Variant report

Variant	nsv1023773
Chromosome Location	chr7:17544993-17635119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17563515-17564310	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17570705-17570973	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17545639-17546113	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:17547356-17547682	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:17582050-17582722	HepG2	liver:	n/a	n/a
6	ATF1	chr7:17556068-17556263	K562	blood:	n/a	n/a
7	ATF2	chr7:17545610-17546051	GM12878	blood:	n/a	n/a
8	ATF2	chr7:17545626-17546038	GM12878	blood:	n/a	n/a
9	ATF3	chr7:17598333-17599109	A549	lung:	n/a	n/a
10	ATF3	chr7:17598348-17598968	A549	lung:	n/a	n/a
11	BATF	chr7:17586358-17586636	GM12878	blood:	n/a	chr7:17586494-17586505 chr7:17586523-17586532
12	BATF	chr7:17545754-17546108	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:17545665-17546083	GM12878	blood:	n/a	n/a
14	BCL3	chr7:17598337-17599111	A549	lung:	n/a	n/a
15	BCL3	chr7:17598160-17599399	A549	lung:	n/a	chr7:17598247-17598256
16	BCL3	chr7:17597307-17597887	A549	lung:	n/a	n/a
17	BCL3	chr7:17545577-17546157	A549	lung:	n/a	n/a
18	BHLHE40	chr7:17570680-17570977	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:17545738-17546036	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:17547300-17547707	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:17547360-17547534	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:17586327-17586569	HepG2	liver:	n/a	n/a
23	BHLHE40	chr7:17545645-17546075	GM12878	blood:	n/a	n/a
24	BRCA1	chr7:17563951-17564339	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr7:17572488-17573127	HCT-116	colon:	n/a	n/a
26	CBX3	chr7:17572366-17573261	HCT-116	colon:	n/a	n/a
27	CEBPB	chr7:17563930-17564321	A549	lung:	n/a	n/a
28	CEBPB	chr7:17564763-17565167	Hela-S3	cervix:	n/a	chr7:17564977-17564988 chr7:17564977-17564990
29	CEBPB	chr7:17563901-17564322	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:17598391-17598933	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:17553900-17554070	Hela-S3	cervix:	n/a	chr7:17553987-17553998
32	CEBPB	chr7:17574009-17574267	IMR90	lung:	n/a	chr7:17574146-17574157
33	CEBPB	chr7:17545765-17546073	HepG2	liver:	n/a	chr7:17545856-17545869
34	CEBPB	chr7:17553882-17554198	A549	lung:	n/a	chr7:17553987-17553998
35	CEBPB	chr7:17574118-17574312	K562	blood:	n/a	chr7:17574146-17574157
36	CEBPB	chr7:17564955-17565053	HepG2	liver:	n/a	chr7:17564977-17564988 chr7:17564977-17564990
37	CEBPB	chr7:17604350-17604644	Hela-S3	cervix:	n/a	chr7:17604492-17604503
38	CEBPB	chr7:17604308-17604693	IMR90	lung:	n/a	chr7:17604492-17604503
39	CEBPB	chr7:17586096-17586561	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:17600087-17600532	A549	lung:	n/a	n/a
41	CEBPB	chr7:17628420-17628522	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:17574007-17574315	Hela-S3	cervix:	n/a	chr7:17574146-17574157
43	CEBPB	chr7:17604355-17604602	HepG2	liver:	n/a	chr7:17604492-17604503
44	CEBPB	chr7:17598451-17598839	A549	lung:	n/a	n/a
45	CEBPB	chr7:17598446-17599042	MCF-7	breast:	n/a	n/a
46	CEBPB	chr7:17597031-17597221	Hela-S3	cervix:	n/a	chr7:17597111-17597124 chr7:17597111-17597122
47	CEBPB	chr7:17586081-17586691	Hela-S3	cervix:	n/a	chr7:17586613-17586624 chr7:17586613-17586626 chr7:17586613-17586626
48	CEBPB	chr7:17553869-17554081	IMR90	lung:	n/a	chr7:17553987-17553998
49	CEBPB	chr7:17563813-17564458	A549	lung:	n/a	n/a
50	CEBPB	chr7:17597063-17597136	HepG2	liver:	n/a	chr7:17597111-17597124 chr7:17597111-17597122

