Variant report

Variant	nsv966726
Chromosome Location	chr7:99473527-99488698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:102)
CpG islands
(count:306)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:102 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:99474151-99474402	K562	blood:	n/a	n/a
2	CCNT2	chr7:99479141-99479415	K562	blood:	n/a	n/a
3	CEBPB	chr7:99483619-99483841	A549	lung:	n/a	chr7:99483733-99483744
4	CEBPB	chr7:99479075-99479187	K562	blood:	n/a	n/a
5	CEBPB	chr7:99483615-99483813	K562	blood:	n/a	chr7:99483733-99483744
6	CEBPB	chr7:99483580-99483857	HepG2	liver:	n/a	chr7:99483733-99483744
7	CEBPB	chr7:99483571-99483872	IMR90	lung:	n/a	chr7:99483733-99483744
8	CEBPD	chr7:99478964-99479384	K562	blood:	n/a	n/a
9	CEBPD	chr7:99478923-99479407	K562	blood:	n/a	n/a
10	CTCF	chr7:99474220-99474370	HepG2	liver:	n/a	n/a
11	CTCF	chr7:99474380-99474530	A549	lung:	n/a	n/a
12	CTCF	chr7:99474340-99474490	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:99474264-99474324	MCF-7	breast:	n/a	n/a
14	CTCF	chr7:99474310-99474442	GM12878	blood:	n/a	n/a
15	CTCF	chr7:99474167-99474529	K562	blood:	n/a	n/a
16	CTCF	chr7:99474235-99474453	K562	blood:	n/a	n/a
17	CTCF	chr7:99474131-99474563	K562	blood:	n/a	n/a
18	CTCF	chr7:99474404-99474411	HepG2	liver:	n/a	n/a
19	CTCF	chr7:99474200-99474350	K562	blood:	n/a	n/a
20	CTCF	chr7:99474138-99474405	K562	blood:	n/a	n/a
21	CTCF	chr7:99474180-99474330	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr7:99474300-99474450	NB4	blood:	n/a	n/a
23	CTCF	chr7:99474277-99474439	GM12878	blood:	n/a	n/a
24	CTCF	chr7:99474229-99474419	HepG2	liver:	n/a	n/a
25	CTCF	chr7:99474283-99474412	NHEK	skin:	n/a	n/a
26	CTCF	chr7:99474300-99474450	HL-60	blood:	n/a	n/a
27	CTCF	chr7:99484360-99484510	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr7:99474319-99474403	HepG2	liver:	n/a	n/a
29	CTCF	chr7:99474280-99474399	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:99474220-99474370	GM12869	blood:	n/a	n/a
31	CTCF	chr7:99474334-99474359	GM10266	blood:	n/a	n/a
32	CTCF	chr7:99474258-99474408	MCF-7	breast:	n/a	n/a
33	CUX1	chr7:99479017-99479244	K562	blood:	n/a	n/a
34	CUX1	chr7:99474293-99474425	K562	blood:	n/a	n/a
35	E2F4	chr7:99481032-99481097	MCF10A-Er-Src	breast:	n/a	n/a
36	ELF1	chr7:99474123-99474573	K562	blood:	n/a	chr7:99474343-99474356
37	EP300	chr7:99478972-99479393	K562	blood:	n/a	n/a
38	GATA1	chr7:99478807-99479579	K562	blood:	n/a	chr7:99479245-99479254
39	GATA2	chr7:99474150-99474503	K562	blood:	n/a	n/a
40	GATA2	chr7:99474221-99474536	K562	blood:	n/a	n/a
41	GATA2	chr7:99474168-99474459	K562	blood:	n/a	n/a
42	GATA2	chr7:99478902-99479415	K562	blood:	n/a	chr7:99479245-99479254
43	GATA2	chr7:99479070-99479238	SH-SY5Y	brain:	n/a	n/a
44	JUND	chr7:99479033-99479282	K562	blood:	n/a	n/a
45	JUND	chr7:99474223-99474383	K562	blood:	n/a	n/a
46	MAFK	chr7:99474329-99474359	K562	blood:	n/a	n/a
47	MAX	chr7:99474002-99474472	NB4	blood:	n/a	chr7:99474175-99474185
48	MAZ	chr7:99474271-99474446	K562	blood:	n/a	n/a
49	MYC	chr7:99474270-99474364	K562	blood:	n/a	n/a
50	MYC	chr7:99474046-99474488	NB4	blood:	n/a	chr7:99474175-99474185

