Variant report

Variant	rs544365440
Chromosome Location	chr9:116917594-116917595
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	YY1	chr9:116917592-116917773	GM12891	blood:	n/a	n/a
2	CTCF	chr9:116917551-116917907	K562	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
3	HCFC1	chr9:116917456-116918137	Hela-S3	cervix:	n/a	n/a
4	RAD21	chr9:116917532-116917937	H1-hESC	embryonic stem cell:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
5	CTCF	chr9:116917487-116917817	ECC-1	luminal epithelium:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
6	YY1	chr9:116917586-116917836	GM12891	blood:	n/a	n/a
7	CTCF	chr9:116917443-116917867	T-47D	breast:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
8	CREB1	chr9:116917536-116918110	A549	lung:	n/a	n/a
9	YY1	chr9:116917487-116917938	H1-hESC	embryonic stem cell:	n/a	n/a
10	RAD21	chr9:116917412-116917986	A549	lung:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
11	MXI1	chr9:116917415-116920656	IMR90	lung:	n/a	n/a
12	CTCF	chr9:116917523-116917881	A549	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
13	CTCF	chr9:116917550-116917975	K562	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
14	CTCF	chr9:116917524-116917869	GM19238	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
15	RAD21	chr9:116917568-116917869	A549	lung:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
16	CTCF	chr9:116917499-116917904	H1-hESC	embryonic stem cell:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
17	RAD21	chr9:116917500-116917975	IMR90	lung:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
18	GABPA	chr9:116917485-116917759	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr9:116917571-116917853	GM13977	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
20	RAD21	chr9:116917525-116917798	GM12878	blood:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
21	RAD21	chr9:116917398-116918023	H1-hESC	embryonic stem cell:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
22	BHLHE40	chr9:116917582-116917706	K562	blood:	n/a	n/a
23	CTCF	chr9:116917551-116917835	Lung_OC	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
24	CTCF	chr9:116917557-116917860	LNCaP	prostate:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
25	RAD21	chr9:116917514-116917910	SK-N-SH_RA	brain:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
26	POLR2A	chr9:116917588-116917982	U87	brain:	n/a	n/a
27	CTBP2	chr9:116917548-116918440	H1-hESC	embryonic stem cell:	n/a	n/a
28	RAD21	chr9:116917523-116917973	ECC-1	luminal epithelium:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
29	CTCF	chr9:116917542-116917878	GM12892	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
30	MAZ	chr9:116915766-116920871	IMR90	lung:	n/a	chr9:116917994-116918004 chr9:116918626-116918636 chr9:116920321-116920330 chr9:116919415-116919424 chr9:116917529-116917539
31	RFX5	chr9:116917566-116917731	HepG2	liver:	n/a	n/a
32	RAD21	chr9:116917423-116917983	HepG2	liver:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
33	MXI1	chr9:116917521-116917935	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:116917541-116917736	HepG2	liver:	n/a	n/a
35	MAX	chr9:116917424-116918034	A549	lung:	n/a	chr9:116917994-116918004 chr9:116917529-116917539
36	CTCF	chr9:116917572-116917847	LNCaP	prostate:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
37	CTCF	chr9:116917545-116917917	Spleen_OC	spleen:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
38	EGR1	chr9:116917573-116917787	K562	blood:	n/a	n/a
39	HDAC2	chr9:116917502-116917878	HepG2	liver:	n/a	chr9:116917811-116917825
40	MAX	chr9:116917554-116917912	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr9:116917513-116917852	A549	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
42	CTCF	chr9:116917273-116918495	A549	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116918452-116918465 chr9:116918402-116918415 chr9:116917712-116917730 chr9:116917705-116917718
43	CTCF	chr9:116917570-116917846	K562	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
44	CTCF	chr9:116917559-116917848	GM10266	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
45	CTCF	chr9:116917577-116917826	A549	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
46	CTCF	chr9:116917383-116917914	MCF-7	breast:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
47	ZBTB7A	chr9:116917448-116918699	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr9:116917578-116917870	Fibrobl	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
49	RAD21	chr9:116917399-116917990	ECC-1	luminal epithelium:	n/a	chr9:116917723-116917742 chr9:116917708-116917718 chr9:116917718-116917728 chr9:116917728-116917740 chr9:116917858-116917870 chr9:116917718-116917730 chr9:116917726-116917739 chr9:116917703-116917722 chr9:116917716-116917729 chr9:116917706-116917719 chr9:116917713-116917732 chr9:116917708-116917720
50	CTCF	chr9:116917551-116917886	NHEK	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:116917422..116918284-chr9:117067805..117069207,4	K562	blood:

