EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS154-00051 
Organism
Homo sapiens 
Tissue/cell
Osteoblast 
Coordinate
chr1:2135350-2137550 
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
ATGCTGCCGC CCGGTGGGGT TGGGGAGGAC TTAGTGGCAC CCACTGACCT CCCACTGGGG 60
ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG GCTCTCCGAG CACCCTGGGG CAGCCCCTCC 120
AGCCTGGGAG AGCCAGCTCA CATCTGGGCA GTTGGTGAGG CCAGCTCCTG CCATCTCGGG 180
TCCCCATGCG CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC TCCACAGACC CTCACAGACG 240
GCCTCACAGG CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG 300
TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA 360
GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG 420
CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG 480
GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT 540
GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC 600
CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC 660
CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC 720
AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC 780
GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC 840
AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC 900
CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG 960
CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC 1020
CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC 1080
AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG 1140
CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG 1200
CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC 1260
GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC 1320
TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT 1380
GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC 1440
CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG 1500
GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG 1560
GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG 1620
AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG 1680
GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC 1740
AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG 1800
TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC 1860
TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG 1920
GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC 1980
ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG 2040
AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT 2100
TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG 2160
CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA 2200