EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS085-00031 
Organism
Homo sapiens 
Tissue/cell
Heart 
Coordinate
chr1:2135650-2137740 
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
TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA 60
GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG 120
CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG 180
GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT 240
GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC 300
CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC 360
CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC 420
AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC 480
GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC 540
AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC 600
CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG 660
CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC 720
CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC 780
AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG 840
CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG 900
CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC 960
GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC 1020
TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT 1080
GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC 1140
CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG 1200
GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG 1260
GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG 1320
AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG 1380
GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC 1440
AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG 1500
TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC 1560
TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG 1620
GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC 1680
ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG 1740
AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT 1800
TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG 1860
CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA GTTCACTTCC CTGTTGGTAC 1920
TCACCCACCT GTCTGTGGAA AGGCAGCAAT GGTCGATTTC CCCCTTAAGA AACAAAGCGT 1980
GAAGGAGGAA GAGAGGCTAC AGGAATCTGC CATCCGGGAG ACCCTGTCTC TAACGGGCCA 2040
TACGGGGTCC CCCTGTGTCT CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2090