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99475820-99475870	MCF-7	breast:	n/a
2	chr7:99475820-99475870	MCF-7	breast:	n/a
3	chr7:99486165-99486215	AoSMC	blood vessel:	n/a
4	chr7:99475824-99475874	ovcar-3	ovarian:	n/a
5	chr7:99486165-99486215	HepG2	liver:	n/a
6	chr7:99486165-99486215	HRE	kidney:	n/a
7	chr7:99474543-99474593	SK-N-SH	brain:	n/a
8	chr7:99475820-99475870	HCPEpiC	choroid plexus:	n/a
9	chr7:99475820-99475870	NHBE	bronchial:	n/a
10	chr7:99475824-99475874	SKMC	muscle:	n/a
11	chr7:99474543-99474593	MCF10A-Er-Src	breast:	n/a
12	chr7:99474543-99474593	U87	brain:	n/a
13	chr7:99474543-99474593	PrEC	prostate:	n/a
14	chr7:99486165-99486215	BE2_C	brain:	n/a
15	chr7:99486165-99486215	Hela-S3	cervix:	n/a
16	chr7:99474543-99474593	IMR90	lung:	fetal
17	chr7:99475824-99475874	GM06990	blood:	n/a
18	chr7:99488474-99488524	GM12892	blood:	n/a
19	chr7:99474543-99474593	HL-60	blood:	n/a
20	chr7:99488474-99488524	HL-60	blood:	n/a
21	chr7:99475824-99475874	Hepatocyte	liver:	n/a
22	chr7:99475820-99475870	Caco-2	colon:	n/a
23	chr7:99486165-99486215	HL-60	blood:	n/a
24	chr7:99475820-99475870	GM06990	blood:	n/a
25	chr7:99486165-99486215	NB4	blood:	n/a
26	chr7:99486165-99486215	MCF-7	breast:	n/a
27	chr7:99488474-99488524	NHDF-neo	bronchial:	n/a
28	chr7:99488474-99488524	HNPCEpiC	eye:	n/a
29	chr7:99475824-99475874	LNCaP	prostate:	n/a
30	chr7:99475824-99475874	HCF	heart:	n/a
31	chr7:99475820-99475870	MCF10A-Er-Src	breast:	n/a
32	chr7:99488474-99488524	SK-N-SH	brain:	n/a
33	chr7:99475824-99475874	H1-hESC	embryonic stem cell:	embryo
34	chr7:99475824-99475874	HCPEpiC	choroid plexus:	n/a
35	chr7:99475820-99475870	ovcar-3	ovarian:	n/a
36	chr7:99488474-99488524	RPTEC	kidney:	n/a
37	chr7:99475820-99475870	BJ	skin:	n/a
38	chr7:99475820-99475870	SK-N-MC	brain:	n/a
39	chr7:99475824-99475874	AG09309	skin:	n/a
40	chr7:99486165-99486215	AG09309	skin:	n/a
41	chr7:99475824-99475874	BJ	skin:	n/a
42	chr7:99486165-99486215	HMEC	breast:	n/a
43	chr7:99474543-99474593	NT2-D1	testis:	n/a
44	chr7:99475824-99475874	NT2-D1	testis:	n/a
45	chr7:99475820-99475870	GM19239	blood:	n/a
46	chr7:99474543-99474593	HEEpiC	esophagus:	n/a
47	chr7:99486165-99486215	Jurkat	blood:	n/a
48	chr7:99475820-99475870	HRPEpiC	eye:	n/a
49	chr7:99486165-99486215	LNCaP	prostate:	n/a
50	chr7:99486165-99486215	GM06990	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:99485783..99488764-chr7:99489956..99491818,2	K562	blood:
2	chr1:37196801..37197670-chr7:99474858..99475858,2	K562	blood:
3	chr7:99462714..99465600-chr7:99478263..99479767,2	K562	blood:
4	chr7:99481318..99483626-chr7:99494027..99496823,2	K562	blood:
5	chr7:99479801..99482615-chr7:99515257..99518045,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP3A43-5	chr7:99476463-99476904	expReg_chr7_6295_+

No data

Variant related genes	Relation type
OR2AE1	TF binding region
OR2AE1	CpG island
ENSG00000146833	chromatin interactions

