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

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EnhancerAtlas ID
HS047-33875 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr9:33138850-33140310 
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: 34             
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_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_53402chr9:33139080-33142103Spleen
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: 1             
ChromosomeStartEnd
chr93313893033139314
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
CCCTCAGCAA CTGACACCAC CATCTCCCCA GGGCAGAAGC TGATACCCGG GTGGTCCATC 60
TTCTATTCCC CCTCCTCTCT CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA 120
CATACACACA CACACACGCC CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA 180
ACCCACAGAA GCCGATCGAG CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC 240
TGCAAACTTG CCCTGTGATA TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT 300
CTGGGTACCT ACTGTGTGCC AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG 360
ACAAGACAAA TCCTGCCTTC CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA 420
AATTACCCTG GTTTAAGGAT GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT 480
TTATCACTGA ACAGCCTCTT CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG 540
CACAACCCCC ATCATGCTTC CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT 600
TGCCAATCTG GCAATTTTTT CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA 660
CAACAGACAG CAGCCCCAGA CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG 720
AGGCCTCCTG AATGCCCTGC ACACCTCCTG CCATACTGCA GGGACCATGC TCTGCTACAC 780
ACCTGGCTCT GTCCCAGTGA GAAACTCCAG AGAGCTCAGA CTCCAGGAAG GCAACGACTA 840
CCTCTGTTCA GAATCATGCA GACCTGCGAC CAGGTTTCAG AGCCACTGCC TGGGGTGGTG 900
GGGAGAAGCT CTGGGAGGAG GCAGAGGGCT GAGGGCTTCA TGACAGGCCT CAAGCCGAGC 960
CAAGGCGCCC TTGCTGTGCG GCGCATGGCG TGTGCTACCA CAGGCTCTCG GCCCCGCTGG 1020
GCTGGCTTGT GTGTTTTCTT GGCTCTGGAA GCTGGGAGGC AGGGTTACGT AAGCAGATGA 1080
GCAGATGTAA GCTGTCCTCG GCTCCCCCAG CTCAAGCCCC GCCACGTGGG CCTCTCGGCT 1140
GGGAGTCCAG GTCATGGCCT TGCATGTAAG TCGCTCAATA ACTTCAATGT GTGAGCTCAA 1200
TTCAGACAAA TTCCACTGCT CCCCTGCCTG GCACAGCAAA CCCAAACACA TACATGCCCC 1260
TCCATCAAAG GCCCTGCTAA TCTAAGCCAA CACCAGCACG GACTCCTGAC TGGTTTTCAT 1320
GCTGGCTGAA GCACTAGTTC AATCCTTTAG CCTCAGCAAA ATAGGCTGAA ACATCTAGTC 1380
ACTGTTTGTC AACTGATTGG CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT GCTTTATTGT 1440
GACAATGTTT CACTAGCCCA 1460