Variant report

Variant	rs943843
Chromosome Location	chr9:117349401-117349402
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:73)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:73 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr9:117349007-117350832	SK-N-MC	brain:	n/a	n/a
2	CHD1	chr9:117349169-117352295	IMR90	lung:	n/a	chr9:117349924-117349934
3	POLR2A	chr9:117349296-117350442	HEK293	kidney:	n/a	n/a
4	MAX	chr9:117349397-117350479	A549	lung:	n/a	chr9:117349987-117350000 chr9:117349989-117349998 chr9:117349989-117349998 chr9:117349987-117350000 chr9:117349989-117349998
5	POLR2A	chr9:117349356-117351283	PBDE	blood:	n/a	n/a
6	POLR2A	chr9:117349133-117351975	IMR90	lung:	n/a	n/a
7	POLR2A	chr9:117349308-117350531	PFSK-1	brain:	n/a	n/a
8	POLR2A	chr9:117349245-117352151	HepG2	liver:	n/a	n/a
9	POLR2A	chr9:117349265-117351466	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr9:117349391-117350549	HepG2	liver:	n/a	n/a
11	POLR2A	chr9:117349253-117350411	HCT-116	colon:	n/a	n/a
12	POLR2A	chr9:117349378-117350793	NB4	blood:	n/a	n/a
13	HEY1	chr9:117349376-117350546	K562	blood:	n/a	n/a
14	TAL1	chr9:117349343-117350810	K562	blood:	n/a	n/a
15	ZMIZ1	chr9:117349363-117350376	K562	blood:	n/a	n/a
16	POLR2A	chr9:117349376-117350319	U87	brain:	n/a	n/a
17	ETS1	chr9:117349367-117350467	A549	lung:	n/a	n/a
18	FOXA1	chr9:117349245-117349677	HepG2	liver:	n/a	chr9:117349415-117349430
19	MAX	chr9:117349309-117350635	HepG2	liver:	n/a	chr9:117349987-117350000 chr9:117349989-117349998 chr9:117349989-117349998 chr9:117349987-117350000 chr9:117349989-117349998
20	HCFC1	chr9:117349157-117351047	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr9:117349354-117351587	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr9:117349371-117351537	GM12878	blood:	n/a	n/a
23	POLR2A	chr9:117349199-117351049	MCF-7	breast:	n/a	n/a
24	POLR2A	chr9:117349331-117352122	K562	blood:	n/a	n/a
25	POLR2A	chr9:117348930-117351418	HepG2	liver:	n/a	n/a
26	POLR2A	chr9:117349365-117350465	K562	blood:	n/a	n/a
27	ARID3A	chr9:117349284-117350227	HepG2	liver:	n/a	n/a
28	POLR2A	chr9:117349401-117350456	GM12878	blood:	n/a	n/a
29	RCOR1	chr9:117349200-117352056	IMR90	lung:	n/a	n/a
30	SRF	chr9:117349329-117350360	MCF-7	breast:	n/a	n/a
31	POLR2A	chr9:117349223-117350862	Hela-S3	cervix:	n/a	n/a
32	REST	chr9:117349331-117350379	A549	lung:	n/a	n/a
33	REST	chr9:117349287-117351575	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr9:117349357-117350411	HUVEC	blood vessel:	n/a	n/a
35	CBX3	chr9:117349322-117350493	K562	blood:	n/a	n/a
36	POLR2A	chr9:117349383-117350365	HCT-116	colon:	n/a	n/a
37	MAFK	chr9:117349381-117350216	K562	blood:	n/a	n/a
38	POLR2A	chr9:117349193-117350860	K562	blood:	n/a	n/a
39	TBP	chr9:117349400-117350285	Hela-S3	cervix:	n/a	n/a
40	NFIC	chr9:117349393-117350359	HepG2	liver:	n/a	n/a
41	MYBL2	chr9:117349286-117350362	HepG2	liver:	n/a	n/a
42	SIX5	chr9:117349302-117350434	A549	lung:	n/a	n/a
43	POLR2A	chr9:117349246-117351372	GM12891	blood:	n/a	n/a
44	MAZ	chr9:117349386-117350178	HepG2	liver:	n/a	chr9:117349987-117350000 chr9:117349989-117349998 chr9:117349989-117349998 chr9:117349987-117350000 chr9:117349989-117349998
45	POLR2A	chr9:117349246-117351532	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr9:117349247-117352088	H1-hESC	embryonic stem cell:	n/a	n/a
47	FOXA1	chr9:117349254-117349596	HepG2	liver:	n/a	chr9:117349415-117349430
48	EP300	chr9:117349393-117350565	A549	lung:	n/a	chr9:117350478-117350492
49	POLR2A	chr9:117349390-117350286	HepG2	liver:	n/a	n/a
50	RAD21	chr9:117349350-117350082	HepG2	liver:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:117344187..117346251-chr9:117348380..117349949,2	K562	blood:
2	chr9:117333105..117337028-chr9:117348080..117351758,7	MCF-7	breast:
3	chr20:49344264..49345857-chr9:117348003..117349598,2	MCF-7	breast:
4	chr9:117346842..117352204-chr9:117370877..117374909,8	K562	blood:
5	chr9:117347997..117349543-chr9:117368915..117371130,2	MCF-7	breast:
6	chr9:117310558..117329379-chr9:117338511..117355772,81	MCF-7	breast:
7	chr3:114343388..114344052-chr9:117349360..117350171,2	Hela-S3	cervix:
8	chr9:117349294..117352043-chr9:117375229..117380114,4	MCF-7	breast:
9	chr9:117348207..117349836-chr9:117361324..117363712,2	K562	blood:
10	chr9:117265762..117270088-chr9:117348229..117352933,7	K562	blood:
