Variant report

Variant	nsv889080
Chromosome Location	chr7:117176248-117238379
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 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	chr7:117195388-117195586	K562	blood:	n/a	n/a
2	ATF2	chr7:117228213-117228911	GM12878	blood:	n/a	n/a
3	ATF2	chr7:117228256-117228885	GM12878	blood:	n/a	n/a
4	ATF3	chr7:117222180-117222830	A549	lung:	n/a	n/a
5	ATF3	chr7:117222102-117222912	A549	lung:	n/a	n/a
6	ATF3	chr7:117228178-117228937	A549	lung:	n/a	n/a
7	BACH1	chr7:117188133-117188349	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:117204164-117204384	GM12878	blood:	n/a	n/a
9	BATF	chr7:117228364-117228827	GM12878	blood:	n/a	chr7:117228615-117228626
10	BCL11A	chr7:117228325-117228839	GM12878	blood:	n/a	n/a
11	BCL3	chr7:117228214-117228853	A549	lung:	n/a	n/a
12	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
13	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
14	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
15	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
17	BHLHE40	chr7:117204094-117204536	GM12878	blood:	n/a	chr7:117204311-117204320 chr7:117204311-117204320
18	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
20	CEBPB	chr7:117213004-117213146	A549	lung:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
21	CEBPB	chr7:117202921-117203156	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
23	CEBPB	chr7:117200161-117200427	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
25	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
26	CEBPB	chr7:117206581-117206695	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:117228036-117228960	A549	lung:	n/a	chr7:117228586-117228597
28	CEBPB	chr7:117222135-117222657	MCF-7	breast:	n/a	chr7:117222302-117222313
29	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
30	CEBPB	chr7:117191755-117191958	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:117202887-117203267	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:117212837-117213239	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
33	CEBPB	chr7:117222236-117222366	HepG2	liver:	n/a	chr7:117222302-117222313
34	CEBPB	chr7:117222054-117222935	A549	lung:	n/a	chr7:117222302-117222313
35	CEBPB	chr7:117222117-117222867	IMR90	lung:	n/a	chr7:117222302-117222313
36	CEBPB	chr7:117202940-117203217	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
38	CEBPB	chr7:117222244-117222431	K562	blood:	n/a	chr7:117222302-117222313
39	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
40	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
41	CEBPB	chr7:117212851-117213351	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
42	CEBPB	chr7:117198075-117198115	A549	lung:	n/a	n/a
43	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
44	CEBPB	chr7:117200159-117200394	IMR90	lung:	n/a	n/a
45	CHD2	chr7:117228282-117228913	GM12878	blood:	n/a	n/a
46	CHD2	chr7:117222172-117222928	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr7:117204156-117204422	GM12878	blood:	n/a	n/a
48	CHD2	chr7:117228247-117228854	Hela-S3	cervix:	n/a	n/a
49	CREB1	chr7:117222364-117222750	A549	lung:	n/a	n/a
50	CREB1	chr7:117222454-117222759	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117228958-117229008	HCF	heart:	n/a
2	chr7:117228958-117229008	GM12878	blood:	n/a
3	chr7:117228958-117229008	PrEC	prostate:	n/a
4	chr7:117228958-117229008	BE2_C	brain:	n/a
5	chr7:117228958-117229008	AG09309	skin:	n/a
6	chr7:117228958-117229008	HL-60	blood:	n/a
7	chr7:117228958-117229008	AG04450	lung:	fetal
8	chr7:117228958-117229008	GM06990	blood:	n/a
9	chr7:117228958-117229008	NB4	blood:	n/a
