Variant report

Variant	esv3393496
Chromosome Location	chr7:64497342-64499890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:466)
CpG islands
(count:305)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:466 , 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	chr7:64499554-64499763	K562	blood:	n/a	n/a
2	ATF3	chr7:64498130-64498270	K562	blood:	n/a	n/a
3	BRCA1	chr7:64498202-64498400	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr7:64498092-64498620	K562	blood:	n/a	n/a
5	CCNT2	chr7:64499237-64499539	K562	blood:	n/a	n/a
6	CCNT2	chr7:64498363-64498944	K562	blood:	n/a	chr7:64498603-64498612
7	CEBPB	chr7:64498204-64498690	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:64498354-64498681	IMR90	lung:	n/a	n/a
9	CEBPB	chr7:64498390-64498522	K562	blood:	n/a	n/a
10	CEBPB	chr7:64498426-64498560	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:64498404-64498657	HepG2	liver:	n/a	n/a
12	CEBPD	chr7:64498325-64498917	HepG2	liver:	n/a	n/a
13	CEBPD	chr7:64498325-64498998	K562	blood:	n/a	n/a
14	CHD1	chr7:64498839-64498936	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr7:64498799-64498925	GM12878	blood:	n/a	n/a
16	CHD2	chr7:64499230-64499430	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr7:64499264-64499446	HepG2	liver:	n/a	n/a
18	CHD2	chr7:64499368-64499426	K562	blood:	n/a	n/a
19	CHD2	chr7:64498789-64498862	K562	blood:	n/a	n/a
20	CHD2	chr7:64498227-64498953	Hela-S3	cervix:	n/a	n/a
21	CREB1	chr7:64498290-64499048	HepG2	liver:	n/a	n/a
22	CREB1	chr7:64498311-64498913	A549	lung:	n/a	n/a
23	CTCF	chr7:64498100-64498250	GM12872	blood:	n/a	n/a
24	CTCF	chr7:64498100-64498250	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr7:64498040-64498190	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr7:64499340-64499490	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr7:64498040-64498190	GM12871	blood:	n/a	n/a
28	CTCF	chr7:64498100-64498250	SAEC	small airway:	n/a	n/a
29	CTCF	chr7:64498120-64498270	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr7:64498080-64498230	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr7:64497993-64498252	K562	blood:	n/a	n/a
32	CTCF	chr7:64498120-64498270	GM12865	blood:	n/a	n/a
33	CTCF	chr7:64498080-64498230	HEK293	kidney:	n/a	n/a
34	CTCF	chr7:64498080-64498230	GM12870	blood:	n/a	n/a
35	CTCF	chr7:64499491-64499508	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr7:64498080-64498230	MCF-7	breast:	n/a	n/a
37	CTCF	chr7:64498172-64498341	GM12878	blood:	n/a	chr7:64498301-64498314
38	CTCF	chr7:64498765-64498787	GM19239	blood:	n/a	n/a
39	CTCF	chr7:64498080-64498230	HMEC	breast:	n/a	n/a
40	CTCF	chr7:64498100-64498250	GM06990	blood:	n/a	n/a
41	CTCF	chr7:64498179-64498224	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr7:64498120-64498270	GM12873	blood:	n/a	n/a
43	CTCF	chr7:64498080-64498230	NB4	blood:	n/a	n/a
44	CTCF	chr7:64498080-64498230	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr7:64498140-64498290	GM12868	blood:	n/a	n/a
46	CTCF	chr7:64498360-64498510	GM12874	blood:	n/a	n/a
47	CTCF	chr7:64498140-64498290	GM12878	blood:	n/a	n/a
48	CTCF	chr7:64498060-64498210	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr7:64498100-64498250	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr7:64498100-64498250	GM12875	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64498472-64498522	HCF	heart:	n/a
2	chr7:64498472-64498522	NHBE	bronchial:	n/a
3	chr7:64498824-64498874	PFSK-1	brain:	n/a
4	chr7:64498472-64498522	HEEpiC	esophagus:	n/a
5	chr7:64498824-64498874	Hela-S3	cervix:	n/a
6	chr7:64499099-64499149	LNCaP	prostate:	n/a
7	chr7:64498824-64498874	BJ	skin:	n/a
8	chr7:64498472-64498522	H1-hESC	embryonic stem cell:	embryo
9	chr7:64498824-64498874	SKMC	muscle:	n/a
10	chr7:64498824-64498874	PrEC	prostate:	n/a
11	chr7:64498773-64498823	Jurkat	blood:	n/a
12	chr7:64499107-64499157	HEEpiC	esophagus:	n/a
13	chr7:64499099-64499149	GM12878	blood:	n/a
14	chr7:64499099-64499149	SK-N-MC	brain:	n/a
15	chr7:64498472-64498522	PFSK-1	brain:	n/a
16	chr7:64499099-64499149	NB4	blood:	n/a
17	chr7:64499107-64499157	K562	blood:	n/a
18	chr7:64499099-64499149	T-47D	breast:	n/a
19	chr7:64498824-64498874	GM12878	blood:	n/a
20	chr7:64498472-64498522	AG04449	skin:	fetal
21	chr7:64498773-64498823	AG09319	gingival:	n/a
22	chr7:64498824-64498874	SK-N-SH_RA	brain:	n/a
23	chr7:64498773-64498823	HRE	kidney:	n/a
24	chr7:64499107-64499157	HCM	heart:	n/a
25	chr7:64499107-64499157	PANC-1	pancreas:	n/a
26	chr7:64498773-64498823	RPTEC	kidney:	n/a
27	chr7:64498824-64498874	NHBE	bronchial:	n/a
28	chr7:64499107-64499157	HRCEpiC	kidney:	n/a
29	chr7:64499099-64499149	HCPEpiC	choroid plexus:	n/a
30	chr7:64498472-64498522	SKMC	muscle:	n/a
31	chr7:64499099-64499149	AG04449	skin:	fetal
32	chr7:64498472-64498522	HCM	heart:	n/a
33	chr7:64499099-64499149	HCM	heart:	n/a
34	chr7:64499099-64499149	HIPEpiC	eye:	n/a
