Variant report

Variant	nsv1028190
Chromosome Location	chr7:110152875-110197412
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	chr7:110162717-110163545	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:110161251-110162197	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	chr7:110162913-110163306	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:110166663-110166922	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:110184991-110185228	HepG2	liver:	n/a	chr7:110185096-110185107
10	CEBPB	chr7:110168937-110169627	HepG2	liver:	n/a	chr7:110169430-110169441
11	CEBPB	chr7:110169305-110169550	HepG2	liver:	n/a	chr7:110169430-110169441
12	CEBPB	chr7:110161316-110161827	HepG2	liver:	n/a	chr7:110161465-110161478
13	CEBPB	chr7:110169292-110169556	Hela-S3	cervix:	n/a	chr7:110169430-110169441
14	CEBPB	chr7:110171283-110171565	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:110176259-110176422	HepG2	liver:	n/a	chr7:110176317-110176328 chr7:110176319-110176330 chr7:110176317-110176330 chr7:110176317-110176330
16	CEBPB	chr7:110162874-110163235	A549	lung:	n/a	n/a
17	CEBPB	chr7:110182130-110182398	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:110184991-110185190	A549	lung:	n/a	chr7:110185096-110185107
19	CEBPB	chr7:110179284-110179632	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:110169268-110169575	A549	lung:	n/a	chr7:110169430-110169441
21	CEBPB	chr7:110162775-110163289	A549	lung:	n/a	n/a
22	CEBPB	chr7:110169270-110169612	IMR90	lung:	n/a	chr7:110169430-110169441
23	CEBPB	chr7:110182172-110182372	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:110169245-110169615	HepG2	liver:	n/a	chr7:110169430-110169441
25	CEBPD	chr7:110169295-110169515	HepG2	liver:	n/a	n/a
26	CEBPD	chr7:110162957-110163255	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	chr7:110174780-110174930	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
31	CTCF	chr7:110174780-110174930	SAEC	small airway:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
32	CTCF	chr7:110184480-110184630	BJ	skin:	n/a	n/a
33	CTCF	chr7:110174752-110174933	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
34	CTCF	chr7:110174787-110174911	ProgFib	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
35	CTCF	chr7:110174780-110174930	HEEpiC	esophagus:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
36	CTCF	chr7:110158870-110158908	GM20000	blood:	n/a	n/a
37	CTCF	chr7:110174757-110174955	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
38	CTCF	chr7:110174760-110174910	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
39	CTCF	chr7:110174653-110175102	MCF-7	breast:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
40	CTCF	chr7:110174780-110174930	NHEK	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
41	CTCF	chr7:110174720-110174870	HepG2	liver:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
42	CTCF	chr7:110174717-110175031	IMR90	lung:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
43	CTCF	chr7:110184400-110184550	AG04449	skin:	n/a	n/a
44	CTCF	chr7:110155363-110155437	GM13976	blood:	n/a	n/a
45	CTCF	chr7:110184393-110184593	IMR90	lung:	n/a	n/a
46	CTCF	chr7:110174700-110174850	HVMF	connective:	n/a	n/a
47	CTCF	chr7:110174780-110174930	AG04449	skin:	n/a	chr7:110174856-110174869 chr7:110174858-110174868
48	CTCF	chr7:110174767-110174933	LNCaP	prostate:	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	GM06990	blood:	n/a