10	chr7:117228958-117229008	AG09319	gingival:	n/a
11	chr7:117228958-117229008	HRCEpiC	kidney:	n/a
12	chr7:117228958-117229008	ProgFib	skin:	n/a
13	chr7:117228958-117229008	IMR90	lung:	fetal
14	chr7:117228958-117229008	HEK293	kidney:	embryo
15	chr7:117228958-117229008	K562	blood:	n/a
16	chr7:117228958-117229008	PANC-1	pancreas:	n/a
17	chr7:117228958-117229008	HNPCEpiC	eye:	n/a
18	chr7:117228958-117229008	HMEC	breast:	n/a
19	chr7:117228958-117229008	HCPEpiC	choroid plexus:	n/a
20	chr7:117228958-117229008	AG04449	skin:	fetal
21	chr7:117228958-117229008	ovcar-3	ovarian:	n/a
22	chr7:117228958-117229008	PFSK-1	brain:	n/a
23	chr7:117228958-117229008	AoSMC	blood vessel:	n/a
24	chr7:117228958-117229008	SK-N-SH_RA	brain:	n/a
25	chr7:117228958-117229008	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:117228958-117229008	HAEpiC	amniotic membrane:	n/a
27	chr7:117228958-117229008	HEEpiC	esophagus:	n/a
28	chr7:117228958-117229008	HCM	heart:	n/a
29	chr7:117228958-117229008	HIPEpiC	eye:	n/a
30	chr7:117228958-117229008	HCT-116	colon:	n/a
31	chr7:117228958-117229008	HepG2	liver:	n/a
32	chr7:117228958-117229008	HUVEC	blood vessel:	n/a
33	chr7:117228958-117229008	T-47D	breast:	n/a
34	chr7:117228958-117229008	NT2-D1	testis:	n/a
35	chr7:117228958-117229008	RPTEC	kidney:	n/a
36	chr7:117228958-117229008	Jurkat	blood:	n/a
37	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
38	chr7:117228958-117229008	MCF10A-Er-Src	breast:	n/a
39	chr7:117228958-117229008	GM12892	blood:	n/a
40	chr7:117228958-117229008	ECC-1	luminal epithelium:	n/a
41	chr7:117228958-117229008	SAEC	small airway:	n/a
42	chr7:117228958-117229008	A549	lung:	n/a
43	chr7:117228958-117229008	CMK	blood:	n/a
44	chr7:117228958-117229008	AG10803	skin:	n/a
45	chr7:117228958-117229008	GM19239	blood:	n/a
46	chr7:117228958-117229008	NH-A	brain:	n/a
47	chr7:117228958-117229008	Caco-2	colon:	n/a
48	chr7:117228958-117229008	SK-N-SH	brain:	n/a
49	chr7:117228958-117229008	HRE	kidney:	n/a
50	chr7:117228958-117229008	Hepatocyte	liver:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:115847372-115857098..7:117194433-117196955	H1-hESC	embryonic stem cell:	embryo
2	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
3	7:115861595-115870968..7:117216968-117220729	H1-hESC	embryonic stem cell:	embryo
4	chr7:117171466..117173089-chr7:117174919..117176705,2	K562	blood:
5	7:117065049-117068137..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
6	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
7	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
8	chr7:117173270..117176194-chr7:117177984..117179733,2	MCF-7	breast:
9	7:115890993-115892266..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
10	chr7:117180519..117183145-chr7:117187916..117190717,2	K562	blood:
11	7:116604327-116608063..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
12	7:115847372-115857098..7:117179549-117182665	H1-hESC	embryonic stem cell:	embryo
13	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:
14	7:117100350-117112126..7:117201648-117203159	H1-hESC	embryonic stem cell:	embryo
15	chr7:117190103..117191769-chr7:117198785..117201652,2	K562	blood:
16	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
17	chr7:117203452..117206266-chr7:117206487..117208495,3	MCF-7	breast:
18	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:
19	chr7:117184115..117186355-chr7:117188163..117190019,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASZ1-1	chr7:117200787-117200846	ENSG00000232661.1
2	lnc-CTTNBP2-4	chr7:117226261-117226470	NONHSAT122949
3	lnc-ASZ1-1	chr7:117204570-117204730	ENSG00000232661.1

