Variant report

Variant	rs34038545
Chromosome Location	chr17:45144907-45144908
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	YY1	chr17:45144560-45145145	SK-N-SH	brain:	n/a	n/a
2	TAF1	chr17:45144596-45145017	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr17:45144840-45144990	HPF	lung:	n/a	n/a
4	HDAC2	chr17:45144650-45145093	K562	blood:	n/a	n/a
5	MXI1	chr17:45144573-45145024	Hela-S3	cervix:	n/a	n/a
6	NR2F2	chr17:45144723-45145061	K562	blood:	n/a	n/a
7	FOXM1	chr17:45144554-45145066	GM12878	blood:	n/a	n/a
8	CCNT2	chr17:45144623-45145013	K562	blood:	n/a	n/a
9	TAF1	chr17:45144471-45145268	ECC-1	luminal epithelium:	n/a	n/a
10	PML	chr17:45144558-45145124	K562	blood:	n/a	n/a
11	PAX5	chr17:45144727-45145063	GM12878	blood:	n/a	n/a
12	POLR2A	chr17:45144106-45145117	HL-60	blood:	n/a	n/a
13	CTCF	chr17:45144800-45144950	HBMEC	blood vessel:	n/a	n/a
14	POLR2A	chr17:45144135-45145051	GM12891	blood:	n/a	n/a
15	NFIC	chr17:45144560-45145158	HepG2	liver:	n/a	n/a
16	CTCF	chr17:45144840-45144990	RPTEC	kidney:	n/a	n/a
17	CTCF	chr17:45144900-45145050	HPAF	blood vessel:	n/a	n/a
18	CTCF	chr17:45144818-45144992	Lung_OC	lung:	n/a	n/a
19	CTCF	chr17:45144812-45144991	GM12891	blood:	n/a	n/a
20	ZEB1	chr17:45144386-45145209	HepG2	liver:	n/a	chr17:45144773-45144782
21	POLR2A	chr17:45144577-45145040	GM12892	blood:	n/a	n/a
22	POLR2A	chr17:45144620-45145010	H1-hESC	embryonic stem cell:	n/a	n/a
23	FOSL1	chr17:45144632-45145020	K562	blood:	n/a	n/a
24	GABPA	chr17:45144461-45145188	A549	lung:	n/a	n/a
25	E2F6	chr17:45144386-45145187	A549	lung:	n/a	n/a
26	RAD21	chr17:45144639-45145103	IMR90	lung:	n/a	n/a
27	SIN3AK20	chr17:45144538-45145100	A549	lung:	n/a	n/a
28	REST	chr17:45144715-45145043	K562	blood:	n/a	n/a
29	NANOG	chr17:45144574-45145006	H1-hESC	embryonic stem cell:	n/a	n/a
30	YY1	chr17:45144574-45145022	K562	blood:	n/a	n/a
31	FOSL2	chr17:45144615-45145078	HepG2	liver:	n/a	n/a
32	CTCF	chr17:45144880-45145030	NHDF-neo	bronchial:	n/a	n/a
33	GABPA	chr17:45144568-45145044	K562	blood:	n/a	n/a
34	YY1	chr17:45144639-45145103	GM12892	blood:	n/a	n/a
35	ZBTB7A	chr17:45144603-45145019	K562	blood:	n/a	n/a
36	TEAD4	chr17:45144632-45145116	K562	blood:	n/a	n/a
37	MBD4	chr17:45144438-45145094	HepG2	liver:	n/a	n/a
38	CTCF	chr17:45144848-45144983	MCF-7	breast:	n/a	n/a
39	ELF1	chr17:45144638-45145059	HepG2	liver:	n/a	n/a
40	RAD21	chr17:45144589-45145044	SK-N-SH_RA	brain:	n/a	n/a
41	MAX	chr17:45144344-45145256	HCT-116	colon:	n/a	n/a
42	CTCF	chr17:45144840-45144990	GM12866	blood:	n/a	n/a
43	ZNF143	chr17:45144674-45145134	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAFK	chr17:45144647-45145070	K562	blood:	n/a	n/a
45	CTCF	chr17:45144840-45144990	HRPEpiC	eye:	n/a	n/a
46	ZBTB33	chr17:45144606-45145158	A549	lung:	n/a	n/a
47	RXRA	chr17:45144742-45145021	GM12878	blood:	n/a	n/a
48	TCF12	chr17:45144584-45145053	H1-hESC	embryonic stem cell:	n/a	n/a
49	ZEB1	chr17:45144607-45145025	GM12878	blood:	n/a	chr17:45144773-45144782
50	CTCF	chr17:45144733-45145051	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45144857-45144907	CMK	blood:	n/a
2	chr17:45144857-45144907	LNCaP	prostate:	n/a
3	chr17:45144857-45144907	GM12878	blood:	n/a
4	chr17:45144857-45144907	HAEpiC	amniotic membrane:	n/a
5	chr17:45144857-45144907	IMR90	lung:	fetal
6	chr17:45144857-45144907	HCPEpiC	choroid plexus:	n/a
7	chr17:45144857-45144907	HRPEpiC	eye:	n/a
8	chr17:45144857-45144907	SKMC	muscle:	n/a
9	chr17:45144857-45144907	AG09319	gingival:	n/a
10	chr17:45144857-45144907	GM06990	blood:	n/a
11	chr17:45144857-45144907	HL-60	blood:	n/a
12	chr17:45144857-45144907	HMEC	breast:	n/a
13	chr17:45144857-45144907	BJ	skin:	n/a
14	chr17:45144857-45144907	H1-hESC	embryonic stem cell:	embryo
15	chr17:45144857-45144907	Hepatocyte	liver:	n/a
16	chr17:45144857-45144907	SK-N-SH	brain:	n/a
17	chr17:45144857-45144907	HIPEpiC	eye:	n/a
18	chr17:45144857-45144907	HRE	kidney:	n/a
19	chr17:45144857-45144907	HPAEpiC	pulmonary alveolar:	n/a
20	chr17:45144857-45144907	AG10803	skin:	n/a
21	chr17:45144857-45144907	PANC-1	pancreas:	n/a
22	chr17:45144857-45144907	Caco-2	colon:	n/a
23	chr17:45144857-45144907	A549	lung:	n/a
24	chr17:45144857-45144907	ovcar-3	ovarian:	n/a
25	chr17:45144857-45144907	HUVEC	blood vessel:	n/a
26	chr17:45144857-45144907	NT2-D1	testis:	n/a
27	chr17:45144857-45144907	NHDF-neo	bronchial:	n/a
28	chr17:45144857-45144907	AG04450	lung:	fetal
29	chr17:45144857-45144907	HCM	heart:	n/a
