Variant report

Variant	nsv878561
Chromosome Location	chr4:7402284-7544610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:826)
CpG islands
(count:3788)
Chromatin interactive
region (count:57)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7532753-7532902	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:7517343-7517590	HepG2	liver:	n/a	n/a
3	ATF3	chr4:7462396-7462591	K562	blood:	n/a	chr4:7462510-7462519
4	BACH1	chr4:7459110-7459520	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:7474386-7474403	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:7431462-7431555	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr4:7415403-7415635	GM12878	blood:	n/a	n/a
8	BCL3	chr4:7544346-7544668	GM12878	blood:	n/a	n/a
9	BCL3	chr4:7418098-7418400	GM12878	blood:	n/a	n/a
10	BCL3	chr4:7544248-7544648	GM12878	blood:	n/a	n/a
11	BCL3	chr4:7418462-7418837	GM12878	blood:	n/a	n/a
12	BCL3	chr4:7452670-7452924	GM12878	blood:	n/a	n/a
13	BCL3	chr4:7418400-7418837	GM12878	blood:	n/a	n/a
14	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
15	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
16	BHLHE40	chr4:7463215-7463337	K562	blood:	n/a	chr4:7463252-7463273 chr4:7463259-7463268
17	BRCA1	chr4:7436571-7436572	HepG2	liver:	n/a	n/a
18	CBX3	chr4:7404211-7405066	HCT-116	colon:	n/a	n/a
19	CCNT2	chr4:7505792-7505967	K562	blood:	n/a	n/a
20	CEBPB	chr4:7517322-7517536	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:7517278-7517645	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:7433501-7433762	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:7433460-7433830	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:7525826-7526412	HepG2	liver:	n/a	chr4:7525982-7525993
25	CEBPB	chr4:7517279-7517633	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:7517417-7517597	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:7446523-7446950	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:7541525-7541851	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:7446529-7446871	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:7446537-7446857	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:7525842-7526080	A549	lung:	n/a	chr4:7525982-7525993
32	CEBPB	chr4:7437550-7437908	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:7462372-7462637	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:7525887-7526098	H1-hESC	embryonic stem cell:	n/a	chr4:7525982-7525993
35	CEBPB	chr4:7404372-7404685	MCF-7	breast:	n/a	n/a
36	CEBPB	chr4:7437595-7437783	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:7446555-7446878	MCF-7	breast:	n/a	n/a
38	CEBPB	chr4:7446635-7446744	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:7472785-7473103	MCF-7	breast:	n/a	n/a
40	CEBPB	chr4:7404223-7405053	HCT-116	colon:	n/a	chr4:7404985-7404993
41	CEBPB	chr4:7446572-7446820	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:7433508-7433674	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:7404489-7404760	A549	lung:	n/a	n/a
44	CEBPB	chr4:7517192-7517635	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:7446628-7446633	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:7525934-7526014	IMR90	lung:	n/a	chr4:7525982-7525993
47	CEBPD	chr4:7517347-7517719	HepG2	liver:	n/a	n/a
48	CEBPD	chr4:7516506-7516755	HepG2	liver:	n/a	n/a
49	CEBPZ	chr4:7539713-7539730	HepG2	liver:	n/a	n/a
50	CHD2	chr4:7436619-7436861	Hela-S3	cervix:	n/a	n/a

(count:3788 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7484382-7484432	GM12878	blood:	n/a
2	chr4:7528296-7528346	HNPCEpiC	eye:	n/a
3	chr4:7511100-7511150	Hela-S3	cervix:	n/a
4	chr4:7437027-7437077	MCF10A-Er-Src	breast:	n/a
5	chr4:7502947-7502997	ovcar-3	ovarian:	n/a
6	chr4:7417336-7417386	HCM	heart:	n/a
7	chr4:7484382-7484432	GM12878	blood:	n/a
8	chr4:7528296-7528346	HNPCEpiC	eye:	n/a
9	chr4:7511100-7511150	Hela-S3	cervix:	n/a
10	chr4:7437027-7437077	MCF10A-Er-Src	breast:	n/a
11	chr4:7502947-7502997	ovcar-3	ovarian:	n/a
12	chr4:7417336-7417386	HCM	heart:	n/a
13	chr4:7502947-7502997	RPTEC	kidney:	n/a
14	chr4:7532607-7532657	NHBE	bronchial:	n/a
15	chr4:7508044-7508094	AoSMC	blood vessel:	n/a
