EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS078-00067 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr1:2136020-2136860 
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: 21             
IDCoordinateTissue/cell
SE_02984chr1:2135742-2136307Bladder
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_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
GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG 60
ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA 120
CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC 180
TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG 240
ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC 300
GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC 360
CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC 420
CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC 480
AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC 540
GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC 600
TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC 660
CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC 720
CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC 780
TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT 840