Variant report

Variant	rs4974567
Chromosome Location	chr4:1167387-1167388
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:1167268-1167551	A549	lung:	n/a	chr4:1167391-1167402
2	CEBPB	chr4:1166998-1167583	HepG2	liver:	n/a	chr4:1167391-1167402
3	CEBPB	chr4:1167200-1167583	IMR90	lung:	n/a	chr4:1167391-1167402
4	STAT3	chr4:1167297-1167589	MCF10A-Er-Src	breast:	n/a	n/a
5	HDAC2	chr4:1167229-1167588	HepG2	liver:	n/a	n/a
6	POLR2A	chr4:1166111-1167892	HepG2	liver:	n/a	n/a
7	FOSL2	chr4:1167188-1167641	A549	lung:	n/a	n/a
8	EP300	chr4:1167246-1167522	HepG2	liver:	n/a	n/a
9	EP300	chr4:1167187-1167685	HepG2	liver:	n/a	chr4:1167225-1167241
10	CEBPB	chr4:1167199-1167586	HepG2	liver:	n/a	chr4:1167391-1167402
11	FOXA1	chr4:1167211-1167778	HepG2	liver:	n/a	n/a
12	FOXA1	chr4:1167202-1167662	HepG2	liver:	n/a	n/a
13	POLR2A	chr4:1167295-1167534	HepG2	liver:	n/a	n/a
14	CEBPB	chr4:1167334-1167486	H1-hESC	embryonic stem cell:	n/a	chr4:1167391-1167402
15	HNF4A	chr4:1167263-1167599	HepG2	liver:	n/a	n/a
16	MYBL2	chr4:1167092-1167760	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:1167347-1167490	K562	blood:	n/a	chr4:1167391-1167402
18	TBP	chr4:1167118-1167617	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:1167318-1167525	HepG2	liver:	n/a	chr4:1167391-1167402
20	POLR2A	chr4:1167122-1167594	HepG2	liver:	n/a	n/a
21	SP1	chr4:1167185-1167723	HepG2	liver:	n/a	chr4:1167201-1167214
22	RFX5	chr4:1167323-1167635	HepG2	liver:	n/a	n/a
23	POLR2A	chr4:1167201-1167477	HepG2	liver:	n/a	n/a
24	POLR2A	chr4:1167302-1167449	HepG2	liver:	n/a	n/a
25	CEBPD	chr4:1167191-1167487	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:1167229-1167577	A549	lung:	n/a	chr4:1167391-1167402
27	CEBPD	chr4:1167228-1167485	HepG2	liver:	n/a	n/a
28	FOXA1	chr4:1167194-1167691	HepG2	liver:	n/a	n/a
29	HEY1	chr4:1167090-1167776	HepG2	liver:	n/a	n/a
30	NFIC	chr4:1167186-1167600	HepG2	liver:	n/a	n/a
31	TCF12	chr4:1167102-1167699	A549	lung:	n/a	chr4:1167215-1167225
32	MBD4	chr4:1167247-1167564	HepG2	liver:	n/a	n/a
33	HEY1	chr4:1167262-1167468	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:1167083-1167697	A549	lung:	n/a	chr4:1167391-1167402
35	POLR2A	chr4:1167192-1167458	HepG2	liver:	n/a	n/a
36	FOXA1	chr4:1167233-1167739	HepG2	liver:	n/a	n/a
37	SMC3	chr4:1167222-1167559	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:1167268-1167617	HepG2	liver:	n/a	chr4:1167391-1167402
39	FOXA2	chr4:1167258-1167664	HepG2	liver:	n/a	n/a
40	ARID3A	chr4:1167268-1167586	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1167369-1167419	ECC-1	luminal epithelium:	n/a
2	chr4:1167369-1167419	Caco-2	colon:	n/a
3	chr4:1167369-1167419	U87	brain:	n/a
4	chr4:1167369-1167419	SKMC	muscle:	n/a
5	chr4:1167369-1167419	Hela-S3	cervix:	n/a
6	chr4:1167369-1167419	HCF	heart:	n/a
7	chr4:1167369-1167419	HCT-116	colon:	n/a
8	chr4:1167369-1167419	HMEC	breast:	n/a
9	chr4:1167369-1167419	HEEpiC	esophagus:	n/a
10	chr4:1167369-1167419	AG04450	lung:	fetal
11	chr4:1167369-1167419	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:1167369-1167419	SK-N-SH_RA	brain:	n/a
13	chr4:1167369-1167419	HEK293	kidney:	embryo
14	chr4:1167369-1167419	AG10803	skin:	n/a
15	chr4:1167369-1167419	GM19239	blood:	n/a
16	chr4:1167369-1167419	AG04449	skin:	fetal
17	chr4:1167369-1167419	LNCaP	prostate:	n/a
18	chr4:1167369-1167419	HRPEpiC	eye:	n/a
19	chr4:1167369-1167419	HRCEpiC	kidney:	n/a
20	chr4:1167369-1167419	ovcar-3	ovarian:	n/a
21	chr4:1167369-1167419	GM12892	blood:	n/a
22	chr4:1167369-1167419	HIPEpiC	eye:	n/a
23	chr4:1167369-1167419	BJ	skin:	n/a
24	chr4:1167369-1167419	HCPEpiC	choroid plexus:	n/a
25	chr4:1167369-1167419	HNPCEpiC	eye:	n/a
26	chr4:1167369-1167419	Jurkat	blood:	n/a
27	chr4:1167369-1167419	PANC-1	pancreas:	n/a
28	chr4:1167369-1167419	SK-N-MC	brain:	n/a
29	chr4:1167369-1167419	MCF10A-Er-Src	breast:	n/a
30	chr4:1167369-1167419	A549	lung:	n/a
31	chr4:1167369-1167419	AoSMC	blood vessel:	n/a
32	chr4:1167369-1167419	SK-N-SH	brain:	n/a
33	chr4:1167369-1167419	ProgFib	skin:	n/a
34	chr4:1167369-1167419	GM12878	blood:	n/a
35	chr4:1167369-1167419	MCF-7	breast:	n/a
36	chr4:1167369-1167419	NHBE	bronchial:	n/a
