Variant report

Variant	nsv1020181
Chromosome Location	chr7:7448657-7484862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:563)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7478472-7478836	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7464097-7464338	HepG2	liver:	n/a	n/a
3	ATF1	chr7:7464065-7464481	K562	blood:	n/a	n/a
4	ATF3	chr7:7478333-7478974	A549	lung:	n/a	n/a
5	BACH1	chr7:7458714-7458862	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr7:7478442-7478892	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr7:7464181-7464259	HepG2	liver:	n/a	n/a
8	BRCA1	chr7:7464042-7464369	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr7:7455775-7456204	HCT-116	colon:	n/a	n/a
10	CBX3	chr7:7478353-7479081	HCT-116	colon:	n/a	n/a
11	CBX3	chr7:7478342-7479021	HCT-116	colon:	n/a	n/a
12	CEBPB	chr7:7464846-7465009	K562	blood:	n/a	n/a
13	CEBPB	chr7:7478474-7478949	A549	lung:	n/a	n/a
14	CEBPB	chr7:7478329-7479033	A549	lung:	n/a	n/a
15	CEBPB	chr7:7462392-7462592	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:7464132-7464268	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:7464047-7464367	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr7:7478008-7479033	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:7478398-7479050	A549	lung:	n/a	n/a
20	CEBPB	chr7:7478047-7478248	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:7478405-7479121	HCT-116	colon:	n/a	n/a
22	CEBPB	chr7:7478454-7479012	Hela-S3	cervix:	n/a	n/a
23	CHD1	chr7:7463743-7464626	IMR90	lung:	n/a	n/a
24	CHD2	chr7:7464056-7464387	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr7:7478517-7478893	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr7:7456427-7456522	Medullo	brain:	n/a	n/a
27	CTCF	chr7:7464160-7464310	AG09319	gingival:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
28	CTCF	chr7:7464100-7464250	Hela-S3	cervix:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
29	CTCF	chr7:7464043-7464352	A549	lung:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
30	CTCF	chr7:7463973-7464522	IMR90	lung:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
31	CTCF	chr7:7464120-7464270	AG04450	lung:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
32	CTCF	chr7:7464140-7464290	NHDF-neo	bronchial:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
33	CTCF	chr7:7464120-7464270	NB4	blood:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
34	CTCF	chr7:7464180-7464330	HFF	foreskin:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
35	CTCF	chr7:7463996-7464005	A549	lung:	n/a	n/a
36	CTCF	chr7:7463963-7463976	GM19240	blood:	n/a	n/a
37	CTCF	chr7:7464160-7464310	GM12873	blood:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
38	CTCF	chr7:7463977-7464422	H1-hESC	embryonic stem cell:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
39	CTCF	chr7:7478710-7478720	ProgFib	skin:	n/a	n/a
40	CTCF	chr7:7464060-7464210	GM12869	blood:	n/a	n/a
41	CTCF	chr7:7464160-7464310	HBMEC	blood vessel:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
42	CTCF	chr7:7478820-7478970	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr7:7464074-7464317	K562	blood:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
44	CTCF	chr7:7464080-7464230	GM12870	blood:	n/a	chr7:7464209-7464227
45	CTCF	chr7:7464160-7464310	NHDF-neo	bronchial:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
46	CTCF	chr7:7464140-7464290	AG04449	skin:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
47	CTCF	chr7:7478660-7478810	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr7:7464180-7464330	GM12875	blood:	n/a	chr7:7464211-7464232 chr7:7464209-7464227
49	CTCF	chr7:7463680-7463830	HVMF	connective:	n/a	n/a
50	CTCF	chr7:7464140-7464290	AoAF	blood vessel:	n/a	chr7:7464211-7464232 chr7:7464209-7464227

