EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-14424 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr14:93509150-93511830 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35584079chr1493511641hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR2MA0258.2chr14:93511661-93511676AGGTCAGAGTGGCCT+6.66
FOSL2MA0478.1chr14:93510658-93510669CTGAGTCACCC-6.02
GATA2MA0036.3chr14:93509989-93510000TTCTTATCTGT+6.14
Gata1MA0035.3chr14:93509989-93510000TTCTTATCTGT+6.62
JUNBMA0490.1chr14:93510658-93510669CTGAGTCACCC-6.02
Klf12MA0742.1chr14:93511071-93511086AAGAAGGGTGTGGCC-6.25
Klf1MA0493.1chr14:93511075-93511086AGGGTGTGGCC-6.32
MYCNMA0104.4chr14:93509512-93509524GGCCACGTGGGC+6.27
MYCNMA0104.4chr14:93509512-93509524GGCCACGTGGGC-6.27
RUNX1MA0002.2chr14:93511647-93511658AAACCACAGAG-6.14
ZNF263MA0528.1chr14:93511134-93511155AAAGGAGGAAGAGGAAGAAGC+6.88
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_03181chr14:93510068-93510583Brain_Angular_Gyrus
SE_03888chr14:93504983-93513044Brain_Anterior_Caudate
SE_04808chr14:93494251-93514329Brain_Cingulate_Gyrus
SE_05777chr14:93493302-93514911Brain_Hippocampus_Middle
SE_06743chr14:93498689-93509524Brain_Hippocampus_Middle_150
SE_06743chr14:93509612-93512256Brain_Hippocampus_Middle_150
SE_07721chr14:93492779-93514769Brain_Inferior_Temporal_Lobe
SE_09265chr14:93510048-93513026CD14
SE_23185chr14:93505279-93514419Colon_Crypt_1
SE_23918chr14:93509314-93512076Colon_Crypt_2
SE_26366chr14:93505659-93512899Duodenum_Smooth_Muscle
SE_26889chr14:93505113-93512411Esophagus
SE_27639chr14:93505251-93519390Fetal_Intestine
SE_28556chr14:93505100-93524844Fetal_Intestine_Large
SE_34796chr14:93505024-93514368HeLa
SE_40660chr14:93505046-93514961Left_Ventricle
SE_41563chr14:93509310-93512004LNCaP
SE_42451chr14:93505095-93514218Lung
SE_48575chr14:93505057-93512067Right_Atrium
SE_49689chr14:93509996-93512067Right_Ventricle
SE_50538chr14:93509223-93514489Sigmoid_Colon
SE_52403chr14:93505242-93519331Small_Intestine
SE_57475chr14:93510071-93511486VACO_503
SE_65267chr14:93507414-93512032Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr149350944693510834
Number: 1             
IDChromosomeStartEnd
GH14I093038chr149350488193524683
Enhancer Sequence
TCAGGAGTTC AAGACCAACC TGAGCAACAT GGTGAAACCC CATCTCTACT AAAAACTCAA 60
GAATTACCCA GGCATGGTGG CGTGCACCTG CAATCGCAGC TACTCGGGAG GCTGAGGCAA 120
GAGAATAGCT TGAACCCAGG AGGCGGAGGT TGTAGTGAGC CAAGATCGCA CCACTGCACC 180
CCAGCCTGGT GACAGAGCGA GACTGTCTCA AAAAAAAAAG TTTCAATCTT AACTCTACAA 240
ATTGACTTGA AGTCCAAACT CTTTCTCATC CAGCTACTGC CAGCTCCCCA CCGAGGCCCA 300
CACTTTGGGG AAAACCCTTA GAAACTTCTT GTCATTGGTT AAAAAAATAT TGACCCAGGA 360
TTGGCCACGT GGGCCACAGG TGGTTTCACA GCACACACAG AACCAGAAGC TGGGGCTCAG 420
