Variant report

Variant	nsv5897
Chromosome Location	chr7:110160821-110208234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:110161251-110162197	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:110162717-110163545	HepG2	liver:	n/a	n/a
3	ATF3	chr7:110162799-110163299	A549	lung:	n/a	n/a
4	BCL3	chr7:110162740-110163442	A549	lung:	n/a	n/a
5	BCL3	chr7:110162678-110163384	A549	lung:	n/a	n/a
6	BHLHE40	chr7:110162911-110163273	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
8	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
9	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
10	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
11	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
12	CEBPB	chr7:110184991-110185190	A549	lung:	n/a	chr7:110185096-110185107
13	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
14	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
15	CEBPB	chr7:110184991-110185228	HepG2	liver:	n/a	chr7:110185096-110185107
16	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
18	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
20	CEBPB	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
21	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
25	CEBPD	chr7:110162957-110163255	HepG2	liver:	n/a	n/a
26	CEBPD	chr7:110169295-110169515	HepG2	liver:	n/a	n/a
27	CREB1	chr7:110162749-110163280	HepG2	liver:	n/a	n/a
28	CREB1	chr7:110162763-110163354	HepG2	liver:	n/a	n/a
29	CREB1	chr7:110162960-110163204	A549	lung:	n/a	n/a
30	CTCF	chr7:110174757-110174955	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
31	CTCF	chr7:110174653-110175102	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
32	CTCF	chr7:110174780-110174930	SAEC	small airway:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
33	CTCF	chr7:110184480-110184630	BJ	skin:	n/a	n/a
34	CTCF	chr7:110174762-110174953	LNCaP	prostate:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
35	CTCF	chr7:110174820-110174970	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
36	CTCF	chr7:110174760-110174910	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
37	CTCF	chr7:110174780-110174930	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110188540-110188690	GM12865	blood:	n/a	n/a
39	CTCF	chr7:110174760-110174910	AG04450	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
40	CTCF	chr7:110174767-110174933	LNCaP	prostate:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
41	CTCF	chr7:110167320-110167470	GM12866	blood:	n/a	n/a
42	CTCF	chr7:110174791-110174942	Hela-S3	cervix:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
43	CTCF	chr7:110174780-110174930	AG09319	gingival:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
44	CTCF	chr7:110163060-110163210	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:110174780-110174930	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
46	CTCF	chr7:110174800-110174950	HMEC	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
47	CTCF	chr7:110184400-110184550	AG04449	skin:	n/a	n/a
48	CTCF	chr7:110174760-110174910	SK-N-SH_RA	brain:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
49	CTCF	chr7:110201843-110201961	GM10248	blood:	n/a	n/a
50	CTCF	chr7:110184460-110184610	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110174780-110174830	HRE	kidney:	n/a
2	chr7:110174780-110174830	NB4	blood:	n/a
3	chr7:110174780-110174830	GM12878	blood:	n/a
4	chr7:110174780-110174830	ProgFib	skin:	n/a
5	chr7:110174780-110174830	HMEC	breast:	n/a
6	chr7:110174780-110174830	Hela-S3	cervix:	n/a
7	chr7:110174780-110174830	SAEC	small airway:	n/a
8	chr7:110174780-110174830	HCF	heart:	n/a
9	chr7:110174780-110174830	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
11	chr7:110174780-110174830	HepG2	liver:	n/a
12	chr7:110174780-110174830	HCM	heart:	n/a
13	chr7:110174780-110174830	ovcar-3	ovarian:	n/a
14	chr7:110174780-110174830	GM12892	blood:	n/a
15	chr7:110174780-110174830	RPTEC	kidney:	n/a
16	chr7:110174780-110174830	PANC-1	pancreas:	n/a
17	chr7:110174780-110174830	HCT-116	colon:	n/a
18	chr7:110174780-110174830	BE2_C	brain:	n/a
19	chr7:110174780-110174830	A549	lung:	n/a
20	chr7:110174780-110174830	AG09319	gingival:	n/a
21	chr7:110174780-110174830	HNPCEpiC	eye:	n/a
22	chr7:110174780-110174830	IMR90	lung:	fetal
23	chr7:110174780-110174830	SK-N-SH	brain:	n/a
24	chr7:110174780-110174830	SKMC	muscle:	n/a
25	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
26	chr7:110174780-110174830	HIPEpiC	eye:	n/a
27	chr7:110174780-110174830	U87	brain:	n/a
28	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
29	chr7:110174780-110174830	NHBE	bronchial:	n/a
30	chr7:110174780-110174830	PFSK-1	brain:	n/a
31	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
32	chr7:110174780-110174830	Jurkat	blood:	n/a
33	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
34	chr7:110174780-110174830	HRPEpiC	eye:	n/a
35	chr7:110174780-110174830	GM12891	blood:	n/a
36	chr7:110174780-110174830	HL-60	blood:	n/a
37	chr7:110174780-110174830	NT2-D1	testis:	n/a
38	chr7:110174780-110174830	NHDF-neo	bronchial:	n/a
39	chr7:110174780-110174830	GM06990	blood:	n/a
40	chr7:110174780-110174830	HRCEpiC	kidney:	n/a
41	chr7:110174780-110174830	MCF10A-Er-Src	breast:	n/a
42	chr7:110174780-110174830	AG04450	lung:	fetal
43	chr7:110174780-110174830	HEK293	kidney:	embryo
44	chr7:110174780-110174830	AG09309	skin:	n/a
45	chr7:110174780-110174830	AoSMC	blood vessel:	n/a
46	chr7:110174780-110174830	LNCaP	prostate:	n/a
47	chr7:110174780-110174830	AG04449	skin:	fetal
48	chr7:110174780-110174830	CMK	blood:	n/a
49	chr7:110174780-110174830	PrEC	prostate:	n/a
50	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
2	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
3	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
4	chr7:110175478..110177187-chr7:110400882..110403616,2	MCF-7	breast:
5	chr7:110204286..110206261-chr7:110213162..110216015,2	MCF-7	breast:
6	chr7:86847727..86850173-chr7:110164264..110166076,2	K562	blood:
7	chr4:4482219..4482825-chr7:110184645..110185165,2	MCF-7	breast:
8	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
9	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
10	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
11	chr7:109858826..109860608-chr7:110161184..110163464,2	MCF-7	breast:
12	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
13	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
14	chr7:110203860..110205462-chr7:110210314..110213055,2	K562	blood:
15	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
16	chr7:110202555..110205359-chr7:110210937..110215614,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMMP2L-1	chr7:110174646-110174811	XLOC_006561
2	lnc-IMMP2L-1	chr7:110165513-110165618	XLOC_006561
3	lnc-IMMP2L-1	chr7:110165513-110165618	XLOC_006561

