Variant report

Variant	nsv824234
Chromosome Location	chr7:99553734-99585424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:612)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 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	ATF1	chr7:99556328-99556705	K562	blood:	n/a	n/a
5	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
6	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
8	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a
9	CBX3	chr7:99580102-99580449	K562	blood:	n/a	n/a
10	CEBPB	chr7:99583119-99583425	Hela-S3	cervix:	n/a	chr7:99583288-99583301
11	CEBPB	chr7:99583168-99583411	A549	lung:	n/a	chr7:99583288-99583301
12	CEBPB	chr7:99565066-99565152	K562	blood:	n/a	n/a
13	CEBPB	chr7:99567060-99567224	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr7:99556353-99556621	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr7:99575690-99575863	HepG2	liver:	n/a	chr7:99575754-99575765
16	CEBPB	chr7:99575708-99575800	K562	blood:	n/a	chr7:99575754-99575765
17	CEBPB	chr7:99573782-99574101	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:99577572-99577727	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:99556368-99556553	K562	blood:	n/a	n/a
20	CEBPB	chr7:99567135-99567143	K562	blood:	n/a	n/a
21	CEBPB	chr7:99575694-99575894	A549	lung:	n/a	chr7:99575754-99575765
22	CEBPB	chr7:99575685-99575889	IMR90	lung:	n/a	chr7:99575754-99575765
23	CEBPB	chr7:99583228-99583367	HepG2	liver:	n/a	chr7:99583288-99583301
24	CEBPB	chr7:99580261-99580324	K562	blood:	n/a	n/a
25	CEBPD	chr7:99573511-99573814	HepG2	liver:	n/a	n/a
26	CHD2	chr7:99577376-99577548	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:99577400-99577550	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr7:99577300-99577450	HCM	heart:	n/a	n/a
29	CTCF	chr7:99577700-99577850	A549	lung:	n/a	n/a
30	CTCF	chr7:99577408-99577736	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr7:99577660-99577810	HAc	cerebellar:	n/a	n/a
32	CTCF	chr7:99577905-99577911	GM19240	blood:	n/a	n/a
33	CTCF	chr7:99577400-99577550	GM12865	blood:	n/a	n/a
34	CTCF	chr7:99577440-99577590	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr7:99577420-99577570	HCPEpiC	choroid plexus:	n/a	n/a
36	CTCF	chr7:99577680-99577830	GM12872	blood:	n/a	n/a
37	CTCF	chr7:99577880-99578030	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr7:99577463-99577604	T-47D	breast:	n/a	n/a
39	CTCF	chr7:99577400-99577550	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr7:99577218-99577880	A549	lung:	n/a	n/a
41	CTCF	chr7:99577414-99577732	GM10266	blood:	n/a	n/a
42	CTCF	chr7:99577284-99577776	HCT-116	colon:	n/a	n/a
43	CTCF	chr7:99577660-99577810	GM06990	blood:	n/a	n/a
44	CTCF	chr7:99577249-99577305	GM12891	blood:	n/a	n/a
45	CTCF	chr7:99577240-99577312	GM10266	blood:	n/a	n/a
46	CTCF	chr7:99577431-99577704	HepG2	liver:	n/a	n/a
47	CTCF	chr7:99576434-99576528	GM19240	blood:	n/a	n/a
48	CTCF	chr7:99577700-99577850	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr7:99576447-99576569	GM19238	blood:	n/a	n/a
50	CTCF	chr7:99577420-99577570	GM12873	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99576547-99576597	IMR90	lung:	fetal
2	chr7:99559579-99559629	HCT-116	colon:	n/a
3	chr7:99576547-99576597	IMR90	lung:	fetal
4	chr7:99559579-99559629	HCT-116	colon:	n/a
5	chr7:99573278-99573328	NHDF-neo	bronchial:	n/a
6	chr7:99574420-99574470	HCT-116	colon:	n/a
7	chr7:99558185-99558235	AG09309	skin:	n/a
8	chr7:99573278-99573328	NT2-D1	testis:	n/a
9	chr7:99576547-99576597	K562	blood:	n/a
10	chr7:99574383-99574433	HEEpiC	esophagus:	n/a
11	chr7:99574383-99574433	NHBE	bronchial:	n/a
12	chr7:99576539-99576589	AG09309	skin:	n/a
13	chr7:99576547-99576597	Caco-2	colon:	n/a
14	chr7:99576547-99576597	LNCaP	prostate:	n/a
15	chr7:99574466-99574516	GM19239	blood:	n/a
16	chr7:99576547-99576597	HepG2	liver:	n/a
17	chr7:99573747-99573797	AG04449	skin:	fetal
18	chr7:99559579-99559629	NHBE	bronchial:	n/a
19	chr7:99559579-99559629	HepG2	liver:	n/a
20	chr7:99573278-99573328	HEK293	kidney:	embryo
21	chr7:99574383-99574433	PFSK-1	brain:	n/a
22	chr7:99558185-99558235	NH-A	brain:	n/a
23	chr7:99576539-99576589	NHDF-neo	bronchial:	n/a
24	chr7:99558185-99558235	HIPEpiC	eye:	n/a
25	chr7:99564474-99564524	SK-N-MC	brain:	n/a
26	chr7:99576539-99576589	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:99574420-99574470	MCF10A-Er-Src	breast:	n/a
28	chr7:99576539-99576589	HEK293	kidney:	embryo
29	chr7:99573278-99573328	AG10803	skin:	n/a
30	chr7:99558185-99558235	AoSMC	blood vessel:	n/a
31	chr7:99574383-99574433	MCF10A-Er-Src	breast:	n/a
32	chr7:99574466-99574516	NHBE	bronchial:	n/a
33	chr7:99576539-99576589	MCF-7	breast:	n/a
34	chr7:99559579-99559629	SK-N-SH_RA	brain:	n/a
35	chr7:99574383-99574433	Jurkat	blood:	n/a
36	chr7:99573278-99573328	SAEC	small airway:	n/a
37	chr7:99574466-99574516	AG04449	skin:	fetal
