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

TagContent
EnhancerAtlas ID
HS146-07488 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr19:13146690-13149010 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr19:13147131-13147143AATTGTTTGTTT+6.22
JUNMA0488.1chr19:13147717-13147730ATGACATCATTGT-6.33
JUND(var.2)MA0492.1chr19:13147716-13147731CATGACATCATTGTT-6.31
MEF2AMA0052.3chr19:13147560-13147572GCTATAAATAGC+6.32
MEF2BMA0660.1chr19:13147560-13147572GCTATAAATAGC+7.22
STAT1MA0137.3chr19:13148905-13148916TTTCTAGGAAA+6.14
Stat4MA0518.1chr19:13148905-13148919TTTCTAGGAAATCG+6.71
TCF7L2MA0523.1chr19:13147938-13147952TTCCTTTCATCTTT-6.1
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00024chr19:13106663-13152679Adipose_Nuclei
SE_01540chr19:13146555-13152186Aorta
SE_02418chr19:13146930-13149222Astrocytes
SE_02988chr19:13146715-13147274Bladder
SE_03137chr19:13146606-13150036Brain_Angular_Gyrus
SE_03859chr19:13122647-13152397Brain_Anterior_Caudate
SE_04900chr19:13122231-13152649Brain_Cingulate_Gyrus
SE_05829chr19:13106701-13152645Brain_Hippocampus_Middle
SE_06678chr19:13122257-13152530Brain_Hippocampus_Middle_150
SE_07717chr19:13121683-13152553Brain_Inferior_Temporal_Lobe
SE_08780chr19:13147656-13147889Brain_Mid_Frontal_Lobe
SE_08780chr19:13147901-13148150Brain_Mid_Frontal_Lobe
SE_24497chr19:13146599-13148284Colon_Crypt_2
SE_26006chr19:13147099-13150343Duodenum_Smooth_Muscle
SE_26520chr19:13115825-13152105Esophagus
SE_29659chr19:13146615-13148669Fetal_Muscle
SE_31390chr19:13146667-13148302Gastric
SE_33451chr19:13144165-13152481H2171
SE_35947chr19:13144135-13150253HMEC
SE_40665chr19:13140190-13152144Left_Ventricle
SE_41557chr19:13146608-13149043LNCaP
SE_44148chr19:13146369-13152359NHDF-Ad
SE_44758chr19:13146614-13149434NHLF
SE_45899chr19:13141968-13150175Osteoblasts
SE_46652chr19:13147816-13148178Ovary
SE_47172chr19:13147501-13149537Panc1
SE_47634chr19:13147043-13147436Pancreas
SE_48559chr19:13146540-13152163Right_Atrium
SE_50434chr19:13146459-13149100Sigmoid_Colon
SE_51076chr19:13106668-13152566Skeletal_Muscle
SE_53207chr19:13146595-13149076Small_Intestine
SE_54519chr19:13146519-13150287Stomach_Smooth_Muscle
SE_56594chr19:13147427-13149541u87
SE_64579chr19:13142213-13148771NHEK
SE_67980chr19:13100968-13183275TC32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr191314742413147812
chr191314721013148787
Number: 1             
IDChromosomeStartEnd
GH19I013030chr191314113613149343
Enhancer Sequence
TTTGTACCCT TGCCCGCATC ATCCCAAGTG CAGAGCCAAT GTCCCTGTCT TCTTTTCCCT 60
GAGGTGACAG TTTCAGCGTG TCATTCCTGG GAGGAGTGAC CAACAGGGCA TGTACTGGTG 120
