EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS092-37936 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr9:33138660-33141630 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3780486chr933139453hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BCL6BMA0731.1chr9:33139223-33139240TGCCTTCCAGGAGTTCC+6.02
NFYBMA0502.1chr9:33140242-33140257CTGATTGGCCAGTGG-6
RARA(var.2)MA0730.1chr9:33141277-33141294AGGTCACCTTGAGGTCA+7.71
RREB1MA0073.1chr9:33138936-33138956CCCCAACACACACACTAACG+6.46
ZNF263MA0528.1chr9:33139345-33139366CTCTTCTCACTCTCCTGCTCC-6.41
Number of super-enhancer constituents: 46             
IDCoordinateTissue/cell
SE_00330chr9:33138866-33141700Adipose_Nuclei
SE_00992chr9:33138818-33140399Adrenal_Gland
SE_00992chr9:33140510-33141415Adrenal_Gland
SE_09459chr9:33134458-33139068CD14
SE_10229chr9:33134720-33146706CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_12090chr9:33136393-33139356CD3
SE_12090chr9:33140249-33142158CD3
SE_14891chr9:33140511-33142287CD4_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_19329chr9:33140372-33141391CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33134255-33146063CD56
SE_22416chr9:33135220-33146719CD8_primiary
SE_26031chr9:33139672-33141321Duodenum_Smooth_Muscle
SE_26859chr9:33139260-33140484Esophagus
SE_26859chr9:33140490-33141363Esophagus
SE_27770chr9:33139911-33141110Fetal_Intestine
SE_29800chr9:33139312-33141840Fetal_Muscle
SE_31534chr9:33139337-33140430Gastric
SE_31534chr9:33140552-33141138Gastric
SE_32659chr9:33135226-33145795GM12878
SE_40894chr9:33138811-33142004Left_Ventricle
SE_41831chr9:33139282-33140314LNCaP
SE_42236chr9:33137933-33140413Lung
SE_42236chr9:33140421-33142021Lung
SE_44340chr9:33139198-33141245NHDF-Ad
SE_45447chr9:33139306-33141157NHLF
SE_45731chr9:33138938-33141879Osteoblasts
SE_46917chr9:33138775-33140378Ovary
SE_46917chr9:33140576-33141301Ovary
SE_47814chr9:33139478-33140178Pancreas
SE_48426chr9:33138706-33140393Psoas_Muscle
SE_48426chr9:33140480-33141409Psoas_Muscle
SE_48738chr9:33136686-33140472Right_Atrium
SE_48738chr9:33140483-33141323Right_Atrium
SE_50176chr9:33134918-33140478Sigmoid_Colon
SE_50176chr9:33140489-33142097Sigmoid_Colon
SE_51651chr9:33138989-33141643Skeletal_Muscle
SE_52621chr9:33139293-33140398Small_Intestine
SE_52621chr9:33140511-33141315Small_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: 4             
ChromosomeStartEnd
chr93313867833138863
chr93313893033139314
chr93313932133140496
chr93314069633141208
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
AGGTCTTTGG TTTAAGCACA TGACAGTTCC CAAACCTCTG TTTCCATCTC ATGTCTCTCT 60
CCTGACCTCA CAGCCAACAG AACATGGCTA GCCATATGTC ATGGGCACCT CAAATTCAAC 120
CTGCCCCAAA TGGATTCTCA TGCAACCCCA CCACCATCAC CACCTACAGC CAGACCTGCT 180
TCTCAGGATT CCCTCAGCAA CTGACACCAC CATCTCCCCA GGGCAGAAGC TGATACCCGG 240
GTGGTCCATC TTCTATTCCC CCTCCTCTCT CCCCAACCCC AACACACACA CTAACGCTCT 300
CTCACCCTCA CATACACACA CACACACGCC CACTCGCTCC CATGCCGGGG CTGTCCACAG 360
CATGCTGACA ACCCACAGAA GCCGATCGAG CACCAAGCCA GAGAGTCTTT ACTCTGAAAT 420
GTCTGTTAAC TGCAAACTTG CCCTGTGATA TGTATCAAGA CCACTTTCAA TTTGTTTCAA 480
