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

TagContent
EnhancerAtlas ID
HS043-45066 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chrX:106989500-106992490 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MSCMA0665.1chrX:106989897-106989907AACAGCTGTT+6.02
MSCMA0665.1chrX:106989897-106989907AACAGCTGTT-6.02
MYF6MA0667.1chrX:106989897-106989907AACAGCTGTT+6.02
MYF6MA0667.1chrX:106989897-106989907AACAGCTGTT-6.02
Myod1MA0499.1chrX:106989813-106989826TCCAGCTGTCCCT+6.16
Pou2f3MA0627.1chrX:106992043-106992059TGCTATGCAAATGCGA+6.06
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01071chrX:106989367-106989918Adrenal_Gland
SE_01071chrX:106990347-106991470Adrenal_Gland
SE_01966chrX:106990173-106990993Aorta
SE_01966chrX:106991004-106992010Aorta
SE_03516chrX:106990283-106990765Brain_Angular_Gyrus
SE_03516chrX:106991039-106991631Brain_Angular_Gyrus
SE_04216chrX:106987744-106989872Brain_Anterior_Caudate
SE_04216chrX:106990152-106991874Brain_Anterior_Caudate
SE_05145chrX:106979146-106992565Brain_Cingulate_Gyrus
SE_06059chrX:106978065-106992474Brain_Hippocampus_Middle
SE_07082chrX:106978329-106992314Brain_Hippocampus_Middle_150
SE_08011chrX:106979346-106992461Brain_Inferior_Temporal_Lobe
SE_26851chrX:106990147-106992432Esophagus
SE_31551chrX:106990250-106992318Gastric
SE_37687chrX:106989580-106992355HSMMtube
SE_40984chrX:106989867-106992527Left_Ventricle
SE_42321chrX:106990010-106992448Lung
SE_46769chrX:106990381-106991059Ovary
SE_46769chrX:106991068-106991402Ovary
SE_46769chrX:106991502-106992365Ovary
SE_48198chrX:106989259-106992458Psoas_Muscle
SE_48777chrX:106989182-106992207Right_Atrium
SE_50259chrX:106990162-106991922Sigmoid_Colon
SE_51615chrX:106989713-106992266Skeletal_Muscle
SE_52487chrX:106990151-106991969Small_Intestine
SE_54817chrX:106990027-106992266Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chrX106990492106991512
Number: 1             
IDChromosomeStartEnd
GH0XI107746chrX106989297106992371
Enhancer Sequence
AAGAAGCAGA GGCAAAGAAC TAAGGAGGTC TGGGAGTGCA GAAAAGGGAA GAGGGGCCAA 60
GACGGTTCTC CCAGGCAGGC CCAAGATTGA GGACAGTCCA GACATATACA CTCTCACTAG 120
ACAGACAAGA CAGACAGACA CACACACACA GACATACACA CACACTCATG CATGCACACA 180
CAGGCAGGCA CACATACCTC CTTCACATAT GCCTTGGTCA TCCTGACTCT CCAGGAGTAC 240
TACTTCCATA TACAGGATTT GACTCAGATA GAGTCACACA CAGAAGAACA CCAACCCTCC 300
CAGATGCTAT ACTTCCAGCT GTCCCTTCAC AAACACAGGT AGGCCCCCAT AAGTATATTT 360
ACCATACATT TTTCCATACC TTTTTTGCAT ACAGCATAAC AGCTGTTTTT TTACGTACAC 420
CCTCATCACT CCTCAAGTCC CTTCCACCCA CTCAAGTCCT GACATATGTA CGGAGTTACA 480
CATACACACA TTCATGTGTG TCCTCCTTCC CAACAAAGGC AAAAGGAGTC TGCGCTCAAT 540
ACATTCTTTG TTCTTTCTTA CTTGGTGGAT TACATTTGAA GGAGTGACTG GACAGCTAGG 600
TGAACTGGAT AAATACTTTT TCCAATGTTT CTTAGCATGA TGGAAAAGTC CATCAAGGAC 660
