EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS136-00025 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr1:2135540-2137740 
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
CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG 60
CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA 120
GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG 180
CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA 240
ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA 300
GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG 360
GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC 420
GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG 480
GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG 540
ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA 600
CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC 660
TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG 720
ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC 780
GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC 840
CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC 900
CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC 960
AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC 1020
GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC 1080
TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC 1140
CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC 1200
CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC 1260
TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT 1320
CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG 1380
CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA 1440
AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA 1500
ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG 1560
CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT 1620
GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG 1680
TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG 1740
GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC 1800
ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG AGAGCCGAGC 1860
TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG 1920
GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG CCACTCTAGC 1980
ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA GTTCACTTCC CTGTTGGTAC TCACCCACCT 2040
GTCTGTGGAA AGGCAGCAAT GGTCGATTTC CCCCTTAAGA AACAAAGCGT GAAGGAGGAA 2100
GAGAGGCTAC AGGAATCTGC CATCCGGGAG ACCCTGTCTC TAACGGGCCA TACGGGGTCC 2160
CCCTGTGTCT CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2200