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

TagContent
EnhancerAtlas ID
HS050-23648 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr15:75951600-75954520 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr15:75954298-75954311GGTGACAGCTGCA-6.5
MyogMA0500.1chr15:75954301-75954312GACAGCTGCAG+6.62
RREB1MA0073.1chr15:75952284-75952304TGGGGGTGGGGGTATTGGGG-6.08
Tcf12MA0521.1chr15:75954301-75954312GACAGCTGCAG+6.14
ZNF263MA0528.1chr15:75951828-75951849CCCCTCTCTCCACCCTGCCCC-6.1
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00448chr15:75950549-75956919Adipose_Nuclei
SE_01620chr15:75949399-75957459Aorta
SE_02426chr15:75952557-75954556Astrocytes
SE_03062chr15:75953622-75954438Bladder
SE_24007chr15:75952770-75953200Colon_Crypt_2
SE_25223chr15:75953125-75954151Colon_Crypt_3
SE_26310chr15:75951695-75954782Duodenum_Smooth_Muscle
SE_26676chr15:75950618-75960618Esophagus
SE_30075chr15:75952287-75954521Fetal_Muscle
SE_31932chr15:75951252-75954515Gastric
SE_34597chr15:75952501-75954488HCT-116
SE_36093chr15:75952406-75954880HMEC
SE_37864chr15:75951836-75955030HSMMtube
SE_41356chr15:75952281-75954601Left_Ventricle
SE_42347chr15:75950358-75957604Lung
SE_44203chr15:75951679-75957628NHDF-Ad
SE_44859chr15:75952132-75954746NHLF
SE_45931chr15:75952243-75954914Osteoblasts
SE_46892chr15:75952424-75952725Ovary
SE_46892chr15:75952820-75954363Ovary
SE_47752chr15:75953278-75953909Pancreas
SE_48850chr15:75951340-75954548Right_Atrium
SE_50411chr15:75951368-75957615Sigmoid_Colon
SE_52931chr15:75952661-75954579Small_Intestine
SE_53820chr15:75951189-75954605Spleen
SE_56214chr15:75952763-75956620u87
SE_64409chr15:75952140-75954652NHEK
SE_65676chr15:75951303-75952771Pancreatic_islets
SE_65676chr15:75952976-75954759Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr157595302475954441
chr157595184675952110
chr157595229475954348
Number: 1             
IDChromosomeStartEnd
GH15I075658chr157595106175963062
Enhancer Sequence
ACTTGGTGGA GGGAGGGCTT CCAGGGTCAA GGCCGTCAGG GAAGGTTGGC TAGACCAGGG 60
ACCAGGGAGC TTGTGCAGGA AGATGGAGAA GGGCCAGCAG GTGCGGTGGG GGAAGGGGCG 120
GGCAGGACTC CCTGTTCAGG GCATAGCGTC CTCAGAGGAA CTTCTGGAAT GGGTCCCCCT 180
GGCCCTTGGT CAACATTAGG TCAGATTTGG GACTTTCTGA GGAATTTTCC CCTCTCTCCA 240
CCCTGCCCCA TTTTCTAACC CATCCGAGGA ACTTCCCGCC CTTAACCTCT TCTCAGCTCT 300
GCCATCCATG TAGCCATCTG CAGAAGGGGC TCTGAGCAGT GGGGGCTGGG CCAGGCCGAG 360
GCAGGGCTGG TGGGAATGCT CCTCCTAACC CATGGTGCCT GGAAAGTCCC CTGCTCATGC 420
TTCCTGCTCT GGGAACAGTG TTGTCCTCTG TGTGCCTTCC TTGAGAGGGG ACCACCTCCC 480
AGGCCTTCCA TCCTCAGGGT GAGGCCATCA GTCTGATACT TTTCTCAGGA GGGACTTGGA 540
TCCAGGAGAA GCATCAGGAA GTGGAGTCTT GGGATAATGC CAGGCCTGCT CCTGGTATCC 600
TGAGGTCTCT GGGCTGGGGC AGGTGTGTGT GTGGCAGGGA GGGAGGCTGT CCTGGCCCTC 660
