Variant report

Variant	nsv887768
Chromosome Location	chr7:16910963-16946486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:397)
CpG islands
(count:430)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:16920513-16920521	K562	blood:	n/a	n/a
2	ATF1	chr7:16938123-16938126	K562	blood:	n/a	n/a
3	ATF3	chr7:16944740-16945401	A549	lung:	n/a	n/a
4	BCL3	chr7:16944794-16945427	A549	lung:	n/a	n/a
5	BCL3	chr7:16944766-16945589	A549	lung:	n/a	n/a
6	CEBPB	chr7:16934273-16934451	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:16939825-16940248	MCF-7	breast:	n/a	chr7:16940012-16940023
8	CEBPB	chr7:16939879-16940162	K562	blood:	n/a	chr7:16940012-16940023
9	CEBPB	chr7:16944788-16945468	A549	lung:	n/a	n/a
10	CEBPB	chr7:16939841-16940168	IMR90	lung:	n/a	chr7:16940012-16940023
11	CEBPB	chr7:16939862-16940157	H1-hESC	embryonic stem cell:	n/a	chr7:16940012-16940023
12	CEBPB	chr7:16939849-16940196	A549	lung:	n/a	chr7:16940012-16940023
13	CEBPB	chr7:16939900-16940158	Hela-S3	cervix:	n/a	chr7:16940012-16940023
14	CEBPB	chr7:16939841-16940183	HepG2	liver:	n/a	chr7:16940012-16940023
15	CEBPB	chr7:16934284-16934399	A549	lung:	n/a	n/a
16	CTCF	chr7:16931120-16931270	HCM	heart:	n/a	chr7:16931142-16931163
17	CTCF	chr7:16930901-16931427	MCF-7	breast:	n/a	chr7:16931142-16931163
18	CTCF	chr7:16931040-16931190	GM12878	blood:	n/a	chr7:16931142-16931163
19	CTCF	chr7:16931880-16932030	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr7:16931066-16931190	SK-N-SH_RA	brain:	n/a	chr7:16931142-16931163
21	CTCF	chr7:16931780-16931930	NHEK	skin:	n/a	n/a
22	CTCF	chr7:16931920-16932070	NHEK	skin:	n/a	n/a
23	CTCF	chr7:16931012-16931270	Hela-S3	cervix:	n/a	chr7:16931142-16931163
24	CTCF	chr7:16931916-16932010	NHEK	skin:	n/a	n/a
25	CTCF	chr7:16930982-16931320	K562	blood:	n/a	chr7:16931142-16931163
26	CTCF	chr7:16931100-16931250	BJ	skin:	n/a	chr7:16931142-16931163
27	CTCF	chr7:16931060-16931210	BE2_C	brain:	n/a	chr7:16931142-16931163
28	CTCF	chr7:16931023-16931269	NHEK	skin:	n/a	chr7:16931142-16931163
29	CTCF	chr7:16931021-16931324	H1-hESC	embryonic stem cell:	n/a	chr7:16931142-16931163
30	CTCF	chr7:16930823-16931442	MCF-7	breast:	n/a	chr7:16931142-16931163
31	CTCF	chr7:16931000-16931150	HAc	cerebellar:	n/a	n/a
32	CTCF	chr7:16931081-16931205	MCF-7	breast:	n/a	chr7:16931142-16931163
33	CTCF	chr7:16931060-16931210	GM12866	blood:	n/a	chr7:16931142-16931163
34	CTCF	chr7:16931080-16931230	MCF-7	breast:	n/a	chr7:16931142-16931163
35	CTCF	chr7:16931060-16931210	AG04449	skin:	n/a	chr7:16931142-16931163
36	CTCF	chr7:16931080-16931230	AG04449	skin:	n/a	chr7:16931142-16931163
37	CTCF	chr7:16931840-16931990	MCF-7	breast:	n/a	n/a
38	CTCF	chr7:16931051-16931203	GM19238	blood:	n/a	chr7:16931142-16931163
39	CTCF	chr7:16931040-16931190	GM12871	blood:	n/a	chr7:16931142-16931163
40	CTCF	chr7:16931043-16931269	Fibrobl	skin:	n/a	chr7:16931142-16931163
41	CTCF	chr7:16931040-16931190	WI-38	lung:	n/a	chr7:16931142-16931163
42	CTCF	chr7:16931120-16931270	NHDF-neo	bronchial:	n/a	chr7:16931142-16931163
43	CTCF	chr7:16931076-16931213	GM10266	blood:	n/a	chr7:16931142-16931163
44	CTCF	chr7:16931040-16931190	HL-60	blood:	n/a	chr7:16931142-16931163
45	CTCF	chr7:16931080-16931230	HMF	breast:	n/a	chr7:16931142-16931163
46	CTCF	chr7:16931120-16931270	HVMF	connective:	n/a	chr7:16931142-16931163
47	CTCF	chr7:16931100-16931250	GM12867	blood:	n/a	chr7:16931142-16931163
48	CTCF	chr7:16931920-16932070	SAEC	small airway:	n/a	n/a
49	CTCF	chr7:16931080-16931230	GM12865	blood:	n/a	chr7:16931142-16931163
50	CTCF	chr7:16931019-16931270	MCF-7	breast:	n/a	chr7:16931142-16931163

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16913845-16913895	HIPEpiC	eye:	n/a
2	chr7:16945442-16945492	AG04450	lung:	fetal
3	chr7:16922492-16922542	HepG2	liver:	n/a
4	chr7:16913845-16913895	HIPEpiC	eye:	n/a
5	chr7:16945442-16945492	AG04450	lung:	fetal
6	chr7:16922492-16922542	HepG2	liver:	n/a
7	chr7:16921699-16921749	RPTEC	kidney:	n/a
8	chr7:16945442-16945492	AG10803	skin:	n/a
9	chr7:16922421-16922471	NT2-D1	testis:	n/a
