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

TagContent
EnhancerAtlas ID
HS063-04428 
Organism
Homo sapiens 
Tissue/cell
GM18505 
Coordinate
chr3:10238860-10241900 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr3:10239073-10239094AAAAAAAAAGAAAAAGAAAAA-6.09
MEF2AMA0052.3chr3:10239716-10239728ACTAAAAATAGA+6.27
MEF2BMA0660.1chr3:10239716-10239728ACTAAAAATAGA+6.32
MEF2CMA0497.1chr3:10239714-10239729CTACTAAAAATAGAA+6.57
ZNF263MA0528.1chr3:10240864-10240885AGTGGAGGAGGGGAGAGGAAG+6.08
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_03544chr3:10240260-10240940Brain_Angular_Gyrus
SE_05284chr3:10239556-10241713Brain_Cingulate_Gyrus
SE_06271chr3:10230310-10239221Brain_Hippocampus_Middle
SE_06271chr3:10239536-10241921Brain_Hippocampus_Middle
SE_07281chr3:10239529-10241372Brain_Hippocampus_Middle_150
SE_08553chr3:10239744-10241777Brain_Inferior_Temporal_Lobe
SE_10483chr3:10239552-10242463CD19_Primary
SE_11117chr3:10230364-10244148CD20
SE_12182chr3:10239800-10241688CD3
SE_18222chr3:10230393-10242416CD4p_CD25-_CD45ROp_Memory
SE_18887chr3:10239325-10242218CD4p_CD25-_Il17-_PMAstim_Th
SE_19527chr3:10237958-10239423CD4p_CD25-_Il17p_PMAstim_Th17
SE_19527chr3:10239586-10241934CD4p_CD25-_Il17p_PMAstim_Th17
SE_20302chr3:10232846-10239394CD56
SE_20302chr3:10239719-10242481CD56
SE_22972chr3:10239783-10241915CD8_primiary
SE_27300chr3:10239815-10241654Esophagus
SE_35045chr3:10239193-10242641HeLa
SE_36305chr3:10239752-10241604HMEC
SE_38379chr3:10239866-10241762HUVEC
SE_46480chr3:10232852-10239588Osteoblasts
SE_46480chr3:10239746-10241594Osteoblasts
SE_55870chr3:10232869-10239613u87
SE_55870chr3:10239757-10241715u87
SE_58615chr3:10208482-10269048Ly1
SE_62498chr3:10211834-10316085Tonsil
SE_64685chr3:10239754-10241685NHEK
SE_67695chr3:10232869-10239613u87
SE_67695chr3:10239757-10241715u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr31023972210241621
chr31023993710241585
chr31024043710240684
chr31024069110241307
Number: 1             
IDChromosomeStartEnd
GH03I010188chr31023045810242599
Enhancer Sequence
AGACCAGCCT GGCCAACATG GTGAAACCCC ATCTCTACTA AAAATACAGA AAAAAAAAAT 60
TAGCTGGATG TGGTGTTGCA AACCTGTAAT CCCAGCTACT CAGGAGGCTG AGGCAGGAGA 120
ATCGCTTGAA TCCAGGAGGC AGAGGTTGCA GTGAGCCGAG ATTCCTCCAC TGTACTCTAG 180
CCTGGGCAAC AGAGTAAGAC TCTGTCTCAA AAAAAAAAAA AAGAAAAAGA AAAAGAAAAC 240
TAAAAGACTC TCATCCTACT CTTCTTATCC TCAATATGTG GACTATTTAA GAGATAACCA 300
ATATTTTAAG ACTATAACCA CCACAGAAAT AAAGGTCCCA TATTTTGAGC TAAGCAGTGT 360
CTCCATTAGT CTTCATAAAA GTTGTCCAAA GGAGGGCCGG GCATGGTGGC TCACACCTGT 420
AATCCCAGCA CTTTGGGAGG CTGAAGAGGG CGGATCATGA GGTCAGGAGA TCGAGACCAT 480
CCTGGCTAAC ACGCTGAAAC CCTGTCTCTA CTAAAAATAC AAAAAATTAG CCGGGTGTGG 540
TGGTGGGCGC CTATAGTCCC AGCTACTCGG GAGGCTGAGG CAGAAGAATG GCGTGAACCT 600
GGGAGGCGGA GCTTGTAGTG AGCCGAGATT GTGCCACTGC ACTCTAGCCT GGGCGACAGA 660
