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

TagContent
EnhancerAtlas ID
HS155-14033 
Organism
Homo sapiens 
Tissue/cell
Ovary 
Coordinate
chr9:33138630-33140320 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
NFYBMA0502.1chr9:33140242-33140257CTGATTGGCCAGTGG-6
RREB1MA0073.1chr9:33138936-33138956CCCCAACACACACACTAACG+6.46
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00330chr9:33138866-33141700Adipose_Nuclei
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_18081chr9:33140148-33141844CD4p_CD25-_CD45ROp_Memory
SE_18665chr9:33135758-33139718CD4p_CD25-_Il17-_PMAstim_Th
SE_18665chr9:33140056-33142210CD4p_CD25-_Il17-_PMAstim_Th
SE_20045chr9:33134255-33146063CD56
SE_22416chr9:33135220-33146719CD8_primiary
SE_26031chr9:33139672-33141321Duodenum_Smooth_Muscle
SE_26859chr9:33139260-33140484Esophagus
SE_27770chr9:33139911-33141110Fetal_Intestine
SE_29800chr9:33139312-33141840Fetal_Muscle
SE_31534chr9:33139337-33140430Gastric
SE_32659chr9:33135226-33145795GM12878
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_47814chr9:33139478-33140178Pancreas
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
CCCCCTTCTC TTCTCACTCT CCCTATACCC AGGTCTTTGG TTTAAGCACA TGACAGTTCC 60
CAAACCTCTG TTTCCATCTC ATGTCTCTCT CCTGACCTCA CAGCCAACAG AACATGGCTA 120
GCCATATGTC ATGGGCACCT CAAATTCAAC CTGCCCCAAA TGGATTCTCA TGCAACCCCA 180
CCACCATCAC CACCTACAGC CAGACCTGCT TCTCAGGATT CCCTCAGCAA CTGACACCAC 240
CATCTCCCCA GGGCAGAAGC TGATACCCGG GTGGTCCATC TTCTATTCCC CCTCCTCTCT 300
CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA CATACACACA CACACACGCC 360
CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA ACCCACAGAA GCCGATCGAG 420
CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC TGCAAACTTG CCCTGTGATA 480
TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT CTGGGTACCT ACTGTGTGCC 540
AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG ACAAGACAAA TCCTGCCTTC 600
CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA AATTACCCTG GTTTAAGGAT 660
GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT TTATCACTGA ACAGCCTCTT 720
CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG CACAACCCCC ATCATGCTTC 780
CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT TGCCAATCTG GCAATTTTTT 840
CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA CAACAGACAG CAGCCCCAGA 900
CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG AGGCCTCCTG AATGCCCTGC 960
ACACCTCCTG CCATACTGCA GGGACCATGC TCTGCTACAC ACCTGGCTCT GTCCCAGTGA 1020
GAAACTCCAG AGAGCTCAGA CTCCAGGAAG GCAACGACTA CCTCTGTTCA GAATCATGCA 1080
GACCTGCGAC CAGGTTTCAG AGCCACTGCC TGGGGTGGTG GGGAGAAGCT CTGGGAGGAG 1140
GCAGAGGGCT GAGGGCTTCA TGACAGGCCT CAAGCCGAGC CAAGGCGCCC TTGCTGTGCG 1200
GCGCATGGCG TGTGCTACCA CAGGCTCTCG GCCCCGCTGG GCTGGCTTGT GTGTTTTCTT 1260
GGCTCTGGAA GCTGGGAGGC AGGGTTACGT AAGCAGATGA GCAGATGTAA GCTGTCCTCG 1320
GCTCCCCCAG CTCAAGCCCC GCCACGTGGG CCTCTCGGCT GGGAGTCCAG GTCATGGCCT 1380
TGCATGTAAG TCGCTCAATA ACTTCAATGT GTGAGCTCAA TTCAGACAAA TTCCACTGCT 1440
CCCCTGCCTG GCACAGCAAA CCCAAACACA TACATGCCCC TCCATCAAAG GCCCTGCTAA 1500
TCTAAGCCAA CACCAGCACG GACTCCTGAC TGGTTTTCAT GCTGGCTGAA GCACTAGTTC 1560
AATCCTTTAG CCTCAGCAAA ATAGGCTGAA ACATCTAGTC ACTGTTTGTC AACTGATTGG 1620
CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT GCTTTATTGT GACAATGTTT CACTAGCCCA 1680
GGAATGAAAT 1690