10	chr7:16922326-16922376	SAEC	small airway:	n/a
11	chr7:16922492-16922542	MCF-7	breast:	n/a
12	chr7:16920271-16920321	HNPCEpiC	eye:	n/a
13	chr7:16922421-16922471	GM06990	blood:	n/a
14	chr7:16920271-16920321	LNCaP	prostate:	n/a
15	chr7:16945442-16945492	SAEC	small airway:	n/a
16	chr7:16945442-16945492	AG04449	skin:	fetal
17	chr7:16922326-16922376	MCF-7	breast:	n/a
18	chr7:16922326-16922376	NT2-D1	testis:	n/a
19	chr7:16922326-16922376	Caco-2	colon:	n/a
20	chr7:16913845-16913895	HRPEpiC	eye:	n/a
21	chr7:16945442-16945492	K562	blood:	n/a
22	chr7:16945442-16945492	Caco-2	colon:	n/a
23	chr7:16945442-16945492	PrEC	prostate:	n/a
24	chr7:16945442-16945492	HAEpiC	amniotic membrane:	n/a
25	chr7:16913845-16913895	BE2_C	brain:	n/a
26	chr7:16921699-16921749	LNCaP	prostate:	n/a
27	chr7:16922326-16922376	HRE	kidney:	n/a
28	chr7:16913845-16913895	GM06990	blood:	n/a
29	chr7:16922421-16922471	Hela-S3	cervix:	n/a
30	chr7:16922492-16922542	GM12891	blood:	n/a
31	chr7:16922421-16922471	AG09319	gingival:	n/a
32	chr7:16945442-16945492	ProgFib	skin:	n/a
33	chr7:16922492-16922542	SKMC	muscle:	n/a
34	chr7:16945442-16945492	GM19239	blood:	n/a
35	chr7:16922326-16922376	AG04450	lung:	fetal
36	chr7:16945442-16945492	HEK293	kidney:	embryo
37	chr7:16913845-16913895	SAEC	small airway:	n/a
38	chr7:16945442-16945492	HCT-116	colon:	n/a
39	chr7:16913845-16913895	H1-hESC	embryonic stem cell:	embryo
40	chr7:16921699-16921749	NT2-D1	testis:	n/a
41	chr7:16913845-16913895	RPTEC	kidney:	n/a
42	chr7:16920271-16920321	PANC-1	pancreas:	n/a
43	chr7:16922492-16922542	BE2_C	brain:	n/a
44	chr7:16921699-16921749	NHBE	bronchial:	n/a
45	chr7:16922421-16922471	SK-N-MC	brain:	n/a
46	chr7:16945442-16945492	AG09309	skin:	n/a
47	chr7:16913845-16913895	CMK	blood:	n/a
48	chr7:16922492-16922542	HUVEC	blood vessel:	n/a
49	chr7:16921699-16921749	PrEC	prostate:	n/a
50	chr7:16922492-16922542	ovcar-3	ovarian:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
2	chr7:16930864..16931608-chr7:16957731..16958689,3	MCF-7	breast:
3	chr7:16834464..16837381-chr7:16917250..16920233,2	MCF-7	breast:
4	chr7:16793190..16795518-chr7:16923523..16926249,2	MCF-7	breast:
5	chr7:16842935..16845400-chr7:16919121..16922153,4	MCF-7	breast:
6	chr7:16929331..16931159-chr7:16956087..16958854,2	MCF-7	breast:
7	chr7:16825159..16826158-chr7:16919904..16920435,2	MCF-7	breast:
8	chr7:16839543..16841251-chr7:16918984..16920555,2	MCF-7	breast:
9	chr7:16928340..16931630-chr7:16941776..16947382,5	MCF-7	breast:
10	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
11	chr7:16944903..16947549-chr7:16951008..16952763,2	MCF-7	breast:
12	chr7:16930305..16931804-chr7:16957626..16958588,7	MCF-7	breast:
13	chr7:16931815..16932543-chr7:16957591..16958753,3	MCF-7	breast:
14	chr7:16840761..16845436-chr7:16917964..16923686,10	MCF-7	breast:
15	chr7:16930587..16933448-chr7:16954480..16956101,2	MCF-7	breast:
16	chr7:16922993..16923881-chr9:94630482..94631276,2	MCF-7	breast:
17	chr7:16942340..16948340-chr7:16954410..16958338,5	MCF-7	breast:
18	chr7:16795433..16797720-chr7:16943125..16945595,2	MCF-7	breast:
19	chr7:16929547..16932168-chr7:17718216..17720768,2	MCF-7	breast:
20	chr7:16909538..16911043-chr7:16914853..16916500,2	K562	blood:
21	chr7:16944622..16945221-chr7:16961355..16961992,2	MCF-7	breast:
22	chr7:16918898..16922214-chr7:16923893..16926911,3	MCF-7	breast:
23	chr7:16920618..16921311-chr8:99380929..99381723,2	MCF-7	breast:
24	chr7:16850191..16850816-chr7:16919955..16920542,2	MCF-7	breast:
25	chr7:16843625..16845723-chr7:16926394..16928363,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN13-1	chr7:16928245-16928509	NONHSAT119308
2	lnc-AGR2-1	chr7:16913040-16913467	NONHSAT119307
3	lnc-AGR2-1	chr7:16918134-16918269	NONHSAT119307
4	lnc-AGR2-1	chr7:16921568-16921597	NONHSAT119307

No data

Variant related genes	Relation type
AGR3	TF binding region
ENSG00000227965	TF binding region
AGR3	CpG island
ENSG00000227965	CpG island
ENSG00000173467	chromatin interactions
ENSG00000228675	chromatin interactions