GTGAGACTCC GTCTCAAAAA AAAAAAAAAA TTATTTAAAA TATCAGTGAC AGTAAAGAAA 720
ACACAAGGAA GAAGCCACTC AGGCCGGGCG CAGTGGCTCA CGCCTGTAAT CCCAGCACTT 780
TGGGAGGCTG AGGAGGGCGG ATCATGACGT CAGGAGATCG AGACCATCCT GGCTAACACA 840
GTGAAACCCT GTCTCTACTA AAAATAGAAA AAATTAGCCG GGCGTGCTGG TGGGCGCCTG 900
TAGTCCCAGC TACACGGGAG GCTGAGGCAG GAGAATGGCG TGAGCCCGAG AATCGGAGCT 960
TGCAGTGAGC CAAGATCACA CCACTGCACT CCAGCCTGGG CGACAGAGCG AGACTCCGTC 1020
TCAAAAAACA AAACAAAACA AAACAAAACG AAAATTTATT TAAAATGTCA GTGACAGTAA 1080
AGAAAACACA AGGACGAAGC CACTCATCAC CCCCCGACAT TCAGCCTTGT TGTTATTTTT 1140
GTGCATTCCC GATGTCTCCC CAACTCCTCC CACCCTGGGG AAGTCAGTGA TCACCCCTTT 1200
GTTCCTGTTT GTCTGGGGAT TGGGGCGTCT GCCCCTGGGG GAATTGGGGC TGGTGGTGGC 1260
AGTGATGGCA GTGGTGTTTC AATAGTTCTG CCCTAGCTGG GTGGGAGACA GTGAAACCAG 1320
TCCCAGGTTT GACTGTTGTT GGCTGTTTTA CTTGACACAA GTCATTTCAC TTATCTGAGC 1380
CTCAATATAC TCAAAAATAA AATGCAGATA AACCTATGAA CTACCAGAGA TTGTTGTGAA 1440
AATTAAATAA ATATGCACGG TGCCATACCA GTGTGGTGCT ATGCAAATTT AGGTCCTATT 1500
ATTTTAGTTC AAAAGCTTGG GTTTGAAAAG TGAGGTCCCA GGGTAACAAT TGGTTTTGTT 1560
TAGAGAGGCA CAGTTGACCA GTTCAAAGAA ATGTTGCTGG AGATGTTTTG TCCCAGCCCT 1620
ACCTGGGACA TCTGTTGTGA CATCCCCTGT GTCATGCTTT ATGTCATGCT CTGTGTGACA 1680
TCAAGCGAGT CAGCAGCCCT TCCTGGGACT TCAGTGCCCC AGTTTTTGTC ATTCTCAAAC 1740
ATGAGTCTAT CCCAAACCAC CAGAGAATGA GGGACTTGAA TGCAGGGCTA TAGCATCAGG 1800
TTTTATCTGG GAGGCAATGG GGAGACAGAA AGATTCAGGC TAAGGAGTGT GGACATTATC 1860
TAGGCAATGG GGAGCCCCAT AAAGGCTTCA AGCAGGGAAG TGACGAGGCC AGATGTATAC 1920
TTTGGTAAGA AGTAGCCTGG CAAGGGTGTG GAGGCTGCCT GAGCTGGCGG CAGGGCCCAG 1980
CCAGAAGGGA TAAGATCAGG GCCCAGTGGA GGAGGGGAGA GGAAGCTGTT TCACAGAGCA 2040
GCTCTGAGAA GCTGGCTGGA AGCTGAGGTT GACACACCCT CGAAGCACCT TTGGGGTTTC 2100
CCAAGTTGAT GTAAAAAGGA AATGATTACC CTCGAGAAGG CAGGGGAGTT CTTCGGCCAG 2160
TCCTGCGTGC CTTTGGCATG TGATCTTAGC AAGTCATTTA ACCTGCTCAG GCCTCAGTTT 2220
CCTCATCTCT GAACAGGGAT GAGAAGCAGA GATGTTGTGA GGATTCATGT CTGTGCAGCT 2280
GGGCCTGGGC CTGGTACAGC CCGTCCTCAG TGGCCATGGC TGCTGTTTTA GGATTCTCAT 2340
CCATCAAGTG GGAAGGATGC GTTTGTCTCC ACTGCGTGAA AGGGAGGTTG TAGGACAGCC 2400
AGAACTTTGA TCCCTAGGGG CTGGAGTGGG AGCTTAGAGG GATGGTGTCT TTGACCCGCT 2460
CACGTGTTCA GGGAAATGTG CAGTCTACAG CGCCCATTCC CATCTCTACT CTCCTTTCCC 2520
ACATGACACC CCAGCGGGAG GCAAACGGAC GCCATTATCA CCTCCGTTTT ATAGGTGAGG 2580
GAAGGGAGAC CGAGAGGAGG AAGGTGACTT GTTGGAGGTC ACACAGCTGG TTGGGTGGAA 2640
GCAGGTGTAT GTGACTTAGC ACGTCAGAGC TCCACCTTCA CCAGGACTGC CATGTTCAGC 2700
CACTGCTCTT TTTTTTTTTT TTTTTTTTTG AGACAGAGTC TTGCTCTGTC GCTCAGGCTG 2760
GAGTGTAGTG GTGCGATCTT GGCTCACTGC AAGCTCCGCC TCCCCGGTTC AAGTGATTCT 2820
CCTGCCTCAG CCTCCCAAGT AGCTGAGACT ACAGCCGTGT GCCACCATGC CCAACTAATT 2880
TTTGTATTTT TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CGAACTCCTG 2940
ACCTCAGGCA GTCCACCCAC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC 3000
CGCGCCTGGT CTACCGCATT TTACAGATGG GGAGGCCGGG 3040