11	chr9:117348104..117352194-chr9:117371141..117379325,14	K562	blood:
12	chr9:117264226..117271307-chr9:117346303..117355535,28	MCF-7	breast:
13	chr9:117335405..117337699-chr9:117348254..117350000,2	MCF-7	breast:
14	chr9:117346757..117362857-chr9:117372020..117377914,21	MCF-7	breast:
15	chr17:57921591..57925193-chr9:117348845..117350845,3	MCF-7	breast:
16	chr9:117264854..117270088-chr9:117348300..117353117,7	K562	blood:
17	chr9:117324281..117328199-chr9:117347808..117351256,4	MCF-7	breast:
18	chr9:117264990..117269271-chr9:117348762..117354798,9	MCF-7	breast:
19	chr9:117349336..117350972-chr9:117372211..117374265,2	MCF-7	breast:

No data

Variant related genes	Relation type
ATP6V1G1	TF binding region
ENSG00000157693	Chromatin interaction
ENSG00000181722	Chromatin interaction
ENSG00000201749	Chromatin interaction
ENSG00000095397	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000235797	Chromatin interaction
ENSG00000272241	Chromatin interaction
ENSG00000238530	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1078349	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982297	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10982327	0.84[ASN][1000 genomes]
rs12551657	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12551962	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12553341	1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12554462	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12554525	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13296652	0.81[ASN][1000 genomes]
rs13297637	0.83[ASN][1000 genomes]
rs16930078	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs2274595	1.00[CEU][hapmap]
rs2418308	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34424883	0.81[ASN][1000 genomes]
rs4978597	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4979425	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56820236	0.82[EUR][1000 genomes]
rs58441304	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60063492	0.82[EUR][1000 genomes]
rs7042157	0.82[EUR][1000 genomes]
rs73557571	0.82[EUR][1000 genomes]
rs7855043	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[EUR][1000 genomes]
rs7855806	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7868842	0.83[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv1051544	chr9:116944940-117443031	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
4	nsv540203	chr9:116944940-117443031	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
5	nsv1048093	chr9:116945025-117456210	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
6	nsv1050991	chr9:116953739-117442999	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
7	nsv1046311	chr9:116953739-117447142	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS 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	157 gene(s)	inside rSNPs	diseases
8	nsv1052877	chr9:116953739-117456210	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
9	nsv1039681	chr9:116953739-117457158	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
10	nsv1051987	chr9:116955841-117453668	Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
11	nsv1044374	chr9:116955841-117460150	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
12	nsv466534	chr9:116956268-117455810	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
13	nsv615234	chr9:116956268-117455810	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv1048817	chr9:116957958-117456210	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
15	nsv615235	chr9:116958144-117367061	ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
16	nsv615236	chr9:116958144-117455810	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
17	nsv466535	chr9:116958144-117456175	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
18	nsv615237	chr9:116958144-117456175	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
19	nsv615238	chr9:116958144-117458475	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
20	nsv430094	chr9:116958446-117456446	Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
21	nsv1053756	chr9:116975934-117443031	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS 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	43 gene(s)	inside rSNPs	diseases
22	nsv540204	chr9:116975934-117443031	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
