr4:7126882-7126932	SK-N-SH	brain:	n/a
4	chr4:7131061-7131111	SK-N-MC	brain:	n/a
5	chr4:7114067-7114117	HUVEC	blood vessel:	n/a
6	chr4:7126882-7126932	GM06990	blood:	n/a
7	chr4:7114067-7114117	HCF	heart:	n/a
8	chr4:7114067-7114117	CMK	blood:	n/a
9	chr4:7114046-7114096	U87	brain:	n/a
10	chr4:7131061-7131111	RPTEC	kidney:	n/a
11	chr4:7114012-7114062	LNCaP	prostate:	n/a
12	chr4:7114046-7114096	SKMC	muscle:	n/a
13	chr4:7131136-7131186	T-47D	breast:	n/a
14	chr4:7114067-7114117	BJ	skin:	n/a
15	chr4:7131136-7131186	GM12878	blood:	n/a
16	chr4:7131247-7131297	SK-N-SH_RA	brain:	n/a
17	chr4:7129440-7129490	HRPEpiC	eye:	n/a
18	chr4:7114046-7114096	PrEC	prostate:	n/a
19	chr4:7131403-7131453	AG04450	lung:	fetal
20	chr4:7131247-7131297	AG10803	skin:	n/a
21	chr4:7114046-7114096	GM12892	blood:	n/a
22	chr4:7131403-7131453	Jurkat	blood:	n/a
23	chr4:7129440-7129490	HEK293	kidney:	embryo
24	chr4:7131478-7131528	U87	brain:	n/a
25	chr4:7129440-7129490	AG10803	skin:	n/a
26	chr4:7126882-7126932	K562	blood:	n/a
27	chr4:7129517-7129567	SAEC	small airway:	n/a
28	chr4:7129517-7129567	U87	brain:	n/a
29	chr4:7131061-7131111	NB4	blood:	n/a
30	chr4:7129517-7129567	AG09319	gingival:	n/a
31	chr4:7131478-7131528	GM06990	blood:	n/a
32	chr4:7126882-7126932	H1-hESC	embryonic stem cell:	embryo
33	chr4:7131136-7131186	K562	blood:	n/a
34	chr4:7131478-7131528	ProgFib	skin:	n/a
35	chr4:7114046-7114096	HEK293	kidney:	embryo
36	chr4:7114067-7114117	HCT-116	colon:	n/a
37	chr4:7129440-7129490	AG04450	lung:	fetal
38	chr4:7131061-7131111	HNPCEpiC	eye:	n/a
39	chr4:7131136-7131186	HCF	heart:	n/a
40	chr4:7129517-7129567	HAEpiC	amniotic membrane:	n/a
41	chr4:7131061-7131111	NHDF-neo	bronchial:	n/a
42	chr4:7131247-7131297	Caco-2	colon:	n/a
43	chr4:7131136-7131186	Hela-S3	cervix:	n/a
44	chr4:7114046-7114096	HepG2	liver:	n/a
45	chr4:7129517-7129567	HCF	heart:	n/a
46	chr4:7129517-7129567	GM06990	blood:	n/a
47	chr4:7131061-7131111	HEK293	kidney:	embryo
48	chr4:7131136-7131186	NHBE	bronchial:	n/a
49	chr4:7131136-7131186	U87	brain:	n/a
50	chr4:7131061-7131111	MCF-7	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7103913..7105517-chr4:7112314..7115141,2	K562	blood:
2	chr4:7106689..7108245-chr4:7109405..7112071,2	MCF-7	breast:
3	chr4:7127382..7129975-chr4:7130114..7132149,2	MCF-7	breast:
4	chr4:7124347..7127288-chr4:7130183..7132382,4	K562	blood:
5	chr4:7124347..7127288-chr4:7130183..7132382,4	K562	blood:
6	chr4:7127382..7129975-chr4:7130114..7132149,2	MCF-7	breast:
7	chr4:7103913..7106622-chr4:7111535..7115141,3	K562	blood:
8	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:
9	chr4:7121664..7124511-chr4:7134767..7137572,2	K562	blood:
10	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
11	chr4:7103610..7105955-chr4:7121635..7124295,2	K562	blood:
12	chr4:7105423..7108283-chr4:7118442..7120103,2	MCF-7	breast:
13	chr4:7136644..7138277-chr4:7150802..7153276,2	MCF-7	breast:
14	chr4:7125529..7126029-chr6:30710536..30711392,2	Hela-S3	cervix:
15	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:
16	chr4:7121664..7124511-chr4:7134767..7137572,2	K562	blood:
17	chr4:7120740..7122988-chr4:7129086..7130661,2	MCF-7	breast:
18	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
19	chr4:7105809..7107677-chr4:7109830..7111435,2	K562	blood:
20	chr4:7120740..7122988-chr4:7129086..7130661,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRPEL1-2	chr4:7133632-7133655	NONHSAT095050
2	lnc-GRPEL1-2	chr4:7132607-7132626	XLOC_003873
3	lnc-GRPEL1-2	chr4:7132819-7133131	XLOC_003873
4	lnc-GRPEL1-2	chr4:7132540-7133055	NONHSAT095050

