EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS064-15627 
Organism
Homo sapiens 
Tissue/cell
GM18507 
Coordinate
chr9:33137850-33139620 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
RREB1MA0073.1chr9:33138936-33138956CCCCAACACACACACTAACG+6.46
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
Number of super-enhancer constituents: 34             
IDCoordinateTissue/cell
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_26859chr9:33139260-33140484Esophagus
SE_29800chr9:33139312-33141840Fetal_Muscle
SE_31534chr9:33139337-33140430Gastric
SE_32659chr9:33135226-33145795GM12878
SE_40894chr9:33134620-33138311Left_Ventricle
SE_40894chr9:33138811-33142004Left_Ventricle
SE_41831chr9:33139282-33140314LNCaP
SE_42236chr9:33137933-33140413Lung
SE_44340chr9:33139198-33141245NHDF-Ad
SE_45447chr9:33139306-33141157NHLF
SE_45731chr9:33138938-33141879Osteoblasts
SE_46917chr9:33138775-33140378Ovary
SE_48426chr9:33138706-33140393Psoas_Muscle
SE_48738chr9:33136686-33140472Right_Atrium
SE_50176chr9:33134918-33140478Sigmoid_Colon
SE_51651chr9:33138989-33141643Skeletal_Muscle
SE_52621chr9:33139293-33140398Small_Intestine
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: 2             
ChromosomeStartEnd
chr93313867833138863
chr93313893033139314
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
CTGCCCAACA CCCAACCCTG GGCAAAGGCT ACTGGGGGGG CCCTGCTGCA CAGTGAACTT 60
GTGAAAAACA TGAAGAAAAG ATCTGTCACA GGGCTCTTTT CACTTCAGAG GGCCCCCACA 120
ACATCTGCAG CCCCCACCCC ACCTTTGGTT CTGAGGATGC TGCTAAACAT AACCGCGTTT 180
TGGGGAACCC AAGAAGCACC TGGGCTGTCA CCCTGCCGAC TTGCTCGTAC CTTCTGAAAC 240
CCACCCAGAA AACAGGAATT CACATGTGGC CTGGCTCGCT TCCGCGGGAC AGACACCTGC 300
AGGCTGGAAA GTGTCCTGGT GTTGCCCCAT CATGGGTTTC AGAAAGGTGG TCCTGAAGTC 360
AAGAGCCCCG GACAGGAGAA GAGATGCCTG GGCCCCGGTC CAGCTCCACC AGTGACTTTC 420
CAGATGATCT TTGGTATCCT GAGAGTGGAT AGTACAGCCA CTCTCAGGGT ACTGGTTTCC 480
TCATTTGTAA ACTGCAGGGA CAGGACTGGA TGCTCTCTAA GGTCTCAGAA CGCCCTGACG 540
TGTCCAGTGA CACTTGGTAA ACCAGGAGGA GTGCAGGGAT CCAAAGCAAG ATCTTTAGAC 600
AAATCCTTGC TCCCACCTTC CCTGCCCTCA GCATGAATTT CCAAGCAGAC AGGAGACGTG 660
AGTGTCCAGC ATAGGAGAGG TGGAAAGAAG CCTTGATCAC CAAGCGTCAC ATTTACCTAC 720
GTCTCCTCTT ACCTCAAATT CCTAGGCTTT CTCAGCTTCT TTCTTGGATG TCCATCTTTG 780
CCCCCTTCTC TTCTCACTCT CCCTATACCC AGGTCTTTGG TTTAAGCACA TGACAGTTCC 840
CAAACCTCTG TTTCCATCTC ATGTCTCTCT CCTGACCTCA CAGCCAACAG AACATGGCTA 900
GCCATATGTC ATGGGCACCT CAAATTCAAC CTGCCCCAAA TGGATTCTCA TGCAACCCCA 960
CCACCATCAC CACCTACAGC CAGACCTGCT TCTCAGGATT CCCTCAGCAA CTGACACCAC 1020
CATCTCCCCA GGGCAGAAGC TGATACCCGG GTGGTCCATC TTCTATTCCC CCTCCTCTCT 1080
CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA CATACACACA CACACACGCC 1140
CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA ACCCACAGAA GCCGATCGAG 1200
CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC TGCAAACTTG CCCTGTGATA 1260
TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT CTGGGTACCT ACTGTGTGCC 1320
AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG ACAAGACAAA TCCTGCCTTC 1380
CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA AATTACCCTG GTTTAAGGAT 1440
GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT TTATCACTGA ACAGCCTCTT 1500
CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG CACAACCCCC ATCATGCTTC 1560
CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT TGCCAATCTG GCAATTTTTT 1620
CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA CAACAGACAG CAGCCCCAGA 1680
CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG AGGCCTCCTG AATGCCCTGC 1740
ACACCTCCTG CCATACTGCA GGGACCATGC 1770