EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS189-00441 
Organism
Homo sapiens 
Tissue/cell
Thymus 
Coordinate
chr10:126345870-126348770 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3781454chr10126348565hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr10:126347190-126347208GGGAGAGAGGGAGGAAGG+6.27
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_03136chr10:126346157-126346906Brain_Angular_Gyrus
SE_03136chr10:126346953-126347668Brain_Angular_Gyrus
SE_03854chr10:126345895-126348505Brain_Anterior_Caudate
SE_04762chr10:126345744-126349551Brain_Cingulate_Gyrus
SE_05766chr10:126345724-126349554Brain_Hippocampus_Middle
SE_06675chr10:126345786-126348484Brain_Hippocampus_Middle_150
SE_07831chr10:126345766-126348583Brain_Inferior_Temporal_Lobe
SE_09159chr10:126345812-126347356CD14
SE_10177chr10:126346118-126348206CD19_Primary
SE_11826chr10:126345840-126348543CD3
SE_14406chr10:126345636-126348604CD4_Memory_Primary_7pool
SE_16286chr10:126345784-126348523CD4_Naive_Primary_8pool
SE_17772chr10:126345653-126350906CD4p_CD25-_CD45ROp_Memory
SE_18306chr10:126345820-126348615CD4p_CD25-_Il17-_PMAstim_Th
SE_19113chr10:126345778-126348493CD4p_CD25-_Il17p_PMAstim_Th17
SE_19980chr10:126345692-126350202CD56
SE_20757chr10:126345857-126348589CD8_Memory_7pool
SE_22300chr10:126345679-126350664CD8_primiary
SE_23768chr10:126347123-126347455Colon_Crypt_2
SE_25345chr10:126345638-126348500DND41
SE_26558chr10:126346495-126347565Esophagus
SE_26558chr10:126347586-126348485Esophagus
SE_30910chr10:126345727-126348379Fetal_Thymus
SE_31435chr10:126346226-126348490Gastric
SE_36994chr10:126345509-126347910HSMMtube
SE_39370chr10:126345763-126348156Jurkat
SE_42109chr10:126346257-126348413Lung
SE_51170chr10:126346111-126347664Skeletal_Muscle
SE_52350chr10:126346143-126348446Small_Intestine
SE_53300chr10:126346160-126347224Spleen
SE_55093chr10:126346222-126347542Thymus
SE_55093chr10:126347742-126348456Thymus
SE_62212chr10:126285528-126438541Tonsil
SE_65502chr10:126346617-126347387Pancreatic_islets
SE_66255chr10:126345763-126348156Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10126347478126347709
Number: 1             
IDChromosomeStartEnd
GH10I124657chr10126345791126350773
Enhancer Sequence
ATGTTTCTTT CCCCTTTTTA AAGCAACAAA TTCGTATTTC TTGTCATTGT TCCACACATT 60
GGTAAATGAT GATTTAAAAT CTGTATTTGC ACCTGTGGAA TCCATGGACT CCTGGGGCTA 120
GAAAGGGTGT CAAGAGTCAC TTCTCAGCGT TATAACTGCT CAGAAAAAGG ACTGCAAGGA 180
ACTACACCAA ATATTTAAAG ATCATTATCT CTGTAGGTGG ATTTCAGAGG AATTTAAATT 240
TCTGTTCTTT TACATTTCCA AACTATATTT TTTCTCTTCT GAACTTTAAA CTTTTTTACA 300
AGTATGCATT AATTTTTTTA ACCAGTAGAA ACAGTAAATG TCAATGAATG TGAAACTGAC 360
ATACTCCTGA GCTGATATAC AAGTGTTTGT GCCCTCTACT AACAAGAATA TTACCATTTA 420
CCATGAATTG AGCATTTGTT GTGTGCTGTT AGCCCTGAGC ATGAGACAGA CATTTCACCT 480
AACTCCCTCT TTTCATGCCC ATTTTACGAA TGAGGAAACA GGATCAGAGA AATCCAATGA 540