Variant related genes	Relation type
COL27A1	TF binding region
ENSG00000196739	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv2422396	chr9:116792944-117354862	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
3	esv2422492	chr9:116811294-117366643	Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS 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 miRNA target site	155 gene(s)	inside rSNPs	diseases
4	esv2761285	chr9:116811897-117103268	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
5	nsv870215	chr9:116842614-117070344	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	124 gene(s)	inside rSNPs	diseases
6	nsv893752	chr9:116899258-116944333	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv466526	chr9:116901926-116924781	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv615226	chr9:116901926-116924781	Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv615227	chr9:116904534-116924781	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv466527	chr9:116907448-116933449	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv615228	chr9:116907448-116933449	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv466529	chr9:116907553-116930194	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv615229	chr9:116907553-116930194	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv466530	chr9:116916931-116935660	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv615230	chr9:116916931-116935660	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv466531	chr9:116916931-116940418	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv615231	chr9:116916931-116940418	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
18	esv3360971	chr9:116917156-116919904	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	esv3449146	chr9:116917406-116919679	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116915800-116917600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
2	chr9:116916000-116917600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
3	chr9:116916000-116917600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
4	chr9:116916000-116917800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:116916000-116917800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
6	chr9:116916200-116917800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
7	chr9:116916400-116917600	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
8	chr9:116916600-116917600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:116916600-116917600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr9:116916600-116917600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:116916600-116917600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr9:116916600-116917600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
13	chr9:116916600-116917600	Flanking Active TSS	Ovary	ovary
14	chr9:116916600-116917600	Bivalent/Poised TSS	HepG2	liver
15	chr9:116916600-116917600	Bivalent Enhancer	HSMMtube	muscle
16	chr9:116916600-116917800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
17	chr9:116916600-116917800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
18	chr9:116916600-116917800	Flanking Active TSS	Liver	Liver
19	chr9:116916600-116918000	Bivalent/Poised TSS	Fetal Thymus	thymus
20	chr9:116916800-116917600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
21	chr9:116916800-116917600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
22	chr9:116916800-116917600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
23	chr9:116916800-116917600	Enhancers	Left Ventricle	heart
24	chr9:116916800-116917600	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
25	chr9:116916800-116917800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
26	chr9:116916800-116918400	Enhancers	Spleen	Spleen
27	chr9:116917000-116917600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:116917000-116917600	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
29	chr9:116917000-116917600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:116917000-116917600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:116917000-116917600	Flanking Active TSS	Brain Anterior Caudate	brain
32	chr9:116917000-116917600	Bivalent/Poised TSS	Colonic Mucosa	Colon
33	chr9:116917000-116917600	Flanking Active TSS	A549	lung
34	chr9:116917000-116917600	Bivalent Enhancer	HUVEC	blood vessel
35	chr9:116917000-116917800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
36	chr9:116917000-116917800	Bivalent Enhancer	Placenta	Placenta
37	chr9:116917200-116917600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:116917200-116917600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
39	chr9:116917200-116917600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr9:116917200-116917600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
41	chr9:116917200-116917600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr9:116917200-116917600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr9:116917200-116917600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
44	chr9:116917200-116917600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
45	chr9:116917200-116917600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
46	chr9:116917200-116917600	Bivalent Enhancer	Esophagus	oesophagus
47	chr9:116917200-116917600	Enhancers	Fetal Heart	heart
48	chr9:116917200-116917600	Bivalent/Poised TSS	Osteobl	bone
49	chr9:116917200-116917800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr9:116917200-116917800	Weak transcription	Lung	lung

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