Variant report

Variant	nsv970912
Chromosome Location	chr7:99567298-99582014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:427)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99578392-99578401	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99577288-99577300	K562	blood:	n/a	n/a
3	ARID3A	chr7:99573511-99574236	HepG2	liver:	n/a	n/a
4	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a
5	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
6	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
7	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
8	CBX3	chr7:99580102-99580449	K562	blood:	n/a	n/a
9	CEBPB	chr7:99575708-99575800	K562	blood:	n/a	chr7:99575754-99575765
10	CEBPB	chr7:99577572-99577727	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr7:99575694-99575894	A549	lung:	n/a	chr7:99575754-99575765
12	CEBPB	chr7:99573782-99574101	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:99580261-99580324	K562	blood:	n/a	n/a
14	CEBPB	chr7:99575690-99575863	HepG2	liver:	n/a	chr7:99575754-99575765
15	CEBPB	chr7:99575685-99575889	IMR90	lung:	n/a	chr7:99575754-99575765
16	CEBPD	chr7:99573511-99573814	HepG2	liver:	n/a	n/a
17	CHD2	chr7:99577376-99577548	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr7:99577680-99577830	HCM	heart:	n/a	n/a
19	CTCF	chr7:99577416-99577712	GM19240	blood:	n/a	n/a
20	CTCF	chr7:99577458-99577682	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr7:99577420-99577570	HepG2	liver:	n/a	n/a
22	CTCF	chr7:99577285-99577289	K562	blood:	n/a	n/a
23	CTCF	chr7:99577440-99577590	GM12864	blood:	n/a	n/a
24	CTCF	chr7:99577680-99577830	RPTEC	kidney:	n/a	n/a
25	CTCF	chr7:99576460-99576610	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr7:99576092-99576142	GM13977	blood:	n/a	n/a
27	CTCF	chr7:99578380-99578530	SAEC	small airway:	n/a	n/a
28	CTCF	chr7:99577400-99577550	GM12870	blood:	n/a	n/a
29	CTCF	chr7:99577660-99577810	GM12873	blood:	n/a	n/a
30	CTCF	chr7:99577405-99577641	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:99577660-99577810	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:99577420-99577570	HEK293	kidney:	n/a	n/a
33	CTCF	chr7:99578734-99578759	LNCaP	prostate:	n/a	n/a
34	CTCF	chr7:99576447-99576569	GM19238	blood:	n/a	n/a
35	CTCF	chr7:99577402-99577704	K562	blood:	n/a	n/a
36	CTCF	chr7:99577420-99577570	WI-38	lung:	n/a	n/a
37	CTCF	chr7:99574100-99574250	BJ	skin:	n/a	n/a
38	CTCF	chr7:99577410-99577757	Medullo	brain:	n/a	n/a
39	CTCF	chr7:99577440-99577590	NHLF	lung:	n/a	n/a
40	CTCF	chr7:99577260-99577410	A549	lung:	n/a	n/a
41	CTCF	chr7:99577347-99577747	GM12878	blood:	n/a	n/a
42	CTCF	chr7:99577400-99577550	AG09319	gingival:	n/a	n/a
43	CTCF	chr7:99577700-99577850	GM12871	blood:	n/a	n/a
44	CTCF	chr7:99577420-99577570	GM12864	blood:	n/a	n/a
45	CTCF	chr7:99577420-99577570	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr7:99576436-99576531	K562	blood:	n/a	n/a
47	CTCF	chr7:99577400-99577550	HFF	foreskin:	n/a	n/a
48	CTCF	chr7:99577240-99577312	GM10266	blood:	n/a	n/a
49	CTCF	chr7:99577700-99577850	HCM	heart:	n/a	n/a
