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

TagContent
EnhancerAtlas ID
HS149-01109 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr8:26465820-26467910 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr8:26467444-26467462CCTTCCTCACCTCCTCCC-6.05
ZNF263MA0528.1chr8:26467440-26467461CTATCCTTCCTCACCTCCTCC-6.11
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00237chr8:26465142-26475244Adipose_Nuclei
SE_00830chr8:26467254-26467615Adipose_Tissue
SE_01375chr8:26465977-26466319Adrenal_Gland
SE_01375chr8:26466404-26467724Adrenal_Gland
SE_01900chr8:26465859-26474746Aorta
SE_03143chr8:26465813-26471505Brain_Angular_Gyrus
SE_03863chr8:26465434-26478517Brain_Anterior_Caudate
SE_04776chr8:26464076-26478256Brain_Cingulate_Gyrus
SE_05786chr8:26465177-26478320Brain_Hippocampus_Middle
SE_06684chr8:26463418-26476093Brain_Hippocampus_Middle_150
SE_07727chr8:26465285-26478125Brain_Inferior_Temporal_Lobe
SE_08783chr8:26466077-26466911Brain_Mid_Frontal_Lobe
SE_08783chr8:26466984-26469137Brain_Mid_Frontal_Lobe
SE_09397chr8:26465423-26471739CD14
SE_25935chr8:26465140-26474279Duodenum_Smooth_Muscle
SE_29761chr8:26465455-26470206Fetal_Muscle
SE_36469chr8:26465475-26470176HMEC
SE_37890chr8:26465139-26470003HSMMtube
SE_38508chr8:26464677-26469653HUVEC
SE_40698chr8:26465830-26476005Left_Ventricle
SE_42132chr8:26465786-26476382Lung
SE_44172chr8:26465502-26472741NHDF-Ad
SE_44989chr8:26465538-26469979NHLF
SE_45747chr8:26464992-26470266Osteoblasts
SE_46934chr8:26465945-26467798Ovary
SE_48590chr8:26465766-26475508Right_Atrium
SE_51048chr8:26465875-26474787Sigmoid_Colon
SE_51461chr8:26465387-26473669Skeletal_Muscle
SE_54115chr8:26465910-26469831Spleen
SE_55019chr8:26465376-26473878Stomach_Smooth_Muscle
SE_55993chr8:26465456-26470105u87
SE_65620chr8:26466545-26469891Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr82646620926466513
Number: 1             
IDChromosomeStartEnd
GH08I026607chr82646471826475916
Enhancer Sequence
AGTGACTTTT TTTGGATGAT TGGATGAGTC ATGGAAGATT TTATTTTTTT TCTCCATTCT 60
TTCTGGTGTT CCAGGGTTTT GGCATTGAAG TACTTTTGTA CTTAGAGGAG TTTTATAAAA 120
AACAAAAGTT CCCTTTGAGG GATACTTTGC ATCTGGACTG TTATCTCTTA CCCACATCAT 180
TCTTGAGGAC GAAGAGAAAA TACCTGTGAG GAAGTATTTA CATTTGTTAC GGTGGTGCTG 240
GGCTGAGTTT GTGTGGACCC TGGACTCCCA GCTGTCCACA CAGTTATAAA GAGTAATTAA 300
AAGCTCCCTG AACAACAGGT CCCTTATCAG CCTTAAACCT TATTGTTCAG ATACATTGGC 360
TTTTATTCAT AGTCTTACTA ATCAACTGGG GACAAAAAAG ACCCATTGAA CCATTAGCCC 420
TCAGCCCGAG ATGAGAAGCG CATGATGGTA CAATGGCCGT GGTTCAGACT CAGATGTTAT 480
GCTATGTTTT GAATTCAGTC CAGGTTCCTA GGAGGAAAAC ACCCATCAAA TTATGTTGGC 540
TTTAGAGCGA TCTCAGTCAA CAGATGACAT CACCGACTTT TCCTTCCCTG CTGGTCTTTA 600
TTTGGAGGGG ATGCAAGAAT TGTGCAACCT TGGAATAAAC AGAATAGAGA CCCGACTCCT 660
CACTCATTGT GTTTCTGAGT TTAGTTTCAA TCCAACAGCG GATCTGTTTT TTTACTCCAT 720
GTAATGGGAC TGTTGCTGCA GCTTTTGTAC AAGGGTGGAG TGGGTGTCCA TTTGCTGACG 780
AGCACCCTGT GTACACGCTA GTTTTTATTT GAACGAGGTG CTCTTGTCTT TATTATGTAT 840
TGTCTGCCCA TAAATGATGT CTTGAAATAG AGGGGTGAGC ATCACCTCAT TTATTTCAAC 900
CCATATTTGT ACAGAAGGAT TTTTGTAATC AAATCATGGG GTTTGTGTGT AGAACTCAGT 960
AAGAAGTAAT CATGACCCTG TCCGTTCATT TGCTCTTTGT TCTTTCCTGT TATTAACAAT 1020
GGCTTTGGGG CTTTTGGGGC GCATTTAGTT CTGCACGTTG TGTATGTAAG TAGATGTTCT 1080
TCTGTGGGGG CTGCAAGTCC TTAAGTTATA GTTGGATTCC CTTCCCAGCA AGGAACCAAC 1140
AGGAAGGAAA ACGAAGTCAA ACCCAGTCTT TGCACGTGGA AGCTTGTGGC GTGACTGTTA 1200
TTTTTTTGTG ATGTTCTGTA CAGCCCTGTA ATCTCTTATT TTTGGCAAGC CAACTCTGAA 1260
TCTGTGGTCC CGTAGCCCCA GGCAACCAAA AGCTGAGACA AACAGAGGAA GTGTCGTTAT 1320
TCACATGTTT CTCTGGCCAC CTCATCGGGC TGGACGCTGC CGGCTGCCAC CCGTCGCTGA 1380
GCTGGAGCTC CCCAGAGTGC AGCCTGGCCA GGCAGGGACT GTTGACCCTG GCCCCTGTAG 1440
GAAGCACCTC TGGCTTGTCC CCCAGCCCCC AGGGTCCCTG CCACTCATTA CTTCTCTGCA 1500
CTCTTTCTGT AATTTGTTCA TCGCCTGGAA TTTATTTCTG GCAGACTTTG TGGTCAAAAC 1560
TGGGAAGTGT CTGTTTCCTT AAAACAGCCT TTCCTCAAAC CCAGGAAGTG AAGTAGGGAG 1620
CTATCCTTCC TCACCTCCTC CCTGTCACAT GCACATGGGC ATACACACAC GTACACACTC 1680
ACCCATGTGC ACACACACAG GCACACACAT GAGAAAGGGA CGGGGAAAGC TAGGGTGTCC 1740
ACCCCAGCCT GGGCTCCTGG TATCCCTAAG GGTTTTGGAA GAAGAGTTTC AGTTTTTCAA 1800
AGCCTGCTGG AGATGTAACT GTCGTGATGT TTCGTGGGAT CTGCAAGAGC CTGTAGCGTC 1860
AGGTTTCTTT CCTTTTGATT GGGATGACAT GAAGTCTGTT AATGCGGGAT CGTTTGTGTT 1920
ATCTGCTCTG ATAGGTGGTT TTACTTGCAT TTGATTTTTG ATAGAATGAG AGATGAATTG 1980
ATTTGTTCCT GATACATTCT GTTGGGATAC AGTCCATTTG ATAGGAAGGT TGTTTACATC 2040
ACAGTGTCCT GTATTTGGGG GCTGCCCTGG GATGTGAAAA GTCTGTTTAT 2090