Variant report

Variant	rs494986
Chromosome Location	chr12:121569936-121569937
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:21 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF217	chr12:121569742-121570076	MCF-7	breast:	n/a	n/a
2	GATA3	chr12:121569540-121570286	MCF-7	breast:	n/a	chr12:121569900-121569908
3	GATA3	chr12:121569676-121570082	T-47D	breast:	n/a	chr12:121569900-121569908
4	HNF4A	chr12:121569890-121570261	HepG2	liver:	n/a	n/a
5	FOXA1	chr12:121569826-121570116	HepG2	liver:	n/a	n/a
6	JUN	chr12:121569328-121571628	K562	blood:	n/a	chr12:121571251-121571261 chr12:121571252-121571260 chr12:121571251-121571261 chr12:121571251-121571261 chr12:121571251-121571261
7	JUND	chr12:121569778-121570035	K562	blood:	n/a	n/a
8	NR2F2	chr12:121569661-121570285	MCF-7	breast:	n/a	n/a
9	GATA3	chr12:121569730-121570073	SH-SY5Y	brain:	n/a	chr12:121569900-121569908
10	SIN3AK20	chr12:121569499-121570202	MCF-7	breast:	n/a	n/a
11	EP300	chr12:121569723-121570191	MCF-7	breast:	n/a	n/a
12	GATA2	chr12:121569738-121570145	SH-SY5Y	brain:	n/a	n/a
13	GATA3	chr12:121569664-121570064	T-47D	breast:	n/a	chr12:121569900-121569908
14	FOXA1	chr12:121569810-121570146	HepG2	liver:	n/a	n/a
15	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
16	KAP1	chr12:121569281-121570057	U2OS	brain:	n/a	n/a
17	NR2F2	chr12:121569651-121570304	MCF-7	breast:	n/a	n/a
18	GATA3	chr12:121569713-121570172	MCF-7	breast:	n/a	chr12:121569900-121569908
19	HNF4A	chr12:121569924-121570164	HepG2	liver:	n/a	n/a
20	SP1	chr12:121569801-121570247	HepG2	liver:	n/a	n/a
21	GATA3	chr12:121569512-121570382	MCF-7	breast:	n/a	chr12:121569900-121569908

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121569924-121569974	ECC-1	luminal epithelium:	n/a
2	chr12:121569924-121569974	SK-N-SH_RA	brain:	n/a
3	chr12:121569924-121569974	PFSK-1	brain:	n/a
4	chr12:121569924-121569974	NHBE	bronchial:	n/a
5	chr12:121569924-121569974	SAEC	small airway:	n/a
6	chr12:121569924-121569974	HRCEpiC	kidney:	n/a
7	chr12:121569924-121569974	CMK	blood:	n/a
8	chr12:121569924-121569974	HIPEpiC	eye:	n/a
9	chr12:121569924-121569974	NT2-D1	testis:	n/a
10	chr12:121569924-121569974	AG09309	skin:	n/a
11	chr12:121569924-121569974	AG10803	skin:	n/a
12	chr12:121569924-121569974	NH-A	brain:	n/a
13	chr12:121569924-121569974	IMR90	lung:	fetal
14	chr12:121569924-121569974	PANC-1	pancreas:	n/a
15	chr12:121569924-121569974	LNCaP	prostate:	n/a
16	chr12:121569924-121569974	GM12892	blood:	n/a
17	chr12:121569924-121569974	H1-hESC	embryonic stem cell:	embryo
18	chr12:121569924-121569974	HMEC	breast:	n/a
19	chr12:121569924-121569974	HUVEC	blood vessel:	n/a
20	chr12:121569924-121569974	MCF10A-Er-Src	breast:	n/a
21	chr12:121569924-121569974	GM06990	blood:	n/a
22	chr12:121569924-121569974	SK-N-SH	brain:	n/a
23	chr12:121569924-121569974	Hela-S3	cervix:	n/a
24	chr12:121569924-121569974	U87	brain:	n/a
25	chr12:121569924-121569974	HNPCEpiC	eye:	n/a
26	chr12:121569924-121569974	AG09319	gingival:	n/a
27	chr12:121569924-121569974	Jurkat	blood:	n/a
28	chr12:121569924-121569974	AoSMC	blood vessel:	n/a
29	chr12:121569924-121569974	K562	blood:	n/a
30	chr12:121569924-121569974	HEEpiC	esophagus:	n/a
31	chr12:121569924-121569974	BE2_C	brain:	n/a
32	chr12:121569924-121569974	GM12878	blood:	n/a
33	chr12:121569924-121569974	Hepatocyte	liver:	n/a
34	chr12:121569924-121569974	BJ	skin:	n/a
35	chr12:121569924-121569974	HEK293	kidney:	embryo
36	chr12:121569924-121569974	NB4	blood:	n/a
37	chr12:121569924-121569974	AG04449	skin:	fetal
38	chr12:121569924-121569974	HRE	kidney:	n/a
39	chr12:121569924-121569974	HCM	heart:	n/a
40	chr12:121569924-121569974	RPTEC	kidney:	n/a
41	chr12:121569924-121569974	HCT-116	colon:	n/a
42	chr12:121569924-121569974	HPAEpiC	pulmonary alveolar:	n/a
43	chr12:121569924-121569974	NHDF-neo	bronchial:	n/a
44	chr12:121569924-121569974	HAEpiC	amniotic membrane:	n/a
45	chr12:121569924-121569974	HepG2	liver:	n/a
46	chr12:121569924-121569974	ProgFib	skin:	n/a
47	chr12:121569924-121569974	GM12891	blood:	n/a
48	chr12:121569924-121569974	PrEC	prostate:	n/a
49	chr12:121569924-121569974	HCPEpiC	choroid plexus:	n/a
50	chr12:121569924-121569974	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:121569636..121570366-chr12:121640682..121641273,2	MCF-7	breast:
2	chr12:121569572..121570160-chr12:121640475..121641223,2	MCF-7	breast:
3	chr12:121569906..121572539-chr12:121647803..121649868,2	MCF-7	breast:
4	chr12:121569648..121570492-chr12:121613509..121614358,5	MCF-7	breast:
5	chr12:121569656..121570427-chr12:121608922..121609716,2	MCF-7	breast:

No data

Variant related genes	Relation type
P2RX7	TF binding region
P2RX7	CpG island
ENSG00000135124	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1180016	1.00[YRI][hapmap]
rs12810503	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12813980	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12814235	0.96[AMR][1000 genomes]
rs12816966	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12817169	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12819523	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12819930	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12820593	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12824585	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12830584	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12832396	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1718153	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17432871	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17434640	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17525809	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1794901	1.00[YRI][hapmap]
rs208285	0.80[AFR][1000 genomes]
rs208302	0.88[ASN][1000 genomes]
rs2260138	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2393752	1.00[ASN][1000 genomes]
rs2393753	0.88[ASN][1000 genomes]
rs2393754	0.91[ASN][1000 genomes]
rs2708094	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs28969465	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28969469	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34185850	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34325588	0.96[AMR][1000 genomes]
rs34449339	0.93[ASN][1000 genomes]
rs34480856	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34572498	0.94[ASN][1000 genomes]
rs34805626	0.93[ASN][1000 genomes]
rs34811727	0.96[AMR][1000 genomes]
rs34934130	0.96[AMR][1000 genomes]
rs35018823	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35076950	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35158421	0.93[ASN][1000 genomes]
rs35237790	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35362296	0.96[AMR][1000 genomes]
rs35455367	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35579189	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35605477	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35607692	0.84[AMR][1000 genomes]
rs35760636	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35869834	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35940217	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs36133237	0.93[ASN][1000 genomes]
rs3861796	1.00[YRI][hapmap]
rs512239	0.80[AFR][1000 genomes]
rs513113	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs514109	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56098349	0.93[ASN][1000 genomes]
rs566496	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs583187	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs584133	0.80[AFR][1000 genomes]
rs585847	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588130	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588510	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs588573	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs599785	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs601636	0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs603505	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs603891	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs618201	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs657172	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs657647	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs66570654	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66811517	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670541	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs675718	1.00[ASN][1000 genomes]
rs676632	1.00[ASN][1000 genomes]
rs67691679	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67739439	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67881993	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67898046	0.96[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs680700	0.80[AFR][1000 genomes]
rs682104	0.80[AFR][1000 genomes]
rs71454676	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71454679	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71454680	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73214191	0.96[AMR][1000 genomes]
rs73214199	0.96[AMR][1000 genomes]
rs73216114	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73218241	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs934353	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs934354	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs934355	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv899559	chr12:121324727-121592689	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	esv2758318	chr12:121415845-121584813	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv2759917	chr12:121415845-121584813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv832531	chr12:121440495-121604232	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv430537	chr12:121487632-121579955	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats 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 target site	25 gene(s)	inside rSNPs	diseases
10	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv899563	chr12:121543011-121600529	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1050519	chr12:121552964-121756420	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121562400-121570600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:121562800-121570400	Weak transcription	Ovary	ovary
3	chr12:121564200-121570600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:121565800-121570600	Enhancers	Placenta	Placenta
5	chr12:121566600-121570200	Weak transcription	Small Intestine	intestine
6	chr12:121566800-121570400	Weak transcription	Gastric	stomach
7	chr12:121567000-121570200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:121567200-121570000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:121567200-121570400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:121567200-121570400	Weak transcription	Fetal Lung	lung
11	chr12:121567200-121570400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr12:121567200-121570400	Weak transcription	HMEC	breast
13	chr12:121567400-121570400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr12:121567400-121570400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr12:121567400-121570400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:121567600-121570000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr12:121567600-121570000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:121567600-121570000	Enhancers	Brain Substantia Nigra	brain
19	chr12:121567600-121570200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr12:121567600-121570200	Weak transcription	Fetal Heart	heart
21	chr12:121567600-121570200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr12:121567600-121570200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr12:121567600-121570400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr12:121567600-121570400	Enhancers	Primary T cells fromperipheralblood	blood
25	chr12:121567600-121570400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:121567600-121570400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr12:121567600-121570400	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr12:121567600-121570400	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr12:121567600-121570400	Weak transcription	Psoas Muscle	Psoas
30	chr12:121567600-121570400	Weak transcription	Right Atrium	heart
31	chr12:121567600-121570400	Weak transcription	Right Ventricle	heart
32	chr12:121567600-121570400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr12:121567600-121570400	Weak transcription	Stomach Mucosa	stomach
34	chr12:121567600-121570400	Weak transcription	NHDF-Ad	bronchial
35	chr12:121567600-121570600	Enhancers	Primary hematopoietic stem cells	blood
36	chr12:121567600-121570600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:121567600-121570600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:121567800-121570000	Enhancers	Brain Hippocampus Middle	brain
39	chr12:121567800-121570200	Weak transcription	Adipose Nuclei	Adipose
40	chr12:121567800-121570200	Weak transcription	Spleen	Spleen
41	chr12:121567800-121570200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr12:121567800-121570400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr12:121567800-121570400	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr12:121567800-121570400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr12:121567800-121570400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:121567800-121570400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:121567800-121570400	Weak transcription	Fetal Muscle Leg	muscle
48	chr12:121567800-121570400	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr12:121567800-121570400	Weak transcription	Thymus	Thymus
50	chr12:121567800-121570400	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links