2	chr7:110174780-110174830	SK-N-SH_RA	brain:	n/a
3	chr7:110174780-110174830	HRE	kidney:	n/a
4	chr7:110174780-110174830	CMK	blood:	n/a
5	chr7:110174780-110174830	A549	lung:	n/a
6	chr7:110174780-110174830	PFSK-1	brain:	n/a
7	chr7:110174780-110174830	MCF-7	breast:	n/a
8	chr7:110174780-110174830	HEEpiC	esophagus:	n/a
9	chr7:110174780-110174830	ovcar-3	ovarian:	n/a
10	chr7:110174780-110174830	AG09309	skin:	n/a
11	chr7:110174780-110174830	SAEC	small airway:	n/a
12	chr7:110174780-110174830	GM12892	blood:	n/a
13	chr7:110174780-110174830	HEK293	kidney:	embryo
14	chr7:110174780-110174830	AG10803	skin:	n/a
15	chr7:110174780-110174830	HNPCEpiC	eye:	n/a
16	chr7:110174780-110174830	AoSMC	blood vessel:	n/a
17	chr7:110174780-110174830	HL-60	blood:	n/a
18	chr7:110174780-110174830	PrEC	prostate:	n/a
19	chr7:110174780-110174830	NH-A	brain:	n/a
20	chr7:110174780-110174830	H1-hESC	embryonic stem cell:	embryo
21	chr7:110174780-110174830	IMR90	lung:	fetal
22	chr7:110174780-110174830	GM12878	blood:	n/a
23	chr7:110174780-110174830	GM12891	blood:	n/a
24	chr7:110174780-110174830	HRPEpiC	eye:	n/a
25	chr7:110174780-110174830	LNCaP	prostate:	n/a
26	chr7:110174780-110174830	RPTEC	kidney:	n/a
27	chr7:110174780-110174830	BE2_C	brain:	n/a
28	chr7:110174780-110174830	Jurkat	blood:	n/a
29	chr7:110174780-110174830	HepG2	liver:	n/a
30	chr7:110174780-110174830	HIPEpiC	eye:	n/a
31	chr7:110174780-110174830	ECC-1	luminal epithelium:	n/a
32	chr7:110174780-110174830	SK-N-MC	brain:	n/a
33	chr7:110174780-110174830	PANC-1	pancreas:	n/a
34	chr7:110174780-110174830	T-47D	breast:	n/a
35	chr7:110174780-110174830	NHBE	bronchial:	n/a
36	chr7:110174780-110174830	Hepatocyte	liver:	n/a
37	chr7:110174780-110174830	HUVEC	blood vessel:	n/a
38	chr7:110174780-110174830	AG09319	gingival:	n/a
39	chr7:110174780-110174830	NB4	blood:	n/a
40	chr7:110174780-110174830	Caco-2	colon:	n/a
41	chr7:110174780-110174830	HCM	heart:	n/a
42	chr7:110174780-110174830	BJ	skin:	n/a
43	chr7:110174780-110174830	MCF10A-Er-Src	breast:	n/a
44	chr7:110174780-110174830	HMEC	breast:	n/a
45	chr7:110174780-110174830	ProgFib	skin:	n/a
46	chr7:110174780-110174830	HAEpiC	amniotic membrane:	n/a
47	chr7:110174780-110174830	HCPEpiC	choroid plexus:	n/a
48	chr7:110174780-110174830	K562	blood:	n/a
49	chr7:110174780-110174830	GM19239	blood:	n/a
50	chr7:110174780-110174830	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
2	chr7:110182691..110184718-chr7:110187881..110190742,2	K562	blood:
3	chr7:109858826..109860608-chr7:110161184..110163464,2	MCF-7	breast:
4	chr7:86847727..86850173-chr7:110164264..110166076,2	K562	blood:
5	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:
6	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
7	chr4:4482219..4482825-chr7:110184645..110185165,2	MCF-7	breast:
8	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
9	chr7:110163317..110164856-chr7:110167030..110169564,2	MCF-7	breast:
10	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
11	chr7:110159826..110161779-chr7:110166390..110168526,2	MCF-7	breast:
12	chr7:110177934..110179982-chr7:110181081..110183744,2	K562	blood:
13	chr7:110175478..110177187-chr7:110400882..110403616,2	MCF-7	breast:
14	chr17:57931575..57933892-chr7:110150089..110152912,2	MCF-7	breast:
15	chr7:110158309..110160168-chr7:110161330..110163385,2	K562	blood:

