EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS082-00040 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr1:2135230-2137740 
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
CCCTGTGACA GAGGTGCTGT CGCGTGGCCC CACTTACAGA TGGGTCAACT GAGGCCCGGG 60
GCATCTGTCC ACTTGTCATG ACAGTGAGCG GCCAAGCTGG ATGTGAACCC AGGTTTTTGT 120
ATGCTGCCGC CCGGTGGGGT TGGGGAGGAC TTAGTGGCAC CCACTGACCT CCCACTGGGG 180
ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG GCTCTCCGAG CACCCTGGGG CAGCCCCTCC 240
AGCCTGGGAG AGCCAGCTCA CATCTGGGCA GTTGGTGAGG CCAGCTCCTG CCATCTCGGG 300
TCCCCATGCG CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC TCCACAGACC CTCACAGACG 360
GCCTCACAGG CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG 420
TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA 480
GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG 540
CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG 600
GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT 660
GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC 720
CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC 780
CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC 840
AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC 900
GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC 960
AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC 1020
CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG 1080
CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC 1140
CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC 1200
AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG 1260
CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG 1320
CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC 1380
GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC 1440
TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT 1500
GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC 1560
CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG 1620
GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG 1680
GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG 1740
AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG 1800
GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC 1860
AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG 1920
TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC 1980
TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG 2040
GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC 2100
ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG 2160
AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT 2220
TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG 2280
CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA GTTCACTTCC CTGTTGGTAC 2340
TCACCCACCT GTCTGTGGAA AGGCAGCAAT GGTCGATTTC CCCCTTAAGA AACAAAGCGT 2400
GAAGGAGGAA GAGAGGCTAC AGGAATCTGC CATCCGGGAG ACCCTGTCTC TAACGGGCCA 2460
TACGGGGTCC CCCTGTGTCT CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2510