Variant report

Variant	nsv878563
Chromosome Location	chr4:7420785-7529367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:632)
CpG islands
(count:3609)
Chromatin interactive
region (count:43)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7517343-7517590	HepG2	liver:	n/a	n/a
2	ATF3	chr4:7462396-7462591	K562	blood:	n/a	chr4:7462510-7462519
3	BACH1	chr4:7474386-7474403	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:7431462-7431555	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:7459110-7459520	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr4:7452670-7452924	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:7462352-7462679	K562	blood:	n/a	chr4:7462508-7462521 chr4:7462511-7462520 chr4:7462510-7462519 chr4:7462509-7462518 chr4:7462510-7462519 chr4:7462504-7462525
8	BHLHE40	chr4:7463215-7463337	K562	blood:	n/a	chr4:7463252-7463273 chr4:7463259-7463268
9	BHLHE40	chr4:7462305-7462695	HepG2	liver:	n/a	chr4:7462508-7462521 chr4:7462511-7462520 chr4:7462510-7462519 chr4:7462509-7462518 chr4:7462510-7462519 chr4:7462504-7462525
10	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
11	CCNT2	chr4:7505792-7505967	K562	blood:	n/a	n/a
12	CEBPB	chr4:7446628-7446633	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:7433501-7433762	MCF-7	breast:	n/a	n/a
14	CEBPB	chr4:7437550-7437908	HepG2	liver:	n/a	n/a
15	CEBPB	chr4:7525887-7526098	H1-hESC	embryonic stem cell:	n/a	chr4:7525982-7525993
16	CEBPB	chr4:7517279-7517633	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:7446635-7446744	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:7437595-7437783	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:7446555-7446878	MCF-7	breast:	n/a	n/a
20	CEBPB	chr4:7517192-7517635	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:7446537-7446857	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:7525934-7526014	IMR90	lung:	n/a	chr4:7525982-7525993
23	CEBPB	chr4:7525826-7526412	HepG2	liver:	n/a	chr4:7525982-7525993
24	CEBPB	chr4:7517278-7517645	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:7517322-7517536	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:7433508-7433674	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr4:7446529-7446871	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:7446572-7446820	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:7462372-7462637	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:7472785-7473103	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:7446523-7446950	MCF-7	breast:	n/a	n/a
32	CEBPB	chr4:7433460-7433830	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:7517417-7517597	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:7525842-7526080	A549	lung:	n/a	chr4:7525982-7525993
35	CEBPD	chr4:7516506-7516755	HepG2	liver:	n/a	n/a
36	CEBPD	chr4:7517347-7517719	HepG2	liver:	n/a	n/a
37	CHD2	chr4:7517348-7517609	HepG2	liver:	n/a	n/a
38	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr4:7525404-7525516	HepG2	liver:	n/a	n/a
40	CHD2	chr4:7441612-7441614	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr4:7464210-7464433	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr4:7512161-7512419	A549	lung:	n/a	n/a
43	CTBP2	chr4:7465845-7466283	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:7528240-7528390	K562	blood:	n/a	n/a
45	CTCF	chr4:7433640-7433790	HMEC	breast:	n/a	n/a
46	CTCF	chr4:7489714-7489764	H1-hESC	embryonic stem cell:	n/a	chr4:7489732-7489745
47	CTCF	chr4:7464438-7464622	K562	blood:	n/a	n/a
48	CTCF	chr4:7528307-7528527	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:7448440-7448590	SK-N-SH_RA	brain:	n/a	chr4:7448490-7448499
50	CTCF	chr4:7528340-7528490	Caco-2	colon:	n/a	n/a