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17552196-17552246	HRE	kidney:	n/a
2	chr7:17582718-17582768	MCF10A-Er-Src	breast:	n/a
3	chr7:17585471-17585521	ovcar-3	ovarian:	n/a
4	chr7:17598458-17598508	Jurkat	blood:	n/a
5	chr7:17552196-17552246	ovcar-3	ovarian:	n/a
6	chr7:17552196-17552246	HIPEpiC	eye:	n/a
7	chr7:17552196-17552246	U87	brain:	n/a
8	chr7:17552196-17552246	HMEC	breast:	n/a
9	chr7:17585471-17585521	AG09319	gingival:	n/a
10	chr7:17582718-17582768	IMR90	lung:	fetal
11	chr7:17582718-17582768	HIPEpiC	eye:	n/a
12	chr7:17598458-17598508	HRE	kidney:	n/a
13	chr7:17585471-17585521	GM06990	blood:	n/a
14	chr7:17582718-17582768	HCPEpiC	choroid plexus:	n/a
15	chr7:17598458-17598508	ovcar-3	ovarian:	n/a
16	chr7:17582718-17582768	ProgFib	skin:	n/a
17	chr7:17582718-17582768	PANC-1	pancreas:	n/a
18	chr7:17585471-17585521	HEEpiC	esophagus:	n/a
19	chr7:17582718-17582768	AG04450	lung:	fetal
20	chr7:17582718-17582768	PFSK-1	brain:	n/a
21	chr7:17582718-17582768	U87	brain:	n/a
22	chr7:17582718-17582768	HEK293	kidney:	embryo
23	chr7:17598458-17598508	BJ	skin:	n/a
24	chr7:17598458-17598508	HMEC	breast:	n/a
25	chr7:17585471-17585521	NH-A	brain:	n/a
26	chr7:17585471-17585521	MCF10A-Er-Src	breast:	n/a
27	chr7:17552196-17552246	AoSMC	blood vessel:	n/a
28	chr7:17598458-17598508	AG04449	skin:	fetal
29	chr7:17552196-17552246	HAEpiC	amniotic membrane:	n/a
30	chr7:17598458-17598508	SK-N-SH	brain:	n/a
31	chr7:17598458-17598508	ECC-1	luminal epithelium:	n/a
32	chr7:17585471-17585521	LNCaP	prostate:	n/a
33	chr7:17585471-17585521	PFSK-1	brain:	n/a
34	chr7:17552196-17552246	NHDF-neo	bronchial:	n/a
35	chr7:17598458-17598508	SKMC	muscle:	n/a
36	chr7:17585471-17585521	Caco-2	colon:	n/a
37	chr7:17585471-17585521	SK-N-SH	brain:	n/a
38	chr7:17552196-17552246	A549	lung:	n/a
39	chr7:17598458-17598508	NHBE	bronchial:	n/a
40	chr7:17585471-17585521	RPTEC	kidney:	n/a
41	chr7:17582718-17582768	HMEC	breast:	n/a
42	chr7:17582718-17582768	H1-hESC	embryonic stem cell:	embryo
43	chr7:17552196-17552246	HepG2	liver:	n/a
44	chr7:17585471-17585521	PANC-1	pancreas:	n/a
45	chr7:17598458-17598508	GM12892	blood:	n/a
46	chr7:17598458-17598508	NB4	blood:	n/a
47	chr7:17552196-17552246	Hepatocyte	liver:	n/a
48	chr7:17552196-17552246	AG04449	skin:	fetal
49	chr7:17598458-17598508	AoSMC	blood vessel:	n/a
50	chr7:17598458-17598508	SAEC	small airway:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17342140..17343219-chr7:17570441..17571204,3	MCF-7	breast:
2	chr7:16974533..16976554-chr7:17579096..17580960,2	K562	blood:
3	chr7:17595637..17596623-chr7:17657831..17658483,2	MCF-7	breast:
4	chr7:17558188..17561143-chr7:17568617..17570224,2	MCF-7	breast:
5	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
6	chr7:17558188..17561143-chr7:17568617..17570224,2	MCF-7	breast:
7	chr7:17102519..17103019-chr7:17570516..17571366,2	MCF-7	breast:
8	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
9	chr7:17585475..17587800-chr7:17685188..17687624,2	MCF-7	breast:
10	chr7:17337629..17339397-chr7:17596553..17598570,2	MCF-7	breast:
11	chr7:17566122..17568059-chr7:17569390..17571113,2	MCF-7	breast:
12	chr7:17514240..17514759-chr7:17570395..17571281,2	MCF-7	breast:
13	chr7:17344294..17345014-chr7:17570513..17571272,2	MCF-7	breast:
14	chr7:17566122..17568059-chr7:17569390..17571113,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-4	chr7:17564901-17565058	NONHSAT119333
2	lnc-SNX13-1	chr7:17598376-17598533	ENSG00000226598
3	lnc-SNX13-3	chr7:17619972-17620082	NONHSAT119341

No data

Variant related genes	Relation type
ENSG00000226598	TF binding region
ENSG00000226598	CpG island
ENSG00000106546	chromatin interactions
ENSG00000237773	chromatin interactions