ATTTGAAATC CCTCACAGAG TTCACTCCCT TGGCCTATAG ACAAGACACC AGTGGTAACC 720
TTTAGTGACT GCCAAAAGCT TCTAAGATTC TCTTAGTCCT GCTATGCTAG CTGACCTTTG 780
CAAGGAATCT TGGGTATTCC AAACTAAGAA CATTTAGTAT AAGAAACAAA ACAAAAACAA 840
AATCTTTCCC TGATGGTTAA GAACAATATG AAAGTATCTG TCCAAATTAG CAGGCCTGGC 900
CTGCGGCAAG ATGGTGAAGA AAGAAAAGTT GACGTGAAAG CCCACTCCAT TGTGTGTCCT 960
CTTGCAGCTT GCTTAGTCCC CCTTATCACA CACGCCCTGG GACCACATCT TGTCCCCTGC 1020
CAGGCTTACT CTGTTCTGGC CAAAGACTCC TAAAACTGGG AAAAGGACTT TTGGATTTGA 1080
CTAGAAGGAA GTCATGGGGA AGCTTAGAAA GAGAAGTGGG TCTGTCAGAT CTAAGCAGAA 1140
TGTAGTGTGA CATCTAAGTG GTGGGCACTG TGATCTACGC AGTGCAGTGT GCACAGAAAA 1200
CCTAGCGACC AGTGAGTTTT TACCCAGTCC CGCTAGCCTG CCCATTAAAA AGTTCAAATG 1260
TGGCTTGGCT GAAAAGCAAT CAGATCTGTT ATTGACACTG TTTCATTCTG AATAGCACAG 1320
AGGACTAAAG GCTTTCTTTA CTTAGTTCAT TAGTTAGCTA ACAAGCATTT TTCAAGCACC 1380
TACTGTGCAT GGAGCACTGT CCCAGACACT CGGCTGTTGC CGTTGCTGCT CTGCTATTGA 1440
ATTTCTAAAT ACAGGCTGTT GCCAGACATC CAATTTTCTG AGTGCTTGCT CTGACAGGGA 1500
ACAATGACTA ATGAACCAAA CATCAGGGAG GGCCCTCTGA TCTCCAGCAC AGAACATGCC 1560
CATAAAGGCA GATTCTAATT TGTTCAGCAA GCAGCTGCCA ATTCTTCTGG GATCTTAATT 1620
ACCTGGAGCA GTTTATGTGG GTGAATCCCC TTGGGAGAGA AACCCTGAAC CCTGTCTTTC 1680
TCATACCCTA TCATACCCCA GGCCCTATAA GTGGCTTTAA CTCTCAGCCA CTGCATATGT 1740
GTCCAAGGTC CAGGCCACAG CAGTTCACCA GATAGGCATT CCAGGCACTG CCCACGGCCT 1800
TCTTCACACC CCTGCACACA CACCCCTGGA CACACCCCTT CACACATGCA CATACATGGA 1860
GGGAGCTGTA TGTAAATAGT GGAAAACTCA ATGGGCTGCA AGTCAAGAGA CAGGAATTTC 1920
AATCCAACTC TGCTTCTTCT CCGTGTGACC TTGGGCAAGA CTTTTTCTAT CTCTGGGCTT 1980
CTATTTCCAC TTCTGGAAAA TGAGGGGCTG GACTAGATAA TCTCTATGAG CCTTTCCAAT 2040
TCTAGCACTT GAAATTCTGC TCCTCAGAAT GAAATGAGAC TCAAGTGAGC TGTGTGACAA 2100
GATCAGATTT GTGGCGTGGG GATGAGATAA GGTAGGGCCA GTGGTCAGCT CAGAAGCCCC 2160
AGAAGTCACC ATCATGGAGA AGGAAAAATC GCTGCCTCCT TGGGTCAGCC CTTCCCAAAG 2220
TTCCATACTG CTTCTGAAAT GGTTCACAAA TAAGGCTGGT GGATCTGGGG CACGGTGGGA 2280
TCTTCCTCCC TTCTGCCTCA TCTCCCTCCC CTTTCATTCC TTTTATAACC CTTGTTCCAA 2340
CTCTTGTTCC CTTTAACCAG CCCATCAGCT CACACCGACT AGTTCTCTTA GCAAACTCTT 2400
CAGAAAGGCC AGCGATTAAA TGATCTCAAG AGTCTCCCGA GTCTGTAAAA TGTAAATAAC 2460
AGCCCCTGCC CTGGCGGCCT TCACAGGCTT TCCAGAGGAT CAAATAAGAT AGAGTCTGTG 2520
AAAGTGCTTT AGAAATTGTC AAGTGCTATG CAAATGCGAG GGATTATTAT TAATGATGGG 2580
TGGGGAGGCA GCCACATGAT GTGAGAAGCA GAGTGCCAAC CTGTCTGCTT TGCTTACCAT 2640
CTTAATTGGG TAAAGGCATT GGCATTGCCA GCCTATAGCC AGCTTGTAGT AGGGACAGTT 2700
ATTTGCTTAG CATCCTCCCC TACTGGACCC CGTCTGCTAG CAGAGGGCAG AGCCAGAGGG 2760
AAGAGGAGAA AAGGACAGGA CAGGTCAGGT GCGGTGGCTC ATGCCTGTGA TCCCAGCATT 2820
TTGGGAGGCC GAAGCGGTTG TATCACCTGA TGTCAGGAGT TCAAGACCAG CCTGGCCAAC 2880
ATGGTGAAAC CCTGTCTCTA CTAAAAATAC ACACACACAC ACACACACAC ACACACACAC 2940
ACACACACAC ACACAAATTA GCCGGGCGTA GTGGTAGGCA CCTGTAATCC 2990