EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS082-03179 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr1:221999520-222001000 
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:221999882-221999900GAAAGAAAGAAAGGAAGA+6.22
EWSR1-FLI1MA0149.1chr1:221999886-221999904GAAAGAAAGGAAGAAAGA+6.22
EWSR1-FLI1MA0149.1chr1:221999901-221999919AGAAAGAAAGAAGGAAGG+6.56
EWSR1-FLI1MA0149.1chr1:222000059-222000077GGGAGGGAGGGAGGAAGG+7.28
EWSR1-FLI1MA0149.1chr1:222000063-222000081GGGAGGGAGGAAGGAAGA+7.39
EWSR1-FLI1MA0149.1chr1:221999905-221999923AGAAAGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr1:222000067-222000085GGGAGGAAGGAAGAAAGA+7
EWSR1-FLI1MA0149.1chr1:221999913-221999931GGAAGGAAGGAAGGAAAA+9.07
EWSR1-FLI1MA0149.1chr1:221999909-221999927AGAAGGAAGGAAGGAAGG+9.09
FOSL2MA0478.1chr1:222000249-222000260GGGTGACTCAG+6.02
IRF1MA0050.2chr1:221999850-221999871AGAAAGAAAGAGAAAGAAAGA-6.76
IRF1MA0050.2chr1:221999955-221999976AGAAAGAAAGAGAAAGAAAGA-6.76
JUNBMA0490.1chr1:222000249-222000260GGGTGACTCAG+6.02
Nr2f6(var.2)MA0728.1chr1:221999616-221999631GAGGTCAAGAGTTCG+6.24
ZNF263MA0528.1chr1:222000065-222000086GAGGGAGGAAGGAAGAAAGAG+6.07
ZNF263MA0528.1chr1:221999914-221999935GAAGGAAGGAAGGAAAAAGGA+6.17
ZNF263MA0528.1chr1:222000068-222000089GGAGGAAGGAAGAAAGAGAGA+6.24
ZNF263MA0528.1chr1:222000061-222000082GAGGGAGGGAGGAAGGAAGAA+6.41
ZNF263MA0528.1chr1:221999910-221999931GAAGGAAGGAAGGAAGGAAAA+6.56
ZNF263MA0528.1chr1:222000072-222000093GAAGGAAGAAAGAGAGAAAGA+6.58
ZNF263MA0528.1chr1:222000057-222000078GAGGGAGGGAGGGAGGAAGGA+7.29
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_35982chr1:221999806-222001200HMEC
SE_52249chr1:222000163-222000869Skeletal_Muscle_Myoblast
SE_55946chr1:221999901-222005096u87
SE_64045chr1:221999986-222000869HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1222000173222000483
Number: 1             
IDChromosomeStartEnd
GH01I221826chr1221999933222001478
Enhancer Sequence
GATGAGAACC AAGGTCGAAA AGTGCAACTC ATGGCTGGGC GCGGTGGCTC ATGCCTGTAA 60
TCCCAGCACT TTGGGAGGCC GAGGTGGGTG GATCACGAGG TCAAGAGTTC GAGACCAGAC 120
TGACCAACAT GGTGAAACCC TGTCTCTACT AAAAATACAA AAATTAGCTG AGCATGGTGG 180
TGCACGTCTG TAATCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATCGCT TCAACCTGGG 240
AGGCAGAGGT TGCAGTGAGC CGAGATGGCG CCATTGCACT CAAGCCTGGG TGACAGAGTG 300
AAACTCCATT TTGAAGGAAA GAAAGAAAGA AGAAAGAAAG AGAAAGAAAG AAAAGAAAGA 360
AAGAAAGAAA GAAAGGAAGA AAGAAAGAAA GAAGGAAGGA AGGAAGGAAA AAGGAAAAGA 420
AAGAAAGAGA GAGAGAGAAA GAAAGAGAAA GAAAGAAAGA AGGAAAGAAA GAAAGAAAGA 480
AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAGAAAGA AAGAAAGAAA GAAAAGAGAG 540
GGAGGGAGGG AGGAAGGAAG AAAGAGAGAA AGAAAGAAGG AAAAGTGCAA CACTCTTCAG 600
TGTTTCCCAG GAAGAAGTTT GGGTATAGGA GTTTTGTAAT TACAGTGGGA ATGTTATTCG 660
ACTAGAGAGT TGCAACCCAG GGGTGGGGGC GGAAGCCCAC TGAGGACCCC TAGGCCAAAT 720
CAAGAGTGAG GGTGACTCAG GTGACACACA GGGAGCCCAG TGGTCAGCTG GTTCAACCTA 780
ATCTGGAGAA TGACTCAACA CCAGGATGCC ACTGCTGTTG GGGGAGGAGG AGGAAGTGCT 840
AAACCCGCTT CAATATTTCC TGTCTTAAGC CCACATTGTT CTGGGGATTG AGATCTGAAG 900
TTGAGGGGTT GGGGGTCAGT GAATCTGGCT ATAGACATTG TAGATCTGCA GATGGAGGGC 960
ATGAAACAGG CTGAAACTGC TGCAATATGT ACTCACCCTG AGGGCCTGAG GACCTAGATG 1020
ATCATCTTAA TTTAGATTGC TCCTTGGCCC ACACAGACAT GATAGTGCCT GCAGACAGTG 1080
GCTCTGGCAC TGGCACCCAT GGTAGCAGTT GGCCTCATTG TGATGGGAAA GCCTCCAGCT 1140
CCCTCCAAGA TGCAGTTAGG GTTTCTGGTC TCATTCTTGG AAGAGTTTTG TTGGATGAAT 1200
TAAACTGGAA TCATCTTCCT TTCCCAGGAA ACTGTTGTCT CTTTTGTCTG CTCTGCCTCT 1260
GGGTGAAATC TGTAGTCCTT ACTTGCTGCT ATTTTCTACC ATCCTAATAA TAGCTCATTG 1320
TTAGGCAGAC ATGACGCAAA TACATTTCTC ACTATCTTGG GAGATTTGGG GGGGGGGTCT 1380
TACCTTCTTA TTTAAGTTCT TTGTTTAATT ATTTAATTCT TTTCTTTTCT TTTTTTTTTT 1440
TTTTTAGTTT GTTCTCTTTG TTTGCCCTTA GTTGGTAAAG 1480