38	chr7:99574383-99574433	Hela-S3	cervix:	n/a
39	chr7:99574466-99574516	H1-hESC	embryonic stem cell:	embryo
40	chr7:99573278-99573328	HCPEpiC	choroid plexus:	n/a
41	chr7:99573747-99573797	HCPEpiC	choroid plexus:	n/a
42	chr7:99564474-99564524	NHDF-neo	bronchial:	n/a
43	chr7:99573747-99573797	HepG2	liver:	n/a
44	chr7:99576539-99576589	SK-N-SH	brain:	n/a
45	chr7:99574466-99574516	PrEC	prostate:	n/a
46	chr7:99574420-99574470	HUVEC	blood vessel:	n/a
47	chr7:99559579-99559629	AG09309	skin:	n/a
48	chr7:99573278-99573328	NH-A	brain:	n/a
49	chr7:99576539-99576589	GM12892	blood:	n/a
50	chr7:99573747-99573797	AG09309	skin:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99513401..99515939-chr7:99585193..99587203,2	K562	blood:
2	chr7:99577726..99579955-chr7:100932141..100934760,2	MCF-7	breast:
3	chr7:99552657..99555253-chr7:99568391..99571946,4	MCF-7	breast:
4	chr7:99561546..99564106-chr7:99573574..99575308,2	K562	blood:
5	chr7:99516941..99519594-chr7:99565743..99568567,2	MCF-7	breast:
6	chr7:99582037..99584694-chr7:99677705..99680267,2	K562	blood:
7	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
8	chr7:99573022..99574848-chr7:99645324..99647689,2	K562	blood:
9	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
10	chr7:99577974..99580142-chr7:99679417..99681794,2	MCF-7	breast:
11	chr7:99584391..99586095-chr7:99609489..99611371,2	K562	blood:
12	chr7:99561135..99564106-chr7:99572617..99575074,2	K562	blood:
13	chr7:99553429..99555510-chr7:99679317..99681058,2	K562	blood:
14	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
15	chr7:99580447..99585207-chr7:99587129..99590928,6	K562	blood:
16	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
17	chr7:99544479..99546185-chr7:99557536..99559733,2	K562	blood:
18	chr7:99552193..99555165-chr7:99565614..99568546,3	K562	blood:
19	chr7:99569355..99572345-chr7:99573855..99575853,2	K562	blood:
20	chr7:99576315..99578805-chr7:99697574..99699659,2	MCF-7	breast:
21	chr7:99546378..99548989-chr7:99551538..99554041,2	MCF-7	breast:
22	chr7:99550695..99553534-chr7:99558845..99560540,2	MCF-7	breast:
23	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
24	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
25	chr7:99577230..99578015-chr7:99588605..99589135,2	MCF-7	breast:
26	chr7:99516441..99518017-chr7:99556643..99558220,2	MCF-7	breast:

No data

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

Extended variants
information (count: 1427 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1427 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529852322	chr7:99553742-99553743	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs117304234	chr7:99553769-99553770	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146394060	chr7:99553770-99553771	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs561869149	chr7:99553793-99553794	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs575246689	chr7:99553820-99553821	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs28707517	chr7:99553894-99553895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs78731432	chr7:99553929-99553930	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78497987	chr7:99553932-99553933	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541697340	chr7:99553957-99553958	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563596136	chr7:99553958-99553959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs529906440	chr7:99554119-99554120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564817974	chr7:99554120-99554121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565712046	chr7:99554121-99554122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530669466	chr7:99554156-99554157	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114498341	chr7:99554174-99554175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564033599	chr7:99554175-99554176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs562867752	chr7:99554186-99554187	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528113760	chr7:99554243-99554244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111290725	chr7:99554251-99554252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs546695115	chr7:99554283-99554284	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568198535	chr7:99554291-99554292	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs193156084	chr7:99554326-99554327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550942862	chr7:99554360-99554361	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200855676	chr7:99554387-99554388	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs141546482	chr7:99554399-99554400	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368484314	chr7:99554425-99554426	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs150714718	chr7:99554456-99554457	