50	CTCF	chr7:99577680-99577830	GM12865	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99574420-99574470	AG09309	skin:	n/a
2	chr7:99574466-99574516	HPAEpiC	pulmonary alveolar:	n/a
3	chr7:99574420-99574470	CMK	blood:	n/a
4	chr7:99573747-99573797	GM12891	blood:	n/a
5	chr7:99574383-99574433	H1-hESC	embryonic stem cell:	embryo
6	chr7:99574420-99574470	PFSK-1	brain:	n/a
7	chr7:99574466-99574516	HIPEpiC	eye:	n/a
8	chr7:99574420-99574470	GM19239	blood:	n/a
9	chr7:99574420-99574470	HCT-116	colon:	n/a
10	chr7:99574383-99574433	MCF-7	breast:	n/a
11	chr7:99576539-99576589	ProgFib	skin:	n/a
12	chr7:99573278-99573328	H1-hESC	embryonic stem cell:	embryo
13	chr7:99576547-99576597	ovcar-3	ovarian:	n/a
14	chr7:99574383-99574433	U87	brain:	n/a
15	chr7:99574420-99574470	HRPEpiC	eye:	n/a
16	chr7:99574383-99574433	NHDF-neo	bronchial:	n/a
17	chr7:99576547-99576597	Jurkat	blood:	n/a
18	chr7:99573278-99573328	NHDF-neo	bronchial:	n/a
19	chr7:99574383-99574433	Caco-2	colon:	n/a
20	chr7:99573278-99573328	GM12878	blood:	n/a
21	chr7:99573747-99573797	HEK293	kidney:	embryo
22	chr7:99573747-99573797	H1-hESC	embryonic stem cell:	embryo
23	chr7:99573278-99573328	AG04449	skin:	fetal
24	chr7:99573278-99573328	GM19239	blood:	n/a
25	chr7:99574466-99574516	HAEpiC	amniotic membrane:	n/a
26	chr7:99574420-99574470	Caco-2	colon:	n/a
27	chr7:99573747-99573797	AG10803	skin:	n/a
28	chr7:99574383-99574433	AoSMC	blood vessel:	n/a
29	chr7:99576539-99576589	H1-hESC	embryonic stem cell:	embryo
30	chr7:99576547-99576597	BE2_C	brain:	n/a
31	chr7:99573278-99573328	MCF-7	breast:	n/a
32	chr7:99573747-99573797	HRPEpiC	eye:	n/a
33	chr7:99574383-99574433	ProgFib	skin:	n/a
34	chr7:99576547-99576597	AG04450	lung:	fetal
35	chr7:99576539-99576589	A549	lung:	n/a
36	chr7:99576539-99576589	GM12892	blood:	n/a
37	chr7:99574420-99574470	PANC-1	pancreas:	n/a
38	chr7:99574420-99574470	HepG2	liver:	n/a
39	chr7:99574466-99574516	H1-hESC	embryonic stem cell:	embryo
40	chr7:99576547-99576597	AG10803	skin:	n/a
41	chr7:99574420-99574470	GM12892	blood:	n/a
42	chr7:99576539-99576589	HepG2	liver:	n/a
43	chr7:99574466-99574516	SAEC	small airway:	n/a
44	chr7:99574383-99574433	GM06990	blood:	n/a
45	chr7:99574383-99574433	NH-A	brain:	n/a
46	chr7:99574383-99574433	HUVEC	blood vessel:	n/a
47	chr7:99574420-99574470	MCF10A-Er-Src	breast:	n/a
48	chr7:99573278-99573328	NHBE	bronchial:	n/a
49	chr7:99574383-99574433	SKMC	muscle:	n/a
50	chr7:99576547-99576597	HRE	kidney:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
2	chr7:99576315..99578805-chr7:99697574..99699659,2	MCF-7	breast:
3	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
4	chr7:99569355..99572345-chr7:99573855..99575853,2	K562	blood:
5	chr7:99516941..99519594-chr7:99565743..99568567,2	MCF-7	breast:
6	chr7:99573022..99574848-chr7:99645324..99647689,2	K562	blood:
7	chr7:99577726..99579955-chr7:100932141..100934760,2	MCF-7	breast:
8	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
9	chr7:99580447..99585207-chr7:99587129..99590928,6	K562	blood:
10	chr7:99577974..99580142-chr7:99679417..99681794,2	MCF-7	breast:
11	chr7:99577230..99578015-chr7:99588605..99589135,2	MCF-7	breast:

No data

Variant related genes	Relation type
AZGP1	TF binding region
AZGP1P1	TF binding region
AZGP1	CpG island
AZGP1P1	CpG island
ENSG00000146833	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000160862	chromatin interactions

Extended variants
information (count: 654 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79039815	chr7:99567380-99567381	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs563904304	chr7:99567396-99567397	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs187075417	chr7:99567416-99567417	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2527923	chr7:99567455-99567456	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs191594465	chr7:99567469-99567470	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs573356459	chr7:99567471-99567472	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs183049437	chr7:99567473-99567474	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556307734	chr7:99567478-99567479	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs374790167	chr7:99567494-99567495	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs578128385	chr7:99567566-99567567	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543264640	chr7:99567679-99567680	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368208508	chr7:99567693-99567694	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs188487094	chr7:99567797-99567798	Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560660495	chr7:99567803-99567804	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs140897498	chr7:99567859-99567860	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs59340776	chr7:99567864-99567865	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111914925	chr7:99567878-99567879	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112176908	chr7:99567891-99567892	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs542607864	chr7:99567903-99567904	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2527917	chr7:99567908-99567909	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs565702110	chr7:99567917-99567918	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34183830	chr7:99567945-99567946	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192951502	chr7:99567969-99567970	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113484180	chr7:99567980-99567981	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35781494	chr7:99567990-99567991	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533014059	chr7:99568030-99568031	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs551644638	chr7:99568052-99568053	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566702002	chr7:99568068-99568069	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534099571	chr7:99568074-99568075	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374977245	chr7:99568086-99568087	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554904949	chr7:99568089-99568090	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566941725	chr7:99568100-99568101	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs537523269	chr7:99568164-99568165	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs184578481	chr7:99568182-99568183	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148697840	chr7:99568190-99568191	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114045383	chr7:99568199-99568200	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554345946	chr7:99568243-99568244	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs539506690	chr7:99568273-99568274	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557843961	chr7:99568282-99568283	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs572610058	chr7:99568284-99568285	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs543358789	chr7:99568307-99568308	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs78932884	chr7:99568322-99568323	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576535482	chr7:99568324-99568325	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372833137	chr7:99568347-99568348	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576109978	chr7:99568382-99568383	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543919933	chr7:99568416-99568417	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs187892991	chr7:99568418-99568419	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200823928	chr7:99568479-99568480	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs146314754	chr7:99568496-99568497	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs139527091	chr7:99568501-99568502	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	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
small cell lung cancer	20016488	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
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
2	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
3	chr7:99563400-99573000	Weak transcription	Gastric	stomach
4	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
6	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
7	chr7:99565800-99568200	Weak transcription	HepG2	liver
8	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
9	chr7:99567000-99569000	Weak transcription	Lung	lung
10	chr7:99567000-99570600	Genic enhancers	Liver	Liver
11	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
13	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
14	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:99568200-99569600	Strong transcription	HepG2	liver
16	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
17	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
18	chr7:99569000-99569600	Enhancers	Lung	lung
19	chr7:99569600-99571600	Weak transcription	HepG2	liver
20	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
21	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
22	chr7:99570600-99570800	Enhancers	Liver	Liver
23	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
24	chr7:99571400-99573800	Active TSS	Liver	Liver
25	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
26	chr7:99571600-99572400	Enhancers	HepG2	liver
27	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
28	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr7:99572400-99572800	Flanking Active TSS	HepG2	liver
30	chr7:99572400-99573600	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr7:99572400-99573600	Active TSS	Right Ventricle	heart
32	chr7:99572600-99573400	Active TSS	Adipose Nuclei	Adipose
33	chr7:99572600-99573800	Active TSS	Pancreas	Pancrea
34	chr7:99572800-99573800	Active TSS	HepG2	liver
35	chr7:99572800-99574000	Active TSS	Brain Substantia Nigra	brain
36	chr7:99572800-99574200	Enhancers	Brain Cingulate Gyrus	brain
37	chr7:99573000-99573600	Active TSS	Duodenum Mucosa	Duodenum
38	chr7:99573000-99573600	Active TSS	Left Ventricle	heart
39	chr7:99573000-99573800	Active TSS	Gastric	stomach
40	chr7:99573000-99574200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr7:99573400-99573800	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr7:99573400-99573800	Active TSS	Brain Anterior Caudate	brain
43	chr7:99573400-99574200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:99573400-99574400	Enhancers	Fetal Intestine Small	intestine
45	chr7:99573400-99574600	Enhancers	Stomach Mucosa	stomach
46	chr7:99573600-99573800	Enhancers	Brain Hippocampus Middle	brain
47	chr7:99573600-99573800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:99573600-99573800	Enhancers	Left Ventricle	heart
49	chr7:99573600-99574000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:99573600-99574200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin

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