EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS007-00027 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr1:2135630-2137040 
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
CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG 60
CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA 120
TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC 180
CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA 240
CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT 300
GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC 360
ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC 420
CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC 480
CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG 540
AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT 600
TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC 660
TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC 720
CCCCTCCCTC CCTTCGGGCC CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG 780
CGCCACGCGC CCCGCCCCTC AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC 840
TCCCACGAGG CTCCCTCACG CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC 900
GCCCCGCCCC TCAAGCCCCG CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC 960
CTCCCCCGGG CTCCCCCCAC GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC 1020
TCCTCCTTCT GGCCCTTCCC TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC 1080
GCCCACACCC CGCCCCTCAT GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC 1140
CGCCCACGTT CCGCCCCACC CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC 1200
GTCCCCGTGA GCCCCGCGAG GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC 1260
AGGTCCACAG GCCCAGCCCG GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC 1320
TTCCGGGGCG GCCGTGCAAG AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG 1380
CCGCCTGCGG ACGGCGAAGG GGCGGGTGAA 1410