Variant report

Variant	nsv1021693
Chromosome Location	chr7:110157227-110197412
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	chr7:110162678-110163384	A549	lung:	n/a	n/a
5	BCL3	chr7:110162740-110163442	A549	lung:	n/a	n/a
6	BHLHE40	chr7:110162911-110163273	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
8	CEBPB	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
10	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
11	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
12	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
14	CEBPB	chr7:110184991-110185228	HepG2	liver:	n/a	chr7:110185096-110185107
15	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
16	CEBPB	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
17	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
19	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
20	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
21	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
22	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:110184991-110185190	A549	lung:	n/a	chr7:110185096-110185107
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	chr7:110162960-110163204	A549	lung:	n/a	n/a
29	CREB1	chr7:110162763-110163354	HepG2	liver:	n/a	n/a
30	CTCF	chr7:110174780-110174930	HCPEpiC	choroid plexus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
31	CTCF	chr7:110174791-110174942	Hela-S3	cervix:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
32	CTCF	chr7:110174760-110174910	HCPEpiC	choroid plexus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
33	CTCF	chr7:110174780-110174930	BE2_C	brain:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
34	CTCF	chr7:110163060-110163210	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:110174780-110174930	HEEpiC	esophagus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
36	CTCF	chr7:110174787-110174911	ProgFib	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
37	CTCF	chr7:110174767-110174933	LNCaP	prostate:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110167320-110167470	GM12866	blood:	n/a	n/a
39	CTCF	chr7:110174757-110174955	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
40	CTCF	chr7:110184480-110184630	BJ	skin:	n/a	n/a
41	CTCF	chr7:110174780-110174930	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
42	CTCF	chr7:110174820-110174970	AG10803	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
43	CTCF	chr7:110174717-110175031	IMR90	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
44	CTCF	chr7:110174780-110174930	AG09319	gingival:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
45	CTCF	chr7:110174653-110175102	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
46	CTCF	chr7:110174780-110174930	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
47	CTCF	chr7:110159697-110159754	Fibrobl	skin:	n/a	n/a
48	CTCF	chr7:110174752-110174933	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
49	CTCF	chr7:110184440-110184590	BJ	skin:	n/a	n/a
50	CTCF	chr7:110174760-110174910	HMF	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:110174780-110174830	T-47D	breast:	n/a
2	chr7:110174780-110174830	RPTEC	kidney:	n/a
3	chr7:110174780-110174830	GM12878	blood:	n/a
4	chr7:110174780-110174830	SKMC	muscle:	n/a
5	chr7:110174780-110174830	PrEC	prostate:	n/a
6	chr7:110174780-110174830	HAEpiC	amniotic membrane:	n/a
7	chr7:110174780-110174830	AG09309	skin:	n/a
8	chr7:110174780-110174830	AG04449	skin:	fetal
9	chr7:110174780-110174830	AG09319	gingival:	n/a
10	chr7:110174780-110174830	GM06990	blood:	n/a
11	chr7:110174780-110174830	HepG2	liver:	n/a
12	chr7:110174780-110174830	GM12892	blood:	n/a
13	chr7:110174780-110174830	ovcar-3	ovarian:	n/a
14	chr7:110174780-110174830	MCF10A-Er-Src	breast:	n/a
15	chr7:110174780-110174830	BJ	skin:	n/a
16	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
17	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
18	chr7:110174780-110174830	NHDF-neo	bronchial:	n/a
19	chr7:110174780-110174830	NHBE	bronchial:	n/a
20	chr7:110174780-110174830	HIPEpiC	eye:	n/a
21	chr7:110174780-110174830	Caco-2	colon:	n/a
22	chr7:110174780-110174830	PANC-1	pancreas:	n/a
23	chr7:110174780-110174830	HCM	heart:	n/a
24	chr7:110174780-110174830	BE2_C	brain:	n/a
25	chr7:110174780-110174830	Hepatocyte	liver:	n/a
26	chr7:110174780-110174830	HNPCEpiC	eye:	n/a
27	chr7:110174780-110174830	NH-A	brain:	n/a
28	chr7:110174780-110174830	AG04450	lung:	fetal
29	chr7:110174780-110174830	AG10803	skin:	n/a
30	chr7:110174780-110174830	HMEC	breast:	n/a
31	chr7:110174780-110174830	GM19239	blood:	n/a
32	chr7:110174780-110174830	LNCaP	prostate:	n/a
33	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a
34	chr7:110174780-110174830	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
36	chr7:110174780-110174830	AoSMC	blood vessel:	n/a
37	chr7:110174780-110174830	K562	blood:	n/a
38	chr7:110174780-110174830	Jurkat	blood:	n/a
39	chr7:110174780-110174830	HRPEpiC	eye:	n/a
40	chr7:110174780-110174830	ProgFib	skin:	n/a
41	chr7:110174780-110174830	Hela-S3	cervix:	n/a
42	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
43	chr7:110174780-110174830	HL-60	blood:	n/a
44	chr7:110174780-110174830	PFSK-1	brain:	n/a
45	chr7:110174780-110174830	NB4	blood:	n/a
46	chr7:110174780-110174830	HRE	kidney:	n/a
47	chr7:110174780-110174830	GM12891	blood:	n/a
48	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
49	chr7:110174780-110174830	CMK	blood:	n/a
50	chr7:110174780-110174830	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
2	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
3	chr4:4482219..4482825-chr7:110184645..110185165,2	MCF-7	breast:
4	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
5	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
6	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
7	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
8	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
9	chr7:86847727..86850173-chr7:110164264..110166076,2	K562	blood:
10	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
11	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
12	chr7:110175478..110177187-chr7:110400882..110403616,2	MCF-7	breast:
13	chr7:109858826..109860608-chr7:110161184..110163464,2	MCF-7	breast:
14	chr7:110158309..110160168-chr7:110161330..110163385,2	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: 1575 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1575 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563238670	chr7:110157240-110157241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6960599	chr7:110157254-110157255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs187989345	chr7:110157280-110157281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191666514	chr7:110157284-110157285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77723688	chr7:110157408-110157409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564999821	chr7:110157421-110157422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138142420	chr7:110157434-110157435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535297833	chr7:110157445-110157446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527785197	chr7:110157452-110157453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs183497633	chr7:110157467-110157468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561144661	chr7:110157506-110157507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530144790	chr7:110157541-110157542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2966417	chr7:110157546-110157547	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs569977676	chr7:110157653-110157654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532335512	chr7:110157669-110157670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552407563	chr7:110157703-110157704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565731282	chr7:110157716-110157717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35143758	chr7:110157730-110157731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200634307	chr7:110157731-110157732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201300810	chr7:110157732-110157733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs71149593	chr7:110157733-110157734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397789917	chr7:110157735-110157736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534729206	chr7:110157837-110157838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577424846	chr7:110157848-110157849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187624136	chr7:110157886-110157887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192608352	chr7:110157903-110157904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537096886	chr7:110157904-110157905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556571719	chr7:110157988-110157989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182141678	chr7:110158007-110158008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113081664	chr7:110158045-110158046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538802161	chr7:110158046-110158047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539396273	chr7:110158083-110158084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572175383	chr7:110158086-110158087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541152775	chr7:110158122-110158123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561458567	chr7:110158128-110158129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574736293	chr7:110158148-110158149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7807567	chr7:110158226-110158227	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1354991	chr7:110158246-110158247	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs532450478	chr7:110158248-110158249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186791427	chr7:110158255-110158256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192703067	chr7:110158265-110158266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs115554783	chr7:110158269-110158270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77312242	chr7:110158296-110158297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73429277	chr7:110158302-110158303	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73429280	chr7:110158324-110158325	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs547906735	chr7:110158365-110158366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184703851	chr7:110158388-110158389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570835649	chr7:110158391-110158392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148189654	chr7:110158403-110158404	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs538964484	chr7:110158427-110158428	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