Variant related genes	Relation type
ENSG00000226965	TF binding region
ENSG00000226965	CpG island
ENSG00000135185	chromatin interactions
ENSG00000200397	chromatin interactions
XIRP2	miRNA target sites
GULP1	miRNA target sites

Extended variants
information (count: 1803 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1803 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73429292	chr7:110160825-110160826	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369096696	chr7:110160834-110160835	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs557480447	chr7:110160871-110160872	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs377412698	chr7:110160909-110160910	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs553821438	chr7:110160917-110160918	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs370478272	chr7:110160971-110160972	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs573656889	chr7:110161047-110161048	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs113315601	chr7:110161050-110161051	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs542579887	chr7:110161064-110161065	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs141151035	chr7:110161091-110161092	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs576140093	chr7:110161192-110161193	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs544896829	chr7:110161234-110161235	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs564815712	chr7:110161239-110161240	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs150164254	chr7:110161343-110161344	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs6975627	chr7:110161348-110161349	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs560590032	chr7:110161395-110161396	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs529393684	chr7:110161400-110161401	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs75907182	chr7:110161457-110161458	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs180890794	chr7:110161461-110161462	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs138414223	chr7:110161468-110161469	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs115695543	chr7:110161517-110161518	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs186363946	chr7:110161519-110161520	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs370483049	chr7:110161541-110161542	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs533948396	chr7:110161548-110161549	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs9691601	chr7:110161560-110161561	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs191270550	chr7:110161600-110161601	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs182797221	chr7:110161615-110161616	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs149245837	chr7:110161616-110161617	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs576101486	chr7:110161624-110161625	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs545060188	chr7:110161638-110161639	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs558448585	chr7:110161644-110161645	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs185989970	chr7:110161655-110161656	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs528201090	chr7:110161670-110161671	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs190846091	chr7:110161682-110161683	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs560537886	chr7:110161706-110161707	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs529528249	chr7:110161740-110161741	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs542734537	chr7:110161768-110161769	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs562690209	chr7:110161770-110161771	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs143424369	chr7:110161772-110161773	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs551371065	chr7:110161855-110161856	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs571179857	chr7:110161877-110161878	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs138026626	chr7:110161914-110161915	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs143490760	chr7:110161939-110161940	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs147306136	chr7:110161973-110161974	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs183438664	chr7:110162037-110162038	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536491648	chr7:110162044-110162045	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs556281956	chr7:110162055-110162056	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs117316012	chr7:110162226-110162227	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs538589703	chr7:110162246-110162247	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs12155419	chr7:110162264-110162265	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:91)

