Variant report

Variant	nsv522109
Chromosome Location	chr7:16908545-16946486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:429)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 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	chr7:16938123-16938126	K562	blood:	n/a	n/a
2	ATF1	chr7:16920513-16920521	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	chr7:16939841-16940183	HepG2	liver:	n/a	chr7:16940012-16940023
7	CEBPB	chr7:16944788-16945468	A549	lung:	n/a	n/a
8	CEBPB	chr7:16934273-16934451	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:16939879-16940162	K562	blood:	n/a	chr7:16940012-16940023
10	CEBPB	chr7:16939825-16940248	MCF-7	breast:	n/a	chr7:16940012-16940023
11	CEBPB	chr7:16939900-16940158	Hela-S3	cervix:	n/a	chr7:16940012-16940023
12	CEBPB	chr7:16939841-16940168	IMR90	lung:	n/a	chr7:16940012-16940023
13	CEBPB	chr7:16934284-16934399	A549	lung:	n/a	n/a
14	CEBPB	chr7:16939849-16940196	A549	lung:	n/a	chr7:16940012-16940023
15	CEBPB	chr7:16939862-16940157	H1-hESC	embryonic stem cell:	n/a	chr7:16940012-16940023
16	CTCF	chr7:16931060-16931210	AG09319	gingival:	n/a	chr7:16931142-16931163
17	CTCF	chr7:16931920-16932070	SAEC	small airway:	n/a	n/a
18	CTCF	chr7:16930823-16931442	MCF-7	breast:	n/a	chr7:16931142-16931163
19	CTCF	chr7:16931080-16931230	AG04449	skin:	n/a	chr7:16931142-16931163
20	CTCF	chr7:16931040-16931190	HEK293	kidney:	n/a	chr7:16931142-16931163
21	CTCF	chr7:16931880-16932030	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr7:16931021-16931324	H1-hESC	embryonic stem cell:	n/a	chr7:16931142-16931163
23	CTCF	chr7:16931040-16931190	K562	blood:	n/a	chr7:16931142-16931163
24	CTCF	chr7:16931840-16931990	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr7:16931020-16931170	NHEK	skin:	n/a	chr7:16931142-16931163
26	CTCF	chr7:16931080-16931230	HVMF	connective:	n/a	chr7:16931142-16931163
27	CTCF	chr7:16931020-16931170	GM12873	blood:	n/a	chr7:16931142-16931163
28	CTCF	chr7:16931080-16931230	HMF	breast:	n/a	chr7:16931142-16931163
29	CTCF	chr7:16931060-16931210	WERI-Rb-1	eye:	n/a	chr7:16931142-16931163
30	CTCF	chr7:16930942-16931341	IMR90	lung:	n/a	chr7:16931142-16931163
31	CTCF	chr7:16931060-16931210	A549	lung:	n/a	chr7:16931142-16931163
32	CTCF	chr7:16931780-16931930	NHEK	skin:	n/a	n/a
33	CTCF	chr7:16931060-16931210	BJ	skin:	n/a	chr7:16931142-16931163
34	CTCF	chr7:16931060-16931210	Hela-S3	cervix:	n/a	chr7:16931142-16931163
35	CTCF	chr7:16931081-16931205	MCF-7	breast:	n/a	chr7:16931142-16931163
36	CTCF	chr7:16931020-16931276	LNCaP	prostate:	n/a	chr7:16931142-16931163
37	CTCF	chr7:16931020-16931170	GM06990	blood:	n/a	chr7:16931142-16931163
38	CTCF	chr7:16931060-16931210	HCPEpiC	choroid plexus:	n/a	chr7:16931142-16931163
39	CTCF	chr7:16931880-16932030	Caco-2	colon:	n/a	n/a
40	CTCF	chr7:16931041-16931246	ProgFib	skin:	n/a	chr7:16931142-16931163
41	CTCF	chr7:16931120-16931270	WI-38	lung:	n/a	chr7:16931142-16931163
42	CTCF	chr7:16930985-16931232	K562	blood:	n/a	chr7:16931142-16931163
43	CTCF	chr7:16931100-16931250	GM12867	blood:	n/a	chr7:16931142-16931163
44	CTCF	chr7:16931040-16931190	GM12870	blood:	n/a	chr7:16931142-16931163
45	CTCF	chr7:16930980-16931130	HCM	heart:	n/a	n/a
46	CTCF	chr7:16931043-16931269	Fibrobl	skin:	n/a	chr7:16931142-16931163
47	CTCF	chr7:16931060-16931210	GM12875	blood:	n/a	chr7:16931142-16931163
48	CTCF	chr7:16931080-16931230	NHDF-neo	bronchial:	n/a	chr7:16931142-16931163
49	CTCF	chr7:16930897-16931342	A549	lung:	n/a	chr7:16931142-16931163
50	CTCF	chr7:16931100-16931250	MCF-7	breast:	n/a	chr7:16931142-16931163

