Variant report

Variant	rs2033385
Chromosome Location	chr14:45605818-45605819
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	POLR2A	chr14:45604842-45605839	K562	blood:	n/a	n/a
2	SIN3AK20	chr14:45604603-45606108	MCF-7	breast:	n/a	n/a
3	REST	chr14:45602751-45605945	H1-neurons	neurons:	n/a	n/a
4	WRNIP1	chr14:45604534-45605879	GM12878	blood:	n/a	n/a
5	MAX	chr14:45604741-45606030	MCF-7	breast:	n/a	n/a
6	MAX	chr14:45604677-45605886	NB4	blood:	n/a	n/a
7	MAX	chr14:45604622-45605988	A549	lung:	n/a	n/a
8	MYC	chr14:45605567-45605998	MCF10A-Er-Src	breast:	n/a	n/a
9	GABPA	chr14:45604455-45605984	MCF-7	breast:	n/a	n/a
10	HCFC1	chr14:45602844-45606700	Hela-S3	cervix:	n/a	n/a
11	MXI1	chr14:45604433-45606343	IMR90	lung:	n/a	n/a
12	MYC	chr14:45603191-45605877	K562	blood:	n/a	chr14:45603665-45603675 chr14:45603452-45603462
13	SIN3AK20	chr14:45604557-45606051	MCF-7	breast:	n/a	n/a
14	MYC	chr14:45605575-45606185	MCF10A-Er-Src	breast:	n/a	n/a
15	MXI1	chr14:45602724-45606159	SK-N-SH	brain:	n/a	n/a
16	MXI1	chr14:45604823-45605975	HepG2	liver:	n/a	n/a
17	POLR2A	chr14:45605647-45606001	MCF10A-Er-Src	breast:	n/a	n/a
18	MXI1	chr14:45604772-45605926	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr14:45604840-45605870	HepG2	liver:	n/a	n/a
20	MYC	chr14:45603257-45605853	NB4	blood:	n/a	chr14:45603665-45603675 chr14:45603452-45603462
21	CEBPB	chr14:45604815-45606009	Hela-S3	cervix:	n/a	chr14:45605057-45605065 chr14:45605542-45605553
22	MXI1	chr14:45605721-45605852	K562	blood:	n/a	n/a
23	SIN3AK20	chr14:45605634-45605919	K562	blood:	n/a	n/a
24	CHD1	chr14:45602891-45606393	IMR90	lung:	n/a	chr14:45603710-45603720
25	GTF2F1	chr14:45604842-45605846	Hela-S3	cervix:	n/a	n/a
26	SIN3A	chr14:45604794-45606001	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr14:45604902-45605975	H1-hESC	embryonic stem cell:	n/a	n/a
28	MXI1	chr14:45604575-45606161	Hela-S3	cervix:	n/a	n/a
29	SREBP1	chr14:45602656-45606838	GM12878	blood:	n/a	n/a
30	MAX	chr14:45604816-45606097	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr14:45604808-45605842	Hela-S3	cervix:	n/a	n/a
32	MYC	chr14:45604791-45606023	K562	blood:	n/a	n/a
33	MAX	chr14:45605598-45605840	K562	blood:	n/a	n/a
34	IRF1	chr14:45604595-45605900	K562	blood:	n/a	chr14:45605056-45605065 chr14:45604736-45604748 chr14:45604608-45604617
35	MAX	chr14:45604870-45605938	K562	blood:	n/a	n/a
36	HA-E2F1	chr14:45604910-45605836	MCF-7	breast:	n/a	chr14:45605056-45605065
37	E2F4	chr14:45604491-45606738	MCF10A-Er-Src	breast:	n/a	chr14:45606613-45606622 chr14:45605056-45605065
38	MAX	chr14:45605654-45605830	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45552000..45555852-chr14:45600098..45605984,10	MCF-7	breast:
2	chr14:45602054..45606945-chr14:45719959..45724414,9	MCF-7	breast:
3	chr14:45365342..45368511-chr14:45602012..45605909,4	MCF-7	breast:
4	chr14:45429027..45431300-chr14:45604077..45605830,2	K562	blood:
5	chr14:45428391..45434782-chr14:45601313..45606393,12	MCF-7	breast:
6	chr14:45428929..45435608-chr14:45601966..45608462,12	MCF-7	breast:
7	chr14:45380875..45383162-chr14:45604875..45606595,2	MCF-7	breast:
8	chr14:45601339..45606570-chr14:45722040..45724234,5	MCF-7	breast:
9	chr14:45601512..45605313-chr14:45605494..45608093,6	K562	blood:
10	chr14:45602011..45605313-chr14:45605492..45607351,3	K562	blood:

Variant related genes	Relation type
FKBP3	TF binding region
ENSG00000198718	Chromatin interaction
ENSG00000100442	Chromatin interaction
ENSG00000249163	Chromatin interaction
ENSG00000179476	Chromatin interaction
ENSG00000179454	Chromatin interaction
ENSG00000258949	Chromatin interaction
ENSG00000129534	Chromatin interaction
ENSG00000185246	Chromatin interaction
ENSG00000258633	Chromatin interaction
ENSG00000187790	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs10129236	1.00[CHB][hapmap]
rs10130368	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10130377	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10131615	0.88[ASW][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs10132389	0.86[YRI][hapmap]
rs10132547	0.88[ASW][hapmap];0.89[JPT][hapmap];0.84[MEX][hapmap];0.86[YRI][hapmap]
rs10132949	0.88[ASW][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs10134071	0.88[ASW][hapmap];1.00[MEX][hapmap];0.86[YRI][hapmap]
rs10134598	1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.89[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs10135085	0.88[ASW][hapmap];1.00[CEU][hapmap];0.88[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.86[YRI][hapmap];0.87[EUR][1000 genomes]
rs10135890	1.00[ASW][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];0.96[YRI][hapmap]
