Variant report

Variant	rs372752209
Chromosome Location	chr7:5458759-5458760
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:187)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:187 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:5458661-5458979	Gliobla	brain:	n/a	n/a
2	ELK1	chr7:5458702-5458902	Hela-S3	cervix:	n/a	n/a
3	POLR2A	chr7:5458245-5459277	HepG2	liver:	n/a	n/a
4	RAD21	chr7:5458307-5458842	IMR90	lung:	n/a	chr7:5458471-5458490
5	POLR2A	chr7:5458557-5459248	U87	brain:	n/a	n/a
6	MAZ	chr7:5457576-5459985	IMR90	lung:	n/a	chr7:5459045-5459055 chr7:5459206-5459216
7	FOSL2	chr7:5458122-5458873	MCF-7	breast:	n/a	chr7:5458823-5458834
8	BCL3	chr7:5458034-5459081	A549	lung:	n/a	n/a
9	EP300	chr7:5458066-5458931	T-47D	breast:	n/a	chr7:5458278-5458288
10	ZKSCAN1	chr7:5458109-5459038	Hela-S3	cervix:	n/a	chr7:5458734-5458747
11	ATF2	chr7:5458219-5458881	H1-hESC	embryonic stem cell:	n/a	n/a
12	TBP	chr7:5457870-5459053	Hela-S3	cervix:	n/a	n/a
13	HMGN3	chr7:5458174-5459075	K562	blood:	n/a	n/a
14	REST	chr7:5457985-5459093	A549	lung:	n/a	chr7:5458637-5458646 chr7:5458179-5458186
15	MAFK	chr7:5458689-5458960	IMR90	lung:	n/a	n/a
16	RCOR1	chr7:5458167-5458858	K562	blood:	n/a	n/a
17	POLR2A	chr7:5458134-5458978	Hela-S3	cervix:	n/a	n/a
18	MYBL2	chr7:5458071-5459120	HepG2	liver:	n/a	n/a
19	MAX	chr7:5458112-5459149	A549	lung:	n/a	chr7:5459045-5459055
20	GTF2F1	chr7:5457810-5458950	Hela-S3	cervix:	n/a	n/a
21	E2F6	chr7:5458144-5459035	H1-hESC	embryonic stem cell:	n/a	chr7:5458631-5458641
22	TAF1	chr7:5457904-5459131	H1-neurons	neurons:	n/a	n/a
23	POLR2A	chr7:5458395-5459190	HepG2	liver:	n/a	n/a
24	MAX	chr7:5458003-5459196	HCT-116	colon:	n/a	chr7:5459045-5459055
25	EP300	chr7:5457950-5458997	A549	lung:	n/a	chr7:5458278-5458288 chr7:5458945-5458958
26	MXI1	chr7:5458312-5458847	H1-hESC	embryonic stem cell:	n/a	n/a
27	GATA3	chr7:5456781-5458965	T-47D	breast:	n/a	chr7:5457594-5457602 chr7:5457443-5457450 chr7:5457436-5457457 chr7:5457443-5457452 chr7:5458506-5458514 chr7:5457589-5457597 chr7:5457823-5457831 chr7:5457632-5457640 chr7:5457442-5457452 chr7:5457614-5457622
28	TCF7L2	chr7:5458003-5458950	HEK293	kidney:	n/a	n/a
29	POLR2A	chr7:5458473-5459083	ECC-1	luminal epithelium:	n/a	n/a
30	POLR2A	chr7:5458103-5459178	MCF-7	breast:	n/a	n/a
31	RCOR1	chr7:5457965-5459010	Hela-S3	cervix:	n/a	n/a
32	TCF12	chr7:5457922-5458864	ECC-1	luminal epithelium:	n/a	n/a
33	KAP1	chr7:5458096-5458855	U2OS	brain:	n/a	n/a
34	MAFK	chr7:5458142-5458972	Hela-S3	cervix:	n/a	n/a
35	ELF1	chr7:5457992-5459351	MCF-7	breast:	n/a	n/a
36	MYC	chr7:5458714-5458955	HUVEC	blood vessel:	n/a	n/a
37	SP1	chr7:5457879-5459050	A549	lung:	n/a	chr7:5458561-5458572 chr7:5458562-5458571
38	ELF1	chr7:5458609-5458938	A549	lung:	n/a	n/a
39	SIN3AK20	chr7:5458552-5459007	A549	lung:	n/a	n/a
40	MXI1	chr7:5458121-5459055	Hela-S3	cervix:	n/a	n/a
41	ZNF263	chr7:5457962-5458988	HEK293-T-REx	kidney:	n/a	n/a
42	POLR2A	chr7:5458486-5458844	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr7:5458094-5459081	Hela-S3	cervix:	n/a	n/a
44	MAX	chr7:5458143-5459154	ECC-1	luminal epithelium:	n/a	chr7:5459045-5459055
45	POLR2A	chr7:5456980-5458909	K562	blood:	n/a	n/a
46	MYC	chr7:5458085-5458941	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr7:5457984-5459231	HCT-116	colon:	n/a	n/a
48	TCF12	chr7:5456880-5459163	A549	lung:	n/a	chr7:5457832-5457839
49	BHLHE40	chr7:5458291-5458835	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:5458710-5459130	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5458719-5458769	K562	blood:	n/a
2	chr7:5458719-5458769	NHBE	bronchial:	n/a
3	chr7:5458719-5458769	T-47D	breast:	n/a
4	chr7:5458719-5458769	ProgFib	skin:	n/a
5	chr7:5458719-5458769	SAEC	small airway:	n/a
6	chr7:5458719-5458769	LNCaP	prostate:	n/a
7	chr7:5458719-5458769	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:5458719-5458769	HEEpiC	esophagus:	n/a
9	chr7:5458719-5458769	ovcar-3	ovarian:	n/a
