Variant report

Variant	rs11794186
Chromosome Location	chr9:115517316-115517317
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	GATA3	chr9:115516879-115517320	MCF-7	breast:	n/a	n/a
2	RUNX3	chr9:115516922-115517375	GM12878	blood:	n/a	n/a
3	SRF	chr9:115516670-115517317	MCF-7	breast:	n/a	chr9:115516978-115516993 chr9:115516980-115516994 chr9:115516981-115516990 chr9:115516976-115516990 chr9:115516980-115516991 chr9:115516977-115516994 chr9:115516977-115516991 chr9:115516979-115516992 chr9:115516981-115516992 chr9:115516976-115516994 chr9:115516979-115516990 chr9:115516974-115516991
4	RCOR1	chr9:115517032-115517348	K562	blood:	n/a	n/a
5	SIN3AK20	chr9:115516708-115517479	MCF-7	breast:	n/a	n/a
6	SPI1	chr9:115517042-115517346	GM12878	blood:	n/a	n/a
7	FOS	chr9:115516911-115517668	MCF10A-Er-Src	breast:	n/a	n/a
8	ZKSCAN1	chr9:115517052-115517561	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:115517273-115517592	IMR90	lung:	n/a	chr9:115517429-115517440
10	GATA3	chr9:115516712-115517359	MCF-7	breast:	n/a	n/a
11	RUNX3	chr9:115516966-115517346	GM12878	blood:	n/a	n/a
12	MYC	chr9:115517013-115517394	MCF10A-Er-Src	breast:	n/a	n/a
13	SPI1	chr9:115517217-115517670	HL-60	blood:	n/a	n/a
14	SPI1	chr9:115517044-115517535	GM12891	blood:	n/a	n/a
15	KAP1	chr9:115516992-115517353	HEK293	kidney:	n/a	chr9:115517245-115517253
16	SPI1	chr9:115516987-115517791	HL-60	blood:	n/a	n/a
17	SRF	chr9:115516667-115517432	MCF-7	breast:	n/a	chr9:115516978-115516993 chr9:115516980-115516994 chr9:115516981-115516990 chr9:115516976-115516990 chr9:115516980-115516991 chr9:115516977-115516994 chr9:115516977-115516991 chr9:115516979-115516992 chr9:115516981-115516992 chr9:115516976-115516994 chr9:115516979-115516990 chr9:115516974-115516991

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:115511365..115514968-chr9:115517023..115521042,5	K562	blood:
2	chr9:115503663..115506191-chr9:115515083..115517470,2	K562	blood:

Variant related genes	Relation type
ENSG00000226609	TF binding region
ENSG00000148158	Chromatin interaction
ENSG00000226609	Chromatin interaction