30	chr17:45144857-45144907	NHBE	bronchial:	n/a
31	chr17:45144857-45144907	ProgFib	skin:	n/a
32	chr17:45144857-45144907	AoSMC	blood vessel:	n/a
33	chr17:45144857-45144907	RPTEC	kidney:	n/a
34	chr17:45144857-45144907	U87	brain:	n/a
35	chr17:45144857-45144907	T-47D	breast:	n/a
36	chr17:45144857-45144907	SK-N-MC	brain:	n/a
37	chr17:45144857-45144907	GM12892	blood:	n/a
38	chr17:45144857-45144907	SAEC	small airway:	n/a
39	chr17:45144857-45144907	MCF-7	breast:	n/a
40	chr17:45144857-45144907	GM12891	blood:	n/a
41	chr17:45144857-45144907	HCT-116	colon:	n/a
42	chr17:45144857-45144907	PrEC	prostate:	n/a
43	chr17:45144857-45144907	NB4	blood:	n/a
44	chr17:45144857-45144907	PFSK-1	brain:	n/a
45	chr17:45144857-45144907	NH-A	brain:	n/a
46	chr17:45144857-45144907	K562	blood:	n/a
47	chr17:45144857-45144907	GM19239	blood:	n/a
48	chr17:45144857-45144907	SK-N-SH_RA	brain:	n/a
49	chr17:45144857-45144907	Jurkat	blood:	n/a
50	chr17:45144857-45144907	AG09309	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45143352..45146051-chr17:45399301..45401762,3	K562	blood:
2	chr1:28655193..28655793-chr17:45144387..45145240,2	Hela-S3	cervix:
3	chr17:45143352..45144907-chr17:45399301..45401186,2	K562	blood:
4	chr17:45144506..45145240-chr9:130213283..130213833,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
ENSG00000262879	TF binding region
ENSG00000262879	CpG island
ENSG00000178852	Chromatin interaction
ENSG00000197958	Chromatin interaction
ENSG00000263293	Chromatin interaction
ENSG00000130772	Chromatin interaction
ENSG00000148356	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10514915	0.91[ASN][1000 genomes]
rs11079748	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11079750	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11079752	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11649887	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11654517	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11658350	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11871052	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11871364	0.87[EUR][1000 genomes]
rs12603447	0.95[ASN][1000 genomes]
rs12939753	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12942936	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12949929	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12950276	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12950699	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1634260	0.91[ASN][1000 genomes]
rs2007723	0.93[ASN][1000 genomes]
rs2316331	0.90[ASN][1000 genomes]
rs2317376	0.91[ASN][1000 genomes]
rs2873131	0.91[ASN][1000 genomes]
rs34314554	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34710835	1.00[ASN][1000 genomes]
rs35721448	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4074247	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4074249	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4968253	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4968301	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4968304	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56362502	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7207418	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7214785	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7215573	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7215903	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7215907	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7219544	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7219899	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7220777	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7222781	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8077021	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9889451	0.95[ASN][1000 genomes]
rs9899078	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3492820	chr17:44174959-45161556	Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	esv3492821	chr17:44174959-45161556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
3	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv833466	chr17:45020360-45204537	Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
7	nsv833467	chr17:45063935-45252624	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
8	nsv522797	chr17:45084279-45183152	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers 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 miRNA target site	12 gene(s)	inside rSNPs	diseases
