EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS055-00004 
Organism
Homo sapiens 
Tissue/cell
FT33 
Coordinate
chr1:2135360-2137740 
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
CCGGTGGGGT TGGGGAGGAC TTAGTGGCAC CCACTGACCT CCCACTGGGG ATCGGGGTCA 60
GGGAGTGAAG TAAGTGCCTG GCTCTCCGAG CACCCTGGGG CAGCCCCTCC AGCCTGGGAG 120
AGCCAGCTCA CATCTGGGCA GTTGGTGAGG CCAGCTCCTG CCATCTCGGG TCCCCATGCG 180
CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG 240
CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA 300
GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG 360
CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA 420
ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA 480
GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG 540
GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC 600
GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG 660
GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG 720
ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA 780
CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC 840
TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG 900
ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC 960
GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC 1020
CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC 1080
CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC 1140
AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC 1200
GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC 1260
TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC 1320
CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC 1380
CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC 1440
TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT 1500
CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG 1560
CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA 1620
AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA 1680
ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG 1740
CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT 1800
GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG 1860
TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG 1920
GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC 1980
ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG AGAGCCGAGC 2040
TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG 2100
GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG CCACTCTAGC 2160
ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA GTTCACTTCC CTGTTGGTAC TCACCCACCT 2220
GTCTGTGGAA AGGCAGCAAT GGTCGATTTC CCCCTTAAGA AACAAAGCGT GAAGGAGGAA 2280
GAGAGGCTAC AGGAATCTGC CATCCGGGAG ACCCTGTCTC TAACGGGCCA TACGGGGTCC 2340
CCCTGTGTCT CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2380