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

TagContent
EnhancerAtlas ID
HS098-00061 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr1:2135590-2137210 
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
GCCTCACAGG CCAACACCCA GCGGCTGCAC TGCCCATGGT CACTATCTCT GCAGCCCGCG 60
TGTGCGGCCA GTGTCCCTCC GGTGACCCCA GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA 120
GCATCGTGAG CCGTGGTCTG CCGTCCTGGC ACATCCTGAA TGGAGGTGCA CGCATAGAGG 180
CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA GGGATTTGCC CCCTTCTGGG ACGTGCCCTG 240
GGGACGGTCA GTTCTCCCAA ATAGTGACTT CCTTTCTCCA CATAATGAGA GCCTTTGGCT 300
GAGGGATTGG GAGGACCAGG AAAAAGCCGC CAGGCCACGT GGGGCGTGAC TTGGCGATCC 360
CGGTGGCTCC GGGCGTCAGC TTGGACCTCA GACGCCCCTC ACAGCTCACA GCCCTGTGGC 420
CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC CCCCGGGAGC CGGAGAACCC GCAGGACGTC 480
AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG ACCCCACTGC CCAGCGCCTT CAGGACTAGC 540
GGATGATGGA CTTGTGCTAA ACTGGCTACG ACCCCTCCGG AGCAGGGTCC TGGGTAAATC 600
AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC 660
CCCACCTCAG ACCCGAGCTA GCTCTCCAGC CTGGTTCCTC TGCCGGACCC TCCTCCCGGG 720
CACCTCCCAC GCCCCGCCCT CAAGCCCCGC CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC 780
CCCCATACCC CGCCCCTCAA GCCCCGCCCC GCCCCCCGGG CGCCACGCGC CCCGCCCCTC 840
AAGCCCCGCC CCTCCCTCCG GGCTCCCCAC GCCCCGCCCC TCCCACGAGG CTCCCTCACG 900
CCCCGTCCCC AAGCCCCGCC CTTCCCCCGG GCTCCCCCAC GCCCCGCCCC TCAAGCCCCG 960
CCCCCCAGGC GCCCCACGCC CCACCCCTCA ATCCCCGCCC CTCCCCCGGG CTCCCCCCAC 1020
GCCCCGCCCC TCTTTCCGGC CCCCTACGCC CCGCCCCCGC TCCTCCTTCT GGCCCTTCCC 1080
TTGCCCCGCC CCTCCCAGTG CCACCGTCCT TCCAGGCAGC GCCCACACCC CGCCCCTCAT 1140
GGGCACCACC CACACAAGCA AGCCCCGCCC CGCAGGGTCC CGCCCACGTT CCGCCCCACC 1200
CCGCCCCAGC TGTGTCCTCG GCGCCCAGCC TGGGGCAGCC GTCCCCGTGA GCCCCGCGAG 1260
GGGAGCCTGT CCCAGCCACC TCGCCGCTTC AATTTCCTCC AGGTCCACAG GCCCAGCCCG 1320
GCGCGCGCCG CTCGTTCTGC GACCTCCAGG GCGAGCGCGC TTCCGGGGCG GCCGTGCAAG 1380
AGGCGTGGGA AGCGCGCGGG GGGTTCTGAG CGTGCAGTCG CCGCCTGCGG ACGGCGAAGG 1440
GGCGGGTGAA ACGAGTTTCC AGCGTCGAGC CTGCTTCGTT TCAAGGTGGA CGCCACATGC 1500
AAGCCACGAG CGCGTCGCCG CACGGTGTAC GCCCACGGTC CGGGCCGGGC GTTCTGCGGG 1560
TGCCCCCGCT GCGCCGCAGG CCTCAGTGGC GCGCCCGGGG ACTGGAAGGC TGAGCCGCCC 1620