35	chr7:64499099-64499149	AG04450	lung:	fetal
36	chr7:64498824-64498874	HepG2	liver:	n/a
37	chr7:64498472-64498522	HL-60	blood:	n/a
38	chr7:64498773-64498823	SK-N-MC	brain:	n/a
39	chr7:64499099-64499149	PFSK-1	brain:	n/a
40	chr7:64498824-64498874	SK-N-MC	brain:	n/a
41	chr7:64498773-64498823	IMR90	lung:	fetal
42	chr7:64499107-64499157	SK-N-SH	brain:	n/a
43	chr7:64498773-64498823	GM19239	blood:	n/a
44	chr7:64498472-64498522	HUVEC	blood vessel:	n/a
45	chr7:64499107-64499157	H1-hESC	embryonic stem cell:	embryo
46	chr7:64499107-64499157	Hela-S3	cervix:	n/a
47	chr7:64498472-64498522	HCPEpiC	choroid plexus:	n/a
48	chr7:64499107-64499157	CMK	blood:	n/a
49	chr7:64498824-64498874	SAEC	small airway:	n/a
50	chr7:64498773-64498823	Caco-2	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64467103..64469967-chr7:64496870..64499849,2	K562	blood:
2	chr7:64498619..64500351-chr7:65337220..65338727,3	MCF-7	breast:
3	chr7:64253690..64256534-chr7:64497237..64499995,2	K562	blood:
4	chr7:64499257..64501633-chr7:64540419..64543070,2	MCF-7	breast:
5	chr7:64498559..64499288-chr7:65338067..65339051,2	NB4	blood:
6	chr7:64465846..64468983-chr7:64497347..64500243,4	MCF-7	breast:
7	chr7:64465739..64467675-chr7:64497142..64500012,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ERV3-1-3	chr7:64498790-64498937	NONHSAT121067

No data

Variant related genes	Relation type
ENSG00000239985	TF binding region
CCT6P3	TF binding region
ENSG00000239985	CpG island
CCT6P3	CpG island
ENSG00000213462	chromatin interactions
ENSG00000197008	chromatin interactions
ENSG00000152926	chromatin interactions
ENSG00000196715	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116508427	chr7:64497378-64497379	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs562423092	chr7:64497401-64497402	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs376206431	chr7:64497422-64497423	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs531358588	chr7:64497471-64497472	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs144118848	chr7:64497473-64497474	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs570114682	chr7:64497581-64497582	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs539080722	chr7:64497626-64497627	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs561662379	chr7:64497668-64497669	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs527866568	chr7:64497674-64497675	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs547723049	chr7:64497734-64497735	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs570801518	chr7:64497746-64497747	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs558424359	chr7:64497756-64497757	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199743396	chr7:64497757-64497758	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs146750176	chr7:64497781-64497782	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs35672059	chr7:64497783-64497784	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs574153460	chr7:64497810-64497811	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184233935	chr7:64497826-64497827	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs550065822	chr7:64497862-64497863	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs186288891	chr7:64497864-64497865	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs535497657	chr7:64497875-64497876	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs555808566	chr7:64497968-64497969	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs572493227	chr7:64497998-64497999	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs190666767	chr7:64498039-64498040	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs201569965	chr7:64498045-64498046	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs572731305	chr7:64498107-64498108	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs201208053	chr7:64498130-64498131	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs534354821	chr7:64498184-64498185	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs182900986	chr7:64498218-64498219	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs7789020	chr7:64498257-64498258	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs62455990	chr7:64498314-64498315	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs74832495	chr7:64498315-64498316	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs571529510	chr7:64498321-64498322	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs562784577	chr7:64498326-64498327	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs370251546	chr7:64498338-64498339	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs192962993	chr7:64498345-64498346	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs35679667	chr7:64498368-64498369	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs561820524	chr7:64498505-64498506	