No data

Variant related genes	Relation type
ENSG00000245468	TF binding region
RN7SKP36	TF binding region
ENSG00000245468	CpG island
RN7SKP36	CpG island
ENSG00000245468	chromatin interactions
ENSG00000272273	chromatin interactions
SPIN4	miRNA target sites
KDELC2	miRNA target sites

Extended variants
information (count: 1460 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1460 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4082843	chr4:7109083-7109084	Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35837216	chr4:7109121-7109122	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs561361183	chr4:7109154-7109155	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs576488226	chr4:7109170-7109171	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs80042202	chr4:7109184-7109185	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs565373315	chr4:7109204-7109205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372094231	chr4:7109232-7109233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374953256	chr4:7109235-7109236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144292655	chr4:7109241-7109242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532754106	chr4:7109289-7109290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541570016	chr4:7109295-7109296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113345760	chr4:7109310-7109311	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146589623	chr4:7109324-7109325	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149127990	chr4:7109341-7109342	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs143239519	chr4:7109359-7109360	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs576412324	chr4:7109374-7109375	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs571562908	chr4:7109380-7109381	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs372196388	chr4:7109423-7109424	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554023394	chr4:7109482-7109483	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531887444	chr4:7109490-7109491	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs566255533	chr4:7109517-7109518	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs117245014	chr4:7109548-7109549	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs554762466	chr4:7109554-7109555	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs368829700	chr4:7109590-7109591	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs576292328	chr4:7109606-7109607	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs76799351	chr4:7109642-7109643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs115329358	chr4:7109669-7109670	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545156270	chr4:7109713-7109714	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs372298745	chr4:7109734-7109735	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs545077852	chr4:7109744-7109745	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs76976023	chr4:7109745-7109746	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs527460520	chr4:7109752-7109753	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs75507883	chr4:7109769-7109770	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs10026013	chr4:7109777-7109778	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs531595471	chr4:7109791-7109792	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550105661	chr4:7109807-7109808	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs373230761	chr4:7109808-7109809	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565711327	chr4:7109810-7109811	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs28401383	chr4:7109830-7109831	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs77625386	chr4:7109869-7109870	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs193193721	chr4:7109891-7109892	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs536360749	chr4:7109916-7109917	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs548331633	chr4:7109929-7109930	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs570173510	chr4:7109933-7109934	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs569916091	chr4:7109934-7109935	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs537345853	chr4:7109995-7109996	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs369363599	chr4:7110000-7110001	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs73796422	chr4:7110026-7110027	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs28629411	chr4:7110049-7110050	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116433226	chr4:7110092-7110093	Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	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
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7105600-7109200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr4:7105800-7111000	Weak transcription	Right Ventricle	heart
3	chr4:7105800-7176000	Weak transcription	Right Atrium	heart
4	chr4:7107400-7114400	Weak transcription	Spleen	Spleen
5	chr4:7107600-7109800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:7108000-7110400	Weak transcription	Fetal Muscle Leg	muscle
7	chr4:7109000-7109200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:7109800-7110600	Bivalent Enhancer	HepG2	liver
9	chr4:7109800-7111000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:7110200-7110400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr4:7110400-7111200	Enhancers	Fetal Muscle Leg	muscle
12	chr4:7110800-7111400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:7110800-7111600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:7111200-7111600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr4:7113200-7113400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr4:7113400-7114200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:7114200-7122000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:7114400-7114600	Enhancers	Spleen	Spleen
19	chr4:7114600-7114800	ZNF genes & repeats	Spleen	Spleen
20	chr4:7114800-7121000	Weak transcription	Spleen	Spleen
21	chr4:7117600-7117800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr4:7117800-7133400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:7118600-7118800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:7121000-7124400	Enhancers	Spleen	Spleen
25	chr4:7121600-7121800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:7122000-7122200	Bivalent/Poised TSS	K562	blood
27	chr4:7122000-7124800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:7122200-7122400	Bivalent Enhancer	K562	blood
29	chr4:7122600-7123000	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr4:7122600-7123200	Enhancers	Stomach Smooth Muscle	stomach
31	chr4:7122600-7123800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:7122600-7123800	Enhancers	Fetal Muscle Trunk	muscle
33	chr4:7122600-7123800	Enhancers	Lung	lung
34	chr4:7122800-7123200	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr4:7122800-7123200	Enhancers	Brain Substantia Nigra	brain
36	chr4:7122800-7123600	Enhancers	Fetal Muscle Leg	muscle
37	chr4:7123000-7123600	Enhancers	Colonic Mucosa	Colon
38	chr4:7123000-7126400	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr4:7123200-7124000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:7123200-7126600	Weak transcription	Stomach Smooth Muscle	stomach
41	chr4:7123200-7128400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:7123400-7125000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:7123600-7123800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:7123600-7124200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:7124000-7124400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:7124000-7126600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:7124200-7124400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:7124400-7126600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:7124800-7129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:7125000-7125200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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