EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS023-17233 
Organism
Homo sapiens 
Tissue/cell
CD8+ 
Coordinate
chr22:38654880-38657520 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr22:38655923-38655933GGCACGTGCC+6.02
HES2MA0616.2chr22:38655923-38655933GGCACGTGCC-6.02
Nr2f6(var.2)MA0728.1chr22:38656134-38656149TGAACTCCTGACCTT-6.04
ZNF263MA0528.1chr22:38656731-38656752TGCTCTCCCACTTCCTCCTTC-6.53
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_01704chr22:38654485-38655844Aorta
SE_01704chr22:38656258-38658843Aorta
SE_03229chr22:38654562-38655687Brain_Angular_Gyrus
SE_03229chr22:38656271-38658009Brain_Angular_Gyrus
SE_04072chr22:38654541-38655905Brain_Anterior_Caudate
SE_04072chr22:38656166-38659059Brain_Anterior_Caudate
SE_04952chr22:38652352-38658959Brain_Cingulate_Gyrus
SE_07869chr22:38652169-38659387Brain_Inferior_Temporal_Lobe
SE_08820chr22:38656929-38657526Brain_Mid_Frontal_Lobe
SE_26802chr22:38654704-38655856Esophagus
SE_26802chr22:38656293-38658929Esophagus
SE_27733chr22:38652410-38655784Fetal_Intestine
SE_27733chr22:38656291-38658176Fetal_Intestine
SE_37347chr22:38655946-38658129HSMMtube
SE_40787chr22:38653157-38655924Left_Ventricle
SE_40787chr22:38656532-38658906Left_Ventricle
SE_44907chr22:38654444-38655775NHLF
SE_44907chr22:38656208-38657716NHLF
SE_45934chr22:38652261-38655398Osteoblasts
SE_45934chr22:38656199-38658738Osteoblasts
SE_46738chr22:38655365-38655720Ovary
SE_46738chr22:38656964-38657522Ovary
SE_50292chr22:38653131-38655881Sigmoid_Colon
SE_50292chr22:38656212-38658953Sigmoid_Colon
SE_52414chr22:38652442-38655903Small_Intestine
SE_52414chr22:38656209-38658945Small_Intestine
SE_59089chr22:38654708-38715012Ly3
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr223865530138655703
chr223865600038656892
Number: 1             
IDChromosomeStartEnd
GH22I038256chr223865228538659058
Enhancer Sequence
GACCGTCTTC CAGAACTGTA GGGAGGCTGA TGAGGAAGCA GACATCCAGT GTCGTTTATT 60
TCTATGTTTA TTTTCAACTG TAATGGTATC CCTCCTCCCA ACCTGAAATC CACTGAGAAT 120
GTGGCAGGAG CTGGCCGTGG GACCCAAAGT CTCACTTCTC CCAAGACTGC CCCACCTCCC 180
TCCTCTTCCA GGAAAGACGT CTTCCGGCTG GCCCCCCATC AGAGACATCC TTTCTCAGAT 240
AAGCTACGCA GCTATGTCGT CACTGAACTT GGCCACCTGC CTTGGAGTTT ATTTCGGGAG 300
CATCCCACCA TCTCACCCAG ATTCTATCGT CAGAGTCATT TTAACTCATG TTTGAGGGAC 360
ACCTTACTGC TGCTATCCCC TCTGCCCATG GATTTTATTA TGTGCTGTGT GGTAGGCTGA 420
AGAATAATCC CCCAAAGATG TTGACATCCT AACCCCCAGA GCCTGTGAAC ATGCTACCTT 480
ACATGGCAAA AGGGACTTTG CAGAAGTGAC TGAATTAAGG GTCCTGAAAT GAGAGATTAT 540