16	chr4:7484382-7484432	ovcar-3	ovarian:	n/a
17	chr4:7427446-7427496	Jurkat	blood:	n/a
18	chr4:7437812-7437862	SKMC	muscle:	n/a
19	chr4:7437156-7437206	Caco-2	colon:	n/a
20	chr4:7502947-7502997	MCF-7	breast:	n/a
21	chr4:7512177-7512227	Hela-S3	cervix:	n/a
22	chr4:7434754-7434804	HCPEpiC	choroid plexus:	n/a
23	chr4:7438613-7438663	BE2_C	brain:	n/a
24	chr4:7434754-7434804	NHDF-neo	bronchial:	n/a
25	chr4:7502429-7502479	AoSMC	blood vessel:	n/a
26	chr4:7511100-7511150	SK-N-MC	brain:	n/a
27	chr4:7435357-7435407	Jurkat	blood:	n/a
28	chr4:7479912-7479962	GM06990	blood:	n/a
29	chr4:7463234-7463284	HRPEpiC	eye:	n/a
30	chr4:7436861-7436911	HL-60	blood:	n/a
31	chr4:7430936-7430986	BJ	skin:	n/a
32	chr4:7512177-7512227	AG04450	lung:	fetal
33	chr4:7518783-7518833	CMK	blood:	n/a
34	chr4:7437027-7437077	ECC-1	luminal epithelium:	n/a
35	chr4:7512177-7512227	U87	brain:	n/a
36	chr4:7532607-7532657	HCM	heart:	n/a
37	chr4:7436239-7436289	BE2_C	brain:	n/a
38	chr4:7436199-7436249	ECC-1	luminal epithelium:	n/a
39	chr4:7526639-7526689	GM12878	blood:	n/a
40	chr4:7528129-7528179	Hepatocyte	liver:	n/a
41	chr4:7463234-7463284	IMR90	lung:	fetal
42	chr4:7434754-7434804	PrEC	prostate:	n/a
43	chr4:7436259-7436309	SKMC	muscle:	n/a
44	chr4:7502947-7502997	K562	blood:	n/a
45	chr4:7528468-7528518	MCF-7	breast:	n/a
46	chr4:7436259-7436309	MCF-7	breast:	n/a
47	chr4:7512278-7512328	Caco-2	colon:	n/a
48	chr4:7435639-7435689	HCT-116	colon:	n/a
49	chr4:7532607-7532657	AG09309	skin:	n/a
50	chr4:7532607-7532657	Caco-2	colon:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:7436453..7438238-chr4:7441242..7443096,2	MCF-7	breast:
2	chr4:7421842..7424756-chr4:7435320..7437360,2	MCF-7	breast:
3	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
4	chr4:7516092..7517714-chr4:7519119..7521315,2	K562	blood:
5	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
6	chr4:7455060..7457538-chr4:7459563..7461357,2	K562	blood:
7	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
8	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
9	chr4:7529694..7531413-chr4:7534964..7537319,2	K562	blood:
10	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
11	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
12	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
13	chr4:7396272..7396793-chr4:7463896..7464564,2	MCF-7	breast:
14	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:
15	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
16	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
17	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:
18	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
19	chr4:7410518..7413253-chr4:7418283..7420136,2	K562	blood:
20	chr4:7475842..7476773-chr4:7652108..7653034,2	MCF-7	breast:
21	chr4:7430206..7433720-chr4:7434978..7437884,3	K562	blood:
22	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
23	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
24	chr4:7509518..7511220-chr4:7514824..7517339,2	K562	blood:
25	chr4:7513451..7515620-chr4:7531524..7533326,2	K562	blood:
26	chr4:7516846..7519696-chr4:7521879..7524111,2	K562	blood:
27	chr4:7420470..7422077-chr4:7425743..7427334,2	MCF-7	breast:
28	chr15:41624966..41625477-chr4:7539151..7539651,2	Hela-S3	cervix:
29	chr4:7444681..7447159-chr4:7457852..7459823,2	MCF-7	breast:
30	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
31	chr4:7445641..7447880-chr4:7451112..7453216,2	K562	blood:
32	chr4:7535311..7535864-chr4:7556278..7556945,2	MCF-7	breast:
33	chr4:7426666..7428188-chr4:7440042..7442576,2	MCF-7	breast:
34	chr4:7539171..7539671-chr6:30709977..30710667,2	Hela-S3	cervix:
35	chr4:7410518..7413253-chr4:7418283..7420136,2	K562	blood:
36	chr4:7421765..7423604-chr4:7439157..7441831,2	K562	blood:
37	chr4:7432269..7435967-chr4:7438458..7442398,4	MCF-7	breast:
38	chr4:7520525..7523407-chr4:7542100..7544094,2	K562	blood:
39	chr4:7452936..7455745-chr4:7457448..7459365,2	MCF-7	breast:
40	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
41	chr4:7524802..7527211-chr4:7527477..7529278,2	MCF-7	breast:
42	chr4:7474972..7476940-chr4:7478120..7479939,2	MCF-7	breast:
43	chr4:7412059..7414681-chr4:7420210..7422240,3	MCF-7	breast:
44	chr4:7540632..7544452-chr4:7547712..7552910,6	MCF-7	breast:
45	chr4:7529694..7531413-chr4:7534964..7537319,2	K562	blood:
46	chr4:7543788..7545988-chr4:7546899..7549006,2	K562	blood:
47	chr12:13044402..13044911-chr4:7539151..7539651,2	Hela-S3	cervix:
48	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
49	chr4:7428532..7430154-chr4:7431457..7433548,3	K562	blood:
50	chr4:7426666..7428188-chr4:7440042..7442576,2	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
ENSG00000137312	chromatin interactions
ENSG00000137804	chromatin interactions
ENSG00000013588	chromatin interactions

Extended variants
information (count: 8046 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:8046 , 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	rs10516186	chr4:7402284-7402285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539613542	chr4:7402290-7402291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77034564	chr4:7402304-7402305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140204813	chr4:7402327-7402328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187698761	chr4:7402355-7402356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114289271	chr4:7402359-7402360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13106023	chr4:7402360-7402361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191461372	chr4:7402441-7402442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184299309	chr4:7402445-7402446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143751210	chr4:7402464-7402465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7441975	chr4:7402476-7402477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7441976	chr4:7402484-7402485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7436489	chr4:7402485-7402486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13140023	chr4:7402497-7402498	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs553923668	chr4:7402504-7402505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs151304564	chr4:7402511-7402512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35527369	chr4:7402529-7402530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370738411	chr4:7402531-7402532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376789830	chr4:7402532-7402533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576507005	chr4:7402544-7402545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7436526	chr4:7402562-7402563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543889440	chr4:7402566-7402567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7441083	chr4:7402593-7402594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558919691	chr4:7402602-7402603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7666482	chr4:7402606-7402607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541199593	chr4:7402616-7402617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7441087	chr4:7402617-7402618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559636585	chr4:7402619-7402620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574752510	chr4:7402627-7402628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564771189	chr4:7402628-7402629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560938855	chr4:7402629-7402630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531349550	chr4:7402633-7402634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549823974	chr4:7402650-7402651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564797247	chr4:7402652-7402653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7434487	chr4:7402691-7402692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7437397	chr4:7402692-7402693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190018622	chr4:7402715-7402716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62644740	chr4:7402746-7402747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565981968	chr4:7402752-7402753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143097263	chr4:7402753-7402754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62644741	