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
Acute myeloid leukemia	16864856	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
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	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
Autism	19401682	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	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110155400-110162600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
3	chr7:110158600-110161000	Weak transcription	Liver	Liver
4	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
5	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr7:110160800-110163600	Enhancers	HepG2	liver
8	chr7:110160800-110163800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:110161000-110161600	Enhancers	Liver	Liver
10	chr7:110161200-110162600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:110161200-110163200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr7:110161400-110163400	Enhancers	Fetal Intestine Large	intestine
13	chr7:110161600-110162000	Enhancers	Psoas Muscle	Psoas
14	chr7:110161600-110162000	Transcr. at gene 5' and 3'	Dnd41	blood
15	chr7:110161600-110162200	Flanking Active TSS	Liver	Liver
16	chr7:110161600-110162200	Enhancers	Duodenum Mucosa	Duodenum
17	chr7:110161600-110162800	Enhancers	Brain Hippocampus Middle	brain
18	chr7:110161600-110163200	Enhancers	Pancreas	Pancrea
19	chr7:110161600-110163400	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr7:110161600-110163600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:110161600-110163800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:110161800-110162200	Enhancers	A549	lung
23	chr7:110161800-110163200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr7:110161800-110163400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:110161800-110163400	Enhancers	Fetal Intestine Small	intestine
26	chr7:110161800-110163600	Enhancers	Fetal Heart	heart
27	chr7:110162000-110162200	Flanking Active TSS	Dnd41	blood
28	chr7:110162000-110162400	Enhancers	Brain Substantia Nigra	brain
29	chr7:110162000-110163000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr7:110162200-110162600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr7:110162200-110162800	Flanking Active TSS	A549	lung
32	chr7:110162200-110163000	Enhancers	Dnd41	blood
33	chr7:110162200-110163600	Enhancers	Liver	Liver
34	chr7:110162200-110164400	Enhancers	Fetal Kidney	kidney
35	chr7:110162400-110163200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr7:110162600-110162800	Enhancers	Duodenum Mucosa	Duodenum
37	chr7:110162600-110163000	Enhancers	Stomach Mucosa	stomach
38	chr7:110162600-110163200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:110162600-110163200	Enhancers	Fetal Lung	lung
40	chr7:110162600-110163200	Enhancers	Fetal Muscle Leg	muscle
41	chr7:110162600-110163400	Enhancers	NHEK	skin
42	chr7:110162600-110163600	Enhancers	Fetal Brain Male	brain
43	chr7:110162800-110163200	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr7:110162800-110163200	Active TSS	A549	lung
45	chr7:110163000-110163400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:110163000-110163600	Flanking Active TSS	Dnd41	blood
47	chr7:110163000-110164200	Weak transcription	Stomach Mucosa	stomach
48	chr7:110163200-110163400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr7:110163200-110163400	Active TSS	Duodenum Mucosa	Duodenum
50	chr7:110163200-110163600	Flanking Active TSS	A549	lung

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