No data

Variant related genes	Relation type
CFTR	TF binding region
ENSG00000234001	TF binding region
ENSG00000232661	TF binding region
CFTR	CpG island
ENSG00000234001	CpG island
ENSG00000232661	CpG island
ENSG00000228368	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000004866	chromatin interactions
ENSG00000135269	chromatin interactions
ENSG00000232661	chromatin interactions
ENSG00000154438	chromatin interactions

Extended variants
information (count: 2442 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2442 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148699	chr7:117176248-117176249	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs7357279	chr7:117176296-117176297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143051292	chr7:117176308-117176309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532529536	chr7:117176338-117176339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551567455	chr7:117176361-117176362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143542722	chr7:117176433-117176434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571754026	chr7:117176438-117176439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532407036	chr7:117176487-117176488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557519394	chr7:117176524-117176525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550552830	chr7:117176547-117176548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34543279	chr7:117176569-117176570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1805176	chr7:117176571-117176572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369149477	chr7:117176587-117176588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs387906367	chr7:117176588-117176589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3034763	chr7:117176590-117176591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs397508793	chr7:117176592-117176593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs193922531	chr7:117176593-117176594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397759426	chr7:117176596-117176597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113744424	chr7:117176613-117176614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191456345	chr7:117176630-117176631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397508794	chr7:117176631-117176632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397508795	chr7:117176633-117176634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148519623	chr7:117176652-117176653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs121908772	chr7:117176661-117176662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs121908773	chr7:117176663-117176664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201016820	chr7:117176664-117176665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193922532	chr7:117176683-117176684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397508799	chr7:117176686-117176687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs397508800	chr7:117176687-117176688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397508801	chr7:117176694-117176695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs397508802	chr7:117176700-117176701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142864834	chr7:117176704-117176705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151073129	chr7:117176711-117176712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397508803	chr7:117176715-117176716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs397508805	chr7:117176717-117176718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs387906380	chr7:117176718-117176719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs397508806	chr7:117176719-117176720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs397508807	chr7:117176720-117176721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs397508808	chr7:117176726-117176727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533959068	chr7:117176732-117176733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1800687	chr7:117176736-117176737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1800503	chr7:117176738-117176739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs79718042	chr7:117176815-117176816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544263779	chr7:117176822-117176823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556200585	chr7:117176846-117176847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574337423	chr7:117176850-117176851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147632822	chr7:117176858-117176859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536919749	chr7:117176873-117176874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560167674	chr7:117176882-117176883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142285107	chr7:117176922-117176923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117164400-117177600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:117171600-117177400	Weak transcription	Colonic Mucosa	Colon
3	chr7:117173000-117208000	Weak transcription	Pancreas	Pancrea
4	chr7:117173400-117178800	Weak transcription	Gastric	stomach
5	chr7:117174000-117179200	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr7:117174600-117178800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr7:117175400-117177800	Weak transcription	Fetal Intestine Large	intestine
8	chr7:117175400-117177800	Weak transcription	Fetal Intestine Small	intestine
9	chr7:117176000-117177800	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr7:117176200-117176400	Enhancers	Stomach Mucosa	stomach
11	chr7:117177400-117178000	Enhancers	Colonic Mucosa	Colon
12	chr7:117177600-117178400	Enhancers	Fetal Heart	heart
13	chr7:117177600-117185800	Strong transcription	Duodenum Mucosa	Duodenum
14	chr7:117177800-117178400	Enhancers	Fetal Intestine Large	intestine
15	chr7:117177800-117178400	Enhancers	Fetal Intestine Small	intestine
16	chr7:117177800-117178800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr7:117178000-117179000	Weak transcription	Colonic Mucosa	Colon
18	chr7:117178400-117179000	Weak transcription	Fetal Intestine Small	intestine
19	chr7:117178400-117180000	Weak transcription	Fetal Intestine Large	intestine
20	chr7:117178800-117179200	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr7:117178800-117179200	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr7:117179000-117179200	Enhancers	Colonic Mucosa	Colon
23	chr7:117179000-117179200	Genic enhancers	Fetal Intestine Small	intestine
24	chr7:117179200-117179400	Enhancers	Gastric	stomach
25	chr7:117179200-117180200	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr7:117179200-117182400	Weak transcription	Colonic Mucosa	Colon
27	chr7:117179200-117182600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:117179200-117183600	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr7:117179200-117191800	Weak transcription	Fetal Intestine Small	intestine
30	chr7:117180000-117181800	Strong transcription	Fetal Intestine Large	intestine
31	chr7:117180200-117181400	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr7:117181400-117213400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr7:117181800-117183200	Weak transcription	Fetal Intestine Large	intestine
34	chr7:117183200-117185800	Strong transcription	Fetal Intestine Large	intestine
35	chr7:117183600-117184200	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr7:117184200-117184600	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr7:117184600-117185800	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr7:117185800-117186400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr7:117185800-117195400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr7:117185800-117203600	Weak transcription	Fetal Intestine Large	intestine
41	chr7:117186400-117187000	Strong transcription	Duodenum Mucosa	Duodenum
42	chr7:117186600-117187000	Enhancers	Stomach Mucosa	stomach
43	chr7:117187000-117193000	Weak transcription	Duodenum Mucosa	Duodenum
44	chr7:117187000-117205200	Weak transcription	Stomach Mucosa	stomach
45	chr7:117187800-117188200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:117187800-117188200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr7:117187800-117188400	Enhancers	A549	lung
48	chr7:117190600-117192000	Enhancers	Dnd41	blood
49	chr7:117191800-117193400	Strong transcription	Fetal Intestine Small	intestine
50	chr7:117192000-117195400	Weak transcription	Dnd41	blood

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