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73156683	chr7:99554472-99554473	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs572875265	chr7:99554509-99554510	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535002308	chr7:99554511-99554512	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs372444246	chr7:99554537-99554538	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184588380	chr7:99554541-99554542	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs573842611	chr7:99554568-99554569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs187808994	chr7:99554575-99554576	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563297871	chr7:99554579-99554580	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs575408123	chr7:99554598-99554599	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191204357	chr7:99554603-99554604	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564399297	chr7:99554604-99554605	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568641098	chr7:99554612-99554613	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs528078768	chr7:99554615-99554616	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547046956	chr7:99554616-99554617	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs115951506	chr7:99554652-99554653	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561766249	chr7:99554680-99554681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528937699	chr7:99554689-99554690	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540757251	chr7:99554697-99554698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550660288	chr7:99554710-99554711	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs569318460	chr7:99554727-99554728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540047598	chr7:99554753-99554754	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs551637407	chr7:99554766-99554767	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566862684	chr7:99554864-99554865	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99550400-99553800	Enhancers	Liver	Liver
2	chr7:99552800-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:99552800-99553800	Enhancers	GM12878-XiMat	blood
4	chr7:99552800-99554000	Enhancers	HepG2	liver
5	chr7:99553000-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:99553800-99563200	Weak transcription	Liver	Liver
7	chr7:99554000-99565000	Weak transcription	HepG2	liver
8	chr7:99556400-99556600	Bivalent/Poised TSS	K562	blood
9	chr7:99560400-99560600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
10	chr7:99561600-99564000	Weak transcription	Pancreas	Pancrea
11	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
12	chr7:99563200-99567000	Strong transcription	Liver	Liver
13	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
14	chr7:99563400-99573000	Weak transcription	Gastric	stomach
15	chr7:99564000-99565600	Strong transcription	Pancreas	Pancrea
16	chr7:99564600-99564800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:99565000-99565800	Strong transcription	HepG2	liver
19	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
20	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
21	chr7:99565800-99568200	Weak transcription	HepG2	liver
22	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
23	chr7:99566800-99567000	Enhancers	Lung	lung
24	chr7:99567000-99569000	Weak transcription	Lung	lung
25	chr7:99567000-99570600	Genic enhancers	Liver	Liver
26	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
28	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
29	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:99568200-99569600	Strong transcription	HepG2	liver
31	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
32	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
33	chr7:99569000-99569600	Enhancers	Lung	lung
34	chr7:99569600-99571600	Weak transcription	HepG2	liver
35	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
36	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
37	chr7:99570600-99570800	Enhancers	Liver	Liver
38	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
39	chr7:99571400-99573800	Active TSS	Liver	Liver
40	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
41	chr7:99571600-99572400	Enhancers	HepG2	liver
42	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
43	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr7:99572400-99572800	Flanking Active TSS	HepG2	liver
45	chr7:99572400-99573600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr7:99572400-99573600	Active TSS	Right Ventricle	heart
47	chr7:99572600-99573400	Active TSS	Adipose Nuclei	Adipose
48	chr7:99572600-99573800	Active TSS	Pancreas	Pancrea
49	chr7:99572800-99573800	Active TSS	HepG2	liver
50	chr7:99572800-99574000	Active TSS	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links