Variant report

Variant	nsv881341
Chromosome Location	chr4:165661477-165721118
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:165669639-165669801	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:165669588-165669845	K562	blood:	n/a	n/a
3	ATF2	chr4:165720564-165721044	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:165720732-165721021	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr4:165700918-165701211	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:165669591-165669785	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:165717007-165717087	GM12878	blood:	n/a	n/a
8	CEBPB	chr4:165692173-165692638	ECC-1	luminal epithelium:	n/a	chr4:165692403-165692414
9	CEBPB	chr4:165692223-165692618	MCF-7	breast:	n/a	chr4:165692403-165692414
10	CEBPB	chr4:165692203-165692553	A549	lung:	n/a	chr4:165692403-165692414
11	CEBPB	chr4:165692232-165692567	K562	blood:	n/a	chr4:165692403-165692414
12	CEBPB	chr4:165692224-165692580	HepG2	liver:	n/a	chr4:165692403-165692414
13	CEBPB	chr4:165692199-165692681	MCF-7	breast:	n/a	chr4:165692403-165692414
14	CEBPB	chr4:165692825-165692980	K562	blood:	n/a	n/a
15	CEBPB	chr4:165692157-165692673	ECC-1	luminal epithelium:	n/a	chr4:165692403-165692414
16	CEBPB	chr4:165720669-165721107	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:165692230-165692583	A549	lung:	n/a	chr4:165692403-165692414
18	CEBPB	chr4:165692225-165692594	IMR90	lung:	n/a	chr4:165692403-165692414
19	CEBPB	chr4:165692217-165692595	Hela-S3	cervix:	n/a	chr4:165692403-165692414
20	CEBPB	chr4:165692281-165692594	H1-hESC	embryonic stem cell:	n/a	chr4:165692403-165692414
21	CHD2	chr4:165693287-165693544	K562	blood:	n/a	n/a
22	CHD2	chr4:165720619-165721136	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr4:165717046-165717101	GM12878	blood:	n/a	n/a
24	CTCF	chr4:165689480-165689630	NHEK	skin:	n/a	n/a
25	CTCF	chr4:165669940-165670090	GM06990	blood:	n/a	n/a
26	CTCF	chr4:165689800-165689950	AoAF	blood vessel:	n/a	chr4:165689860-165689878 chr4:165689865-165689873 chr4:165689861-165689877 chr4:165689862-165689883
27	CTCF	chr4:165689639-165690076	MCF-7	breast:	n/a	chr4:165689860-165689878 chr4:165689865-165689873 chr4:165689861-165689877 chr4:165689862-165689883
28	CTCF	chr4:165669667-165669754	GM10266	blood:	n/a	chr4:165669714-165669730 chr4:165669718-165669726 chr4:165669708-165669729 chr4:165669713-165669731 chr4:165669715-165669728
29	CTCF	chr4:165689860-165690010	NHDF-neo	bronchial:	n/a	chr4:165689861-165689877 chr4:165689862-165689883 chr4:165689865-165689873 chr4:165689860-165689878
30	CTCF	chr4:165689740-165689890	HMEC	breast:	n/a	chr4:165689860-165689878 chr4:165689865-165689873 chr4:165689861-165689877 chr4:165689862-165689883
31	CTCF	chr4:165669960-165670110	AG09309	skin:	n/a	n/a
32	CTCF	chr4:165669660-165669810	HUVEC	blood vessel:	n/a	chr4:165669714-165669730 chr4:165669718-165669726 chr4:165669708-165669729 chr4:165669713-165669731 chr4:165669715-165669728
33	CTCF	chr4:165669600-165669750	SK-N-SH_RA	brain:	n/a	chr4:165669714-165669730 chr4:165669718-165669726 chr4:165669708-165669729 chr4:165669713-165669731 chr4:165669715-165669728
34	CTCF	chr4:165689800-165689950	GM12865	blood:	n/a	chr4:165689860-165689878 chr4:165689865-165689873 chr4:165689861-165689877 chr4:165689862-165689883
35	CTCF	chr4:165701020-165701170	GM12801	blood:	n/a	chr4:165701081-165701099
36	CTCF	chr4:165700975-165701199	A549	lung:	n/a	chr4:165701081-165701099
37	CTCF	chr4:165700955-165701236	MCF-7	breast:	n/a	chr4:165701081-165701099
38	CTCF	chr4:165689680-165689830	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:165701080-165701230	HCT-116	colon:	n/a	chr4:165701081-165701099
40	CTCF	chr4:165700970-165701203	Kidney_OC	kidney:	n/a	chr4:165701081-165701099
41	CTCF	chr4:165681220-165681370	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr4:165701080-165701230	A549	lung:	n/a	chr4:165701081-165701099
43	CTCF	chr4:165700943-165701157	A549	lung:	n/a	chr4:165701081-165701099
44	CTCF	chr4:165690080-165690230	NHLF	lung:	n/a	n/a
45	CTCF	chr4:165669640-165669790	GM12873	blood:	n/a	chr4:165669714-165669730 chr4:165669718-165669726 chr4:165669708-165669729 chr4:165669713-165669731 chr4:165669715-165669728
46	CTCF	chr4:165701020-165701170	RPTEC	kidney:	n/a	chr4:165701081-165701099
