Variant report

Variant	esv3353578
Chromosome Location	chr7:99553048-99586040
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:512)
CpG islands
(count:610)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99553594-99553700	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99573511-99574236	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:99577288-99577300	K562	blood:	n/a	n/a
4	ARID3A	chr7:99578392-99578401	HepG2	liver:	n/a	n/a
5	ATF1	chr7:99556328-99556705	K562	blood:	n/a	n/a
6	BATF	chr7:99552903-99553159	GM12878	blood:	n/a	chr7:99553049-99553060 chr7:99553050-99553060
7	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
10	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
11	CBX3	chr7:99580102-99580449	K562	blood:	n/a	n/a
12	CEBPB	chr7:99583168-99583411	A549	lung:	n/a	chr7:99583288-99583301
13	CEBPB	chr7:99580261-99580324	K562	blood:	n/a	n/a
14	CEBPB	chr7:99567135-99567143	K562	blood:	n/a	n/a
15	CEBPB	chr7:99583228-99583367	HepG2	liver:	n/a	chr7:99583288-99583301
16	CEBPB	chr7:99575708-99575800	K562	blood:	n/a	chr7:99575754-99575765
17	CEBPB	chr7:99583119-99583425	Hela-S3	cervix:	n/a	chr7:99583288-99583301
18	CEBPB	chr7:99556353-99556621	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr7:99575690-99575863	HepG2	liver:	n/a	chr7:99575754-99575765
20	CEBPB	chr7:99575694-99575894	A549	lung:	n/a	chr7:99575754-99575765
21	CEBPB	chr7:99565066-99565152	K562	blood:	n/a	n/a
22	CEBPB	chr7:99575685-99575889	IMR90	lung:	n/a	chr7:99575754-99575765
23	CEBPB	chr7:99577572-99577727	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:99573782-99574101	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:99556368-99556553	K562	blood:	n/a	n/a
26	CEBPB	chr7:99567060-99567224	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPD	chr7:99573511-99573814	HepG2	liver:	n/a	n/a
28	CHD2	chr7:99577376-99577548	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr7:99577660-99577810	GM12875	blood:	n/a	n/a
30	CTCF	chr7:99577680-99577830	HVMF	connective:	n/a	n/a
31	CTCF	chr7:99576443-99576562	GM12891	blood:	n/a	n/a
32	CTCF	chr7:99577700-99577850	A549	lung:	n/a	n/a
33	CTCF	chr7:99577120-99577270	GM12866	blood:	n/a	n/a
34	CTCF	chr7:99577356-99577742	IMR90	lung:	n/a	n/a
35	CTCF	chr7:99577387-99577738	GM13977	blood:	n/a	n/a
36	CTCF	chr7:99577440-99577590	HCM	heart:	n/a	n/a
37	CTCF	chr7:99577471-99577586	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:99577680-99577830	HCM	heart:	n/a	n/a
39	CTCF	chr7:99573689-99573696	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr7:99577440-99577590	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr7:99577420-99577570	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr7:99577660-99577810	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr7:99577660-99577810	GM06990	blood:	n/a	n/a
44	CTCF	chr7:99576460-99576610	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr7:99577440-99577590	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr7:99576436-99576531	K562	blood:	n/a	n/a
47	CTCF	chr7:99565020-99565170	K562	blood:	n/a	n/a
48	CTCF	chr7:99577438-99577681	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:99577280-99577430	HAc	cerebellar:	n/a	n/a
50	CTCF	chr7:99577700-99577850	NHDF-neo	bronchial:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99576539-99576589	IMR90	lung:	fetal
2	chr7:99574383-99574433	SK-N-SH_RA	brain:	n/a
3	chr7:99576547-99576597	HRE	kidney:	n/a
4	chr7:99558185-99558235	GM06990	blood:	n/a
5	chr7:99574383-99574433	K562	blood:	n/a
6	chr7:99574383-99574433	LNCaP	prostate:	n/a
7	chr7:99574420-99574470	Jurkat	blood:	n/a
8	chr7:99558185-99558235	SK-N-SH_RA	brain:	n/a
9	chr7:99574383-99574433	HL-60	blood:	n/a
10	chr7:99558185-99558235	GM19239	blood:	n/a
11	chr7:99559579-99559629	LNCaP	prostate:	n/a
12	chr7:99564474-99564524	HRPEpiC	eye:	n/a
13	chr7:99564474-99564524	AG10803	skin:	n/a
14	chr7:99576547-99576597	AG09319	gingival:	n/a
15	chr7:99576547-99576597	IMR90	lung:	fetal
16	chr7:99574420-99574470	SAEC	small airway:	n/a
17	chr7:99574420-99574470	AG10803	skin:	n/a
18	chr7:99558185-99558235	HIPEpiC	eye:	n/a
19	chr7:99576539-99576589	SKMC	muscle:	n/a
20	chr7:99573747-99573797	AG10803	skin:	n/a
21	chr7:99574420-99574470	Caco-2	colon:	n/a
22	chr7:99574383-99574433	HIPEpiC	eye:	n/a
23	chr7:99576547-99576597	GM12878	blood:	n/a
24	chr7:99574383-99574433	Hepatocyte	liver:	n/a
25	chr7:99564474-99564524	AG09309	skin:	n/a
26	chr7:99558185-99558235	Hepatocyte	liver:	n/a
27	chr7:99574466-99574516	HUVEC	blood vessel:	n/a
28	chr7:99574383-99574433	HAEpiC	amniotic membrane:	n/a
29	chr7:99574383-99574433	GM12892	blood:	n/a
30	chr7:99559579-99559629	Caco-2	colon:	n/a
31	chr7:99573278-99573328	HAEpiC	amniotic membrane:	n/a
32	chr7:99559579-99559629	AG09319	gingival:	n/a
33	chr7:99573747-99573797	H1-hESC	embryonic stem cell:	embryo
34	chr7:99574383-99574433	HUVEC	blood vessel:	n/a
35	chr7:99576539-99576589	HL-60	blood:	n/a
36	chr7:99574420-99574470	Hela-S3	cervix:	n/a
37	chr7:99576539-99576589	GM12892	blood:	n/a
38	chr7:99576539-99576589	K562	blood:	n/a
39	chr7:99573747-99573797	HCPEpiC	choroid plexus:	n/a
