Variant report

Variant	nsv970504
Chromosome Location	chr7:64361813-64366077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:406)
CpG islands
(count:671)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:406 , 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	chr7:64365875-64366480	K562	blood:	n/a	n/a
2	ATF1	chr7:64363473-64363703	K562	blood:	n/a	n/a
3	ATF1	chr7:64365697-64365833	K562	blood:	n/a	n/a
4	BHLHE40	chr7:64363248-64363868	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:64363471-64363888	K562	blood:	n/a	n/a
6	BRCA1	chr7:64363243-64363817	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr7:64363296-64364102	K562	blood:	n/a	n/a
8	CBX3	chr7:64363347-64363683	K562	blood:	n/a	n/a
9	CBX3	chr7:64364313-64364731	K562	blood:	n/a	n/a
10	CCNT2	chr7:64363483-64364106	K562	blood:	n/a	n/a
11	CEBPB	chr7:64364353-64364520	K562	blood:	n/a	n/a
12	CEBPB	chr7:64365877-64366191	K562	blood:	n/a	chr7:64365898-64365906
13	CHD1	chr7:64363296-64364276	GM12878	blood:	n/a	n/a
14	CHD1	chr7:64364037-64364487	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr7:64363364-64363999	K562	blood:	n/a	n/a
16	CHD2	chr7:64363374-64363853	GM12878	blood:	n/a	n/a
17	CHD2	chr7:64364437-64364557	K562	blood:	n/a	n/a
18	CHD2	chr7:64363407-64363745	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr7:64363378-64363989	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr7:64363472-64363651	HepG2	liver:	n/a	n/a
21	CTCF	chr7:64363578-64363599	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr7:64363676-64363817	K562	blood:	n/a	n/a
23	CTCF	chr7:64363546-64363679	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr7:64366056-64366282	K562	blood:	n/a	n/a
25	CTCF	chr7:64363740-64363890	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr7:64363800-64363950	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr7:64363980-64364130	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr7:64363720-64363870	SK-N-SH_RA	brain:	n/a	n/a
29	CUX1	chr7:64363708-64363855	K562	blood:	n/a	n/a
30	CUX1	chr7:64364079-64364278	K562	blood:	n/a	n/a
31	E2F4	chr7:64363350-64363856	K562	blood:	n/a	n/a
32	E2F4	chr7:64363357-64363848	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr7:64363476-64363830	GM12878	blood:	n/a	n/a
34	E2F6	chr7:64363483-64363732	K562	blood:	n/a	n/a
35	EBF1	chr7:64363545-64363742	GM12878	blood:	n/a	n/a
36	EGR1	chr7:64363338-64363661	K562	blood:	n/a	chr7:64363536-64363549 chr7:64363535-64363550 chr7:64363536-64363549
37	EGR1	chr7:64365562-64365920	K562	blood:	n/a	n/a
38	EGR1	chr7:64365598-64365832	K562	blood:	n/a	n/a
39	EGR1	chr7:64363276-64363672	K562	blood:	n/a	chr7:64363536-64363549 chr7:64363535-64363550 chr7:64363536-64363549
40	ELF1	chr7:64363297-64364120	GM12878	blood:	n/a	n/a
41	ELF1	chr7:64363232-64364097	HCT-116	colon:	n/a	n/a
42	ELF1	chr7:64363242-64364119	SK-N-SH	brain:	n/a	n/a
43	ELF1	chr7:64363338-64364030	K562	blood:	n/a	n/a
44	ELF1	chr7:64363441-64363981	A549	lung:	n/a	n/a
45	ELF1	chr7:64363304-64364222	MCF-7	breast:	n/a	n/a
46	ELF1	chr7:64363203-64364113	MCF-7	breast:	n/a	n/a
47	ELF1	chr7:64363360-64364154	K562	blood:	n/a	n/a
48	ELF1	chr7:64363383-64363980	SK-N-SH	brain:	n/a	n/a
49	ELF1	chr7:64363385-64363809	HepG2	liver:	n/a	n/a
50	ELF1	chr7:64363360-64363878	A549	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64363590-64363640	SK-N-SH	brain:	n/a
2	chr7:64363546-64363596	SK-N-SH	brain:	n/a
3	chr7:64362320-64362370	HRCEpiC	kidney:	n/a
4	chr7:64362320-64362370	GM19239	blood:	n/a
5	chr7:64363624-64363674	IMR90	lung:	fetal
6	chr7:64363590-64363640	U87	brain:	n/a
7	chr7:64363421-64363471	NT2-D1	testis:	n/a
8	chr7:64363546-64363596	GM12892	blood:	n/a
9	chr7:64363575-64363625	A549	lung:	n/a
10	chr7:64363934-64363984	HCT-116	colon:	n/a
11	chr7:64363877-64363927	GM19239	blood:	n/a
12	chr7:64363590-64363640	GM12878	blood:	n/a
13	chr7:64363877-64363927	A549	lung:	n/a
14	chr7:64363082-64363132	H1-hESC	embryonic stem cell:	embryo
15	chr7:64363624-64363674	AG04449	skin:	fetal
16	chr7:64363624-64363674	A549	lung:	n/a
17	chr7:64363575-64363625	HIPEpiC	eye:	n/a
18	chr7:64363082-64363132	MCF10A-Er-Src	breast:	n/a
19	chr7:64363575-64363625	GM12891	blood:	n/a
20	chr7:64363421-64363471	AG10803	skin:	n/a
21	chr7:64363624-64363674	Caco-2	colon:	n/a
22	chr7:64363546-64363596	Hela-S3	cervix:	n/a
23	chr7:64363590-64363640	SK-N-SH_RA	brain:	n/a
24	chr7:64363624-64363674	HIPEpiC	eye:	n/a
25	chr7:64363590-64363640	T-47D	breast:	n/a
26	chr7:64363624-64363674	HCT-116	colon:	n/a
27	chr7:64363590-64363640	HEEpiC	esophagus:	n/a
28	chr7:64363877-64363927	ECC-1	luminal epithelium:	n/a
29	chr7:64363546-64363596	HEEpiC	esophagus:	n/a
30	chr7:64363624-64363674	AG04450	lung:	fetal
31	chr7:64363421-64363471	CMK	blood:	n/a