9	esv1851648	chr17:45091619-45146146	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
10	esv1846431	chr17:45092987-45145946	ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
11	esv3332795	chr17:45116212-45209297	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS 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	13 gene(s)	inside rSNPs	diseases
12	esv3386521	chr17:45116232-45209267	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	esv21010	chr17:45125753-45177221	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv1059766	chr17:45130765-45203468	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription 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	9 gene(s)	inside rSNPs	diseases
15	esv2760450	chr17:45130777-45225222	Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
16	esv9886	chr17:45142849-45153796	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs34038545	GOSR2	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45143600-45145000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr17:45143600-45145000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr17:45143600-45145000	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr17:45143600-45145000	Active TSS	Lung	lung
5	chr17:45143600-45145000	Active TSS	HSMM	muscle
6	chr17:45143800-45145000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr17:45143800-45145000	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr17:45143800-45145200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr17:45143800-45145200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr17:45143800-45145200	Active TSS	NHEK	skin
11	chr17:45144000-45145000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr17:45144000-45145000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr17:45144000-45145000	Active TSS	Cortex derived primary cultured neurospheres	brain
14	chr17:45144000-45145000	Active TSS	Brain Substantia Nigra	brain
15	chr17:45144000-45145000	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr17:45144000-45145000	Active TSS	K562	blood
17	chr17:45144000-45145000	Active TSS	NHDF-Ad	bronchial
18	chr17:45144000-45145000	Active TSS	NHLF	lung
19	chr17:45144000-45145200	Active TSS	Brain Germinal Matrix	brain
20	chr17:45144000-45145200	Active TSS	Fetal Kidney	kidney
21	chr17:45144200-45145000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr17:45144200-45145000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr17:45144200-45145000	Active TSS	H9 Cell Line	embryonic stem cell
24	chr17:45144200-45145000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr17:45144200-45145000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr17:45144200-45145000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr17:45144200-45145000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr17:45144200-45145000	Active TSS	Aorta	Aorta
29	chr17:45144200-45145000	Active TSS	Esophagus	oesophagus
30	chr17:45144200-45145000	Active TSS	Fetal Intestine Large	intestine
31	chr17:45144200-45145000	Active TSS	Fetal Intestine Small	intestine
32	chr17:45144200-45145000	Active TSS	Fetal Muscle Trunk	muscle
33	chr17:45144200-45145000	Active TSS	Placenta	Placenta
34	chr17:45144200-45145000	Active TSS	Fetal Stomach	stomach
35	chr17:45144200-45145000	Active TSS	Ovary	ovary
36	chr17:45144200-45145000	Active TSS	Pancreas	Pancrea
37	chr17:45144200-45145000	Active TSS	Placenta Amnion	Placenta Amnion
38	chr17:45144200-45145000	Active TSS	Right Ventricle	heart
39	chr17:45144200-45145000	Active TSS	Small Intestine	intestine
40	chr17:45144200-45145000	Active TSS	Stomach Smooth Muscle	stomach
41	chr17:45144200-45145200	Active TSS	Fetal Brain Female	brain
42	chr17:45144200-45145200	Active TSS	HepG2	liver
43	chr17:45144400-45145000	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr17:45144400-45145000	Active TSS	H1 Cell Line	embryonic stem cell
45	chr17:45144400-45145000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr17:45144400-45145000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr17:45144400-45145000	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr17:45144400-45145000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr17:45144400-45145000	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr17:45144400-45145000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links