Variant report

Variant	rs1293309
Chromosome Location	chr8:11723775-11723776
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	CTCF	chr8:11723667-11724140	A549	lung:	n/a	chr8:11723924-11723945 chr8:11723922-11723940 chr8:11724050-11724063 chr8:11723925-11723934 chr8:11723895-11723904
2	POLR2A	chr8:11723684-11724022	HepG2	liver:	n/a	n/a
3	RAD21	chr8:11723724-11724054	HepG2	liver:	n/a	chr8:11723923-11723942
4	POLR2A	chr8:11723622-11725666	PBDE	blood:	n/a	n/a
5	CTCF	chr8:11723748-11724065	A549	lung:	n/a	chr8:11723924-11723945 chr8:11723922-11723940 chr8:11724050-11724063 chr8:11723925-11723934 chr8:11723895-11723904
6	POLR2A	chr8:11723723-11726721	HepG2	liver:	n/a	n/a
7	SMARCB1	chr8:11723731-11725527	Hela-S3	cervix:	n/a	chr8:11724117-11724126
8	RAD21	chr8:11723713-11724243	A549	lung:	n/a	chr8:11723923-11723942
9	HCFC1	chr8:11723755-11724002	K562	blood:	n/a	n/a
10	CHD1	chr8:11723365-11726352	IMR90	lung:	n/a	n/a
11	BHLHE40	chr8:11723577-11724531	K562	blood:	n/a	chr8:11724440-11724456
12	POLR2A	chr8:11723732-11723790	K562	blood:	n/a	n/a
13	MYC	chr8:11723702-11723904	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr8:11723577-11726448	MCF10A-Er-Src	breast:	n/a	n/a
15	MXI1	chr8:11723737-11724166	HepG2	liver:	n/a	n/a
16	POLR2A	chr8:11723707-11725173	K562	blood:	n/a	n/a
17	POLR2A	chr8:11723563-11724136	IMR90	lung:	n/a	n/a
18	RAD21	chr8:11723701-11724191	A549	lung:	n/a	chr8:11723923-11723942 chr8:11723701-11723715
19	SMC3	chr8:11723734-11724113	HepG2	liver:	n/a	chr8:11723924-11723938
20	RAD21	chr8:11723748-11724102	A549	lung:	n/a	chr8:11723923-11723942
21	POLR2A	chr8:11723619-11723976	K562	blood:	n/a	n/a
22	CBX3	chr8:11723728-11724492	K562	blood:	n/a	n/a
23	POLR2A	chr8:11717595-11726429	MCF10A-Er-Src	breast:	n/a	n/a
24	CTCF	chr8:11723680-11723830	A549	lung:	n/a	n/a
25	POLR2A	chr8:11723658-11724028	HepG2	liver:	n/a	n/a
26	POLR2A	chr8:11723599-11726575	K562	blood:	n/a	n/a
27	CTCF	chr8:11723552-11724303	A549	lung:	n/a	chr8:11723924-11723945 chr8:11723922-11723940 chr8:11724050-11724063 chr8:11723925-11723934 chr8:11723895-11723904
28	MAZ	chr8:11723679-11726511	K562	blood:	n/a	chr8:11724739-11724749 chr8:11725956-11725966 chr8:11726080-11726090
29	NR2F2	chr8:11723452-11725221	K562	blood:	n/a	n/a
30	POLR2A	chr8:11720772-11734387	K562	blood:	n/a	n/a
31	POLR2A	chr8:11723624-11724197	K562	blood:	n/a	n/a
32	POLR2A	chr8:11723548-11725869	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:11708825..11713035-chr8:11718721..11724039,7	MCF-7	breast:
2	chr8:11701711..11703998-chr8:11723479..11725596,2	K562	blood:
3	chr8:11708512..11715317-chr8:11723234..11727095,9	MCF-7	breast:
4	chr8:11695946..11697771-chr8:11722616..11724742,2	MCF-7	breast:

Variant related genes	Relation type
CTSB	TF binding region
ENSG00000164733	Chromatin interaction
ENSG00000269899	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1293303	0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs1293306	0.96[CHB][hapmap];0.86[ASN][1000 genomes]
rs1293310	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1293311	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1296022	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1296023	0.89[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1299525	0.83[CHB][hapmap];0.88[ASN][1000 genomes]
rs1619003	0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1619200	0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1620833	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1624088	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1692803	0.84[EUR][1000 genomes]
rs1692804	0.82[CHB][hapmap];0.81[JPT][hapmap];0.84[ASN][1000 genomes]
rs1692807	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1692808	0.81[JPT][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1736117	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1736118	0.84[EUR][1000 genomes]
rs1736119	0.84[EUR][1000 genomes]
rs1736120	0.84[EUR][1000 genomes]
rs1736121	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2201680	1.00[YRI][hapmap]
rs2250903	0.81[JPT][hapmap];0.84[EUR][1000 genomes]
rs2294137	1.00[YRI][hapmap]
rs2472430	0.84[EUR][1000 genomes]
rs2645412	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2645415	0.87[CHB][hapmap];0.84[ASN][1000 genomes]
rs2740596	0.81[ASN][1000 genomes]
rs2740597	0.81[JPT][hapmap]
rs2740600	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2740601	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2740602	0.84[EUR][1000 genomes]
rs3104255	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3116070	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3116071	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3735809	1.00[YRI][hapmap]
rs7828791	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7844154	0.84[EUR][1000 genomes]
rs8191595	1.00[YRI][hapmap]
rs904016	0.84[EUR][1000 genomes]
rs904017	0.84[EUR][1000 genomes]
rs9644756	0.85[CHB][hapmap]
rs966785	0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS 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 target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