TCTGAGTGGT TAGGATCCCA CTCTGGGGGA TTCCTGCTGG TGGTATAACC CCGACCACAG 180
AAGTCAGGGC CTAAGCCTCA GCCTGCCCTG AGATCCCCAC CAAGGGGGCT GCGGCTGGAG 240
GGAGGGGCCC CTGGGAAGTA TCCTGCTTGG CTGCACCTGG CTTGGCCTCT GGAGTCGACT 300
TCCCAAGTCT CCTAGGAAGG CGAGGGCTCT CCTTCGTGTG GAGTAGACCC TTCGCCAACT 360
GGCCTGGCGT GTCCGGGAGG CTTCCTTTCT TAAAATGGGG GGATGAAGCG TCAGTCATGC 420
TTCCAGGATT TATTTCATCA TAATTGTTTG TTTTGGGTTT AACAATACAG CAGGGAGAAG 480
AGTGGCAGAG GAAGAAGAGC GTCCTCTCCA GGCCAGGGGT GGGGCTGTGG AAATGAGAAA 540
CCGGACGAGA CAGAGAGGGA ATCCAGAGAG GGCTTTGCGG TTGAGTCTGC CAGTCTGGAG 600
AAGGCTGCTC TCCAGACAGC TGAGAGTAGG GTGACACCTG GTGACTCTTG TGGACTGGGC 660
GGAGCTGTGT GGAGCGATCG GGAGATCCCC GGAGGCGACC TGCAGGAGGC CAGCCGAGTG 720
CAGCCCTTGG GGAGTGTGTC CTTATTATGC CTGCAGATTA TATCCCCATT AGCGCATAAT 780
TATTATATAA TGGGCGTTAT TGCATAATGG CAGTTATATA ACAGGTGGCC CAGAATACAG 840
ACAGGGGGTG TAATAAGTGT ATATCCTCTG GCTATAAATA GCCACCAGCC CCACACCAAA 900
TATGTGGTCA CACCAGAGCC ACCTTATAAA TACCCGTGCT GGGCTATAAA TTTCTGAGCA 960
GTGACGTCAG CGGGCATGGT ACCTAGTTAG GGGGTGGTAG GAGGGACCTG CGGCCCCACC 1020
CGGACACATG ACATCATTGT TTCCTTAGTA ACAGGAATGC TCCCGGGGGA CCAAGTGAAG 1080
AAAGGCCTTT AAAGGGAGGA GGCAAATGGA TAGGAAGCTT GAGTTGGGGG TGGGTGCTAA 1140
GCCTGGGCTG AACAGGGTGA GGTCTCCTGG GCAGAGTCCT TAATGGGTGA GACAGGCCAT 1200
CTGCCCTTGG GTATTTGACC CAACGGGAAG CAAGGCAGTA GACTCCGTTT CCTTTCATCT 1260
TTAGGGGGTC TCAAGTCCCC TTTCCTGTGT GTAGCAGATT CTGCCAGCCT TGGCTGTGTG 1320
TCAGGGAGAA GAGGGGAGCT ACAGAGTCTT CCCTGTCCTT CTCTCTCCCA GGTGACCTCT 1380
ACAGGGCTCT GGGGCCACTT GCTTAAGGGA GACCCGACTT CTGCACCCGG TCATATCCTC 1440
CCCAGGGCAT GACCACTTCC CCTACCAGAC GTAGTAGGCC AGTTTCAGCC TTAGTAATCT 1500
AAGAAATATG TGAGCAATTT GATGCGGATC TCAGAGAGCC TCGTGGAAGT AATGGCGCTG 1560
AGAGATGGCG CCTGGGGAAG AAAGAGGAGA CAAGGATAGT ATTCTGGCCC CAGAAGAAAC 1620
TATGAGGTGG GATATAATCT TTTTAGGTGT ATGGGAGATT GCTTCATATA GGGTGGGGAA 1680
GAACTAGTCT TCATAGCCCT GAGCATAGAG GAGGAAATTT GCCTTTGGCA GATGAGGGGA 1740
TTGGAAGAAG GCTGGATGAC CAACTCGTCC TGGTTTGCTC AGAGTTTCAC AGCCCCTCAC 1800
CTCGGTAAAC CCCTCAGTCT CCAGCAAACT GGGATTGTTG GTCACCCTAG AACAGTGATT 1860
TTCAACCAAG GGCAATTTTG TCCCGCAGGG AACATTTGGC AATGTCTGTG AACACTTTTG 1920
GTTGTCACAG TTGTGGGGGG AGGGTGCTAT TGGAATCTAG TGGGAAGAGT CTACTGCATA 1980
TGACAGTCCC CCAGGAACAA AGAATCATCT CGCCCCCAAA CGTCACAAGT GCGGAGGTGG 2040
AGAAACCCAG CCTTAGAGGG AGAATAAGCA GACCCTGCTG TGCGTGGTCT CTCCTCAGGA 2100
CGCCTCTTGC CTCTGCTAGC AGAGTGGGCT GCTTGGCTGC CTTCCTGAAT TTCTTGCAGC 2160
TCTTGTTTTC TGTGCTTTGA TTGGTTGTGT TTAGGGTTCT GTGGCCTGGA AACCTTTTCT 2220
AGGAAATCGT GTGGCTTCTG AGAGGGTCTT TCCCATCTCA AAGCTCAGAG ACCCTTTGAG 2280
ACAGTGCCAT CTCAAAGTGA GACAGTGCTG ACAGCAAGCC 2320