CCTGGATAAC CTGGGTGGGC CCATGTCATC ACAAGGGTCC TCGTAGGAGG AAGGCAGGAG 600
GTAGAGAGCG AGAAGAGGGC AGCGTGACAA AGGAAGCAGA GAGAGGAAAG TGGAAGCTGC 660
TACGCTGCTG CCCTTGCAGA TGGCGAAAGG CGCCACAAGC CACAGATGGA GGTGGTCTCT 720
AGGAGCTGGA AGAGGCAGGG AAATAATTCT CCCCCAGAGC CTCCAGAAGG AGTATGGCCC 780
TGCCAACACC TCGATTTTAG TCCAGTGAAA CACATTCTGG ACCTGACCTC CAAAACTGTG 840
AGATAATTAA TGTGTGCGCA TGCATTTTAT TGGTTTTTCT TATTGTAAGT AATCTATAAT 900
TTGTGTTTGT TTTGTTTTTG AGAAGGAGTC TCACTCTGTG GCCCAGGCTG GAGTGCAGTG 960
GTGCGATCTC GGCTCACTGC AACCTCTGCC TCCTGGGTTC AAGCAATTCT CCCACCTCAG 1020
CCTCCAGAGT AGCTGGGGTT ACAGGCACGT GCCACCACGC CTGGCTTTTT TTTTTTTTTT 1080
TTTTTGTGAG ACGGAGTCTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGGC GTGATCTTGG 1140
CTCACTGCAA CCTCCGCCTC CCAGTAACTG GGACTACAGG CGCGTGCCAC CACGTCCTGC 1200
TAATTTTGTA TTCTTAGTAG AGACAGGCTT TCACCATATT GGTCAGGCTG GTCTTGAACT 1260
CCTGACCTTG TGTTCCGCCC ACCTTGTCCT CCCAAAGTTC TGGGATTACA GGCGTGATCC 1320
ACCACACCCG GCCAAATGCC TGGCTAATTT TTTATATTTT TGTTAGAGAC AGGGTTTCAT 1380
CATGTTGGCC AGGCTGGTCT CGAACTCCTG ACCTCAAGTG ATCCACTCAC CTCAGCCTCC 1440
CAAAGTGCTG GGATTACAGA TGTGAGCCAC CGCACCCGAC CTAATTTGTG TTTTAAGTCA 1500
CTAAGTTTCT GGTAATTTGT TGCAGCAGCA AGCAGCTTGC AGATGCAAAA CAGAGGTTTG 1560
AAGGGCTGAC GTCATTTGCC CACAATCACC TGACAAATGG TTCTTCCGAC TGCCACTGCC 1620
GTGCTGTGAA ATCCGCAGAA CTCTGGAGCC TGACCACCTA GACCTGACCT CCAGCTTTGC 1680
CACTGGCTAG CTTTGTGTCT GTGAGCAAGT TACACAACCT CTCCTTGCCT TAGCTTCCTC 1740
ATCTATAAAA TGGGGAAGCA GCCATACCTG CCTCTGAGAG AGAGGGACGG AATAATGAGT 1800
GAACACAGAA AGCACTGAGA AGGTCTGGCA CCATGTGATG TCAGCTGCCA TTGCTCTCCC 1860
ACTTCCTCCT TCGGCCAGCC TGGGATTTCA TGCTCCCAAC AGTCTCTGGG ACCCAGGTTC 1920
TGTTGCTGGG TATTTGCTCT CTTTAAATCT TCTGAGGTCA TATTTTCATT CATTAGTTTC 1980
AGATCCAAAC CCTTTAGAGC TGCAGCCACG AAGTGCTCAC TCAGGCGGCT GCCACCCACA 2040
GGCCAAGCTA AACTGGCAAC CCGTTCACAT ATATATCCCT GGAATATTCA TGCAGCCTGG 2100
GAGGGCTTTT GTTCTCTTAT TTAATATAGA TGGAGAACCT TCCATCTTAC CATAACTCGC 2160
TGGTTGGGGT CAGACTCGAG CACTGTTCAT CTGAACTGAC CGCTCTGCTC CCACTCCAGC 2220
CGCCTGGGAA TGACAACGGG AATGACAGCC GGCCCTCCTG CCTTTGGGGG TTGCCTGGGC 2280
TCTCTGAGCT TCTGGGCAGC TGCATTATTG GGGGAGGCTG ATCCACATCA GAGCAGGTCA 2340
GCAACCCACA GCCTGGCCCT TCTCCAGAGG GGATTAGAGG GAAAGAGCGG CCCCTGGCCA 2400
GGCACTTCTG CCTGGTGAGC CTTTTGAAAA GGATCACATG CCCTCACAAG GGGTCAGGGG 2460
TCCACAGCTC TCCTTCCGTC TCCCCTTCAA TCAACACAAA CAAGCGGAGG CCACTCTAGC 2520
GGCTCCACAT TTCTCCCCCT TCTCCTGGGC CAAGTTCCCA GGAATCTCTC AACCAGGAAA 2580
GCAAAATCAT CCAATCATGT ACATATCTGT CACTTGGGTG GGGGTGCAGA AATAAAGGGG 2640