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

TagContent
EnhancerAtlas ID
HS007-13810 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr5:139075810-139078650 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr5:139077207-139077218GGCCACACCCA+6.62
RREB1MA0073.1chr5:139076961-139076981CCCCCATTCACCCACCCCCG+6.5
ZNF263MA0528.1chr5:139076727-139076748AGAGCAGGGAAGGGGGAGGGA+6.26
ZNF263MA0528.1chr5:139078403-139078424CCTCCCTGCTCCCTCTGCTCC-6.43
ZNF740MA0753.2chr5:139078572-139078585ACACCCCCCCCAC+6.82
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_03140chr5:139077222-139079757Brain_Angular_Gyrus
SE_03865chr5:139075665-139079795Brain_Anterior_Caudate
SE_04768chr5:139075791-139079817Brain_Cingulate_Gyrus
SE_05771chr5:139074803-139079842Brain_Hippocampus_Middle
SE_06683chr5:139075852-139079604Brain_Hippocampus_Middle_150
SE_07722chr5:139075367-139079904Brain_Inferior_Temporal_Lobe
SE_08785chr5:139076058-139076350Brain_Mid_Frontal_Lobe
SE_08785chr5:139077255-139077604Brain_Mid_Frontal_Lobe
SE_13414chr5:139075806-139078377CD34_Primary_RO01536
SE_25255chr5:139076350-139077533Colon_Crypt_3
SE_27739chr5:139075790-139079429Fetal_Intestine
SE_28684chr5:139075714-139079698Fetal_Intestine_Large
SE_29581chr5:139075776-139079395Fetal_Muscle
SE_30930chr5:139075948-139078068Fetal_Thymus
SE_31417chr5:139075889-139079477Gastric
SE_33374chr5:139076434-139077140H1
SE_33677chr5:139075744-139077639H2171
SE_34346chr5:139075888-139078466HCT-116
SE_36941chr5:139068133-139079024HSMMtube
SE_40547chr5:139075555-139079970K562
SE_40649chr5:139075743-139079459Left_Ventricle
SE_42197chr5:139075725-139079407Lung
SE_45813chr5:139071957-139078550Osteoblasts
SE_47460chr5:139075818-139078710Pancreas
SE_48055chr5:139075785-139078204Psoas_Muscle
SE_48579chr5:139075882-139079587Right_Atrium
SE_49460chr5:139076628-139077101Right_Ventricle
SE_51090chr5:139075721-139079481Skeletal_Muscle
SE_53351chr5:139075859-139079558Spleen
SE_55117chr5:139076126-139077598Thymus
SE_55730chr5:139075803-139078946u87
SE_58504chr5:139012442-139092243Ly1
SE_59951chr5:139067745-139092302Ly4
SE_63555chr5:139075583-139078253HSMM
SE_65250chr5:139075601-139078895Pancreatic_islets
SE_67548chr5:139075803-139078946u87
SE_68692chr5:139075792-139079343H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5139076374139076603
chr5139077054139077268
chr5139078128139078514
Number: 1             
IDChromosomeStartEnd
GH05I139683chr5139062979139081910
Enhancer Sequence
ATTGCATCAT TGCACTCCAG CCTGGATAAC AAGAGTGAGA CTCAGTCTCA ACAAAAAAAC 60
AACAAAAAAA GAAAGTACCC AACCTAGGGC CCGGTACATA GTAGGTGTTC ATTAAATAGC 120
CTTGATTGCC AGGGATATCA TCAACACCGT CATCATGACT GAGTCCCTTC CAGCAGCTGG 180
CCCTGAGCCG AGGGCTTTAC AGATATCTGT CACCATTAGC ACATGGTGCT GTCGTCCCAT 240
TCTGCGGAAA GCAAGGCTCA GGCTAGGGGA ATAAGAGTCC AGGGTCACAC AGCCTTTGAG 300
GTAGGTGGCC TTGCTGTATT TCAGGTTCCT AGAGGAAGAG CCCTAGGAAC AGCACTCCCA 360
CACAGTGCTC TGCTTCTCGA GCTGAAGAGG TTTCATTGAC TCCTTTTTTC TGCACCTGCC 420
