Variant report

Variant	rs564037149
Chromosome Location	chr7:3340464-3340465
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr7:3340453-3340653	MCF-7	breast:	n/a	chr7:3340556-3340566
2	CTCF	chr7:3340418-3340766	GM10266	blood:	n/a	chr7:3340483-3340496
3	YY1	chr7:3340430-3340933	ECC-1	luminal epithelium:	n/a	chr7:3340750-3340759 chr7:3340664-3340678 chr7:3340464-3340475 chr7:3340661-3340675 chr7:3340745-3340759 chr7:3340666-3340675
4	RUNX3	chr7:3340464-3340779	GM12878	blood:	n/a	n/a
5	MAZ	chr7:3340423-3340911	GM12878	blood:	n/a	chr7:3340556-3340566
6	RAD21	chr7:3340160-3340979	MCF-7	breast:	n/a	n/a
7	MAX	chr7:3340236-3341061	HCT-116	colon:	n/a	chr7:3340556-3340566
8	POLR2A	chr7:3340452-3340913	HUVEC	blood vessel:	n/a	n/a
9	CTCF	chr7:3340358-3340781	MCF-7	breast:	n/a	chr7:3340483-3340496
10	CTCF	chr7:3340445-3340787	GM13977	blood:	n/a	chr7:3340483-3340496
11	CTCF	chr7:3339276-3341235	SK-N-SH	brain:	n/a	chr7:3339295-3339303 chr7:3340483-3340496 chr7:3339382-3339390
12	EP300	chr7:3340260-3341049	SK-N-SH	brain:	n/a	chr7:3340459-3340475 chr7:3340748-3340757 chr7:3340695-3340704 chr7:3340638-3340647 chr7:3340735-3340751
13	CTCF	chr7:3340433-3340874	A549	lung:	n/a	chr7:3340483-3340496
14	CTCF	chr7:3340464-3340760	Fibrobl	skin:	n/a	chr7:3340483-3340496
15	MAX	chr7:3340278-3341002	H1-hESC	embryonic stem cell:	n/a	chr7:3340556-3340566
16	RAD21	chr7:3340369-3340901	HCT-116	colon:	n/a	n/a
17	RAD21	chr7:3340445-3340896	HepG2	liver:	n/a	n/a
18	RAD21	chr7:3340288-3340949	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr7:3340214-3341121	MCF-7	breast:	n/a	n/a
20	YY1	chr7:3340284-3340751	GM12891	blood:	n/a	chr7:3340664-3340678 chr7:3340464-3340475 chr7:3340661-3340675 chr7:3340666-3340675
21	MAX	chr7:3340431-3340992	K562	blood:	n/a	chr7:3340556-3340566
22	RAD21	chr7:3340369-3340948	SK-N-SH_RA	brain:	n/a	n/a
23	RAD21	chr7:3340392-3340764	A549	lung:	n/a	n/a
24	E2F6	chr7:3340434-3340956	K562	blood:	n/a	chr7:3340661-3340671 chr7:3340635-3340645 chr7:3340638-3340647 chr7:3340765-3340774 chr7:3340640-3340652 chr7:3340748-3340758 chr7:3340731-3340740 chr7:3340437-3340451 chr7:3340641-3340652 chr7:3340557-3340566 chr7:3340695-3340705
25	YY1	chr7:3340300-3340931	HepG2	liver:	n/a	chr7:3340750-3340759 chr7:3340664-3340678 chr7:3340464-3340475 chr7:3340661-3340675 chr7:3340745-3340759 chr7:3340666-3340675
26	ZNF143	chr7:3340427-3340811	GM12878	blood:	n/a	chr7:3340695-3340705 chr7:3340638-3340648 chr7:3340748-3340758 chr7:3340556-3340566
27	BHLHE40	chr7:3340409-3341002	HepG2	liver:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
28	FOXP2	chr7:3340409-3340756	PFSK-1	brain:	n/a	n/a
29	RAD21	chr7:3340329-3340836	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr7:3340179-3341039	A549	lung:	n/a	chr7:3340483-3340496
31	SIN3AK20	chr7:3339879-3341185	PANC-1	pancreas:	n/a	n/a
32	MAX	chr7:3340376-3340867	A549	lung:	n/a	chr7:3340556-3340566
33	JUN	chr7:3340371-3341094	K562	blood:	n/a	chr7:3340690-3340699 chr7:3340730-3340739
34	POLR2A	chr7:3340297-3341084	PANC-1	pancreas:	n/a	n/a
35	MAZ	chr7:3340273-3340943	HepG2	liver:	n/a	chr7:3340556-3340566
36	CTCF	chr7:3340401-3340939	MCF-7	breast:	n/a	chr7:3340483-3340496
37	CTCF	chr7:3340413-3340826	Spleen_OC	spleen:	n/a	chr7:3340483-3340496
38	RAD21	chr7:3340235-3340997	IMR90	lung:	n/a	n/a
39	ELF1	chr7:3340417-3340943	GM12878	blood:	n/a	chr7:3340532-3340544
40	SMC3	chr7:3339220-3341228	SK-N-SH	brain:	n/a	n/a
41	YY1	chr7:3340271-3340885	GM12892	blood:	n/a	chr7:3340750-3340759 chr7:3340664-3340678 chr7:3340464-3340475 chr7:3340661-3340675 chr7:3340745-3340759 chr7:3340666-3340675
42	POLR2A	chr7:3339844-3341257	MCF-7	breast:	n/a	n/a
43	MAX	chr7:3339896-3341192	HepG2	liver:	n/a	chr7:3340556-3340566
44	CTCF	chr7:3340444-3340732	K562	blood:	n/a	chr7:3340483-3340496
45	CTCF	chr7:3340447-3340745	GM12891	blood:	n/a	chr7:3340483-3340496
46	FOXA1	chr7:3340404-3340781	HepG2	liver:	n/a	n/a
47	RAD21	chr7:3340345-3340892	SK-N-SH_RA	brain:	n/a	n/a
48	EGR1	chr7:3340407-3341021	K562	blood:	n/a	chr7:3340549-3340563 chr7:3340553-3340562 chr7:3340903-3340917 chr7:3340752-3340762 chr7:3340690-3340700 chr7:3340730-3340740
