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

TagContent
EnhancerAtlas ID
HS073-14277 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr9:33135420-33139500 
Target genes
Number: 5             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
ESR2MA0258.2chr9:33137832-33137847AGGTCAGCCAGGCCT+6.25
RREB1MA0073.1chr9:33138936-33138956CCCCAACACACACACTAACG+6.46
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
ZfxMA0146.2chr9:33137840-33137854CAGGCCTGGGCTGC-6.2
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00330chr9:33134396-33136684Adipose_Nuclei
SE_00330chr9:33138866-33141700Adipose_Nuclei
SE_00992chr9:33134966-33138299Adrenal_Gland
SE_00992chr9:33138818-33140399Adrenal_Gland
SE_09459chr9:33134458-33139068CD14
SE_10229chr9:33134720-33146706CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33136393-33139356CD3
SE_14891chr9:33136466-33138896CD4_Memory_Primary_7pool
SE_18665chr9:33135758-33139718CD4p_CD25-_Il17-_PMAstim_Th
SE_19329chr9:33136605-33138149CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33134255-33146063CD56
SE_22416chr9:33135220-33146719CD8_primiary
SE_26859chr9:33135768-33137338Esophagus
SE_27770chr9:33133434-33136209Fetal_Intestine
SE_28724chr9:33133427-33136185Fetal_Intestine_Large
SE_29800chr9:33134401-33137058Fetal_Muscle
SE_31534chr9:33135301-33136542Gastric
SE_32659chr9:33135226-33145795GM12878
SE_40894chr9:33134620-33138311Left_Ventricle
SE_40894chr9:33138811-33142004Left_Ventricle
SE_42236chr9:33134930-33137913Lung
SE_42236chr9:33137933-33140413Lung
SE_45731chr9:33138938-33141879Osteoblasts
SE_46917chr9:33134890-33136451Ovary
SE_46917chr9:33138775-33140378Ovary
SE_48426chr9:33138706-33140393Psoas_Muscle
SE_48738chr9:33136686-33140472Right_Atrium
SE_50176chr9:33134918-33140478Sigmoid_Colon
SE_51651chr9:33134813-33136290Skeletal_Muscle
SE_51651chr9:33138989-33141643Skeletal_Muscle
SE_53402chr9:33134893-33138878Spleen
SE_53402chr9:33139080-33142103Spleen
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 6             
ChromosomeStartEnd
chr93313571233136351
chr93313653133137040
chr93313704133137549
chr93313760833138604
chr93313867833138863
chr93313893033139314
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
CACTAGAGAG GTGGAGGGAG GGAGAAGTTA GCAGGCCACA GGACTCGCCA CCGCTCCACA 60
GGCTGCATCA GATGGCCAGG CTGCAGCTGC AGCTGCAGAG GAAATGTCTC CTCCTGGGAG 120
