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

TagContent
EnhancerAtlas ID
HS050-68413 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:33138800-33141930 
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: 45             
IDCoordinateTissue/cell
SE_00330chr9:33138866-33141700Adipose_Nuclei
SE_00992chr9:33138818-33140399Adrenal_Gland
SE_00992chr9:33140510-33141415Adrenal_Gland
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: 3             
ChromosomeStartEnd
chr93313893033139314
chr93313932133140496
chr93314069633141208
Number: 1             
IDChromosomeStartEnd
GH09I033133chr93313369733146567
Enhancer Sequence
TGCAACCCCA CCACCATCAC CACCTACAGC CAGACCTGCT TCTCAGGATT CCCTCAGCAA 60
CTGACACCAC CATCTCCCCA GGGCAGAAGC TGATACCCGG GTGGTCCATC TTCTATTCCC 120
CCTCCTCTCT CCCCAACCCC AACACACACA CTAACGCTCT CTCACCCTCA CATACACACA 180
CACACACGCC CACTCGCTCC CATGCCGGGG CTGTCCACAG CATGCTGACA ACCCACAGAA 240
GCCGATCGAG CACCAAGCCA GAGAGTCTTT ACTCTGAAAT GTCTGTTAAC TGCAAACTTG 300
CCCTGTGATA TGTATCAAGA CCACTTTCAA TTTGTTTCAA TTGATACTTT CTGGGTACCT 360
ACTGTGTGCC AGCCCAAGGA GGAGTGGGTT GAGGTAGGGA GGGAGGATGG ACAAGACAAA 420
TCCTGCCTTC CAGGAGTTCC CTGCTGAGCG TGTGGCAGAA CCTAAATGAA AATTACCCTG 480
GTTTAAGGAT GGTCAAGGAG CTTGCTCCTC CAATGGCTCT GTGCAGAGCT TTATCACTGA 540
ACAGCCTCTT CTCACTCTCC TGCTCCCTTC TGAACTCGCT GTGCCCCTTG CACAACCCCC 600
ATCATGCTTC CAACACACTG AGACACCTTG ACCCCCAATC CTGCCCTTCT TGCCAATCTG 660
GCAATTTTTT CTCCACAACT CTAAGGATCT TGCAGCTCAC ACCTTTGAGA CAACAGACAG 720
CAGCCCCAGA CCTGGCGTTG AATGACTAAT TGGGTCGAGT GCCAGCCAGG AGGCCTCCTG 780
AATGCCCTGC ACACCTCCTG CCATACTGCA GGGACCATGC TCTGCTACAC ACCTGGCTCT 840
GTCCCAGTGA GAAACTCCAG AGAGCTCAGA CTCCAGGAAG GCAACGACTA CCTCTGTTCA 900
GAATCATGCA GACCTGCGAC CAGGTTTCAG AGCCACTGCC TGGGGTGGTG GGGAGAAGCT 960
CTGGGAGGAG GCAGAGGGCT GAGGGCTTCA TGACAGGCCT CAAGCCGAGC CAAGGCGCCC 1020
TTGCTGTGCG GCGCATGGCG TGTGCTACCA CAGGCTCTCG GCCCCGCTGG GCTGGCTTGT 1080
GTGTTTTCTT GGCTCTGGAA GCTGGGAGGC AGGGTTACGT AAGCAGATGA GCAGATGTAA 1140
GCTGTCCTCG GCTCCCCCAG CTCAAGCCCC GCCACGTGGG CCTCTCGGCT GGGAGTCCAG 1200
GTCATGGCCT TGCATGTAAG TCGCTCAATA ACTTCAATGT GTGAGCTCAA TTCAGACAAA 1260
TTCCACTGCT CCCCTGCCTG GCACAGCAAA CCCAAACACA TACATGCCCC TCCATCAAAG 1320
