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

TagContent
EnhancerAtlas ID
HS180-30202 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr20:47354630-47356380 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6066835chr2047355009hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr20:47355227-47355240GGGGACAGCTGCT-7.04
MyogMA0500.1chr20:47355230-47355241GACAGCTGCTG+6.14
SOX10MA0442.2chr20:47355989-47356000TCCTTTGTTTT-6.32
Sox3MA0514.1chr20:47355990-47356000CCTTTGTTTT+6.02
Tcf12MA0521.1chr20:47355230-47355241GACAGCTGCTG+6.02
Number of super-enhancer constituents: 23             
IDCoordinateTissue/cell
SE_01671chr20:47354368-47357034Aorta
SE_03141chr20:47353753-47357193Brain_Angular_Gyrus
SE_03860chr20:47352646-47357274Brain_Anterior_Caudate
SE_04767chr20:47330290-47357597Brain_Cingulate_Gyrus
SE_05768chr20:47330773-47357344Brain_Hippocampus_Middle
SE_06681chr20:47321409-47357433Brain_Hippocampus_Middle_150
SE_07719chr20:47329977-47357562Brain_Inferior_Temporal_Lobe
SE_08847chr20:47354585-47355007Brain_Mid_Frontal_Lobe
SE_09151chr20:47353839-47357374CD14
SE_11697chr20:47353783-47356584CD20
SE_14588chr20:47354199-47356996CD4_Memory_Primary_7pool
SE_16488chr20:47355140-47356190CD4_Naive_Primary_8pool
SE_18054chr20:47354068-47357368CD4p_CD25-_CD45ROp_Memory
SE_18819chr20:47354063-47357233CD4p_CD25-_Il17-_PMAstim_Th
SE_19386chr20:47354052-47357337CD4p_CD25-_Il17p_PMAstim_Th17
SE_20065chr20:47354132-47357341CD56
SE_22493chr20:47354199-47357283CD8_primiary
SE_32607chr20:47354044-47358612GM12878
SE_42516chr20:47353714-47355907Lung
SE_42516chr20:47355916-47357322Lung
SE_50554chr20:47354020-47356510Sigmoid_Colon
SE_53697chr20:47354561-47355631Spleen
SE_65415chr20:47354581-47356039Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr204735599447356352
Number: 1             
IDChromosomeStartEnd
GH20I048738chr204735407447357229
Enhancer Sequence
TCTCCACAGA GATGAAGGGA AGGGACTGGG CCAGAAAGCA GGGACAAATC GGTTTCTTCC 60
CACATACCAA CCCCAGTCAC TGGGTAGTGC CAGCTGGAAC ACTGGTGAGG AGGATTCTGG 120
GGCCCCACAG GAAGCCTAGA GACAGAATGC TGTGATTGAT TAGGAATGTC TGCCACAGGT 180
GCAGGAGAGG GGGTAACAAG CTCACCACTG GTTTGTCATT CCTCATCCCC TGAGCCCCCT 240
TCTACGACAA GGTCTGCAAT GTTTTCCTCT CCTTCAGCCT GTGGGAAGGG CAGGGGCCCA 300
ACGCTTGAGG CTTGGAGAAG TTAAATTTAG CAAAGGACAA CATCCCCTCT GCAGCACCGT 360
GCCCAGTTCA ATCACGCCTG TGTCCTTTCA TCCAGCCTGA CCCCAGCTGC ATCTCAGGCC 420
TGAGACCCTG CAAATACGGA AACGCTGCTC TTGACAGCTC AGAGTCCAAG TGTTCCATTT 480
CCTCCTGGAG GCCCGACATG GGGCTCTGAT TGCTTTGCCA GGAAGAAACG GACAAACAGT 540
TGTGCATACA CAGATGTGGT GGGTACGGAA CATGTGGCTG TGGGTTTGGG GGGAGAAGGG 600
GACAGCTGCT GGCTGGAAAC AGCCAGGGGA GGGGAGCTCA CCCCCAGGAA AGGCTCAAGG 660
ATTGTGAGAG GTGGCAGCTG CTGTCCACAA TACCCAGGTG ACAGTGGCTC CACAGAGACC 720
ATCAGCTCCA AACCACTCAT TTCACAGCCA GCAAGACTAA GACCCAGAAG AGGGAAGGAG 780
CTGGCCCATG CAGACATATT CTCCAGTGGG GAGGAGAGAA GTGAGAATCA GGTCTCAGTT 840
TCTCAACAGT CTCCCCAAAT TATTTACCCA TCCATACAGC TGTGGGGAGA GGGGGGTTAA 900
AACAGAAATC AGACCACACT ACTCCCGTGC TTAAAACCTG CAATGGCTTT CACTGACTCA 960
GAATAAGATC TACAGTCCTC ACCTCGGCAC GCAAAGCCCT ACAGGATCTG CCCTGCCCCC 1020
ACTATGACAC CCTCAAACTC TCTCTATCAC TCACTCTGCT CTGGCCACGC CAGTCTCCCT 1080
TCTTCTCTCA AATGAGCTAA GCTTGCTCCC AGCTCAGGGC TTCTGCCCTT TCTCACCTTG 1140
GTCCAGACCA CCCTCCCCAA GATCATCCCA TTCCAACCCC TCAGAAAGGC CATCCCACCC 1200
TTGGGTTGCC AGATATAAAA TAAACCCCAG GATGCCCAGG TGAATGCTCA TTTCAGACAC 1260
ATATTTTTTT TAGTATAAGT ATGTCTCAAA TATTCCATAA GACATGTTTC CACTAAAAAA 1320
TTATTTGATG TTTACCTGAA ATTCCAATTT CCCTGGGTGT CCTTTGTTTT CATTTGCTAA 1380
ATCTAGCAGC CCTGGCCCTG ACCTCCCGAT TGAAAGCAAC CTCAGGCAGA GTCACTCTTT 1440
ACCACATCTG CATTTTATGT TCTTCACAGT CTGCACTGGC ATCTGAAATG ACCTCATTTG 1500
TTAAATTACC CTCTGTTTCT CCCACCTACG AGCCGCGTGG CAGCACGGAG CAAGTCTGTC 1560
TTACTTAGTA CAGCATCCCC AGGGTCTAGT GCAGAGCCTG GCACACAGGA GATGCTTACT 1620
ATGTATTTCA GGAGACCTCA TCACATAAGA GTAAAAAACA CAGACTCTAC AGCCTGACTG 1680
TGTCAGCTCA AATCCTGGCT CTGATGCTTC CTAGCTCTGT AAGCTTGCCC TATAACTTAA 1740
TCTCTCTGGG 1750