EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-21526 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr14:93509230-93512030 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs35584079chr1493511641hg19
TF binding sites/motifs
Number: 14             
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
HES2MA0616.2chr14:93511862-93511872GGCACGTGCC+6.02
HES2MA0616.2chr14:93511862-93511872GGCACGTGCC-6.02
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
ZNF263MA0528.1chr14:93511890-93511911GGAGGAGGAGGTGAGAGGAGG+7.65
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
CGTGCACCTG CAATCGCAGC TACTCGGGAG GCTGAGGCAA GAGAATAGCT TGAACCCAGG 60
AGGCGGAGGT TGTAGTGAGC CAAGATCGCA CCACTGCACC CCAGCCTGGT GACAGAGCGA 120
GACTGTCTCA AAAAAAAAAG TTTCAATCTT AACTCTACAA ATTGACTTGA AGTCCAAACT 180
CTTTCTCATC CAGCTACTGC CAGCTCCCCA CCGAGGCCCA CACTTTGGGG AAAACCCTTA 240
GAAACTTCTT GTCATTGGTT AAAAAAATAT TGACCCAGGA TTGGCCACGT GGGCCACAGG 300
TGGTTTCACA GCACACACAG AACCAGAAGC TGGGGCTCAG AGAAGCAAAA TAACTTGCCC 360
AAGATCACAC AGCTAAGGAG ATCGGATTGA AATCCACCCC AGTTTATGTG CACAGACAGA 420
AGGGGAGAAA AGAGATGTGG GGCAGGTGGA TTTCTGAGGG CAGGAAATAC CAGTGGGAAA 480
GCCGAAGACA GCACAGTAGA GACTGCAAAA GCCCAGTGCT CTGTGGAGTC ACTGCAGAAA 540
GCACCGAACA CATCCAAGGC TCAACCCATC AGGCACTCTT TCCTTTGGGG CTACTTCCAA 600
CAGGAAATTC CAAGTGTCCC TGTCAAGCAG GGGAAATGCC ATCCTGGGTC CAAGGCAGCA 660
GGGCAGCCTC CCTGCCCCGC CCAGCCCCAC CTACATGAAG AACAAAGTGC ACCAGGCAGG 720
AATGTGCACT CAGGCCGTAG CCAGCCTCAG CCTGGCTCAT TCTTATCTGT GGCTTGATTA 780
AAACAAGCTT GGATTACACC ACAATCTTTA AGCCCCAAGG CTGGGGGTGG TGTCACCAGG 840
AATCTGTTCC AAGCGCACGT CATGCCCAGG CCACCGTTCT CCTTCCCCTC ATTGGTGGCA 900
GGCTGGCATC CTGCAGGAGG CCCTTCCCAG ACCACAGCCC CACCCTTCCT CTCCTGCCGC 960
CCACCTGAAG GCCCCAATAC ACATCTTCCT ACAGTTCTGG CTTCAACTCT GTTCCTGAGA 1020
CCTTTACTGC CCCAAGTCCA CTACCCTGAG TTCTGGGCAA ATGAAAAATC TTTTCCCCTT 1080
CACCAGATTT CTCAAATCCA ACCATTCTGG AACCCGGCTT GTGGATGGCT AGGCTCTAGC 1140
CTCCCTCCTC TTCTGTCCCA TCACCCTGGG AAGACAGAGC CAGAGGGTAC TGAGGAATTC 1200
AGGTGGGAGG GGTTGGGGGG GAGGTGAGGA GGGGGTCCTA GGAGCAAATG GAGGGTCACA 1260
AACTGAAGCG CCCATGGGGC AAATGTAAAC CATGAGGCTG GTGGTGTGGG ACAACAGAGA 1320
ATGGTGGGGC CTAAGGGGCA ACCAGCTTAA ACACTGGCAA CAAATTCAAA GGAAAGAATG 1380
TAAAATTCCT GTGTGGGCCA AACAGATTGC ATGCAGGCCC AGGTATATCT GAGTCACCCA 1440
CGTGTAATCT GGTCCAACCC CCTCCGCAGA GATAGGAAAG CTGAAATCCA GACACAAGGA 1500
AGGGACCATG AATAAGTTTG TGCTGGCGAT TACTGAGAAA GTCTAGCATA AAAATTAAAC 1560
CGAAGCCTAG GCCGAACACT GGCATCCCTC TGCTTGGCTG TGAAGCTGGT GAGGATGCTG 1620
CACTCGGCCT GGCAGCAGAT GGAAACTCTG GAACTCGAGG GCCACGGATG AGCCACAGGG 1680
CCCCCCAGGT AAAGGACTGA CAGCCAGCCA TGCAAGCCCC TGGGACTGAC CCAGATGCAG 1740
AACTGACCAA TGTGGCGACA ACCATCACCC AACCCTGTGG GGCTGTAGAT CTCAGAGGAG 1800
GTGGGACAGT GGCCCAGCGG ACAGCAACAC GGCAGAGAGG GAAGAAGGGT GTGGCCTCTG 1860
TCTATGGCCT GGCCAGAAGG GCCACCGCAA GCACCAAGGC TAGCAAAGGA GGAAGAGGAA 1920
GAAGCAAGAA AAACCCGACA CCGTGACGGA CTAGCGTGGG CCGCAAGTCA GGGTTGTGGT 1980
TCTTTAGGAT ATATCTTAAC AGGGTAAGGG CCTTAAATGC CCTTTCCCCA CCAACCTGAC 2040
AGGGTTTAGC ACCAGGACTC CTGGCCAGGG CAGGCCCCAG GGCTCTAGGA TCTGTCAGAT 2100
CAGGAAGAAA GGGGCATTTA AGGTCTCCCT CCTGTAAGAT CTACCTTAAA GAACCAGATC 2160
CCTGACTTTG CAGCCCAGTG CCATGCTGCT TTTGAGCCTG AAATGGAAGT CTGTGCCTTA 2220
GTTCCAAGTC ACCAGGCACT GGTTCCTTGC CCTTGCAGGC ACAGGGCATC AAGATCAAAC 2280
CAAACCTCCA AGCCTCACCT CTCACAAATA AGCAGAGGCC AGTTACCCCT CTGGGCAAGA 2340
CCTCAGGCCC CTGTCCCTGC CAGTCAGCAG CTCTGCCTCC CGCAGCGCTT GAGGGCTGGT 2400
CCATGCAGCC GGCCAGGAAA CCACAGAGGC CAGGTCAGAG TGGCCTTTTA ATTCAACTCC 2460
CCTGGTGACC CTGAAGAGCA CTGCCGCAGA CTGAGAGGCT GGAAGTAGGC TATGCTGCCC 2520
CTGCCCCATA ACAAAGACTC TACAGCAAAT CACCAGGATG GGGGAAGATT AGCGCAAAGT 2580
GGGTGGAGAG TCTCCCTGAA ACGTACTGAC AGCACTTAAA AACCAATTAG ATGGCACGTG 2640
CCTGTAGTCC CAGCTACTCA GGAGGAGGAG GTGAGAGGAG GATCACTGGA GCCCAGGAGT 2700
TCAAGGCTGA AGTGCGCTAT GATTGCATCT GTGAAATAGC CACTGTACTC CAGCCTGGGC 2760
AACACAGCGA AACCCTATCT AAGAAAATCC AATTAGAGAC 2800