40	chr7:99574383-99574433	HEK293	kidney:	embryo
41	chr7:99564474-99564524	NHBE	bronchial:	n/a
42	chr7:99558185-99558235	AG04449	skin:	fetal
43	chr7:99559579-99559629	GM19239	blood:	n/a
44	chr7:99574420-99574470	HRCEpiC	kidney:	n/a
45	chr7:99573747-99573797	NH-A	brain:	n/a
46	chr7:99576547-99576597	SAEC	small airway:	n/a
47	chr7:99573278-99573328	HRE	kidney:	n/a
48	chr7:99576547-99576597	ProgFib	skin:	n/a
49	chr7:99574420-99574470	AoSMC	blood vessel:	n/a
50	chr7:99576547-99576597	ovcar-3	ovarian:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99552193..99555165-chr7:99565614..99568546,3	K562	blood:
2	chr7:99515983..99517855-chr7:99552009..99553690,2	MCF-7	breast:
3	chr7:99582037..99584694-chr7:99677705..99680267,2	K562	blood:
4	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
5	chr7:99550695..99553534-chr7:99558845..99560540,2	MCF-7	breast:
6	chr7:99516441..99518017-chr7:99556643..99558220,2	MCF-7	breast:
7	chr7:99569355..99572345-chr7:99573855..99575853,2	K562	blood:
8	chr7:99577974..99580142-chr7:99679417..99681794,2	MCF-7	breast:
9	chr7:99584391..99586095-chr7:99609489..99611371,2	K562	blood:
10	chr7:99561135..99564106-chr7:99572617..99575074,2	K562	blood:
11	chr7:99550695..99553534-chr7:99558845..99560540,2	MCF-7	breast:
12	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
13	chr7:99577726..99579955-chr7:100932141..100934760,2	MCF-7	breast:
14	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
15	chr7:99580447..99585207-chr7:99587129..99590928,6	K562	blood:
16	chr7:99515474..99518311-chr7:99585562..99587097,2	K562	blood:
17	chr7:99552657..99555253-chr7:99568391..99571946,4	MCF-7	breast:
18	chr7:99516941..99519594-chr7:99565743..99568567,2	MCF-7	breast:
19	chr7:99546378..99548989-chr7:99551538..99554041,2	MCF-7	breast:
20	chr7:99573022..99574848-chr7:99645324..99647689,2	K562	blood:
21	chr7:99513401..99515939-chr7:99585193..99587203,2	K562	blood:
22	chr7:99544479..99546185-chr7:99557536..99559733,2	K562	blood:
23	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
24	chr16:3072904..3075257-chr7:99551706..99553216,2	MCF-7	breast:
25	chr7:99576315..99578805-chr7:99697574..99699659,2	MCF-7	breast:
26	chr7:99553429..99555510-chr7:99679317..99681058,2	K562	blood:
27	chr7:99577524..99578039-chr7:99588237..99589217,3	K562	blood:
28	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
29	chr7:99525542..99528041-chr7:99585746..99587767,2	MCF-7	breast:
30	chr7:99561546..99564106-chr7:99573574..99575308,2	K562	blood:
31	chr7:99577230..99578015-chr7:99588605..99589135,2	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
ENSG00000131652	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000160862	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000237640	chromatin interactions
ENSG00000103145	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000176402	chromatin interactions

Extended variants
information (count: 1475 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117268080	chr7:99553066-99553067	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs528612114	chr7:99553087-99553088	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs79335386	chr7:99553092-99553093	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs114313339	chr7:99553147-99553148	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs115292693	chr7:99553163-99553164	Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs2525548	chr7:99553167-99553168	Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs532103703	chr7:99553234-99553235	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs550424782	chr7:99553239-99553240	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs563139684	chr7:99553335-99553336	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530516873	chr7:99553336-99553337	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs143365014	chr7:99553360-99553361	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191365439	chr7:99553361-99553362	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570465003	chr7:99553434-99553435	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35180763	chr7:99553437-99553438	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs562661782	chr7:99553507-99553508	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs183619425	chr7:99553528-99553529	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs553116272	chr7:99553529-99553530	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs199796601	chr7:99553541-99553542	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs564339619	chr7:99553595-99553596	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs148347774	chr7:99553616-99553617	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs535700609	chr7:99553647-99553648	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs188204635	chr7:99553655-99553656	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs575891869	chr7:99553664-99553665	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs370544008	chr7:99553667-99553668	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs142099766	chr7:99553672-99553673	