EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-35239 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr9:137272010-137273650 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs62573099chr9137272245hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GLIS2MA0736.1chr9:137272026-137272040GGCCCCCCGCGGTG+6.16
ZIC1MA0696.1chr9:137272026-137272040GGCCCCCCGCGGTG+6.89
ZIC3MA0697.1chr9:137272026-137272041GGCCCCCCGCGGTGT+6.69
ZIC4MA0751.1chr9:137272026-137272041GGCCCCCCGCGGTGT+7.12
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_00860chr9:137261032-137275300Adrenal_Gland
SE_02933chr9:137267847-137274105Bladder
SE_05812chr9:137261360-137282798Brain_Hippocampus_Middle
SE_09174chr9:137271959-137278823CD14
SE_23121chr9:137268064-137272180Colon_Crypt_1
SE_23121chr9:137273109-137276118Colon_Crypt_1
SE_23757chr9:137272192-137272594Colon_Crypt_2
SE_23757chr9:137273008-137273550Colon_Crypt_2
SE_24707chr9:137267912-137275776Colon_Crypt_3
SE_26524chr9:137261081-137273486Esophagus
SE_28276chr9:137272422-137275612Fetal_Intestine
SE_29238chr9:137272293-137275657Fetal_Intestine_Large
SE_33498chr9:137264862-137274948H2171
SE_34123chr9:137269284-137272233HCC1954
SE_34906chr9:137261183-137274052HeLa
SE_40986chr9:137262434-137273204Left_Ventricle
SE_41556chr9:137243649-137273607LNCaP
SE_42130chr9:137261389-137273101Lung
SE_43440chr9:137267839-137274060MCF-7
SE_48050chr9:137252285-137278501Psoas_Muscle
SE_52424chr9:137273350-137275415Small_Intestine
SE_53315chr9:137273283-137275051Spleen
SE_65247chr9:137261076-137277919Pancreatic_islets
SE_68695chr9:137267831-137275219H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr9137272600137273400
chr9137272238137272364
chr9137272366137272506
chr9137272755137272852
chr9137272864137273054
Number: 1             
IDChromosomeStartEnd
GH09I134369chr9137261189137279971
Enhancer Sequence
TGCGTGTGTT GGGGGTGGCC CCCCGCGGTG TAGGCCGGAG GTGGCGTGCC GGCCCCGTGA 60
GTCACGCCGA TCCCAGGATG GGAGTGGGGG TGGCCGGGGC ACTGTGAGCT GGCGTGCTGA 120
GGCTGGCCTG CCCGTGGCTT GGCCTGGGGG CAGGGGTAGG GTGGGGTCCT GCCCGGGTTC 180
TCCTGGAGAA CCTGGGTCAG GAGCCAGGGG CCAGATCAGG GCTGGGGACT TCGCCTGGGG 240
TCGGATAGGG GCTGGGGTGG CCATGAGAAG TGAGGAGCCT CCCATGACCC AGTGGTTGCA 300
AGGAGCAGAT GCCGCCTGTC AGGTGGGCGG CCCCCCCTGG GAGGAGGCTG CAGGCTGGGA 360
GGTAGACAGG ACGGGCCCCT CGGTGTGATG GTTGGGGTGT CCAGGGACTG GACTTGGGAA 420
GGGTTGGTGA CCTAGTGCCA TGGGGTCCCT GCTCTCTGTG GCTGCCTCTG TGGCCAGGCC 480
TTGGCCCTCC TATTGCTGCC CCACGACACC TGGCTGTGGC TTGTCCCAGC TCCTGGGCCA 540
GGTGGGGAGT GCAGCTGGCC ACCGAGCCTC ATGAAGCACC TTTCCAGTTC CCCGGCACCT 600
GGGTCTGGCC GAGGTCTGAG GCCAGAGGAA AGGCCTCCTC CAGAATCCAG GGCTGCCCGT 660
CCTGAGGTAA GGGGCTTTGA GCTGCAGGCA GACGGCACCT TCTACCCATG GCCGGATCCC 720
CCCCTGTCAA TCTGCAGTAG AGACAGCAGA GCCCCCGGGA ACCCCTCCCA GCAGCTGAGG 780
GTTCAGGGGG TGCCCCTCAC TGTACTGGGG AAATGTGGCC CCAGCGGGCA GGAGGTGCAG 840
GGCCCAGTCA GAGACTGAGT CTGAACCCGG TGGGGCCTCA GGCCAGCTCT GTGACCCGGA 900
CAAGGGGTTT TCCTTCTCTG AGCCCCAGTT GCTGCTGTCA GAGCCTGCGG TGGGCACTGA 960
TTTGAGGAAG GACAGACATG GGCTGGGAGG GTTGAGGGAG GCCCTGGAGA GGGGGACCCT 1020
GGGGAGGGAG ATCTTGGAGC TGCAGAGGCT TTGAAGAGGC AGGCGTATGG GAGTGCGTGG 1080
CCAGGTTGCC CGGCCTGGGC TGGGGGCTGG GTCCAGGGAT GCAGCTGGCC TCACCTGCTG 1140
GTAGAGCCCT GTCTGGAGGA GTTGAGCTCA GACCTTAGCT AGTGCTGACC GCGCTGGGGC 1200
AGAGTGCTGA GAGGGGCTCT CTCAGGGCCG TCTCTCAGGG CTGGGCCCTG TTGGATCTTC 1260
TAACTGTCTG AGCGGGAGAG GGAAGGCTTC CTGGAGGAGG TGTCCCTGGT AGGAAGACGC 1320
AGAGGGAATG ATTGTGTGTG CTGTAAGGGC CAGGCCCAGG GCTGAGAGGG GCTGGTGGAG 1380
ATGGTGGGGG CTGGGTGGGG CAGGACACCA TGGTCTATGT GGCGCCCGCC CTTCTCCCTC 1440
CTCCATGGCC ACAAGGCCCC TCTGGTACAG AGGGTGGTGC TGGCCTTGAG GGATCTGGCC 1500
GGCAGGTAGG CAAGTGAATG ACAGAGCCCC TCAGGTGGAC TTGGGGGTGG GGCCTCCTGG 1560
TTCTGCCTAT TTTCTTCAGC GGCCCTGGTT AGGGCTTTGA AGGGGCTTCA CTGCAAATTA 1620
GCCCCGACCT CCCCGGGGTG 1640