32	chr7:64363624-64363674	SAEC	small airway:	n/a
33	chr7:64363934-64363984	AG09319	gingival:	n/a
34	chr7:64363615-64363665	U87	brain:	n/a
35	chr7:64363877-64363927	CMK	blood:	n/a
36	chr7:64362326-64362376	MCF10A-Er-Src	breast:	n/a
37	chr7:64363934-64363984	GM12878	blood:	n/a
38	chr7:64363575-64363625	MCF10A-Er-Src	breast:	n/a
39	chr7:64363575-64363625	AG09319	gingival:	n/a
40	chr7:64363082-64363132	IMR90	lung:	fetal
41	chr7:64363421-64363471	ProgFib	skin:	n/a
42	chr7:64363615-64363665	NT2-D1	testis:	n/a
43	chr7:64363590-64363640	AG10803	skin:	n/a
44	chr7:64363877-64363927	GM12892	blood:	n/a
45	chr7:64363082-64363132	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:64362320-64362370	NH-A	brain:	n/a
47	chr7:64362326-64362376	GM12891	blood:	n/a
48	chr7:64363624-64363674	AoSMC	blood vessel:	n/a
49	chr7:64363624-64363674	U87	brain:	n/a
50	chr7:64363421-64363471	GM12878	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:64351381..64353400-chr7:64363667..64366418,2	K562	blood:
2	chr7:64363939..64365901-chr7:64381813..64383330,2	K562	blood:
3	chr11:62432738..62433244-chr7:64363197..64364194,2	NB4	blood:
4	chr7:64364987..64367738-chr7:64372489..64374310,3	K562	blood:
5	chr7:64365012..64367238-chr7:64400877..64402549,2	MCF-7	breast:
6	chr7:64365308..64368250-chr7:64464896..64466671,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF273-1	chr7:64363620-64363797	NR_003099

No data

Variant related genes	Relation type
ZNF273	TF binding region
ZNF273	CpG island
ENSG00000206597	chromatin interactions
ENSG00000214756	chromatin interactions

Extended variants
information (count: 160 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:160 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372958799	chr7:64361830-64361831	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375115436	chr7:64361842-64361843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548878400	chr7:64361856-64361857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372514205	chr7:64361860-64361861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144892163	chr7:64361894-64361895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10264026	chr7:64361941-64361942	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs552491587	chr7:64361995-64361996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76897101	chr7:64362005-64362006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531348903	chr7:64362007-64362008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10282599	chr7:64362012-64362013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs568184583	chr7:64362031-64362032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191187005	chr7:64362100-64362101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147963145	chr7:64362109-64362110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185728748	chr7:64362130-64362131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539694804	chr7:64362155-64362156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562346624	chr7:64362158-64362159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190588188	chr7:64362167-64362168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1966140	chr7:64362191-64362192	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs542228783	chr7:64362196-64362197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372404709	chr7:64362297-64362298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370122710	chr7:64362312-64362313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571182183	chr7:64362324-64362325	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs184439766	chr7:64362326-64362327	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs181762968	chr7:64362437-64362438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373120486	chr7:64362491-64362492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114415327	chr7:64362606-64362607	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs376289019	chr7:64362650-64362651	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545741341	chr7:64362721-64362722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs547224617	chr7:64362772-64362773	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs562819957	chr7:64362832-64362833	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs531182190	chr7:64362833-64362834	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs10237833	chr7:64362836-64362837	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs141522814	chr7:64362933-64362934	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs62455117	chr7:64362965-64362966	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185105441	chr7:64363005-64363006	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs571014319	