CTGTGCTCCT GGCCTGGTCC GGTAGCGGGA CGGGGGCGAT CAGTCTGGAG AGAAGACAGC 480
CCCAGGAACT AAGTCCCAAA GGAGTGTTCT AACCAGAGCT TGTGGGAGAT AGACGGGCCT 540
CCTTGGGCGG CGGGGGGCTG TGACTGCGGA CTGCCCCGAG GTGCGAGCTG GTTCAGTGTT 600
CTAAGAAACT GAGAGAATGG AGGATGGGCA AGGCAGGTAG CAGGACCTGC AGGAGCAGAA 660
CGGGGAGGCT GGAAAGCCTG GGGCCAGGCC TGTGGTGGGC AGGGGAGGGT GCATGATGAG 720
GGGGTGGGAA CACGGAGCGG GTGAGTCACC GTTTCTGGGC CAGGCAGGCG GCGGCTGCAG 780
AGCGGGGGGC GCATTCCTGG CTGGCAGGGC GGCCGGCACT AATGTCTTTC CCACATGGCC 840
CCGAATTCCC CGCTCGGCAC GATCACACGG GCAAGACGCT CCCGCGGCCA CCCCCGCCCC 900
AGCTGCCTCC TTCCCACAGA GCAGGGAAGG GGGAGGGAGT GTGGTGGAGG CTGGCGGAAC 960
CGGCCCCTCC TGGGGCGGGG TGGGGGTCTC TAGCGTGGCC TCCCTGGGGC CTGCGCCCAC 1020
GGTGTCGGCA CGCGATGAGC GACTCACAGG GCAGCTGCAG TCACAGTGAG AGCAGGGCCG 1080
CGCTTGTGAA GCGGAGAAGG AAGGAGGCCG GGAACCGCCT TGGGTCTTTG GCCACGTCTC 1140
TCCTTCCCTG GCCCCCATTC ACCCACCCCC GCCCTGGGTC AGGCTTTCCC TCGCGCTGCG 1200
GCTGTCGGAG GGCCGCGGCC GGATAGGGAC AAGCGGCGGA GCAGCAGCAA GTCCGGCCGC 1260
CTCCGATCCT ACGCCTTCTG GCCCTCCCCT CCTTCCCGAC CTCTGGGCCT GGCTGGTGGG 1320
GGGCGGAGTG GGGAGTGGGG GGACTGTGCC GCTGCCGCTG CATCCGGCGG GGGCCTGCTG 1380
GGGTGGTTCC TGGAAGAGGC CACACCCAGT CCCTCCCTCC GTGGGATGGA GGCCAGCCCT 1440
TGCTAAGGCG AAGGGAACTA GGAGCGCCGC TCTCCCACGC AGCCCCTGTC CCCAGGCCAG 1500
GTCCTGGAGA GGGGGGAAAC TGAGGCTGCT GAGAGGGCGG CCCACCCAGA GCTCCCTGTG 1560
CTGGGAGAGG TTGGCCGCTG TCCCTCCCAG CTGGGCTCAG AGGCGCTAAT GAGAGTTAAA 1620
TGTAGGACGT GAGTCACCTC TAGGAGGGGG CTGGGACCAC CCCCAGATGT GGGTCCAGAC 1680
GCTCAGGCTT TTTCCTACTC CCCTGTGTGT CACCCCCTAC CCTTGGCAGG GTGGGGCATG 1740
AGTTCTGACC TTGCTGACCA GGCTCTGTCA CCCTGGACCA GCCTCACTTA AATGGCTGGC 1800
TGCCTCAGGA GCGGGTGCTG TGGGACCACA GGAGACTCTA AATCCCGGGA TAGGCCCAGT 1860
GGACCCTGAG GACTTAGGGG ATGGACCAAC ACCTGGGGTC TCTAGTGGCC GTGAGCCCTG 1920
GGGTGTGGTC ATGGGTCTTG GGATGGGGGT GGGCAAAGGG CCCAGGCCAC CCTGAAGATT 1980
TCCCCACCCT TCTGCCTGCC TGGCTTTGCT CAGGCCACGA GGCTCTGACC ACACAGGGTG 2040
CCTGTTCCCC CACTCCCCAA AGTCCCACTC TCTGACCTTC AGCCGGCACA AGGACCTCAG 2100
TCTGAAGTCC TTATGGCAGG GCAGGCAGTT TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 2160
TGTGTGTGTG TACACACGTG TGCCTCTGCG GCTGGGTCTA TTTGTGCCGC TGTGTGTATT 2220
TATGACTGAA TGTACAATCG TGTATATTTA TGTGTGACTG GCTGTCTCTG AGGGGTCTCT 2280
CAGTGTTGCA GGGGGCTTGA CAGGGAATGT GCATTTCTGC GTCTGTATCT GTTTGTTCCT 2340
TCTATGTCTA CATGTGGGTC TTTCTGTGTG ACTGTGTTTG TGTCAGCCTG GCCCCATCTA 2400
TGGGGTCCCT GCCTCCTCAA GCACCCCACC ATCACCAGGA GCCACAGGCA TCTGGGAGGA 2460
GACTCGGGAG GTGAAGCGCC TGCTGTTCCC CAAATGGAAT GGCTTAGCTG GGTGGGCAGC 2520
ACCAGGGGGT GGGCGTGGGC AGCCACAGGA GAGAGAAAAG TGGAGGCCGG GGAGGAGCCC 2580
TACTCAGCAG TCCCCTCCCT GCTCCCTCTG CTCCCAGCTC AGCGCCTCCT GGCAAGAGCT 2640
TATTTGCATG GTATTTACAT TTCATTTGCA TCGTGTTCAA TTAAAAACCT GACCAGCTCC 2700
CGCCTGCCTG GCGCTGCCCG CCCAGCCTGG TGAAAATGTT GGTTGGGCAT GACAGCCTTC 2760
CCACACCCCC CCCACGCCCC CACGGACTGA CCGATGTGGG AGGGGTCCTC CCCTCATTGA 2820
GATCATGCAA GTCACCCACT 2840