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16920271-16920321	HMEC	breast:	n/a
2	chr7:16922492-16922542	LNCaP	prostate:	n/a
3	chr7:16920271-16920321	HMEC	breast:	n/a
4	chr7:16922492-16922542	LNCaP	prostate:	n/a
5	chr7:16922421-16922471	MCF10A-Er-Src	breast:	n/a
6	chr7:16922492-16922542	ovcar-3	ovarian:	n/a
7	chr7:16922421-16922471	GM19239	blood:	n/a
8	chr7:16920271-16920321	SKMC	muscle:	n/a
9	chr7:16921699-16921749	SAEC	small airway:	n/a
10	chr7:16922326-16922376	HCM	heart:	n/a
11	chr7:16922492-16922542	HepG2	liver:	n/a
12	chr7:16920271-16920321	GM12891	blood:	n/a
13	chr7:16922326-16922376	RPTEC	kidney:	n/a
14	chr7:16922421-16922471	HCPEpiC	choroid plexus:	n/a
15	chr7:16922421-16922471	GM06990	blood:	n/a
16	chr7:16913845-16913895	IMR90	lung:	fetal
17	chr7:16921699-16921749	HCF	heart:	n/a
18	chr7:16921699-16921749	SK-N-MC	brain:	n/a
19	chr7:16920271-16920321	ProgFib	skin:	n/a
20	chr7:16945442-16945492	Caco-2	colon:	n/a
21	chr7:16922421-16922471	HCF	heart:	n/a
22	chr7:16922492-16922542	AG09309	skin:	n/a
23	chr7:16920271-16920321	HUVEC	blood vessel:	n/a
24	chr7:16922421-16922471	SAEC	small airway:	n/a
25	chr7:16922421-16922471	GM12878	blood:	n/a
26	chr7:16920271-16920321	LNCaP	prostate:	n/a
27	chr7:16922326-16922376	ProgFib	skin:	n/a
28	chr7:16922326-16922376	AG09309	skin:	n/a
29	chr7:16922326-16922376	K562	blood:	n/a
30	chr7:16922492-16922542	GM19239	blood:	n/a
31	chr7:16913845-16913895	HCPEpiC	choroid plexus:	n/a
32	chr7:16922421-16922471	H1-hESC	embryonic stem cell:	embryo
33	chr7:16920271-16920321	SK-N-SH_RA	brain:	n/a
34	chr7:16922421-16922471	BE2_C	brain:	n/a
35	chr7:16922421-16922471	U87	brain:	n/a
36	chr7:16922492-16922542	U87	brain:	n/a
37	chr7:16913845-16913895	HNPCEpiC	eye:	n/a
38	chr7:16922492-16922542	PFSK-1	brain:	n/a
39	chr7:16920271-16920321	A549	lung:	n/a
40	chr7:16922326-16922376	HEEpiC	esophagus:	n/a
41	chr7:16913845-16913895	PFSK-1	brain:	n/a
42	chr7:16945442-16945492	U87	brain:	n/a
43	chr7:16922326-16922376	HRPEpiC	eye:	n/a
44	chr7:16920271-16920321	HCT-116	colon:	n/a
45	chr7:16921699-16921749	HL-60	blood:	n/a
46	chr7:16920271-16920321	HRCEpiC	kidney:	n/a
47	chr7:16945442-16945492	SAEC	small airway:	n/a
48	chr7:16920271-16920321	SAEC	small airway:	n/a
49	chr7:16922492-16922542	HMEC	breast:	n/a
50	chr7:16922326-16922376	HCF	heart:	n/a

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

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

(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	chr7:16918134-16918269	NONHSAT119307
3	lnc-AGR2-1	chr7:16913040-16913467	NONHSAT119307
4	lnc-AGR2-1	chr7:16921568-16921597	NONHSAT119307

No data

Variant related genes	Relation type
AGR3	TF binding region
ENSG00000227965	TF binding region
RAD17P1	TF binding region
AGR3	CpG island
ENSG00000227965	CpG island
RAD17P1	CpG island
ENSG00000106541	chromatin interactions
ENSG00000173467	chromatin interactions
ENSG00000228675	chromatin interactions