GCAACGTGGC CACGGAGAGG GCCCTCCTGC CCAGCATCAG GCACCACATC CAGCATTAGG 180
GTGACCAACC ATCCCCAGAA ACCCCCTTCA GTGTGGGGCA AACCTAGATG GTTGGTCACT 240
CTGTGAAGCA CTCGCCTGCC CAGGACCCTC CCCGCTCTGA CTCCACTGTA AAATGGAAGT 300
AATTTCTACC CAGACTTCCT GACAGGCTGT TGTAGAAATC AGTGATCACG GATGAGAAGG 360
CAATTTCTCA AAACCCCTGA GGTTGAGACT TAGCTCTGTG ACCTCCCAGC TGCGTGGCCT 420
TGGACAAATG GCTGACATCA TCTCTCTGAT TCTAGCCTAA CTGGGGAAGT GTGTGTGTGT 480
GTGTGTGTAT GTGTGTGTGT GTGTGTGTGT GTGTATGCAT GCATGTTGGG GACGTCAGTG 540
TGGAGGGAGT TAGCTTCGAA GTGGAAGGTA GCAGGAGTGG CATGAGTGCC CATGTCCCAG 600
GAAGGGACTC GATGGAAGGT GAACCAAGGT CTGGGAGAGA TGGAGGCAAA GAAACCCCAA 660
AGGAGACCGA GGGAAAATAA AAGAAATAGC TGGAAACACA GAAGAATGTT TAGTAACAGA 720
GGGGATAAAG TAACAAAGAG GAAGAAGAAG TAACAAAGAG GGAGGGATGA CTCCCAAGTT 780
TCTGGCCTAG AAGAACATGG ATGCAGATGA GATAAGTAAG TTAGTAAGAG AGTGCTTGCC 840
TCAGAAGAAA AATGGATGAG GTGCAGATTG TGGATTGTGA GGTAACGGCA GGTGGGAAGA 900
GGGATGAGGA AAACGTCACA TACCGGGTAT GTGGTACACG TGGTGCAGTC CAGGCAACAC 960
AGGGAATCAA GGCTCTGCTG AGAGTCAAGA GCCAAGGCTT GAACCCAGGC TCCCCATACT 1020
CTCTGCAGAC CAGACCGCCT CAAAATGGGT TCCAGAAAAC ATCAGACCCA GCAAGATGCT 1080
TAATGGAAAA ACATGTCTCG TGGTCAAATA AGAACGGGAA TGCTGCGTAT TAAATCCTGC 1140
TTCTGCAAAG TCACGACACA CACCAAAGGC TCTGAGAAGT TGTGCAGTCG AAAAACCCCC 1200
TTCGTTATAT TTAACCCACC ATTTCCCAAG CTTATTTGGC TACAGAACCA TTTTTCCAGG 1260
GAACACACTT TGGGAACTGT TACTCTAGTG TAACCAGCTT CACCTGTGAA GCAAATGAGC 1320
CACAAGAACA AAGGAAGGAA CCTAGAGAAC AGGTAGGAAC ACCAACCACA AGCACAGATC 1380
AAAACCTGAA ACATGCTGGT GAGAACCCGC CCAGGGCCAG TGAGCAGGCT TCAGCCTGCC 1440
CTGTTTATCA ATAACGCGTG GCTCTCCAAG CACCCCCTAC TCCCGGAATC ACTCGCCCTT 1500
CTGAATTCAA CAGCTTGAGA AAAAAAGCTG TGGGCCTGCT TCCTCTCACC AGATAGCTGC 1560
CACTTCCACC CCCTTCCCCA GTACACATCT CACATCTTCC CTCCCTCCGT AGCTGACCCA 1620
GGTCCACCAT CACAGGACCT GTTCCCATTA GTTTGTTTTC TTCTGAGATA CAGCCCCGAC 1680
CATATTACTT TCCCACTAAA ACCTCCAGTG GCTCTAAGGC TGTGTGTCCC TGCACAAGGG 1740
AAGGCCAAGG CCCACAGCTG AGCAAAAGGC CCTTCACCCT CAGCTCTGTC TGTCTCCCTC 1800
CCCATCCCTT AAGCCATGCC TGTCCACACT TTTCTCTTTG CCAGAAATGC CCTTCCCACT 1860
CTCCTCTTAA CTAGCAAACT TTCGCATTGA GAGATAGGCC TCAATCAAGC TTGATCCTTT 1920
TACTCTCTGC GCTATCACAG AGCTCAGGCA GCAGACCCTC TGGGGCAGGG AAGAAGATCC 1980
TCAGGCCTCC CTCTCTGGTC ATGCACCTCC CTCCTGGAGG GACAGAGGCC TTGAAGCTCA 2040
GTCCCTTATA AGACTGCCTG CTGAGCCAGC TCCCACCTCC CAGGGTGCCC TAAAGTGAGC 2100