GCCCTGCTAA TCTAAGCCAA CACCAGCACG GACTCCTGAC TGGTTTTCAT GCTGGCTGAA 1380
GCACTAGTTC AATCCTTTAG CCTCAGCAAA ATAGGCTGAA ACATCTAGTC ACTGTTTGTC 1440
AACTGATTGG CCAGTGGGTC GAAAGAAGCG TTGGCCTGAT GCTTTATTGT GACAATGTTT 1500
CACTAGCCCA GGAATGAAAT CACAGAAGTA AAGACCATGT AGGTGTTTTT TAATTAAACT 1560
AAAGGTAATC AAAGTATAGG AATGCCCTTT CTTCCAAGAT TAAGTGCTTC TTACTCTTTG 1620
AATATTAAAA TGTCCTTTCT CTTATGAAAT CATCATAGAT TTTCATGCTG GACTGATTTT 1680
TAAAATTTAA TTTAAAAAAA AAATCCTTCC TTGGCAGCCA TGGGTCAGGC CTCTAAGTTT 1740
GTTTTGAAAA TTCTCTGGAC AGGAAATCCA AGTATTCAGG AAACATTTGG GAACACGTGG 1800
AACTAGGCAG TGCCTAGAAC TCTGTGATTC TGAGAGCTGG GATACTGGAA TTTCTTCCTG 1860
GGTCTCAGAC CTGACAGTAC ACTGCACAGC CCCTCTTCAC AAATCAGCTC CCCCACCAGT 1920
GCTGTTCCAC AGGCTCATGT GGATGGGCCG CTTCTCTCTG TACCAATCTT CCAAAGGCCA 1980
GGTGCGCACC GCAAGCTGAG CCAGGCATTA CCACCAAATT CCCCAGCTTG AGAAAAGATT 2040
TGCTTGCAGC ATTCTCGTGA AATCACGGTG CCCCTTGAGG CCCCTTGGGC TAGAAATGAG 2100
AAGCACCATT TACTGTACGT GGCTCACCCG TCATTCTGGG AAGAGCACAA GCTCTCTAAG 2160
TCTGCAAGGG CTTCAGTCTA ACAAATCTAA CAGCTGCCTG GCCTTAGCTC AAACACCACC 2220
CTCCCAGGAA GCCTTCCCAG ACCACTCAAG GTTGGTTCTT AAGCATTTCA CCCACTTCCC 2280
CTAAGCATTC ACAGCACCAC ATCCATTCAT ATTCAAACAT GTACCCAGTT AGTATGTATC 2340
ATGTGCCAGG TGGTATAGGG CATGCAGGGG TTGGTAGGGG AGTGGGCGGC AGGGTGAGCA 2400
AGTAAAGAAG AGGTCTTTGA GGCTGGGCAT GGTGGCTCAT GTCTGTAATC CCAGCACTTT 2460
GGGAGGCTGA GACAGGCAGG TCACCTTGAG GTCAGGGGCT TGAGACCAGC CTGGCCAACA 2520
TGGTGAAACC CCATCTCTAC TAAACCCCAT CTCTATTAAA AATACAAAAA TTAACCGGGT 2580
GTGGTGTAGC TGTAATCCCA GCTACTTAGG AGGCTGAGGC AGGAGAATCT CTTGAACCTG 2640
GGAGGTGAAG GTTGCAGTGA GCCGAAATCA CGCCATTGCA CTCCAGCCTG GGCGACAGAG 2700
CAAGACTCTG TCTCAACAAC AACAACAAAA GGTCTTTACC CCCAGTAGTC AAGGAGACCA 2760
GCAAAGCCAA CAGTACTGCT AAGTGTGACA GGTAACAAAC AATAAGCTAA AACTAGCACA 2820
GAAGGGGAAT CAACTAGGGG ACAGGAAGAG AGTCAAGGAA AGCTTTGCAA AGAAGCAGCT 2880
CCTCCATCAG GGCCCCTCAG TTCTCTTGGG AGGATTCATC ACAGAGTTGT GTCCACTTGG 2940
CTGCCATGCA CGTGGGAGTA CGCCAATAAA TCCTAGCTGT GTGGGTGGCG CGCAGCTATC 3000
CTCTCTGCTT CTCTGCCACC TGCACAAGTA ACAAAGGTTT CCATAAACCT ACAAGAAAAC 3060
CTGACAGAAG AGCAGGGGAT GGAGAGCCAC CAGAAGGGAC TCTCGATTCT CACGTGAAGC 3120
ATTTTGCACT 3130