Extended variants
information (count: 4652 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4652 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1868358	chr7:17544993-17544994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373434369	chr7:17545000-17545001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189483312	chr7:17545005-17545006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117220082	chr7:17545065-17545066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540234492	chr7:17545091-17545092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62444696	chr7:17545099-17545100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148442737	chr7:17545106-17545107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565403914	chr7:17545119-17545120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1868359	chr7:17545170-17545171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs5882608	chr7:17545203-17545204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113031137	chr7:17545209-17545210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547793950	chr7:17545219-17545220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75413781	chr7:17545260-17545261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527586014	chr7:17545261-17545262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10224965	chr7:17545326-17545327	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs181086960	chr7:17545345-17545346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1868360	chr7:17545357-17545358	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537652366	chr7:17545395-17545396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185917408	chr7:17545428-17545429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549436463	chr7:17545512-17545513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150993081	chr7:17545515-17545516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73071149	chr7:17545544-17545545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs373753522	chr7:17545565-17545566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367905013	chr7:17545566-17545567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372074285	chr7:17545568-17545569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375364978	chr7:17545569-17545570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72104199	chr7:17545570-17545571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72130091	chr7:17545574-17545575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7802643	chr7:17545576-17545577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7802647	chr7:17545578-17545579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529174748	chr7:17545580-17545581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs59708473	chr7:17545612-17545613	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs7802666	chr7:17545631-17545632	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572048258	chr7:17545657-17545658	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12670915	chr7:17545679-17545680	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116254657	chr7:17545734-17545735	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs187157644	chr7:17545744-17545745	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs544048473	chr7:17545746-17545747	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs149804464	chr7:17545865-17545866	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs138748920	chr7:17545893-17545894	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs191173186	chr7:17545897-17545898	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs560742143	chr7:17545928-17545929	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs7803349	chr7:17545963-17545964	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73071153	chr7:17545964-17545965	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs537827140	chr7:17545984-17545985	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs73071155	chr7:17545998-17545999	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548957802	chr7:17546008-17546009	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs552807467	chr7:17546041-17546042	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs561257801	chr7:17546052-17546053	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs531368117	chr7:17546109-17546110	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22495309	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:684 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17537600-17546400	Weak transcription	Ovary	ovary
2	chr7:17542200-17545800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:17542200-17547400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:17542800-17545800	Weak transcription	NHLF	lung
5	chr7:17542800-17547400	Enhancers	Liver	Liver
6	chr7:17543200-17548000	Enhancers	HepG2	liver
7	chr7:17543600-17545000	Weak transcription	Fetal Intestine Small	intestine
8	chr7:17543600-17550600	Weak transcription	NHDF-Ad	bronchial
9	chr7:17544600-17545600	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr7:17544600-17545800	Enhancers	Fetal Lung	lung
11	chr7:17544600-17545800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:17544600-17546800	Enhancers	GM12878-XiMat	blood
13	chr7:17544600-17547800	Enhancers	Fetal Intestine Large	intestine
14	chr7:17544800-17545800	Weak transcription	Esophagus	oesophagus
15	chr7:17544800-17545800	Weak transcription	Gastric	stomach
16	chr7:17544800-17546400	Weak transcription	Pancreas	Pancrea
17	chr7:17544800-17547600	Enhancers	Stomach Mucosa	stomach
18	chr7:17545000-17545200	Enhancers	Fetal Intestine Small	intestine
19	chr7:17545000-17546600	Enhancers	Small Intestine	intestine
20	chr7:17545200-17545600	Weak transcription	Fetal Intestine Small	intestine
21	chr7:17545600-17546000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr7:17545600-17547800	Enhancers	Fetal Intestine Small	intestine
23	chr7:17545800-17546000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:17545800-17546000	Flanking Active TSS	Fetal Lung	lung
25	chr7:17545800-17546200	Enhancers	Esophagus	oesophagus
26	chr7:17545800-17546200	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr7:17545800-17546200	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr7:17545800-17546200	Enhancers	NHLF	lung
29	chr7:17545800-17546600	Enhancers	Fetal Stomach	stomach
30	chr7:17545800-17546600	Enhancers	Gastric	stomach
31	chr7:17545800-17546600	Enhancers	A549	lung
32	chr7:17545800-17546800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr7:17546000-17546200	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr7:17546000-17546400	Enhancers	Fetal Lung	lung
35	chr7:17546200-17556000	Weak transcription	NHLF	lung
36	chr7:17546400-17546600	Enhancers	Ovary	ovary
37	chr7:17546400-17546600	Enhancers	Pancreas	Pancrea
38	chr7:17546400-17546800	Enhancers	Colon Smooth Muscle	Colon
39	chr7:17546400-17546800	Flanking Active TSS	Fetal Lung	lung
40	chr7:17546600-17547400	Enhancers	Duodenum Mucosa	Duodenum
41	chr7:17546600-17547400	Weak transcription	Ovary	ovary
42	chr7:17546600-17551800	Weak transcription	A549	lung
43	chr7:17546800-17551800	Weak transcription	Fetal Lung	lung
44	chr7:17547200-17547600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr7:17547400-17547600	Enhancers	Ovary	ovary
46	chr7:17547400-17547800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:17547400-17547800	Flanking Active TSS	Liver	Liver
48	chr7:17547600-17551200	Weak transcription	Stomach Mucosa	stomach
49	chr7:17547800-17548800	Weak transcription	Liver	Liver
50	chr7:17548800-17549000	ZNF genes & repeats	Liver	Liver

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