Variant report

Variant	rs34789323
Chromosome Location	chr9:116917685-116917686
allele	-/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	chr9:116917640-116917790	AG10803	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
3	CTCF	chr9:116917600-116917750	GM12873	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
4	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
5	MYC	chr9:116917636-116917836	MCF10A-Er-Src	breast:	n/a	n/a
6	CTCF	chr9:116917660-116917810	GM12864	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
7	HCFC1	chr9:116917456-116918137	Hela-S3	cervix:	n/a	n/a
8	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
9	CTCF	chr9:116917620-116917770	GM12878	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
10	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
11	RAD21	chr9:116917601-116917770	K562	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
12	CTCF	chr9:116917640-116917790	HPAF	blood vessel:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
13	CTCF	chr9:116917660-116917810	HEEpiC	esophagus:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
14	CTCF	chr9:116917640-116917790	SAEC	small airway:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
15	YY1	chr9:116917586-116917836	GM12891	blood:	n/a	n/a
16	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
17	CREB1	chr9:116917536-116918110	A549	lung:	n/a	n/a
18	CTCF	chr9:116917600-116917750	GM12865	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
19	CTCF	chr9:116917640-116917790	BJ	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
20	CTCF	chr9:116917640-116917790	AG04449	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
21	CTCF	chr9:116917600-116917817	HUVEC	blood vessel:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
22	CTCF	chr9:116917660-116917810	NHEK	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
23	CTCF	chr9:116917680-116917830	HAc	cerebellar:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
24	YY1	chr9:116917487-116917938	H1-hESC	embryonic stem cell:	n/a	n/a
25	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
26	CTCF	chr9:116917620-116917770	AG09309	skin:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
27	MXI1	chr9:116917415-116920656	IMR90	lung:	n/a	n/a
28	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
29	TEAD4	chr9:116917600-116917900	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:116917640-116917790	GM12868	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
31	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
32	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
33	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
34	CTCF	chr9:116917620-116917770	NB4	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
35	CTCF	chr9:116917620-116917770	Hela-S3	cervix:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
36	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
37	CTCF	chr9:116917680-116917830	HCM	heart:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
38	CTCF	chr9:116917640-116917790	HMEC	breast:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
39	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
40	GABPA	chr9:116917485-116917759	H1-hESC	embryonic stem cell:	n/a	n/a
41	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
42	CTCF	chr9:116917620-116917770	AG04450	lung:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
43	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
44	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
45	CTCF	chr9:116917640-116917790	HUVEC	blood vessel:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
46	BHLHE40	chr9:116917582-116917706	K562	blood:	n/a	n/a
47	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
48	POLR2A	chr9:116917683-116917899	A549	lung:	n/a	n/a
49	CTCF	chr9:116917620-116917770	HRE	kidney:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
50	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

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:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116916000-116917800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:116916000-116917800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
3	chr9:116916200-116917800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
4	chr9:116916600-116917800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
5	chr9:116916600-116917800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
6	chr9:116916600-116917800	Flanking Active TSS	Liver	Liver
7	chr9:116916600-116918000	Bivalent/Poised TSS	Fetal Thymus	thymus
8	chr9:116916800-116917800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
9	chr9:116916800-116918400	Enhancers	Spleen	Spleen
10	chr9:116917000-116917800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
11	chr9:116917000-116917800	Bivalent Enhancer	Placenta	Placenta
12	chr9:116917200-116917800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr9:116917200-116917800	Weak transcription	Lung	lung
14	chr9:116917200-116918200	Bivalent Enhancer	Fetal Brain Male	brain
15	chr9:116917200-116919000	Active TSS	Right Atrium	heart
16	chr9:116917200-116919200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr9:116917200-116919400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr9:116917400-116917800	Enhancers	Primary B cells from cord blood	blood
19	chr9:116917400-116917800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr9:116917400-116917800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr9:116917400-116917800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr9:116917400-116917800	Enhancers	Brain Substantia Nigra	brain
23	chr9:116917400-116917800	Bivalent Enhancer	Small Intestine	intestine
24	chr9:116917400-116918000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
25	chr9:116917400-116918000	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr9:116917400-116918000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr9:116917400-116918600	Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr9:116917400-116918800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
29	chr9:116917400-116918800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr9:116917400-116918800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr9:116917400-116918800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
32	chr9:116917400-116918800	Active TSS	Gastric	stomach
33	chr9:116917400-116918800	Active TSS	Pancreas	Pancrea
34	chr9:116917400-116919000	Active TSS	Duodenum Mucosa	Duodenum
35	chr9:116917400-116919200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr9:116917400-116919200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:116917400-116919200	Active TSS	Rectal Smooth Muscle	rectum
38	chr9:116917400-116919400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
39	chr9:116917400-116919600	Active TSS	Hela-S3	cervix
40	chr9:116917400-116919800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr9:116917600-116917800	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
42	chr9:116917600-116917800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr9:116917600-116917800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr9:116917600-116917800	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
45	chr9:116917600-116917800	Active TSS	Adipose Nuclei	Adipose
46	chr9:116917600-116917800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
47	chr9:116917600-116917800	Weak transcription	Left Ventricle	heart
48	chr9:116917600-116917800	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr9:116917600-116917800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr9:116917600-116917800	Flanking Active TSS	Stomach Mucosa	stomach

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