Variant report

Variant	rs10914018
Chromosome Location	chr1:180491100-180491101
allele	A/G
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	TCF7L2	chr1:180490654-180491556	HEK293	kidney:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
2	CREB1	chr1:180490601-180491121	HepG2	liver:	n/a	n/a
3	POLR2A	chr1:180489708-180492117	MCF10A-Er-Src	breast:	n/a	n/a
4	FOS	chr1:180490664-180491947	MCF10A-Er-Src	breast:	n/a	n/a
5	STAT3	chr1:180490620-180492058	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
6	CEBPB	chr1:180490629-180491818	Hela-S3	cervix:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
7	GTF2F1	chr1:180490692-180491606	Hela-S3	cervix:	n/a	n/a
8	FOS	chr1:180490693-180491869	MCF10A-Er-Src	breast:	n/a	n/a
9	CEBPB	chr1:180490643-180491660	HepG2	liver:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
10	FOS	chr1:180490628-180492057	MCF10A-Er-Src	breast:	n/a	n/a
11	TBP	chr1:180490718-180491567	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:180490499-180491275	HCT-116	colon:	n/a	chr1:180491245-180491256 chr1:180491245-180491258 chr1:180491245-180491256 chr1:180491245-180491258
13	MAX	chr1:180490502-180491386	HCT-116	colon:	n/a	n/a
14	MYC	chr1:180490667-180491990	MCF10A-Er-Src	breast:	n/a	n/a
15	TCF7L2	chr1:180490603-180491456	HCT-116	colon:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
16	TCF7L2	chr1:180490657-180491371	Hela-S3	cervix:	n/a	chr1:180490862-180490876
17	POLR2A	chr1:180490663-180491601	HepG2	liver:	n/a	n/a
18	CREB1	chr1:180490586-180491154	HepG2	liver:	n/a	n/a
19	TCF7L2	chr1:180490675-180491586	MCF-7	breast:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
20	POLR2A	chr1:180489712-180492297	MCF10A-Er-Src	breast:	n/a	n/a
21	SP1	chr1:180490488-180491209	HCT-116	colon:	n/a	n/a
22	STAT3	chr1:180490715-180491757	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
23	RAD21	chr1:180491083-180491285	HepG2	liver:	n/a	n/a
24	MYC	chr1:180490643-180491502	K562	blood:	n/a	n/a
25	MYC	chr1:180490627-180492029	MCF10A-Er-Src	breast:	n/a	n/a
26	STAT3	chr1:180490631-180492130	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
27	USF1	chr1:180490486-180491197	HCT-116	colon:	n/a	chr1:180490845-180490856
28	STAT3	chr1:180490601-180492165	MCF10A-Er-Src	breast:	n/a	chr1:180491461-180491481 chr1:180491467-180491475
29	SP1	chr1:180490548-180491160	HCT-116	colon:	n/a	n/a
30	TEAD4	chr1:180490490-180491139	HepG2	liver:	n/a	n/a
31	MAX	chr1:180491075-180491726	HepG2	liver:	n/a	n/a
32	TCF7L2	chr1:180490733-180491382	HepG2	liver:	n/a	chr1:180490862-180490876
33	JUN	chr1:180490693-180491160	HepG2	liver:	n/a	n/a
34	MAX	chr1:180490470-180491176	HCT-116	colon:	n/a	n/a
35	FOS	chr1:180490600-180492102	MCF10A-Er-Src	breast:	n/a	n/a
36	TCF7L2	chr1:180490581-180491744	Hela-S3	cervix:	n/a	chr1:180491376-180491390 chr1:180490862-180490876
37	KAP1	chr1:180490647-180491763	U2OS	brain:	n/a	n/a
38	USF1	chr1:180490559-180491134	HCT-116	colon:	n/a	chr1:180490845-180490856