(count:3609 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7502429-7502479	SAEC	small airway:	n/a
2	chr4:7486195-7486245	HNPCEpiC	eye:	n/a
3	chr4:7526639-7526689	ProgFib	skin:	n/a
4	chr4:7462664-7462714	AG04449	skin:	fetal
5	chr4:7427446-7427496	BE2_C	brain:	n/a
6	chr4:7473106-7473156	HRPEpiC	eye:	n/a
7	chr4:7472958-7473008	H1-hESC	embryonic stem cell:	embryo
8	chr4:7482223-7482273	NHBE	bronchial:	n/a
9	chr4:7528296-7528346	HIPEpiC	eye:	n/a
10	chr4:7512425-7512475	HIPEpiC	eye:	n/a
11	chr4:7502429-7502479	SAEC	small airway:	n/a
12	chr4:7486195-7486245	HNPCEpiC	eye:	n/a
13	chr4:7526639-7526689	ProgFib	skin:	n/a
14	chr4:7462664-7462714	AG04449	skin:	fetal
15	chr4:7427446-7427496	BE2_C	brain:	n/a
16	chr4:7473106-7473156	HRPEpiC	eye:	n/a
17	chr4:7472958-7473008	H1-hESC	embryonic stem cell:	embryo
18	chr4:7482223-7482273	NHBE	bronchial:	n/a
19	chr4:7528296-7528346	HIPEpiC	eye:	n/a
20	chr4:7512425-7512475	HIPEpiC	eye:	n/a
21	chr4:7485948-7485998	NB4	blood:	n/a
22	chr4:7462468-7462518	NHBE	bronchial:	n/a
23	chr4:7449747-7449797	SKMC	muscle:	n/a
24	chr4:7436239-7436289	GM12878	blood:	n/a
25	chr4:7438613-7438663	AG04449	skin:	fetal
26	chr4:7430936-7430986	HCF	heart:	n/a
27	chr4:7436861-7436911	AG09319	gingival:	n/a
28	chr4:7508044-7508094	SK-N-SH_RA	brain:	n/a
29	chr4:7512016-7512066	RPTEC	kidney:	n/a
30	chr4:7484382-7484432	NHBE	bronchial:	n/a
31	chr4:7528129-7528179	HCM	heart:	n/a
32	chr4:7436874-7436924	GM12878	blood:	n/a
33	chr4:7508044-7508094	PANC-1	pancreas:	n/a
34	chr4:7463234-7463284	GM19239	blood:	n/a
35	chr4:7508044-7508094	ProgFib	skin:	n/a
36	chr4:7435357-7435407	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:7473297-7473347	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:7463007-7463057	IMR90	lung:	fetal
39	chr4:7511100-7511150	PrEC	prostate:	n/a
40	chr4:7449747-7449797	IMR90	lung:	fetal
41	chr4:7435357-7435407	HUVEC	blood vessel:	n/a
42	chr4:7434754-7434804	HUVEC	blood vessel:	n/a
43	chr4:7462664-7462714	HRCEpiC	kidney:	n/a
44	chr4:7512498-7512548	GM19239	blood:	n/a
45	chr4:7437156-7437206	T-47D	breast:	n/a
46	chr4:7512425-7512475	HCM	heart:	n/a
47	chr4:7484382-7484432	AG04450	lung:	fetal
48	chr4:7512425-7512475	HMEC	breast:	n/a
49	chr4:7518783-7518833	Hela-S3	cervix:	n/a
50	chr4:7479912-7479962	BJ	skin:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
2	chr4:7475842..7476773-chr4:7652108..7653034,2	MCF-7	breast:
3	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
4	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
5	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
6	chr4:7396272..7396793-chr4:7463896..7464564,2	MCF-7	breast:
7	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
8	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
9	chr4:7430206..7433720-chr4:7434978..7437884,3	K562	blood:
10	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
11	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
12	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
13	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
14	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
15	chr4:7436453..7438238-chr4:7441242..7443096,2	MCF-7	breast:
16	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
17	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
18	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
19	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
20	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
21	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
22	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
23	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
24	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
25	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
26	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
27	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
28	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
29	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
30	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
31	chr4:7421842..7424756-chr4:7435320..7437360,2	MCF-7	breast:
32	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
33	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
34	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
35	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
36	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
37	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
38	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
39	chr4:7512552..7515805-chr4:7517576..7521782,4	MCF-7	breast:
40	chr4:7430997..7432542-chr4:7435254..7438169,2	MCF-7	breast:
41	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
42	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:
43	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSAPL1-1	chr4:7432021-7433304	NONHSAT095056

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4274	chr4:7461818-7461835	MIMAT0016906

No data

Variant related genes	Relation type
MIR4274	TF binding region
PSAPL1	TF binding region
MIR4274	CpG island
PSAPL1	CpG island
ENSG00000178597	chromatin interactions