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7474236-7474286	AoSMC	blood vessel:	n/a
2	chr7:7478820-7478870	AoSMC	blood vessel:	n/a
3	chr7:7474236-7474286	H1-hESC	embryonic stem cell:	embryo
4	chr7:7474236-7474286	NT2-D1	testis:	n/a
5	chr7:7478820-7478870	HL-60	blood:	n/a
6	chr7:7478820-7478870	K562	blood:	n/a
7	chr7:7478820-7478870	HCF	heart:	n/a
8	chr7:7478820-7478870	GM19239	blood:	n/a
9	chr7:7478820-7478870	AG10803	skin:	n/a
10	chr7:7478820-7478870	Jurkat	blood:	n/a
11	chr7:7474236-7474286	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:7474236-7474286	ECC-1	luminal epithelium:	n/a
13	chr7:7478820-7478870	HIPEpiC	eye:	n/a
14	chr7:7474236-7474286	ovcar-3	ovarian:	n/a
15	chr7:7478820-7478870	A549	lung:	n/a
16	chr7:7474236-7474286	HRPEpiC	eye:	n/a
17	chr7:7474236-7474286	HRCEpiC	kidney:	n/a
18	chr7:7478820-7478870	AG09319	gingival:	n/a
19	chr7:7478820-7478870	NHBE	bronchial:	n/a
20	chr7:7474236-7474286	Hepatocyte	liver:	n/a
21	chr7:7474236-7474286	MCF10A-Er-Src	breast:	n/a
22	chr7:7474236-7474286	GM12891	blood:	n/a
23	chr7:7478820-7478870	HMEC	breast:	n/a
24	chr7:7478820-7478870	ECC-1	luminal epithelium:	n/a
25	chr7:7478820-7478870	Caco-2	colon:	n/a
26	chr7:7478820-7478870	HCPEpiC	choroid plexus:	n/a
27	chr7:7478820-7478870	GM06990	blood:	n/a
28	chr7:7474236-7474286	HCPEpiC	choroid plexus:	n/a
29	chr7:7478820-7478870	NB4	blood:	n/a
30	chr7:7478820-7478870	HRCEpiC	kidney:	n/a
31	chr7:7478820-7478870	NHDF-neo	bronchial:	n/a
32	chr7:7478820-7478870	HRPEpiC	eye:	n/a
33	chr7:7474236-7474286	ProgFib	skin:	n/a
34	chr7:7478820-7478870	ProgFib	skin:	n/a
35	chr7:7478820-7478870	U87	brain:	n/a
36	chr7:7474236-7474286	HepG2	liver:	n/a
37	chr7:7474236-7474286	NB4	blood:	n/a
38	chr7:7474236-7474286	GM12892	blood:	n/a
39	chr7:7478820-7478870	RPTEC	kidney:	n/a
40	chr7:7478820-7478870	GM12878	blood:	n/a
41	chr7:7474236-7474286	GM06990	blood:	n/a
42	chr7:7474236-7474286	AG04450	lung:	fetal
43	chr7:7474236-7474286	U87	brain:	n/a
44	chr7:7474236-7474286	AG09319	gingival:	n/a
45	chr7:7474236-7474286	HUVEC	blood vessel:	n/a
46	chr7:7478820-7478870	PFSK-1	brain:	n/a
47	chr7:7478820-7478870	HAEpiC	amniotic membrane:	n/a
48	chr7:7478820-7478870	HCM	heart:	n/a
49	chr7:7478820-7478870	SK-N-MC	brain:	n/a
50	chr7:7474236-7474286	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:7141034..7143515-chr7:7462815..7464467,2	MCF-7	breast:
2	chr7:7394315..7395000-chr7:7458752..7459656,3	MCF-7	breast:
3	chr7:7457672..7460558-chr7:7460578..7462678,3	MCF-7	breast:
4	chr7:7446277..7450841-chr7:7451007..7455027,4	K562	blood:
5	chr7:7445984..7447777-chr7:7451084..7453972,2	K562	blood:
6	chr7:7142761..7143623-chr7:7463315..7464213,2	MCF-7	breast:
7	chr7:7463700..7464480-chr7:7580427..7581567,10	MCF-7	breast:
8	chr7:7394187..7395000-chr7:7458752..7459656,4	MCF-7	breast:
9	chr7:7465052..7465954-chr7:7580703..7581616,2	K562	blood:
10	chr7:7361031..7361660-chr7:7458707..7459324,2	MCF-7	breast:
11	chr7:7464180..7464696-chr7:7579103..7579829,2	MCF-7	breast:
12	chr7:7456758..7459628-chr7:7464929..7467571,2	K562	blood:
13	chr7:7463756..7464685-chr7:7580802..7582089,8	MCF-7	breast:
14	chr7:7484454..7487980-chr7:7492862..7495926,3	MCF-7	breast:
15	chr7:7457858..7459653-chr7:7472855..7475146,2	K562	blood:
16	chr7:7470914..7472671-chr7:7492916..7494632,2	MCF-7	breast:
17	chr7:7446277..7450841-chr7:7451007..7455027,4	K562	blood:
18	chr7:7463681..7464442-chr7:7580757..7581561,4	K562	blood:
19	chr7:7467878..7469732-chr7:7578364..7581316,2	K562	blood:
20	chr7:7463581..7464271-chr7:8335248..8335877,2	K562	blood:
21	chr7:7457858..7459653-chr7:7472855..7475146,2	K562	blood:
22	chr7:7473373..7475762-chr7:7594753..7597282,2	MCF-7	breast:
23	chr7:7391197..7393340-chr7:7455899..7457673,2	MCF-7	breast:
24	chr7:7456758..7459628-chr7:7464929..7467571,2	K562	blood:
25	chr7:7456425..7458799-chr7:7459595..7461119,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPA3-5	chr7:7459516-7459941	NONHSAT119111
2	lnc-RPA3-5	chr7:7457263-7457558	NONHSAT119111

No data

Variant related genes	Relation type
COL28A1	TF binding region
COL28A1	CpG island
ENSG00000201218	chromatin interactions
ENSG00000215018	chromatin interactions