AGGCACTGTG CTCTTCAGAG AAGACCAGGA CTCAGTCAGT GGTCACCCTG GACAAGTTTT 2160
TCCCAAACCT ATCACAAGAA TTGCTTGAGG AAGTTAGTAC AAGTACAGCA TCTCGGGCCC 2220
TTCCCTTAGA GAGTCTGTGG ATTTTGGGAA GGACCTAAAT GGCTACCTAA CAAGGAGCCC 2280
AGATGATTCT CACTGGGCAA GCTGGGTAGT AGGGCTCCGA TGGACCATCT GATGGGCATC 2340
TGATGTCAAG GCTTAGGGCT TTCGGGCAAA GAGGGCCCTC GGGGATTCCC ACCATTCACA 2400
CCCTTCCCCA CAAGGTCAGC CAGGCCTGGG CTGCCCAACA CCCAACCCTG GGCAAAGGCT 2460
ACTGGGGGGG CCCTGCTGCA CAGTGAACTT GTGAAAAACA TGAAGAAAAG ATCTGTCACA 2520
GGGCTCTTTT CACTTCAGAG GGCCCCCACA ACATCTGCAG CCCCCACCCC ACCTTTGGTT 2580
CTGAGGATGC TGCTAAACAT AACCGCGTTT TGGGGAACCC AAGAAGCACC TGGGCTGTCA 2640
CCCTGCCGAC TTGCTCGTAC CTTCTGAAAC CCACCCAGAA AACAGGAATT CACATGTGGC 2700
CTGGCTCGCT TCCGCGGGAC AGACACCTGC AGGCTGGAAA GTGTCCTGGT GTTGCCCCAT 2760
CATGGGTTTC AGAAAGGTGG TCCTGAAGTC AAGAGCCCCG GACAGGAGAA GAGATGCCTG 2820
GGCCCCGGTC CAGCTCCACC AGTGACTTTC CAGATGATCT TTGGTATCCT GAGAGTGGAT 2880
AGTACAGCCA CTCTCAGGGT ACTGGTTTCC TCATTTGTAA ACTGCAGGGA CAGGACTGGA 2940
TGCTCTCTAA GGTCTCAGAA CGCCCTGACG TGTCCAGTGA CACTTGGTAA ACCAGGAGGA 3000
GTGCAGGGAT CCAAAGCAAG ATCTTTAGAC AAATCCTTGC TCCCACCTTC CCTGCCCTCA 3060
GCATGAATTT CCAAGCAGAC AGGAGACGTG AGTGTCCAGC ATAGGAGAGG TGGAAAGAAG 3120
CCTTGATCAC CAAGCGTCAC ATTTACCTAC GTCTCCTCTT ACCTCAAATT CCTAGGCTTT 3180
CTCAGCTTCT TTCTTGGATG TCCATCTTTG CCCCCTTCTC TTCTCACTCT CCCTATACCC 3240
AGGTCTTTGG TTTAAGCACA TGACAGTTCC CAAACCTCTG TTTCCATCTC ATGTCTCTCT 3300
CCTGACCTCA CAGCCAACAG AACATGGCTA GCCATATGTC ATGGGCACCT CAAATTCAAC 3360
CTGCCCCAAA TGGATTCTCA TGCAACCCCA CCACCATCAC CACCTACAGC CAGACCTGCT 3420
TCTCAGGATT CCCTCAGCAA CTGACACCAC CATCTCCCCA GGGCAGAAGC TGATACCCGG 3480
GTGGTCCATC TTCTATTCCC CCTCCTCTCT CCCCAACCCC AACACACACA CTAACGCTCT 3540
CTCACCCTCA CATACACACA CACACACGCC CACTCGCTCC CATGCCGGGG CTGTCCACAG 3600
CATGCTGACA ACCCACAGAA GCCGATCGAG CACCAAGCCA GAGAGTCTTT ACTCTGAAAT 3660
GTCTGTTAAC TGCAAACTTG CCCTGTGATA TGTATCAAGA CCACTTTCAA TTTGTTTCAA 3720
TTGATACTTT CTGGGTACCT ACTGTGTGCC AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA 3780
GGGAGGATGG ACAAGACAAA TCCTGCCTTC CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA 3840
CCTAAATGAA AATTACCCTG GTTTAAGGAT GGTCAAGGAG CTTGCTCCTC CAATGGCTCT 3900
GTGCAGAGCT TTATCACTGA ACAGCCTCTT CTCACTCTCC TGCTCCCTTC TGAACTCGCT 3960
GTGCCCCTTG CACAACCCCC ATCATGCTTC CAACACACTG AGACACCTTG ACCCCCAATC 4020
CTGCCCTTCT TGCCAATCTG GCAATTTTTT CTCCACAACT CTAAGGATCT TGCAGCTCAC 4080