Variant report

Variant	nsv888689
Chromosome Location	chr7:87093247-87110017
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:432)
CpG islands
(count:915)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:87105129-87105319	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:87103805-87104061	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:87093353-87093783	HepG2	liver:	n/a	n/a
4	ATF2	chr7:87103357-87104743	GM12878	blood:	n/a	chr7:87104394-87104401
5	ATF2	chr7:87103159-87104838	GM12878	blood:	n/a	chr7:87104394-87104401
6	BACH1	chr7:87104693-87104885	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:87094518-87094660	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:87103714-87104408	GM12878	blood:	n/a	chr7:87104368-87104377
9	BATF	chr7:87103408-87104590	GM12878	blood:	n/a	chr7:87104368-87104377
10	BCL11A	chr7:87103389-87104608	GM12878	blood:	n/a	chr7:87103426-87103435
11	BCL11A	chr7:87103765-87104455	GM12878	blood:	n/a	n/a
12	BCL3	chr7:87103771-87104306	GM12878	blood:	n/a	n/a
13	BCL3	chr7:87103501-87104527	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:87103241-87104577	GM12878	blood:	n/a	chr7:87103426-87103435
15	BCLAF1	chr7:87103284-87104672	GM12878	blood:	n/a	chr7:87103426-87103435
16	BHLHE40	chr7:87093399-87093797	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:87105560-87105599	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:87103333-87105002	GM12878	blood:	n/a	n/a
19	BRCA1	chr7:87104037-87104253	GM12878	blood:	n/a	n/a
20	BRCA1	chr7:87093351-87093701	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:87105230-87105252	GM12878	blood:	n/a	n/a
22	CCNT2	chr7:87105224-87105341	K562	blood:	n/a	n/a
23	CEBPB	chr7:87103220-87104832	GM12878	blood:	n/a	n/a
24	CEBPB	chr7:87104216-87104585	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:87103821-87104498	GM12878	blood:	n/a	n/a
26	CEBPB	chr7:87104255-87104498	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr7:87104230-87104587	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:87093392-87093696	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:87104372-87104706	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr7:87104253-87104485	K562	blood:	n/a	n/a
31	CEBPB	chr7:87104224-87104575	A549	lung:	n/a	n/a
32	CEBPD	chr7:87094462-87094862	HepG2	liver:	n/a	n/a
33	CEBPD	chr7:87104723-87105270	HepG2	liver:	n/a	n/a
34	CHD1	chr7:87103651-87105326	GM12878	blood:	n/a	chr7:87104889-87104899
35	CHD1	chr7:87104723-87104848	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr7:87105625-87106080	GM12878	blood:	n/a	n/a
37	CHD1	chr7:87102462-87102974	GM12878	blood:	n/a	n/a
38	CHD1	chr7:87103203-87103403	GM12878	blood:	n/a	n/a
39	CHD2	chr7:87103416-87105339	GM12878	blood:	n/a	chr7:87104889-87104899
40	CHD2	chr7:87104791-87105412	HepG2	liver:	n/a	chr7:87104889-87104899
41	CHD2	chr7:87094469-87094656	HepG2	liver:	n/a	n/a
42	CHD2	chr7:87102329-87102373	GM12878	blood:	n/a	n/a