chr4:7402754-7402755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201543461	chr4:7402764-7402765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111161305	chr4:7402767-7402768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182846678	chr4:7402772-7402773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62644742	chr4:7402779-7402780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570017391	chr4:7402794-7402795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199997744	chr4:7402796-7402797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200651773	chr4:7402799-7402800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537176646	chr4:7402818-7402819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531477051	chr4:7402820-7402821	Weak transcription	n/a	n/a	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1180 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7399800-7404200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr4:7400000-7404800	Weak transcription	Left Ventricle	heart
3	chr4:7400200-7404800	Weak transcription	Pancreas	Pancrea
4	chr4:7400800-7404200	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:7400800-7404200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:7403200-7405400	Enhancers	Stomach Mucosa	stomach
7	chr4:7404000-7405400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:7404000-7405400	Enhancers	HMEC	breast
9	chr4:7404200-7405200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:7404200-7405400	Enhancers	Colon Smooth Muscle	Colon
11	chr4:7404200-7405400	Enhancers	Rectal Smooth Muscle	rectum
12	chr4:7404200-7405400	Enhancers	Stomach Smooth Muscle	stomach
13	chr4:7404400-7405200	Enhancers	Fetal Stomach	stomach
14	chr4:7404400-7405200	Enhancers	Right Ventricle	heart
15	chr4:7404400-7405200	Enhancers	NHEK	skin
16	chr4:7404600-7405400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:7404600-7405400	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr4:7404800-7405200	Enhancers	Fetal Intestine Small	intestine
19	chr4:7404800-7405200	Enhancers	Gastric	stomach
20	chr4:7404800-7405200	Enhancers	Pancreas	Pancrea
21	chr4:7404800-7405400	Enhancers	Left Ventricle	heart
22	chr4:7405000-7405200	Enhancers	NH-A	brain
23	chr4:7408800-7409200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr4:7410800-7411400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
25	chr4:7411000-7411200	Enhancers	Psoas Muscle	Psoas
26	chr4:7411400-7411600	Enhancers	Stomach Smooth Muscle	stomach
27	chr4:7411400-7413400	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr4:7411400-7414400	Enhancers	Colon Smooth Muscle	Colon
29	chr4:7411400-7415000	Enhancers	Fetal Brain Male	brain
30	chr4:7411600-7412000	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr4:7411600-7412800	Enhancers	Fetal Muscle Leg	muscle
32	chr4:7411600-7413200	Enhancers	Fetal Intestine Small	intestine
33	chr4:7411800-7412600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:7411800-7412800	Enhancers	Fetal Lung	lung
35	chr4:7411800-7413800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr4:7411800-7414000	Enhancers	Fetal Stomach	stomach
37	chr4:7411800-7414400	Enhancers	Rectal Smooth Muscle	rectum
38	chr4:7412000-7412200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:7412000-7412200	Enhancers	Aorta	Aorta
40	chr4:7412000-7412400	Enhancers	Stomach Smooth Muscle	stomach
41	chr4:7412200-7413600	Weak transcription	Aorta	Aorta
42	chr4:7412400-7412600	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr4:7412400-7414000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr4:7412600-7413200	Enhancers	Stomach Smooth Muscle	stomach
45	chr4:7412600-7415800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:7412800-7413200	Weak transcription	Fetal Lung	lung
47	chr4:7412800-7413200	Weak transcription	Fetal Muscle Leg	muscle
48	chr4:7412800-7413800	Enhancers	Fetal Muscle Trunk	muscle
49	chr4:7413000-7415000	Enhancers	Brain Germinal Matrix	brain
50	chr4:7413200-7413400	Flanking Active TSS	Stomach Smooth Muscle	stomach

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