chr7:64363038-64363039	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs115028737	chr7:64363043-64363044	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550179606	chr7:64363071-64363072	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs113632881	chr7:64363092-64363093	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs112787709	chr7:64363093-64363094	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs370123740	chr7:64363101-64363102	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs570307016	chr7:64363127-64363128	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs143676234	chr7:64363131-64363132	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs569965560	chr7:64363161-64363162	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs148111502	chr7:64363207-64363208	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs572154903	chr7:64363273-64363274	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs377508456	chr7:64363287-64363288	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs71567877	chr7:64363298-64363299	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs4717223	chr7:64363299-64363300	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs200788266	chr7:64363303-64363304	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64351200-64363200	Weak transcription	Psoas Muscle	Psoas
2	chr7:64351400-64363000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr7:64351400-64363200	Weak transcription	Brain Angular Gyrus	brain
4	chr7:64352000-64363000	Weak transcription	Ovary	ovary
5	chr7:64352800-64362800	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:64353000-64363000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:64353200-64363200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr7:64353400-64363000	Weak transcription	Brain Anterior Caudate	brain
9	chr7:64353800-64363200	Weak transcription	Fetal Brain Male	brain
10	chr7:64356200-64363000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr7:64357800-64363400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:64360200-64362800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:64360800-64363200	Weak transcription	Small Intestine	intestine
14	chr7:64361200-64362800	Weak transcription	HepG2	liver
15	chr7:64361800-64362000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr7:64362000-64363000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr7:64362600-64362800	Enhancers	Dnd41	blood
18	chr7:64362600-64362800	Enhancers	K562	blood
19	chr7:64362800-64363000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr7:64362800-64363000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr7:64362800-64363000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr7:64362800-64363000	Enhancers	Adipose Nuclei	Adipose
23	chr7:64362800-64363000	Enhancers	Brain Hippocampus Middle	brain
24	chr7:64362800-64363000	Enhancers	Placenta	Placenta
25	chr7:64362800-64363200	Enhancers	Primary T cells fromperipheralblood	blood
26	chr7:64362800-64363200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr7:64362800-64363200	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr7:64362800-64363200	Enhancers	Fetal Muscle Trunk	muscle
29	chr7:64362800-64363400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:64362800-64363400	Flanking Active TSS	Dnd41	blood
31	chr7:64362800-64363400	Flanking Active TSS	K562	blood
32	chr7:64362800-64363600	Active TSS	HepG2	liver
33	chr7:64362800-64364200	Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr7:64362800-64364200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr7:64362800-64364600	Active TSS	Stomach Smooth Muscle	stomach
36	chr7:64362800-64364800	Active TSS	Duodenum Mucosa	Duodenum
37	chr7:64362800-64365000	Active TSS	A549	lung
38	chr7:64362800-64366000	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr7:64362800-64366000	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr7:64362800-64366400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:64363000-64363200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr7:64363000-64363200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:64363000-64363200	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr7:64363000-64363200	Enhancers	Primary B cells from cord blood	blood
45	chr7:64363000-64363200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr7:64363000-64363200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr7:64363000-64363200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr7:64363000-64363200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:64363000-64363200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr7:64363000-64363200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links