10	chr7:5458719-5458769	Caco-2	colon:	n/a
11	chr7:5458719-5458769	HUVEC	blood vessel:	n/a
12	chr7:5458719-5458769	PFSK-1	brain:	n/a
13	chr7:5458719-5458769	PANC-1	pancreas:	n/a
14	chr7:5458719-5458769	MCF10A-Er-Src	breast:	n/a
15	chr7:5458719-5458769	CMK	blood:	n/a
16	chr7:5458719-5458769	HCT-116	colon:	n/a
17	chr7:5458719-5458769	Jurkat	blood:	n/a
18	chr7:5458719-5458769	SK-N-MC	brain:	n/a
19	chr7:5458719-5458769	HNPCEpiC	eye:	n/a
20	chr7:5458719-5458769	BJ	skin:	n/a
21	chr7:5458719-5458769	ECC-1	luminal epithelium:	n/a
22	chr7:5458719-5458769	NB4	blood:	n/a
23	chr7:5458719-5458769	Hepatocyte	liver:	n/a
24	chr7:5458719-5458769	GM19239	blood:	n/a
25	chr7:5458719-5458769	HRE	kidney:	n/a
26	chr7:5458719-5458769	AG04449	skin:	fetal
27	chr7:5458719-5458769	GM12878	blood:	n/a
28	chr7:5458719-5458769	AG10803	skin:	n/a
29	chr7:5458719-5458769	HepG2	liver:	n/a
30	chr7:5458719-5458769	AG04450	lung:	fetal
31	chr7:5458719-5458769	AoSMC	blood vessel:	n/a
32	chr7:5458719-5458769	HRCEpiC	kidney:	n/a
33	chr7:5458719-5458769	BE2_C	brain:	n/a
34	chr7:5458719-5458769	HCPEpiC	choroid plexus:	n/a
35	chr7:5458719-5458769	PrEC	prostate:	n/a
36	chr7:5458719-5458769	GM06990	blood:	n/a
37	chr7:5458719-5458769	IMR90	lung:	fetal
38	chr7:5458719-5458769	H1-hESC	embryonic stem cell:	embryo
39	chr7:5458719-5458769	HMEC	breast:	n/a
40	chr7:5458719-5458769	HAEpiC	amniotic membrane:	n/a
41	chr7:5458719-5458769	SKMC	muscle:	n/a
42	chr7:5458719-5458769	SK-N-SH	brain:	n/a
43	chr7:5458719-5458769	U87	brain:	n/a
44	chr7:5458719-5458769	A549	lung:	n/a
45	chr7:5458719-5458769	Hela-S3	cervix:	n/a
46	chr7:5458719-5458769	HRPEpiC	eye:	n/a
47	chr7:5458719-5458769	HCM	heart:	n/a
48	chr7:5458719-5458769	SK-N-SH_RA	brain:	n/a
49	chr7:5458719-5458769	NHDF-neo	bronchial:	n/a
50	chr7:5458719-5458769	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:5456513..5458866-chr7:5593273..5595987,2	MCF-7	breast:
2	chr7:5458614..5460773-chr7:5569317..5571189,3	K562	blood:
3	chr7:5458325..5469295-chr7:5567159..5574053,21	MCF-7	breast:
4	chr7:5458325..5461852-chr7:5568883..5572530,6	MCF-7	breast:
5	chr7:5458255..5459132-chr7:5468021..5469070,3	MCF-7	breast:
6	chr7:5405158..5408659-chr7:5455520..5459271,4	MCF-7	breast:
7	chr7:5405741..5406385-chr7:5458033..5458970,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000188365	TF binding region
ENSG00000241269	TF binding region
ENSG00000241269	CpG island
ENSG00000188365	CpG island
ENSG00000075624	Chromatin interaction
ENSG00000273084	Chromatin interaction
ENSG00000263900	Chromatin interaction
ENSG00000234432	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	nsv887391	chr7:5224407-5572132	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	292 gene(s)	inside rSNPs	diseases
5	nsv823996	chr7:5285503-5465988	Flanking Active TSS Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv887396	chr7:5305297-5475409	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	esv1814049	chr7:5314993-5675131	Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	333 gene(s)	inside rSNPs	diseases
8	esv1820266	chr7:5332088-5665173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
9	nsv533965	chr7:5370746-5548397	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
10	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
11	nsv887401	chr7:5393243-5539958	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
12	nsv887402	chr7:5394951-5494677	Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
13	nsv887404	chr7:5402606-5667645	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
14	nsv887405	chr7:5409059-5552436	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
15	nsv887406	chr7:5414602-5552436	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	52 gene(s)	inside rSNPs	diseases
16	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
17	nsv887407	chr7:5432672-5605130	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	302 gene(s)	inside rSNPs	diseases