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs557820073	chr7:99553730-99553731	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529852322	chr7:99553742-99553743	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs117304234	chr7:99553769-99553770	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs146394060	chr7:99553770-99553771	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs561869149	chr7:99553793-99553794	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs575246689	chr7:99553820-99553821	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28707517	chr7:99553894-99553895	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78731432	chr7:99553929-99553930	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs78497987	chr7:99553932-99553933	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs541697340	chr7:99553957-99553958	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563596136	chr7:99553958-99553959	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529906440	chr7:99554119-99554120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs564817974	chr7:99554120-99554121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs565712046	chr7:99554121-99554122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530669466	chr7:99554156-99554157	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs114498341	chr7:99554174-99554175	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564033599	chr7:99554175-99554176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs562867752	chr7:99554186-99554187	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs528113760	chr7:99554243-99554244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs111290725	chr7:99554251-99554252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546695115	chr7:99554283-99554284	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs568198535	chr7:99554291-99554292	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs193156084	chr7:99554326-99554327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550942862	chr7:99554360-99554361	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200855676	chr7:99554387-99554388	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:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99550400-99553800	Enhancers	Liver	Liver
2	chr7:99550800-99553200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr7:99552800-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:99552800-99553800	Enhancers	GM12878-XiMat	blood
5	chr7:99552800-99554000	Enhancers	HepG2	liver
6	chr7:99553000-99553800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr7:99553800-99563200	Weak transcription	Liver	Liver
8	chr7:99554000-99565000	Weak transcription	HepG2	liver
9	chr7:99556400-99556600	Bivalent/Poised TSS	K562	blood
10	chr7:99560400-99560600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
11	chr7:99561600-99564000	Weak transcription	Pancreas	Pancrea
12	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
13	chr7:99563200-99567000	Strong transcription	Liver	Liver
14	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
15	chr7:99563400-99573000	Weak transcription	Gastric	stomach
16	chr7:99564000-99565600	Strong transcription	Pancreas	Pancrea
17	chr7:99564600-99564800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:99565000-99565800	Strong transcription	HepG2	liver
20	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
21	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
22	chr7:99565800-99568200	Weak transcription	HepG2	liver
23	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
24	chr7:99566800-99567000	Enhancers	Lung	lung
25	chr7:99567000-99569000	Weak transcription	Lung	lung
26	chr7:99567000-99570600	Genic enhancers	Liver	Liver
27	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
29	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
30	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:99568200-99569600	Strong transcription	HepG2	liver
32	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
33	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
34	chr7:99569000-99569600	Enhancers	Lung	lung
35	chr7:99569600-99571600	Weak transcription	HepG2	liver
36	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
37	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
38	chr7:99570600-99570800	Enhancers	Liver	Liver
39	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
40	chr7:99571400-99573800	Active TSS	Liver	Liver
41	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
42	chr7:99571600-99572400	Enhancers	HepG2	liver
43	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
44	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr7:99572400-99572800	Flanking Active TSS	HepG2	liver
46	chr7:99572400-99573600	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr7:99572400-99573600	Active TSS	Right Ventricle	heart
48	chr7:99572600-99573400	Active TSS	Adipose Nuclei	Adipose
49	chr7:99572600-99573800	Active TSS	Pancreas	Pancrea
50	chr7:99572800-99573800	Active TSS	HepG2	liver

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