49	E2F6	chr7:3340331-3341223	K562	blood:	n/a	chr7:3340661-3340671 chr7:3340635-3340645 chr7:3340638-3340647 chr7:3340765-3340774 chr7:3340640-3340652 chr7:3340748-3340758 chr7:3340731-3340740 chr7:3340437-3340451 chr7:3340641-3340652 chr7:3340557-3340566 chr7:3340695-3340705
50	MAFK	chr7:3340286-3340713	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3340459-3340509	GM12891	blood:	n/a
2	chr7:3340459-3340509	IMR90	lung:	fetal
3	chr7:3340459-3340509	U87	brain:	n/a
4	chr7:3340459-3340509	SKMC	muscle:	n/a
5	chr7:3340459-3340509	NB4	blood:	n/a
6	chr7:3340459-3340509	NT2-D1	testis:	n/a
7	chr7:3340459-3340509	LNCaP	prostate:	n/a
8	chr7:3340459-3340509	HUVEC	blood vessel:	n/a
9	chr7:3340459-3340509	HRCEpiC	kidney:	n/a
10	chr7:3340459-3340509	ECC-1	luminal epithelium:	n/a
11	chr7:3340459-3340509	HRE	kidney:	n/a
12	chr7:3340459-3340509	Caco-2	colon:	n/a
13	chr7:3340459-3340509	PrEC	prostate:	n/a
14	chr7:3340459-3340509	CMK	blood:	n/a
15	chr7:3340459-3340509	PANC-1	pancreas:	n/a
16	chr7:3340459-3340509	HRPEpiC	eye:	n/a
17	chr7:3340459-3340509	GM12878	blood:	n/a
18	chr7:3340459-3340509	BE2_C	brain:	n/a
19	chr7:3340459-3340509	AG04449	skin:	fetal
20	chr7:3340459-3340509	GM19239	blood:	n/a
21	chr7:3340459-3340509	HCPEpiC	choroid plexus:	n/a
22	chr7:3340459-3340509	Hela-S3	cervix:	n/a
23	chr7:3340459-3340509	HEK293	kidney:	embryo
24	chr7:3340459-3340509	NHDF-neo	bronchial:	n/a
25	chr7:3340459-3340509	HEEpiC	esophagus:	n/a
26	chr7:3340459-3340509	A549	lung:	n/a
27	chr7:3340459-3340509	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:3340459-3340509	AG09319	gingival:	n/a
29	chr7:3340459-3340509	HL-60	blood:	n/a
30	chr7:3340459-3340509	HepG2	liver:	n/a
31	chr7:3340459-3340509	HIPEpiC	eye:	n/a
32	chr7:3340459-3340509	H1-hESC	embryonic stem cell:	embryo
33	chr7:3340459-3340509	Hepatocyte	liver:	n/a
34	chr7:3340459-3340509	MCF10A-Er-Src	breast:	n/a
35	chr7:3340459-3340509	NH-A	brain:	n/a
36	chr7:3340459-3340509	SK-N-MC	brain:	n/a
37	chr7:3340459-3340509	HCF	heart:	n/a
38	chr7:3340459-3340509	K562	blood:	n/a
39	chr7:3340459-3340509	AoSMC	blood vessel:	n/a
40	chr7:3340459-3340509	ovcar-3	ovarian:	n/a
41	chr7:3340459-3340509	AG10803	skin:	n/a
42	chr7:3340459-3340509	HCM	heart:	n/a
43	chr7:3340459-3340509	AG09309	skin:	n/a
44	chr7:3340459-3340509	BJ	skin:	n/a
45	chr7:3340459-3340509	NHBE	bronchial:	n/a
46	chr7:3340459-3340509	ProgFib	skin:	n/a
47	chr7:3340459-3340509	HCT-116	colon:	n/a
48	chr7:3340459-3340509	HMEC	breast:	n/a
49	chr7:3340459-3340509	GM06990	blood:	n/a
50	chr7:3340459-3340509	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:
2	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
3	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
4	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island
ENSG00000211544	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464264	chr7:3194156-3349625	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv605880	chr7:3194156-3349625	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1023127	chr7:3216344-3466223	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2758100	chr7:3286625-3560229	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv2759500	chr7:3286625-3560229	Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1019515	chr7:3300048-3479972	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv887324	chr7:3308195-3400105	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv1803572	chr7:3327994-3341589	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
13	nsv605885	chr7:3337081-3340551	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	esv19885	chr7:3339551-3341631	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
15	esv3328363	chr7:3339726-3342349	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	esv3345863	chr7:3339851-3342399	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	esv1802865	chr7:3339987-3341589	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
18	nsv605886	chr7:3340090-3340969	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv605887	chr7:3340187-3341488	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