ENSG00000106541	chromatin interactions

Extended variants
information (count: 1668 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12672303	chr7:16910963-16910964	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535877993	chr7:16910968-16910969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149299902	chr7:16910969-16910970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576035274	chr7:16911019-16911020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79971236	chr7:16911020-16911021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189010875	chr7:16911024-16911025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543985797	chr7:16911038-16911039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs180840059	chr7:16911068-16911069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs577096975	chr7:16911077-16911078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541300487	chr7:16911101-16911102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559638216	chr7:16911108-16911109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376682588	chr7:16911131-16911132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs185879054	chr7:16911139-16911140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563800297	chr7:16911192-16911193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190164021	chr7:16911202-16911203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549934377	chr7:16911204-16911205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372901084	chr7:16911241-16911242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571438904	chr7:16911279-16911280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144521719	chr7:16911306-16911307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181712256	chr7:16911335-16911336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186600561	chr7:16911350-16911351	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536238833	chr7:16911359-16911360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553476306	chr7:16911381-16911382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572988996	chr7:16911385-16911386	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139787390	chr7:16911402-16911403	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370958845	chr7:16911412-16911413	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540860544	chr7:16911420-16911421	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558254728	chr7:16911422-16911423	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6949436	chr7:16911439-16911440	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs6969588	chr7:16911443-16911444	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553206980	chr7:16911450-16911451	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541484498	chr7:16911451-16911452	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140713118	chr7:16911453-16911454	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142373899	chr7:16911460-16911461	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13237263	chr7:16911517-16911518	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563568158	chr7:16911522-16911523	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs151277206	chr7:16911530-16911531	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs573836872	chr7:16911543-16911544	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545941741	chr7:16911549-16911550	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs115886932	chr7:16911584-16911585	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532298449	chr7:16911607-16911608	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74349257	chr7:16911612-16911613	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547658607	chr7:16911639-16911640	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145717971	chr7:16911666-16911667	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565968188	chr7:16911673-16911674	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529975087	chr7:16911697-16911698	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs548145913	chr7:16911702-16911703	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373883510	chr7:16911721-16911722	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368508755	chr7:16911722-16911723	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371864765	chr7:16911728-16911729	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16891800-16920200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:16892600-16915600	Weak transcription	Stomach Mucosa	stomach