37	chr4:1167369-1167419	CMK	blood:	n/a
38	chr4:1167369-1167419	GM12891	blood:	n/a
39	chr4:1167369-1167419	GM06990	blood:	n/a
40	chr4:1167369-1167419	HCM	heart:	n/a
41	chr4:1167369-1167419	RPTEC	kidney:	n/a
42	chr4:1167369-1167419	PrEC	prostate:	n/a
43	chr4:1167369-1167419	T-47D	breast:	n/a
44	chr4:1167369-1167419	HUVEC	blood vessel:	n/a
45	chr4:1167369-1167419	HL-60	blood:	n/a
46	chr4:1167369-1167419	HepG2	liver:	n/a
47	chr4:1167369-1167419	NH-A	brain:	n/a
48	chr4:1167369-1167419	IMR90	lung:	fetal
49	chr4:1167369-1167419	H1-hESC	embryonic stem cell:	embryo
50	chr4:1167369-1167419	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:1159479..1162008-chr4:1166717..1168665,3	MCF-7	breast:
2	chr4:1161114..1165211-chr4:1166165..1170804,4	MCF-7	breast:

No data

Variant related genes	Relation type
SPON2	TF binding region
SPON2	CpG island
ENSG00000159674	Chromatin interaction
ENSG00000273179	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10008164	1.00[TSI][hapmap]
rs10011708	1.00[TSI][hapmap]
rs10013662	1.00[ASW][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11931513	1.00[EUR][1000 genomes]
rs11932895	1.00[EUR][1000 genomes]
rs1250087	1.00[TSI][hapmap]
rs1250104	1.00[TSI][hapmap]
rs1272043	1.00[ASW][hapmap];1.00[TSI][hapmap]
rs13115935	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1383658	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1383659	1.00[TSI][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1481168	1.00[ASW][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1680075	1.00[EUR][1000 genomes]
rs1680082	1.00[EUR][1000 genomes]
rs17164618	1.00[EUR][1000 genomes]
rs1732105	1.00[EUR][1000 genomes]
rs1871758	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2127911	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28750743	1.00[ASW][hapmap]
rs34082974	1.00[EUR][1000 genomes]
rs4246689	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs4336168	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4465987	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974580	1.00[EUR][1000 genomes]
rs4974581	1.00[EUR][1000 genomes]
rs4974634	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974635	0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs4974636	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974641	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4974645	1.00[ASW][hapmap];1.00[TSI][hapmap]
rs57461362	1.00[EUR][1000 genomes]
rs59318613	1.00[EUR][1000 genomes]
rs59669372	1.00[EUR][1000 genomes]
rs60410862	1.00[EUR][1000 genomes]
rs6818213	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6834402	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6835204	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6836809	1.00[ASW][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6836952	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs73069991	1.00[EUR][1000 genomes]
rs73069994	1.00[EUR][1000 genomes]
rs73071910	1.00[EUR][1000 genomes]
rs73071925	1.00[EUR][1000 genomes]
rs73073722	1.00[EUR][1000 genomes]
rs73073725	1.00[EUR][1000 genomes]
rs73073727	1.00[EUR][1000 genomes]
rs73073729	1.00[EUR][1000 genomes]
rs73796061	1.00[EUR][1000 genomes]
rs7660109	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7676912	1.00[ASW][hapmap];1.00[TSI][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7691582	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs922697	1.00[ASW][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9997694	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	nsv1009619	chr4:901897-1215657	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv1003876	chr4:927509-1191316	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv1000381	chr4:927509-1198766	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
6	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
7	nsv1005990	chr4:1015652-1167619	Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv1012892	chr4:1086871-1176630	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv829835	chr4:1097586-1304239	Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription 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	59 gene(s)	inside rSNPs	diseases
