EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS120-00023 
Organism
Homo sapiens 
Tissue/cell
LNCaP-abl 
Coordinate
chr1:2136100-2137370 
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr1:2136395-2136406GCCCCGCCCCC+6.02
KLF16MA0741.1chr1:2136544-2136555GCCCCGCCCCC+6.02
KLF16MA0741.1chr1:2136637-2136648GCCCCGCCCCC+6.02
KLF5MA0599.1chr1:2136333-2136343GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136390-2136400GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136395-2136405GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136418-2136428GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136432-2136442GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136460-2136470GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136530-2136540GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136544-2136554GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136610-2136620GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136637-2136647GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136672-2136682GCCCCGCCCC+6.02
KLF5MA0599.1chr1:2136751-2136761GCCCCGCCCC+6.02
SP1MA0079.4chr1:2136330-2136345CAAGCCCCGCCCCTC+6.34
SP1MA0079.4chr1:2136429-2136444CAAGCCCCGCCCCTC+6.34
SP1MA0079.4chr1:2136541-2136556CAAGCCCCGCCCCCC+6.86
SP2MA0516.2chr1:2136606-2136623CCACGCCCCGCCCCTCT+6.04
SP2MA0516.2chr1:2136329-2136346TCAAGCCCCGCCCCTCA+6.16
SP2MA0516.2chr1:2136428-2136445TCAAGCCCCGCCCCTCC+6.29
SP2MA0516.2chr1:2136540-2136557TCAAGCCCCGCCCCCCA+7.04
SP3MA0746.2chr1:2136394-2136407CGCCCCGCCCCCC+6.11
SP4MA0685.1chr1:2136330-2136347CAAGCCCCGCCCCTCAA+6.09
SP4MA0685.1chr1:2136541-2136558CAAGCCCCGCCCCCCAG+6.37
SP4MA0685.1chr1:2136429-2136446CAAGCCCCGCCCCTCCC+6.4
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_02984chr1:2135742-2136307Bladder
SE_02984chr1:2136784-2137318Bladder
SE_07454chr1:2136659-2137763Brain_Hippocampus_Middle_150
SE_24063chr1:2135543-2136326Colon_Crypt_2
SE_24063chr1:2136771-2137584Colon_Crypt_2
SE_28207chr1:2135320-2136370Fetal_Intestine
SE_28207chr1:2136651-2137279Fetal_Intestine
SE_29530chr1:2135575-2136399Fetal_Intestine_Large
SE_29530chr1:2136675-2137395Fetal_Intestine_Large
SE_40333chr1:2135518-2136309K562
SE_40333chr1:2136793-2137298K562
SE_46689chr1:2135346-2136306Ovary
SE_46689chr1:2136752-2137641Ovary
SE_47622chr1:2135695-2136333Pancreas
SE_47622chr1:2136690-2137347Pancreas
SE_54645chr1:2135111-2136378Stomach_Smooth_Muscle
SE_54645chr1:2136671-2142113Stomach_Smooth_Muscle
SE_55632chr1:2136634-2137365Thymus
SE_62490chr1:2120386-2191742Tonsil
SE_68393chr1:2120436-2162432TC32
SE_68394chr1:2120436-2162432TC32
SE_69135chr1:2135338-2136316H9
SE_69135chr1:2136731-2137456H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr121366422136736
Number: 1             
IDChromosomeStartEnd
GH01I002203chr121346022142348
Enhancer Sequence
ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG 60
ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC 120
GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC 180
CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC 240
CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC 300
GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC 360
GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG 420
GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA 480
ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC 540
CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT 600
TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC 660
CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC 720
TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC 780
AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG 840
GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG 900
CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC 960
CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC 1020
GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC 1080
GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC 1140
ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG 1200
GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA 1260
AAGGTCTTCA 1270