No.	Distal block	Cell Line	Cell type
1	chr1:180472964..180474571-chr1:180490356..180493108,2	MCF-7	breast:
2	chr1:180470877..180472880-chr1:180490627..180493125,2	K562	blood:
3	chr1:180489178..180492158-chr1:180598991..180600573,2	K562	blood:
4	chr1:180490294..180492192-chr1:180552011..180554702,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000206905	TF binding region
ENSG00000135847	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10158367	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10465516	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10494527	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs10737342	0.86[CHB][hapmap]
rs10753209	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs10753211	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10753212	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10753216	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10798745	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs10798746	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs10798756	0.85[EUR][1000 genomes]
rs10798757	0.85[EUR][1000 genomes]
rs10798759	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap];0.85[EUR][1000 genomes]
rs10798760	0.85[EUR][1000 genomes]
rs10798761	0.81[CHB][hapmap]
rs10798762	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs10798766	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10798767	0.86[CHB][hapmap]
rs10798769	1.00[CEU][hapmap];0.86[CHB][hapmap];0.88[GIH][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10798770	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10798771	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10798775	0.82[EUR][1000 genomes]
rs10913974	0.85[EUR][1000 genomes]
rs10913976	0.85[EUR][1000 genomes]
rs10913978	0.85[EUR][1000 genomes]
rs10913980	1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes]
rs10913981	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.86[EUR][1000 genomes]
rs10913982	0.85[EUR][1000 genomes]
rs10913983	0.86[EUR][1000 genomes]
rs10913984	0.84[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs10913985	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs10913986	0.81[EUR][1000 genomes]
rs10913987	1.00[CEU][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes]
rs10913998	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10914001	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10914002	0.86[CHB][hapmap]
rs10914005	1.00[CEU][hapmap];0.86[CHB][hapmap];0.86[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];0.98[TSI][hapmap];0.89[EUR][1000 genomes]
rs10914010	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10914014	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10914016	1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10914017	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10914023	1.00[CEU][hapmap];0.81[CHB][hapmap];0.95[GIH][hapmap];0.80[MEX][hapmap];0.95[TSI][hapmap];0.91[EUR][1000 genomes]
rs10914028	0.83[EUR][1000 genomes]
rs11580793	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11799870	1.00[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.91[YRI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12024201	0.96[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12034217	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes]
rs12041620	0.82[ASN][1000 genomes]
rs12121043	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12122338	0.81[EUR][1000 genomes]
rs12127886	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12128560	0.81[EUR][1000 genomes]
rs12129511	0.86[EUR][1000 genomes]
rs12129784	0.85[EUR][1000 genomes]
rs12131071	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12132837	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12135463	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12136111	0.91[EUR][1000 genomes]
rs12141348	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.85[YRI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12141848	1.00[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes]
rs12143350	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12561776	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12565492	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12691484	0.86[CHB][hapmap]
rs12730889	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12733492	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1416821	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1416823	0.86[CHB][hapmap];0.86[CHD][hapmap];0.82[ASN][1000 genomes]
rs1418102	0.86[CHB][hapmap]
rs1538620	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1538622	1.00[CEU][hapmap];0.81[CHB][hapmap];0.93[GIH][hapmap];0.93[TSI][hapmap];0.84[EUR][1000 genomes]
rs16856086	0.82[ASN][1000 genomes]
rs1934410	0.82[EUR][1000 genomes]
rs2105232	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3806300	0.81[CHB][hapmap]
rs3806301	0.80[CHB][hapmap];0.90[CHD][hapmap]
rs3923222	0.82[EUR][1000 genomes]
rs4076403	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.85[EUR][1000 genomes]
rs4142992	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4418555	0.89[EUR][1000 genomes]
rs4420052	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4421553	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs4442335	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];0.91[GIH][hapmap];0.90[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.85[EUR][1000 genomes]
rs4483365	0.86[CHB][hapmap]
rs4578179	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.91[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs4607831	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4634864	0.85[EUR][1000 genomes]
rs4642852	0.86[CHB][hapmap]
rs4651064	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4652496	0.86[CHB][hapmap]
rs4652498	0.86[CHB][hapmap]
rs4652499	0.85[CHB][hapmap]
rs4652505	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6425625	0.86[CHB][hapmap]
rs6661208	0.81[CHB][hapmap]
rs6665719	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs6670544	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6674244	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6680368	0.86[CHB][hapmap]
rs6697924	1.00[CEU][hapmap];0.86[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6700986	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6704334	0.85[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap]
rs6704437	0.86[CHB][hapmap];0.86[CHD][hapmap];0.87[JPT][hapmap]
rs72720922	0.82[ASN][1000 genomes]
rs7523857	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7528650	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.84[MKK][hapmap];0.98[TSI][hapmap];0.92[YRI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7532806	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.86[EUR][1000 genomes]
rs7539910	0.86[CHB][hapmap]
rs7540276	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7543366	1.00[CEU][hapmap];0.90[CHB][hapmap];0.87[JPT][hapmap];0.82[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs822706	0.86[CHB][hapmap]
rs9726041	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs9730180	0.84[CHB][hapmap];0.86[JPT][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762200	chr1:180300936-180493841	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
3	nsv949311	chr1:180438895-180692815	ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10914018	ACBD6	cis	parietal	SCAN
rs10914018	RNASEL	cis	cerebellum	SCAN

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180481800-180491200	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:180485800-180491200	Weak transcription	HSMMtube	muscle
3	chr1:180486000-180493400	Weak transcription	Fetal Stomach	stomach
4	chr1:180486000-180499400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:180486400-180493800	Weak transcription	Fetal Lung	lung
6	chr1:180488000-180500400	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr1:180488200-180492200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:180488600-180497000	Enhancers	Placenta	Placenta
9	chr1:180488800-180491800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:180489400-180494400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:180489800-180494400	Weak transcription	HUVEC	blood vessel
12	chr1:180490400-180492000	Enhancers	Placenta Amnion	Placenta Amnion
13	chr1:180490600-180491200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:180490600-180491200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr1:180490600-180491200	Enhancers	Hela-S3	cervix
16	chr1:180490600-180491200	Enhancers	K562	blood
17	chr1:180490600-180491400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:180490600-180491400	Enhancers	Right Ventricle	heart
19	chr1:180490600-180491400	Enhancers	A549	lung
20	chr1:180490600-180491600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:180490600-180491600	Enhancers	Liver	Liver
22	chr1:180490600-180491600	Enhancers	Psoas Muscle	Psoas
23	chr1:180490600-180491600	Enhancers	Right Atrium	heart
24	chr1:180490600-180491800	Enhancers	Pancreas	Pancrea
25	chr1:180490600-180492000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr1:180490600-180492000	Enhancers	H9 Cell Line	embryonic stem cell
27	chr1:180490600-180492000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr1:180490600-180492400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr1:180490600-180492600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:180490600-180492800	Enhancers	HMEC	breast
31	chr1:180490800-180491400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:180490800-180491400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:180490800-180491400	Enhancers	Fetal Muscle Leg	muscle
34	chr1:180490800-180491400	Weak transcription	Left Ventricle	heart
35	chr1:180490800-180491600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:180490800-180491600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:180490800-180491800	Flanking Active TSS	HepG2	liver
38	chr1:180490800-180492000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:180490800-180492000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr1:180490800-180492200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr1:180490800-180492600	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr1:180490800-180493800	Weak transcription	Lung	lung
43	chr1:180491000-180491200	Flanking Active TSS	Fetal Heart	heart
44	chr1:180491000-180492000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr1:180491000-180492000	Flanking Active TSS	NHEK	skin
46	chr1:180491000-180499400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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