EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-00102 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:2135070-2137740 
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
TGAGCGGAGG GAAGATATCA GGCTGGGGCC GGCTGCTGGG CCTGTCCTCT CTGAGTTGCC 60
TCAAATCCCC TGTTCCTTGA GCGGTCCTGG AGCCTGGCCT CAGGCCTCAG GGCACCACAC 120
TACTTGCCTC CAGGGACCAG CCTGTTCACC CCACACCCAG CCCTGTGACA GAGGTGCTGT 180
CGCGTGGCCC CACTTACAGA TGGGTCAACT GAGGCCCGGG GCATCTGTCC ACTTGTCATG 240
ACAGTGAGCG GCCAAGCTGG ATGTGAACCC AGGTTTTTGT ATGCTGCCGC CCGGTGGGGT 300
TGGGGAGGAC TTAGTGGCAC CCACTGACCT CCCACTGGGG ATCGGGGTCA GGGAGTGAAG 360
TAAGTGCCTG GCTCTCCGAG CACCCTGGGG CAGCCCCTCC AGCCTGGGAG AGCCAGCTCA 420
CATCTGGGCA GTTGGTGAGG CCAGCTCCTG CCATCTCGGG TCCCCATGCG CTTCTCAGAT 480
GTGAAAGCCC CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG CCAACACCCA 540
GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC 600
GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG 660
CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG 720
CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA 780
ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG 840
AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC 900
TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC 960
GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC 1020
ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA 1080
ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA 1140
GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA 1200
GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT 1260
CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA 1320
GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG 1380
GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC 1440
CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC 1500
CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC 1560
CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG 1620
CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA 1680
AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG 1740
GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC 1800
TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC 1860
GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG 1920
GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA ACGAGTTTCC 1980
AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC AAGCCACGAG CGCGTCGCCG 2040
CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG TGCCCCCGCT GCGCCGCAGG 2100
CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC TCCTCCCATG TGCGCGGGAG 2160
TCCCTCCGCC ACTGTGCCCA GATCGCCGGC GAAGCGCAGG GGGAGGCTGG GAAGGGCATC 2220
GGGAGACACG GGCCTGCGCC CCCTACCCGG GCCCCGGCCC ACCTGTCCGC ACACCTGTCC 2280
GAAGCCTTAA AAGGTCTTCA TTCCTTTTCG GTCTGATCTG AGAGCCGAGC TCTCGGCAGG 2340
GATGGGGACC CAGGGCTCGG CCTGCAGGTG CCGTGCCAAT TAGGGCCCAG GCAGGAGAGG 2400
GGCGTCCCTG CACTGGGGCT CCATCATTAC GTTCGCATGG CCACTCTAGC ATGGGAGGGG 2460
GGCAGGGCCT TTCCCTGTTA GTTCACTTCC CTGTTGGTAC TCACCCACCT GTCTGTGGAA 2520
AGGCAGCAAT GGTCGATTTC CCCCTTAAGA AACAAAGCGT GAAGGAGGAA GAGAGGCTAC 2580
AGGAATCTGC CATCCGGGAG ACCCTGTCTC TAACGGGCCA TACGGGGTCC CCCTGTGTCT 2640
CCTGCAGCCC TGCACAGCCC CGGTCTGAGG 2670