Extended variants
information (count: 1662 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1662 , 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	rs1297791	chr7:7448657-7448658	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560878616	chr7:7448669-7448670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191370354	chr7:7448693-7448694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546882708	chr7:7448762-7448763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571603986	chr7:7448784-7448785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533343862	chr7:7448795-7448796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551533468	chr7:7448826-7448827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570128544	chr7:7448863-7448864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142367629	chr7:7448875-7448876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555835769	chr7:7448877-7448878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567489437	chr7:7448896-7448897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576041070	chr7:7448898-7448899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553233756	chr7:7448967-7448968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577943533	chr7:7449010-7449011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150844836	chr7:7449024-7449025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556722677	chr7:7449062-7449063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575204055	chr7:7449100-7449101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542331192	chr7:7449111-7449112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1294600	chr7:7449148-7449149	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528280673	chr7:7449206-7449207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540462165	chr7:7449210-7449211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376955966	chr7:7449232-7449233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532490760	chr7:7449235-7449236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550864544	chr7:7449264-7449265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7807860	chr7:7449281-7449282	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs530954081	chr7:7449312-7449313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549171653	chr7:7449318-7449319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567453672	chr7:7449319-7449320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534864398	chr7:7449337-7449338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575042376	chr7:7449378-7449379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184567807	chr7:7449413-7449414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139290615	chr7:7449451-7449452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs80352409	chr7:7449473-7449474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557636100	chr7:7449503-7449504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373993116	chr7:7449508-7449509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149934074	chr7:7449509-7449510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189882831	chr7:7449539-7449540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573022999	chr7:7449631-7449632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1294601	chr7:7449636-7449637	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147602990	chr7:7449691-7449692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1294602	chr7:7449727-7449728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545853672	chr7:7449776-7449777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35323342	chr7:7449806-7449807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192886037	chr7:7449904-7449905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73674530	chr7:7449918-7449919	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs185472360	chr7:7449931-7449932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs548991487	chr7:7449975-7449976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12333776	chr7:7449976-7449977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114979405	chr7:7449978-7449979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546696974	chr7:7449980-7449981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	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
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7447600-7448800	Enhancers	Stomach Mucosa	stomach
2	chr7:7447600-7448800	Enhancers	NHEK	skin
3	chr7:7447600-7450200	Enhancers	Fetal Intestine Large	intestine
4	chr7:7447600-7450200	Enhancers	Fetal Intestine Small	intestine
5	chr7:7447800-7463800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr7:7447800-7464200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr7:7448000-7452800	Weak transcription	Colonic Mucosa	Colon
8	chr7:7448200-7448800	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr7:7448200-7450200	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr7:7448400-7449200	Enhancers	Duodenum Mucosa	Duodenum
11	chr7:7448800-7451200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr7:7448800-7455000	Weak transcription	Stomach Mucosa	stomach
13	chr7:7449200-7449600	Weak transcription	Duodenum Mucosa	Duodenum
14	chr7:7449400-7450200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr7:7449600-7449800	Enhancers	Duodenum Mucosa	Duodenum
16	chr7:7449800-7453800	Weak transcription	Duodenum Mucosa	Duodenum
17	chr7:7450200-7450600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:7450200-7452600	Weak transcription	Fetal Intestine Large	intestine
19	chr7:7450200-7452800	Weak transcription	Fetal Intestine Small	intestine
20	chr7:7450200-7453800	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr7:7450600-7451200	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr7:7451000-7451200	Enhancers	Gastric	stomach
23	chr7:7451200-7451600	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr7:7451200-7453600	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr7:7451200-7464000	Weak transcription	Gastric	stomach
26	chr7:7451600-7454000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr7:7452600-7456400	Enhancers	Fetal Intestine Large	intestine
28	chr7:7452800-7453000	Enhancers	Colonic Mucosa	Colon
29	chr7:7452800-7457000	Enhancers	Fetal Intestine Small	intestine
30	chr7:7453000-7454000	Weak transcription	Colonic Mucosa	Colon
31	chr7:7453600-7457000	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr7:7453800-7454200	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr7:7453800-7455400	Enhancers	Duodenum Mucosa	Duodenum
34	chr7:7454000-7454200	Flanking Active TSS	Colonic Mucosa	Colon
35	chr7:7454000-7454400	Enhancers	Small Intestine	intestine
36	chr7:7454000-7454600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr7:7454200-7454400	Active TSS	Colonic Mucosa	Colon
38	chr7:7454200-7456000	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr7:7454400-7464200	Weak transcription	Small Intestine	intestine
40	chr7:7454600-7455200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr7:7454800-7455000	Weak transcription	Pancreas	Pancrea
42	chr7:7455000-7455200	Enhancers	Pancreas	Pancrea
43	chr7:7455000-7457000	Enhancers	Stomach Mucosa	stomach
44	chr7:7455000-7458000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr7:7455200-7456600	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr7:7455200-7478600	Weak transcription	Pancreas	Pancrea
47	chr7:7455400-7455800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:7455600-7456200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:7455600-7457000	Enhancers	Primary T cells fromperipheralblood	blood
50	chr7:7455600-7457000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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