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10759584	0.88[ASN][1000 genomes]
rs10817370	1.00[YRI][hapmap]
rs10817374	1.00[YRI][hapmap]
rs10817380	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10817381	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10817383	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10817385	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10817387	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10817388	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10817390	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10817393	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs10817394	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs10981483	1.00[YRI][hapmap]
rs10981497	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981498	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10981500	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981501	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981506	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10981510	0.85[ASN][1000 genomes]
rs10981512	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10981517	1.00[EUR][1000 genomes]
rs10981520	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs10981522	0.82[JPT][hapmap]
rs10981524	1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs10981525	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs10981527	0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11790110	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11792606	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12235123	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12685108	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1361719	0.92[ASN][1000 genomes]
rs1361720	0.82[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1517079	1.00[YRI][hapmap]
rs1891403	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1965335	0.92[ASN][1000 genomes]
rs2645993	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2796037	0.95[ASN][1000 genomes]
rs28494060	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2935476	0.85[ASN][1000 genomes]
rs4979148	0.88[ASN][1000 genomes]
rs4979150	0.88[ASN][1000 genomes]
rs4979153	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs59721032	1.00[EUR][1000 genomes]
rs72768411	0.92[ASN][1000 genomes]
rs73534733	0.82[ASN][1000 genomes]
rs7859381	0.88[ASN][1000 genomes]
rs7862183	0.98[ASN][1000 genomes]
rs7863952	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7868830	0.82[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7872308	0.84[ASN][1000 genomes]
rs787269	0.88[ASN][1000 genomes]
rs787270	0.88[ASN][1000 genomes]
rs787271	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs787272	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs787274	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs787275	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs787276	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs787279	0.92[ASN][1000 genomes]
rs787280	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs787284	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs787292	0.89[ASN][1000 genomes]
rs787295	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs787297	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs787298	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs787301	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs813101	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9409123	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758198	chr9:115240454-116002951	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	esv2759710	chr9:115240454-116002951	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv515899	chr9:115359049-115593870	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv34346	chr9:115360505-115581453	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1038999	chr9:115367078-115590950	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	esv2757350	chr9:115371397-115594108	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv471317	chr9:115375153-115558246	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	esv2761275	chr9:115376461-115590962	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv1035169	chr9:115378282-115573581	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS 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	15 gene(s)	inside rSNPs	diseases
10	nsv1049451	chr9:115378282-115585109	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1047374	chr9:115378282-115590950	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1038306	chr9:115379305-115595695	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv540194	chr9:115379305-115595695	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1051909	chr9:115379505-115588377	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
15	nsv540195	chr9:115379505-115588377	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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	15 gene(s)	inside rSNPs	diseases
16	nsv915763	chr9:115379600-115588349	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	esv3693040	chr9:115381164-115578065	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv515121	chr9:115383227-115585827	Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
19	nsv1044168	chr9:115383253-115585109	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
20	nsv1048327	chr9:115383253-115589646	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv1044381	chr9:115383253-115590950	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv442163	chr9:115383255-115590578	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
23	esv35051	chr9:115383332-115573581	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
24	esv34763	chr9:115383332-115581453	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
25	nsv430090	chr9:115383445-115594445	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv1041424	chr9:115389428-115590950	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	nsv1050186	chr9:115390759-115550453	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer 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	15 gene(s)	inside rSNPs	diseases
28	nsv1047625	chr9:115390759-115587347	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
29	nsv540196	chr9:115390759-115587347	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
30	nsv615198	chr9:115397206-115589251	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
31	nsv893733	chr9:115397206-115712068	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
32	nsv1051808	chr9:115397891-115590950	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
33	esv34739	chr9:115409445-115581453	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:115514000-115518000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr9:115514200-115518000	Enhancers	Fetal Thymus	thymus
3	chr9:115514200-115518000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr9:115514200-115518200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr9:115514200-115518600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr9:115514400-115517400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:115514400-115517400	Weak transcription	Right Atrium	heart
8	chr9:115514400-115517400	Weak transcription	Small Intestine	intestine
9	chr9:115514400-115517600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr9:115514400-115517800	Enhancers	Primary B cells from cord blood	blood
11	chr9:115514400-115517800	Enhancers	NH-A	brain
12	chr9:115514400-115518000	Enhancers	Hela-S3	cervix
13	chr9:115514400-115518200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr9:115514400-115518400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr9:115514400-115518400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr9:115514400-115518600	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr9:115514400-115518600	Enhancers	NHLF	lung
18	chr9:115514400-115518800	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr9:115514400-115519200	Weak transcription	K562	blood
20	chr9:115514400-115520400	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr9:115514400-115520600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:115514400-115521000	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr9:115514600-115517400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr9:115514600-115517400	Weak transcription	Ovary	ovary
25	chr9:115514600-115517400	Enhancers	NHDF-Ad	bronchial
26	chr9:115514600-115517600	Enhancers	Fetal Heart	heart
27	chr9:115514600-115517600	Enhancers	Rectal Smooth Muscle	rectum
28	chr9:115514600-115517800	Enhancers	Lung	lung
29	chr9:115514600-115518200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr9:115514600-115518200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:115514600-115518200	Enhancers	Adipose Nuclei	Adipose
32	chr9:115514600-115518400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr9:115514600-115518400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr9:115514600-115518600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr9:115514600-115518800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:115514600-115519400	Enhancers	Fetal Intestine Large	intestine
37	chr9:115514600-115520200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:115514600-115520400	Enhancers	Colon Smooth Muscle	Colon
39	chr9:115514600-115523600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr9:115514600-115526400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:115514600-115526400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:115514800-115517400	Weak transcription	Psoas Muscle	Psoas
43	chr9:115514800-115517400	Weak transcription	Spleen	Spleen
44	chr9:115514800-115517600	Weak transcription	Fetal Stomach	stomach
45	chr9:115514800-115517600	Weak transcription	Pancreas	Pancrea
46	chr9:115514800-115517800	Enhancers	Brain Anterior Caudate	brain
47	chr9:115514800-115519400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr9:115514800-115520000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:115514800-115520000	Enhancers	Osteobl	bone
50	chr9:115514800-115523400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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