Extended variants
information (count: 6402 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:6402 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4292336	chr4:7420785-7420786	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs55739999	chr4:7420826-7420827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538589855	chr4:7420853-7420854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs76117917	chr4:7420854-7420855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7692426	chr4:7420858-7420859	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs115522420	chr4:7420869-7420870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186044828	chr4:7420896-7420897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76930175	chr4:7420954-7420955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543722089	chr4:7420958-7420959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377378964	chr4:7421002-7421003	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs7663695	chr4:7421007-7421008	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs531068189	chr4:7421014-7421015	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs35618033	chr4:7421046-7421047	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs7663860	chr4:7421048-7421049	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs73796563	chr4:7421065-7421066	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs190501694	chr4:7421134-7421135	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs150773858	chr4:7421146-7421147	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs563924954	chr4:7421169-7421170	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs530986431	chr4:7421174-7421175	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs375569353	chr4:7421177-7421178	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs552840941	chr4:7421191-7421192	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs564730306	chr4:7421193-7421194	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs6446599	chr4:7421198-7421199	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543874154	chr4:7421278-7421279	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs184130896	chr4:7421279-7421280	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs188593853	chr4:7421283-7421284	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs6821163	chr4:7421305-7421306	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs546692158	chr4:7421306-7421307	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs192736857	chr4:7421316-7421317	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs182532846	chr4:7421363-7421364	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs568036244	chr4:7421381-7421382	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs536804419	chr4:7421404-7421405	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs558462064	chr4:7421407-7421408	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs11414942	chr4:7421428-7421429	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs397700678	chr4:7421430-7421431	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs377012816	chr4:7421431-7421432	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs4689740	chr4:7421443-7421444	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs557154969	chr4:7421450-7421451	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs144743725	chr4:7421490-7421491	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs4689741	chr4:7421498-7421499	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs574705610	chr4:7421537-7421538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs147490774	chr4:7421549-7421550	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs563588338	chr4:7421582-7421583	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs575806497	chr4:7421632-7421633	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs546411360	chr4:7421700-7421701	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs564817507	chr4:7421747-7421748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs528773691	chr4:7421775-7421776	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs370186862	chr4:7421777-7421778	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs539744352	chr4:7421789-7421790	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs547451439	chr4:7421874-7421875	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7414200-7421400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr4:7414600-7422200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr4:7418800-7429200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:7420800-7421000	Enhancers	Stomach Smooth Muscle	stomach
5	chr4:7421000-7422000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:7421000-7422200	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:7421200-7421800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr4:7421200-7422800	Enhancers	Brain Substantia Nigra	brain
9	chr4:7421400-7423000	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr4:7421600-7422200	Enhancers	Colon Smooth Muscle	Colon
11	chr4:7421600-7422800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr4:7421600-7424200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:7421800-7422800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
14	chr4:7421800-7425200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr4:7422000-7422600	Enhancers	Stomach Smooth Muscle	stomach
16	chr4:7422000-7422800	Enhancers	Brain Cingulate Gyrus	brain
17	chr4:7422000-7423000	Enhancers	Esophagus	oesophagus
18	chr4:7422200-7422400	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr4:7422200-7422600	Enhancers	Brain Anterior Caudate	brain
20	chr4:7422200-7422600	Enhancers	Right Ventricle	heart
21	chr4:7422200-7422800	Enhancers	Lung	lung
22	chr4:7422200-7423000	Enhancers	Fetal Muscle Leg	muscle
23	chr4:7422400-7422800	Enhancers	Brain Angular Gyrus	brain
24	chr4:7422600-7425200	Weak transcription	Brain Anterior Caudate	brain
25	chr4:7422600-7425400	Weak transcription	Brain Hippocampus Middle	brain
26	chr4:7422800-7425400	Weak transcription	Brain Substantia Nigra	brain
27	chr4:7422800-7425600	Weak transcription	Brain Angular Gyrus	brain
28	chr4:7422800-7425600	Weak transcription	Brain Cingulate Gyrus	brain
29	chr4:7423000-7425000	Weak transcription	Fetal Muscle Leg	muscle
30	chr4:7423000-7425200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr4:7423000-7425600	Weak transcription	Esophagus	oesophagus
32	chr4:7423200-7436200	Weak transcription	Right Atrium	heart
33	chr4:7423400-7423800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:7423800-7424000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:7423800-7424000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:7424000-7424600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:7424000-7426400	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr4:7424200-7425600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr4:7424400-7425600	Weak transcription	Spleen	Spleen
40	chr4:7424600-7425600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:7424800-7425000	Enhancers	Brain Germinal Matrix	brain
42	chr4:7425000-7425600	Weak transcription	Brain Germinal Matrix	brain
43	chr4:7425000-7430400	Enhancers	Fetal Muscle Leg	muscle
44	chr4:7425200-7426200	Enhancers	Brain Anterior Caudate	brain
45	chr4:7425200-7426200	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr4:7425200-7426200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr4:7425200-7430400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr4:7425400-7426000	Enhancers	Brain Hippocampus Middle	brain
49	chr4:7425400-7426200	Enhancers	Brain Substantia Nigra	brain
50	chr4:7425600-7425800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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