10	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
11	nsv878329	chr4:1147407-1254930	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
12	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
13	nsv519106	chr4:1158991-1174861	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv593276	chr4:1159680-1227469	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
15	nsv461151	chr4:1159680-1236840	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv593277	chr4:1159680-1236840	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	nsv878331	chr4:1159680-1254930	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
18	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
19	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:1166000-1167400	Enhancers	Lung	lung
2	chr4:1166400-1167400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr4:1166400-1167400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
4	chr4:1166400-1168000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:1166600-1167400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:1166600-1167400	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:1166600-1167800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
8	chr4:1166600-1167800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr4:1166600-1167800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr4:1166600-1167800	Enhancers	Left Ventricle	heart
11	chr4:1166600-1168000	Enhancers	Right Ventricle	heart
12	chr4:1166600-1168000	Enhancers	NHLF	lung
13	chr4:1166600-1168200	Bivalent Enhancer	Placenta	Placenta
14	chr4:1166600-1169200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr4:1166600-1169600	Enhancers	Psoas Muscle	Psoas
16	chr4:1166600-1170800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr4:1166600-1171000	Weak transcription	Gastric	stomach
18	chr4:1166800-1167400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:1166800-1167400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:1166800-1167400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr4:1166800-1167400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:1166800-1167400	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr4:1166800-1167400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
24	chr4:1166800-1167800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:1166800-1167800	Bivalent Enhancer	Fetal Heart	heart
26	chr4:1166800-1167800	Bivalent Enhancer	Fetal Lung	lung
27	chr4:1166800-1167800	Enhancers	HSMMtube	muscle
28	chr4:1166800-1168000	Flanking Active TSS	HepG2	liver
29	chr4:1167000-1167400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
30	chr4:1167000-1167600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
31	chr4:1167000-1167800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr4:1167000-1168000	Enhancers	Ovary	ovary
33	chr4:1167000-1168000	Enhancers	A549	lung
34	chr4:1167000-1169800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr4:1167000-1174200	Weak transcription	Primary T cells from cord blood	blood
36	chr4:1167200-1167400	Bivalent Enhancer	HMEC	breast
37	chr4:1167200-1167600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:1167200-1167600	Enhancers	Liver	Liver
39	chr4:1167200-1167600	Bivalent Enhancer	Fetal Intestine Small	intestine
40	chr4:1167200-1167800	Enhancers	Esophagus	oesophagus
41	chr4:1167200-1167800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr4:1167200-1167800	Enhancers	Osteobl	bone
43	chr4:1167200-1168000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:1167200-1168000	Enhancers	NHDF-Ad	bronchial
45	chr4:1167200-1168200	Bivalent Enhancer	Fetal Stomach	stomach
46	chr4:1167200-1168200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
47	chr4:1167200-1169000	Weak transcription	Pancreas	Pancrea
48	chr4:1167200-1169200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:1167200-1169600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:1167200-1170000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

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