18	nsv887408	chr7:5432672-5667645	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
19	nsv508443	chr7:5447283-5501122	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
20	nsv526194	chr7:5452756-5592436	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	278 gene(s)	inside rSNPs	diseases
21	nsv823997	chr7:5457916-5463961	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
22	esv3428734	chr7:5458676-5468674	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5456800-5458800	Enhancers	Fetal Heart	heart
2	chr7:5457000-5459000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:5457000-5459400	Flanking Active TSS	Stomach Smooth Muscle	stomach
4	chr7:5457000-5461400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:5457200-5458800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:5457200-5458800	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:5457200-5458800	Flanking Active TSS	NHDF-Ad	bronchial
8	chr7:5457200-5459200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
9	chr7:5457200-5459400	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr7:5457200-5461000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
11	chr7:5457400-5458800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:5457400-5459400	Flanking Active TSS	A549	lung
13	chr7:5457600-5458800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr7:5457600-5458800	Flanking Active TSS	Colon Smooth Muscle	Colon
15	chr7:5457600-5461000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:5457800-5458800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:5457800-5458800	Bivalent Enhancer	Primary B cells from cord blood	blood
18	chr7:5457800-5458800	Flanking Active TSS	Fetal Brain Male	brain
19	chr7:5457800-5458800	Flanking Active TSS	Stomach Mucosa	stomach
20	chr7:5457800-5459000	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr7:5457800-5459200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
22	chr7:5457800-5459200	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr7:5457800-5459200	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr7:5457800-5459600	Flanking Active TSS	Hela-S3	cervix
25	chr7:5457800-5459800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
26	chr7:5457800-5461400	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:5458000-5458800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr7:5458000-5458800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
29	chr7:5458000-5459000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
30	chr7:5458000-5459000	Flanking Active TSS	Brain Cingulate Gyrus	brain
31	chr7:5458000-5459000	Flanking Active TSS	Ovary	ovary
32	chr7:5458000-5459000	Flanking Active TSS	HSMM	muscle
33	chr7:5458000-5459000	Flanking Active TSS	K562	blood
34	chr7:5458000-5459200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
35	chr7:5458000-5459200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
36	chr7:5458000-5459200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:5458000-5459200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr7:5458000-5459200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:5458000-5459200	Flanking Active TSS	Colonic Mucosa	Colon
40	chr7:5458000-5459200	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
41	chr7:5458000-5459200	Flanking Active TSS	Pancreas	Pancrea
42	chr7:5458000-5459200	Flanking Active TSS	HUVEC	blood vessel
43	chr7:5458000-5459200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr7:5458000-5459200	Flanking Active TSS	NHEK	skin
45	chr7:5458000-5459200	Flanking Active TSS	Osteobl	bone
46	chr7:5458000-5459400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
47	chr7:5458000-5459400	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr7:5458000-5459400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr7:5458000-5459400	Flanking Active TSS	NH-A	brain
50	chr7:5458000-5460200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links