CTCTCTCTTT TCTTTCTGCC TCTATGGGGG TGGGGGTATT GGGGGAACTT GGGGCCGTTC 720
TGGGGTAGCT AAGCCCCTTT CAGCAGGAGA TTGGGGGACC AGTGTTGGGG GCATCCTGGT 780
GATGGCCGAT TCCTGCCTCG TCACATGCCA GGCAGATGTT CCCGACTCGG CTGGACCCAG 840
CTGCCTCGTT TCCTCCCTTA CTTTGCTCTG AGGGGGTGGA AAACAAGGCT TCTCTTTCTG 900
CCCTGGACAG CTACCAGCAC CCGGGGTAGG GGATCCCCTG GTCACCAGTC TTGGCCCAGT 960
ACAGGAAAAG GAATCCGCTT TGTGGCCACA GATGGGGGCT GGGGATGGAA GCAGACCTCA 1020
GATCCTGCAT CTCTTCACCC GCTGGACACA GGAGGGCTAT GAACCACTGT GCCGTGGCTG 1080
CACCACTGGC TGGAGCAGAG CCAGGCCTGG GAGAGGCAGG TGGCCCCATC GGCCCCTGCT 1140
CTGCACCACC CCTCCCAGAT GACAGAGCCA TATGTCTTCC ACGTGTCTAC ACACTCACAG 1200
ACTCACGAAT GTAATCGCTC AGTCTCACAA CAAGCACACG CAGTCACACA CCTGCCCACA 1260
GGCACATACG CCACATAAGC ATGCCTGTAT GCTCACACAG TCATACTGCC ACACGCTATT 1320
ACACATTCAC AGCCACAGCC ACACATGCCT TGCCATCCAT TCAAAGCACC AGTGGCTACT 1380
TTGTCAGACA CAGCCACACC ACAGTCCTAT GCACATGGTC ATAGCCTCAC ACAGTGACAC 1440
ATACTCGGGC ACACACCGCC ACAAAGCCAT GCTTGCACAG AGCAAAGGTG TCATAAGCAT 1500
CTCTGTGCCT GGACTGCACC TGCATGACCT CCCAGGGTCC CCACCTCATC AGAGATTAAG 1560
GAGAGCTTTG CTTGGAGACA CCACCCCTGG AGGGGGTGTC TCCAAGGGGG AGTAGAGCCA 1620
GTCACAAGCA CCACATACAG GCACACAGCC TGAGGTCTAG GGATGCAATT GGGATGACTG 1680
GATACCACCA AGTTCAGCTC CTTATTGAAC AGATGGGCGC CTGAGGCCCA GGGAGCAGTG 1740
GTGGCTGGCC TTATCACCCA GCAGGGCAGG GGATACTCTG GGGCCAGAGC CTGGCTCTGG 1800
GCAGACTCTG TTTCCTGGCC CTGCCCTCCC CTGGGCCAAT CCTCTGGGCC AGGCTGCCTC 1860
TGAAGGCCCC TGGCTGAACC GATCCAGCAG AGCTCCAGGC AGCTCCCTTC TCAAGCTAGA 1920
GCTGAGCTGC AGTGGCCACG GGAGCCGGAG CCAGGATGCG GTGGGCAGGG CCTAGGCCTG 1980
GGCGGGAGGA ACATTCCTGC ACCATCTCCT CCCCAAGCAT GTGAGGACCC AGCCCGCCCT 2040
GCCCGCCTGC CCGCTGACTC AGGCCTCCAG GAGCCAAGCC TGCTCAGCTC CCCCACCCAC 2100
CCTAACCTGC TTCCCCACTA GTTCGGCTCT GGTTCCCCTC TCCACTGGCT GGGGCAGGAG 2160
AAGACGGTGA GCCCTGGTAG GAAGACCATG GGGAAAAATC AAACCTCACC ACCCCCCGAC 2220
ATAGCTCAGA AGGGCTGATT GTGAAACCCA GCTCTGTTCA ACATAGTTGA ACACAAACTT 2280
TTTTTTTCTT TTGGTTTGGT TTTGTTTTGT TGGTCAAACC CCAGTGCAGT GCAGTCTGTT 2340
TAAGAAGTAG TGTCGCATAG CTGTGGCCTG GATCTGCTCA GCAGCCCCAG TAGGCAGCAT 2400
TTATTCCCTT TCGCAACAAA GAGACTGAGA CTTGGCCAGA GGGAAGATGG GACCTGCCTA 2460
GGTTCACACA GGGAATCTCT GGCGGGGCTG GACTCAAACC CAGCTCCCTG CCATCACTCC 2520
TTAGAGTCAC ACTGATGAAC TCATTTAGGG CCAAAGGAAG AAGGGGAGGC AGATTTCCCC 2580
TCTAGATGAG TGAAGGGATA GGAGGCTGGT GAACCCAACG GCTGAAATGT GAAGGGTGAG 2640
AGGGTAGGGT GAGTCCCCCC AGCCCTGAGG GATGAAGGGT CTGAAGATGG CACTGCACGG 2700
TGACAGCTGC AGTGACTCAG GAGCTCCGTT TACAAAGGAA CATGAGTGAG GAACATAACT 2760
TAATTTTTTT TTATATCTGA CCTGAATTTC TGTTTTCCTC CCCCATTCCC CACATGGTAG 2820
AAGTGTAATC TCACATCAAT TTGGGGACCC TTTCTTTCCC CAGGGATGTG TAGAACTTTT 2880
GGGGATGGCA CATTTGAAGA CCTTAGGGAG CTTTGCATTT 2920