EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-00061 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr1:2135100-2137740 
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
GGCTGCTGGG CCTGTCCTCT CTGAGTTGCC TCAAATCCCC TGTTCCTTGA GCGGTCCTGG 60
AGCCTGGCCT CAGGCCTCAG GGCACCACAC TACTTGCCTC CAGGGACCAG CCTGTTCACC 120
CCACACCCAG CCCTGTGACA GAGGTGCTGT CGCGTGGCCC CACTTACAGA TGGGTCAACT 180
GAGGCCCGGG GCATCTGTCC ACTTGTCATG ACAGTGAGCG GCCAAGCTGG ATGTGAACCC 240
AGGTTTTTGT ATGCTGCCGC CCGGTGGGGT TGGGGAGGAC TTAGTGGCAC CCACTGACCT 300
CCCACTGGGG ATCGGGGTCA GGGAGTGAAG TAAGTGCCTG GCTCTCCGAG CACCCTGGGG 360
CAGCCCCTCC AGCCTGGGAG AGCCAGCTCA CATCTGGGCA GTTGGTGAGG CCAGCTCCTG 420
CCATCTCGGG TCCCCATGCG CTTCTCAGAT GTGAAAGCCC CTTGCTGGCC TCCACAGACC 480
CTCACAGACG GCCTCACAGG CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT 540
GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT 600
GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA 660
CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG 720
ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA 780
GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC 840
TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA 900
GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC 960
GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT 1020
CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC 1080
TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC 1140
GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC 1200
TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC 1260
CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC 1320
CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG 1380
CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC 1440
TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG 1500
CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT 1560
GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC 1620
CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT 1680
CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA 1740
GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG 1800
GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG 1860
GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG 1920
ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA 1980
CGCCACATGC AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC 2040
GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC 2100
TGAGCCGCCC TCCTCCCATG TGCGCGGGAG TCCCTCCGCC ACTGTGCCCA GATCGCCGGC 2160
GAAGCGCAGG GGGAGGCTGG GAAGGGCATC GGGAGACACG GGCCTGCGCC CCCTACCCGG 2220
GCCCCGGCCC ACCTGTCCGC ACACCTGTCC GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG 2280
GTCTGATCTG AGAGCCGAGC TCTCGGCAGG GATGGGGACC CAGGGCTCGG CCTGCAGGTG 2340
CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG GGCGTCCCTG CACTGGGGCT CCATCATTAC 2400
GTTCGCATGG CCACTCTAGC ATGGGAGGGG GGCAGGGCCT TTCCCTGTTA GTTCACTTCC 2460
CTGTTGGTAC TCACCCACCT GTCTGTGGAA AGGCAGCAAT GGTCGATTTC CCCCTTAAGA 2520
AACAAAGCGT GAAGGAGGAA GAGAGGCTAC AGGAATCTGC CATCCGGGAG ACCCTGTCTC 2580
TAACGGGCCA TACGGGGTCC CCCTGTGTCT CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2640