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs71533994	chr7:64498522-64498523	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs547100298	chr7:64498529-64498530	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs564295081	chr7:64498561-64498562	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs527433566	chr7:64498641-64498642	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs533371483	chr7:64498670-64498671	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs550027163	chr7:64498673-64498674	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs570041149	chr7:64498674-64498675	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs140721023	chr7:64498681-64498682	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
46	rs139476739	chr7:64498715-64498716	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs78001727	chr7:64498748-64498749	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs182969532	chr7:64498755-64498756	Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
49	rs534760424	chr7:64498764-64498765	Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs34438629	chr7:64498782-64498783	Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:81)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	17426248	CNVD
Williams Syndrome	20824207	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Cancer	21272361	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64493800-64498200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:64493800-64498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:64496200-64498000	Enhancers	HepG2	liver
4	chr7:64496200-64498200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr7:64496400-64498000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:64496600-64498000	Enhancers	K562	blood
7	chr7:64496600-64498200	Weak transcription	Right Atrium	heart
8	chr7:64496600-64498200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:64496600-64498200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:64496800-64497800	Weak transcription	Placenta	Placenta
11	chr7:64496800-64498000	Weak transcription	Brain Hippocampus Middle	brain
12	chr7:64496800-64498600	Weak transcription	Primary B cells from cord blood	blood
13	chr7:64497000-64498200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:64497000-64498200	Enhancers	Adipose Nuclei	Adipose
15	chr7:64497000-64498400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr7:64497000-64498600	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr7:64497000-64498800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:64497200-64497400	Enhancers	GM12878-XiMat	blood
19	chr7:64497200-64497800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr7:64497200-64498200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr7:64497800-64498000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:64497800-64498000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:64497800-64498000	Enhancers	Placenta	Placenta
24	chr7:64497800-64498000	Enhancers	Dnd41	blood
25	chr7:64497800-64498200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:64497800-64498200	Enhancers	Fetal Stomach	stomach
27	chr7:64497800-64498400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr7:64498000-64498200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr7:64498000-64498200	Enhancers	Brain Hippocampus Middle	brain
30	chr7:64498000-64498200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr7:64498000-64498200	Enhancers	Fetal Intestine Large	intestine
32	chr7:64498000-64498400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr7:64498000-64498400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr7:64498000-64498400	Flanking Active TSS	Placenta	Placenta
35	chr7:64498000-64498400	Flanking Active TSS	Dnd41	blood
36	chr7:64498000-64498400	Flanking Active TSS	K562	blood
37	chr7:64498000-64498600	Enhancers	Primary B cells from peripheral blood	blood
38	chr7:64498000-64498600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr7:64498000-64498800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:64498000-64499400	Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr7:64498000-64499400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:64498000-64499400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:64498000-64499400	Active TSS	HepG2	liver
44	chr7:64498000-64499600	Active TSS	Colon Smooth Muscle	Colon
45	chr7:64498000-64499800	Active TSS	Brain Angular Gyrus	brain
46	chr7:64498000-64499800	Active TSS	Brain Cingulate Gyrus	brain
47	chr7:64498000-64500000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:64498000-64500000	Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr7:64498000-64500000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:64498000-64500000	Active TSS	Brain Anterior Caudate	brain

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