EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-00064 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr1:2135320-2137740 
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
GCCAAGCTGG ATGTGAACCC AGGTTTTTGT ATGCTGCCGC CCGGTGGGGT TGGGGAGGAC 60
TTAGTGGCAC CCACTGACCT CCCACTGGGG ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG 120
GCTCTCCGAG CACCCTGGGG CAGCCCCTCC AGCCTGGGAG AGCCAGCTCA CATCTGGGCA 180
GTTGGTGAGG CCAGCTCCTG CCATCTCGGG TCCCCATGCG CTTCTCAGAT GTGAAAGCCC 240
CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG CCAACACCCA GCGGCTGCAC 300
TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA 360
GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC 420
ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA 480
GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT 540
CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC 600
CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA 660
GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC 720
CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG 780
ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG 840
ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC 900
GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC 960
CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC 1020
CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC 1080
GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC 1140
GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG 1200
GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA 1260
ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC 1320
CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT 1380
TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC 1440
CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC 1500
TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC 1560
AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG 1620
GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG 1680
CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC 1740
CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC 1800
GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC 1860
GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC 1920
ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG 1980
GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA 2040
AAGGTCTTCA TTCCTTTTCG GTCTGATCTG AGAGCCGAGC TCTCGGCAGG GATGGGGACC 2100
CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG 2160
CACTGGGGCT CCATCATTAC GTTCGCATGG CCACTCTAGC ATGGGAGGGG GGCAGGGCCT 2220
TTCCCTGTTA GTTCACTTCC CTGTTGGTAC TCACCCACCT GTCTGTGGAA AGGCAGCAAT 2280
GGTCGATTTC CCCCTTAAGA AACAAAGCGT GAAGGAGGAA GAGAGGCTAC AGGAATCTGC 2340
CATCCGGGAG ACCCTGTCTC TAACGGGCCA TACGGGGTCC CCCTGTGTCT CCTGCAGCCC 2400
TGCACAGCCC CGGTCTGAGG 2420