AGAAGCAAAA TAACTTGCCC AAGATCACAC AGCTAAGGAG ATCGGATTGA AATCCACCCC 480
AGTTTATGTG CACAGACAGA AGGGGAGAAA AGAGATGTGG GGCAGGTGGA TTTCTGAGGG 540
CAGGAAATAC CAGTGGGAAA GCCGAAGACA GCACAGTAGA GACTGCAAAA GCCCAGTGCT 600
CTGTGGAGTC ACTGCAGAAA GCACCGAACA CATCCAAGGC TCAACCCATC AGGCACTCTT 660
TCCTTTGGGG CTACTTCCAA CAGGAAATTC CAAGTGTCCC TGTCAAGCAG GGGAAATGCC 720
ATCCTGGGTC CAAGGCAGCA GGGCAGCCTC CCTGCCCCGC CCAGCCCCAC CTACATGAAG 780
AACAAAGTGC ACCAGGCAGG AATGTGCACT CAGGCCGTAG CCAGCCTCAG CCTGGCTCAT 840
TCTTATCTGT GGCTTGATTA AAACAAGCTT GGATTACACC ACAATCTTTA AGCCCCAAGG 900
CTGGGGGTGG TGTCACCAGG AATCTGTTCC AAGCGCACGT CATGCCCAGG CCACCGTTCT 960
CCTTCCCCTC ATTGGTGGCA GGCTGGCATC CTGCAGGAGG CCCTTCCCAG ACCACAGCCC 1020
CACCCTTCCT CTCCTGCCGC CCACCTGAAG GCCCCAATAC ACATCTTCCT ACAGTTCTGG 1080
CTTCAACTCT GTTCCTGAGA CCTTTACTGC CCCAAGTCCA CTACCCTGAG TTCTGGGCAA 1140
ATGAAAAATC TTTTCCCCTT CACCAGATTT CTCAAATCCA ACCATTCTGG AACCCGGCTT 1200
GTGGATGGCT AGGCTCTAGC CTCCCTCCTC TTCTGTCCCA TCACCCTGGG AAGACAGAGC 1260
CAGAGGGTAC TGAGGAATTC AGGTGGGAGG GGTTGGGGGG GAGGTGAGGA GGGGGTCCTA 1320
GGAGCAAATG GAGGGTCACA AACTGAAGCG CCCATGGGGC AAATGTAAAC CATGAGGCTG 1380
GTGGTGTGGG ACAACAGAGA ATGGTGGGGC CTAAGGGGCA ACCAGCTTAA ACACTGGCAA 1440
CAAATTCAAA GGAAAGAATG TAAAATTCCT GTGTGGGCCA AACAGATTGC ATGCAGGCCC 1500
AGGTATATCT GAGTCACCCA CGTGTAATCT GGTCCAACCC CCTCCGCAGA GATAGGAAAG 1560
CTGAAATCCA GACACAAGGA AGGGACCATG AATAAGTTTG TGCTGGCGAT TACTGAGAAA 1620
GTCTAGCATA AAAATTAAAC CGAAGCCTAG GCCGAACACT GGCATCCCTC TGCTTGGCTG 1680
TGAAGCTGGT GAGGATGCTG CACTCGGCCT GGCAGCAGAT GGAAACTCTG GAACTCGAGG 1740
GCCACGGATG AGCCACAGGG CCCCCCAGGT AAAGGACTGA CAGCCAGCCA TGCAAGCCCC 1800
TGGGACTGAC CCAGATGCAG AACTGACCAA TGTGGCGACA ACCATCACCC AACCCTGTGG 1860
GGCTGTAGAT CTCAGAGGAG GTGGGACAGT GGCCCAGCGG ACAGCAACAC GGCAGAGAGG 1920
GAAGAAGGGT GTGGCCTCTG TCTATGGCCT GGCCAGAAGG GCCACCGCAA GCACCAAGGC 1980
TAGCAAAGGA GGAAGAGGAA GAAGCAAGAA AAACCCGACA CCGTGACGGA CTAGCGTGGG 2040
CCGCAAGTCA GGGTTGTGGT TCTTTAGGAT ATATCTTAAC AGGGTAAGGG CCTTAAATGC 2100
CCTTTCCCCA CCAACCTGAC AGGGTTTAGC ACCAGGACTC CTGGCCAGGG CAGGCCCCAG 2160
GGCTCTAGGA TCTGTCAGAT CAGGAAGAAA GGGGCATTTA AGGTCTCCCT CCTGTAAGAT 2220
CTACCTTAAA GAACCAGATC CCTGACTTTG CAGCCCAGTG CCATGCTGCT TTTGAGCCTG 2280
AAATGGAAGT CTGTGCCTTA GTTCCAAGTC ACCAGGCACT GGTTCCTTGC CCTTGCAGGC 2340
ACAGGGCATC AAGATCAAAC CAAACCTCCA AGCCTCACCT CTCACAAATA AGCAGAGGCC 2400
AGTTACCCCT CTGGGCAAGA CCTCAGGCCC CTGTCCCTGC CAGTCAGCAG CTCTGCCTCC 2460
CGCAGCGCTT GAGGGCTGGT CCATGCAGCC GGCCAGGAAA CCACAGAGGC CAGGTCAGAG 2520
TGGCCTTTTA ATTCAACTCC CCTGGTGACC CTGAAGAGCA CTGCCGCAGA CTGAGAGGCT 2580
GGAAGTAGGC TATGCTGCCC CTGCCCCATA ACAAAGACTC TACAGCAAAT CACCAGGATG 2640
GGGGAAGATT AGCGCAAAGT GGGTGGAGAG TCTCCCTGAA 2680