23	nsv1047704	chr9:116978041-117399362	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
24	nsv540205	chr9:116978041-117399362	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
25	nsv530950	chr9:117009156-117399361	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
26	nsv916139	chr9:117009169-117399454	Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
27	nsv530951	chr9:117032675-117439804	Flanking Active TSS Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
28	nsv831694	chr9:117328640-117502785	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer 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	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117344800-117349600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:117346200-117349600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:117349000-117349600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr9:117349000-117350800	Active TSS	Rectal Smooth Muscle	rectum
5	chr9:117349200-117349600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr9:117349200-117349600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr9:117349200-117349600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:117349200-117349600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:117349200-117349600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr9:117349200-117349600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr9:117349200-117349600	Flanking Active TSS	Fetal Intestine Large	intestine
12	chr9:117349200-117349600	Flanking Active TSS	Fetal Stomach	stomach
13	chr9:117349200-117349600	Flanking Active TSS	A549	lung
14	chr9:117349200-117349800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:117349200-117349800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr9:117349200-117349800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr9:117349200-117349800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr9:117349200-117349800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
19	chr9:117349200-117349800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:117349200-117349800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:117349200-117349800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr9:117349200-117349800	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr9:117349200-117349800	Flanking Active TSS	Fetal Brain Male	brain
24	chr9:117349200-117349800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
25	chr9:117349200-117349800	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr9:117349200-117349800	Flanking Active TSS	Dnd41	blood
27	chr9:117349200-117349800	Flanking Active TSS	Hela-S3	cervix
28	chr9:117349200-117349800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr9:117349200-117350200	Active TSS	Brain Germinal Matrix	brain
30	chr9:117349200-117350800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr9:117349200-117350800	Active TSS	Fetal Lung	lung
32	chr9:117349200-117350800	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr9:117349200-117350800	Active TSS	Rectal Mucosa Donor 31	rectum
34	chr9:117349200-117351000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr9:117349200-117351000	Active TSS	Brain Hippocampus Middle	brain
36	chr9:117349200-117351000	Active TSS	Colon Smooth Muscle	Colon
37	chr9:117349200-117351000	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr9:117349200-117351000	Active TSS	Fetal Kidney	kidney
39	chr9:117349200-117351200	Active TSS	Fetal Intestine Small	intestine
40	chr9:117349200-117351400	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr9:117349200-117351600	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr9:117349200-117351800	Active TSS	Colonic Mucosa	Colon
43	chr9:117349400-117349600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
44	chr9:117349400-117349600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr9:117349400-117349600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr9:117349400-117349600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr9:117349400-117349600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr9:117349400-117349600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr9:117349400-117349600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
50	chr9:117349400-117349600	Flanking Active TSS	Brain Cingulate Gyrus	brain

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