Extended variants
information (count: 1774 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2471907	chr7:16908545-16908546	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs113930465	chr7:16908554-16908555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192925074	chr7:16908568-16908569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533090738	chr7:16908584-16908585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7787112	chr7:16908585-16908586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567099317	chr7:16908588-16908589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77210081	chr7:16908617-16908618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183842027	chr7:16908620-16908621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7804221	chr7:16908621-16908622	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs7804082	chr7:16908631-16908632	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs558535762	chr7:16908639-16908640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs556568296	chr7:16908690-16908691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs151219286	chr7:16908697-16908698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117942360	chr7:16908711-16908712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537478357	chr7:16908725-16908726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4521666	chr7:16908741-16908742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs573924743	chr7:16908745-16908746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571330539	chr7:16908762-16908763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540045157	chr7:16908771-16908772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs555194195	chr7:16908778-16908779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543126299	chr7:16908831-16908832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573921642	chr7:16908896-16908897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139723659	chr7:16908908-16908909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186979857	chr7:16908932-16908933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2471906	chr7:16908956-16908957	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571910428	chr7:16908979-16908980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7787787	chr7:16909013-16909014	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs201011514	chr7:16909039-16909040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564078060	chr7:16909077-16909078	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117697267	chr7:16909090-16909091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145350910	chr7:16909091-16909092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549602735	chr7:16909142-16909143	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs573923200	chr7:16909158-16909159	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs567861347	chr7:16909162-16909163	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs2254186	chr7:16909168-16909169	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532065678	chr7:16909266-16909267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs549885050	chr7:16909277-16909278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567095909	chr7:16909297-16909298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373236083	chr7:16909298-16909299	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs5012362	chr7:16909302-16909303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372484586	chr7:16909303-16909304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201202406	chr7:16909304-16909305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201983765	chr7:16909307-16909308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76838818	chr7:16909308-16909309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs71007797	chr7:16909318-16909319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542896968	chr7:16909436-16909437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11769254	chr7:16909487-16909488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142447908	chr7:16909511-16909512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565837767	chr7:16909530-16909531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs533732018	chr7:16909531-16909532	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:182 , 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	chr7:16906200-16909000	Weak transcription	Fetal Intestine Large	intestine
8	chr7:16908200-16909000	Weak transcription	Fetal Intestine Small	intestine
9	chr7:16909000-16909400	Strong transcription	Fetal Intestine Large	intestine
10	chr7:16909000-16909400	Strong transcription	Fetal Intestine Small	intestine
11	chr7:16909400-16910600	Weak transcription	Fetal Intestine Large	intestine
12	chr7:16909400-16911000	Weak transcription	Fetal Intestine Small	intestine
13	chr7:16910600-16915600	Strong transcription	Fetal Intestine Large	intestine
14	chr7:16911000-16911600	Strong transcription	Fetal Intestine Small	intestine
15	chr7:16911400-16914000	Strong transcription	Duodenum Mucosa	Duodenum
16	chr7:16911600-16914200	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr7:16911600-16917000	Weak transcription	Fetal Intestine Small	intestine
18	chr7:16911800-16913800	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr7:16912600-16920000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:16913000-16914400	Enhancers	Placenta Amnion	Placenta Amnion
21	chr7:16913800-16917800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr7:16914000-16918000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr7:16914200-16919000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr7:16914400-16920200	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr7:16915600-16916200	Weak transcription	Fetal Intestine Large	intestine
26	chr7:16915600-16916600	Enhancers	Stomach Mucosa	stomach
27	chr7:16915800-16916200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr7:16916200-16917000	Enhancers	Fetal Intestine Large	intestine
29	chr7:16916600-16917800	Weak transcription	Stomach Mucosa	stomach
30	chr7:16917000-16917400	Weak transcription	Fetal Intestine Large	intestine
31	chr7:16917000-16918200	Enhancers	Fetal Intestine Small	intestine
32	chr7:16917400-16918200	Enhancers	Fetal Intestine Large	intestine
33	chr7:16917800-16918000	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr7:16917800-16918000	Enhancers	Stomach Mucosa	stomach
35	chr7:16918000-16918200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr7:16918000-16920200	Weak transcription	Stomach Mucosa	stomach
37	chr7:16918000-16921600	Active TSS	Duodenum Mucosa	Duodenum
38	chr7:16918200-16918400	Flanking Active TSS	Fetal Intestine Large	intestine
39	chr7:16918200-16918400	Enhancers	Small Intestine	intestine
40	chr7:16918200-16918600	Flanking Active TSS	Fetal Intestine Small	intestine
41	chr7:16918200-16922000	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr7:16918400-16922000	Active TSS	Fetal Intestine Large	intestine
43	chr7:16918600-16922000	Active TSS	Fetal Intestine Small	intestine
44	chr7:16919000-16922000	Active TSS	Rectal Mucosa Donor 31	rectum
45	chr7:16919400-16921200	Active TSS	Colonic Mucosa	Colon
46	chr7:16919600-16920000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:16919600-16921200	Active TSS	Rectal Smooth Muscle	rectum
48	chr7:16920000-16920400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:16920000-16921800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr7:16920200-16920800	Active TSS	Duodenum Smooth Muscle	Duodenum

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