EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-00054 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:2135380-2137630 
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
TTAGTGGCAC CCACTGACCT CCCACTGGGG ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG 60
GCTCTCCGAG CACCCTGGGG CAGCCCCTCC AGCCTGGGAG AGCCAGCTCA CATCTGGGCA 120
GTTGGTGAGG CCAGCTCCTG CCATCTCGGG TCCCCATGCG CTTCTCAGAT GTGAAAGCCC 180
CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG CCAACACCCA GCGGCTGCAC 240
TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA 300
GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC 360
ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA 420
GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT 480
CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC 540
CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA 600
GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC 660
CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG 720
ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG 780
ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC 840
GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC 900
CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC 960
CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC 1020
GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC 1080
GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG 1140
GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA 1200
ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC 1260
CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT 1320
TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC 1380
CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC 1440
TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC 1500
AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG 1560
GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG 1620
CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC 1680
CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC 1740
GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC 1800
GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC 1860
ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG 1920
GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA 1980
AAGGTCTTCA TTCCTTTTCG GTCTGATCTG AGAGCCGAGC TCTCGGCAGG GATGGGGACC 2040
CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG 2100
CACTGGGGCT CCATCATTAC GTTCGCATGG CCACTCTAGC ATGGGAGGGG GGCAGGGCCT 2160
TTCCCTGTTA GTTCACTTCC CTGTTGGTAC TCACCCACCT GTCTGTGGAA AGGCAGCAAT 2220
GGTCGATTTC CCCCTTAAGA AACAAAGCGT 2250