EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS080-00056 
Organism
Homo sapiens 
Tissue/cell
H9 
Coordinate
chr1:2135330-2137740 
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
ATGTGAACCC AGGTTTTTGT ATGCTGCCGC CCGGTGGGGT TGGGGAGGAC TTAGTGGCAC 60
CCACTGACCT CCCACTGGGG ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG GCTCTCCGAG 120
CACCCTGGGG CAGCCCCTCC AGCCTGGGAG AGCCAGCTCA CATCTGGGCA GTTGGTGAGG 180
CCAGCTCCTG CCATCTCGGG TCCCCATGCG CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC 240
TCCACAGACC CTCACAGACG GCCTCACAGG CCAACACCCA GCGGCTGCAC TGCCCATGGT 300
CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG 360
CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA 420
TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC 480
CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA 540
CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT 600
GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC 660
ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC 720
CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC 780
CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG 840
AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT 900
TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC 960
TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC 1020
CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG 1080
CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC 1140
TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC 1200
GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC 1260
CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC 1320
TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC 1380
GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC 1440
CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC 1500
GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC 1560
AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC 1620
TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG 1680
CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT 1740
TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC 1800
CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG 1860
ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA 1920
GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC 1980
CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA 2040
TTCCTTTTCG GTCTGATCTG AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG 2100
CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT 2160
CCATCATTAC GTTCGCATGG CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA 2220
GTTCACTTCC CTGTTGGTAC TCACCCACCT GTCTGTGGAA AGGCAGCAAT GGTCGATTTC 2280
CCCCTTAAGA AACAAAGCGT GAAGGAGGAA GAGAGGCTAC AGGAATCTGC CATCCGGGAG 2340
ACCCTGTCTC TAACGGGCCA TACGGGGTCC CCCTGTGTCT CCTGCAGCCC TGCACAGCCC 2400
CGGTCTGAGG 2410