20	esv1803913	chr7:3340187-3341589	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
21	esv1836877	chr7:3340187-3341589	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
22	nsv605888	chr7:3340187-3341589	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv605889	chr7:3340187-3342276	Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
24	esv3421283	chr7:3340376-3342024	Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
25	nsv605890	chr7:3340396-3341488	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
26	esv1833976	chr7:3340396-3341589	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3339400-3340600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:3339400-3340600	Bivalent Enhancer	Placenta	Placenta
3	chr7:3339600-3342600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
4	chr7:3339800-3340600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr7:3339800-3340600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
6	chr7:3339800-3340600	Active TSS	Brain Substantia Nigra	brain
7	chr7:3339800-3340600	Enhancers	Fetal Brain Male	brain
8	chr7:3339800-3341600	Active TSS	Fetal Brain Female	brain
9	chr7:3339800-3342200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:3339800-3342200	Active TSS	HSMMtube	muscle
11	chr7:3340000-3340600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:3340000-3340600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
13	chr7:3340000-3340600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
14	chr7:3340000-3340600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr7:3340000-3340600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
16	chr7:3340000-3340600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:3340000-3340600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr7:3340000-3340600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr7:3340000-3340600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr7:3340000-3340600	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr7:3340000-3340600	Flanking Active TSS	Colonic Mucosa	Colon
22	chr7:3340000-3340600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
23	chr7:3340000-3340600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
24	chr7:3340000-3340600	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr7:3340000-3341600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:3340000-3341600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:3340000-3342200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:3340000-3342200	Active TSS	HepG2	liver
29	chr7:3340000-3342200	Active TSS	HSMM	muscle
30	chr7:3340000-3342400	Active TSS	Right Atrium	heart
31	chr7:3340000-3342600	Active TSS	H9 Cell Line	embryonic stem cell
32	chr7:3340000-3342600	Active TSS	Rectal Smooth Muscle	rectum
33	chr7:3340000-3343400	Active TSS	Aorta	Aorta
34	chr7:3340200-3340600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr7:3340200-3340600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:3340200-3340600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:3340200-3340600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
38	chr7:3340200-3340600	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
39	chr7:3340200-3340600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
40	chr7:3340200-3340600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
41	chr7:3340200-3340600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr7:3340200-3340600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr7:3340200-3340600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr7:3340200-3340600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:3340200-3340600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr7:3340200-3340600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:3340200-3340600	Flanking Active TSS	Liver	Liver
48	chr7:3340200-3340600	Active TSS	Brain Angular Gyrus	brain
49	chr7:3340200-3340600	Active TSS	Colon Smooth Muscle	Colon
50	chr7:3340200-3340600	Bivalent/Poised TSS	Fetal Intestine Small	intestine

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