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

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

Extended variants
information (count: 1728 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73429261	chr7:110152882-110152883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537830073	chr7:110152921-110152922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187046348	chr7:110152942-110152943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573142471	chr7:110152966-110152967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542130187	chr7:110152977-110152978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190332518	chr7:110153018-110153019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146272554	chr7:110153020-110153021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550794776	chr7:110153022-110153023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560132691	chr7:110153059-110153060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138085381	chr7:110153141-110153142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532864922	chr7:110153184-110153185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1532974	chr7:110153191-110153192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs566144992	chr7:110153202-110153203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183344657	chr7:110153214-110153215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548449755	chr7:110153234-110153235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573453145	chr7:110153241-110153242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188799447	chr7:110153261-110153262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73429263	chr7:110153289-110153290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577239225	chr7:110153309-110153310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539957141	chr7:110153351-110153352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553540473	chr7:110153405-110153406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573254978	chr7:110153479-110153480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542292923	chr7:110153481-110153482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142362384	chr7:110153495-110153496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575507475	chr7:110153563-110153564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1508202	chr7:110153569-110153570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs1532973	chr7:110153599-110153600	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs544424217	chr7:110153666-110153667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546101954	chr7:110153673-110153674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73429267	chr7:110153718-110153719	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs193092473	chr7:110153808-110153809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559843178	chr7:110153813-110153814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528854136	chr7:110153816-110153817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530435041	chr7:110153837-110153838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2966415	chr7:110153849-110153850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs62465629	chr7:110153866-110153867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374511913	chr7:110153886-110153887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552192742	chr7:110153901-110153902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1508201	chr7:110153909-110153910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370871274	chr7:110154027-110154028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550861029	chr7:110154047-110154048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34072578	chr7:110154056-110154057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367989098	chr7:110154072-110154073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571010448	chr7:110154098-110154099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375295262	chr7:110154139-110154140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540067751	chr7:110154187-110154188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112827881	chr7:110154193-110154194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553503708	chr7:110154200-110154201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs80192074	chr7:110154239-110154240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377061800	chr7:110154244-110154245	Weak transcription	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:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:110152600-110154600	Weak transcription	Dnd41	blood
2	chr7:110154600-110155400	Enhancers	Dnd41	blood
3	chr7:110155000-110155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:110155200-110155400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:110155400-110156000	Enhancers	Right Atrium	heart
6	chr7:110155400-110156000	Genic enhancers	Dnd41	blood
7	chr7:110155400-110162600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:110155600-110155800	Enhancers	Pancreas	Pancrea
9	chr7:110155800-110158800	Weak transcription	Pancreas	Pancrea
10	chr7:110156000-110157600	Enhancers	Dnd41	blood
11	chr7:110157000-110158800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:110157200-110158600	Enhancers	Liver	Liver
13	chr7:110157400-110157600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr7:110157600-110158400	Weak transcription	Dnd41	blood
15	chr7:110158400-110161600	ZNF genes & repeats	Dnd41	blood
16	chr7:110158600-110161000	Weak transcription	Liver	Liver
17	chr7:110158800-110159400	ZNF genes & repeats	Pancreas	Pancrea
18	chr7:110158800-110159800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr7:110158800-110160200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:110159400-110161600	Weak transcription	Pancreas	Pancrea
21	chr7:110159800-110170400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:110160000-110160200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
23	chr7:110160200-110163000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr7:110160800-110163600	Enhancers	HepG2	liver
25	chr7:110160800-110163800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:110161000-110161600	Enhancers	Liver	Liver
27	chr7:110161200-110162600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:110161200-110163200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:110161400-110163400	Enhancers	Fetal Intestine Large	intestine
30	chr7:110161600-110162000	Enhancers	Psoas Muscle	Psoas
31	chr7:110161600-110162000	Transcr. at gene 5' and 3'	Dnd41	blood
32	chr7:110161600-110162200	Flanking Active TSS	Liver	Liver
33	chr7:110161600-110162200	Enhancers	Duodenum Mucosa	Duodenum
34	chr7:110161600-110162800	Enhancers	Brain Hippocampus Middle	brain
35	chr7:110161600-110163200	Enhancers	Pancreas	Pancrea
36	chr7:110161600-110163400	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr7:110161600-110163600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:110161600-110163800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:110161800-110162200	Enhancers	A549	lung
40	chr7:110161800-110163200	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr7:110161800-110163400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:110161800-110163400	Enhancers	Fetal Intestine Small	intestine
43	chr7:110161800-110163600	Enhancers	Fetal Heart	heart
44	chr7:110162000-110162200	Flanking Active TSS	Dnd41	blood
45	chr7:110162000-110162400	Enhancers	Brain Substantia Nigra	brain
46	chr7:110162000-110163000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr7:110162200-110162600	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:110162200-110162800	Flanking Active TSS	A549	lung
49	chr7:110162200-110163000	Enhancers	Dnd41	blood
50	chr7:110162200-110163600	Enhancers	Liver	Liver

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