3	chr7:16901200-16911800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:16902000-16911400	Weak transcription	Duodenum Mucosa	Duodenum
5	chr7:16902200-16911600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr7:16905800-16913000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr7:16909400-16911000	Weak transcription	Fetal Intestine Small	intestine
8	chr7:16910600-16915600	Strong transcription	Fetal Intestine Large	intestine
9	chr7:16911000-16911600	Strong transcription	Fetal Intestine Small	intestine
10	chr7:16911400-16914000	Strong transcription	Duodenum Mucosa	Duodenum
11	chr7:16911600-16914200	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr7:16911600-16917000	Weak transcription	Fetal Intestine Small	intestine
13	chr7:16911800-16913800	Strong transcription	Rectal Mucosa Donor 29	rectum
14	chr7:16912600-16920000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:16913000-16914400	Enhancers	Placenta Amnion	Placenta Amnion
16	chr7:16913800-16917800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr7:16914000-16918000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr7:16914200-16919000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr7:16914400-16920200	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:16915600-16916200	Weak transcription	Fetal Intestine Large	intestine
21	chr7:16915600-16916600	Enhancers	Stomach Mucosa	stomach
22	chr7:16915800-16916200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr7:16916200-16917000	Enhancers	Fetal Intestine Large	intestine
24	chr7:16916600-16917800	Weak transcription	Stomach Mucosa	stomach
25	chr7:16917000-16917400	Weak transcription	Fetal Intestine Large	intestine
26	chr7:16917000-16918200	Enhancers	Fetal Intestine Small	intestine
27	chr7:16917400-16918200	Enhancers	Fetal Intestine Large	intestine
28	chr7:16917800-16918000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr7:16917800-16918000	Enhancers	Stomach Mucosa	stomach
30	chr7:16918000-16918200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:16918000-16920200	Weak transcription	Stomach Mucosa	stomach
32	chr7:16918000-16921600	Active TSS	Duodenum Mucosa	Duodenum
33	chr7:16918200-16918400	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr7:16918200-16918400	Enhancers	Small Intestine	intestine
35	chr7:16918200-16918600	Flanking Active TSS	Fetal Intestine Small	intestine
36	chr7:16918200-16922000	Active TSS	Rectal Mucosa Donor 29	rectum
37	chr7:16918400-16922000	Active TSS	Fetal Intestine Large	intestine
38	chr7:16918600-16922000	Active TSS	Fetal Intestine Small	intestine
39	chr7:16919000-16922000	Active TSS	Rectal Mucosa Donor 31	rectum
40	chr7:16919400-16921200	Active TSS	Colonic Mucosa	Colon
41	chr7:16919600-16920000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:16919600-16921200	Active TSS	Rectal Smooth Muscle	rectum
43	chr7:16920000-16920400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:16920000-16921800	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr7:16920200-16920800	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr7:16920200-16920800	Active TSS	Stomach Mucosa	stomach
47	chr7:16920200-16921400	Active TSS	Fetal Stomach	stomach
48	chr7:16920200-16921400	Active TSS	Placenta Amnion	Placenta Amnion
49	chr7:16920400-16920600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr7:16920400-16920600	Enhancers	Pancreas	Pancrea

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