47	CTCF	chr4:165681180-165681330	HCT-116	colon:	n/a	n/a
48	CTCF	chr4:165701040-165701190	HCM	heart:	n/a	chr4:165701081-165701099
49	CTCF	chr4:165669840-165669990	GM12871	blood:	n/a	n/a
50	CTCF	chr4:165669645-165669911	GM13977	blood:	n/a	chr4:165669714-165669730 chr4:165669718-165669726 chr4:165669708-165669729 chr4:165669713-165669731 chr4:165669715-165669728

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165675138-165675188	SK-N-SH_RA	brain:	n/a
2	chr4:165675138-165675188	SK-N-SH_RA	brain:	n/a
3	chr4:165675069-165675119	PrEC	prostate:	n/a
4	chr4:165675069-165675119	HCT-116	colon:	n/a
5	chr4:165675069-165675119	GM12878	blood:	n/a
6	chr4:165675069-165675119	HRE	kidney:	n/a
7	chr4:165675138-165675188	GM12892	blood:	n/a
8	chr4:165675069-165675119	RPTEC	kidney:	n/a
9	chr4:165675138-165675188	SKMC	muscle:	n/a
10	chr4:165675069-165675119	ovcar-3	ovarian:	n/a
11	chr4:165672394-165672444	HEK293	kidney:	embryo
12	chr4:165675069-165675119	MCF-7	breast:	n/a
13	chr4:165675138-165675188	PFSK-1	brain:	n/a
14	chr4:165675138-165675188	NHDF-neo	bronchial:	n/a
15	chr4:165675138-165675188	HEK293	kidney:	embryo
16	chr4:165675138-165675188	AG09309	skin:	n/a
17	chr4:165672394-165672444	AG09309	skin:	n/a
18	chr4:165672394-165672444	HCPEpiC	choroid plexus:	n/a
19	chr4:165675069-165675119	PANC-1	pancreas:	n/a
20	chr4:165675069-165675119	NHBE	bronchial:	n/a
21	chr4:165675069-165675119	AoSMC	blood vessel:	n/a
22	chr4:165675138-165675188	Caco-2	colon:	n/a
23	chr4:165675069-165675119	CMK	blood:	n/a
24	chr4:165675138-165675188	GM12878	blood:	n/a
25	chr4:165675138-165675188	HIPEpiC	eye:	n/a
26	chr4:165675069-165675119	HL-60	blood:	n/a
27	chr4:165675069-165675119	AG04449	skin:	fetal
28	chr4:165675138-165675188	RPTEC	kidney:	n/a
29	chr4:165675069-165675119	GM12891	blood:	n/a
30	chr4:165675138-165675188	HCT-116	colon:	n/a
31	chr4:165672394-165672444	PFSK-1	brain:	n/a
32	chr4:165675069-165675119	HRCEpiC	kidney:	n/a
33	chr4:165675069-165675119	AG04450	lung:	fetal
34	chr4:165672394-165672444	NT2-D1	testis:	n/a
35	chr4:165675138-165675188	HNPCEpiC	eye:	n/a
36	chr4:165672394-165672444	ovcar-3	ovarian:	n/a
37	chr4:165675138-165675188	HRE	kidney:	n/a
38	chr4:165675138-165675188	BJ	skin:	n/a
39	chr4:165672394-165672444	LNCaP	prostate:	n/a
40	chr4:165672394-165672444	HCF	heart:	n/a
41	chr4:165675138-165675188	CMK	blood:	n/a
42	chr4:165672394-165672444	NB4	blood:	n/a
43	chr4:165675069-165675119	T-47D	breast:	n/a
44	chr4:165675138-165675188	GM06990	blood:	n/a
45	chr4:165675069-165675119	MCF10A-Er-Src	breast:	n/a
46	chr4:165672394-165672444	HRCEpiC	kidney:	n/a
47	chr4:165675069-165675119	AG09319	gingival:	n/a
48	chr4:165672394-165672444	SK-N-MC	brain:	n/a
49	chr4:165675138-165675188	NH-A	brain:	n/a
50	chr4:165675138-165675188	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:165700594..165701568-chr4:166017670..166018467,3	K562	blood:
2	chr4:165701014..165701543-chr4:165856051..165856573,2	MCF-7	breast:
3	chr4:165700661..165701216-chr4:165804953..165805488,2	MCF-7	breast:
4	chr4:165698401..165701010-chr4:165876309..165878904,2	MCF-7	breast:
5	chr4:165680979..165683517-chr4:165704780..165706574,2	K562	blood:
6	chr4:165662552..165665240-chr4:165667378..165668885,2	K562	blood:
7	chr4:165662552..165665240-chr4:165667378..165668885,2	K562	blood:
8	chr2:164115997..164116846-chr4:165677534..165678338,2	MCF-7	breast:
9	chr4:165699281..165700032-chr4:165856272..165857241,2	MCF-7	breast:
10	chr4:164470993..164471692-chr4:165669595..165670148,2	MCF-7	breast:
11	chr4:165700977..165701537-chr4:165804617..165805893,3	MCF-7	breast:
12	chr4:165717917..165720004-chr4:165723969..165725996,2	MCF-7	breast:
13	chr4:165694682..165697477-chr4:165698117..165700423,3	K562	blood:
14	chr4:165689047..165689634-chr4:165918458..165919146,2	MCF-7	breast:
15	chr4:165694682..165697477-chr4:165698117..165700423,3	K562	blood:
16	chr4:165680979..165683517-chr4:165704780..165706574,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-2	chr4:165691571-165691707	ENSG00000248771
2	lnc-C4orf39-2	chr4:165718691-165718758	NONHSAT099078
3	lnc-C4orf39-2	chr4:165675283-165675563	ENSG00000248771
4	lnc-C4orf39-2	chr4:165691571-165691836	NONHSAT099075
5	lnc-C4orf39-2	chr4:165676874-165677139	FPKM1_group_24399_transcript_1
6	lnc-C4orf39-2	chr4:165675216-165675327	ENSG00000248771