CTTGCTCAAA GTCCCACAGC TAGAGCCGCA ACCAGCTCCA TCTGCTCCAA AGGCCTTGCT 600
TGCAGCCAGC CTACTCCACA GCTTCTCCGC AGCCAGGAAG GTTCCTTTCT GCTTGCTTGC 660
TTTTCTACGC GGCCACTGAA AGCAGCTGTG ACGATATGTA GGTCATACTA ACCACAAATA 720
TTACCAAGAC CACGGAACTG GGTGGGCACT TTGGCAGCAT CTTGGTTGTG ACTGGTGACT 780
TTTCTCCCAC AGTCAAAGAA CCAGGTCAGT TCCCAGGCTC ACCCAGCAGA CAGTCTGGGG 840
CAGAGACAGG GGCAGCGAGC AAGAACCCAG GGGAGGGGCT TTGCTACGCA AGAAACTAAG 900
GAAAACACTG GTGTGCTTGG GGATAGGGAT CCCGCTTGGC AAATGCGGAG GCCTCTGGCC 960
ATATTCGGTG CTGCCATACA CAATGCCACC CAAGGAGGTT TCAGGTCCAG AAGCGCCCCA 1020
GGTCACCTCA GCAGGAGTCC CAGGCTATGG ACCTCTGAAT AGATGTCAAG GGGGACCCTC 1080
CTGCCCATTG CCACATCCCT ACCCTGGTTA CATGTTACTG GTGTTTCTCA AAGGCTGCTT 1140
TGCCAAGTGG GTGGCCCCCA CTCATACATG CAAAATGGGC TAAGAGGAGT ATTCTTCACC 1200
CCTTCTAGGA GACACAAGCA TATTCAGACC TGGAGAAGTG TCACCTTAGT GAGATCTATT 1260
TAATGGTGCT GGACCTTTGA GAACCATCCA TACAAGTCCT GGAGAACAGC AAACTACCGT 1320
GGGAGAGAGG GAGGAAGGTG CACACGGCAT GTGGAGGAAG CTGAGATCCT AGGAGCAGGC 1380
CAGGTGCCTC CAGCAACATC CCTGCACTTC ACCCCGGCAA CCCAGGCCAC AACTGCAGTG 1440
CAGTGAGCTA AAGGGCCACA GCCTGGGGAT GGAACACCAA GGCCACGTTC CCTGCCTCCA 1500
CCCATGCTCC CCGTGTCCGC CTGTCAAAGC TTCTCCAGCC TGCTGGTCCT CAAACCCTGC 1560
TCCCTGTGCC CCCACTGAGG CTGCGCTGCA CGGGCTCAGC ACACAGACTG CTAGCCACAC 1620
CACCCAAGTT CAAATCCCTT ACCTGCCTAG AACCGGCACC ATGGCCCTAG GTGAGTTATT 1680
TAATTAGGTC TGTGCTTCTG TGTCTGTGGT GGTAACCTGG CATGACAATA ACAGTAGCTG 1740
TGTCCCAGAT ACTGGGATGG CGATGGTGGG GATGGGCAGG TTTGGTGGCT GACGTGCACC 1800
CACCCCTTCT GCCAGCATCT TGCACATCAT GGGAGCTCAG TGTACACTGA CAGGACTTGC 1860
AGGACACATA CAGCCTTTGA AGCTAAACTA CCCTTTGGAG AATCGTGACT CCCTCCACCT 1920
CTAGCCTTCC TGCTTTCAGC CATGATAGGC CTAAAGTCTG AGCAGAGCTG CTCACCAAGG 1980
AAGGACTAAG AGGAGCCACA AGGAGCAGCT TTATTTAAAG GGAGAGATAC AACTGATCAG 2040
CAGCTTTTCC TCCTTGCCCC TCATCTTTTC ATTGTCAGTT TCAAAACAGG CCAGTGCTAG 2100
GGCCAGAGCT AATAGCAGTG GTGGAAGTGG TCTTGGTTAC AGTAAGAACT TTCTAACACA 2160
TTTCTGGGTC CCCAAAGATG CTCCAGCCCA CGCAACAGCC TCCTGGCTCC AGGCTGGCTG 2220
CTGCAGGTTT CTCAGACAAT GGCAGCATCT GCCCTGGGAC AGCCTCCACT GCCTAACTTT 2280
GAGGTGGGGC ACAGGATAAA ACCACAGCCA GCTGAGGCTT TTAAATCTGA GCCAACCATC 2340
CCCACCCTTA TTTTCACAGA GTGGCTGCAA AACCACCTTG CCGGGCCAAG CTCCATTACC 2400
ACAAGCTCAT CTCCTCTAGC AACTTCTGAG CTGGCTGTCC ACCTAAGGGG CCAGAAGATA 2460
TCTGGCTGAC AGAGTTTTCT GGGTCCCAGG CCAGAGTCAA CTTTGCTTTT GTTTTGTTTT 2520
TTGAGACGGA GTCTCGCTCT TGTCACCCAG GCTGGAGTGC CATGGCACAA TCTCAGCTCA 2580
CTGCAACCTC TGCCTCCCGA GTTCAAGCAA TTCTCCCGCC TCAGCCTCCC GAGTAGCTGG 2640
GATTACAGGT GTGCACCACC ATGCCCAGCT AATTTTTGTA TTTGTAGTAT AGACGGGGTT 2700
TTGCCATGTT GGCCAGGCTG GTCTCAAACT CCTGACCTCA AGTGACCCAC CCGCCTTGGC 2760
CTTCCAACGT TCTGGGATTA CAGGCATGAG CCGCTGTGCC TGGCCCAGAG CGAACTTTCT 2820
AGGGGTTTGT CTTCAGTGGC GAGAAGCCCA GTGCTGCCCT CGCTGTTCAC GTTTGGGTTT 2880
CGTTCCACCA TATGGAGCGG 2900