TTGATACTTT CTGGGTACCT ACTGTGTGCC AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA 540
GGGAGGATGG ACAAGACAAA TCCTGCCTTC CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA 600
CCTAAATGAA AATTACCCTG GTTTAAGGAT GGTCAAGGAG CTTGCTCCTC CAATGGCTCT 660
GTGCAGAGCT TTATCACTGA ACAGCCTCTT CTCACTCTCC TGCTCCCTTC TGAACTCGCT 720
GTGCCCCTTG CACAACCCCC ATCATGCTTC CAACACACTG AGACACCTTG ACCCCCAATC 780
CTGCCCTTCT TGCCAATCTG GCAATTTTTT CTCCACAACT CTAAGGATCT TGCAGCTCAC 840
ACCTTTGAGA CAACAGACAG CAGCCCCAGA CCTGGCGTTG AATGACTAAT TGGGTCGAGT 900
GCCAGCCAGG AGGCCTCCTG AATGCCCTGC ACACCTCCTG CCATACTGCA GGGACCATGC 960
TCTGCTACAC ACCTGGCTCT GTCCCAGTGA GAAACTCCAG AGAGCTCAGA CTCCAGGAAG 1020
GCAACGACTA CCTCTGTTCA GAATCATGCA GACCTGCGAC CAGGTTTCAG AGCCACTGCC 1080
TGGGGTGGTG GGGAGAAGCT CTGGGAGGAG GCAGAGGGCT GAGGGCTTCA TGACAGGCCT 1140
CAAGCCGAGC CAAGGCGCCC TTGCTGTGCG GCGCATGGCG TGTGCTACCA CAGGCTCTCG 1200
GCCCCGCTGG GCTGGCTTGT GTGTTTTCTT GGCTCTGGAA GCTGGGAGGC AGGGTTACGT 1260
AAGCAGATGA GCAGATGTAA GCTGTCCTCG GCTCCCCCAG CTCAAGCCCC GCCACGTGGG 1320
CCTCTCGGCT GGGAGTCCAG GTCATGGCCT TGCATGTAAG TCGCTCAATA ACTTCAATGT 1380
GTGAGCTCAA TTCAGACAAA TTCCACTGCT CCCCTGCCTG GCACAGCAAA CCCAAACACA 1440
TACATGCCCC TCCATCAAAG GCCCTGCTAA TCTAAGCCAA CACCAGCACG GACTCCTGAC 1500
TGGTTTTCAT GCTGGCTGAA GCACTAGTTC AATCCTTTAG CCTCAGCAAA ATAGGCTGAA 1560
ACATCTAGTC ACTGTTTGTC AACTGATTGG CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT 1620
GCTTTATTGT GACAATGTTT CACTAGCCCA GGAATGAAAT CACAGAAGTA AAGACCATGT 1680
AGGTGTTTTT TAATTAAACT AAAGGTAATC AAAGTATAGG AATGCCCTTT CTTCCAAGAT 1740
TAAGTGCTTC TTACTCTTTG AATATTAAAA TGTCCTTTCT CTTATGAAAT CATCATAGAT 1800
TTTCATGCTG GACTGATTTT TAAAATTTAA TTTAAAAAAA AAATCCTTCC TTGGCAGCCA 1860
TGGGTCAGGC CTCTAAGTTT GTTTTGAAAA TTCTCTGGAC AGGAAATCCA AGTATTCAGG 1920
AAACATTTGG GAACACGTGG AACTAGGCAG TGCCTAGAAC TCTGTGATTC TGAGAGCTGG 1980
GATACTGGAA TTTCTTCCTG GGTCTCAGAC CTGACAGTAC ACTGCACAGC CCCTCTTCAC 2040
AAATCAGCTC CCCCACCAGT GCTGTTCCAC AGGCTCATGT GGATGGGCCG CTTCTCTCTG 2100
TACCAATCTT CCAAAGGCCA GGTGCGCACC GCAAGCTGAG CCAGGCATTA CCACCAAATT 2160
CCCCAGCTTG AGAAAAGATT TGCTTGCAGC ATTCTCGTGA AATCACGGTG CCCCTTGAGG 2220
CCCCTTGGGC TAGAAATGAG AAGCACCATT TACTGTACGT GGCTCACCCG TCATTCTGGG 2280
AAGAGCACAA GCTCTCTAAG TCTGCAAGGG CTTCAGTCTA ACAAATCTAA CAGCTGCCTG 2340
GCCTTAGCTC AAACACCACC CTCCCAGGAA GCCTTCCCAG ACCACTCAAG GTTGGTTCTT 2400
AAGCATTTCA CCCACTTCCC CTAAGCATTC ACAGCACCAC ATCCATTCAT ATTCAAACAT 2460
GTACCCAGTT AGTATGTATC ATGTGCCAGG TGGTATAGGG CATGCAGGGG TTGGTAGGGG 2520
AGTGGGCGGC AGGGTGAGCA AGTAAAGAAG AGGTCTTTGA GGCTGGGCAT GGTGGCTCAT 2580
GTCTGTAATC CCAGCACTTT GGGAGGCTGA GACAGGCAGG TCACCTTGAG GTCAGGGGCT 2640
TGAGACCAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC TAAACCCCAT CTCTATTAAA 2700
AATACAAAAA TTAACCGGGT GTGGTGTAGC TGTAATCCCA GCTACTTAGG AGGCTGAGGC 2760
AGGAGAATCT CTTGAACCTG GGAGGTGAAG GTTGCAGTGA GCCGAAATCA CGCCATTGCA 2820
CTCCAGCCTG GGCGACAGAG CAAGACTCTG TCTCAACAAC AACAACAAAA GGTCTTTACC 2880
CCCAGTAGTC AAGGAGACCA GCAAAGCCAA CAGTACTGCT AAGTGTGACA GGTAACAAAC 2940
AATAAGCTAA AACTAGCACA GAAGGGGAAT 2970