7	lnc-C4orf39-2	chr4:165675241-165675563	NONHSAT099075
8	lnc-C4orf39-2	chr4:165675463-165675563	ENSG00000248771
9	lnc-C4orf39-2	chr4:165691571-165691707	ENSG00000248771
10	lnc-C4orf39-2	chr4:165675241-165675563	FPKM1_group_24399_transcript_1

Variant related genes	Relation type
RNU6-668P	TF binding region
ENSG00000248771	TF binding region
RNU6-668P	CpG island
ENSG00000248771	CpG island
ENSG00000250486	chromatin interactions

Extended variants
information (count: 2121 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2121 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117590146	chr4:165670025-165670026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553125500	chr4:165670040-165670041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566517656	chr4:165670080-165670081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28396291	chr4:165670091-165670092	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549019720	chr4:165670095-165670096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567867165	chr4:165670172-165670173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114537374	chr4:165670264-165670265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28587555	chr4:165670272-165670273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs184228994	chr4:165670273-165670274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539332517	chr4:165670274-165670275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557798037	chr4:165670279-165670280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572832055	chr4:165670288-165670289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540351327	chr4:165670325-165670326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201491280	chr4:165670330-165670331	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs199629241	chr4:165670345-165670346	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs561596291	chr4:165670347-165670348	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs539281673	chr4:165670357-165670358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs112295059	chr4:165670364-165670365	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs28708774	chr4:165670367-165670368	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs77342750	chr4:165670387-165670388	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs75699942	chr4:165670408-165670409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28871390	chr4:165670427-165670428	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557196128	chr4:165670431-165670432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs11734006	chr4:165670469-165670470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533095687	chr4:165670474-165670475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs28763310	chr4:165670503-165670504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560115155	chr4:165670510-165670511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74350954	chr4:165670551-165670552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79021201	chr4:165670561-165670562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189454974	chr4:165670563-165670564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549472387	chr4:165670571-165670572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567687394	chr4:165670575-165670576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374923429	chr4:165670584-165670585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150165759	chr4:165670590-165670591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs202026267	chr4:165670591-165670592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56933140	chr4:165670607-165670608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62352371	chr4:165670617-165670618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs180908492	chr4:165670630-165670631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573759017	chr4:165670655-165670656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539344605	chr4:165670664-165670665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539995729	chr4:165670687-165670688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554477558	chr4:165670689-165670690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572895269	