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:178 , 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	chr7:110155800-110158800	Weak transcription	Pancreas	Pancrea
3	chr7:110156000-110157600	Enhancers	Dnd41	blood
4	chr7:110157000-110158800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:110157200-110158600	Enhancers	Liver	Liver
6	chr7:110157400-110157600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:110157600-110158400	Weak transcription	Dnd41	blood
8	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
9	chr7:110158600-110161000	Weak transcription	Liver	Liver
10	chr7:110158800-110159400	ZNF genes & repeats	Pancreas	Pancrea
11	chr7:110158800-110159800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:110158800-110160200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
14	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:110160000-110160200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
16	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr7:110160800-110163600	Enhancers	HepG2	liver
18	chr7:110160800-110163800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr7:110161000-110161600	Enhancers	Liver	Liver
20	chr7:110161200-110162600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:110161200-110163200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr7:110161400-110163400	Enhancers	Fetal Intestine Large	intestine
23	chr7:110161600-110162000	Enhancers	Psoas Muscle	Psoas
24	chr7:110161600-110162000	Transcr. at gene 5' and 3'	Dnd41	blood
25	chr7:110161600-110162200	Flanking Active TSS	Liver	Liver
26	chr7:110161600-110162200	Enhancers	Duodenum Mucosa	Duodenum
27	chr7:110161600-110162800	Enhancers	Brain Hippocampus Middle	brain
28	chr7:110161600-110163200	Enhancers	Pancreas	Pancrea
29	chr7:110161600-110163400	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr7:110161600-110163600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:110161600-110163800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:110161800-110162200	Enhancers	A549	lung
33	chr7:110161800-110163200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr7:110161800-110163400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:110161800-110163400	Enhancers	Fetal Intestine Small	intestine
36	chr7:110161800-110163600	Enhancers	Fetal Heart	heart
37	chr7:110162000-110162200	Flanking Active TSS	Dnd41	blood
38	chr7:110162000-110162400	Enhancers	Brain Substantia Nigra	brain
39	chr7:110162000-110163000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:110162200-110162600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr7:110162200-110162800	Flanking Active TSS	A549	lung
42	chr7:110162200-110163000	Enhancers	Dnd41	blood
43	chr7:110162200-110163600	Enhancers	Liver	Liver
44	chr7:110162200-110164400	Enhancers	Fetal Kidney	kidney
45	chr7:110162400-110163200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:110162600-110162800	Enhancers	Duodenum Mucosa	Duodenum
47	chr7:110162600-110163000	Enhancers	Stomach Mucosa	stomach
48	chr7:110162600-110163200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr7:110162600-110163200	Enhancers	Fetal Lung	lung
50	chr7:110162600-110163200	Enhancers	Fetal Muscle Leg	muscle

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