Variant report

Variant	rs6477091
Chromosome Location	chr9:6567464-6567465
allele	A/T
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	GATA2	chr9:6566400-6567569	HUVEC	blood vessel:	n/a	chr9:6567215-6567222 chr9:6566672-6566682
2	YY1	chr9:6567324-6567628	HCT-116	colon:	n/a	n/a
3	FOS	chr9:6566370-6567598	MCF10A-Er-Src	breast:	n/a	chr9:6567211-6567221 chr9:6566601-6566612 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
4	EP300	chr9:6566113-6567841	SK-N-SH	brain:	n/a	chr9:6566309-6566323 chr9:6566308-6566322
5	PBX3	chr9:6566317-6567777	SK-N-SH	brain:	n/a	n/a
6	MXI1	chr9:6566385-6567534	Hela-S3	cervix:	n/a	n/a
7	GTF2F1	chr9:6566344-6567658	Hela-S3	cervix:	n/a	n/a
8	JUND	chr9:6566243-6567826	SK-N-SH	brain:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
9	POLR2A	chr9:6565867-6567710	HUVEC	blood vessel:	n/a	n/a
10	JUND	chr9:6566221-6567828	SK-N-SH	brain:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
11	POLR2A	chr9:6566359-6567837	IMR90	lung:	n/a	n/a
12	TCF12	chr9:6566144-6567850	SK-N-SH	brain:	n/a	chr9:6566490-6566498
13	MYC	chr9:6567089-6567621	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr9:6566254-6567809	U87	brain:	n/a	n/a
15	STAT3	chr9:6566277-6567631	MCF10A-Er-Src	breast:	n/a	chr9:6567275-6567283
16	SP1	chr9:6566298-6567723	A549	lung:	n/a	n/a
17	FOSL1	chr9:6566097-6567815	HCT-116	colon:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
18	POLR2A	chr9:6567324-6567649	HCT-116	colon:	n/a	n/a
19	GATA3	chr9:6566211-6567833	SK-N-SH	brain:	n/a	chr9:6567733-6567740 chr9:6567215-6567222 chr9:6567733-6567740 chr9:6567726-6567747 chr9:6566672-6566682 chr9:6567733-6567740
20	MAFK	chr9:6566461-6567600	IMR90	lung:	n/a	chr9:6567062-6567073 chr9:6566626-6566635
21	EP300	chr9:6566294-6567636	Hela-S3	cervix:	n/a	chr9:6566309-6566323 chr9:6566308-6566322
22	STAT3	chr9:6566280-6567631	MCF10A-Er-Src	breast:	n/a	chr9:6567275-6567283
23	RAD21	chr9:6566458-6567718	IMR90	lung:	n/a	n/a
24	MAX	chr9:6567046-6567668	SK-N-SH	brain:	n/a	n/a
25	SMC3	chr9:6566409-6568638	SK-N-SH	brain:	n/a	n/a
26	TBP	chr9:6566281-6567732	Hela-S3	cervix:	n/a	n/a
27	GATA3	chr9:6566279-6567693	A549	lung:	n/a	chr9:6567215-6567222 chr9:6566672-6566682
28	CHD2	chr9:6566415-6567623	Hela-S3	cervix:	n/a	n/a
29	MAX	chr9:6566351-6567611	Hela-S3	cervix:	n/a	n/a
30	STAT3	chr9:6567098-6567633	Hela-S3	cervix:	n/a	chr9:6567275-6567283
31	POLR2A	chr9:6566254-6567803	U87	brain:	n/a	n/a
32	TCF7L2	chr9:6566464-6567578	HCT-116	colon:	n/a	chr9:6567183-6567192
33	MAX	chr9:6566204-6567693	A549	lung:	n/a	n/a
34	POLR2A	chr9:6566318-6567675	SK-N-SH	brain:	n/a	n/a
35	JUND	chr9:6566173-6567762	Hela-S3	cervix:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
36	USF2	chr9:6566500-6567577	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:6566241-6567786	HCT-116	colon:	n/a	n/a
38	POLR2A	chr9:6566417-6567742	MCF10A-Er-Src	breast:	n/a	n/a
39	PBX3	chr9:6566252-6567812	SK-N-SH	brain:	n/a	n/a
40	ZKSCAN1	chr9:6566517-6567543	Hela-S3	cervix:	n/a	n/a
41	JUND	chr9:6566221-6567917	HCT-116	colon:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
42	EP300	chr9:6566154-6567666	SK-N-SH	brain:	n/a	chr9:6566309-6566323 chr9:6566308-6566322
43	JUN	chr9:6566318-6567618	HUVEC	blood vessel:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
44	POLR2A	chr9:6566313-6567728	HUVEC	blood vessel:	n/a	n/a
45	POLR2A	chr9:6565947-6567850	HUVEC	blood vessel:	n/a	n/a
46	CEBPB	chr9:6566289-6567541	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr9:6566794-6567745	HCT-116	colon:	n/a	n/a
48	SP1	chr9:6566231-6567881	HCT-116	colon:	n/a	n/a
49	FOS	chr9:6566281-6567562	MCF10A-Er-Src	breast:	n/a	chr9:6567211-6567221 chr9:6566601-6566612 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221
50	JUND	chr9:6566248-6567807	HCT-116	colon:	n/a	chr9:6567211-6567221 chr9:6567182-6567193 chr9:6567211-6567221 chr9:6566627-6566637 chr9:6567332-6567341 chr9:6567182-6567192 chr9:6566627-6566637 chr9:6567183-6567191 chr9:6567211-6567221 chr9:6566629-6566640 chr9:6566626-6566638 chr9:6567182-6567192 chr9:6567211-6567221