Extended variants
information (count: 675 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:675 , 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	rs559180555	chr7:99473574-99473575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs571100460	chr7:99473587-99473588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1025576	chr7:99473624-99473625	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs57619271	chr7:99473650-99473651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540756783	chr7:99473655-99473656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574517281	chr7:99473693-99473694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs367594084	chr7:99473713-99473714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200086548	chr7:99473714-99473715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541886063	chr7:99473723-99473724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146943316	chr7:99473737-99473738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs137913586	chr7:99473744-99473745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548139758	chr7:99473772-99473773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73403577	chr7:99473801-99473802	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs150118912	chr7:99473808-99473809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576165620	chr7:99473814-99473815	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138428749	chr7:99473815-99473816	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149412845	chr7:99473821-99473822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs199575787	chr7:99473825-99473826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532405967	chr7:99473839-99473840	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs17161997	chr7:99473858-99473859	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs369186811	chr7:99473895-99473896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559363136	chr7:99473903-99473904	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77351044	chr7:99473908-99473909	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373813784	chr7:99473909-99473910	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs372431371	chr7:99473922-99473923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201572604	chr7:99473923-99473924	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143060332	chr7:99473924-99473925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376481425	chr7:99473940-99473941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552496714	chr7:99473943-99473944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368379164	chr7:99473962-99473963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552455865	chr7:99473968-99473969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140031758	chr7:99473970-99473971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534917452	chr7:99473974-99473975	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60737583	chr7:99474007-99474008	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115589005	chr7:99474016-99474017	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs371922555	chr7:99474026-99474027	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs369288362	chr7:99474079-99474080	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs139298936	chr7:99474087-99474088	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs535487871	chr7:99474094-99474095	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs200544126	chr7:99474126-99474127	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs114518763	chr7:99474143-99474144	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs539930180	chr7:99474146-99474147	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs145563974	chr7:99474149-99474150	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs115450325	chr7:99474158-99474159	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs145303813	chr7:99474167-99474168	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs373434015	chr7:99474174-99474175	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs200782836	chr7:99474175-99474176	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs62474462	chr7:99474195-99474196	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs200183500	chr7:99474198-99474199	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs147632802	chr7:99474207-99474208	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	19212409	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99458200-99489600	Weak transcription	Pancreas	Pancrea
2	chr7:99465200-99475400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:99468400-99487200	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:99470000-99489600	Weak transcription	Gastric	stomach
5	chr7:99470400-99486800	Weak transcription	Primary T cells from cord blood	blood
6	chr7:99470400-99487000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:99470600-99474000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:99471400-99487000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr7:99472000-99473800	Weak transcription	Adipose Nuclei	Adipose
10	chr7:99472400-99487200	Weak transcription	Brain Anterior Caudate	brain
11	chr7:99472400-99487400	Weak transcription	Aorta	Aorta
12	chr7:99472600-99487000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr7:99472600-99487200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr7:99472600-99487600	Weak transcription	Lung	lung
15	chr7:99472600-99488800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr7:99472800-99476200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:99473000-99487200	Weak transcription	Brain Substantia Nigra	brain
18	chr7:99473200-99487200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:99473600-99474600	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr7:99473800-99474600	Strong transcription	Adipose Nuclei	Adipose
21	chr7:99474000-99474600	Bivalent Enhancer	K562	blood
22	chr7:99474000-99475400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr7:99474200-99474600	Enhancers	Esophagus	oesophagus
24	chr7:99474600-99487000	Weak transcription	Adipose Nuclei	Adipose
25	chr7:99474800-99487000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr7:99475400-99477400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:99476000-99487000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr7:99476200-99476800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:99478200-99487000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr7:99479000-99479200	Enhancers	Thymus	Thymus
31	chr7:99479200-99488800	Weak transcription	Thymus	Thymus
32	chr7:99479800-99499200	Weak transcription	Small Intestine	intestine
33	chr7:99480400-99487800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:99480800-99487200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr7:99482600-99487400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr7:99483000-99487200	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr7:99484000-99487000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr7:99484000-99487200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:99484200-99487000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr7:99484400-99484600	Active TSS	Spleen	Spleen
41	chr7:99484600-99484800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:99484600-99487200	Weak transcription	Brain Hippocampus Middle	brain
43	chr7:99484600-99487200	Weak transcription	Spleen	Spleen
44	chr7:99484800-99487000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:99484800-99487000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:99484800-99487000	Weak transcription	Placenta	Placenta
47	chr7:99484800-99487200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:99484800-99487200	Weak transcription	Fetal Muscle Trunk	muscle
49	chr7:99485000-99486800	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr7:99485000-99487000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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