EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS088-00115 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr1:2135930-2137740 
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
GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC 60
ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC 120
CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC 180
CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG 240
AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT 300
TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC 360
TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC 420
CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG 480
CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC 540
TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC 600
GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC 660
CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC 720
TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC 780
GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC 840
CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC 900
GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC 960
AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC 1020
TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG 1080
CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT 1140
TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC 1200
CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG 1260
ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA 1320
GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC 1380
CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA 1440
TTCCTTTTCG GTCTGATCTG AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG 1500
CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT 1560
CCATCATTAC GTTCGCATGG CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA 1620
GTTCACTTCC CTGTTGGTAC TCACCCACCT GTCTGTGGAA AGGCAGCAAT GGTCGATTTC 1680
CCCCTTAAGA AACAAAGCGT GAAGGAGGAA GAGAGGCTAC AGGAATCTGC CATCCGGGAG 1740
ACCCTGTCTC TAACGGGCCA TACGGGGTCC CCCTGTGTCT CCTGCAGCCC TGCACAGCCC 1800
CGGTCTGAGG 1810