9	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
12	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
14	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
17	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
18	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv1016952	chr8:11679271-11849955	Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv1029093	chr8:11679271-11858466	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
21	nsv539478	chr8:11679271-11858466	Bivalent/Poised TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv1017334	chr8:11688534-11732949	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
23	nsv539479	chr8:11688534-11732949	Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
24	nsv1019738	chr8:11696393-11732949	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
25	nsv539480	chr8:11696393-11732949	Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
26	nsv1031972	chr8:11696393-11805961	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	nsv539481	chr8:11696393-11805961	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	esv34042	chr8:11698337-11726817	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
29	nsv610293	chr8:11698747-11929734	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
30	nsv516685	chr8:11698747-12570199	Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	74 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1293309	CTSB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11706600-11724400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:11706800-11724400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:11708600-11724600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:11711600-11723800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:11712000-11724600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr8:11718400-11723800	Enhancers	Stomach Mucosa	stomach
7	chr8:11719000-11724400	Weak transcription	Aorta	Aorta
8	chr8:11719800-11723800	Enhancers	Placenta Amnion	Placenta Amnion
9	chr8:11720000-11724000	Enhancers	Ovary	ovary
10	chr8:11720400-11723800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:11720400-11723800	Weak transcription	Brain Germinal Matrix	brain
12	chr8:11720400-11723800	Genic enhancers	Fetal Stomach	stomach
13	chr8:11720800-11723800	Weak transcription	GM12878-XiMat	blood
14	chr8:11721000-11723800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:11721000-11724000	Transcr. at gene 5' and 3'	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:11721200-11723800	Transcr. at gene 5' and 3'	Osteobl	bone
17	chr8:11721200-11724800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr8:11721600-11723800	Enhancers	Pancreas	Pancrea
19	chr8:11721600-11724000	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr8:11721600-11724200	Enhancers	Fetal Heart	heart
21	chr8:11721600-11724400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:11721600-11724800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
23	chr8:11721800-11725000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
24	chr8:11722000-11724200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr8:11722200-11723800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:11722200-11723800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr8:11722200-11723800	Weak transcription	Fetal Lung	lung
28	chr8:11722400-11724400	Enhancers	Fetal Brain Male	brain
29	chr8:11722400-11724400	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr8:11722400-11724600	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr8:11722600-11723800	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr8:11722600-11723800	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr8:11722600-11723800	Enhancers	Small Intestine	intestine
34	chr8:11722600-11724000	Transcr. at gene 5' and 3'	NHLF	lung
35	chr8:11722600-11724200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr8:11722600-11724600	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:11722600-11724600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr8:11722600-11724600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr8:11722600-11724600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
40	chr8:11722600-11724600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:11722600-11724600	Active TSS	Right Atrium	heart
42	chr8:11722600-11724800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
43	chr8:11722800-11723800	Active TSS	Esophagus	oesophagus
44	chr8:11722800-11723800	Enhancers	Left Ventricle	heart
45	chr8:11722800-11723800	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr8:11722800-11723800	Weak transcription	Thymus	Thymus
47	chr8:11722800-11723800	Weak transcription	HSMMtube	muscle
48	chr8:11722800-11724200	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr8:11722800-11724800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr8:11723000-11724200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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