43	CHD2	chr7:87093418-87093639	HepG2	liver:	n/a	n/a
44	CHD2	chr7:87094526-87094716	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:87103692-87104672	GM12878	blood:	n/a	n/a
46	CREB1	chr7:87103262-87105411	GM12878	blood:	n/a	n/a
47	CTCF	chr7:87094675-87094813	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:87094680-87094830	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:87104690-87104698	GM12892	blood:	n/a	n/a
50	CTCF	chr7:87094660-87094810	A549	lung:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:87105216-87105266	Hela-S3	cervix:	n/a
2	chr7:87104724-87104774	HCM	heart:	n/a
3	chr7:87105216-87105266	AG09309	skin:	n/a
4	chr7:87109370-87109420	AG04450	lung:	fetal
5	chr7:87104879-87104929	MCF10A-Er-Src	breast:	n/a
6	chr7:87102261-87102311	HRE	kidney:	n/a
7	chr7:87104932-87104982	PFSK-1	brain:	n/a
8	chr7:87109370-87109420	ProgFib	skin:	n/a
9	chr7:87105022-87105072	GM12878	blood:	n/a
10	chr7:87105398-87105448	HepG2	liver:	n/a
11	chr7:87109370-87109420	SK-N-SH	brain:	n/a
12	chr7:87105216-87105266	U87	brain:	n/a
13	chr7:87105398-87105448	ProgFib	skin:	n/a
14	chr7:87104932-87104982	LNCaP	prostate:	n/a
15	chr7:87104932-87104982	HCM	heart:	n/a
16	chr7:87105416-87105466	AG09319	gingival:	n/a
17	chr7:87109799-87109849	Jurkat	blood:	n/a
18	chr7:87104879-87104929	HNPCEpiC	eye:	n/a
19	chr7:87105216-87105266	SK-N-SH_RA	brain:	n/a
20	chr7:87105293-87105343	ProgFib	skin:	n/a
21	chr7:87109799-87109849	GM12891	blood:	n/a
22	chr7:87102261-87102311	Caco-2	colon:	n/a
23	chr7:87105022-87105072	NT2-D1	testis:	n/a
24	chr7:87102261-87102311	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:87093634-87093684	GM12892	blood:	n/a
26	chr7:87109799-87109849	HCF	heart:	n/a
27	chr7:87105022-87105072	SK-N-SH	brain:	n/a
28	chr7:87109799-87109849	RPTEC	kidney:	n/a
29	chr7:87105416-87105466	HMEC	breast:	n/a
30	chr7:87109799-87109849	SKMC	muscle:	n/a
31	chr7:87105293-87105343	Jurkat	blood:	n/a
32	chr7:87093634-87093684	K562	blood:	n/a
33	chr7:87105022-87105072	T-47D	breast:	n/a
34	chr7:87105416-87105466	HEK293	kidney:	embryo
35	chr7:87104932-87104982	HepG2	liver:	n/a
36	chr7:87109799-87109849	HL-60	blood:	n/a
37	chr7:87093634-87093684	AG09309	skin:	n/a
38	chr7:87105216-87105266	BJ	skin:	n/a
39	chr7:87109799-87109849	HRPEpiC	eye:	n/a
40	chr7:87102261-87102311	RPTEC	kidney:	n/a
41	chr7:87102261-87102311	K562	blood:	n/a
42	chr7:87102261-87102311	MCF-7	breast:	n/a
43	chr7:87105293-87105343	NT2-D1	testis:	n/a
44	chr7:87105416-87105466	Jurkat	blood:	n/a
45	chr7:87103624-87103674	SK-N-MC	brain:	n/a
46	chr7:87104724-87104774	CMK	blood:	n/a
47	chr7:87109799-87109849	NHDF-neo	bronchial:	n/a
48	chr7:87104879-87104929	Hela-S3	cervix:	n/a
49	chr7:87105216-87105266	HUVEC	blood vessel:	n/a
50	chr7:87105293-87105343	HPAEpiC	pulmonary alveolar:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:87105847..87108201-chr7:87108317..87110707,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CROT-1	chr7:87105081-87107196	NONHSAT121834