rs10137415	1.00[CHB][hapmap]
rs10138272	0.89[YRI][hapmap]
rs10138997	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10140049	0.88[ASW][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs10140222	0.88[ASW][hapmap];0.83[MEX][hapmap];0.86[YRI][hapmap]
rs10141474	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10143508	1.00[CHB][hapmap]
rs10143794	0.86[CHB][hapmap]
rs10143806	1.00[CEU][hapmap];0.89[JPT][hapmap];0.82[YRI][hapmap];0.91[EUR][1000 genomes]
rs10145092	0.83[ASW][hapmap];0.90[YRI][hapmap]
rs10145267	0.83[YRI][hapmap]
rs10147499	0.90[YRI][hapmap]
rs10149578	0.86[CHB][hapmap]
rs10152101	0.83[ASW][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap]
rs11157423	0.80[YRI][hapmap]
rs11157424	0.83[ASW][hapmap];1.00[MEX][hapmap];0.80[YRI][hapmap]
rs11157433	1.00[CHB][hapmap];0.82[MKK][hapmap]
rs11844832	0.80[EUR][1000 genomes]
rs11845088	0.90[YRI][hapmap]
rs11845507	1.00[CHB][hapmap];0.84[CHD][hapmap];0.82[MKK][hapmap]
rs11845956	0.88[ASW][hapmap];1.00[MEX][hapmap];0.89[YRI][hapmap]
rs11847336	1.00[CEU][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.94[TSI][hapmap];0.91[EUR][1000 genomes]
rs11850363	0.86[YRI][hapmap]
rs12100842	1.00[ASW][hapmap];0.88[JPT][hapmap];0.93[LWK][hapmap];0.90[MEX][hapmap];0.96[MKK][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes]
rs12433547	0.86[CHB][hapmap]
rs12433565	0.86[CHB][hapmap]
rs1252959	0.86[CHB][hapmap]
rs1252960	0.86[CHB][hapmap]
rs1252966	0.86[CHB][hapmap]
rs1266209	0.86[CHB][hapmap]
rs1268576	0.86[CHB][hapmap]
rs1367580	0.86[CHB][hapmap]
rs1431050	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs17115718	0.83[YRI][hapmap]
rs17115787	0.88[ASW][hapmap];1.00[MEX][hapmap];0.86[YRI][hapmap]
rs17115809	0.88[ASW][hapmap];1.00[CEU][hapmap];0.88[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.86[YRI][hapmap];0.91[EUR][1000 genomes]
rs17115811	0.88[ASW][hapmap];0.88[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.86[YRI][hapmap];0.91[EUR][1000 genomes]
rs17115860	1.00[CHB][hapmap]
rs17115912	0.86[CHB][hapmap]
rs17636302	0.86[CHB][hapmap]
rs1969713	0.83[ASN][1000 genomes]
rs2016738	0.82[CHD][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs2145148	0.86[CHB][hapmap]
rs2750119	0.86[CHB][hapmap]
rs28370281	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28448551	0.88[ASW][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap]
rs28637857	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3736772	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs3783700	0.89[JPT][hapmap]
rs3783702	1.00[CEU][hapmap];0.89[JPT][hapmap];0.93[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3825624	0.86[CHB][hapmap]
rs3825625	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3825627	0.88[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.91[EUR][1000 genomes]
rs3825628	0.91[EUR][1000 genomes]
rs3825629	0.86[YRI][hapmap]
rs3916169	0.86[CHB][hapmap]
rs4900664	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs4900667	0.86[CHB][hapmap]
rs4906564	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs4906568	1.00[CHB][hapmap];0.82[MKK][hapmap]
rs56836063	0.80[EUR][1000 genomes]
rs57003561	0.91[EUR][1000 genomes]
rs57602646	0.91[EUR][1000 genomes]
rs58826926	0.91[EUR][1000 genomes]
rs59353994	0.91[EUR][1000 genomes]
rs61155826	0.91[EUR][1000 genomes]
rs6572296	1.00[CHB][hapmap];0.86[MKK][hapmap]
rs7141145	0.86[CHB][hapmap]
rs7146566	0.86[YRI][hapmap];0.80[EUR][1000 genomes]
rs7147246	0.86[CHB][hapmap]
rs7148613	1.00[CHB][hapmap];0.90[MKK][hapmap]
rs7158846	0.83[ASW][hapmap];1.00[MEX][hapmap];0.83[YRI][hapmap]
rs7160373	0.86[CHB][hapmap]
rs72474138	0.91[EUR][1000 genomes]
rs73340611	0.91[EUR][1000 genomes]
rs73340622	0.91[EUR][1000 genomes]
rs73340626	0.91[EUR][1000 genomes]
rs73340655	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73340659	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73349820	0.80[EUR][1000 genomes]
rs73349842	0.87[EUR][1000 genomes]
rs73349853	0.91[EUR][1000 genomes]
rs73349857	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73349858	0.91[EUR][1000 genomes]
rs73349868	0.91[EUR][1000 genomes]
rs8006685	0.88[ASW][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs8009193	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8015453	0.80[AFR][1000 genomes]
rs8017844	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8020533	1.00[CHB][hapmap];0.84[CHD][hapmap]
rs8022008	0.88[ASW][hapmap];1.00[MEX][hapmap];0.90[YRI][hapmap]
rs8022499	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8022608	1.00[CEU][hapmap];0.89[YRI][hapmap]