chr4:165670724-165670725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185791029	chr4:165670774-165670775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10025404	chr4:165670811-165670812	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs573703607	chr4:165670815-165670816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544284016	chr4:165670868-165670869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116384256	chr4:165670869-165670870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577368147	chr4:165670915-165670916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544920825	chr4:165670996-165670997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165670000-165670400	Enhancers	Fetal Intestine Small	intestine
2	chr4:165670400-165671600	Weak transcription	Fetal Intestine Small	intestine
3	chr4:165671600-165671800	Enhancers	Fetal Intestine Small	intestine
4	chr4:165673400-165687000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:165674400-165675200	Enhancers	Colonic Mucosa	Colon
6	chr4:165674600-165674800	Flanking Active TSS	Duodenum Mucosa	Duodenum
7	chr4:165674600-165674800	Enhancers	Fetal Intestine Small	intestine
8	chr4:165674600-165674800	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr4:165674600-165674800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr4:165674600-165675000	Enhancers	Fetal Intestine Large	intestine
11	chr4:165674800-165676400	Active TSS	Fetal Intestine Small	intestine
12	chr4:165674800-165677200	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr4:165674800-165678200	Active TSS	Duodenum Mucosa	Duodenum
14	chr4:165674800-165678200	Active TSS	Rectal Mucosa Donor 31	rectum
15	chr4:165675200-165675600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:165675200-165675600	Enhancers	Liver	Liver
17	chr4:165675200-165675600	Active TSS	Colonic Mucosa	Colon
18	chr4:165675200-165675600	Enhancers	Fetal Stomach	stomach
19	chr4:165675200-165675800	Active TSS	Fetal Intestine Large	intestine
20	chr4:165675200-165676000	Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr4:165675400-165675600	Flanking Active TSS	Stomach Mucosa	stomach
22	chr4:165675600-165681000	Weak transcription	Stomach Mucosa	stomach
23	chr4:165676400-165676600	Flanking Active TSS	Fetal Intestine Small	intestine
24	chr4:165676600-165676800	Enhancers	Fetal Intestine Small	intestine
25	chr4:165676800-165677000	Flanking Active TSS	Fetal Intestine Small	intestine
26	chr4:165677000-165680800	Weak transcription	Fetal Intestine Small	intestine
27	chr4:165677200-165678000	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr4:165678000-165678400	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr4:165678200-165678400	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr4:165678200-165681400	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr4:165678400-165681000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr4:165678400-165682600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr4:165680800-165687200	Enhancers	Fetal Intestine Small	intestine
34	chr4:165681000-165681400	Enhancers	Duodenum Mucosa	Duodenum
35	chr4:165681000-165681400	Enhancers	Stomach Mucosa	stomach
36	chr4:165681200-165684400	Enhancers	Fetal Intestine Large	intestine
37	chr4:165681400-165681600	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr4:165681400-165682600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr4:165681400-165682600	Weak transcription	Stomach Mucosa	stomach
40	chr4:165681400-165685000	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr4:165681600-165682600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:165682600-165683400	Enhancers	Duodenum Mucosa	Duodenum
43	chr4:165682600-165683400	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr4:165682600-165683400	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr4:165682600-165683400	Enhancers	Stomach Mucosa	stomach
46	chr4:165683400-165684800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr4:165683400-165686200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr4:165683400-165686400	Weak transcription	Stomach Mucosa	stomach
49	chr4:165684400-165684800	Weak transcription	Fetal Intestine Large	intestine
50	chr4:165684800-165685000	Enhancers	Fetal Intestine Large	intestine

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