No data

Variant related genes	Relation type
ABCB4	TF binding region
ABCB4	CpG island
ENSG00000005471	chromatin interactions

Extended variants
information (count: 614 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs988448	chr7:87093247-87093248	Enhancers Strong transcription Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377365516	chr7:87093309-87093310	Enhancers Strong transcription Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557161474	chr7:87093311-87093312	Enhancers Strong transcription Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34519968	chr7:87093371-87093372	Enhancers Strong transcription Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373547992	chr7:87093411-87093412	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140624937	chr7:87093422-87093423	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544724821	chr7:87093446-87093447	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs542769374	chr7:87093584-87093585	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs370768927	chr7:87093592-87093593	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs561491057	chr7:87093704-87093705	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs528699810	chr7:87093734-87093735	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs563009114	chr7:87093753-87093754	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs530505494	chr7:87093757-87093758	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs548933214	chr7:87093781-87093782	Enhancers Strong transcription Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs138320831	chr7:87093808-87093809	Enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113761912	chr7:87093851-87093852	Enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182658255	chr7:87093946-87093947	Enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550621837	chr7:87093965-87093966	Enhancers Flanking Active TSS Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568783783	chr7:87094028-87094029	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs45619732	chr7:87094059-87094060	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185505518	chr7:87094073-87094074	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190807995	chr7:87094097-87094098	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567448626	chr7:87094129-87094130	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528412999	chr7:87094143-87094144	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs45547236	chr7:87094170-87094171	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs570449536	chr7:87094174-87094175	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537769636	chr7:87094211-87094212	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111406304	chr7:87094224-87094225	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557288648	chr7:87094241-87094242	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10452935	chr7:87094247-87094248	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs45454596	chr7:87094274-87094275	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10452936	chr7:87094306-87094307	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs573462772	chr7:87094324-87094325	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10452937	chr7:87094333-87094334	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs374159560	chr7:87094348-87094349	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565554451	chr7:87094363-87094364	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577587185	chr7:87094394-87094395	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113184620	chr7:87094462-87094463	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144233742	chr7:87094488-87094489	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188857893	chr7:87094491-87094492	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529662914	chr7:87094503-87094504	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548264957	chr7:87094512-87094513	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559855841	chr7:87094521-87094522	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192189371	chr7:87094525-87094526	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376261206	chr7:87094526-87094527	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138866544	chr7:87094548-87094549	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183000288	chr7:87094550-87094551	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537705934	chr7:87094618-87094619	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs549809542	chr7:87094627-87094628	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs569231548	chr7:87094667-87094668	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87075600-87094800	Strong transcription	Primary B cells from peripheral blood	blood
2	chr7:87084400-87094000	Strong transcription	Primary B cells from cord blood	blood
3	chr7:87086200-87094200	Weak transcription	Fetal Heart	heart
4	chr7:87092600-87093400	Enhancers	HepG2	liver
5	chr7:87092600-87094800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr7:87092800-87094800	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr7:87093000-87093400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:87093000-87094200	Enhancers	H9 Cell Line	embryonic stem cell
9	chr7:87093000-87094400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr7:87093000-87095000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:87093000-87095000	Enhancers	Psoas Muscle	Psoas
12	chr7:87093200-87093400	Flanking Active TSS	Liver	Liver
13	chr7:87093200-87093400	Weak transcription	Left Ventricle	heart
14	chr7:87093200-87093600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr7:87093200-87093600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:87093200-87094200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr7:87093400-87093600	Enhancers	Liver	Liver
18	chr7:87093400-87093600	Enhancers	Left Ventricle	heart
19	chr7:87093400-87093800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:87093400-87093800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr7:87093400-87094000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr7:87093400-87094000	Flanking Active TSS	HepG2	liver
23	chr7:87093400-87094200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:87093400-87094200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr7:87093400-87094200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr7:87093600-87093800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:87093600-87093800	Flanking Active TSS	Liver	Liver
28	chr7:87093600-87094200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:87093600-87094400	Weak transcription	Left Ventricle	heart
30	chr7:87093600-87102400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr7:87093800-87094000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:87093800-87094200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr7:87093800-87094200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:87093800-87094200	Enhancers	Liver	Liver
35	chr7:87093800-87094200	Enhancers	Pancreatic Islets	Pancreatic Islet
36	chr7:87093800-87094200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr7:87094000-87094200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr7:87094000-87094200	Active TSS	HepG2	liver
39	chr7:87094000-87094800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:87094000-87101000	Weak transcription	Primary B cells from cord blood	blood
41	chr7:87094200-87094400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
42	chr7:87094200-87094400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr7:87094200-87094400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr7:87094200-87094400	Flanking Active TSS	Liver	Liver
45	chr7:87094200-87094400	Enhancers	Stomach Mucosa	stomach
46	chr7:87094200-87094400	Flanking Active TSS	HepG2	liver
47	chr7:87094200-87094600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr7:87094200-87094600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr7:87094200-87094600	Enhancers	Fetal Heart	heart
50	chr7:87094200-87094600	Enhancers	Pancreas	Pancrea

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