rs911041	1.00[CHB][hapmap]
rs9323106	0.90[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901841	chr14:45198196-45719643	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	esv1795667	chr14:45361680-45721052	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	esv1794986	chr14:45368685-45650813	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv1803131	chr14:45441932-45726848	Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv933364	chr14:45467086-45705844	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv901842	chr14:45506857-45713358	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers 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	32 gene(s)	inside rSNPs	diseases
7	nsv901843	chr14:45506857-45833490	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer 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	40 gene(s)	inside rSNPs	diseases
8	nsv832785	chr14:45520670-45710741	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
9	esv1800510	chr14:45572528-45650813	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv530814	chr14:45604432-46198418	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2033385	FANCM	cis	lymphoblastoid	seeQTL

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45600600-45608600	Active TSS	GM12878-XiMat	blood
2	chr14:45602000-45606600	Active TSS	HUES64 Cell Line	embryonic stem cell
3	chr14:45602000-45607400	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr14:45602000-45607400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr14:45602000-45608200	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr14:45602200-45606000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr14:45602200-45606000	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr14:45602200-45606200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:45602200-45606400	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr14:45602200-45607200	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr14:45602200-45607600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:45602200-45607600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr14:45602200-45608000	Active TSS	K562	blood
14	chr14:45602400-45606000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:45602400-45606400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:45602400-45606600	Active TSS	Hela-S3	cervix
17	chr14:45602400-45606800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr14:45602600-45606000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr14:45602600-45606200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:45602600-45606200	Active TSS	Right Atrium	heart
21	chr14:45602600-45606400	Active TSS	Right Ventricle	heart
22	chr14:45602600-45606400	Active TSS	HSMMtube	muscle
23	chr14:45602600-45606600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:45602600-45606600	Active TSS	Muscle Satellite Cultured Cells	--
25	chr14:45602600-45606600	Active TSS	Fetal Kidney	kidney
26	chr14:45602600-45606600	Active TSS	HSMM	muscle
27	chr14:45602600-45606800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr14:45602600-45606800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr14:45602600-45606800	Active TSS	H9 Cell Line	embryonic stem cell
30	chr14:45602600-45607000	Active TSS	H1 Cell Line	embryonic stem cell
31	chr14:45602600-45607400	Active TSS	NHLF	lung
32	chr14:45602800-45606000	Active TSS	Aorta	Aorta
33	chr14:45602800-45606000	Active TSS	Fetal Heart	heart
34	chr14:45602800-45606000	Active TSS	Fetal Intestine Small	intestine
35	chr14:45602800-45606000	Active TSS	Fetal Muscle Trunk	muscle
36	chr14:45602800-45606200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr14:45602800-45606200	Active TSS	Fetal Stomach	stomach
38	chr14:45602800-45606200	Active TSS	Ovary	ovary
39	chr14:45602800-45606400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr14:45602800-45606400	Active TSS	A549	lung
41	chr14:45602800-45606400	Active TSS	NHEK	skin
42	chr14:45602800-45606600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:45602800-45606600	Active TSS	Fetal Intestine Large	intestine
44	chr14:45602800-45606600	Active TSS	Fetal Muscle Leg	muscle
45	chr14:45602800-45607200	Active TSS	Fetal Thymus	thymus
46	chr14:45602800-45608000	Active TSS	NHDF-Ad	bronchial
47	chr14:45603000-45606000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:45603000-45606000	Active TSS	Left Ventricle	heart
49	chr14:45603000-45606200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:45603000-45606600	Active TSS	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links