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:6411889..6413422-chr9:6565833..6568598,2	K562	blood:

Variant related genes	Relation type
ENSG00000252110	TF binding region
GLDC	TF binding region
ENSG00000237158	TF binding region
ENSG00000147854	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs7027507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7039182	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7859893	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7870809	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031086	chr9:5806949-6630686	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv539967	chr9:5806949-6630686	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv933124	chr9:6099101-6644738	Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Active TSS 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	28 gene(s)	inside rSNPs	diseases
4	nsv1029000	chr9:6188652-6687205	Enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
5	nsv1031459	chr9:6216913-6657192	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS 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	29 gene(s)	inside rSNPs	diseases
6	nsv948562	chr9:6222553-6684955	Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	nsv1032350	chr9:6328167-6630686	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv831497	chr9:6377501-6612402	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
9	nsv892162	chr9:6480005-6788085	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
10	nsv831498	chr9:6496021-6689728	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
11	nsv934176	chr9:6517535-6644738	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv892163	chr9:6523056-6632061	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1025627	chr9:6523056-6648098	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	esv2752308	chr9:6523060-6899149	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	73 gene(s)	inside rSNPs	diseases
15	nsv613206	chr9:6525753-6686738	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
16	esv3324686	chr9:6528411-6728310	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
17	nsv1028402	chr9:6542253-6874231	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
18	nsv1018308	chr9:6544766-6869653	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
19	nsv1015462	chr9:6544766-6874231	Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
20	nsv1018870	chr9:6548393-6708345	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
21	nsv892164	chr9:6555079-6664282	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
22	nsv931094	chr9:6558442-6672439	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
23	nsv870402	chr9:6565246-7016784	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
24	nsv1016600	chr9:6566610-6695986	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
25	nsv1033539	chr9:6566610-7022554	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6532000-6570400	Strong transcription	Liver	Liver
2	chr9:6554600-6568600	Weak transcription	Fetal Intestine Small	intestine
3	chr9:6558600-6586600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:6558800-6580800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr9:6559200-6583400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr9:6559600-6568200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:6559800-6567600	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:6560200-6569400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:6560200-6572200	Weak transcription	GM12878-XiMat	blood
10	chr9:6561200-6591000	Weak transcription	Placenta	Placenta
11	chr9:6563400-6583000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr9:6564400-6568000	Enhancers	Brain Hippocampus Middle	brain
13	chr9:6564600-6568000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:6564800-6568200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr9:6565400-6575200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr9:6565400-6586400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:6565600-6568200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr9:6565600-6569400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:6565600-6577000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr9:6566400-6575400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:6566600-6567600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:6566600-6567600	Enhancers	K562	blood
23	chr9:6566600-6579800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr9:6566800-6567600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr9:6566800-6567600	Enhancers	Brain Angular Gyrus	brain
26	chr9:6566800-6567600	Flanking Active TSS	Hela-S3	cervix
27	chr9:6566800-6567600	Flanking Active TSS	HSMM	muscle
28	chr9:6566800-6567600	Flanking Active TSS	Osteobl	bone
29	chr9:6566800-6567800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr9:6566800-6567800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:6566800-6567800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr9:6566800-6567800	Flanking Active TSS	HUVEC	blood vessel
33	chr9:6566800-6567800	Flanking Active TSS	NH-A	brain
34	chr9:6566800-6568000	Flanking Active TSS	NHDF-Ad	bronchial
35	chr9:6566800-6568200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:6566800-6568200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr9:6566800-6572800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr9:6567000-6567600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:6567000-6567600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr9:6567000-6568200	Enhancers	Brain Cingulate Gyrus	brain
41	chr9:6567000-6575400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr9:6567000-6581000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr9:6567200-6567600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr9:6567200-6567600	Flanking Active TSS	HSMMtube	muscle
45	chr9:6567200-6567800	Flanking Active TSS	A549	lung
46	chr9:6567200-6568200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:6567200-6568200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr9:6567200-6568400	Enhancers	Placenta Amnion	Placenta Amnion
49	chr9:6567200-6569200	Enhancers	HMEC	breast
50	chr9:6567400-6567600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung

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